SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs4131850 | snp | C/T | 0.240478 | 0.249819 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110374748 | CATAAGAACATGGGA[C/T]ACCTATACTCAGAGA | 51434 |
rs4131851 | snp | A/G | 0.240478 | 0.249819 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110374540 | CAAATTGAGAACTCT[A/G]AAAATTAGGAAGAGA | 51434 |
rs4131852 | snp | C/G | 0.222928 | 0.24853 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110374852 | AAGCCTTGGGTCCTG[C/G]GGTCTGACCTAGGTG | 51434 |
rs6606746 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110378889 | cctgggtgacagagc[A/G]agactccatttcaaa | 51434 |
rs11554605 | snp | A/G | 0 | 0 | utr-variant-3-prime, intron-variant | ANAPC7 | GRCh38.p7 | 12:110375877 | CAGTTCTCTAATGTT[A/G]TTAATATATTTTAAG | 51434 |
rs28368965 | snp | C/G | 0 | 0 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387337 | AGAGAGAGAGAGAGG[C/G]AGAGAGAGAGAGAGA | 51434 |
rs28397252 | snp | A/C | 0.240478 | 0.249819 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110378145 | CGTTGCCCAGGCTGG[A/C]GCGCAATGGCGCCAT | 51434 |
rs28407893 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110376566 | AGAGCGAGACTCCAT[C/T]TCAAAAAAAAAAAAA | 51434 |
rs28408745 | snp | A/G | 0 | 0 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110384722 | AAAAACCAAAGGAGC[A/G]GAACAACCTACCTCA | 51434 |
rs28429955 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403005 | CCTCGGCCTCCCAAA[A/G]GGCTCGTATTAGAGG | 51434 |
rs28439824 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110376399 | ACAGTGAAACCCCGT[C/T]TCTACTAAAAATACA | 51434 |
rs28473443 | snp | C/T | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110401760 | GGAGGCCGAGGCGGG[C/T]GGATCACGAGGTCAG | 51434 |
rs28480627 | snp | C/T | 0.247621 | 0.249989 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110396854 | ATATATCTATCCATA[C/T]TCTCATATTAAGATG | 51434 |
rs28482181 | snp | C/T | 0.0711525 | 0.174681 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110385919 | CCTAATTACTGCCTT[C/T]AATCACCTTATCCCT | 51434 |
rs28489972 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, utr-variant-5-prime | ANAPC7 | GRCh38.p7 | 12:110401388 | GCATGTGAGTGCTTA[C/T]TGCGCACAGCCACTG | 51434 |
rs28505800 | snp | A/C | 0.0633504 | 0.166319 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388174 | TCCGAGAAGCTGGGA[A/C]TACAGGCACGCGCCA | 51434 |
rs28525480 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110376401 | AGTGAAACCCCGTCT[C/T]TACTAAAAATACAAA | 51434 |
rs28537922 | snp | A/C | 0.0471551 | 0.14613 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110378383 | ACAGGCGTAAGCCAC[A/C]GTGCCTGGCCTGGCT | 51434 |
rs28539050 | snp | A/G | 0 | 0 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387336 | GAGAGAGAGAGAGAG[A/G]CAGAGAGAGAGAGAG | 51434 |
rs28554115 | snp | C/G | 0.247337 | 0.249986 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110398186 | AGGAGGCAGAGGTTG[C/G]GGTGAGCCAAGATCG | 51434 |
rs28555214 | snp | A/C | 0.435407 | 0.167703 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110391231 | ATTTTAAAAATAGAT[A/C]CTCACTTAAAAACAT | 51434 |
rs28562304 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, utr-variant-5-prime | ANAPC7 | GRCh38.p7 | 12:110401405 | GCGCACAGCCACTGC[A/G]CTTTCAATTGGTGGG | 51434 |
rs28562888 | snp | C/T | 0.240478 | 0.249819 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380637 | GCCTGGGTGACAGGG[C/T]GAGACTCTGTCTCAA | 51434 |
rs28566000 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395635 | TCTCGTTCTGTCACC[C/G]AGGCTGGTGTCTCCT | 51434 |
rs28569834 | snp | G/T | 0.300421 | 0.244863 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388403 | ACTAAATCACTCTCT[G/T]CAGGGGAACTTTTAA | 51434 |
rs28580853 | snp | C/G | 0.300421 | 0.244863 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388404 | CTAAATCACTCTCTT[C/G]AGGGGAACTTTTAAA | 51434 |
rs28586930 | snp | A/G | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110373819 | ATGTCACAGAACACT[A/G]TCTATTCCTTGAGCT | 51434 |
rs28592908 | snp | C/T | 0.24019 | 0.249807 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383204 | AGCACTTTAAGAAGC[C/T]GAGGCAGGTGGATCA | 51434 |
rs28595030 | snp | C/T | 0.0154538 | 0.0865337 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110405095 | ATAGGCAAAACTCCT[C/T]AGACACCAAGTTAAA | 51434 |
rs28601692 | snp | A/C | 0.5 | 0 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110394665 | CAAGAGTGAAATTCC[A/C]CCTCAAAAAAAAAAA | 51434 |
rs28602314 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388253 | TGTTGCCCAGGCTGG[G/T]CTCGACCTGCTGAGC | 51434 |
rs28609096 | snp | A/G | 0.489376 | 0.0721049 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110378117 | TATTTTTTTTGCGAC[A/G]GAGTTTCACTCTCGT | 51434 |
rs28610169 | snp | A/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382461 | AAAAAAAAAAAAAAA[A/T]ATATATATATATATA | 51434 |
rs28617452 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381398 | CTGGAGTGCAGTGGC[A/G]CAATCTTGGCTCACT | 51434 |
rs28626965 | snp | A/T | 0.480853 | 0.0959518 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110390253 | TTTTTTTTGTATTTT[A/T]AGTAGAGATGGTGTT | 51434 |
rs28630671 | snp | C/T | 0 | 0 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388778 | CAGACTGACCCCATT[C/T]TTCAAAAGAAAGAAG | 51434 |
rs28637922 | snp | G/T | 0.395818 | 0.203069 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381334 | GGATGATGTTTTTTT[G/T]TTGTTGTTGTTGTTG | 51434 |
rs28653722 | snp | C/G | 0.240765 | 0.249829 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110396801 | ATTACAGGCGTGAGC[C/G]ATCATGCCTGGCCAC | 51434 |
rs28654519 | snp | A/C | 0.32 | 0.24 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110392092 | CAAGACTCCACCTCA[A/C]AAAAAAAAAAAAAAA | 51434 |
rs28657702 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383292 | AAATACAAAAAATTA[A/G]CCGGGCATAGTGGCA | 51434 |
rs28670084 | snp | A/C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383033 | CATACAGGAGTAGCA[A/C/T]CCAACATCAGACCCC | 51434 |
rs28670753 | snp | C/T | 0.244659 | 0.249943 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388658 | AGATAGCAAAATAAG[C/T]GTATATTGCAAAGAA | 51434 |
rs28692795 | snp | C/T | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110401751 | AGCACTTTGGGAGGC[C/T]GAGGCGGGCGGATCA | 51434 |
rs28694740 | snp | A/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110376564 | ACAGAGCGAGACTCC[A/T]TCTCAAAAAAAAAAA | 51434 |
rs28695619 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389711 | CCGAGGTGGGTGGAT[C/T]ACGAGGTCAGGAGAT | 51434 |
rs28703074 | snp | A/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382463 | AAAAAAAAAAAAAAA[A/T]ATATATATATATATA | 51434 |
rs28713182 | snp | C/T | 0.00994328 | 0.0699023 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382716 | TTGAGATTACAGGCA[C/T]GAGCCACCATGCCTG | 51434 |
rs28713419 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110376542 | CCACTACACTCCAGT[C/T]TGGGCAACAGAGCGA | 51434 |
rs28801481 | snp | A/C | | | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110405607 | GGGTGGTGTGTGGGA[A/C]CCTAGAGTGGGAGAG | 51434 |
rs28813775 | snp | A/G | 0.400682 | 0.199487 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110405656 | TTTGTGGTAAGGGAC[A/G]ATATTGTGGGGTTGT | 51434 |
rs28816104 | snp | A/G | 0.357877 | 0.225527 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110384134 | TTGAACTCAGAGGGC[A/G]GATGTTGCAGTGAGC | 51434 |
rs28828437 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383899 | AAAAAAAAAAAAAAA[A/G]AAAAAAAAAAGAAAA | 51434 |
rs28840829 | snp | C/T | 0.00279162 | 0.0372561 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110405697 | ATTTGTCGTATAGAA[C/T]GATTGGTGATGGCCT | 51434 |
rs34090832 | in-del | -/G | | | frameshift-variant, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110386344 | TTATCAGATAAGGAT[-/G]CCAACATCTGTGCCT | 51434 |
rs34130472 | in-del | -/A | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110391930 | AACCCCGTCTCCACT[-/A]AAATGCAAAAAAGTA | 51434 |
rs34363447 | in-del | -/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389886 | CAGTGAGCCGAGATC[-/T]GTGCCACTGCACTCC | 51434 |
rs34369524 | in-del | -/C | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110391051 | AAAATTAGGCAGGTG[-/C]CAGCGGTACGCGCCT | 51434 |
rs34681975 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389331 | AAAGTGAGAAACTCT[C/T]GACATAGCTAGTTAA | 51434 |
rs34713439 | in-del | -/T | 0.5 | 0 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395319 | ATGACCCAGCAATTC[-/T]TTTTTTTTTTTTTGA | 51434 |
rs34812107 | in-del | -/A | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380650 | GCGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 51434 |
rs34840178 | snp | A/G | 0.48955 | 0.071525 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110394222 | TAGGCTTGGAGTGGC[A/G]TCTCACACCTGTAAT | 51434 |
rs35026231 | snp | A/G | 0.247337 | 0.249986 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110394320 | ACACAGTGGAACCTT[A/G]TCTCTACCAAAAATA | 51434 |
rs35149960 | in-del | -/A | 0.5 | 0 | intron-variant, downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110377137 | GCAAGATGCCGTCTC[-/A]AAAAAAAAAAAAAAA | 51434 |
rs35685027 | in-del | -/A | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383471 | AGCTGGGCGTGGTGG[-/A]CTCACACCTGTAATC | 51434 |
rs35699984 | in-del | -/A | 0.31357 | 0.241783 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381955 | CTGTGACAGCTGGAG[-/A]AAAAAAAAAAAAAAA | 51434 |
rs35975593 | in-del | -/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110398399 | CCAGCCTGGGCAACA[-/G]GGGAATGAAACCCTG | 51434 |
rs55634798 | snp | G/T | 0.241978 | 0.253716 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395943 | AATTTTTCCACAGAT[G/T]GGGGGTGAGGGGGTG | 51434 |
rs55805203 | snp | G/T | 0.134119 | 0.221521 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381337 | TGATGTTTTTTTGTT[G/T]TTGTTGTTGTTGTTT | 51434 |
rs55913108 | snp | C/T | 0.247337 | 0.249986 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110378702 | CTTTTTGGCACAAAG[C/T]GCTCATCAAAACAAA | 51434 |
rs55946301 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403216 | GAAGGATTCAGCCTA[A/G]CGATGTGACAGTCGC | 51434 |
rs56122570 | snp | A/G | 0.237593 | 0.249692 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110378486 | TCTTTTATTTGAAAC[A/G]TAACAGCTGTCTCAA | 51434 |
rs56127909 | snp | A/G | 0.240478 | 0.249819 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395958 | GGGGGGTGAGGGGGT[A/G]GTTTCAGGATGAAAC | 51434 |
rs56130410 | snp | C/T | 0.139868 | 0.224435 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110386307 | ACAGCCACTGTCTTC[C/T]TGCCCCAAGAATTAC | 51434 |
rs56184938 | snp | C/T | 0.240765 | 0.249829 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110379388 | ACCTAAATCTCCAAA[C/T]GGCAGCTTAAGAAGC | 51434 |
rs56209636 | snp | C/T | 0.247337 | 0.249986 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110404193 | CCTTGGTTCGAGGGG[C/T]ATATTTCCCCATGTA | 51434 |
rs56251637 | snp | G/T | 0.240478 | 0.249819 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110396064 | TCACAATAGGGTTTG[G/T]GTTCCTATAAGAATC | 51434 |
rs56264688 | snp | A/T | 0.237303 | 0.249677 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110401789 | AGGAGATCGAGACCA[A/T]CGTGAAACCCTGTCT | 51434 |
rs56355505 | in-del | -/A | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110398432 | TCAGAAAAAAAAAAA[-/A]GTAAACTTCACTAGC | 51434 |
rs56750920 | snp | C/G | 0.496937 | 0.0390173 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387383 | AGAGAGAGAGAGAGA[C/G]AGAGAGAGAGAGAGA | 51434 |
rs57010575 | in-del | -/AA | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110400900 | AAAAAAAAAAAAAAA[-/AA]TTAGCTGGGCGTGGT | 51434 |
rs57102821 | snp | C/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387375 | AGAGAGACAGAGAGA[C/G]AGAGAGACAGAGAGA | 51434 |
rs57154770 | snp | C/T | 0.240478 | 0.249819 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110376610 | CAGTTTGAATTATAA[C/T]GTTTTAAATGGGCTC | 51434 |
rs57198298 | snp | A/G | 0.0123036 | 0.0774623 | downstream-variant-500B, intron-variant | ANAPC7 | GRCh38.p7 | 12:110375174 | TCGTCTCCTGGTTGA[A/G]GCCTTCCACATCCTG | 51434 |
rs57434475 | in-del | -/AAAAAAA/AAAAAAAA/AAAAAAAAA/AAAAAAAAAA | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110376586 | AAAAAAAAAAAAAAA[lengthTooLong]GAAATTTGCAGTTTG | 51434 |
rs57660651 | in-del | -/GC | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387343 | GAGAGAGGCAGAGAG[-/GC]AGAGAGAGACAGAGA | 51434 |
rs57821814 | snp | A/C | 0.205417 | 0.245993 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110391449 | CATTCATTTAGACAC[A/C]TTTTGACTCACTTCC | 51434 |
rs57846014 | snp | C/G | 0.250168 | 0.25 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387433 | AGAGAGAGAGAGAGA[C/G]CGACCTTGTCTCAAA | 51434 |
rs58142028 | snp | C/G | 0.487049 | 0.0794222 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387367 | ACAGAGAGAGAGAGA[C/G]AGAGAGAGAGAGAGA | 51434 |
rs58202031 | snp | C/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387359 | AGAGAGAGACAGAGA[C/G]AGAGAGACAGAGAGA | 51434 |
rs58225143 | snp | C/G | 0.498794 | 0.0245311 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387287 | AGAGAGAGAGAGAGA[C/G]AGAGAGAGAGAGAGA | 51434 |
rs58413984 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110399273 | GATCCACCCGCCTCA[A/G]CCTCCCAAAGTGCTG | 51434 |
rs59022837 | snp | A/G | 0.195526 | 0.243993 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389704 | TGGGAGGCCGAGGTG[A/G]GTGGATTACGAGGTC | 51434 |
rs59080238 | in-del | -/CA | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387308 | AGAGAGAGAGAGAGA[-/CA]GACAGAGAGACAGAG | 51434 |
rs59393659 | in-del | -/A | 0.248188 | 0.249993 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110400104 | TCCCCAGAAAAACAG[-/A]AAAAAAACAACAAAA | 51434 |
rs59398345 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110376587 | AAAAAAAAAAAAAAA[A/G]AAATTTGCAGTTTGA | 51434 |
rs59509298 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110391923 | ATGGTGAAACCCCGT[C/T]TCCACTAAAATGCAA | 51434 |
rs59550005 | in-del | -/CA | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387390 | AGAGAGACAGAGAGA[-/CA]GAGAGAGAGAGAGAG | 51434 |
rs60143179 | snp | A/C/T | 0.0193772 | 0.0965046 | downstream-variant-500B, intron-variant | ANAPC7 | GRCh38.p7 | 12:110375137 | CTACCGATATAAATG[A/C/T]GGACCGATCTGTAAC | 51434 |
rs60339427 | snp | A/G | 0.247337 | 0.249986 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110386666 | AAGAATAAAGCAGAA[A/G]TCTCTCAGTACCAAC | 51434 |
rs60436466 | snp | A/C | 0.250168 | 0.25 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387434 | GAGAGAGAGAGAGAC[A/C]GACCTTGTCTCAAAA | 51434 |
rs60687245 | snp | C/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387353 | AGAGAGAGAGAGAGA[C/G]AGAGAGAGAGAGACA | 51434 |
rs60764482 | in-del | -/A | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110399811 | AAAAAAAAAAAAAAA[-/A]GGGGCCAGGCGCGGT | 51434 |
rs61198310 | in-del | -/CA | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387296 | AGAGACAGAGAGAGA[-/CA]GAGAGAGAGAGAGAC | 51434 |
rs61216094 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403139 | AGCGCATAAAAACCA[C/G/T]GAGGCTGGGTCCCTG | 51434 |
rs61244835 | snp | C/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387311 | AGAGAGAGAGAGAGA[C/G]AGAGAGACAGAGAGA | 51434 |
rs61363009 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387327 | AGAGAGACAGAGAGA[C/G]AGAGAGAGGCAGAGA | 51434 |
rs61754907 | snp | A/G | 0.00750344 | 0.06079 | synonymous-codon, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110387786 | AGTGTGCACAAAAGC[A/G]TACGCTTTGATCCAC | 51434 |
rs61942584 | snp | A/G | 0.5 | 0 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110376724 | AAAAAAAAAAAAAGG[A/G]CCAAACGGGAAGTCA | 51434 |
rs61942585 | snp | A/G | 0.0397176 | 0.135208 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381955 | CTGTGACAGCTGGAG[A/G]AAAAAAAAAAAAAAA | 51434 |
rs61942587 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388330 | GTGTAAGCCACCATG[A/C]CCGGCCAAAAACCAT | 51434 |
rs61942589 | snp | A/C | | | missense, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110396415 | AATCTGCATGATACA[A/C]CAAAAGCTGGTACTT | 51434 |
rs66967302 | in-del | AAAA/TAT | 0.5 | 0 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382465 | AAAAAAAAAAAAAAA[AAAA/TAT]ATATATATATATATA | 51434 |
rs71083120 | in-del | -/GAGAGA | 0 | 0 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387310 | AGAGAGAGAGAGAGA[-/GAGAGA]CAGAGAGACAGAGAG | 51434 |
rs71083121 | in-del | -/AG | 0 | 0 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387387 | GAGAGAGAGACAGAG[-/AG]AGAGAGAGAGAGAGA | 51434 |
rs71445504 | in-del | -/G | 0.5 | 0 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380676 | AAAAAAACAGGACCC[-/G]GGGCACGGTGGCTCA | 51434 |
rs73206866 | snp | A/G | 0.0482946 | 0.147699 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110378700 | AACTTTTTGGCACAA[A/G]GTGCTCATCAAAACA | 51434 |
rs73206868 | snp | G/T | 0.247337 | 0.249986 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110379030 | TGCCTGGCTAAATTT[G/T]TTTCTATTTTTAGTA | 51434 |
