SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs144815310 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145023791 | GATCAGGGTGGTGTC[A/G]CTGAAGGTTTGGGTG | 10393 |
rs144822528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145056582 | GGACCCCTTTCCTTG[C/T]AACATCTTTCTGGCG | 10393 |
rs144824864 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144984256 | AGTAGCTGATGGCTT[C/G]TTATCCTCCTTTTGC | 10393 |
rs144837276 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145057679 | TTGAAGAGATACCAG[A/G]TATCAGTGACCAAAA | 10393 |
rs144850085 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145019231 | TAAATTTAAGAAAAC[C/T]GAAATTATATCAAGG | 10393 |
rs144947146 | snp | A/C | 0.0209421 | 0.100162 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144993016 | TGCATAGAGGTTACA[A/C]CTTGGCTAAAGCTTC | 10393 |
rs144966959 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145080704 | CACAAGGTCAGGAGT[C/T]CCAGACCAGCCTGAC | 10393 |
rs144980504 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145076982 | ACGCGGGTGGATCAC[A/G]AGGTCAGGAGATCGA | 10393 |
rs145052986 | in-del | -/GTGTGTGTGTGTGT | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054605 | GGGACATACTGAATA[-/GTGTGTGTGTGTGT]GTGTGTGTGTGTGTG | 10393 |
rs145081854 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145059260 | GAAATATTATTTTAT[C/G]AGAAGAACTGACATA | 10393 |
rs145087904 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145032415 | TGGAAAATTGGTGAC[C/T]AAGAAATTTAGGGAA | 10393 |
rs145088560 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145005282 | TCATAATAGTCTCTC[A/T]GGGATTTTGGATTTC | 10393 |
rs145093294 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081152 | ACATTCAAAGCATTG[A/G]AAAACATGTGGCTGT | 10393 |
rs145112807 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145078495 | ATTCCAATCAAACTA[C/T]TGACAGTTTTCACAG | 10393 |
rs145148267 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | ANAPC10 | GRCh38.p7 | 4:145033268 | TGAAAATGGTACCAC[C/G]ATCACCCCTGGTGAT | 10393 |
rs145148360 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145080447 | TTATGCACTGTGTAG[G/T]GCCACCTTTGTGCCA | 10393 |
rs145197632 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145020452 | AATAAAAGCCATCTA[C/T]GACAAACCCACAGCA | 10393 |
rs145228876 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145039478 | ATTTTTCCTTTTCTA[C/T]GAGATAATAATAAAT | 10393 |
rs145311503 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144971004 | AGAAAACAATCCACA[A/C]TGGGTGGAAAAACCC | 10393 |
rs145333524 | snp | A/C | | | upstream-variant-2KB, intron-variant, missense, utr-variant-5-prime | ABCE1, ANAPC10 | GRCh38.p7 | 4:145097508 | ACCGTTTCCTTGACA[A/C]CTCCCATTGTATCCG | 10393 |
rs145351782 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145014226 | CCCACTGCCTGGAAA[C/T]AGACTCAGTGCTGTT | 10393 |
rs145364802 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145091275 | AAACCAGTGACTGGT[A/G]CAATATTGTGATAGT | 10393 |
rs145400873 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145025553 | ACACACACAGTTATC[A/G]ATTGGGTTTGCCATC | 10393 |
rs145401246 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144978863 | CTCGCAGAGTGGCTC[A/C]GAACTAAAGTTAGAT | 10393 |
rs145470839 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145086239 | AAGTGCTTAGATTAC[C/T]GGCATGAGCCACCGT | 10393 |
rs145505072 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145022050 | TCAGGGAACACTTCT[A/G]CACTGCTGGAATGTA | 10393 |
rs145529881 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145039653 | TGGCTGGAGTGCAGT[C/G]GCTAGATCTTGGAGC | 10393 |
rs145552638 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144986460 | GAGATTCAACTTCTT[C/T]CTGATTTAGTCTTGG | 10393 |
rs145576733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144982187 | ATTTGCCAGGCACTG[C/T]GCTAAGTGCTTACAG | 10393 |
rs145607782 | snp | A/G | 0.0119091 | 0.0762411 | utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995283 | AAAATTAGATATAAC[A/G]GATGCCTTGTTCAAT | 10393 |
rs145619414 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145079226 | GCAAAGGACATGAAC[A/G]GACATTCCTCAAAAG | 10393 |
rs145679062 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081958 | CAAGTGATCCTCCTG[C/T]CTTGGCCTCCCAAAG | 10393 |
rs145720810 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145055568 | GTCTCAATAAATAAA[A/T]AAAAAATTAAATAAA | 10393 |
rs145724641 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144993197 | TGGTATTCACTTCAT[C/T]GTGTGGTGGTCTGGA | 10393 |
rs145746210 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145040985 | TTACTACAGATCTAC[A/G]CAGAGGTAAAAATCC | 10393 |
rs145815971 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145051148 | CATCATTAGTTAGAG[A/G]CCTAATTGAATCAAG | 10393 |
rs145838340 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145037845 | TCAGCTACTCAGGAG[A/G]CTGAGGCAGGAGGAT | 10393 |
rs145894020 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144996406 | GAGATCTAGAGACAC[A/G]GCTGCTGCTGCTGTG | 10393 |
rs145916143 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145098019 | TGACCCACCGGCCTT[A/G]AGGAAAGCGCAAACG | 10393 |
rs145929458 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145049939 | AATGAAGCCTTCAGA[A/C]CCTCAAAGTTATTCA | 10393 |
rs145931383 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144973753 | AATAAATTTATGCCA[A/G]TAATTTTGAAAATGT | 10393 |
rs145940572 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145095215 | TGCAGTTTCATCTCC[A/G]CAGTTTCAGTTACCC | 10393 |
rs145964344 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144979930 | TTCACTTTCTTTTAC[A/G]TTCCACCTTATCTAA | 10393 |
rs146050324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145068863 | TGCTGTGAGCCAAGA[C/T]TGCGCTACTGTACTC | 10393 |
rs146087803 | snp | A/T | 0.144969 | 0.226867 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144998505 | AACTGAACAACCTGC[A/T]CCTGAATGACTACTG | 10393 |
rs146105846 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145049024 | GTCAGTCATACAATG[C/T]TTTGGTTTCTCAGTG | 10393 |
rs146152427 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145050438 | GGATTATTAGAATAG[C/T]GAGGGCTGCCTTCAA | 10393 |
rs146174860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145012828 | ATATAGTTTGGGTCT[A/G]TGTCCCTGCCCAAAT | 10393 |
rs146269199 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145069706 | ATCAGCAAGGTCAGA[A/T]CTATTTTCTTAATAT | 10393 |
rs146273278 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145011372 | AAAATAAAATAAAAT[A/G]AAATAAAATAAAATA | 10393 |
rs146291608 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145031905 | CTATCATGAACTGGG[C/T]GCTTTCTGACCCATC | 10393 |
rs146302065 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145073147 | AATCCTCCTACCTCA[C/G]CCTCCCAAAGTGTTG | 10393 |
rs146325680 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145035283 | TTGGTCAAAGAGGAC[A/G]ACCCTCCCTAATAGA | 10393 |
rs146390772 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145090693 | TAGTACAACTTCATA[C/T]ATAACTTTTGAAAAC | 10393 |
rs146423881 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145046315 | CCTGTAAATATTGTA[A/T]TTCTTTTTAAAAATA | 10393 |
rs146425784 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144970585 | GAAAAAGAAAAAACA[C/T]AGGAGATGAGAACTT | 10393 |
rs146437098 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145052836 | AAGGTTGCAGTGAGC[A/C/T]GAGATTGCACCACTG | 10393 |
rs146491466 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145025644 | TGATCACAGATGACC[A/G]TAACAGGTATAATAT | 10393 |
rs146515418 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144988928 | TATTGCTGAGTAGCA[G/T]TTCATTATATGTATA | 10393 |
rs146527216 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145028931 | TCAAATCTGCTAAGA[C/T]TGCCCTAAGTGGGAG | 10393 |
rs146543785 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145026261 | ATTTATTGATTGACT[-/G]AATGACTATTTTGTG | 10393 |
rs146548884 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144991589 | TCACCATGTTAGCAG[A/G]ATGGTCTCGATCTCC | 10393 |
rs146576984 | in-del | -/T | 0.00874735 | 0.0655527 | utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144994912 | CCAGTATTAAAAGAA[-/T]AACCTTCCTCTGGGT | 10393 |
rs146613710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145041094 | AGGATCTATGACTTC[C/T]AGTGGTCCCATAATT | 10393 |
rs146635271 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145004611 | TGATCACATGCTTTT[G/T]GTTTTCAGTTGTTTA | 10393 |
rs146646213 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145046754 | CTGTCCAGTTGCAAC[A/G]GAGAAAACACTGATA | 10393 |
rs146733872 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145059677 | GTCTAAAAAACACTT[C/T]AGTTTCATATTTAAG | 10393 |
rs146767098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145065080 | TAAGTACTTACTTCA[C/T]TTCCTATATTAAATA | 10393 |
rs146787682 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145028088 | AAAGAGCTGTTAGAT[A/G]GTGTGATGGTTAATA | 10393 |
rs146832477 | in-del | -/T | | | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145099055 | TTTTTGGTACGCTTT[-/T]GTAGCACTAGGCACT | 10393 |
rs146875163 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145040597 | CCAATTTATAGTTAA[C/T]TTATAGGTAACTGAA | 10393 |
rs146886650 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145086522 | CATGTATCAGAAACT[C/T]TGAGAGCTCAGCCCT | 10393 |
rs146898058 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145067014 | TTATCGTAAGGTTCA[C/T]GTACCCACAGAAATC | 10393 |
rs146918946 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145030297 | ACAGACCAGAACCCC[C/T]TGAATGAAGGAGAGG | 10393 |
rs146941258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145026371 | GTTCTAGTAATAAAC[A/G]TAATCGATAAGTGAT | 10393 |
rs147004737 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145088921 | GCTCTCCAGCCCCTA[C/T]AGCCTTCTTTCTGAA | 10393 |
rs147005360 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145011784 | TCTGAAGTTGCCTAG[A/G]ATAGGTTGCTGAAAG | 10393 |
rs147024465 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145048287 | TGTCCTTGTGCTAAC[A/C]AAAGCCATCAAAGAT | 10393 |
rs147026242 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144972884 | TACCTTGAAAATCTC[C/T]ATATATTTAAGGAGA | 10393 |
rs147047474 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145092293 | TGTCACAAACCTGCA[C/T]ATCCTACACATGTAC | 10393 |
rs147050670 | in-del | -/A | 0.0509478 | 0.151255 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145060577 | TCATAATTTCTAGTG[-/A]AAAAAAAAAGGAAAA | 10393 |
rs147068777 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144976640 | AATTATTCATATACA[C/G]AATCTTTTCATTAAA | 10393 |
rs147110974 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145030852 | AAGGACTTGAAGGAC[A/G]TGGGGGTGGTAATTC | 10393 |
rs147152631 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144990639 | CAGATCTCCTGTGAA[C/T]TCAGAGTGAGAACTC | 10393 |
rs147183198 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145044579 | TCTGGGGTTTTCATT[C/T]GCAATGTTGTTTGCA | 10393 |
rs147195699 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145039557 | AGAACTATAGATGTA[C/T]TGATTTTTTTCCAGC | 10393 |
rs147212831 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145003393 | CCCTTGGGTATATAC[C/T]GAATAATGGAATTTG | 10393 |
rs147256019 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145006762 | CTTAGCCTTTTTTCT[A/G]TCAGTATTTGGTGCA | 10393 |
rs147289916 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145062475 | AGCTGGGCATGGTGG[C/T]GCATTCCTGTAATCC | 10393 |
rs147309950 | snp | C/T | 0.029116 | 0.117091 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144986499 | ATGTGTCGAGGAATT[C/T]ATCCATTTCTTCTAG | 10393 |
rs147395967 | snp | A/C | 0.0205511 | 0.0992634 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145084988 | TATTGGACAGTCATG[A/C]TTCAAATCATGCTTC | 10393 |
rs147396741 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145007678 | GACACATTTAAAGCA[A/G]TGTGTAGAGGGAAAT | 10393 |
rs147407239 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145004249 | TTGGGGCAGAGTAAC[C/T]ATGGTGTTTGTGTAG | 10393 |
rs147513253 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145023823 | CTGTAGAAATTTCTT[A/G]AAATAAGACAACAAT | 10393 |
rs147532919 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144985643 | TTCAAGATTTGTCAG[C/T]GTTTTAGTCATTGAA | 10393 |
rs147659019 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144977051 | AGAGACTTATTTGGA[G/T]CTGTGTACAATTTCT | 10393 |
rs147688078 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144981529 | TTGCTGACATTGCTT[A/C]TCAGCTTAAGAATCT | 10393 |
rs147690371 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145055277 | CTTTAAAAAAAAGGA[A/G]GCCAGTGAGGTAGCT | 10393 |
rs147700476 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145052159 | ATAAAATTTCGGTGA[C/G]GCATAAGAAATAAGT | 10393 |
rs147795539 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145076390 | AACTAAACCCAACTT[G/T]TACCACAGTAAAACC | 10393 |
rs147796980 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144999811 | CAAACTATACTACAC[A/G]GCTACAGTAACCTAA | 10393 |
rs147805275 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145071360 | GCAGTGAGCCAAGAT[C/T]GTGCCATTGCACTCC | 10393 |
rs147806650 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144996633 | AAAGATGGGGAGAAA[C/T]CAGAGCAGAAAAGCT | 10393 |
rs147902102 | snp | A/C/T | 0.0158469 | 0.0875917 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145019548 | GGAACTAGAGAAACA[A/C/T]GAACAAACCAAACCC | 10393 |
rs147911397 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145092016 | AGAACTACCCTGCCT[A/C]TCCCTTTCAGGAGCT | 10393 |
rs147923453 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144980622 | GTTCACTCTGATGAT[C/T]GTTTCTTTTGCTGTG | 10393 |
rs147932121 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144976058 | TCGATCTAACCATAT[A/G]TGTATCTAACAGAAA | 10393 |
rs148017643 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144990222 | AGAGGATGAGACAGA[A/T]CCCAGGACCACAGAG | 10393 |
rs148019526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145060055 | AGAAAGACAGTGTAG[A/G]CTCAGAAATGCTAAA | 10393 |
rs148058486 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145015619 | TCACAAAAAGATCAT[A/C]ACCTAGGCACACTGT | 10393 |
rs148082500 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145079636 | TCAACCTAGATGCCC[A/G]TCAACAGTGGACTGG | 10393 |
rs148092951 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145003351 | ACATACATGTGCATA[G/T]GTCTTTATGGTAGAA | 10393 |
rs148144848 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145072392 | CTGAGAAACTGCTAC[A/G]TAAATCGAGAGTTGC | 10393 |
rs148175169 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145031041 | GTATCTGGTATCCAA[C/T]CATTGACTTGGCAAA | 10393 |
rs148212153 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145089819 | TATCTGATTTATCGC[A/G]TCTCCTGATTTCCTT | 10393 |
rs148216946 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144984734 | GTGAAATACCATTTC[C/T]TGAAATAAAAATTCA | 10393 |
rs148227460 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145025763 | CACTGATAGACTTGC[A/T]CAATGCAGAGTTGCC | 10393 |
rs148260763 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145084502 | TGTCTAATCTTTTGG[A/C]TTCCCTGGGCCACAC | 10393 |
rs148262219 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145053053 | CCTAAGAAACCTTAT[C/T]CTGACTGATGAGGAA | 10393 |
rs148272558 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144978577 | TGTAATCTCAACTAC[C/T]TAGGAGGCCGAGGTG | 10393 |
rs148303342 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145038239 | TAACTAGGGCCGGGC[A/C]TGGTGGTTCATGTCT | 10393 |
rs148351709 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145005689 | AGTTTCAAATAATTT[C/G]TTGATTTCTGCCTTA | 10393 |
rs148396341 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145039811 | ATGTTGGCCAGGATG[C/G]TCTCGATCTCTTGAC | 10393 |
rs148416777 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145049483 | AGCACCTTCACACAC[C/T]AAAAACTACTTTCTT | 10393 |
rs148544653 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant, utr-variant-3-prime | ANAPC10 | GRCh38.p7 | 4:145063489 | TAAATTTAGAGACAC[A/G]GTCTTAATATAAACA | 10393 |
rs148573614 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145018592 | GCAGTGAGCCGAGAT[C/G/T]GTGCCATTGCACTCA | 10393 |
rs148595555 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145057719 | TTATCTAAGTCCCTT[C/T]CTCTCTGCCCCTCCC | 10393 |
rs148628024 | snp | C/T | 0.170733 | 0.237101 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145012195 | ATATATATATATATA[C/T]ACACACACACATATA | 10393 |
rs148658579 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145074728 | CTATACAAATAAATA[A/T]CCAGGTTCAAAATTT | 10393 |
rs148670600 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144968646 | TTGATTAGGTCAAAG[A/G/T]TGAGGATCCCAGGAC | 10393 |
rs148701136 | snp | C/G | 0.00716266 | 0.059414 | intron-variant, downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:145032837 | CTTCCATCATGGAAA[C/G]GGCAGAGGTTTGTCT | 10393 |
rs148733267 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144987703 | CAGGAAGTAAACTTA[A/C]ATCTCCTCTACACTC | 10393 |
rs148756736 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145027627 | TACTTGAGAGAAAAA[C/T]AGATCACATGCAAAG | 10393 |
rs148785612 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144980497 | TCCTTGTTGATTCTG[C/G]ATATTAGACCTTTCA | 10393 |
rs148843717 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144989830 | TTTATTACTGATACG[C/G]AGAAAGTTTGAGTGG | 10393 |
rs148895352 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144982123 | TGCTGGGATTACAGG[C/T]GTGAGCCACCGCACC | 10393 |
rs148948325 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145051887 | TATCTATTAAATAAT[C/T]GCAGAGTACCTTTTA | 10393 |
rs148977430 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145010282 | ATTCCTCAGGGATCT[A/G]GAACTAGAAATACCA | 10393 |
rs149008186 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145072121 | AACTTTAAAGCAAGA[C/T]TGAGGCTTTCACTAC | 10393 |
rs149028589 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145004448 | AATGCTTCCAGCTTT[C/T]GCCCATTCAGTATGA | 10393 |
rs149038375 | snp | A/G | 0.201418 | 0.245234 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145016226 | TTAGAAAACCCCACC[A/G]TCTCAGCCCAAAATC | 10393 |
rs149049383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145025666 | GTATAATATTGGTGA[A/G]AAAGTTTGAAGTTTG | 10393 |
rs149059502 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145065902 | TGGGACCATAGGAGA[C/T]CTTTATTTTCTTCTT | 10393 |
rs149156036 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145091756 | TTTCTGGTTCTACAT[C/T]TTTGAGGACTCGCCA | 10393 |
rs149185812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145047091 | CAAACAAGACAGGCA[C/T]TGTAATTTTCATTTT | 10393 |
rs149186850 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144971564 | TAATGCCTTATAGAT[C/T]AATGATCAATATATT | 10393 |
rs149191476 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145078494 | TATTCCAATCAAACT[A/C]CTGACAGTTTTCACA | 10393 |
rs149199277 | in-del | -/G | 0.00636936 | 0.0560724 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145073896 | TGTAGAAATTTTGAT[-/G]GAAGGCAGATCAAAC | 10393 |
rs149243738 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144980296 | TTGACTTTTTAATAA[C/T]AGCCATTCTGATTGG | 10393 |
rs149252673 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145100228 | GGGTAGTGACATGCA[C/T]CTATAGTCCCAGCTA | 10393 |
rs149253292 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145022416 | AAGTCACTCAGGAAC[A/G]GAGAACCAAACATCG | 10393 |
rs149292253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144973463 | CCTCAGCATCATGCA[A/G]TATACCTATGTAACA | 10393 |
rs149294542 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145049448 | TCTAAATTCTTTGTT[G/T]TCATTTCAAGAATGT | 10393 |
rs149304632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145094150 | ACACCCATATTGTGG[A/G]ACAGTAATCAACAAT | 10393 |
rs149350411 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145044231 | TACTCATTATAGCAA[A/C/T]GTGTTTGACAAAAAT | 10393 |
rs149379725 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145001865 | AGAGCAGATGTAACC[C/T]GCTAGGCATGCACTG | 10393 |
rs149432738 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144997499 | ACTAAGCTTCATAAG[C/T]GAAGGAGAAATAAAA | 10393 |
rs149464478 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145057558 | GCTTCTATTTACACA[C/G]TGATGATTCCAAAAT | 10393 |
rs149509735 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145011944 | CCTTGAGGGGCTAGG[A/C]CCCAGAAGTGTTAAA | 10393 |
rs149519450 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054236 | TTAATCAGCAACATG[A/T]TAGTCGCCAGAAATA | 10393 |
rs149560000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145083162 | TTAACAACAATAATA[A/G]CAATAACAAACACTG | 10393 |
rs149561404 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145006460 | ATAGCAATGAATAAA[A/G]GAATGTAGGGCAGTA | 10393 |
rs149590963 | in-del | -/C | 0.030665 | 0.119967 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144968413 | AAATACAATTTAATA[-/C]TTTTCTCTGTATTAA | 10393 |
rs149594872 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145068668 | TGTAATCCCAGCACT[C/T]TGGGAGGCTGAGGCA | 10393 |
rs149624312 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145027165 | AGTGCCACCACACTC[A/G]GCTAATTTTTGTATT | 10393 |
rs149653686 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145085929 | AGTGCAGTGGCGCGA[C/T]TTCAGCTCACTGCAA | 10393 |
rs149688218 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145070845 | ACACATGCTACAACA[C/T]GAATGAACCTTGAAA | 10393 |
rs149696447 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145039652 | CTGGCTGGAGTGCAG[A/T]GGCTAGATCTTGGAG | 10393 |
rs149780032 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145025331 | TTTTGGCTTTCAACA[C/T]GCCCCCCCCCCCTTT | 10393 |
rs149781527 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995277 | ATATACAAAATTAGA[C/T]ATAACGGATGCCTTG | 10393 |
rs149815066 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145050740 | TCATGAACCAACCTC[A/G]GCTAGTTTCAAGCTT | 10393 |
rs149821825 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144976044 | TATCTGTCTATCAAT[C/T]GATCTAACCATATGT | 10393 |
rs149833799 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144991139 | AATAATTTAGTAGAG[C/T]AGAGGAGAACCTGGG | 10393 |
rs149838060 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145096901 | GAACAGTCATACCTG[C/T]CCTCTAGCTGTCAAA | 10393 |
rs149867580 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145046167 | TAATGGAAAAGTCTG[C/T]AAAAATATTTGTGCA | 10393 |
rs149909888 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145004308 | GTTAGTTTGAGTTCC[C/G]ATCTTCCTATTTGGA | 10393 |
rs149958366 | snp | A/C/T | 0.00676609 | 0.0577691 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144998990 | ATACTATAAACACCT[A/C/T]TACGCAAATAAACTA | 10393 |
rs149961216 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145073818 | AAATCATTTTAATAT[A/G]ATTAAAAATGTTGTA | 10393 |
rs149973448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145019824 | TTTATGGGCATAAAC[C/T]TGAAAACCTAGAAGA | 10393 |
rs149996050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145059006 | AATCTTTTAAACTAG[C/T]TAAATTCAACAAAAA | 10393 |
rs150023668 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145091123 | CACTACTGAACTTCA[G/T]GAATTTCATACTCAA | 10393 |
rs150025022 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145014172 | TTTATTTCATAGCTC[A/G]GAGGTGGGTACCATG | 10393 |
rs150067027 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144970951 | ACAGACAAAGCCCTG[A/C]TGAAGATAAGCTCAC | 10393 |
rs150089521 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145060826 | ATTGTGGTAGAATAA[C/G]AGAAAAAATAAAATC | 10393 |
rs150130793 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145093275 | GGAATTTGAAGCCTG[G/T]GAGACACTGAAGGTA | 10393 |
rs150171630 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144973323 | GGATTCACATGAACA[C/T]GAAGATAGTAACAAT | 10393 |
rs150185931 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145088401 | TTTCAACTAGAAAAA[C/T]AGGCATTGCAAAATT | 10393 |
rs150223036 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144967310 | TCCATATAAAAATTG[G/T]ATCCTTTCATTGCCA | 10393 |
rs150309446 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144996819 | TATTCGAACCCATCG[C/T]AAAGAAGCTAAAAAC | 10393 |
rs150342302 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:145053628 | ATCTACAAATCCTTG[C/T]AGGAAGAATTCTCTT | 10393 |
rs150358154 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144993002 | TGAGACTCTCCACCT[A/G]CATAGAGGTTACAAC | 10393 |
rs150433615 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145006180 | TTAAGTCCTCTTCTT[C/G]AATTGAGCTCTTTAC | 10393 |
rs150486520 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145000636 | ATTGTGGAAGACAGT[A/G]TGGTGACTGCTCAGA | 10393 |
rs150501996 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145022353 | AAAGGAATGAATTAA[C/T]GGCATTCGCAGCGAC | 10393 |
rs150530819 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145008310 | CAATCAATAGAAAAA[C/G]AGGGAATCCTCCCTA | 10393 |
rs150536148 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145085500 | TTCACAACTTTATTA[C/T]GTATGTGCTCAAAGA | 10393 |
rs150548781 | in-del | -/TA | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145026932 | ATACATATATATATA[-/TA]TATATATATATATGT | 10393 |
rs150588124 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145079856 | TAGTGGCTCACACGT[A/G]TAATCCCAGCACTTT | 10393 |
rs150617132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145035540 | AGATCTTCCTGCAGG[C/T]TCTCCAACTCCTAGG | 10393 |
rs150655265 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144990958 | CCCCAGCCCTGGAAA[C/G]TCTGCTCTGTAACTC | 10393 |
rs150678034 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145031233 | ACAAGATATCACACT[G/T]GTCCATTACATTGAT | 10393 |
rs150701988 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145096320 | CCCAACACTTTGGGA[A/G]GCTGAGACAGGAGGA | 10393 |
rs150705999 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144985078 | AATAAACTGATCTGT[A/G]AGGCTTTCTTTCTCA | 10393 |
rs150741242 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144968785 | TCAGGCAGCTGATTT[A/C]TTATAGCATTCTGCC | 10393 |
rs150743665 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145045496 | GTCATCTTGTAAAAC[C/T]GGATTACAGAATACT | 10393 |
rs150792356 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145039299 | TCGCAATCCTATGTA[C/G]GTAATGAATAAGATG | 10393 |
rs150869399 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054870 | TTTTATTCATTCTAC[A/G]CCATTCTGTGTCTTC | 10393 |
rs150880870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145068327 | ATCTAGTAAAGCACA[A/G]AGCCAGAATTTAATC | 10393 |
rs150888246 | snp | C/T | 0.00517822 | 0.0506191 | utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144994728 | TTCCATAAGTACTGC[C/T]AGATTATACAGGCAA | 10393 |
rs150931312 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145000134 | ATACCATTCAGGACA[C/T]AGGCATGGCCAAGAA | 10393 |
rs150986307 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144996217 | CGAAACAGGCTTATA[G/T]GATCTTAGTGATGAC | 10393 |
rs151037982 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, utr-variant-3-prime | ANAPC10 | GRCh38.p7 | 4:145063856 | GAGTGAAAGAAGCCA[C/T]ACATAAAAGTTATAT | 10393 |
rs151060473 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145011116 | GCAAGTGGATCACCC[A/G]AGGTCAGGAGTTCGA | 10393 |
rs151104891 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145080950 | ATAAATGGAACAAGA[C/T]AGCTGAGTTAACTGG | 10393 |
rs151110058 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144975079 | CGGTTCAAACAAATC[A/G]ATAAAGAGGTTCAAA | 10393 |
rs151148471 | snp | C/G/T | 0.0111256 | 0.0738101 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145036912 | AAAAAGGAAGGATCA[C/G/T]AGTTTTCCCTAAAGG | 10393 |
rs151187165 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144992927 | TTTAAGAAATTGCCA[C/G]AGCCCTGTCAGCATT | 10393 |
rs151233911 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145097777 | TAAAAAAAGATAGAA[A/C]TAAAGCCCATCTTTA | 10393 |
rs151238778 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144988373 | ATTAAAATTTTTCAT[A/G]TAACTGCAGTTTGTC | 10393 |
rs151272509 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145047602 | TTTCTCAAAGTCAGG[A/C]ACACTTCTCAATGCC | 10393 |
rs151320797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145013473 | ATGTGACAAAATTCA[A/G]TACTCATTTATGATT | 10393 |
rs180773663 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144976548 | GACAAAATCAGCCAA[G/T]GATTACAGTAGACAG | 10393 |
rs180845442 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145013713 | CAGACCCTCTGAAAA[A/C]AGCGGTCTGCTCCTG | 10393 |
rs180849260 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145001411 | TGAGGTACTTAAGAG[C/T]AGTCAAAAATCATAG | 10393 |
rs180857033 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144985806 | ATAACTAGCTGATAT[C/T]ACAAATAGTTTTTCC | 10393 |
rs180862607 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145021999 | CAGGAATGGCCATAA[G/T]CAAAAAATCAGTAGA | 10393 |
rs180879633 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144967307 | GCATCCATATAAAAA[G/T]TGGATCCTTTCATTG | 10393 |
rs180895225 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145086108 | GCTGGGATTACAGGC[A/G]CCTGCCAACACGCCC | 10393 |
rs180903828 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145071674 | ATAACCTGAAGGGTT[A/G]TCTTAGTTTCTTTCT | 10393 |
rs180915294 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145031867 | GACTATGGGTCATCA[A/G]GTCACCATGCAACCT | 10393 |
rs180918183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145053898 | AGCACTTTCAGCTGA[C/T]TACTACTGTGTGTGT | 10393 |
rs181079056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145016702 | AGCTGGAGGCATCAT[A/G]CTACCTCACTTCAAA | 10393 |
rs181084468 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144981397 | CTCCTAGGTATTTTA[C/T]TCTCTTTGTAGCAAT | 10393 |
rs181095743 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145004347 | TTTATTTCTCTTGCC[G/T]GATTGCTCTGGCTAG | 10393 |
rs181105511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144990939 | AGGGAGGTAGGACTA[C/T]CATCCCCAGCCCTGG | 10393 |
rs181145584 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081101 | CATAGCGGCCAACTG[C/T]CTCTTATTTAAAATT | 10393 |
rs181153205 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145049992 | CCAAACTAATGTTAA[C/T]GTTCATATTTTGACC | 10393 |
rs181158424 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145068271 | TACAGATGCAGAAAC[C/T]GAGGTTCACATCAGG | 10393 |
rs181160509 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145075121 | ACCAGGAGGTCTTCA[C/T]AGATTCTGTGCTTAC | 10393 |
rs181168895 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145056795 | CCAGTATGTTTTCCT[A/T]ATAAGAGGGATTGAT | 10393 |
rs181170897 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145036003 | AAGAAAGAGTTTATA[A/C]TCTGTCAGAGAATTT | 10393 |
rs181171031 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144998387 | ACAAACTGTCTCTAA[A/G]ACCACAGTGCAATCA | 10393 |
rs181176888 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145028868 | GATGAAAGAAAATGA[G/T]GAACTCAGGGATTCT | 10393 |
rs181177458 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145009884 | ATCAGAGTGAAAAGG[A/C]AACCTACAAAATGGG | 10393 |
rs181283177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145045894 | AATAACTTTTTCATA[C/T]TGTAATTTTAAAAAA | 10393 |
rs181293034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145022911 | AAAGTTTTAGGGTAC[C/T]TGTGCACAACATGCA | 10393 |
rs181322941 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144985319 | AAAGATCTGCAAAGC[A/C]AAAATATTCACATGT | 10393 |
rs181347082 | snp | G/T | | | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145096581 | AGAGGTTCACTTGAT[G/T]ATTTTTACTTCTACA | 10393 |
rs181354466 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145062569 | CCAAGATCATACCAC[C/T]GCACTCCAGTGTGGG | 10393 |
rs181359356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145078826 | ACTGGCTAGCCATAC[A/G]CAGAAGATTGAAATC | 10393 |
rs181366280 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145085664 | GCTTAGAAAGTATCA[C/T]AGTACAACTAAGCAG | 10393 |
rs181388817 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:145053227 | AGAAAATTCACATAG[A/C]TACTCAGGAAACATG | 10393 |
rs181391782 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145000991 | TAAATGGGAATTGAA[C/T]AATGAGAACACTTGG | 10393 |
rs181413150 | snp | C/T | 0.00204574 | 0.0319169 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144995649 | TTTATTCAACAAATA[C/T]AATTTATAACAATGA | 10393 |
rs181417665 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145013189 | CAATCTAAGAACAGA[A/G]TAACAGAGGCCTGCA | 10393 |
rs181500610 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145070710 | CAATGTTCATAACAG[C/T]ATTATTTACAACAGC | 10393 |
rs181502066 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145005044 | CTGTTTAGGGATTCA[A/G]TATCTTCCTTGTTCA | 10393 |
rs181511871 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145049571 | AATTTGGTCGCATCT[G/T]CAGGCTCCATTTCTT | 10393 |
rs181520899 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145008090 | AGAAGATGAAGAAGA[A/C]ATGGATAAATTCCTG | 10393 |
rs181525648 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145031342 | GGATGGGAAATAAAT[C/T]CAACTAAAATTCCGG | 10393 |
rs181534948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144991823 | ATAAGGGATGAAGGT[A/G]GCTACACTAAACAAT | 10393 |
rs181538637 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144972553 | TCAAAACATATAAAG[A/T]GACAATTGACAGAAT | 10393 |
rs181540966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144978378 | TGAAAAAAGCTGCAA[C/T]GTTTTCCTCCTGGAA | 10393 |
rs181569362 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145080815 | GGAAGGCTGAGGCAG[A/G]AGAATCGCTTGAACC | 10393 |
rs181577106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145067898 | AGATTTAAACAAAAT[A/G]ATGGTGTGTACTAAA | 10393 |
rs181579184 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145039061 | ACTAAGGCAAAACCT[A/G]TAAGAAGCAGGCAAC | 10393 |
rs181580798 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145018333 | GCAGTACTACAGAAT[G/T]GATAAGCATTCACCA | 10393 |
rs181703697 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145009547 | TCTGATGTTTGACAA[A/T]CCTGACAAAAACAAG | 10393 |
rs181714943 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144980594 | AAATTTTCTCCCATT[A/C]TGTAGGTTGTCTGTT | 10393 |
rs181725862 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145007908 | AGGAGCTGGTTTTTT[C/G]AAAAGATCAACAAAA | 10393 |
rs181727847 | snp | A/G | 0.00142745 | 0.0266775 | utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995359 | CGTTTAATGATTTTC[A/G]TCTCATTTTAAAGTC | 10393 |
rs181732948 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145076013 | TCCCAGGGTCCCTGC[C/T]TGGCCATGTCTGATT | 10393 |
rs181735335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144977388 | GTCTCTTTCACAACA[C/T]ATAATAATGGGTGGT | 10393 |
rs181785831 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145045614 | AGATACAATACTCCA[C/T]TTTTTTTCATATCAC | 10393 |
rs181789450 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145028166 | GGTGTGCCTGTGTGT[A/G]TGTTGCCAAAAGAGA | 10393 |
rs181799855 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145022415 | GAAGTCACTCAGGAA[C/T]GGAGAACCAAACATC | 10393 |
rs181816862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145072223 | TACCAAAAAGTGTGC[C/T]ATATGCTCCCCACCA | 10393 |
rs181849095 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144998065 | ACCCAATACAGGAGC[A/C]CCCAGATTCATAAAG | 10393 |
rs181886101 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145086975 | CTGCACTCCAGTCAA[C/T]AACGGGGCTAAATCA | 10393 |
rs181918324 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145092085 | AAACCAAACACCACA[C/T]GTTCTCGCTTATAAA | 10393 |
rs181961937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145095725 | TTTATTACTTTATTA[C/T]TTCTATTGTTATAAT | 10393 |
rs181976770 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145032015 | CCGGAAGGCACAAGT[G/T]ACATGAGGAAGTGGC | 10393 |
rs181984531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145061676 | TCTACTTATAAAAGG[C/T]TTACCAATATGAGTG | 10393 |
rs182007901 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145057706 | AAAATTAATCTCATT[A/C]TCTAAGTCCCTTTCT | 10393 |
rs182075688 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145068678 | GCACTTTGGGAGGCT[A/G]AGGCAGGCAGATCAC | 10393 |
rs182080483 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081608 | GTTAATAAAATAGAT[C/T]TATTTGTCTATAACC | 10393 |
rs182087445 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145091721 | TATACCCAGTGATGG[A/G]ATTGCTGAGTCAAAT | 10393 |
rs182209749 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054811 | CAGCCACTTGCTCAA[C/G]TTTATTGTTCTTTCT | 10393 |
rs182210152 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ANAPC10 | GRCh38.p7 | 4:145033156 | GACTGGGGCAAAGTT[A/C]TCCAGAAGGCTGTGT | 10393 |
rs182221230 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145057525 | GTTCCAGCCCTAGCA[C/T]TCTTCTTTCATATCT | 10393 |
rs182222605 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145015188 | AAGGAAATCCAAAAA[A/T]TGATACAAGAAGTGA | 10393 |
rs182224207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145003302 | CTGATGGGCTTTTAG[A/G]TTGATTCCATGTCTT | 10393 |
rs182242723 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054417 | CAAAAAATTAGCCGG[G/T]CATGGTGGCAGGCGC | 10393 |
rs182247751 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145017447 | ACCAGTTAGAATGGC[A/G]ATCATTAAAAAGTCA | 10393 |
rs182258040 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144991208 | AATGGTAAAGATTTG[C/T]TAAGAGCAAGGTGAA | 10393 |
rs182260488 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144978938 | CCTATTTCTGGGAAT[C/G]AGCATGTGTCTTAAA | 10393 |
rs182261323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145077967 | AGAACCAGAACAAGA[C/T]AAAGATGCCCACTCT | 10393 |
rs182264131 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145014341 | TTCCCTGACAACCTG[C/T]GTGACTCAGCAGAGG | 10393 |
rs182267098 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145088758 | TCTGTATCAGATCAT[A/C]TTCCTCTCCTGCTTA | 10393 |
rs182279191 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145072887 | TTAAGCCTAGTATCT[A/C]TTACGTATCTGTTTT | 10393 |
rs182405391 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145011097 | AGCACTTTTGGAGGC[C/G/T]GAGGCAAGTGGATCA | 10393 |
rs182412755 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145039635 | CAGTCTCGCTCTGTC[A/G]CCTGGCTGGAGTGCA | 10393 |
rs182412988 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144999554 | AATGAAATGAAAGAG[G/T]ACACAAACAAATGGA | 10393 |
rs182415769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145018769 | GGCATTTCATGTAAA[C/T]GGACACCAAAAGTGA | 10393 |
rs182417404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144984184 | GGCACTATTTTTTGA[C/T]AAACAGTAAAATCCC | 10393 |
rs182441672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144971053 | TTCACATAATGAAAG[C/T]GTCTTACAGAGATTA | 10393 |
rs182468340 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145092472 | TTGTCCCAACTGTAG[C/T]AGAGCATAGGAGGAA | 10393 |
rs182478977 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145058012 | CCCATTCCCATGATT[A/C]AGCTGTGTTGATGTT | 10393 |
rs182480222 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145076448 | AAAAAAGTCCCATCT[A/G]AAGGACAGCAACTTC | 10393 |
rs182493313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145075548 | GAAGGCATTGAGAGT[A/G]GACAGAGGGAGGACC | 10393 |
rs182501164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145037129 | CCAGAACACAGTTGC[A/G]GAGCTCCTCATGCTA | 10393 |
rs182519949 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145004669 | TCTGCATGTGTTGAA[A/C]CAACTTTGTATTCCA | 10393 |
rs182579224 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145078958 | ATACCTAGAAATACC[C/T]AGAACATAGGACCTA | 10393 |
rs182604672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145046018 | TAATTTGTTCAATTG[C/T]TGGGCCAAACTGCCC | 10393 |
rs182609004 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144987754 | TCACGACTTTCTAAT[A/T]TCTGGCTTGATTGGT | 10393 |
rs182626482 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145003137 | TTTCTGTTCCTGTGT[C/T]AGTTTGCTTAGGATA | 10393 |
rs182637567 | snp | A/C/T | 0.00835859 | 0.0641884 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144987411 | CAAAAAACCAAACAC[A/C/T]GCATGTTCTCACTCA | 10393 |
rs182641955 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144968415 | ATACAATTTAATACT[G/T]TTCTCTGTATTAAAT | 10393 |
rs182708675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145014895 | AAACGGGGAGAGTGC[C/T]ACATCAAGGGAACAG | 10393 |
rs182782824 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144996087 | ACCAGAAGTAATTAA[C/T]GACAGGGTTCGAGGT | 10393 |
rs182810136 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145066381 | AGCAAAGAAGGACAG[C/G]AAATTTTTGAAGACC | 10393 |
rs182824748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145047289 | CTCACCCTTCTGTCC[C/T]ACTCTGAAAACAATA | 10393 |
rs182845239 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145005342 | CATTTCTGACTGTAT[C/T]TTGGATCTTTTCTCT | 10393 |
rs182859539 | snp | C/T | 0 | 0 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144973030 | TAAACTAGAGCTGCA[C/T]TTGGAGGAAACTTTA | 10393 |
rs182877761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ANAPC10 | GRCh38.p7 | 4:145063312 | AACAATGAATATCTC[A/G]AAAGACAAAACAACA | 10393 |
rs182886037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145024415 | GCAGCTAATGCCTTA[C/T]GAAATGTATATCTTA | 10393 |
rs182888456 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145079796 | CCAAATATTGCATGT[C/T]CTCACTTATAAGTGG | 10393 |
rs182894025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144969157 | TCTCCAATCTGAAAG[A/G]GAGATAATAAGACCT | 10393 |
rs182896142 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145098992 | CAGCGTGTACGCAGC[C/T]ATGACTGGGGTTGTC | 10393 |
rs182901267 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145069684 | GACCTCAAGACTCTT[A/T]CAGAGGATCAGCAAG | 10393 |
rs182921442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145030569 | TCAGGTAATTAATGG[A/G]GTTTTAGCTTAGGTC | 10393 |
rs182938303 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | ABCE1, ANAPC10 | GRCh38.p7 | 4:145097596 | AACGGACTGTAAACT[C/T]TGGCAAGGCCTGAGG | 10393 |
rs183046209 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145069189 | CTGAGCAACAGGCAG[C/T]ACAGGCCTCTAGGTC | 10393 |
rs183113970 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145082463 | CGGATACATTTTAAA[G/T]AACGTATGTATTTAA | 10393 |
rs183117510 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145059629 | TGTTTCTCATATAAC[A/C/G]ATATAGAAATAATTT | 10393 |
rs183153797 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144992168 | CTTGGAAAAAAGATT[A/C]TTTCAAAATATTACT | 10393 |
rs183189053 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145083335 | AATTATCTCACCACA[A/C]CTCTGCAGAACATTT | 10393 |
rs183195842 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145051638 | AATTTTTAAAGAACT[A/G]TTCTTTTTTTTCATG | 10393 |
rs183197708 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145026019 | ACCTGAATATAAAGC[A/G]AACTGTACAACTGGA | 10393 |
rs183201575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145087484 | ATTTTAACTGAGGCA[A/G]ATGTCTTAACTATGA | 10393 |
rs183203906 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054653 | TGTGCGCGCGCGCGC[A/G]CGTGCGTGCAGCGCA | 10393 |
rs183219790 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144996818 | ATATTCGAACCCATC[A/G]CAAAGAAGCTAAAAA | 10393 |
rs183259094 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145025626 | AGTAGCATCAAAGAT[G/T]ATTGATCACAGATGA | 10393 |
rs183267565 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145008624 | AGAAAAGGCCTTTGA[A/C]AAAATTCAACACAGC | 10393 |
rs183272254 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144996356 | AGATCCTGGAGCAAC[A/C]TCAGCTGGGCGCCAC | 10393 |
rs183277734 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144979110 | AACTTTTTTTCCTTC[A/C]ACTATTATTTTCAGT | 10393 |
rs183311314 | snp | G/T | | | intron-variant, utr-variant-3-prime | ANAPC10 | GRCh38.p7 | 4:145064156 | TTAAAAAATGAAAAT[G/T]AAGCAAATGTTGATA | 10393 |
rs183319617 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145046436 | TAAATTCCATAAGCA[A/C]AAACAATTTCAAGAA | 10393 |
rs183433415 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145072794 | ATAATTCAATATGTA[A/G]GTGACTAGTAAAGTC | 10393 |
rs183450516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145008713 | AAGAGCTATTTATGA[C/T]AAACCCACAGCCAAT | 10393 |
rs183453031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145051330 | GAGCATGGTTCATGG[C/T]GTCCCAAAACAATTA | 10393 |
rs183456416 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:145032780 | ACCATTCCTCAGAGT[A/G]ATCAGCCAGCTACCT | 10393 |
rs183458922 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145010957 | GGGACCAGGTATCCA[C/T]GGAAGGCACGGCAAG | 10393 |
rs183476240 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145083858 | CTGATAGATTAAAAA[A/G]ATTGTATTTCACATT | 10393 |
rs183485384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144983185 | AATAAAATAAAAACA[A/G]ATAAAAATAATTATT | 10393 |
rs183488159 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145070240 | ACACTCCGTCATATA[C/T]ACATTGTCTATGGGA | 10393 |
rs183498762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145010414 | AATAGCAAAGACTTG[A/G]AACCAACCCAAATGA | 10393 |
rs183503789 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144973967 | AATTTAAAACGTTTT[C/T]TATTTTTTGAGGCCA | 10393 |
rs183509308 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144998899 | AAGAAAAGAGAAAAG[A/C]AGCAAATAGACACAA | 10393 |
rs183515668 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144982671 | TGATCTAAAAATTAT[C/G]AGAAAGCCTCTAGGA | 10393 |
rs183525868 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145077011 | GAGACCATTCTGGCT[A/G]AAACGGTGAAACCCT | 10393 |
rs183595165 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145050457 | GGCTGCCTTCAACTT[G/T]AAGTCACTAGCTGCA | 10393 |
rs183630315 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144997168 | GAAATCACTCTTCAG[C/G]ATATTGCCCAGAAGA | 10393 |
rs183637756 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144979908 | CAGACACCGCTTCCC[A/C]TTCCTCTTCACTTTC | 10393 |
rs183643718 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144967704 | CCCAAGGAATAAGAC[A/C]ACAGAAAGCTCAAAA | 10393 |
rs183713199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144999168 | CCAGATGGATTAAGA[A/G]ACGAATTCTACCAGA | 10393 |
rs183733360 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145002659 | GTCAATTAAAAAGAA[C/T]AATTTTATCAAAAGC | 10393 |
rs183737255 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145094271 | AGTATTTATATCGGC[A/C]TTCTGGGAAAGGCGA | 10393 |
rs183787831 | snp | A/C/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145098281 | CGCGCGCGCACTACG[A/C/T]CCTATGGCTTGCGCG | 10393 |
rs183845842 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145057180 | TATAATAAGAAAAGA[C/T]AGAATTCCTGCTATT | 10393 |
rs183853612 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145075496 | GAGAAACCAGACCAT[A/C]AAGAAGACAAGCATA | 10393 |
rs183861952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145036725 | AACTCAAAGTTAGTA[C/T]AACTGAAAATAAAAA | 10393 |
rs183863531 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145017095 | AACACCAAAAGCAAT[A/C/G]GCAACAAAAGCCAAA | 10393 |
rs183923817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145091103 | AAGTAAGACATATGA[C/T]ATTGCACTACTGAAC | 10393 |
rs183945407 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144986302 | TTTTTCTACTGATTG[A/G]AATAGTTTCAGAAGG | 10393 |
rs183987181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145079284 | AAGATGGTCAACCTC[A/G]CTAATCACTGGAGAA | 10393 |
rs183999242 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144993288 | ACATTGTTGTCAACA[C/T]GTGGAATAATCATTT | 10393 |
rs184063580 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145092922 | AACAGTCCTTTCTCA[G/T]AGTGAGGCAGAAAAC | 10393 |
rs184066588 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145058924 | AAATTATGTGTATCA[C/T]ACCAAAACATTCTAC | 10393 |
rs184075430 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145031583 | CTGACAGTTTTGAGT[A/G]GGGTCCAGAACAGGA | 10393 |
rs184075664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145060015 | ATGCACAAAAGTAAC[C/T]CAACTGAGATGAAGC | 10393 |
rs184078735 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145077186 | CCTGGGCGACAGAGC[A/G]AGACTCTGTCTCAAA | 10393 |
rs184080885 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145019295 | ATCAATTCCAAAAGG[A/T]ACCTTCAAAACATGC | 10393 |
rs184091411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145042902 | TTTAAAATAACAGGT[A/G]AAGAAAAAATTGTCT | 10393 |
rs184100039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145095428 | TTTGTCCAGCATATC[C/T]ACACTGTGTATACTA | 10393 |
rs184138184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145061178 | CTTAGAAAAAATTAA[A/G]AGACTACCTATAAGA | 10393 |
rs184147032 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145022098 | TGGAAAACAGTATGG[A/C]GATTCCTTAAAGAGC | 10393 |
rs184162764 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145094921 | AGAATTCTATCCCAA[A/C]AAAGAGTAAAAGGAA | 10393 |
rs184171885 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145080833 | AATCGCTTGAACCTG[C/G]GAGGCGGAGGTTGCA | 10393 |
rs184202434 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145076917 | AAAATAAAAAAGAAT[C/T]TGCCAGGCGTGGTGG | 10393 |
rs184234059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145040194 | TTGCTCTTGATGCCC[A/G]GGCTGGAGTACAATG | 10393 |
rs184246845 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145006221 | TGCCCTTTTTGTCTT[A/T]TGTGATCTTTGTTGT | 10393 |
rs184262104 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145077465 | AGAGCTGGTATCAAC[C/T]CTACTGAAACGATTG | 10393 |
rs184288368 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145045081 | CAGAAAGCACTAATA[C/G]TCTCCAAAAGCTAAT | 10393 |
rs184316735 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145016341 | ACAAACAAACAGAGA[A/G]CCAAATCATGAGTGA | 10393 |
rs184319726 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145004068 | CCCCTCCTTGGTTAC[A/G]TGTATTCCTAGGCAG | 10393 |
rs184327861 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144989633 | ACCAGTTTCTCACTT[A/T]AATACAAAAGCTAGA | 10393 |
rs184334458 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144970505 | AGTAGTCTATCCTGT[C/G]TTTGCCTCGATGGTG | 10393 |
rs184348749 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145009005 | GTCTCAGGATACAAA[A/C]TCAATGTGTAAAAAT | 10393 |
rs184383334 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145084350 | CAGCAAAGAGATAAG[C/T]ATATAATGTCATGAA | 10393 |
rs184427766 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145048721 | AATTGCTAAAGAACA[C/T]GTATGTTTTTCAAGC | 10393 |
rs184446637 | snp | A/C/T | 0.0107286 | 0.0724924 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144990999 | GATGCCACATCAGAG[A/C/T]GGCTGTTCAGCAGCA | 10393 |
rs184482419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144971018 | ACTGGGTGGAAAAAC[C/T]CATAGAAATACCCAA | 10393 |
rs184546587 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145020689 | CAAAAATCCTAAAGA[C/T]TCCTCCAGAAAGCTC | 10393 |
rs184546961 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145007068 | CGAATAAGAACAGCT[C/G]CAGTGCACAGGTCAC | 10393 |
rs184556659 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | ANAPC10 | GRCh38.p7 | 4:144993600 | GCTTTGTTAATATAA[C/T]GCATTATCTGTATTT | 10393 |
rs184562595 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145066818 | AATAACTGGCTTAAG[A/G]TCAAAAAGCTAGTAG | 10393 |
rs184564290 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144975130 | GCTCAAATACATATC[A/G]CACATACATGGATAC | 10393 |
rs184570942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145004415 | AGGCATCCTTGTTTC[A/G]TTCCAGTTTTCAAGA | 10393 |
rs184578153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145026605 | ATGAACACAAATGGT[C/T]CCAAACTTATTATCT | 10393 |
rs184600935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144976225 | AACTTGAATATATAT[C/T]ACAAAAATCATGTTG | 10393 |
rs184610657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145049473 | GAATGTTCACAGCAC[C/T]TTCACACACTAAAAA | 10393 |
rs184617255 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145089447 | TAAATTTGTTTTTCA[A/C]CATTGGATTAATTTG | 10393 |
rs184624228 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145041763 | AACTGGTTCCAGATA[C/T]ACAGCAATATTATCC | 10393 |
rs184626080 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145027148 | AGCTGAGACTACAGG[C/T]GAGTGCCACCACACT | 10393 |
rs184630723 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145009404 | AAAAGAACAAAGCTG[C/G]AGGCATCACGCTACT | 10393 |
rs184642363 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144997778 | CCAATTGAAAGACAC[A/G]GACTGGCAAATTAGA | 10393 |
rs184651583 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144980086 | ATGTGCTGTCATGGC[A/G]ACTGGCCAAGGCAGC | 10393 |
rs184681083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145007324 | CTCTCCACCCCAGAT[A/G]AACAGAATATACATT | 10393 |
rs184701920 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145067464 | CGCTTTCTCCTGAGA[A/C]AGAGCTTCTGGCAGG | 10393 |
rs184706425 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145080651 | CAGTGGCTCACGCCT[A/G]TAATCCCAGCACTTT | 10393 |
rs184741088 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145071171 | CAACACTTTGGGAGG[C/T]TGAGGAGGGCAGAGC | 10393 |
rs184817104 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145021135 | CACTGCAATCCCCAT[C/G]AAAATACCATCATCA | 10393 |
rs184845577 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995273 | AAACATATACAAAAT[A/T]AGATATAACGGATGC | 10393 |
rs184849483 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145030881 | TCCCACCACATCCCC[A/G]TTCAACTCTCCCATC | 10393 |
rs184853884 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145011742 | TCAAATACATGGCCT[A/C]TTTTTCCCTCACAAT | 10393 |
rs184854026 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144976745 | GAAACTGTGCTTACA[C/T]TATATTCTTGATTCT | 10393 |
rs184858801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145000232 | TAAAGAGCTTCTGCA[C/T]GGCAAAAGAAACTAC | 10393 |
rs184871826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145085871 | AATTTTTTTTCTTTT[C/T]TTTTTTTTTTAAGAT | 10393 |
rs184873848 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:145053288 | TTTAGGCTCAATAAA[G/T]ATTAAAATAGATAGC | 10393 |
rs184984701 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144979677 | GGTCTTTGAGGAATC[A/G]CCACATTGTTATGGG | 10393 |
rs184988091 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145089911 | CTGATTGTTTTACTC[C/T]GTTACTTACCTTTTC | 10393 |
rs185020768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145056481 | TCATTCCTCTACTTC[C/T]TTAAAAAACTCGCTT | 10393 |
rs185107531 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145074811 | TTCCAATTTTTAAAA[A/G]TTTTCTTTATACTAA | 10393 |
rs185124524 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145071949 | TTCTTTTCTTACCTC[C/T]TCTTCGTTCCCATAC | 10393 |
rs185129097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145008418 | ATATCCCTGATGAAC[A/G]TCGGTGCAAAAATCA | 10393 |
rs185135320 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145031868 | ACTATGGGTCATCAA[C/G]TCACCATGCAACCTG | 10393 |
rs185135396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054159 | TGATCTGCCCGCTGC[A/G]GCCTCCCAAAGTGCT | 10393 |
rs185150085 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145013915 | AGGGGTAGAGAAAGC[A/C]GTGGAAAAGGCCCTG | 10393 |
rs185178078 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144985234 | CTTCCAAATACCATA[A/C]CCCAGGGAGTCATAG | 10393 |
rs185181430 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145092677 | TGGGAGAGGGGAAGA[C/G]ACTAAACAGCCTAAG | 10393 |
rs185188943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145058051 | TAATGTCTGCCATTA[C/T]GTACAATCTGACTAT | 10393 |
rs185191949 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145076550 | CAGAGTGTCTTCTTA[C/T]ATCCAAATGAGCACA | 10393 |
rs185203883 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145086222 | CTGGCCTCAGTCTCC[C/T]AAAGTGCTTAGATTA | 10393 |
rs185238469 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145052842 | GCAGTGAGCCGAGAT[A/T]GCACCACTGCACTCC | 10393 |
rs185288378 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145000809 | CAACTGTCCATCAGT[A/G]ATAGACTGGATTAAG | 10393 |
rs185353813 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145070510 | CAAATGTTGGCATGG[A/T]TGTGGAGAAACTGGA | 10393 |
rs185370157 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145031197 | TCTTATTCGAAGAGA[A/C]CTTGATCACTTTTCC | 10393 |
rs185381531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145010119 | AAATCAAAACCACAA[C/T]GAGATACCATCTCAC | 10393 |
rs185385912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144998453 | AAATTAAAACTCAGG[A/G]TTAAGAAACTCACTC | 10393 |
rs185393750 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144982124 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCACCC | 10393 |
rs185423442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144969986 | CAATTCCCCTGTTTC[A/G]TAGAACTCAAGGTAA | 10393 |
rs185426562 | snp | C/G/T | 0.00239393 | 0.0345281 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145078847 | GATTGAAATCAGACC[C/G/T]CTCCCTTTCACCATA | 10393 |
rs185432906 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145096621 | AGTTCTATAATTCTG[G/T]GCCTGAAAATTCAAA | 10393 |
rs185436918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:145062950 | GATCTTATTTACATA[C/T]GGAATATTAAAAAGT | 10393 |
rs185478578 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145073219 | TAAATGACATCAGCA[C/T]TTTAATTTTTCCATT | 10393 |
rs185483745 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145034832 | TCAGATGACTCAACG[C/T]CTCCCAGGAATGAGC | 10393 |
rs185503733 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145003931 | TAAATAGCTTTGGGC[A/G]GTATGGCCTTTTAAC | 10393 |
rs185545805 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144988867 | CTCTTAAAATAATTA[C/T]TTTGGACATTTAGCT | 10393 |
rs185601131 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145055134 | CTTAAGATAAGTGTA[A/C]ATCCACTGTTCACAG | 10393 |
rs185615576 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145013522 | TGGAAACAGAATGCA[A/G]TCATTAATAAAAAAC | 10393 |
rs185625940 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145001032 | CACCCCGGGGCCTGT[C/G]GTAGGGTGCAGGGCA | 10393 |
rs185630799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145015399 | AGACAAAGAAAAAAG[A/G]ATAAGAAAATATGAA | 10393 |
rs185634289 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144985493 | TAGCAGTAACAATTT[C/T]CTAAAACACTAGATA | 10393 |
rs185644264 | snp | A/G | 0.00159617 | 0.0282053 | downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:144966844 | AAATACAGTGGTGTT[A/G]GAGTTTTCAACATTT | 10393 |
rs185677599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145039295 | GTTATCGCAATCCTA[C/T]GTAGGTAATGAATAA | 10393 |
rs185677860 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145057770 | GTATGCCATTACTAG[C/T]AAATGCCAACTTTCA | 10393 |
rs185690596 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145068137 | TCCTGGACTGCCAGG[A/C]TCCTCTTACACGAAG | 10393 |
rs185692684 | snp | A/C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145018623 | GCCTGGGTGACAGAG[A/C/T]GAGACTCCATCTCAA | 10393 |
rs185694533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145005196 | GCTGGGATTACAGGC[A/G]TGAACCACCATACCT | 10393 |
rs185705231 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144991899 | CACCTTGGATTTTCA[A/T]AGCTAGAGGAAAGTC | 10393 |
rs185714852 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144972607 | ACAATCATATGGAAG[A/G]GTTTCATACAACTTT | 10393 |
rs185767040 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145025425 | GACACTTAGAGACCA[C/T]TGTCAAGTTACTAAA | 10393 |
rs185791138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145001739 | TGGTGTAAACAGGAT[C/T]CATTAGAGTTTCTCT | 10393 |
rs185818965 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | ABCE1, ANAPC10 | GRCh38.p7 | 4:145097647 | TTTACTGAATGAATA[A/C]ACAGATGAATAGGTT | 10393 |
rs185838205 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145007563 | GAAACTGAACAACCT[A/G]CTCCTGAATGACTAC | 10393 |
rs185849857 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant, utr-variant-3-prime | ANAPC10 | GRCh38.p7 | 4:145063597 | AACCACCAGATTTTA[A/C]TGATTATTTGGGCTT | 10393 |
rs185873986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144984893 | GGTAATCATGGAATA[C/T]ATAATATTAAAAAAT | 10393 |
rs185919077 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145045659 | CACTCTCACATATAT[G/T]AATGTATACGTGATC | 10393 |
rs185927661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145022551 | AATACTACAAACAGG[A/G]TGGTGCAATGTATAC | 10393 |
rs185934083 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144985917 | ATTATTTTGAGATAC[A/G]TCCCATCAATACCTA | 10393 |
rs185942587 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144968285 | TAAGAAGGACGGGGG[A/G]AAAAGAGACACATCA | 10393 |
rs185942924 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145007928 | GATCAACAAAATTGA[C/T]AGACCGCTAGCAAGA | 10393 |
rs185949172 | snp | C/T | 1.65715e-05 | 0.00287845 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995525 | CAGCAATCTGTATCA[C/T]GAATGTACGAGTTGG | 10393 |
rs185956442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144977849 | TATGAAAGTATGGAA[A/G]GAAAAACAGAGAATA | 10393 |
rs185963303 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145079033 | ATGTAAATTGACAAG[C/T]GGGACCTAATTAAAC | 10393 |
rs185977074 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145046040 | AAACTGCCCTAAAAG[C/G]AAATGCCCTGTTACA | 10393 |
rs186004384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145061740 | AAATACAATTTAATA[C/T]GTCAAGTCATCAGAG | 10393 |
rs186011799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145078000 | CCACTTCTATTCAAC[A/G]TAGTTCTAGAGGTCC | 10393 |
rs186085746 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081344 | TGATACATTAAGGTA[A/C/T]TGTATTGGGCCATAA | 10393 |
rs186093848 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145050265 | TCAACAAGCATAGTG[A/T]TTTGAAATAAATCTT | 10393 |
rs186135427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145028894 | ATTCTAACTCCTGGC[C/T]TCAGAAGCAGGTATT | 10393 |
rs186184633 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144971993 | TATTGTTCACCTGTT[C/T]AAAACCCTTTAATGA | 10393 |
rs186230107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145068296 | ATCAGGTTAAGCAAG[C/T]GGTCCTTGTTTACAC | 10393 |
rs186266289 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144978497 | AAAAATGGACACTTT[A/T]GATCATTCCCCTTTT | 10393 |
rs186335035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145045934 | CTAATAAGCCAACTT[A/G]ACATATGTTCTAGCA | 10393 |
rs186347938 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145008167 | TCAATAGACCAATAA[C/G]AGGCTCTGAAATTGA | 10393 |
rs186399359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145069097 | CATCTGCTCATGAAG[A/G]TTAACTGCTACATGA | 10393 |
rs186418134 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144995711 | ACATTTTGCTCAACG[A/G]AAGAATGACAATATG | 10393 |
rs186418753 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145050706 | TTTATGTTATGCAGA[C/T]GGCTTCTTCACTGAA | 10393 |
rs186424711 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145029390 | CTAGACCTATAATTA[G/T]ACTAAAGTCCTGGCA | 10393 |
rs186429207 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145010488 | CCATGGAATACTATG[C/T]AGCCATAAAAAAGGA | 10393 |
rs186432301 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144998994 | TATAAACACCTCTAC[A/G]CAAATAAACTAGAAA | 10393 |
rs186469050 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145082341 | TTTAGTAGAGAAGGC[A/G]TTTCTCCATGTGGGT | 10393 |
rs186503553 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144998087 | TTCATAAAGCAAGTC[C/T]TTAGAGATCTATAAA | 10393 |
rs186523953 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145088856 | TAATCTGTCCCACCA[C/T]GTCTAATTACATTTC | 10393 |
rs186542251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145023092 | CAACATGGAATACTA[C/T]ATAGCAGTGAGGATG | 10393 |
rs186546462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054822 | TCAAGTTTATTGTTC[C/T]TTCTCCTTGTTATGT | 10393 |
rs186559323 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145033387 | CTGGAGACACAACAA[C/T]GATTCCATTAAACTG | 10393 |
rs186575937 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145028404 | GCTGGTTCTCCTTGC[C/T]CTTCAGCTTGCAGAC | 10393 |
rs186619497 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145092176 | GTCAGGATGGGGTAG[C/G]GGGAGGGAGAGCATT | 10393 |
rs186627078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144996100 | AACGACAGGGTTCGA[A/G]GTAGCTTGCCCAGGC | 10393 |
rs186631035 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144979007 | ACATTAGCAAGTTTT[A/T]TTGGGTATTCTTTGA | 10393 |
rs186726219 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144980756 | GAATGGTATTATCTA[A/G]ATTTTCTTCTAGGGT | 10393 |
rs186753983 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145030702 | CCCCACATTGGCTCC[A/C]TGACTGGTAGGGTGA | 10393 |
rs186764059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145039665 | AGTGGCTAGATCTTG[A/G]AGCACTGCAACCTCC | 10393 |
rs186769866 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144999640 | GCCCAAGGTAATTTA[C/T]AGATTCAATGCTATC | 10393 |
rs186777130 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144984332 | GTGATTGTTATAAAT[G/T]TCAACAGTTGAAAAA | 10393 |
rs186808346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145014418 | CACCCCTATCCCCCA[C/T]AGCAGCTGCACCAAG | 10393 |
rs186809909 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145049663 | TGGCTCACTGGAACC[A/G]CCGCCACCTAGGCTT | 10393 |
rs186824419 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145009573 | ACAAGAAATGGGGAA[A/C]GGATTCCCTATTTAA | 10393 |
rs186837206 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144987124 | CTAGGAATACCATTT[A/G]ACCAGCCATCCCATT | 10393 |
rs186863709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145076093 | ATAGCTTTTTCACCA[A/G]CAGACCCCACCTAAC | 10393 |
rs186896262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145087001 | AATCATGACTTACTT[C/T]AGTCAATACACTGTG | 10393 |
rs186906797 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054453 | GTCCCAGCTACTTGG[A/G]AGGCTGAGGCAGGAG | 10393 |
rs186973015 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054696 | TGCCTGTGTGTGTGC[A/C]TGTGTGTGTGTGCAT | 10393 |
rs186978030 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:145032831 | GGACTTCTTCCATCA[C/T]GGAAACGGCAGAGGT | 10393 |
rs186979654 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145015041 | GCTCCTTAACACCCC[A/C]CAAAAAATCATATTG | 10393 |
rs186993969 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145003147 | TGTGTCAGTTTGCTT[A/C]GGATACTGGCATCCA | 10393 |
rs187009102 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144987585 | CACCAACATGGCACA[C/T]GTATACATATGTAAC | 10393 |
rs187015160 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144968753 | ATCAACATCAATAAG[C/T]ATTCTACCACCTAGC | 10393 |
rs187028380 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145003041 | CTCAAGAAAGTCCCA[A/G]CCACTATTGTTCCCT | 10393 |
rs187098292 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144982765 | ACTTACTTAAGTCAG[C/T]GTAGTAGGGGTTTCT | 10393 |
rs187102680 | snp | A/C/T | 0.000351297 | 0.0132486 | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145096144 | ATGCACACATTGTAT[A/C/T]AGGAACTGGGCATCT | 10393 |
rs187107052 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145004905 | CCTCAAAATTTCAGT[A/T]GGATTAGTAACCAGC | 10393 |
rs187107422 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145072417 | AGTTGCTTATTTTCT[A/G]TGTGAAGAAAAAACA | 10393 |
rs187112662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145032235 | AGGACATCCCTGAAG[A/G]ACAGCGGTGAAAGGA | 10393 |
rs187157241 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145075763 | ATCTGAACCAGCAGG[A/G]AGTGCTGCTTGGAGA | 10393 |
rs187173539 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145037970 | AAAAAAAAAAAAAAT[A/C]CAGTTGAAGCAGAAA | 10393 |
rs187190532 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145079912 | TGAGGTCAGGAGTTT[A/G]AGACCAGCCTGGCCA | 10393 |
rs187194157 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145099501 | TTTGGGGTTTGTGAG[C/T]TTTTTGAGAACTTAG | 10393 |
rs187286124 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144991334 | ATGGCTTTGAATGCA[C/G]CTCAATAAAAATTTG | 10393 |
rs187353474 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144975206 | CTTCAGCAAATGGTA[A/C]TGAGTCAATTGACTA | 10393 |
rs187365443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145091810 | CTAATTTACATTTCC[A/G]CCAACACTGTAAACA | 10393 |
rs187365641 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145057542 | CTTCTTTCATATCTA[A/C]GCTTCTATTTACACA | 10393 |
rs187381068 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144967336 | TGCCATTTGGTCAAG[A/G]AACAAGATGAAACAT | 10393 |
rs187381667 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145017760 | TAAGAAAATGTGGCA[C/T]ATACACACCATGGAA | 10393 |
rs187401646 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145077015 | CCATTCTGGCTGAAA[C/T]GGTGAAACCCTGTCT | 10393 |
rs187403657 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145041804 | CAAGAAACAATAATT[A/G]AAAGATTCATACAAC | 10393 |
rs187406850 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145059718 | TCTACAATAATTTTT[A/T]AAAACAACAATAACT | 10393 |
rs187410248 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145020961 | AGACAACACAAACAA[A/T]TGGAAACACATCCCA | 10393 |
rs187425510 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145007196 | AATAATAATGGGAGA[A/C]TTTAACACCCCACTG | 10393 |
rs187430507 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime, intron-variant | ANAPC10 | GRCh38.p7 | 4:144994397 | TCACTATTTAATACT[G/T]TAGTGTACCCAGCAA | 10393 |
rs187431229 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145003526 | TTTTGTATACAGTGT[A/G]AGGAAGGGATCCAGT | 10393 |
rs187446511 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144969403 | TATTAAAAGATGTAA[A/G]TGAACAAGATCACCA | 10393 |
rs187471490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145094395 | CAATGTTATATATTC[A/G]ATTATAATGCTGCTT | 10393 |
rs187606454 | snp | A/T | | | intron-variant, utr-variant-3-prime | ANAPC10 | GRCh38.p7 | 4:145064307 | AACAACTGAAGAATC[A/T]AGGAAGTGAGTATAC | 10393 |
rs187609873 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145079449 | TGTAAATTAGTTCAG[C/T]CACTGTGGAAAGCAG | 10393 |
rs187611408 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145046437 | AAATTCCATAAGCAC[A/C]AACAATTTCAAGAAC | 10393 |
rs187622779 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144989047 | CACATACAAGTCTTT[G/T]TATGGATATATGTTT | 10393 |
rs187622918 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145025641 | TATTGATCACAGATG[A/C]CCGTAACAGGTATAA | 10393 |
rs187626431 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145008660 | ATGCTAAAAACTCTC[A/C]ATAAACTAGGAATTG | 10393 |
rs187637474 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144996489 | GGTCCCAACTGACCA[A/G]CTGCAGGCTGTTGTT | 10393 |
rs187646275 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144993233 | ACCTGCAGCATCTCT[G/T]AGATATGCCTGTACC | 10393 |
rs187679286 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145098331 | CATTTTGGCCGGTGG[C/G]CGTGAGAACACGCTG | 10393 |
rs187680386 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145051681 | TTCATGAAAAATTCA[G/T]GCAGTTAGAGGAATA | 10393 |
rs187690608 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144988578 | GTACAATAAGTTATT[C/T]TTAAAATCAGTTCTG | 10393 |
rs187717876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145019158 | ACACAATCTATTCAA[C/T]AGCGCATGGGACTTT | 10393 |
rs187757129 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145084292 | AATTTCAAATTACTA[C/G]TTAGCTAGATAAAGA | 10393 |
rs187761292 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145015200 | AAAATGATACAAGAA[A/G]TGAAAGGAGAGATAT | 10393 |
rs187779139 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145070246 | CGTCATATACACATT[A/G]TCTATGGGAGCTTTA | 10393 |
rs187782540 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145083615 | ATTTTGATGACTTTG[G/T]ATGACAAAAACTTTA | 10393 |
rs187789601 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145051894 | TAAATAATCGCAGAG[A/T]ACCTTTTAGTCAACC | 10393 |
rs187881030 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144975012 | CATTAGAATGTATTA[C/T]GATTCAACACTAATT | 10393 |
rs187931734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144973420 | ATTATGTTTATGTCC[C/T]GGGTGACGGAATCAC | 10393 |
rs187940326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145008714 | AGAGCTATTTATGAC[A/G]AACCCACAGCCAATA | 10393 |
rs187954536 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144979825 | ACATGCCATAGTACC[A/G]GGCATTATCAGTACC | 10393 |
rs188011744 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145005741 | CACTCGAAGCAGGCT[A/G]TTTCATTTCCATGTA | 10393 |
rs188017256 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145026943 | TATATATATATATAT[A/G]TATGTGTGTGTGTGT | 10393 |
rs188019726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145072821 | AGTCCAATGAATATC[C/T]AGTTGAGTCTAATGA | 10393 |
rs188027554 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145047481 | ATGATAATTCCATGC[G/T]ACCGATAATCCTGAA | 10393 |
rs188033255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145009171 | CAAACCACTCCTCAA[C/T]GAAATAAAAGAGGAC | 10393 |
rs188040441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144997188 | TGCCCAGAAGAACTT[C/T]CCCAATCTAGCAAGG | 10393 |
rs188048667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144979912 | CACCGCTTCCCCTTC[C/T]TCTTCACTTTCTTTT | 10393 |
rs188058288 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145069685 | ACCTCAAGACTCTTT[A/C]AGAGGATCAGCAAGG | 10393 |
rs188189829 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, synonymous-codon | ANAPC10 | GRCh38.p7 | 4:144999280 | ATGAGGCCAGCATCA[C/T]CCTGATACCAAAGCC | 10393 |
rs188209687 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145091167 | GATCCTGCCACTCCT[C/T]TAGTAGCAGTAACTA | 10393 |
rs188217562 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145057247 | AACAATTACTCCAAA[A/G]AGTGCTTAAACAAGT | 10393 |
rs188220003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145075502 | CCAGACCATCAAGAA[A/G]ACAAGCATACTTTAA | 10393 |
rs188226980 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144996824 | GAACCCATCGCAAAG[A/G]AGCTAAAAACCTTGA | 10393 |
rs188274132 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145029873 | AAAACAGATTTGTGA[A/G]GGCAGCACCCCCATT | 10393 |
rs188290867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145087587 | CTATATACATTTAAA[C/T]GAAGTAAAATTAAAA | 10393 |
rs188298964 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145066445 | TGGTCTTTCTTCTTA[C/T]GGAGAGATCAAAGAT | 10393 |
rs188309266 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145026050 | CATTTAACAGTAAAA[A/T]CTCACCTCCCTTCCT | 10393 |
rs188384849 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144985683 | ATGAGAATAAATGTA[C/T]AAAACATCACTTGGT | 10393 |
rs188393234 | snp | C/T | 0.0023933 | 0.0345097 | downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:144967016 | TTAAATCTTATAACC[C/T]TGAAATAAGAATCTA | 10393 |
rs188431522 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145071488 | AAAATCTTTACTGTT[C/T]ATTACTCACCATCTC | 10393 |
rs188445442 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145077203 | GACTCTGTCTCAAAA[A/T]AAATAAATAAATAGA | 10393 |
rs188453450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145095159 | AGCATCTAAACAAAA[A/G]GAATATTAAAATCAG | 10393 |
rs188454746 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:145053554 | GAGATGGCTAAGCTA[A/C]GGTTTCTGTTTTGTA | 10393 |
rs188459705 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145031629 | GGTCCAGGCTGCTGT[A/G]CAAGCTGCTCTGCCA | 10393 |
rs188461730 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145013709 | CCCACAGACCCTCTG[A/G]AAAAAGCGGTCTGCT | 10393 |
rs188464898 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145011058 | GAGGATTGCCTGAAC[A/G]CAGTGGCTCACGTCT | 10393 |
rs188485255 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144983312 | GTAAAATATTCATAA[A/G]TTAACACAGGTTGAG | 10393 |
rs188493722 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145016059 | CTTTGAAAACTGGCA[C/T]GAGACAGGGATGCCC | 10393 |
rs188527990 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145082504 | TTGTGCTTTTTGCAA[C/G]CTGATAGTAAAAATG | 10393 |
rs188543013 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145051339 | TCATGGCGTCCCAAA[A/C]CAATTACAATAGTAT | 10393 |
rs188561892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145089665 | ATGAAATATTGAACC[A/G]TTATTTCAAAGATAC | 10393 |
rs188563906 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145055266 | TATTCTTTGGTCTTT[A/T]AAAAAAAGGAGGCCA | 10393 |
rs188629807 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144990669 | CACTTATCACCAACG[A/G/T]GATGGCACCAAGCCA | 10393 |
rs188638114 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144970506 | GTAGTCTATCCTGTG[C/T]TTGCCTCGATGGTGG | 10393 |
rs188680569 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145074936 | AAATCCTTCAAATTA[C/T]GGAAAGAAAGCTACC | 10393 |
rs188696992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145035917 | CTTCCACTGGTAGCA[A/G]ATGAGCTGGAAGTCC | 10393 |
rs188697370 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145056627 | TATAGTGTGGAAATC[C/T]CCGACCCAAAGGTTA | 10393 |
rs188710967 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145016638 | TAAAGTTCATATGGA[A/G]CCAAAAGGGAGTCCA | 10393 |
rs188712386 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144979589 | CATGTATCTTTATAA[C/T]AGAATTATTTATATT | 10393 |
rs188714895 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145004219 | TGTTGAAGTCATTTA[A/T]CAGATCAAGGAGCTT | 10393 |
rs188732512 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145041228 | CAATAGTTAAGGTGA[A/C]ATTTTACAAAATGAA | 10393 |
rs188747305 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145006500 | TCAGACCAGATGATA[A/C]AAGAAGACCTAGATT | 10393 |
rs188760710 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145035053 | AAGCTAGTCTAAAGT[A/C]CATTTCTCAAGACTC | 10393 |
rs188783971 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145003957 | TTAACAATATTGAGT[C/G]TTCCTATCCATGAGC | 10393 |
rs188800916 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145076942 | TGGTGGCTCACACCT[A/G]TAATCCCAGCACTTT | 10393 |
rs188835818 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145073822 | CATTTTAATATAATT[A/T]AAAATGTTGTATAAT | 10393 |
rs188858769 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145062171 | AGCTGATTTATTTAT[G/T]AATCTATTCAAGCAC | 10393 |
rs188861093 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145078099 | CTTTGTTTGCAGACA[A/G]TATAATTCTACACCT | 10393 |
rs188867734 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145045665 | CACATATATGAATGT[A/T]TACGTGATCTTCTAC | 10393 |
rs189013423 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145019536 | GTCACACCTCAAGGA[A/C]CTAGAGAAACACGAA | 10393 |
rs189032114 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145067034 | CCACAGAAATCGTAC[A/G]TATAATTTGCTATAT | 10393 |
rs189032179 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145004475 | ATGATGTTGGCTGTG[C/G]GTTTGTCAAAGATGT | 10393 |
rs189052635 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144971024 | TGGAAAAACCCATAG[A/C/G]AATACCCAAGAAATT | 10393 |
rs189087451 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145080661 | CGCCTGTAATCCCAG[C/T]ACTTTGGGAGGCCGA | 10393 |
rs189090117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145093116 | TTCTACAGCTGGAGG[C/T]AGGGCAAGAGCATGG | 10393 |
rs189097078 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145067768 | GACATTAGTGACATA[C/T]TCCTAGTTGCCTAAC | 10393 |
rs189104336 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145059068 | TTCTGTCTTATCAAA[C/T]CAATTTATGTTTATA | 10393 |
rs189119498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145049544 | GTTCAAGTTTTATAA[C/T]GAGATTGCTGCAATT | 10393 |
rs189122602 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145036923 | ATCATAGTTTTCCCT[A/G]AAGGGTAGGGGAAGG | 10393 |
rs189125580 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145028165 | GGGTGTGCCTGTGTG[G/T]GTGTTGCCAAAAGAG | 10393 |
rs189127400 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145009501 | GGAACAGAACAGAGG[C/T]CTCAGAAATAATACC | 10393 |
rs189207717 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144970367 | ATAAAAACTCTCCTG[C/T]TAGATAAACTGGAAA | 10393 |
rs189277948 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145021947 | ATGATCAGGCAAATG[C/T]GAATTAAAATCACAA | 10393 |
rs189288280 | snp | C/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995023 | ATTACTCTAATGTAT[C/G]AACACTAATGAAATA | 10393 |
rs189310421 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145049070 | CACTCTACTGTAGTC[C/T]ATTAAGTGTGTAATA | 10393 |
rs189311822 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145017155 | GAGCTTCTGCACAGC[A/C]AAAGAAACTACCATC | 10393 |
rs189326693 | snp | C/G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144991007 | ATCAGAGTGGCTGTT[C/G/T]AGCAGCACCATGCTG | 10393 |
rs189332384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145086007 | TGGCTGAAGCTCACC[C/T]TTGCAGGGGGCAGAG | 10393 |
rs189349999 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145007812 | GCTAGCAGAAGGCAA[C/G]AAATAACTAAGATCA | 10393 |
rs189351647 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145060578 | TCATAATTTCTAGTG[A/G]AAAAAAAAGGAAAAT | 10393 |
rs189355148 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145031070 | AATGCCTTTTTCTCC[A/C]TTCCTGTCCATAAGG | 10393 |
rs189361431 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995286 | ATTAGATATAACGGA[C/T]GCCTTGTTCAATAAA | 10393 |
rs189369880 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144977366 | AAAATGTAGTTGTTA[G/T]TCCAGAGTCTCTTTC | 10393 |
rs189370102 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145012379 | TTTTCCAGTGTCTGA[C/T]AATCAGAAATGACTA | 10393 |
rs189402711 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145080193 | AGACATGGGTGCCTA[C/G]TTGAGGTGAAGGAAA | 10393 |
rs189568990 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145007374 | CTTATTCCAAAATTG[A/G]CCACATAGTTGGAAG | 10393 |
rs189583981 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144976345 | ATTTAATTCAGGATA[C/T]GGGTTAATCTTGGAG | 10393 |
rs189585945 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145009880 | TACCATCAGAGTGAA[A/C]AGGCAACCTACAAAA | 10393 |
rs189607464 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144980971 | TGGCTGTAGGTGTGC[A/G]GTCTTATTTCTGGGT | 10393 |
rs189654058 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145044042 | TCTTTCTCTCTTTCT[A/G]TGTTTCTTCCCAACA | 10393 |
rs189661019 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081000 | ATTCAGCCAGGCCCA[C/G]TGGTTCATGCCTGGA | 10393 |
rs189675270 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145049715 | CTCCCAAGTAGATGG[A/G]ACTACAGATGTGCAT | 10393 |
rs189693388 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145076713 | AATCTAAGGAATCCA[A/G]TAAAATGAATCAAGA | 10393 |
rs189707319 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144982453 | CTGATTTTCAGACAC[A/G]TTTGCTTCCTTCTAG | 10393 |
rs189759725 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145050447 | GAATAGTGAGGGCTG[A/C]CTTCAACTTGAAGTC | 10393 |
rs189774226 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145029027 | TGGCTGACCTGCAAC[A/G]AAAGATGCATGTACA | 10393 |
rs189780514 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145010181 | GGAAACCCCAGGTGC[C/T]GGAGGGGATGTGGAG | 10393 |
