SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs1612 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | CDC27 | GRCh38.p7 | 17:47178214 | cactcaatggaaaat[A/G]ttagagtgtatcata | 996 |
rs9979 | snp | A/G | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47120835 | TGAGCTGGCGGTGTC[A/G]TCGTCCGTCACTTAT | 996 |
rs183402 | snp | G/T | 0.499121 | 0.020948 | intron-variant | CDC27 | GRCh38.p7 | 17:47173894 | TGTTGGCCAGGCTGG[G/T]CTTGAATTCCTGACC | 996 |
rs188799 | snp | A/G | 0.402982 | 0.197728 | intron-variant | CDC27 | GRCh38.p7 | 17:47151675 | GAAGATGTAAAATTT[A/G]AAACCTCTAACTTAC | 996 |
rs221596 | snp | A/G | 0.498734 | 0.0251279 | intron-variant | CDC27 | GRCh38.p7 | 17:47152945 | GAAATAATAATTGAA[A/G]CTATTAAAATGACCA | 996 |
rs221597 | snp | C/T | 0.4021 | 0.198407 | intron-variant | CDC27 | GRCh38.p7 | 17:47152356 | AGAACTGTTACCAAG[C/T]GCCAAAGGAGTATAA | 996 |
rs221598 | snp | G/T | 0.4021 | 0.198407 | intron-variant | CDC27 | GRCh38.p7 | 17:47188084 | ATGAAAGTAGTGATA[G/T]ATTAAAATATTTACT | 996 |
rs221599 | snp | A/T | 0.402277 | 0.198272 | intron-variant | CDC27 | GRCh38.p7 | 17:47187014 | ATTGATCTTTATCAT[A/T]GTAGCCAAAGTTGCT | 996 |
rs221600 | snp | A/G | 0.0799831 | 0.183287 | intron-variant | CDC27 | GRCh38.p7 | 17:47186208 | ATGAATAACCATTAT[A/G]TGAGCAGAAGAGTTT | 996 |
rs221601 | snp | C/T | 0 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47175025 | TCTCTCTCTCTTTCT[C/T]TCTTTCTTTCTTTCT | 996 |
rs221602 | snp | C/T | 0.4021 | 0.198407 | intron-variant | CDC27 | GRCh38.p7 | 17:47174513 | GCAATATATTATGGA[C/T]CTTATAATTCTAATC | 996 |
rs221603 | snp | A/G | 0.49907 | 0.0215454 | intron-variant | CDC27 | GRCh38.p7 | 17:47172271 | TTTCCTTGGTTTCTT[A/G]TAGAGAAAAGTAATC | 996 |
rs221604 | snp | C/T | 0.498927 | 0.0231381 | intron-variant | CDC27 | GRCh38.p7 | 17:47169422 | tgacctcaaggtgat[C/T]cacctgcctcagcct | 996 |
rs221605 | snp | A/T | 0.498908 | 0.0233371 | intron-variant | CDC27 | GRCh38.p7 | 17:47169351 | gccCCATGTTAGTTT[A/T]TTTTACCTTGGGTGA | 996 |
rs221606 | snp | A/C | 0.498832 | 0.0241331 | intron-variant | CDC27 | GRCh38.p7 | 17:47178810 | gtctcaaaaaaaaaa[A/C]ggaaaaaggaaagag | 996 |
rs221607 | snp | C/T | 0.498927 | 0.0231381 | intron-variant | CDC27 | GRCh38.p7 | 17:47177296 | AGCCACTGTATCCGG[C/T]CTTTATTTTTTAATA | 996 |
rs701982 | snp | A/C | 0.453453 | 0.145282 | intron-variant | CDC27 | GRCh38.p7 | 17:47167456 | CAACATCTCATATCT[A/C]TAGAGTGACTTCCAG | 996 |
rs731789 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47121434 | GGTTTATGGGGTCAG[G/T]CTatcagtcaatcaa | 996 |
rs731790 | snp | A/G | 0.142087 | 0.22551 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47120977 | CAGCATGACAGATGC[A/G]GATGACACACAACTT | 996 |
rs764791 | snp | A/G | 0 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47179918 | AACTATAATAAACTA[A/G]AAACTGCCTATTCTT | 996 |
rs764792 | snp | A/G | 0.402277 | 0.198272 | intron-variant | CDC27 | GRCh38.p7 | 17:47180251 | AAAGAAGATTATACA[A/G]TAGATTAATCTACTC | 996 |
rs858674 | snp | A/G | 0.0637235 | 0.166737 | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47190127 | AATTTCTAATGGCCT[A/G]TTGAGCTTTTCCATG | 996 |
rs858675 | snp | A/G | 0.499087 | 0.0213463 | intron-variant | CDC27 | GRCh38.p7 | 17:47167230 | AAAGTTGCATTAGAT[A/G]ATAAAAAGTCACACA | 996 |
rs858676 | snp | C/T | 0.117537 | 0.212022 | intron-variant | CDC27 | GRCh38.p7 | 17:47167102 | tttgggaggccaagg[C/T]gggtggatcacctga | 996 |
rs858677 | snp | A/G | 0.394721 | 0.203852 | intron-variant | CDC27 | GRCh38.p7 | 17:47165364 | ctaaaaataaaaact[A/G]ctgacaataccaagt | 996 |
rs858678 | snp | C/G | 0.297636 | 0.24542 | intron-variant | CDC27 | GRCh38.p7 | 17:47163605 | ATACATATATGTAAA[C/G]AAGGAAGTTCTTTTT | 996 |
rs858679 | snp | C/T | 0.402277 | 0.198272 | intron-variant | CDC27 | GRCh38.p7 | 17:47151103 | TGTAAAAATAATTTC[C/T]GATTTGTACATTTCA | 996 |
rs858680 | snp | C/T | 0.499017 | 0.0221427 | intron-variant | CDC27 | GRCh38.p7 | 17:47150947 | cctcccgggttcaag[C/T]gattctcctgcctca | 996 |
rs858681 | snp | A/G | 0.394721 | 0.203852 | intron-variant | CDC27 | GRCh38.p7 | 17:47147255 | cgcgccaccatgccc[A/G]gctaatttttgtatt | 996 |
rs858682 | snp | C/T | 0 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47175013 | tctctctttctttct[C/T]tctctctctcctttc | 996 |
rs865750 | snp | G/T | 0.43555 | 0.167544 | intron-variant | CDC27 | GRCh38.p7 | 17:47149976 | tttttatagagtttt[G/T]tttttgtttttgttt | 996 |
rs866502 | snp | A/G | 0.113334 | 0.209338 | intron-variant | CDC27 | GRCh38.p7 | 17:47163914 | cagctgggcgtggtg[A/G]cacgagcctgtaatc | 996 |
rs938904 | snp | A/G | 0.481517 | 0.0943397 | intron-variant | CDC27 | GRCh38.p7 | 17:47121034 | TTTAAAAATAAAACA[A/G]AAGTCCACAGTAAGT | 996 |
rs954344 | snp | A/G | 0.109108 | 0.206518 | intron-variant | CDC27 | GRCh38.p7 | 17:47179456 | TACTCTTGGGAAAGC[A/G]GAATCAGACAGATTA | 996 |
rs954345 | snp | A/G | 0.109461 | 0.206758 | intron-variant | CDC27 | GRCh38.p7 | 17:47179598 | TAGAGTACCTAGTAT[A/G]CAGTAAGAAATCAAT | 996 |
rs1058201 | snp | G/T | 0 | 0 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47171964 | GTATTTGCATTGCGG[G/T]GTAGTACAACTGTGT | 996 |
rs1064545 | snp | C/T | 0 | 0 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47143885 | ATCTTTAAATTACCT[C/T]GGTTGTGGAGCTGTC | 996 |
rs1102461 | snp | C/G | 0.498908 | 0.0233371 | intron-variant | CDC27 | GRCh38.p7 | 17:47164133 | taggcagttataaca[C/G]tatggtaaatatttg | 996 |
rs1102462 | snp | C/T | 0.498945 | 0.022939 | intron-variant | CDC27 | GRCh38.p7 | 17:47146956 | cccacttcaggctcc[C/T]gggtagctggaacta | 996 |
rs1141701 | snp | A/C | 0 | 0 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47143907 | GGAGCTGTCACTAGT[A/C]AAGAGTCGTGAACTT | 996 |
rs1476498 | snp | A/T | 0.396546 | 0.202545 | intron-variant | CDC27 | GRCh38.p7 | 17:47126511 | GTGGGGTTTTCTTTG[A/T]TTGTTTAATTAGGCA | 996 |