rs73206870 | snp | C/T | 0.196149 | 0.244131 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382148 | ATTTTTAAGGGGAAA[C/T]CTTGATATGGAAGAG | 51434 |
rs73206871 | snp | G/T | 0.0205511 | 0.0992634 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110385526 | TGCCAGACTAGTATT[G/T]CTAAAACATCATTTT | 51434 |
rs73206878 | snp | A/C | 0.137187 | 0.223099 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110397210 | TCTCAACAACAACAA[A/C]AAAAAACCAATGCAC | 51434 |
rs73206880 | snp | G/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110397347 | ATCACAAGATCACAA[G/T]ATCGAGATCATCCTG | 51434 |
rs73206881 | snp | A/C | 0.255503 | 0.249939 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110397573 | AAAAAAAAAAAAAAA[A/C]ACTAAAAACTAAAGA | 51434 |
rs73206882 | snp | A/G | 0.237303 | 0.249677 | intron-variant, upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110402710 | AAGGAAACATGAAAG[A/G]CGCCACGCCCACCCA | 51434 |
rs73417362 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110377905 | TGTGAGCACCCCATC[C/T]GACCACTGGAAGAAT | 51434 |
rs73417366 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381026 | CATATTAATGAGTAC[A/G]CCACACTGGATGGGG | 51434 |
rs74361481 | snp | A/C | 0.0146672 | 0.084371 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381972 | AAAAAAAAAAAAAAA[A/C]ACACAAAAACCCCAG | 51434 |
rs74731088 | snp | A/G | 0 | 0 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383902 | AAAAAAAAAAAAGAA[A/G]AAAAAAAGAAAAAAG | 51434 |
rs74840214 | snp | C/T | 0.00358779 | 0.0422022 | utr-variant-3-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110373829 | ACACTGTCTATTCCT[C/T]GAGCTTTTGGATTTA | 51434 |
rs74951779 | snp | A/C | 0 | 0 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110391202 | CTCAAACAAACAAAC[A/C]AAAAAAGTCAACTAT | 51434 |
rs74973042 | snp | G/T | 0 | 0 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110390085 | TTAGATTTTTTTTTT[G/T]GAGACGGAGTTTCAC | 51434 |
rs75347070 | snp | A/G | 0.0442319 | 0.141984 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403574 | GCTGAGGAGCCGCAC[A/G]TTGGAGTGCAGCCCC | 51434 |
rs75531218 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110384981 | AAAGATCACTGCCTC[A/G]GGCTGGGTGCAGTGG | 51434 |
rs75590061 | in-del | -/AA | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110397215 | ACAACAACAAAAAAA[-/AA]CCAATGCACAAAAAG | 51434 |
rs75664229 | snp | A/C | 0.5 | 0 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110404648 | TTACAGTAGTAGATG[A/C]AAAAAAAATGCTCTG | 51434 |
rs76468288 | in-del | -/TT | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395609 | CTTCTTTTTTTTTTT[-/TT]GAGACAGAGTCTCGT | 51434 |
rs76524211 | snp | A/C | 0.5 | 0 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110399817 | AAAAAAAAAAGGGGC[A/C]AGGCGCGGTGGCTCA | 51434 |
rs77023110 | snp | A/G | 0.000319481 | 0.0126348 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395056 | TGGAGAGAGGGAGCA[A/G]GGTTAGGAGAGCTGA | 51434 |
rs77132224 | snp | A/G | 0.0327036 | 0.123622 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381958 | TGACAGCTGGAGAAA[A/G]AAAAAAAAAAAAAAA | 51434 |
rs77384020 | snp | A/C | 0 | 0 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110384685 | TCTCACAAAAAAAAA[A/C]CAAAAAAAAACAAAA | 51434 |
rs77558255 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382162 | ATCTTGATATGGAAG[A/G]GAAAAATTATGAAAA | 51434 |
rs77622018 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110400225 | GTATTATTACATCCA[C/T]AGAAAGCATTCAGAT | 51434 |
rs78123354 | snp | A/G | 0.0509478 | 0.151255 | downstream-variant-500B, intron-variant | ANAPC7 | GRCh38.p7 | 12:110375017 | CCCAAGCCAGCAGGC[A/G]TCCCACGCCTAGCAA | 51434 |
rs78217750 | snp | A/G | 0.12371 | 0.215756 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381956 | TGTGACAGCTGGAGA[A/G]AAAAAAAAAAAAAAA | 51434 |
rs78283777 | snp | A/T | 0 | 0 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110394697 | AAAAAAAAAAAAAAA[A/T]TAGCTGGGTGTGGCA | 51434 |
rs78660520 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110393268 | TGTACACCTATGGAA[C/G]GCAAAAAATGAAGTT | 51434 |
rs78843188 | snp | C/G | 0.240765 | 0.249829 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110390118 | TTGTCACCCAGGCTA[C/G]AGTGCGATGGCACGA | 51434 |
rs79060677 | snp | G/T | 0.5 | 0 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395611 | TCTTTTTTTTTTTTT[G/T]AGACAGAGTCTCGTT | 51434 |
rs79071195 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110400528 | CATGGGCTAAACTTC[A/G]TCTAGCCAGAGAATT | 51434 |
rs79239201 | snp | C/T | 0.0446081 | 0.142528 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388462 | CAAGATTGAGAACTA[C/T]TATCTTTGACAGTAA | 51434 |
rs79387430 | in-del | -/AAAAA | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381969 | GAAAAAAAAAAAAAA[-/AAAAA]CACAAAAACCCCAGA | 51434 |
rs79447402 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110398516 | CCAATGTTTTAAAAC[C/T]GTTTAACCTTGAGTA | 51434 |
rs79846732 | snp | A/G | 0.00146936 | 0.0270651 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388495 | ATGCCATGAAAACAG[A/G]CAGGAAATATCTCTA | 51434 |
rs80038381 | snp | A/G | 0.00755907 | 0.0610114 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110404843 | TTTTTTCTTTTTTTC[A/G]AGACGGAGTTTTGCT | 51434 |
rs80072218 | snp | A/G | 0.5 | 0 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110376721 | TGAAAAAAAAAAAAA[A/G]GGGCCAAACGGGAAG | 51434 |
rs111298771 | snp | C/T | 0.19334 | 0.243495 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110405608 | GGTGGTGTGTGGGAA[C/T]CTAGAGTGGGAGAGA | 51434 |
rs111406162 | in-del | -/A/AA/G | 0.306899 | 0.266374 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381954 | CTGTGACAGCTGGAG[-/A/AA/G]AAAAAAAAAAAAAAA | 51434 |
rs111419116 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110397061 | TACAAAAAATTAGCC[A/G]GGCGTGGTGGCAGGC | 51434 |
rs111438435 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110393590 | AAAAAAAAATTGGCC[A/G]GGCATGGTGGCTCCC | 51434 |
rs111566188 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110393877 | CCTCTCAAAAAAAAA[A/G]AAAAAAAAAAAATAG | 51434 |
rs111608830 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110400313 | ACGAAAAAATAGTTA[C/G/T]TGCCTCTGGAGAAAG | 51434 |
rs111661323 | snp | C/T | 0.5 | 0 | missense, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110374301 | TCCATCTTCTGCATC[C/T]CCTCTAGAGACTTCT | 51434 |
rs111908272 | snp | A/C/G | 0 | 0 | splice-donor-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403526 | ACCCGCCTCAACTCA[A/C/G]GGGTTGTTATTACTC | 51434 |
rs111966274 | in-del | -/C | 0.5 | 0 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110404199 | TCGAGGGGTATATTT[-/C]CCCCATGTAAAATTA | 51434 |
rs112118902 | in-del | -/CC | 0.5 | 0 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387433 | AGAGAGAGAGAGAGA[-/CC]GACCTTGTCTCAAAA | 51434 |
rs112291494 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime, downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110373191 | GACCAGTGACAGACT[A/G]CTGGAACCAGACCCC | 51434 |
rs112318897 | snp | A/T | 0.5 | 0 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110391620 | CTGACAAATGCAGAC[A/T]CATACAGGTGCTCTA | 51434 |
rs112322226 | snp | C/G | 0.00279162 | 0.0372561 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110403894 | GCAAACTTTACTGAG[C/G]ATTTACAATGAGACA | 51434 |
rs112377299 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110403858 | TATTTTTACGCAAAA[A/G]TCACGTTATCATCCT | 51434 |
rs112381706 | snp | G/T | 0.5 | 0 | missense, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110395150 | AGTATAGCAATGGCA[G/T]CTTTATCTTGTTTTA | 51434 |
rs112395747 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110404945 | CCTGCCTCAGCTTCC[C/T]GAGTAGCTGGGATTA | 51434 |
rs112400225 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380718 | CTAGCACTTTGGGAG[A/G]CCGAGGCGGGCGGAT | 51434 |
rs112470258 | snp | A/T | 0.031825 | 0.122064 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389984 | AGCCAGAAAATCTAA[A/T]AGTTCCTAAGAATGT | 51434 |
rs112490118 | snp | A/C/T | 0 | 0 | splice-donor-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403525 | TACCCGCCTCAACTC[A/C/T]CGGGTTGTTATTACT | 51434 |
rs112533160 | snp | A/G | 0.002083 | 0.032205 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110377678 | CCAACCCATGCTTCC[A/G]CTCTGACAGCTCTCC | 51434 |
rs112552996 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110391731 | TACAAATATCCACAG[A/G]TCATTATGAAGGAGA | 51434 |
rs112626804 | snp | A/C | 0.5 | 0 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110399647 | TTGCATTATTGTGGC[A/C]ATGTGCGGTGGCTTA | 51434 |
rs112916395 | in-del | -/A | 0 | 0 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110384676 | GAGACTCTGTCTCAC[-/A]AAAAAAAAACAAAAA | 51434 |
rs113011403 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110385307 | CTCTCCGCAGCCCCC[A/G]CTTTATTCTCACCCA | 51434 |
rs113013763 | in-del | -/T | 0 | 0 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110396684 | TTTGTTTTTTTTTTT[-/T]AGTAGACATGGGGTT | 51434 |
rs113505920 | snp | G/T | 0 | 0 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395947 | TTTCCACAGATGGGG[G/T]GTGAGGGGGTGGTTT | 51434 |
rs113598382 | snp | A/G | 0.5 | 0 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110390421 | CTAGATCATTAACCT[A/G]AGGAAGCAGTCAATG | 51434 |
rs113660973 | in-del | -/T | 0.237303 | 0.249677 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110392379 | GGAGGTGCTTAAACA[-/T]TGTTCTCATCAAGTT | 51434 |
rs113786094 | snp | C/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383975 | TGGGAGGCTGAGGCA[C/G]GTGGATCACGAGGTC | 51434 |
rs113838372 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383465 | AAAACCCAGCTGGGC[A/G]TGGTGGCTCACACCT | 51434 |
rs113974545 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403145 | TAAAAACCAGGAGGC[C/T]GGGTCCCTGAGCTGC | 51434 |
rs114106793 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110386232 | ACACCATTTCTATGA[A/C]ACTTGGTATCGAGTA | 51434 |
rs114362038 | snp | A/G | 0.0138799 | 0.0821421 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110405312 | CCGGGAAGTTTCACA[A/G]TGTCTTTCTATAATC | 51434 |
rs114890469 | snp | A/G | 0.0103295 | 0.0711199 | downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110372654 | CCTCCTGAGTATTGA[A/G]TAGCTGGGATTATAG | 51434 |
rs114913824 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110374777 | TGATGTAATTAAACA[A/T]AGCAGCATTTCAGGA | 51434 |
rs115166185 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389200 | CCAGTAATATCTGAA[C/T]AAAAGACGCTGCCCT | 51434 |
rs115287726 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382699 | CTCAGTCTCCCAAAG[C/T]GTTGAGATTACAGGC | 51434 |
rs115298242 | snp | G/T | 0.0418186 | 0.138422 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110391057 | TAGGCAGGTGCAGCG[G/T]TACGCGCCTGTAGTA | 51434 |
rs115504359 | snp | A/C | 0.0637235 | 0.166737 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110397344 | CAGATCACAAGATCA[A/C]AAGATCGAGATCATC | 51434 |
rs115691916 | snp | C/T | 0.0256215 | 0.110247 | downstream-variant-500B, intron-variant | ANAPC7 | GRCh38.p7 | 12:110375340 | AGCATCTCCAGTTGT[C/T]ACTGAGATGCTAGGC | 51434 |
rs115733813 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110379241 | AATAGTTTTACTTCC[C/T]TGCTAAAGCCCTACT | 51434 |
rs115810235 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381312 | CAGGATATTGAAAAG[C/T]TTCCCCGGATGATGT | 51434 |
rs116034519 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110400162 | TCTTCAAACTCTGTG[A/C]TTCTATGTATGTAGT | 51434 |
rs116185196 | snp | A/G | 0.0637235 | 0.166737 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110404089 | CTAACGGCCTTTACA[A/G]TGGCGCATGCGCACC | 51434 |
rs116225614 | snp | C/T | 0.0256215 | 0.110247 | utr-variant-3-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110373993 | TTAGAAATGAAGTCA[C/T]GACTAGGAATTGGGA | 51434 |
rs116491199 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395945 | TTTTTCCACAGATGG[C/G]GGGTGAGGGGGTGGT | 51434 |
rs116572599 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381161 | AAATCCAGTGAAAGC[C/T]CTAAATAAATGTAAA | 51434 |
rs116793868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110385617 | GTGCAAACAAATCCA[C/T]CCTTCTAGATCTGCT | 51434 |
rs116862125 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110372649 | CTCAGCCTCCTGAGT[A/C]TTGAGTAGCTGGGAT | 51434 |
rs116863163 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110374867 | CCAGGACCCAAGGCT[A/T]CCCCTACCCAAGCAT | 51434 |
rs117200300 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388078 | TCTTGTTCTGTCCCC[C/T]TGGGCTGGAATGCAG | 51434 |
rs117278527 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110398891 | CAGAGGTTGCGGTGA[G/T]CCAAGATAGTGTGCC | 51434 |
rs117311384 | snp | A/G | 0.0232847 | 0.105357 | intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403143 | CATAAAAACCAGGAG[A/G]CTGGGTCCCTGAGCT | 51434 |
rs117338451 | snp | A/G | 0.00914312 | 0.0669923 | downstream-variant-500B, intron-variant | ANAPC7 | GRCh38.p7 | 12:110375118 | ACCCATGTTGGCACC[A/G]TTTCTACCGATATAA | 51434 |
rs117447857 | snp | C/T | 0.0023933 | 0.0345097 | downstream-variant-500B, intron-variant | ANAPC7 | GRCh38.p7 | 12:110375317 | GAGACTGACAGCTCC[C/T]GAAACATAGCATCTC | 51434 |
rs117462029 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395455 | GAGTACTACAGGTAT[A/G]TGCCACCATGCCGTT | 51434 |
rs117586468 | snp | A/G | 0.0221141 | 0.102801 | utr-variant-3-prime, downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110373392 | CTGGCAAATAATTCT[A/G]GGGCTGAATCAATGC | 51434 |
rs117665213 | snp | A/G | 0.0232847 | 0.105357 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110404175 | TTCGGCCCTGGGGGA[A/G]CTCCTTGGTTCGAGG | 51434 |
rs117814277 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110384213 | TCTAAAACATAAAAT[A/G]AAATAAAGTAAAATA | 51434 |
rs117945406 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110392601 | TGACAGTATTATTAG[A/T]ATATTAAATACTGAT | 51434 |
rs117985339 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110378551 | AACAGTACTTACCAC[A/G]TGCACCAAACAGACT | 51434 |
rs118018382 | snp | C/T | 0.0217236 | 0.101931 | intron-variant, downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110377288 | CTGCTGCAAAAGGCA[C/T]ACACCTGTCTAGTCA | 51434 |
rs137890406 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110385593 | GCACTTGAGGTGAGG[A/G]GAGATCTTGTGCAAA | 51434 |
rs137996217 | in-del | -/AAAA | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382442 | GCTGATTATCCTTTT[-/AAAA]AAAAAAAAAAAAAAA | 51434 |
rs138053799 | snp | C/T | 3.32182e-05 | 0.00407529 | synonymous-codon, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110374168 | GCCGAACCACTGCTC[C/T]TGGTCAGCCCACTGG | 51434 |
rs138172421 | snp | A/G | 0.118933 | 0.212888 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110399910 | ACCAGCCTGGCCAAC[A/G]TGTTGAAACCTCGTC | 51434 |
rs138239979 | in-del | -/AAA | 0.0448719 | 0.142907 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389398 | TACAGAAAGACAGAT[-/AAA]GAAGTATAATACTTG | 51434 |
rs138247171 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110378139 | CACTCTCGTTGCCCA[A/G]GCTGGAGCGCAATGG | 51434 |
rs138302941 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110402922 | TTAATTTTTACTTTT[C/G]GTAGAGGCAGGGTCT | 51434 |
rs138429015 | in-del | -/TAC | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110400587 | TTAAGAACTAAGAGT[-/TAC]AACTAGGGCCTAAAT | 51434 |
rs138434229 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110390621 | AACAATGGAATAATG[A/C]AATACTAAAAATAAA | 51434 |
rs138457092 | snp | C/G | 0.0155422 | 0.0867729 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403634 | CACATTCATCCTGCT[C/G]TGCAAAGCCGCGGGC | 51434 |
rs138556976 | snp | C/G | 0.027123 | 0.113256 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381708 | TCTGAGGGCTGCTGC[C/G]ACACCCACGGATTCA | 51434 |
rs138657867 | snp | C/T | 0.000395309 | 0.0140534 | synonymous-codon, intron-variant, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110377460 | CAGGGCTTTATCTAA[C/T]AATGTTTTGGCTTTC | 51434 |
rs138673465 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387154 | AGGATGGTTTGAGCC[C/T]GGGAGATTGACAGGT | 51434 |
rs138788614 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395729 | ATTTTTAGTAGAGAC[A/G]GCGTTTCACCGTGTT | 51434 |
rs138932824 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110400138 | GTATAGTCTAGATGA[C/G]TTAAGTTCTCTTCAA | 51434 |
rs139092205 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110397624 | AATGGGGGGCTGGGC[A/G]TGGTGGCTCATGCCT | 51434 |
rs139260438 | snp | A/C | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387280 | GAGAGAGAGAGAGAG[A/C]GAGAGACAGAGAGAG | 51434 |
rs139413364 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110395116 | TTTGGGAGTTCTTTG[C/T]CTTGAAGGGATCCCA | 51434 |
rs139448442 | snp | C/T | 0.0151814 | 0.0857917 | utr-variant-3-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110374136 | GCGGCCATGGAGCTG[C/T]CGCCCCCTCACTGCA | 51434 |
rs139455135 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110379485 | TGAGCTCTGGTGAAA[C/T]AGGCATGCAGTATAA | 51434 |
rs139552832 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380390 | GGTTGTGGTGGCTCA[C/T]GCCTGTAATCCCAGA | 51434 |