rs189790832 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144998822 | AAAAAATCAATGAAT[A/C]CAGGAGCTGGTTTTT | 10393 |
rs189841337 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145031210 | GACCTTGATCACTTT[C/T]CCCTTCCACAAGATA | 10393 |
rs189853502 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145028576 | AATATTAAGGATGGG[G/T]TTGTTTCATTGGTTT | 10393 |
rs189868220 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145003222 | ATGGCTGCACAGTAT[C/T]CCATTATGTGAAATT | 10393 |
rs189870055 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144998096 | CAAGTCCTTAGAGAT[A/C]TATAAAGAGACTTAG | 10393 |
rs189911759 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145088379 | ACAGTCAATTGCTTA[A/C]TAAACATTTCAACTA | 10393 |
rs189926020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145072876 | ATACACTGTGATTAA[A/G]CCTAGTATCTATTAC | 10393 |
rs189932680 | snp | A/C | 0 | 0 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145090252 | CCTAATATAATGTAA[A/C]TATGTAAAAAGTTGT | 10393 |
rs189933955 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145070602 | GGTGACTCAAAAACT[G/T]AAACATAGAATTACC | 10393 |
rs189941784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:145032857 | GAGGTTTGTCTTCAC[C/T]GGAATAGACACTTAC | 10393 |
rs189942172 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054790 | AATGAAGACTATAAG[A/T]GACCCCAGCCACTTG | 10393 |
rs189943524 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145068144 | CTGCCAGGCTCCTCT[C/T]ACACGAAGAGGTAGA | 10393 |
rs189960074 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145015090 | CAAACCAAAAAGAAA[C/T]CCCTGACTTACCTGA | 10393 |
rs190092050 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144997843 | GGAGACCCATCTCAC[A/G]TGCAGAGACACACAC | 10393 |
rs190109744 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145005323 | GTGGTTACATCCCTC[C/T]TGTCATTTCTGACTG | 10393 |
rs190110917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145012631 | GTAGAAAAATCTGAA[C/T]AGAATGACATTTATT | 10393 |
rs190117744 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144992075 | GCTCTGCCTGTGGAA[A/C]AACAAAGCCTGGATG | 10393 |
rs190125251 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144985263 | AGTAGAAGACTGGAA[A/G]GCCAAAATAATATGG | 10393 |
rs190159239 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145092337 | CTTAAAATTTAAATT[A/T]AAAAAAATCACCTCC | 10393 |
rs190175798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145084812 | ACACACTGGTTTGAA[A/G]ATTAGGACAAAATGT | 10393 |
rs190177337 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145076345 | AGCTGAGCCTTGGTA[C/T]CCTGAAATCATCCAG | 10393 |
rs190184055 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145052843 | CAGTGAGCCGAGATT[A/G]CACCACTGCACTCCT | 10393 |
rs190186140 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145057941 | CCTTAATTAAATCCT[C/T]GTAATTTTTACCTGG | 10393 |
rs190188161 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145039340 | ACTTCAATATAATCT[A/C]AATATGCTTTGTGGA | 10393 |
rs190192236 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145018757 | GGAGTGGAAAAAGGC[A/T]TTTCATGTAAATGGA | 10393 |
rs190234452 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145091827 | CAACACTGTAAACAC[A/G]TGGAGTACTATCCAG | 10393 |
rs190347633 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144984945 | AAATAACCTTAACTT[G/T]TCACATAAAATTGCC | 10393 |
rs190353695 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144968310 | ACATCATGCTTTACA[C/T]GGCTCAGTTTAGATT | 10393 |
rs190354123 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144980588 | TAGCAAAAATTTTCT[C/G]CCATTCTGTAGGTTG | 10393 |
rs190357898 | snp | C/G | 0.00195568 | 0.0312092 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995564 | GATTGTCAGTTAAGG[C/G]AACATGAATCCAGCC | 10393 |
rs190389184 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145045575 | CAACAACTTGAAGGA[C/G]ATTAATGAAGTAAAA | 10393 |
rs190447066 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145007942 | ATAGACCGCTAGCAA[C/G]ACTAATAAAGAAGAA | 10393 |
rs190474255 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145075972 | GGGGCCAGTCTGATC[C/T]GAGCAACACTTTGTC | 10393 |
rs190475409 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145077590 | AACCTCAGGCCAATA[C/T]TCTTGATGAACATCG | 10393 |
rs190592335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145000606 | CTGTTGGTGGGACTG[C/T]AAACTAGTTCAACCA | 10393 |
rs190647336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145061499 | CTTAGTACAAATAGG[C/T]TACGAAACTAGAAAA | 10393 |
rs190658701 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145022156 | CAATCTCAATACTGG[A/G]TATCTACCCAGAGTA | 10393 |
rs190682250 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145004988 | TTTTCCTGGTTGGTA[C/G]GCTTTTTATTACTGA | 10393 |
rs190683910 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145039863 | CTTCCCAAAGTGCTG[C/G]AATTACAGGCGTAAG | 10393 |
rs190685977 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145068636 | AAAAATGGGGGCCGG[A/G]TGCAGTGGCACACGC | 10393 |
rs190686310 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144991734 | TTAGTGTATTCTATG[A/C/T]GAGGTCCAAGACAAT | 10393 |
rs190697137 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144972312 | TAGCAAATAAAAGAA[A/T]GGAAAAAAACATAGC | 10393 |
rs190701625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145005912 | GTGCCACATGTAGAT[A/G]AGAAAAATGTATATT | 10393 |
rs190710647 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145095499 | AATCATCAACATCAT[A/C]GTGGCTTGATGATCC | 10393 |
rs190720822 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144973583 | CAATAAACCCACAAG[G/T]TTGTTCTTAGAAAAG | 10393 |
rs190849202 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145082363 | CATGTGGGTCAGGCC[A/G]GTCTCGAACTCCCAA | 10393 |
rs190861739 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145069148 | AACTAGAATACTGGA[G/T]AACATATCTGAAGCA | 10393 |
rs190880000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145029685 | AGCTGAAATATGGAT[C/T]AAAAAATGGCCCACT | 10393 |
rs190881938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145050912 | AGTAATAAGGCTGTA[C/T]TGCTTTCTTATTATT | 10393 |
rs190937556 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145023321 | AGTATAAGGATTTTT[A/G]TTATAAAATAACACA | 10393 |
rs190945892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081407 | AAATAAATTATATTG[A/G]AAAGTATATTTGAGA | 10393 |
rs190954525 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145019210 | AGGCCACAAAATGAG[C/T]TGTAATAAATTTAAG | 10393 |
rs190957568 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144995829 | AATAAAAATAGATGT[G/T]CTTCATGTTTACTGA | 10393 |
rs190963519 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144993256 | CCTGTACCAGCAGTG[C/T]GAAGTGCATTTTCTC | 10393 |
rs191018774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145058918 | GCCTAAAAATTATGT[A/G]TATCACACCAAAACA | 10393 |
rs191042966 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144979085 | GGTTTTCTTTGAATA[C/T]TAAATTATAAACTTT | 10393 |
rs191100120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145046200 | TAGGATAGACAGCGC[C/T]TTCTTGAAAATACTG | 10393 |
rs191100199 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145086927 | GTAAATATTCATGCT[C/T]CTCTCCCCACTCTCC | 10393 |
rs191108658 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145025587 | CATGGGCTTAAGTTC[A/G]TGGGGACCCATAACA | 10393 |
rs191117778 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145072021 | AACACAAAAAAAACA[A/C]AAAAAAACTAGGTAG | 10393 |
rs191125747 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145008530 | TGCAAGGCTGGTTCA[A/G]CATATGCAAATCAAT | 10393 |
rs191126044 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054347 | ATGAGGTCAGGAGAT[C/T]GAGACCATCCTGGCC | 10393 |
rs191130291 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144996286 | ATAAGCTGTCTACAG[A/T]CTGTAAAGAGACGTT | 10393 |
rs191183871 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145045992 | TTGCTTTATAAATTT[C/T]CAAACATAACTAATT | 10393 |
rs191189507 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145000127 | CTAGGTAATACCATT[C/T]AGGACATAGGCATGG | 10393 |
rs191195533 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144984477 | ATCTCTAGCCACAGA[C/T]GAATGCCAGCGTAAA | 10393 |
rs191200317 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145008198 | GGCAATAATTAATAG[C/G]TTACCAACCAAAACA | 10393 |
rs191213327 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144978828 | AAAAATAGACAGGAA[A/T]AAAAGAATAAAAAAT | 10393 |
rs191239272 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145051573 | AGGTGAAAAGCATAA[A/C]ATGAGGTAGGCCTGT | 10393 |
rs191245449 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145070232 | ACTAAGTGACACTCC[G/T]TCATATACACATTGT | 10393 |
rs191256987 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145078922 | CTACAACTATAAAAA[C/T]CCAGGTAGAAAACCT | 10393 |
rs191269776 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145051718 | CAGCCACATAGTTAT[C/T]ATTGCATACAGTTAT | 10393 |
rs191272791 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145030827 | GGTTGCAAAGATTAG[C/T]GCCACCATCAAGGAC | 10393 |
rs191276483 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145011484 | TTTATAGGTATCAGA[A/G]ACAAGCAAAAAGCAA | 10393 |
rs191329692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145083011 | ATACAAGCAGTCATA[C/T]ATGTATTCTTTCTAT | 10393 |
rs191440451 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144972620 | AGAGTTTCATACAAC[C/T]TTCTTATTAACCGAT | 10393 |
rs191444185 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144987705 | GGAAGTAAACTTACA[C/T]CTCCTCTACACTCTC | 10393 |
rs191447901 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144978231 | CTTACATTGAGTATG[A/T]GTAAATGTCTCTGTG | 10393 |
rs191450557 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144969042 | ACACATACACGTACA[A/C/T]ACATGCATACGTATA | 10393 |
rs191475178 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145095389 | GTCCAGCACATCCAC[A/C]ACTTTGTCCAGCACA | 10393 |
rs191477788 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145069501 | CCAAACAATTTCCAG[C/T]GGGCACAGAGGACTG | 10393 |
rs191495358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:145032556 | TGGATAGGATGACCC[A/G]TTCTGTGGACACCAC | 10393 |
rs191510417 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145003080 | TCCATGTGTATTCAA[G/T]GTTTAGCTCCCACTT | 10393 |
rs191572324 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145072431 | TATGTGAAGAAAAAA[C/T]ATCTAAGGAACCAAA | 10393 |
rs191667386 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145090959 | AAATATCTGACCCTA[A/G]AGAAGCAAAGATCGA | 10393 |
rs191737617 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054505 | AGAGCTTGCAGTGAG[C/T]GAGATCGCGCCACTG | 10393 |
rs191748015 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145057607 | CTTCTTTCCTTAGGT[A/T]CAGATCCATATACCA | 10393 |
rs191754880 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144999028 | TACAAGAAATGGATA[A/C]ATTCCTGGACAAATA | 10393 |
rs191757121 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145018126 | GTATAATAAAAAAAA[A/T]ATATATATATATAAA | 10393 |
rs191778590 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144983604 | AAAGTGACAAAATTA[C/T]AGGCCATCAGATGCT | 10393 |
rs191827005 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145020974 | AAATGGAAACACATC[C/T]CATGTTCATGGAATG | 10393 |
rs191833310 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145007290 | ATGCACCAAGCAGAC[A/C]TAATAGACATCCATA | 10393 |
rs191850557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145087142 | TCACAGCCTAAAGCC[A/G]AGCCATCACCAAAGC | 10393 |
rs191878636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145094918 | CCAAGAATTCTATCC[C/T]AACAAAGAGTAAAAG | 10393 |
rs191886788 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145059957 | TTAAGAATTTAAAAA[C/G]TACCATCTTGATTTG | 10393 |
rs191886953 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145077131 | GTGAAACCGGGAGGC[A/G]GAGCTTGCAGTGAGC | 10393 |
rs191892268 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145042860 | AATGGAATTTCAATA[A/C]CCTAACTGCTTATTT | 10393 |
rs191967006 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145014186 | CGGAGGTGGGTACCA[C/T]GGGGCAAGTTCTCAG | 10393 |
rs191982708 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144986141 | ATGTGTGGCTGGATT[C/T]GGTTTGCCAGTATTT | 10393 |
rs192010848 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145079083 | AAAAGAAACTATTAA[C/T]GGAGTAAACAGACAA | 10393 |
rs192046040 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145010844 | ATAAATAAATAAATC[A/C/G]CTTGATCTTTAACCA | 10393 |
rs192053297 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145037999 | AAGATACATGGACAC[C/T]AACCTACCTTTTAAA | 10393 |
rs192060986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144989267 | TAAGCAAGTCTATCA[A/G]TGCTATTTTTCCAAC | 10393 |
rs192061103 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145025727 | GTGACATAAAATGAG[A/C]ACATGCTGCTGGAAA | 10393 |
rs192063336 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145008683 | AGGAATTGATGGGAC[A/G]TATCTCAAAATAATA | 10393 |
rs192063846 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144982977 | CATCCTGGCTAACAC[A/G]GTGAAACCCCGTCTC | 10393 |
rs192073093 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144970480 | CAACTGAAAACCGGA[A/C]TGGCACATGAGTAGT | 10393 |
rs192126993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | ABCE1, ANAPC10 | GRCh38.p7 | 4:145098432 | CAGGTACGTGAATAG[C/T]CCGGAGAGGTTTGGC | 10393 |
rs192133104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145066320 | GGCCAAAGGTATCAA[A/G]CTGACATCTTTCTCT | 10393 |
rs192139109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145016323 | CATTCTTATACACCA[A/G]TAACAAACAAACAGA | 10393 |
rs192141357 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145079540 | TGGGTATATATCCAA[A/G]GGGATTTAAATCATT | 10393 |
rs192154375 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145004040 | TTTGAGTAGTATCTT[G/T]TAATTCTCATTTCCC | 10393 |
rs192154548 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145046448 | GCACAAACAATTTCA[A/T]GAACAGAGAACAAAA | 10393 |
rs192287533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145044326 | AAGATACAGAACAAG[A/G]GTAAAAAAATGAAAA | 10393 |
rs192305503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145052793 | CTCGGGAGGCTGAGA[C/T]AGGAGAAGCGCTTGA | 10393 |
rs192308067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144993310 | TAATCATTTTCACTG[C/T]AGTCATTCTAGTGGC | 10393 |
rs192309021 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145001968 | GTCAAATATTAAGTA[C/T]AAAACTGTTTACATG | 10393 |
rs192314392 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144975059 | GATGATTGGAGCTTC[A/C]TACTCGGTTCAAACA | 10393 |
rs192325128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144967477 | TGCTTTAAGAATTTG[C/T]GAAAAAATGGGCATG | 10393 |
rs192366064 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145077345 | AGAAACAACAAGCAA[A/G]CTGGAAAATATATTT | 10393 |
rs192367652 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | ANAPC10 | GRCh38.p7 | 4:145063816 | CACATTCAACTACGT[A/G]GACAAATCTCAAAAA | 10393 |
rs192377737 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145084325 | TAGAATGGTAAGATT[C/G]AGGGGCATTCAGCAA | 10393 |
rs192381092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145020527 | AACTGGAACAAAACA[A/G]GGATGCCCACTCTCA | 10393 |
rs192385194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145007036 | CATCTCCTGGGAGGC[A/G]CGGGTCCCAAGATGG | 10393 |
rs192396250 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145070443 | AGCACAAAACATTAG[A/G]GAAATGAAAATCAAA | 10393 |
rs192399207 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145031906 | TATCATGAACTGGGC[A/G]CTTTCTGACCCATCT | 10393 |
rs192449223 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, intron-variant, missense | ABCE1, ANAPC10 | GRCh38.p7 | 4:145098221 | AGCTCAATGACGTCA[C/T]ATCTCCCTACCTACC | 10393 |
rs192535849 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145066463 | AGAGATCAAAGATCA[C/T]GAAGATGGCTCTTAA | 10393 |
rs192546799 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145026079 | CTCTTGCTCAGCTAC[A/G]AGAACACTGACTCCT | 10393 |
rs192554294 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145009270 | GCCCAAGGTAATTTA[C/T]AGATTCAATGTCATC | 10393 |
rs192558633 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144997412 | AACTCTACAAGCCAG[A/C]AGAGAGTGGGGGCCA | 10393 |
rs192562120 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144997133 | TACCTGAAAGTGACG[C/G]CCAGAATGGAACCAA | 10393 |
rs192571209 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144979914 | CCGCTTCCCCTTCCT[C/G]TTCACTTTCTTTTAC | 10393 |
rs192622384 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145067051 | ATAATTTGCTATATA[C/T]ATAGTTTCATTAAAT | 10393 |
rs192633263 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145049145 | TTTTACTGCTAAAAA[C/T]TGCTAACAATCCCCT | 10393 |
rs192637819 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145089362 | AGATGTTCACAAAAT[A/G]CAGCCATACTGAATC | 10393 |
rs192647870 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145073164 | CTCCCAAAGTGTTGG[A/G]ATTATAGGCGTGAGC | 10393 |
rs192676984 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145060746 | TCATAAAAATTCACA[C/T]TATTTTAATAACTTG | 10393 |
rs192698924 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145083738 | TTTTTAACGTTGTTG[C/T]TAGATAATTTTAAAT | 10393 |
rs192740121 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144994806 | ATTCCGTGAAGGTGA[A/G]TATGAGACAATTAAT | 10393 |
rs192745215 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145011073 | GCAGTGGCTCACGTC[A/T]GTAATCCCAGCACTT | 10393 |
rs192824447 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145048475 | GGTTCTGACACAGTA[C/T]AGAGATTCTTCTACT | 10393 |
rs192827859 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145008933 | ATGATTATATATTTA[A/G]AAAACCCCACTGTCT | 10393 |
rs192837953 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144979897 | CTAGCTCATTACAGA[A/C]ACCGCTTCCCCTTCC | 10393 |
rs192859789 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145079924 | TTTGAGACCAGCCTG[A/G]CCAACATGGTGAAAC | 10393 |
rs192867242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144979657 | AAATGGTATTTATGC[C/T]TCTAGGTCTTTGAGG | 10393 |
rs192881028 | snp | G/T | 0 | 0 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145074613 | ACAAAAAAAGCATGC[G/T]AAACATTCAGCAAGT | 10393 |
rs192892504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145035656 | TGATTCCAGTTCATC[C/T]TCATGGGTTCCAGCC | 10393 |
rs192949797 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145029999 | TTGAATCCCAAGGTG[C/G]CAGGCGCTAAGTGGC | 10393 |
rs192952691 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144975342 | TCATGATGTTCAGGT[G/T]GAAAACAATTTTTTA | 10393 |
rs192955075 | snp | C/T | | | intron-variant, splice-acceptor-variant | ANAPC10 | GRCh38.p7 | 4:144999295 | TCCTGATACCAAAGC[C/T]TGGCAGAGACACAAC | 10393 |
rs193006390 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145031124 | AGCTAGCAAGGCCAG[C/T]AATTTACCTTACTGT | 10393 |
rs193013425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145059427 | AAGCCTCCTTTTAAA[A/G]AAAATCACTTGGTAA | 10393 |
rs193014902 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145000680 | AAATACTATTTGACC[C/G]AGCATTCCCATTACT | 10393 |
rs193046943 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145093679 | ACAAATAAAAAATAT[A/G]ATATCACAGATGAAA | 10393 |
rs193070215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144996537 | ACCACACTCCCCACA[A/G]CTTCTTGTCCATGCT | 10393 |
rs193088929 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145089879 | CATCCTCCACACTTC[C/G/T]CAAATATGAACAAAC | 10393 |
rs193114899 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145015225 | AGATATTCAAGGAAA[C/T]AGATAGCATAAAGAA | 10393 |
rs193119805 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144988580 | ACAATAAGTTATTTT[A/T]AAAATCAGTTCTGTT | 10393 |
rs193131422 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145080412 | GATAAAATTTAATTA[C/G]AACAGCTAAATTCTG | 10393 |
rs193136060 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054896 | TCTTCCCGTATCTTA[C/T]AGTTGTACTCTTCTA | 10393 |
rs193204769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145076968 | ACTTTGGGAGGCCAA[C/T]GCGGGTGGATCACGA | 10393 |
rs193207675 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145012472 | AATTAGAATACACTT[C/T]TAATAAAAATTCTAC | 10393 |
rs193212714 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144985188 | GCAGCTTCCTTGTAG[A/C]AGACTGGTAAACAGC | 10393 |
rs193268855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145033758 | AAGGGAATACAGAAC[A/G]GGTAGTAGAAGAAGG | 10393 |
rs193271381 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145003614 | TCCTTCCCCCATTGC[C/T]TGTTTTTGTCGACTT | 10393 |
rs193276241 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144969637 | TTTTCAACAGGCATG[A/G]GAGAAAAGAGAGTCT | 10393 |
rs199509337 | in-del | -/A | 0.0437281 | 0.141251 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145078431 | GAATCAATATTGTTT[-/A]AAAAAAAAATGGTCA | 10393 |
rs199567889 | in-del | -/GATAGATAGATA | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144980531 | ATAGATAGATAGATC[-/GATAGATAGATA]GATAGATAGATAGAT | 10393 |
rs199570289 | snp | A/G | 0.00199792 | 0.0315431 | missense, intron-variant | ANAPC10 | GRCh38.p7 | 4:145096003 | GTTTGCAAGATGAGA[A/G]TGACCAAACAGCTTG | 10393 |
rs199591692 | in-del | -/A | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144987646 | AACTTAAAGTATAAT[-/A]AAAAAAAATGTCTTC | 10393 |
rs199615804 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145045990 | TTTTGCTTTATAAAT[A/T]TTCAAACATAACTAA | 10393 |
rs199639427 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145026941 | TATATATATATATAT[A/G]TATATGTGTGTGTGT | 10393 |
rs199643136 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145004679 | TTGAACCAACTTTGT[A/T]TTCCAGGGATGAAGC | 10393 |
rs199651500 | snp | C/T | 0.000338829 | 0.0130115 | utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995336 | AAATACAGGATAAAA[C/T]AAAGATACGTTTAAT | 10393 |
rs199666053 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145090185 | GCACAAGTCCCTTAT[C/T]TAAAATGGCTCCTCT | 10393 |
rs199671091 | snp | A/C/G | 1.65767e-05 | 0.00287891 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995540 | TGAATGTACGAGTTG[A/C/G]CTTCTTATGATTGTC | 10393 |
rs199728554 | in-del | -/AACAT | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081448 | TAAAAGGAACTATGC[-/AACAT]ACCATAAGAAAATTC | 10393 |
rs199734599 | in-del | -/AA | 0.164741 | 0.235012 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145007869 | CAAAAAAAACCCTTC[-/AA]AAAAAAAAAAATCAA | 10393 |
rs199775794 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145016060 | TTTGAAAACTGGCAC[A/G]AGACAGGGATGCCCT | 10393 |
rs199788158 | snp | A/C | 0.0014571 | 0.0269523 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995514 | ATTGGCTAGAACAGC[A/C]ATCTGTATCATGAAT | 10393 |
rs199807447 | in-del | -/G | 0.0115144 | 0.0749975 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145091875 | ATAATGTCCTTTGCA[-/G]GGACTTGGACAAAAG | 10393 |
rs199933816 | in-del | -/ATAG | 0.0150606 | 0.0854603 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144980512 | GATATTAGACCTTTC[-/ATAG]ATAGATAGATAGATC | 10393 |
rs199948892 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145092947 | GAAAACTCTTTACCA[A/C]AAAAGACCAGCCACA | 10393 |
rs199977910 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145011240 | TACTCAGGAGGCTGA[A/G]GCAGGAGAATTGCTT | 10393 |
rs200088692 | in-del | -/A | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145055565 | ACTGTCTCAATAAAT[-/A]AAAAAAAAATTAAAT | 10393 |
rs200114650 | snp | A/G | 8.27986e-05 | 0.0064337 | upstream-variant-2KB, missense, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145096033 | GTGACCCAATTTCCC[A/G]TACTGTTCCAGTCCT | 10393 |
rs200128698 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145019061 | CAGAAAGTCAACAAA[G/T]AAACAATGGATTTAA | 10393 |
rs200158028 | in-del | -/AAAC | 0.030665 | 0.119967 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145043279 | ATTATTTTGACTAAA[-/AAAC]AATTCTAATTATAGA | 10393 |
rs200201430 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145016575 | GATTCAATGCCATCC[A/C]CATCAAGCTACCAAT | 10393 |
rs200203924 | in-del | -/A | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145018479 | CTCTACTAAAAATAC[-/A]AAAAAAAAATAAGCC | 10393 |
rs200209460 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144998875 | AGACCGCTAGCAACA[C/T]TAATAAAGAAGAAAA | 10393 |
rs200248505 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145011873 | GGAGGGAAGCACTAG[A/G]GTTTAGAACTTGCCA | 10393 |
rs200295830 | snp | A/G | 3.31378e-05 | 0.00407036 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995496 | GTCTCTTCCATTCTG[A/G]TGATTGGCTAGAACA | 10393 |
rs200306281 | in-del | -/A | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145085552 | TTGTTCTTAAAATGC[-/A]AAAAAAAAAATTAAA | 10393 |
rs200372164 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145012164 | ACAAGCTATATGTAT[A/G]TGTGTGTGTGTGTAT | 10393 |
rs200373978 | in-del | -/AC | 0.0352966 | 0.128072 | utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995066 | TATAATTGTGTATAT[-/AC]ACTGAAATTTTCAGT | 10393 |
rs200378004 | in-del | -/A | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145071999 | GAAATGTGAAAGGAC[-/A]AAAAAAAACACAAAA | 10393 |
rs200457388 | in-del | -/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144984061 | CTAAAAATTTCAAGA[-/C]AGAAATAAATTTTGT | 10393 |
rs200486982 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144997216 | AGGCAGGCCAACATT[C/T]AAATTCAGGAAATAC | 10393 |
rs200552388 | in-del | -/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145087358 | TTTGCTAAGGGGCTG[-/T]TTTTTTCTTTTTTTT | 10393 |
rs200563461 | in-del | -/TGTA | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145037037 | GTGTGTGTGTGTGTG[-/TGTA]TGTGTGTGCATGCAT | 10393 |
rs200738760 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145018308 | GGCCTAAATGCTCCA[C/T]TTAAAAGATGCAGTA | 10393 |
rs200740929 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145090972 | TAGAGAAGCAAAGAT[C/T]GAGCAATCACTTTCT | 10393 |
rs200819764 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145018073 | GTATACATATGTAAC[A/T]AACCTGCACGTTGTG | 10393 |
rs200888562 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144971180 | CATAAAAATAAAAAA[G/T]GGAGAGCCACTGTTA | 10393 |
rs200919705 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145005576 | AATTGAGATCTTTCT[A/G]ACTTTTTGATGTGGG | 10393 |
rs200924236 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144982514 | CAATGAGACATAAGA[A/C]GTATGCTGAATATTT | 10393 |
rs200962707 | snp | C/T | 0.00199806 | 0.0315443 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995394 | TATTGAACGATACAT[C/T]ATGAAATCTATAGTT | 10393 |
rs200996035 | in-del | -/ATTT | 0.00795532 | 0.062565 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081606 | ATGTTAATAAAATAG[-/ATTT]ATTTGTCTATAACCT | 10393 |
rs201017904 | in-del | -/A | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145018652 | AAAATCTCGAAATCT[-/A]AAAAAAAAAAAAAAA | 10393 |
rs201034162 | snp | C/T | 0.029116 | 0.117091 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054646 | GTGTGTGTGTGCGCG[C/T]GCGCGCGCGTGCGTG | 10393 |
rs201053830 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145072929 | AGGAGACAGGGTCTC[G/T]CTCTGTCACCCAGGC | 10393 |
rs201054817 | in-del | -/A | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145072019 | AAACACAAAAAAAAC[-/A]AAAAAAAAACTAGGT | 10393 |
rs201073598 | snp | A/C/T | 0.000266478 | 0.01154 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081800 | AAAAAGAAACAACTA[A/C/T]ACATGCAAAACATAA | 10393 |
rs201134151 | in-del | -/A | 0.00478085 | 0.0486577 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145023218 | CATCTATGCAAAGTG[-/A]AAAAAAAACCAACAA | 10393 |
rs201246162 | snp | C/T | 0.00199792 | 0.0315431 | missense, nc-transcript-variant | ANAPC10 | GRCh38.p7 | 4:145081708 | CCATCTGATTGCCAA[C/T]AAGTTTCTAGATTGT | 10393 |
rs201262683 | in-del | -/GTGTGTGTGT | 0.345925 | 0.230864 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054605 | GGGACATACTGAATA[-/GTGTGTGTGT]GTGTGTGTGTGTGTG | 10393 |
rs201284772 | snp | A/C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144984062 | TAAAAATTTCAAGAC[A/C/G]GAAATAAATTTTGTT | 10393 |
rs201292137 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145084285 | TGCATTGAATTTCAA[A/C]TTACTAGTTAGCTAG | 10393 |
rs201301796 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145041279 | CAAATTTTATTTTAC[A/G]TGAATTTTTAAAATA | 10393 |
rs201315122 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144980534 | GATAGATAGATCGAT[A/C]GATAGATAGATAGAT | 10393 |
rs201317623 | in-del | -/A | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144978817 | TCTCCAAAAAAAAAA[-/A]TAGACAGGAAAAAAA | 10393 |
rs201412996 | in-del | -/CC | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054683 | ATGTGTGTGTGTGTG[-/CC]TGTGTGTGTGCCTGT | 10393 |
rs201493778 | in-del | -/AT | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145012175 | TATATGTGTGTGTGT[-/AT]GTATATATATATATA | 10393 |
rs201506564 | snp | G/T | | | intron-variant, utr-variant-3-prime | ANAPC10 | GRCh38.p7 | 4:145063639 | GACCAAAAAATGTCA[G/T]CAGCCACAGCTTCAC | 10393 |
rs201518162 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant, downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:145032577 | TGGACACCACACAAC[C/G]TCTTTCCCCAGCCAC | 10393 |
rs201522548 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145017329 | TGAACAGACACTTCT[C/T]AAAAGAAGACATTTA | 10393 |
rs201553695 | in-del | -/A | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081227 | TTAAAGGTTCTAAGT[-/A]AAAAAAAAAAAAAAA | 10393 |
rs201572407 | in-del | -/A | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145072010 | GGACAAAAAAAACAC[-/A]AAAAAAAACAAAAAA | 10393 |
rs201579388 | in-del | -/A | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145089308 | TAACTCAATGTCTTC[-/A]AAAAAAAAACAGGGA | 10393 |
rs201645751 | in-del | -/TG | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145012165 | CAAGCTATATGTATA[-/TG]TGTGTGTGTGTATAT | 10393 |
rs201693751 | in-del | -/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144993086 | GGTATACATACATTG[-/T]TTTTTTTTTAGACTA | 10393 |
rs201700839 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145022506 | CAATGGACTTTGGGG[A/T]CTTGGGGGAAAGTGG | 10393 |
rs201702086 | snp | A/G | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | ABCE1, ANAPC10 | GRCh38.p7 | 4:145097547 | CTTTAATCGGCACAC[A/G]AGCACTTGATACTTA | 10393 |
rs201733381 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145043840 | TTCCAGATAAAATTC[-/T]TTTTTTTTCCCTTTG | 10393 |
rs201752128 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145018586 | GAGTTTGCAGTGAGC[C/T]GAGATCGTGCCATTG | 10393 |
rs201780921 | snp | G/T | | | utr-variant-5-prime, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145098311 | GTGCGGCGGCTGGGC[G/T]CCGCCATTTTGGCCG | 10393 |
rs201782585 | in-del | -/CTT | 0.0352966 | 0.128072 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145028338 | CTCCCATGATGGATG[-/CTT]CCTGCCTTCGAACAT | 10393 |
rs201846338 | in-del | -/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145067049 | GTATAATTTGCTATA[-/T]ACATAGTTTCATTAA | 10393 |
rs201853860 | snp | A/G | | | synonymous-codon, utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995561 | TATGATTGTCAGTTA[A/G]GGGAACATGAATCCA | 10393 |
rs201865251 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145057899 | CCTTTTAATTTATTT[G/T]AAATATAGGGAACCC | 10393 |
rs201900885 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145008707 | AATAATAAGAGCTAT[C/T]TATGACAAACCCACA | 10393 |
rs201935464 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145019903 | AGAATTAGATACCCT[A/G]AACAGACCAATAACA | 10393 |
rs201988495 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145040135 | TGTGTGTGTATGTGT[A/G]TGTGTGTGTGTGTGT | 10393 |
rs201990708 | in-del | -/A | 0.0174175 | 0.0916809 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145085254 | GTGCGAGAAACGGAC[-/A]AAAAAAATAAAAATA | 10393 |
rs202023299 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145080139 | AAAAAAAAAAAAAAA[G/T]ACACATTGAATACAC | 10393 |
rs202052896 | in-del | -/A | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145042927 | TGTCTAAAAAAAAAA[-/A]CAAAATAAAGTGTTT | 10393 |
rs202100756 | in-del | -/GTGTGTGTGTGT | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145036996 | TACCAAATAGATAAC[-/GTGTGTGTGTGT]GTGTGTGTGTGTGTG | 10393 |
rs202196239 | snp | A/C | 0.00199802 | 0.0315439 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995464 | GGTGTGTATATTTTA[A/C]TTTGTCTCATATGGG | 10393 |
rs202235812 | snp | C/T | | | intron-variant, utr-variant-3-prime | ANAPC10 | GRCh38.p7 | 4:145063472 | CTAACTCAGATTAAA[C/T]ATAAATTTAGAGACA | 10393 |
rs207465152 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145024288 | CTCTTGTTAATGTTC[A/G]TATTTTGACCTTCTC | 10393 |
rs367570508 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145053809 | AAGGTTCCTGACTAG[A/G]CTCACCTCTATTAAG | 10393 |
rs367578686 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145071296 | CTGTAATCCCAGCTA[C/G]TTGGGAGGCTGAGGC | 10393 |
rs367579546 | snp | C/T | | | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145098757 | CTGGAGAGGAAGGCA[C/T]CTTTAGAACTTACAG | 10393 |
rs367580450 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145016324 | ATTCTTATACACCAA[C/T]AACAAACAAACAGAG | 10393 |
rs367589449 | snp | G/T | | | intron-variant, downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:145033034 | CTCATGGAATTCACT[G/T]GTCTTACCATGTTCC | 10393 |
rs367601165 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144998569 | GTTCTTTGAAACTAA[C/T]GAGAACAAAGACACA | 10393 |
rs367675019 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145053937 | TTTTTTTAGATGAAG[C/T]CTCTCTCTGTCACCA | 10393 |
rs367716697 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145071641 | CAAGAAACTGGGAAA[A/G]GGGAACTTTATAACC | 10393 |
rs367804171 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145026418 | ATAAAAAGTGCATGG[C/G]AAAAAAACAGAGCAG | 10393 |
rs367816175 | in-del | -/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144991396 | GCATTTTTTTTTTTT[-/T]GAGACGAGTCTCATT | 10393 |
rs367819066 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145080071 | GTGAACAGAGATCAC[A/G]CCACTGCGCTCCAGC | 10393 |
rs367832245 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145091687 | CTTTGTAAAATAATA[A/G]TTTATATTCTTTTGG | 10393 |
rs367836208 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145047343 | TGAAACAGACTGGGT[A/T]TTTCCGTCTGTAAGC | 10393 |
rs367836889 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145022981 | TGCACCCATTAACTC[A/G]TCATTTACATTAGGT | 10393 |
rs367846593 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145059933 | ACATAATGCTAAAAC[A/G]CAAGGGATTTAAGAA | 10393 |
rs367933408 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144999457 | ACAAAGAAAATAAAA[C/T]ACCTAGGAATACAAC | 10393 |
rs367961757 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145015060 | AAAATCATATTGGCT[C/G/T]ACCAGCAGTGGATCC | 10393 |
rs367990392 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145085232 | ACTGCACTCTAGCCT[A/G]GGCAACAGTGCGAGA | 10393 |
rs368046550 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145041539 | TGGCAATCAAGAAAC[A/T]CAGACATCGTAGGCC | 10393 |
rs368050164 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144967345 | GTCAAGGAACAAGAT[A/G]AAACATGAAAATAAC | 10393 |
rs368130181 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145036174 | AATAATGAAAACATG[C/T]ATAATGATTTCAGCA | 10393 |
rs368177513 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145025646 | ATCACAGATGACCGT[A/C]ACAGGTATAATATTG | 10393 |
rs368211942 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145045728 | ATACACACATACTCA[C/T]CTAAAATGTCACACG | 10393 |
rs368237464 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145079578 | AAGACAAATGCACAC[A/G]TATGTTGATTGCAGC | 10393 |
rs368246155 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145006276 | TATAGCAACCCAGAC[-/T]TTTTATCTGAAAAAT | 10393 |
rs368265818 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145042654 | AGAATCCCTCACAAA[C/T]TGAAAAATATAAGAA | 10393 |
rs368364068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145090244 | TTATAATACCTAATA[C/T]AATGTAAATATGTAA | 10393 |
rs368373832 | snp | A/G | | | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145100133 | TTTCTTAAATGCATT[A/G]CAATTTATCACTATT | 10393 |
rs368383718 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145072825 | CAATGAATATCTAGT[C/T]GAGTCTAATGATTTC | 10393 |
rs368387716 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144998895 | AAAGAAGAAAAGAGA[A/T]AAGAAGCAAATAGAC | 10393 |
rs368475195 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145041202 | TAGCTAAATCTAGAA[C/T]ATCTGTCTAACAATA | 10393 |
rs368479547 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145078311 | CACCTGGGAATACAG[C/T]TAACCAAGGAGGCAA | 10393 |
rs368483351 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144977833 | GAGTAAAATTATCTA[A/C]TATGAAAGTATGGAA | 10393 |
rs368493676 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144971922 | TCCCTACCTTTATTG[G/T]CTCTAGTGCTTGCTG | 10393 |
rs368583128 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145023872 | TGACTCTTCCTTTCA[C/T]GGAAAATTCATCTGT | 10393 |
rs368631389 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145026961 | TGTGTGTGTGTGTAT[A/G]TATATATATATATAT | 10393 |
rs368642867 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145018593 | CAGTGAGCCGAGATC[A/G]TGCCATTGCACTCAG | 10393 |
rs368681385 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145013623 | GGATGAACAGAGCAG[C/G]ATGTGGAGGCTCATA | 10393 |
rs368685820 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145091381 | ATCTCATTACTGACA[C/T]AATATGGCACCAGTC | 10393 |
rs368724329 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145019741 | AACCTCAATAAGAAA[A/T]GAAACAGGAGACATT | 10393 |
rs368742261 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145085917 | CGCCCAGGCTGCAGT[G/T]CAGTGGCGCGATTTC | 10393 |
rs368783750 | in-del | -/GATTT | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145053873 | AGGTAGTTTCAGCAA[-/GATTT]ACTGCAGCACTTTCA | 10393 |
rs368787590 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145088506 | ACTCAGGAAACAGTA[C/T]GAGTTGTTCTGCCAG | 10393 |
rs368815187 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144999961 | ATGGGGAAAGGATTC[C/T]CTATTTAATAAATGG | 10393 |
rs368854191 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145018238 | TATACAGGCAACAAA[C/T]AGCATGATGAATGGA | 10393 |
rs368882031 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144978685 | AATTATGTGGTCATG[G/T]TGGTTTGCACCTGTA | 10393 |
rs368971108 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145077153 | GCAGTGAGCCGAGAT[A/C]GTGCCACTGCACTCC | 10393 |
rs368979908 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144987766 | AATTTCTGGCTTGAT[G/T]GGTTAGAGACCTATT | 10393 |
rs369071567 | in-del | -/TAAAG | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144975723 | ACTTTTATAAATCAA[-/TAAAG]TAAAGACTTTTAAAA | 10393 |
rs369097251 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145065310 | AAAAAATGCAAGTGG[A/C]CAACAAAACATGAAA | 10393 |
rs369129534 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145079862 | CTCACACGTATAATC[C/T]CAGCACTTTGGGAGG | 10393 |
rs369185241 | in-del | -/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145018123 | GAGTATAATAAAAAA[-/T]AATATATATATATAT | 10393 |
rs369237421 | in-del | -/C | | | intron-variant, utr-variant-3-prime | ANAPC10 | GRCh38.p7 | 4:145063639 | ACCAAAAAATGTCAA[-/C]CAGCCACAGCTTCAC | 10393 |
rs369258627 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145087738 | TAGATTATAATATGA[A/T]GTATTAGTACAACAA | 10393 |
rs369263028 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144969605 | ATAGACTGGATCTTG[C/T]TGTCAGTCGTGTGAT | 10393 |
rs369267412 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145027096 | GCAACCTCTGCCACC[C/T]GGGTTCAAGCAATTC | 10393 |
rs369273194 | snp | A/C | 4.96833e-05 | 0.00498389 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145095936 | GATGCCTGTACAAGG[A/C]AACTGCAAGTGACTA | 10393 |
rs369278822 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144985738 | CAAATTAATTGTTGT[A/T]ACTCACATAAAAACA | 10393 |
rs369412881 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145093713 | TTCTTAGGCAGAATT[A/G]TCAGTATATTCAATA | 10393 |
rs369425590 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145062327 | TCTTAAAAGTAAGGG[C/T]TGGGCATGGTGGCTC | 10393 |
rs369440678 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime, intron-variant | ANAPC10 | GRCh38.p7 | 4:144994255 | AATAATACAATTCTT[C/T]CCAGAACTTACAGGA | 10393 |
rs369443296 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145025472 | TTGTTGTGTCTCAAC[A/C]AATAAGGAGGCCCAA | 10393 |
rs369523731 | snp | C/T | 1.68425e-05 | 0.00290189 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145064719 | AAAGTAAAAATAACA[C/T]GCACTTCATCATATG | 10393 |
rs369557836 | snp | A/G | | | intron-variant, utr-variant-3-prime | ANAPC10 | GRCh38.p7 | 4:145063843 | AAAACCCTAGGCTGA[A/G]TGAAAGAAGCCATAC | 10393 |
rs369567656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144990494 | CTGTACAGGAAGCTG[A/G]TGCCAGCATCTGCTT | 10393 |
rs369625686 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145049394 | AGTTCTTTTAAAATT[G/T]GAGTCAGTCTTCTTT | 10393 |
rs369637473 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145001686 | CATCACTCAATATTC[G/T]TTCGTTGATATCAGC | 10393 |
rs369648056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144968311 | CATCATGCTTTACAC[A/G]GCTCAGTTTAGATTA | 10393 |
rs369676390 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144980623 | TTCACTCTGATGATC[A/G]TTTCTTTTGCTGTGC | 10393 |
rs369686595 | in-del | -/AAAAT/AAAATAAAAT | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145011336 | ATGAGACTGTCTTAA[-/AAAAT/AAAATAAAAT]AAAATAAAATAAAAT | 10393 |
rs369716788 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145055999 | CTTTGAAGCAAACTA[C/T]ACAAGCATGGGTCAA | 10393 |
rs369719785 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144984152 | ATTAGTTGCTGAATG[C/T]TACTCTAAAAAAAAT | 10393 |
rs369778610 | snp | C/T | 0.000169986 | 0.00921758 | missense, intron-variant | ANAPC10 | GRCh38.p7 | 4:145064588 | CGAATTTCTTGAAGG[C/T]TGTGAAAATTATTTC | 10393 |
rs369818220 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145065881 | AAATTAACTGTTTTC[A/G]TGGGATGGGACCATA | 10393 |
rs369831396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145028700 | TGTAAACTGTTTAGA[A/G]AGTTATGCAAAATAA | 10393 |
rs369864520 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145022365 | TAACGGCATTCGCAG[C/T]GACCTGGATGAGATC | 10393 |
rs369896986 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145086800 | CAGTAATCACAACAA[A/T]CAAAAATATCTCCAG | 10393 |
rs369903661 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145048335 | AAATATGCCATAATA[C/T]GACAAAATAAATAAC | 10393 |
rs369904183 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145017037 | AAGAAAACCTAGGCA[A/T]TACCATTCAGGACAT | 10393 |
rs369921129 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145007934 | CAAAATTGATAGACC[A/G]CTAGCAAGACTAATA | 10393 |
rs369942751 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145095767 | ATTATTAATTATTGT[C/T]AATCTCTTACTGTGC | 10393 |
rs369951164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145028637 | ATTAGACCCAAAACT[A/G]CTAAGGACTCTACTT | 10393 |
rs369985701 | in-del | -/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145082391 | AACTTCAAGTGATCC[-/C]AGCCGCCTCAGCTTC | 10393 |
rs370113295 | in-del | -/TA/TATATA | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145034523 | TAACAAACTCTCCTT[-/TA/TATATA]TATATATATATATAT | 10393 |
rs370126263 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145066716 | AATGCTCTATACATA[C/T]TGTCTCATTTATTTC | 10393 |
rs370172289 | in-del | -/CAC | 0.00478085 | 0.0486577 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145023041 | GATTATCAAAATACA[-/CAC]CAATAGTCAAGTGGA | 10393 |
rs370252588 | in-del | -/A | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145046800 | CAACCTTAAAAAAAA[-/A]CACTTCATGCTTAGA | 10393 |
rs370253194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145024698 | TCCATTTATAGCACA[C/T]GAGTAGAACAGATTT | 10393 |
rs370274078 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145077373 | TTTGAGGATACTGTC[C/T]ATGAAAATTTCCCCG | 10393 |
rs370286264 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145040868 | GAAGGGGACTGAGAA[A/G]GAAGAAACTAATTCA | 10393 |
rs370298728 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144997894 | GAGGAAGATCTACCA[A/C]GCAAATGGAAAACAA | 10393 |
rs370339378 | snp | A/T | | | downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:144966722 | TCTTTGCCAAATCCA[A/T]CTGTAAAGATTCAGT | 10393 |
rs370419352 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144977192 | ATGATTCCACAAGTA[A/C/T]CATCCTCTAGAGAAT | 10393 |
rs370461117 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145091589 | CATTTTCTTTATTCA[A/G]TCTATCACTGATGGG | 10393 |
rs370468563 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145059838 | ATGTTCTTTGGTCCA[C/T]TGCTCTAAATGATAA | 10393 |
rs370482464 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145022570 | TGCAATGTATACTGC[C/T]TGGGTGATGGGTGCA | 10393 |
rs370555829 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144969502 | TTAAAAGGACCTTTT[A/T]AGCAAAGAATACGAT | 10393 |
rs370693269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145031553 | TCCAGCCCACTTATC[A/G]AGTGACCTGAAAGGC | 10393 |
rs370730116 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145026963 | TGTGTGTGTGTATAT[A/G]TATATATATATATAT | 10393 |
rs370740919 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144997326 | GGAAAAATATTAAGG[G/T]CAGCCAGACAGAAAG | 10393 |
rs370744555 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145031477 | ACCAAGAAAGAGGCA[C/T]GACACCTAGTGGGTC | 10393 |
rs370774950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145014126 | GCATCCAGTGTGCAG[C/T]CTCCACAGGTGGAGG | 10393 |
rs370805837 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145002965 | TTATTTAGTCACCCA[C/G]GTAGTAGGCATAATA | 10393 |
rs370917185 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145071323 | AGGCAGGAGAATTGC[A/T]TGAATCTGGGAGGCA | 10393 |
rs370917823 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145026357 | CTCTTGTAAGTGATG[C/T]TCTAGTAATAAACGT | 10393 |
rs371035372 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145090440 | TTAGTGAAATCTTAT[C/T]CTTGCTTCATCATAC | 10393 |
rs371050751 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145005129 | TTTGAAGGCTCACTG[A/C]AAACTCTGCCTCTCA | 10393 |
rs371052387 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145095626 | CTCGCTCTCATCACA[C/T]AGACATTTTATCTCT | 10393 |
rs371079111 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145051219 | TTGTGTCTCAGGGAA[C/T]AGGAAAACACAATTA | 10393 |
rs371097577 | snp | A/C | | | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145098904 | CATCTTGCCGCCATG[A/C]AGTCGAATACTCGCT | 10393 |
rs371140771 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144979096 | AATATTAAATTATAA[A/T]CTTTTTTTCCTTCAA | 10393 |
rs371150711 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145025823 | TTTATCAAAGAGAAG[G/T]GCAATAAAATGAGGT | 10393 |
rs371165602 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145052169 | GGTGAGGCATAAGAA[A/G]TAAGTTCAAGTCATC | 10393 |
rs371180291 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144979320 | GTGTCCGTGCTCTCA[C/T]TGATCAACTCCCACT | 10393 |
rs371212343 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144982915 | CCTGTAATCCCAGCA[-/C]TTTGGGAGGCCAAGG | 10393 |
rs371266451 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145048198 | CTGCAGAAATAAATT[G/T]CACAAATATTAACTG | 10393 |
rs371272666 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145080099 | AGCCTGGGCAACAGA[A/G]AGAGACTCTGTCTCA | 10393 |
rs371279324 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145082148 | AAAAAACATCTTCTA[A/G]GAGATATTATATTTT | 10393 |
rs371287528 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145033456 | TACCTTTAAGTCAAT[A/G]GGCTAAAAAGGGAGT | 10393 |
rs371289852 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145051879 | AAGGACACTATCTAT[C/T]AAATAATCGCAGAGT | 10393 |
rs371292560 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145090017 | ATACAGCTTCACATA[C/T]GCCATTTCCCTATTT | 10393 |
rs371296973 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144972030 | TAACAATAAAAAAAT[A/C]AAAATCCTTCAATGG | 10393 |
rs371359794 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145092103 | TCTCGCTTATAAATA[A/G]GAGCTAAACAATGAC | 10393 |
rs371367523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145023665 | TACATCTAAGAAAAC[A/G]ATTTAAGAATGTTTT | 10393 |
rs371391953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144969052 | GTACATACATGCATA[C/T]GTATATAGGGGGAGT | 10393 |
rs371393537 | snp | C/T | 7.07272e-05 | 0.00594631 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144995654 | TCAACAAATATAATT[C/T]ATAACAATGAATGCA | 10393 |
rs371419028 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145018383 | TCACACCTATAATCC[C/G]AAGGCTTTGGGAGGC | 10393 |
rs371419563 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145012197 | ATATATATATATATA[C/T]ACACACACATATATA | 10393 |
rs371502191 | in-del | -/CTTT | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145075063 | CACATCCTAGACCTT[-/CTTT]ATCAGTGTTAGCAGG | 10393 |
rs371515912 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145071401 | ACGAGAGTGAAACTC[C/T]GTCTCAAAATAAATA | 10393 |
rs371545831 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145012301 | ATATTGAAAATATTG[C/T]CACTTGAACATGTTT | 10393 |
rs371550169 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145015278 | CATTGGATATACTTA[C/T]AGAAATGCAAAATGC | 10393 |
rs371595145 | in-del | -/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145077504 | GAGAGGAAGAATTCC[-/C]TCCCTAACTCATTCT | 10393 |
rs371617333 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144999533 | GAGAACTACAAACCA[C/G]TGCTCAATGAAATGA | 10393 |
rs371640424 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145060356 | AAGGAAGGGTCTGAT[A/G]CCTTTGTAGAGAGTT | 10393 |
rs371727965 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144973048 | GGAGGAAACTTTACA[A/G]CCTTTAAGTATATAT | 10393 |
rs371910469 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145041756 | ATTTAATAACTGGTT[C/T]CAGATATACAGCAAT | 10393 |
rs371924329 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144967508 | GATGTTCTTCGTAAA[C/T]AATAAAATATTTTAC | 10393 |
rs371939778 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145017386 | GCTCATCATCACTGG[C/T]CATCAGAGAAATGCA | 10393 |
rs371989149 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145036325 | TATAGATACGTACAC[A/G]TTATTTAGAATTGTA | 10393 |
rs372063941 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145026215 | AAGAAAAGACCTATA[C/T]ATAATGATGTGTGAA | 10393 |
rs372131460 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145007231 | TATTAGACACATCTA[C/T]GAGACAGAAGGTTGA | 10393 |
rs372262329 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144996189 | ATGGAGATATCCCCA[C/G]GGCTCTACACTCCGA | 10393 |
rs372310865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144982294 | GGCTATGCGTGGCAG[A/G]TATTATTCACTGTCT | 10393 |
rs372372870 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145056257 | AACCAAGATGGCCAC[A/G]AGAGTGACCTCTGGT | 10393 |
rs372401997 | snp | A/C/G | 0.000282912 | 0.0118905 | missense, synonymous-codon, intron-variant | ANAPC10 | GRCh38.p7 | 4:145064590 | AATTTCTTGAAGGTT[A/C/G]TGAAAATTATTTCCT | 10393 |
rs372431479 | in-del | -/A | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145007855 | AGGACACAGAGACAC[-/A]AAAAAAACCCTTCAA | 10393 |
rs372438414 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144968515 | AAGCAATGAGCTTAT[C/G]TGCCAAATAAATAGG | 10393 |
rs372474450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145035115 | AAGAGTTCTTTTCAT[A/G]CAAGATTTGGAAAGC | 10393 |
rs372540570 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145095125 | TAAAAAAAAATTCAG[A/T]GCATTAGAATTAAAA | 10393 |
rs372544647 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145027242 | CTCTTCACCTCAGGT[G/T]ATCTGCCCGCCTCAG | 10393 |
rs372645589 | snp | C/T | | | downstream-variant-500B, intron-variant | ANAPC10 | GRCh38.p7 | 4:144993980 | AGACCCTGTTGTTTA[C/T]TTGACTGTTTTCCTT | 10393 |
rs372675173 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145093646 | AGATGAAAATTCTAC[A/G]AGTCAAATGGAAGAG | 10393 |
rs372701826 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144970065 | GTTACTTCCTCAGGC[A/T]AAGTTAAAACAGCCA | 10393 |
rs372807818 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145016329 | TATACACCAATAACA[A/G]ACAAACAGAGAGCCA | 10393 |
rs372858642 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145067848 | CAACTTCCCTTAAAG[G/T]TAGGTAGAGCCATAT | 10393 |
rs372866692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145064863 | AAATATAGGTCCAGA[C/T]AGTATGTTAAATATA | 10393 |
rs372867447 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144992969 | ACCCTGATAAGTCAG[C/T]AGCCATCAACACCTA | 10393 |
rs372943163 | snp | C/T | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | ABCE1, ANAPC10 | GRCh38.p7 | 4:145097374 | CTAAGTCTATTCATA[C/T]GTGAAAAAACACTTC | 10393 |
rs372956268 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145069075 | AATAAAACAAGAAAG[C/T]CCGAGACATCTGCTC | 10393 |
rs372958361 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145038343 | CATGGCAAAACCCCG[C/T]CTCTATTAAAAATAC | 10393 |
rs373056348 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145038870 | ACTAAGGCAAAACCT[A/G]TAAGAAGCAGGCAAC | 10393 |
rs373063214 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145076308 | GGCCCTCTGGATTAC[A/C]GCATGCAACCCACAA | 10393 |
rs373103625 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145096279 | TTAAATCTTAGGGGC[C/T]GGGCATGGTGGCTCA | 10393 |
rs373116687 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144991671 | GTGAGCTACCATGCC[C/T]GGCCAGGAATTTTTT | 10393 |
rs373134435 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145011593 | AACAGGAGCATTTGT[C/T]GATGCTGGTAAAGGG | 10393 |
rs373248336 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144969845 | TCTTTAACAATTATT[A/T]TTATTATCAAATATT | 10393 |
rs373249480 | in-del | -/CCCTGTCTC | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145037938 | GGTGACAGAGCAAAA[-/CCCTGTCTC]AAAAAAAAAAAAAAA | 10393 |
rs373284229 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145018401 | GGCTTTGGGAGGCTC[A/T]GGCGGGCAGATTACT | 10393 |
rs373301066 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145067218 | AAATAGCAATGCATG[C/T]CATAAGATTAAACAT | 10393 |
rs373316661 | snp | A/G | 0.000169985 | 0.00921758 | utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995327 | ATATTATTTAAATAC[A/G]GGATAAAACAAAGAT | 10393 |
rs373329577 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145028704 | AACTGTTTAGAGAGT[G/T]ATGCAAAATAAATGT | 10393 |
rs373349588 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145051548 | ATGCAGTTATCTATA[A/C]AGTGCAATAAGGTGA | 10393 |
rs373447086 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144967553 | ATTTACTTTCATTTT[A/G]TGTGTATAAAAATGA | 10393 |
rs373474862 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145010187 | CCCAGGTGCTGGAGG[A/G]GATGTGGAGAAATAG | 10393 |
rs373536178 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145058143 | ATGGGAACCATGTTA[A/C]ATCACAATATATGTG | 10393 |
rs373557540 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145017557 | CATTGTGGAAGACAG[G/T]GTGGCAATTCCTCAG | 10393 |
rs373575263 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145075846 | AAATGGCTACAGTGG[A/C]GCACAGCCAGGGATG | 10393 |
rs373580896 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145000072 | ATGGATTAAAGACTT[A/G]AATGTTAGACCTAAA | 10393 |
rs373642093 | snp | A/G | | | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145097884 | TCCCGGCCCTGAACT[A/G]ACCACACAGTTGAGA | 10393 |
rs373715273 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145034215 | GGGTATGCCTGTGTC[C/G]GTGTTACCAAAAGAG | 10393 |
rs373739561 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145098092 | GCTAGGACCACGCTC[C/G]ACGTCGGAGAAAAGC | 10393 |
rs373758860 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145085885 | TTTTTTTTTTTTAAG[A/G]TGGAGTCTCACTTTG | 10393 |
rs373806267 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145048573 | AAGCAACTACTAATA[C/G]CATCTACTGGTAGTT | 10393 |
rs373886326 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144992101 | GGATGACAGTACCAC[C/T]GTTTAGAGCATAATT | 10393 |
rs373888798 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145022758 | ACACTGGAATTGTTG[C/G]GTCATAGGCAAGTTT | 10393 |
rs373900165 | snp | A/C | 3.32309e-05 | 0.00407607 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081792 | TCCCTGTGAAAAAGA[A/C]ACAACTATACATGCA | 10393 |
rs373905802 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145024832 | AAGTTTTCAAGCCAG[A/G]CATTGACTTCTCCTC | 10393 |
rs373924584 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144983611 | CAAAATTACAGGCCA[C/T]CAGATGCTACACATT | 10393 |
rs373973088 | snp | C/G | 0.000636663 | 0.0178305 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144995611 | TCAAGTTGCTGCCAA[C/G]GGAAAAAAAATCAGA | 10393 |
rs374011485 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145091592 | TTTCTTTATTCAATC[G/T]ATCACTGATGGGCGT | 10393 |
rs374092355 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145052459 | AGAGGTGGAATCCGC[G/T]TATTTTCTAATTTTA | 10393 |
rs374095890 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145014975 | CTCTGACAGAGGCTA[C/T]GCAAATGAGAAAGAA | 10393 |
rs374112875 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144984365 | AATAGCTGGCTGAAC[C/T]CTCTGCTTCAGTCTT | 10393 |
rs374157937 | in-del | -/TTCT | 0.0245799 | 0.108101 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145065206 | GAATTCTGCTGCTGA[-/TTCT]TTCTTTCTTTCTTTC | 10393 |
rs374278301 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145073888 | AATAAAATTTGTAGA[A/C]ATTTTGATGAAGGCA | 10393 |
rs374321985 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145042701 | TACACTCAGAAAACA[C/T]AGAGTCTTTATTCCA | 10393 |
rs374333640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144972121 | AAATCTGGCCTCAAA[C/T]TATCTTTCTAAAGTT | 10393 |
rs374345655 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145022187 | AATGAAGTCATTATA[A/T]GAAAAAGATACTTGC | 10393 |
rs374363598 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144995892 | CCAGAATAAAACAAA[A/T]ACACTAGAAAGTACA | 10393 |
rs374395202 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145070736 | ACAGCCGAAAGGTAG[A/C]AACAACCCAATGTCC | 10393 |
rs374425497 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145082235 | GCTCATTGCAACCTC[C/T]GCCTCCCGGATTCAA | 10393 |
rs374468205 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145056629 | TAGTGTGGAAATCCC[C/T]GACCCAAAGGTTAAC | 10393 |
rs374508075 | in-del | -/A | 0.00478085 | 0.0486577 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145082996 | AGATACTATATGCAT[-/A]TACAAGCAGTCATAT | 10393 |
rs374520864 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144985139 | AAAACTGCACAAAAA[C/T]AATCCCAACTAAATG | 10393 |
rs374572053 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145006283 | ACCCAGACTTTTTAT[C/T]TGAAAAATCTGCCAA | 10393 |
rs374622813 | in-del | -/AGAT | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144980526 | CATAGATAGATAGAT[-/AGAT]CGATAGATAGATAGA | 10393 |
rs374656881 | in-del | -/TTAGT | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144988784 | CTGATCTGCTGTCAC[-/TTAGT]TTATATTTTCTAGAA | 10393 |
rs374669789 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145045669 | TATATGAATGTATAC[A/G]TGATCTTCTACACAC | 10393 |
rs374672811 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144969539 | TCAACCTATTACTAT[C/T]CCAGATAATGCTGGA | 10393 |
rs374675595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145061588 | AAAACATTTTATTGC[C/T]AGTGTTTCACTTATC | 10393 |
rs374682029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145035021 | ACACCTGTGGCGACT[C/T]TGTAATGTGTCAACT | 10393 |
rs374721010 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144993399 | GAGCATCTTTTTGTA[A/C]AATTACTTGCCAATC | 10393 |
rs374754373 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144979135 | TTCAGTTCCAGGGTA[A/C]CTGTGCAGGATGTGG | 10393 |
rs374767651 | in-del | -/AAG | 0.00835141 | 0.0640778 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145020009 | TCTACCAGACTTTCA[-/AAG]AAGAATTGGTACCGA | 10393 |
rs374803156 | in-del | -/ACCT | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145034117 | CAGATACATATAGGT[-/ACCT]TCAAGTTGACAAGGG | 10393 |
rs374849635 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145095112 | CAGAGATATATGATA[A/G]AAAAAAATTCAGTGC | 10393 |
rs374902605 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145084527 | CCACACTGGAAGAAG[A/T]ACTGTCTTGGGCCAC | 10393 |
rs374905811 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145055324 | GCACTTTGAGAGGCC[A/G]AGGCGGCCAGATCAC | 10393 |
rs374978618 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145037878 | ATTGAACCTAGAAGG[C/T]CTAGGCCCCAGTGAA | 10393 |
rs375085916 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145038265 | TGTCTATAATCCTCG[A/C]ACTTTGGGAGGCCAA | 10393 |
rs375095644 | in-del | -/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145018124 | AGTATAATAAAAAAA[-/T]ATATATATATATATA | 10393 |
rs375118593 | in-del | -/A | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145043118 | TATTATTTGCTAAAA[-/A]TGCACTAGCTGCCAA | 10393 |
rs375239648 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145090228 | ATCATCTCTAGATTA[C/T]TTATAATACCTAATA | 10393 |
rs375241516 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145018524 | GCACCTATAATCCCA[A/G]CTACTTAGGAGGCTG | 10393 |
rs375244402 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145080043 | CACTTGAACCTGGGA[A/G]GTAGAGGTTGCAGTG | 10393 |
rs375253206 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145059049 | AGACTTGATAAATTA[C/T]ACTTTCTGTCTTATC | 10393 |
rs375254987 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144977695 | TACTTAAATCTGCAC[A/G]TTGTTCTGGAACCAG | 10393 |
rs375259919 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145005550 | CTTTTAGTTATGATC[A/G]TAGGTTGTTAAATTG | 10393 |
rs375291541 | in-del | -/ACAA | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145043281 | TATTTTGACTAAAAA[-/ACAA]TTCTAATTATAGATA | 10393 |
rs375343998 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:144966881 | CACAGTTGCCTACTT[G/T]GAGCTAACACTGCTC | 10393 |
rs375387922 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145075989 | AGCAACACTTTGTCT[G/T]CCAGTCTCTCCCAGG | 10393 |
rs375395549 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145051930 | GGATTTCACATAGTC[G/T]GATTACTTAGGTTAA | 10393 |
rs375397936 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145038385 | AGGCATGGTGGTGCA[C/T]GCCTGTAATCCCAGC | 10393 |
rs375403403 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144979122 | TTCAACTATTATTTT[C/G]AGTTCCAGGGTACCT | 10393 |
rs375440822 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145056265 | TGGCCACGAGAGTGA[A/C/T]CTCTGGTAGTCCTCA | 10393 |
rs375494061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145040482 | CTATAAAAACATAAC[A/G]AATTTTAATGGCTTT | 10393 |
rs375502265 | snp | C/T | 0 | 0 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145048303 | AAAGCCATCAAAGAT[C/T]TGTGGGCCCTGAAAA | 10393 |
rs375508323 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145007933 | ACAAAATTGATAGAC[C/T]GCTAGCAAGACTAAT | 10393 |
rs375519056 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144973561 | AAATATATGCAACAG[A/T]AGGGATCAATAAACC | 10393 |
rs375562397 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145093704 | ATGAAAAATTTCTTA[C/G]GCAGAATTATCAGTA | 10393 |
rs375569697 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145048760 | TTTAAAAAAAAAAAG[A/G]AAATTCAACCATTGG | 10393 |
rs375679251 | snp | C/T | 1.66147e-05 | 0.0028822 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995389 | CACCTTATTGAACGA[C/T]ACATCATGAAATCTA | 10393 |
rs375690033 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144968031 | AAGGGTGTTATCAGA[G/T]TAGGACTTAGATTAG | 10393 |
rs375698408 | snp | A/G | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant, synonymous-codon | ABCE1, ANAPC10 | GRCh38.p7 | 4:145098141 | CAGACCTGGCTGCTT[A/G]CCGAAACTCAGATTC | 10393 |
rs375704197 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145079513 | TACTATTTGACCAAG[A/C]AATCCCATTACTGGG | 10393 |
rs375757648 | in-del | -/ATTT | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144978438 | GTAAACATTTTGTTT[-/ATTT]GATAGGGATGAGCAA | 10393 |
rs375770796 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145095404 | CACTTTGTCCAGCAC[A/G]TCCACCACTTTGTCC | 10393 |
rs375842127 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145016592 | ATCAAGCTACCAATG[A/C]CTTTCTTCACAGAAT | 10393 |
rs375853219 | in-del | -/GTCTT | | | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145099909 | ATTTTGAACACTTTT[-/GTCTT]CGAATCTGAAATATC | 10393 |
rs375911670 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | ABCE1, ANAPC10 | GRCh38.p7 | 4:145097523 | CCTCCCATTGTATCC[A/G]AAGTTGTTCTTTAAT | 10393 |
rs375925291 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145069578 | ATACCTAAGACATTC[A/G]TTTGAGATCCCAGAT | 10393 |
rs376073789 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145026949 | TATATATATATATGT[A/G]TGTGTGTGTATATAT | 10393 |
rs376074955 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144980103 | CTGGCCAAGGCAGCA[A/C]CCCTCTGGGCAGAAG | 10393 |
rs376110348 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995040 | ACACTAATGAAATAA[A/T]CACCTAGCTATTATA | 10393 |
rs376111564 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145072062 | GCAAACTACACCCAA[C/G]TTGCAACAAGCCCAA | 10393 |
rs376113879 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145095492 | GATATCCAATCATCA[A/T]CATCATCGTGGCTTG | 10393 |
rs376118702 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145080114 | GAGAGACTCTGTCTC[A/C]AAAAAAAAAAAAAAA | 10393 |
rs376125489 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145047022 | CTAAGAATCTATACA[C/T]ATTAGGTTCATGGTA | 10393 |
rs376130138 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145091504 | AAGAACCCAAAAGAA[A/C]GCTGAAAAAGCTTTT | 10393 |
rs376196228 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144987384 | ATTATTCTCAGTAAA[C/G]TATCGCAAGGACAAA | 10393 |
rs376287235 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145077779 | AACAAAAACCACATC[A/G]TCATCTCAAGAGATG | 10393 |
rs376295141 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145003818 | AGATCATCTTGGCTA[C/T]TTAAGCTCTTTTTTG | 10393 |
rs376308689 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144971469 | CACACCAAAGCTCAC[A/G/T]TGATAGTTTTAAAGT | 10393 |
rs376315209 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144993226 | GAATTGAACCTGCAG[C/T]ATCTCTGAGATATGC | 10393 |
rs376317926 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145015651 | ATCAGGTAATGTAAA[A/G]TTAAGACAAAGGAAA | 10393 |
rs376336672 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145093900 | TAGAAAGATAATAGA[C/G]AAGCAATAGGGCAAA | 10393 |
rs376383360 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145087465 | TAGGCTCTGCTAGGG[C/G]GCTATTTTAACTGAG | 10393 |
rs376424802 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144967768 | ATCTTTCTAAGAAAG[G/T]CTGTAGAAGAGGGAT | 10393 |
rs376448732 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145031874 | GGTCATCAAGTCACC[A/G]TGCAACCTGAACTGA | 10393 |
rs376474517 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995018 | AAACCATTACTCTAA[C/T]GTATGAACACTAATG | 10393 |
rs376482123 | in-del | -/A | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145029691 | AATATGGATTAAAAA[-/A]TGGCCCACTGTGAGA | 10393 |
rs376484957 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144990397 | TAGAAGTTTTAGTCC[A/G]TTTTTGCCTCTCTAT | 10393 |
rs376517176 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145009217 | AACATTCCATGCTCA[C/T]GGATAGGAAGAATCA | 10393 |
rs376572135 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145078406 | AAACATCCCATGCTC[A/T]TGGATAGGAAGAATC | 10393 |
rs376669739 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145076518 | ACCAGAGCAAGAATT[A/C]TGGCAAGTCTAAAAC | 10393 |
rs376689123 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145002635 | ATTCTGAATAAATGT[A/G]AAGCCAATGTCAATT | 10393 |
rs376719852 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144983511 | GATATAGAATAAAAA[A/C]AATTAAAATATACAG | 10393 |
rs376811267 | snp | A/C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145094343 | GGCCCAGAAGACTGA[A/C/T]CATAAAGAGACATGA | 10393 |
rs376818954 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145026553 | GTGAGGCTTCCAGAC[G/T]GGCTACACTATAGGA | 10393 |
rs376827906 | snp | A/T | 3.3896e-05 | 0.00411666 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145064540 | AGTAAAAGTTAAAGG[A/T]TGACATATTTTTAAA | 10393 |
rs376850805 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145052013 | ATTTTAAAAAATTGG[A/G]GTGAAAAAAGAACTG | 10393 |
rs376904561 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145017424 | ACCACAATGAGATAC[C/T]ATCTCACACCAGTTA | 10393 |
rs376920297 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145089659 | ATCTGAATGAAATAT[C/T]GAACCATTATTTCAA | 10393 |
rs376926053 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145020338 | AAACAAAAATCACAT[A/G]ATCATCTCACCAGAT | 10393 |
rs376933195 | snp | A/G | 6.62723e-05 | 0.00575602 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995490 | ATGGGTGTCTCTTCC[A/G]TTCTGGTGATTGGCT | 10393 |
rs376998760 | snp | A/T | 0.000169986 | 0.00921758 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145064716 | AATAAAGTAAAAATA[A/T]CATGCACTTCATCAT | 10393 |
rs377018864 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145056828 | TCTGCATTTCTAAAA[C/G]CATGTCATTTTCATT | 10393 |
rs377058541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145080680 | TTGGGAGGCCGAGGC[A/G]GGTTGAATCACAAGG | 10393 |
rs377108553 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime, intron-variant | ANAPC10 | GRCh38.p7 | 4:144994120 | TTCTACCCTACCCAG[C/T]ATCTGACAAGTATAA | 10393 |
rs377151283 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144997612 | GAACAACCAGTACCA[C/G]ACACTGCAAAAACAG | 10393 |
rs377159579 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145050930 | CTTTCTTATTATTCA[C/T]GTGTTCACTAGAGTA | 10393 |
rs377218814 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144969302 | GTTTATGCAAGGAAT[C/T]AAGCAGGGTGTCAGG | 10393 |
rs377287821 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145038974 | AAATCAAAAGTGGCA[C/T]TGTATTTCTCAACAT | 10393 |
rs377323874 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145018405 | TTGGGAGGCTCAGGC[A/G]GGCAGATTACTTGAG | 10393 |
rs377329954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144976213 | TTTACAGAAAGTAAC[C/T]TGAATATATATTACA | 10393 |
rs377339394 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081973 | CCTTGGCCTCCCAAA[G/T]TGCAGTGATTACAGG | 10393 |
rs377344308 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145051725 | ATAGTTATTATTGCA[C/T]ACAGTTATTGTAAAG | 10393 |
rs377352500 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145011767 | CACAATATTTGCCAC[A/G]TTCTGAAGTTGCCTA | 10393 |
rs377407088 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144970036 | ATTTATTCACATGGG[G/T]TGCATTCTTCAGGGT | 10393 |
rs377408936 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145082509 | CTTTTTGCAAGCTGA[C/T]AGTAAAAATGACTAA | 10393 |
rs377450288 | multinucleotide-polymorphism | GG/TT | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144967427 | TTCGTCTGTCCTGTG[GG/TT]GGTGACACACCTGCT | 10393 |
rs377457021 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145057468 | GCTTTCTTCACTGGA[A/T]AACCTTTTCCTATCC | 10393 |
rs377477089 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145058603 | ATTCACAGAATAAAG[A/C]ATGAATCTGTTTTGT | 10393 |
rs377535871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145047038 | ATTAGGTTCATGGTA[A/G]ATGTTTTTACACTGC | 10393 |
rs377537608 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145010196 | TGGAGGGGATGTGGA[C/G]AAATAGGAACATTTT | 10393 |
rs377727615 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145005942 | TCTGCTGTTTTGGAG[A/T]GGAGAGTTCTGTAGA | 10393 |
rs386401758 | in-del | -/A | 0 | 0 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145002902 | AGAGGCACACGTGCA[-/A]GTTTATTATAAAGGT | 10393 |
rs386401759 | in-del | -/TA | | | intron-variant, utr-variant-3-prime | ANAPC10 | GRCh38.p7 | 4:145063474 | ACTCAGATTAAACAT[-/TA]AAATTTAGAGACACG | 10393 |
rs386401760 | in-del | -/AA | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145080137 | AAAAAAAAAAAAAAA[-/AA]ACACACATTGAATAC | 10393 |
rs386680445 | multinucleotide-polymorphism | CAT/TAG | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144988926 | TTTATTGCTGAGTAG[CAT/TAG]TTCATTATATGTATA | 10393 |
rs386680446 | multinucleotide-polymorphism | AG/GA | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145004429 | CGTTCCAGTTTTCAA[AG/GA]GGAATGCTTCCAGCT | 10393 |
rs386680447 | in-del | CGCC/TG | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145025331 | TTTTGGCTTTCAACA[CGCC/TG]CCCCCCCCCTTTTAA | 10393 |
rs386680448 | multinucleotide-polymorphism | CAT/GAG | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145036910 | ATAAAAAGGAAGGAT[CAT/GAG]AGTTTTCCCTAAAGG | 10393 |
rs386680449 | multinucleotide-polymorphism | AGC/GAT | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145047760 | TTTTTAAATTGATGA[AGC/GAT]TATTGTTCAACTAGA | 10393 |
rs397742192 | in-del | -/A | 0 | 0 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145066787 | GATTTAAAAAAAAAA[-/A]CATAACACTTAGGTT | 10393 |
rs397897193 | in-del | -/TT | 0.433171 | 0.170142 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145002473 | TCTCTGTATAGAAAC[-/TT]TTCCGATTTTCTAGT | 10393 |
rs397995668 | in-del | -/T | 0 | 0 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144991702 | TTTTTTTTTTTTTTT[-/T]AGCTCATCAGCTATC | 10393 |
rs398064113 | in-del | -/TA | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145067049 | GTATAATTTGCTATA[-/TA]CATAGTTTCATTAAA | 10393 |
rs527245801 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144979865 | TCCTTTCCTTATTTG[A/G]AAAGAGGACTAACTT | 10393 |
rs527246599 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144970843 | ATTACAAAGAAATAG[A/G]TCCCAAGCCAGGGAT | 10393 |
rs527281335 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145069563 | GTAAGTCCTCTTCAA[A/G]TACCTAAGACATTCG | 10393 |
rs527304289 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145028528 | CCATGACTAATACAG[C/T]TTTTGGTACCAGGAG | 10393 |
rs527330338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145071990 | AACAAATTCAGAAAT[A/G]TGAAAGGACAAAAAA | 10393 |
rs527344931 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145065595 | ATGCAGAAAAATCTT[C/G]TCCTGTGATTAAATC | 10393 |
rs527384403 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145013702 | AAGAGGACCCACAGA[A/C]CCTCTGAAAAAAGCG | 10393 |
rs527408216 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145065260 | TATACATATCCTAGG[G/T]AAAGAAGAAACACAT | 10393 |
rs527408701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145013136 | CAATTAAGTGTCTTT[C/T]CTTTACAAATTATCC | 10393 |
rs527422533 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145019959 | AAAAATTATCAACAA[A/C]AAAAAAGGCCAGGCC | 10393 |
rs527454813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144985898 | TTTGTCATAGATAGC[C/T]CTTATTATTTTGAGA | 10393 |
rs527475612 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145041613 | CTTCTAGAAGGCATA[G/T]GCAAGATATGTCTTG | 10393 |
rs527495676 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145000349 | TAAAAAGAACTTAAA[C/T]AAATTTACAAGAAAA | 10393 |
rs527517422 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | ANAPC10 | GRCh38.p7 | 4:144993832 | AAGACACTAGATAGT[A/G]TATGTGATCATTAGT | 10393 |
rs527519179 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145000986 | ACTCATAAATGGGAA[C/T]TGAACAATGAGAACA | 10393 |
rs527533532 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145027789 | TTGAGGGTGAGATTA[A/G]AATAAAGTTTTCAGT | 10393 |
rs527570958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145079986 | GGGCGTGGTGGCAGG[C/T]ACCTGTAATCCCAGC | 10393 |
rs527597738 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145083713 | AGAATAATTGCACTT[C/T]TATAAAATTTTTTTA | 10393 |
rs527616391 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144998117 | GAGACTTAGACTCCC[-/A]ACACAATAATAATGG | 10393 |
rs527687432 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145012168 | GCTATATGTATATGT[A/G]TGTGTGTGTATATAT | 10393 |
rs527697945 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144991674 | AGCTACCATGCCCGG[A/C]CAGGAATTTTTTTTT | 10393 |
rs527715109 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145055159 | TCACAGCACTACTAT[G/T]CACATTAGGCAAGAG | 10393 |
rs527728018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144969196 | GGAATGTTGTAGGAA[C/T]TAAATATTACATAAA | 10393 |
rs527734218 | in-del | -/AAC | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145034510 | TGTAAGTTAACACTT[-/AAC]AAACTCTCCTTTATA | 10393 |
rs527748464 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145041031 | TTATATTAAAAAAAA[A/C]AACTGAAGTAGCTCC | 10393 |
rs527847530 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144977297 | AACCACAGATAATTT[A/G]TATACGACAAATATT | 10393 |
rs527857263 | snp | A/C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145097179 | TGCACTCCAGCCTGC[A/C/G]TAACAGAGCAAGACA | 10393 |
rs527902553 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145025694 | TTGAAATACTACAAG[A/T]ATTACCAAAATATGA | 10393 |
rs527906948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144984862 | AAAGACAAGAGGGAC[A/G]CTTAATGGTCGTGGA | 10393 |
rs527909153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144976455 | CAATGACTAAATTCA[C/T]TGAGCTGGTGTTTGG | 10393 |
rs527940674 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145070727 | TTATTTACAACAGCC[A/G]AAAGGTAGAAACAAC | 10393 |
rs527966290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145018234 | AAGGTATACAGGCAA[C/T]AAATAGCATGATGAA | 10393 |
rs527968509 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145011571 | GTCTTTCTGCACCCA[C/T]TTTAACAACAGGAGC | 10393 |
rs527994313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144968650 | TTAGGTCAAAGGTGA[A/G]GATCCCAGGACAACA | 10393 |
rs527997145 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145010975 | AAGGCACGGCAAGAC[A/T]GAAAGCTTCCACAAT | 10393 |
rs527999467 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145071004 | AGAAAAGGAAATTGG[G/T]TGGTTATTATTTAAT | 10393 |
rs528005718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145061900 | ATCACTTGAGGTCAG[A/G]AGTTTGAGATCAGCC | 10393 |
rs528111262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145009438 | CTTCAAAATATACTA[A/G]AACCAAAACAGCATG | 10393 |
rs528118170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145059434 | CTTTTAAAAAAAATC[A/G]CTTGGTAACAGCTTT | 10393 |
rs528139625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145037904 | GTGAACCATGATTGC[A/G]CTACTGCACTCAAGC | 10393 |
rs528153136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145019865 | TTCCTGGAGGTGTAC[A/G]CCCCTCCCAGCTTAA | 10393 |
rs528153864 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145046433 | AAATAAATTCCATAA[C/G]CACAAACAATTTCAA | 10393 |
rs528162828 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145091400 | ATGGCACCAGTCTAG[G/T]CATACTAATAGATCA | 10393 |
rs528176140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145045889 | AGTTGAATAACTTTT[C/T]CATACTGTAATTTTA | 10393 |
rs528204517 | snp | A/C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant, synonymous-codon | ABCE1, ANAPC10 | GRCh38.p7 | 4:145098159 | GAAACTCAGATTCTC[A/C/G]GCACCTCCAGCAGCT | 10393 |
rs528204753 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145000445 | CCAACACACACTAAA[A/C]CATGCTCATCATCAC | 10393 |
rs528224812 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145067281 | ACTGCTCAAAACCAT[A/C]ATTATAATAATAATC | 10393 |
rs528259260 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145018608 | GTGCCATTGCACTCA[G/T]CCTGGGTGACAGAGC | 10393 |
rs528292115 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145092137 | AAATGGACACAGGGA[A/G]GGGAACATCACACAC | 10393 |
rs528311244 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145021769 | TCTTCACAATCTATA[A/C]ATCTGAAAATGGACT | 10393 |
rs528316247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144972934 | TAAATAAACTGTGGG[C/T]CAAAAAAAGCCATTC | 10393 |
rs528338436 | in-del | -/TAAGATTGTTT | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145089582 | AATTGTGCTGAATTG[-/TAAGATTGTTT]TAAGATTGTTTTGTG | 10393 |
rs528377835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145015441 | AGAAGTCCAGGATTA[C/T]GTGAAACAACCAAAC | 10393 |
rs528402362 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145037890 | AGGTCTAGGCCCCAG[C/T]GAACCATGATTGCGC | 10393 |
rs528404410 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145015021 | TGGTAATATGACAAA[A/C]CAAGGCTCCTTAACA | 10393 |
rs528432070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081446 | CATAAAAGGAACTAT[A/G]CAACATACCATAAGA | 10393 |
rs528455341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145035975 | GGAACTGAGAGTTAC[A/G]TATTGCTGTTTCAAG | 10393 |
rs528543395 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145082215 | AGTGCAATGGCACAA[A/T]CTCGGCTCATTGCAA | 10393 |
rs528547903 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145020737 | ATTCAGTAAAGTTTC[A/C]AGATACAAGAATAAT | 10393 |
rs528549808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145029975 | AAAATTTAAATAAAA[C/T]GGGAATAATTGAATC | 10393 |
rs528612760 | in-del | -/TAAC | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145070003 | TTTATTTTTAGTGAA[-/TAAC]TAAATAATTTAAAGT | 10393 |
rs528640205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145029458 | GAGGTGCACTACAAC[C/T]GAAAAGAACTGTTTG | 10393 |
rs528650776 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145057734 | TCTCTCTGCCCCTCC[C/T]CCTCAGAATGTTCCT | 10393 |
rs528656430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145001770 | ATGAAGACATCGACA[C/T]CTCTCAGTCTGGCTT | 10393 |
rs528690384 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145014002 | AGGAGGGCGGCCAGC[A/G]GTGCGGAGAAAATGC | 10393 |
rs528743403 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145044127 | ACAAAAAATAGATTC[A/C]AGGAGATAATGCTGC | 10393 |
rs528756767 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145011293 | AGTAAGCCAAGATTG[C/T]GCCACTGTACTCTGG | 10393 |
rs528760334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145051897 | ATAATCGCAGAGTAC[C/T]TTTTAGTCAACCTCA | 10393 |
rs528767636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054415 | TACAAAAAATTAGCC[A/G]GGCATGGTGGCAGGC | 10393 |
rs528770009 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145096904 | CAGTCATACCTGCCC[A/T]CTAGCTGTCAAAAGT | 10393 |
rs528794112 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145002384 | CCCTAGTGAAGAAGG[C/T]GACCACCTAAGAAGA | 10393 |
rs528807783 | snp | A/G | 4.99555e-05 | 0.00499752 | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145096126 | TCTATGTAGAAAACA[A/G]GAATGCACACATTGT | 10393 |
rs528865136 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:145032695 | ACTCACCAAGGCTGA[C/T]GTGGCTACGGCCACT | 10393 |
rs528879855 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144972223 | GTCTCATCAGAGTCA[A/G]ACTGAGTAAAAAACA | 10393 |
rs528893002 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145004279 | GGTCTAGCATCATAT[C/T]ATCTGCAAACAGTGT | 10393 |