rs1515754 | snp | A/G | 0.0629771 | 0.165899 | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47190263 | ACATAAGTTCAGAGA[A/G]GTAATTTGCCAAGGA | 996 |
rs1634261 | snp | G/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47174990 | CTCCTTTCCTTTCCT[G/T]TCCTGTCCTGTCCTG | 996 |
rs1634265 | snp | A/G | 0.396727 | 0.202413 | intron-variant | CDC27 | GRCh38.p7 | 17:47159838 | GATCAAGTCCCTGGA[A/G]GAGATCTATCTCTTC | 996 |
rs1634268 | snp | A/G | 0.403509 | 0.197319 | intron-variant | CDC27 | GRCh38.p7 | 17:47125823 | CAGGCGCAGCAGCTC[A/G]CGCCTGTAATCCCAG | 996 |
rs1634269 | snp | G/T | 0.498982 | 0.0225409 | intron-variant | CDC27 | GRCh38.p7 | 17:47123725 | AGTTCTAACACTTAA[G/T]AAAATGATATCCTAG | 996 |
rs1713493 | snp | C/T | 0.403158 | 0.197592 | downstream-variant-500B | CDC27 | GRCh38.p7 | 17:47117396 | CTCACCCCACCTTCA[C/T]ATGTTTTTCCCTGTT | 996 |
rs1713494 | snp | C/T | 0.40386 | 0.197046 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47118824 | CTTTGAAAGTAGGTA[C/T]GAGGAAAAATAAAAT | 996 |
rs1713495 | snp | C/T | 0.403684 | 0.197183 | intron-variant | CDC27 | GRCh38.p7 | 17:47123106 | ATAATCAGACATTAT[C/T]TTCAGAATTCCTTGC | 996 |
rs1986817 | snp | C/T | 0.190205 | 0.242744 | intron-variant | CDC27 | GRCh38.p7 | 17:47180148 | AAATTTTTAAAAATA[C/T]AGCAAAATATGGGGC | 996 |
rs2040602 | snp | A/G | 0.105569 | 0.204058 | intron-variant | CDC27 | GRCh38.p7 | 17:47127152 | aggactacaggcata[A/G]gccaccatgctcagc | 996 |
rs2285591 | snp | C/G | 0.033811 | 0.125614 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47189213 | GGAGCCGCTACAGGG[C/G]GGGCCTGAGGCACTG | 996 |
rs2317378 | snp | C/T | 0.110167 | 0.207236 | intron-variant | CDC27 | GRCh38.p7 | 17:47121737 | catgcctggcATATA[C/T]ATACttttttttttt | 996 |
rs2905371 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47181188 | agctcactgcaacct[C/T]tacctcccaggctca | 996 |
rs2956063 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47169175 | ttttatttttttgta[A/G]agatggggtcttggt | 996 |
rs2956064 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47169426 | tgaggcaggtggatc[A/C]ccttgaggtcaggag | 996 |
rs3032863 | in-del | -/A | | | intron-variant | CDC27 | GRCh38.p7 | 17:47178554 | ATAAATAAAAATAAG[-/A]AAAAAAAAAAAAAAC | 996 |
rs3208627 | snp | A/G | 0 | 0 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47181605 | AACCGCATCTCGGTA[A/G]GCATAGTGGTTTAGT | 996 |
rs3208659 | snp | G/T | 0.46875 | 0.121031 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47156977 | CAGTTTTTGGTTTAT[G/T]TTGAACCTGTTTAGA | 996 |
rs3809858 | snp | A/C | 0.289424 | 0.246872 | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47189846 | ATAGCTTCTGTCTTC[A/C]AGGAGATTAAGGTCT | 996 |
rs3815040 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | CDC27 | GRCh38.p7 | 17:47138499 | TCGAGATTTGACTAC[A/G]TTAAATTTGCTGTTG | 996 |
rs4968254 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | CDC27 | GRCh38.p7 | 17:47158835 | ttgatgcccaggcgg[A/G]tcttgaactcatgag | 996 |
rs4968306 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | CDC27 | GRCh38.p7 | 17:47122280 | GACTCATTATCTGAC[C/T]TTATATGCATTTTGT | 996 |
rs5820646 | in-del | -/A | 0.0111196 | 0.0737302 | intron-variant | CDC27 | GRCh38.p7 | 17:47187851 | ATCTACAGCCAGAAT[-/A]AAAAAAAAATCTTAA | 996 |
rs6504743 | snp | A/T | 0.49706 | 0.0382258 | intron-variant | CDC27 | GRCh38.p7 | 17:47141421 | GTAAAAAGCCTTGTA[A/T]TAAAGACATTGTGTC | 996 |
rs6504744 | snp | C/T | 0.499382 | 0.017561 | intron-variant | CDC27 | GRCh38.p7 | 17:47141475 | ATAGCATTCTTCAAG[C/T]TTATAAAACATATTC | 996 |
rs6504745 | snp | A/G | 0.458775 | 0.137524 | intron-variant | CDC27 | GRCh38.p7 | 17:47141491 | TTATAAAACATATTC[A/G]ATGTCAAAAATTCAC | 996 |
rs7220394 | snp | A/G | 0.0846316 | 0.187492 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47141988 | ACACAAAGCTAAATA[A/G]CCTTTCCCCATTTCA | 996 |
rs7222028 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | CDC27 | GRCh38.p7 | 17:47186252 | TAAATCTAAATTTCT[C/T]ATTGAGTAGCCAAAA | 996 |
rs7222294 | snp | G/T | 0.482384 | 0.0921818 | intron-variant | CDC27 | GRCh38.p7 | 17:47175098 | AAGGAAGGAAGGAAG[G/T]AAGTTGTAGCAGCAC | 996 |
rs7222999 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47126169 | CCTTGATTTTCATTT[A/T]GGAGCCAGAAAATCT | 996 |
rs7350889 | snp | C/T | 0.00241097 | 0.0346363 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47156961 | CCTAATAAACTTCGA[C/T]CAGTTTTTGGTTTAT | 996 |
rs7350908 | snp | A/G/T | 0.00151503 | 0.0274829 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157031 | GTGGGACAGTATCAG[A/G/T]TGAAATTACAGCTGA | 996 |
rs7501655 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47169669 | aaaaaaaaaaTAGAA[A/T]CAAACAAAAAAACCT | 996 |
rs7502265 | snp | C/T | 0.109108 | 0.206518 | intron-variant | CDC27 | GRCh38.p7 | 17:47176592 | AAGATGGCCAAATTG[C/T]GCAGGGCTTTGTAAA | 996 |
rs8065815 | snp | A/G | 0.115788 | 0.21092 | intron-variant | CDC27 | GRCh38.p7 | 17:47139547 | GCTGGGATTACAGGC[A/G]TGAGCCACCACACCT | 996 |
rs8070852 | snp | A/G | 0 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47175042 | gaaagagagagagag[A/G]aaggaaggaaggaag | 996 |
rs8071243 | snp | C/T | 0.132653 | 0.220748 | intron-variant | CDC27 | GRCh38.p7 | 17:47140010 | AAAGGAAAAGAAATT[C/T]TCACAGTTTAGTTTA | 996 |
rs8071382 | snp | C/T | 0.401924 | 0.198543 | intron-variant | CDC27 | GRCh38.p7 | 17:47145454 | aatttgtctggtcca[C/T]gtcccaggctcctga | 996 |
rs8073936 | snp | C/G | 0.498945 | 0.022939 | intron-variant | CDC27 | GRCh38.p7 | 17:47133905 | aggcatgtgtcacca[C/G]gcccagctaattttc | 996 |
rs8074188 | snp | A/G | 0 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47175043 | aaagagagagagagg[A/G]aggaaggaaggaagg | 996 |
rs8075445 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | CDC27 | GRCh38.p7 | 17:47143255 | aggcgtgagccactg[C/T]gtccgCCGGGTCTCC | 996 |