rs139745807 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110393074 | TGCTGGGATTACAGG[C/T]ATGAGCCACCATGCC | 51434 |
rs139780260 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110396107 | TGATCTGACAGGAGG[C/T]GGAGCTCAGGCAGTA | 51434 |
rs139835127 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383628 | TGGTTCATGCCTGTA[A/C]ACCCAGCACTTTGGG | 51434 |
rs139899913 | snp | C/T | 0.0170251 | 0.090679 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110405688 | AAAAGGAGCATTTGT[C/T]GTATAGAATGATTGG | 51434 |
rs139954100 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387961 | CATGCAAGGAGCAAC[A/G]GGCTACATCTTCCCT | 51434 |
rs139997986 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388319 | TAGAATTACAGGTGT[A/G]AGCCACCATGCCCGG | 51434 |
rs140037413 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110394666 | AAGAGTGAAATTCCA[C/T]CTCAAAAAAAAAAAA | 51434 |
rs140147934 | in-del | -/ACAAAAAAAAA | 0.138546 | 0.223781 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110384674 | GTGAGACTCTGTCTC[-/ACAAAAAAAAA]ACAAAAAAAAACAAA | 51434 |
rs140259017 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110400819 | GGGAGGCCTAAGTCA[C/T]GGGGATCACTTGAGG | 51434 |
rs140284932 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382024 | CAAAGAAAGTTGATC[A/C]AAAAATCATATTGAA | 51434 |
rs140374912 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110404517 | GCCAATGAGGCAGTT[C/T]AGGTCGTTGAGTCAG | 51434 |
rs140605189 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110399492 | ATAGGCATCATACAT[C/T]AGTGTTTGCGGGAGG | 51434 |
rs140612337 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110402641 | GCCCGGCCAATAAAG[A/G]ATATTAAGCAGGAGA | 51434 |
rs140644527 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388913 | GTGAAACCCCGTCTC[G/T]ACTAAAAAATACAAA | 51434 |
rs140833670 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110385647 | TTCCTCATCTAAACG[C/T]TTGGGATGGCCCCTT | 51434 |
rs140857540 | snp | A/G | 0.0486741 | 0.148216 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383221 | AGGCAGGTGGATCAC[A/G]AGGTCAGGAGATCGA | 51434 |
rs140917138 | snp | A/G | 0.0027308 | 0.0368503 | synonymous-codon, intron-variant, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110377505 | GTCTTCAAGACAAAC[A/G]GTGGCTAAAAGGGTA | 51434 |
rs140956581 | snp | A/C/T | 0.000296841 | 0.0121793 | missense, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110382913 | CAAGGTTCTCAACAT[A/C/T]CTCTAGCCGCCCTTC | 51434 |
rs141097298 | snp | C/T | 1.66893e-05 | 0.00288867 | missense, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110374328 | TTCTGGTCATTGGGG[C/T]CCAAACTAGGGGACA | 51434 |
rs141147170 | snp | C/T | 0.0844695 | 0.187349 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403632 | ATCACATTCATCCTG[C/T]TCTGCAAAGCCGCGG | 51434 |
rs141246304 | snp | C/G | 0.0256215 | 0.110247 | intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110402962 | GCCCAGGTTGGTCTT[C/G]AACTCCTGGGCTCAA | 51434 |
rs141563182 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110378614 | ACAGCGAGACGCCCT[A/G]TGAGGAGGCCACCTT | 51434 |
rs141583697 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110392144 | AAGGAAGATACCTTG[A/G]GCATTGCAGCAGACA | 51434 |
rs141661991 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110373385 | TCTATTTCTGGCAAA[G/T]AATTCTGGGGCTGAA | 51434 |
rs141787858 | in-del | -/A | | | utr-variant-3-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110373859 | AGAAATTAGTTATAT[-/A]AAAAGTACTCTTGGC | 51434 |
rs141870646 | snp | A/C | 0.0232847 | 0.105357 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110374930 | CCACCCCCACCCCCA[A/C]AGTTCAGAGCCTCTA | 51434 |
rs141902221 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395547 | CTCCTACCTCCGCCT[C/G]TGGAAGTGCTTGGAT | 51434 |
rs142280830 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110398259 | CAAAAAAAAAGAAAA[C/T]ACAAAAATTAGCCAG | 51434 |
rs142395617 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110396991 | GGCGGATCTCGAGGT[C/T]AGGAGATCGAGACCA | 51434 |
rs142621431 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380093 | CAGTGGTTCACGTCT[A/G]TAATCCCAGCACTTT | 51434 |
rs142682099 | snp | G/T | 0.0414363 | 0.137845 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382514 | TAGAGACAGGGTCTT[G/T]CTACATTGCCCATGC | 51434 |
rs142722780 | snp | C/G/T | 0.00398564 | 0.0444627 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110404739 | GAAGCTCCTGTAGAT[C/G/T]CTTTTCCCATCTCAT | 51434 |
rs142843654 | snp | C/G | 0.0696718 | 0.173152 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388105 | GCAGTGGCACAATCT[C/G]AGCTCACTGCAACCT | 51434 |
rs142843807 | snp | C/T | 0.0267878 | 0.112589 | intron-variant, downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110377009 | GGGCATGGTGGTGCA[C/T]GCCTGTAGTCCCAGC | 51434 |
rs142918860 | in-del | -/GCACATGTAAGGAACCT | 0.00159617 | 0.0282053 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110377867 | TAGGGAAGGAAACAA[-/GCACATGTAAGGAACCT]GCAGCATGTGAGCAC | 51434 |
rs143019127 | snp | C/T | 0.0174803 | 0.0918399 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110396471 | GAAAACAAGAGAAAA[C/T]GTAATACATCTTTTC | 51434 |
rs143048404 | snp | G/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389631 | ATGCAACTGGGAAAT[G/T]AGAAAATCTAAAAGT | 51434 |
rs143061580 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110378164 | CAATGGCGCCATCTC[A/G]GCTCACTGCAATCTC | 51434 |
rs143082802 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110399921 | CAACATGTTGAAACC[C/T]CGTCTCTACTAAAAA | 51434 |
rs143236660 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403268 | CAGGAAACCCTCGCC[C/T]GGGTCGTCCTCAGAG | 51434 |
rs143247464 | snp | C/G | 0.00358779 | 0.0422022 | downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110372449 | TGAGGCTGCATCCTG[C/G]ACAGCATGCCTAGGC | 51434 |
rs143332061 | in-del | -/A | 0.0486741 | 0.148216 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110397779 | CATGCCTGTAATCCC[-/A]ACCTACTCGGGAGGT | 51434 |
rs143532376 | in-del | -/C/CC | 0.000148582 | 0.00861795 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110386280 | CCTATTATCTCTGAT[-/C/CC]CCCCCCCAACAACAG | 51434 |
rs143538351 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110399319 | GCCACTGCGCCCAGC[C/T]GAGTCGAATAATTCT | 51434 |
rs143543688 | snp | G/T | 0.00318978 | 0.0398085 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110403848 | AATGAGTTGTTATTT[G/T]TACGCAAAAATCACG | 51434 |
rs143562818 | snp | A/C | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387274 | GAGAGAGAGAGAGAG[A/C]GAGAGAGAGAGACAG | 51434 |
rs143586209 | in-del | -/GA | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387214 | TGCACTCTAGCCTGG[-/GA]GAGAGAGAGAGAGAG | 51434 |
rs143660720 | snp | A/G | 4.95683e-05 | 0.00497812 | missense, nc-transcript-variant, intron-variant | ANAPC7 | GRCh38.p7 | 12:110381785 | GACAAGGTGCGAGCC[A/G]TATGGCCTCCCGAAA | 51434 |
rs143938358 | snp | C/G | 7.67062e-05 | 0.00619251 | synonymous-codon, nc-transcript-variant, intron-variant | ANAPC7 | GRCh38.p7 | 12:110381924 | GAGGGCCCGGGAGTA[C/G]CGTTTGCTATAGAAG | 51434 |
rs144086470 | snp | C/T | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110401805 | CGTGAAACCCTGTCT[C/T]TACTAAAAATACAAA | 51434 |
rs144122821 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110376689 | AACCAAATTATGAGT[G/T]TATCATAAATCAGGA | 51434 |
rs144182436 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110400966 | GAGGTGGGAGGATCG[A/C]TTGAGCCTGGGAGGT | 51434 |
rs144236946 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110391764 | ATGGTATATTTCTAA[C/T]AAAGTAAGGAATAGT | 51434 |
rs144448426 | in-del | -/C | 0.0170251 | 0.090679 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110404117 | ACCAGGCTAGGGCCG[-/C]CGCGCCCCTCCTCAG | 51434 |
rs144450515 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110393087 | GGCATGAGCCACCAT[A/G]CCCAGCCGACACCAG | 51434 |
rs144489946 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110398292 | ATGGTGGTGCATGCC[C/T]GTAATCCCAGCTACT | 51434 |
rs144664720 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380824 | CCAGGTGTAATCCTA[C/G]CTACTGGGGAGGCTG | 51434 |
rs144672647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383410 | GCCACTGCACTGCCT[A/G]GGTGACAGACTGAGA | 51434 |
rs144782037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110400392 | TGCCCCTTCTCCACT[A/G]TTTGAATTTAACAGT | 51434 |
rs144846977 | snp | C/G/T | 9.8841e-05 | 0.00702935 | missense, intron-variant, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110377443 | TAATCTGGCCTTTGG[C/G/T]TCAGGGCTTTATCTA | 51434 |
rs144978882 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110402598 | CTCGGCCTCCCAAAG[C/T]GCTGGGATTACAGGC | 51434 |
rs144994558 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110376801 | TTATATTCAGCTCCA[A/G]CTAATTCAGGACAAC | 51434 |
rs145073369 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110397820 | GAATCGCTTGAACCC[A/G]GGAGGCAGAGGTTGC | 51434 |
rs145084671 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110400677 | GCATAAACACATAAG[C/G]CTGACAGAGACCAGG | 51434 |
rs145251143 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382076 | TCCAAACCACACTTA[C/T]AGTTTTAACCTAAGA | 51434 |
rs145316741 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110385487 | GATTCCAAGCTGCCA[C/T]TGCCATTCCAAGCTG | 51434 |
rs145424066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110384362 | TGTTTGTGCCACTCC[C/T]GCCTGAGTGACAGAG | 51434 |
rs145483086 | snp | A/G | 1.74653e-05 | 0.00295505 | missense, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110396441 | TACTTCTGAGGTGGG[A/G]AGAATAACTCACTAG | 51434 |
rs145518850 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110397118 | CTGAAGCAGGAGACT[A/G]GCATGAACCCAGGAG | 51434 |
rs145572127 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110398308 | GTAATCCCAGCTACT[C/T]AGGAGGCTAAGACAG | 51434 |
rs145642626 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110399683 | ATAATCCTAGCTACT[C/T]AGAGGCTGAGGCAGG | 51434 |
rs145665414 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110378304 | TCTCCATGTTGGTCA[A/G]GCTGCTCTCGAACTC | 51434 |
rs145953141 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110390581 | TATAAAACAATCTAA[C/T]ATAGCATTGATTCAC | 51434 |
rs145983141 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395467 | TATGTGCCACCATGC[C/T]GTTTTGTAAAGACAG | 51434 |
rs146089351 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387272 | GAGAGAGAGAGAGAG[A/G]GAGAGAGAGAGAGAC | 51434 |
rs146123778 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110396763 | CAAGTGATCTACCTG[C/T]GTCGGCCTCCCAAAG | 51434 |
rs146182299 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110378975 | GCAATTCTCCTGCCT[C/T]AGCCTCCCAAGTAGC | 51434 |
rs146237743 | in-del | -/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380677 | AAAAAACAGGACCCG[-/G]GGCACGGTGGCTCAC | 51434 |
rs146284266 | snp | C/T | 0.0023933 | 0.0345097 | downstream-variant-500B, intron-variant | ANAPC7 | GRCh38.p7 | 12:110375080 | TTTCTCACTTGCTTC[C/T]GAGATTCTAAAAAGC | 51434 |
rs146300604 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110396091 | AATCTAATGCCGCAG[C/G]TGATCTGACAGGAGG | 51434 |
rs146338310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110377734 | ACAAAGGGCAGGCCA[C/T]GGGAAACTGATGGTG | 51434 |
rs146402871 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110392973 | GCTAATTTTATATTT[C/T]TAGTAGAGACGGGGT | 51434 |
rs146462528 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389410 | GATAAAGAAGTATAA[C/T]ACTTGGCTTTTCTTT | 51434 |
rs146604329 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110393150 | ACTATAATATGCTGC[C/T]AAATCAAACACAAAG | 51434 |
rs146835582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110385262 | CAAGAGTGAAACTCC[A/G]TCTCAAACAAACAAA | 51434 |
rs146853753 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388772 | TAAAGGCAGACTGAC[C/T]CCATTCTTCAAAAGA | 51434 |
rs146925612 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110394130 | GCAATGAGCCGAGAT[C/T]GCACCACTGCACTCC | 51434 |
rs147001395 | snp | A/C | 0.0197687 | 0.0974348 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389959 | AAAAAACCCACAAAA[A/C]CAAAAAAAAAGCCAG | 51434 |
rs147082419 | snp | C/T | 0.00636936 | 0.0560724 | downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110372648 | CCTCAGCCTCCTGAG[C/T]ATTGAGTAGCTGGGA | 51434 |
rs147090898 | snp | C/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110377926 | CTGGAAGAATAAATG[C/G]GACACTAATGATTAG | 51434 |
rs147107313 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381111 | AAAACCAGAAAAAAA[A/G]TCAGAAAAAATGGAT | 51434 |
rs147146618 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110400770 | CATTAATGAGGCTGG[C/G]CTCGGTGGCTCACGC | 51434 |
rs147653855 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110394334 | TATCTCTACCAAAAA[C/T]AAAAAAAATTGGCCA | 51434 |
rs147873940 | snp | A/C | 0.0260105 | 0.111035 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380944 | CTCTGTCTCAAAAAA[A/C]AGAGGAGTAAGAGAA | 51434 |
rs147921327 | snp | G/T | 0.0217236 | 0.101931 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110394876 | GTTAAACATAAAAAA[G/T]AAAAAAGAAAAAACA | 51434 |
rs147964086 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110377810 | TTCCCCAGAGAACTT[C/G]ATGGATGTAGAAAAA | 51434 |
rs148019779 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110373102 | ATACTCAGAGCCATC[A/G]CAACTTAAGGCACAA | 51434 |
rs148022338 | snp | A/C/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387255 | AGAGAGACAGAGAGA[A/C/G]AGAGAGAGAGAGAGA | 51434 |
rs148083718 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110392058 | GATTGTGCCACTGCA[C/T]TCCAGCCTGGCAACA | 51434 |
rs148111109 | snp | A/G | 1.70898e-05 | 0.00292311 | synonymous-codon, nc-transcript-variant, intron-variant | ANAPC7 | GRCh38.p7 | 12:110381870 | TAGCAGAGCTTGAAC[A/G]CTATTACTGTTCAGC | 51434 |
rs148216735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110378197 | CCTCCCGGGTTCAAG[C/T]GATTCTCCTCCCTCA | 51434 |
rs148234937 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395542 | AAGTCCTCCTACCTC[C/T]GCCTCTGGAAGTGCT | 51434 |
rs148268689 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383185 | GGCTCACACCTGTAA[C/T]TCCAGCACTTTAAGA | 51434 |
rs148336599 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110399328 | CCCAGCCGAGTCGAA[C/T]AATTCTGTAGATAGT | 51434 |
rs148387490 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403381 | CTCCGAAGTCTGCTC[C/G]GCTCCAGGACGCCCT | 51434 |
rs148432234 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110400611 | CCTAAATCTCCAAAC[A/G]TGGAAACTGTATGCT | 51434 |
rs148484057 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110405244 | GAGAGAGTCGTGATC[A/G]ATTGAGTAAGCAGGG | 51434 |
rs148536135 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110376826 | GACAACTCAAACCAG[A/G]TAACAGTGAGCCGAG | 51434 |
rs148709290 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110392017 | GAATCGCTTGAACCC[A/G]GGAGGTGGAGGTTGC | 51434 |
rs148822220 | snp | A/G | 0.0217236 | 0.101931 | intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403402 | AGGACGCCCTCGCAG[A/G]CCCCGGAGCCTCCGC | 51434 |
rs148833222 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110393736 | GTTGGGCATGGTGGC[A/G]CATGCCTGTAATCCC | 51434 |
rs148885004 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110398530 | CTGTTTAACCTTGAG[C/T]ATTACAGTCAAGAAT | 51434 |
rs149058367 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389489 | TTGGCCCGTAGGTAC[C/T]AACTCACTAAAGTAA | 51434 |
rs149218420 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110384637 | TGCAGTGAGCCGAGA[C/T]TGCACCACTGCACTC | 51434 |
rs149357519 | snp | C/G | 0.247621 | 0.249989 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395731 | TTTTAGTAGAGACGG[C/G]GTTTCACCGTGTTAG | 51434 |
rs149509859 | snp | A/T | 0.0217236 | 0.101931 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110390365 | AGGCGTGAGCCACCG[A/T]GTCTGGCAAAATTAG | 51434 |
rs149587001 | in-del | -/CA | 0.435694 | 0.167385 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110392090 | AGCAAGACTCCACCT[-/CA]CAAAAAAAAAAAAAA | 51434 |
rs149663405 | snp | C/T | 1.6495e-05 | 0.0028718 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110395170 | ATCTTGTTTTAGCAT[C/T]GTATAACATTCAGCC | 51434 |
rs149680156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110393539 | TTGGGACCAACCTGG[A/G]CAAATGGTGGAGACC | 51434 |
rs149838646 | snp | C/T | 4.94352e-05 | 0.00497143 | missense, intron-variant, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110388538 | TCAAGGGCTAATGGG[C/T]ACTGCCTCAGCACCT | 51434 |
rs150013087 | snp | C/T | 0.139903 | 0.224452 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380409 | TGTAATCCCAGAACT[C/T]TGGGAGGCCAAGGCA | 51434 |
rs150081950 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110386242 | TATGAAACTTGGTAT[C/T]GAGTATTAATGCTGC | 51434 |
rs150215847 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110394516 | CGCCTATAATCCCAG[C/T]TACTCGGGAGGCTGA | 51434 |
rs150240373 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381484 | TGGGACTACAGGTGT[A/G]AGCCACCATGCCCAG | 51434 |
rs150510693 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110373409 | GGCTGAATCAATGCA[C/T]TGCGAATAAGACAAA | 51434 |