rs528951378 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145026347 | AATCCCTGTTCTCTT[A/G]TAAGTGATGTTCTAG | 10393 |
rs528953514 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145017700 | GCACTACTCACAATA[A/G]CAAAGACTTGGAACC | 10393 |
rs528956184 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145001256 | AGGGAGGGAGGGAGG[A/G]AGGGAGGGAAAGAAA | 10393 |
rs528959580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145070299 | CAATTGCAGCAGGAC[A/G]TATAAAGAAGTCTTA | 10393 |
rs528968514 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144977342 | ATTTACACAACATTA[G/T]TGCCTCAAAAAATGT | 10393 |
rs529021167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, missense | ANAPC10 | GRCh38.p7 | 4:145033316 | GCTTCCTGTTCCCAC[A/G]ACATTACGTTCTGCT | 10393 |
rs529037980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145005957 | TGGAGAGTTCTGTAG[A/G]TATCTATTAGGCCCA | 10393 |
rs529050708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145047443 | ATGACTATAACTTCA[A/G]GTTAAATGGAGTTCA | 10393 |
rs529052691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054874 | ATTCATTCTACACCA[C/T]TCTGTGTCTTCCCGT | 10393 |
rs529160173 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145040253 | CTCCCAGGTTCAAAC[A/G]ATTCTCCTGCCTCAG | 10393 |
rs529161891 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145048119 | AATCTGCCTTGGATT[C/G]TTTTCCTCAGTAAAG | 10393 |
rs529169124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144992448 | TGATTTAAGGGAGAA[A/G]GTCAAAATAGCAACT | 10393 |
rs529181667 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145093555 | AATAACTATAACTAT[A/G]AGTAAGATGTTAAAA | 10393 |
rs529198597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144999389 | CATTCCTCTACACCA[A/G]TAACAGACAAACAGA | 10393 |
rs529267799 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145024792 | CCAGCTGCATCAGCC[C/T]CTAACAAAATCAGCT | 10393 |
rs529288314 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144976346 | TTTAATTCAGGATAC[A/G]GGTTAATCTTGGAGA | 10393 |
rs529288821 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145016320 | AAGCATTCTTATACA[C/G]CAATAACAAACAAAC | 10393 |
rs529289980 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144967172 | ACTTCTGAGATACAG[A/T]ACACAGGGCGAGAAG | 10393 |
rs529344240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145077147 | GAGCTTGCAGTGAGC[C/T]GAGATCGTGCCACTG | 10393 |
rs529350424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144975732 | AATCAATAAAGTAAA[A/G]ACTTTTAAAATATGA | 10393 |
rs529375605 | in-del | -/A | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145007881 | TTCAAAAAAAAAAAA[-/A]TCAATGAATCCAGGA | 10393 |
rs529413731 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145060997 | AAGCTAGGCACTAAC[A/G]ATTTAAAGCAACATC | 10393 |
rs529467121 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145038585 | ATCCCAGCATTTTGG[G/T]AGGCCAAGGCAGGAG | 10393 |
rs529472295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145084007 | ACAGGGTCTTGCTCT[A/G]ACACACAGGCTGGAA | 10393 |
rs529479953 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144998226 | CAGCTCTGCACCAAG[C/T]GGACCTAATAGACAT | 10393 |
rs529491863 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145092031 | CTCCCTTTCAGGAGC[C/T]GGAAGCCATCATCCT | 10393 |
rs529492957 | in-del | -/TA | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145073545 | ATATTGGTATTAAAG[-/TA]TATATATAGGATTTT | 10393 |
rs529511826 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145083009 | ATATACAAGCAGTCA[C/T]ATATGTATTCTTTCT | 10393 |
rs529585416 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145031423 | TAAGATATTCCTTCT[A/C]AGGTGAAGGATAAGT | 10393 |
rs529589336 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145076482 | GATTAAAGGAACATT[C/T]TCCCACACAGATAAG | 10393 |
rs529598708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144983143 | CCAGCCTGGGCAACA[A/G]AGTGAGAATCCATCC | 10393 |
rs529618096 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145066109 | CCTTGAACAGAAGTA[C/T]TCTGTGTCAAAAGTC | 10393 |
rs529661085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145020596 | AGCAATCAAACAAGC[A/G]AAAGAAATAAAGGAC | 10393 |
rs529661189 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145013799 | GAAGATCCTCCACCC[C/G]CAAGCACACACTCCT | 10393 |
rs529700784 | in-del | -/ATC | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145065387 | AGAGATATTAGTTTT[-/ATC]ATCATATTGGAAAAT | 10393 |
rs529735200 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145008465 | AAACCGAATCCAGCA[A/G]CACATCAAAAAGCTT | 10393 |
rs529740344 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145065333 | ACATGAAAATGTGTT[C/T]AACGTCTAATAATCA | 10393 |
rs529756218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145073473 | ACAGTGTAATTTGGG[A/G]AGGAGGGTAAATAAA | 10393 |
rs529760149 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145083582 | AAAAGTTGGTATGTT[A/C]TGAAATTAATATACC | 10393 |
rs529764331 | snp | A/G | | | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145096788 | CACCTTGCTTCAAGC[A/G]ATCCTCCCACCTCAG | 10393 |
rs529769730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145014405 | GACCTGGGAACCTCA[C/T]CCCTATCCCCCACAG | 10393 |
rs529870484 | snp | A/C | 6.96419e-05 | 0.00590052 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144995651 | TATTCAACAAATATA[A/C]TTTATAACAATGAAT | 10393 |
rs529871281 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144979243 | CATCCATTAGCTATT[C/G]TTCCTGATGCTCTCC | 10393 |
rs529895218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145020123 | CAAAACCAGGAAAGG[A/G]CATAACCAGAAAGAA | 10393 |
rs529895918 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144997804 | TTAGATAAAGAGTCA[A/G]GACCCATCAGTGTGC | 10393 |
rs529910130 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145031609 | CAGGAGAAGGCTCTG[A/C]AACAGGTCCAGGCTG | 10393 |
rs529927217 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145055742 | ACTAGAACAGTGCTC[A/C]CCAGGGCCTGGAGAA | 10393 |
rs529932555 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144987011 | ACAGGTGCTGGAGAG[A/G]ATGTGGAGAAATAGG | 10393 |
rs529942921 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145082253 | CTCCCGGATTCAAGC[A/G]ATTCTCCTGCCTCAG | 10393 |
rs530049463 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145018336 | GTACTACAGAATGGA[G/T]AAGCATTCACCAACT | 10393 |
rs530073651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145056383 | ACGAATAATCCACCC[C/T]TTGTTTAGCATATCA | 10393 |
rs530107885 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145057375 | TGCCTAGATAATCCT[A/G]ACTTTATATGACTTC | 10393 |
rs530112539 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144988326 | CTCATAAACTGATTT[C/T]GAAAGTGTCTTATAC | 10393 |
rs530179835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145034725 | CAGATGGTGATGCAG[A/G]TTCGACCCAGGGGAC | 10393 |
rs530180031 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145014972 | TCCCTCTGACAGAGG[C/T]TATGCAAATGAGAAA | 10393 |
rs530201515 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145087743 | TATAATATGAAGTAT[C/T]AGTACAACAATAAAG | 10393 |
rs530214941 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144969529 | CGATTCAAATTCAAC[C/T]TATTACTATTCCAGA | 10393 |
rs530229058 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145041754 | AAATTTAATAACTGG[C/T]TCCAGATATACAGCA | 10393 |
rs530271071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145071068 | ATGGAGGTGGTAGTG[A/G]TTGCACAACACTGTA | 10393 |
rs530274887 | in-del | -/AAGAC | 0.00438332 | 0.0466095 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144984848 | TTCTACTCGGCAGAA[-/AAGAC]AAGAGGGACACTTAA | 10393 |
rs530274999 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144978275 | CTCATAAGCTAGACT[A/C]TAAGTTCTTTCTGAG | 10393 |
rs530335842 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145018278 | CACATCTCAATACTA[A/C]CATTGAATGTAAATG | 10393 |
rs530350274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ANAPC10 | GRCh38.p7 | 4:145064043 | GGTGGAAATGTTCTA[C/T]ATTTTAACAGGAGTT | 10393 |
rs530383005 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144988155 | TAATTATTTTTTTAA[A/G]TTTTTGTAGTGACAA | 10393 |
rs530435624 | snp | A/C/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145098666 | CTGCCACACCCGCGA[A/C/G]GGACTTCGAGAATGG | 10393 |
rs530447052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145055843 | GTGTATTCATAACCA[C/T]GTGAATACCATATAT | 10393 |
rs530455551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145012266 | AAAAAGAAATGAGTG[A/G]TATTAAATTTATACT | 10393 |
rs530512834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144991447 | CAGTGTCGCGATCTC[A/G]GCTCACTGCAAGCTC | 10393 |
rs530554800 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145033457 | ACCTTTAAGTCAATA[A/G]GCTAAAAAGGGAGTT | 10393 |
rs530561141 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054090 | ATTTTTCTAATTTTA[A/G]TAGAGATGGGGTTTC | 10393 |
rs530608309 | in-del | -/AAAAAGCTAGTAGGAGGGAACAGTTGAAAT | 0.0023933 | 0.0345097 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145066821 | AACTGGCTTAAGGTC[lengthTooLong]TAAAAAATGTGTCTG | 10393 |
rs530629179 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145038814 | GAGACAGAGTGAGAC[A/T]CTGTCTCAAAAAAAA | 10393 |
rs530671579 | snp | C/G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145085168 | TGGCTGAGGCAGGGG[C/G/T]ATCACTTGAGTCCTG | 10393 |
rs530694873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145004179 | TGCTACTGATTTTTG[C/T]ACACTGGTTTTGTAT | 10393 |
rs530732861 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:145053405 | TGCTTAGAAAGCTTC[C/T]TCTACGTACTGCCTC | 10393 |
rs530781173 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144974520 | ATAAATAAAAGACAC[A/G]AGAAAAGAAAAAGAA | 10393 |
rs530784340 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144981833 | ATTTTTTATTTTTTT[A/T]ATTTTTTTGAGATGG | 10393 |
rs530815812 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081968 | TCCTGCCTTGGCCTC[C/G]CAAAGTGCAGTGATT | 10393 |
rs530829283 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145009942 | ACAGAGGGCTAATAT[A/C]CAGAATCTACAAAGA | 10393 |
rs530854083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145060001 | AATAACATGAATTCA[C/T]GCACAAAAGTAACCC | 10393 |
rs530893226 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145075731 | TAGTGGCAGGAGGCC[C/G]CACAACCCCCCCAGG | 10393 |
rs530918904 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144973850 | TCTAAATAGTTTTCT[A/C/T]TATAGATATATCAAT | 10393 |
rs531008541 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145052628 | TCGGGGGCTGGGTGC[A/G]GTGGCTCATGCCTAT | 10393 |
rs531020435 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145050103 | AGATCCATCAGATCA[C/T]TTGCCACTATTTATG | 10393 |
rs531052320 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145045242 | ATGTGAATAAGTACT[C/T]TGCAAACTTTATCCT | 10393 |
rs531081519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145036858 | TGAGGTACATATTCA[C/T]AGTGGTAAAACTATA | 10393 |
rs531102249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145090349 | ACTATTTTCAACCCT[C/T]AGTTAGTTGAATCCA | 10393 |
rs531105172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145089817 | CCTATCTGATTTATC[A/G]CGTCTCCTGATTTCC | 10393 |
rs531122478 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145045168 | TATTATTTATTTTTT[A/T]AAAAACACACCCAAA | 10393 |
rs531193845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145034486 | GCCTATTGTGGGACC[C/T]TGTGATTCTGTAAGT | 10393 |
rs531204395 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145046015 | AACTAATTTGTTCAA[C/T]TGTTGGGCCAAACTG | 10393 |
rs531226902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144996888 | CAGCAAAGAGAAGAC[C/T]TTAAATGACCCCATG | 10393 |
rs531248346 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145036054 | CATTTTAAAAATTAA[C/G]AAACAAGGTAAAGTA | 10393 |
rs531259955 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | ABCE1, ANAPC10 | GRCh38.p7 | 4:145097451 | TACTGCTACTGAACA[C/T]TGTTATATATGCTAT | 10393 |
rs531269154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145018992 | ATAGACAGCAACACC[A/G]TAACAGTGGGGGACT | 10393 |
rs531299728 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144986779 | GGGCTAATATCCAGA[A/C]TCTGCAATGAACTCC | 10393 |
rs531326379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145071792 | CAGATAAATCATCCA[C/T]AGCATTAAGTGAATG | 10393 |
rs531327139 | in-del | -/AT | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145000834 | TTAAGAAAATGTGAC[-/AT]ATATATATACCATGG | 10393 |
rs531344956 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145037214 | TGCTGCTACATGATA[C/T]TGAAACGTATCTTTT | 10393 |
rs531363547 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144985849 | TCTCAACAATGTCCT[C/T]TTTTTGCCCATTCAG | 10393 |
rs531382937 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145079216 | TAAAAAATGGGCAAA[A/G]GACATGAACGGACAT | 10393 |
rs531399919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145040362 | CATGTTGGTCAGGCT[A/G]GTCTCGAACTCCTGA | 10393 |
rs531422255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145006606 | GAATCATATCAAATT[A/G]TCATTTTTGTAGGTC | 10393 |
rs531431107 | in-del | -/A | 0.00478085 | 0.0486577 | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145097211 | TGTCCCAAAAAGCAC[-/A]AAAATAAGAAAAAAA | 10393 |
rs531504735 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145094096 | GACCATTTTGAAAGC[C/T]AGCTACTACTAATCT | 10393 |
rs531510070 | snp | C/G | 0 | 0 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145040959 | AATGCATGACAATGG[C/G]AACAAAGTTCTTACT | 10393 |
rs531542426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145093573 | TAAGATGTTAAAAAA[A/G]AAAAACAAAAACCTA | 10393 |
rs531554556 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144971378 | TAAACTGATGCTCTT[C/T]CATCAAAAGGGCCTA | 10393 |
rs531617573 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145017515 | GAACACTTTTCCACT[G/T]TTGGTCAGACTGTGA | 10393 |
rs531617960 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145010967 | ATCCACGGAAGGCAC[A/G]GCAAGACAGAAAGCT | 10393 |
rs531629749 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144984969 | AATTGCCATGGATTA[C/T]AGACATTCTCTTAGA | 10393 |
rs531631338 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | ANAPC10 | GRCh38.p7 | 4:144993645 | TAAGGGGAAGCATTA[C/T]CTTCATAATCCTCAG | 10393 |
rs531640066 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145061059 | GCAGAAAAGTAGTAT[A/G]TTCATTAAGTTTTCC | 10393 |
rs531656098 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144977253 | CCTTTTTATCCCAGG[A/C]AAACTTCTGATCGCC | 10393 |
rs531657217 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144968332 | GTTTAGATTAAATCA[C/T]ATTAATATTTTCTAA | 10393 |
rs531660588 | in-del | -/AC | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145039617 | TTTTTTTTGTTTGAA[-/AC]ACAGTCTCGCTCTGT | 10393 |
rs531667241 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145003533 | TACAGTGTAAGGAAG[A/G]GATCCAGTTTCAATC | 10393 |
rs531692878 | in-del | -/A | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144994601 | TCTTTTAATATATAT[-/A]AAAAAATTTCACATA | 10393 |
rs531694813 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145061840 | AGGCCAGGCGCGGTG[C/G]CTCAAACCTGTAATC | 10393 |
rs531720742 | in-del | -/A | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144994929 | CCTTCCTCTGGGTAG[-/A]AAAAAATAGTAATTT | 10393 |
rs531723445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144968610 | TTCCCTAACAAGTGA[A/G]GTGAAGAGAGAAGAT | 10393 |
rs531752700 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145005499 | CTTCTTGTATTCTGC[G/T]AGACTTGGGGTTGGT | 10393 |
rs531778722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144967927 | CTTGCATCTTTACAA[C/T]GTTTTTGGACACCTG | 10393 |
rs531797456 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145069822 | AAAGATTTAATGAAC[A/T]AGCAGAAATGAGACT | 10393 |
rs531799658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145023945 | TTTCAAAATTGGAGT[C/T]GGTCCTTTCAGACCC | 10393 |
rs531809627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145006112 | TAGGTCTCTAAGAAC[C/T]TGCTTTATGAATTTG | 10393 |
rs531815752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144992061 | CCTACTCTGCCTGTG[C/T]TCTGCCTGTGGAACA | 10393 |
rs531838196 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144983235 | GCTGAGAATTGTAAT[A/C]AAACAAATATAGAAG | 10393 |
rs531844891 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145016888 | GGATTCCCTATTTAA[C/T]AAATGGTGTTGGGAA | 10393 |
rs531852814 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145055125 | ATAAAGGATCTTAAG[A/T]TAAGTGTACATCCAC | 10393 |
rs531899837 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144984112 | TCGAAGAAAATTTCT[A/G]AAGAATAGGTTATTT | 10393 |
rs531920814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145031972 | TATCAAATGGAAGTG[A/G]TATATACGTGATCAG | 10393 |
rs531978347 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145084839 | ATGTAAAATATGTCA[C/T]TAGTAATAGTAGTCC | 10393 |
rs531981758 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145008549 | ATGCAAATCAATAAA[C/T]GTAATCCATCATATA | 10393 |
rs531987014 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145076623 | AAATGACAGACATTT[C/G]GAATTCAGAATTCAG | 10393 |
rs532004870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145014956 | CTTCAGCCCTAGACC[C/T]TCCCTCTGACAGAGG | 10393 |
rs532075725 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145045236 | CAGGTAATGTGAATA[A/G]GTACTTTGCAAACTT | 10393 |
rs532080621 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145025157 | GGCTTTGACTTAAGG[A/G]AATGTTGTGGCTGGT | 10393 |
rs532100130 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145052604 | AGGTTTTCCTATTTA[A/G]AAAAAATATCGGGGG | 10393 |
rs532114760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145052729 | ACACAGTGAAAACCC[A/G]TCTCAAAAATTAGCC | 10393 |
rs532115249 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145008879 | AAGGGCATTCAATTA[C/G/T]GAAAAGAGGAAGTCA | 10393 |
rs532134118 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145026263 | TTATTGATTGACTGA[A/G]TGACTATTTTGTGCA | 10393 |
rs532138100 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144980550 | GATAGATAGATAGAT[A/C]GATAGATAGATAGAT | 10393 |
rs532167980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145073578 | TAAATTTATAAAGTA[C/T]TTTCTGTTCAAAGTG | 10393 |
rs532168759 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144992107 | CAGTACCACTGTTTA[C/G]AGCATAATTTACTGC | 10393 |
rs532171302 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144973573 | CAGAAGGGATCAATA[A/T]ACCCACAAGTTTGTT | 10393 |
rs532173608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145057857 | CCAATATTCTGAATA[C/T]ACCCCAGGTAGCAAT | 10393 |
rs532180855 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145022947 | GTTACATATGTTTAC[A/G]TGTGCCATGTTGGTG | 10393 |
rs532194500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145029271 | CCTTTGTCTGAGAAG[A/G]TAAACCCTGTGCTGC | 10393 |
rs532201169 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144979948 | CCACCTTATCTAAAA[A/T]AAATTCAAATGTTTA | 10393 |
rs532235139 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145014433 | CAGCAGCTGCACCAA[G/T]GCCCACCCAAGGAAA | 10393 |
rs532273016 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145062557 | GGTTGCAGTGAGCCA[A/C]GATCATACCACTGCA | 10393 |
rs532306557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144972743 | AAAACTCAAGGGTAA[A/G]TACTATTTTCATGAA | 10393 |
rs532339160 | in-del | -/A | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145064984 | GGTACTTTATCATGC[-/A]AAACAAGCATTAAGG | 10393 |
rs532345624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145088408 | TAGAAAAATAGGCAT[C/T]GCAAAATTAACATAT | 10393 |
rs532352124 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145020656 | GTCACTGTTTACTGA[A/C]AATATAATCGTTTAC | 10393 |
rs532354189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144995822 | TAGACAAAATAAAAA[C/T]AGATGTGCTTCATGT | 10393 |
rs532382825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145095810 | TTACACTTTATCACA[A/G]GTATTTATGTATAGG | 10393 |
rs532406978 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054549 | GCAATGGAGAGAGAC[A/T]CTATCTCAAAAAAAA | 10393 |
rs532416807 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145001717 | TGCTATGGTATGAAA[A/C]CTACAGTGGTGTAAA | 10393 |
rs532451988 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145089513 | CTATTATACGGTAGC[A/C]GTCATAACACAAATT | 10393 |
rs532457934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144987501 | GGCCTGTTGTGGGGT[A/G]GGGGGAGGGGGGAGG | 10393 |
rs532463723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145066231 | TTAAGCACTTTTCCT[C/T]GGATCAAGAGGTAAA | 10393 |
rs532541707 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145014268 | CAGTGTGAGTGAGAC[C/T]GGCCCTTTGGATTGT | 10393 |
rs532560968 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145065147 | GCAAAGAGAAAACTA[C/T]CTTTCCTAAAAAATA | 10393 |
rs532597893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ANAPC10 | GRCh38.p7 | 4:145064217 | GGTGAAATGGACAAA[C/T]ATGCACAAGTTATTT | 10393 |
rs532610804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145028679 | GAAAATACTGATAGT[C/T]CTTGGTGTAAACTGT | 10393 |
rs532621454 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145080799 | GTAATCCCAGTTACT[C/T]GGAAGGCTGAGGCAG | 10393 |
rs532648763 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145088111 | CACTTGTTTCCTCTT[A/G]ACTTCTATCCATGAT | 10393 |
rs532693163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145035268 | CCCAAAGCTGTGTGC[C/T]TGGTCAAAGAGGACG | 10393 |
rs532699641 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145057234 | CTATAAATTTAGAAA[A/C]AATTACTCCAAAGAG | 10393 |
rs532740735 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145093443 | TATTTGGCACTCAAT[A/T]AAAAAAAAAGACAAA | 10393 |
rs532745415 | in-del | -/TTGT | 0.0023933 | 0.0345097 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144980454 | CACTTTTTAATGGGG[-/TTGT]TTGTTTTTTCTTGTA | 10393 |
rs532769093 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144987389 | TCTCAGTAAAGTATC[A/G]CAAGGACAAAAAACC | 10393 |
rs532776124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145092709 | CAGTGCTACAGATAC[A/G]GAGGAGGGGACTGAC | 10393 |
rs532777081 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145013090 | AGGCTTCCCCAGACA[G/T]GCTTCCTGTACAGCC | 10393 |
rs532818512 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145001133 | GTACATGTATACCTA[C/T]GTAACAAACCTGCAC | 10393 |
rs532821047 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145041836 | ATTATGAAATGTAAA[C/T]GTGCATCTGAATTTT | 10393 |
rs532833297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145008013 | GGGGATATCACCACC[A/G]ATCCCACAGAAGTAC | 10393 |
rs532848783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145085760 | ACTTTTGCTTCTTCA[A/G]TATGCCTTACAAACG | 10393 |
rs532885052 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144985479 | TACTAAGAATTTTAT[A/G]GCAGTAACAATTTTC | 10393 |
rs532895422 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145007452 | GTCTCTCAGACCACA[A/G]TGCAATCAAATCACA | 10393 |
rs532927105 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145040020 | AGCCCATGCTCTTGG[A/T]TCTTTAACAACCCAA | 10393 |
rs532937734 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145039640 | TCGCTCTGTCGCCTG[A/G]CTGGAGTGCAGTGGC | 10393 |
rs532951666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145060950 | AAAGATGTATAATTA[A/G]AAGATAAAAGTATTC | 10393 |
rs532957688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144976134 | CACCATTATTTGTAA[C/T]AACAACTCCAATTAC | 10393 |
rs532974926 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054176 | CCTCCCAAAGTGCTG[G/T]TATTACAGGCCTGAG | 10393 |
rs532988005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145060092 | CTTCTATATAGAAAT[A/G]GTCTCTTGTGTAGAA | 10393 |
rs533008958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:145032604 | CCACCACTGTCATCG[C/T]CCAATGGGCCCATGA | 10393 |
rs533061434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054512 | GCAGTGAGCGAGATC[A/G]CGCCACTGCACTCCA | 10393 |
rs533098357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145032193 | ACCACCTGCAAGTGG[A/G]CAGCTGCAGCACTAC | 10393 |
rs533109129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145098780 | ACTTACAGCACTCTC[C/T]AGTACCCCCACACTC | 10393 |
rs533117446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145068102 | GGGTCCACAAACACA[C/T]TGTGAGGCTGCCATA | 10393 |
rs533128499 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145082821 | CAGACTTTTTAATAA[A/G]AGAAATAAGTTTAAC | 10393 |
rs533142918 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144974698 | TAGCATCAAAATTAT[C/G]AAATTCCTAGGAATA | 10393 |
rs533169813 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145031348 | GAAATAAATCCAACT[A/G]AAATTCCGGGACCGT | 10393 |
rs533186690 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145022654 | AATAACCTATGGAAA[A/T]TTTTTTTTTAATTAA | 10393 |
rs533187926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145010036 | CAGACACTTCTCAAA[A/G]GAAGACATTTATGCA | 10393 |
rs533195784 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:144967107 | AGCAGTAACTTAAAC[A/G]TTTTTTTAGTGATAA | 10393 |
rs533219256 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145075821 | GTGGAGCCCAGAGGG[C/T]TTGGCATGGAAATGG | 10393 |
rs533238264 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145005278 | GGGTTCATAATAGTC[A/T]CTCAGGGATTTTGGA | 10393 |
rs533301716 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145010758 | CAGCACACCAACATG[A/G]CACATGTATACATAT | 10393 |
rs533309385 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145094334 | GCTTGGAAAGGCCCA[-/G]AAGACTGACCATAAA | 10393 |
rs533319363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145076421 | CTCGATGACATCAAA[A/G]AAGATAAAAGCAAAA | 10393 |
rs533334186 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144982991 | CGGTGAAACCCCGTC[G/T]CTACTAAAAATACAA | 10393 |
rs533339140 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145045911 | GTAATTTTAAAAAAC[A/G]ATCTGATCTAATAAG | 10393 |
rs533353379 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145041378 | TCATTTTGAGAAAAA[C/T]GTTTTAACTTGTTTC | 10393 |
rs533374141 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144997127 | TTGGTATACCTGAAA[A/G]TGACGGCCAGAATGG | 10393 |
rs533413589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145083847 | TATTTACTCACCTGA[C/T]AGATTAAAAAAATTG | 10393 |
rs533443227 | in-del | -/AT | 0.00755907 | 0.0610114 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145083008 | CATATACAAGCAGTC[-/AT]ATATGTATTCTTTCT | 10393 |
rs533453996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145016227 | TAGAAAACCCCACCG[C/T]CTCAGCCCAAAATCT | 10393 |
rs533472231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144975377 | ACAAAAAACACAAAA[C/T]ATTATAAAAAGACCA | 10393 |
rs533486217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145037742 | CCTGGAGCCCAGGAG[C/T]TTCAGAGCAGCCTGG | 10393 |
rs533494545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145023745 | TTTTTGCTGGTGTAA[A/G]GTCTTGCCTTAATGT | 10393 |
rs533506533 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145056039 | TATGAACTTCTGGTA[C/T]TGTCAGAGGCGTGTG | 10393 |
rs533516145 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144989550 | TTCCCTGAGACCCAA[C/T]AATATTGAAATTAGG | 10393 |
rs533548785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145045670 | ATATGAATGTATACG[C/T]GATCTTCTACACACA | 10393 |
rs533569133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145012564 | CATACATCATAAGAC[A/G]AAATGGATAAATTCC | 10393 |
rs533577179 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145090448 | ATCTTATTCTTGCTT[C/T]ATCATACAGAATAAG | 10393 |
rs533597091 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144970136 | CTTTGAGTAGAATTT[A/C]TGAAGTGGCAAGGTT | 10393 |
rs533654256 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144984077 | AGAAATAAATTTTGT[C/T]CTAATCTGCCCAGAG | 10393 |
rs533656220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144990571 | AGAGCCAGCATCACA[C/T]GGTGAGAACAGGAGC | 10393 |
rs533800720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145018404 | TTTGGGAGGCTCAGG[C/T]GGGCAGATTACTTGA | 10393 |
rs533822698 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145062453 | TCTACTAAAAATAGA[A/T]AAAATTAGCTGGGCA | 10393 |
rs533839518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145024691 | TTGTTCTTCCATTTA[C/T]AGCACATGAGTAGAA | 10393 |
rs533840151 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145094858 | CATGGCAAAAGAAGA[C/T]AGTGAAAGAGCATTC | 10393 |
rs533856367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145000575 | GAGGATGTGGAGAAA[C/T]AGGAACACTTTTACA | 10393 |
rs533856667 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145007534 | AAACTCACTCAAAAC[C/G]GCTCAACTACAGGGA | 10393 |
rs533876504 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145026744 | GGAACTCCAAAGAGA[C/G]GCAGTGAAGAAGTAC | 10393 |
rs533920039 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145007046 | GAGGCGCGGGTCCCA[A/G]GATGGACGAATAAGA | 10393 |
rs533929485 | in-del | -/GTTAT | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145071006 | AAAGGAAATTGGGTG[-/GTTAT]GTTATTATTTAATGG | 10393 |
rs533945027 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144977701 | AATCTGCACGTTGTT[A/C]TGGAACCAGAATGTA | 10393 |
rs533992354 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145078302 | AAAATAAAACACCTG[G/T]GAATACAGCTAACCA | 10393 |
rs534032633 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145032425 | GTGACCAAGAAATTT[A/C]GGGAAGAGGTATGTG | 10393 |
rs534036294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145040450 | ACCATGCCCAGCCTA[C/T]TGTATGCTTTTAAGA | 10393 |
rs534047563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145011790 | GTTGCCTAGGATAGG[C/T]TGCTGAAAGGTTAAG | 10393 |
rs534098806 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144968105 | ATTTTAATTGAGATT[A/T]TACTAATTCATTTAT | 10393 |
rs534101965 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144968963 | CAAGTGATGTCAAAT[G/T]ATTGCTATGAGGTAT | 10393 |
rs534136603 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145017932 | ATGAGAATACTTGGA[C/T]ACAGGAAGGGAAACA | 10393 |
rs534171838 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144998553 | AGGCAGAAATAAAGA[C/T]GTTCTTTGAAACTAA | 10393 |
rs534176072 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145069517 | GGGCACAGAGGACTG[C/G]GAATCATTAAAGCTC | 10393 |
rs534181648 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145090833 | TTAAAGCTATACTTC[A/C]TCCACTAAATTGTGA | 10393 |
rs534187975 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145039785 | TTTTTCAGTAGAGAC[A/G]TGGTTTCACCATGTT | 10393 |
rs534206641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145005523 | GGTTGGTTTGCTCTC[A/G]GTTCCCTAGTTCTTT | 10393 |
rs534225940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145047572 | AACACAAGGCAAATC[C/T]TCATTCAAAATAAGT | 10393 |
rs534256573 | snp | C/G | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant, missense | ABCE1, ANAPC10 | GRCh38.p7 | 4:145098217 | TCGCAGCTCAATGAC[C/G]TCATATCTCCCTACC | 10393 |
rs534268672 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145004996 | GTTGGTAGGCTTTTT[A/G]TTACTGATTCAGTTT | 10393 |
rs534277956 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144997142 | GTGACGGCCAGAATG[C/G]AACCAAGGTGGAAAT | 10393 |
rs534285920 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144984544 | CAGTTTGGGCCATTA[G/T]TTCTGGGACCACAGG | 10393 |
rs534296246 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145052837 | AGGTTGCAGTGAGCC[A/G]AGATTGCACCACTGC | 10393 |
rs534312997 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145085388 | AATCACGATTCTTCC[A/G]TAAAAGCTCCACAGT | 10393 |
rs534327729 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144989197 | TACCTAATTTTATTG[C/T]ACTTCACAGATAACT | 10393 |
rs534336637 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144996701 | AGAAATGCAGCTCCT[C/T]GCCAGCAACGGAACA | 10393 |
rs534341454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145061228 | AATGTTTCAGCACTT[A/G]GATGACATAATAGAA | 10393 |
rs534357142 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145044496 | CCACCCACCATGACC[C/G]ACCTCCACCCACAGT | 10393 |
rs534371660 | snp | A/T | | | intron-variant, downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:145063193 | AAGTGGTATGTGAAG[A/T]AATGCATATGTTAAC | 10393 |
rs534420482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145029835 | GGAGGGTCCAGAAGA[C/T]ATACCCTTGACCAAT | 10393 |
rs534431558 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145060675 | AAAAGATTTAGGTGG[A/G]TTTTCCACTCAGTTA | 10393 |
rs534434090 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144967338 | CCATTTGGTCAAGGA[A/T]CAAGATGAAACATGA | 10393 |
rs534437376 | in-del | -/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145059879 | TCACACATTATTTTT[-/C]CTTCTGAGAGCAAAA | 10393 |
rs534507956 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144985892 | TGTGGGTTTGTCATA[C/G]ATAGCTCTTATTATT | 10393 |
rs534508955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054659 | CGCGCGCGCGCGTGC[A/G]TGCAGCGCATGTGTG | 10393 |
rs534512018 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145015545 | AGGAAAACTTCCTGG[C/T]CTTGCTAGAGACCTA | 10393 |
rs534515833 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145008269 | GGTACAAAGAGGAGC[A/T]GGTACCATTCCTTCT | 10393 |
rs534567816 | in-del | -/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145055758 | CCAGGGCCTGGAGAA[-/G]GGGGAAACTGGGAGT | 10393 |
rs534588516 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145087093 | CTCCACTAAGAGAAT[A/T]TGCCTGGACAAATGG | 10393 |
rs534589715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145002803 | TGTACATAGTAAAAA[C/T]TTTTTAAACTTACAA | 10393 |
rs534644851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145002079 | CTCTCACTACTTCTC[C/T]TTTACTAACCATATC | 10393 |
rs534669152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144971269 | ACATTGAATTATTTG[C/T]CACTGGCTTGCATTG | 10393 |
rs534670281 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144979986 | GAGATTAGTTTAGAT[G/T]GTACAACCCGACCCT | 10393 |
rs534692201 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144987804 | CAGTAGACTGTAAGC[-/A]ACTGGAAGGCAAGGT | 10393 |
rs534698374 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145008718 | CTATTTATGACAAAC[C/G]CACAGCCAATATCAT | 10393 |
rs534745859 | snp | C/T | 0 | 0 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145090565 | TAGTGGAAAGCACTA[C/T]TGTGTAATGGAGTCT | 10393 |
rs534764428 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145013955 | TGGGTCCCCAGGCAG[A/G]CCATTCTTGCCTGGC | 10393 |
rs534771802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145057923 | GGAACCCAACTGCCA[C/T]AGCCTTAATTAAATC | 10393 |
rs534833730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145014526 | AGTTGAAGACAAAGG[A/G]CATACTCTCTTGGGA | 10393 |
rs534867244 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995195 | GAGCTTTATTACATG[C/T]TAAAGAAAATAAAGA | 10393 |
rs534882555 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145012715 | CTTTATCAGTTGGAC[C/T]GGCTTCTTCTAAATA | 10393 |
rs534896858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145042120 | GATGCTGTATGAATC[C/T]GAATGAAGGTTGAGA | 10393 |
rs534914466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145050543 | ACTTCTCCTCTCTAA[C/T]CTTAGCTGGCATCTT | 10393 |
rs534938434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145052166 | TTCGGTGAGGCATAA[A/G]AAATAAGTTCAAGTC | 10393 |
rs534964100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145008602 | ACATGATTTTCTCAA[C/T]AGATGCAGAAAAGGC | 10393 |
rs534966820 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145057798 | TCAACCAGTTGCCTA[A/C]GCTGAGAATTCCAGA | 10393 |
rs534974029 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145088752 | AAAAATTCTGTATCA[A/G]ATCATCTTCCTCTCC | 10393 |
rs534995818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145028721 | TGCAAAATAAATGTG[C/T]TTGACACTTGATTCA | 10393 |
rs534997631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145019612 | AGAGCATAACTAAAT[A/G]AAACTAAAACAAAAT | 10393 |
rs535007026 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144987195 | AAAGACACATGCACA[C/T]GTGTGTTTATTGTGG | 10393 |
rs535020591 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145072146 | CACTACTCACTAGAA[A/C]TGAACACTTCTATTT | 10393 |
rs535054377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144987666 | AAAATGTCTTCTTTA[A/G]CTTCACCTCTATCTT | 10393 |
rs535055199 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144967386 | AAGTCAGAAGACCTG[A/G]GTCATTTACTACTTG | 10393 |
rs535084969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145077388 | CATGAAAATTTCCCC[A/G]ATCTCGCTAAGGAGG | 10393 |
rs535109417 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145069063 | GTCTTAAAATAAAAT[A/C]AAACAAGAAAGTCCG | 10393 |
rs535116262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144976188 | TGCAATAGTAAATGA[A/G]CAAACTATATTTACA | 10393 |
rs535122546 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145035300 | CCCTCCCTAATAGAG[A/G]AGGACCACTCTTTGG | 10393 |
rs535168262 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145020302 | AGTCAATAAATGTGA[C/T]ACACCACATAAACAG | 10393 |
rs535187556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144968170 | TCTAAGTGCCTCAGA[A/G]CCAAAGTTACTTACA | 10393 |
rs535241581 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime, intron-variant | ANAPC10 | GRCh38.p7 | 4:144994490 | AAATAACCATCCCCC[A/G]AAAAAAAGTAATACA | 10393 |
rs535242894 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145093514 | AGAGATGACCCAGTT[A/G]TTGGAACTACCAGAC | 10393 |
rs535255533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145001228 | AGGGAGGGAGGGAGG[A/G]AAGGAGGGAGTGAGG | 10393 |
rs535291935 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145035285 | GGTCAAAGAGGACGA[A/C]CCTCCCTAATAGAGG | 10393 |
rs535302599 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145046706 | TAAAATAATTTTTTT[A/T]AAAATCCAAATAACC | 10393 |
rs535303063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145028229 | GATCCAGCCTTAATC[C/T]GGTGGGCACAATCTA | 10393 |
rs535311191 | snp | G/T | | | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145097229 | AATAAGAAAAAAATG[G/T]TAAAAGTTCACTTAC | 10393 |
rs535357776 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145032244 | CTGAAGGACAGCGGT[G/T]AAAGGAAATCTTCCC | 10393 |
rs535389284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145084381 | TCAAGAAAAATGGCA[C/T]ACATGGAAAACAACA | 10393 |
rs535395847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145069644 | AGAGAAATGATCTTA[A/G]AGAGTGGTCTGGGGA | 10393 |
rs535418691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:145053623 | CAAATATCTACAAAT[C/T]CTTGTAGGAAGAATT | 10393 |
rs535424699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145016423 | TACAAGGGATGTGAA[A/G]GACCTCTTCAAGGAG | 10393 |
rs535427217 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145025339 | TTCAACACGCCCCCC[C/G]CCCCTTTTAAGCTCA | 10393 |
rs535433659 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145067447 | TCCCCTCACTCACTA[C/T]ACGCTTTCTCCTGAG | 10393 |
rs535490697 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145011127 | ACCCGAGGTCAGGAG[G/T]TCGAGACCAACCTGG | 10393 |
rs535491038 | in-del | -/TTATG | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144969778 | AATGCCCTGTATATC[-/TTATG]TTATATGAAATTAAA | 10393 |
rs535496500 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145098332 | ATTTTGGCCGGTGGC[C/T]GTGAGAACACGCTGT | 10393 |
rs535533274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145091606 | CTATCACTGATGGGC[A/G]TTTGGGTTGATTCCA | 10393 |
rs535575557 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054278 | TTTACCACACCAGGC[A/G]CGGTAGCTCACACCT | 10393 |
rs535589565 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145017151 | TAAAGAGCTTCTGCA[C/T]AGCAAAAGAAACTAC | 10393 |
rs535596738 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144991627 | GTGATCCACCCGCCT[C/T]GGCATCCCAAAGTGC | 10393 |
rs535619167 | in-del | -/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145039599 | CTATGAGGTATACTC[-/T]TTTTTTTTTTGTTTG | 10393 |
rs535621649 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145077198 | AGCAAGACTCTGTCT[C/T]AAAAAAAATAAATAA | 10393 |
rs535637279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145039192 | ACATTTACAATAAAA[A/G]CAATGAGGAAGTGGA | 10393 |
rs535640640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145067676 | GTTGATATTTTGGCC[A/G]CCTCCTGCTACCACA | 10393 |
rs535656093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145092209 | GAAAAATAGCTAATG[C/T]ATGCTGGGCTTAATA | 10393 |
rs535665932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144998473 | GAAACTCACTCAAAA[C/T]GGCTCAACTACATGG | 10393 |
rs535687817 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144971935 | TGTCTCTAGTGCTTG[C/T]TGCTCCATTTGAATC | 10393 |
rs535719000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145024274 | CAACTTCTTCCAAAC[C/T]CTTGTTAATGTTCGT | 10393 |
rs535735028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144983590 | CATAAACTGTTAGAA[A/G]AGTGACAAAATTACA | 10393 |
rs535738062 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145029823 | TCATCCCAGCTGGGA[A/G]GGTCCAGAAGATATA | 10393 |
rs535743424 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145009236 | TAGGAAGAATCAATA[A/T]CATGAAAATGGCCAT | 10393 |
rs535748127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145031645 | CAAGCTGCTCTGCCA[C/T]TTGGGCCATATAACT | 10393 |
rs535849649 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145009636 | GTAGAAAGCTGAAAC[A/T]GGATCCCTTCCTTAC | 10393 |
rs535857984 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144989953 | AGAGAGGTAAGGAAG[C/T]TACAGAAGTTTGAAG | 10393 |
rs535875725 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145007590 | CTACTGGGTACATAA[A/C]GAAATGAAAGCAGAA | 10393 |
rs535917822 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145019254 | TATCAAGGACTCTCT[C/G]AGACCACAGTGGAAT | 10393 |
rs535935178 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145004776 | AGATTTTTGCATCTA[A/T]GTTCATGAAGGATAT | 10393 |
rs535937071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144997904 | TACCAAGCAAATGGA[A/G]AACAAAAAAAACCAG | 10393 |
rs535962599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145042322 | AAAATTTGACTAACT[C/T]ATAACAATACTATCA | 10393 |
rs536022631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145018460 | CCAACATGGTGAAAC[C/T]CCATCTCTACTAAAA | 10393 |
rs536031469 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144974167 | AAAGCTGGATTTATT[C/G]CAGGATCGATAGTTG | 10393 |
rs536059930 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145075480 | AAGAGCTTCATTCAC[C/G]GAGAAACCAGACCAT | 10393 |
rs536083148 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144982051 | TGGGTTTCACCATGC[C/T]GCCAGGCTGGTCTTG | 10393 |
rs536092091 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144978586 | AACTACTTAGGAGGC[C/T]GAGGTGGGAGAATTG | 10393 |
rs536095170 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145034188 | GATTGAGGGATACAA[A/G]GTATTAATCCTGGGT | 10393 |
rs536101299 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145016014 | TCACAGCCAATATCA[C/T]ACTGAATGGGCAAAA | 10393 |
rs536139076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145064470 | AATATTTTTCTCTTA[C/T]ATATTAACATTTTAA | 10393 |
rs536163951 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144974850 | TTTTCCTCAGATTGA[G/T]CTATAGTATAGGGTC | 10393 |
rs536311564 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145059574 | AAACCAAAGGACAAC[A/T]TTCACATATGCTGAA | 10393 |
rs536317728 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145026833 | CATCCATGAAACAAG[A/C]ACAGAATGTTAATTT | 10393 |
rs536354693 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145026092 | ACGAGAACACTGACT[C/T]CTAGGCAGATCACTT | 10393 |
rs536376504 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145090277 | AGTTGTACAGTGTTG[C/T]TTTTCTATTTGTGTT | 10393 |
rs536376625 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145056244 | CCAAACCCACCAAAA[C/T]CAAGATGGCCACGAG | 10393 |
rs536418861 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145072020 | AAACACAAAAAAAAC[A/C]AAAAAAAACTAGGTA | 10393 |
rs536459802 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145068549 | TAAACACAGTCCACA[C/T]AGTTGTTTAAATCAG | 10393 |
rs536464754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145011608 | TGATGCTGGTAAAGG[A/G]CGAGAGGCTAAAAAC | 10393 |
rs536514202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145007160 | CCTTAGAGACATACA[A/G]AGAGACTTAGACTCC | 10393 |
rs536520227 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144992666 | TCGTGGATGAGGAAT[A/G]AAATTGGTTTTTTGA | 10393 |
rs536521161 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145073360 | AGGTCCTGTTGTTCA[C/G]CTGTTACCTGATATT | 10393 |
rs536527679 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144999767 | CTACGCAAAAAGAAC[A/G]AAGTTGGAGGCATCA | 10393 |
rs536536024 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145068817 | TGGGAGGCTGAGGCA[A/G]GAGAATCGCTTGAAC | 10393 |
rs536565331 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145030242 | TGAATTATAAAAACA[A/G]AGAATCACAGCCTCT | 10393 |
rs536586771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145006273 | AATTATAGCAACCCA[A/G]ACTTTTTATCTGAAA | 10393 |
rs536591774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144999073 | TAAGCCAGGAAGAAG[C/T]TGAATCCCTGAATAG | 10393 |
rs536594480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145012645 | ATAGAATGACATTTA[C/T]TAAGGAAACTGACTC | 10393 |
rs536617792 | in-del | -/A | 0.00874735 | 0.0655527 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145071468 | TATTTCACTACAAAT[-/A]AAAAAAAATCTTTAC | 10393 |
rs536665046 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144989767 | TTCTTGGAGGAAATT[A/G]TAAGTACTACACTAG | 10393 |
rs536716613 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144982326 | CCAAATACCCATGCT[G/T]CCTTCTTCCTTGCAT | 10393 |
rs536736262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144974278 | AAGTTTTGTATACTC[A/G]ATATTCATTCATGAT | 10393 |
rs536736936 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145079567 | CATTTCACCATAAGA[C/T]AAATGCACACATATG | 10393 |
rs536747851 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144977928 | TGCAACCAGCTATAA[C/T]GTGATTCTCAGGAAT | 10393 |
rs536806117 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145091074 | CTGATAGACTCAAAG[C/T]TCAAAATCACATGAA | 10393 |
rs536838858 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145012192 | TATATATATATATAT[A/G]TATACACACACACAT | 10393 |
rs536857298 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145002935 | ATTGCATATCATGAG[G/T]ATTTGGTATAAAGAT | 10393 |
rs536871823 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, missense | ABCE1, ANAPC10 | GRCh38.p7 | 4:145097259 | CATATGCTCTTACCA[C/T]AGAAGATAAGGTCAG | 10393 |
rs536882131 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145087972 | AGAATCACTTGAACC[C/T]GGGAGGTGGAGGTTG | 10393 |
rs536892528 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054666 | GCGCGTGCGTGCAGC[A/G]CATGTGTGTGTGTGT | 10393 |
rs536894057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145052228 | TAATAATATATTGTA[C/T]ACTTGAAAATTGCTA | 10393 |
rs536897463 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145052748 | CAAAAATTAGCCAGG[C/T]GTGGTGGTGCACACC | 10393 |
rs536904493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145093779 | CCAATGAAAAATACC[A/G]GAATTGAAACACAAC | 10393 |
rs536909250 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145083166 | CAACAATAATAACAA[A/T]AACAAACACTGATAT | 10393 |
rs536965060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145048439 | CTTCCTGACAGTCAA[C/T]ACGAAGTGGGTATCA | 10393 |
rs537000192 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145010992 | AAAGCTTCCACAATA[A/G]AAGTCACATGAAGAA | 10393 |
rs537022930 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145083103 | ATTTTACTTAACATA[A/T]CTGGAGTTTTTTACC | 10393 |
rs537030520 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145002161 | GAAGCAGCAGATTCT[A/G]GAATTTTAACCATCC | 10393 |
rs537032077 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145041610 | CCCCTTCTAGAAGGC[A/T]TATGCAAGATATGTC | 10393 |
rs537126109 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145076094 | TAGCTTTTTCACCAA[C/G]AGACCCCACCTAACC | 10393 |
rs537131530 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145057994 | TCTAGGTGCTCCAGC[G/T]CCCCCATTCCCATGA | 10393 |
rs537174543 | in-del | -/A | 0.00835141 | 0.0640778 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145066759 | ATAGGAACTTTTATT[-/A]TCTTCATTTTTCTGA | 10393 |
rs537217479 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145080997 | TAAATTCAGCCAGGC[C/G]CAGTGGTTCATGCCT | 10393 |
rs537253858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145009014 | TACAAAATCAATGTG[C/T]AAAAATCACAAGTAT | 10393 |
rs537280184 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145043272 | TTGATACATTATTTT[A/G]ACTAAAAAACAATTC | 10393 |
rs537313823 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145048152 | AAAACGGACGCCCCT[C/G]CACTATCTTTAAAAT | 10393 |
rs537319650 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144970477 | AAGCAACTGAAAACC[A/G]GACTGGCACATGAGT | 10393 |
rs537319751 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145006065 | TGTTAAAGTCTCCCC[A/G]CTATTATTGTGGGGT | 10393 |
rs537329834 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145073016 | ATCCATGTCAGCTTC[C/T]TGAATAGCTGAGACT | 10393 |
rs537335158 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144980085 | GATGTGCTGTCATGG[C/T]GACTGGCCAAGGCAG | 10393 |
rs537403752 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145062254 | TAAATTAAAAGAAAA[C/G]TAATTTACAACAATT | 10393 |
rs537406463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144968786 | CAGGCAGCTGATTTC[C/T]TATAGCATTCTGCCC | 10393 |
rs537469495 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144977396 | CACAACATATAATAA[A/T]GGGTGGTGTGTGATA | 10393 |
rs537496340 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145065719 | ATTTAAAATAATCAT[A/G]TACATATATAGTTAC | 10393 |
rs537510384 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145074456 | TCCTCCAAAGAAAAA[C/T]CAAGAAATATGAAAA | 10393 |
rs537562902 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145003783 | TAATATGATGCTTCT[A/T]GCTTTGTTCTTCTTG | 10393 |
rs537657835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144996088 | CCAGAAGTAATTAAC[A/G]ACAGGGTTCGAGGTA | 10393 |
rs537669342 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144987220 | TTGTGGCACTATTCA[C/T]GATAGCAAAGACTTG | 10393 |
rs537683069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145039699 | TCCCGGATTCAAGCA[A/G]TTCTCCTGCCTTAGC | 10393 |
rs537713471 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145020389 | AATCCAGCATCCCTT[A/T]ATGATTAAAACTCAG | 10393 |
rs537733182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081511 | ATGCTAATAATCTAA[C/T]TGAACTGAAAAATAA | 10393 |
rs537734261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145078168 | TGATGAACAACTTCA[A/G]CAAAGTTTCAGGATA | 10393 |
rs537771400 | in-del | -/T | 0.0103295 | 0.0711199 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145013944 | TGGGAGCTTGCTGGG[-/T]CCCCAGGCAGGCCAT | 10393 |
rs537827066 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145011238 | TCTACTCAGGAGGCT[A/G]AGGCAGGAGAATTGC | 10393 |
rs537827119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145017785 | ATGGAATACTATGCA[C/T]CCATAAAAAAGGATG | 10393 |
rs537847188 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144998625 | GTAAAGCAGTGTGTC[A/C/G]AGGGAAATTTATAGC | 10393 |
rs537858679 | in-del | -/TTGTC | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145099907 | CAATTTTGAACACTT[-/TTGTC]TTCGAATCTGAAATA | 10393 |
rs537874262 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144968303 | AAGAGACACATCATG[A/C]TTTACACGGCTCAGT | 10393 |
rs537900984 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145067690 | CGCCTCCTGCTACCA[A/C]AGATACGAGCATCTG | 10393 |
rs537910672 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144996204 | CGGCTCTACACTCCG[A/T]AACAGGCTTATAGGA | 10393 |
rs537918360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145031752 | GAATCACAGTGGAGG[C/T]CTCTTGGATTTCACA | 10393 |
rs537932690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144998951 | CACCACTGAACCAAC[A/G]GAAATACAAACTACC | 10393 |
rs537952613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145084532 | CTGGAAGAAGAACTG[C/T]CTTGGGCCACACATA | 10393 |
rs537969650 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145047472 | CAGTGAGTCATGATA[A/C]TTCCATGCTACCGAT | 10393 |
rs537972162 | in-del | -/A | 0.00358779 | 0.0422022 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145085553 | TTGTTCTTAAAATGC[-/A]AAAAAAAAATTAAAC | 10393 |
rs537994262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144984369 | GCTGGCTGAACTCTC[C/T]GCTTCAGTCTTTTGG | 10393 |
rs538009859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145059824 | ACATCTAAAATATAA[C/T]GTTCTTTGGTCCATT | 10393 |
rs538015591 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145077511 | AAGAATTCCTCCCTA[A/T]CTCATTCTATAAGGC | 10393 |
rs538033630 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145016096 | ACCACTCCTATTCAA[A/C]ATAGTGTTGGAAGTT | 10393 |
rs538042149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145032366 | TGTAGCCAATGGATC[A/G]GCTGGATGGTCAGGG | 10393 |
rs538051300 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144983700 | TGCAGCAAAAAGGCT[C/G]AGAATAATGAAAAAC | 10393 |
rs538052749 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145085127 | CAAAAAATAAAAAAA[A/C]TTAGCCAGGCGTGAT | 10393 |
rs538055607 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144992524 | ATTGAGGGGTTTACG[A/C]CTTCAGTGGAAAAAG | 10393 |
rs538102688 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145025310 | AAGAGGTTAGCTTTT[A/G]GCCTATTTTGGCTTT | 10393 |
rs538109532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145010296 | TAGAACTAGAAATAC[C/T]ATTTGACCCAGCCAT | 10393 |
rs538112486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145017198 | CAACCTACAGAATTG[A/G]AGAAAATTTTTGCAA | 10393 |
rs538153106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145025441 | TGTCAAGTTACTAAA[C/T]GGCCTAATTTCAATA | 10393 |
rs538167194 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145094726 | GGGTGAGAAAAGATA[C/T]CTGGCAAATGCCATG | 10393 |
rs538174909 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:145053661 | TTCCTTTATGAAGGA[C/G]AAATGGACACAGAAA | 10393 |
rs538195777 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145009707 | AATGTTAGACCTAAA[A/C]CCATAAAAACCCTAG | 10393 |
rs538240877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145043562 | ACTGAGCTGTAAAAC[C/T]GCAAAATCCCTTATT | 10393 |
rs538262675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145099159 | ATACCTTTATTATCT[C/T]TTCAGGGCTTCGTAC | 10393 |
rs538286145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145051591 | GAGGTAGGCCTGTAT[A/G]GTACTTAGTATACAA | 10393 |
rs538300839 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145055865 | ACCATATATGTAGCA[C/G]TACTGAACTAACTAC | 10393 |
rs538310405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145036228 | TAAGATGAAGATAAG[A/G]GAAGTAGATGAGAGA | 10393 |
rs538347201 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145035434 | CAAGACAAGCAGGCG[C/T]TTTTATAGATCATAT | 10393 |
rs538376557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144998539 | ACATAACAAAATGAA[A/G]GCAGAAATAAAGATG | 10393 |
rs538394660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144996138 | TCACTCACAGCCAGG[A/G]GAGGCTCCTGGATGT | 10393 |
rs538415283 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145029078 | TTAAAGTGAGGGCAT[C/T]GATTGGAAAAGAATG | 10393 |
rs538453196 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144989677 | AATGAGGAAGGCATA[C/T]TGAAAACTGAGATAG | 10393 |
rs538459487 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145013294 | AATGAAAAAAACCTA[A/G]AACAAATACTAGCAA | 10393 |
rs538460131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144975013 | ATTAGAATGTATTAC[A/G]ATTCAACACTAATTA | 10393 |
rs538508143 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145008255 | CAAATTCTACCAGAG[A/G]TACAAAGAGGAGCTG | 10393 |
rs538513985 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145018845 | ATGGCAGTTAAAAAA[C/G]ACAAAGAGGGACATT | 10393 |
rs538538917 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144967318 | AAAATTGGATCCTTT[C/G]ATTGCCATTTGGTCA | 10393 |
rs538543233 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145004183 | ACTGATTTTTGTACA[C/T]TGGTTTTGTATCTGA | 10393 |
rs538597592 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145007809 | GAAGCTAGCAGAAGG[C/G]AAGAAATAACTAAGA | 10393 |
rs538597752 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144987087 | GTGGAAGTCAGTGTG[C/G]AGATTCCTCAGGGAT | 10393 |
rs538612660 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145059176 | TTTGGGATCAACAAA[C/T]AGAGCCAGAACTTTT | 10393 |
rs538621182 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145052127 | GGGGGACAGTTGGGA[A/G]ATGTTGGTCGAAGGA | 10393 |
rs538630100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145080267 | TTACTACCTGGATGA[C/T]GAAATTTGTACACCA | 10393 |
rs538658463 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145087821 | GGAGGCTGAGGTGGG[C/T]GGATCACTTGAGGTC | 10393 |
rs538661203 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145096291 | GGCTGGGCATGGTGG[C/T]TCACACCTGTAATCC | 10393 |
rs538662764 | snp | G/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995075 | TGTATATACTGAAAT[G/T]TTCAGTTCAACTCTT | 10393 |
rs538681708 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145012816 | TATAAGGCCTTGATA[C/T]AGTTTGGGTCTGTGT | 10393 |
rs538708124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145019439 | ACCTGTGGGATACAG[C/T]AAAGGTGGTGCCCAG | 10393 |
rs538715552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144987771 | CTGGCTTGATTGGTT[A/G]GAGACCTATTGTTTC | 10393 |
rs538732710 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145044459 | CTCCTTTCTATCCTT[C/T]GCATTTCCTTCCCCC | 10393 |
rs538735932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145089906 | AAACACTGATTGTTT[C/T]ACTCTGTTACTTACC | 10393 |
rs538763325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145002685 | AAAGCCCAAGATAGT[A/G]AACACATTTTAAGAA | 10393 |
rs538771814 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145097111 | GGGGGGCTGAGACAG[A/G]AGGATCACCTGAACT | 10393 |
rs538790279 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144971999 | TCACCTGTTTAAAAC[C/G]CTTTAATGAAAATAA | 10393 |
rs538801359 | in-del | -/A | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | ABCE1, ANAPC10 | GRCh38.p7 | 4:145097575 | TTACTAAATAACGGC[-/A]GACACAACGGACTGT | 10393 |
rs538812827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145020220 | ATCCAACAACATACC[A/G]AAAAGATAAACTACC | 10393 |
rs538837741 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145087856 | GTTTGAGATCAGCCT[-/G]GCCAACATGGTGAAA | 10393 |
rs538859333 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145006930 | TCTGTCCTAAAATTA[G/T]TCCCACAATACAGGC | 10393 |
rs538911582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145001416 | TACTTAAGAGTAGTC[A/G]AAAATCATAGACACA | 10393 |
rs538979049 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144978778 | ATCCCACTGCTTCCA[A/G]CCTAGGTGACAAAGT | 10393 |
rs538982836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145094630 | ACTAAACTAATAACA[C/T]TATAAAGTCCCTCAA | 10393 |
rs538986880 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144993391 | ATGAAGTTGAGCATC[G/T]TTTTGTACAATTACT | 10393 |
rs539001724 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145027230 | GCTAGTCTTGAACTC[C/T]TCACCTCAGGTGATC | 10393 |
rs539004264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145000511 | AGATACCATCTCACA[C/T]CAGTTAGAATGGCAA | 10393 |
rs539012856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145034770 | GGCTGGGTGGATGTG[C/T]GTTAGGCTGCAGTGC | 10393 |
rs539021669 | in-del | -/T | 0.0142736 | 0.0832652 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145070361 | AAAGAGGGAAGGGAC[-/T]TTAAGCAGTCATTTC | 10393 |
rs539027323 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144982118 | CAAAGTGCTGGGATT[A/T]CAGGCGTGAGCCACC | 10393 |
rs539041393 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145011977 | ACAGAACTAGAGAGA[A/G]CCTTGCAAGAACTGC | 10393 |
rs539043161 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145023445 | TTTACCTATATAATC[G/T]GTAGTAATGCAGAAA | 10393 |
rs539063598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145076188 | GCTTTGACTGCACCC[C/T]TCATTGGAGTGTTGT | 10393 |
rs539103524 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145009147 | TGTGAAGGACCTCTT[C/T]AGGAACCACAAACCA | 10393 |
rs539119282 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145072093 | GTTTAGGGAGAGGAA[A/T]AAAACTTAAAGAAAC | 10393 |
rs539138306 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144976088 | ATGCACATGCAATAT[G/T]AGTCAAAAGACAGGT | 10393 |
rs539168254 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145067379 | GTGGGGAAGGAAGAG[A/G]GCAATACTTTCCTAT | 10393 |
rs539187151 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144972505 | CAGAAAGATACAATA[A/G]TTCTAAATATGTATG | 10393 |
rs539205263 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145037490 | TTTAAGTAAACGTGT[A/C]AGAAATATATCTAAG | 10393 |
rs539227686 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145040536 | GAGCTGCTAGTATGT[C/T]CCAGGCACTTAAAAC | 10393 |
rs539235439 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145046973 | ACAAAGCTAACAGAG[A/C]AAAGTAGTATGGATG | 10393 |
rs539252598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145048501 | CTACTTACAGATTCA[C/T]TTCCAAAGGGTCATC | 10393 |
rs539263358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145090762 | CTTAGAACAGCATCT[A/G]TCACTTAGTAAGCAC | 10393 |
rs539277842 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144997217 | GGCAGGCCAACATTT[A/C]AATTCAGGAAATACA | 10393 |
rs539281081 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145045462 | AAAATATGAGTAAAT[G/T]CCCTGGTCATCTCCC | 10393 |
rs539302859 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145033691 | AACAAAGCTTTGGGT[C/G]ACTCCACCAGGAAAA | 10393 |
rs539337878 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145083341 | CTCACCACACCTCTG[A/C]AGAACATTTAGGTTG | 10393 |
rs539344634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145041289 | TTTACATGAATTTTT[A/G]AAATACTGAACTAAC | 10393 |
rs539360587 | in-del | -/CT | 0.00755907 | 0.0610114 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145057447 | TCTTTCTGAGAGTTC[-/CT]CTCAGCTTTCTTCAC | 10393 |
rs539376619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145091529 | GCTTTTAAAAAACGG[A/G]GGGAGGGGGAAATCA | 10393 |
rs539388954 | in-del | -/TGAA | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145035777 | TGTTTACATCAGATG[-/TGAA]TGAAAACAACAGTCT | 10393 |
rs539431260 | in-del | -/A | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145074060 | TTCCCAATATTCCTT[-/A]AAAAAATTATTAACG | 10393 |
rs539471760 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145016408 | CCTAGGAATCCAACT[A/T]ACAAGGGATGTGAAG | 10393 |
rs539486952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145058068 | TACAATCTGACTATA[C/T]ATTTTCACTGAAACA | 10393 |
rs539503062 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145097833 | GGACTGGACGCCACC[A/G]AGTGGATAAAATATG | 10393 |
rs539506217 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145069003 | ACAAAGACCATGTTT[G/T]GAAAGGATATATGAG | 10393 |
rs539558366 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145024094 | GCTCATCAATAAGAT[C/G]CAACTCCTCATCAGT | 10393 |
rs539561600 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145059565 | AGAAGCAATAAACCA[A/G]AGGACAACTTTCACA | 10393 |
rs539564935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145052858 | GCACCACTGCACTCC[C/T]GCCTGGGCAACAGAG | 10393 |
rs539566738 | snp | C/T | | | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145098597 | GGGCGACGCCGAGAG[C/T]TTGGGGGCGCCTCGG | 10393 |
rs539580190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144997842 | AGGAGACCCATCTCA[C/T]GTGCAGAGACACACA | 10393 |
rs539608866 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145045974 | TTATGATTATCTATG[C/T]TTTTGCTTTATAAAT | 10393 |
rs539619584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145029727 | GGAAATACCTGATCT[C/T]CCTTTGTTTAATGTA | 10393 |
rs539636778 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145098272 | TCTATGTCGCGCGCG[A/C]GCACTACGTCCTATG | 10393 |
rs539646173 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:145053502 | TATTAATTAGCTATC[A/T]AATTACAAAGTAGGC | 10393 |
rs539657406 | snp | C/T | 6.62745e-05 | 0.00575612 | synonymous-codon, nc-transcript-variant | ANAPC10 | GRCh38.p7 | 4:145081716 | TTGCCAATAAGTTTC[C/T]AGATTGTCATCTCGT | 10393 |
rs539674480 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145077476 | CAACCCTACTGAAAC[A/G]ATTGCAAAAAACTGA | 10393 |
rs539686940 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145043421 | GTTCACATGATAGAA[C/G]AATGGGAAAATTTTC | 10393 |
rs539711828 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144999008 | CGCAAATAAACTAGA[A/G]AATCTACAAGAAATG | 10393 |
rs539716830 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144990885 | GCATCATGACTGCCT[G/T]AAGGTATAAATATCT | 10393 |
rs539783128 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145030307 | ACCCCTTGAATGAAG[G/T]AGAGGCCAGGTCCCC | 10393 |
rs539784305 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145020945 | CACTGAAAGAAATCA[C/T]AGACAACACAAACAA | 10393 |
rs539814839 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145073800 | AATTTCTTTGCGACA[C/T]AGAAATCATTTTAAT | 10393 |
rs539837732 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145042533 | ACTTTCTAATTTCAT[G/T]TTTTCATTATTTTAT | 10393 |
rs539849916 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145050264 | GTCAACAAGCATAGT[A/G]TTTTGAAATAAATCT | 10393 |
rs539851632 | snp | A/T | 0 | 0 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144974025 | AGAAAAATACAAAAA[A/T]AGGAATATCACAGGT | 10393 |
rs539852135 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145048454 | CACGAAGTGGGTATC[A/G]TTACTGGTTCTGACA | 10393 |
rs539863614 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145070454 | TTAGGGAAATGAAAA[A/T]CAAAACTATAATGAG | 10393 |
rs539890477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145055415 | ATACAAAAGTTAGCC[A/G]GGCATGGTGGTGTGT | 10393 |
rs539896438 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145086464 | GTGTCGTTCCTGAAC[C/G]AGCAGCATCATTACC | 10393 |
rs539927173 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145009567 | ACAAAAACAAGAAAT[C/G]GGGAAAGGATTCCCT | 10393 |
rs539927269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145003620 | CCCCATTGCTTGTTT[C/T]TGTCGACTTCGTTGA | 10393 |
rs539934622 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144993453 | CTGTTCAAATATTTT[C/G]CTCATTTTTAAATTG | 10393 |
rs539998985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145082210 | GCTGGAGTGCAATGG[C/T]ACAATCTCGGCTCAT | 10393 |
rs540001119 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145049082 | GTCTATTAAGTGTGT[A/C]ATAGCATTATGTCTA | 10393 |
rs540034767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145017384 | ATGCTCATCATCACT[A/G]GTCATCAGAGAAATG | 10393 |
rs540054838 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144980104 | TGGCCAAGGCAGCAC[A/C]CCTCTGGGCAGAAGT | 10393 |
rs540056338 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145069907 | CTTCTCACTATTTTT[C/G]TTGTTGTTCATTTGG | 10393 |
rs540080187 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144988637 | GTGCCTATTTAAAGT[A/G]TATAATTTGATGAGA | 10393 |
rs540090298 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145014616 | GGAAAGCGCCACCTC[A/C]TGGCAGGACAACCAG | 10393 |
rs540123382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054854 | TCTACCCTCGCATCT[A/G]TTTTATTCATTCTAC | 10393 |
rs540129877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144981900 | GCAATCTTGGCTCAC[C/T]GCAACCTCCGTCTTC | 10393 |
rs540153408 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145092625 | CACACTGACTCTCAG[A/G]CTCTTTTGCAAGGGC | 10393 |
rs540187113 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145040067 | ATGTAATGAAAACTC[A/T]TAATTTCATGAGATT | 10393 |
rs540205161 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145093445 | TTTGGCACTCAATAA[A/T]AAAAAAAGACAAACA | 10393 |
rs540242038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144999249 | GAAAAAGAGGGAATC[C/T]TCCCTACCTCATTTG | 10393 |
rs540256928 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145023746 | TTTTGCTGGTGTAAG[G/T]TCTTGCCTTAATGTT | 10393 |
rs540270918 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145047995 | CAAATTAGGATTGCC[C/G]TATATTCCCCAAAGC | 10393 |
rs540284120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145076438 | AGATAAAAGCAAAAA[A/G]GTCCCATCTAAAGGA | 10393 |
rs540289382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144990667 | CTCACTTATCACCAA[C/T]GGGATGGCACCAAGC | 10393 |
rs540296508 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145039377 | GAATTCTGAAAGAGA[C/T]TGGGAAGAAAAGTAG | 10393 |
rs540360711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145077597 | GGCCAATATTCTTGA[C/T]GAACATCGACACAAA | 10393 |
rs540367223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144993014 | CCTGCATAGAGGTTA[C/T]AACTTGGCTAAAGCT | 10393 |
rs540408220 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145010803 | CGTTGTGCACATGTA[C/G]CCTAGAACTTAAAAT | 10393 |
rs540437621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145004377 | GAACTTCCAGGACTA[C/T]GCTGAATAGGAGTGG | 10393 |
rs540449351 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144986996 | AAAAGTCAGGAAACC[A/C]CAGGTGCTGGAGAGG | 10393 |
rs540466012 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144976903 | AGTAATTTGACTTGA[A/G]AGAGTATGAATTGGA | 10393 |
rs540477923 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144997601 | AATATGGAAAGGAAC[A/T]ACCAGTACCAGACAC | 10393 |
rs540504004 | in-del | -/CTAA | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144970049 | GGTGCATTCTTCAGG[-/CTAA]GTTACTTCCTCAGGC | 10393 |
rs540505009 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145005869 | TAGGATTGTTTTATG[A/C]CTGATTGTGTGGTTA | 10393 |
rs540518821 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145045742 | ATCTAAAATGTCACA[C/T]GTCAATACTCCTGAT | 10393 |
rs540540350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145038461 | GAAGTTGCAGAGTGC[C/T]GAGATGGTGCCACTA | 10393 |
rs540555789 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144998620 | CACATGTAAAGCAGT[A/G]TGTCGAGGGAAATTT | 10393 |
rs540583890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145046847 | TGAATCCAAGACAAC[C/T]TATCCATTTTCCATA | 10393 |
rs540594436 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144983858 | ATAGGATGGAATATC[A/C]TTTGAATAACTATTT | 10393 |
rs540612649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145099321 | CATGTTTTATTTTTT[C/T]ACTCTTTCCCAACAG | 10393 |
rs540620172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145029143 | GACTCTGATGAAGCT[A/G]GGGACACTGAGTTCG | 10393 |
rs540643312 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145084675 | CGATAAAATGTAAAA[A/C]TTGGGCTATTACTTC | 10393 |
rs540649415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144983023 | AACTTAGCCAGGCAT[A/G]GTGGCAAGCAACTGT | 10393 |
rs540657644 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145028558 | GTGGTTCTAGAGGAA[C/G]AGAATATTAAGGATG | 10393 |
rs540680474 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145045451 | TCGGCCTAAAAAAAA[A/T]ATGAGTAAATTCCCT | 10393 |
rs540694737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145021021 | GAAAATGACCATACC[A/G]CCAAAAGCAACCTAC | 10393 |
rs540711577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145069255 | AACAACTGAGTTTTC[C/T]GGCTGCAGGCAATTT | 10393 |
rs540733926 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145020559 | CACTCGTCTTCAACA[C/T]AGTACTGGAAGTCCT | 10393 |
rs540746140 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145078508 | TACTGACAGTTTTCA[C/G]AGAATTAGAGAACTA | 10393 |
rs540749264 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145077080 | GGCAGGCACCTGTAG[A/T]CCCAGCTACTCAGGA | 10393 |
rs540773832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145046355 | TAGAAAGTATAAGGG[C/T]TAAGAAGTAAAATTC | 10393 |
rs540802472 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145098549 | CAGCGCGTGGCAGCG[A/G]TTCCTGCGGGACAGC | 10393 |
rs540808330 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145020170 | CCCTGATGAACATAA[A/T]TGCTAAAATCCTTAA | 10393 |
rs540877649 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145053786 | AAACATGAGGCTGAA[A/C]AAAAAAAAAGGTTCC | 10393 |
rs540883965 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145056549 | AGATATAAGAACCCC[C/G]TCTTGGGGTCTGGAT | 10393 |
rs540939286 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145088086 | TGAAGAATTAACTAA[C/T]TTCCTGAAACACTTG | 10393 |
rs540988147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144980362 | TTTCTCTAATGATCA[A/G]TGATGTTGAGATTTT | 10393 |
rs541000582 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144975746 | AGACTTTTAAAATAT[A/G]AGTGAAAGAAAATGA | 10393 |
rs541059136 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144970549 | AGTTGTCATCTAGGA[C/G]TTTGATTTTTCAGGG | 10393 |
rs541063924 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145007399 | TGGAAGTAAAGCATC[A/C]CTCAGCAAATGTAAA | 10393 |
rs541068664 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144970638 | GAAACTAAGATCTCT[A/G]TATAAAACTCGAAGA | 10393 |
rs541076820 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime | ANAPC10 | GRCh38.p7 | 4:145064000 | TGAAGACTGAACTGC[A/G]AACAGATATGATGGA | 10393 |
rs541118672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145074242 | TTCATTTTCTTATTA[C/T]ATTTTTTCCTTCCCC | 10393 |
rs541122192 | in-del | -/G | 0.00318978 | 0.0398085 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144991380 | ACAAAGAGTTTTTTT[-/G]GCATTTTTTTTTTTT | 10393 |
rs541126979 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144972497 | TGATCTGCCAGAAAG[A/T]TACAATAATTCTAAA | 10393 |
rs541129999 | in-del | -/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145002607 | ATAGAGTGTTCTACT[-/C]ATCTGCATGACAATT | 10393 |
rs541159225 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145007350 | ACATTCTTCTCAGCA[C/T]CCCACACGCTTATTC | 10393 |
rs541159837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145082396 | TCAAGTGATCCAGCC[A/G]CCTCAGCTTCCCAAA | 10393 |
rs541189917 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144978218 | CACTCACTGTCACCT[G/T]ACATTGAGTATGTGT | 10393 |
rs541244037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145087141 | CTCACAGCCTAAAGC[C/T]GAGCCATCACCAAAG | 10393 |
rs541284144 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145080670 | TCCCAGCACTTTGGG[A/T]GGCCGAGGCGGGTTG | 10393 |
rs541300171 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144996203 | ACGGCTCTACACTCC[A/G]AAACAGGCTTATAGG | 10393 |
rs541325180 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144969401 | AGTATTAAAAGATGT[A/G]AGTGAACAAGATCAC | 10393 |
rs541341055 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145043635 | CTTTCCATTATAAAT[A/C]TTTTTTTATTACTAT | 10393 |
rs541377601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145088360 | AGCAGAGCTCCCAGC[C/T]TCTACAGTCAATTGC | 10393 |
rs541388710 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145064917 | ACAGACACCTATGTA[C/G]AACATGGTCAAGAGC | 10393 |
rs541432016 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145060815 | TATATTTAGATATTG[C/T]GGTAGAATAACAGAA | 10393 |
rs541461665 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:144966673 | CAAACCATTAAAAAT[A/G]TATCCCCAATTGGGC | 10393 |
rs541490321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144998242 | GGACCTAATAGACAT[C/T]CACAGAACTTTCCAC | 10393 |
rs541500906 | snp | C/T | | | downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:144966769 | TTCCCATTTTGCTCA[C/T]GATCCTAAGTTATTT | 10393 |
rs541522516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145057055 | TCTTGAAAGAAAATT[C/T]ATCAACTTCTAAGTT | 10393 |
rs541524383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145050267 | AACAAGCATAGTGTT[C/T]TGAAATAAATCTTTT | 10393 |
rs541528161 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145005083 | AGATTATATTTCCAA[G/T]AATGTATCCATTTCT | 10393 |
rs541555964 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145013484 | TTCAATACTCATTTA[C/T]GATTTTAAAACTCTT | 10393 |
rs541572287 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145098594 | CGCGGGCGACGCCGA[C/G]AGCTTGGGGGCGCCT | 10393 |
rs541575400 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145011427 | GTGGCAAGCCAATGC[C/T]CCTGCTGAGAATGCT | 10393 |
rs541620257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144982855 | GATTTGTTAGTGAAC[A/G]ATTTTATTTAAAAAT | 10393 |
rs541640403 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145026240 | TGTGAATGTCCTCAA[C/T]TTAACATTTATTGAT | 10393 |
rs541640539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145033811 | TCTTGTGACCAGCTG[C/T]AGAAATGAGGACTGT | 10393 |
rs541659512 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145082811 | TGGTAAAATGCAGAC[C/T]TTTTAATAAGAGAAA | 10393 |
rs541685907 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144969893 | GTAGAGCATATAATG[A/G]ACCCCTGGGTATATA | 10393 |
rs541718345 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144975157 | ATACTTGATTTCAAA[A/T]AAATAAGGCATTACA | 10393 |
rs541718715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145018261 | TGAATGGAATGGTAC[C/T]TCACATCTCAATACT | 10393 |
rs541752994 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145076254 | ACAGCAGTTGCTTAT[C/G]TTGAAGGGCCAGAGA | 10393 |
rs541766905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145015456 | TGTGAAACAACCAAA[C/T]TTAAGAATAATCGGT | 10393 |
rs541789262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145067909 | AAATGATGGTGTGTA[C/T]TAAAGAAAGTTTCTT | 10393 |
rs541814620 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145089084 | AAGAGGCCTTCCATA[A/G]TCCCACAAACTAATG | 10393 |
rs541815339 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145053983 | GTGCAATCTCAGCTC[A/G]CTGCAACCTCTGCCT | 10393 |
rs541835104 | snp | A/G | | | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145099802 | CGTTACAATTATTTT[A/G]GCTTTAGACTGTAAA | 10393 |
rs541869463 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145052883 | ACAGAGCGAGACTCT[C/G]TCTCAAAAAAAAAAA | 10393 |
rs541875630 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145082492 | AAACTCAGTTTCTTG[G/T]GCTTTTTGCAAGCTG | 10393 |
rs541895689 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145021638 | TTTCATGACCAAGAA[C/G]CCCAAAGCAAATGCA | 10393 |
rs541901859 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145045095 | ACTCTCCAAAAGCTA[A/C]TGTAAAAATAAATTT | 10393 |
rs541934804 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145091916 | ACCAGCCACAGATAC[A/G]AGGCTATCTTGAATA | 10393 |
rs541938385 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145001498 | ACATGGTAGAGAGTT[-/A]AAAGTTTTACAAAAT | 10393 |
rs541984498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145000318 | CCCATCTGACAGAGG[A/G]CTAATATCCAGAATC | 10393 |
rs541990033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145058198 | TCTTTCTTACCACTC[C/T]CTCAGACCTATCCAG | 10393 |
rs541999659 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144989322 | TGTCATTTTGGTAAT[C/T]CTCTATCTCAAACTT | 10393 |
rs542027072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145057743 | CCCTCCCCCTCAGAA[C/T]GTTCCTTCTCTGTAT | 10393 |
rs542050795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145008454 | AAAATACTGGCAAAC[C/T]GAATCCAGCAGCACA | 10393 |
rs542078761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145030586 | TTTTAGCTTAGGTCT[A/G]ACTTACACTGGGTCC | 10393 |
rs542095457 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145071263 | AATACAAAATTAGCC[A/G]GGCGTGGTGATGCAT | 10393 |
rs542097457 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145031698 | GGTATCAGTGGCAGA[C/T]AGGGATGCTGTTTGG | 10393 |
rs542100324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145052575 | CTATATTGATTTCTA[C/T]TGTAAAATTAGGGAG | 10393 |
rs542100737 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145068427 | TATGTGATAGACGAT[A/C]GCTTTACATTTAAAG | 10393 |
rs542117627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145016204 | TGCAGATGACATGAT[C/T]GTATATTTAGAAAAC | 10393 |
rs542118270 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | ABCE1, ANAPC10 | GRCh38.p7 | 4:145097425 | ATGTAAAACTGCTTT[G/T]GTAGCGCAGTTACTG | 10393 |
rs542152473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145023612 | CAAATAAAAGCTGTG[C/T]TACACTATACTAGAG | 10393 |
rs542158752 | in-del | -/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145069201 | CAGCACAGGCCTCTA[-/G]GTCCTGAGAGAAAGA | 10393 |
rs542182693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145026677 | TGGTATGTAAGAAAC[A/G]AGACAAAATAAGACA | 10393 |
rs542184823 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | ABCE1, ANAPC10 | GRCh38.p7 | 4:145097921 | TGAGGCCTAGAAGAG[C/G]GCGCAACAGTAAGCC | 10393 |
rs542222925 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145018915 | CAATCCTAAACATAT[A/G]TGCACATAACACTGG | 10393 |
rs542248181 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144996848 | ACCTTGAAAAAAGAT[C/T]AGACGAATGGCTAAC | 10393 |
rs542252028 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145003778 | TCAGGTAATATGATG[C/G]TTCTAGCTTTGTTCT | 10393 |
rs542277345 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144983984 | AAAATATCTGCAGGA[C/G]TCAGAGTTACTGAGT | 10393 |
rs542278156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145094905 | AAAGGACTGCCACCC[A/G]AGAATTCTATCCCAA | 10393 |
rs542311856 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145079751 | ATGCAGCTGGAGGCC[A/G]GCATCCTAAGAGAAC | 10393 |
rs542334754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145037423 | CCAGCCCTATCACCA[C/T]AAATTTTAACAGTAA | 10393 |
rs542337596 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144986485 | TCTTGGGAGGGTGTA[C/T]GTGTCGAGGAATTTA | 10393 |
rs542380593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145034152 | ACTTGCGATGGTTAA[C/T]ACTGAAAGTCAACTT | 10393 |
rs542382263 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145013281 | TCTCATGAGCACAAA[C/T]GAAAAAAACCTAGAA | 10393 |
rs542387297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144997271 | CGAGAAGAGCAACAC[C/T]AAGATACATACTTGT | 10393 |
rs542390325 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145014745 | TGAGAGACCCACAGA[C/T]GGTTCACATCACAGG | 10393 |
rs542418637 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145066991 | AATTTTTTCTAAGCC[A/C]TGAGTTATTATCGTA | 10393 |
rs542427498 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145055560 | TAGACACTGTCTCAA[C/T]AAATAAAAAAAAAAT | 10393 |
rs542438909 | in-del | -/A | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145089112 | TGTAGCCTCCCACTT[-/A]AAAGTTACTTTCTAT | 10393 |
rs542472009 | snp | C/T | | | downstream-variant-500B, intron-variant | ANAPC10 | GRCh38.p7 | 4:144993831 | TAAGACACTAGATAG[C/T]ATATGTGATCATTAG | 10393 |
rs542478881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144973329 | ACATGAACACGAAGA[C/T]AGTAACAATAAACAC | 10393 |
rs542496096 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145049005 | GAGTATCACAATAAA[G/T]TGAGTCAGTCATACA | 10393 |
rs542507936 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145003048 | AAGTCCCAGCCACTA[C/T]TGTTCCCTTCTTTGT | 10393 |