rs8076808 | snp | C/T | 0.393619 | 0.204631 | intron-variant | CDC27 | GRCh38.p7 | 17:47138170 | ATTCAAGATTATAAT[C/T]CACAATCTATCTCTG | 996 |
rs8077506 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | CDC27 | GRCh38.p7 | 17:47127851 | gagagtacaggcaca[C/T]gtcaccacacctggc | 996 |
rs8081278 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | CDC27 | GRCh38.p7 | 17:47183244 | TTAAAAAGGTTACAA[C/T]GGAAACCAGTAAAAT | 996 |
rs9630738 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | CDC27 | GRCh38.p7 | 17:47142596 | GGTCTTCAAAGTCAT[A/T]TAATTTTAAACACAG | 996 |
rs9747135 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47133524 | agctcaccacaacct[A/C]cgcctcccaggttca | 996 |
rs9747143 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47133028 | atatatatatatata[C/T]acacacacacacaca | 996 |
rs9747171 | snp | A/G | 0.498158 | 0.0302955 | intron-variant | CDC27 | GRCh38.p7 | 17:47133507 | tgcaatggcatgatc[A/G]cagctcaccacaacc | 996 |
rs9747451 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47133759 | TACATATAttttttt[C/T]cttttttgagacagt | 996 |
rs9890214 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | CDC27 | GRCh38.p7 | 17:47123630 | ttggtcaggctggtc[C/T]taaactcctgacctc | 996 |
rs9891209 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47145877 | attgcagcctgggcg[A/G]caacagcgaaactct | 996 |
rs9892830 | snp | A/G | 0 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47155031 | GATCTCAGGAGATTT[A/G]TTAGAAATAAAGAAG | 996 |
rs9895155 | snp | A/G | 0 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47160661 | ATGGAAAAAAATTCA[A/G]AACAGCAATTCTTCC | 996 |
rs9897015 | snp | A/G | 0.404733 | 0.196361 | intron-variant | CDC27 | GRCh38.p7 | 17:47125392 | gctggaattacaggc[A/G]tgtgccaccatgcct | 996 |
rs9903593 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47131857 | aattttttttgtaga[A/G]atggggtctcgctat | 996 |
rs9903595 | snp | G/T | 0.489796 | 0.070696 | intron-variant | CDC27 | GRCh38.p7 | 17:47131860 | TTTTTTTGTAGAGAT[G/T]GGGTCTCGCTATGTT | 996 |
rs9903611 | snp | G/T | 0.49655 | 0.04139 | intron-variant | CDC27 | GRCh38.p7 | 17:47131876 | GGGTCTCGCTATGTT[G/T]CCCAGGCTGGTCTCC | 996 |
rs9904549 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47180943 | AATACAGACTCTTTT[C/T]TTaaaaaaaaaaaaa | 996 |
rs9905231 | snp | C/G | 0.49655 | 0.04139 | intron-variant | CDC27 | GRCh38.p7 | 17:47131877 | GGTCTCGCTATGTTG[C/G]CCAGGCTGGTCTCCA | 996 |
rs9905595 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47180971 | aaaaaaaaaaaaaaT[A/C]CATggcatggtggcc | 996 |
rs9905948 | snp | C/T | 0.407845 | 0.193868 | intron-variant | CDC27 | GRCh38.p7 | 17:47140063 | TCTTAATGAAATGAG[C/T]ATGACAGAAAATAAG | 996 |
rs9905958 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47169164 | cccagctaatttttt[A/T]tttttttgtagagat | 996 |
rs9909415 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47123596 | tttgtatttttagta[A/G]aggtcaggtttcacc | 996 |
rs9909538 | snp | A/G | 0 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47181415 | TAAGGGAACTACACA[A/G]AAAAAAAGTAAAGAT | 996 |
rs9909569 | snp | A/G | 0 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47181452 | AACTAGTGTCAATCA[A/G]AAAAACAACAAGATG | 996 |
rs9911450 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47168999 | tttttttttttcttt[C/T]tttttttttggaaac | 996 |
rs9911821 | snp | A/T | 0.375 | 0.216506 | intron-variant | CDC27 | GRCh38.p7 | 17:47131851 | tttttaaattttttt[A/T]gtagagatggggtct | 996 |
rs9911893 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47169165 | ccagctaatttttta[A/T]ttttttgtagagatg | 996 |
rs10636944 | in-del | -/TTA | 0.394721 | 0.203852 | intron-variant | CDC27 | GRCh38.p7 | 17:47157589 | GATAAAGCTGTAAAT[-/TTA]GAAAATAAACTACAA | 996 |
rs10700260 | in-del | -/AAGGA | 0 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47175004 | CAGGAAAGGAAAGGA[-/AAGGA]GAGAGAGAAAGAAAG | 996 |
rs11079757 | snp | A/G | 0.316968 | 0.240864 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47118484 | AACAAGTGTGTGCGC[A/G]TATATATATATGTAT | 996 |
rs11079759 | snp | C/G | 0.109108 | 0.206518 | intron-variant | CDC27 | GRCh38.p7 | 17:47152470 | AATTAATGAAGATTA[C/G]AAAAACTAAGCAATA | 996 |
rs11079760 | snp | C/T | 0.316243 | 0.241064 | intron-variant | CDC27 | GRCh38.p7 | 17:47153061 | CCAATTTGGAAAAGG[C/T]GGAGGAAGGCTTATG | 996 |
rs11079761 | snp | C/G | 0.109461 | 0.206758 | intron-variant, upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47189066 | CCACTCCGCGGCCTG[C/G]TGCGGCCTAGGCCCG | 996 |
rs11372544 | in-del | -/A/AA/AAA | 0.596568 | 0.113873 | intron-variant | CDC27 | GRCh38.p7 | 17:47157394 | ACAAAAAAAAAAAAA[-/A/AA/AAA]GTTTGTCTCTGAGGA | 996 |
rs11422815 | in-del | -/G | 0.498908 | 0.0233371 | intron-variant | CDC27 | GRCh38.p7 | 17:47179334 | AACTGATATTGTCCA[-/G]CCAAGAAAACTGTTG | 996 |
rs11464067 | in-del | -/T | 0.392511 | 0.205404 | intron-variant | CDC27 | GRCh38.p7 | 17:47137805 | TCTTTTTTTTTTTTT[-/T]GAGATCTGGTCTTGT | 996 |
rs11491191 | snp | A/G | 0.0671218 | 0.170457 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47142303 | CCTTCTGAAATGATG[A/G]AAGAGTCCAATTTTG | 996 |
rs11570440 | snp | A/C | 0.00636936 | 0.0560724 | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47190748 | TGGCTACTTTCCAGG[A/C]CAGTGTAAAAGTCTG | 996 |
rs11570441 | snp | C/G | 0.106278 | 0.204558 | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47190619 | TATACAGTGACAAGA[C/G]AAGGCGGTGGAGAAG | 996 |
rs11570442 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47190193 | GGCCTCTGAATTTCC[A/G]ACCCCCTACTCTTCC | 996 |
rs11570443 | snp | A/G | 0.0287284 | 0.116357 | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47190171 | TACTCTTCCCACCAC[A/G]GCGGAATGCCTCACC | 996 |