rs150562694 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380294 | AAGTGGAGGTTGCAG[C/T]GAGCTGAGATTGCAC | 51434 |
rs150701875 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110399958 | AATTAGCCAGGCATG[G/T]TGGTGGGCGCCTGTA | 51434 |
rs150708550 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110378329 | GAACTCCTGACCTCA[A/G]GTGATCCGCCCAGCT | 51434 |
rs150770522 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383212 | AAGAAGCCGAGGCAG[C/G]TGGATCACGAGGTCA | 51434 |
rs150897727 | snp | A/T | 8.24817e-05 | 0.00642137 | missense, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110387821 | AGAGCCAGTCCAAGT[A/T]AGGCACGGTTTGGAT | 51434 |
rs150915394 | in-del | -/AG | 0.00953873 | 0.0683987 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110399541 | ATTACTAATAGACAC[-/AG]GGTTTCTTTTTGTTG | 51434 |
rs151041709 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110377326 | CTAGCTGGGACAAGG[A/G]GCTCCAACTGAGGTC | 51434 |
rs151094104 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381377 | GAGTCTTGCTCTGTC[A/G]CCAGGCTGGAGTGCA | 51434 |
rs151228959 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110400996 | TGGAGGCTGTAGTCA[C/G]CCGAGATCGCACCAC | 51434 |
rs180860755 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110385944 | ATCCCTTTCTTATTC[C/T]TTTTTAATTATACTA | 51434 |
rs181111888 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110391388 | ACTGGAATTTTCCTT[A/T]AAAATGTGAGGGAAT | 51434 |
rs181145208 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant, upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110402568 | CTCGATCTCCTGACC[A/T]CGTGATCCGCCCGCC | 51434 |
rs181145437 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381112 | AAACCAGAAAAAAAA[A/T]CAGAAAAAATGGATT | 51434 |
rs181284233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110374939 | CCCCCAAAGTTCAGA[A/G]CCTCTAGAACATTCA | 51434 |
rs181300585 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110396140 | ATTCACTAGCCCTCC[A/G]CCCACCTCCTGCTGT | 51434 |
rs181368825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110385612 | ATCTTGTGCAAACAA[A/G]TCCATCCTTCTAGAT | 51434 |
rs181535046 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380862 | AGAATGGCATTAACC[C/T]GGGAGGTGGAGCCTG | 51434 |
rs181540613 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110400977 | ATCGATTGAGCCTGG[C/G]AGGTGGAGGCTGTAG | 51434 |
rs181758785 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110374578 | CTCCACAAATTTCTT[A/T]AACTTTTTCATACCT | 51434 |
rs181879395 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110391821 | GCTTCTTGGCCGGGC[A/G]TGGTGGCTCATGCCT | 51434 |
rs181954385 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395679 | AAGTAGCTGGGACTA[A/C]AGGCATCCACCACCA | 51434 |
rs182032398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110402928 | TTTACTTTTCGTAGA[A/G]GCAGGGTCTCCCTAT | 51434 |
rs182219209 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389070 | CTGGGCTACAGAGTG[A/C]GACTCCATCTTAAAA | 51434 |
rs182229965 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110391516 | CTAACAGACAAGAAA[A/G]AAAAACTGTAAATGT | 51434 |
rs182259769 | snp | A/T | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110386331 | GAATTACTTACCTTT[A/T]ATCAGATAAGGATCC | 51434 |
rs182427620 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110392957 | TGCGCCACCACACCC[A/G]GCTAATTTTATATTT | 51434 |
rs182568063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110376425 | ATACAAAAAATTAGC[C/T]GGGCTTGGTGGCAGG | 51434 |
rs182602155 | snp | A/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387364 | GAGACAGAGAGAGAG[A/T]GACAGAGAGAGAGAG | 51434 |
rs182811458 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110378910 | GTCACCCAGGCTGGA[C/G]GGCAGTGGTGACATC | 51434 |
rs182818511 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110398080 | GTGAAACCCCGTCTC[C/T]AGTAAAAATACAAAA | 51434 |
rs182860198 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110397020 | CATCCTGGCTAACGC[A/G]GTGAAACCCCATCTC | 51434 |
rs182876361 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110404298 | TCTGGCACACTTAAC[A/G]TTTTAGGAAAGTTTT | 51434 |
rs183043127 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382756 | TTACCTCTTAAACCT[A/G]TGCTTTCAATTTATA | 51434 |
rs183056626 | snp | A/G | 0.00264949 | 0.0363005 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403678 | CTGACTCGAAAAGCC[A/G]GTAGAGGATCCTTAG | 51434 |
rs183064103 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110372687 | GTGTACCACCATGCC[C/T]GGTTAATTTTTGTAT | 51434 |
rs183089014 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110399022 | GTGAGCTGAATAATT[C/T]TTTTTTTTTTTTTTT | 51434 |
rs183169973 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383709 | GGTGAAACCCCATCT[C/G]TACTAAAAATACAAA | 51434 |
rs183282424 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110377266 | ACCAATCCAAGCAGG[A/C]TCAGACCTGCTGCAA | 51434 |
rs183285866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110397537 | GCACTCCAGCCTGGC[A/G]ACAGAGCGAGATCTC | 51434 |
rs183512687 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381465 | CTTCAGCCTCCCAAG[G/T]AGCTGGGACTACAGG | 51434 |
rs183708557 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110393948 | GAGGCCGTGGCAGGC[A/G]AATCACAAAGTCAGG | 51434 |
rs183857144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110391460 | ACACATTTTGACTCA[C/T]TTCCTTGTCCTTTAC | 51434 |
rs184049005 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110393636 | ACTCTGTGAGGCCGA[A/G]GTGGGTGGATCACCT | 51434 |
rs184067954 | snp | A/G | 0.00318978 | 0.0398085 | utr-variant-3-prime, downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110373099 | TGTATACTCAGAGCC[A/G]TCGCAACTTAAGGCA | 51434 |
rs184387651 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110405707 | TAGAATGATTGGTGA[C/T]GGCCTGGATGCAGTT | 51434 |
rs184394299 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110379622 | ACAAAGACAATACTC[C/T]TTCCCCCTCAACAAA | 51434 |
rs184522048 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110399093 | TGGCACAATCTCGGC[C/T]CACTACGACCCCTGC | 51434 |
rs184622932 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380415 | CCCAGAACTTTGGGA[A/G]GCCAAGGCAGGCAGC | 51434 |
rs184638754 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110399771 | CTCCAGCCTGGGTGA[C/T]GAGAGAGAGACTCTG | 51434 |
rs184813611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110385707 | GCTCATAAGACTGTT[C/T]ATTGTCACAAGGCCC | 51434 |
rs184847858 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110384616 | CTTAAACCAGGAGGT[G/T]GAGGTTGCAGTGAGC | 51434 |
rs184855416 | snp | A/C | 0.0023933 | 0.0345097 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110404785 | CCTGGATGTGTGAGA[A/C]CTTCTATTTGATTTT | 51434 |
rs184914089 | snp | C/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110387849 | GATCACATTCATTGT[C/G]ATGGATGCCACCTCT | 51434 |
rs184960021 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110390973 | GAGGTGGGTGGATCA[C/T]GAGGTCAGGAGATCG | 51434 |
rs185118784 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110386046 | GCACACCATAAATTT[A/G]TAAGTCATAAGGAGG | 51434 |
rs185176040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110393030 | GAACTCCCAACCTCA[A/G]ATGATTCACCCACCT | 51434 |
rs185228167 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110385155 | GCCTATAATCCCAGC[C/T]ACTCGGGAGGCTGAG | 51434 |
rs185409201 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | ANAPC7 | GRCh38.p7 | 12:110375599 | AATAAGGTAGCTAGA[C/T]ATAGACAAGGAAATG | 51434 |
rs185422809 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110396573 | TGGAGTGCAGTGGCA[C/G]GATCTCGGCTCACTG | 51434 |
rs185591016 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110390126 | CAGGCTAGAGTGCGA[C/T]GGCACGATCTCAGCT | 51434 |
rs185690256 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110392342 | CAAAAACTCAGAAAA[C/T]AGTAAATAATACCTT | 51434 |
rs185751816 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110394984 | GAAGAGGAAGAAAAT[G/T]AGAATTAGAATCATG | 51434 |
rs185787465 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110397065 | AAAAATTAGCCAGGC[A/G]TGGTGGCAGGCGCCT | 51434 |
rs185865381 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110373735 | CCCTAGGGCCAGATC[A/G]TGCTGCCATCCAACT | 51434 |
rs185918144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110376730 | AAAAAAAGGGCCAAA[C/T]GGGAAGTCATAAAAT | 51434 |
rs185937582 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110374843 | ACTTGTAAACACCTA[G/T]GTCAGACCCCAGGAC | 51434 |
rs185944784 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395728 | TATTTTTAGTAGAGA[C/T]GGCGTTTCACCGTGT | 51434 |
rs186176603 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110402616 | TGGGATTACAGGCAT[A/G]AGCCACTACGCCCGG | 51434 |
rs186400366 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382553 | AATTTCTGGCCTCAA[A/G]TAATTACCTCTTTTT | 51434 |
rs186412198 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403096 | CCTGATACACTTAAC[A/G]GGGGGACCAATCTCA | 51434 |
rs186528084 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389312 | ATGAACTATCTCACA[G/T]AAGAAAGTGAGAAAC | 51434 |
rs186758153 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380925 | CCTGGGCAACAAAGC[A/G]AGACTCTGTCTCAAA | 51434 |
rs186867183 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110386888 | GTTAGACACTGCAAT[A/G]AACCAAGCTTCTGGT | 51434 |
rs186982914 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388003 | CAACTGCTTCCCTAT[G/T]CTGAGCGATGCATGA | 51434 |
rs187180225 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389398 | TACAGAAAGACAGAT[A/G]AAGAAGTATAATACT | 51434 |
rs187328807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110391743 | CAGGTCATTATGAAG[A/G]AGATTATGGTATATT | 51434 |
rs187400714 | snp | A/G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110373040 | TTGGACTAATTTTTG[A/G/T]ATTTGGGATTAGCTG | 51434 |
rs187405409 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110394270 | CCAAAGTGGGAGGAC[A/G]GTTTGAGCCCAGGAG | 51434 |
rs187601659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110378215 | TTCTCCTCCCTCAGC[C/T]TCCCGAGTAGCTGGG | 51434 |
rs187611048 | snp | A/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110400588 | TTAAGAACTAAGAGT[A/T]ACTAGGGCCTAAATC | 51434 |
rs187703059 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383932 | GAAGGGCCAGGCGCG[C/G]TGGCTCATGCCTGTA | 51434 |
rs187752065 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110384884 | ACCATCAGAAATACA[A/C]TGCTGAAAAGCCAAT | 51434 |
rs187767061 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110405259 | GATTGAGTAAGCAGG[G/T]GGTACATGACATGCA | 51434 |
rs187960730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110378932 | GGTGACATCTCGGCT[C/T]ACTGCAACCCATGTC | 51434 |
rs187993707 | snp | A/C | 0.00557542 | 0.0525036 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110404649 | TACAGTAGTAGATGC[A/C]AAAAAAATGCTCTGA | 51434 |
rs188178013 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110391473 | CACTTCCTTGTCCTT[C/T]ACATAGACTGAGAAG | 51434 |
rs188221379 | snp | G/T | 0.000609075 | 0.0174404 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403691 | CCGGTAGAGGATCCT[G/T]AGGGAAGACTCCAAA | 51434 |
rs188264056 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110398366 | AGTTGCAGTGGGCCA[A/G]GATCATGCCATTTGT | 51434 |
rs188419180 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110394722 | GTGGCAGCATGCAAC[C/T]GTAATCCCAGCTATT | 51434 |
rs188431616 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110385926 | ACTGCCTTTAATCAC[C/G]TTATCCCTTTCTTAT | 51434 |
rs188502030 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110390319 | CCTCAGGTGATCCAA[C/T]CACCTCGGCCTCCCA | 51434 |
rs188507486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383025 | GGGTCCCACATACAG[A/G]AGTAGCACCCAACAT | 51434 |
rs188685102 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110391259 | CATCATAAAGCCACA[C/T]TCCACCAGTTATAAA | 51434 |
rs188841046 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110374892 | AAGCATTCACATTTA[C/G]CAGCTGAGTGTCAGT | 51434 |
rs188845505 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395776 | ATCTCCTGACCTCGT[C/G]ATCCGCCCGCCTAGG | 51434 |
rs189041053 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110393679 | TCAAGACCAGCCTGA[A/C]CAACATGGAGAAACC | 51434 |
rs189042575 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110399362 | TTTCTCAACAAGCTA[C/G]GCACAGTGGCTCACA | 51434 |
rs189072819 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380770 | CCATCCTGGCTAGCA[C/T]GGTGAAACACTGTCT | 51434 |
rs189087296 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110399948 | AAAATACGAAAATTA[C/G]CCAGGCATGGTGGTG | 51434 |
rs189330568 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380311 | AGCTGAGATTGCACC[A/C]CTGCACTCCAGCCTG | 51434 |
rs189582824 | snp | C/G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110373189 | CTGACCAGTGACAGA[C/G/T]TGCTGGAACCAGACC | 51434 |
rs189603285 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381104 | CTCACCAAAAACCAG[A/T]AAAAAAATCAGAAAA | 51434 |
rs189878414 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110402294 | AGATATTTGCCTTCA[A/G]AGGCCATGGGAAAGA | 51434 |
rs189908061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388888 | GATTGAGACCATCCC[A/G]GCTAACACAGTGAAA | 51434 |
rs190127388 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110385324 | TTTATTCTCACCCAC[A/G]TTCTATAAAAAGGGA | 51434 |
rs190147020 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110392942 | CTGAGATTACAGGCA[C/T]GCGCCACCACACCCG | 51434 |
rs190160850 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110391804 | AGTTTATAATTAAAA[C/T]GGCTTCTTGGCCGGG | 51434 |
rs190404812 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110373856 | TTTAGAAATTAGTTA[C/T]ATAAAAAGTACTCTT | 51434 |
rs190449093 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389108 | AAAAAAAAAAGAAAA[A/G]AAAAGAAATTACTAC | 51434 |
rs190658674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395399 | GATTTACTGCAGTCT[C/T]AGACTCCTAGTCTCA | 51434 |
rs190698439 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110402718 | ATGAAAGGCGCCACG[A/C]CCACCCATTAATGGA | 51434 |
rs190814685 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382747 | TCCAGGTGATTACCT[C/G]TTAAACCTGTGCTTT | 51434 |
rs190834930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403118 | CCAATCTCAGATGCG[A/G]GGGCTAGCGCATAAA | 51434 |
rs190961315 | snp | A/C/G | 0.00597678 | 0.0543977 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110393497 | ATTTGGGAGGCTAAG[A/C/G]GGGGAGGACAACTTG | 51434 |
rs190967024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110396932 | GCACAGGCTGGGTGC[A/G]GTGGCTTACGCCTGT | 51434 |
rs191193656 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110376413 | TCTCTACTAAAAATA[C/T]AAAAAATTAGCCGGG | 51434 |
rs191221024 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383985 | AGGCAGGTGGATCAC[A/G]AGGTCAGGAGTTCAA | 51434 |
rs191233320 | snp | A/T | | | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110404668 | AAAATGCTCTGAAAA[A/T]ATCACAGTGTATCTT | 51434 |
rs191256143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383254 | CCATCCTGGCTAACA[C/T]GGTGAAACCTCATCT | 51434 |
rs191488398 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110404244 | GGAAATAAAGGCTGG[A/G]TCCAGGAATTAGCTG | 51434 |
rs191761851 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387590 | GATTACATTTGGGAC[C/T]ATTCAGTATAAAAGA | 51434 |
rs191851189 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110373052 | TTGAATTTGGGATTA[A/G]CTGTGACACCCACCC | 51434 |
rs191856105 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110394625 | TGCAGTGAGCCCCCA[C/T]GCTATTGCACTCCAG | 51434 |
rs191986345 | snp | C/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387357 | AGAGAGAGAGACAGA[C/G]AGAGAGAGACAGAGA | 51434 |
rs192011009 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110376850 | AGCCGAGGCTGGGCA[C/G]GGTGGCTCACACCTA | 51434 |
rs192085565 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110378547 | GATGAACAGTACTTA[A/C]CACATGCACCAAACA | 51434 |
rs192098181 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110397851 | TGTGAGCCGAGATTG[C/T]GCCACTACACTCCAG | 51434 |
rs192242344 | snp | A/C | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381058 | CGAGCGGTGGGAGGA[A/C]AAAAAAAAAAAACCC | 51434 |
rs192316415 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110384978 | ATTAAAGATCACTGC[C/T]TCGGGCTGGGTGCAG | 51434 |
rs192335190 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110405341 | TCTGTAGATAACATC[A/G]GTTGCTAGGTCAGGG | 51434 |
rs192353241 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110397370 | TCATCCTGGCCAACA[C/G]GGTGGAACCCCAGCT | 51434 |
rs192546749 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110398861 | GAGGCAGGAGAATCA[C/T]TTGAATCTGGGAGGC | 51434 |
rs192584053 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389738 | AGATTGAGACCATCC[C/T]GGCTAACACAGTGAA | 51434 |
rs192603745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380393 | TGTGGTGGCTCATGC[C/T]TGTAATCCCAGAACT | 51434 |
rs192701036 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110394835 | TGGGTGACAGTGAGA[C/T]TCTGTCTCAAAAAAT | 51434 |