rs542541269 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145008769 | AAGCATTCCCTTTGA[A/C]AACTGGCACGAGACA | 10393 |
rs542569875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, missense | ANAPC10 | GRCh38.p7 | 4:145033323 | GTTCCCACGACATTA[C/T]GTTCTGCTGGCCTAG | 10393 |
rs542608074 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144977186 | ATTTCTATGATTCCA[C/G]AAGTATCATCCTCTA | 10393 |
rs542627860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145086555 | TGAGAGTTTATGTTG[C/T]GATAAATCCTCTAGG | 10393 |
rs542668703 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145016799 | TGCAACAGAACAGAG[C/G]CCTCAGAAATAATAC | 10393 |
rs542671426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144984764 | ACTCAAAATGTTTCA[C/T]AAGAATACAGAACAA | 10393 |
rs542682691 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145017990 | GGGGGAGGGGGGAGG[A/G]ATAGCATTAGGTGGT | 10393 |
rs542693587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145032458 | TGGGCCTCTCTTGAG[C/T]GGTCAAAAGCTGAAT | 10393 |
rs542703551 | in-del | -/A | 0.0103295 | 0.0711199 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145029686 | GCTGAAATATGGATT[-/A]AAAAATGGCCCACTG | 10393 |
rs542706792 | in-del | -/ATTT | 0.00119856 | 0.0244508 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145062161 | GAAGACTAAGAGCTG[-/ATTT]ATTTATTAATCTATT | 10393 |
rs542723311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145017481 | AACAACAGGTGCTGG[A/G]GAGGATGTGGAGAAA | 10393 |
rs542788173 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144994599 | AAATCTTTTAATATA[C/T]ATAAAAAATTTCACA | 10393 |
rs542797354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145006079 | CACTATTATTGTGGG[A/G]TTTTCTAAGTCTCTT | 10393 |
rs542839556 | snp | C/T | | | intron-variant, utr-variant-3-prime | ANAPC10 | GRCh38.p7 | 4:145063769 | TCAAACAGTGAAATA[C/T]AACTCAGAAGTAAAA | 10393 |
rs542850346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054904 | TATCTTATAGTTGTA[C/T]TCTTCTACTTTATAA | 10393 |
rs542864765 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145094080 | GGCAAGGATAACTGG[C/G]GACCATTTTGAAAGC | 10393 |
rs542891903 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054234 | TTTTAATCAGCAACA[C/T]GTTAGTCGCCAGAAA | 10393 |
rs542893015 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144992798 | TTGAGAGGATTGACT[C/G]CAATTTTGAAAGAAG | 10393 |
rs542910657 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145000080 | AAGACTTAAATGTTA[A/G]ACCTAAAACCATAAA | 10393 |
rs542916945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145005531 | TGCTCTCGGTTCCCT[A/G]GTTCTTTTAGTTATG | 10393 |
rs542954535 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144991967 | CTTGTTAGCAGCTAA[G/T]GCAGCTGGTGACTTT | 10393 |
rs542971512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145039816 | GGCCAGGATGGTCTC[A/G]ATCTCTTGACCTTGT | 10393 |
rs543050243 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145077939 | CAAAAACTGGAAGGA[A/G]GCATTCCACTTAAGA | 10393 |
rs543051800 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145077628 | AATCCTCAATAACAT[A/G]CTAGCAAACTGAAAC | 10393 |
rs543058048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144976350 | ATTCAGGATACGGGT[C/T]AATCTTGGAGAGGAT | 10393 |
rs543087334 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145015324 | CAATAGAAATGAACA[A/T]GCAGAAGAAAGAAAT | 10393 |
rs543087863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145061786 | AAATGTATCAGATAT[A/G]TGACTAAAAGAAGGG | 10393 |
rs543100687 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145008854 | GGCAATCAGGCAGGA[A/G]AAAGAAATAAAGGGC | 10393 |
rs543126035 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145014884 | CATCCATAGGAAAAC[A/G]GGGAGAGTGCTACAT | 10393 |
rs543131502 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145058408 | CTGGGCTTTAAAAAC[C/T]ACAAAACAATATTGT | 10393 |
rs543164748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145039514 | TAAACATTTTGGAAG[C/T]ACTTTTTCTTTGGCA | 10393 |
rs543214102 | snp | C/G | 0 | 0 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144996252 | ACACTCTACCAACTA[C/G]GGCCTTGGGCCTGAC | 10393 |
rs543227489 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145092591 | AGCAACACTGAGAGC[A/C]CAAAACACAAGGTGA | 10393 |
rs543258227 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145050184 | TTGATCCATGGGCTG[A/C]AGAATACATGTTGTG | 10393 |
rs543276318 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145089438 | TTTTTCCCCTAAATT[G/T]GTTTTTCAACATTGG | 10393 |
rs543276839 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145020639 | AAAGAGGAAGTCAAA[C/T]TGTCACTGTTTACTG | 10393 |
rs543285410 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144984026 | GGAGTCAAAATTACA[A/C]CCAGTTACCAATCTA | 10393 |
rs543293232 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144989083 | TTTGGGGGGTAAATA[C/T]GTAGAAGTGGAATGA | 10393 |
rs543314843 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145007118 | ATATGCACCCAATAC[A/G]GGAGCACCCAGATTC | 10393 |
rs543332464 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145040826 | AAGCCATAATTCTAC[A/G]TATGCTATAAAGAGA | 10393 |
rs543337104 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145077177 | GCACTCCAGCCTGGG[C/T]GACAGAGCAAGACTC | 10393 |
rs543338757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145084718 | TAAATCTGCACTGTC[C/T]AATACGGTAGCCACT | 10393 |
rs543350421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144988219 | TCCTGGGCTCAAGCA[A/G]TCCTCCCACCTTGGC | 10393 |
rs543358853 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145082049 | CTTCTACCCTTTTAT[A/T]CAGAGCTCAACTCTT | 10393 |
rs543374271 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145044132 | AAATAGATTCAAGGA[A/G]ATAATGCTGCCCTTG | 10393 |
rs543388512 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081332 | GTTTACTTAATATGA[A/T]ACATTAAGGTATTGT | 10393 |
rs543418818 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144981216 | TAGTTTAATGAGAAT[A/G]GCATTGAATCTATAA | 10393 |
rs543441083 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145040106 | AAGCAAACTATTGTA[C/T]GCTTTTGTTTTAGTG | 10393 |
rs543441233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145029866 | GCCTTGCAAAACAGA[C/T]TTGTGAGGGCAGCAC | 10393 |
rs543441946 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145007953 | GCAAGACTAATAAAG[A/C]AGAAAAGAGAAAAGA | 10393 |
rs543450824 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145074420 | TTGTAAGTTTTCTGC[A/G]TGGCTGATAGAACAG | 10393 |
rs543473163 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145096607 | CTACAATGCTATGCA[G/T]TTCTATAATTCTGTG | 10393 |
rs543496304 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145057182 | TAATAAGAAAAGATA[G/T]AATTCCTGCTATTAA | 10393 |
rs543512736 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145034959 | CAGCTGGAGCCATCA[G/T]TCAGTTACTGTTTGT | 10393 |
rs543526362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145067721 | CTGAATAATTTCTCA[C/T]TGGGTTTGGAACCCA | 10393 |
rs543556257 | in-del | -/AC | 0.00438332 | 0.0466095 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145039117 | GAGACATCACTTTCT[-/AC]AGAGAAAAATAGGTC | 10393 |
rs543558955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145095792 | CTGTGCCTAATTTAT[A/G]AATTACACTTTATCA | 10393 |
rs543560693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144970617 | ACTCTTGCAATGTGG[C/T]ATACTGAAACTAAGA | 10393 |
rs543580362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145001654 | ACTTCTGAATAGGAA[C/T]CACCCACCACCTTTC | 10393 |
rs543616032 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145080451 | GCACTGTGTAGGGCC[A/C]CCTTTGTGCCATAAC | 10393 |
rs543667794 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144978886 | AGTTAGATACAGTAA[C/G]AATTGCTAGAGTGTC | 10393 |
rs543696011 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081881 | ATATTAATTTTTTTT[A/T]ATTTATTTTTTGTAG | 10393 |
rs543698220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144971391 | TTTCATCAAAAGGGC[C/T]TACAAAAACACAGAC | 10393 |
rs543722042 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145036556 | GTCTTACTATGTTGT[A/C]CAAGCTGGCCTTGAA | 10393 |
rs543731603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145090044 | ATTTCTAGTCTCATT[C/T]ACTACATGAAATTAA | 10393 |
rs543738311 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145065116 | AAATAACTAGCTAAG[A/T]GAGGAACTGGGTCCA | 10393 |
rs543738590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145073503 | ACTAATTTGTATGAT[C/T]TGGCTTAAGCAATTT | 10393 |
rs543754228 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145057649 | CCATGGACTACCTAC[G/T]GAAAATCCCTCCATT | 10393 |
rs543781495 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144990066 | ATATCTCTGTCATGC[C/T]TACCTTTGAAGAAAA | 10393 |
rs543792932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145051154 | TAGTTAGAGGCCTAA[C/T]TGAATCAAGCCAATT | 10393 |
rs543816121 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054802 | AAGAGACCCCAGCCA[C/G]TTGCTCAAGTTTATT | 10393 |
rs543868145 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144992074 | TGCTCTGCCTGTGGA[A/T]CAACAAAGCCTGGAT | 10393 |
rs543889593 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144977193 | TGATTCCACAAGTAT[C/G]ATCCTCTAGAGAATG | 10393 |
rs543919072 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145031355 | ATCCAACTAAAATTC[C/T]GGGACCGTCGACCTC | 10393 |
rs543922832 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145008353 | AGGTCAGCATCATCC[C/T]GATACCAAAGTCTGG | 10393 |
rs543935535 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144999153 | AAAACAAGTCTAGGA[C/T]CAGATGGATTAAGAG | 10393 |
rs543950766 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145042742 | TCAGTAAAAAAAAAA[A/T]GATGTGTGAACAGCA | 10393 |
rs543956512 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:144966903 | ACACTGCTCTTGAGG[A/G]ATGAATGACACAGCA | 10393 |
rs543963387 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant, utr-variant-3-prime | ANAPC10 | GRCh38.p7 | 4:145064109 | CCAAGTAATATACTT[A/T]AGATTATGCAAAATT | 10393 |
rs543988805 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145047762 | TTTAAATTGATGAGA[C/T]TATTGTTCAACTAGA | 10393 |
rs544102867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145013572 | TCAGAGACTTCATCA[C/T]GGTGGATGGGAGGCA | 10393 |
rs544137363 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145019801 | CATTCAAGGCTACTA[C/T]GAATATGTTTATGGG | 10393 |
rs544139384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145012998 | GACACCTCCCTCTTC[C/T]CTCTCTTCCTCCAAC | 10393 |
rs544146311 | in-del | -/ATATATATATATACAC | 0.00358779 | 0.0422022 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145012184 | TGTGTGTGTATATAT[-/ATATATATATATACAC]ACACACATATATATA | 10393 |
rs544146431 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145047046 | CATGGTAGATGTTTT[G/T]ACACTGCTTATCTAA | 10393 |
rs544207633 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145005175 | CCTACCTCAGTCTCC[A/T]GTGTAGCTGGGATTA | 10393 |
rs544229205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145037674 | GATGAAGGCGAGGCA[C/T]AATGGCTCACACCTA | 10393 |
rs544281247 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144998007 | ACATAATGGTAAAGG[C/G]ATCAATTCAACAAGA | 10393 |
rs544316708 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145057033 | AAGTGACCTTACAGG[A/G]CAATGCTCTTGAAAG | 10393 |
rs544324446 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145079167 | ATCCAGAAACTATAA[A/G]GAACTTAAATTTACA | 10393 |
rs544380017 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145088948 | TGAACCTCTAAAATG[C/T]CAAATCAACTAACTT | 10393 |
rs544394559 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145016225 | TTTAGAAAACCCCAC[C/T]GTCTCAGCCCAAAAT | 10393 |
rs544468857 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145010615 | ACTCATAGATGGGAA[C/T]TGAACAATGAGAACA | 10393 |
rs544517808 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145098818 | ACCCAAAATGGATAT[A/T]TTGTCACATGTGCAT | 10393 |
rs544521274 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145052671 | TTGCGAGGCTCAGGC[A/G]GGCACAGATCACATG | 10393 |
rs544528325 | snp | A/G | | | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145096622 | GTTCTATAATTCTGT[A/G]CCTGAAAATTCAAAT | 10393 |
rs544556626 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145009991 | GAAAAAATCAAACAA[A/C]CCCATCAAAAAGTGG | 10393 |
rs544563625 | in-del | -/C | 0.469014 | 0.120553 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145025334 | TGGCTTTCAACACGC[-/C]CCCCCCCCCTTTTAA | 10393 |
rs544620073 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144990363 | ACAATTTCTACACTG[C/G]AAAGAAATGAGATTG | 10393 |
rs544630790 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145042415 | AGATGTATAATCCAG[C/T]CAAGATATACTTTAT | 10393 |
rs544635182 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145034490 | ATTGTGGGACCTTGT[G/T]ATTCTGTAAGTTAAC | 10393 |
rs544649260 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145012940 | GTGCTGTTCTCATGA[C/T]AGTGAGTGAGTTATC | 10393 |
rs544656499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145069367 | AAAACTCCAGAAATA[C/T]GCGTGGGGTCCCCTT | 10393 |
rs544658516 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145023673 | AGAAAACAATTTAAG[A/G]ATGTTTTACTGCTAA | 10393 |
rs544663512 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145010805 | TTGTGCACATGTACC[A/C]TAGAACTTAAAATAT | 10393 |
rs544695139 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145031303 | AATACACTGGACTTA[C/T]TGGTGAGACATTTGC | 10393 |
rs544744551 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145053004 | AGTGTACTATAAATA[C/T]TATTATTATTTTAGC | 10393 |
rs544781473 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145009289 | TTCAATGTCATCCCC[A/C]TCAAACTACCAATGA | 10393 |
rs544795322 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145050082 | GATTTTCAATTTGCT[A/T]TGCCTAGATCCATCA | 10393 |
rs544801799 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145080620 | GAATGTTAAAATAGA[C/T]GGTATAGGCCAGGTA | 10393 |
rs544814868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145007304 | CCTAATAGACATCCA[C/T]AGAACTCTCCACCCC | 10393 |
rs544831840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145059127 | TCAAATTGTTTAAAA[C/T]AGGCCCCTCATAAGA | 10393 |
rs544866803 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144990699 | ATTCCTGAGGAATCC[A/G]CCCCCATGATCCAAA | 10393 |
rs544877154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | ABCE1, ANAPC10 | GRCh38.p7 | 4:145098434 | GGTACGTGAATAGCC[C/T]GGAGAGGTTTGGCCG | 10393 |
rs544887216 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145057639 | ACCCTACTATCCATG[C/G]ACTACCTACTGAAAA | 10393 |
rs544909851 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145060642 | CCCTCCAGTGGGCAA[A/G]CATCCACGGAAAAAT | 10393 |
rs544915515 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145056212 | CTAATAAAACAGGCT[A/G]CAGTAAAGAAGCTGG | 10393 |
rs544980615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144987323 | TGCAGCCATAAAAAA[C/T]GATGAGTTCATGTCC | 10393 |
rs545027567 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144969171 | GAGAGATAATAAGAC[C/T]TATTTTGTAGGAATG | 10393 |
rs545045590 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144986791 | AGAATCTGCAATGAA[C/T]TCCAACAAATTTACA | 10393 |
rs545050980 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145012798 | ACACTTTTTAACTAT[A/T]TTTATAAGGCCTTGA | 10393 |
rs545051545 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145018140 | ATATATATATATATA[A/T]ATAAAATAAAGCACA | 10393 |
rs545073028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145006607 | AATCATATCAAATTG[C/T]CATTTTTGTAGGTCA | 10393 |
rs545122254 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144979804 | TTGCCTTTGTTAGAT[A/G]CCCAGACATGCCATA | 10393 |
rs545138104 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145011998 | CAAGAACTGCAAAGC[A/C]GCTTCCACTGCAAAG | 10393 |
rs545141186 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144974514 | AATAAAATAAATAAA[A/C]GACACGAGAAAAGAA | 10393 |
rs545275728 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145087466 | AGGCTCTGCTAGGGG[G/T]CTATTTTAACTGAGG | 10393 |
rs545304907 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081381 | TATATCTTTCTGAAA[A/G]TACCCGCAAAAAATA | 10393 |
rs545361959 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145094968 | TTATCACTCATTTAT[C/T]CAATTGAGAGAAACG | 10393 |
rs545384799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145062602 | ACAGAGTAAGACTCC[A/G]TCTCCAAAGAAAAGA | 10393 |
rs545401099 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144968643 | TATTTGATTAGGTCA[A/C]AGGTGAGGATCCCAG | 10393 |
rs545430773 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145070900 | AGACACCAAAGGACA[A/C]ATATTATATAATTCC | 10393 |
rs545446330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145009822 | CCAAAATTGACAAAT[A/G]GGATCTAACTAAACT | 10393 |
rs545543162 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant, stop-gained | ABCE1, ANAPC10 | GRCh38.p7 | 4:145098125 | ACACACTCACAGTTT[A/C]CAGACCTGGCTGCTT | 10393 |
rs545545293 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145041316 | TAACTCTATTACTTA[C/G/T]AGCTTAGATAGCATG | 10393 |
rs545555568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144989979 | TGAAGCTAGCAGAGA[C/T]TGCTTCAGAAGGTTT | 10393 |
rs545567488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145053054 | CTAAGAAACCTTATC[C/T]TGACTGATGAGGAAG | 10393 |
rs545586101 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144970044 | ACATGGGGTGCATTC[-/T]TCAGGGTTACTTCCT | 10393 |
rs545606034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145085649 | TGTCTCTAATTTATT[A/G]CTTAGAAAGTATCAT | 10393 |
rs545620951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145016114 | AGTGTTGGAAGTTCT[A/G]GCCAGGGCAATCAGG | 10393 |
rs545625583 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145014570 | CGCCCACCGTCTGAT[C/G]CTCCCTATACTACCA | 10393 |
rs545648292 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145039909 | AAGGTACATTCTTTT[A/C]ATCTTCACTTTAGAT | 10393 |
rs545648822 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145017521 | TTTTCCACTGTTGGT[C/G]AGACTGTGAACTAGT | 10393 |
rs545663162 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144977258 | TTATCCCAGGCAAAC[G/T]TCTGATCGCCTTCTC | 10393 |
rs545677460 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145079379 | GTCAAAAAAAAATAA[C/T]AGATGCTGGTGAAGT | 10393 |
rs545688630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144982140 | TGAGCCACCGCACCC[A/G]GCCAGCAGCTACTTT | 10393 |
rs545694514 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081894 | TTTATTTATTTTTTG[C/T]AGACAGGGTCTTGCT | 10393 |
rs545706967 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144988836 | CACATATATGTACTC[-/T]TTTTTTGTACAGCTT | 10393 |
rs545720376 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145077850 | AAAATCCTCAACAAA[C/G]TAGGCATTGAAGGAT | 10393 |
rs545745638 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145014984 | AGGCTATGCAAATGA[C/G]AAAGAACCAGAAAAC | 10393 |
rs545746557 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144987690 | CTATCTTCTTCAGCA[A/G]GAAGTAAACTTACAT | 10393 |
rs545768360 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145096686 | CTTTTATTCTAGGAA[A/T]ATATAAATATTGATC | 10393 |
rs545782235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145021476 | TGGCTAGACACATAT[A/G]GGACAATGAAACTGG | 10393 |
rs545791224 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145059423 | TTTCAAGCCTCCTTT[A/T]AAAAAAAATCACTTG | 10393 |
rs545793824 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145037455 | TAAATATTGAAAAGA[A/T]AGAAAGGTTAAAACT | 10393 |
rs545804683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145074649 | ATAATGTATTTTAAT[C/T]AGACCTAATCAGAAC | 10393 |
rs545815890 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145067806 | CCCTTTATCCCCTCT[G/T]TCTTCATAACATCTG | 10393 |
rs545818386 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144974412 | AAAATTTTCACATTG[C/T]GATCAGAAACAAGAA | 10393 |
rs545848546 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145026874 | CAAAGAACAAGAAGA[A/C]GTCTTAGAAATTTAT | 10393 |
rs545879157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144988524 | GAAATATAGTTACTT[C/T]AAATCTAGCATCTTT | 10393 |
rs545888239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145002293 | GTGTTAAAAGGAAGC[A/G]GCTACCACAAAAGCA | 10393 |
rs545901356 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145059847 | GGTCCATTGCTCTAA[A/C]TGATAAAAAAAAAAT | 10393 |
rs545921162 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144994705 | TTCCATAAGTACTGC[C/T]AGAACTCTTCCATAA | 10393 |
rs545987980 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145065232 | TTTCTTTCTTTTGCT[A/C/G]TTGATTTTAAAATAT | 10393 |
rs546013658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145037237 | TATCTTTTATCTTAG[A/G]ACAAAAATGAAACAG | 10393 |
rs546013700 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145029933 | GTATGTCAGATCTAA[C/T]GATGAGAACCACGGT | 10393 |
rs546044933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145022366 | AACGGCATTCGCAGC[A/G]ACCTGGATGAGATCG | 10393 |
rs546064924 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145003207 | ATCTCATTCTCTTTT[A/C]TGGCTGCACAGTATT | 10393 |
rs546067082 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145075603 | AGTAAGCTAGGAACC[A/G]TGAATGGGGTTGCTG | 10393 |
rs546078484 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145039826 | GTCTCGATCTCTTGA[C/G]CTTGTGATCTGCCTG | 10393 |
rs546109082 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145067119 | TAATTAAAAGGTAGA[C/G]TAAAAAATTTTAAAA | 10393 |
rs546125631 | snp | A/T | 0 | 0 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145030532 | CTCCAGTTAAAGCAG[A/T]TAAAGTAGGGGCTTA | 10393 |
rs546132550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145052331 | TTAGTCAGTCTACAA[C/T]GTATAAAAATATCAA | 10393 |
rs546137591 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145036425 | ACAAAAATTGGCTAA[C/T]ATAGCTAACAGGATT | 10393 |
rs546166602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145084961 | TGTATATATATTTCA[C/T]GTCACATATTCTATT | 10393 |
rs546197146 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144983559 | TAAACGCTCCCAGGG[A/G]GTGACTTTTGAGTGA | 10393 |
rs546271807 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144984863 | AAGACAAGAGGGACA[A/C]TTAATGGTCGTGGAG | 10393 |
rs546274002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144976527 | CACTTAAAAGGAAAA[C/T]AGACCGACAAAATCA | 10393 |
rs546287236 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144992321 | CTTATTGTTTCAGAA[A/G]TACATTTCATAAGGC | 10393 |
rs546293666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145044790 | TAGTTTATCTTAGTG[A/G]CACACTATAGTTAAT | 10393 |
rs546295635 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145064406 | AAAAAATAAAGAGAA[A/C]AATCAGAATTCAGAA | 10393 |
rs546326300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145003000 | ATAGGTAGTTTTCCA[C/T]TCCCACCCTCCTCCC | 10393 |
rs546335012 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144984167 | CTACTCTAAAAAAAA[A/T]AGGCACTATTTTTTG | 10393 |
rs546335156 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145020368 | TGCAGAAAAAGCATT[A/T]GACAAAATCCAGCAT | 10393 |
rs546335723 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145035939 | TGGAAGTCCAGGAGG[G/T]ATGTTACCCAGAAAA | 10393 |
rs546372105 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145000771 | GTGGCACTATTCACA[A/G]TAGCAAAGACTTGGA | 10393 |
rs546389939 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145073174 | GTTGGGATTATAGGC[A/G]TGAGCCACTGCACCC | 10393 |
rs546400353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054197 | CAGGCCTGAGCCACC[A/G]TGCCCAGCCTGATTA | 10393 |
rs546423025 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145061834 | AATAAGAGGCCAGGC[A/G]CGGTGGCTCAAACCT | 10393 |
rs546455780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145092712 | TGCTACAGATACAGA[A/G]GAGGGGACTGACCAC | 10393 |
rs546486352 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145058991 | CTACTTTTTTAAAAA[A/T]ATCTTTTAAACTAGC | 10393 |
rs546492716 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145092152 | GGGGAACATCACACA[C/G]TAGGGCCTGTCAGGA | 10393 |
rs546492835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145008411 | TAGACCAATATCCCT[A/G]ATGAACATCGGTGCA | 10393 |
rs546513287 | in-del | -/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144991384 | AAGAGTTTTTTTGCA[-/T]TTTTTTTTTTTTGAG | 10393 |
rs546523196 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145038028 | AACAACTGATAACAA[C/T]GAAGCCTTTAAAAGG | 10393 |
rs546546804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144998865 | CAAAATTGATAGACC[A/G]CTAGCAACACTAATA | 10393 |
rs546554298 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145008082 | AATAAACTAGAAGAT[A/G]AAGAAGAAATGGATA | 10393 |
rs546581154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145099798 | ACAGCGTTACAATTA[C/T]TTTGGCTTTAGACTG | 10393 |
rs546629063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145069539 | TTAAAGCTCCCAATA[A/G]CCGAAGTGGTAAGTC | 10393 |
rs546662568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145031599 | GGGTCCAGAACAGGA[A/G]AAGGCTCTGCAACAG | 10393 |
rs546686578 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145060163 | TTGGTTTTCAATTTA[C/T]GTGGAATAGGATATT | 10393 |
rs546735929 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145025323 | TTGGCCTATTTTGGC[C/T]TTCAACACGCCCCCC | 10393 |
rs546739624 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:145032614 | CATCGCCCAATGGGC[C/T]CATGAACAAAGCAGC | 10393 |
rs546743490 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144991038 | TTATGTTCCACAGGT[A/C]CCTTGGGCACAAACC | 10393 |
rs546746697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145046571 | TTATTAGCTAAATAC[C/T]AGGAAGCTTAAAATT | 10393 |
rs546751327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145037802 | AAACACAAAAATTAG[C/T]AGAGCATGGTAGCAT | 10393 |
rs546773700 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime | ANAPC10 | GRCh38.p7 | 4:144967135 | TAAGAGCTTCACCTC[C/T]TCCATTCTCACTTGA | 10393 |
rs546783777 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145016250 | CAAAATCTCCTTAAG[C/G]TAATAAGCAACTTCA | 10393 |
rs546787799 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145080022 | GGGATCCTGAGGCAG[A/G]AGAATCACTTGAACC | 10393 |
rs546806332 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145068682 | TTTGGGAGGCTGAGG[C/G]AGGCAGATCACAAGG | 10393 |
rs546844393 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144991597 | TTAGCAGGATGGTCT[A/C]GATCTCCTGACCTTG | 10393 |
rs546905830 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144998430 | GTCTCTCAGACCACA[G/T]GGCAATAAAATTAAA | 10393 |
rs546910943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145030851 | CAAGGACTTGAAGGA[C/T]GTGGGGGTGGTAATT | 10393 |
rs546933103 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144981885 | CTGGAGTGCAGTGGC[A/G]CAATCTTGGCTCACC | 10393 |
rs546967171 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145015804 | TTCCTCAAACAAAAT[C/T]ATCAGCCAAGAATTT | 10393 |
rs546986488 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145019973 | AAAAAAAAGGCCAGG[C/T]CCAGAAATTCACAGC | 10393 |
rs546999758 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145087420 | GGAGTACAGTGGTAC[A/G]ATCACAGCTCACTGC | 10393 |
rs547018904 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145075157 | TGCATCCCAAAATCA[C/T]ACTAGCTTTTTTAGC | 10393 |
rs547023238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145019182 | GGACTTTCTCCAAGA[C/T]GGACCACATGATAGG | 10393 |
rs547036458 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145061456 | TCCAGGAAAAACAAG[C/T]ACAACTAAGATTACA | 10393 |
rs547040769 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144974743 | ACATAAAATATCTCT[C/G]TAGAAAACAATAAAA | 10393 |
rs547045096 | in-del | -/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145051641 | TTTAAAGAACTATTC[-/T]TTTTTTTTCATGAAT | 10393 |
rs547062151 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145082242 | GCAACCTCCGCCTCC[C/T]GGATTCAAGCGATTC | 10393 |
rs547071019 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145004272 | TTGTGTAGGTCTAGC[A/T]TCATATCATCTGCAA | 10393 |
rs547083878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145057295 | TTCAGAATTGCATTA[A/G]GTAAATTACATTAAG | 10393 |
rs547111717 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145046351 | TGCATAGAAAGTATA[A/C]GGGCTAAGAAGTAAA | 10393 |
rs547122645 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145056630 | AGTGTGGAAATCCCC[A/G]ACCCAAAGGTTAACA | 10393 |
rs547178972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144989598 | AATGGCCTCTAAGTG[C/T]TCAAGTGAAAGGAAG | 10393 |
rs547197502 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145091318 | TTCAGTGCTAGTTTA[C/T]CAAGGAAGGTAAACT | 10393 |
rs547214818 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144984094 | TAATCTGCCCAGAGA[A/G]CTTCGAAGAAAATTT | 10393 |
rs547238996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145033489 | CAGTGTTGGCTGGGA[C/T]GACTGACCTGGACTA | 10393 |
rs547300554 | in-del | -/ATATAT | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145026921 | TTTGCCTATACATAC[-/ATATAT]ATATATATATATATA | 10393 |
rs547301356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144982388 | GTAGGCTATGTGTTT[A/G]GCCCCAGAAAACAGT | 10393 |
rs547310987 | in-del | -/GAAGAAAATAAT | 0.0107246 | 0.0724382 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144973150 | AGCCCAAAGAAAATA[-/GAAGAAAATAAT]GAAGAGCGTGCAGCC | 10393 |
rs547330637 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145072012 | GACAAAAAAAACACA[A/C]AAAAAACAAAAAAAA | 10393 |
rs547360129 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145082826 | TTTTTAATAAGAGAA[A/G]TAAGTTTAACTTACA | 10393 |
rs547366348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144981910 | CTCACCGCAACCTCC[A/G]TCTTCCAGGTTCAAG | 10393 |
rs547380901 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145006748 | TCAGTTTGAACCTTC[G/T]TAGCCTTTTTTCTGT | 10393 |
rs547380953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144999684 | CAATGACTTTCTTCA[C/T]AGAACTGGAAAAAAC | 10393 |
rs547387655 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145072724 | TCCTAAATTATACCA[G/T]ATGGTTCAGTCACAA | 10393 |
rs547424411 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145008181 | ACAGGCTCTGAAATT[A/G]AGGCAATAATTAATA | 10393 |
rs547435383 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145078946 | AAAACCTAGGAAATA[A/C]CTAGAAATACCTAGA | 10393 |
rs547505865 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145020385 | ACAAAATCCAGCATC[C/T]CTTTATGATTAAAAC | 10393 |
rs547526826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145034633 | TATGTATTATATATA[A/G]TATCCTATATACAGG | 10393 |
rs547540686 | snp | A/C | 0.000798403 | 0.0199641 | downstream-variant-500B, utr-variant-3-prime, intron-variant | ANAPC10 | GRCh38.p7 | 4:144994100 | TCTTCTCCTTCAATC[A/C]TCTCTTCTACCCTAC | 10393 |
rs547554524 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145041049 | CTGAAGTAGCTCCCC[A/C]ACCCAATGACCCACA | 10393 |
rs547593885 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145087588 | TATATACATTTAAAC[A/G]AAGTAAAATTAAAAA | 10393 |
rs547608042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144977299 | CCACAGATAATTTAT[A/G]TACGACAAATATTAA | 10393 |
rs547619821 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145041723 | ATCATTCATTGACTA[C/T]TGGATCTATTGACTA | 10393 |
rs547632641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145079471 | GGAAAGCAGTTTGGA[A/G]ATTTCTCAAAGAATT | 10393 |
rs547637589 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144968653 | GGTCAAAGGTGAGGA[A/T]CCCAGGACAACATTG | 10393 |
rs547668756 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145017680 | GCACACGTATGTTTA[C/T]TGCAGCACTACTCAC | 10393 |
rs547689709 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145070244 | TCCGTCATATACACA[C/T]TGTCTATGGGAGCTT | 10393 |
rs547690646 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145070279 | ACTACAATGGCAAAG[C/T]TGAGCAATTGCAGCA | 10393 |
rs547699351 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144979113 | TTTTTTTCCTTCAAC[A/T]ATTATTTTCAGTTCC | 10393 |
rs547712366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145071266 | ACAAAATTAGCCAGG[C/T]GTGGTGATGCATGCC | 10393 |
rs547716167 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144986973 | ACCAGTTAGAATGGC[A/G]ATCATTAAAAAGTCA | 10393 |
rs547739033 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145040455 | GCCCAGCCTATTGTA[A/T]GCTTTTAAGACCTAT | 10393 |
rs547754104 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144978547 | GTATTGCAGCTGGGC[A/C]TGGTGGCTCATGCCT | 10393 |
rs547774767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145004158 | GATGTTGTTGGAGTA[C/T]AGGTATGCTACTGAT | 10393 |
rs547776377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144997151 | AGAATGGAACCAAGG[C/T]GGAAATCACTCTTCA | 10393 |
rs547776936 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145048357 | ATAAATAACTGAGGG[A/C]CAAGATTAGTGTATA | 10393 |
rs547835494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145095002 | AAAAAAAATAAATGA[A/G]TAACAACTGAATCAT | 10393 |
rs547870437 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145086942 | TCTCTCCCCACTCTC[A/C]ATGGGAGGGATACGA | 10393 |
rs547933189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145092097 | ACATGTTCTCGCTTA[C/T]AAATAGGAGCTAAAC | 10393 |
rs547978411 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145040006 | CAGATGACTCCAAAG[-/C]CCCATGCTCTTGGAT | 10393 |
rs547997129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144973770 | AATTTTGAAAATGTA[C/T]AGGAAATGGATAAAC | 10393 |
rs548003062 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145017096 | ACACCAAAAGCAATC[A/G]CAACAAAAGCCAAAA | 10393 |
rs548030508 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145061229 | ATGTTTCAGCACTTA[C/G]ATGACATAATAGAAG | 10393 |
rs548036016 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145003356 | CATGTGCATATGTCT[G/T]TATGGTAGAACGATT | 10393 |
rs548065424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:145062835 | AATATTATACAGCCC[C/T]AAAGAGAAGGAAATC | 10393 |
rs548106518 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145055176 | ACATTAGGCAAGAGG[G/T]GGGAACAACCCAAGT | 10393 |
rs548118656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145014542 | CATACTCTCTTGGGA[A/G]TTCTAGGCCCCCCGC | 10393 |
rs548124676 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144997844 | GAGACCCATCTCACG[G/T]GCAGAGACACACACA | 10393 |
rs548141181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145062057 | GACAGAGCAAGACTC[C/T]GTCAAAAAAAGAAAA | 10393 |
rs548196750 | snp | C/T | 0 | 0 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081447 | ATAAAAGGAACTATG[C/T]AACATACCATAAGAA | 10393 |
rs548201350 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145083705 | AGAAAAATAGAATAA[A/C/T]TGCACTTTTATAAAA | 10393 |
rs548201450 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145020595 | GAGCAATCAAACAAG[C/T]GAAAGAAATAAAGGA | 10393 |
rs548215163 | in-del | -/A | 0.00438332 | 0.0466095 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144970249 | AATGTAATGTTCTTT[-/A]AAAAAAAAATCAAGT | 10393 |
rs548215830 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145045310 | TTCACCTATTCTATA[C/T]ATGAGGAAACTGAGG | 10393 |
rs548250968 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145037910 | CATGATTGCGCTACT[A/G]CACTCAAGCATGGGT | 10393 |
rs548255291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144972985 | TGTAACTGAATAATT[A/G]TGAATAATTAAGTGT | 10393 |
rs548289071 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145057711 | TAATCTCATTATCTA[A/C]GTCCCTTTCTCTCTG | 10393 |
rs548299785 | snp | G/T | | | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145096880 | ATATTCATTGAGTGA[G/T]GCAGAGAACAGTCAT | 10393 |
rs548299837 | snp | C/T | | | intron-variant, downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:145062929 | ACAGAAAGACAAATA[C/T]CACATGATCTTATTT | 10393 |
rs548310405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145091403 | GCACCAGTCTAGTCA[C/T]ACTAATAGATCAAAC | 10393 |
rs548311971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145093507 | CAGACCCAGAGATGA[C/T]CCAGTTGTTGGAACT | 10393 |
rs548333266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145058757 | CTTTTCTGTATAACA[C/T]ATTTTAGTTCCAAAA | 10393 |
rs548346670 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144985805 | AATAACTAGCTGATA[C/T]TACAAATAGTTTTTC | 10393 |
rs548371361 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145067321 | TGAATGCTCACTATA[C/G]GCCAGGCATCGTGCT | 10393 |
rs548382893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145051340 | CATGGCGTCCCAAAA[C/T]AATTACAATAGTATC | 10393 |
rs548406859 | in-del | -/AAAGAAAAAAGAA | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145015388 | CAACCAAACAAAGAC[-/AAAGAAAAAAGAA]TAAGAAAATATGAAC | 10393 |
rs548418481 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144995699 | AACTTATAATTAACA[C/T]TTTGCTCAACGAAAG | 10393 |
rs548449898 | in-del | -/TT | 0.00279162 | 0.0372561 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144991953 | GGAAGAGAATAACTC[-/TT]GTTAGCAGCTAATGC | 10393 |
rs548464539 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145043107 | ACTAGAAACAGTATT[A/T]TTTGCTAAAAATGCA | 10393 |
rs548481365 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145027935 | AAAGTGAAGGAAATT[C/T]CCAGGATGATCTTAA | 10393 |
rs548498270 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145052801 | GCTGAGACAGGAGAA[A/G]CGCTTGAACCTGGGA | 10393 |
rs548513637 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145057056 | CTTGAAAGAAAATTC[A/G]TCAACTTCTAAGTTT | 10393 |
rs548564733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145029490 | GTTCTCTAATTAATA[C/T]AAACAGAAATCTAGA | 10393 |
rs548589955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145078110 | GACAATATAATTCTA[C/T]ACCTAGAAAACCCCA | 10393 |
rs548615418 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145018354 | GCATTCACCAACTGG[C/T]CGGGCACCGCGGCTC | 10393 |
rs548665147 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145071069 | TGGAGGTGGTAGTGG[C/T]TGCACAACACTGTAA | 10393 |
rs548702294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145070390 | TCTCTGAAGAAGATA[C/T]ACAAATAACCAGGAA | 10393 |
rs548722455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145048141 | TCAGTAAAGCTAAAA[C/T]GGACGCCCCTCCACT | 10393 |
rs548722913 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145020776 | ATCAGTAGCTCTCCC[A/G]TACACCAACAGCAAC | 10393 |
rs548730248 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:145032701 | CAAGGCTGACGTGGC[C/T]ACGGCCACTGATGAA | 10393 |
rs548791160 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145001847 | CTGGCTGTGACTTAC[G/T]TAAGAGCAGATGTAA | 10393 |
rs548806913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145047464 | ATGGAGTTCAGTGAG[C/T]CATGATAATTCCATG | 10393 |
rs548853848 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145086620 | CCTCTAAGGCAAGGT[G/T]TCTCAATCATGGCAG | 10393 |
rs548866594 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144996415 | AGACACGGCTGCTGC[G/T]GCTGTGCTGGTCTAA | 10393 |
rs548880605 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145040334 | TGTATTGTTAATAGA[A/G]ACGGGGTTTCTCCAT | 10393 |
rs548909967 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145096983 | TGGGAGGCCAAGGCA[A/G]GTGGATTGCTTGAGC | 10393 |
rs548929448 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145044062 | TCTTCCCAACACTTT[-/C]CCCCTTCCTCCTGCA | 10393 |
rs548931239 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145002418 | CTTTGAAAGTCAAAA[C/T]CAGTCCCCCTGCTAA | 10393 |
rs548934219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054280 | TACCACACCAGGCGC[A/G]GTAGCTCACACCTGT | 10393 |
rs548960103 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145025785 | AGAGTTGCCACAAAT[C/T]TTCGATTTGTAAAAA | 10393 |
rs548965114 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144991708 | TTTTTTTTTTAGCTC[A/G]TCAGCTATCGTTAGT | 10393 |
rs549001388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145016322 | GCATTCTTATACACC[A/G]ATAACAAACAAACAG | 10393 |
rs549038636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144978354 | ATTCAATAATACACA[C/T]TGATTGTTTGAAAAA | 10393 |
rs549046531 | snp | C/T | 0.332568 | 0.235971 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054642 | GTGTGTGTGTGTGTG[C/T]GCGCGCGCGCGCGTG | 10393 |
rs549053758 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145062221 | GCATGGCCTGTCAGA[A/C]AAAAGAAGAAATGTT | 10393 |
rs549094155 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145030489 | GAGCTGACATTGATT[C/G]CAGGGGACCCAAAGA | 10393 |
rs549114998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145039682 | GCACTGCAACCTCCA[C/T]CTCCCGGATTCAAGC | 10393 |
rs549142329 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144981084 | TTTGAAGTCCAGTAG[A/C]ATGATGCCTCCAGCT | 10393 |
rs549169309 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145070962 | CACAGAGGCAAAAAA[C/T]AAAACAGCGATTATC | 10393 |
rs549203878 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144977756 | TCCTGATGATTCCCA[A/C]CTGGAAGGAAGCTCA | 10393 |
rs549220479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145010882 | GAGAGGTATATGGGG[A/G]AAAAAAAACAAAAAT | 10393 |
rs549230262 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145011011 | TCACATGAAGAAGGT[C/G]TGGACTTTTAAAATG | 10393 |
rs549262642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144993101 | GTTTTTTTTTAGACT[A/G]CAACAGTGTAAACAA | 10393 |
rs549274536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145032320 | GGAAGGAGAAATGGC[C/T]GGATGTACAATTATA | 10393 |
rs549308868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145085079 | AAAAAGCTGTTTTAC[C/T]AGCCTGTGCAACATA | 10393 |
rs549313349 | in-del | -/ATAA | 0.0063719 | 0.0560834 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144973735 | TCATAAAATGATAAT[-/ATAA]ATAAATTTATGCCAA | 10393 |
rs549324093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144992456 | GGGAGAAGGTCAAAA[C/T]AGCAACTTTAACAGG | 10393 |
rs549324109 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144999472 | TACCTAGGAATACAA[C/G]TTACAAGGGATGTGA | 10393 |
rs549341018 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145014410 | GGGAACCTCACCCCT[A/G]TCCCCCACAGCAGCT | 10393 |
rs549357586 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145038622 | TTGAGGTCAGGAGTT[C/T]GAGACCAGCCTAACA | 10393 |
rs549361814 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145008620 | ATGCAGAAAAGGCCT[C/T]TGACAAAATTCAACA | 10393 |
rs549364233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145060473 | TATTGCTAAATAAGG[C/T]AGCTATATGCTTTTC | 10393 |
rs549384564 | in-del | -/ACA | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145041815 | AATTAAAAGATTCAT[-/ACA]ACAATTATGAAATGT | 10393 |
rs549427143 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145046025 | TTCAATTGTTGGGCC[A/G]AACTGCCCTAAAAGC | 10393 |
rs549450987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144983155 | ACAGAGTGAGAATCC[A/G]TCCCAAAATAAATAA | 10393 |
rs549468095 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145099946 | CAAATCCTTCTTTGT[G/T]TGCAGGAGCCTGTTA | 10393 |
rs549470724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145004874 | CTTCACAGAATGAAT[C/T]AGGGGAGTCCCTCTT | 10393 |
rs549475640 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145051487 | AAAAAATGGTGCCAA[C/T]AGACTTCCTTGACAC | 10393 |
rs549510519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145008226 | ACAAGTCCAGGACCA[A/G]ATGGATTCACAGACA | 10393 |
rs549512687 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145057509 | TATTGGCATCTTCAT[G/T]GTTCCAGCCCTAGCA | 10393 |
rs549549101 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145000938 | TCTAAGCCAACTATC[A/G]CAAGGACAGAAAACC | 10393 |
rs549554595 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144982462 | AGACACATTTGCTTC[C/G]TTCTAGATGGAGGTG | 10393 |
rs549567054 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144987442 | TAGGTGGGAATTGAA[A/C]AATGAGAACACATGG | 10393 |
rs549593111 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145011251 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCCTGGAG | 10393 |
rs549601567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145030988 | AGCTGCTGTACCAGA[C/T]GTGGTTTCATTGCTT | 10393 |
rs549608681 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145037480 | AAAACTAGCCTTTAA[C/G]TAAACGTGTCAGAAA | 10393 |
rs549617368 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145084096 | CCACCTCAGTCATCT[A/T]GGTAGCTGGAACCAC | 10393 |
rs549621115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145076029 | TGGCCATGTCTGATT[A/G]CAGCACAGCCTCAGA | 10393 |
rs549628248 | snp | A/G | 0 | 0 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145013803 | ATCCTCCACCCCCAA[A/G]CACACACTCCTACTG | 10393 |
rs549646580 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145068824 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCCAGGAG | 10393 |
rs549665385 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145020154 | AACCACAGACCCATA[A/T]CCCTGATGAACATAA | 10393 |
rs549674382 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144975774 | TGATATTTCACAAAA[C/G]AGGCTATCTAAATTG | 10393 |
rs549716089 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145057816 | TGAGAATTCCAGATG[C/T]CCCTTTCTGCTTATT | 10393 |
rs549731386 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145076568 | CCAAATGAGCACACT[A/C]GTTGCCCAGCAATGG | 10393 |
rs549735284 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144974970 | ACTATTAAGAAAGAA[C/G]AAGCTGAGAGAACTT | 10393 |
rs549737754 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145028032 | AATTTAGTAGGGGAA[A/G]TATCTGTAAGAGAAA | 10393 |
rs549806168 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145066207 | TTCATTAGAAAGGAA[C/T]AGGGAAAGTTAAGCA | 10393 |
rs549828148 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145052048 | TTCTCATTTATACAC[A/G]GAATCTAAAGTTGAA | 10393 |
rs549861217 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145033472 | GGCTAAAAAGGGAGT[A/T]ACAGTGTTGGCTGGG | 10393 |
rs549873801 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145097096 | ACACCTGTAGTCCCA[A/G]GGGGGCTGAGACAGG | 10393 |
rs549883374 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145071893 | TACAGAGAACATCAA[C/T]GCTATATCACCAAGA | 10393 |
rs549935540 | in-del | -/TATAT | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145034602 | CATACATATCCTATA[-/TATAT]TATAACAAGGATATG | 10393 |
rs549970876 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144987023 | GAGGATGTGGAGAAA[C/T]AGGAACACTTTTACA | 10393 |
rs549976339 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144969581 | AGTTGGAAATAGCAT[A/C]CTCGCTGGATAGACT | 10393 |
rs550012596 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145000465 | CTCATCATCACTGGT[C/T]ATCAGAGAAATGCAA | 10393 |
rs550021767 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145034729 | TGGTGATGCAGGTTC[A/G/T]ACCCAGGGGACAGGG | 10393 |
rs550033454 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145094610 | TTTCTGAAAGAAAGA[A/T]GACTACTAAACTAAT | 10393 |
rs550040609 | in-del | -/A | 0.00517822 | 0.0506191 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144974019 | TGACAAGAAAAATAC[-/A]AAAAAAAGGAATATC | 10393 |
rs550056610 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145087753 | AGTATTAGTACAACA[A/C]TAAAGAGATGAGGCC | 10393 |
rs550061455 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144971574 | TAGATTAATGATCAA[C/T]ATATTCACCACTGTT | 10393 |
rs550063794 | snp | A/G | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | ABCE1, ANAPC10 | GRCh38.p7 | 4:145097917 | AAGTTGAGGCCTAGA[A/G]GAGCGCGCAACAGTA | 10393 |
rs550072984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145055875 | TAGCACTACTGAACT[A/G]ACTACATAAAAAATG | 10393 |
rs550089867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145065382 | CACACAGAGATATTA[A/G]TTTTATCATCATATT | 10393 |
rs550112239 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:145063070 | TCAGTTAGATAGGAA[A/G]AATAAAATCAAGAGA | 10393 |
rs550124301 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144968438 | TATTAAATCAATCTC[C/T]TCCTCTCCACCTCTC | 10393 |
rs550139386 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145092131 | GACAACAAATGGACA[A/C]AGGGAGGGGAACATC | 10393 |
rs550172069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144990846 | CCCTTGCAAGAGACC[C/T]GTACCTGCCTTAACA | 10393 |
rs550211429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145088402 | TTCAACTAGAAAAAT[A/G]GGCATTGCAAAATTA | 10393 |
rs550220824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145006805 | AAATGTCCTGTTTTG[C/T]TGCCTCTGTGATTCC | 10393 |
rs550240817 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145041140 | TTACTTATAGAAGTA[C/T]AAAAATTAGCCAAAA | 10393 |
rs550245673 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144983300 | ACAATATACACAGTA[A/C]AATATTCATAAATTA | 10393 |
rs550268794 | in-del | -/TA | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145012174 | GTATATGTGTGTGTG[-/TA]TGTATATATATATAT | 10393 |
rs550279978 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145059194 | AGCCAGAACTTTTGT[C/G]TGCATCTTCTTACTC | 10393 |
rs550309185 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144991527 | GGACTACAGGCACCC[A/G]CCACCACGCCCGGCT | 10393 |
rs550318108 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144998347 | TAAAGCACTCCTCAG[A/C]AAATATAAAAGAACA | 10393 |
rs550327624 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054425 | TAGCCGGGCATGGTG[G/T]CAGGCGCCTGTAGTC | 10393 |
rs550362251 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145043756 | CCTCCTACAGTATTA[C/T]AAATGAAGGCTGATA | 10393 |
rs550365300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145084880 | GATTTAAAAATATTA[C/T]TACAATTAATTTCAC | 10393 |
rs550366227 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145028024 | ATACAAGAAATTTAG[C/T]AGGGGAAATATCTGT | 10393 |
rs550376235 | in-del | -/TTG | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145069905 | CTCTTCTCACTATTT[-/TTG]TTGTTGTTCATTTGG | 10393 |
rs550386536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145011650 | CCAGGTAGAGAGTTG[C/T]TTCTTGAAGTCAGAG | 10393 |
rs550391904 | in-del | -/TTC | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145003790 | ATGCTTCTAGCTTTG[-/TTC]TTCTTGTGTAAGATC | 10393 |
rs550400670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145007412 | TCCCTCAGCAAATGT[A/G]AAAGAACAGAAATCA | 10393 |
rs550425617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145091526 | AAAGCTTTTAAAAAA[C/T]GGGGGGAGGGGGAAA | 10393 |
rs550427487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145098766 | AAGGCACCTTTAGAA[C/T]TTACAGCACTCTCTA | 10393 |
rs550545722 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145038915 | CTTCTGATGACGAGA[A/C]ATCACTTTCTACAGA | 10393 |
rs550575990 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145004496 | TCAAAGATGTCTCCT[A/G]TTATTTTGAAGTATG | 10393 |
rs550578081 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054158 | GTGATCTGCCCGCTG[A/C]GGCCTCCCAAAGTGC | 10393 |
rs550585755 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145074979 | GTTTTCGGCAGACCA[C/T]AGGTTCCAAATTTTT | 10393 |
rs550601656 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145076701 | CCCAATCCAAGGAAT[A/C]TAAGGAATCCAGTAA | 10393 |
rs550634249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145038047 | GCCTTTAAAAGGCCA[C/T]TTTATGACTGGGCCT | 10393 |
rs550668628 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145031527 | ACACATTTCTCATTT[C/G]AATGTGTTACTCCAG | 10393 |
rs550680990 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145090060 | ACTACATGAAATTAA[C/T]TGACTAAGCCATGTT | 10393 |
rs550690436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145084273 | GAAAATGAGTTTTGC[A/G]TTGAATTTCAAATTA | 10393 |
rs550696761 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145075738 | AGGAGGCCCCACAAC[C/G]CCCCCAGGCATCTGA | 10393 |
rs550716828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:145053410 | AGAAAGCTTCCTCTA[C/T]GTACTGCCTCTGTCC | 10393 |
rs550753742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145059492 | AAATTCACTTAAGCA[C/T]TCGATCTTGTGCTCT | 10393 |
rs550777362 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144974619 | TTGCCAATACAAAGT[C/G]AAGACACAAAAATAA | 10393 |
rs550795832 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145022588 | GGTGATGGGTGCACC[A/C]AAATCACCACTAAAG | 10393 |
rs550808071 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145052171 | TGAGGCATAAGAAAT[A/G]AGTTCAAGTCATCTA | 10393 |
rs550823890 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144997815 | GTCAAGACCCATCAG[G/T]GTGCTGCATTCAGGA | 10393 |
rs550870023 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145045954 | ATGTTCTAGCAAAAA[A/T]TATATTATGATTATC | 10393 |
rs550942447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145021953 | AGGCAAATGCGAATT[A/G]AAATCACAATGTGAC | 10393 |
rs550956570 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144981848 | TATTTTTTTGAGATG[C/G]AGTCTTGCTCTGTCA | 10393 |
rs550958991 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144980802 | TTTTACATTTAAGTC[G/T]TTAATCCATCTTGAG | 10393 |
rs550977273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145030005 | CCCAAGGTGGCAGGC[A/G]CTAAGTGGCAGCACT | 10393 |
rs550998847 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144997489 | ATCCAGCCAAACTAA[A/G]CTTCATAAGTGAAGG | 10393 |
rs551020833 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144976286 | TTTTGTACATATGTA[C/T]CTAATGTTTATTATG | 10393 |
rs551029831 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145014615 | TGGAAAGCGCCACCT[C/G]CTGGCAGGACAACCA | 10393 |
rs551038880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081567 | GTTAAGTGTATTTCA[C/T]TGTAATTTCTATCTT | 10393 |
rs551056004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145009055 | TAATAACAGACAGAG[A/G]GCCAAATCATGAGTG | 10393 |
rs551060032 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ANAPC10 | GRCh38.p7 | 4:145064299 | AAAATATTAACAACT[A/G]AAGAATCTAGGAAGT | 10393 |
rs551064949 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145086454 | GGTTCGTACAGTGTC[A/G]TTCCTGAACCAGCAG | 10393 |
rs551082190 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145008302 | AACTATTCCAATCAA[G/T]AGAAAAAGAGGGAAT | 10393 |
rs551092911 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145012068 | GTCTATCTGCTTAGC[A/G]GGAGAAAAAGTGAAC | 10393 |
rs551093668 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145089166 | AAAGCAAATATCACT[A/C]TTCAACTCAGAAATC | 10393 |
rs551095382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144973853 | AAATAGTTTTCTATA[C/T]AGATATATCAATTCA | 10393 |
rs551104115 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145071178 | TTGGGAGGCTGAGGA[C/G]GGCAGAGCACCTGAA | 10393 |
rs551120757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145026648 | TAAATAAGAGAAAAT[A/G]GTCAAGGATCTCCTG | 10393 |
rs551135589 | in-del | -/T | 0.00755907 | 0.0610114 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145006210 | CATTATGTAATGCCC[-/T]TTTTTGTCTTTTGTG | 10393 |
rs551179482 | snp | A/C/G | 0.000185856 | 0.00963813 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | ABCE1, ANAPC10 | GRCh38.p7 | 4:145097480 | ATTCAAAATAGGTGC[A/C/G]ATAGTTCTGCATACC | 10393 |
rs551201471 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145040378 | GTCTCGAACTCCTGA[C/G]CTCAGGTGATCCACC | 10393 |
rs551215349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145082098 | GCACATACAAACCCT[A/G]TATTAGGATCAAGTT | 10393 |
rs551219926 | in-del | -/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145052112 | TGGGGCTGGGAGTAA[-/G]GGGGACAGTTGGGAG | 10393 |
rs551255170 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144987964 | TATTTTTAAATTCAA[C/T]AATTTTTGTTTTTTT | 10393 |
rs551259301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144989491 | CCCTGACTGCTCCAT[C/T]GACCAGCTGTTCCTA | 10393 |
rs551280856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145033470 | TAGGCTAAAAAGGGA[A/G]TTACAGTGTTGGCTG | 10393 |
rs551305234 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145090403 | GAAGGCTAACTGTCC[A/C]ATTTCCCTTGCTTTT | 10393 |
rs551324278 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144996915 | CATGAAGCTGAAAAC[A/C]ATGGCACGAGAACTA | 10393 |
rs551338504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145011536 | ATTCGAGGGAGGAGA[A/G]AGCCTCAGGGAGGTG | 10393 |
rs551453461 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145006968 | TATATAACTGTCCAG[A/G]TCCATCACTTCTGGT | 10393 |
rs551461492 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145013101 | GACATGCTTCCTGTA[C/T]AGCCTGTGGAACTGT | 10393 |
rs551474906 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144972609 | AATCATATGGAAGAG[A/T]TTCATACAACTTTCT | 10393 |
rs551478974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145071931 | GGCAATTACAGACTT[C/T]CCTTCTTTTCTTACC | 10393 |
rs551505752 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145012553 | AGCAGATTATACATA[A/C]ATCATAAGACAAAAT | 10393 |
rs551551874 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145016372 | ACTCCCATTCACAAT[C/T]GCCTCAAAGACAATA | 10393 |
rs551556963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144999556 | TGAAATGAAAGAGGA[C/T]ACAAACAAATGGAAG | 10393 |
rs551561732 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144984115 | AAGAAAATTTCTGAA[G/T]AATAGGTTATTTGCA | 10393 |
rs551578995 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145094102 | TTTGAAAGCTAGCTA[A/C]TACTAATCTGGTGAA | 10393 |
rs551619333 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145006137 | AATTTGGGTGCTTCT[C/G]TGTTGACTGCATATA | 10393 |
rs551636077 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144977453 | TCCAATGCTTTAGTA[C/T]AGCATATATAATATA | 10393 |
rs551659859 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145016972 | CACAAAAATTAATTC[A/C]AGATGGATTAAAGAC | 10393 |
rs551669891 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145026005 | GACTAGATGGCAGCA[C/G]CTGAATATAAAGCGA | 10393 |
rs551672295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145025188 | TTGATTTTCTATCCA[A/G]AACATTCTTTCTCCA | 10393 |
rs551687336 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144985855 | CAATGTCCTCTTTTT[G/T]CCCATTCAGTATGAT | 10393 |
rs551694455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145078219 | CAATAGCATTTCTAT[A/G]TACCAATAACATACA | 10393 |
rs551700752 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B, intron-variant | ANAPC10 | GRCh38.p7 | 4:144993679 | CCAAGTTTTCCCACA[C/T]CTAATAAGATAGCCA | 10393 |
rs551711721 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145077188 | TGGGCGACAGAGCAA[G/T]ACTCTGTCTCAAAAA | 10393 |
rs551739155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145086710 | AAGGTATTTAGCTGT[A/G]TCCCTGGGCTCTACC | 10393 |
rs551749808 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145002733 | TTGGACTGAAAAAAG[C/T]AAAACTATTTCCAGA | 10393 |
rs551750033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145005513 | CTAGACTTGGGGTTG[A/G]TTTGCTCTCGGTTCC | 10393 |
rs551751587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145008915 | TCCCTGTTTGCAGAT[A/G]ACATGATTATATATT | 10393 |
rs551781553 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145041421 | TCATTGATAACTGAG[G/T]AGAAAAAGCAAAGAC | 10393 |
rs551792250 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145100073 | AATTGAATTAAAAGT[G/T]TTCACACAGTTAATT | 10393 |
rs551800375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145061859 | AAACCTGTAATCTCA[A/G]CACTTTGGGAGGCCG | 10393 |
rs551828387 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144976409 | AAAGAGGGCTTCCAG[C/G]GTACTGATGTGCTCT | 10393 |
rs551862401 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145044466 | CTATCCTTTGCATTT[A/C]CTTCCCCCCAACTCC | 10393 |
rs551863386 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145093593 | ACAAAAACCTAGAAA[A/G]GTAGATGAAATGTGT | 10393 |
rs551874892 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145097157 | CAGTGAGCCGAGATC[A/G]TGCTACTGCACTCCA | 10393 |
rs551881144 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145033530 | ATCAGTCTACTACTC[C/T]ACAATGGAAGTAAGG | 10393 |
rs551885784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144998987 | AGAATACTATAAACA[C/T]CTCTACGCAAATAAA | 10393 |
rs551897560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145052137 | TGGGAGATGTTGGTC[A/G]AAGGACATAAAATTT | 10393 |
rs552009203 | in-del | -/GTGT | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145040161 | TGTGTGTGTGTGTGT[-/GTGT]TTTGAGACGGAGTTT | 10393 |
rs552010826 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145008567 | AATCCATCATATAAA[A/C]AGAACCAAAGACAAA | 10393 |
rs552017169 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145068895 | AGCCTGGTGACAGAG[A/C]GAAACTCCATCTCAA | 10393 |
rs552020029 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144996545 | CCCCACAGCTTCTTG[A/T]CCATGCTGCTTGCCT | 10393 |
rs552118013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145020238 | AAGATAAACTACCAC[A/G]AGCAAGTGGGTTTCA | 10393 |
rs552123173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145052781 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGACAGG | 10393 |
rs552128905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145088555 | TTCCTCCTGTGAATC[A/G]TAATTATTCCACCTC | 10393 |
rs552159587 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144987092 | AGTCAGTGTGGAGAT[A/T]CCTCAGGGATCTAGA | 10393 |
rs552174954 | in-del | -/TG | 0.0103295 | 0.0711199 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145053904 | TCAGCTGATTACTAC[-/TG]TGTGTGTGTGTGTGT | 10393 |
rs552213766 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145058515 | TATGAAGTGCTCAAA[A/G]GCAGAAACTGTGACT | 10393 |
rs552219213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144997132 | ATACCTGAAAGTGAC[A/G]GCCAGAATGGAACCA | 10393 |
rs552224401 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145090233 | CTCTAGATTACTTAT[A/C]ATACCTAATATAATG | 10393 |
rs552235088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144979964 | AAATTCAAATGTTTA[A/G]CCAACCGAGATTAGT | 10393 |
rs552235526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145045263 | ACTTTATCCTACTTA[A/G]TTCTTTCTGGAATCC | 10393 |
rs552235922 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144996053 | AAGGCTAGGATTCAT[C/T]AGGGAAGAGATGGGA | 10393 |
rs552255983 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145066415 | TTCCTTGATGAGCCA[C/T]AAGCAGGAAGTAAAT | 10393 |
rs552268972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145090492 | AAGACTTCCATGATC[A/G]TTTCAAGCAAAGTAA | 10393 |
rs552297116 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145028496 | TATCTCCCATTAGCT[C/T]TTTCCCTCAAAAAGA | 10393 |
rs552302511 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144987509 | GTGGGGTGGGGGGAG[C/G]GGGGAGGGATAGCAT | 10393 |
rs552305607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144972749 | CAAGGGTAAATACTA[C/T]TTTCATGAAACATTA | 10393 |
rs552342392 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145020665 | TACTGACAATATAAT[A/C]GTTTACCTCAAAAAT | 10393 |
rs552373018 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145085443 | TTTTTTTTTCAGTTA[C/T]TTTATTTTGGCTACC | 10393 |
rs552410179 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144989467 | AGTTACTCCATAAAT[A/G]TCATATGTCCCTGAC | 10393 |
rs552410510 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144970908 | TATTCTGAAAGACAA[-/T]TCTTAACCCAGGCTG | 10393 |
rs552421097 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145087878 | ATGGTGAAACCCTGT[C/T]TAAACTAAAAATAAA | 10393 |
rs552424072 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145065530 | AATACAGTAACACAA[G/T]CACTCAAAAATTGAT | 10393 |
rs552430690 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145080801 | AATCCCAGTTACTCG[C/G]AAGGCTGAGGCAGGA | 10393 |
rs552450777 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145014507 | CTTCCCTATCCACCC[C/T]GGTAGTTGAAGACAA | 10393 |
rs552477420 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145026390 | TCGATAAGTGATTAC[A/T]TAGCATATAAGTATA | 10393 |
rs552521555 | snp | C/T | | | intron-variant, downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:145053296 | CAATAAAGATTAAAA[C/T]AGATAGCTAACATAT | 10393 |
rs552558900 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145035282 | CTTGGTCAAAGAGGA[C/T]GACCCTCCCTAATAG | 10393 |
rs552564272 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995077 | TATATACTGAAATTT[C/T]CAGTTCAACTCTTTT | 10393 |
rs552567123 | snp | A/G | | | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145097098 | ACCTGTAGTCCCAGG[A/G]GGGCTGAGACAGGAG | 10393 |
rs552581833 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145042890 | TCTCTGTACATCTTT[A/G]AAATAACAGGTAAAG | 10393 |
rs552594103 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081387 | TTTCTGAAAGTACCC[A/G]CAAAAAATAAATTAT | 10393 |
rs552596609 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144991809 | CCCCAATCTAGAACA[C/T]AAGGGATGAAGGTGG | 10393 |
rs552627159 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145001190 | AAGTATAATAAATGA[A/C]TGAAAGAAAGAAAGA | 10393 |
rs552632651 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145049565 | TGCTGCAATTTGGTC[A/G]CATCTTCAGGCTCCA | 10393 |
rs552650136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145034787 | TTAGGCTGCAGTGCC[A/G]GTCTAAGGAAAATCT | 10393 |
rs552674020 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145076885 | AGACTGGTTCTTCAA[A/C]TCAATTCAGCTAGAC | 10393 |
rs552740528 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145091557 | TCACCGCTACAGTAT[G/T]CCATAGTGTATATGT | 10393 |
rs552780224 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144967351 | GAACAAGATGAAACA[C/T]GAAAATAACTCTAGT | 10393 |
rs552801081 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145007490 | GTCTCTCAGACCACA[A/G]TGCAATCAAATTACA | 10393 |
rs552808474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145001729 | AAACCTACAGTGGTG[C/T]AAACAGGATCCATTA | 10393 |
rs552812458 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145051297 | CAATATTTACCAATT[A/C]AGTTTGCTATATTAT | 10393 |
rs552820258 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144982770 | CTTAAGTCAGTGTAG[G/T]AGGGGTTTCTGTTAT | 10393 |
rs552835489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145069014 | GTTTTGAAAGGATAT[A/G]TGAGACCTTAATGCA | 10393 |
rs552842735 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145015546 | GGAAAACTTCCTGGC[C/T]TTGCTAGAGACCTAC | 10393 |
rs552852955 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145083410 | ACACCTAGCTGTCTA[C/T]AATCTTTAAATATAT | 10393 |
rs552858791 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145012876 | TCCCCAATGATGGAG[C/G]GGGGCCTGGTGGGAA | 10393 |
rs552891805 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145016124 | GTTCTGGCCAGGGCA[A/T]TCAGGCAGGAGAAAG | 10393 |
rs552901471 | in-del | -/T | 0.00676609 | 0.0577691 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144996735 | TGGACGGAGAATGAC[-/T]TTTGACGAGTTGAGA | 10393 |
rs552940078 | in-del | -/CATT | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144993082 | ATAAAGGTATACATA[-/CATT]GTTTTTTTTTAGACT | 10393 |
rs552960919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145024207 | ATGCATCTGCAGTTA[C/T]TTTCTCAACTGAAGT | 10393 |
rs552971847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145058945 | AACATTCTACAATGA[C/T]TTCAAAGATGAACTA | 10393 |
rs553025679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144990914 | CTGTGAGGACAAGCA[A/G]AGACAAACTAGGGAG | 10393 |
rs553053402 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145009845 | ACTAAACTAAAGAGC[G/T]TCTGCACAGCAAAAG | 10393 |
rs553084376 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145052874 | GCCTGGGCAACAGAG[C/T]GAGACTCTGTCTCAA | 10393 |
rs553123901 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144974108 | TCAGCAAATTATTAG[C/T]AAACAAAATTAAGTG | 10393 |
rs553145029 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145037412 | AGTCACTACACCCAG[A/C]CCTATCACCATAAAT | 10393 |
rs553148647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145059879 | TCACACATTATTTTT[C/T]CTTCTGAGAGCAAAA | 10393 |
rs553177434 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145030551 | AGTAGGGGCTTACAG[A/C]GGTCAGGTAATTAAT | 10393 |
rs553186993 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145006879 | TCTCTGCAGAGACTC[C/G]TCTGTATGTTCCTTA | 10393 |
rs553194858 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145029804 | TTAGTCACTTTAGAC[A/C]TACTCATCCCAGCTG | 10393 |
rs553333401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144985916 | TATTATTTTGAGATA[C/T]GTCCCATCAATACCT | 10393 |
rs553344526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145067479 | AAGAGCTTCTGGCAG[A/G]AACCAAACATTTGCT | 10393 |
rs553372344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145056049 | TGGTATTGTCAGAGG[C/T]GTGTGAAACCAGAGC | 10393 |
rs553383415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145009196 | GAGGACACAAACAAA[C/T]GGAAGAACATTCCAT | 10393 |
rs553383473 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145003031 | ATCTTCCACCCTCAA[A/G]AAAGTCCCAGCCACT | 10393 |
rs553386331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144997237 | CAGGAAATACAGAGA[A/G]CACCACAAAGATACT | 10393 |
rs553427318 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145045482 | GGTCATCTCCCCATG[G/T]CATCTTGTAAAACTG | 10393 |
rs553441793 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145097864 | GAGCTCGGAAAAGAT[G/T]GGATTCCCGGCCCTG | 10393 |
rs553460913 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145035690 | GCTCATAGGTTCCAG[A/G]TTGTTTTTGTTCCCC | 10393 |
rs553474285 | in-del | -/ATTGTGTTTTTAAACACAATATTCC | 0.00755907 | 0.0610114 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145058418 | AAACCACAAAACAAT[-/ATTGTGTTTTTAAACACAATATTCC]ATTGTGTTCCCATAG | 10393 |
rs553483189 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145049754 | TCAGTTAATTTTTTT[C/G]AATTTCTTTTGTAGA | 10393 |
rs553512203 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145042763 | GTGAACAGCAGACAC[C/T]GATGTTCACACAAGC | 10393 |
rs553543183 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime, intron-variant | ANAPC10 | GRCh38.p7 | 4:144994542 | AATCAAATCTACTCA[C/T]TTTAAACCATGGAAA | 10393 |
rs553559139 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145093604 | GAAAGGTAGATGAAA[C/T]GTGTTAACAGACAGG | 10393 |
rs553585615 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145012509 | AAACTAAAATATCTG[C/T]AACTAAGAATTCATC | 10393 |
rs553599403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145026073 | CCCTTCCTCTTGCTC[A/G]GCTACGAGAACACTG | 10393 |
rs553614486 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144980902 | TAGCACCATTTATTA[A/C]ATAGGGAACCCTTTC | 10393 |
rs553646618 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145017958 | AAACATCACACACCG[A/G]GGCCTGTTGTGGGGT | 10393 |
rs553647591 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144978487 | TTTAATAATTAAAAA[G/T]GGACACTTTTGATCA | 10393 |
rs553674117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145066926 | GCTTAGCTCATTCAA[C/T]AGTCATTGATACGAG | 10393 |
rs553724612 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145032440 | AGGGAAGAGGTATGT[A/G]GATGGGCCTCTCTTG | 10393 |
rs553764105 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145012623 | ATAAAGAAGTAGAAA[A/C]ATCTGAATAGAATGA | 10393 |
rs553779025 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144999982 | TAATAAATGGTGCTG[A/G]GAAAACTGGCTAGCC | 10393 |
rs553800688 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145095400 | CCACCACTTTGTCCA[C/G]CACATCCACCACTTT | 10393 |
rs553809794 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145000706 | TTACTGGGTATATAC[C/T]CAAAGGATTATAAAT | 10393 |
rs553812073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145062456 | ACTAAAAATAGAAAA[A/G]ATTAGCTGGGCATGG | 10393 |
rs553832870 | snp | A/C | | | intron-variant, utr-variant-3-prime | ANAPC10 | GRCh38.p7 | 4:145063951 | TCAATCAATAAAATC[A/C]GTATAATAGTTATTT | 10393 |
rs553856570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145001267 | GAGGGAGGGAGGGAA[A/G]GAAAGAAGAAAAGAA | 10393 |
rs553887096 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145039786 | TTTTCAGTAGAGACG[G/T]GGTTTCACCATGTTG | 10393 |
rs553953920 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145098402 | TGCTCCCCTCCGCAA[A/G]GGGATCGTTTTCTCC | 10393 |
rs553981167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145077308 | CAAAACTACAACTCA[C/T]TGGGGTCCCTGACAG | 10393 |
rs554011953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144968429 | TTTTCTCTGTATTAA[A/G]TCAATCTCCTCCTCT | 10393 |
rs554036948 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145034229 | CGGTGTTACCAAAAG[A/G]GATTAACATCTGAGT | 10393 |
rs554049104 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145030271 | CTCAATTTCCAGACT[G/T]GAGCCAGTTTACAGA | 10393 |
rs554055747 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145018426 | ATTACTTGAGGTCAG[C/G]AATTTGAAACCAGCC | 10393 |
rs554059554 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144998624 | TGTAAAGCAGTGTGT[A/C]GAGGGAAATTTATAG | 10393 |
rs554061508 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145005529 | TTTGCTCTCGGTTCC[C/G]TAGTTCTTTTAGTTA | 10393 |
rs554091278 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145075212 | ACTAAACTCACTGTC[A/G]ACTAAAACTGCTTAA | 10393 |
rs554094924 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144970144 | AGAATTTATGAAGTG[G/T]CAAGGTTTAATGATA | 10393 |
rs554096151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145029843 | CAGAAGATATACCCT[C/T]GACCAATGCCTTGCA | 10393 |
rs554104028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145010383 | GCACACTTATGTTTA[C/T]TGTGGCACTATTCAC | 10393 |
rs554148207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144969037 | GTCTAACACATACAC[A/G]TACATACATGCATAC | 10393 |
rs554156263 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145068089 | AGAGAAGGAAACTGG[A/G]TCCACAAACACACTG | 10393 |
rs554193148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145085403 | GTAAAAGCTCCACAG[C/T]TTAATGTTCTATTGA | 10393 |
rs554240553 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145037054 | TATGTGTGTGCATGC[A/G]TGAATGTGTGTTTTA | 10393 |
rs554249134 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145090568 | TGGAAAGCACTATTG[A/T]GTAATGGAGTCTGTC | 10393 |
rs554257745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145021061 | CACATCCCATGTTCA[C/T]GGAATGGTAGAATCA | 10393 |
rs554270539 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144993259 | GTACCAGCAGTGCGA[A/C]GTGCATTTTCTCCAC | 10393 |
rs554288685 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145095468 | TAGCCATCAACATCA[C/T]CTGCTCCTGATATCC | 10393 |
rs554320974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145002090 | TCTCCTTTACTAACC[A/G]TATCTGTGACTTAAT | 10393 |
rs554330820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144982095 | GTGATCCATTTGCCT[C/T]GGCCTCCCAAAGTGC | 10393 |
rs554352431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145077604 | ATTCTTGATGAACAT[C/T]GACACAAAAATCCTC | 10393 |
rs554352748 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145086119 | AGGCGCCTGCCAACA[A/C]GCCCAGCTAATTTTT | 10393 |
rs554353296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145030466 | GGGGACTACTGGACA[C/T]TGGCTCTGAGCTGAC | 10393 |
rs554398142 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144989654 | AAAAGCTAGAAAGGA[C/T]TAAGTTTAATGAGGA | 10393 |
rs554401340 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144991944 | AAGTTTCAAGGAAGA[C/G]AATAACTCTTGTTAG | 10393 |
rs554426249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054419 | AAAAATTAGCCGGGC[A/G]TGGTGGCAGGCGCCT | 10393 |
rs554440138 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144996626 | AAACCACAAAGATGG[C/G]GAGAAACCAGAGCAG | 10393 |
rs554442346 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145039447 | GGCTGACTCCATTCA[A/C]GTTTTCTTGCTTTAG | 10393 |
rs554456183 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145092479 | AACTGTAGTAGAGCA[C/T]AGGAGGAAGGAACAA | 10393 |
rs554457786 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145002836 | TTATATACATAATAT[G/T]ATTTTTGTTGTAAAA | 10393 |
rs554465818 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145096545 | TTGAGTAGGTCTGGG[A/C]TTTATTTCCTCTCCT | 10393 |
rs554482989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145046938 | GTCATGTACGAGTAA[A/G]GATAAAGCAAGCAGC | 10393 |
rs554513553 | in-del | -/TTTA | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144978435 | GTTGTAAACATTTTG[-/TTTA]TTTGATAGGGATGAG | 10393 |
rs554538937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054661 | CGCGCGCGCGTGCGT[A/G]CAGCGCATGTGTGTG | 10393 |
rs554543954 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144971323 | AGTTGTAAATGCACA[A/T]TTTAGCTACTGCAGG | 10393 |
rs554545776 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144980018 | GCCAATGGGGAAAGG[G/T]TACAGGGGCATGACT | 10393 |
rs554560178 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145028708 | GTTTAGAGAGTTATG[C/T]AAAATAAATGTGTTT | 10393 |
rs554564007 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145072948 | TGTCACCCAGGCTGG[A/G]GTGCAGTGGCATGAC | 10393 |
rs554580020 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145089432 | TACTTATTTTTCCCC[A/T]AAATTTGTTTTTCAA | 10393 |
rs554584288 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144992945 | CCCTGTCAGCATTCA[A/C]CAACCACCACCCTGA | 10393 |
rs554589363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145036336 | ACACGTTATTTAGAA[C/T]TGTACACATCTAATA | 10393 |
rs554591698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081838 | ATATGTATTTGTCCA[A/G]AAATTTTGATAAACA | 10393 |
rs554640331 | in-del | -/AGAAGAA | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145019572 | AAACCCAAACCCAGC[-/AGAAGAA]AGAAGAAAGGAAATG | 10393 |
rs554663831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145075481 | AGAGCTTCATTCACC[A/G]AGAAACCAGACCATC | 10393 |
rs554681060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144981173 | ATTTTTAAATAGTTT[C/T]TTCTAATTCTATAAA | 10393 |
rs554682941 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144972122 | AATCTGGCCTCAAAC[C/T]ATCTTTCTAAAGTTT | 10393 |
rs554723825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145087973 | GAATCACTTGAACCC[A/G]GGAGGTGGAGGTTGC | 10393 |
rs554725909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145079705 | CACAATCATAAAAAA[A/G]AATGAAATCATGTCC | 10393 |
rs554751908 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145074279 | ACGTTAGGACTTATT[G/T]CTCCTAACTGCCAAG | 10393 |
rs554755884 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145068659 | GCACACGCCTGTAAT[C/G]CCAGCACTTTGGGAG | 10393 |
rs554807123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145051699 | AGTTAGAGGAATAAG[C/T]CAACAGCCACATAGT | 10393 |
rs554824120 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145089985 | AAAGTCTTCTATAAT[C/T]AGGCTTCTACCTAAC | 10393 |
rs554855090 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145097226 | AAAAATAAGAAAAAA[A/G]TGTTAAAAGTTCACT | 10393 |
rs554857527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144986426 | GCCTCAATTTCAGAG[C/T]CTGTTATTGGTCTAT | 10393 |
rs554873918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145033997 | TATGTACTAGTATTT[A/G]GGTTGGGGATTGATG | 10393 |
rs554882560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145044504 | CATGACCCACCTCCA[C/T]CCACAGTCTGCTAAC | 10393 |
rs554886379 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145095614 | TTCTTCACCTCACTC[A/G]CTCTCATCACATAGA | 10393 |
rs554932836 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145014169 | CCTTTTATTTCATAG[C/T]TCGGAGGTGGGTACC | 10393 |
rs554954844 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145056568 | TGGGGTCTGGATTGG[C/G]ACCCCTTTCCTTGTA | 10393 |
rs554963136 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145020367 | ATGCAGAAAAAGCAT[C/T]TGACAAAATCCAGCA | 10393 |
rs555050572 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145028771 | AGTTTAATGACACTA[C/T]ACATAATACCTTTGA | 10393 |
rs555060611 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144982356 | TAAAAAAATACTGTT[G/T]GTCTGTTTGTTTTCA | 10393 |
rs555068543 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145013977 | TTGCCTGGCATCACA[A/G]GGATCCTTCAGGAGG | 10393 |
rs555073721 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145060646 | CCAGTGGGCAAACAT[C/T]CACGGAAAAATAAAA | 10393 |
rs555076529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145065560 | TGTCTAATGAAGGCT[A/G]GCCTTGGAGAAAAAA | 10393 |
rs555085835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144968243 | TTCAATAGTTCAAGA[C/T]GAAGTTTGGAGATAC | 10393 |
rs555152654 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145042130 | GAATCTGAATGAAGG[C/T]TGAGACTGCCAACAC | 10393 |
rs555158272 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054679 | GCGCATGTGTGTGTG[A/T]GTGCCTGTGTGTGTG | 10393 |
rs555167156 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145056250 | CCACCAAAACCAAGA[C/T]GGCCACGAGAGTGAC | 10393 |
rs555167450 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145090551 | ACTGAGCCCATATTT[A/G]GTGGAAAGCACTATT | 10393 |
rs555170340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145011149 | CCAACCTGGCCAAAA[C/T]GGTGGAACCCCATCT | 10393 |
rs555202546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145069078 | AAAACAAGAAAGTCC[A/G]AGACATCTGCTCATG | 10393 |
rs555203671 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145070272 | CTTTAATACTACAAT[G/T]GCAAAGTTGAGCAAT | 10393 |
rs555260065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145084436 | ATACATTGGTGTGAA[A/G]CAGGAAATAAGCCAG | 10393 |
rs555285918 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145028257 | CTAATCAGCTTCCAG[C/G]GAATATAAAGCAGGC | 10393 |
rs555309526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145046060 | GCCCTGTTACAGGAG[C/T]GCACCCTAAGCATTT | 10393 |
rs555328119 | in-del | -/A | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145093566 | TATGAGTAAGATGTT[-/A]AAAAAAAAAAAACAA | 10393 |
rs555330385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145010527 | TGTCCTTTGTAGGGA[C/T]ATGCATGAAGGTGAA | 10393 |
rs555341367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144976197 | AAATGAACAAACTAT[A/G]TTTACAGAAAGTAAC | 10393 |
rs555348534 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144976660 | TTTTCATTAAAATAA[C/T]ATTTCCTCTTATTAT | 10393 |
rs555356625 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145060823 | GATATTGTGGTAGAA[A/T]AACAGAAAAAATAAA | 10393 |
rs555365967 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145009651 | TGGATCCCTTCCTTA[A/C]ACCTTACACAAAAAT | 10393 |
rs555427006 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145016509 | TTCCATGCTCATGGA[C/T]AGGAAGAATCAATAT | 10393 |
rs555429019 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145025340 | TCAACACGCCCCCCC[C/G]CCCTTTTAAGCTCAG | 10393 |
rs555451697 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145004329 | CCTATTTGGATGTCT[G/T]TATTTATTTCTCTTG | 10393 |
rs555517104 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145009639 | GAAAGCTGAAACTGG[A/T]TCCCTTCCTTACACC | 10393 |
rs555530067 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144982939 | GCCAAGGAGGGTAGA[C/T]CACGAGGTCAGGAGT | 10393 |
rs555539738 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144978295 | TTCTTTCTGAGTAGA[A/G]AATATGTTTTCTACT | 10393 |
rs555568272 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145039244 | GAAAATTATTTTCAA[A/C]CTAGAATTCCACAGC | 10393 |
rs555589640 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144991640 | CTCGGCATCCCAAAG[C/T]GCTGGGATTAGAGGA | 10393 |
rs555592345 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144973576 | AAGGGATCAATAAAC[C/T]CACAAGTTTGTTCTT | 10393 |
rs555628771 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144979900 | GCTCATTACAGACAC[C/T]GCTTCCCCTTCCTCT | 10393 |