rs11570444 | snp | C/T | 0.00332778 | 0.0406548 | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47190040 | TTTTTCCTCCCTTCA[C/T]TTTCCTATACTTCTT | 996 |
rs11570445 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47189948 | CTTTCCTTATCTTAT[C/T]ACAATTGCCCTCTCT | 996 |
rs11570446 | in-del | -/C | 0.00914312 | 0.0669923 | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47189946 | TTCCTTATCTTATCA[-/C]AATTGCCCTCTCTGA | 996 |
rs11570447 | snp | A/C | 0.00597247 | 0.0543191 | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47189377 | GGTATTTCCGACTCC[A/C]TTCGGGCTTTTCCGT | 996 |
rs11570448 | snp | A/G | 0.00146044 | 0.0269831 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47189219 | CGGGCCGGAGCCGCT[A/G]CAGGGGGGGCCTGAG | 996 |
rs11570449 | snp | C/T | 0.0341408 | 0.126114 | intron-variant, upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47189068 | GGCCACTCCGCGGCC[C/T]GGTGCGGCCTAGGCC | 996 |
rs11570450 | in-del | -/C | 0.0185938 | 0.0946107 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47188957 | GTGTTACCTCTGGCC[-/C]TACATTACTTCACCC | 996 |
rs11570451 | snp | A/G | 0.108755 | 0.206276 | intron-variant, utr-variant-5-prime | CDC27 | GRCh38.p7 | 17:47188797 | AGCGCTCTCTTGCCT[A/G]AAAGATGATCGAGAA | 996 |
rs11570452 | in-del | -/TTGAT | 0.0138799 | 0.0821421 | intron-variant, utr-variant-5-prime | CDC27 | GRCh38.p7 | 17:47188771 | GATCGAGAAGCACAT[-/TTGAT]CGGAGCTTGTGTGAT | 996 |
rs11570453 | in-del | -/GTGATCTTCGTGACGGT | 0.0116955 | 0.0755709 | intron-variant | CDC27 | GRCh38.p7 | 17:47188744 | TTGATCGGAGCTTGT[-/GTGATCTTCGTGACGGT]AGGGCAAGTTTACGG | 996 |
rs11570454 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | CDC27 | GRCh38.p7 | 17:47188327 | TTTAAGTGTGTGATG[C/G]GGTGCCAAGTCATTT | 996 |
rs11570455 | snp | A/G | 0.00335007 | 0.0407899 | intron-variant | CDC27 | GRCh38.p7 | 17:47188120 | CTTCATATTGCCCTT[A/G]AAAGGCTTGAGGTAT | 996 |
rs11570456 | snp | A/C | 0.0383715 | 0.133092 | intron-variant | CDC27 | GRCh38.p7 | 17:47182327 | ATGTCCTTCTATCTC[A/C]TATATACTTTAGGTT | 996 |
rs11570457 | in-del | -/AT | 0.0112991 | 0.0743093 | intron-variant | CDC27 | GRCh38.p7 | 17:47182281 | AAAGAGAAAACATAT[-/AT]TCAAAAAATTAAAAG | 996 |
rs11570458 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CDC27 | GRCh38.p7 | 17:47182214 | CCAATATGCTTCCTG[A/G]AGTGGATGAGAATTG | 996 |
rs11570459 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | CDC27 | GRCh38.p7 | 17:47182045 | TGTTAACAAATAACC[A/T]TGTTATGAGTGCTCT | 996 |
rs11570460 | snp | A/G | 0.104504 | 0.2033 | intron-variant | CDC27 | GRCh38.p7 | 17:47181970 | GGAAAGCTTTATGGG[A/G]CAGATGTTATTTAAG | 996 |
rs11570461 | snp | A/C | 0.0249937 | 0.10896 | intron-variant | CDC27 | GRCh38.p7 | 17:47181656 | ATGTATATTTATGTT[A/C]TTTTTCCTCCATTTG | 996 |
rs11570462 | snp | A/G/T | 5.27821e-05 | 0.00513695 | synonymous-codon, missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47181593 | TGCTTACCGAGATGC[A/G/T]GTTTTCCTCGCAGAA | 996 |
rs11570463 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | CDC27 | GRCh38.p7 | 17:47181501 | TATGAAATTCCATAA[C/T]TTTTTATCACTGTAA | 996 |
rs11570464 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | CDC27 | GRCh38.p7 | 17:47180206 | AAAGTGATGTTTATT[C/G]TGAATAATCTATTTA | 996 |
rs11570465 | in-del | -/G | 0.191775 | 0.243125 | intron-variant | CDC27 | GRCh38.p7 | 17:47173692 | ACTAAAATTACACAC[-/G]CACATGTACACACAA | 996 |
rs11570466 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CDC27 | GRCh38.p7 | 17:47173221 | GGTTTTTGCTTGCAC[A/G]TATCTGTGACAAAAA | 996 |
rs11570467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47170992 | CATCTCAGCCTCCCA[C/T]GTAGCTGGAGCTGCA | 996 |
rs11570468 | snp | A/G | 0.318415 | 0.240457 | intron-variant | CDC27 | GRCh38.p7 | 17:47170926 | TTTTGTATAGATGGG[A/G]TCTCACTATGTTGCC | 996 |
rs11570469 | snp | A/G | 0.0460142 | 0.144533 | intron-variant | CDC27 | GRCh38.p7 | 17:47170823 | TTGAGCCACTGTGCC[A/G]GGCATAAGTATGCAA | 996 |
rs11570470 | snp | A/T | 0.0376037 | 0.131863 | intron-variant | CDC27 | GRCh38.p7 | 17:47170506 | TTGTAATTAAAAAAA[A/T]TTTTTTTTACAAAAA | 996 |
rs11570471 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47170505 | TGTAATTAAAAAAAA[A/T]TTTTTTTACAAAAAA | 996 |
rs11570472 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | CDC27 | GRCh38.p7 | 17:47170277 | CCAGGAATTTGAGGC[C/T]ATGTGAACTATGATT | 996 |
rs11570473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47170223 | TAACAAAGCAAGACC[C/T]TATCTCTTTAAAGAA | 996 |
rs11570475 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47170140 | GAGAGAAAAAATTTG[A/T]GTCTCCATAGTTAGA | 996 |
rs11570476 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | CDC27 | GRCh38.p7 | 17:47169483 | TAATTTTTGTATTTT[G/T]GGTAGACAGGGTTTT | 996 |
rs11570477 | snp | C/G | 0.0912534 | 0.193131 | intron-variant | CDC27 | GRCh38.p7 | 17:47169409 | ATCCACCTGCCTCAG[C/G]CTCCCAAAGTGCTGG | 996 |
rs11570478 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CDC27 | GRCh38.p7 | 17:47169367 | TGAGCCACCGTACCC[A/G]GCCCCATGTTAGTTT | 996 |
rs11570479 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CDC27 | GRCh38.p7 | 17:47169156 | AAAAAAATAAAAAAT[C/T]AGCTGGGTGTGGTGG | 996 |
rs11570480 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | CDC27 | GRCh38.p7 | 17:47168960 | ACAAGTAACTCTGCC[C/T]ATGGGAATGCTTCAC | 996 |
rs11570481 | snp | C/T | 0.190519 | 0.242821 | intron-variant | CDC27 | GRCh38.p7 | 17:47158054 | ATAAGTTAGAATCTT[C/T]GGTATGTTTCAAGAA | 996 |
rs11570482 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CDC27 | GRCh38.p7 | 17:47158018 | TAACTGAAAATTACA[C/T]AAAGATTAAATCCAG | 996 |
rs11570483 | in-del | -/TT/TTA | 0.00159617 | 0.0282053 | intron-variant | CDC27 | GRCh38.p7 | 17:47157802 | TTTGGCCTAGGATAC[-/TT/TTA]ATAAAGGACCATTTT | 996 |
