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 |