rs555633000 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145052903 | AAAAAAAAAAAAAAA[A/G]GGGATACTCATTTAT | 10393 |
rs555703488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145042334 | ACTCATAACAATACT[A/G]TCAAGAAGCCAACAT | 10393 |
rs555740213 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145050852 | TAAGGGAATGTTGTA[A/G]CTGGTTTAATCTTCC | 10393 |
rs555755323 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145010996 | CTTCCACAATAGAAG[A/T]CACATGAAGAAGGTC | 10393 |
rs555793829 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145098384 | GAGCTGATTTGGCCT[C/T]TGTGCTCCCCTCCGC | 10393 |
rs555831223 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145035104 | AGGTGAGACACAAGA[C/G]TTCTTTTCATGCAAG | 10393 |
rs555912336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144997906 | CCAAGCAAATGGAAA[A/G]CAAAAAAAACCAGGG | 10393 |
rs555948267 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145067687 | GGCCGCCTCCTGCTA[C/T]CACAGATACGAGCAT | 10393 |
rs555967107 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145018484 | ACTAAAAATACAAAA[A/C]AAAATAAGCCAGGCA | 10393 |
rs555998051 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144974195 | TTGATTTAACATTCA[A/C]ATATCAACCAATATA | 10393 |
rs556025731 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145009244 | ATCAATATCATGAAA[A/G]TGGCCATATTGCCCA | 10393 |
rs556054649 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145058986 | TGAAACTACTTTTTT[A/T]AAAAAATCTTTTAAA | 10393 |
rs556103206 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145094884 | CATTCATAAATTTTT[A/G]AGAGAAAAGGACTGC | 10393 |
rs556124336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145001328 | CAACATGGATGAACC[C/T]TGAGGACATTATTCT | 10393 |
rs556184344 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145095503 | ATCAACATCATCGTG[G/T]CTTGATGATCCAGAA | 10393 |
rs556209371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145056083 | TCCATCTTGAATACG[A/G]GCTGGGTAAAATGAA | 10393 |
rs556215581 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145091623 | TTGGGTTGATTCCAC[A/C]TCTTTGCTATTATGA | 10393 |
rs556235603 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145026128 | TTTCCTACAAATCTC[A/G]CCTCCCATCCCTTGC | 10393 |
rs556252799 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145018090 | ACCTGCACGTTGTGC[A/T]CATGTACCCTAGAAC | 10393 |
rs556267371 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144987221 | TGTGGCACTATTCAC[A/G]ATAGCAAAGACTTGG | 10393 |
rs556274320 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144985369 | ATATTCCCTGTTTTA[C/T]GTAACATATTTTGCA | 10393 |
rs556296112 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145096220 | ACCCTGACATTAATC[A/G]TTTATTCTGAAGAAT | 10393 |
rs556321337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:145033003 | ACAGCTAAAGAAGTA[C/T]GGCAGTGGGCACATG | 10393 |
rs556338259 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144999138 | AATAGCCTACCAACC[A/C]AAACAAGTCTAGGAC | 10393 |
rs556357408 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145070726 | ATTATTTACAACAGC[C/T]GAAAGGTAGAAACAA | 10393 |
rs556384632 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145007617 | AGAAATAAAGATGTT[C/T]TTTGAAACCAATGAG | 10393 |
rs556395917 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144970351 | ATATGGAAAACTATA[C/G]ATAAAAACTCTCCTG | 10393 |
rs556411391 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144977932 | ACCAGCTATAACGTG[A/C]TTCTCAGGAATTCAT | 10393 |
rs556413190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145056791 | ATTCCCAGTATGTTT[C/T]CCTTATAAGAGGGAT | 10393 |
rs556472321 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145033600 | TCTTAATATTACTAT[A/G]CCCTGTGATTAAGGT | 10393 |
rs556506333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145029612 | TAAGTAGGGACTCTG[C/T]TTTTAATGTTGCAGC | 10393 |
rs556553444 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145086289 | TAATTTAAACAAAAG[A/T]ACTAAAACAAAGACG | 10393 |
rs556569898 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145067322 | GAATGCTCACTATAC[A/G]CCAGGCATCGTGCTA | 10393 |
rs556586965 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144978623 | CCCAGGAGTTCAAGA[C/T]CAGCCTGGGCAACCT | 10393 |
rs556638975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145031044 | TCTGGTATCCAACCA[C/T]TGACTTGGCAAATGC | 10393 |
rs556645893 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144986021 | ATATGGTTTTTGTCA[C/T]TGGTTCTGTTTATAT | 10393 |
rs556653887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145015353 | ATTCAGAGCTTGAAG[A/G]CAAGGTCTTTGAATT | 10393 |
rs556656707 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145071355 | AGGTTGCAGTGAGCC[A/G]AGATCGTGCCATTGC | 10393 |
rs556684245 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144982737 | GATTTTTTAATATAT[G/T]AGAAATATAGAAACT | 10393 |
rs556693147 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145006318 | GTGGAAAAGATAAAG[A/G]GAATTTGTTTGGCAA | 10393 |
rs556725306 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145090125 | TTTCTTGGCATCCAA[C/T]GAGGATTGGTACCAG | 10393 |
rs556737341 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144996789 | AATAACAAACTTCTC[A/C]GAGCTAAAGGAGGAT | 10393 |
rs556768229 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, synonymous-codon | ABCE1, ANAPC10 | GRCh38.p7 | 4:145097260 | ATATGCTCTTACCAT[A/G]GAAGATAAGGTCAGG | 10393 |
rs556795900 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145047760 | TTTTTAAATTGATGA[A/G]ATTATTGTTCAACTA | 10393 |
rs556816805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145076127 | CAGAAAGCTTTAGCA[A/G]ATGGGCTGCTGCCAG | 10393 |
rs556822265 | snp | A/G | | | downstream-variant-500B, intron-variant | ANAPC10 | GRCh38.p7 | 4:144993683 | GTTTTCCCACACCTA[A/G]TAAGATAGCCAGCTG | 10393 |
rs556837605 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144989707 | GGCCGAAAGCTAGGC[C/T]TCTTTCTCCAAACAG | 10393 |
rs556837914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145090711 | AACTTTTGAAAACCT[C/T]ACTGAGATAACTGGT | 10393 |
rs556874405 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144989109 | AATGACTGGTACACA[C/T]AGTAGGTGGATGTTT | 10393 |
rs556875739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145040504 | AATGGCTTTGCTCCT[C/T]TCAGCTACCATTCAC | 10393 |
rs556878469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145004359 | GCCTGATTGCTCTGG[C/T]TAGAACTTCCAGGAC | 10393 |
rs556949907 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145066788 | GATTTAAAAAAAAAA[A/C]ATAACACTTAGGTTA | 10393 |
rs556958680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145030513 | CCAAAGAGTCATTTC[A/G]GTCCTCCAGTTAAAG | 10393 |
rs556986482 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145019116 | TAACAGCTATATACA[A/G]AACATTCCATCCAAG | 10393 |
rs557011025 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144997172 | TCACTCTTCAGGATA[C/T]TGCCCAGAAGAACTT | 10393 |
rs557063295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145008356 | TCAGCATCATCCTGA[C/T]ACCAAAGTCTGGCAC | 10393 |
rs557082103 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144973159 | AAAATAGAAGAAAAT[A/G]ATGAAGAGCGTGCAG | 10393 |
rs557095817 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145087773 | GAGATGAGGCCAGGC[A/G]CAATGACTCATGCCT | 10393 |
rs557104283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145020922 | CTACAAGGAAAACTA[C/T]AAAACACCACTGAAA | 10393 |
rs557157272 | snp | A/C/G | 0.00199529 | 0.0315338 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145045438 | CTATCAACATCACTC[A/C/G]GCCTAAAAAAAATAT | 10393 |
rs557193567 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145073987 | ATCAGCAAACAAGTA[C/T]ATTAGTCCCTATAAT | 10393 |
rs557195992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145044626 | TAAGTGTTTCTATTA[C/T]ACTGACAGGGTCAAT | 10393 |
rs557237359 | in-del | -/A | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145085614 | AATGTCCTATAATTC[-/A]AAACTGATCATTTAA | 10393 |
rs557249572 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145068212 | AAAAGCTCTGCTACT[A/G]TATGTTCTGATTTCT | 10393 |
rs557280271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144979696 | CATTGTTATGGGATA[C/T]GATAAAGTTTCTTTT | 10393 |
rs557417544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145052257 | TAAGACAGATTTAAG[C/T]GTTCACACCACAAAG | 10393 |
rs557485110 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145028907 | GCTTCAGAAGCAGGT[A/G]TTAACCCCTCAAATC | 10393 |
rs557502116 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145009473 | TGGTACCAAAACAGA[C/G]ATGTAGACCAATGGA | 10393 |
rs557543495 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145037628 | TAAATCATTTAACTA[C/T]TAAGTAAACAATTGC | 10393 |
rs557571697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145032409 | CATGATTGGAAAATT[A/G]GTGACCAAGAAATTT | 10393 |
rs557591865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145061555 | GAGGTTTCAAATATA[C/T]ACCACGTATATCAAA | 10393 |
rs557602682 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145055355 | CTGAGGTCAGGAGTT[A/C]GAGACTAGCCTGCCC | 10393 |
rs557617238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144972267 | TTTTGTTTACAGAAA[A/G]CATATAATAAATACA | 10393 |
rs557622840 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145025526 | GGCTGGTTAGGTGCT[A/G]GAGTAGTCAGAACAC | 10393 |
rs557645433 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145077565 | CTGCCAGAGATCCAG[C/T]AAAAGAAGAAACCTC | 10393 |
rs557669819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145069736 | TTACTAAGATGTAAT[C/T]TGCCTTTTTCAGAAT | 10393 |
rs557701204 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145075565 | ACAGAGGGAGGACCA[A/C]GCAGACCCTGGGCTG | 10393 |
rs557753962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144968913 | GCTACATCCTACCTA[C/T]GTATTGTAACAGTGA | 10393 |
rs557766000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145017799 | ACCCATAAAAAAGGA[C/T]GAGTTCATGTCCTTT | 10393 |
rs557769287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145005811 | ATCTTTATTGCATTG[C/T]AGTCTAAGGACATGG | 10393 |
rs557784978 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145017229 | TCTACTCATCTGACA[A/G]AGGGCTAATATCCAG | 10393 |
rs557808359 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145039702 | CGGATTCAAGCAATT[A/C]TCCTGCCTTAGCCTC | 10393 |
rs557813892 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145077632 | CTCAATAACATACTA[C/G]CAAACTGAAACCAGC | 10393 |
rs557816460 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145011250 | GCTGAGGCAGGAGAA[C/T]TGCTTGAACCCTGGA | 10393 |
rs557862764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144998572 | CTTTGAAACTAATGA[A/G]AACAAAGACACAACA | 10393 |
rs557877145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145046770 | GAGAAAACACTGATA[C/T]CGAAATGCCAAATAT | 10393 |
rs557905916 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145047548 | ATCTGCCTTAGACAA[C/T]TCCCTCTCAACACAA | 10393 |
rs557906329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145006446 | ATAAGAAAGGAACGA[C/T]AGCAATGAATAAAAG | 10393 |
rs557922965 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145009736 | AGAAGAAAACCTAGG[C/T]AATACCATTCAGGAC | 10393 |
rs557938583 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144976248 | TCATGTTGAATAAAA[G/T]AAATCCAACACAAAA | 10393 |
rs557957418 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145007053 | GGGTCCCAAGATGGA[C/T]GAATAAGAACAGCTC | 10393 |
rs557958184 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145016098 | CACTCCTATTCAACA[C/T]AGTGTTGGAAGTTCT | 10393 |
rs557974969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145024435 | TGTATATCTTAAATA[A/G]TAAGAATTGAAAGTT | 10393 |
rs557996007 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144984466 | TTAAAATCTGGATCT[A/C]TAGCCACAGACGAAT | 10393 |
rs558027791 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145002026 | AAGGAAGGAAAAACT[A/G]CTTGATAGTTGCTTC | 10393 |
rs558033704 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145010345 | CCCAAAGGATTATAA[A/T]TCAAGCTGCTATAAA | 10393 |
rs558041919 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145038937 | TTCTACAGAGAAAAA[C/T]AGGTCACATGCAAAG | 10393 |
rs558099472 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145035468 | TTGTCATTATCTACT[C/G]CTTCACACCATTGTC | 10393 |
rs558103738 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144970222 | ACCATTTTAAGGCCA[A/C]AACAACTGTGAAATG | 10393 |
rs558109672 | snp | A/G | | | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145099540 | TATTTTAAAAAAGGG[A/G]GTTTTTTTGTTTGTT | 10393 |
rs558126520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145004923 | ATTAGTAACCAGCTC[C/T]TCCTTACACAACCAG | 10393 |
rs558146533 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145075621 | AATGGGGTTGCTGAG[C/T]ACCAGGACTCATTTC | 10393 |
rs558165508 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054396 | CTCTACTAAAAAAAA[A/T]ATATACAAAAAATTA | 10393 |
rs558209070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145099198 | CATTTAATACGTATT[A/G]TGAATGAATGACAGC | 10393 |
rs558213634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145036269 | TTATAGAGCTAAATC[C/T]TGATGTGTTATAGCA | 10393 |
rs558237229 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145084594 | CTAAAAAAAAAAAAA[A/T]TCATAATGTTTCAAA | 10393 |
rs558258020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144992568 | GGTAGAAATAGCAAG[A/G]GAACAAGAATTAGAA | 10393 |
rs558258329 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144983793 | CTTACATAGGTTAAT[G/T]TATATAGGTAATATG | 10393 |
rs558315558 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144991718 | AGCTCATCAGCTATC[A/G]TTAGTGTATTCTATG | 10393 |
rs558327950 | in-del | -/CTAGAGAC | 0.00358779 | 0.0422022 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145015550 | AACTTCCTGGCCTTG[-/CTAGAGAC]CTACACATCCAAATA | 10393 |
rs558336931 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145073176 | TGGGATTATAGGCGT[A/G]AGCCACTGCACCCAA | 10393 |
rs558340858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144988831 | TGAAACCACATATAT[A/G]TACTCTTTTTTGTAC | 10393 |
rs558354415 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144993169 | CCACTTTATTGTGAT[A/T]GTCACTTTACTGTGG | 10393 |
rs558375112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081102 | ATAGCGGCCAACTGT[C/T]TCTTATTTAAAATTT | 10393 |
rs558445818 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145008261 | CTACCAGAGGTACAA[A/G]GAGGAGCTGGTACCA | 10393 |
rs558500567 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145098543 | CAGCAGCAGCGCGTG[G/T]CAGCGGTTCCTGCGG | 10393 |
rs558520927 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144996170 | GGGAAACAATATGAG[A/C]GATATGGAGATATCC | 10393 |
rs558534711 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145043601 | TCTTTCTTACTTTAG[A/G]TGAAATATACCATCA | 10393 |
rs558552897 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145096299 | ATGGTGGCTCACACC[G/T]GTAATCCCAACACTT | 10393 |
rs558573681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145042439 | ACTTTATAAATAAAA[C/T]AGATTTTAAAGGGCA | 10393 |
rs558598858 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145001553 | CTTAAATACTGTAAG[A/T]TTAAATACTATTGTA | 10393 |
rs558615379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145050949 | TTCACTAGAGTAGCA[C/T]GTTTAATTTCCGTCA | 10393 |
rs558641856 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145088438 | TATAAATTAAATTAT[G/T]TATTTTTTGACCCAA | 10393 |
rs558657511 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144978457 | GATAGGGATGAGCAA[C/T]AATTTTATATTATTT | 10393 |
rs558658818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144980222 | TTGAACTAATTTACA[C/T]TCCCAACAGTGTAAA | 10393 |
rs558675741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144979352 | GCAAGTGAGAATATG[C/T]GGTGTTTGGTTTACT | 10393 |
rs558678548 | snp | C/T | | | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145098631 | TCCCCTCCAGCCGAC[C/T]CGGCTGTCGCCGCTG | 10393 |
rs558681548 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144993130 | AATTTTATAAGCACT[C/G]GGAAACCAAAACGTT | 10393 |
rs558719671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145086443 | TCTAATGCAGTGGTT[C/T]GTACAGTGTCGTTCC | 10393 |
rs558727411 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145027322 | AACTTCTTAATTTAA[G/T]AGAAGTTAAATGAAT | 10393 |
rs558773905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145002018 | AATAAAAGAAGGAAG[A/G]AAAAACTACTTGATA | 10393 |
rs558795398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144986163 | CCAGTATTTTATTTA[A/G]GATTTTTGCATCGAT | 10393 |
rs558810184 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145056938 | TTTTGTCTTCTTTGC[A/C]CTAGGCTGTTACCAT | 10393 |
rs558813659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145051593 | GGTAGGCCTGTATAG[C/T]ACTTAGTATACAATG | 10393 |
rs558869971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145028094 | CTGTTAGATGGTGTG[A/G]TGGTTAATACCGAGT | 10393 |
rs558878677 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144993400 | AGCATCTTTTTGTAC[A/C]ATTACTTGCCAATCA | 10393 |
rs558890572 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145080268 | TACTACCTGGATGAC[A/G]AAATTTGTACACCAA | 10393 |
rs558893500 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145010494 | AATACTATGCAGCCA[G/T]AAAAAAGGATGAGTT | 10393 |
rs558950730 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145008919 | TGTTTGCAGATGACA[A/T]GATTATATATTTAGA | 10393 |
rs558953044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145079640 | CCTAGATGCCCATCA[A/G]CAGTGGACTGGATAA | 10393 |
rs558995289 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144971227 | CTGCACTTTTGGGGA[C/T]GATCAAGGCAAAATC | 10393 |
rs559008557 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145007847 | AGAATTGAAGGACAC[A/G]GAGACACAAAAAAAA | 10393 |
rs559058794 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144975829 | TGACTTCATTAGTTA[C/T]CAGGGAAAAGAAAAT | 10393 |
rs559102684 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145000525 | ATCAGTTAGAATGGC[A/G]ATCATTAAAAAGTCA | 10393 |
rs559111297 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144981527 | CTTTGCTGACATTGC[A/T]TATCAGCTTAAGAAT | 10393 |
rs559166076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:145033023 | GTGGGCACATGCTCA[C/T]GGAATTCACTGGTCT | 10393 |
rs559168164 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145041307 | ATACTGAACTAACTC[A/T]ATTACTTACAGCTTA | 10393 |
rs559168180 | snp | C/G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145020237 | AAAGATAAACTACCA[C/G/T]GAGCAAGTGGGTTTC | 10393 |
rs559250996 | snp | C/T | 0.000800961 | 0.019996 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144973734 | ATCATAAAATGATAA[C/T]ATAAATAAATTTATG | 10393 |
rs559251951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145090850 | CCACTAAATTGTGAA[A/G]TCCTTGACAGTAAAG | 10393 |
rs559277974 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145033734 | CTGATGAGGTGCTTG[A/C]TGAAGGCAAAGGGAA | 10393 |
rs559372321 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144980589 | AGCAAAAATTTTCTC[C/T]CATTCTGTAGGTTGT | 10393 |
rs559392230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081912 | ACAGGGTCTTGCTGT[A/G]TTGCCCAGGCTGGCC | 10393 |
rs559428979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145090239 | ATTACTTATAATACC[C/T]AATATAATGTAAATA | 10393 |
rs559431537 | in-del | -/CT | 0.00755907 | 0.0610114 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145039596 | GCCCTATGAGGTATA[-/CT]CTCTTTTTTTTTTGT | 10393 |
rs559442694 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145025418 | TCACTTGGACACTTA[C/G]AGACCATTGTCAAGT | 10393 |
rs559448339 | snp | A/G | 0.000251984 | 0.0112218 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145053827 | CACCTCTATTAAGAT[A/G]TACTTTTAAATTATG | 10393 |
rs559466638 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145083181 | TAACAAACACTGATA[C/T]CACATTAACTATGTG | 10393 |
rs559471462 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145021585 | TTCTAGAAGATTAAC[A/G]TTGGAAAAACCCTTC | 10393 |
rs559486573 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | ABCE1, ANAPC10 | GRCh38.p7 | 4:145097348 | ATCTTTCACATCTTT[G/T]GTTAATTTTACTAAG | 10393 |
rs559502646 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145065925 | TTCTTCTTTATGATT[C/T]TTAAAGTTTCTGAAC | 10393 |
rs559520016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145053089 | TTCAGAGAAGATTAT[A/G]TATTTTCAATATGAG | 10393 |
rs559584682 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145015014 | CCAACCCTGGTAATA[A/T]GACAAAACAAGGCTC | 10393 |
rs559592659 | in-del | -/AA | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144979700 | GTTATGGGATATGAT[-/AA]AGTTTCTTTTCAAAT | 10393 |
rs559600125 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145029945 | TAACGATGAGAACCA[C/T]GGTCACTCAACTACA | 10393 |
rs559623212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145044961 | TTATAGAAGTTCACT[A/G]TAAACATTCGGAAGT | 10393 |
rs559633315 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144967189 | CACAGGGCGAGAAGA[A/G]TCAAAGTTAGTTAAC | 10393 |
rs559642238 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145058539 | TGTGACTTTATTGTA[G/T]CCCCAGTATCTAACA | 10393 |
rs559644904 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145067277 | TCAAACTGCTCAAAA[A/C]CATCATTATAATAAT | 10393 |
rs559711301 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144969913 | CTGGGTATATACTAC[C/T]GGCTTAAGAAATGAA | 10393 |
rs559718017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145085811 | CTTATGTGCCAATCC[C/T]GTCTCAACCTCTTTT | 10393 |
rs559718496 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145044109 | CCTATACTAAAAAAC[A/C]AAACAAAAAATAGAT | 10393 |
rs559719927 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145076333 | CCACAAGCACTGAGC[C/T]GAGCCTTGGTACCCT | 10393 |
rs559772367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144977322 | AATATTAACTAAATA[A/G]TTTGATTTACACAAC | 10393 |
rs559788940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145079019 | CAATTAAAACAAAAA[C/T]GTAAATTGACAAGTG | 10393 |
rs559793126 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144970764 | GAGAATCCATAATAT[A/G]AGCCTGAACTCATAC | 10393 |
rs559815696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144988568 | TGTAAAACAAGTACA[A/G]TAAGTTATTTTTAAA | 10393 |
rs559827837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145002381 | CTGCCCTAGTGAAGA[A/G]GGCGACCACCTAAGA | 10393 |
rs559858690 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:145032670 | CATGGGCTCAGCAAC[A/T]TGGACTTCCACTCAC | 10393 |
rs559913137 | snp | A/G | | | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145100016 | TTCTATTGAAAAACA[A/G]GTAGGGAATCCCCTT | 10393 |
rs559922152 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145035967 | AAAAATGTGGAACTG[A/C]GAGTTACGTATTGCT | 10393 |
rs559931366 | snp | C/T | 0.323197 | 0.239044 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054638 | GTGTGTGTGTGTGTG[C/T]GTGCGCGCGCGCGCG | 10393 |
rs559943069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145013653 | ATCGTGAATTTTAGC[C/T]CCAGAGTGATTGCAG | 10393 |
rs560005902 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144983567 | CCCAGGGAGTGACTT[A/T]TGAGTGACATAAACT | 10393 |
rs560006300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145048092 | TGCTAGAGTCGAATC[A/G]ATTTTAGAACTAATC | 10393 |
rs560060142 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145040695 | AAAGTAATTACCCAA[C/T]CAAAATCCTGAACAT | 10393 |
rs560060908 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145000336 | AATATCCAGAATCTA[A/C]AAAGAACTTAAACAA | 10393 |
rs560093779 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145094037 | ACACAATTTGGAAGC[A/G]GTCCACAGAAGGGCA | 10393 |
rs560137261 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145010843 | AATAAATAAATAAAT[C/T]GCTTGATCTTTAACC | 10393 |
rs560170069 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, synonymous-codon | ANAPC10 | GRCh38.p7 | 4:145033315 | TGCTTCCTGTTCCCA[C/T]GACATTACGTTCTGC | 10393 |
rs560206232 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144993503 | GAGTTGTAAGGGATT[G/T]TTATATATTCTAAAT | 10393 |
rs560230759 | snp | C/G | | | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145096981 | TTTGGGAGGCCAAGG[C/G]AGGTGGATTGCTTGA | 10393 |
rs560235060 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145020715 | GCTCCTAGAACTGAC[-/A]AAAAGAATTCAGTAA | 10393 |
rs560252981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145099827 | TGTAAATGCTTCTAA[A/G]TATTCCTCACTTCCT | 10393 |
rs560255054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145011294 | GTAAGCCAAGATTGC[A/G]CCACTGTACTCTGGC | 10393 |
rs560338273 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145060973 | AAGTATTCATATCAC[C/G]AGCTGCAAAAGCTAG | 10393 |
rs560346428 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144967721 | CAGAAAGCTCAAAAT[C/G]TGGCATCAGGGAGAA | 10393 |
rs560353618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145005317 | GGGTCAGTGGTTACA[C/T]CCCTCTTGTCATTTC | 10393 |
rs560370643 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145016590 | ACATCAAGCTACCAA[G/T]GACTTTCTTCACAGA | 10393 |
rs560379582 | in-del | -/AAAA | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144997908 | AAGCAAATGGAAAAC[-/AAAA]AAAACCAGGGGTTGC | 10393 |
rs560394328 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145066131 | TCAAAAGTCAGCCTA[C/T]AAAAACAGCAGGGGC | 10393 |
rs560410598 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145031364 | AAATTCCGGGACCGT[C/T]GACCTCAGTAAAATT | 10393 |
rs560426162 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145069298 | GTGAAGAGGGAGATG[A/C]CAAAGAGAATCTAGT | 10393 |
rs560426210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145047319 | ATTTAAAACCCAGAT[C/T]GCAGGTTATGAAACA | 10393 |
rs560458051 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145083122 | GAGTTTTTTACCATA[C/T]GAATATTTATTCCAT | 10393 |
rs560461744 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145035222 | CTAGATTGGTATTAA[A/C]TTCCTCCCTCACTGC | 10393 |
rs560476616 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145071582 | ACCATATGATCCGTA[C/T]GAACAGATACAGAAA | 10393 |
rs560487649 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144975639 | AAACAATGAAAATTC[A/C]ACCCACAAGAGTGGA | 10393 |
rs560511809 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145016300 | AATCAATGTGCAAAA[A/C]TCACAAGCATTCTTA | 10393 |
rs560522119 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145068793 | CATGTGCCTGTAGTA[A/C]CAGCTACTTGGGAGG | 10393 |
rs560531975 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144983878 | AATAACTATTTTAGC[A/T]TAAACTAAAGGCTAG | 10393 |
rs560541673 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145046430 | ACAAAATAAATTCCA[C/T]AAGCACAAACAATTT | 10393 |
rs560558926 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145098586 | TGATGGAGCGCGGGC[C/G]ACGCCGAGAGCTTGG | 10393 |
rs560587455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145020025 | AGAAGAATTGGTACC[A/G]ATCCTACTGACACTA | 10393 |
rs560629237 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime, intron-variant | ANAPC10 | GRCh38.p7 | 4:144994281 | CAGGAAGAAGAGCAG[A/G]GTTTTTAATGAGTGA | 10393 |
rs560663355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144967169 | TTCACTTCTGAGATA[C/T]AGAACACAGGGCGAG | 10393 |
rs560699084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145065331 | AAACATGAAAATGTG[C/T]TCAACGTCTAATAAT | 10393 |
rs560704796 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145091319 | TCAGTGCTAGTTTAC[C/T]AAGGAAGGTAAACTT | 10393 |
rs560717892 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145041917 | TCTTTATAAAAAATA[A/G]TCAAAATGGTAAAAA | 10393 |
rs560719007 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144983121 | GCCAAGATCGTGCCA[C/T]TACACTCCAGCCTGG | 10393 |
rs560735816 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145084695 | GCTATTACTTCTTCC[A/G]TAACTCTTAAATCTG | 10393 |
rs560774154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145067003 | GCCATGAGTTATTAT[C/T]GTAAGGTTCACGTAC | 10393 |
rs560777283 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144997604 | ATGGAAAGGAACAAC[C/G]AGTACCAGACACTGC | 10393 |
rs560787078 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145001632 | CCAACCCAAAGACTG[C/T]CAGGTCACTTCTGAA | 10393 |
rs560809979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145076439 | GATAAAAGCAAAAAA[A/G]TCCCATCTAAAGGAC | 10393 |
rs560824982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145028572 | ACAGAATATTAAGGA[C/T]GGGGTTGTTTCATTG | 10393 |
rs560852806 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145073461 | TAAAATTTATGAACA[G/T]TGTAATTTGGGGAGG | 10393 |
rs560860810 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144971889 | GTCCTAAGTGCTACC[C/T]TATTAAAAGAATTTC | 10393 |
rs560897008 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144986999 | AGTCAGGAAACCACA[A/G]GTGCTGGAGAGGATG | 10393 |
rs560902038 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145022918 | TAGGGTACCTGTGCA[A/C]AACATGCAGGTTTGT | 10393 |
rs560925424 | in-del | -/CTTT | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145043367 | ACTTTCTAATTAATC[-/CTTT]TTTTGTAAGTTATTG | 10393 |
rs560927523 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145034715 | CTGACTAATACAGAT[G/T]GTGATGCAGGTTCGA | 10393 |
rs560960374 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145087622 | AGTTCCTCAGTAACA[C/G]TAGTAACATTTCAAA | 10393 |
rs560971715 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145019015 | GGGGGACTTAAATAC[G/T]CCACTGACAGCACTA | 10393 |
rs561048329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145001023 | CACAGGGCCCACCCC[A/G]GGGCCTGTCGTAGGG | 10393 |
rs561052035 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145014368 | GAGGCAGCCATAATT[A/C]TCCTAAGTACACAAC | 10393 |
rs561101438 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145035215 | TAGCTGGCTAGATTG[G/T]TATTAACTTCCTCCC | 10393 |
rs561140124 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145072750 | CACAATCTTTGACAA[G/T]AAATATTTAACATTT | 10393 |
rs561172544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145095740 | CTTCTATTGTTATAA[C/T]TGTTCTATTTTATTA | 10393 |
rs561226008 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145082120 | GATCAAGTTATTTTG[C/T]TGTCACCTTTTTAAA | 10393 |
rs561283508 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145056346 | TCAGGAAGTTACCCT[A/T]TATGGTCTAAAAAGG | 10393 |
rs561302670 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145098606 | CGAGAGCTTGGGGGC[A/G]CCTCGGTCTTCCCCT | 10393 |
rs561308112 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145071052 | ATGAAAAGTTCTGAA[A/G]ATGGAGGTGGTAGTG | 10393 |
rs561320606 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144979943 | CGTTCCACCTTATCT[-/A]AAAAAAAATTCAAAT | 10393 |
rs561362392 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145051149 | ATCATTAGTTAGAGG[C/T]CTAATTGAATCAAGC | 10393 |
rs561383450 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145012920 | GGTGATGGATTTCCC[C/T]TTTGGTGCTGTTCTC | 10393 |
rs561406601 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144991439 | TTGGAGTGCAGTGTC[A/G]CGATCTCGGCTCACT | 10393 |
rs561408470 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144998688 | CTAAAATTGACACAA[A/T]AACATCACAATTAAA | 10393 |
rs561411387 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145012196 | TATATATATATATAT[A/G]CACACACACATATAT | 10393 |
rs561419185 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145018272 | GTACCTCACATCTCA[A/G]TACTAACATTGAATG | 10393 |
rs561471794 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144998296 | CTTATCAGCACCACA[A/T]TGCACTTATTCCAAA | 10393 |
rs561481136 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144983529 | TTAAAATATACAGGA[C/T]TAAAGTCAGGCAAGT | 10393 |
rs561488257 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145075933 | TGGACCTGCACAATA[C/T]AGGGCTGTCTTACCC | 10393 |
rs561536777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144974517 | AAAATAAATAAAAGA[C/T]ACGAGAAAAGAAAAA | 10393 |
rs561544165 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054414 | ATACAAAAAATTAGC[C/T]GGGCATGGTGGCAGG | 10393 |
rs561555965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145009892 | GAAAAGGCAACCTAC[A/G]AAATGGGAGAAAATT | 10393 |
rs561606428 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145040894 | ATTCAACTGGGTGAA[A/C]GTCTCATAATACTTA | 10393 |
rs561609744 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145085950 | CTCACTGCAACCTCC[A/G]CCTCCTGGGTTCAAG | 10393 |
rs561673024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145071578 | AAAAACCATATGATC[C/T]GTATGAACAGATACA | 10393 |
rs561682897 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054057 | GAGATTACAGGCACT[C/G]GCCACCATTCCCAGC | 10393 |
rs561693691 | in-del | -/TG | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145044396 | AATCATTTCAAAAAA[-/TG]TGTGTTTCTCTCTAA | 10393 |
rs561745336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081966 | CCTCCTGCCTTGGCC[C/T]CCCAAAGTGCAGTGA | 10393 |
rs561810381 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145038688 | TTAGCTGGGTGTGGT[A/G]GTGAATGCCTGTAAT | 10393 |
rs561815041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145023632 | CTATACTAGAGTCTA[C/T]TAAGTATGCAATAGC | 10393 |
rs561816963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145015468 | AAACTTAAGAATAAT[C/T]GGTGTTCCTGAAGAA | 10393 |
rs561821537 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145075704 | CACTCTCACCATGTA[A/T]CTCCAGAATTCTAGT | 10393 |
rs561848924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054450 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 10393 |
rs561858629 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145074829 | TTCTTTATACTAAGC[C/T]ATAACTGGTCTTTGT | 10393 |
rs561899703 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145073267 | TAAGGGGAAAATGCA[A/G]TAAAGTATTCTATAA | 10393 |
rs561904195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145022427 | GAACGGAGAACCAAA[C/T]ATCGTATATTCTCAC | 10393 |
rs561906899 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145067938 | TTTAAAAGAAAAACA[C/T]GCCCCTTTTACCTTT | 10393 |
rs561958143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145051957 | TTAACTCCTACAAAA[C/T]TGAAAAACTGTATGT | 10393 |
rs561978219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145016215 | TGATTGTATATTTAG[A/G]AAACCCCACCGTCTC | 10393 |
rs561995528 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144982202 | CGCTAAGTGCTTACA[C/G]TTGTTATCTCACTCA | 10393 |
rs562003982 | in-del | -/AT | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145018122 | AGAGTATAATAAAAA[-/AT]AAATATATATATATA | 10393 |
rs562018141 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145030649 | CCCCAGTGCCAGAAT[G/T]CATAATTGGCATAGA | 10393 |
rs562032986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145045099 | TCCAAAAGCTAATGT[A/G]AAAATAAATTTGCAT | 10393 |
rs562039725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144997315 | GTTGATATGAAGGAA[A/G]AATATTAAGGGCAGC | 10393 |
rs562042642 | in-del | -/TTCT | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145075061 | AGCACATCCTAGACC[-/TTCT]TTATCAGTGTTAGCA | 10393 |
rs562044502 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144997588 | GAAGGAAGCACTAAA[C/T]ATGGAAAGGAACAAC | 10393 |
rs562090941 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144989332 | GTAATTCTCTATCTC[A/C]AACTTTTTCATTATT | 10393 |
rs562099261 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | ABCE1, ANAPC10 | GRCh38.p7 | 4:145097944 | AGTAAGCCGTGTCGG[C/T]ACCAGACTCTGTTGG | 10393 |
rs562102260 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144994679 | GTCAGACACAAATTT[A/G]AAAATAACTCTTCCA | 10393 |
rs562113375 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145036846 | CTCAATTAATGCTGA[C/G]GTACATATTCACAGT | 10393 |
rs562130449 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145008778 | CTTTGAAAACTGGCA[C/G]GAGACAGGGATGCCC | 10393 |
rs562169509 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145014791 | TGCCCAGTACCAGTC[C/T]GGAGGCTGGTAGACT | 10393 |
rs562202538 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144999907 | AACACCACATATCTA[C/T]AACCATCTCATCTTT | 10393 |
rs562203892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144996725 | CGGAACAAAGCTGGA[C/T]GGAGAATGACTTTGA | 10393 |
rs562207439 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145071745 | ACCATGTAAAAAAGA[A/T]GATGATTAATATACC | 10393 |
rs562227218 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144981803 | TCATAAATGGAATAG[A/C]AGTTACTTTATTTTA | 10393 |
rs562254057 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145002468 | TTTAGACTAGAAAAT[C/T]GGAAAAGTTTCTATA | 10393 |
rs562329462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144996853 | GAAAAAAGATTAGAC[A/G]AATGGCTAACTAGAA | 10393 |
rs562357510 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145048145 | TAAAGCTAAAACGGA[C/T]GCCCCTCCACTATCT | 10393 |
rs562391798 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145003070 | CTTCTTTGTGTCCAT[A/G]TGTATTCAATGTTTA | 10393 |
rs562422991 | in-del | -/T | | | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145096723 | TATTTACTTAATTCC[-/T]TTTTTTTTTAGAGAC | 10393 |
rs562431732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145040904 | GTGAAAGTCTCATAA[C/T]ACTTATTGTTTTATA | 10393 |
rs562467292 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144994717 | TGCTAGAACTCTTCC[A/G]TAAGTACTGCTAGAT | 10393 |
rs562494957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145017505 | GGAGAAATAGGAACA[C/T]TTTTCCACTGTTGGT | 10393 |
rs562495340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145087419 | TGGAGTACAGTGGTA[C/T]GATCACAGCTCACTG | 10393 |
rs562541555 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081806 | AAACAACTATACATG[C/T]AAAACATAAAATTAA | 10393 |
rs562584426 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145027587 | TGAATTTTCAGAATA[A/T]CAAGGATAAGGAGAT | 10393 |
rs562589310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145006080 | ACTATTATTGTGGGG[C/T]TTTCTAAGTCTCTTT | 10393 |
rs562657948 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145011440 | GCCCCTGCTGAGAAT[C/G]CTTATAGGTAAAACA | 10393 |
rs562680509 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145088957 | AAAATGCCAAATCAA[C/G]TAACTTAGAGCCTTT | 10393 |
rs562688793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145006604 | ATGAATCATATCAAA[C/T]TGTCATTTTTGTAGG | 10393 |
rs562736793 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145072007 | AAAGGACAAAAAAAA[-/C]CACAAAAAAAACAAA | 10393 |
rs562739324 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054480 | GGAGAATGGAGTGAA[C/T]CCAGGAGGCAGAGCT | 10393 |
rs562741652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144991997 | TAAGTTGAAGCCAAT[A/G]CTTATTTACCATTCT | 10393 |
rs562752263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145068436 | GACGATAGCTTTACA[C/T]TTAAAGCTAAATGTA | 10393 |
rs562784745 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145094090 | ACTGGGGACCATTTT[A/G]AAAGCTAGCTACTAC | 10393 |
rs562793708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054911 | TAGTTGTACTCTTCT[A/G]CTTTATAACTTCAGT | 10393 |
rs562822966 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145025120 | TTATAGAATTCAAGA[C/G]TTAGGGTCTTACTGT | 10393 |
rs562857754 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145070208 | TTTTGTAAATAAAAT[G/T]TTATTGAAACTAAGT | 10393 |
rs562865092 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145018221 | AAACCAAAAAATCAA[G/T]GTATACAGGCAACAA | 10393 |
rs562879204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145061801 | GTGACTAAAAGAAGG[A/G]CTGTCAATTGGTCCA | 10393 |
rs562909365 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145031914 | ACTGGGCGCTTTCTG[A/T]CCCATCTAACTATAA | 10393 |
rs562966730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145092615 | AAGGTGAATTCACAC[C/T]GACTCTCAGACTCTT | 10393 |
rs562970192 | in-del | -/A | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144983506 | GAAGAGATATAGAAT[-/A]AAAAAAATTAAAATA | 10393 |
rs563000362 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144968527 | TATCTGCCAAATAAA[C/T]AGGAAACAATATAGC | 10393 |
rs563012138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144976365 | TAATCTTGGAGAGGA[C/T]AAAGGAAATAGTGGT | 10393 |
rs563042835 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145020661 | TGTTTACTGACAATA[C/T]AATCGTTTACCTCAA | 10393 |
rs563050959 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145008868 | AAAAAGAAATAAAGG[A/G]CATTCAATTACGAAA | 10393 |
rs563099453 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145086519 | AGACATGTATCAGAA[A/G]CTTTGAGAGCTCAGC | 10393 |
rs563138523 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145069369 | AACTCCAGAAATATG[C/T]GTGGGGTCCCCTTCA | 10393 |
rs563140162 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145077709 | TCCTCGGATGTAAGA[G/T]AGGCTCCACATATGC | 10393 |
rs563141925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144988252 | CCCAAAGTGCTATTA[C/T]AGCTGTGAGCCATTG | 10393 |
rs563143633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144973564 | TATATGCAACAGAAG[A/G]GATCAATAAACCCAC | 10393 |
rs563164849 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144990710 | ATCCGCCCCCATGAT[C/T]CAAATACCTCCCACC | 10393 |
rs563169346 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144984816 | ATTTTGCTTCTGTTT[C/G]CAAAATAGCAAGCTG | 10393 |
rs563177632 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145032496 | TATCCCATATGAGTG[A/C]TCGCCAACAAGTGAC | 10393 |
rs563258973 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145067053 | AATTTGCTATATACA[A/T]AGTTTCATTAAATTT | 10393 |
rs563262249 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144987734 | TCATTCACTGATTAG[A/T]GAGCTCACGACTTTC | 10393 |
rs563299168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145095805 | ATAAATTACACTTTA[C/T]CACAGGTATTTATGT | 10393 |
rs563355757 | snp | A/G | | | intron-variant, downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:145032930 | GACTACCAACCGTGG[A/G]CTCACAGAATGCCTT | 10393 |
rs563357735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145052713 | GAGACCATCCTGGGT[A/G]ACACAGTGAAAACCC | 10393 |
rs563398005 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144987486 | AACATCACACACCAG[C/G]GCCTGTTGTGGGGTG | 10393 |
rs563405702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144981229 | ATAGCATTGAATCTA[C/T]AAAATACTTTGGGCA | 10393 |
rs563435878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081883 | ATTAATTTTTTTTTA[C/T]TTATTTTTTGTAGAC | 10393 |
rs563445225 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145058427 | AAACAATATTGTGTT[C/G]CCATAGCCACCTCCA | 10393 |
rs563463996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145029230 | CAACATCCCCTCCCC[A/G]ACCCACACTGCCATC | 10393 |
rs563488151 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081342 | TATGATACATTAAGG[C/T]ATTGTATTGGGCCAT | 10393 |
rs563517852 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145072262 | TCCAGAGCAGAGAAA[C/G]AGCTTGTTCTAATTT | 10393 |
rs563525866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ANAPC10 | GRCh38.p7 | 4:145064195 | AATATATCACACTGG[C/T]ATTTGGGGTGAAATG | 10393 |
rs563540432 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145074524 | GATACTTAATTGCTA[G/T]TGTGTCTATTCTTGA | 10393 |
rs563567752 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144972632 | AACTTTCTTATTAAC[C/T]GATAGACCAAGCAGA | 10393 |
rs563577333 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145073534 | ACATCCATACATATA[C/T]TGGTATTAAAGTATA | 10393 |
rs563579619 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145020640 | AAGAGGAAGTCAAAC[C/T]GTCACTGTTTACTGA | 10393 |
rs563631021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144980531 | ATAGATAGATAGATC[A/G]ATAGATAGATAGATA | 10393 |
rs563658788 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145051773 | TATATATATGGATTG[A/G]CCAGATTCACCATAA | 10393 |
rs563683532 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145001689 | CACTCAATATTCTTT[C/T]GTTGATATCAGCTGC | 10393 |
rs563724366 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145051164 | CCTAATTGAATCAAG[C/T]CAATTAATTAGGTTA | 10393 |
rs563762243 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145043871 | AAAACCAAACCCTTA[C/T]ACTAGAGTTCACCAA | 10393 |
rs563768370 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145035262 | ATCTCTCCCAAAGCT[C/G]TGTGCTTGGTCAAAG | 10393 |
rs563780037 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145014592 | ATACTACCACAGCTG[A/T]TGCTCTCTGGAAAGC | 10393 |
rs563797157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144984117 | GAAAATTTCTGAAGA[A/G]TAGGTTATTTGCATA | 10393 |
rs563804612 | in-del | -/TA | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145045955 | TGTTCTAGCAAAAAT[-/TA]TATTATGATTATCTA | 10393 |
rs563807537 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145042802 | GACAACCCAGCAGGC[A/G]GTTTTCTGTTTTTTT | 10393 |
rs563826532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145019817 | GAATATGTTTATGGG[C/T]ATAAACTTGAAAACC | 10393 |
rs563826644 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145013000 | CACCTCCCTCTTCCC[G/T]CTCTTCCTCCAACTC | 10393 |
rs563836231 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145007431 | GAACAGAAATCACAA[C/T]AAACTGTCTCTCAGA | 10393 |
rs563856015 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145093297 | CTGAAGGTAACCATA[A/G]CAATAACAAAACTCA | 10393 |
rs563865117 | snp | A/G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145079406 | AAGTTGTGAAAAAAA[A/G/T]GGAATACTTATACAC | 10393 |
rs563871518 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145050083 | ATTTTCAATTTGCTT[C/T]GCCTAGATCCATCAG | 10393 |
rs563875346 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145056552 | TATAAGAACCCCCTC[C/T]TGGGGTCTGGATTGG | 10393 |
rs563889624 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145036503 | TTGTTGCAAGTGCTA[A/C]TGCAAATATTTCACA | 10393 |
rs563897900 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145037774 | CAATATGGCAAAACC[C/G]TGTCTCTACAAAAAA | 10393 |
rs563909241 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144998826 | AATCAATGAATACAG[A/G/T]AGCTGGTTTTTTGAA | 10393 |
rs563913080 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145018916 | AATCCTAAACATATA[C/T]GCACATAACACTGGA | 10393 |
rs563916422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144970639 | AAACTAAGATCTCTG[C/T]ATAAAACTCGAAGAG | 10393 |
rs563966544 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145099738 | AGACTATTTCATGTG[A/T]TACTAAACATCATTA | 10393 |
rs563985487 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081543 | CTATAAGACTTCAGA[C/G]TTTAAAAAGTTAAGT | 10393 |
rs563986770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145013603 | GTAGATTGCAGCTCT[A/G]ACTCGGATGAACAGA | 10393 |
rs564086467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145060932 | ACAGTATAAATCTCA[C/T]ACAAAGATGTATAAT | 10393 |
rs564114579 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144997243 | ATACAGAGAACACCA[A/C]AAAGATACTCCTCGA | 10393 |
rs564149632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145038299 | AGGTGGATTGCCTGA[A/G]GTCAGGAGTTCAAGA | 10393 |
rs564164381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145032087 | TCCCCCAGCCTGCAC[C/T]GATGGCCTCATGGGA | 10393 |
rs564186047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054506 | GAGCTTGCAGTGAGC[A/G]AGATCGCGCCACTGC | 10393 |
rs564227557 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144994796 | GGCTGTAAGTATTCC[A/G]TGAAGGTGAATATGA | 10393 |
rs564231092 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145010013 | AAAAAGTGGGTGAAG[G/T]ATATGAACAGACACT | 10393 |
rs564244503 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145047936 | AAAGTACCTTGCTTA[A/T]CATATTTAGCCAGAG | 10393 |
rs564246745 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145069735 | ATTACTAAGATGTAA[C/T]TTGCCTTTTTCAGAA | 10393 |
rs564253034 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144982134 | CAGGCGTGAGCCACC[A/G]CACCCGGCCAGCAGC | 10393 |
rs564262804 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145016533 | TCAATATTGTGAAAA[A/T]GGCCATATTGCCCAA | 10393 |
rs564335459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144968137 | ATTTTTGCTAATCCA[A/G]TGAAGGACCCCTAAT | 10393 |
rs564360033 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145003368 | TCTTTATGGTAGAAC[A/G]ATTTATATTCCCTTG | 10393 |
rs564364555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145045230 | TGTGACCAGGTAATG[C/T]GAATAAGTACTTTGC | 10393 |
rs564384681 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145009354 | GTTCATATGGAACCA[A/C]AAAAGAGCCCACATT | 10393 |
rs564390806 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145010672 | ACCCTGGGGCCTGTC[A/G]TGGGGTGGGGAAAGA | 10393 |
rs564397626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144975372 | AGCACACAAAAAACA[C/T]AAAACATTATAAAAA | 10393 |
rs564407232 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145023697 | CTGCTAAAAAGTGCT[A/G]ACAATCATCTGGGCC | 10393 |
rs564412169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145004604 | ATTGAAATGATCACA[C/T]GCTTTTTGTTTTCAG | 10393 |
rs564437897 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145037682 | CGAGGCACAATGGCT[A/C]ACACCTATAATCCCA | 10393 |
rs564450575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144967502 | GGCATGGATGTTCTT[C/T]GTAAACAATAAAATA | 10393 |
rs564470650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144982377 | TTTGTTTTCAAGTAG[A/G]CTATGTGTTTAGCCC | 10393 |
rs564475170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145045668 | ATATATGAATGTATA[C/T]GTGATCTTCTACACA | 10393 |
rs564475426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145022601 | CCCAAATCACCACTA[A/G]AGAACTTACACATGT | 10393 |
rs564483003 | in-del | -/AT | 0.00676609 | 0.0577691 | downstream-variant-500B, intron-variant | ANAPC10 | GRCh38.p7 | 4:144993738 | ATAAAAGTAGAAAAC[-/AT]ATTGATTTTCTCAAC | 10393 |
rs564506611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145003949 | ATGGCCTTTTAACAA[C/T]ATTGAGTCTTCCTAT | 10393 |
rs564514310 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145030818 | CCCTGGAGGGGTTGC[A/C]AAGATTAGTGCCACC | 10393 |
rs564535810 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145082725 | ACATAAATGAAGTTG[C/T]ACAATCCTGTGTTTT | 10393 |
rs564545172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145035159 | AATCCGGCTGCGACA[C/T]CTGTCACCCCACTAA | 10393 |
rs564548917 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145053047 | GCAAACCCTAAGAAA[A/C]CTTATCCTGACTGAT | 10393 |
rs564551140 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145027748 | TTATTTCCAAACTAG[A/T]ATTCCATACCTAGCC | 10393 |
rs564591564 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145050385 | TCCATTTATAGCACA[C/T]GGGCAGAATAAATTT | 10393 |
rs564607708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144982988 | ACACGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 10393 |
rs564608253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145065247 | ATTGATTTTAAAATA[C/T]ACATATCCTAGGGAA | 10393 |
rs564641979 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144974696 | AATAGCATCAAAATT[A/C]TCAAATTCCTAGGAA | 10393 |
rs564644323 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144997451 | CATTCTTAAAGAAAA[C/G]AATTTTCAAGCCAGA | 10393 |
rs564686338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144996922 | CTGAAAACCATGGCA[C/T]GAGAACTATGTGACG | 10393 |
rs564699000 | in-del | -/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145022655 | ATAACCTATGGAAAA[-/T]TTTTTTTTAATTAAA | 10393 |
rs564709537 | snp | C/T | 0.000557258 | 0.0166829 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | ABCE1, ANAPC10 | GRCh38.p7 | 4:145097492 | TGCAATAGTTCTGCA[C/T]ACCGTTTCCTTGACA | 10393 |
rs564729476 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145024421 | AATGCCTTATGAAAT[A/G]TATATCTTAAATAAT | 10393 |
rs564836451 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145034551 | TATATATATGTGTGT[A/G]TGTGTGTGTGTGTGT | 10393 |
rs564870884 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144987338 | TGATGAGTTCATGTC[C/G]TTTGTAGGGACATGG | 10393 |
rs564903677 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145088278 | CTAGATGAGTTAGTC[C/T]AGTTCCCTTAGAATA | 10393 |
rs564910220 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | ANAPC10 | GRCh38.p7 | 4:144993830 | ATAAGACACTAGATA[G/T]TATATGTGATCATTA | 10393 |
rs564955807 | snp | A/C | | | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145096201 | AATTTAATGGAACTC[A/C]TATACCCTGACATTA | 10393 |
rs564965337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144971718 | ACACATAAGCAGTCA[A/G]TGAGTTCTGTCTATT | 10393 |
rs564976250 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145000254 | AGAAACTACCATTGG[A/T]GTGAAAAGGCAAAAA | 10393 |
rs564977184 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145019911 | ATACCCTAAACAGAC[C/G]AATAACAAGCAACAA | 10393 |
rs564999537 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145077303 | GAGACCAAAACTACA[A/C]CTCATTGGGGTCCCT | 10393 |
rs565003109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145079938 | GGCCAACATGGTGAA[A/G]CCTTGTCTCTACTAA | 10393 |
rs565042963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145006609 | TCATATCAAATTGTC[A/G]TTTTTGTAGGTCAAA | 10393 |
rs565070336 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145094983 | CCAATTGAGAGAAAC[A/G]GCCAAAAAAAATAAA | 10393 |
rs565095667 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145034421 | TCAGACTGCAAGTTC[-/T]TTAGTTTTGGGACTC | 10393 |
rs565108232 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145050229 | ATCTCCATCAAAGCT[C/G]TTGGGTGACTATGTC | 10393 |
rs565109828 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145094108 | AGCTAGCTACTACTA[A/C]TCTGGTGAATGGATA | 10393 |
rs565112144 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145061916 | AGTTTGAGATCAGCC[C/T]GGCCAACATGGCAAA | 10393 |
rs565130554 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144986887 | TTTATGCAGCCAAAA[A/G]ACACATGAAAAAAAT | 10393 |
rs565134053 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144984841 | AAGCTGGTTCTACTC[A/G]GCAGAAAAGACAAGA | 10393 |
rs565202088 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144994830 | AATTAATTATACTCC[C/T]CATATTAGATTGGTT | 10393 |
rs565211649 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144978027 | GAAGGTAATATTTTG[A/G]CCTTCATCTTCACTA | 10393 |
rs565216395 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145041592 | GACTTGGTGCTTTCA[A/C]TTCCCCTTCTAGAAG | 10393 |
rs565218713 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145092721 | TACAGAGGAGGGGAC[C/T]GACCACCAGTGAAGG | 10393 |
rs565302778 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145003307 | GGGCTTTTAGGTTGA[G/T]TCCATGTCTTTACTA | 10393 |
rs565331090 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145077870 | CATTGAAGGATCATA[A/T]TTCAAAATAATAAGG | 10393 |
rs565364357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145002794 | ACATACATATGTACA[C/T]AGTAAAAATTTTTTA | 10393 |
rs565371706 | in-del | -/AA | 0.00358779 | 0.0422022 | intron-variant, downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:145063144 | TTCTTGAAGATTGCT[-/AA]GAGAGTGGATTTTGA | 10393 |
rs565450064 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144987368 | GATGAAGCTGGAAAC[C/G]ATTATTCTCAGTAAA | 10393 |
rs565475147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144977286 | CTCCATGCTCCAACC[A/G]CAGATAATTTATATA | 10393 |
rs565488104 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145008268 | AGGTACAAAGAGGAG[C/G]TGGTACCATTCCTTC | 10393 |
rs565527104 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144972844 | GACCACAGAGCAATT[A/T]TTCTGTAAGTCAATG | 10393 |
rs565539236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145070938 | TCAGGTCCCCAGAAC[A/G]GTGAAATACACAGAG | 10393 |
rs565548116 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145061873 | AGCACTTTGGGAGGC[A/C]GAGGTGGATAGATCA | 10393 |
rs565562672 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145018110 | TACCCTAGAACTTAG[A/G]GTATAATAAAAAAAA | 10393 |
rs565627028 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145008595 | AAAAACCACATGATT[G/T]TCTCAATAGATGCAG | 10393 |
rs565630204 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145056597 | TAACATCTTTCTGGC[A/G]ACCACTGAAGGGACT | 10393 |
rs565639815 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144969914 | TGGGTATATACTACC[A/G]GCTTAAGAAATGAAA | 10393 |
rs565660626 | in-del | -/T | 0.0337553 | 0.125452 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145036522 | AAATATTTCACACTA[-/T]TTTTTTTAAGAGATT | 10393 |
rs565666207 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145045270 | CCTACTTAATTCTTT[C/T]TGGAATCCAATAAGA | 10393 |
rs565713117 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144979429 | TGTCCCTGCAAAGGA[C/T]ATGATCTTGTTCCTT | 10393 |
rs565716879 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145066364 | AAGGAGACAGGAGAG[C/G]AAGCAAAGAAGGACA | 10393 |
rs565753877 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144972343 | ATTCAAACATTAATC[A/T]AAAGAAACTAGTATA | 10393 |
rs565768625 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145088623 | CAACAGTTCTTAATC[C/T]TAGTCCAAATCAACA | 10393 |
rs565794516 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145036304 | TGATTAGATCACAGC[C/T]TTAAATATAGATACG | 10393 |
rs565863663 | in-del | -/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145028912 | AGAAGCAGGTATTAA[-/C]CCCTCAAATCTGCTA | 10393 |
rs565877894 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145013945 | GGGAGCTTGCTGGGT[A/C]CCCAGGCAGGCCATT | 10393 |
rs565983005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144995848 | CATGTTTACTGAACT[C/T]GTACAATTTATACAA | 10393 |
rs566011629 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145073816 | AGAAATCATTTTAAT[A/G]TAATTAAAAATGTTG | 10393 |
rs566021960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145057903 | TTAATTTATTTCAAA[C/T]ATAGGGAACCCAACT | 10393 |
rs566051629 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145087890 | TGTCTAAACTAAAAA[C/T]AAAAAAAATTAGCTG | 10393 |
rs566101869 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145001708 | GATATCAGCTGCTAT[A/G]GTATGAAACCTACAG | 10393 |
rs566110600 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144976155 | CTCCAATTACAAACA[A/T]GTAGAAGGGTAAATA | 10393 |
rs566131788 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145065533 | ACAGTAACACAATCA[A/C]TCAAAAATTGATGTC | 10393 |
rs566164476 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145020273 | AGGGATGCAGGGATG[A/G]TTTAACATCCACAAG | 10393 |
rs566169908 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145000547 | AAAAAGTCAGGAAAC[A/C]ACAGGTGCTGGAGAG | 10393 |
rs566172651 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145072903 | TTACGTATCTGTTTT[G/T]TTTTTTTTTTAGGAG | 10393 |
rs566186060 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144968141 | TTGCTAATCCAATGA[A/C]GGACCCCTAATTGTC | 10393 |
rs566247573 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145050522 | AAGCTTTCAAGCCAG[G/T]CATTGACTTCTCCTC | 10393 |
rs566305278 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145007522 | CTCAGGATTAAGAAA[C/T]TCACTCAAAACCGCT | 10393 |
rs566309285 | in-del | -/AT | 0.00318978 | 0.0398085 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145012206 | TATATACACACACAC[-/AT]ATATATACATATATA | 10393 |
rs566409422 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145061383 | CAGATACCTAGAAAT[A/T]TCATATGAATATGTA | 10393 |
rs566434094 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145028148 | TACAAAGTATTAATC[C/T]TGGGTGTGCCTGTGT | 10393 |
rs566474840 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145024253 | GTCATCAATGCAGAC[G/T]GGAATCAACTTCTTC | 10393 |
rs566496229 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145024419 | CTAATGCCTTATGAA[A/G]TGTATATCTTAAATA | 10393 |
rs566509105 | in-del | -/G | 0.00279162 | 0.0372561 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145077492 | ATTGCAAAAAACTGA[-/G]AGGAAGAATTCCTCC | 10393 |
rs566535190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145070287 | GGCAAAGTTGAGCAA[C/T]TGCAGCAGGACATAT | 10393 |
rs566569449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145046634 | ATAATGCCACTGATG[C/T]TGTAGTTTCAAAGAA | 10393 |
rs566607110 | snp | C/T | | | intron-variant, downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:145063098 | AGATCCAGTATATAA[C/T]AGTGACTACATTAAT | 10393 |
rs566657430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144991622 | ACCTTGTGATCCACC[C/T]GCCTCGGCATCCCAA | 10393 |
rs566683559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145039101 | AGATACTTCTGATGA[C/T]GAGACATCACTTTCT | 10393 |
rs566687167 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145059906 | AAAAGAAAAGAACAA[C/T]ATTAAATCAAAACAT | 10393 |
rs566687404 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145022091 | GCCACTATGGAAAAC[A/T]GTATGGAGATTCCTT | 10393 |
rs566699609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144997900 | GATCTACCAAGCAAA[C/T]GGAAAACAAAAAAAA | 10393 |
rs566699892 | in-del | -/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144995773 | ACCATGGTCTACTTA[-/T]TAGTTGCTAAGCACT | 10393 |
rs566703930 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145009597 | TATTTAACAAATGGT[A/G]CTGGGAAAACTGGCT | 10393 |
rs566763577 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145015916 | CTGCCAAGCCACCAT[G/T]ACAAGAACTGCTGAA | 10393 |
rs566781944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145092731 | GGGACTGACCACCAG[C/T]GAAGGAAAGCAAAAC | 10393 |
rs566790765 | snp | C/G | 0.0116393 | 0.0753936 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | ABCE1, ANAPC10 | GRCh38.p7 | 4:145097446 | GCAGTTACTGCTACT[C/G]AACATTGTTATATAT | 10393 |
rs566821743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145022854 | TTTTAGGATGATTAA[C/T]ATATGAGTCATTCTT | 10393 |
rs566917197 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145083992 | TTTTTTCTTTTTGAG[A/G]CAGGGTCTTGCTCTG | 10393 |
rs566942825 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145010150 | ACCAGTTAGAATGGC[A/G]ATCATTAAAAAGTCA | 10393 |
rs566951484 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145093560 | CTATAACTATGAGTA[A/C]GATGTTAAAAAAAAA | 10393 |
rs566974183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145051368 | ATCATTAAGAATCAC[C/T]GATCACAGATCACCA | 10393 |
rs567025071 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145068176 | GAAATAAATTTCCAC[C/G]TTGTAGAAAACACCA | 10393 |
rs567050761 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144982033 | TTTGTTTTCAGTAGA[A/G]ACTGGGTTTCACCAT | 10393 |
rs567052237 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145075179 | TTTTTTAGCAACCAC[A/T]TCACACTGTTAATTG | 10393 |
rs567065034 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145082910 | AAGACACAGTGAAAA[C/G]TCACTATCTACCATC | 10393 |
rs567089922 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145002802 | ATGTACATAGTAAAA[A/G]TTTTTTAAACTTACA | 10393 |
rs567107118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145082236 | CTCATTGCAACCTCC[A/G]CCTCCCGGATTCAAG | 10393 |
rs567124871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145026792 | AAACAAAGCATCATT[A/G]ATATCCTCAGTGATA | 10393 |
rs567129173 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145015140 | GTTATTAAGCTATTT[C/T]GAGAGGCACCAGAGA | 10393 |
rs567143154 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145055405 | TACACTAAAAATACA[A/G]AAGTTAGCCGGGCAT | 10393 |
rs567163878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145067671 | ATAAAGTTGATATTT[C/T]GGCCGCCTCCTGCTA | 10393 |
rs567188188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144974143 | CCACAAAAGGATACT[A/G]CCCATAACAAAGCTG | 10393 |
rs567203126 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145042242 | CATAATCAAAAATTA[A/C]AAATTATTCTAAGCA | 10393 |
rs567219634 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995265 | ATATTTTTAAACATA[C/T]ACAAAATTAGATATA | 10393 |
rs567285794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145000419 | CTTCTCAAAAGAAGA[C/T]ATTTATACAGCCAAC | 10393 |
rs567292865 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145013231 | CCAAAATTTGATAAG[A/G]ATAGTATAAGAAAGA | 10393 |
rs567379513 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145001285 | AAGAAGAAAAGAAAA[G/T]AAAAGAAATTAATTC | 10393 |
rs567413829 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145015401 | ACAAAGAAAAAAGAA[C/T]AAGAAAATATGAACA | 10393 |
rs567466771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144979124 | CAACTATTATTTTCA[A/G]TTCCAGGGTACCTGT | 10393 |
rs567468217 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145080079 | AGATCACGCCACTGC[A/G]CTCCAGCCTGGGCAA | 10393 |
rs567515853 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145064467 | TCCAATATTTTTCTC[C/T]TATATATTAACATTT | 10393 |
rs567546126 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145057617 | TAGGTTCAGATCCAT[A/G]TACCATACCCTACTA | 10393 |
rs567564146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145040477 | AAGACCTATAAAAAC[A/G]TAACAAATTTTAATG | 10393 |
rs567574127 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145041947 | ACCCAGTTTCAGATA[C/T]GTATATTTATTCCTT | 10393 |
rs567577293 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145072016 | AAAAAAACACAAAAA[A/G]AACAAAAAAAAACTA | 10393 |
rs567583267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144970241 | AACTGTGAAATGTAA[C/T]GTTCTTTAAAAAAAA | 10393 |
rs567592413 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145093775 | CAGGCCAATGAAAAA[C/T]ACCAGAATTGAAACA | 10393 |
rs567623002 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145046057 | AATGCCCTGTTACAG[A/G]AGCGCACCCTAAGCA | 10393 |
rs567631634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145006262 | GTTTTGTCTGAAATT[A/G]TAGCAACCCAGACTT | 10393 |
rs567682276 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145031991 | ATACGTGATCAGGCT[C/T]GAGCAGGTCCGGAAG | 10393 |
rs567683807 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145079651 | ATCAACAGTGGACTG[A/G]ATAAAGAAAATATTG | 10393 |
rs567685127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:145032867 | TTCACTGGAATAGAC[A/G]CTTACCAGATATGGT | 10393 |
rs567705140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144997767 | GGCTAAATGCTCCAA[C/T]TGAAAGACACAGACT | 10393 |
rs567728413 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144981525 | GACTTTGCTGACATT[A/G]CTTATCAGCTTAAGA | 10393 |
rs567737674 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145033490 | AGTGTTGGCTGGGAT[G/T]ACTGACCTGGACTAT | 10393 |
rs567760043 | snp | C/G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant, synonymous-codon, missense | ABCE1, ANAPC10 | GRCh38.p7 | 4:145098183 | AGCAGCTGGCTTCGC[C/G/T]AACGGCGTTGAACAA | 10393 |
rs567765119 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144997164 | GGTGGAAATCACTCT[G/T]CAGGATATTGCCCAG | 10393 |
rs567770821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145086951 | ACTCTCCATGGGAGG[A/G]ATACGATTCTGCACT | 10393 |
rs567794440 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145077161 | CCGAGATCGTGCCAC[G/T]GCACTCCAGCCTGGG | 10393 |
rs567826140 | snp | C/G | 0.00199601 | 0.0315281 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145062160 | AGAAGACTAAGAGCT[C/G]ATTTATTTATTAATC | 10393 |
rs567887567 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145017684 | ACGTATGTTTATTGC[A/G]GCACTACTCACAATA | 10393 |
rs567915242 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145091409 | GTCTAGTCATACTAA[C/T]AGATCAAACAGTGAA | 10393 |
rs567930097 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144977921 | TAGTCAATGCAACCA[A/G]CTATAACGTGATTCT | 10393 |
rs567999573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145082299 | GGATTACAGGCACAC[A/G]CCACCACGCCAGACT | 10393 |
rs567999835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145055212 | CTGAGAGATGAATAG[A/G]TAAGCAAAATGAAAT | 10393 |
rs568021030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144982487 | GAGGTGGTTGTGTGA[C/T]CCAGTTCTTACCAAT | 10393 |
rs568025711 | in-del | -/TTCT | 0.0104583 | 0.0715525 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145065209 | TCTGCTGCTGATTCT[-/TTCT]TTCTTTCTTTCTTTC | 10393 |
rs568044144 | in-del | -/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144968640 | TTTATTTGATTAGGT[-/C]CAAAGGTGAGGATCC | 10393 |
rs568054661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145030989 | GCTGCTGTACCAGAT[A/G]TGGTTTCATTGCTTG | 10393 |
rs568063938 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145037099 | CAGGGAAACACTAAG[G/T]ACCCAACAGAAACTC | 10393 |
rs568089491 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145037930 | CAAGCATGGGTGACA[C/G]AGCAAAACCCTGTCT | 10393 |
rs568094599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145004176 | GTATGCTACTGATTT[C/T]TGTACACTGGTTTTG | 10393 |
rs568102072 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145073842 | TGTTGTATAATGTTA[C/T]TACCATGATAAAAAT | 10393 |
rs568105783 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144998864 | ACAAAATTGATAGAC[C/T]GCTAGCAACACTAAT | 10393 |
rs568110381 | snp | C/T | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | ABCE1, ANAPC10 | GRCh38.p7 | 4:145098003 | ACTAAGGCTCCACTC[C/T]TGACCCACCGGCCTT | 10393 |
rs568137767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145058827 | TTGGAAATAAGTGAT[A/G]CATACAATAATAAAT | 10393 |
rs568142423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081452 | AGGAACTATGCAACA[C/T]ACCATAAGAAAATTC | 10393 |
rs568167502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144982121 | AGTGCTGGGATTACA[A/G]GCGTGAGCCACCGCA | 10393 |
rs568170898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144973826 | CTTACACAAGAAGAT[A/G]TACAAAAATCTAAAT | 10393 |
rs568177645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145030483 | GGCTCTGAGCTGACA[C/T]TGATTCCAGGGGACC | 10393 |
rs568189866 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145037512 | ATATCTAAGAAAACA[C/G]GCTATTTGATATCAT | 10393 |
rs568217470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145002872 | AATATCTTTTTCTAA[C/T]TTTTATTTTAGGTTC | 10393 |
rs568244644 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144971858 | ATTGCAAGCTTACTA[C/T]GTATCAGGTACTATT | 10393 |
rs568247289 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145052173 | AGGCATAAGAAATAA[C/G]TTCAAGTCATCTACT | 10393 |
rs568279195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145008636 | TGACAAAATTCAACA[C/T]AGCCCATCATGCTAA | 10393 |
rs568312542 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:145053315 | TAGCTAACATATTAT[C/G]TGAACAATTTCCCTA | 10393 |
rs568314682 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145045367 | AGATTCACACAGCTA[C/G]TAAGTAGCAAAACTA | 10393 |
rs568334391 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144985984 | TTTGTCAAAGGCCTT[C/T]TCTGCATCTATTGAG | 10393 |
rs568358924 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144980684 | TGTCAATTTTTGCTT[C/T]TGTTGTGATTGCTTT | 10393 |
rs568385518 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144976714 | TATGGAAAATGATTA[G/T]TATTATTTAAAATGG | 10393 |
rs568403292 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145052823 | AACCTGGGAGGCGAA[C/G]GTTGCAGTGAGCCGA | 10393 |
rs568436895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145067340 | AGGCATCGTGCTATA[C/T]TCGTAGCATAAGATA | 10393 |
rs568446826 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145067334 | TACGCCAGGCATCGT[C/G]CTATATTCGTAGCAT | 10393 |
rs568468678 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145020379 | CATTTGACAAAATCC[A/G]GCATCCCTTTATGAT | 10393 |
rs568502438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145070423 | ACATGAAAAAAATGC[C/T]TGATAGCACAAAACA | 10393 |
rs568518356 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145033474 | CTAAAAAGGGAGTTA[A/C]AGTGTTGGCTGGGAT | 10393 |
rs568539321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145078112 | CAATATAATTCTACA[C/T]CTAGAAAACCCCATA | 10393 |
rs568544038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145021909 | TGGCCAACAAACATA[C/T]GAAAAAATGCTCAGC | 10393 |
rs568546008 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145014563 | GGCCCCCCGCCCACC[A/G]TCTGATCCTCCCTAT | 10393 |
rs568553634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145066546 | TTTTGCTCAGAATAA[C/T]TACGTTTCTAAATTG | 10393 |
rs568581447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144969591 | AGCATACTCGCTGGA[C/T]AGACTGGATCTTGTT | 10393 |
rs568585523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:145063154 | TTGCTAAGAGAGTGG[A/G]TTTTGAGAGTTCTCA | 10393 |
rs568613468 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145071120 | CTGTACATTTAAAAA[C/T]GGCTGGCCAGGAACA | 10393 |
rs568619412 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144988636 | TGTGCCTATTTAAAG[C/T]GTATAATTTGATGAG | 10393 |
rs568653820 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145036013 | TTATAATCTGTCAGA[G/T]AATTTAGACATATGT | 10393 |
rs568674405 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145089698 | AAAGATTTTTGCAAA[G/T]CCATGTGCCACCTAC | 10393 |
rs568677882 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145096188 | TTTTACCAAGAAAAA[G/T]TTAATGGAACTCATA | 10393 |
rs568695938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144980056 | GGAATAAAGGCTCTC[A/G]TGCCCTTTGTTCAGA | 10393 |
rs568706592 | in-del | -/T | 0.00150414 | 0.0273826 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144998932 | AAAATGATAAAGCAA[-/T]TATCACCACTGAACC | 10393 |
rs568713437 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145062635 | AAAAAAAAGTAAATT[A/G]AGATAATTGTCTATA | 10393 |
rs568719962 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145001855 | GACTTACTTAAGAGC[A/C]GATGTAACCCGCTAG | 10393 |
rs568733295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145039688 | CAACCTCCACCTCCC[A/G]GATTCAAGCAATTCT | 10393 |
rs568758853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144987700 | CAGCAGGAAGTAAAC[C/T]TACATCTCCTCTACA | 10393 |
rs568792323 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144992505 | TTCAACCTTCATGGA[A/T]GACATTGAGGGGTTT | 10393 |
rs568792729 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144983936 | GACCTAGAATGATGT[A/G]AAAGGGGTGAAACTA | 10393 |
rs568793140 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144996425 | GCTGCTGCTGTGCTG[G/T]TCTAAGGAGGGAGAA | 10393 |
rs568827507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145077469 | CTGGTATCAACCCTA[C/T]TGAAACGATTGCAAA | 10393 |
rs568832826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145055284 | AAAAAGGAGGCCAGT[A/G]AGGTAGCTCAGGCCT | 10393 |
rs568837576 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145017782 | ACCATGGAATACTAT[G/T]CACCCATAAAAAAGG | 10393 |
rs568838742 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145025919 | TTGATGGTTTCCTTT[A/C]CCACTCTTATAGAAA | 10393 |
rs568840155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145040336 | TATTGTTAATAGAGA[C/T]GGGGTTTCTCCATGT | 10393 |
rs568852601 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145059468 | ATCTGAAGACAAAAA[C/G]AGAGCTTAAAATTCA | 10393 |
rs568869620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145062237 | AAAAGAAGAAATGTT[C/T]TTAAATTAAAAGAAA | 10393 |
rs568914593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145085108 | TAGTGAGACACTGTC[C/T]ATACAAAAAATAAAA | 10393 |
rs568954860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145011670 | TGAAGTCAGAGAAAC[A/G]TGCAGAGCTATTACT | 10393 |
rs568970059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145047467 | GAGTTCAGTGAGTCA[C/T]GATAATTCCATGCTA | 10393 |
rs568999684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145092779 | AACCCTTCTCTCCCA[C/T]AGAGGAAAGGACTTA | 10393 |
rs569002029 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145090207 | GGCTCCTCTTGTATA[C/T]TTCAAATCATCTCTA | 10393 |
rs569024264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145093564 | AACTATGAGTAAGAT[A/G]TTAAAAAAAAAAAAC | 10393 |
rs569030063 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145028355 | TCCTGCCTTCGAACA[C/T]AGGACTCCCAAGTTG | 10393 |
rs569075350 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144984364 | AAATAGCTGGCTGAA[C/G]TCTCTGCTTCAGTCT | 10393 |
rs569077581 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145016080 | AGGGATGCCCTCTCT[C/T]ACCACTCCTATTCAA | 10393 |
rs569077643 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145023899 | CTGTAGCATGCAATG[C/G]TGTTTAGTAGTATTT | 10393 |
rs569128247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145004892 | GGGAGTCCCTCTTCC[C/T]CAAAATTTCAGTAGG | 10393 |
rs569142196 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145004387 | GACTATGCTGAATAG[C/G]AGTGGTGAGTGAAGG | 10393 |
rs569144645 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054312 | ATTCCAGCACTTTGG[G/T]AGGCCGAGGAGGGCA | 10393 |
rs569164204 | in-del | -/TAACTAAGATAGA | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144967201 | AGAATCAAAGTTAGT[-/TAACTAAGATAGA]ATTTATCAACCATTA | 10393 |
rs569189397 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145075241 | AAATATCTTTCACAC[-/T]TCTGGCTTTGTCCTC | 10393 |
rs569231133 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145014652 | AAATAAAGCATTAAA[C/T]CATCAAAGCTAAGAA | 10393 |
rs569239915 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145099019 | TGTCCCAAGTAGTTT[C/G]CCAGTAGAAATCCTA | 10393 |
rs569248505 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144997528 | AATACTTTACAGACA[A/G]GCAAATGCTGAGTTC | 10393 |
rs569261175 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145090977 | AAGCAAAGATCGAGC[A/G]ATCACTTTCTCATGC | 10393 |
rs569279174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145008536 | GCTGGTTCAACATAT[A/G]CAAATCAATAAACGT | 10393 |
rs569295607 | in-del | -/TGTGTGTGTGCC | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054673 | CGTGCAGCGCATGTG[-/TGTGTGTGTGCC]TGTGTGTGTGCCTGT | 10393 |
rs569311805 | in-del | -/A | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145060578 | TCATAATTTCTAGTG[-/A]AAAAAAAAGGAAAAT | 10393 |
rs569314763 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145092278 | GGACACATTTACCTA[C/T]GTCACAAACCTGCAC | 10393 |
rs569342930 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145005422 | CCAGCTCCTAGATTC[A/C]ATGATCCTTTGTATG | 10393 |
rs569343171 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145008228 | AAGTCCAGGACCAGA[C/T]GGATTCACAGACAAA | 10393 |
rs569348597 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145100042 | CCCTTGCCCCAATTA[C/T]TGAAACTGATACAGA | 10393 |
rs569381952 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054643 | TGTGTGTGTGTGTGC[A/G]CGCGCGCGCGCGTGC | 10393 |
rs569383060 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144998508 | TGAACAACCTGCTCC[C/T]GAATGACTACTGGGT | 10393 |
rs569423573 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145060535 | CAAATCAACAATTAC[A/C]AAAAATAAGCATCTC | 10393 |
rs569439085 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145031478 | CCAAGAAAGAGGCAC[A/G]ACACCTAGTGGGTCT | 10393 |
rs569456768 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145043495 | ACAATACATTATATG[C/G]TAGCATAACCTGCCA | 10393 |
rs569461931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145076592 | GCAATGGTTCTTAAC[C/T]GGATTGAAATGACAG | 10393 |
rs569463248 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145084097 | CACCTCAGTCATCTA[C/G]GTAGCTGGAACCACA | 10393 |
rs569463785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145068249 | TACAGCATTACTGTG[C/T]CTGTATTACAGATGC | 10393 |
rs569464189 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145087918 | CTGAGTGTGGTGGTG[C/T]GCACCTATAATCTTA | 10393 |
rs569483076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145013286 | TGAGCACAAATGAAA[A/G]AAACCTAGAACAAAT | 10393 |
rs569568185 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144975951 | AGCAACTTTTATACC[C/T]GGCTGTTGAAATGTG | 10393 |
rs569571540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145068840 | GCTTGAACCCAGGAG[A/G]TGGAGGTTGCTGTGA | 10393 |
rs569581724 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144992891 | AGTCTATCAATGAAG[A/C]AAAGTTCATTGCTGT | 10393 |
rs569596378 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145013816 | AAGCACACACTCCTA[C/G]TGGGGAAACTGAAGG | 10393 |
rs569638923 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145026032 | GCGAACTGTACAACT[C/G]GACATTTAACAGTAA | 10393 |
rs569697625 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144986125 | GTGGATAAGCTTTTG[C/G]ATGTGTGGCTGGATT | 10393 |
rs569699398 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145052100 | ATGATGGTTACCTGG[A/G]GCTGGGAGTAAGGGG | 10393 |
rs569701034 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145042392 | ACAAGACATTTATGA[-/T]TATTTTCAGATGTAT | 10393 |
rs569721623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145020172 | CTGATGAACATAAAT[A/G]CTAAAATCCTTAACA | 10393 |
rs569745980 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145097101 | TGTAGTCCCAGGGGG[G/T]CTGAGACAGGAGGAT | 10393 |
rs569761026 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime, intron-variant | ANAPC10 | GRCh38.p7 | 4:144994378 | ACTATTTTTTAAATA[A/G]TATTCACTATTTAAT | 10393 |
rs569769274 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145047664 | CTCAACACAAGGCAA[C/T]TCTTCATTCACAATA | 10393 |
rs569776074 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144996106 | AGGGTTCGAGGTAGC[C/T]TGCCCAGGCAGGGAA | 10393 |
rs569781081 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145080764 | AATACAAAATTAGCC[A/G]GGCGTGGTGGCGCAT | 10393 |
rs569788019 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145052670 | TTTGCGAGGCTCAGG[C/T]GGGCACAGATCACAT | 10393 |
rs569834585 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144987083 | CATTGTGGAAGTCAG[C/T]GTGGAGATTCCTCAG | 10393 |
rs569851742 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145079931 | CCAGCCTGGCCAACA[C/T]GGTGAAACCTTGTCT | 10393 |
rs569862410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145064498 | TAACCTGTCTAATGT[A/G]ATGTCAACTGTGACT | 10393 |
rs569879620 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144972616 | TGGAAGAGTTTCATA[A/C]AACTTTCTTATTAAC | 10393 |
rs569895288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145072047 | GGTAGGGTAAGAGAA[A/G]CAAACTACACCCAAC | 10393 |
rs569968044 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145074434 | CATGGCTGATAGAAC[A/C]GCACCTTCCTCCAAA | 10393 |
rs569970043 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145033668 | ACAAATGACCCAGAC[C/T]CTTCAGGAACAAAGC | 10393 |
rs569972939 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145021039 | AAAAGCAACCTACAA[A/G]TGGAAACACATCCCA | 10393 |
rs569975074 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145065471 | ACCAGTTAGTAGAAA[C/T]ACAACCTTTGACCTA | 10393 |
rs569989781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145087772 | AGAGATGAGGCCAGG[C/T]GCAATGACTCATGCC | 10393 |
rs569994310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145094618 | AGAAAGATGACTACT[A/G]AACTAATAACATTAT | 10393 |
rs569997479 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145001110 | AATGGGTGCAGCAAA[C/G]CAACATGGTACATGT | 10393 |
rs570088588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145041822 | AGATTCATACAACAA[C/T]TATGAAATGTAAACG | 10393 |
rs570091964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144982738 | ATTTTTTAATATATG[A/G]GAAATATAGAAACTT | 10393 |
rs570130274 | snp | C/T | | | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145096285 | CTTAGGGGCTGGGCA[C/T]GGTGGCTCACACCTG | 10393 |
rs570132133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145028054 | TAAGAGAAAATGGGG[A/G]GGGAGCCAGGGGAAG | 10393 |
rs570148470 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145092138 | AATGGACACAGGGAG[A/G]GGAACATCACACACT | 10393 |