rs11570485 | snp | A/G/T | 0.00430297 | 0.0461852 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157251 | TGAGACAGTTCTTAC[A/G/T]GAAACACCCCAGGAC | 996 |
rs11570486 | snp | C/G | 0.0295035 | 0.117819 | intron-variant | CDC27 | GRCh38.p7 | 17:47156141 | AAAAAAAAAATTGGA[C/G]GAAAATTTAAAACTC | 996 |
rs11570487 | snp | G/T | 0.105214 | 0.203807 | intron-variant | CDC27 | GRCh38.p7 | 17:47155900 | AGTGGCACAATCATA[G/T]CTCACTGCAGCCTCA | 996 |
rs11570488 | snp | C/T | 0.0894459 | 0.191631 | intron-variant | CDC27 | GRCh38.p7 | 17:47155406 | TTACAAAAATTAGCC[C/T]GGCATGGTGACACAT | 996 |
rs11570489 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CDC27 | GRCh38.p7 | 17:47155389 | GCATGGTGACACATA[C/T]GTGTAATCCCAGGTA | 996 |
rs11570490 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CDC27 | GRCh38.p7 | 17:47155364 | CAGGTACTTTGGGGG[C/T]TGAGGCACAAGAATC | 996 |
rs11570491 | snp | A/G | 0.0074128 | 0.0604272 | intron-variant | CDC27 | GRCh38.p7 | 17:47154850 | GACCTTCTAATTTAA[A/G]TATACTGCTGCTTTA | 996 |
rs11570492 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | CDC27 | GRCh38.p7 | 17:47154482 | TCTTGGTTACAGTAG[A/G]AGACAGACTTCTTAC | 996 |
rs11570493 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CDC27 | GRCh38.p7 | 17:47154008 | TCTACCTCCCAGGCT[C/T]AAGTGATCCTTCCAC | 996 |
rs11570494 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | CDC27 | GRCh38.p7 | 17:47153948 | GTGTACACCACCACA[A/C]CCAGCTAATTTTTTT | 996 |
rs11570495 | snp | C/T | 0.191461 | 0.24305 | intron-variant | CDC27 | GRCh38.p7 | 17:47153598 | TGTGAATAACAGTTA[C/T]ACTCTCTTTACCTTA | 996 |
rs11570496 | snp | G/T | 0.0222194 | 0.103034 | intron-variant | CDC27 | GRCh38.p7 | 17:47153002 | AGATGAAAATATTCA[G/T]TAGAAAGTTAGTCAT | 996 |
rs11570497 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | CDC27 | GRCh38.p7 | 17:47152932 | AAGCTATTAAAATGA[C/G]CAGGCTCTCCTAGGG | 996 |
rs11570498 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | CDC27 | GRCh38.p7 | 17:47152918 | ACCAGGCTCTCCTAG[A/G]GAAAGAAAGAGTAGC | 996 |
rs11570499 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47152563 | CTAGATGGTGGAAAT[C/G]AATAGAAATAAGGGA | 996 |
rs11570500 | snp | A/G | 0.0111728 | 0.0739025 | intron-variant | CDC27 | GRCh38.p7 | 17:47152559 | ATGGTGGAAATGAAT[A/G]GAAATAAGGGAATAA | 996 |
rs11570501 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | CDC27 | GRCh38.p7 | 17:47152446 | AGCAATATTAACTCT[A/G]AAGAACAATATCCTT | 996 |
rs11570502 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | CDC27 | GRCh38.p7 | 17:47152434 | TCTAAAGAACAATAT[A/C]CTTAGGTTTTGGAAA | 996 |
rs11570503 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | CDC27 | GRCh38.p7 | 17:47152234 | CCCCAAATAGAGAAG[G/T]TATGTAATAAATGGA | 996 |
rs11570504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47152156 | CTTTGAAACAAAAAG[C/T]GAAAGATGAAAAGAC | 996 |
rs11570505 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | CDC27 | GRCh38.p7 | 17:47151737 | CATTTCTTTAATTTA[G/T]GCAGATAGTGACTCT | 996 |
rs11570506 | snp | A/G | 0.109108 | 0.206518 | intron-variant | CDC27 | GRCh38.p7 | 17:47151730 | TTAATTTAGGCAGAT[A/G]GTGACTCTCGTGGAT | 996 |
rs11570507 | snp | C/T | 0.0588605 | 0.161139 | intron-variant | CDC27 | GRCh38.p7 | 17:47151721 | GCAGATAGTGACTCT[C/T]GTGGATTCTAGAATA | 996 |
rs11570508 | snp | G/T | 0.219349 | 0.248114 | intron-variant | CDC27 | GRCh38.p7 | 17:47151194 | AAGTCTAATCCTCTT[G/T]AGTGCCAGCTTGCAG | 996 |
rs11570509 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | CDC27 | GRCh38.p7 | 17:47150956 | CAACCTCCGCCTCCC[A/G]GGTTCAAGCGATTCT | 996 |
rs11570510 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CDC27 | GRCh38.p7 | 17:47145424 | TCTTTATTATATAAC[A/C]CTCAAACACCTACAC | 996 |
rs11570511 | snp | C/T | 0.318656 | 0.240388 | intron-variant | CDC27 | GRCh38.p7 | 17:47144711 | TTTAGATAGTTTAGT[C/T]CACAAGTTTACCCAC | 996 |
rs11570512 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | CDC27 | GRCh38.p7 | 17:47144414 | AAATGAAGGGTAAAA[-/A]TAATTGATTTATAGA | 996 |
rs11570513 | snp | A/T | 0.217851 | 0.247924 | intron-variant | CDC27 | GRCh38.p7 | 17:47144393 | GATTTATAGATGTGC[A/T]TATCATTTGTCGATC | 996 |
rs11570514 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | CDC27 | GRCh38.p7 | 17:47144312 | GTGAAGATCTATGCT[A/G]TAATCTTTACTATTT | 996 |
rs11570515 | in-del | -/T | 0.00755907 | 0.0610114 | intron-variant | CDC27 | GRCh38.p7 | 17:47144263 | TATTTTTATTTTTTT[-/T]ATATGAAGGAAAGTT | 996 |
rs11570516 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | CDC27 | GRCh38.p7 | 17:47144151 | GAGTCCCTCATTTTT[-/T]AAATACTGTGTTTTC | 996 |
rs11570517 | in-del | -/T | 0.193966 | 0.243639 | intron-variant | CDC27 | GRCh38.p7 | 17:47143985 | TTTATAATTTTTTTT[-/T]AGTACAACACCTCAG | 996 |
rs11570518 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | CDC27 | GRCh38.p7 | 17:47143678 | TTTTTTAATTAAAAA[A/C]TTTTTTTTCTCAAGT | 996 |
rs11570519 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47143319 | CACATGTTATCATTT[A/G]CAGAAGAGTGAGTCT | 996 |
rs11570520 | snp | A/T | 0.105569 | 0.204058 | intron-variant | CDC27 | GRCh38.p7 | 17:47142913 | CAAGGCAGGCAGATC[A/T]CCTAAGGTCAGGAGT | 996 |
rs11570521 | snp | A/T | 0.0124219 | 0.0778244 | intron-variant | CDC27 | GRCh38.p7 | 17:47142892 | GGTCAGGAGTTCGAG[A/T]CCAGCCTGACCAACG | 996 |
rs11570522 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CDC27 | GRCh38.p7 | 17:47142878 | GACCAGCCTGACCAA[C/T]GTGGAGAAATCCAGT | 996 |
rs11570523 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | CDC27 | GRCh38.p7 | 17:47142781 | TGAAGCAGGAGAATC[A/G]CTTGAACCCGGGAGG | 996 |
rs11570524 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47142772 | AGAATCGCTTGAACC[C/T]GGGAGGCAGAGGTTG | 996 |
rs11570525 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47142526 | TAATCAAGATTGTAC[A/G]TTTATTTTATATCTA | 996 |