rs192824417 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110379428 | CAACTGGGAAACATC[C/T]GCTGTCCAAATATTA | 51434 |
rs192895554 | snp | A/C | | | intron-variant, utr-variant-5-prime | ANAPC7 | GRCh38.p7 | 12:110401394 | GAGTGCTTATTGCGC[A/C]CAGCCACTGCGCTTT | 51434 |
rs193006432 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110393791 | AGAACTGCTTGAACC[C/T]GGGAGGCAGAGGTTG | 51434 |
rs193089961 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110390656 | TTTTTTACTTGGCCT[C/T]AGATTTTCCATATTA | 51434 |
rs193279619 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110399542 | ATTACTAATAGACAC[A/G]GTTTCTTTTTGTTGG | 51434 |
rs199558275 | in-del | -/T | 0.0225045 | 0.103662 | downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110372535 | ATCTGTGGGGCTTTA[-/T]TTTTTTTTTAAACAC | 51434 |
rs199561791 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389103 | AAAAAAAAAAAAAAA[C/T]AAAAGAAAAGAAATT | 51434 |
rs199642159 | snp | A/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110400310 | CACACGAAAAAATAG[A/T]TATTGCCTCTGGAGA | 51434 |
rs199724894 | in-del | -/CT | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110400588 | TAAGAACTAAGAGTA[-/CT]ACTAGGGCCTAAATC | 51434 |
rs199766537 | snp | C/G | 0.00169695 | 0.0290791 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382813 | TTAATCTACTGACAA[C/G]TGGGGAGAAAAGAGA | 51434 |
rs199792027 | snp | A/G | 0.00210272 | 0.0323564 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403665 | AGCGGCGGCAGCACT[A/G]ACTCGAAAAGCCGGT | 51434 |
rs199793096 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380171 | GCCTGGCTAACATGG[C/T]GAAACCCCATCTCTA | 51434 |
rs199834205 | in-del | -/TTTTTA | 0.00676609 | 0.0577691 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382564 | TCAAGTAATTACCTC[-/TTTTTA]TTTTTATTTATTTAT | 51434 |
rs199898262 | snp | C/G | 0.00199792 | 0.0315431 | missense, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110387810 | GATCCACACAGAGAG[C/G]CAGTCCAAGTTAGGC | 51434 |
rs199917341 | snp | C/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387243 | AGAGAGAGAGACAGA[C/G]AGACAGAGAGACAGA | 51434 |
rs199941223 | snp | G/T | 0.000201056 | 0.0100243 | missense, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110395217 | CAATTTCAGATGGAA[G/T]ACACTAAAAGACAAT | 51434 |
rs199956013 | snp | C/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387319 | AGAGAGACAGAGAGA[C/G]AGAGAGAGAGAGAGA | 51434 |
rs200045076 | in-del | -/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110400586 | TTTAAGAACTAAGAG[-/T]TAACTAGGGCCTAAA | 51434 |
rs200047744 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382770 | TGTGCTTTCAATTTA[C/T]ATTCTCTTCAAGAGC | 51434 |
rs200086640 | snp | C/G | 0.000151353 | 0.00869792 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395058 | GAGAGAGGGAGCAGG[C/G]TTAGGAGAGCTGAGG | 51434 |
rs200115169 | in-del | -/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110396682 | ACCCAGCTAATTTTT[-/G]GTTTTTTTTTTTAGT | 51434 |
rs200196047 | snp | A/G | 0.000399281 | 0.0141238 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403656 | GCCGCGGGCAGCGGC[A/G]GCAGCACTGACTCGA | 51434 |
rs200316709 | snp | C/G/T | 0.000118131 | 0.00768459 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110396461 | TAACTCACTAGAAAA[C/G/T]AAGAGAAAATGTAAT | 51434 |
rs200361388 | snp | C/T | 0.000280013 | 0.0118291 | synonymous-codon, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110376137 | GAAATCTCCTAGGAT[C/T]CGATGCAGGACACAG | 51434 |
rs200364295 | in-del | -/GC | 0.00993419 | 0.0697739 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387102 | TGGGTGTGGTGGCAT[-/GC]GCCTGTAGTCCCAGA | 51434 |
rs200412886 | snp | C/G | 1.64757e-05 | 0.00287012 | missense, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110386444 | GGTCCACGTTATCTC[C/G]CAATAAGGATTTTTT | 51434 |
rs200431504 | in-del | -/TA | 0.0176699 | 0.0923187 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381735 | TTCACACCATTCACC[-/TA]TGTTTTCTTTCTTAC | 51434 |
rs200556644 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381954 | GCTGTGACAGCTGGA[A/G]AAAAAAAAAAAAAAA | 51434 |
rs200588429 | in-del | -/G | | | intron-variant, upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110402032 | TAACAAAAATTAGCT[-/G]GGGCGTGTGGCGCTC | 51434 |
rs200704477 | snp | A/G | 1.76914e-05 | 0.00297412 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381728 | CCACGGATTCACACC[A/G]TTCACCTATGTTTTC | 51434 |
rs200761710 | in-del | -/GAA | 0.00953873 | 0.0683987 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110378517 | AGGCACTTGCTGAGG[-/GAA]GCTTCCCTAAACGAG | 51434 |
rs200871554 | snp | C/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380274 | GAGAATCACTTAAAC[C/G]CGGCAAGTGGAGGTT | 51434 |
rs201117642 | snp | A/G | 0.00092936 | 0.0215364 | utr-variant-3-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110374127 | CAGGCCACTGCGGCC[A/G]TGGAGCTGCCGCCCC | 51434 |
rs201160899 | snp | A/G | 3.92457e-05 | 0.00442959 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110396458 | GAATAACTCACTAGA[A/G]AACAAGAGAAAATGT | 51434 |
rs201208334 | snp | C/T | 0.00199805 | 0.0315441 | utr-variant-3-prime, intron-variant | ANAPC7 | GRCh38.p7 | 12:110376022 | AGCTCACTGCCTCCT[C/T]TACCCTCCTCAGTGG | 51434 |
rs201209979 | snp | A/G | 0.00199792 | 0.0315431 | missense, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110387889 | ACAGAAAGGGACAAC[A/G]AGCCTAAACCAACAG | 51434 |
rs201267311 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387392 | GAGAGACAGAGAGAG[A/G]GAGAGAGAGAGAGAG | 51434 |
rs201366440 | in-del | -/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110396528 | TTCTTTTTTTTTTTT[-/T]GAAATAGATTCTCAC | 51434 |
rs201370750 | in-del | -/AC | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387289 | GAGAGAGAGAGACAG[-/AC]AGAGAGAGAGAGAGA | 51434 |
rs201397523 | in-del | -/C | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110397573 | AAAAAAAAAAAAAAA[-/C]ACTAAAAACTAAAGA | 51434 |
rs201398895 | in-del | -/AG | 0.00993419 | 0.0697739 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110384127 | GAATTGCTTGAACTC[-/AG]AGGGCGGATGTTGCA | 51434 |
rs201433415 | in-del | -/T | 0.00597247 | 0.0543191 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382079 | AAACCACACTTATAG[-/T]TTTAACCTAAGATAT | 51434 |
rs201440638 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380299 | GAGGTTGCAGTGAGC[C/T]GAGATTGCACCACTG | 51434 |
rs201458718 | in-del | -/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381326 | CTTCCCCGGATGATG[-/T]TTTTTTTGTTGTTGT | 51434 |
rs201481931 | snp | A/G | 3.38748e-05 | 0.00411537 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403622 | CACGTGGTCTATCAC[A/G]TTCATCCTGCTCTGC | 51434 |
rs201523244 | snp | A/C/T | 4.94257e-05 | 0.004971 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110386310 | GCCACTGTCTTCCTG[A/C/T]CCCAAGAATTACTTA | 51434 |
rs201531982 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110377590 | GCTTCTCGAATACTG[C/T]TGGAGGCTAAGTAAC | 51434 |
rs201586482 | in-del | -/TTTA | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382572 | TTACCTCTTTTTATT[-/TTTA]TTTATTTATTTTTGA | 51434 |
rs201746238 | snp | G/T | 0.00199805 | 0.0315442 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110386499 | TTAAACATTGAACCT[G/T]TAAATCTATTATAAA | 51434 |
rs201808610 | snp | A/T | 0.00199802 | 0.0315439 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387923 | GCAGAAGAAAGAAAG[A/T]AAGGCACGATATCTC | 51434 |
rs201940515 | snp | C/G | 1.64882e-05 | 0.00287121 | missense, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110395160 | TGGCATCTTTATCTT[C/G]TTTTAGCATTGTATA | 51434 |
rs202028995 | snp | C/G | 1.6473e-05 | 0.00286988 | missense, intron-variant, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110377490 | CTCCTGTGTCACTGG[C/G]TCTTCAAGACAAACG | 51434 |
rs202155296 | in-del | -/A | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381070 | GACAAAAAAAAAAAA[-/A]CCCCATCCCAACTAT | 51434 |
rs202161891 | snp | A/G | 0.00174961 | 0.0295253 | intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403498 | GCCGCTTTCTCCTCA[A/G]CCCCAGGCAGCTACC | 51434 |
rs367618463 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110401937 | CAAGATCGTGCAGAG[C/T]GAGACTCCGTCTCAA | 51434 |
rs367644409 | snp | A/G | 1.64844e-05 | 0.00287087 | missense, intron-variant, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110377614 | AAGTAACATTCGATA[A/G]GACCTGAAAAAAGTA | 51434 |
rs367762819 | snp | C/G | 1.64963e-05 | 0.00287192 | missense, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110387757 | ATGGTACTGATTGCT[C/G]TTGAGTTGTCACCAG | 51434 |
rs367895598 | in-del | -/CT | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383428 | TGACAGACTGAGACT[-/CT]GTCTCAAAAAAAGAA | 51434 |
rs367996316 | snp | C/T | | | missense, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110382948 | GCCAGTAGGTAGCCA[C/T]ATACATCCATTCCTA | 51434 |
rs368036319 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110397018 | ACCATCCTGGCTAAC[G/T]CGGTGAAACCCCATC | 51434 |
rs368038734 | snp | C/T | | | utr-variant-3-prime, intron-variant | ANAPC7 | GRCh38.p7 | 12:110375847 | TATAGTGGTGTGGGA[C/T]GGTTATGAGTGAAAC | 51434 |
rs368110252 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382090 | ATAGTTTTAACCTAA[A/C/G]ATATTAGTAGAAAAG | 51434 |
rs368122318 | snp | C/T | 6.58935e-05 | 0.00573955 | synonymous-codon, intron-variant, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110377481 | TTTGGCTTTCTCCTG[C/T]GTCACTGGGTCTTCA | 51434 |
rs368191452 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382334 | ATGCTTAACCCTAGA[A/G]GGAGAGGTTATTAGC | 51434 |
rs368224612 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383931 | AGAAGGGCCAGGCGC[A/G]GTGGCTCATGCCTGT | 51434 |
rs368232311 | snp | A/G | 0.000592905 | 0.0172076 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110386316 | GTCTTCCTGCCCCAA[A/G]AATTACTTACCTTTT | 51434 |
rs368320792 | in-del | A/TACT | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110400588 | TTAAGAACTAAGAGT[A/TACT]ACTAGGGCCTAAATC | 51434 |
rs368416947 | snp | A/G | 5.08798e-05 | 0.00504354 | intron-variant, downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110377351 | GAGGTCAGGTTTTAT[A/G]AAAATTAATGATGAA | 51434 |
rs368603305 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110396603 | GCAACCTCCACCTCC[C/T]GGGTTCAAGTGATTC | 51434 |
rs368734362 | snp | A/G | 0.000488489 | 0.0156207 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387932 | AGAAAGTAAGGCACG[A/G]TATCTCTCTTCCACA | 51434 |
rs368802086 | snp | A/G | 5.28648e-05 | 0.00514097 | utr-variant-3-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110374123 | AGGGCAGGCCACTGC[A/G]GCCATGGAGCTGCCG | 51434 |
rs368825963 | snp | C/T | 1.78261e-05 | 0.00298542 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381726 | ACCCACGGATTCACA[C/T]CATTCACCTATGTTT | 51434 |
rs368951209 | snp | C/T | 1.65655e-05 | 0.00287793 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388475 | TACTATCTTTGACAG[C/T]AAACATGCCATGAAA | 51434 |
rs369086956 | snp | C/T | | | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110404912 | GCAACCTCTGTCACC[C/T]GGGTTCAAGGAATTC | 51434 |
rs369130684 | snp | C/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403425 | GCCTCCGCTGGCGCC[C/G]GCGGCCGCTCCTTCC | 51434 |
rs369251759 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110385197 | ACTTTAACCAGGAGG[C/T]GGAGGTTGCAGTGAG | 51434 |
rs369274675 | snp | A/C/T | 0.00597455 | 0.054357 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388161 | CATGCCCCAGCCTTC[A/C/T]GAGAAGCTGGGACTA | 51434 |
rs369285072 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110393604 | CGGGCATGGTGGCTC[C/T]CACCTGTAACCCCAG | 51434 |
rs369339122 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110373159 | AGCCCCAGAGCTCAG[A/G]GTGTGATACTCAGGC | 51434 |
rs369373794 | snp | A/G | 8.19325e-05 | 0.00639996 | synonymous-codon, nc-transcript-variant, intron-variant | ANAPC7 | GRCh38.p7 | 12:110381939 | GCGTTTGCTATAGAA[A/G]CTGTGACAGCTGGAG | 51434 |
rs369493772 | snp | A/G | 1.64841e-05 | 0.00287085 | synonymous-codon, intron-variant, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110388522 | TCTACCTAGAATGGC[A/G]TCAAGGGCTAATGGG | 51434 |
rs369511874 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110399099 | AATCTCGGCTCACTA[C/T]GACCCCTGCCTCCCG | 51434 |
rs369544514 | snp | C/T | 0.000153988 | 0.00877327 | intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403509 | CTCAGCCCCAGGCAG[C/T]TACCCGCCTCAACTC | 51434 |
rs369613988 | in-del | -/A | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110396226 | CTTGGAGTCTTTCTC[-/A]AAAAAAAAAAAAAAA | 51434 |
rs369686449 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110397764 | GACGGGTGTGGTGGC[A/G]CATGCCTGTAATCCC | 51434 |
rs369958598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110378650 | GAGTCAACTCTCAAC[C/T]CTTCATGCCAGTAAG | 51434 |
rs370096501 | snp | C/T | 1.64781e-05 | 0.00287033 | synonymous-codon, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110374267 | CTCCTGAGTGGCATC[C/T]GTGGGACTCTCCTCC | 51434 |
rs370143087 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110392945 | AGATTACAGGCATGC[A/G]CCACCACACCCGGCT | 51434 |
rs370167189 | snp | G/T | 0.000165 | 0.00908146 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110395119 | GGGAGTTCTTTGTCT[G/T]GAAGGGATCCCATCA | 51434 |
rs370179211 | snp | A/C | 1.67421e-05 | 0.00289323 | utr-variant-3-prime, intron-variant | ANAPC7 | GRCh38.p7 | 12:110376033 | TCCTCTACCCTCCTC[A/C]GTGGCCTTCCCCCAA | 51434 |
rs370370004 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395572 | TTGGATTACAGGTGT[A/G]AGCCACTGTGCCTGG | 51434 |
rs370419897 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110394759 | GCTGAGGTGGGAGGA[C/T]TGCTTAAGCCTGGGA | 51434 |
rs370452700 | snp | C/T | | | synonymous-codon, intron-variant, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110388555 | CTGCCTCAGCACCTC[C/T]TTATAGCTGGTGACT | 51434 |
rs370532761 | in-del | -/CT | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110378891 | TGAAATGGAGTCTTG[-/CT]CTGTCACCCAGGCTG | 51434 |
rs370764449 | snp | C/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110386435 | TTCCCAATAGGTCCA[C/T]GTTATCTCGCAATAA | 51434 |
rs370848986 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110401045 | ACAAAGCAAGACTCC[A/G]TCTGAAAAGCAAAAC | 51434 |
rs370892553 | snp | A/G | 3.43849e-05 | 0.00414624 | missense, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110396435 | AGCTGGTACTTCTGA[A/G]GTGGGGAGAATAACT | 51434 |
rs370909299 | snp | A/G | 0.00557542 | 0.0525036 | downstream-variant-500B, intron-variant | ANAPC7 | GRCh38.p7 | 12:110375161 | CTGTAACATCTCCTC[A/G]TCTCCTGGTTGAAGC | 51434 |
rs371040337 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110386997 | CACTTTGGGAGGCCC[A/C]CGTGGGAGAATCACT | 51434 |
rs371060796 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382991 | ATAGTGAGAAGAGGT[A/G]TTTTAAGAAGAGAAG | 51434 |
rs371085821 | snp | C/T | | | downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110372537 | TCTGTGGGGCTTTAT[C/T]TTTTTTTAAACACTG | 51434 |
rs371110033 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110376211 | CTTCATATTTCTGTT[C/T]TCTGCCTGGGGGAAT | 51434 |
rs371264796 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110391984 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGTAG | 51434 |
rs371289531 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380435 | AGGCAGGCAGCTCAC[A/G]AGGTCAGGAGTTCGA | 51434 |
rs371334932 | snp | C/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110377974 | AGATCAAAGTAGTGA[C/G]AGATGATGTTCCCAA | 51434 |
rs371341310 | snp | G/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110390161 | GCAACCTCTGCCTCC[G/T]GGGTTCAAGTGATTC | 51434 |
rs371352820 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387333 | ACAGAGAGAGAGAGA[A/G]AGGCAGAGAGAGAGA | 51434 |
rs371661838 | snp | C/T | 5.0508e-05 | 0.00502508 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110387888 | TACAGAAAGGGACAA[C/T]AAGCCTAAACCAACA | 51434 |
rs371683997 | snp | A/G | 0.000153988 | 0.00877328 | missense, intron-variant, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110388526 | CCTAGAATGGCATCA[A/G]GGGCTAATGGGCACT | 51434 |
rs371733605 | snp | A/G | | | intron-variant, upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110402275 | GTCGCAGAGAGTGGA[A/G]GGCAGATATTTGCCT | 51434 |
rs371818494 | in-del | -/TTC | 0.00478085 | 0.0486577 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388041 | ACCATAATTTAGTAT[-/TTC]TTTTCTTTTTGAGAC | 51434 |
rs371877997 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383852 | CTGCACTCTAGCCTT[A/G]GCTACAGAGCGAGAC | 51434 |
rs372040468 | snp | C/T | 6.58903e-05 | 0.00573941 | missense, intron-variant, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110377555 | CCAGAGTTTTGTAAA[C/T]GTTGTTAGCCATTAC | 51434 |
rs372195221 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389805 | GGCGTGGTGGCGGGC[A/G]CCTGTAGTCCCAGCT | 51434 |
rs372266566 | in-del | -/A | 0.445196 | 0.1562 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387446 | GACCGACCTTGTCTC[-/A]AAAAAAAAAAAAAAA | 51434 |