rs570185652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145006360 | TTTGCTGGGCAGATC[C/T]CTTTACCTTCAGACT | 10393 |
rs570196760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145034753 | GACAGGGAAGGAAGG[C/T]AGGCTGGGTGGATGT | 10393 |
rs570213947 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145050445 | TAGAATAGTGAGGGC[G/T]GCCTTCAACTTGAAG | 10393 |
rs570215874 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145055878 | CACTACTGAACTAAC[C/T]ACATAAAAAATGGTT | 10393 |
rs570272080 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145098267 | CACGCTCTATGTCGC[A/G]CGCGCGCACTACGTC | 10393 |
rs570304243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145012485 | TTTTAATAAAAATTC[C/T]ACAGTTGAAAACTAA | 10393 |
rs570335145 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145000491 | TGCAAATCAAAACCA[A/C]AATGAGATACCATCT | 10393 |
rs570349317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145084286 | GCATTGAATTTCAAA[C/T]TACTAGTTAGCTAGA | 10393 |
rs570365095 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145041497 | AATGGCTGTATGCCA[A/G]GTTGCCCTGTGAAGA | 10393 |
rs570406524 | in-del | -/GTAAT | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145045224 | TTACTATGTGACCAG[-/GTAAT]GTGAATAAGTACTTT | 10393 |
rs570435290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145091528 | AGCTTTTAAAAAACG[A/G]GGGGAGGGGGAAATC | 10393 |
rs570435348 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145098779 | AACTTACAGCACTCT[C/T]TAGTACCCCCACACT | 10393 |
rs570470475 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144998353 | ACTCCTCAGCAAATA[G/T]AAAAGAACAGAAATT | 10393 |
rs570481362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145038963 | CAAAGCATCAGAAAT[C/T]AAAAGTGGCATTGTA | 10393 |
rs570487439 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145031050 | ATCCAACCATTGACT[C/T]GGCAAATGCCTTTTT | 10393 |
rs570504901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145067450 | CCTCACTCACTACAC[A/G]CTTTCTCCTGAGAAA | 10393 |
rs570538419 | snp | A/G | | | intron-variant, downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:145032547 | ATAATCACATGGATA[A/G]GATGACCCGTTCTGT | 10393 |
rs570540414 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144996194 | GATATCCCCACGGCT[C/T]TACACTCCGAAACAG | 10393 |
rs570657010 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145003534 | ACAGTGTAAGGAAGG[C/G]ATCCAGTTTCAATCT | 10393 |
rs570661509 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144991942 | CAAAGTTTCAAGGAA[C/G]AGAATAACTCTTGTT | 10393 |
rs570683615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145046515 | TAGAAAATATCTAAT[A/G]TTTTGACACAACGGA | 10393 |
rs570690309 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145009562 | ACCTGACAAAAACAA[A/G]AAATGGGGAAAGGAT | 10393 |
rs570716458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145038072 | GGGCCTGGTGGTTCA[C/T]GCCTGTAATCTCAAC | 10393 |
rs570763982 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145034157 | CGATGGTTAATACTG[A/C]AAGTCAACTTGATTG | 10393 |
rs570830791 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145015073 | CTCACCAGCAGTGGA[A/T]CCAAACCAAAAAGAA | 10393 |
rs570907098 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145066416 | TCCTTGATGAGCCAT[A/G]AGCAGGAAGTAAATG | 10393 |
rs570940726 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145015663 | AAAGTTAAGACAAAG[A/G]AAAGAATCTTAAGAG | 10393 |
rs570950732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145009089 | TCCCATTCACAACTG[C/T]TACAAAGAAAATAAA | 10393 |
rs570970449 | snp | A/T | | | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145097212 | GTCCCAAAAAGCACA[A/T]AAATAAGAAAAAAAT | 10393 |
rs570980930 | snp | A/G | 6.62701e-05 | 0.00575593 | synonymous-codon, nc-transcript-variant | ANAPC10 | GRCh38.p7 | 4:145081707 | ACCATCTGATTGCCA[A/G]TAAGTTTCTAGATTG | 10393 |
rs571011725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145090410 | AACTGTCCCATTTCC[C/T]TTGCTTTTATGTCCT | 10393 |
rs571038436 | snp | A/T | | | intron-variant, utr-variant-3-prime | ANAPC10 | GRCh38.p7 | 4:145063233 | TCAGTCATTCTACAA[A/T]GTATATATATTTCAA | 10393 |
rs571052406 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145064430 | TTCAGAAGAAAAAAA[A/T]TTTACACTCAAACAT | 10393 |
rs571073367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145082189 | AGTTTCACTCTCGTG[A/G]CCCAAGCTGGAGTGC | 10393 |
rs571085696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144973168 | GAAAATAATGAAGAG[C/T]GTGCAGCCATAAAAA | 10393 |
rs571108630 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145089900 | ATGAACAAACACTGA[C/T]TGTTTTACTCTGTTA | 10393 |
rs571136945 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145002615 | TTCTACTCATCTGCA[C/T]GACAATTCTGAATAA | 10393 |
rs571141529 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145074047 | TCCTTAAAATATTAT[C/T]CCCAATATTCCTTAA | 10393 |
rs571149256 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145094634 | AACTAATAACATTAT[A/G]AAGTCCCTCAAGCTA | 10393 |
rs571184190 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145018624 | CCTGGGTGACAGAGC[A/G]AGACTCCATCTCAAA | 10393 |
rs571184269 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144980822 | TCCATCTTGAGTTAA[A/T]TTGTGTATAAGGTGT | 10393 |
rs571188887 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145068035 | ACCATAAGACAACCT[G/T]GAGGATAAAATCTAC | 10393 |
rs571209040 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145049666 | CTCACTGGAACCGCC[A/G]CCACCTAGGCTTAAG | 10393 |
rs571211658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144970081 | AAGTTAAAACAGCCA[A/G]TCTTCTATCAATCTT | 10393 |
rs571236210 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145087468 | GCTCTGCTAGGGGGC[C/T]ATTTTAACTGAGGCA | 10393 |
rs571239306 | snp | C/G | 0 | 0 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145013110 | CCTGTACAGCCTGTG[C/G]AACTGTGAGCCAATT | 10393 |
rs571244951 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145015939 | CTGCTGAAAGGAGCT[C/T]GAAACCTTAAAACAA | 10393 |
rs571273571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145006148 | TTCTGTGTTGACTGC[A/G]TATATATTTAGGGCA | 10393 |
rs571298903 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145004210 | CTGAAACTTTGTTGA[A/G]GTCATTTATCAGATC | 10393 |
rs571337183 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145005522 | GGGTTGGTTTGCTCT[C/T]GGTTCCCTAGTTCTT | 10393 |
rs571348468 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145078271 | CACAATTCCACTCAA[A/T]ACAGCCACAAAAAAA | 10393 |
rs571405538 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144968914 | CTACATCCTACCTAC[A/G]TATTGTAACAGTGAC | 10393 |
rs571448268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145017885 | AAAAAACCAAACACC[A/G]TGTGTTCTCACTGAT | 10393 |
rs571452838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145039742 | TAGGACTACAGGCAC[A/G]CACCACCACACCCAC | 10393 |
rs571462182 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144993250 | GATATGCCTGTACCA[C/G]CAGTGCGAAGTGCAT | 10393 |
rs571463130 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145086722 | TGTATCCCTGGGCTC[C/T]ACCCACTAGATGCCA | 10393 |
rs571479801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145010364 | AGCTGCTATAAAGAC[A/G]CACGCACACTTATGT | 10393 |
rs571488682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145071205 | TGAAGTTGGGATTTC[A/G]AGAATAGCCCGACCA | 10393 |
rs571490872 | in-del | -/TC | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145059054 | TGATAAATTACACTT[-/TC]TGTCTTATCAAACCA | 10393 |
rs571513586 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144979265 | ATGCTCTCCCCCTGC[A/C]CCTCTATAGGTGCCC | 10393 |
rs571518774 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144978507 | ACTTTTGATCATTCC[C/T]CTTTTAAGTAAATAT | 10393 |
rs571535879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145047562 | ATTCCCTCTCAACAC[A/G]AGGCAAATCTTCATT | 10393 |
rs571580313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144977661 | CATGCCTAAAATACC[C/T]TCTTGTGTTATTTAT | 10393 |
rs571592676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145011033 | TTTAAAATGTCTCTT[C/T]TAAATTCAAGAGGAT | 10393 |
rs571599645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145100212 | TGTAAAAATCAAGCC[A/G]GGGTAGTGACATGCA | 10393 |
rs571656278 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144992589 | AGAATTAGAAATGGA[A/G]CCTAAAAATGTGTCT | 10393 |
rs571692312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145008944 | TTTAGAAAACCCCAC[C/T]GTCTCAGCCCAAAAT | 10393 |
rs571694596 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145087576 | CTACACTGTGGCTAT[A/T]TACATTTAAACGAAG | 10393 |
rs571717889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144999568 | GGACACAAACAAATG[A/G]AAGAACATTCCATGC | 10393 |
rs571732910 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant, utr-variant-3-prime | ANAPC10 | GRCh38.p7 | 4:145064028 | GGAATTCTCTGGAGT[A/G]GTGGAAATGTTCTAT | 10393 |
rs571756751 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145016402 | AAAATACCTAGGAAT[A/C]CAACTTACAAGGGAT | 10393 |
rs571782902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145017073 | TGGGCAAGGACTTCA[C/T]GTCTAAAACACCAAA | 10393 |
rs571789850 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145093645 | GAGATGAAAATTCTA[C/T]GAGTCAAATGGAAGA | 10393 |
rs571798646 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145029805 | TAGTCACTTTAGACC[G/T]ACTCATCCCAGCTGG | 10393 |
rs571809316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144976437 | TCTAGTCTTTGCCAG[A/G]TGCAATGACTAAATT | 10393 |
rs571818001 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054654 | GTGCGCGCGCGCGCG[C/T]GTGCGTGCAGCGCAT | 10393 |
rs571819480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145025220 | ATTAGCAATAAGGCT[A/G]TTTTGCTTTCTTATC | 10393 |
rs571863527 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145069508 | ATTTCCAGTGGGCAC[A/C]GAGGACTGGGAATCA | 10393 |
rs571911607 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144988022 | CTCTGTCACCCAGAC[A/T]AGAGTGCAGTGGTGT | 10393 |
rs571936317 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145071852 | GCATCCATAAGATAA[C/T]AGTCAGCTTTAAACA | 10393 |
rs571943741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144968072 | AACAGCAATGGTAAA[C/T]TGGATAGATGAAATA | 10393 |
rs571956277 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144981991 | ACCACACACAGCTTT[C/G]TTTTTTTTAGTAGAG | 10393 |
rs571996548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145002025 | GAAGGAAGGAAAAAC[C/T]ACTTGATAGTTGCTT | 10393 |
rs572097670 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145020549 | CCACTCTCACCACTC[A/G]TCTTCAACATAGTAC | 10393 |
rs572118226 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145067952 | ATGCCCCTTTTACCT[A/T]TCTCATCTACTCCTT | 10393 |
rs572119900 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145026873 | TCAAAGAACAAGAAG[A/T]AGTCTTAGAAATTTA | 10393 |
rs572140699 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145015952 | CTCGAAACCTTAAAA[C/T]AAATCCTGGAAACAC | 10393 |
rs572178457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145095686 | TAATATTTTGAGAGC[A/G]AGAGAGACCACTTTC | 10393 |
rs572186406 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145051091 | TTGAGTTAAAGTGAG[A/C]GATGTGAAACTCTTC | 10393 |
rs572234613 | snp | A/G | | | intron-variant, utr-variant-3-prime | ANAPC10 | GRCh38.p7 | 4:145064125 | AGATTATGCAAAATT[A/G]TGCATAAATTTTATC | 10393 |
rs572264538 | in-del | -/T | 0.00478085 | 0.0486577 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145089432 | TACTTATTTTTCCCC[-/T]AAATTTGTTTTTCAA | 10393 |
rs572269666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144985571 | ATATATTAATTTCTA[C/T]TAAATTACTAGTCAT | 10393 |
rs572284743 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145039738 | TAGCTAGGACTACAG[G/T]CACGCACCACCACAC | 10393 |
rs572293988 | snp | A/G | 0.000449233 | 0.0149805 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995383 | TAAAGTCACCTTATT[A/G]AACGATACATCATGA | 10393 |
rs572332485 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145075443 | TGATCAGAGCCAAGA[C/T]GGCCAACTAGATGTG | 10393 |
rs572349408 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145042547 | TTTTTTCATTATTTT[A/C]TAGTATATAAATACA | 10393 |
rs572353219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145094778 | ACCTTAGATGCTTCC[A/G]GAAAAAAACAAGTTA | 10393 |
rs572353339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145086444 | CTAATGCAGTGGTTC[A/G]TACAGTGTCGTTCCT | 10393 |
rs572356693 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145088329 | TTCAAATTTGTATCT[C/G]CAACCCAGAACTTCA | 10393 |
rs572368075 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145012894 | GGCCTGGTGGGAAAT[A/G]ACTGGATCATGGTGA | 10393 |
rs572406385 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144986300 | TCTTTTTCTACTGAT[G/T]GGAATAGTTTCAGAA | 10393 |
rs572410498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144978110 | ACCTCTACATACATA[A/G]ATTTCTATCTTTCCA | 10393 |
rs572439321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145071513 | CATCTCAACAGAATA[C/T]TAAATAAATAATATT | 10393 |
rs572462005 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | ANAPC10 | GRCh38.p7 | 4:145063965 | CAGTATAATAGTTAT[A/T]TCTGAGGGTAGGATA | 10393 |
rs572462806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144971228 | TGCACTTTTGGGGAC[A/G]ATCAAGGCAAAATCA | 10393 |
rs572475715 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | ABCE1, ANAPC10 | GRCh38.p7 | 4:145098491 | GAATGTAGGGACGTT[C/T]TCCGAGAGCCTTTGG | 10393 |
rs572483051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145019552 | CTAGAGAAACACGAA[C/T]AAACCAAACCCAAAC | 10393 |
rs572539241 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145057023 | CACTTGAAAAAAGTG[A/G]CCTTACAGGACAATG | 10393 |
rs572545322 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145043261 | AAGTTTTGATTTTGA[C/T]ACATTATTTTGACTA | 10393 |
rs572546879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144975135 | AATACATATCACACA[C/T]ACATGGATACTTGAT | 10393 |
rs572575836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145064882 | ATGTTAAATATAGGC[C/T]CAGATAATATGTTAA | 10393 |
rs572622005 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144967383 | CAGAAGTCAGAAGAC[C/G]TGAGTCATTTACTAC | 10393 |
rs572625245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144993419 | ACTTGCCAATCATAT[A/G]ACTTCCTTGGTAAAG | 10393 |
rs572662663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145083502 | ATAAATATTGCCAAA[C/T]TGTCCTCTAAAACAT | 10393 |
rs572685487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144982188 | TTTGCCAGGCACTGC[A/G]CTAAGTGCTTACAGT | 10393 |
rs572687313 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144996775 | TTCAGATGATCAGAA[A/G]TAACAAACTTCTCCG | 10393 |
rs572722892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145079672 | GAAAATATTGTAAAC[A/G]TACACCATGGAACAC | 10393 |
rs572730794 | snp | C/G | 0.000798403 | 0.0199641 | downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:144966649 | TTAGCTTTTACTCTA[C/G]ACTACCTGCAAACCA | 10393 |
rs572740073 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145082466 | ATACATTTTAAAGAA[C/T]GTATGTATTTAAACT | 10393 |
rs572751479 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145016135 | GGCAATCAGGCAGGA[A/G]AAAGAAATAAAGGGT | 10393 |
rs572757060 | in-del | -/AGG | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144999488 | TTACAAGGGATGTGA[-/AGG]AGAACTACACAACCA | 10393 |
rs572762217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145016420 | ACTTACAAGGGATGT[A/G]AAGGACCTCTTCAAG | 10393 |
rs572766550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145027470 | CTATCAAAGAACACA[A/G]GAGTGTCTCCAGGAC | 10393 |
rs572773666 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144990416 | TTGCCTCTCTATAAA[C/T]AAATACTTGAGACTG | 10393 |
rs572787811 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145068424 | ATATATGTGATAGAC[A/G]ATAGCTTTACATTTA | 10393 |
rs572795982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145069056 | AGATACGGTCTTAAA[A/G]TAAAATAAAACAAGA | 10393 |
rs572803592 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145026220 | AAGACCTATACATAA[G/T]GATGTGTGAATGTCC | 10393 |
rs572824534 | snp | A/T | 0 | 0 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145076241 | TGGCCCCTCCAGTAC[A/T]GCAGTTGCTTATCTT | 10393 |
rs572826021 | in-del | -/A | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144983484 | ACTGGCGGATTACAC[-/A]AATGCTGAAGAGATA | 10393 |
rs572879364 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145052875 | CCTGGGCAACAGAGC[A/G]AGACTCTGTCTCAAA | 10393 |
rs572883995 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145049931 | CTCCCTCCAATGAAG[C/G]CTTCAGACCCTCAAA | 10393 |
rs572894531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145060706 | AATCAGTACTATAAC[C/T]AATGAAATGATGACT | 10393 |
rs572900294 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144988799 | TTAGTTTATATTTTC[C/T]AGAATTTTATAAAAA | 10393 |
rs572929299 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144986893 | CAGCCAAAAGACACA[C/T]GAAAAAAATGCTCAC | 10393 |
rs572937843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054423 | ATTAGCCGGGCATGG[C/T]GGCAGGCGCCTGTAG | 10393 |
rs572942517 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145095642 | AGACATTTTATCTCT[C/T]ACATCATCGCAGGAG | 10393 |
rs572945203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145075623 | TGGGGTTGCTGAGCA[C/T]CAGGACTCATTTCTG | 10393 |
rs573001957 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144990054 | TAAAATGGCAGTATA[G/T]CTCTGTCATGCCTAC | 10393 |
rs573010591 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145019590 | AAGAAAGGAAATGAC[C/G]AAGATCAGAGCATAA | 10393 |
rs573011953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145038176 | CTATCTCTACAAAAT[A/G]AAAATAAATAATAGA | 10393 |
rs573095860 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144982854 | GGATTTGTTAGTGAA[C/T]GATTTTATTTAAAAA | 10393 |
rs573120842 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145097882 | ATTCCCGGCCCTGAA[C/T]TGACCACACAGTTGA | 10393 |
rs573163662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145052480 | TCTAATTTTAGTTGT[C/T]CTCACAGATAAAATA | 10393 |
rs573164405 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144996828 | CCATCGCAAAGAAGC[G/T]AAAAACCTTGAAAAA | 10393 |
rs573165747 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145058963 | CAAAGATGAACTAAA[G/T]TTAGTTATGAAACTA | 10393 |
rs573193479 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | ABCE1, ANAPC10 | GRCh38.p7 | 4:145097408 | ACTGGATCGTGAACA[A/G]TATGTAAAACTGCTT | 10393 |
rs573204603 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145071030 | TTAATGGGTTCCACA[C/T]AGGATGATGAAAAGT | 10393 |
rs573213096 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145037414 | TCACTACACCCAGCC[C/T]TATCACCATAAATTT | 10393 |
rs573226123 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145009223 | CCATGCTCATGGATA[A/G]GAAGAATCAATATCA | 10393 |
rs573233766 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145090869 | TTGACAGTAAAGATT[A/G]TGTCTTTTTTGTCTT | 10393 |
rs573259178 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145086005 | GGTGGCTGAAGCTCA[C/T]CTTTGCAGGGGGCAG | 10393 |
rs573278689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145049882 | TCCATTTCTAATGGT[A/G]GTTATCTTGCTGTTT | 10393 |
rs573320947 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145014742 | GGCTGAGAGACCCAC[A/T]GACGGTTCACATCAC | 10393 |
rs573339668 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144989488 | TGTCCCTGACTGCTC[A/C]ATCGACCAGCTGTTC | 10393 |
rs573339736 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145056587 | CCTTTCCTTGTAACA[C/T]CTTTCTGGCGACCAC | 10393 |
rs573385274 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145017149 | ACTAAAGAGCTTCTG[C/G/T]ACAGCAAAAGAAACT | 10393 |
rs573396423 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime, intron-variant | ANAPC10 | GRCh38.p7 | 4:144994426 | AATGCATGAACCACA[A/G]AGAGCAATCTTTTCC | 10393 |
rs573411746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145065975 | GTGCTATTTGGCCAC[C/T]AGGAAAAAAAAAATC | 10393 |
rs573411880 | in-del | -/A | 0.0993497 | 0.199511 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145007870 | AAAAAAAACCCTTCA[-/A]AAAAAAAAAAATCAA | 10393 |
rs573474935 | in-del | -/A | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145059851 | ATTGCTCTAAATGAT[-/A]AAAAAAAAAATCTCA | 10393 |
rs573504550 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145017962 | ATCACACACCGGGGC[C/G]TGTTGTGGGGTGGGG | 10393 |
rs573519578 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144972378 | TATTAAATCAGACAA[A/C]GTAGATTTTATAGCA | 10393 |
rs573519978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144980970 | ATGGCTGTAGGTGTG[C/T]GGTCTTATTTCTGGG | 10393 |
rs573535398 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145040799 | CAAGTGAATAAATAC[C/T]GACAACTCAAAAAGC | 10393 |
rs573544633 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145094876 | TGAAAGAGCATTCAT[A/C]AATTTTTGAGAGAAA | 10393 |
rs573556243 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145094077 | GAAGGCAAGGATAAC[G/T]GGGGACCATTTTGAA | 10393 |
rs573563330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145048809 | CAGGAATAACTGAAA[C/T]TATCAGTATCTCAGT | 10393 |
rs573577081 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145008721 | TTTATGACAAACCCA[C/G]AGCCAATATCATACT | 10393 |
rs573635340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145034034 | TGGTTGTACGAAGGA[C/T]AGTTGTATTATGTTA | 10393 |
rs573653939 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B, intron-variant | ANAPC10 | GRCh38.p7 | 4:144993545 | TCAAATATATAATTT[A/G]CACTTTAGAAAGTAA | 10393 |
rs573657175 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144970615 | TAACTCTTGCAATGT[A/G]GCATACTGAAACTAA | 10393 |
rs573657576 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145087253 | ACAACACCACTAGAG[A/T]CATATTTGAGCAGCC | 10393 |
rs573715449 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145000001 | AACTGGCTAGCCATA[C/T]GGAGAAAGCTGAAAC | 10393 |
rs573721017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145041412 | AAATGATAATCATTG[A/G]TAACTGAGGAGAAAA | 10393 |
rs573746167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145011839 | CACAGCAGAGTTTTT[A/G]GCAATTTTTCAGGGC | 10393 |
rs573774840 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145012402 | AATGACTATGATTAA[C/T]ATGCTTAAGAAATGA | 10393 |
rs573780195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145062468 | AAAAATTAGCTGGGC[A/G]TGGTGGCGCATTCCT | 10393 |
rs573787740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145017478 | GGAAACAACAGGTGC[C/T]GGAGAGGATGTGGAG | 10393 |
rs573791194 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145061741 | AATACAATTTAATAC[A/G]TCAAGTCATCAGAGA | 10393 |
rs573802715 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144979958 | TAAAAAAAATTCAAA[C/T]GTTTAGCCAACCGAG | 10393 |
rs573875171 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145006556 | GAAGCAAATTACTTA[C/T]GCTAGCTAACCTTTA | 10393 |
rs573913818 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145009848 | AAACTAAAGAGCTTC[C/T]GCACAGCAAAAGAAA | 10393 |
rs573931239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145005060 | TATCTTCCTTGTTCA[A/G]TCTTCAGAGATTATA | 10393 |
rs573996900 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145032455 | GGATGGGCCTCTCTT[C/G]AGTGGTCAAAAGCTG | 10393 |
rs574018811 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145011387 | AAAATAAAATAAAAT[A/T]AAATTCAAGAGGATG | 10393 |
rs574025696 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144992796 | ACTTGAGAGGATTGA[A/C]TCCAATTTTGAAAGA | 10393 |
rs574040797 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144973750 | ATAAATAAATTTATG[C/T]CAATAATTTTGAAAA | 10393 |
rs574083095 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144979469 | GCATGGTATTCCATG[A/G]TGATTATGTACCATA | 10393 |
rs574084500 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145000172 | TCTAAACACCAAAAG[C/T]AGTGGCAACAAAAGC | 10393 |
rs574116008 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145092590 | CAGCAACACTGAGAG[A/C]CCAAAACACAAGGTG | 10393 |
rs574123532 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145085438 | AAGGTTTTTTTTTTC[A/G]GTTATTTTATTTTGG | 10393 |
rs574157015 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145099491 | CCAAAAGCTGTTTGG[A/C/G]GTTTGTGAGCTTTTT | 10393 |
rs574203284 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144977061 | TTGGAGCTGTGTACA[A/T]TTTCTGATGGTCTCG | 10393 |
rs574222417 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145021123 | AACCTACAAATTCAC[G/T]GCAATCCCCATCAAA | 10393 |
rs574262244 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145047007 | GTAAAGTTATATTGA[C/G]TAAGAATCTATACAT | 10393 |
rs574263012 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144991954 | GAAGAGAATAACTCT[C/T]GTTAGCAGCTAATGC | 10393 |
rs574263178 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144996223 | AGGCTTATAGGATCT[G/T]AGTGATGACAGAAAC | 10393 |
rs574332926 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144981215 | GTAGTTTAATGAGAA[C/T]AGCATTGAATCTATA | 10393 |
rs574365625 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145029846 | AAGATATACCCTTGA[C/G]CAATGCCTTGCAAAA | 10393 |
rs574366320 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145084701 | ACTTCTTCCGTAACT[C/G]TTAAATCTGCACTGT | 10393 |
rs574388588 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081872 | AGGTCAGAAATATTA[A/T]TTTTTTTTTATTTAT | 10393 |
rs574423680 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144980434 | GTCTGTTCATACTTT[C/T]TGCCCACTTTTTAAT | 10393 |
rs574424047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145047640 | AAATTTCCTCAGAGA[C/T]AATTCCCTCTCAACA | 10393 |
rs574431919 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144974209 | AAATATCAACCAATA[C/T]AATTCAACATAATAA | 10393 |
rs574438493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145074373 | GTAAGTTTTTAATAT[A/G]TTCTATTCAAATTTT | 10393 |
rs574472704 | snp | C/T | | | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145099512 | TGAGCTTTTTGAGAA[C/T]TTAGTTCTCCCCTAT | 10393 |
rs574498916 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145061323 | TCTCAAAATCCTTAT[C/T]TAATGTCAGTAAAAT | 10393 |
rs574542728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145089434 | CTTATTTTTCCCCTA[A/G]ATTTGTTTTTCAACA | 10393 |
rs574543126 | in-del | -/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145035166 | CTGCGACATCTGTCA[-/C]CCCACTAATCACCAG | 10393 |
rs574562817 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145091641 | TTTGCTATTATGAAT[A/G]GTGCTGCAATGAACA | 10393 |
rs574580338 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144981992 | CCACACACAGCTTTC[-/T]TTTTTTTAGTAGAGA | 10393 |
rs574581475 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145096595 | TGATTTTTACTTCTA[C/T]AATGCTATGCAGTTC | 10393 |
rs574588803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145001635 | ACCCAAAGACTGCCA[A/G]GTCACTTCTGAATAG | 10393 |
rs574625201 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145090036 | ATTTCCCTATTTCTA[G/T]TCTCATTTACTACAT | 10393 |
rs574632983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145029201 | AGAAAGAGCTTCACC[A/G]TCCCCAGTAGTGGCA | 10393 |
rs574669148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145043768 | TTACAAATGAAGGCT[A/G]ATATCTGCTGCATAA | 10393 |
rs574679385 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145074768 | GTAGCAACTATTACT[A/G]TCAAGCAGTTAAATT | 10393 |
rs574682434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144988165 | TTTAAATTTTTGTAG[C/T]GACAAGGTCTTGCTA | 10393 |
rs574731469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145079750 | GATGCAGCTGGAGGC[C/T]GGCATCCTAAGAGAA | 10393 |
rs574763983 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081244 | AAAAAAAAAAAAAAA[A/T]TTTCCAAATAAAAGT | 10393 |
rs574773630 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145020937 | CAAAACACCACTGAA[A/G]GAAATCATAGACAAC | 10393 |
rs574808366 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145072205 | ACATAAAACTGGGTA[C/G]GTTACCAAAAAGTGT | 10393 |
rs574812524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144970610 | GAACTTAACTCTTGC[A/G]ATGTGGCATACTGAA | 10393 |
rs574849237 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145057625 | GATCCATATACCATA[C/T]CCTACTATCCATGGA | 10393 |
rs574849923 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144986403 | TGGTTGGTAAGCTAT[A/T]AATTATTGCCTCAAT | 10393 |
rs574866332 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145099629 | AGAGTTCTTCTAAAT[A/G]TCTTAAACTTAAAAC | 10393 |
rs574920981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144987206 | CACACGTGTGTTTAT[C/T]GTGGCACTATTCACG | 10393 |
rs574960040 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144978872 | TGGCTCAGAACTAAA[G/T]TTAGATACAGTAAGA | 10393 |
rs574972044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145087994 | TGGAGGTTGCAGTGA[A/G]CTGAGATCGCACCAC | 10393 |
rs574995728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145051150 | TCATTAGTTAGAGGC[C/T]TAATTGAATCAAGCC | 10393 |
rs575050200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145068499 | AATCGTTCTTCTTAA[C/T]GTGCTAGATATATTA | 10393 |
rs575102205 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145027529 | AAACCATTGAGCACC[C/G]TGCACAATAAAGGAA | 10393 |
rs575137129 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145076297 | GTCTGTTCAAAGGCC[C/T]TCTGGATTACAGCAT | 10393 |
rs575150153 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145016723 | TCACTTCAAACTATA[C/G]TACAAGGCTACAGTA | 10393 |
rs575155674 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144967470 | ACAGGGTTGCTTTAA[C/G]AATTTGCGAAAAAAT | 10393 |
rs575191535 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144989787 | TACTACACTAGTGAA[C/T]CCATGAATGATAAGA | 10393 |
rs575204337 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145019652 | TAAATGAAACAAAAA[C/G]CTGCTTGTTTGAAAA | 10393 |
rs575208593 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145039996 | TCAAACTCCAGCAGA[C/T]GACTCCAAAGCCCAT | 10393 |
rs575239782 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145028258 | TAATCAGCTTCCAGC[G/T]AATATAAAGCAGGCA | 10393 |
rs575273813 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145056186 | ATAAGATACAGGTCA[C/T]AAAGACCTTGCTAAT | 10393 |
rs575281533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145011150 | CAACCTGGCCAAAAC[A/G]GTGGAACCCCATCTC | 10393 |
rs575317700 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145010545 | GCATGAAGGTGAAAA[A/T]CATCATTCTGAGCAA | 10393 |
rs575319344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145017172 | AAGAAACTACCATCG[A/G]AGTAAACAGGCAACC | 10393 |
rs575329380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145013275 | AATCTTTCTCATGAG[C/T]ACAAATGAAAAAAAC | 10393 |
rs575384141 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145047761 | TTTTAAATTGATGAG[A/G]TTATTGTTCAACTAG | 10393 |
rs575397324 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144982946 | AGGGTAGACCACGAG[A/G]TCAGGAGTTCGAGAC | 10393 |
rs575416264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145031725 | TTGGAGCCTTTGGCA[A/G]GCCCCCATAGTGAAT | 10393 |
rs575439179 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145015242 | GATAGCATAAAGAAA[A/C]AACAATCAAACTTCA | 10393 |
rs575517370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145091723 | TACCCAGTGATGGGA[C/T]TGCTGAGTCAAATGG | 10393 |
rs575553231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144991665 | AGAGGAGTGAGCTAC[C/T]ATGCCCGGCCAGGAA | 10393 |
rs575581206 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145037521 | AAAACAGGCTATTTG[A/C]TATCATGCCACTGGA | 10393 |
rs575613508 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145042394 | CAAGACATTTATGAT[A/C]TTTTCAGATGTATAA | 10393 |
rs575626256 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145004336 | GGATGTCTTTATTTA[C/T]TTCTCTTGCCTGATT | 10393 |
rs575641149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145016219 | TGTATATTTAGAAAA[C/T]CCCACCGTCTCAGCC | 10393 |
rs575677877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144997915 | TGGAAAACAAAAAAA[A/G]CCAGGGGTTGCAATC | 10393 |
rs575706721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145009271 | CCCAAGGTAATTTAT[A/G]GATTCAATGTCATCC | 10393 |
rs575742642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144997353 | AAAGGTCGGGTTGCC[C/T]ACAAAGGGAAGCCCA | 10393 |
rs575790340 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145053933 | GTTTTTTTTTTAGAT[C/G]AAGTCTCTCTCTGTC | 10393 |
rs575814520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145008801 | GGATGCCCTCTCTCA[C/T]CACTCCTATTCAACA | 10393 |
rs575830872 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145058331 | GATTTTGCACCTGAA[C/T]AGGCTTTGTATTTAT | 10393 |
rs575832353 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145038427 | CTGAGGCAGGAGAAC[C/T]GCTTGAACCCAGGAG | 10393 |
rs575841241 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145068351 | TTTAATCCAGGTCTA[C/T]GTGACTACATTATAT | 10393 |
rs575850406 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144979667 | TATGCCTCTAGGTCT[C/T]TGAGGAATCGCCACA | 10393 |
rs575858895 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145052972 | TCAGGGAAGAAGTAG[A/G]AAAAACAGCAGTTGC | 10393 |
rs575900695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145041547 | AAGAAACTCAGACAT[C/T]GTAGGCCCTTAGAAA | 10393 |
rs575914277 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145014746 | GAGAGACCCACAGAC[A/G]GTTCACATCACAGGA | 10393 |
rs575918091 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145085680 | AGTACAACTAAGCAG[G/T]TCTAATATCTTCAAG | 10393 |
rs575936908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145067696 | CTGCTACCACAGATA[C/T]GAGCATCTGCTGAAT | 10393 |
rs575981476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145077921 | AGACAACATCATACC[A/G]AGCAAAAACTGGAAG | 10393 |
rs576049612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145028477 | CTCATATCATATATA[C/T]ACATATCTCCCATTA | 10393 |
rs576122765 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145018579 | AGAGGCAGAGTTTGC[A/T]GTGAGCCGAGATCGT | 10393 |
rs576125055 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144968294 | CGGGGGAAAAAGAGA[C/T]ACATCATGCTTTACA | 10393 |
rs576152544 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145095524 | TGATCCAGAATCACC[A/C]GAAGCAGATGCTCCT | 10393 |
rs576182103 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145056148 | AAGGCATGCTAAGTC[A/T]CCAGATGAGATACAA | 10393 |
rs576185158 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145088939 | CCTTCTTTCTGAACC[A/T]CTAAAATGCCAAATC | 10393 |
rs576189716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145055653 | AAGTGAAGTAAGCTA[A/G]TCAAAAAAGGACAAA | 10393 |
rs576197278 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145093863 | ATGGTCTAGCATATG[C/T]ATAATTGGATTCCCA | 10393 |
rs576209175 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144987308 | CACCATGGAATACTA[C/T]GCAGCCATAAAAAAT | 10393 |
rs576227858 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145050906 | CATATCAGTAATAAG[A/G]CTGTATTGCTTTCTT | 10393 |
rs576292076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145049989 | CTTCCAAACTAATGT[C/T]AATGTTCATATTTTG | 10393 |
rs576306721 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144970408 | AAATACATGAACTTA[C/T]AATGCTTAGCTGAGC | 10393 |
rs576314089 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145079602 | TTGCAGCACTACGCA[A/C]AATAGCAAAGACAAG | 10393 |
rs576314468 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145043710 | AAAAGATGTCTTTTA[C/T]AAAAAGAAAATGCAA | 10393 |
rs576322312 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145007115 | TATATATGCACCCAA[C/T]ACGGGAGCACCCAGA | 10393 |
rs576337469 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144984836 | ATAGCAAGCTGGTTC[G/T]ACTCGGCAGAAAAGA | 10393 |
rs576399956 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145034860 | AGCCTGCTTTAGTGT[C/T]CCTGTTGTGCTCAGC | 10393 |
rs576403688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145026147 | CCCATCCCTTGCCAC[A/G]TGCCCCAGGCCAGAG | 10393 |
rs576421328 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144970476 | GAAGCAACTGAAAAC[C/T]GGACTGGCACATGAG | 10393 |
rs576425958 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145078849 | TTGAAATCAGACCCC[C/T]CCCTTTCACCATATA | 10393 |
rs576459741 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145070850 | TGCTACAACATGAAT[G/T]AACCTTGAAAACATT | 10393 |
rs576469361 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144982136 | GGCGTGAGCCACCGC[A/G]CCCGGCCAGCAGCTA | 10393 |
rs576484487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144978727 | TTGGGAGGATCCCTT[C/T]AGCCCAGTAGTTTGA | 10393 |
rs576488750 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145031131 | AAGGCCAGCAATTTA[A/C]CTTACTGTCCTACCT | 10393 |
rs576506314 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145009392 | CAATCCTAAGCAAAA[A/C]GAACAAAGCTGCAGG | 10393 |
rs576511802 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145070499 | ATGACTATTATCAAA[C/T]GTTGGCATGGATGTG | 10393 |
rs576516831 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145077189 | GGGCGACAGAGCAAG[A/C]CTCTGTCTCAAAAAA | 10393 |
rs576527665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145085542 | CAAAATAGTATTTGT[C/T]CTTAAAATGCAAAAA | 10393 |
rs576565376 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145015387 | CCAACCAAACAAAGA[A/C]AAAGAAAAAAGAATA | 10393 |
rs576588024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145090723 | CCTTACTGAGATAAC[C/T]GGTTATTTTATGCAT | 10393 |
rs576596487 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144989133 | GATGTTTAATTTTTT[A/T]AAAATTACCAAACTG | 10393 |
rs576609615 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144999151 | CCAAAACAAGTCTAG[G/T]ACCAGATGGATTAAG | 10393 |
rs576634585 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:145033009 | AAAGAAGTATGGCAG[C/T]GGGCACATGCTCATG | 10393 |
rs576641738 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145077712 | TCGGATGTAAGATAG[C/G]CTCCACATATGCAAA | 10393 |
rs576671280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145090126 | TTCTTGGCATCCAAC[A/G]AGGATTGGTACCAGG | 10393 |
rs576708479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145032539 | GGAGTTTAATAATCA[C/T]ATGGATAGGATGACC | 10393 |
rs576728191 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144981381 | TCCCTTGTTAGTTGT[A/C]CTCCTAGGTATTTTA | 10393 |
rs576741194 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144974325 | ATTTGGTAAACTAGG[A/T]AATAGCATTAATTTG | 10393 |
rs576768634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145076155 | CAGCATACATTTGCC[C/T]ACAGACTTCCCCTGA | 10393 |
rs576856727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145040526 | ACCATTCACTGAGCT[A/G]CTAGTATGTTCCAGG | 10393 |
rs576857885 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145066809 | ACTTAGGTTAATAAC[A/T]GGCTTAAGGTCAAAA | 10393 |
rs576870341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145016100 | CTCCTATTCAACATA[A/G]TGTTGGAAGTTCTGG | 10393 |
rs576913328 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, missense | ABCE1, ANAPC10 | GRCh38.p7 | 4:145097295 | TGGCTTCAAGATTTT[G/T]AAGTGAATAACTGGC | 10393 |
rs576968311 | in-del | -/TTTAT | 0.00159617 | 0.0282053 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144981810 | TGGAATAGCAGTTAC[-/TTTAT]TTTATTTTTTATTTT | 10393 |
rs576980955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145059843 | CTTTGGTCCATTGCT[C/T]TAAATGATAAAAAAA | 10393 |
rs577019606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145068325 | ACATCTAGTAAAGCA[C/T]AGAGCCAGAATTTAA | 10393 |
rs577084693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145082369 | GGTCAGGCCGGTCTC[A/G]AACTCCCAACTTCAA | 10393 |
rs577097846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145036685 | ACATGTTTTACTGTA[A/G]TAAAAAGAAACATTA | 10393 |
rs577115114 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145029926 | CTTCTCTGTATGTCA[G/T]ATCTAACGATGAGAA | 10393 |
rs577116998 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145098789 | ACTCTCTAGTACCCC[C/T]ACACTCCTCCAGCAC | 10393 |
rs577124663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145002277 | TTCAGAAGTTCCAAA[C/T]GTGTTAAAAGGAAGC | 10393 |
rs577132609 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144972710 | TAATTACTTGACATA[A/C]ATAGAACACTGCACC | 10393 |
rs577160884 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145056804 | TTTCCTTATAAGAGG[G/T]ATTGATAATCTGCAT | 10393 |
rs577162212 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145091041 | TATGTAAAATGCTAA[C/T]CATATAATGATATTT | 10393 |
rs577164803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145051796 | CACCATAATTAAGTG[A/G]AATGAGAGAAGGAGC | 10393 |
rs577171681 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145030520 | GTCATTTCGGTCCTC[C/T]AGTTAAAGCAGTTAA | 10393 |
rs577174363 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145088742 | GTCATCTTTTAAAAA[A/T]TCTGTATCAGATCAT | 10393 |
rs577176951 | snp | A/G | | | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145096578 | TAAAGAGGTTCACTT[A/G]ATGATTTTTACTTCT | 10393 |
rs577199804 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145055414 | AATACAAAAGTTAGC[A/C]GGGCATGGTGGTGTG | 10393 |
rs577200945 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145057700 | GTGACCAAAATTAAT[C/T]TCATTATCTAAGTCC | 10393 |
rs577259174 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145037221 | ACATGATATTGAAAC[A/G]TATCTTTTATCTTAG | 10393 |
rs577276015 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145052258 | AAGACAGATTTAAGC[A/G]TTCACACCACAAAGA | 10393 |
rs577305715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145093950 | ATGGACACAATGTCT[C/T]TTACAACCTAGTCTC | 10393 |
rs577344330 | snp | A/C | 0 | 0 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144971535 | ATCTTTACATGTTTT[A/C]TTATATATATTTGTA | 10393 |
rs577344549 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145049678 | GCCGCCACCTAGGCT[A/T]AAGCAATCCTCCCAC | 10393 |
rs577382559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145044757 | AACATGACAATACTG[A/G]CTAACTAATGGGCTT | 10393 |
rs577386199 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145028914 | AAGCAGGTATTAACC[A/C]CTCAAATCTGCTAAG | 10393 |
rs577406546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081088 | CCAGCTTGGCCAACA[C/T]AGCGGCCAACTGTCT | 10393 |
rs577407918 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144979746 | TTTATTCTTTAATTC[A/C]TAGTTACACCCACCC | 10393 |
rs577466513 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145025155 | TAGGCTTTGACTTAA[A/G]GGAATGTTGTGGCTG | 10393 |
rs577466678 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144990690 | CACCAAGCCATTCCT[A/G]AGGAATCCGCCCCCA | 10393 |
rs577473273 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144969585 | GGAAATAGCATACTC[A/G]CTGGATAGACTGGAT | 10393 |
rs577483907 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145062377 | TTTGGGAGGCCGAGA[A/G]AGGCAGATCACTTGA | 10393 |
rs577492074 | in-del | -/GA | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144985940 | AATACCTAATTTATT[-/GA]GAGTTTTTTGGATGA | 10393 |
rs577493283 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145060622 | TCAATACACACTACA[C/T]TACACCCTCCAGTGG | 10393 |
rs577516057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144999178 | TAAGAGACGAATTCT[A/G]CCAGAGGTACAAAGA | 10393 |
rs577528325 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145020382 | TTGACAAAATCCAGC[A/C]TCCCTTTATGATTAA | 10393 |
rs577600962 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145093293 | GACACTGAAGGTAAC[C/T]ATAGCAATAACAAAA | 10393 |
rs577621124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145040613 | TTATAGGTAACTGAA[A/G]TTCATAGAAAGGTTA | 10393 |
rs577657721 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144999858 | ACCAAAACAGAGATA[C/T]AGACCAATGCAACAG | 10393 |
rs577691398 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145085244 | CCTGGGCAACAGTGC[A/G]AGAAACGGACAAAAA | 10393 |
rs577708419 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145048661 | TAAGAAGAAATTCTA[C/T]GAAAACAATTTTCTA | 10393 |
rs577738687 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144967562 | CATTTTATGTGTATA[A/C]AAATGAAATATATTT | 10393 |
rs577762308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145031857 | CTGAATGTTTGACTA[C/T]GGGTCATCAAGTCAC | 10393 |
rs577763804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145069893 | TAAACAATGACACTC[C/T]TCTCACTATTTTTGT | 10393 |
rs577785187 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145016541 | GTGAAAATGGCCATA[C/T]TGCCCAAGGTAATTT | 10393 |
rs577789950 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145025550 | AGAACACACACAGTT[A/T]TCGATTGGGTTTGCC | 10393 |
rs577795336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145069229 | AGAAAATAAATGAGG[C/T]GAGCCCTACAAACAA | 10393 |
rs577826023 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145009738 | AAGAAAACCTAGGTA[A/T]TACCATTCAGGACAT | 10393 |
rs577870937 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145029261 | AGTCTTTCCACCTTT[-/G]TCTGAGAAGATAAAC | 10393 |
rs577888315 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144976871 | AAGAAAATTTTCTTA[A/T]TTTGAATCCAAAAAA | 10393 |
rs577905786 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145017271 | AACTCAAACAAATTT[A/C]CAAGAAAAAAAAACA | 10393 |
rs577907667 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144983243 | TTGTAATAAAACAAA[G/T]ATAGAAGATAAATAA | 10393 |
rs577949321 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144976282 | CATATTTTGTACATA[A/T]GTACCTAATGTTTAT | 10393 |
rs577992724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144998619 | ACACATGTAAAGCAG[C/T]GTGTCGAGGGAAATT | 10393 |
rs578027714 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144974418 | TTCACATTGTGATCA[A/G]AAACAAGAATGGCTG | 10393 |
rs578040133 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145084661 | TGGGCCATATATGTC[A/G]ATAAAATGTAAAAAT | 10393 |
rs578048732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145077060 | AAAAATTAGGTGGGC[A/G]TGGTGGCAGGCACCT | 10393 |
rs578065196 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144970786 | AACTCATACAGGATT[C/G]AAATTATCTCAAATG | 10393 |
rs578087062 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145098544 | AGCAGCAGCGCGTGG[C/T]AGCGGTTCCTGCGGG | 10393 |
rs578095910 | snp | C/T | 0.000197453 | 0.00993416 | intron-variant, missense | ANAPC10 | GRCh38.p7 | 4:145053776 | TTCACATGTAAAACA[C/T]GAGGCTGAAAAAAAA | 10393 |
rs578103218 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145092342 | AATTTAAATTAAAAA[A/G]AATCACCTCCATCCA | 10393 |
rs578115082 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081182 | TTTTTCCTTTCCCCT[C/G]AAAAAGCATTATCAA | 10393 |
rs578144687 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145035700 | TCCAGATTGTTTTTG[C/T]TCCCCACCACTTTAC | 10393 |
rs578149253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144983856 | CCATAGGATGGAATA[C/T]CATTTGAATAACTAT | 10393 |
rs578171653 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145006992 | TTCTGGTACCTCAAG[C/T]GGCTATATGCTGAAG | 10393 |
rs578175174 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145046831 | TCTGATAGTAAGGAA[C/T]TGAATCCAAGACAAC | 10393 |
rs578178970 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144998071 | TACAGGAGCACCCAG[A/G]TTCATAAAGCAAGTC | 10393 |
rs578187435 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145099231 | AAGCCGAATTCCCAC[A/C]TCCCATTAACTACAT | 10393 |
rs578237267 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145013527 | ACAGAATGCAATCAT[G/T]AATAAAAAACAGCAT | 10393 |
rs578246780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145091826 | CCAACACTGTAAACA[C/T]GTGGAGTACTATCCA | 10393 |
rs745320444 | in-del | -/TAGT | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145084290 | TGAATTTCAAATTAC[-/TAGT]TAGCTAGATAAAGAG | 10393 |
rs745321167 | snp | C/T | | | downstream-variant-500B, intron-variant | ANAPC10 | GRCh38.p7 | 4:144993724 | AATACGTAAGGAGAA[C/T]AAAAGTAGAAAACAT | 10393 |
rs745325330 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145024566 | TAGGTACATTGTCAA[C/T]GAGCAGTAATATTTT | 10393 |
rs745384092 | in-del | -/AA | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145049944 | AGCCTTCAGACCCTC[-/AA]AGTTATTCATGAGGC | 10393 |
rs745440253 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145079417 | AAAAGGGAATACTTA[C/T]ACACTGCTGGTGGTA | 10393 |
rs745446604 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144990770 | TTTCAACATGAAATT[A/T]GGAGGTAAAAAACAT | 10393 |
rs745446801 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145028230 | ATCCAGCCTTAATCT[C/G]GTGGGCACAATCTAA | 10393 |
rs745472572 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145090786 | TAAGCACTAAATAAA[A/T]GTTATTAATTATTAC | 10393 |
rs745497225 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145055282 | AAAAAAAGGAGGCCA[A/G]TGAGGTAGCTCAGGC | 10393 |
rs745548443 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145056259 | CCAAGATGGCCACGA[C/G]AGTGACCTCTGGTAG | 10393 |
rs745552537 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145039784 | ATTTTTCAGTAGAGA[C/T]GTGGTTTCACCATGT | 10393 |
rs745553036 | snp | A/C | 1.65776e-05 | 0.00287898 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995430 | TCTAGGAAATTTACC[A/C]ATGGAGCTCTCTTCT | 10393 |
rs745596190 | snp | C/T | 0.000185822 | 0.00963724 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | ABCE1, ANAPC10 | GRCh38.p7 | 4:145097445 | CGCAGTTACTGCTAC[C/T]GAACATTGTTATATA | 10393 |
rs745621420 | snp | A/T | | | downstream-variant-500B, intron-variant | ANAPC10 | GRCh38.p7 | 4:144993588 | TTAGATAATTATGCT[A/T]TGTTAATATAATGCA | 10393 |
rs745631722 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145007357 | TCTCAGCACCCCACA[C/T]GCTTATTCCAAAATT | 10393 |
rs745642291 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144978043 | CCTTCATCTTCACTA[C/T]TTATTTCATTTCTCA | 10393 |
rs745711564 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145051503 | AGACTTCCTTGACAC[A/G]GTTGCCACAAAGCTT | 10393 |
rs745724396 | snp | C/G | | | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145100308 | GTAGTGTCCTGTGAT[C/G]ACTGCCCTCAGCCAG | 10393 |
rs745724545 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145086759 | ACACTCCCCCAACTC[C/T]CCAACTCCCCCCACC | 10393 |
rs745729057 | in-del | -/TTG | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144984422 | ATCAGTATTTTGATA[-/TTG]TTGTAGTAATAACAG | 10393 |
rs745766585 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145080364 | AAGTCAGAAGGAAAA[C/T]AAATAAATCCTGCCT | 10393 |
rs745768627 | snp | C/T | | | intron-variant, utr-variant-3-prime | ANAPC10 | GRCh38.p7 | 4:145063497 | GAGACACGGTCTTAA[C/T]ATAAACACTAAGTCA | 10393 |
rs745814866 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145049564 | TTGCTGCAATTTGGT[C/T]GCATCTTCAGGCTCC | 10393 |
rs745820020 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145065100 | TATATTAAATACTTG[A/C]AAATAACTAGCTAAG | 10393 |
rs745854313 | snp | C/T | 0.000149033 | 0.00863099 | upstream-variant-2KB, synonymous-codon, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145096046 | CCGTACTGTTCCAGT[C/T]CTTTCCAACTGCTTG | 10393 |
rs745859841 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144970282 | AGGATATTTAGAAAC[A/G]TGTGAAAAAAGACTT | 10393 |
rs745866070 | in-del | -/GGG | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145040336 | ATTGTTAATAGAGAC[-/GGG]GGGGTTTCTCCATGT | 10393 |
rs745869962 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145058796 | GCCCCAAATGCATAG[C/T]TACCTCAACTCCATT | 10393 |
rs745895930 | snp | A/G | 1.68318e-05 | 0.00290096 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081618 | TAGATTTATTTGTCT[A/G]TAACCTACAGTAGAT | 10393 |
rs745899942 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145021066 | CCCATGTTCATGGAA[C/T]GGTAGAATCAAAATT | 10393 |
rs745904075 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145001819 | ATTAGCAACCTTTAA[C/G]TCACTATCTACTCTG | 10393 |
rs746015225 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145037706 | AATCCCATGTCTTTC[A/G]GAGGCCAAGGCAGGC | 10393 |
rs746020099 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144979896 | TCTAGCTCATTACAG[A/C]CACCGCTTCCCCTTC | 10393 |
rs746066243 | in-del | -/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144991680 | ATGCCCGGCCAGGAA[-/T]TTTTTTTTTTTTTTT | 10393 |
rs746076052 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145095496 | TCCAATCATCAACAT[C/T]ATCGTGGCTTGATGA | 10393 |
rs746092592 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145034028 | CATTTCTGGTTGTAC[A/G]AAGGATAGTTGTATT | 10393 |
rs746102445 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145074915 | TCTAATTCCTCCACA[A/T]AGTATAAATCCTTCA | 10393 |
rs746117398 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145035702 | CAGATTGTTTTTGTT[C/G]CCCACCACTTTACAT | 10393 |
rs746178319 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145029428 | GGAGGTGAAGTTGAG[A/T]GTGTGATCCATGAGG | 10393 |
rs746194376 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144973972 | AAAACGTTTTTTATT[C/T]TTTGAGGCCAAACTG | 10393 |
rs746207699 | snp | C/T | | | intron-variant, utr-variant-3-prime | ANAPC10 | GRCh38.p7 | 4:145063660 | ACAGCTTCACAATTA[C/T]GTAGTTCAAAGTCAT | 10393 |
rs746271826 | in-del | -/GTGTAT | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145037036 | TGTGTGTGTGTGTGT[-/GTGTAT]GTGTGTGCATGCATG | 10393 |
rs746281523 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145007637 | AAACCAATGAGAACA[A/C]AGACACAACAAACCA | 10393 |
rs746288617 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145083138 | GAATATTTATTCCAT[A/G]TCAATAAATTAACAA | 10393 |
rs746349315 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145025237 | TTTGCTTTCTTATCA[C/T]TCATGTGTTCACTAG | 10393 |
rs746363108 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145059934 | CATAATGCTAAAACG[C/T]AAGGGATTTAAGAAT | 10393 |
rs746378181 | snp | A/C | 9.93575e-05 | 0.00704761 | upstream-variant-2KB, synonymous-codon, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145096022 | CCAAACAGCTTGTGA[A/C]CCAATTTCCCGTACT | 10393 |
rs746409372 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145045529 | CAAGTTCCAAAGCCA[C/T]TCTACAAAAGAATAT | 10393 |
rs746465574 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145055141 | TAAGTGTACATCCAC[C/T]GTTCACAGCACTACT | 10393 |
rs746469397 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145037684 | AGGCACAATGGCTCA[C/G]ACCTATAATCCCATG | 10393 |
rs746491628 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144997048 | AGAGAAAAAAGAGTA[A/G]AAAGAAATGAACAAA | 10393 |
rs746576967 | snp | C/G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145090678 | AAATGGTAAAAGAAA[C/G/T]AGTACAACTTCATAT | 10393 |
rs746643742 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145068939 | AAATGTCCTCTGTAT[C/T]AATGTTAACTAGATG | 10393 |
rs746723322 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145041093 | TAGGATCTATGACTT[C/T]TAGTGGTCCCATAAT | 10393 |
rs746751654 | snp | A/T | | | intron-variant, utr-variant-3-prime | ANAPC10 | GRCh38.p7 | 4:145063286 | ATACAATATTTAATA[A/T]TTTTTTTAAAAACAA | 10393 |
rs746754967 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145006201 | AGCTCTTTACCATTA[G/T]GTAATGCCCTTTTTG | 10393 |
rs746816192 | in-del | -/T | | | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145099493 | AAAAGCTGTTTGGGG[-/T]TTGTGAGCTTTTTGA | 10393 |
rs746817788 | in-del | -/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144993257 | TGTACCAGCAGTGCG[-/T]AAGTGCATTTTCTCC | 10393 |
rs746878555 | snp | A/G | | | downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:144967012 | TTAATTAAATCTTAT[A/G]ACCCTGAAATAAGAA | 10393 |
rs746880572 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144983126 | GATCGTGCCACTACA[C/T]TCCAGCCTGGGCAAC | 10393 |
rs746944828 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145062351 | GTGGCTCACGCCTGT[A/C]ATCCTAGCACTTTGG | 10393 |
rs746960435 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145023292 | AGAGTCAGAATAACC[A/G]TTAGCCTTCAGGAAG | 10393 |
rs746961101 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145024310 | GACCTTCTCACATGA[A/T]TCATAAATGTTCTTA | 10393 |
rs747074985 | snp | C/T | | | intron-variant, missense | ANAPC10 | GRCh38.p7 | 4:145033294 | GTGATCCACTGGCAA[C/T]ATTTTTGCTTCCTGT | 10393 |
rs747094764 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145020067 | AGAGAAAGAGGGAAC[A/C]CTCCCTAATTCATTC | 10393 |
rs747148650 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144982580 | GACAGATGTGGCCAG[C/T]ATCACTCTTCTCCTT | 10393 |
rs747155860 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145072687 | CAAGTGCTAAAAAAA[C/T]CTACCCAATCCTAAA | 10393 |
rs747161156 | snp | G/T | | | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145098672 | CACCCGCGAGGGACT[G/T]CGAGAATGGACCTAG | 10393 |
rs747173372 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145036493 | AGAAGTATGATTGTT[A/G]CAAGTGCTACTGCAA | 10393 |
rs747190415 | snp | A/G | 1.66941e-05 | 0.00288908 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081627 | TTGTCTATAACCTAC[A/G]GTAGATGAAAAATTT | 10393 |
rs747236717 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145050399 | ATGGGCAGAATAAAT[C/T]TAGCATAATTCTTAA | 10393 |
rs747242644 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145049222 | CTTAATGATGACGGC[C/T]ACTGACAGATTAAGG | 10393 |
rs747277685 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145043553 | AACACATGCACTGAG[C/T]TGTAAAACCGCAAAA | 10393 |
rs747296441 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144993251 | ATATGCCTGTACCAG[C/G]AGTGCGAAGTGCATT | 10393 |
rs747297622 | snp | C/T | 1.65712e-05 | 0.00287843 | missense, nc-transcript-variant | ANAPC10 | GRCh38.p7 | 4:145081738 | TCATCTCGTAACTGA[C/T]CCACTCCAAATCCTA | 10393 |
rs747317084 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145004231 | TTATCAGATCAAGGA[C/G]CTTTGGGGCAGAGTA | 10393 |
rs747321621 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145094504 | TCAAGAAAGTGCTCA[C/T]AGAAAGACAGAGAAG | 10393 |
rs747327271 | snp | C/T | 1.65767e-05 | 0.00287891 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995437 | AATTTACCAATGGAG[C/T]TCTCTTCTACTGGTG | 10393 |
rs747341825 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144985869 | TGCCCATTCAGTATG[A/T]TACTGGCTGTGGGTT | 10393 |
rs747417617 | in-del | -/TTCACTG | 3.33431e-05 | 0.00408294 | frameshift-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:145064675 | TAAATACATAATGTC[-/TTCACTG]TTGTTTTTCTTCTAA | 10393 |
rs747429954 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145080675 | GCACTTTGGGAGGCC[A/G]AGGCGGGTTGAATCA | 10393 |
rs747432070 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145094657 | TCAAGCTAAAGAAAT[G/T]TCTCCAAGCTTGAGT | 10393 |
rs747441857 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145000658 | CTGCTCAGAGATCTA[C/G]AACTAGAAATACTAT | 10393 |
rs747478225 | in-del | -/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145002329 | GAAGAAAGACAGACT[-/C]CCAACTCAAAAGGCT | 10393 |
rs747479844 | in-del | -/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145059862 | ATGATAAAAAAAAAA[-/T]CTCACACATTATTTT | 10393 |
rs747500967 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145074760 | TCTGACAGGTAGCAA[C/G]TATTACTATCAAGCA | 10393 |
rs747542013 | in-del | -/CTAGAGAC | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145015549 | AACTTCCTGGCCTTG[-/CTAGAGAC]CTAGAGACCTACACA | 10393 |
rs747548251 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144969708 | AACTTACTCTCTGAC[A/G]TCTTTGGGATGAAAA | 10393 |
rs747549560 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145068721 | TCGAGACCATCCTGG[C/G]CAACATGGTGAAATC | 10393 |
rs747552050 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145058155 | TTACATCACAATATA[C/T]GTGTTGAATGAATAA | 10393 |
rs747572023 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145015623 | AAAAAGATCATCACC[C/T]AGGCACACTGTCATC | 10393 |
rs747600723 | in-del | -/GGAT | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145094557 | GAGGCTTGGTTGAGA[-/GGAT]GGATACAGGAGTCAT | 10393 |
rs747606011 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145001527 | ATGAAGAGTTTTGAC[A/G]ATGTATAGTTCTTAA | 10393 |
rs747614417 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144995643 | TATGCTTTTATTCAA[C/T]AAATATAATTTATAA | 10393 |
rs747614455 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145012210 | TACACACACACATAT[A/G]TATACATATATATAA | 10393 |
rs747625162 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054829 | TATTGTTCTTTCTCC[G/T]TGTTATGTATCTACC | 10393 |
rs747667689 | in-del | -/AG | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144998581 | AATGAGAACAAAGAC[-/AG]ACAACATACCAGAAT | 10393 |
rs747669938 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145094220 | CACAAGTGAATTATG[C/T]TAAATGAAAGACACT | 10393 |
rs747831942 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145045023 | CTACTTTTGCTTATA[C/T]GTTTATACAACTAAA | 10393 |
rs747860418 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145067030 | GTACCCACAGAAATC[A/G]TACGTATAATTTGCT | 10393 |
rs747879037 | in-del | -/A | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145071925 | ACAAATGGCAATTAC[-/A]GACTTTCCTTCTTTT | 10393 |
rs747881365 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145029317 | TGATCTGAGGTAGCT[G/T]CCAGGCAAGAAAATG | 10393 |
rs747949347 | snp | A/T | | | downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:144966675 | AACCATTAAAAATGT[A/T]TCCCCAATTGGGCTC | 10393 |
rs747972626 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144981251 | CTTTGGGCAGTATGG[C/T]CATTTTCACAATATT | 10393 |
rs747993342 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145089625 | CTAAGCTGAATCTAC[G/T]AAACACATTCCAACT | 10393 |
rs747999007 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145060481 | AATAAGGCAGCTATA[C/T]GCTTTTCTCAACTTA | 10393 |
rs748039842 | in-del | -/AAG | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145009764 | GACATAGGCATGGGC[-/AAG]GACTTCATGTCTAAA | 10393 |
rs748045184 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145077387 | CCATGAAAATTTCCC[C/T]GATCTCGCTAAGGAG | 10393 |
rs748055905 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145040843 | ATGCTATAAAGAGAT[A/G]TGGAACTTTGAAGGG | 10393 |
rs748081378 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145036044 | TGGTAACCAACATTT[G/T]AAAAATTAAGAAACA | 10393 |
rs748115885 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145031202 | TTCGAAGAGACCTTG[A/T]TCACTTTTCCCTTCC | 10393 |
rs748131188 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145090496 | CTTCCATGATCGTTT[C/G]AAGCAAAGTAAATCA | 10393 |
rs748132806 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145037160 | TCCATGAGGTTTAGT[A/T]TTTTCCAAGTCCTTC | 10393 |
rs748147744 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144996936 | ACGAGAACTATGTGA[C/T]GCATGCACAAGCTTC | 10393 |
rs748170675 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145048598 | GTAGTTGACAGCGCT[A/G]ACATATTTCTCCCCC | 10393 |
rs748172940 | in-del | -/AA | 1.65796e-05 | 0.00287916 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081762 | AATCCTAAAAACACC[-/AA]AAGTGTCAATAAATC | 10393 |
rs748207251 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144976175 | AAGGGTAAATATATG[A/C]AATAGTAAATGAACA | 10393 |
rs748295391 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145010486 | CACCATGGAATACTA[G/T]GCAGCCATAAAAAAG | 10393 |
rs748296089 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145085367 | TTCCCTAGTAAAGGA[A/T]AACTAAATCACGATT | 10393 |
rs748322115 | snp | C/T | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | ABCE1, ANAPC10 | GRCh38.p7 | 4:145097399 | CACTTCAATACTGGA[C/T]CGTGAACAATATGTA | 10393 |
rs748345170 | in-del | -/TAT | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145045153 | GCTTAAGTTGTAAAA[-/TAT]TATTTATTTTTTTAA | 10393 |
rs748352138 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145061977 | CTGAGGCAGGAGAAT[A/C]ACTTGAACCTGGGAG | 10393 |
rs748391594 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145056508 | GCTTTCACTTTATGG[A/C]TTTGCCCTGAATTCC | 10393 |
rs748397159 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145047385 | AACTCTGCGTTCAAT[A/G]GCGAGTACAATATGA | 10393 |
rs748420594 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145019931 | ACAAGCAACAAGATT[C/G]AAATGGTAATTTAAA | 10393 |
rs748458276 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144990604 | GAGAGGGATTTGGTG[C/T]CACACTCTTTTAAAA | 10393 |
rs748459625 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145035433 | TCAAGACAAGCAGGC[A/G]CTTTTATAGATCATA | 10393 |
rs748499295 | snp | A/G | 5.10391e-05 | 0.00505143 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145064524 | TGACTATCTTCTAAT[A/G]AGTAAAAGTTAAAGG | 10393 |
rs748508127 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145092223 | GCATGCTGGGCTTAA[C/T]ACTTATGTGATAAGT | 10393 |
rs748523246 | in-del | -/ATGAG | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145039477 | GATTTTTCCTTTTCT[-/ATGAG]ATAATAATAAATAAC | 10393 |
rs748582571 | snp | C/T | | | intron-variant, downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:145032925 | GCCAAGACTACCAAC[C/T]GTGGACTCACAGAAT | 10393 |
rs748629001 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144999979 | ATTTAATAAATGGTG[C/T]TGGGAAAACTGGCTA | 10393 |
rs748633453 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145086303 | GAACTAAAACAAAGA[C/T]GTATCTATGATAACT | 10393 |
rs748643192 | snp | A/G | 1.6593e-05 | 0.00288031 | synonymous-codon, utr-variant-3-prime, missense, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995568 | GTCAGTTAAGGGAAC[A/G]TGAATCCAGCCACTT | 10393 |
rs748680743 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145032275 | AGTGGGCAGAACTTC[A/G]AGCAGTGCACCTGAT | 10393 |
rs748686283 | in-del | -/TA | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145034525 | ACAAACTCTCCTTTA[-/TA]TATATATATATATAT | 10393 |
rs748724417 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144977300 | CACAGATAATTTATA[C/T]ACGACAAATATTAAC | 10393 |
rs748738061 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145018219 | AAAAACCAAAAAATC[A/G]AGGTATACAGGCAAC | 10393 |
rs748744901 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145028128 | AACTTAATTGGATTG[G/T]GGGATACAAAGTATT | 10393 |
rs748745055 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145007265 | GGATATTCAGGACTT[G/T]AACTCAGCTATGCAC | 10393 |
rs748791552 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145091087 | AGCTCAAAATCACAT[C/G]AAGTAAGACATATGA | 10393 |
rs748838277 | snp | C/T | 3.31741e-05 | 0.00407259 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995405 | ACATCATGAAATCTA[C/T]AGTTGTACATCTAGG | 10393 |
rs748884165 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145041366 | CATGAATAATCATCA[C/T]TTTGAGAAAAATGTT | 10393 |
rs748891663 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145065510 | AACTTCTGAGAATGC[A/G]TTAAAATACAGTAAC | 10393 |
rs748976543 | snp | A/G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144982957 | CGAGGTCAGGAGTTC[A/G/T]AGACCATCCTGGCTA | 10393 |
rs748982138 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145026242 | TGAATGTCCTCAATT[C/T]AACATTTATTGATTG | 10393 |
rs748983418 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145080564 | TTGCTGATTTGTACT[C/T]TAGGACAATAAAAGC | 10393 |
rs749013519 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144985569 | TAATATATTAATTTC[C/T]ACTAAATTACTAGTC | 10393 |
rs749034185 | snp | A/C | 3.31488e-05 | 0.00407103 | missense, nc-transcript-variant | ANAPC10 | GRCh38.p7 | 4:145081748 | ACTGATCCACTCCAA[A/C]TCCTAAAAACACCAA | 10393 |
rs749038027 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145035974 | TGGAACTGAGAGTTA[C/T]GTATTGCTGTTTCAA | 10393 |
rs749088913 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144981053 | CTGTTTTGGTTACTG[C/T]AGCCTTGTAGTATAG | 10393 |
rs749128438 | snp | C/G | | | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145100513 | TTGTAGAAAGGCATT[C/G]AGTATTTAAATTAGA | 10393 |
rs749136151 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145089548 | CTTTTGTTTTTCCAG[C/T]CTCTTAGGTAGAGAC | 10393 |
rs749138393 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145075128 | GGTCTTCATAGATTC[C/T]GTGCTTACCTTATTG | 10393 |
rs749155389 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145066619 | GGCAAGTTTAGAAAA[A/G]CAAAGAATACTAAAA | 10393 |
rs749159901 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145014954 | GCCTTCAGCCCTAGA[A/C]CTTCCCTCTGACAGA | 10393 |
rs749195391 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145076605 | ACCGGATTGAAATGA[A/C]AGAAATGACAGACAT | 10393 |
rs749226072 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145088079 | AGAGAAATGAAGAAT[C/T]AACTAACTTCCTGAA | 10393 |
rs749241858 | snp | C/T | | | synonymous-codon, utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995541 | GAATGTACGAGTTGG[C/T]TTCTTATGATTGTCA | 10393 |
rs749262511 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145045863 | CTTTGCAAAGAAGAA[C/T]TTTTAAAATAAGTTG | 10393 |
rs749286891 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145004278 | AGGTCTAGCATCATA[A/T]CATCTGCAAACAGTG | 10393 |
rs749297537 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145061788 | ATGTATCAGATATGT[C/G]ACTAAAAGAAGGGCT | 10393 |
rs749333004 | snp | A/G | | | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145100468 | ATTTATCCCCTGGAG[A/G]GGAATTCATTATGCT | 10393 |
rs749383240 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144990429 | AATAAATACTTGAGA[C/G]TGGGTAATTTATAAA | 10393 |
rs749436030 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145005485 | TCTGATTTTGGTTAC[A/T]TCTTGTATTCTGCTA | 10393 |
rs749451108 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081824 | AACATAAAATTAACA[C/T]ATGTATTTGTCCAGA | 10393 |
rs749492628 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145060334 | AAATACACATTCTAG[A/G]GTATTAAAGGAAGGG | 10393 |
rs749498395 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144975532 | ACATACATATATGTT[G/T]TGAAATGATTACCAC | 10393 |
rs749519025 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145022449 | TATTCTCACTGATAT[A/G]TGGGAGCTAAGCTAT | 10393 |
rs749524575 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145021296 | TAAGGACATAGTCAC[C/G]AAAACAGCATGGTAC | 10393 |
rs749628625 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145079308 | TGGAGAAATACAAAT[C/G]AAAACCACAATGAGA | 10393 |
rs749629061 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145070468 | ATCAAAACTATAATG[A/T]GACAGACTCATTAGG | 10393 |
rs749677506 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144975860 | TAAAACTACAAAAAG[C/T]TAATATTATACTCAC | 10393 |
rs749682400 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145070427 | GAAAAAAATGCTTGA[C/T]AGCACAAAACATTAG | 10393 |
rs749729135 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145068131 | TACCACTCCTGGACT[A/G]CCAGGCTCCTCTTAC | 10393 |
rs749760745 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145083248 | ATCTAATATTTATTA[A/G]CTCATATAACAACAT | 10393 |
rs749768418 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145085093 | CCAGCCTGTGCAACA[C/T]AGTGAGACACTGTCT | 10393 |
rs749794176 | snp | A/G | 1.69812e-05 | 0.00291382 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145064538 | TGAGTAAAAGTTAAA[A/G]GATGACATATTTTTA | 10393 |
rs749802756 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145029680 | TGGTTAGCTGAAATA[C/T]GGATTAAAAAATGGC | 10393 |
rs749813688 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145069004 | CAAAGACCATGTTTT[G/T]AAAGGATATATGAGA | 10393 |
rs749816535 | snp | A/T | | | downstream-variant-500B, utr-variant-3-prime, intron-variant | ANAPC10 | GRCh38.p7 | 4:144994179 | TTTTGGCTACAGACT[A/T]TTTGGTGATCCCACA | 10393 |
rs749856017 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145031069 | AAATGCCTTTTTCTC[C/T]ATTCCTGTCCATAAG | 10393 |
rs749858654 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144991579 | AGATGGGGTTTCACC[A/T]TGTTAGCAGGATGGT | 10393 |
rs749902571 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144967956 | TGTGAAATTCTGAAG[G/T]CAAAACAAAACATCT | 10393 |
rs749907563 | snp | C/T | 1.65718e-05 | 0.00287848 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995520 | TAGAACAGCAATCTG[C/T]ATCATGAATGTACGA | 10393 |
rs749914515 | snp | A/C | 0.000430107 | 0.0146584 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144999330 | AAAGAGAATTTTAGA[A/C]CAATATGTTTCAGGA | 10393 |
rs749917324 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145020524 | GAGAACTGGAACAAA[A/T]CAAGGATGCCCACTC | 10393 |
rs749955445 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145093182 | AGCACAGGAAAACTG[C/G]AGTGGAACTATTATA | 10393 |
rs749959899 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144981265 | GCCATTTTCACAATA[C/T]TACTTATTCTTATTC | 10393 |
rs750015564 | in-del | -/A | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145022798 | AAAAACTGCCAAACC[-/A]AAAAAAAAAAAAAAA | 10393 |
rs750017992 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145070305 | CAGCAGGACATATAA[A/G]GAAGTCTTACAGCTT | 10393 |
rs750027962 | in-del | -/TA | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145034575 | GTGTGTGTGTGTGTG[-/TA]TATATATCCCACATA | 10393 |
rs750071183 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145073723 | TCTCTTTAAAATGAA[G/T]CAAACCAGCACAACT | 10393 |
rs750078346 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145087205 | AGACTAGGGTTGTTC[A/G]TTAAGCAGCATTAGT | 10393 |
rs750137229 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144978889 | TAGATACAGTAAGAA[A/T]TGCTAGAGTGTCCTT | 10393 |
rs750147203 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144973058 | TTACAGCCTTTAAGT[A/G]TATATTTTAGAAAAG | 10393 |
rs750176558 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145082568 | CTAATAAGTTCAATA[C/T]GCCATGCTTACTGAG | 10393 |
rs750180528 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145093522 | CCCAGTTGTTGGAAC[C/T]ACCAGACAGGAATCT | 10393 |
rs750182221 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145028886 | ACTCAGGGATTCTAA[C/T]TCCTGGCTTCAGAAG | 10393 |
rs750248503 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144971868 | TACTATGTATCAGGT[A/G]CTATTGTCCTAAGTG | 10393 |
rs750266001 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144999090 | GAATCCCTGAATAGA[C/G]CAATAACAGGCTCTG | 10393 |
rs750305501 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145090498 | TCCATGATCGTTTCA[A/G]GCAAAGTAAATCACT | 10393 |
rs750335001 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144968044 | GAGTAGGACTTAGAT[A/T]AGACCACATGTAAAC | 10393 |
rs750367027 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145059446 | ATCACTTGGTAACAG[A/C]TTTATTATCTGAAGA | 10393 |
rs750403742 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081149 | AATACATTCAAAGCA[C/T]TGAAAAACATGTGGC | 10393 |
rs750413295 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145044272 | CTTTCAGAAAAGAGC[C/T]CAATGCAACAATGAC | 10393 |
rs750440669 | snp | A/C | 4.98923e-05 | 0.00499436 | missense, intron-variant | ANAPC10 | GRCh38.p7 | 4:145064607 | GAAAATTATTTCCTA[A/C]TCTGACTGAGATCTT | 10393 |
rs750450406 | in-del | -/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145024861 | TCTCTAGCTATGGAA[-/G]TCGTAGTTGGCATCT | 10393 |
rs750470289 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145036564 | ATGTTGTCCAAGCTG[C/G]CCTTGAACTCCTGGG | 10393 |
rs750494788 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144996798 | CTTCTCCGAGCTAAA[C/G]GAGGATATTCGAACC | 10393 |
rs750499870 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144982091 | CCTGGTGATCCATTT[C/G]CCTCGGCCTCCCAAA | 10393 |
rs750510655 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145022325 | TACATGGTGGGATAC[C/T]ACTCAGCCATAAAAA | 10393 |
rs750518191 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144992276 | CCATTCTGTAGCCCA[A/T]GAACCAAGCAGTCAT | 10393 |
rs750552997 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144980925 | ACCCTTTCCCCATTG[C/T]TTGTTTTCATCAGGT | 10393 |
rs750566066 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145090170 | ACGAAATCCACTGAT[A/G]CACAAGTCCCTTATT | 10393 |
rs750573161 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145027222 | TTGGCCAGGCTAGTC[G/T]TGAACTCTTCACCTC | 10393 |
rs750595008 | in-del | -/A | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144996729 | CAAAGCTGGACGGAG[-/A]AATGACTTTGACGAG | 10393 |
rs750635268 | in-del | -/CTAA | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145002868 | GCTAAATATCTTTTT[-/CTAA]CTTTTATTTTAGGTT | 10393 |
rs750648661 | in-del | -/TGTGTG | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145040132 | TAGTGTGTGTGTATG[-/TGTGTG]TGTGTGTGTGTGTGT | 10393 |
rs750653563 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145089200 | TAACTCAAAGGCCAT[A/T]ATTGTCAGTTATAGC | 10393 |
rs750680367 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145043942 | AAGCTGATATATTGC[A/T]TTGGGAAGTTCTTTA | 10393 |
rs750695036 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145053020 | TATTATTATTTTAGC[C/T]AAGTGTGCCAGGCAA | 10393 |
rs750713970 | snp | C/G | 1.66529e-05 | 0.00288551 | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145096124 | ATTCTATGTAGAAAA[C/G]AAGAATGCACACATT | 10393 |
rs750723395 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145013175 | GAATTTCTTTACAGC[A/C]ATCTAAGAACAGAAT | 10393 |
rs750760998 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145047053 | GATGTTTTTACACTG[C/T]TTATCTAATTTTCAC | 10393 |
rs750806920 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145006530 | TTGAATTTCACTTCT[A/G]ATCAGGAATTGAAGC | 10393 |
rs750851445 | in-del | -/TAAA | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145083227 | ACATTTTATATATGT[-/TAAA]TAATCTAATATTTAT | 10393 |
rs750870702 | snp | A/C | | | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145097223 | CACAAAAATAAGAAA[A/C]AAATGTTAAAAGTTC | 10393 |
rs750970998 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145012404 | TGACTATGATTAACA[C/T]GCTTAAGAAATGAGG | 10393 |
rs750986340 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145004194 | TACACTGGTTTTGTA[A/T]CTGAAACTTTGTTGA | 10393 |
rs750990106 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145023559 | TTTCAACCAGTTTGC[A/G]ATAAAGCAAGTCACA | 10393 |
rs750993798 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145015471 | CTTAAGAATAATCGG[C/T]GTTCCTGAAGAAGAA | 10393 |
rs750994895 | snp | A/C | 1.65608e-05 | 0.00287752 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145095957 | CAAGTGACTATTTCC[A/C]ACAGCTTTTTTGTTT | 10393 |
rs751002613 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145071541 | ATTGAATTTTATTAT[G/T]CACCATCTCAACAGA | 10393 |
rs751074331 | snp | C/T | 1.66557e-05 | 0.00288575 | missense, intron-variant | ANAPC10 | GRCh38.p7 | 4:145064658 | CAGATTTGTAGTCTG[C/T]ATAAATACATAATGT | 10393 |
rs751076494 | snp | C/T | | | intron-variant, downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:145032947 | TCACAGAATGCCTTA[C/T]CCATTGTCATGGTAT | 10393 |
rs751105349 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144978106 | ATATACCTCTACATA[A/C]ATAAATTTCTATCTT | 10393 |
rs751137240 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145098228 | TGACGTCATATCTCC[C/G]TACCTACCTCCAGGG | 10393 |
rs751162628 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145009447 | ATACTAAAACCAAAA[C/G]AGCATGGTGCTGGTA | 10393 |
rs751164190 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144974475 | TTAATACCTTACTGC[A/G]GGGCCTAGCGAGTAC | 10393 |
rs751232197 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145027848 | ATGTGGAGGATGTAG[G/T]CCACCAATAAAGGAA | 10393 |
rs751238558 | in-del | -/AAT | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145070049 | ATTTCTAAAATAGTA[-/AAT]AATGAGATACATATA | 10393 |
rs751266024 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145042756 | ATGATGTGTGAACAG[C/T]AGACACTGATGTTCA | 10393 |
rs751309537 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145031892 | CAACCTGAACTGACT[A/G]TCATGAACTGGGCGC | 10393 |
rs751322400 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144969806 | AATTAAAGATGTGGT[A/G]CTGTTTGCATTATGG | 10393 |
rs751322608 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145025892 | TTACCTGCCCCCAGT[A/G]TGAGCAGGCAGTTGA | 10393 |
rs751337099 | in-del | -/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145041449 | ACCGTTTTTGTTCTA[-/T]TTCACAAGTACCAAC | 10393 |
rs751387570 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144987750 | GAGCTCACGACTTTC[C/T]AATTTCTGGCTTGAT | 10393 |
rs751467968 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144979966 | ATTCAAATGTTTAGC[C/G]AACCGAGATTAGTTT | 10393 |
rs751489309 | in-del | -/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081244 | AAAAAAAAAAAAAAA[-/T]TTTCCAAATAAAAGT | 10393 |
rs751544256 | snp | C/T | 1.65603e-05 | 0.00287747 | synonymous-codon, intron-variant | ANAPC10 | GRCh38.p7 | 4:145095998 | ACCTGGTTTGCAAGA[C/T]GAGAGTGACCAAACA | 10393 |
rs751557670 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145040942 | TTAATATGCACAGAA[A/T]TAATGCATGACAATG | 10393 |
rs751562278 | in-del | -/TA | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145082156 | TCTTCTAGGAGATAT[-/TA]TATTTTTTTGAGACA | 10393 |
rs751577522 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144985110 | CATCTCCCTCTCTCC[A/G]AGGCTTTCTGGATAA | 10393 |
rs751583134 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144999822 | ACACGGCTACAGTAA[A/C]CTAAACAGCATGGTA | 10393 |
rs751599417 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145051562 | AAAGTGCAATAAGGT[C/G]AAAAGCATAAAATGA | 10393 |
rs751630216 | in-del | -/A | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145017869 | AACTATCTCAAGGAT[-/A]AAAAAACCAAACACC | 10393 |
rs751644049 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145022600 | ACCCAAATCACCACT[A/G]AAGAACTTACACATG | 10393 |
rs751651295 | in-del | -/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145091877 | AATGTCCTTTGCAGG[-/G]ACTTGGACAAAAGAC | 10393 |
rs751664837 | snp | C/T | 1.67116e-05 | 0.0028906 | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145096143 | AATGCACACATTGTA[C/T]CAGGAACTGGGCATC | 10393 |
rs751720144 | snp | C/G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145064974 | AAGCCAAATTAGGTA[C/G/T]TTTATCATGCAAACA | 10393 |
rs751729861 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145087825 | GCTGAGGTGGGCGGA[C/T]CACTTGAGGTCAAGA | 10393 |
rs751799758 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145071848 | AAAAGCATCCATAAG[A/G]TAATAGTCAGCTTTA | 10393 |
rs751810007 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144987460 | TGAGAACACATGGAC[A/G]CAAGAAGGGGAACAT | 10393 |
rs751810413 | in-del | -/TAAAG | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145043022 | AGGGGAAAAAAGAAA[-/TAAAG]TAATGTTCCAAAGGT | 10393 |
rs751821003 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081051 | TGAGGTGGGAGGAAT[A/G]CTTGAGGCCAGGAGT | 10393 |
rs751822061 | snp | C/G | | | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145100174 | TCAGTTTATTAACCA[C/G]TTCTGGTATGTTTTT | 10393 |
rs751835993 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144971658 | TAGCATGATATTCAT[A/G]TCTGTTAATTAACTT | 10393 |
rs751838191 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145066153 | AGCAGGGGCTCTGTA[C/G]CTCTTAGTAAGGAGA | 10393 |
rs751882699 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145022162 | CAATACTGGGTATCT[A/C]CCCAGAGTAAATGAA | 10393 |
rs751916722 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145059729 | TTTTAAAAACAACAA[C/T]AACTAGTTAGCAAAC | 10393 |
rs751958778 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145010716 | CATTAGGAGATATAC[C/T]TAATGTAAATGACGA | 10393 |
rs751992536 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145089112 | ATGTAGCCTCCCACT[G/T]AAAGTTACTTTCTAT | 10393 |