rs11570526 | snp | A/G | 0.0115603 | 0.0751433 | intron-variant | CDC27 | GRCh38.p7 | 17:47141449 | GCTATAAAGAAAATT[A/G]TGCTGAATTGAGGAC | 996 |
rs11570527 | in-del | -/TG | 0.0110494 | 0.0735024 | intron-variant | CDC27 | GRCh38.p7 | 17:47141066 | TTTCTTGCCTCTGTG[-/TG]GAGCTTACATTCTAG | 996 |
rs11570528 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | CDC27 | GRCh38.p7 | 17:47141058 | CTGTGTGGAGCTTAC[A/G]TTCTAGCAACAGACA | 996 |
rs11570529 | snp | G/T | 0.109108 | 0.206518 | intron-variant | CDC27 | GRCh38.p7 | 17:47140946 | AATGAAGTATGGTGT[G/T]TTTGTTTTTATGTAC | 996 |
rs11570530 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | CDC27 | GRCh38.p7 | 17:47140802 | ATAGTACAGAACAGA[C/G]AGTTGAAGACAGAAA | 996 |
rs11570531 | in-del | -/A | 0.0118339 | 0.076006 | intron-variant | CDC27 | GRCh38.p7 | 17:47140686 | TCGGAAAAGCCATTT[-/A]AAAAATTATTTCTAA | 996 |
rs11570532 | snp | C/T | 0.375 | 0.216506 | intron-variant | CDC27 | GRCh38.p7 | 17:47139972 | TTTTTATTACCTAGA[C/T]CTTTTCTGGCAGCTG | 996 |
rs11570533 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | CDC27 | GRCh38.p7 | 17:47139716 | TATATTCAGGGCTCA[A/G]TAGGATTTATAACCA | 996 |
rs11570534 | snp | C/T | 0.031825 | 0.122064 | intron-variant | CDC27 | GRCh38.p7 | 17:47139642 | TCTGGCACAACCTCT[C/T]GGTAAAAATTGTTCA | 996 |
rs11570535 | snp | C/T | 0.0114282 | 0.0747228 | intron-variant | CDC27 | GRCh38.p7 | 17:47139510 | GGAGGCCGAGGCGGG[C/T]GGATCACAAGGTCAG | 996 |
rs11570536 | snp | C/G/T | 0.0114282 | 0.0747228 | intron-variant | CDC27 | GRCh38.p7 | 17:47139306 | GCACTCCAGCCTGGG[C/G/T]GACAGAGTGAGACTC | 996 |
rs11570537 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | CDC27 | GRCh38.p7 | 17:47138975 | CAGCATTTAGATCCT[A/G]TGAAGATAATGACCA | 996 |
rs11570538 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CDC27 | GRCh38.p7 | 17:47138637 | TTTAGTGTCACCCAC[A/G]CTTATTTCTTTTTTT | 996 |
rs11570539 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CDC27 | GRCh38.p7 | 17:47138591 | CAGGGACTCAGAGAG[G/T]AAGAGAAAGTCCTAG | 996 |
rs11570540 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | CDC27 | GRCh38.p7 | 17:47138377 | ACATAGGTGCAATTA[A/G]TGTACATGCTCTAAT | 996 |
rs11570541 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | CDC27 | GRCh38.p7 | 17:47138061 | ATAATCCCAGCACTT[C/T]GGGAGGCTGAGGCAG | 996 |
rs11570542 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | CDC27 | GRCh38.p7 | 17:47137843 | ACTGCCCTCCAGCCC[A/G]GACAACAGAACAAGA | 996 |
rs11570543 | snp | A/G | 0.128538 | 0.218511 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137319 | CAGTCTGCAACGGGA[A/G]CATGATATTGCAATT | 996 |
rs11570544 | snp | C/T | 0.49872 | 0.0252688 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137265 | AGTTGATCCAAATTA[C/T]GCTTATGCCTATACT | 996 |
rs11570545 | snp | C/T | 0.00279385 | 0.0372709 | intron-variant | CDC27 | GRCh38.p7 | 17:47136431 | TTTTTTTGTCAGATA[C/T]GGTTATCTTTGGGGT | 996 |
rs11570546 | snp | C/T | 0.316485 | 0.240998 | intron-variant | CDC27 | GRCh38.p7 | 17:47132137 | ACAGTATTCTGGAGC[C/T]TATTACACCCAAAAA | 996 |
rs11570547 | in-del | -/AAAA | 0.32103 | 0.243215 | intron-variant | CDC27 | GRCh38.p7 | 17:47132093 | CATTTGGCTTAGCAT[-/AAAA]AAAAAATCACAGAAT | 996 |
rs11570548 | snp | C/T | 0.184203 | 0.241186 | intron-variant | CDC27 | GRCh38.p7 | 17:47131353 | GACATAGTCCAGCAC[C/T]GTAAGACAGGGCAAG | 996 |
rs11570549 | snp | C/T | 0.0667028 | 0.170006 | intron-variant | CDC27 | GRCh38.p7 | 17:47130865 | TTTGAGATGGAGTTT[C/T]GCTCTTGTTGCCCAG | 996 |
rs11570550 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | CDC27 | GRCh38.p7 | 17:47130825 | CAGTGGCACAATCTC[A/G]GCTTACCACAACCTC | 996 |
rs11570551 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CDC27 | GRCh38.p7 | 17:47130602 | CAGGCGTGAGCCACC[A/G]GGCCCAGCCCACCCC | 996 |
rs11570552 | in-del | -/TTT | 0.401924 | 0.198543 | intron-variant | CDC27 | GRCh38.p7 | 17:47129995 | GTAAACAGGAGTGTT[-/TTT]AACACAGTTTTGAGA | 996 |
rs11570553 | snp | A/G | 0.0879971 | 0.190408 | intron-variant | CDC27 | GRCh38.p7 | 17:47129848 | GGTAACCAAATATCT[A/G]CTCTAAAGATAGACT | 996 |
rs11570554 | snp | C/G | 0.0456336 | 0.143994 | intron-variant | CDC27 | GRCh38.p7 | 17:47129781 | GATTTTTATCACAGA[C/G]CAAATTATTTAAGAT | 996 |
rs11570555 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | CDC27 | GRCh38.p7 | 17:47129780 | ATTTTTATCACAGAG[C/T]AAATTATTTAAGATC | 996 |
rs11570556 | in-del | -/A | 0.0112991 | 0.0743093 | intron-variant | CDC27 | GRCh38.p7 | 17:47129690 | TAGAGATAATCTATT[-/A]ATCATTTGGTAATTA | 996 |
rs11570557 | snp | A/G | 0.109108 | 0.206518 | intron-variant | CDC27 | GRCh38.p7 | 17:47128744 | AAACAGAAAAAGAAA[A/G]CGAATGTGTGTGCAT | 996 |
rs11570558 | snp | A/T | 0.0119756 | 0.0764486 | intron-variant | CDC27 | GRCh38.p7 | 17:47128536 | TAAGTTATGAGAGCT[A/T]ATAACACGGAGACTA | 996 |
rs11570559 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | CDC27 | GRCh38.p7 | 17:47128324 | TAAATTCAGGGCTGG[G/T]CGCAGTGGCTCACAC | 996 |
rs11570560 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CDC27 | GRCh38.p7 | 17:47128323 | AAATTCAGGGCTGGG[C/T]GCAGTGGCTCACACC | 996 |
rs11570561 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | CDC27 | GRCh38.p7 | 17:47127987 | TTAATACTAATAAAA[A/T]TCCCTATAATCCCGT | 996 |
rs11570562 | snp | A/G | 0.105569 | 0.204058 | intron-variant | CDC27 | GRCh38.p7 | 17:47127505 | TGAGGCAGGAGAATC[A/G]CTTGAAACTGGAAGG | 996 |
rs11570563 | snp | G/T | 0.0341408 | 0.126114 | intron-variant | CDC27 | GRCh38.p7 | 17:47125972 | GGGATAGGCATGCTG[G/T]TTGCATGAAATGTTG | 996 |
rs11570564 | snp | A/G | 0.0633504 | 0.166319 | intron-variant | CDC27 | GRCh38.p7 | 17:47125915 | AAAGAAAACATATCA[A/G]TTCTGAATTGTGTGT | 996 |
rs11570565 | snp | C/G | 0.228796 | 0.255082 | intron-variant | CDC27 | GRCh38.p7 | 17:47125778 | GAGGCGGGTGGATCA[C/G]GAGGTCAGGAGTTCA | 996 |