rs372296802 | snp | A/G | 8.27616e-05 | 0.00643226 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388480 | TCTTTGACAGTAAAC[A/G]TGCCATGAAAACAGG | 51434 |
rs372340116 | snp | C/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110397798 | TACTCGGGAGGTTGA[C/G]ACAGGAGAATCGCTT | 51434 |
rs372348208 | snp | A/G | 3.34801e-05 | 0.00409132 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110377636 | AAAAAAGTAAAACAC[A/G]TGAAGACATTCAATG | 51434 |
rs372373517 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387935 | AAGTAAGGCACGATA[C/T]CTCTCTTCCACATGC | 51434 |
rs372409572 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388657 | CAGATAGCAAAATAA[C/G]CGTATATTGCAAAGA | 51434 |
rs372627134 | snp | A/C | 0.00187419 | 0.0305546 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110403751 | CACACGCGGCACCAC[A/C]CCCAAGCAAGAGGTA | 51434 |
rs372651086 | snp | A/C | 1.64746e-05 | 0.00287002 | missense, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110376118 | ACTCATTGACAGCTA[A/C]AAGGAAATCTCCTAG | 51434 |
rs372779812 | snp | C/T | 6.59718e-05 | 0.00574296 | missense, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110382882 | TGCTGATCAGAGATA[C/T]TGAAAAGGCGGCATC | 51434 |
rs373040490 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110404710 | TTTTCAGCTCTTAAC[A/G]TTTTGTCACAGTTGA | 51434 |
rs373126088 | in-del | -/C | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403035 | GCGTGAGCCACCGCG[-/C]CCGGCCCCGTTTTCA | 51434 |
rs373159742 | snp | A/G | | | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110405030 | CTTTGTGTGAGCAAC[A/G]AGGCTGTTTGTTTCA | 51434 |
rs373181694 | snp | C/T | 0.000338061 | 0.0129968 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388662 | AGCAAAATAAGCGTA[C/T]ATTGCAAAGAAAATC | 51434 |
rs373208750 | snp | C/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395395 | ACATGATTTACTGCA[C/G]TCTTAGACTCCTAGT | 51434 |
rs373220522 | snp | A/G | | | downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110372403 | TCTCATCACAGTATG[A/G]CAGGTCATGGAGCTG | 51434 |
rs373261312 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110398717 | AATCCCAGCACTTTG[C/T]GAGGCCAAGGTGGGT | 51434 |
rs373276328 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110374051 | TCACATGCTGAATCA[C/T]TGTCCTTCTGAGAGC | 51434 |
rs373287464 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110392987 | TTTAGTAGAGACGGG[A/G]TTTCTCCATGTTGGT | 51434 |
rs373288136 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389318 | TATCTCACATAAGAA[A/G]GTGAGAAACTCTTGA | 51434 |
rs373516411 | snp | C/T | 1.82703e-05 | 0.00302239 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381712 | AGGGCTGCTGCCACA[C/T]CCACGGATTCACACC | 51434 |
rs373539186 | snp | A/C/G | 0.00860819 | 0.0650535 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110386292 | TGATCCCCCCCAACA[A/C/G]CAGCCACTGTCTTCC | 51434 |
rs373690811 | snp | A/G | 1.70685e-05 | 0.00292129 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387897 | GGACAACAAGCCTAA[A/G]CCAACAGAAAGCAGA | 51434 |
rs373846073 | snp | A/G | 1.64781e-05 | 0.00287033 | missense, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110374268 | TCCTGAGTGGCATCC[A/G]TGGGACTCTCCTCCT | 51434 |
rs373891142 | in-del | -/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389103 | AAAAAAAAAAAAAAA[-/G]AAAAGAAAAGAAATT | 51434 |
rs374088588 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110402309 | GAGGCCATGGGAAAG[A/C]ATTTTCATAAGTGCA | 51434 |
rs374122177 | in-del | -/A | 0.367503 | 0.220665 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110398421 | GAAACCCTGTCTCAG[-/A]AAAAAAAAAAAGTAA | 51434 |
rs374213907 | snp | A/G | | | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110405166 | CCTGTCTCAAGAGCC[A/G]AGCTCCCCGAGTGAG | 51434 |
rs374270104 | snp | C/T | 0.00108944 | 0.0233138 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403589 | GTTGGAGTGCAGCCC[C/T]GCGGCCGCCATGTCC | 51434 |
rs374271620 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110390226 | GGCACCCGCCACCAC[A/G]CCCAGCTAATTTTTT | 51434 |
rs374276809 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110401108 | CCAATGGGCAGCAGC[A/T]GCTGCATTGTAAGCA | 51434 |
rs374392897 | snp | A/G | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110401851 | CGGTGGCGGGCGCCT[A/G]TAGTCCCAGCTACTC | 51434 |
rs374404661 | snp | A/G/T | 0.00017156 | 0.00926028 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395252 | ATATTTCTTTGAAAC[A/G/T]TTATTCCAACAATAT | 51434 |
rs374563770 | snp | C/T | 0.000894754 | 0.0211324 | missense, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403720 | AAATGGCGGCGTCGC[C/T]GGGGTCCATCGGGTC | 51434 |
rs374781177 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110391411 | GAGGGAATATGTGGC[A/G]ATGTTTACCATATAT | 51434 |
rs374842303 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110384547 | AAAAACTAGCCAGGC[A/G]TGGTGGCACACACCT | 51434 |
rs374920125 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110400174 | GTGATTCTATGTATG[C/T]AGTGAGAAATAACCA | 51434 |
rs374985758 | snp | A/G/T | 0.000798403 | 0.0199641 | downstream-variant-500B, intron-variant | ANAPC7 | GRCh38.p7 | 12:110375255 | CCTTCCCTTCTACAG[A/G/T]CTACTATGAAAGCCC | 51434 |
rs375107592 | snp | C/T | 8.39736e-05 | 0.00647918 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387704 | CAGACAAGCAAAGGG[C/T]CTCAAGAACACTGAA | 51434 |
rs375151847 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant, intron-variant | ANAPC7 | GRCh38.p7 | 12:110381872 | GCAGAGCTTGAACAC[C/T]ATTACTGTTCAGCTG | 51434 |
rs375232096 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388499 | CATGAAAACAGGCAG[A/G]AAATATCTCTACCTA | 51434 |
rs375282612 | snp | A/G/T | 3.98527e-05 | 0.00446375 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110396463 | ACTCACTAGAAAACA[A/G/T]GAGAAAATGTAATAC | 51434 |
rs375350273 | snp | C/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389736 | GGAGATTGAGACCAT[C/G]CCGGCTAACACAGTG | 51434 |
rs375383581 | multinucleotide-polymorphism | CA/GG | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110398186 | AGGAGGCAGAGGTTG[CA/GG]GTGAGCCAAGATCGT | 51434 |
rs375392456 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380574 | GAGAATGGTTTGAAC[C/T]CGGAAGGTGGAGGTT | 51434 |
rs375415723 | snp | A/C/G | 9.91677e-05 | 0.00704095 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110376221 | CTGTTCTCTGCCTGG[A/C/G]GGAATAAAAAAGACC | 51434 |
rs375419042 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381332 | CCGGATGATGTTTTT[C/T]TGTTGTTGTTGTTGT | 51434 |
rs375431802 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110394076 | AGCTACCCAGGAGGC[C/T]GAGGCAGGAGAATCA | 51434 |
rs375521345 | snp | C/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388681 | GCAAAGAAAATCTCT[C/G]ACCATGAAAAAGTCC | 51434 |
rs375619361 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110397885 | GGGCGACAAGAGTGA[A/G]ACTCTGTCTTTTAAA | 51434 |
rs375690201 | snp | C/T | 0.000296492 | 0.012172 | missense, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110376187 | CGTTCCTCAGCAAAG[C/T]AATTCCATCTTCATA | 51434 |
rs375718605 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383862 | GCCTTGGCTACAGAG[C/G]GAGACTCCGTCTCAA | 51434 |
rs375786350 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382967 | CATCCATTCCTAGAA[A/G]AGAAGGACATAGTGA | 51434 |
rs375836640 | snp | C/T | 1.73258e-05 | 0.00294323 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110374361 | AAAACAAAGGAGAGG[C/T]CTGAATCTCTGCCTT | 51434 |
rs376051317 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110398806 | CAAAATTAGCCTGGC[A/G]TGGTGGCACATGCCT | 51434 |
rs376089150 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380209 | TACAAAAATGAGCTG[A/G]GTGTGGTGGTGTATG | 51434 |
rs376138291 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380821 | TAGCCAGGTGTAATC[C/T]TAGCTACTGGGGAGG | 51434 |
rs376141390 | snp | A/G | | | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110405181 | GAGCTCCCCGAGTGA[A/G]CAATTCCTGTCCCTT | 51434 |
rs376157991 | snp | C/T | 1.65127e-05 | 0.00287334 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110395113 | TACTTTGGGAGTTCT[C/T]TGTCTTGAAGGGATC | 51434 |
rs376439064 | snp | C/T | | | intron-variant, utr-variant-5-prime | ANAPC7 | GRCh38.p7 | 12:110401426 | AATTGGTGGGTGATG[C/T]GAAGGGTAGAAAAGT | 51434 |
rs376495881 | snp | C/T | | | downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110372493 | GCTTCTTCTACTGGC[C/T]GCACACTCACCTGGT | 51434 |
rs376533103 | snp | A/G | 5.19116e-05 | 0.00509442 | utr-variant-3-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110374138 | GGCCATGGAGCTGCC[A/G]CCCCCTCACTGCATG | 51434 |
rs376571153 | in-del | -/A | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388932 | AAAAATACAAAAAAA[-/A]TTAGCTGGGCGTGGT | 51434 |
rs376652055 | snp | A/G | 6.58903e-05 | 0.00573941 | synonymous-codon, intron-variant, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110377556 | CAGAGTTTTGTAAAC[A/G]TTGTTAGCCATTACC | 51434 |
rs376654075 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395016 | GTAAAATGTTCACAC[A/G]GACTCCTTAATGCAT | 51434 |
rs376661785 | snp | C/T | 0.000374589 | 0.0136804 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110377658 | CATTCAATGCCATTA[C/T]CATTCCAACCCATGC | 51434 |
rs376816346 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110374360 | CAAAACAAAGGAGAG[A/G]CCTGAATCTCTGCCT | 51434 |
rs376884195 | snp | C/T | | | downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110372814 | TTACAGGTGTGAGCA[C/T]GCCTAGCCTTATATG | 51434 |
rs376913408 | snp | A/C | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383551 | CAAGACCAGCCTGGG[A/C]AATATGGTGAGACCC | 51434 |
rs376974095 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403122 | TCTCAGATGCGGGGG[C/T]TAGCGCATAAAAACC | 51434 |
rs377148261 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110400390 | CATGCCCCTTCTCCA[C/T]TGTTTGAATTTAACA | 51434 |
rs377333706 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382309 | CACAATGCATTCACC[-/A]ACTCAGTTAATGCTT | 51434 |
rs377365901 | in-del | -/G | 0.0466883 | 0.14548 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381953 | GCTGTGACAGCTGGA[-/G]GAAAAAAAAAAAAAA | 51434 |
rs377423031 | snp | A/G | 1.66907e-05 | 0.00288879 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382983 | AGAAGGACATAGTGA[A/G]AAGAGGTGTTTTAAG | 51434 |
rs377434453 | in-del | -/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382463 | AAAAAAAAAAAAAAA[-/T]ATATATATATATATA | 51434 |
rs377477700 | snp | A/G | 0.000124339 | 0.0078838 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403590 | TTGGAGTGCAGCCCC[A/G]CGGCCGCCATGTCCC | 51434 |
rs377571077 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388901 | CCGGCTAACACAGTG[A/G]AACCCCGTCTCTACT | 51434 |
rs377659178 | snp | A/G | 1.67393e-05 | 0.00289299 | missense, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110396417 | TCTGCATGATACACC[A/G]AAAGCTGGTACTTCT | 51434 |
rs377710126 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110394490 | AAAAATTAGCCTGGC[A/G]TGGTGGCAGGCGCCT | 51434 |
rs377749384 | snp | C/T | 4.98293e-05 | 0.00499121 | missense, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110374322 | AGAGACTTCTGGTCA[C/T]TGGGGTCCAAACTAG | 51434 |
rs377751164 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110399821 | AAAAAAGGGGCCAGG[A/C]GCGGTGGCTCACGCC | 51434 |
rs386766336 | multinucleotide-polymorphism | GG/TC | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388403 | ACTAAATCACTCTCT[GG/TC]AGGGGAACTTTTAAA | 51434 |
rs398021054 | in-del | -/A | 0 | 0 | intron-variant, downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110377158 | AAAAAAAAAAAAAAA[-/A]TTAGTGAGCCGAATA | 51434 |
rs398116863 | in-del | -/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110396694 | TTTGTTTTTTTTTTT[-/T]AGTAGACATGGGGTT | 51434 |
rs527323085 | snp | G/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110379735 | ATCTTCCTGTTAAGA[G/T]CAAATCACTCCTAGA | 51434 |
rs527401954 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110405504 | ATAAAACGAAATAGT[C/T]GTAAAGTGTTGCGGC | 51434 |
rs527526870 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110399111 | CTACGACCCCTGCCT[C/T]CCGGGTTCAAGCAAT | 51434 |
rs527554151 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110393064 | CCTCCCAAAGTGCTG[A/G]GATTACAGGCATGAG | 51434 |
rs527563285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110385597 | TTGAGGTGAGGGGAG[A/G]TCTTGTGCAAACAAA | 51434 |
rs527575185 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403159 | CTGGGTCCCTGAGCT[A/G]CAGCGAGAGAAAAAA | 51434 |
rs527710032 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110404518 | CCAATGAGGCAGTTT[A/G]GGTCGTTGAGTCAGA | 51434 |
rs527724598 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110396684 | CCCAGCTAATTTTTG[G/T]TTTTTTTTTTAGTAG | 51434 |
rs527752280 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110390346 | CCCAAAGTGCTGGGA[G/T]TACAGGCGTGAGCCA | 51434 |
rs527820451 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110372421 | GGTCATGGAGCTGAG[A/G]AAGCCCATGAAGTGA | 51434 |
rs527825447 | in-del | -/AAC | 0.00119737 | 0.0244387 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110384393 | TGAGACCCTGTCTCT[-/AAC]AACAAAACCAAAACC | 51434 |
rs527853412 | snp | G/T | | | downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110372505 | GGCCGCACACTCACC[G/T]GGTGTGACCCCAACT | 51434 |
rs527881116 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110384457 | TGCCTATAATCCCAG[C/G]ACTTTGGGAGGCCGA | 51434 |
rs527883768 | snp | A/G | 6.79302e-05 | 0.00582756 | intron-variant, downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110377343 | CTCCAACTGAGGTCA[A/G]GTTTTATAAAAATTA | 51434 |
rs527915562 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110397040 | AACCCCATCTCTACT[A/G]AAAAATACAAAAAAT | 51434 |
rs528000359 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110376517 | GAGCTTGCAGTGAGC[C/T]GTGATTGTGCCACTA | 51434 |
rs528203367 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | ANAPC7 | GRCh38.p7 | 12:110375392 | GTGCTGAACAATTGA[A/G]TGTGATCAGACTCTA | 51434 |
rs528320975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110386748 | TTAAAGGTAATGTCA[C/T]TCACAAGTGACACCT | 51434 |
rs528338500 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110404017 | ATAAAATACAGTAAG[G/T]TGAGGAAAAACGCTC | 51434 |
rs528515188 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110373838 | ATTCCTTGAGCTTTT[A/G]GATTTAGAAATTAGT | 51434 |
rs528765544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395785 | CCTCGTGATCCGCCC[A/G]CCTAGGCCTCCCAAA | 51434 |
rs529107057 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110400619 | TCCAAACGTGGAAAC[C/T]GTATGCTTTGGCAAA | 51434 |
rs529158388 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110405333 | TTCTATAATCTGTAG[A/G]TAACATCAGTTGCTA | 51434 |
rs529174929 | snp | G/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110386602 | CGTAATAAAAAACTT[G/T]AAGCTTATGACTTTA | 51434 |
rs529552007 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395921 | GGGGACCAGTTTCAT[C/G]AAAGACAATTTTTCC | 51434 |
rs529621556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110394521 | ATAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 51434 |
rs529658837 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110384955 | TAGTTCTATCCAGAA[C/T]GCAGTTCATTAAAGA | 51434 |
rs529699455 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, missense, upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110401587 | TAGAGAACACGCTTG[C/G]TGCATTCAAATAACA | 51434 |
rs529772700 | snp | C/T | 0.02016 | 0.0983543 | intron-variant, downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110377236 | GCCAGCTACGTTTGG[C/T]TGGGCTAAATATAAA | 51434 |
rs529794345 | snp | G/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395472 | GCCACCATGCCGTTT[G/T]GTAAAGACAGGGGTC | 51434 |
rs529844364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388407 | AATCACTCTCTTCAG[A/G]GGAACTTTTAAAAAA | 51434 |
rs529845970 | snp | A/C | 0.000399281 | 0.0141238 | missense, nc-transcript-variant, intron-variant | ANAPC7 | GRCh38.p7 | 12:110381946 | CTATAGAAGCTGTGA[A/C]AGCTGGAGAAAAAAA | 51434 |
rs529861305 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395563 | TGGAAGTGCTTGGAT[C/T]ACAGGTGTGAGCCAC | 51434 |
rs529902000 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381213 | AAACCTGTCTGCACA[G/T]TGGTAACCCCTGGGG | 51434 |
rs530017744 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110390818 | CTGATGGACTATCTT[C/T]CTCAACAAATATCAA | 51434 |
rs530101309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110379916 | AAAATATTACATAAC[A/G]AAACAAAGTTGGACC | 51434 |
rs530115905 | snp | A/G | 1.6483e-05 | 0.00287076 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110386278 | CTCCCTATTATCTCT[A/G]ATCCCCCCCAACAAC | 51434 |
rs530737763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110374919 | CAGTACATACGCCAC[C/T]CCCACCCCCAAAGTT | 51434 |
rs530780620 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387231 | AGAGAGAGAGAGAGA[C/G]AGAGAGACAGAGAGA | 51434 |
rs530915258 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388794 | TTCAAAAGAAAGAAG[A/T]AATTGGCCAGGTGCA | 51434 |