rs752037929 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145075971 | GGGGGCCAGTCTGAT[C/T]TGAGCAACACTTTGT | 10393 |
rs752107237 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145030655 | TGCCAGAATGCATAA[C/T]TGGCATAGACATACT | 10393 |
rs752112134 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145036428 | AAAATTGGCTAACAT[A/G]GCTAACAGGATTGCT | 10393 |
rs752127787 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144990890 | ATGACTGCCTGAAGG[C/T]ATAAATATCTGTGAG | 10393 |
rs752133662 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144981274 | ACAATATTACTTATT[C/G]TTATTCATGAGTATA | 10393 |
rs752140754 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145084440 | ATTGGTGTGAAGCAG[A/G]AAATAAGCCAGACAT | 10393 |
rs752142311 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145089983 | ATAAAGTCTTCTATA[A/G]TCAGGCTTCTACCTA | 10393 |
rs752161588 | snp | C/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | ABCE1, ANAPC10 | GRCh38.p7 | 4:145098431 | CCAGGTACGTGAATA[C/G]CCCGGAGAGGTTTGG | 10393 |
rs752206743 | snp | A/G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145048087 | TAGGCTGCTAGAGTC[A/G/T]AATCAATTTTAGAAC | 10393 |
rs752221364 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144975208 | TCAGCAAATGGTAAT[A/G]AGTCAATTGACTATC | 10393 |
rs752240412 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144969053 | TACATACATGCATAC[A/G]TATATAGGGGGAGTT | 10393 |
rs752268468 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145062476 | GCTGGGCATGGTGGC[A/G]CATTCCTGTAATCCC | 10393 |
rs752288152 | in-del | -/TTAC | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145041309 | ACTGAACTAACTCTA[-/TTAC]TTACAGCTTAGATAG | 10393 |
rs752293823 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145003886 | GTGAACAATGTCATT[C/G]GTAATTTGATAGGTA | 10393 |
rs752295107 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144973639 | TGAGATTGATAAAGA[A/G]GAAAAAAGAGAAGTC | 10393 |
rs752299095 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145042205 | ACTCAGTAGCATAAG[A/G]GTAAAAATAAATGAT | 10393 |
rs752362780 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145005061 | ATCTTCCTTGTTCAA[C/T]CTTCAGAGATTATAT | 10393 |
rs752371902 | snp | C/T | | | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145097168 | GATCGTGCTACTGCA[C/T]TCCAGCCTGCGTAAC | 10393 |
rs752387023 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145056068 | TGAAACCAGAGCAAC[A/T]CCATCTTGAATACGA | 10393 |
rs752394727 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145061212 | CTTTTTCTATATGGC[C/T]AATGTTTCAGCACTT | 10393 |
rs752416580 | in-del | -/TTA | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144982782 | TAGTAGGGGTTTCTG[-/TTA]TTGATAGCTAAATGC | 10393 |
rs752455250 | snp | C/T | 1.65682e-05 | 0.00287817 | missense, nc-transcript-variant | ANAPC10 | GRCh38.p7 | 4:145081694 | AATGAGGCTGGGAAC[C/T]ATCTGATTGCCAATA | 10393 |
rs752463619 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144989783 | TAAGTACTACACTAG[C/T]GAACCCATGAATGAT | 10393 |
rs752463772 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144983019 | CAAAAACTTAGCCAG[A/G]CATGGTGGCAAGCAA | 10393 |
rs752481765 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145027746 | AATTATTTCCAAACT[A/G]GAATTCCATACCTAG | 10393 |
rs752504950 | snp | A/G | 1.65688e-05 | 0.00287821 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995498 | CTCTTCCATTCTGGT[A/G]ATTGGCTAGAACAGC | 10393 |
rs752515033 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144999397 | TACACCAATAACAGA[A/C]AAACAGAGAGCCAAA | 10393 |
rs752544180 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145040568 | TTTGTTGCAATCATC[C/T]CAACATCATATCTCC | 10393 |
rs752606723 | in-del | -/GTGTGC | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054637 | TGTGTGTGTGTGTGT[-/GTGTGC]GCGCGCGCGCGCGTG | 10393 |
rs752719408 | snp | C/T | | | intron-variant, utr-variant-3-prime | ANAPC10 | GRCh38.p7 | 4:145064130 | ATGCAAAATTGTGCA[C/T]AAATTTTATCTTAAA | 10393 |
rs752719429 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145014099 | CAGAACTCAGGGGAG[A/G]GCCCAAATCCAGCAT | 10393 |
rs752741327 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145015042 | CTCCTTAACACCCCC[C/T]AAAAAATCATATTGG | 10393 |
rs752781906 | snp | A/G | | | intron-variant, downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:145053666 | TTATGAAGGAGAAAT[A/G]GACACAGAAAAGTAT | 10393 |
rs752805572 | in-del | -/GT | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054642 | TGTGTGTGTGTGTGC[-/GT]GCGCGCGCGCGCGTG | 10393 |
rs752831443 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144969753 | TGACAAGCACACATG[A/C]CAAATGCCAAATGCC | 10393 |
rs752840479 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145008012 | AGGGGATATCACCAC[C/T]GATCCCACAGAAGTA | 10393 |
rs752841403 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144993172 | CTTTATTGTGATAGT[C/T]ACTTTACTGTGGTAT | 10393 |
rs752878480 | snp | G/T | | | utr-variant-5-prime, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145098365 | GGCTGAAAAGTGAAG[G/T]CAAGAGCTGATTTGG | 10393 |
rs752981048 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144984488 | CAGACGAATGCCAGC[A/G]TAAAAAGGAGAGCTA | 10393 |
rs752990778 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145016645 | CATATGGAACCAAAA[C/G]GGAGTCCACATTGCC | 10393 |
rs753022196 | snp | A/C | 1.69198e-05 | 0.00290854 | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145096155 | GTATCAGGAACTGGG[A/C]ATCTTTCTACAAAAG | 10393 |
rs753052403 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144986782 | CTAATATCCAGAATC[C/T]GCAATGAACTCCAAC | 10393 |
rs753064193 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145035239 | TCCTCCCTCACTGCT[C/T]TGTGTGCATCTCTCC | 10393 |
rs753114735 | snp | C/T | | | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145099852 | CTTCCTTTTTTCCTC[C/T]CAGCTGTAAGAATGA | 10393 |
rs753117596 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145020724 | AACTGACAAAAGAAT[A/T]CAGTAAAGTTTCCAG | 10393 |
rs753167430 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145076216 | TGTTGCCAGCACACT[A/G]GAAACACTGTGGCCC | 10393 |
rs753190495 | snp | A/G | | | intron-variant, synonymous-codon | ANAPC10 | GRCh38.p7 | 4:145033324 | TTCCCACGACATTAC[A/G]TTCTGCTGGCCTAGA | 10393 |
rs753197858 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145065722 | TAAAATAATCATGTA[C/T]ATATATAGTTACAGT | 10393 |
rs753215088 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144994657 | ACTGCCCAGGGAATG[C/T]TACAATGTCAGACAC | 10393 |
rs753235531 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145044632 | TTTCTATTATACTGA[C/G]AGGGTCAATTAGTCT | 10393 |
rs753253089 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145051456 | ATAGAAACAGGAATT[C/G]AGCACAAGCTGTTAA | 10393 |
rs753332008 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144999372 | TGTGCAAAAATCACA[A/C]GCATTCCTCTACACC | 10393 |
rs753347206 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145029205 | AGAGCTTCACCATCC[C/T]CAGTAGTGGCAACAT | 10393 |
rs753373422 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144988241 | CACCTTGGCCTCCCA[A/T]AGTGCTATTACAGCT | 10393 |
rs753373506 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145003809 | TCTTGTGTAAGATCA[G/T]CTTGGCTATTTAAGC | 10393 |
rs753411545 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145093898 | CTTAGAAAGATAATA[G/T]AGAAGCAATAGGGCA | 10393 |
rs753412622 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145095535 | CACCAGAAGCAGATG[C/T]TCCTCCTTCTGAAGT | 10393 |
rs753419836 | in-del | -/GTGTG | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054635 | TGTGTGTGTGTGTGT[-/GTGTG]TGCGCGCGCGCGCGC | 10393 |
rs753426424 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144989484 | CATATGTCCCTGACT[C/G]CTCCATCGACCAGCT | 10393 |
rs753454949 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145035027 | GTGGCGACTTTGTAA[C/T]GTGTCAACTCAAGCT | 10393 |
rs753476644 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145059579 | AAAGGACAACTTTCA[C/T]ATATGCTGAAAGTGT | 10393 |
rs753500684 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145094464 | CACCTAAAAAGGGTA[A/G]GTTTTATAGTATGTA | 10393 |
rs753520014 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145057981 | TATCTACCTGGTCTC[C/T]AGGTGCTCCAGCTCC | 10393 |
rs753595528 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144996844 | AAAAACCTTGAAAAA[A/G]GATTAGACGAATGGC | 10393 |
rs753608365 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145002532 | GTTAAGATTATATAG[C/T]TTAACTAGTCTTAAA | 10393 |
rs753633160 | snp | C/T | | | intron-variant, downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:145053513 | TATCTAATTACAAAG[C/T]AGGCAACAGATTCTA | 10393 |
rs753686189 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144968740 | ATCCACACATACCAT[C/G]AACATCAATAAGTAT | 10393 |
rs753722675 | snp | C/T | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant, synonymous-codon | ABCE1, ANAPC10 | GRCh38.p7 | 4:145098174 | GGCACCTCCAGCAGC[C/T]GGCTTCGCCAACGGC | 10393 |
rs753774593 | snp | A/G | 1.65696e-05 | 0.00287828 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995511 | GTGATTGGCTAGAAC[A/G]GCAATCTGTATCATG | 10393 |
rs753790805 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145082642 | ATTCTGAAGCCAAAT[A/G]CTTCTGATTAAAATT | 10393 |
rs753829448 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145030516 | AAGAGTCATTTCGGT[A/C]CTCCAGTTAAAGCAG | 10393 |
rs753831185 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145011779 | CACATTCTGAAGTTG[C/G]CTAGGATAGGTTGCT | 10393 |
rs753847513 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145078754 | TGATCTTCAACAAAG[C/T]TGGCAATAACAAGCA | 10393 |
rs753849810 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145050294 | TTTTTCTCTGAGCAG[C/T]AGGTCTTTACAGTGG | 10393 |
rs753873095 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145025217 | CATATTAGCAATAAG[C/G]CTGTTTTGCTTTCTT | 10393 |
rs753874774 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144973401 | GAAGAACCACCTATT[C/G]AGTATTATGTTTATG | 10393 |
rs753911631 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145023898 | TCTGTAGCATGCAAT[A/G]CTGTTTAGTAGTATT | 10393 |
rs753922075 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145086070 | CGTAAGAGTGAAGAC[C/T]TGCCTCAGCCTCCCC | 10393 |
rs753926918 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145040349 | GACGGGGTTTCTCCA[C/T]GTTGGTCAGGCTGGT | 10393 |
rs753928478 | in-del | -/AC | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145042698 | CACTACACTCAGAAA[-/AC]ACAGAGTCTTTATTC | 10393 |
rs753932791 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144967503 | GCATGGATGTTCTTC[A/G]TAAACAATAAAATAT | 10393 |
rs753969268 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144982940 | CCAAGGAGGGTAGAC[C/T]ACGAGGTCAGGAGTT | 10393 |
rs753975837 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145090354 | TTTCAACCCTCAGTT[A/G]GTTGAATCCATGAAA | 10393 |
rs754022129 | snp | A/G | | | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995534 | GTATCATGAATGTAC[A/G]AGTTGGCTTCTTATG | 10393 |
rs754077724 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145077016 | CATTCTGGCTGAAAC[A/G]GTGAAACCCTGTCTC | 10393 |
rs754081873 | in-del | -/AG | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145009974 | TTAAACAAATTTACA[-/AG]AGAAAAAATCAAACA | 10393 |
rs754105326 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145031934 | TCTAACTATAAAGTG[C/G]GTTGTGCACAGCAGC | 10393 |
rs754111989 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054786 | AGTAAATGAAGACTA[C/T]AAGAGACCCCAGCCA | 10393 |
rs754112771 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145091294 | TATTGTGATAGTAAT[A/G]AGGTACGATTCAGTG | 10393 |
rs754186405 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145049901 | ATCTTGCTGTTTCCA[C/T]TACATCTGCAGTTAC | 10393 |
rs754230717 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime, intron-variant | ANAPC10 | GRCh38.p7 | 4:144994519 | CATCTAGAGAAAACA[A/G]CATACAAAATCAAAT | 10393 |
rs754231259 | snp | C/T | | | intron-variant, downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:145033020 | GCAGTGGGCACATGC[C/T]CATGGAATTCACTGG | 10393 |
rs754255416 | in-del | -/AGTTTATTATA | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145002902 | CAGAGGCACACGTGC[-/AGTTTATTATA]AAGGTAAATTGCATA | 10393 |
rs754290286 | in-del | -/A | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145091384 | CATTACTGACACAAT[-/A]ATGGCACCAGTCTAG | 10393 |
rs754314453 | in-del | -/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144983834 | TGATATCAATAATTA[-/C]AGAATGCCATAGGAT | 10393 |
rs754320272 | snp | C/T | | | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145099574 | TTGTTGGAAGAGCAT[C/T]TAACAATTGGGAGAG | 10393 |
rs754327067 | snp | A/G | | | intron-variant, downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:145063094 | CAAGAGATCCAGTAT[A/G]TAACAGTGACTACAT | 10393 |
rs754369024 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145006755 | GAACCTTCTTAGCCT[G/T]TTTTCTGTCAGTATT | 10393 |
rs754376797 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144983943 | AATGATGTGAAAGGG[A/G]TGAAACTAAAAGTGA | 10393 |
rs754386228 | snp | A/G | | | intron-variant, utr-variant-3-prime | ANAPC10 | GRCh38.p7 | 4:145063923 | GCAATATGGATCTAT[A/G]ATAAAAAATCAATCA | 10393 |
rs754408003 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145098275 | ATGTCGCGCGCGCGC[A/G]CTACGTCCTATGGCT | 10393 |
rs754452493 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144999868 | AGATATAGACCAATG[C/G]AACAGAACAGAGGCC | 10393 |
rs754472209 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145095570 | TCAGAAGGTTAATAG[C/T]AGCCTAACACTACAT | 10393 |
rs754489353 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145082712 | CTCCATCCATTCTAC[A/G]TAAATGAAGTTGTAC | 10393 |
rs754495302 | snp | C/T | 1.65836e-05 | 0.0028795 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081767 | TAAAAACACCAAAAG[C/T]GTCAATAAATCCCTG | 10393 |
rs754507833 | in-del | -/GATAGATA | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144980531 | ATAGATAGATAGATC[-/GATAGATA]GATAGATAGATAGAT | 10393 |
rs754544543 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145043322 | AAAATACATAGTACT[A/G]TATTAAAACAATAAG | 10393 |
rs754546170 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145029220 | CCAGTAGTGGCAACA[A/T]CCCCTCCCCGACCCA | 10393 |
rs754553782 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145066756 | TCAAATAGGAACTTT[A/T]ATTTCTTCATTTTTC | 10393 |
rs754558448 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145094494 | AAATTATACCTCAAG[A/G]AAGTGCTCATAGAAA | 10393 |
rs754570947 | in-del | -/GTGTGTGC | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054635 | TGTGTGTGTGTGTGT[-/GTGTGTGC]GCGCGCGCGCGCGTG | 10393 |
rs754571258 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145002602 | ACTAGATAGAGTGTT[C/G]TACTCATCTGCATGA | 10393 |
rs754595030 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144969007 | ATATTATGTAGAAGA[A/G]ATGATAGAAAGATAG | 10393 |
rs754604368 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145008143 | taaaccaggaagaag[C/T]tgaatccctcaatag | 10393 |
rs754670337 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145044862 | CCCAAATTGGTGGTA[C/T]ATTATTTGATATAAA | 10393 |
rs754675535 | in-del | -/AAAAT | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145009097 | ACAACTGCTACAAAG[-/AAAAT]AAAATACCTAGGAAT | 10393 |
rs754700610 | snp | C/T | 1.66715e-05 | 0.00288712 | missense, intron-variant | ANAPC10 | GRCh38.p7 | 4:145064673 | CATAAATACATAATG[C/T]CTTCACTGTTGTTTT | 10393 |
rs754707714 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144996856 | AAAAGATTAGACGAA[C/T]GGCTAACTAGAATAA | 10393 |
rs754714657 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144988403 | CCAATACTCAAAAGC[A/C]CTGACTGACTGCAAA | 10393 |
rs754826554 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145068633 | GTGAAAAATGGGGGC[C/T]GGGTGCAGTGGCACA | 10393 |
rs754831670 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145090387 | AGAACCTACAGATAT[A/G]GAAGGCTAACTGTCC | 10393 |
rs754851997 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145018256 | CATGATGAATGGAAT[A/G]GTACCTCACATCTCA | 10393 |
rs754853030 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145080072 | TGAACAGAGATCACG[C/T]CACTGCGCTCCAGCC | 10393 |
rs754874168 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145036962 | AGGAACTGAGATACT[A/C]ATAATGTTCTATTTC | 10393 |
rs754904746 | in-del | -/TCT | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144978567 | GGCTCATGCCTGTAA[-/TCT]CAACTACTTAGGAGG | 10393 |
rs754951565 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145069849 | GACTCCAGCTATTTT[C/T]TGTGAACCAAAAAGG | 10393 |
rs754963106 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144988904 | TGGCACATATCAATC[A/G]TTCATTTTTATTGCT | 10393 |
rs754967157 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144973427 | TTATGTCCTGGGTGA[C/T]GGAATCACTAGGAGC | 10393 |
rs755041919 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145061860 | AACCTGTAATCTCAG[A/C]ACTTTGGGAGGCCGA | 10393 |
rs755082990 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145050812 | TGAAGAGAATTAGGA[C/T]CATACTGTGGATTAG | 10393 |
rs755097430 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145091328 | GTTTACCAAGGAAGG[C/T]AAACTTTACCAAAGG | 10393 |
rs755128768 | snp | C/T | | | upstream-variant-2KB, intron-variant, synonymous-codon | ABCE1, ANAPC10 | GRCh38.p7 | 4:145097314 | TGAATAACTGGCCCA[C/T]TCTAAAAAGGTTGAC | 10393 |
rs755150807 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144979828 | TGCCATAGTACCAGG[A/C]ATTATCAGTACCAGC | 10393 |
rs755175055 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145023909 | CAATGCTGTTTAGTA[A/G]TATTTTACTTAAGGC | 10393 |
rs755191192 | in-del | -/AAGAG | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145013415 | TTGTTAATAGTAGAA[-/AAGAG]AAAACTCATACTGTC | 10393 |
rs755201680 | in-del | -/A | | | intron-variant, downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:145053596 | AATTTCAAATACAAG[-/A]GGAAAGATTCCCAAA | 10393 |
rs755218478 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145038264 | ATGTCTATAATCCTC[A/G]CACTTTGGGAGGCCA | 10393 |
rs755237352 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144982203 | GCTAAGTGCTTACAG[C/T]TGTTATCTCACTCAG | 10393 |
rs755241784 | snp | A/T | 1.65603e-05 | 0.00287747 | missense, intron-variant | ANAPC10 | GRCh38.p7 | 4:145096002 | GGTTTGCAAGATGAG[A/T]GTGACCAAACAGCTT | 10393 |
rs755246209 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145010177 | GTCAGGAAACCCCAG[C/G]TGCTGGAGGGGATGT | 10393 |
rs755336009 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144979145 | GGGTACCTGTGCAGG[A/T]TGTGGAGGTTTGTTA | 10393 |
rs755380407 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145086259 | TGAGCCACCGTGTCC[C/G]GCCCTGAATTGTTTT | 10393 |
rs755387301 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144976997 | TTTCAAAAACTCAAA[A/T]TTTTTTTTTAACTCA | 10393 |
rs755412343 | in-del | -/A | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145092812 | CTACTGTAGGAGGAG[-/A]ATCAACCCTGTTGAC | 10393 |
rs755428606 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145035174 | TCTGTCACCCCACTA[A/G]TCACCAGAGTTGATT | 10393 |
rs755431439 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145087220 | GTTAAGCAGCATTAG[C/T]GGAGCAAGAGCACTA | 10393 |
rs755468564 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145048522 | AAGGGTCATCATTAA[A/G]TCTACTTAATCACAT | 10393 |
rs755493311 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145006759 | CTTCTTAGCCTTTTT[C/T]CTGTCAGTATTTGGT | 10393 |
rs755570840 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144996436 | GCTGGTCTAAGGAGG[C/G]AGAAGGGAGACTTGG | 10393 |
rs755582781 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145031584 | TGACAGTTTTGAGTG[A/G]GGTCCAGAACAGGAG | 10393 |
rs755607254 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145094355 | TGACCATAAAGAGAC[A/T]TGAGGGAACTTTGTG | 10393 |
rs755626327 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145093244 | GTTCTCACAGTAAGC[A/C]CAGGGCATCTTTAGA | 10393 |
rs755627283 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145002443 | TGCTAAACATGGTCA[A/G]ATCATTCATTTTAGA | 10393 |
rs755643430 | in-del | -/TG | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145028160 | TCCTGGGTGTGCCTG[-/TG]TGTGTGTGTTGCCAA | 10393 |
rs755676707 | in-del | -/GAA | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145015478 | ATAATCGGTGTTCCT[-/GAA]GAAGAAGAGAAATCT | 10393 |
rs755683226 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145043126 | GCTAAAAATGCACTA[C/G]CTGCCAAGAGCTATG | 10393 |
rs755696637 | snp | C/T | 1.65682e-05 | 0.00287817 | missense, nc-transcript-variant | ANAPC10 | GRCh38.p7 | 4:145081696 | TGAGGCTGGGAACCA[C/T]CTGATTGCCAATAAG | 10393 |
rs755704014 | in-del | -/A/AA | 0.464568 | 0.150345 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145053783 | TAAAACATGAGGCTG[-/A/AA]AAAAAAAAAAAAGGT | 10393 |
rs755730366 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144999093 | TCCCTGAATAGACCA[A/G]TAACAGGCTCTGAAA | 10393 |
rs755803180 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145019619 | AACTAAATGAAACTA[A/C]AACAAAATTACAAAA | 10393 |
rs755842061 | snp | A/G | 0.000682191 | 0.0184562 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995507 | TCTGGTGATTGGCTA[A/G]AACAGCAATCTGTAT | 10393 |
rs755862868 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145000664 | AGAGATCTAGAACTA[C/G]AAATACTATTTGACC | 10393 |
rs755870646 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145011610 | ATGCTGGTAAAGGGC[A/G]AGAGGCTAAAAACTA | 10393 |
rs755877219 | in-del | -/TAAG | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145005386 | GTCTAGCTAGCAGTC[-/TAAG]TATCTTATTCTTTCA | 10393 |
rs755885128 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145080838 | CTTGAACCTGGGAGG[C/T]GGAGGTTGCAGTAAC | 10393 |
rs755892922 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145093859 | ACAAATGGTCTAGCA[C/T]ATGTATAATTGGATT | 10393 |
rs755958833 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144971918 | TCAGTCCCTACCTTT[A/G]TTGTCTCTAGTGCTT | 10393 |
rs755965337 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145066245 | TCGGATCAAGAGGTA[A/G]AACACTAAATACCCA | 10393 |
rs755999390 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144988069 | AGCCTCAACCTCCTG[A/T]GCTCAAACAATCTTC | 10393 |
rs756008124 | in-del | -/ATAT | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145026921 | TTTGCCTATACATAC[-/ATAT]ATATATATATATATA | 10393 |
rs756017095 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145028105 | TGTGATGGTTAATAC[C/T]GAGTGTCAACTTAAT | 10393 |
rs756018397 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145068365 | ATGTGACTACATTAT[A/G]TAAGAGTAACTAATA | 10393 |
rs756030092 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145009422 | GCATCACGCTACTTC[A/G]CTTCAAAATATACTA | 10393 |
rs756052512 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145014618 | AAAGCGCCACCTCCT[G/T]GCAGGACAACCAGCA | 10393 |
rs756072041 | snp | A/G | 3.3248e-05 | 0.00407712 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995387 | GTCACCTTATTGAAC[A/G]ATACATCATGAAATC | 10393 |
rs756083908 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144970400 | CTGGGAAAAAATACA[C/T]GAACTTATAATGCTT | 10393 |
rs756089956 | in-del | -/GTG | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054633 | TGTGTGTGTGTGTGT[-/GTG]TGTGTGCGCGCGCGC | 10393 |
rs756170010 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145090180 | CTGATGCACAAGTCC[A/C]TTATTTAAAATGGCT | 10393 |
rs756259993 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145089396 | TCTTTGTATCAAATA[C/T]AGAGTTAAGCACAGC | 10393 |
rs756276856 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144992359 | GGTAAGTGATTCTTC[C/T]GATGGATCTCAGCAA | 10393 |
rs756284211 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145008170 | ATAGACCAATAACAG[C/G]CTCTGAAATTGAGGC | 10393 |
rs756308485 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145036654 | TACCCAGCTCTTTCA[C/T]GCTTTTAACCTACAT | 10393 |
rs756322522 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145035703 | AGATTGTTTTTGTTC[C/G]CCACCACTTTACATA | 10393 |
rs756329110 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144996799 | TTCTCCGAGCTAAAG[A/G]AGGATATTCGAACCC | 10393 |
rs756346784 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144996163 | GGATGTGGGGAAACA[A/G]TATGAGAGATATGGA | 10393 |
rs756362579 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145053051 | ACCCTAAGAAACCTT[A/G]TCCTGACTGATGAGG | 10393 |
rs756377117 | snp | C/G | 1.69117e-05 | 0.00290785 | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145096158 | TCAGGAACTGGGCAT[C/G]TTTCTACAAAAGTTT | 10393 |
rs756401233 | in-del | -/ATG | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145091048 | AATGCTAATCATATA[-/ATG]ATATTTCACTGATAG | 10393 |
rs756463964 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145084887 | AAATATTATTACAAT[G/T]AATTTCACCTATTTT | 10393 |
rs756506618 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145009952 | AATATCCAGAATCTA[A/C]AAAGAACTTAAACAA | 10393 |
rs756566218 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145070410 | ATAACCAGGAAGCAC[A/G]TGAAAAAAATGCTTG | 10393 |
rs756571582 | snp | C/G | 3.36973e-05 | 0.00410457 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145064720 | AAGTAAAAATAACAT[C/G]CACTTCATCATATGA | 10393 |
rs756580598 | snp | C/G | | | intron-variant, downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:145062721 | AGATGGCACTCCCAT[C/G]TTCACTGCAGCATTA | 10393 |
rs756606015 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145030825 | GGGGTTGCAAAGATT[A/G]GTGCCACCATCAAGG | 10393 |
rs756644246 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145005330 | CATCCCTCTTGTCAT[G/T]TCTGACTGTATTTTG | 10393 |
rs756686800 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145067922 | TACTAAAGAAAGTTT[A/C]TTTAAAAGAAAAACA | 10393 |
rs756754441 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145071544 | GAATTTTATTATTCA[A/C]CATCTCAACAGAATA | 10393 |
rs756756092 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145055269 | TCTTTGGTCTTTAAA[A/G]AAAAGGAGGCCAGTG | 10393 |
rs756763420 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145019238 | AAGAAAACTGAAATT[A/G]TATCAAGGACTCTCT | 10393 |
rs756782266 | snp | C/T | 1.65817e-05 | 0.00287933 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995417 | CTATAGTTGTACATC[C/T]AGGAAATTTACCAAT | 10393 |
rs756795097 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145067386 | AGGAAGAGGGCAATA[C/T]TTTCCTATTTCTGAT | 10393 |
rs756849057 | in-del | -/A | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145003228 | GCACAGTATTCCATT[-/A]TGTGAAATTTGGAAT | 10393 |
rs756861499 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145091647 | ATTATGAATAGTGCT[G/T]CAATGAACATACATG | 10393 |
rs756885574 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144976874 | AAAATTTTCTTATTT[C/T]GAATCCAAAAAAAAG | 10393 |
rs756895343 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145031101 | CCCACCAGAAGCAAT[C/T]TGCCTTCAGCTAGCA | 10393 |
rs756926589 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144993257 | CTGTACCAGCAGTGC[A/G]AAGTGCATTTTCTCC | 10393 |
rs756948435 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145027865 | CACCAATAAAGGAAG[G/T]AAACCAAGAATGATG | 10393 |
rs756992626 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145015483 | CGGTGTTCCTGAAGA[A/C]GAAGAGAAATCTAAA | 10393 |
rs757011429 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144996190 | TGGAGATATCCCCAC[C/G]GCTCTACACTCCGAA | 10393 |
rs757042400 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144971681 | ATTAACTTTAACATA[A/G]ACTTGAAATTTCTGC | 10393 |
rs757103432 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145040981 | GTTCTTACTACAGAT[A/C]TACGCAGAGGTAAAA | 10393 |
rs757136845 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145086412 | CCAATGCAGTTATTA[C/T]ATGATGTACTGGTTC | 10393 |
rs757147480 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145027770 | TACCTAGCCAAATCA[A/T]CCCTTGAGGGTGAGA | 10393 |
rs757156185 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145025949 | AACTAAGGTCTTACC[A/G]GTTAGACAGATTAAA | 10393 |
rs757188249 | snp | A/C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145007054 | GGTCCCAAGATGGAC[A/C/G]AATAAGAACAGCTCC | 10393 |
rs757202052 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145042766 | AACAGCAGACACTGA[C/T]GTTCACACAAGCATA | 10393 |
rs757206682 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145093161 | TGTAGCACAAGTGTG[C/T]GCCAAAGCACAGGAA | 10393 |
rs757228371 | in-del | -/TTG | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144970013 | GTAATCACACTGAAT[-/TTG]TTGTTATTTATTCAC | 10393 |
rs757231420 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144983321 | TCATAAATTAACACA[G/T]GTTGAGCATCCCAAA | 10393 |
rs757274827 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145087900 | AAAAATAAAAAAAAT[C/T]AGCTGAGTGTGGTGG | 10393 |
rs757355086 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144995956 | GATGGCTGACTAGAC[A/C]CAAGTAGTATGTGCC | 10393 |
rs757370184 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145066172 | TTAGTAAGGAGACCA[A/G]ACTTCTGTAGCCTAA | 10393 |
rs757370634 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144985298 | AAGAAGATAATCCTG[A/G]TTTTAAAAGATCTGC | 10393 |
rs757385456 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145035521 | AACTGACCCTCATTC[C/T]CTTAGATCTTCCTGC | 10393 |
rs757401001 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145089137 | TTCTATTATATTGCT[A/G]TCTTATTTTCTGCAA | 10393 |
rs757404691 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145039923 | TAATCTTCACTTTAG[A/G]TACTAGAAATCTGAG | 10393 |
rs757424939 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145022633 | ACTAAACATCACCTG[C/T]ACTCCAATAACCTAT | 10393 |
rs757460604 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145050680 | CAGCACTTGCTGCTT[A/C]ACCTGGCTCTTTTAT | 10393 |
rs757463921 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145079885 | TTGGGAGGCCGAGGC[A/G]GCTAGATCACCTGAG | 10393 |
rs757500747 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145004056 | TAATTCTCATTTCCC[A/C]TCCTTGGTTACGTGT | 10393 |
rs757586529 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995027 | CTCTAATGTATGAAC[A/C]CTAATGAAATAATCA | 10393 |
rs757643054 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145043159 | CCATCTAAAGCAAAA[C/T]GCTTAAGATGGAAAC | 10393 |
rs757727366 | snp | A/C | 1.68599e-05 | 0.00290338 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145064722 | GTAAAAATAACATGC[A/C]CTTCATCATATGAAA | 10393 |
rs757731349 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145021010 | ATCAAAATTGTGAAA[A/G]TGACCATACCACCAA | 10393 |
rs757731403 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145036434 | GGCTAACATAGCTAA[C/T]AGGATTGCTCCCAAA | 10393 |
rs757734903 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145076011 | TCTCCCAGGGTCCCT[G/T]CTTGGCCATGTCTGA | 10393 |
rs757744092 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145061235 | CAGCACTTAGATGAC[A/G]TAATAGAAGCAAAGA | 10393 |
rs757780229 | snp | C/T | 1.65685e-05 | 0.00287819 | missense, nc-transcript-variant | ANAPC10 | GRCh38.p7 | 4:145081723 | TAAGTTTCTAGATTG[C/T]CATCTCGTAACTGAT | 10393 |
rs757784290 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145022209 | GATACTTGCACACAC[A/G]TTTATAGCAGCACAA | 10393 |
rs757803341 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144974499 | CGAGTACAATAAGAA[A/C]ATAAAATAAATAAAA | 10393 |
rs757843995 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144980691 | TTTTGCTTTTGTTGT[C/G]ATTGCTTTTGGCATT | 10393 |
rs757844244 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145059846 | TGGTCCATTGCTCTA[A/T]ATGATAAAAAAAAAA | 10393 |
rs757847139 | snp | A/G | | | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145099287 | TAAAAATCTATAAGA[A/G]GAAGAACTGTCCAAA | 10393 |
rs757903034 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145068737 | CAACATGGTGAAATC[A/C]CGTCTCCACTAAAAA | 10393 |
rs757913733 | snp | A/C | 0.000204436 | 0.0101082 | intron-variant, missense | ANAPC10 | GRCh38.p7 | 4:145053735 | CATTCCTTTATCCTG[A/C]GACTTGAAGATTCAT | 10393 |
rs757923262 | snp | G/T | | | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145098628 | TCTTCCCCTCCAGCC[G/T]ACCCGGCTGTCGCCG | 10393 |
rs757952240 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145070179 | TTGCAGGCTAAATGT[A/G]GACCGCCACCTATTT | 10393 |
rs757955104 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145029370 | CCCGACACCCTTGTT[C/T]GCTTCTAGACCTATA | 10393 |
rs757988825 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145082919 | TGAAAAGTCACTATC[A/T]ACCATCTCATTCTTC | 10393 |
rs757996365 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145013845 | GGTCTCATTTGAGGA[A/G]GAAGATTCTGACCTT | 10393 |
rs758028397 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144975300 | CTGTTCAACAAACCT[G/T]CTAGAATATAATACA | 10393 |
rs758081251 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144973790 | AATGGATAAACTCTC[A/T]GAAAAATATAAATTC | 10393 |
rs758083557 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145046605 | AAATTCTTGCTTTAC[A/T]TATGCCACAAAAAAT | 10393 |
rs758084456 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145030729 | GTGAGAACTATCATG[C/G]TGGGAAAGGCCAAAT | 10393 |
rs758111039 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144991018 | TGTTCAGCAGCACCA[C/T]GCTGTTATGTTCCAC | 10393 |
rs758123577 | in-del | -/TGTGTAT | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145037035 | GTGTGTGTGTGTGTG[-/TGTGTAT]GTGTGTGCATGCATG | 10393 |
rs758137022 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145027822 | TGCAAGGTTTCAACA[A/G]TTTACCTCCCATGTG | 10393 |
rs758230816 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054965 | CCACCCTTTTCCATA[C/T]CACTATCTCTCAGTA | 10393 |
rs758243801 | in-del | -/A | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144967606 | TTATTAAAATCTTTC[-/A]AAAGGTCTTCTAAAA | 10393 |
rs758244340 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144983053 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 10393 |
rs758249568 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145015170 | AAAGGCAAAGCCCAA[C/T]GCAAGGAAATCCAAA | 10393 |
rs758256904 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145091541 | CGGGGGGAGGGGGAA[A/G]TCACCGCTACAGTAT | 10393 |
rs758280057 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145039197 | TACAATAAAAACAAT[C/G]AGGAAGTGGAAAATG | 10393 |
rs758280502 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145040590 | CATATCTCCAATTTA[C/T]AGTTAATTTATAGGT | 10393 |
rs758297394 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144982429 | AGTCAACAATGACAA[C/T]CCTGTTCCCTGATTT | 10393 |
rs758313732 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144996941 | AACTATGTGACGCAT[A/G]CACAAGCTTCAATAG | 10393 |
rs758332962 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145024089 | TCTTTGCTCATCAAT[A/G]AGATGCAACTCCTCA | 10393 |
rs758357933 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145016721 | CCTCACTTCAAACTA[C/T]ACTACAAGGCTACAG | 10393 |
rs758365127 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144998787 | CAGGACTGAAGGAGA[C/T]AGAGACACAAAAAAC | 10393 |
rs758370570 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145056215 | ATAAAACAGGCTGCA[A/G]TAAAGAAGCTGGCCC | 10393 |
rs758388154 | in-del | -/TTTT | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145022655 | ATAACCTATGGAAAA[-/TTTT]TTTTTAATTAAAAAG | 10393 |
rs758434069 | in-del | -/T | | | downstream-variant-500B, intron-variant | ANAPC10 | GRCh38.p7 | 4:144993714 | CATATGAAAAATACG[-/T]TAAGGAGAATAAAAG | 10393 |
rs758499403 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144969760 | CACACATGACAAATG[C/T]CAAATGCCCTGTATA | 10393 |
rs758505936 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145014185 | TCGGAGGTGGGTACC[A/G]TGGGGCAAGTTCTCA | 10393 |
rs758533136 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145050306 | CAGTAGGTCTTTACA[A/G]TGGGATTAAAATATT | 10393 |
rs758538462 | snp | A/G | | | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145100038 | AATCCCCTTGCCCCA[A/G]TTATTGAAACTGATA | 10393 |
rs758568951 | snp | A/G | 3.31389e-05 | 0.00407042 | stop-gained, nc-transcript-variant | ANAPC10 | GRCh38.p7 | 4:145081730 | CTAGATTGTCATCTC[A/G]TAACTGATCCACTCC | 10393 |
rs758581442 | in-del | -/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144989071 | TATGTTTTATATTTT[-/G]GGGGGTAAATACGTA | 10393 |
rs758582213 | in-del | -/GTGTGTGT | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145036996 | TACCAAATAGATAAC[-/GTGTGTGT]GTGTGTGTGTGTGTG | 10393 |
rs758621585 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145020804 | AACCAACTAGAGAAT[C/T]GAATCAAGAACTCAA | 10393 |
rs758626195 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145048610 | GCTGACATATTTCTC[C/T]CCCAACCACCTCCCT | 10393 |
rs758647395 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144968191 | GTTACTTACACAAGG[C/T]CAAAATAATTAAACA | 10393 |
rs758701683 | in-del | -/A | 0.000222 | 0.0105333 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145053806 | AAAAGGTTCCTGACT[-/A]AGGCTCACCTCTATT | 10393 |
rs758718981 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145001403 | TGCTTAGATGAGGTA[C/T]TTAAGAGTAGTCAAA | 10393 |
rs758722569 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145006928 | GTTCTGTCCTAAAAT[C/T]AGTCCCACAATACAG | 10393 |
rs758741839 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145058041 | TTTCCTCATTTAATG[C/T]CTGCCATTACGTACA | 10393 |
rs758807608 | snp | A/T | 3.31246e-05 | 0.00406955 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145095976 | GCTTTTTTGTTTGTT[A/T]GTTTTTACCTGGTTT | 10393 |
rs758819094 | in-del | -/A | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145079366 | TATTACTAAAAAGTC[-/A]AAAAAAAAATAACAG | 10393 |
rs758834735 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145094259 | TAAGCTACATACAGT[A/G]TTTATATCGGCATTC | 10393 |
rs758838253 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144977313 | TATACGACAAATATT[A/G]ACTAAATAGTTTGAT | 10393 |
rs758867863 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145036024 | CAGAGAATTTAGACA[C/T]ATGTTGGTAACCAAC | 10393 |
rs758869519 | snp | C/T | | | intron-variant, synonymous-codon | ANAPC10 | GRCh38.p7 | 4:145033363 | TTTCAGAGGGAGGAA[C/T]GCTGCCACCTGGAGA | 10393 |
rs758887448 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145075625 | GGGTTGCTGAGCACC[A/G]GGACTCATTTCTGGC | 10393 |
rs758914964 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145005004 | GCTTTTTATTACTGA[C/T]TCAGTTTCAGAAATC | 10393 |
rs758935112 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144994704 | CTTCCATAAGTACTG[C/T]TAGAACTCTTCCATA | 10393 |
rs758965944 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145020015 | AGACTTTCAAAGAAG[A/G]ATTGGTACCGATCCT | 10393 |
rs759023280 | snp | C/T | 3.31614e-05 | 0.00407181 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081657 | TGAAAATGTATTAAT[C/T]ACCTGAATTGGATGT | 10393 |
rs759028026 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145039729 | CCTCCTGAGTAGCTA[C/G]GACTACAGGCACGCA | 10393 |
rs759033789 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145046334 | TTTTTAAAAATACAT[A/C]CTGCATAGAAAGTAT | 10393 |
rs759071131 | in-del | -/AAGTGTTT | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145041180 | ATAATTTACTTTCAA[-/AAGTGTTT]AGCTAAATCTAGAAC | 10393 |
rs759075773 | snp | C/T | | | utr-variant-3-prime | ANAPC10 | GRCh38.p7 | 4:144967154 | ATTCTCACTTGATTC[C/T]TCACTTCTGAGATAC | 10393 |
rs759084256 | in-del | -/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145040820 | CTCAAAAAGCCATAA[-/T]TCTACATATGCTATA | 10393 |
rs759088205 | snp | G/T | | | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145096604 | CTTCTACAATGCTAT[G/T]CAGTTCTATAATTCT | 10393 |
rs759120009 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145080763 | AAATACAAAATTAGC[A/C]GGGCGTGGTGGCGCA | 10393 |
rs759144262 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145023409 | TTTATCTTGAACAGT[C/G]CTTTGCCTCACTAAC | 10393 |
rs759162554 | in-del | -/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145036493 | GAAGTATGATTGTTG[-/C]CAAGTGCTACTGCAA | 10393 |
rs759167514 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145037877 | GATTGAACCTAGAAG[A/G]TCTAGGCCCCAGTGA | 10393 |
rs759183738 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145062516 | AGAGGCTGAGGTTTA[A/G]GAATTGTTTGAACCT | 10393 |
rs759187271 | snp | C/T | | | intron-variant, downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:145032805 | CTACCTGGTGGCAGG[C/T]TGATTATATTGGACT | 10393 |
rs759205758 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145022029 | ATGTTGCTGGGGATG[A/C]AGTGATCAGGGAACA | 10393 |
rs759225288 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145076732 | AATGAATCAAGAGCT[A/G]AAAGACGAAATAGCT | 10393 |
rs759237586 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145047458 | GGTTAAATGGAGTTC[A/G]GTGAGTCATGATAAT | 10393 |
rs759265932 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145014890 | TAGGAAAACGGGGAG[A/C]GTGCTACATCAAGGG | 10393 |
rs759309973 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144976908 | TTTGACTTGAGAGAG[C/T]ATGAATTGGACCCAA | 10393 |
rs759381610 | snp | G/T | 1.66007e-05 | 0.00288098 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081782 | TGTCAATAAATCCCT[G/T]TGAAAAAGAAACAAC | 10393 |
rs759422954 | snp | C/T | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant, missense | ABCE1, ANAPC10 | GRCh38.p7 | 4:145098161 | AACTCAGATTCTCGG[C/T]ACCTCCAGCAGCTGG | 10393 |
rs759469337 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145084353 | CAAAGAGATAAGCAT[A/G]TAATGTCATGAATCA | 10393 |
rs759495252 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144975095 | ATAAAGAGGTTCAAA[C/G]AAATTGAACCGAGTA | 10393 |
rs759495515 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145047874 | AAGGTAGAACAGTGA[A/C]GGCAGAAAGAGATTT | 10393 |
rs759516373 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145006443 | GGAATAAGAAAGGAA[C/T]GATAGCAATGAATAA | 10393 |
rs759544452 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144990800 | TCCAAACCATATCAG[C/T]AGTCAATCAGCTTTC | 10393 |
rs759547046 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145031562 | CTTATCGAGTGACCT[A/G]AAAGGCTGACAGTTT | 10393 |
rs759590199 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144998789 | GGACTGAAGGAGATA[C/G]AGACACAAAAAACCT | 10393 |
rs759599267 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144992381 | TCTCAGCAAAACAAA[C/T]GGAGAACTTTCTGGA | 10393 |
rs759621748 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145041843 | AATGTAAACGTGCAT[C/T]TGAATTTTGATCAAG | 10393 |
rs759647579 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145055855 | CCACGTGAATACCAT[A/G]TATGTAGCACTACTG | 10393 |
rs759746192 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144998679 | AGGACAGATCTAAAA[C/T]TGACACAATAACATC | 10393 |
rs759790944 | snp | C/T | 1.68128e-05 | 0.00289933 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145064559 | CATATTTTTAAAAAT[C/T]TGAAAGACATACCCG | 10393 |
rs759792614 | in-del | -/TA | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145037039 | GTGTGTGTGTGTGTG[-/TA]TGTGTGTGCATGCAT | 10393 |
rs759795842 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145055694 | TTTCACTTATATGAG[A/G]TATCTAAAGCAGTCA | 10393 |
rs759797469 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144999307 | AGCCTGGCAGAGACA[C/T]AACAAGAAAAGAGAA | 10393 |
rs759828014 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145056886 | GAATCATATCCTGTC[A/G]TATGGTTAAATAAAG | 10393 |
rs759835705 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145060156 | TAAATTGTTGGTTTT[C/T]AATTTATGTGGAATA | 10393 |
rs759844034 | in-del | -/TT | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144987973 | TTCAACAATTTTTGT[-/TT]TTTTTTTTGTTGTTG | 10393 |
rs759850398 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145021415 | ACTACACAAAAACAT[A/T]AAGTGGGGAAAGGAC | 10393 |
rs759856583 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144983964 | CTAAAAGTGATAATG[C/T]GGAGAAAATATCTGC | 10393 |
rs759859661 | snp | G/T | | | downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:144967081 | CCATTTATTACATGC[G/T]TACCATCTGCAGCAG | 10393 |
rs759911640 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145016496 | AAATGGAAGAACATT[A/C]CATGCTCATGGATAG | 10393 |
rs759946756 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144995772 | TTACCATGGTCTACT[C/T]ATAGTTGCTAAGCAC | 10393 |
rs759965808 | snp | A/G | | | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145099740 | ACTATTTCATGTGAT[A/G]CTAAACATCATTAGT | 10393 |
rs759979871 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145026932 | ATACATATATATATA[C/T]ATATATATATATATG | 10393 |
rs759997473 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145080792 | CATGCCTGTAATCCC[A/G]GTTACTCGGAAGGCT | 10393 |
rs759998955 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145007779 | GAACTAGAGAAGCAA[C/G]AGCAAACAAATTCAG | 10393 |
rs759999493 | snp | G/T | | | intron-variant, utr-variant-3-prime | ANAPC10 | GRCh38.p7 | 4:145063955 | TCAATAAAATCAGTA[G/T]AATAGTTATTTCTGA | 10393 |
rs760042262 | snp | A/G/T | 3.31286e-05 | 0.00406982 | upstream-variant-2KB, missense, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145096078 | GGTCAGCACCAGGAG[A/G/T]TGTCTTGTTTGGTGT | 10393 |
rs760052983 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145065633 | AATTAAAAACAGCCT[A/G]AATATCCATGACAAT | 10393 |
rs760080484 | in-del | -/ACC | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145018895 | GTCCAACAGGAAAAT[-/ACC]ACCACAATCCTAAAC | 10393 |
rs760159857 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145028358 | TGCCTTCGAACATAG[A/G]ACTCCCAAGTTGCTC | 10393 |
rs760204877 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145021845 | ATTAATCCCATCAAA[A/G]AGTGGGCTAAGGACA | 10393 |
rs760214324 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144981779 | AGTATGATATTGGCT[A/G]TGGGTTTGTCATAAA | 10393 |
rs760267465 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144980480 | TTCTTGTAAATTTAA[A/G]TTCCTTGTTGATTCT | 10393 |
rs760275089 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145036179 | TGAAAACATGCATAA[C/T]GATTTCAGCAAATAC | 10393 |
rs760300259 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145052764 | GTGGTGGTGCACACC[A/T]GTAATCCCAGCTACT | 10393 |
rs760349800 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145035220 | GGCTAGATTGGTATT[A/T]ACTTCCTCCCTCACT | 10393 |
rs760377384 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144974896 | AAATTCTGTCAGGTT[G/T]TGTGTGTACATGTGT | 10393 |
rs760383246 | snp | C/T | | | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145096449 | TCATATGACCAGATA[C/T]GCAAAGCAGTGAGCT | 10393 |
rs760409655 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145089786 | AAATTTCTTAAAATT[C/G]TCCTTTATATCACTT | 10393 |
rs760430102 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145020557 | ACCACTCGTCTTCAA[C/G]ATAGTACTGGAAGTC | 10393 |
rs760434413 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145084165 | TAACACTATGTCTGT[A/T]CCACGTAATCCAAAC | 10393 |
rs760544567 | in-del | -/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145073192 | AGCCACTGCACCCAA[-/T]CTACTATTTTTTAAA | 10393 |
rs760588236 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144971679 | TAATTAACTTTAACA[A/T]AAACTTGAAATTTCT | 10393 |
rs760625125 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145046147 | TCAGGGCTTCATTCA[A/C]TGCTTAATGGAAAAG | 10393 |
rs760661324 | in-del | -/TGTGTGTGTATATATA | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145012169 | CTATATGTATATGTG[-/TGTGTGTGTATATATA]TATATATATATACAC | 10393 |
rs760673475 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144999176 | ATTAAGAGACGAATT[C/T]TACCAGAGGTACAAA | 10393 |
rs760681301 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145003595 | CCATTTATTGAATAG[G/T]AAGTCCTTCCCCCAT | 10393 |
rs760713844 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144989346 | CAAACTTTTTCATTA[G/T]TCTTATATCTCTTAT | 10393 |
rs760717543 | snp | A/G | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | ABCE1, ANAPC10 | GRCh38.p7 | 4:145097670 | AATAGGTTCAGTTAT[A/G]AACTAGTTGTCACTT | 10393 |
rs760740758 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145004749 | GGATTCAGTTTGCTA[A/G]TATTTTGTTGAAGAT | 10393 |
rs760782566 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145091237 | GCATTTTCAGGAAAC[C/T]GGTGACATGTGTTGC | 10393 |
rs760834771 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144982769 | ACTTAAGTCAGTGTA[A/G]TAGGGGTTTCTGTTA | 10393 |
rs760854864 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145029984 | ATAAAATGGGAATAA[C/T]TGAATCCCAAGGTGG | 10393 |
rs760870338 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145031437 | TAAGGTGAAGGATAA[A/G]TTGCTGCATTTGGCC | 10393 |
rs760874292 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145088421 | ATTGCAAAATTAACA[C/T]ATATAAATTAAATTA | 10393 |
rs760879888 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145038157 | CTGGCAACATAGTGA[A/G]ACCCTATCTCTACAA | 10393 |
rs760927345 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145085844 | AAAGCTTCCCACTCA[C/G]TATTGTATTTGAATT | 10393 |
rs760936757 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145069370 | ACTCCAGAAATATGC[A/G]TGGGGTCCCCTTCAT | 10393 |
rs760970351 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145006632 | AGGTCAAAAATAAAA[C/T]GACGATAATTTTATT | 10393 |
rs760977688 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145055192 | GGGAACAACCCAAGT[C/G]ACCACTGAGAGATGA | 10393 |
rs760988171 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054756 | AGGAAAAAGTGGTCA[A/G]GTATGAAAGAGGTCA | 10393 |
rs760994307 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145070792 | GGCACAGTCATACAA[C/T]GGAATATTATTCATC | 10393 |
rs761031700 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145092030 | TCTCCCTTTCAGGAG[C/G]TGGAAGCCATCATCC | 10393 |
rs761038413 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145026404 | CATAGCATATAAGTA[C/T]AAAAAGTGCATGGGA | 10393 |
rs761050211 | in-del | -/C | 0.000118202 | 0.00768682 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145064728 | TAACATGCACTTCAT[-/C]CATATGAAAAGATTT | 10393 |
rs761059657 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145040219 | ACAATGGCACGATCT[A/G]GGCTCACCGCACCTC | 10393 |
rs761121731 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145078599 | AGAACAAAGCTGGAG[C/G]CATCACATTACCCCC | 10393 |
rs761148011 | snp | G/T | | | utr-variant-5-prime, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145098243 | CTACCTACCTCCAGG[G/T]TTCCGCCTCACGCTC | 10393 |
rs761156990 | snp | C/T | | | intron-variant, utr-variant-3-prime | ANAPC10 | GRCh38.p7 | 4:145063867 | GCCATACATAAAAGT[C/T]ATATCCTGTATGACT | 10393 |
rs761271933 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144978625 | CAGGAGTTCAAGACC[A/G]GCCTGGGCAACCTAG | 10393 |
rs761278129 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145073495 | GTAAATAAACTAATT[C/T]GTATGATTTGGCTTA | 10393 |
rs761337478 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145065529 | AAATACAGTAACACA[A/G]TCACTCAAAAATTGA | 10393 |
rs761337710 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145035147 | GGATGTGAGGGCAAT[C/T]CGGCTGCGACATCTG | 10393 |
rs761337919 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144981692 | CAATACTATGGTGAA[C/T]AGAAGTGGTGAGAGA | 10393 |
rs761375874 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144980210 | CTTCCACAATGGTTG[A/G]ACTAATTTACACTCC | 10393 |
rs761434998 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145088590 | AATATATCCCAAAGC[C/T]ATCATTCCTTTCCAT | 10393 |
rs761442053 | snp | A/G | 1.66007e-05 | 0.00288098 | upstream-variant-2KB, utr-variant-5-prime, synonymous-codon, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145096109 | AGTCATTTTTAAAAT[A/G]TTCTATGTAGAAAAC | 10393 |
rs761443090 | in-del | -/TGTATATGTGTG | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145012159 | CAATTACAAGCTATA[-/TGTATATGTGTG]TGTGTGTATATATAT | 10393 |
rs761450280 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144992774 | TAGTTGATAAAGCAA[C/T]AGCAGGACTTGAGAG | 10393 |
rs761452341 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145074258 | ATTTTTTCCTTCCCC[C/T]TCTCTACGTTAGGAC | 10393 |
rs761501764 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime, intron-variant | ANAPC10 | GRCh38.p7 | 4:144994138 | CTGACAAGTATAATG[C/T]GCTTAATTTGGTGAT | 10393 |
rs761584997 | snp | A/G | | | intron-variant, downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:145032959 | TTATCCATTGTCATG[A/G]TATTCCACACAGCAT | 10393 |
rs761610901 | snp | C/T | 1.66341e-05 | 0.00288388 | missense, intron-variant | ANAPC10 | GRCh38.p7 | 4:145064600 | AGGTTGTGAAAATTA[C/T]TTCCTACTCTGACTG | 10393 |
rs761619178 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144987879 | CCAATAGATATGCAC[A/G]CACACCAAAACACAA | 10393 |
rs761631863 | in-del | -/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145001725 | TATGAAACCTACAGT[-/G]GTGTAAACAGGATCC | 10393 |
rs761665630 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145044130 | AAAAATAGATTCAAG[A/G]AGATAATGCTGCCCT | 10393 |
rs761683481 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145094302 | AACCAAAGGGACCCA[A/G]AACTGAGCTGTCAGG | 10393 |
rs761739940 | snp | A/G | 3.52044e-05 | 0.00419535 | utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995345 | ATAAAACAAAGATAC[A/G]TTTAATGATTTTCGT | 10393 |
rs761754359 | in-del | -/CAAAAAAAAAA | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145039010 | ATAAAAACAATGTCT[-/CAAAAAAAAAA]AAAAAAAAAAAAAAA | 10393 |
rs761766229 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145075293 | CTCTTCAAAAGGAAG[G/T]AAGAGAAGTGGATTA | 10393 |
rs761826488 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145020433 | AAGGAACATACCTCA[A/G]TGTAATAAAAGCCAT | 10393 |
rs761849694 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145002119 | ATGAAATTCTGTAGA[A/C]TCTTACTACGAGAAC | 10393 |
rs761863093 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144980205 | ATTGTCTTCCACAAT[A/G]GTTGAACTAATTTAC | 10393 |
rs761879511 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145021715 | TTTGCATGGCAAAAG[G/T]AACAGTCAGCAGAGT | 10393 |
rs761922242 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145028792 | ATACCTTTGACCATA[C/T]GTGGAGAACCAAGGA | 10393 |
rs761936639 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145026396 | AGTGATTACATAGCA[C/T]ATAAGTATAAAAAGT | 10393 |
rs761967777 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144972951 | AAAAAAAGCCATTCT[C/T]ATAGAAATTAGAAAA | 10393 |
rs762004700 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145046114 | AATCCTCTGCCTTCA[C/T]ATTGGCTACAGTGAC | 10393 |
rs762034186 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145048976 | GGTCTGGTTCCAGAC[C/T]ACAGCAATAAAGTGA | 10393 |
rs762038893 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145069327 | GTAGTCTACTGAATT[C/G]ATAAGGAATAAGCTA | 10393 |
rs762075571 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145082252 | CCTCCCGGATTCAAG[A/C]GATTCTCCTGCCTCA | 10393 |
rs762077388 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145076919 | AATAAAAAAGAATTT[G/T]CCAGGCGTGGTGGCT | 10393 |
rs762096338 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145029512 | AAATCTAGAGAACAA[G/T]CATGGGAATGGATAT | 10393 |
rs762097496 | snp | A/G | 1.65614e-05 | 0.00287757 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145095943 | GTACAAGGAAACTGC[A/G]AGTGACTATTTCCAA | 10393 |
rs762103343 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145023472 | GAAATAAATTTACAC[A/G]ATGAAGATTTCATTT | 10393 |
rs762116914 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145008212 | gcttaccaaccaaaa[A/C]aagtccaggaccaga | 10393 |
rs762129434 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145029980 | TTAAATAAAATGGGA[A/G]TAATTGAATCCCAAG | 10393 |
rs762130850 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145083787 | TACATTTCTGTTGGA[A/T]AGCACTGCTCTGCAC | 10393 |
rs762141834 | in-del | -/A | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145082622 | ATTTTCAAAAGGCAT[-/A]ATATATTCTGAAGCC | 10393 |
rs762142804 | in-del | -/CAGG | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144994737 | TACTGCTAGATTATA[-/CAGG]CAATCTTTACATAAT | 10393 |
rs762181486 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145089992 | TCTATAATCAGGCTT[C/G]TACCTAACTATACAG | 10393 |
rs762227349 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144967305 | AAGCATCCATATAAA[A/G]ATTGGATCCTTTCAT | 10393 |
rs762285047 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145078447 | AAAAAAAAATGGTCA[C/T]AACTGCCCAAAGCAA | 10393 |
rs762322503 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144992563 | CATGTGGTAGAAATA[A/G]CAAGAGAACAAGAAT | 10393 |
rs762332572 | snp | A/C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145038100 | AACATTTTAGGAGGC[A/C/G]TAAAGGGGAGGATAG | 10393 |
rs762350424 | in-del | -/A | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145052602 | GAGGTTTTCCTATTT[-/A]AAAAAAAATATCGGG | 10393 |
rs762361714 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144982009 | TTTTTTAGTAGAGAC[C/T]GGGTTTTTTTTGTTT | 10393 |
rs762368861 | snp | C/T | 3.31428e-05 | 0.00407066 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995457 | TTCTACTGGTGTGTA[C/T]ATTTTAATTTGTCTC | 10393 |
rs762369477 | snp | C/G | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant, stop-gained | ABCE1, ANAPC10 | GRCh38.p7 | 4:145098193 | TTCGCCAACGGCGTT[C/G]AACAAGGGTCGCAGC | 10393 |
rs762406841 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144996722 | CAACGGAACAAAGCT[A/G]GACGGAGAATGACTT | 10393 |
rs762446826 | in-del | -/CAAA | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144988073 | TCAACCTCCTGAGCT[-/CAAA]CAATCTTCCTGCTCT | 10393 |
rs762447297 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144969165 | CTGAAAGAGAGATAA[C/T]AAGACCTATTTTGTA | 10393 |
rs762447820 | in-del | -/AATTTG | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145014055 | GCTGAATTTTGTAAC[-/AATTTG]AACTAGTCAAGAAGG | 10393 |
rs762528189 | snp | C/T | | | downstream-variant-500B, intron-variant | ANAPC10 | GRCh38.p7 | 4:144993861 | GTCTTCCTCCTTTTT[C/T]CTTTTAAGCAAACTT | 10393 |
rs762548009 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144976771 | ATTCTTCCATATCAC[C/T]AGTATATTTCATGCT | 10393 |
rs762560690 | snp | G/T | | | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145098855 | TTGTGGGAAGTCGTG[G/T]CTTCCACGTTTTGTT | 10393 |
rs762584536 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145024835 | TTTTCAAGCCAGGCA[C/T]TGACTTCTCCTCTCT | 10393 |
rs762601945 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145020340 | ACAAAAATCACATGA[A/T]CATCTCACCAGATGC | 10393 |
rs762615604 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145026617 | GGTTCCAAACTTATT[A/G]TCTGTGCCTCACTCT | 10393 |
rs762616914 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145049651 | ATGGCATGATCATGG[A/C]TCACTGGAACCGCCG | 10393 |
rs762653925 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145062634 | AAAAAAAAAGTAAAT[C/T]AAGATAATTGTCTAT | 10393 |
rs762678941 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144999510 | CTACACAACCACTTC[G/T]CTTCAAGGAGAACTA | 10393 |
rs762737877 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145069814 | ATATTGTAAAAGATT[G/T]AATGAACAAGCAGAA | 10393 |
rs762756875 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145030710 | TGGCTCCCTGACTGG[A/T]AGGGTGAGAACTATC | 10393 |
rs762758735 | in-del | -/ATG | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145041399 | AACTTGTTTCCAAAA[-/ATG]ATAATCATTGATAAC | 10393 |
rs762840074 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145071301 | ATCCCAGCTACTTGG[A/G]AGGCTGAGGCAGGAG | 10393 |
rs762868083 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144980900 | CCTAGCACCATTTAT[C/T]AAATAGGGAACCCTT | 10393 |
rs762879744 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145073192 | AGCCACTGCACCCAA[C/T]CTACTATTTTTTAAA | 10393 |
rs762890471 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144978537 | TTTATAAACTGTATT[A/G]CAGCTGGGCATGGTG | 10393 |
rs762927130 | snp | A/G | | | intron-variant, downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:145032838 | TTCCATCATGGAAAC[A/G]GCAGAGGTTTGTCTT | 10393 |
rs762927789 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144972847 | CACAGAGCAATTATT[C/T]TGTAAGTCAATGATA | 10393 |
rs762962943 | snp | A/T | 1.66294e-05 | 0.00288347 | missense, intron-variant | ANAPC10 | GRCh38.p7 | 4:145064612 | TTATTTCCTACTCTG[A/T]CTGAGATCTTGCTTG | 10393 |
rs762967341 | snp | C/G | 6.64695e-05 | 0.00576457 | missense, utr-variant-3-prime, synonymous-codon, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995579 | GAACATGAATCCAGC[C/G]ACTTGGTTCCACCAA | 10393 |
rs762980032 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145019126 | ATACAGAACATTCCA[C/T]CCAAGAACCACAGAA | 10393 |
rs762981587 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144988896 | CTGTGCTGTGGCACA[C/T]ATCAATCGTTCATTT | 10393 |
rs763003639 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145082171 | TATATTTTTTTGAGA[C/G]AGAGTTTCACTCTCG | 10393 |
rs763015630 | snp | C/T | 1.65938e-05 | 0.00288039 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081648 | TGAAAAATTTGAAAA[C/T]GTATTAATTACCTGA | 10393 |
rs763021506 | in-del | -/A | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145073851 | TGTTATTACCATGAT[-/A]AAAAATAGCAAGATT | 10393 |
rs763025340 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144971308 | TAATAATAAATATAA[A/T]GTTGTAAATGCACAT | 10393 |
rs763041765 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145060649 | GTGGGCAAACATCCA[C/T]GGAAAAATAAAAAAG | 10393 |
rs763060393 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145028729 | AAATGTGTTTGACAC[C/T]TGATTCACCACTCTT | 10393 |
rs763133863 | snp | G/T | | | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145097138 | AACTGGGAGGCGGAG[G/T]TTGCAGTGAGCCGAG | 10393 |
rs763157995 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145002006 | ACTGCCATGGAAAAT[A/G]AAAGAAGGAAGGAAA | 10393 |
rs763164313 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144984731 | AATGTGAAATACCAT[A/T]TCCTGAAATAAAAAT | 10393 |
rs763202359 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145059112 | CCATTCCACTTTATA[C/T]CAAATTGTTTAAAAT | 10393 |
rs763220878 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145094182 | AAAAGGAATAAACTA[C/T]AGATATGTGCCCCAG | 10393 |
rs763223911 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145089001 | GGTGTCAAGAAAGTT[A/C]TTCTCTGAAATCTTT | 10393 |
rs763236619 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145036324 | ATATAGATACGTACA[C/T]GTTATTTAGAATTGT | 10393 |
rs763273273 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144980578 | GATAGATAGATAGCA[A/C]AAATTTTCTCCCATT | 10393 |
rs763276159 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145095020 | ACAACTGAATCATAG[C/T]AGAGATAGAGGAGGA | 10393 |
rs763283310 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145025510 | GAGGGAGATGGGAAA[C/T]GGCTGGTTAGGTGCT | 10393 |
rs763330575 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144996648 | CCAGAGCAGAAAAGC[C/T]GAAAATTCTAAAAAT | 10393 |
rs763339501 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145067980 | CTTCCTGCTGCCTGG[A/G]ATATGGACATGATAG | 10393 |
rs763373469 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054179 | CCCAAAGTGCTGGTA[C/T]TACAGGCCTGAGCCA | 10393 |
rs763388211 | in-del | -/TGTA | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145012175 | GTATATGTGTGTGTG[-/TGTA]TATATATATATATAT | 10393 |
rs763413148 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144995863 | CGTACAATTTATACA[A/G]CTTGTACTCTCTGCC | 10393 |
rs763419885 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145051543 | ATAAAATGCAGTTAT[A/C]TATAAAGTGCAATAA | 10393 |
rs763423202 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145080847 | GGGAGGCGGAGGTTG[C/T]AGTAACCCGAGATCA | 10393 |
rs763428696 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145089904 | ACAAACACTGATTGT[G/T]TTACTCTGTTACTTA | 10393 |
rs763514714 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145084925 | TTTAAACGTAGCTAC[C/T]ATAAAATTCCCCATG | 10393 |
rs763592419 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144976841 | ATATTGTTTCAAACA[C/T]TTCTTCAGTTTTAAA | 10393 |
rs763595370 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145012879 | CCAATGATGGAGGGG[A/G]GCCTGGTGGGAAATG | 10393 |
rs763605452 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145071535 | AATAATATTGAATTT[C/T]ATTATTCACCATCTC | 10393 |
rs763614458 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144991154 | CAGAGGAGAACCTGG[A/G]CTTAAGGAACCACAG | 10393 |
rs763631439 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145086002 | GCAGGTGGCTGAAGC[C/T]CACCTTTGCAGGGGG | 10393 |
rs763697345 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145006525 | TAGATTTGAATTTCA[C/T]TTCTGATCAGGAATT | 10393 |
rs763734691 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145007929 | ATCAACAAAATTGAT[A/G]GACCGCTAGCAAGAC | 10393 |
rs763740566 | snp | C/T | | | intron-variant, downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:145032945 | ACTCACAGAATGCCT[C/T]ATCCATTGTCATGGT | 10393 |
rs763746059 | in-del | -/AT | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145067248 | TACAGACTATTACAC[-/AT]AGAGGCAGTAGCTCA | 10393 |
rs763774466 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144982648 | ACTATCTTTGGACCA[C/T]GACATAATGATCTAA | 10393 |
rs763775171 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145048123 | TGCCTTGGATTCTTT[C/T]CCTCAGTAAAGCTAA | 10393 |
rs763795479 | in-del | -/AGGCTGGTCTT | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144988189 | CTTGCTATGTTGCCC[-/AGGCTGGTCTT]AAACTCCTGGGCTCA | 10393 |
rs763817697 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144984887 | CGTGGAGGTAATCAT[A/G]GAATATATAATATTA | 10393 |
rs763869070 | snp | A/C | 0.000182272 | 0.00954477 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995510 | GGTGATTGGCTAGAA[A/C]AGCAATCTGTATCAT | 10393 |
rs763869375 | snp | A/G | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant, synonymous-codon | ABCE1, ANAPC10 | GRCh38.p7 | 4:145098204 | CGTTGAACAAGGGTC[A/G]CAGCTCAATGACGTC | 10393 |
rs763879940 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144978034 | ATATTTTGGCCTTCA[A/T]CTTCACTATTTATTT | 10393 |
rs763904280 | in-del | -/TG | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145029151 | TGAAGCTGGGGACAC[-/TG]AGTTCGTAAACTCTG | 10393 |
rs763923853 | snp | G/T | 1.90116e-05 | 0.00308309 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144995634 | AAATCAGATTATGCT[G/T]TTATTCAACAAATAT | 10393 |
rs763943873 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144999781 | CAAAGTTGGAGGCAT[C/T]ATGCTACCTCACTTC | 10393 |
rs763962169 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144978554 | AGCTGGGCATGGTGG[C/T]TCATGCCTGTAATCT | 10393 |
rs763967421 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145080222 | AAGGAAGAAGGTGAG[A/G]ACCCAAAAACTACCT | 10393 |
rs763998668 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145094268 | TACAGTATTTATATC[A/G]GCATTCTGGGAAAGG | 10393 |
rs764003470 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145056218 | AAACAGGCTGCAGTA[A/C]AGAAGCTGGCCCAAA | 10393 |
rs764036397 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145087369 | GCTGTTTTTTTCTTT[G/T]TTTTTGAGACAGGGT | 10393 |
rs764060440 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145065830 | TCTATATTTGTATAT[A/C]GAAAAAGACCTAGGT | 10393 |
rs764077012 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145028768 | AGGAGTTTAATGACA[C/T]TACACATAATACCTT | 10393 |
rs764156474 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145034082 | ATATTGTCTTTATAT[A/G]AAGATTATGTAGGAT | 10393 |
rs764165046 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144987437 | ACTCATAGGTGGGAA[C/T]TGAACAATGAGAACA | 10393 |
rs764165525 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145043962 | GAAGTTCTTTAATAT[A/G]TAATTTTGATCATTA | 10393 |
rs764221880 | in-del | -/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144989071 | ATGTTTTATATTTTG[-/G]GGGGGTAAATACGTA | 10393 |
rs764236630 | in-del | -/ATA | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145064886 | TAAATATAGGCCCAG[-/ATA]ATATGTTAATTATAC | 10393 |
rs764278246 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144971464 | CTCTACACACCAAAG[A/C]TCACGTGATAGTTTT | 10393 |
rs764288012 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145022086 | GTACAGCCACTATGG[A/T]AAACAGTATGGAGAT | 10393 |
rs764297957 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144981901 | CAATCTTGGCTCACC[A/G]CAACCTCCGTCTTCC | 10393 |
rs764320115 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145027619 | ATAAAAGCTACTTGA[A/G]AGAAAAATAGATCAC | 10393 |
rs764323449 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145011324 | CCTGGATGACAGAAT[A/G]AGACTGTCTTAAAAA | 10393 |
rs764331282 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144969783 | CCTGTATATCTTATG[A/T]TATATGAAATTAAAG | 10393 |
rs764439219 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145048645 | ATAGGTCCATGGATA[A/C]TAAGAAGAAATTCTA | 10393 |
rs764445253 | in-del | -/AT | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145037040 | TGTGTGTGTGTGTGT[-/AT]GTGTGTGCATGCATG | 10393 |
rs764517612 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145052803 | TGAGACAGGAGAAGC[A/G]CTTGAACCTGGGAGG | 10393 |
rs764527358 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145035327 | TTGGTCAAGAATATA[C/T]GAGTAGCTGTGCTTC | 10393 |
rs764576977 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145076745 | CTGAAAGACGAAATA[C/G]CTATTTTAAGAAAGA | 10393 |
rs764624304 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145007271 | TCAGGACTTGAACTC[A/C]GCTATGCACCAAGCA | 10393 |
rs764635332 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145003703 | CCATTGGTGTATGTG[G/T]CTGTTTTTGTATCAC | 10393 |
rs764647261 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144980607 | TTCTGTAGGTTGTCT[A/G]TTCACTCTGATGATC | 10393 |
rs764655039 | snp | C/T | 1.76971e-05 | 0.0029746 | utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995342 | AGGATAAAACAAAGA[C/T]ACGTTTAATGATTTT | 10393 |
rs764657088 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144995931 | AACTTTTAAAAATAT[A/G]TGAAACACAGATGGC | 10393 |
rs764688473 | snp | A/G | | | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145097134 | CCTGAACTGGGAGGC[A/G]GAGGTTGCAGTGAGC | 10393 |
rs764741448 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145084368 | ATAATGTCATGAATC[A/C]AGAAAAATGGCATAC | 10393 |
rs764788931 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145046391 | CATCCATATTATAAA[A/G]TCAGCTTTACTTTTT | 10393 |
rs764821964 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145023416 | TGAACAGTCCTTTGC[C/T]TCACTAACTATATTT | 10393 |
rs764822259 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145041872 | AGAAACTCAGAGTGA[A/C]ATTCAGAGACAAACA | 10393 |
rs764828409 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145062534 | ATTGTTTGAACCTGG[A/G]AGGTGGAGGTTGCAG | 10393 |
rs764841694 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145030631 | CTCATCCTGTGGTCA[C/T]TTCCCCAGTGCCAGA | 10393 |
rs764874852 | snp | C/T | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant, synonymous-codon | ABCE1, ANAPC10 | GRCh38.p7 | 4:145098189 | TGGCTTCGCCAACGG[C/T]GTTGAACAAGGGTCG | 10393 |
rs764916437 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145061205 | AAGAGCTCTTTTTCT[A/G]TATGGCTAATGTTTC | 10393 |
rs764921179 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054848 | TATGTATCTACCCTC[A/G]CATCTATTTTATTCA | 10393 |
rs764952041 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145005058 | AATATCTTCCTTGTT[C/T]AATCTTCAGAGATTA | 10393 |
rs764971454 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144976918 | GAGAGTATGAATTGG[A/G]CCCAAAGGAATCAAA | 10393 |
rs765014899 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145014939 | AGAATCTGAACAATA[A/G]CCTTCAGCCCTAGAC | 10393 |
rs765059054 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145071244 | AAACCCCATCTCTAT[C/T]AAAAATACAAAATTA | 10393 |
rs765066363 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145018853 | TAAAAAAGACAAAGA[A/G]GGACATTAAATAATG | 10393 |
rs765070026 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144998689 | TAAAATTGACACAAT[A/G]ACATCACAATTAAAA | 10393 |
rs765085711 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145091463 | ACAGGAATATTTGAT[A/T]CAATAATGGATATTA | 10393 |
rs765089127 | snp | C/T | 3.32624e-05 | 0.004078 | synonymous-codon, intron-variant | ANAPC10 | GRCh38.p7 | 4:145064605 | GTGAAAATTATTTCC[C/T]ACTCTGACTGAGATC | 10393 |
rs765148471 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145027667 | TTAAAAGTGGCATTG[G/T]ATTTCTCAACATTTA | 10393 |
rs765158563 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145069876 | AAGGTTCACAAAAAA[C/T]GTAAACAATGACACT | 10393 |
rs765158817 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144969665 | TCTAGTATGGGGATA[A/G]CTAAATCTTAACAGT | 10393 |
rs765243402 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144976533 | AAAGGAAAATAGACC[A/G]ACAAAATCAGCCAAG | 10393 |
rs765279464 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145051260 | GATAAAAAAGCAGCC[A/T]GTTGGTGGAGTAGTC | 10393 |
rs765283242 | snp | A/T | 1.65701e-05 | 0.00287833 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995469 | GTATATTTTAATTTG[A/T]CTCATATGGGTGTCT | 10393 |
rs765357337 | snp | C/T | 1.73957e-05 | 0.00294916 | utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995351 | CAAAGATACGTTTAA[C/T]GATTTTCGTCTCATT | 10393 |
rs765360985 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144984484 | GCCACAGACGAATGC[C/T]AGCGTAAAAAGGAGA | 10393 |
rs765372905 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145016502 | AAGAACATTCCATGC[A/T]CATGGATAGGAAGAA | 10393 |
rs765407699 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144999310 | CTGGCAGAGACACAA[C/G]AAGAAAAGAGAATTT | 10393 |
rs765418043 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145016251 | AAAATCTCCTTAAGC[A/T]AATAAGCAACTTCAG | 10393 |
rs765455611 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145027370 | AAAGAAGTAGAAAAT[A/G]AGAAAATTAGGGGTC | 10393 |
rs765497254 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145040514 | CTCCTTTCAGCTACC[A/G]TTCACTGAGCTGCTA | 10393 |
rs765575474 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145051451 | ATGTGATAGAAACAG[A/G]AATTGAGCACAAGCT | 10393 |
rs765581744 | snp | A/G | 1.65605e-05 | 0.0028775 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145095951 | AAACTGCAAGTGACT[A/G]TTTCCAACAGCTTTT | 10393 |
rs765604149 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145021898 | AGATATACAAATGGC[C/T]AACAAACATACGAAA | 10393 |
rs765610276 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144984051 | AATCTAGCAACTAAA[A/T]ATTTCAAGACAGAAA | 10393 |
rs765625527 | in-del | -/A | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145026775 | AAGAATTTAAAAAAC[-/A]AAAACAAAGCATCAT | 10393 |
rs765638815 | snp | A/G | 1.6631e-05 | 0.00288362 | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145096118 | TAAAATATTCTATGT[A/G]GAAAACAAGAATGCA | 10393 |
rs765654675 | in-del | -/AA | 0.0276742 | 0.114329 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145053784 | TAAAACATGAGGCTG[-/AA]AAAAAAAAAAGGTTC | 10393 |
rs765667446 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145065687 | AATATAGCCATTCAA[C/T]GAACTGCTATAGAAC | 10393 |
rs765669229 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145011156 | GGCCAAAACGGTGGA[A/G]CCCCATCTCTACTAA | 10393 |
rs765712856 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145088829 | CTTTTTCAGGGCCTA[C/G]AAGAGTTCATATAAT | 10393 |
rs765732228 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145007781 | ACTAGAGAAGCAAGA[C/G]CAAACAAATTCAGAA | 10393 |
rs765775444 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145034766 | GGCAGGCTGGGTGGA[A/T]GTGTGTTAGGCTGCA | 10393 |
rs765783303 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144994576 | CCACATTTCCATGTA[C/T]TTCTTTAAAATCTTT | 10393 |
rs765802979 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145039265 | ATTCCACAGCTAAGC[A/G]ATTCTTACTGCAAGG | 10393 |
rs765810403 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145095507 | ACATCATCGTGGCTT[C/G]ATGATCCAGAATCAC | 10393 |
rs765818479 | in-del | -/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145019263 | CTCTCTCAGACCACA[-/G]TGGAATAAAACTGGA | 10393 |
rs765822012 | snp | A/G | | | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145099750 | GTGATACTAAACATC[A/G]TTAGTTAACAGCAGT | 10393 |
rs765831335 | in-del | -/A | 0.0502877 | 0.150383 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145053784 | TAAAACATGAGGCTG[-/A]AAAAAAAAAAAGGTT | 10393 |
rs765840856 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145060773 | CTTGTTTTAGTATAT[C/G]AGTCAGAAGCAGCAA | 10393 |
rs765850219 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145078633 | TTCAAACTAAACTTC[A/C]AAACAACAGTAGCCA | 10393 |
rs765872888 | in-del | -/AC | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144976500 | TTATGCTACATACAT[-/AC]ACACACACACACACT | 10393 |
rs765891079 | in-del | -/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145072899 | TCTATTACGTATCTG[-/T]TTTTTTTTTTTTTTA | 10393 |
rs765895534 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145059470 | CTGAAGACAAAAACA[A/G]AGCTTAAAATTCACT | 10393 |
rs765941115 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145044610 | AAGAGAATTTTATTT[G/T]TAAGTGTTTCTATTA | 10393 |
rs765968325 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145076559 | TTCTTACATCCAAAT[A/G]AGCACACTAGTTGCC | 10393 |
rs766006255 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145036237 | GATAAGGGAAGTAGA[C/T]GAGAGAAGGAATGGG | 10393 |
rs766028459 | snp | C/T | 1.66324e-05 | 0.00288374 | synonymous-codon, intron-variant | ANAPC10 | GRCh38.p7 | 4:145064620 | TACTCTGACTGAGAT[C/T]TTGCTTGGAGTATAG | 10393 |
rs766058129 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145021852 | CCATCAAAAAGTGGG[C/G]TAAGGACATGAATAG | 10393 |
rs766072533 | in-del | -/CT | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145016800 | CAACAGAACAGAGCC[-/CT]CTCAGAAATAATACC | 10393 |
rs766115221 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145038244 | AGGGCCGGGCATGGT[A/G]GTTCATGTCTATAAT | 10393 |
rs766167993 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145084170 | CTATGTCTGTTCCAC[A/G]TAATCCAAACATGAA | 10393 |
rs766168740 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145046248 | GGCAGTTAAGATGTA[C/T]ATAAATAACTTTTAA | 10393 |
rs766208776 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144973347 | TAACAATAAACACTG[C/G]ATTCCAAACGCGGGG | 10393 |
rs766210335 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145031471 | CCTACAACCAAGAAA[C/G]AGGCACGACACCTAG | 10393 |
rs766210477 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145013233 | AAAATTTGATAAGGA[C/T]AGTATAAGAAAGAAC | 10393 |
rs766237571 | in-del | -/AT | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144989053 | CAAGTCTTTGTATGG[-/AT]ATATGTTTTATATTT | 10393 |
rs766284290 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145082638 | ATATATTCTGAAGCC[A/C]AATGCTTCTGATTAA | 10393 |
rs766303145 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145069436 | AAAACTTCACAAGGA[C/T]AGGCAAAGAACAAGC | 10393 |
rs766306698 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144982789 | GGTTTCTGTTATTGA[C/T]AGCTAAATGCAATCC | 10393 |
rs766345015 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144971913 | GAATTTCAGTCCCTA[A/C]CTTTATTGTCTCTAG | 10393 |
rs766370853 | snp | A/T | 1.6585e-05 | 0.00287962 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081654 | ATTTGAAAATGTATT[A/T]ATTACCTGAATTGGA | 10393 |
rs766378805 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145065279 | GAAGAAACACATAAT[A/G]GAAAACGAACCTCAG | 10393 |
rs766459656 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145078611 | GAGGCATCACATTAC[C/T]CCCAACTTCAAACTA | 10393 |
rs766459736 | snp | A/C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145092561 | AAGACCAAATGCAGG[A/C/G]TAGCATAATAGTACA | 10393 |
rs766482336 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145061452 | ATTCTCCAGGAAAAA[C/T]AAGTACAACTAAGAT | 10393 |
rs766522258 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145088737 | ACACAGTCATCTTTT[A/T]AAAATTCTGTATCAG | 10393 |
rs766544071 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145014810 | GGCTGGTAGACTTGC[C/T]GGATGGCCAGACCCA | 10393 |
rs766603046 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145050236 | TCAAAGCTCTTGGGT[A/G]ACTATGTCCATTGTC | 10393 |
rs766604556 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145040331 | TTTTGTATTGTTAAT[A/C]GAGACGGGGTTTCTC | 10393 |
rs766628132 | snp | C/T | | | intron-variant, utr-variant-3-prime | ANAPC10 | GRCh38.p7 | 4:145063897 | TCTGTTCATATGACA[C/T]TGTAAAACAGGCAAT | 10393 |
rs766633875 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145090220 | TACTTCAAATCATCT[C/T]TAGATTACTTATAAT | 10393 |
rs766645824 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054785 | CAGTAAATGAAGACT[A/G]TAAGAGACCCCAGCC | 10393 |
rs766652898 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145086120 | GGCGCCTGCCAACAC[A/G]CCCAGCTAATTTTTG | 10393 |
rs766681296 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145049737 | GATGTGCATCACCAC[A/G]CTCAGTTAATTTTTT | 10393 |
rs766709460 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145013149 | TTTCTTTACAAATTA[A/T]CCAGCCTCAAGAATT | 10393 |
rs766740632 | snp | G/T | 1.66646e-05 | 0.00288652 | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145096130 | TGTAGAAAACAAGAA[G/T]GCACACATTGTATCA | 10393 |
rs766742659 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144983942 | GAATGATGTGAAAGG[G/T]GTGAAACTAAAAGTG | 10393 |
rs766787057 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144992814 | CAATTTTGAAAGAAG[C/T]TCTATTGTGAGTAAA | 10393 |
rs766797098 | snp | A/C | | | utr-variant-5-prime, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145098253 | CCAGGGTTCCGCCTC[A/C]CGCTCTATGTCGCGC | 10393 |
rs766876937 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145006661 | TTTCTGTATAATTGT[C/T]ATACTTTCCTCAGAA | 10393 |
rs766934082 | snp | G/T | 1.65699e-05 | 0.00287831 | missense, nc-transcript-variant | ANAPC10 | GRCh38.p7 | 4:145081672 | TACCTGAATTGGATG[G/T]TCACTAAATGAGGCT | 10393 |
rs766935518 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144984308 | TTTGTCTCCATATCC[A/G]TTTAACATGTGATTG | 10393 |
rs766940703 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145016191 | AATTGTCCCTGTTTG[C/T]AGATGACATGATTGT | 10393 |
rs766954520 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145075470 | TGTGGCCAGGAAGAG[C/G]TTCATTCACCGAGAA | 10393 |
rs766965333 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144969448 | TAATTCACATGAACA[A/C]AAAAATAAAATCAGC | 10393 |
rs766974282 | snp | A/G | | | intron-variant, downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:145062984 | ACTCAGAAGCAGAAG[A/G]AGAATGATAGTTTCT | 10393 |
rs767012207 | in-del | -/A | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144984061 | TAAAAATTTCAAGAC[-/A]AGAAATAAATTTTGT | 10393 |
rs767049383 | in-del | -/ATAGATAG | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144980512 | GATATTAGACCTTTC[-/ATAGATAG]ATAGATAGATCGATA | 10393 |
rs767094112 | in-del | -/A | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145003820 | TCATCTTGGCTATTT[-/A]AAGCTCTTTTTTGGT | 10393 |
rs767107772 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144976898 | AAAAAAGTAATTTGA[C/T]TTGAGAGAGTATGAA | 10393 |
rs767133272 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145019436 | AAAACCTGTGGGATA[C/G]AGCAAAGGTGGTGCC | 10393 |