rs11570566 | snp | A/C | 0.0114282 | 0.0747228 | intron-variant | CDC27 | GRCh38.p7 | 17:47125722 | ACCCCATCTCTACTA[A/C]AAATACAAAAATTAG | 996 |
rs11570567 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | CDC27 | GRCh38.p7 | 17:47124026 | TGGGAAATCAAATAA[G/T]TAAAAACGCTTGGTC | 996 |
rs11570568 | snp | C/G | 0.109108 | 0.206518 | intron-variant | CDC27 | GRCh38.p7 | 17:47123622 | gagtttaagaccagc[C/G]tgaccaacatggtga | 996 |
rs11570569 | snp | A/C | 0.0232526 | 0.105288 | intron-variant | CDC27 | GRCh38.p7 | 17:47123584 | CCTCTACTAAAAATA[A/C]AAAAAATTAGCTGGG | 996 |
rs11570570 | snp | A/G | 0.109108 | 0.206518 | intron-variant | CDC27 | GRCh38.p7 | 17:47123146 | GAGTGATATTTATTG[A/G]AAACTTACTACCTGA | 996 |
rs11570571 | in-del | -/TA | 0.0170927 | 0.0908527 | intron-variant | CDC27 | GRCh38.p7 | 17:47122664 | ATAAGTATATATATA[-/TA]GTTAGAATTTTATAG | 996 |
rs11570572 | snp | A/G | 0.000332602 | 0.0128915 | intron-variant | CDC27 | GRCh38.p7 | 17:47122440 | AAGAACAGATCAGTA[A/G]GTATCATACATATGA | 996 |
rs11570573 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CDC27 | GRCh38.p7 | 17:47121929 | AACATGGTGAAACCT[C/T]GTCTCTACTAAAAAT | 996 |
rs11570574 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | CDC27 | GRCh38.p7 | 17:47121189 | ATATCAGACCTATTA[C/T]AAAGTTAGGAAACTT | 996 |
rs11570575 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47120379 | ATCTCCCATAAACAA[A/G]TGTAATGGGCATATT | 996 |
rs11570576 | snp | C/T | 0.00398564 | 0.0444627 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47120357 | GGGCATATTGGGACT[C/T]GTATGTAGGAATCAA | 996 |
rs11570577 | snp | C/G | 0.00755907 | 0.0610114 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47119968 | TCAAAACATCCCTTT[C/G]ACTTTTCTAAGTGTT | 996 |
rs11570578 | snp | C/G | 0.0573587 | 0.15934 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47119951 | CTTTTCTAAGTGTTT[C/G]CTTAAGCAGAGTGTA | 996 |
rs11570579 | snp | A/G | 0.213333 | 0.247296 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47119930 | GCAGAGTGTAAGAAT[A/G]TGTGGTTACCTTTGG | 996 |
rs11570580 | snp | G/T | 0.00874735 | 0.0655527 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47119291 | GATATTTAACAGATT[G/T]CCCTACCTAAATTTA | 996 |
rs11570581 | snp | A/T | 0.0178098 | 0.0926698 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47119243 | AAACAATACTTTTTT[A/T]AAAAAAAGGAACAGT | 996 |
rs11570582 | snp | A/C | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47119068 | AACAGTGTCATTTAG[A/C]GTTTTATAGAAAGCT | 996 |
rs11570583 | snp | C/G | 0.00336134 | 0.0408579 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47119017 | TAAAGCCTGGAGAAA[C/G]CTAAGCTTAGAACAT | 996 |
rs11570584 | snp | C/T | 0.0267878 | 0.112589 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47118778 | AAGCCTTATTTCCCA[C/T]GTAGTAACACTTTCT | 996 |
rs11570585 | in-del | -/AAATT | 0.0227243 | 0.104143 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47118631 | AAGTTTATTTTACAG[-/AAATT]AAATTAAGTAGTTTG | 996 |
rs11570586 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47118561 | CATAAGTAATTGTGG[C/T]TTTTGCCATGACTTT | 996 |
rs11570587 | snp | C/T | 0.0460142 | 0.144533 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47118459 | CTTGTTCAGAAGTTA[C/T]GTTGTGGCCTTGGAT | 996 |
rs11570588 | snp | G/T | 0.0618563 | 0.164627 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47118455 | TTCAGAAGTTATGTT[G/T]TGGCCTTGGATTTGT | 996 |
rs11650540 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47185533 | ATTACAAAAAATTTG[G/T]TTACTTGTTTTTGTT | 996 |
rs11868039 | snp | C/T | 0.125182 | 0.216612 | intron-variant | CDC27 | GRCh38.p7 | 17:47133632 | ttagtaaagacaggg[C/T]ttctccatgttggtc | 996 |
rs11871023 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47181115 | aaaaaattagccagg[C/G]gtggtggtccgtgcc | 996 |
rs12449604 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47133110 | ACACAAatatacata[A/T]atatatatatatata | 996 |
rs12449605 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47133116 | atatacatatatata[C/T]atatatatatatata | 996 |
rs12451317 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47133096 | acacaaacacacaca[A/C]acaaatatacatata | 996 |
rs12452346 | snp | A/C | 0 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47180267 | TGTATAATCTTCTTT[A/C]TAAGCCTTCCATTCC | 996 |
rs12453390 | snp | A/G | 0.00947846 | 0.0681864 | intron-variant | CDC27 | GRCh38.p7 | 17:47154123 | CTCATGAAACTTGCC[A/G]CAATATTTACTATAA | 996 |
rs12453762 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47133086 | acacacacacacaca[A/C]acacacacacacaaa | 996 |
rs12601027 | snp | C/T | 0.316726 | 0.240931 | intron-variant | CDC27 | GRCh38.p7 | 17:47126102 | TAAATATCAGTACAG[C/T]ACATTAAATAAGGTG | 996 |
rs12936578 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47181206 | gttgcagtgagctga[A/G]atggtcccactgtac | 996 |
rs12936612 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47131948 | agcgctggcattaca[A/G]gcatgagccactgca | 996 |
rs12937292 | snp | C/T | 0.109108 | 0.206518 | intron-variant | CDC27 | GRCh38.p7 | 17:47130933 | ATGTATGAATGTGGC[C/T]GCAGAACTTTAACAA | 996 |
rs12938584 | snp | C/T | 0.490618 | 0.0678448 | intron-variant | CDC27 | GRCh38.p7 | 17:47131890 | TGCCCAGGCTGGTCT[C/T]CAACTCCTGACCTTA | 996 |
rs12938585 | snp | C/G | 0.490618 | 0.0678448 | intron-variant | CDC27 | GRCh38.p7 | 17:47131891 | GCCCAGGCTGGTCTC[C/G]AACTCCTGACCTTAA | 996 |
rs12938619 | snp | C/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47131922 | gtgattcacctgcct[C/T]ggcctcctaaagcgc | 996 |
rs12938636 | snp | C/G | 0 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47131941 | ctcctaaagcgctgg[C/G]attacaggcatgagc | 996 |
rs12938648 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47131950 | cgctggcattacagg[C/T]atgagccactgcaac | 996 |