rs530921690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381077 | AAAAAAAAACCCCAT[C/T]CCAACTATACCCTCA | 51434 |
rs530928311 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110372753 | GCTGGTCTCAAACTC[C/G]TGGCCTCAAGTGATC | 51434 |
rs530934462 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380567 | GAGGCAGGAGAATGG[C/T]TTGAACCCGGAAGGT | 51434 |
rs531234417 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110399780 | GGGTGACGAGAGAGA[A/G]ACTCTGTCTCAGACA | 51434 |
rs531274525 | in-del | -/A | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110399463 | GAGATCTTGTCTCTT[-/A]AAAAAAAAAAAAAAT | 51434 |
rs531319971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110399267 | CCTCATGATCCACCC[A/G]CCTCAGCCTCCCAAA | 51434 |
rs531388914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110399893 | CTGAGGTCAGGAGTT[C/T]GACCAGCCTGGCCAA | 51434 |
rs531446106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110400716 | CAACATGAAGTGGAT[A/G]GTGGCAAAATGTGGG | 51434 |
rs531576990 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110393102 | GCCCAGCCGACACCA[G/T]ATCTTTTGATTTTAG | 51434 |
rs531577757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110391421 | GTGGCGATGTTTACC[A/G]TATATTAACAGACAT | 51434 |
rs531599536 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387104 | GGTGTGGTGGCATGC[A/G]CCTGTAGTCCCAGAT | 51434 |
rs531621023 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387167 | CCCGGGAGATTGACA[-/G]GTCAAGGCTACACTG | 51434 |
rs531634957 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110390513 | GCCAGATATTTATAG[A/G]AAGAGTGGCTCTAAA | 51434 |
rs531660531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110391996 | ACTCGGGAGGCTGAG[A/G]TAGGGGAATCGCTTG | 51434 |
rs531660876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110384507 | CCTGGCCAAGATAGT[A/G]AAACCCCATCTCTAC | 51434 |
rs531682002 | in-del | -/AGG | 0.00557542 | 0.0525036 | cds-indel, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110373712 | ATGACTTCTGGGAAC[-/AGG]AAGCTCCCTAGGGCC | 51434 |
rs531777200 | snp | C/T | | | missense, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110395139 | GGATCCCATCAAGTA[C/T]AGCAATGGCATCTTT | 51434 |
rs531794606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110385306 | CCTCTCCGCAGCCCC[C/T]GCTTTATTCTCACCC | 51434 |
rs531818893 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110378156 | CTGGAGCGCAATGGC[A/G]CCATCTCGGCTCACT | 51434 |
rs531911247 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110373252 | AGACGCAGCTGAAAT[A/C]TGGCCAAAGACTCTC | 51434 |
rs531925552 | snp | A/G | | | downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110372561 | AACACTGTCTCTGTC[A/G]CCCAGGCTGGAGTGC | 51434 |
rs531949020 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110397326 | TTGGGAGGCTGAGGC[A/G]GGCAGATCACAAGAT | 51434 |
rs531967056 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110400784 | GGCTCGGTGGCTCAC[A/G]CCTGCAATCCAAGCA | 51434 |
rs532024156 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110400793 | GCTCACGCCTGCAAT[C/T]CAAGCACTTTGGGAG | 51434 |
rs532206551 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110393800 | TGAACCCGGGAGGCA[C/G]AGGTTGCAGTGAGCT | 51434 |
rs532207744 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387977 | GGCTACATCTTCCCT[G/T]GGCTAAAAGGCAACT | 51434 |
rs532216386 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110394398 | TTGGGAGGCCGAGGT[A/G]GGCGGATCACCTGAG | 51434 |
rs532346970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380608 | ATGAGCCAAGATCAT[A/G]CCACTGCACTCCAGC | 51434 |
rs532348358 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387227 | TGGGAGAGAGAGAGA[C/G]AGAGAGAGAGACAGA | 51434 |
rs532505818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110386218 | AGTATAAGTTTTATA[C/T]ACCATTTCTATGAAA | 51434 |
rs532551229 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110392123 | AAAAAAAAAGGCTTC[C/T]TACAAAAGGAAGATA | 51434 |
rs532589691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110379846 | ACTGAGTCACCAAAC[A/G]TTGCTGAAACTGGCA | 51434 |
rs532947681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110377883 | CACATGTAAGGAACC[C/T]GCAGCATGTGAGCAC | 51434 |
rs532960188 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110377292 | TGCAAAAGGCACACA[A/C]CTGTCTAGTCATCTG | 51434 |
rs532968730 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110398278 | AAAATTAGCCAGGCA[C/T]GGTGGTGCATGCCCG | 51434 |
rs533050549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110391467 | TTGACTCACTTCCTT[A/G]TCCTTTACATAGACT | 51434 |
rs533189910 | snp | A/C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110405375 | AGTTAAGGCAGGAAC[A/C/T]GGCCCTTTTCACTTC | 51434 |
rs533203306 | snp | C/G | 0.000805883 | 0.0200572 | intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403494 | CGCCGCCGCTTTCTC[C/G]TCAGCCCCAGGCAGC | 51434 |
rs533229323 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110399059 | GGAGTCTTACTCTGT[C/T]GCCCAGGCTAGAATG | 51434 |
rs533372227 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389875 | AGGCAGAGCTTGCAG[C/T]GAGCCGAGATCGTGC | 51434 |
rs533391826 | in-del | -/AGA | | | intron-variant, downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110377043 | TCAGGAGGCTGAGGC[-/AGA]AGAATTGCTTGAACC | 51434 |
rs533546702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110390278 | GGTGTTTCACCATGT[C/T]GGCCAGGCTGGTCTT | 51434 |
rs533564452 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383255 | CATCCTGGCTAACAC[A/G]GTGAAACCTCATCTC | 51434 |
rs533630733 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383774 | CCAGCTACTCAGGAG[C/G]CTGAGGCAGGAGAAT | 51434 |
rs533827526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110390740 | TGATGTCAATACTTG[C/T]AAAGAATAAAAAGTT | 51434 |
rs533829159 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110398328 | GGCTAAGACAGGACA[A/G]TCGCTTGAGCCCAGG | 51434 |
rs533829829 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110404991 | ACTGTCATGTGCGTC[C/T]GTGTGAAGAGACCAC | 51434 |
rs533891371 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110397725 | CAACATGGTGAAACC[A/G]TCTCTACTAAAAATA | 51434 |
rs533924949 | snp | C/T | 4.94849e-05 | 0.00497393 | missense, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110382925 | CATCCTCTAGCCGCC[C/T]TTCTCGTGCCAGTAG | 51434 |
rs533932787 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110400470 | CAGAACTTAAACATG[C/T]CCTGAAGCTAGGAAA | 51434 |
rs533969688 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110384695 | AAAAAACAAAAAAAA[A/C]CAAAAAAAACAAAAA | 51434 |
rs533984133 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389317 | CTATCTCACATAAGA[A/C]AGTGAGAAACTCTTG | 51434 |
rs534021396 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388985 | TACTCGGGAGGCTGA[A/G]GCAGGAGAATGGTGT | 51434 |
rs534056887 | snp | A/C | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110401676 | CGGCGGGATCACCAG[A/C]GGTCAGGAGTTGAAG | 51434 |
rs534060677 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110378248 | TACAAGCATGCACCA[A/C]CACACCCGGCTAGTT | 51434 |
rs534091362 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110377931 | AGAATAAATGCGACA[C/T]TAATGATTAGTCTGT | 51434 |
rs534179400 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389949 | AAAACAACAAAAAAA[A/C]CCCACAAAAACAAAA | 51434 |
rs534271698 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383309 | CGGGCATAGTGGCAC[A/G]CGCCTGTAATCCCAG | 51434 |
rs534317864 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110374962 | AACATTCATTTATTT[C/G]CCTCCTAAGCAATCT | 51434 |
rs534328972 | snp | C/T | 3.30338e-05 | 0.00406397 | synonymous-codon, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110374186 | GTCAGCCCACTGGGC[C/T]GCCTCACTGTCGCTG | 51434 |
rs534402832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110376839 | AGATAACAGTGAGCC[A/G]AGGCTGGGCACGGTG | 51434 |
rs534477578 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110404263 | AGGAATTAGCTGATA[C/T]CCATATAAACCAGTA | 51434 |
rs534538986 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403086 | AGTGGACCCTCCTGA[A/T]ACACTTAACGGGGGG | 51434 |
rs534562353 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110396013 | TTAGTCAGATTATAA[C/T]AAGGAACACACAACC | 51434 |
rs534621470 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395676 | CCCAAGTAGCTGGGA[A/C]TACAGGCATCCACCA | 51434 |
rs534955703 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381386 | TCTGTCGCCAGGCTG[C/G]AGTGCAGTGGCGCAA | 51434 |
rs534967789 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110404194 | CTTGGTTCGAGGGGT[A/G]TATTTCCCCATGTAA | 51434 |
rs535074484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110394267 | AGGCCAAAGTGGGAG[A/G]ACAGTTTGAGCCCAG | 51434 |
rs535077457 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110401869 | GTCCCAGCTACTCGG[A/G/T]AGGCTGAGGCAGGAT | 51434 |
rs535305525 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110378103 | TTTATTTTATTATTT[-/A]TTTTTTTTGCGACAG | 51434 |
rs535318349 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389969 | CAAAAACAAAAAAAA[A/C]GCCAGAAAATCTAAA | 51434 |
rs535434223 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | ANAPC7 | GRCh38.p7 | 12:110375825 | CTATACAAATGAACA[C/G]AGATGTTATAGTGGT | 51434 |
rs535495722 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110401867 | TAGTCCCAGCTACTC[C/G]GGAGGCTGAGGCAGG | 51434 |
rs535509914 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110401993 | CCAGACTGGTCAATA[C/T]AGTGAAACTCTGTTT | 51434 |
rs535737917 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | ANAPC7 | GRCh38.p7 | 12:110375054 | CCTCTAATGGAAGTC[C/T]GATATTTTATTTTCT | 51434 |
rs535791838 | snp | C/T | | | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110403983 | TCTCAGAAATTAAAA[C/T]GTGTGGGTATTTACC | 51434 |
rs535850311 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387235 | AGAGAGAGAGAGAGA[C/G]AGACAGAGAGACAGA | 51434 |
rs535902911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388225 | TATTTTTAGTAGAGA[C/T]GGGGTTGTGCCATGT | 51434 |
rs535905221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395496 | AGGGGTCTCACTATG[C/T]TGCCAAGGCTAGTCT | 51434 |
rs535934219 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380665 | CAAAAAAAAAAAAAA[A/C]AAACAGGACCCGGGC | 51434 |
rs535944189 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380448 | ACGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 51434 |
rs536098722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388704 | AAAAGTCCTAATTTT[C/T]ATTACCAGTTATTTA | 51434 |
rs536265582 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389887 | CAGTGAGCCGAGATC[A/G]TGCCACTGCACTCCA | 51434 |
rs536287867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110386587 | AAATATAAAATTCTT[C/T]GTAATAAAAAACTTT | 51434 |
rs536542391 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387964 | GCAAGGAGCAACGGG[C/T]TACATCTTCCCTTGG | 51434 |
rs536564806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110400143 | GTCTAGATGACTTAA[A/G]TTCTCTTCAAACTCT | 51434 |
rs536564871 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110392816 | TTTGTTTTTTTTGAG[A/C]TGGAGTTTCACTCTT | 51434 |
rs536665095 | in-del | -/A | 0.167809 | 0.236103 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110397558 | GCGAGATCTCGTCTC[-/A]AAAAAAAAAAAAAAC | 51434 |
rs536688034 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388113 | ACAATCTCAGCTCAC[G/T]GCAACCTCTGCCTCC | 51434 |
rs536688151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380717 | CCTAGCACTTTGGGA[A/G]GCCGAGGCGGGCGGA | 51434 |
rs536713543 | snp | A/G | 6.99545e-05 | 0.00591374 | utr-variant-3-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110374132 | CACTGCGGCCATGGA[A/G]CTGCCGCCCCCTCAC | 51434 |
rs536814947 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110385586 | GGAATAAGCACTTGA[A/G]GTGAGGGGAGATCTT | 51434 |
rs536909558 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403026 | GTATTAGAGGCGTGA[G/T]CCACCGCGCCCGGCC | 51434 |
rs537029211 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110373171 | CAGGGTGTGATACTC[A/G]GGCTGACCAGTGACA | 51434 |
rs537075350 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110385408 | TCCCTTCAGATTCCC[A/G]TGAAAATTCCTCTCA | 51434 |
rs537132490 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389795 | AAATTAGCTGGGCGT[A/G]GTGGCGGGCGCCTGT | 51434 |
rs537337913 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383200 | TTCCAGCACTTTAAG[A/G]AGCCGAGGCAGGTGG | 51434 |
rs537403045 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110391172 | TCCAGCCTGGGCAAC[A/G]GAGAGAGACTCCATC | 51434 |
rs537514714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110400231 | TTACATCCACAGAAA[A/G]CATTCAGATATGCAT | 51434 |
rs537674546 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387199 | GCTGTGACTGCGCCA[C/T]TGCACTCTAGCCTGG | 51434 |
rs537709868 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110400965 | TGAGGTGGGAGGATC[A/G]ATTGAGCCTGGGAGG | 51434 |
rs537712589 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380079 | TAACAGGCCATGTAC[A/G]GTGGTTCACGTCTGT | 51434 |
rs537825711 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383909 | AAAAAGAAAAAAAAA[A/G]GAAAAAAGAAGGGCC | 51434 |
rs537889918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383404 | GATCACGCCACTGCA[C/T]TGCCTGGGTGACAGA | 51434 |
rs538021673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110379089 | CTGGTCTCGAACTCC[C/T]GACGTCAGGTGTTCC | 51434 |
rs538130688 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110397790 | ATCCCACCTACTCGG[A/G]AGGTTGAGACAGGAG | 51434 |
rs538241457 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110393229 | TTCAAAACAAAGGAA[A/T]AAAACCACCCCCATT | 51434 |
rs538536865 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110392793 | CCAGATCTTTTTTTG[C/T]TTGTTTTTTTGTTTT | 51434 |
rs538611025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110385884 | CTTTTTCAAGATCAG[C/T]GATTTTTCTGTTGTT | 51434 |
rs538658588 | snp | C/T | 0 | 0 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110377676 | TTCCAACCCATGCTT[C/T]CACTCTGACAGCTCT | 51434 |
rs538673651 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110392732 | TGGTAACTTGCCCAA[G/T]TTCACACTGCACACA | 51434 |
rs538707198 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110379386 | TGACCTAAATCTCCA[A/C]ATGGCAGCTTAAGAA | 51434 |
rs538848174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380148 | TTAAGCCCAGGAGTT[C/T]GGGACCAGCCTGGCT | 51434 |
rs538950437 | snp | A/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382441 | GGCTGATTATCCTTT[A/T]AAAAAAAAAAAAAAA | 51434 |
rs538968339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110398805 | ACAAAATTAGCCTGG[C/T]GTGGTGGCACATGCC | 51434 |
rs539303525 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110390035 | AAAAGACCTTCCTAA[C/T]AGTACACAGATAAAC | 51434 |
rs539452112 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110403891 | ACTGCAAACTTTACT[G/T]AGGATTTACAATGAG | 51434 |
rs539498817 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395594 | TGTGCCTGGCCTCAT[C/G]TTCTTTTTTTTTTTT | 51434 |
rs539610451 | in-del | -/GTA | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380219 | GCTGGGTGTGGTGGT[-/GTA]GTATGCCTGTAATCC | 51434 |
rs539641816 | snp | A/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, intron-variant | ANAPC7 | GRCh38.p7 | 12:110375899 | TATTTTAAGAAAAAA[A/T]TTTTAGAAGTCATGA | 51434 |
rs539674077 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110378198 | CTCCCGGGTTCAAGC[A/G]ATTCTCCTCCCTCAG | 51434 |
rs539796838 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110398319 | TACTTAGGAGGCTAA[A/G]ACAGGACAATCGCTT | 51434 |
rs539826713 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388764 | TGTGCAAATAAAGGC[A/T]GACTGACCCCATTCT | 51434 |
rs539894119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389197 | GGCCCAGTAATATCT[A/G]AACAAAAGACGCTGC | 51434 |
rs539913470 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382233 | TTCAGAGAATTTGTA[A/C]AGCCAGGTTAATAAA | 51434 |
rs540017247 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110377767 | ATTAGACTGGCAAGA[C/G]TGTTGATGGAATAGC | 51434 |
rs540170396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110376753 | CATAAAATCATCCAG[A/G]TAGCTCCACTCAAAA | 51434 |
rs540260808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110396966 | CCCAGCACTTTGGGA[A/G]GCTGAGGGGGGCGGA | 51434 |
rs540279090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383630 | GTTCATGCCTGTAAA[C/T]CCAGCACTTTGGGAG | 51434 |
rs540324317 | in-del | -/A | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381059 | GAGCGGTGGGAGGAC[-/A]AAAAAAAAAAACCCC | 51434 |
rs540338571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110390100 | TGAGACGGAGTTTCA[C/T]GCTTGTCACCCAGGC | 51434 |
rs540664350 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382495 | ATATATATATATATA[G/T]TTATAGAGACAGGGT | 51434 |
rs540671531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110374811 | AACCAAAAACATCAC[A/G]CTGTACCATGGAACA | 51434 |
rs540721563 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110394432 | AGGAGTTCAAGACCA[C/G]CCTGGCCAACATGGC | 51434 |
rs540795808 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403271 | GAAACCCTCGCCTGG[A/G]TCGTCCTCAGAGCCT | 51434 |