rs767143852 | snp | A/T | 1.67846e-05 | 0.0028969 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145064703 | TTCTTCTAAAAGCAA[A/T]AAAGTAAAAATAACA | 10393 |
rs767143908 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145051331 | AGCATGGTTCATGGC[A/G]TCCCAAAACAATTAC | 10393 |
rs767162544 | in-del | -/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144988336 | GATTTTGAAAGTGTC[-/T]TATACCCAGATTATA | 10393 |
rs767182257 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145020484 | ATATAATACTGAATG[C/G]CAAAAAGTTGAAAGC | 10393 |
rs767224979 | snp | A/G | | | intron-variant, downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:145033004 | CAGCTAAAGAAGTAT[A/G]GCAGTGGGCACATGC | 10393 |
rs767234981 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144971866 | CTTACTATGTATCAG[G/T]TACTATTGTCCTAAG | 10393 |
rs767238162 | in-del | -/A | 1.74296e-05 | 0.00295204 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144995613 | AGTTGCTGCCAAGGG[-/A]AAAAAAAATCAGATT | 10393 |
rs767299427 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145095219 | GTTTCATCTCCGCAG[C/T]TTCAGTTACCCTTGG | 10393 |
rs767307439 | in-del | -/ACT | | | intron-variant, downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:145063103 | CAGTATATAACAGTG[-/ACT]ACATTAATAAACAAT | 10393 |
rs767322651 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145038132 | TTGAGGCCAGAAGTT[C/G]CAGACAAGCCTGGCA | 10393 |
rs767341110 | snp | C/T | 1.66721e-05 | 0.00288717 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995378 | CATTTTAAAGTCACC[C/T]TATTGAACGATACAT | 10393 |
rs767356853 | in-del | -/GTGTGTGTGC | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054633 | TGTGTGTGTGTGTGT[-/GTGTGTGTGC]GCGCGCGCGCGCGTG | 10393 |
rs767371885 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145059302 | TGTCAAAGTACCATA[C/T]ATGGACTCACATGGT | 10393 |
rs767376635 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081092 | CTTGGCCAACATAGC[A/G]GCCAACTGTCTCTTA | 10393 |
rs767379769 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145042897 | ACATCTTTAAAATAA[C/G]AGGTAAAGAAAAAAT | 10393 |
rs767399903 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145094310 | GGACCCAAAACTGAG[C/T]TGTCAGGGGCTTGGA | 10393 |
rs767411595 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144989250 | TTCTGGCAATCCTGC[A/G]TTAAGCAAGTCTATC | 10393 |
rs767413281 | in-del | -/TGTG | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145040134 | GTGTGTGTGTATGTG[-/TGTG]TGTGTGTGTGTGTGT | 10393 |
rs767471337 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145053011 | TATAAATACTATTAT[C/T]ATTTTAGCTAAGTGT | 10393 |
rs767473203 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144967644 | AATAAAATTTTCTAG[C/T]TCTTATCATAAACAT | 10393 |
rs767482042 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145002032 | GGAAAAACTACTTGA[C/T]AGTTGCTTCAGTAGT | 10393 |
rs767503467 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145003588 | CCCAACACCATTTAT[G/T]GAATAGGAAGTCCTT | 10393 |
rs767528563 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145036521 | CAAATATTTCACACT[A/G]TTTTTTTTAAGAGAT | 10393 |
rs767583677 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145030244 | AATTATAAAAACAGA[A/G]AATCACAGCCTCTCA | 10393 |
rs767586354 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145090092 | TGTTTAAGTTGTATA[A/C]CTCTGCACATATTAT | 10393 |
rs767614203 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144987792 | CTATTGTTTCCTCAG[G/T]AGACTGTAAGCAACT | 10393 |
rs767636867 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145013092 | GCTTCCCCAGACATG[C/T]TTCCTGTACAGCCTG | 10393 |
rs767649103 | in-del | -/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144996007 | AATACTAAGTAGATA[-/C]CTCATATTTTGAACA | 10393 |
rs767651560 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145088514 | AACAGTATGAGTTGT[C/T]CTGCCAGAAAGGTCA | 10393 |
rs767678902 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145069334 | ACTGAATTGATAAGG[A/C]ATAAGCTACACAAAG | 10393 |
rs767683041 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145026664 | GTCAAGGATCTCCTG[G/T]TATGTAAGAAACAAG | 10393 |
rs767700422 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144992227 | AGAGCTCTGATGGAG[A/G]GTTATGTTGTTTTCA | 10393 |
rs767741375 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145078452 | AAAATGGTCATAACT[A/G]CCCAAAGCAATTTAT | 10393 |
rs767750039 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144973051 | GGAAACTTTACAGCC[C/T]TTAAGTATATATTTT | 10393 |
rs767782048 | snp | A/G | | | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145097217 | AAAAAGCACAAAAAT[A/G]AGAAAAAAATGTTAA | 10393 |
rs767794177 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145062644 | TAAATTAAGATAATT[A/G]TCTATAACAAGACCA | 10393 |
rs767857393 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144995968 | GACACAAGTAGTATG[G/T]GCCTCCTCCATGAAA | 10393 |
rs767867086 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145023544 | AAGGCCCCTGTAGAC[A/T]TTCAACCAGTTTGCA | 10393 |
rs767892373 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145061348 | TAAAATTTACAATAG[A/C]ATACAAAACATCTTT | 10393 |
rs767916759 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145068188 | CACCTTGTAGAAAAC[A/G]CCATTATCAAAAGCT | 10393 |
rs767920273 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145024841 | AGCCAGGCATTGACT[C/T]CTCCTCTCTAGCTAT | 10393 |
rs767966719 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145052778 | CTGTAATCCCAGCTA[C/G]TCGGGAGGCTGAGAC | 10393 |
rs768007570 | snp | A/G | | | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145099209 | TATTGTGAATGAATG[A/G]CAGCCAAAGCCGAAT | 10393 |
rs768067472 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145091037 | TTAATATGTAAAATG[C/T]TAATCATATAATGAT | 10393 |
rs768075117 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145091105 | GTAAGACATATGACA[C/T]TGCACTACTGAACTT | 10393 |
rs768076165 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144978861 | TTCTCGCAGAGTGGC[C/T]CAGAACTAAAGTTAG | 10393 |
rs768112782 | in-del | -/A | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145015203 | ATGATACAAGAAGTG[-/A]AAGGAGAGATATTCA | 10393 |
rs768116869 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144982735 | CAGATTTTTTAATAT[A/G]TGAGAAATATAGAAA | 10393 |
rs768117822 | snp | G/T | | | downstream-variant-500B, intron-variant | ANAPC10 | GRCh38.p7 | 4:144993981 | GACCCTGTTGTTTAC[G/T]TGACTGTTTTCCTTA | 10393 |
rs768170052 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144982027 | GTTTTTTTTGTTTTC[A/T]GTAGAGACTGGGTTT | 10393 |
rs768200859 | in-del | -/GGCA | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145029402 | TTAGACTAAAGTCCT[-/GGCA]GGACCCTGGAGGTGA | 10393 |
rs768210518 | snp | C/T | 0.000185822 | 0.00963724 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | ABCE1, ANAPC10 | GRCh38.p7 | 4:145097488 | TAGGTGCAATAGTTC[C/T]GCATACCGTTTCCTT | 10393 |
rs768255111 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145026323 | CAGTGAAACCAAGAA[C/T]AACAACAAAATCCCT | 10393 |
rs768310338 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145007315 | TCCATAGAACTCTCC[A/T]CCCCAGATGAACAGA | 10393 |
rs768312252 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145089570 | GGTAGAGACTAACAA[C/T]TGTGCTGAATTGTAA | 10393 |
rs768319025 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145050983 | ACTTTTCCCTTATAT[C/T]CACAACTTCGCTGTT | 10393 |
rs768361645 | in-del | -/GTCAA | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145061741 | AATACAATTTAATAC[-/GTCAA]GTCATCAGAGAACTA | 10393 |
rs768371072 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144969257 | CTCAGTAAATGTTAA[C/T]TATTTTTAATGTTGT | 10393 |
rs768386455 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144970483 | CTGAAAACCGGACTG[A/G]CACATGAGTAGTCTA | 10393 |
rs768395918 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144981153 | TCTTTATTGGTTCCA[C/T]ATGAATTTTTAAATA | 10393 |
rs768395966 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145021307 | TCACCAAAACAGCAT[A/G]GTACTGGTATAAAAA | 10393 |
rs768409256 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145015101 | GAAATCCCTGACTTA[C/T]CTGAAAAAGAATTTG | 10393 |
rs768417003 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145075148 | TTACCTTATTGCATC[A/C]CAAAATCATACTAGC | 10393 |
rs768467875 | in-del | -/CATT | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144993081 | ATAAAGGTATACATA[-/CATT]CATTGTTTTTTTTTA | 10393 |
rs768521374 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145037862 | TGAGGCAGGAGGATC[A/G]ATTGAACCTAGAAGG | 10393 |
rs768563625 | in-del | -/ATC | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144977191 | TATGATTCCACAAGT[-/ATC]ATCCTCTAGAGAATG | 10393 |
rs768574237 | in-del | -/A | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144983456 | GGATAAGGTATACTC[-/A]AACCTGCATAGTACT | 10393 |
rs768608059 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144980186 | TTTGAGCGTTATTCC[C/T]AACATTGTCTTCCAC | 10393 |
rs768646682 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145020411 | AAAACTCAGCAAAAT[C/T]GGCATAAAGGAACAT | 10393 |
rs768653237 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144971435 | CTACCCTATATAGCA[A/T]CTAGAGGATGTTGCT | 10393 |
rs768654677 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144990480 | CATGGTTCTGCAGAC[C/T]GTACAGGAAGCTGGT | 10393 |
rs768670204 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145034980 | TACTGTTTGTGGGCA[C/G]AGATCTGAGAGGAAC | 10393 |
rs768671597 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145047349 | AGACTGGGTTTTTCC[A/G]TCTGTAAGCCAAGGT | 10393 |
rs768701869 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145088297 | TCCCTTAGAATATCA[C/T]TGGCACACTGATGAC | 10393 |
rs768722828 | snp | C/T | 1.65726e-05 | 0.00287855 | synonymous-codon, nc-transcript-variant | ANAPC10 | GRCh38.p7 | 4:145081740 | ATCTCGTAACTGATC[C/T]ACTCCAAATCCTAAA | 10393 |
rs768728819 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145003400 | GTATATACCGAATAA[C/T]GGAATTTGTGGGTGA | 10393 |
rs768738905 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144974494 | CCTAGCGAGTACAAT[A/C]AGAAAATAAAATAAA | 10393 |
rs768779740 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145045910 | TGTAATTTTAAAAAA[C/T]GATCTGATCTAATAA | 10393 |
rs768791499 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144972857 | TTATTCTGTAAGTCA[A/T]TGATAAAAGGATACC | 10393 |
rs768815069 | in-del | -/CAAAAAAAAAAA | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145039010 | ATAAAAACAATGTCT[-/CAAAAAAAAAAA]AAAAAAAAAAAAAAA | 10393 |
rs768821542 | snp | C/G | | | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145096170 | CATCTTTCTACAAAA[C/G]TTTTTTACCAAGAAA | 10393 |
rs768823387 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145082185 | ACAGAGTTTCACTCT[C/T]GTGGCCCAAGCTGGA | 10393 |
rs768865292 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145026250 | CTCAATTTAACATTT[A/G]TTGATTGACTGAATG | 10393 |
rs768876683 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145083251 | TAATATTTATTAGCT[C/T]ATATAACAACATAAA | 10393 |
rs768888304 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054210 | CCGTGCCCAGCCTGA[C/T]TACTACTGTTTTAAT | 10393 |
rs768889791 | in-del | -/TG | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145028159 | AATCCTGGGTGTGCC[-/TG]TGTGTGTGTTGCCAA | 10393 |
rs768976594 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145069008 | GACCATGTTTTGAAA[C/G]GATATATGAGACCTT | 10393 |
rs769050995 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145038060 | CATTTTATGACTGGG[C/T]CTGGTGGTTCACGCC | 10393 |
rs769054381 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145095037 | GAGATAGAGGAGGAA[A/C]AGAGAAGACCTTATG | 10393 |
rs769066940 | in-del | -/TGA | | | intron-variant, cds-indel | ANAPC10 | GRCh38.p7 | 4:145064167 | AAATTAAGCAAATGT[-/TGA]TAACTCTACCAATAT | 10393 |
rs769090314 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145090813 | TTACATTATGTAGTA[A/G]TAGTTTAAAGCTATA | 10393 |
rs769102718 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145055329 | TTGAGAGGCCGAGGC[A/G]GCCAGATCACCTGAG | 10393 |
rs769112526 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144976038 | TCTATCTATCTGTCT[A/C]TCAATCGATCTAACC | 10393 |
rs769194497 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144997165 | GTGGAAATCACTCTT[A/C]AGGATATTGCCCAGA | 10393 |
rs769201897 | snp | G/T | 3.31636e-05 | 0.00407194 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995552 | TTGGCTTCTTATGAT[G/T]GTCAGTTAAGGGAAC | 10393 |
rs769210126 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144997279 | GCAACACCAAGATAC[A/G]TACTTGTCAGATTCA | 10393 |
rs769243303 | in-del | -/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145050746 | ACCAACCTCGGCTAG[-/T]TTCAAGCTTTTCTTC | 10393 |
rs769246237 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145006456 | AACGATAGCAATGAA[C/T]AAAAGAATGTAGGGC | 10393 |
rs769297785 | snp | C/T | 3.31526e-05 | 0.00407127 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995445 | AATGGAGCTCTCTTC[C/T]ACTGGTGTGTATATT | 10393 |
rs769310336 | snp | A/G | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant, missense | ABCE1, ANAPC10 | GRCh38.p7 | 4:145098169 | TTCTCGGCACCTCCA[A/G]CAGCTGGCTTCGCCA | 10393 |
rs769355578 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145026172 | CCAGAGAATGCATTA[C/T]TATTTTATGGGCAAA | 10393 |
rs769388289 | snp | C/T | 0.000928246 | 0.0215235 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | ABCE1, ANAPC10 | GRCh38.p7 | 4:145097560 | ACAAGCACTTGATAC[C/T]TACTAAATAACGGCA | 10393 |
rs769390341 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145039869 | AAAGTGCTGGAATTA[C/G]AGGCGTAAGTCACTG | 10393 |
rs769403906 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145079419 | AAGGGAATACTTATA[C/T]ACTGCTGGTGGTAAT | 10393 |
rs769443564 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145041052 | AAGTAGCTCCCCAAC[C/G]CAATGACCCACAAAC | 10393 |
rs769506283 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145078114 | ATATAATTCTACACC[C/T]AGAAAACCCCATAGT | 10393 |
rs769509095 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144982618 | CTCTCAAGTGCCAAT[A/G]TGATAGTTACATCAA | 10393 |
rs769509735 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145073079 | TTAAGTTTTTTATAG[A/T]GACAGAATCTTGCTT | 10393 |
rs769510263 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145051560 | ATAAAGTGCAATAAG[C/G]TGAAAAGCATAAAAT | 10393 |
rs769528121 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145034096 | TGAAGATTATGTAGG[A/G]TCTCAGCAGATACAT | 10393 |
rs769546402 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144969654 | AGAAAAGAGAGTCTA[C/G]TATGGGGATAACTAA | 10393 |
rs769547883 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145072398 | AACTGCTACATAAAT[C/T]GAGAGTTGCTTATTT | 10393 |
rs769559046 | snp | A/T | | | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145100369 | AAAAAATTGTCTTTT[A/T]CAGTCTTTTGGTTTT | 10393 |
rs769641671 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145086774 | CCCAACTCCCCCCAC[C/T]CTCATGTCCCCAGTA | 10393 |
rs769680990 | snp | G/T | 1.66067e-05 | 0.00288151 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081641 | CAGTAGATGAAAAAT[G/T]TGAAAATGTATTAAT | 10393 |
rs769706930 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145050933 | TCTTATTATTCATGT[A/G]TTCACTAGAGTAGCA | 10393 |
rs769777805 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144978157 | CTACACTGGGCACTG[A/G]TAATATCTGTCCTTA | 10393 |
rs769788889 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145094982 | TCCAATTGAGAGAAA[C/T]GGCCAAAAAAAATAA | 10393 |
rs769794970 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145001670 | CACCCACCACCTTTC[C/G]CATCACTCAATATTC | 10393 |
rs769805019 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145059937 | AATGCTAAAACGCAA[C/G]GGATTTAAGAATTTA | 10393 |
rs769850255 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145056901 | ATATGGTTAAATAAA[C/G]GGTTTTTAGATTTTG | 10393 |
rs769915383 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145000724 | AAGGATTATAAATCA[C/T]GCTACTATAAAGACA | 10393 |
rs769923189 | in-del | -/C | 1.65605e-05 | 0.0028775 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145095949 | GGAAACTGCAAGTGA[-/C]TATTTCCAACAGCTT | 10393 |
rs769967200 | in-del | -/ATTTT | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145004009 | TTTGTATCATCTCTG[-/ATTTT]ATTTTATTTTTTTTG | 10393 |
rs769984805 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144986092 | TTGCATCCCAGGCAT[A/G]AAGCCCACTTGATCA | 10393 |
rs770020016 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145001895 | GATTTACAGTATTAA[C/T]TGCAGCATAAACAAA | 10393 |
rs770034992 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145043815 | TGGAGGATCCATATT[A/G]CCTAAAATGTTTCCA | 10393 |
rs770048467 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144970863 | AAGCCAGGGATCTCT[A/G]GAGAGTACATGCAGA | 10393 |
rs770072446 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145021095 | TTGTGAAAATGACCA[C/T]ACCACCAAAAGCAAC | 10393 |
rs770103174 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145005099 | AATGTATCCATTTCT[A/T]TTTCCTTTTCTTTTT | 10393 |
rs770130790 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145067458 | ACTACACGCTTTCTC[A/C]TGAGAAAGAGCTTCT | 10393 |
rs770135553 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145082156 | TCTTCTAGGAGATAT[C/T]ATATTTTTTTGAGAC | 10393 |
rs770152906 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144979997 | AGATTGTACAACCCG[A/C]CCCTGGCCAATGGGG | 10393 |
rs770167955 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144972725 | CATAGAACACTGCAC[A/C]CCAAAACTCAAGGGT | 10393 |
rs770185793 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145068941 | ATGTCCTCTGTATCA[A/C]TGTTAACTAGATGCT | 10393 |
rs770221015 | snp | A/G | 1.69934e-05 | 0.00291486 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145064528 | TATCTTCTAATGAGT[A/G]AAAGTTAAAGGATGA | 10393 |
rs770252114 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144974048 | TCACAGGTCAATCTC[A/G]CTCATAATGCAAAAA | 10393 |
rs770254559 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145012803 | TTTTAACTATTTTTA[A/T]AAGGCCTTGATATAG | 10393 |
rs770267765 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144990820 | AATCAGCTTTCCCAT[C/T]ATCTTGGATTCCCTT | 10393 |
rs770295488 | snp | C/T | 0.00123196 | 0.0247883 | missense, utr-variant-3-prime, synonymous-codon, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995573 | TTAAGGGAACATGAA[C/T]CCAGCCACTTGGTTC | 10393 |
rs770313466 | in-del | -/GTTG | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144987982 | TTTTTGTTTTTTTTT[-/GTTG]TTGTTGTTTTTGAGA | 10393 |
rs770319794 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145028312 | AGCCTAGCCTCCCAG[A/C]CTGCATCTTTCTCCC | 10393 |
rs770377293 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145045532 | GTTCCAAAGCCATTC[C/T]ACAAAAGAATATCCA | 10393 |
rs770423342 | in-del | -/ATAG | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144980516 | TTAGACCTTTCATAG[-/ATAG]ATAGATAGATCGATA | 10393 |
rs770455721 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145024712 | ATGAGTAGAACAGAT[A/T]TAGCATAATTCTTAA | 10393 |
rs770492635 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144982533 | TGCTGAATATTTCCA[A/G]GTTCCGGAAACGTTT | 10393 |
rs770493120 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145037762 | GAGCAGCCTGGCCAA[C/T]ATGGCAAAACCCTGT | 10393 |
rs770507991 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144986124 | GGTGGATAAGCTTTT[C/G]GATGTGTGGCTGGAT | 10393 |
rs770513463 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144997050 | AGAAAAAAGAGTAAA[A/T]AGAAATGAACAAAGC | 10393 |
rs770521335 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054063 | ACAGGCACTCGCCAC[C/T]ATTCCCAGCTAATTT | 10393 |
rs770524321 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145039593 | AATAGCCCTATGAGG[A/T]ATACTCTTTTTTTTT | 10393 |
rs770545634 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144981814 | ATAGCAGTTACTTTA[C/T]TTTATTTTTTATTTT | 10393 |
rs770629954 | snp | A/G | | | intron-variant, utr-variant-3-prime | ANAPC10 | GRCh38.p7 | 4:145063380 | TTTGTCAATACATAT[A/G]CAAGTTTTACGAGAA | 10393 |
rs770638921 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145084202 | GGATTTGTATCTTAA[A/G]TTTGCATCTGCTGCC | 10393 |
rs770656429 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145085532 | GTTCAAAGAACAAAA[C/T]AGTATTTGTTCTTAA | 10393 |
rs770681185 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145049291 | TTAAAATAACACTGA[A/C]GTTTACCTCATTTAT | 10393 |
rs770682613 | snp | C/T | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | ABCE1, ANAPC10 | GRCh38.p7 | 4:145097677 | TCAGTTATGAACTAG[C/T]TGTCACTTGCCTGCA | 10393 |
rs770737622 | snp | A/C | | | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145098673 | ACCCGCGAGGGACTT[A/C]GAGAATGGACCTAGA | 10393 |
rs770774138 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145089808 | ATATCACTTCCTATC[C/T]GATTTATCGCGTCTC | 10393 |
rs770815419 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144968542 | TAGGAAACAATATAG[C/T]CTGGCCTTCTTTTCA | 10393 |
rs770845090 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145062470 | AAATTAGCTGGGCAT[A/G]GTGGCGCATTCCTGT | 10393 |
rs770863368 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145024499 | GATGTTGTATCAGCA[A/C]ACATGAAAACATTAA | 10393 |
rs770895434 | in-del | -/TGTGTA | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145037035 | GTGTGTGTGTGTGTG[-/TGTGTA]TGTGTGTGCATGCAT | 10393 |
rs770910770 | snp | C/T | 3.31203e-05 | 0.00406928 | upstream-variant-2KB, missense, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145096032 | TGTGACCCAATTTCC[C/T]GTACTGTTCCAGTCC | 10393 |
rs770957962 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145004856 | GTGTCAGGATGCTGT[A/T]GGCTTCACAGAATGA | 10393 |
rs770995618 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145070828 | AAAGGAATGAAATTC[G/T]GACACATGCTACAAC | 10393 |
rs771000852 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081761 | AAATCCTAAAAACAC[C/T]AAAAGTGTCAATAAA | 10393 |
rs771008932 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145006305 | ATCTGCCAATCAAGT[A/G]GAAAAGATAAAGGGA | 10393 |
rs771068095 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145076457 | CCATCTAAAGGACAG[C/T]AACTTCAAAGATTAA | 10393 |
rs771075791 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144976408 | CAAAGAGGGCTTCCA[A/G]GGTACTGATGTGCTC | 10393 |
rs771101609 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145032498 | TCCCATATGAGTGCT[C/T]GCCAACAAGTGACCT | 10393 |
rs771118905 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145086644 | ATGGCAGTACTGATA[C/T]TTTGGACTGAATAAT | 10393 |
rs771148648 | snp | A/T | 1.66178e-05 | 0.00288247 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995582 | CATGAATCCAGCCAC[A/T]TGGTTCCACCAACTC | 10393 |
rs771149851 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144977912 | TTCCTGCCCTAGTCA[A/G]TGCAACCAGCTATAA | 10393 |
rs771152635 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145018501 | AAATAAGCCAGGCAT[A/G]GTGGCAGGCACCTAT | 10393 |
rs771221193 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145036839 | ACAAGCACTCAATTA[A/C]TGCTGAGGTACATAT | 10393 |
rs771262649 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145001073 | TAGCATTAGGAGAAA[C/T]ACCTAATGTAAATGA | 10393 |
rs771306910 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145094767 | TAAAGAGAAAAACCT[C/T]AGATGCTTCCAGAAA | 10393 |
rs771316366 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145082034 | AAATTAACCAGAATT[A/C]TTCTACCCTTTTATT | 10393 |
rs771343229 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145026482 | TGTACAGCTTTAAAT[A/G]AGGTGGTCAGAATAG | 10393 |
rs771365448 | in-del | -/AAC | | | intron-variant, cds-indel | ANAPC10 | GRCh38.p7 | 4:145063321 | TATCTCAAAAGACAA[-/AAC]AACAACAAAAATACC | 10393 |
rs771425912 | snp | A/C | | | downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:144966744 | AGATTCAGTATAAAA[A/C]ACCTTTTATTTCCCA | 10393 |
rs771449743 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145088686 | TCCTCCATTGGTGTT[C/T]ACCATTATGCCACTA | 10393 |
rs771458925 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145077882 | ATAATTCAAAATAAT[A/G]AGGGCCATCTATGAC | 10393 |
rs771502839 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145059350 | ACACAAGTAGAGAGC[A/G]AAAGGCCACATGAAA | 10393 |
rs771518059 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145058292 | CTTTATGTACATCAT[G/T]ACCCTGCTAGAATGC | 10393 |
rs771633872 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145089632 | GAATCTACTAAACAC[A/T]TTCCAACTTTAATCT | 10393 |
rs771634226 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145015936 | GAACTGCTGAAAGGA[C/G]CTCGAAACCTTAAAA | 10393 |
rs771641110 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144980283 | CATCTGTTGCTTTTT[C/G]ACTTTTTAATAATAG | 10393 |
rs771643615 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145012289 | TTTATACTTAACATA[C/T]TGAAAATATTGTCAC | 10393 |
rs771659414 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145067206 | ATGCTATGTTTCAAA[G/T]AGCAATGCATGTCAT | 10393 |
rs771664218 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145019309 | GAACCTTCAAAACAT[G/T]CAAATACATGGAAAT | 10393 |
rs771676468 | in-del | -/AGTA | | | downstream-variant-500B, intron-variant | ANAPC10 | GRCh38.p7 | 4:144993892 | AATAAATAAGCAGTC[-/AGTA]AGAAGTAACATTATT | 10393 |
rs771776475 | snp | A/C | | | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145096233 | TCATTTATTCTGAAG[A/C]ATGCAGTTAATATAA | 10393 |
rs771814674 | snp | A/G | 1.6577e-05 | 0.00287893 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995431 | CTAGGAAATTTACCA[A/G]TGGAGCTCTCTTCTA | 10393 |
rs771817627 | snp | A/G | | | downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:144966682 | AAAAATGTATCCCCA[A/G]TTGGGCTCATGGTTA | 10393 |
rs771828054 | in-del | -/CTAA | | | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145099342 | TTCCCAACAGGACTG[-/CTAA]CTAGTCATTTATGAT | 10393 |
rs771861652 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144972324 | GAATGGAAAAAAACA[C/T]AGCATTCAAACATTA | 10393 |
rs771862321 | snp | A/G | 1.65608e-05 | 0.00287752 | upstream-variant-2KB, synonymous-codon, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145096064 | TTCCAACTGCTTGGG[A/G]TCAGCACCAGGAGGT | 10393 |
rs771890496 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145046135 | CTACAGTGACTTTCA[C/G]GGCTTCATTCACTGC | 10393 |
rs771898743 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145061989 | AATCACTTGAACCTG[A/G]GAGGCAGAGGCTGCA | 10393 |
rs771975602 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145076393 | TAAACCCAACTTGTA[C/G]CACAGTAAAACCCTC | 10393 |
rs772004111 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145037231 | GAAACGTATCTTTTA[C/T]CTTAGAACAAAAATG | 10393 |
rs772041489 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145005389 | CTAGCTAGCAGTCTA[G/T]CTTATTCTTTCAAAT | 10393 |
rs772054364 | in-del | -/TATA | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145012161 | ATTACAAGCTATATG[-/TATA]TGTGTGTGTGTGTAT | 10393 |
rs772055732 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145004478 | ATGTTGGCTGTGGGT[C/T]TGTCAAAGATGTCTC | 10393 |
rs772064407 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145040973 | GGAACAAAGTTCTTA[C/G]TACAGATCTACGCAG | 10393 |
rs772090557 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145021780 | TATACATCTGAAAAT[A/G]GACTAATATCCAGAA | 10393 |
rs772146010 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144980446 | TTTTTGCCCACTTTT[G/T]AATGGGGTTGTTTGT | 10393 |
rs772149497 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145023137 | TACCCAATTGTACCA[A/G]TGACTGTCACAAACA | 10393 |
rs772156642 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144974821 | TAAAAGACTCAATAT[G/T]GTAAAAGTATCATTT | 10393 |
rs772159109 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144990636 | AATCAGATCTCCTGT[A/G]AACTCAGAGTGAGAA | 10393 |
rs772193343 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145032336 | GGATGTACAATTATA[A/C]ACTGATTCATGGGCT | 10393 |
rs772195837 | snp | C/T | 1.68043e-05 | 0.0028986 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081619 | AGATTTATTTGTCTA[C/T]AACCTACAGTAGATG | 10393 |
rs772229783 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145047456 | CAGGTTAAATGGAGT[C/T]CAGTGAGTCATGATA | 10393 |
rs772251283 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145014398 | CTCCATTGACCTGGG[A/C]ACCTCACCCCTATCC | 10393 |
rs772255772 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145068458 | CTAAATGTAAAAAAC[A/C]AAATAGTTATAAAAC | 10393 |
rs772322459 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145039952 | AGGCTAACATTCCAA[C/G]GTTCATGGTTAAATG | 10393 |
rs772341241 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145031253 | ATTACATTGATGACA[C/T]TGTGCTGACTGGATC | 10393 |
rs772366073 | snp | A/G | | | intron-variant, utr-variant-3-prime | ANAPC10 | GRCh38.p7 | 4:145033161 | GGGCAAAGTTCTCCA[A/G]AAGGCTGTGTATGCT | 10393 |
rs772396176 | in-del | -/TC | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144978567 | GGCTCATGCCTGTAA[-/TC]TCAACTACTTAGGAG | 10393 |
rs772397606 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145055522 | AATATCACGTCACTG[C/T]ACTCCAGCCTGGGTG | 10393 |
rs772398161 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145006100 | TAAGTCTCTTTGTAG[G/T]TCTCTAAGAACTTGC | 10393 |
rs772508461 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145079596 | TGTTGATTGCAGCAC[C/T]ACGCACAATAGCAAA | 10393 |
rs772531118 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145041377 | ATCATTTTGAGAAAA[A/G]TGTTTTAACTTGTTT | 10393 |
rs772537558 | in-del | -/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145055919 | ATTTTGTGGTATATG[-/T]TTTTTGCAATTAAAA | 10393 |
rs772563438 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054888 | ATTCTGTGTCTTCCC[A/G]TATCTTATAGTTGTA | 10393 |
rs772599827 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144997494 | GCCAAACTAAGCTTC[A/G]TAAGTGAAGGAGAAA | 10393 |
rs772617825 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145037629 | AAATCATTTAACTAT[G/T]AAGTAAACAATTGCT | 10393 |
rs772623363 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145091919 | AGCCACAGATACAAG[C/G]CTATCTTGAATAGGA | 10393 |
rs772634466 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144983849 | CAGAATGCCATAGGA[C/T]GGAATATCATTTGAA | 10393 |
rs772648444 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145015977 | AAACACATCAAAACA[C/G]AACCTCTTTAAAGCA | 10393 |
rs772651181 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145072609 | ACTTATATAATAGAG[A/G]TAGGAAAGTTAGTTC | 10393 |
rs772699199 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144996453 | GAAGGGAGACTTGGC[A/G]CTCCCATGCACCCCT | 10393 |
rs772726791 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144999063 | CACCCAAGACTAAGC[A/C]AGGAAGAAGTTGAAT | 10393 |
rs772745294 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145036123 | TAAGCATTAGGACAT[G/T]GTATGATTCAGGCAT | 10393 |
rs772757346 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145000370 | TACAAGAAAAAAAAA[A/C]CATCAAAAAGTGGGC | 10393 |
rs772769033 | in-del | -/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144999900 | AGAAATAACACCACA[-/T]TATCTACAACCATCT | 10393 |
rs772770916 | in-del | -/TA | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145012176 | ATATGTGTGTGTGTG[-/TA]TATATATATATATAT | 10393 |
rs772778097 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145019678 | GAAAAGATAAACTGA[C/T]AGACCATTAGCAAGA | 10393 |
rs772789115 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144995709 | TAACATTTTGCTCAA[C/T]GAAAGAATGACAATA | 10393 |
rs772792025 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145089678 | CCATTATTTCAAAGA[C/T]ACAAAAAGATTTTTG | 10393 |
rs772829050 | in-del | -/A | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144967478 | CTTTAAGAATTTGCG[-/A]AAAAAATGGGCATGG | 10393 |
rs772867180 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144989327 | TTTTGGTAATTCTCT[A/C]TCTCAAACTTTTTCA | 10393 |
rs772871552 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145021781 | ATACATCTGAAAATG[A/G]ACTAATATCCAGAAT | 10393 |
rs772947444 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145046138 | CAGTGACTTTCAGGG[C/G]TTCATTCACTGCTTA | 10393 |
rs772977697 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145052458 | CAGAGGTGGAATCCG[C/T]GTATTTTCTAATTTT | 10393 |
rs772979978 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145002121 | GAAATTCTGTAGAAT[C/T]TTACTACGAGAACTG | 10393 |
rs772991722 | snp | C/G | | | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145096326 | ACTTTGGGAGGCTGA[C/G]ACAGGAGGATCATGT | 10393 |
rs773002305 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145047475 | TGAGTCATGATAATT[C/G]CATGCTACCGATAAT | 10393 |
rs773029381 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145088710 | GCCACTATCAACCAT[C/T]ATCCACAGTGGACAC | 10393 |
rs773044375 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145095305 | TTTTAAACTGTGTAC[C/T]GTCTGAGTAGTGTGA | 10393 |
rs773076888 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145060610 | TATTAAAACATTTCA[A/G]TACACACTACACTAC | 10393 |
rs773113228 | snp | C/G | 1.66023e-05 | 0.00288113 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081643 | GTAGATGAAAAATTT[C/G]AAAATGTATTAATTA | 10393 |
rs773120368 | in-del | -/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145072690 | TGCTAAAAAAATCTA[-/C]CCCAATCCTAAATCA | 10393 |
rs773123716 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145004696 | TCCAGGGATGAAGCC[C/G]ACTTGATGTTGGTGA | 10393 |
rs773139684 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145005758 | TTCATTTCCATGTAA[C/T]TGCATGGTTTTCAGT | 10393 |
rs773191493 | snp | C/T | 1.6601e-05 | 0.00288101 | stop-gained, utr-variant-3-prime, missense, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995574 | TAAGGGAACATGAAT[C/T]CAGCCACTTGGTTCC | 10393 |
rs773213526 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145003592 | ACACCATTTATTGAA[C/T]AGGAAGTCCTTCCCC | 10393 |
rs773215774 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145023238 | AAAACCAACAAATAA[C/T]AACAGGCAAACAAAA | 10393 |
rs773227799 | in-del | -/TTTG | 1.65608e-05 | 0.00287752 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145095966 | ATTTCCAACAGCTTT[-/TTTG]TTTGTTAGTTTTTAC | 10393 |
rs773254847 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144991923 | GAAAGTCAATGCCTG[C/G]CTTCAAAGTTTCAAG | 10393 |
rs773292468 | snp | C/T | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | ABCE1, ANAPC10 | GRCh38.p7 | 4:145097580 | AAATAACGGCAGACA[C/T]AACGGACTGTAAACT | 10393 |
rs773306468 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144976357 | ATACGGGTTAATCTT[G/T]GAGAGGATAAAGGAA | 10393 |
rs773311137 | snp | C/T | 1.65693e-05 | 0.00287826 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995486 | TCATATGGGTGTCTC[C/T]TCCATTCTGGTGATT | 10393 |
rs773345320 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145085466 | TGGCTACCTCAGCTA[C/G]GTTTTTTTTCTCCTC | 10393 |
rs773373672 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145070786 | AAATGTGGCACAGTC[A/G]TACAATGGAATATTA | 10393 |
rs773380438 | in-del | -/TATGTTCCTGG | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145068600 | CTATATTCTTCCATA[-/TATGTTCCTGG]TATAAAAGTGAAAAA | 10393 |
rs773390455 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145079633 | GAATCAACCTAGATG[C/T]CCATCAACAGTGGAC | 10393 |
rs773507796 | in-del | -/A | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145091993 | TGCTGCTGCACTAGG[-/A]AAAACAGAGAACTAC | 10393 |
rs773522816 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144997795 | ACTGGCAAATTAGAT[A/G]AAGAGTCAAGACCCA | 10393 |
rs773575903 | snp | C/T | | | intron-variant, utr-variant-3-prime | ANAPC10 | GRCh38.p7 | 4:145033214 | GTACAGTTTCTCCCA[C/T]AGCCAGGATTCACAG | 10393 |
rs773593061 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145024924 | AAAATGTATTGCTTA[C/T]TGTATCTACCCTCAT | 10393 |
rs773606417 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145069356 | TACACAAAGAAAAAA[C/T]TCCAGAAATATGCGT | 10393 |
rs773632384 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145088295 | GTTCCCTTAGAATAT[C/T]ATTGGCACACTGATG | 10393 |
rs773666034 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144969341 | GACATTCAAAGGGAC[C/T]TGGGTCCCTCTAAAT | 10393 |
rs773707795 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144999170 | AGATGGATTAAGAGA[C/T]GAATTCTACCAGAGG | 10393 |
rs773717503 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145010551 | AGGTGAAAATCATCA[C/T]TCTGAGCAAACTATC | 10393 |
rs773738648 | in-del | -/TAAGA | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145055121 | CTGAATAAAGGATCT[-/TAAGA]TAAGTGTACATCCAC | 10393 |
rs773738671 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145092304 | TGCACATCCTACACA[C/T]GTACCCCAGAACTTA | 10393 |
rs773781015 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145052369 | TTATAAGCACCATAA[A/G]TATACACAATTTTCT | 10393 |
rs773824030 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145040018 | AAAGCCCATGCTCTT[A/G]GATCTTTAACAACCC | 10393 |
rs773836771 | snp | C/T | | | downstream-variant-500B, intron-variant | ANAPC10 | GRCh38.p7 | 4:144994021 | AGGAAAACATCAGTG[C/T]CTAGTGTATATTTCT | 10393 |
rs773837091 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145010546 | CATGAAGGTGAAAAT[C/G]ATCATTCTGAGCAAA | 10393 |
rs773840694 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145087115 | GACAAATGGAGCAGA[A/C]TTGAACCTGACTCAC | 10393 |
rs773873237 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144978587 | ACTACTTAGGAGGCC[A/G]AGGTGGGAGAATTGC | 10393 |
rs773890703 | in-del | -/TA | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145039586 | GCCTTGCAATAGCCC[-/TA]TGAGGTATACTCTTT | 10393 |
rs773904372 | in-del | -/AATA | | | downstream-variant-500B, intron-variant | ANAPC10 | GRCh38.p7 | 4:144993877 | CTTTTAAGCAAACTT[-/AATA]AATAAGCAGTCAGTA | 10393 |
rs773944451 | in-del | -/A | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145033702 | GGTCACTCCACCAGG[-/A]AAAAAAAATCCATGA | 10393 |
rs773951618 | in-del | -/GTGTGT | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145036998 | CCAAATAGATAACGT[-/GTGTGT]GTGTGTGTGTGTGTG | 10393 |
rs773954221 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145051094 | AGTTAAAGTGAGAGA[C/T]GTGAAACTCTTCCTT | 10393 |
rs773983535 | in-del | -/TAAA | | | intron-variant, downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:145062788 | TCATCAATGAATGGG[-/TAAA]TAAACTGTGGGGTAT | 10393 |
rs773995614 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145002027 | AGGAAGGAAAAACTA[A/C]TTGATAGTTGCTTCA | 10393 |
rs774014927 | snp | A/G | 1.65833e-05 | 0.00287948 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081655 | TTTGAAAATGTATTA[A/G]TTACCTGAATTGGAT | 10393 |
rs774014958 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145035080 | ACTCCCTTACCCACA[A/G]TTCTGGTTAGGTGAG | 10393 |
rs774068906 | in-del | -/AC | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145051701 | TAGAGGAATAAGCCA[-/AC]ACAGCCACATAGTTA | 10393 |
rs774072558 | snp | A/G | | | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145099302 | GGAAGAACTGTCCAA[A/G]TAACATGTTTTATTT | 10393 |
rs774079962 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145059193 | GAGCCAGAACTTTTG[C/T]CTGCATCTTCTTACT | 10393 |
rs774096487 | in-del | -/TAT | 1.79245e-05 | 0.00299365 | utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995328 | ATTATTTAAATACAG[-/TAT]GATAAAACAAAGATA | 10393 |
rs774099224 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145065528 | AAAATACAGTAACAC[A/T]ATCACTCAAAAATTG | 10393 |
rs774100536 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144983549 | GTCAGGCAAGTAAAC[A/G]CTCCCAGGGAGTGAC | 10393 |
rs774134761 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145060468 | TAATTTATTGCTAAA[C/T]AAGGCAGCTATATGC | 10393 |
rs774138595 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145088407 | CTAGAAAAATAGGCA[C/T]TGCAAAATTAACATA | 10393 |
rs774175568 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145074182 | GAGAAGCAAAAAGCT[C/T]CTCTATTTTCCATTT | 10393 |
rs774203290 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145043978 | TAATTTTGATCATTA[C/T]CAAAAAAAGAGAAAA | 10393 |
rs774207747 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144980191 | GCGTTATTCCTAACA[C/T]TGTCTTCCACAATGG | 10393 |
rs774231421 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145003410 | AATAATGGAATTTGT[A/G]GGTGAAATGGTAATT | 10393 |
rs774262788 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145021311 | CAAAACAGCATGGTA[A/C]TGGTATAAAAATAGG | 10393 |
rs774267019 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145029710 | CCCACTGTGAGAGAG[A/G]TGGAAATACCTGATC | 10393 |
rs774275739 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145037900 | CCCAGTGAACCATGA[C/T]TGCGCTACTGCACTC | 10393 |
rs774289609 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144990538 | CAGAAAGCTTACAAT[C/T]GTGGTGGAAGGTCAA | 10393 |
rs774308600 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145075175 | TAGCTTTTTTAGCAA[C/T]CACATCACACTGTTA | 10393 |
rs774367721 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144974337 | AGGAAATAGCATTAA[C/T]TTGATTAAGGATTTC | 10393 |
rs774385668 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144991526 | GGGACTACAGGCACC[C/T]GCCACCACGCCCGGC | 10393 |
rs774390312 | snp | C/T | 1.69372e-05 | 0.00291004 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145064544 | AAAGTTAAAGGATGA[C/T]ATATTTTTAAAAATT | 10393 |
rs774419054 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144972870 | CAATGATAAAAGGAT[A/G]CCTTGAAAATCTCTA | 10393 |
rs774498220 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144989084 | TTGGGGGGTAAATAC[A/G]TAGAAGTGGAATGAC | 10393 |
rs774509559 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145090835 | AAAGCTATACTTCCT[A/C]CACTAAATTGTGAAG | 10393 |
rs774510107 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145083697 | ACATACTGAGAAAAA[C/T]AGAATAATTGCACTT | 10393 |
rs774515112 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145031189 | TGTCATAATCTTATT[C/T]GAAGAGACCTTGATC | 10393 |
rs774537856 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145055392 | GTGAAACCCTGTCTA[A/C]ACTAAAAATACAAAA | 10393 |
rs774539989 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144982637 | TAGTTACATCAACTA[C/T]CTTTGGACCATGACA | 10393 |
rs774546910 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145050058 | TAGAATGGTAAGTTA[C/T]TTCCAGAAGATTTTC | 10393 |
rs774595946 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145012935 | CTTTGGTGCTGTTCT[C/T]ATGATAGTGAGTGAG | 10393 |
rs774625119 | snp | A/C | 1.66485e-05 | 0.00288513 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995591 | AGCCACTTGGTTCCA[A/C]CAACTCAAGTTGCTG | 10393 |
rs774641916 | in-del | -/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144977634 | AACCTTCACACTCCA[-/C]CACTTGTTTTCCATG | 10393 |
rs774687941 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145095079 | TAAATCTAACTAGGG[A/T]ATAGTAAAGAAATTG | 10393 |
rs774721385 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145085347 | TTTTAGTACTAGTTT[C/T]TGAGTTCCCTAGTAA | 10393 |
rs774743066 | snp | A/G | | | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145096182 | AAAGTTTTTTACCAA[A/G]AAAAATTTAATGGAA | 10393 |
rs774825779 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995357 | TACGTTTAATGATTT[-/T]CGTCTCATTTTAAAG | 10393 |
rs774828431 | snp | C/G | 1.66457e-05 | 0.00288489 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081797 | GTGAAAAAGAAACAA[C/G]TATACATGCAAAACA | 10393 |
rs774829635 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145029158 | GGGGACACTGAGTTC[A/G]TAAACTCTGATGAGG | 10393 |
rs774842962 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144997378 | AGCCCATCAGACTAA[C/T]AGCAGATCTCTCACC | 10393 |
rs774907879 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145084759 | GGCTACTTGAAATAT[A/T]GCAAGTCCAAATTGA | 10393 |
rs774915897 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145069228 | AAGAAAATAAATGAG[A/G]TGAGCCCTACAAACA | 10393 |
rs774934892 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145014243 | GACTCAGTGCTGTTG[A/G]TGGGGGGCACAGTGT | 10393 |
rs774969029 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054254 | GTCGCCAGAAATATT[C/T]ACGCAAAATTTACCA | 10393 |
rs774989970 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145078362 | AAAACACTGCTGAAG[A/G]AAATCAGACATGACA | 10393 |
rs775029438 | in-del | -/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145060664 | CGGAAAAATAAAAAA[-/G]ATTTAGGTGGATTTT | 10393 |
rs775055407 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144967222 | AGATAGAATTTATCA[A/G]CCATTAACAGTTATA | 10393 |
rs775083414 | snp | A/T | 1.65641e-05 | 0.00287781 | upstream-variant-2KB, synonymous-codon, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145096076 | GGGGTCAGCACCAGG[A/T]GGTGTCTTGTTTGGT | 10393 |
rs775085970 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145069495 | AGTAAGCCAAACAAT[C/T]TCCAGTGGGCACAGA | 10393 |
rs775090682 | snp | C/T | | | intron-variant, utr-variant-3-prime | ANAPC10 | GRCh38.p7 | 4:145063652 | CAACAGCCACAGCTT[C/T]ACAATTATGTAGTTC | 10393 |
rs775097759 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144992522 | ACATTGAGGGGTTTA[C/T]GACTTCAGTGGAAAA | 10393 |
rs775116696 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145018957 | TTATAAAACAATTAC[C/T]AATAGACCTAAAAAA | 10393 |
rs775143501 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145049650 | AATGGCATGATCATG[A/G]CTCACTGGAACCGCC | 10393 |
rs775158791 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144977086 | GTCTCGCTTACAAGT[A/G]AATTTTTCTAAGAAT | 10393 |
rs775193382 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145024797 | TGCATCAGCCCCTAA[C/T]AAAATCAGCTTGTCT | 10393 |
rs775203975 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144968975 | AATTATTGCTATGAG[G/T]TATTCGATACTAGAC | 10393 |
rs775217899 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145073173 | TGTTGGGATTATAGG[C/T]GTGAGCCACTGCACC | 10393 |
rs775244842 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145079512 | CTACTATTTGACCAA[A/G]CAATCCCATTACTGG | 10393 |
rs775258946 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144983717 | GAATAATGAAAAACA[A/G]TTTTTGAAAAGTCAG | 10393 |
rs775280570 | snp | G/T | | | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145098842 | TGTGCATATTTGGTT[G/T]TGGGAAGTCGTGGCT | 10393 |
rs775283338 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145008949 | AAAACCCCACTGTCT[C/G]AGCCCAAAATCTCCT | 10393 |
rs775361585 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145056990 | CAGTGCAGGTCTTCT[A/G]TAACTGCTGCAAAAG | 10393 |
rs775382194 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145020309 | AAATGTGATACACCA[C/T]ATAAACAGAATGAAA | 10393 |
rs775390886 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144971282 | TGCCACTGGCTTGCA[C/T]TGGCACCGTGTAATA | 10393 |
rs775393135 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145043853 | TTCTTTTTTTTCCCT[G/T]TGAAAACCAAACCCT | 10393 |
rs775397885 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145085908 | TCACTTTGCCGCCCA[C/G]GCTGCAGTGCAGTGG | 10393 |
rs775449346 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145086899 | ATTCATCTATGGTTA[C/T]TGTTATTGTTTGGTA | 10393 |
rs775512028 | in-del | -/TA | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145002347 | ACTCAAAAGGCTCAC[-/TA]TATGGAAAGCAAGCT | 10393 |
rs775594027 | in-del | -/A | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145080907 | GCAAAACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 10393 |
rs775609459 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145094178 | AATAAAAAGGAATAA[A/G]CTACAGATATGTGCC | 10393 |
rs775623912 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145058958 | GACTTCAAAGATGAA[C/T]TAAAGTTAGTTATGA | 10393 |
rs775624488 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145050961 | GCACGTTTAATTTCC[A/G]TCAGGAACTTTTCCC | 10393 |
rs775624563 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144976634 | AGAGAAAATTATTCA[C/T]ATACAGAATCTTTTC | 10393 |
rs775657344 | snp | C/T | | | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145097108 | CCAGGGGGGCTGAGA[C/T]AGGAGGATCACCTGA | 10393 |
rs775715216 | snp | A/G | 3.3605e-05 | 0.00409895 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081620 | GATTTATTTGTCTAT[A/G]ACCTACAGTAGATGA | 10393 |
rs775730416 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145036299 | AGATATGATTAGATC[A/G]CAGCTTTAAATATAG | 10393 |
rs775764783 | in-del | -/A | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145021952 | AGGCAAATGCGAATT[-/A]AAAATCACAATGTGA | 10393 |
rs775781987 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145092899 | CTATACCTGAGAGAG[A/G]GGCAAACAACAGTCC | 10393 |
rs775835758 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054149 | CTTGACTTTGTGATC[G/T]GCCCGCTGCGGCCTC | 10393 |
rs775890066 | snp | A/G | | | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145100252 | CCAGCTATTCGGGAG[A/G]CTAAAGCAAGAGGAT | 10393 |
rs775903593 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144995849 | ATGTTTACTGAACTC[A/G]TACAATTTATACAAC | 10393 |
rs775935627 | snp | A/T | | | downstream-variant-500B, intron-variant | ANAPC10 | GRCh38.p7 | 4:144993931 | AACTTCCTGTACTTT[A/T]AAAAAAATTAGATTT | 10393 |
rs775970095 | snp | A/C | 3.59202e-05 | 0.00423778 | utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995326 | TATATTATTTAAATA[A/C]AGGATAAAACAAAGA | 10393 |
rs776028479 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145024523 | ACATTAATTTCCTTG[A/T]ACATCTCCATCAAAG | 10393 |
rs776029022 | snp | A/G | 1.65767e-05 | 0.00287891 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995436 | AAATTTACCAATGGA[A/G]CTCTCTTCTACTGGT | 10393 |
rs776037667 | in-del | -/ATGT | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145037040 | TGTGTGTGTGTGTGT[-/ATGT]GTGTGCATGCATGAA | 10393 |
rs776063007 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145082169 | ATTATATTTTTTTGA[A/G]ACAGAGTTTCACTCT | 10393 |
rs776063514 | in-del | -/TGTGTGTG | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145040130 | TTTAGTGTGTGTGTA[-/TGTGTGTG]TGTGTGTGTGTGTGT | 10393 |
rs776070386 | snp | A/T | | | downstream-variant-500B, utr-variant-3-prime | ANAPC10 | GRCh38.p7 | 4:144967136 | AAGAGCTTCACCTCC[A/T]CCATTCTCACTTGAT | 10393 |
rs776114001 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144972738 | ACCCCAAAACTCAAG[G/T]GTAAATACTATTTTC | 10393 |
rs776207303 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145029641 | GCTCAAGGAGTTAAA[A/G]AAGGTTCTAATAGGT | 10393 |
rs776207990 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144982541 | ATTTCCAGGTTCCGG[A/T]AACGTTTTCCTTCCT | 10393 |
rs776230497 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145004981 | TCTGGGCTTTTCCTG[A/G]TTGGTAGGCTTTTTA | 10393 |
rs776233837 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145077723 | ATAGGCTCCACATAT[C/G]CAAATCAATAAATGT | 10393 |
rs776288708 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145008785 | AACTGGCACGAGACA[A/G]GGATGCCCTCTCTCA | 10393 |
rs776324816 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145037854 | CAGGAGGCTGAGGCA[G/T]GAGGATCGATTGAAC | 10393 |
rs776331064 | snp | C/T | 1.65647e-05 | 0.00287786 | upstream-variant-2KB, synonymous-codon, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145096079 | GTCAGCACCAGGAGG[C/T]GTCTTGTTTGGTGTA | 10393 |
rs776343240 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145046590 | AAGCTTAAAATTGCT[A/C]AATTCTTGCTTTACA | 10393 |
rs776369575 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145006352 | TAAAGGGATTTGCTG[C/G]GCAGATCCCTTTACC | 10393 |
rs776379399 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145041132 | AACAGATTTTACTTA[C/T]AGAAGTATAAAAATT | 10393 |
rs776429740 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145085613 | AAATGTCCTATAATT[C/G]AAAACTGATCATTTA | 10393 |
rs776432282 | snp | C/T | | | intron-variant, downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:145032644 | CCATGGTAGCAGGAA[C/T]GGAGGTTACACATGG | 10393 |
rs776449891 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145084225 | CTGCTGCCTTTATTG[C/T]GCATACTAGTGGATA | 10393 |
rs776467941 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145076581 | CTAGTTGCCCAGCAA[G/T]GGTTCTTAACCGGAT | 10393 |
rs776525280 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144976517 | CACACACACACACTT[A/T]AAAGGAAAATAGACC | 10393 |
rs776538472 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144984368 | AGCTGGCTGAACTCT[C/T]TGCTTCAGTCTTTTG | 10393 |
rs776543037 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145006561 | AAATTACTTATGCTA[C/G]CTAACCTTTATTTCT | 10393 |
rs776557070 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144999303 | CCAAAGCCTGGCAGA[A/G]ACACAACAAGAAAAG | 10393 |
rs776557949 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144992361 | TAAGTGATTCTTCTG[A/T]TGGATCTCAGCAAAA | 10393 |
rs776565466 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145036888 | AAAGACAATTAAGAA[A/G]GTTAACATAAAAAGG | 10393 |
rs776582995 | snp | C/T | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant, missense | ABCE1, ANAPC10 | GRCh38.p7 | 4:145098155 | TGCCGAAACTCAGAT[C/T]CTCGGCACCTCCAGC | 10393 |
rs776607336 | in-del | -/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145001042 | CTGTCGTAGGGTGCA[-/G]GGGCAGGGGGAGGGA | 10393 |
rs776654197 | in-del | -/CAT | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145073211 | CTATTTTTTAAATGA[-/CAT]CAGCACTTTAATTTT | 10393 |
rs776731300 | in-del | -/C | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995150 | TAAAATGATTGGCTT[-/C]AAATCCATTTTTAGT | 10393 |
rs776767553 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145072797 | ATTCAATATGTAGGT[A/G]ACTAGTAAAGTCCAA | 10393 |
rs776813227 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145056675 | GTGGGGTCCTGTAAC[A/G]GTGTGGTTATTTAAC | 10393 |
rs776836033 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145028296 | GTGAAAAGGAGAGAC[A/G]AGCCTAGCCTCCCAG | 10393 |
rs776862492 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145041750 | ACTAAAATTTAATAA[A/C]TGGTTCCAGATATAC | 10393 |
rs776872612 | snp | C/T | 1.76783e-05 | 0.00297302 | utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995344 | GATAAAACAAAGATA[C/T]GTTTAATGATTTTCG | 10393 |
rs776888472 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145010904 | AACAAAAATATACAT[C/T]TCTTTTTTAGAAGGC | 10393 |
rs776910392 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145070916 | ATATTATATAATTCC[A/T]CTTATATCAGGTCCC | 10393 |
rs776943730 | in-del | -/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144980696 | CTTTTGTTGTGATTG[-/C]TTTTGGCATTTTTGT | 10393 |
rs776952534 | snp | A/C | | | downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:144966965 | GACTTGTGTGTGCAG[A/C]CCCACAAAGCTCCCA | 10393 |
rs776956326 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144986334 | ATGGTATCAGCTCCT[C/T]CTTGTACCTCTGGTA | 10393 |
rs776963628 | in-del | -/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145060150 | TGTTCTTAAATTGTT[-/G]GTTTTCAATTTATGT | 10393 |
rs777016985 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145055422 | AGTTAGCCGGGCATG[G/T]TGGTGTGTGCCTGTA | 10393 |
rs777046379 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145055789 | TGTTATTTAATGACT[A/G]TGATTTTTGGTTTTG | 10393 |
rs777111196 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145079853 | GTGTAGTGGCTCACA[C/T]GTATAATCCCAGCAC | 10393 |
rs777129042 | in-del | -/A | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145047131 | TAAACAGAGGCTCAG[-/A]AAAAAACAGAGAAAT | 10393 |
rs777131265 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145021130 | AAATTCACTGCAATC[A/C]CCATCAAAATACCAT | 10393 |
rs777164120 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145080767 | ACAAAATTAGCCGGG[C/T]GTGGTGGCGCATGCC | 10393 |
rs777168827 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144974111 | GCAAATTATTAGCAA[A/G]CAAAATTAAGTGATT | 10393 |
rs777182077 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145093947 | ATAATGGACACAATG[A/T]CTTTTACAACCTAGT | 10393 |
rs777235752 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145070214 | AAATAAAATTTTATT[G/T]AAACTAAGTGACACT | 10393 |
rs777254478 | in-del | -/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144990051 | TTTAAAATGGCAGTA[-/T]TATCTCTGTCATGCC | 10393 |
rs777258057 | in-del | -/A | | | intron-variant, downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:145063173 | GAGAGTTCTCACCAC[-/A]AAAAAAGTGGTATGT | 10393 |
rs777307870 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145024427 | TTATGAAATGTATAT[A/C]TTAAATAATAAGAAT | 10393 |
rs777309193 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144996964 | TTCAATAGCTGATTC[A/G]ATCAAGTGGAAGAAA | 10393 |
rs777346824 | snp | A/G | 1.65743e-05 | 0.00287869 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995452 | CTCTCTTCTACTGGT[A/G]TGTATATTTTAATTT | 10393 |
rs777365640 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145055121 | CTGAATAAAGGATCT[C/T]AAGATAAGTGTACAT | 10393 |
rs777391568 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145079085 | AAGAAACTATTAACG[A/G]AGTAAACAGACAACC | 10393 |
rs777408424 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145040651 | TGCCCAAGGGTCACC[C/T]AGCTAGTGACCTAGC | 10393 |
rs777419763 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145012755 | TAACCTAAATTTTCC[A/G]CCAACACAGAGAATA | 10393 |
rs777444043 | snp | C/T | | | intron-variant, utr-variant-3-prime | ANAPC10 | GRCh38.p7 | 4:145063237 | TCATTCTACAAAGTA[C/T]ATATATTTCAAAACA | 10393 |
rs777446464 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145027847 | CATGTGGAGGATGTA[C/G]TCCACCAATAAAGGA | 10393 |
rs777460093 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145068755 | TCTCCACTAAAAATA[A/C]AAAATGTAGCTGGGT | 10393 |
rs777463885 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145084732 | CCAATACGGTAGCCA[C/G]TAGCCACATGTGGCT | 10393 |
rs777482661 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144968269 | GATACATGAATTTCT[C/T]TAAGAAGGACGGGGG | 10393 |
rs777502568 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145030754 | CCAAATGGAAGCCAA[C/T]AGAGCTACCTTTACT | 10393 |
rs777525851 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145050975 | CGTCAGGAACTTTTC[C/T]CTTATATTCACAACT | 10393 |
rs777569048 | in-del | -/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145034689 | TTAGTTCTGTCCCTC[-/T]TAAGAGAAACCTGAC | 10393 |
rs777573071 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145086304 | AACTAAAACAAAGAC[A/G]TATCTATGATAACTG | 10393 |
rs777599663 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081039 | ATTTTGGGAGGCTGA[C/G]GTGGGAGGAATGCTT | 10393 |
rs777639824 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145008616 | ATAGATGCAGAAAAG[A/G]CCTTTGACAAAATTC | 10393 |
rs777680703 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144983122 | CCAAGATCGTGCCAC[C/T]ACACTCCAGCCTGGG | 10393 |
rs777699619 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145071822 | GTGGGTGGCTGATTC[C/T]CTCAACCCACAAAAG | 10393 |
rs777701101 | in-del | -/TGTATGT | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145037037 | GTGTGTGTGTGTGTG[-/TGTATGT]GTGTGCATGCATGAA | 10393 |
rs777719940 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145087528 | GATACAAATGGTCTC[G/T]GTAGAGAAGTTCATC | 10393 |
rs777743545 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145025675 | TGGTGAAAAAGTTTG[A/G]AGTTTGAAATACTAC | 10393 |
rs777747747 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145006160 | TGCATATATATTTAG[A/G]GCAGTTAAGTCCTCT | 10393 |
rs777757464 | snp | C/T | | | downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:144967011 | TTTAATTAAATCTTA[C/T]AACCCTGAAATAAGA | 10393 |
rs777805354 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144982545 | CCAGGTTCCGGAAAC[A/G]TTTTCCTTCCTGTCA | 10393 |
rs777809479 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145050308 | GTAGGTCTTTACAGT[A/G]GGATTAAAATATTCA | 10393 |
rs777849657 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145090646 | TTAATCTTTCTGTAC[G/T]AGTTTCCTCATTTGG | 10393 |
rs777855636 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144977543 | GATAAATTTCACCTC[A/G]CTCTACCCTTCTCTT | 10393 |
rs777883112 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145015862 | ATGAAGGAAAGATAC[A/G]GTGTTTTCCAGACAA | 10393 |
rs777907335 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145091546 | GGAGGGGGAAATCAC[C/T]GCTACAGTATTCCAT | 10393 |
rs777950134 | in-del | -/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144989317 | TCTGTGTCATTTTGG[-/T]TAATTCTCTATCTCA | 10393 |
rs777990231 | snp | C/G/T | 6.74359e-05 | 0.00580638 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145064721 | AGTAAAAATAACATG[C/G/T]ACTTCATCATATGAA | 10393 |
rs777992678 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145001487 | AATTTATTGTTTACA[A/T]GGTAGAGAGTTAAAG | 10393 |
rs778007423 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145072639 | CTCAAGTGCTAAAAA[A/C]ATCTACCCAATAGAG | 10393 |
rs778082902 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145020024 | AAGAAGAATTGGTAC[C/T]GATCCTACTGACACT | 10393 |
rs778097542 | snp | A/G | | | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145098602 | ACGCCGAGAGCTTGG[A/G]GGCGCCTCGGTCTTC | 10393 |
rs778124928 | in-del | -/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144987519 | GGGAGGGGGGAGGGA[-/T]AGCATTAGGAGATAT | 10393 |
rs778138927 | in-del | -/AT | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054668 | GCGTGCGTGCAGCGC[-/AT]GTGTGTGTGTGTGCC | 10393 |
rs778180868 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144979311 | CCCTACCATGTGTCC[A/G]TGCTCTCATTGATCA | 10393 |
rs778193642 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145020822 | ATCAAGAACTCAATC[C/T]TTTTTACAATAGCTG | 10393 |
rs778246783 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145002605 | AGATAGAGTGTTCTA[C/T]TCATCTGCATGACAA | 10393 |
rs778247485 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145039741 | CTAGGACTACAGGCA[C/T]GCACCACCACACCCA | 10393 |
rs778248655 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145067022 | AGGTTCACGTACCCA[A/C]AGAAATCGTACGTAT | 10393 |
rs778255473 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145058052 | AATGTCTGCCATTAC[C/G]TACAATCTGACTATA | 10393 |
rs778272927 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145029232 | ACATCCCCTCCCCGA[A/C]CCACACTGCCATCAG | 10393 |
rs778273686 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144969411 | GATGTAAGTGAACAA[G/T]ATCACCAAATAACAA | 10393 |
rs778279410 | snp | C/G | 1.6998e-05 | 0.00291525 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145064532 | TTCTAATGAGTAAAA[C/G]TTAAAGGATGACATA | 10393 |
rs778280525 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145094267 | ATACAGTATTTATAT[C/T]GGCATTCTGGGAAAG | 10393 |
rs778303714 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145052224 | TTAATAATAATATAT[G/T]GTATACTTGAAAATT | 10393 |
rs778306608 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145059686 | ACACTTTAGTTTCAT[A/G]TTTAAGTACAAAATA | 10393 |
rs778315621 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144985347 | TGTAACCATAACTAC[A/G]TTAATTATATTCCCT | 10393 |
rs778322204 | snp | A/T | 1.65701e-05 | 0.00287833 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995518 | GCTAGAACAGCAATC[A/T]GTATCATGAATGTAC | 10393 |
rs778335096 | in-del | -/A | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145045330 | GGAAACTGAGGTTTC[-/A]AAAGAGCCAAATATA | 10393 |
rs778360923 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145044986 | GGAAGTTTTTTTTTA[A/G]AACAATAATCAGCTA | 10393 |
rs778378987 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145094036 | GACACAATTTGGAAG[C/T]GGTCCACAGAAGGGC | 10393 |
rs778448870 | in-del | -/TG | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145071080 | GTGGTTGCACAACAC[-/TG]TAAATGTACTTAAGG | 10393 |
rs778469780 | snp | C/T | 1.65789e-05 | 0.0028791 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995428 | CATCTAGGAAATTTA[C/T]CAATGGAGCTCTCTT | 10393 |
rs778478473 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145004205 | TGTATCTGAAACTTT[A/G]TTGAAGTCATTTATC | 10393 |
rs778502209 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145068647 | CCGGGTGCAGTGGCA[C/T]ACGCCTGTAATCCCA | 10393 |
rs778518393 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144982287 | TTAGAGAGGCTATGC[A/G]TGGCAGATATTATTC | 10393 |
rs778522250 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145090393 | TACAGATATGGAAGG[C/T]TAACTGTCCCATTTC | 10393 |
rs778533935 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145094632 | TAAACTAATAACATT[A/G]TAAAGTCCCTCAAGC | 10393 |
rs778578014 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145062309 | TAGTTTTCAAGAAGG[A/G]TTTCTTAAAAGTAAG | 10393 |
rs778587349 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081878 | GAAATATTAATTTTT[A/T]TTTATTTATTTTTTG | 10393 |
rs778660321 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145018257 | ATGATGAATGGAATG[G/T]TACCTCACATCTCAA | 10393 |
rs778664346 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144988553 | TTTAGGTGATTCTTA[C/T]GTAAAACAAGTACAA | 10393 |
rs778739690 | snp | G/T | | | | | GRCh38.p7 | 4:145023371 | GGTCCTGCATGATTT[G/T]GGTCTCTGCTTACCT | 10393 |
rs778771181 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144996240 | GTGATGACAGAAACA[A/C]TCTACCAACTAGGGC | 10393 |
rs778773045 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145040500 | TTTTAATGGCTTTGC[C/T]CCTTTCAGCTACCAT | 10393 |
rs778822335 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144996931 | ATGGCACGAGAACTA[C/T]GTGACGCATGCACAA | 10393 |
rs778825936 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145037138 | AGTTGCGGAGCTCCT[C/T]ATGCTATCCATGAGG | 10393 |
rs778878895 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145022937 | ATGCAGGTTTGTTAC[A/G]TATGTTTACATGTGC | 10393 |
rs778878942 | snp | A/T | 1.69352e-05 | 0.00290987 | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145096160 | AGGAACTGGGCATCT[A/T]TCTACAAAAGTTTTT | 10393 |
rs778934959 | snp | C/T | | | intron-variant, downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:145063157 | CTAAGAGAGTGGATT[C/T]TGAGAGTTCTCACCA | 10393 |
rs778936767 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145010342 | ATACCCAAAGGATTA[C/T]AAATCAAGCTGCTAT | 10393 |
rs778978735 | snp | A/G | | | intron-variant, downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:145053611 | AGGAAAGATTCCCAA[A/G]TATCTACAAATCCTT | 10393 |
rs778983524 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145048576 | CAACTACTAATACCA[C/T]CTACTGGTAGTTGAC | 10393 |
rs778991784 | snp | A/G | 1.68997e-05 | 0.00290682 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081610 | TAATAAAATAGATTT[A/G]TTTGTCTATAACCTA | 10393 |
rs779023742 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145047369 | TAAGCCAAGGTTAGA[A/G]AACTCTGCGTTCAAT | 10393 |
rs779042105 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145005759 | TCATTTCCATGTAAT[C/T]GCATGGTTTTCAGTG | 10393 |
rs779075473 | snp | A/C | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | ABCE1, ANAPC10 | GRCh38.p7 | 4:145097344 | CCTCATCTTTCACAT[A/C]TTTTGTTAATTTTAC | 10393 |
rs779160230 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145061862 | CCTGTAATCTCAGCA[C/T]TTTGGGAGGCCGAGG | 10393 |
rs779179208 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144983483 | TACTGGCGGATTACA[C/T]AAATGCTGAAGAGAT | 10393 |
rs779218054 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145032274 | CAGTGGGCAGAACTT[C/T]GAGCAGTGCACCTGA | 10393 |
rs779218443 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145023982 | TACTTTTTCAACTAA[A/G]TTGATGTAATATTCT | 10393 |
rs779320810 | snp | C/G | | | intron-variant, utr-variant-3-prime | ANAPC10 | GRCh38.p7 | 4:145033186 | TATGCTCTGAATCAG[C/G]GTCCAATATATGGTA | 10393 |
rs779333814 | snp | C/T | 4.97063e-05 | 0.00498505 | missense, nc-transcript-variant | ANAPC10 | GRCh38.p7 | 4:145081727 | TTTCTAGATTGTCAT[C/T]TCGTAACTGATCCAC | 10393 |
rs779345394 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145056327 | TACAAATGCCATGGC[A/G]AAGTCAGGAAGTTAC | 10393 |
rs779376491 | in-del | -/AACAT | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144998154 | TAACACCCCACTGTC[-/AACAT]AACATTAGACAGATC | 10393 |
rs779377495 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145080470 | TTGTGCCATAACAGT[A/G]GAACTGAGCACTGTA | 10393 |
rs779382963 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144977191 | TATGATTCCACAAGT[A/G]TCATCCTCTAGAGAA | 10393 |
rs779417390 | snp | C/G | | | intron-variant, downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:145032817 | AGGTTGATTATATTG[C/G]ACTTCTTCCATCATG | 10393 |
rs779438800 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144999926 | CATCTCATCTTTGAT[A/T]AACCTGACAAAAACA | 10393 |
rs779466867 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145070643 | GCAATTCCACCTGTG[A/G]ATATATATCCAAAAG | 10393 |
rs779513174 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145043141 | GCTGCCAAGAGCTAT[A/G]GTCCATCTAAAGCAA | 10393 |
rs779519379 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145026214 | TAAGAAAAGACCTAT[A/T]CATAATGATGTGTGA | 10393 |
rs779556714 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145098347 | CGTGAGAACACGCTG[C/T]GTGGCTGAAAAGTGA | 10393 |
rs779558420 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145085211 | GTAGTAAGCCATGAC[A/T]GTACCACTGCACTCT | 10393 |
rs779567111 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145094383 | GTGGGATGATGGCAA[A/T]GTTATATATTCGATT | 10393 |
rs779568348 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145028106 | GTGATGGTTAATACC[A/G]AGTGTCAACTTAATT | 10393 |
rs779610004 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145086285 | GTTTTAATTTAAACA[A/G]AAGAACTAAAACAAA | 10393 |
rs779610648 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145093456 | ATAAAAAAAAAAGAC[A/G]AACAAAAAGAAAAAC | 10393 |
rs779611589 | snp | C/T | | | upstream-variant-2KB, missense, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145096039 | CAATTTCCCGTACTG[C/T]TCCAGTCCTTTCCAA | 10393 |
rs779635496 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145057943 | TTAATTAAATCCTCG[C/T]AATTTTTACCTGGCT | 10393 |
rs779709207 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145011763 | CCCTCACAATATTTG[C/T]CACATTCTGAAGTTG | 10393 |
rs779738023 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145035935 | GAGCTGGAAGTCCAG[A/G]AGGGATGTTACCCAG | 10393 |
rs779740664 | snp | C/T | | | intron-variant, utr-variant-3-prime | ANAPC10 | GRCh38.p7 | 4:144999259 | GAATCCTCCCTACCT[C/T]ATTTGATGAGGCCAG | 10393 |
rs779760571 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144996186 | GATATGGAGATATCC[C/T]CACGGCTCTACACTC | 10393 |
rs779763179 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145088044 | CAGAGCGAGACTCCA[C/T]CTCAAAGAATAAAAA | 10393 |
rs779765693 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144988190 | TTGCTATGTTGCCCA[A/G]GCTGGTCTTAAACTC | 10393 |
rs779785171 | snp | A/G | 0.000371747 | 0.0136285 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | ABCE1, ANAPC10 | GRCh38.p7 | 4:145097465 | ATTGTTATATATGCT[A/G]TTCAAAATAGGTGCA | 10393 |
rs779792432 | snp | C/T | 3.31543e-05 | 0.00407137 | missense, utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995533 | TGTATCATGAATGTA[C/T]GAGTTGGCTTCTTAT | 10393 |
rs779855477 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144985560 | TTTATATTGTAATAT[A/G]TTAATTTCTACTAAA | 10393 |
rs779900815 | snp | A/C | 1.65721e-05 | 0.0028785 | missense, nc-transcript-variant | ANAPC10 | GRCh38.p7 | 4:145081741 | TCTCGTAACTGATCC[A/C]CTCCAAATCCTAAAA | 10393 |
rs779961668 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145052045 | ATCTTCTCATTTATA[C/T]ACGGAATCTAAAGTT | 10393 |
rs779977769 | in-del | -/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144987981 | TTTTTGTTTTTTTTT[-/G]GTTGTTGTTGTTTTT | 10393 |
rs779983258 | snp | C/T | 1.65715e-05 | 0.00287845 | synonymous-codon, nc-transcript-variant | ANAPC10 | GRCh38.p7 | 4:145081734 | ATTGTCATCTCGTAA[C/T]TGATCCACTCCAAAT | 10393 |
rs780036319 | in-del | -/TATGTGTGTGCA | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145037039 | GTGTGTGTGTGTGTG[-/TATGTGTGTGCA]TGCATGAATGTGTGT | 10393 |
rs780068470 | snp | A/T | | | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145100385 | CAGTCTTTTGGTTTT[A/T]AAAATAGTTTGAAAA | 10393 |
rs780074747 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144972026 | ATAATAACAATAAAA[A/C]AATAAAAATCCTTCA | 10393 |
rs780100950 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145009973 | ACTTAAACAAATTTA[A/C]AAGAAAAAATCAAAC | 10393 |
rs780140941 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145060116 | TGTAGAAGCAATAAA[C/T]TGCAAACATCTTATA | 10393 |
rs780155219 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145082907 | AACAAGACACAGTGA[A/G]AAGTCACTATCTACC | 10393 |
rs780194727 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145066615 | TCAGGGCAAGTTTAG[A/C]AAAGCAAAGAATACT | 10393 |
rs780215010 | snp | C/T | 1.65603e-05 | 0.00287747 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145095981 | TTTGTTTGTTAGTTT[C/T]TACCTGGTTTGCAAG | 10393 |
rs780246029 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145089507 | AAGACCCTATTATAC[A/G]GTAGCAGTCATAACA | 10393 |
rs780259697 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145036663 | CTTTCACGCTTTTAA[C/T]CTACATACATGTTTT | 10393 |
rs780303136 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145076260 | GTTGCTTATCTTGAA[A/G]GGCCAGAGAACAAGG | 10393 |
rs780337564 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145008298 | CTGAAACTATTCCAA[A/T]CAATAGAAAAAGAGG | 10393 |
rs780408779 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144975744 | AAAGACTTTTAAAAT[A/G]TGAGTGAAAGAAAAT | 10393 |
rs780420521 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144974069 | AATGCAAAAATCCTG[C/T]GATACACATAGATAA | 10393 |
rs780429965 | in-del | -/A | 1.70087e-05 | 0.00291617 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145064528 | TATCTTCTAATGAGT[-/A]AAAGTTAAAGGATGA | 10393 |
rs780470090 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145070323 | AGTCTTACAGCTTAA[A/C]AACAAAAAGACAACC | 10393 |
rs780477863 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145083223 | CTAAACATTTTATAT[A/G]TGTTAAATAATCTAA | 10393 |
rs780488932 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145005441 | ATCCTTTGTATGGTT[C/T]TTCATGTCTCAATTT | 10393 |
rs780491045 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144990263 | ACTTCAAGCAGATGA[C/T]AGGAGAATCAGACTT | 10393 |
rs780496133 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145047209 | CTGACAGGCTCCAAA[C/T]CCCATGATTAAAGCA | 10393 |
rs780522992 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145091667 | GAACATACATGTGCA[G/T]GTATCTTTGTAAAAT | 10393 |
rs780547176 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145030910 | TCTGGCCTGTGCAGA[A/G]GACAGATGGATCCTG | 10393 |
rs780597830 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145014082 | TCAAGAAGGCTCCTG[A/G]CCAGAACTCAGGGGA | 10393 |
rs780648609 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145056253 | CCAAAACCAAGATGG[C/T]CACGAGAGTGACCTC | 10393 |
rs780743130 | snp | A/G | | | upstream-variant-2KB, intron-variant, synonymous-codon | ABCE1, ANAPC10 | GRCh38.p7 | 4:145097245 | TAAAAGTTCACTTAC[A/G]TATGCTCTTACCATA | 10393 |
rs780766051 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145071579 | AAAACCATATGATCC[A/G]TATGAACAGATACAG | 10393 |
rs780842089 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144997156 | GGAACCAAGGTGGAA[A/G]TCACTCTTCAGGATA | 10393 |
rs780862200 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145050693 | TTCACCTGGCTCTTT[C/T]ATGTTATGCAGATGG | 10393 |
rs780910207 | snp | A/G | | | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145098729 | CCCCACTCCCGCCCT[A/G]AAGCTAAACCTGCTG | 10393 |
rs781009289 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145054078 | CATTCCCAGCTAATT[C/T]TTCTAATTTTAGTAG | 10393 |
rs781040323 | in-del | -/TGTC | | | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145100296 | AGTCCCAGTCTGTAG[-/TGTC]TGTCCTGTGATCACT | 10393 |
rs781096117 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144969954 | TGTAATTGAAACCCC[C/G]CTGTGTTCTCATTTC | 10393 |
rs781104489 | in-del | -/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144972029 | ATAACAATAAAAAAA[-/T]AAAAATCCTTCAATG | 10393 |
rs781133360 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145090428 | GCTTTTATGTCCTTA[A/G]TGAAATCTTATTCTT | 10393 |
rs781144646 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144985037 | ATTTTTCCTGTTGAT[A/G]GGATAAATCATGATC | 10393 |
rs781145481 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144968594 | TCCTGCATCACCCCT[C/T]TTCCCTAACAAGTGA | 10393 |
rs781148125 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145076132 | AGCTTTAGCAGATGG[A/G]CTGCTGCCAGCATAC | 10393 |
rs781174875 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144993505 | GTTGTAAGGGATTTT[C/T]ATATATTCTAAATAT | 10393 |
rs781200296 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145010701 | GAGGGGGAGGGATAG[C/T]ATTAGGAGATATACC | 10393 |
rs781227817 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145020216 | CTGAATCCAACAACA[C/T]ACCAAAAAGATAAAC | 10393 |
rs781282591 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145021060 | ACACATCCCATGTTC[A/G]TGGAATGGTAGAATC | 10393 |
rs781293359 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145074901 | ACACATACAAAACAT[C/T]TAATTCCTCCACAAA | 10393 |
rs781302207 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145076480 | AAGATTAAAGGAACA[G/T]TTTCCCACACAGATA | 10393 |
rs781311833 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145035636 | TTGGAGGCAGTGAAC[A/G]TGAATGATTCCAGTT | 10393 |
rs781337227 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145034011 | TGGGTTGGGGATTGA[C/T]GCATTTCTGGTTGTA | 10393 |
rs781400763 | snp | G/T | | | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145099664 | TGAAATCAGAGCCGT[G/T]TACCACTCCTAACTT | 10393 |
rs781408903 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144988663 | TGAGATTTGGCATAT[A/G]TACAGACCCATAAAA | 10393 |
rs781409737 | snp | C/T | 1.67913e-05 | 0.00289748 | upstream-variant-2KB, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145096151 | CATTGTATCAGGAAC[C/T]GGGCATCTTTCTACA | 10393 |
rs781441929 | snp | A/T | 1.70061e-05 | 0.00291595 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145064521 | CTGTGACTATCTTCT[A/T]ATGAGTAAAAGTTAA | 10393 |
rs781473374 | in-del | -/AA | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144991368 | ACTTTCTTAAAACAC[-/AA]AGAGTTTTTTTGCAT | 10393 |
rs781487651 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145040172 | GTGTGTGTTTTGAGA[C/T]GGAGTTTTGCTCTTG | 10393 |
rs781488027 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145082094 | ACTTGCACATACAAA[C/T]CCTATATTAGGATCA | 10393 |
rs781501474 | snp | C/T | 3.31203e-05 | 0.00406928 | upstream-variant-2KB, stop-gained, intron-variant | ABCE1, ANAPC10 | GRCh38.p7 | 4:145096008 | CAAGATGAGAGTGAC[C/T]AAACAGCTTGTGACC | 10393 |
rs781517806 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | ANAPC10 | GRCh38.p7 | 4:144995214 | AGAAAATAAAGATAA[C/T]ATGACCCCAAATTTA | 10393 |
rs781530475 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145087936 | ACCTATAATCTTAGC[C/T]ACCTGGGAGGCTAAG | 10393 |
rs781533177 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145004107 | CTCTGTGGCTACTGT[C/G]AATAGAACTGCATTC | 10393 |
rs781538894 | in-del | -/C | 8.35834e-05 | 0.00646411 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081626 | TTTGTCTATAACCTA[-/C]AGTAGATGAAAAATT | 10393 |
rs781542900 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145051864 | AATTTAATTTAGTCT[A/G]AGGACACTATCTATT | 10393 |
rs781558739 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144979881 | AAAGAGGACTAACTT[C/T]CTAGCTCATTACAGA | 10393 |
rs781590993 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145094882 | AGCATTCATAAATTT[C/T]TGAGAGAAAAGGACT | 10393 |
rs781623840 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145022217 | CACACACGTTTATAG[A/C]AGCACAATTCACAAT | 10393 |
rs781638322 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145029425 | CCTGGAGGTGAAGTT[C/G]AGAGTGTGATCCATG | 10393 |
rs781658844 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144989952 | GAGAGAGGTAAGGAA[A/G]CTACAGAAGTTTGAA | 10393 |
rs781673126 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144970538 | TGGTGAGTAGGAGTT[A/G]TCATCTAGGAGTTTG | 10393 |
rs781673152 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145045397 | AAGATCTGAAACCAG[A/T]TCTGTCTACTTTGCC | 10393 |
rs781673853 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145014555 | GAGTTCTAGGCCCCC[C/T]GCCCACCGTCTGATC | 10393 |
rs781708173 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145046673 | GTATATCTACTCGAA[G/T]GCCAGGGGAAATTTC | 10393 |
rs781781651 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145059868 | AAAAAAAAATCTCAC[A/C]CATTATTTTTCCTTC | 10393 |
rs796106126 | in-del | -/A | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145062069 | CTCTGTCAAAAAAAG[-/A]AAAAAAAAAAAGATT | 10393 |
rs796111961 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144980768 | CTAGATTTTCTTCTA[A/G]GGTTTTAATAGTTTT | 10393 |
rs796166680 | multinucleotide-polymorphism | ATA/TTT | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144971323 | GTTGTAAATGCACAT[ATA/TTT]AGCTACTGCAGGAAA | 10393 |
rs796201517 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145009415 | GCTGCAGGCATCACG[C/T]TACTTCACTTCAAAA | 10393 |
rs796279464 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144980730 | GAAATCTTTGCCCAT[A/G]CCTATATCCTGAATG | 10393 |
rs796308238 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144980775 | TTCTTCTAGGGTTTT[A/T]ATAGTTTTGGGTTTT | 10393 |
rs796326222 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144980771 | GATTTTCTTCTAGGG[G/T]TTTAATAGTTTTGGG | 10393 |
rs796349851 | multinucleotide-polymorphism | CC/GT | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144970505 | GTAGTCTATCCTGTG[CC/GT]TGCCTCGATGGTGGG | 10393 |
rs796431199 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144980505 | GATTCTGGATATTAG[A/C]CCTTTCATAGATAGA | 10393 |
rs796453008 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144967982 | CATCTGCTCACACTC[A/C]TGCCTCTGAGTCTTA | 10393 |
rs796490709 | in-del | -/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145025332 | TTGGCTTTCAACACG[-/C]CCCCCCCCCCCTTTT | 10393 |
rs796551640 | multinucleotide-polymorphism | AAC/CAT | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145055134 | TTAAGATAAGTGTAC[AAC/CAT]CACTGTTCACAGCAC | 10393 |
rs796585801 | in-del | -/A | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145084593 | GCTAAAAAAAAAAAA[-/A]TTCATAATGTTTCAA | 10393 |
rs796610853 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145030661 | AATGCATAATTGGCA[C/T]AGACATACTTAGCAG | 10393 |
rs796824851 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145010979 | CACGGCAAGACAGAA[A/G]GCTTCCACAATAGAA | 10393 |
rs796841890 | in-del | -/AA | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145094800 | AACAAGTTACTTAGG[-/AA]AAAAAAAAAAGAGAG | 10393 |
rs796860913 | snp | A/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145052937 | AAAAATCACATTTCT[A/T]TAGCAGCATATATAC | 10393 |
rs796916293 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144980789 | TAATAGTTTTGGGTT[G/T]TACATTTAAGTCTTT | 10393 |
rs796921032 | in-del | -/A | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145094800 | AACAAGTTACTTAGG[-/A]AAAAAAAAAAAGAGA | 10393 |
rs797013323 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144980726 | TCATGAAATCTTTGC[C/T]CATACCTATATCCTG | 10393 |