rs540914098 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110378090 | GACTCCTAGGGTCTT[C/T]ATTTTATTATTTATT | 51434 |
rs540918548 | snp | A/G | 4.94539e-05 | 0.00497238 | missense, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110396330 | GAAGTTTTACTTAGC[A/G]CTTTCTTCTGCTGTA | 51434 |
rs540976117 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110384094 | GTAATACCAGCTACT[C/T]GGGAGGCTGAGGCAG | 51434 |
rs541124171 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110386915 | TGGTGAGTGCAAAAT[G/T]ATTTTCTTCCAGGCT | 51434 |
rs541183864 | snp | A/G | | | intron-variant, upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110402469 | CGAGTAGCTGGGACT[A/G]CAGGCGCCCGCCACC | 51434 |
rs541211750 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110372678 | ATTATAGGTGTGTAC[C/G]ACCATGCCCGGTTAA | 51434 |
rs541222109 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110376522 | TGCAGTGAGCCGTGA[C/T]TGTGCCACTACACTC | 51434 |
rs541244027 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110399114 | CGACCCCTGCCTCCC[A/G]GGTTCAAGCAATTCT | 51434 |
rs541275031 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388823 | CAGTGGCTCACGCCT[G/T]TAATCCCAGCACTTT | 51434 |
rs541298806 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110373241 | AAGAGCCAGGCAGAC[A/G]CAGCTGAAATCTGGC | 51434 |
rs541445766 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110393015 | GGTCAAGCTGGTCTC[A/G]AACTCCCAACCTCAG | 51434 |
rs541512996 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388439 | ATAAAGTTATTCTAA[G/T]GTACAGGCAAGATTG | 51434 |
rs541772918 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382499 | ATATATATATATTTA[G/T]AGAGACAGGGTCTTG | 51434 |
rs541910606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403120 | AATCTCAGATGCGGG[A/G]GCTAGCGCATAAAAA | 51434 |
rs541949667 | snp | A/C | | | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110405474 | CATTCCTGTCTTCTT[A/C]CGTTAACAAGAAGAA | 51434 |
rs542058162 | snp | A/G | 6.75356e-05 | 0.00581062 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383010 | TAAGAAGAGAAGCAG[A/G]GGTCCCACATACAGG | 51434 |
rs542059055 | in-del | -/CT | 0.00279162 | 0.0372561 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383426 | GGTGACAGACTGAGA[-/CT]CTGTCTCAAAAAAAG | 51434 |
rs542205658 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110378256 | TGCACCACCACACCC[A/G]GCTAGTTTTGTATTT | 51434 |
rs542206560 | snp | C/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110396994 | GGATCTCGAGGTCAG[C/G]AGATCGAGACCATCC | 51434 |
rs542266370 | snp | A/G | | | downstream-variant-500B, intron-variant | ANAPC7 | GRCh38.p7 | 12:110375438 | CACCATAACCTTACA[A/G]ACACACAGACAACCC | 51434 |
rs542268673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110386998 | ACTTTGGGAGGCCCA[C/T]GTGGGAGAATCACTT | 51434 |
rs542300911 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110379478 | GCATCCCTGAGCTCT[A/G]GTGAAATAGGCATGC | 51434 |
rs542322727 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380460 | GTTCGAGACCAGCCT[C/G]GCCAACATGGTGAAA | 51434 |
rs542356588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387619 | GACTAACACATCCCA[A/G]AGACTGGCTGCAGCA | 51434 |
rs542450662 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110392984 | ATTTTTAGTAGAGAC[A/G]GGGTTTCTCCATGTT | 51434 |
rs542542198 | in-del | -/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388444 | TTATTCTAATGTACA[-/G]GGCAAGATTGAGAAC | 51434 |
rs542701118 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110391410 | TGAGGGAATATGTGG[C/T]GATGTTTACCATATA | 51434 |
rs542715267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110398075 | ATAAGGTGAAACCCC[A/G]TCTCTAGTAAAAATA | 51434 |
rs542842052 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110391964 | GGGCGTGGTGGCACA[C/T]GCCTGTAGTCCCAGC | 51434 |
rs542875476 | in-del | -/AAAAAAAAAAG | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383889 | TCAAAAAAAAAAAAA[-/AAAAAAAAAAG]AAAAAAAAAAGAAAA | 51434 |
rs542968893 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110405298 | CAGAGTGAAACAGAC[C/T]GGGAAGTTTCACAAT | 51434 |
rs543171219 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110376500 | CCTGAACCCAGGAGG[C/T]GGAGCTTGCAGTGAG | 51434 |
rs543286589 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | ANAPC7 | GRCh38.p7 | 12:110401369 | TCCTCAACACACTCA[A/G]TAAGCATGTGAGTGC | 51434 |
rs543324061 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110385184 | AGGTGGGAGAGTCAC[C/T]TTAACCAGGAGGCGG | 51434 |
rs543376184 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110394363 | CAGGTGCGGTGGCTC[A/C]CGCCTGTAATCCCAA | 51434 |
rs543636301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110393753 | ATGCCTGTAATCCCA[A/G]CTATTTGGGAGACTG | 51434 |
rs543656445 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110386121 | GGGGAGAAGACACTT[C/G]AATTCAAGCAAAAAC | 51434 |
rs543661103 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110394903 | AACAAAGAATAAGCA[C/T]GTGTAGTATTCTCCA | 51434 |
rs543678111 | snp | A/G | | | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110405061 | CCTGGGTGCAGGCAG[A/G]ATGGTAGCAGCACGA | 51434 |
rs543680948 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380361 | ATCTCAAATAAAAAT[A/T]AAAAAAATAGGCCGG | 51434 |
rs543702060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387952 | TCTCTTCCACATGCA[A/G]GGAGCAACGGGCTAC | 51434 |
rs543849354 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110377279 | GGCTCAGACCTGCTG[C/T]AAAAGGCACACACCT | 51434 |
rs543922042 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382693 | ACCTGTCTCAGTCTC[C/T]CAAAGTGTTGAGATT | 51434 |
rs543958762 | snp | A/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387031 | GCCCAGGAATTCAAG[A/T]CCAGCTTGGGCAACA | 51434 |
rs543981809 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110379629 | CAATACTCTTTCCCC[A/C]TCAACAAATCCAGAG | 51434 |
rs544248996 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110377839 | AAGACTGCCTTCAAA[A/G]GCACCTTCAGTTTAG | 51434 |
rs544252256 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110391130 | AGGAGGTGGAGGTTG[C/T]AGTGAGCTGAGATCA | 51434 |
rs544339462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110384228 | AAAATAAAGTAAAAT[A/G]AAATAGAAAGAAAAA | 51434 |
rs544355186 | snp | A/G | 0.00011931 | 0.00772276 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110403770 | AAGCAAGAGGTAACT[A/G]CTGAAGTGCCCGAAT | 51434 |
rs544419844 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110393798 | CTTGAACCCGGGAGG[C/T]AGAGGTTGCAGTGAG | 51434 |
rs544615838 | in-del | -/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110400606 | AGGGCCTAAATCTCC[-/T]AAACGTGGAAACTGT | 51434 |
rs544723198 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110385050 | GGGTGGATTACCTAA[A/G]GTCAGGAGTTGCAGA | 51434 |
rs544818917 | snp | A/C | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388759 | AACCCTGTGCAAATA[A/C]AGGCAGACTGACCCC | 51434 |
rs544829457 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110404382 | CTTCCCACAAGGGAA[G/T]AAACTGCCTGCTTAA | 51434 |
rs544881263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110390244 | CAGCTAATTTTTTTT[C/T]TGTATTTTAAGTAGA | 51434 |
rs544914094 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110397008 | GGAGATCGAGACCAT[A/C]CTGGCTAACGCGGTG | 51434 |
rs545078605 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110405226 | TTCTAAGGGGGTCCG[C/T]GTGAGAGAGTCGTGA | 51434 |
rs545115978 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110404507 | AGGTAACTGAGCCAA[C/T]GAGGCAGTTTAGGTC | 51434 |
rs545302806 | in-del | -/A | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387445 | GACCGACCTTGTCTC[-/A]AAAAAAAAAAAAAAA | 51434 |
rs545336178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110391870 | GAGGCCAAGGCAGGC[A/G]GATCACCTAAGGTCA | 51434 |
rs545514654 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395780 | CCTGACCTCGTGATC[C/T]GCCCGCCTAGGCCTC | 51434 |
rs545580293 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383428 | TGACAGACTGAGACT[C/G]TGTCTCAAAAAAAGA | 51434 |
rs545600187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388974 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 51434 |
rs545616009 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110397897 | TGAAACTCTGTCTTT[A/T]AAAAAAAAAAAGATC | 51434 |
rs545637555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383126 | ACTATTTCCAGTTTC[C/T]TACAAAGTGACTATT | 51434 |
rs545668055 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110377169 | AAAAATTAGTGAGCC[A/G]AATAGATACCAACCA | 51434 |
rs545675078 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110384316 | GCAGGAGGATTGCTT[A/G]AGCCCAGGAGGTCAA | 51434 |
rs545703820 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110391251 | CTTAAAAACATCATA[A/T]AGCCACATTCCACCA | 51434 |
rs545841023 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389498 | AGGTACTAACTCACT[A/G]AAGTAATGCTACAAA | 51434 |
rs545904343 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110396181 | TCCTAACAGACCAGG[A/C]ACTGGGGCCTGGGGA | 51434 |
rs546205002 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381509 | GCCCAGCTAATTTTT[G/T]TATTTTTAGTAGAGA | 51434 |
rs546233621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110396579 | GCAGTGGCACGATCT[C/T]GGCTCACTGCAACCT | 51434 |
rs546240887 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110376665 | TTGCCAACTAGCCCA[A/C]ATTCAATGAACCAAA | 51434 |
rs546353794 | in-del | -/ACTCAACTCACTCAACTCACTCAACTCACTCAACT | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110402122 | GAGGCTGCAGTGAGC[lengthTooLong]CAAGACTGCGCCACT | 51434 |
rs546354598 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395704 | CCACCATGCCTGGCT[A/G]ATTTTTTGTATTTTT | 51434 |
rs546510610 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389007 | GAATGGTGTGAAACC[A/C/G]GGAGGCGGAGCTTGC | 51434 |
rs546515447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110403201 | GAAGGAGCCGAGAGG[A/G]AAGGATTCAGCCTAG | 51434 |
rs546614434 | snp | A/G | 0.000115364 | 0.00759399 | synonymous-codon, intron-variant, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110377610 | GGCTAAGTAACATTC[A/G]ATAAGACCTGAAAAA | 51434 |
rs546909927 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110404076 | GCCAGGGACAGACCT[A/G]ACGGCCTTTACAGTG | 51434 |
rs546955891 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110400797 | ACGCCTGCAATCCAA[A/G]CACTTTGGGAGGCCT | 51434 |
rs546965741 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382087 | CTTATAGTTTTAACC[G/T]AAGATATTAGTAGAA | 51434 |
rs546979832 | snp | C/T | 6.77966e-05 | 0.00582183 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110388664 | CAAAATAAGCGTATA[C/T]TGCAAAGAAAATCTC | 51434 |
rs546991100 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110391120 | GCTTGAACCCAGGAG[A/G]TGGAGGTTGCAGTGA | 51434 |
rs547093419 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110402793 | CACGGTAAAGGACAA[A/T]GATGCGATCACGGCT | 51434 |
rs547154967 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110401885 | AGGCTGAGGCAGGAT[A/G]ATGGCGTGAACCCAG | 51434 |
rs547178458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110393895 | AAAAAAAAAATAGCC[A/G]GACATGGTGGCTCAC | 51434 |
rs547284708 | in-del | -/AAGGTC | 0.00279162 | 0.0372561 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110390455 | GGGCACAAAAGAAAA[-/AAGGTC]AACCCCCAATCTCTT | 51434 |
rs547321372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395883 | ATCATCTAAATCAGC[A/G]GTCCCCAACCTTTTT | 51434 |
rs547336950 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110393248 | ACCACCCCCATTACC[A/C]AATGTGTACACCTAT | 51434 |
rs547445791 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110379860 | CGTTGCTGAAACTGG[C/T]ACAGCTCCTTTGAAC | 51434 |
rs547501394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110378927 | GCAGTGGTGACATCT[C/T]GGCTCACTGCAACCC | 51434 |
rs547616991 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110400786 | CTCGGTGGCTCACGC[C/T]TGCAATCCAAGCACT | 51434 |
rs547642139 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380615 | AAGATCATGCCACTG[C/T]ACTCCAGCCTGGGTG | 51434 |
rs547648084 | snp | C/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110379736 | TCTTCCTGTTAAGAG[C/T]AAATCACTCCTAGAC | 51434 |
rs547686264 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110381159 | ACAAATCCAGTGAAA[C/G]CCCTAAATAAATGTA | 51434 |
rs547791179 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383808 | TTGAATCAGGGAGGC[A/G]GAGGTTGCAGTGAGC | 51434 |
rs547818547 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110394551 | GGAGAATCACTTGTA[C/T]TTGGGAGATGGAGGT | 51434 |
rs548024052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110401205 | AGAGTAAAAGTTTCC[A/G]TTATAACGCCATTTG | 51434 |
rs548130956 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | ANAPC7 | GRCh38.p7 | 12:110374122 | CAGGGCAGGCCACTG[C/T]GGCCATGGAGCTGCC | 51434 |
rs548319231 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110379972 | CAATGAACAGACCCA[G/T]TCCCACAGCCAACAC | 51434 |
rs548472237 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110393949 | AGGCCGTGGCAGGCG[A/T]ATCACAAAGTCAGGA | 51434 |
rs548612753 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110400910 | AAAAAATTAGCTGGG[C/T]GTGGTGGTGCGAATC | 51434 |
rs548771933 | snp | A/G/T | 0.00119737 | 0.0244387 | downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110372715 | TATTTTTAACAGAGC[A/G/T]GGGGTTTCACCATGT | 51434 |
rs548914121 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110405562 | GAGATAATGGGCGAT[A/G]TTTTTCAGGGCTGCT | 51434 |
rs548930175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110397323 | ACTTTGGGAGGCTGA[A/G]GCGGGCAGATCACAA | 51434 |
rs548996491 | snp | C/G/T | 0.000346055 | 0.0131496 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110386284 | ATTATCTCTGATCCC[C/G/T]CCCAACAACAGCCAC | 51434 |
rs549074591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110399149 | CCTCAGCCTCCCGAG[C/T]AGCTAGGATTATAGG | 51434 |
rs549162514 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110392388 | TTAAACATGTTCTCA[C/T]CAAGTTTGGTTACTT | 51434 |
rs549337411 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110384470 | AGCACTTTGGGAGGC[C/T]GAGGTGGAAATTCAA | 51434 |
rs549427425 | snp | A/G | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110382300 | AGTACTAAGCACAAT[A/G]CATTCACCAACTCAG | 51434 |
rs549439691 | snp | C/T | | | downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110372864 | GATCAAGTGATGTTG[C/T]GCAGGCTTTGGGTCT | 51434 |
rs549444225 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383867 | GGCTACAGAGCGAGA[A/C]TCCGTCTCAAAAAAA | 51434 |
rs549579155 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ANAPC7 | GRCh38.p7 | 12:110377372 | TAATGATGAACAGGA[C/G]AGAAAATAAGACACA | 51434 |
rs549606724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110393104 | CCAGCCGACACCAGA[C/T]CTTTTGATTTTAGTT | 51434 |
rs549721827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110399296 | AAGTGCTGGGATTAC[A/G]GGCGTGAGCCACTGC | 51434 |
rs549800469 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383915 | AAAAAAAAAAGAAAA[A/C]AGAAGGGCCAGGCGC | 51434 |
rs549856953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110392644 | TCATGAATTTATTTG[A/G]TATTTATAAAAGTAA | 51434 |
rs549886501 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110384517 | ATAGTGAAACCCCAT[C/G]TCTACTAAAAATACA | 51434 |
rs549980027 | in-del | -/ATA | 0.00159617 | 0.0282053 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110376606 | TTTGCAGTTTGAATT[-/ATA]ATGTTTTAAATGGGC | 51434 |
rs550118191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110380087 | CATGTACAGTGGTTC[A/G]CGTCTGTAATCCCAG | 51434 |
rs550395838 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ANAPC7 | GRCh38.p7 | 12:110404186 | GGGAACTCCTTGGTT[C/T]GAGGGGTATATTTCC | 51434 |
rs550571187 | snp | A/T | | | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387578 | AGATGATTACATGAT[A/T]ACATTTGGGACCATT | 51434 |
rs550597232 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110376711 | AAATCAGGACTGAAA[A/G]AAAAAAAAAAGGGCC | 51434 |
rs550598316 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110398187 | GGAGGCAGAGGTTGG[A/G]GTGAGCCAAGATCGT | 51434 |
rs550860567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110397493 | AGGAGGTGGAGGTTA[C/T]AGTAAGCCGAGATCG | 51434 |
rs550943142 | in-del | -/CAT | 0.00636936 | 0.0560724 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395693 | ACAGGCATCCACCAC[-/CAT]GCCTGGCTAATTTTT | 51434 |
rs550950964 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | ANAPC7 | GRCh38.p7 | 12:110375884 | CTAATGTTGTTAATA[C/T]ATTTTAAGAAAAAAT | 51434 |
rs551050739 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110395925 | ACCAGTTTCATGAAA[C/G]ACAATTTTTCCACAG | 51434 |
rs551234332 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110389098 | AAAAAAAAAAAAAAA[A/G]AAAAGAAAAGAAAAG | 51434 |
rs551256936 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110383238 | GGTCAGGAGATCGAG[A/C]CCATCCTGGCTAACA | 51434 |
rs551438692 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANAPC7 | GRCh38.p7 | 12:110387027 | TTGAGCCCAGGAATT[C/T]AAGACCAGCTTGGGC | 51434 |