rs12938790 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47180946 | ACAGACTCTTTTCTT[A/C]aaaaaaaaaaaaaaa | 996 |
rs12939693 | snp | A/G | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47131900 | ggtctccaactcctg[A/G]ccttaagtgattcac | 996 |
rs12939729 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47140708 | CTTTTCCGAACACAG[C/T]TCTTGCCTGTCTGTG | 996 |
rs12939749 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47181255 | gtgagaccctgtttc[A/C]aaaaaaaaaaaaaaa | 996 |
rs12940134 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47133056 | acacacacacacaca[C/T]acatatacacacaca | 996 |
rs12940177 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47133124 | atatatatatatata[C/T]atatatatatataat | 996 |
rs12941464 | snp | A/G | 0.105569 | 0.204058 | intron-variant | CDC27 | GRCh38.p7 | 17:47149390 | gtggtgcacacctgt[A/G]gtcccagctactcgg | 996 |
rs12941737 | snp | A/G | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47119385 | GTTCAAATGAGATTA[A/G]CAGTAAATTATAGAA | 996 |
rs12944893 | snp | G/T | 0 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47160031 | CAAACAAACTAGAGG[G/T]GGTAGGTCTTTTTCC | 996 |
rs12945126 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47160065 | CCTCTCCCCTCAAGA[A/T]CTGTTTGTGGAGGAT | 996 |
rs12947008 | snp | A/G | 0.109108 | 0.206518 | intron-variant | CDC27 | GRCh38.p7 | 17:47175218 | ACCTTGCATCCTCCA[A/G]ATACATTTACATCAA | 996 |
rs12948241 | snp | A/C | 0.109108 | 0.206518 | intron-variant | CDC27 | GRCh38.p7 | 17:47174920 | gagatcatgccactg[A/C]actccagcctgggca | 996 |
rs12948252 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47140709 | TTTTCCGAACACAGC[A/T]CTTGCCTGTCTGTGT | 996 |
rs12950715 | snp | C/T | 0.105569 | 0.204058 | intron-variant | CDC27 | GRCh38.p7 | 17:47149267 | actgtaatcccagca[C/T]ttcgggaggccaagg | 996 |
rs13341533 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | CDC27 | GRCh38.p7 | 17:47184968 | AGCCAAAAAGAACAA[C/T]GCTCCTCTCCCTCTC | 996 |
rs16941622 | snp | C/T | 0.319616 | 0.240112 | intron-variant | CDC27 | GRCh38.p7 | 17:47175523 | GACACATGTTTCAAA[C/T]TGATTATCTGGGCCA | 996 |
rs16941626 | snp | C/T | 0.217551 | 0.247885 | intron-variant | CDC27 | GRCh38.p7 | 17:47177974 | TAGCACTTATTTCTA[C/T]TCATTCTTAACAGTT | 996 |
rs16941628 | snp | A/G | 0.216048 | 0.247684 | intron-variant | CDC27 | GRCh38.p7 | 17:47179166 | GACAAAGAACTAGTG[A/G]AACTGAGAAATTATT | 996 |
rs16941635 | snp | A/G | 0.18989 | 0.242666 | intron-variant | CDC27 | GRCh38.p7 | 17:47184589 | AGGTATCATATTCAA[A/G]AGTTGTATCCATTTC | 996 |
rs16941640 | snp | A/T | 0.105924 | 0.204309 | intron-variant | CDC27 | GRCh38.p7 | 17:47187155 | TGGACAATGCTGCTA[A/T]GAAAAAGAAGCAAAT | 996 |
rs17856362 | snp | C/G/T | 6.75425e-05 | 0.00581091 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47142400 | TTCTGTTTGGGATTT[C/G/T]AGGTGGAAACTTCAT | 996 |
rs28687093 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | CDC27 | GRCh38.p7 | 17:47159726 | TGCCCTGGCTGGCAC[A/G]GGTCTGCTTCTGCAC | 996 |
rs28687157 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47178645 | TGTGCCAGAAACTAC[A/G]GCAGACTCTTTACAT | 996 |
rs28768531 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47133136 | ATATATATATATATA[A/T]AATATATATGTATTT | 996 |
rs28792509 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47133090 | ACACACACACAAACA[A/C]ACACACACAAATATA | 996 |
rs28805895 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47133094 | ACACACAAACACACA[A/C]ACACAAATATACATA | 996 |
rs28812244 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47133108 | ACACACAAATATACA[A/T]ATATATATATATATA | 996 |
rs28817085 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47133137 | TATATATATATATAT[A/T]ATATATATGTATTTT | 996 |
rs28854256 | snp | C/T | 0 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47133064 | ACACACATACATATA[C/T]ACACACACACACACA | 996 |
rs28874001 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47133114 | AAATATACATATATA[C/T]ATATATATATATATA | 996 |
rs33982980 | in-del | -/TTA | | | intron-variant | CDC27 | GRCh38.p7 | 17:47157590 | ATAAAGCTGTAAATG[-/TTA]AAAATAAACTACAAG | 996 |
rs34006043 | snp | A/G | 0.105569 | 0.204058 | intron-variant | CDC27 | GRCh38.p7 | 17:47149495 | CAGCCTGGTGACAGA[A/G]TGAGACTCTGTCTTA | 996 |
rs34022421 | in-del | -/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47119739 | TTTTCCAAAGACACC[-/T]AATCTATATTATGAC | 996 |
rs34061862 | in-del | -/C/CAAAA/TAAAAAA | 0.00279162 | 0.0372561 | intron-variant | CDC27 | GRCh38.p7 | 17:47180945 | ACAGACTCTTTTCTT[-/C/CAAAA/TAAAAAA]AAAAAAAAAAAAAAA | 996 |
rs34104273 | in-del | -/A | | | intron-variant | CDC27 | GRCh38.p7 | 17:47181286 | AAAAAAAAAAAAAAA[-/A]CCCAAAACAACAAAA | 996 |
rs34229894 | in-del | -/TAT | | | intron-variant | CDC27 | GRCh38.p7 | 17:47132781 | TATTATTATTATTAT[-/TAT]ATTTTAAAGATAGCA | 996 |
rs34275901 | in-del | -/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47124624 | TAACTATATAATTTT[-/T]CAGAACAACAAAAAG | 996 |
rs34350181 | in-del | -/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47180900 | GTTCCAAGGCTATAG[-/C]AGTCTAAATCCATGT | 996 |
rs34375130 | in-del | -/A | 0 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47149530 | AAAAAAAAAAAAAAA[-/A]GAAATGTTAAAAAGA | 996 |
rs34439261 | in-del | -/A | | | intron-variant | CDC27 | GRCh38.p7 | 17:47123437 | CTTTCTGAGACAGAA[-/A]TCTTGTTCTCTTGCC | 996 |
rs34575855 | in-del | -/T | | | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47190372 | TCTCATATTTCCTTT[-/T]CTGCTCCCCTTCTCC | 996 |
rs34577330 | in-del | -/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47162505 | AGTAGCCCCGTCCCC[-/C]TTGCTTTGCCAGCAG | 996 |
rs34577788 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | CDC27 | GRCh38.p7 | 17:47125438 | TTTTAGTAGACACGC[A/G]GTTTCACCATATTGG | 996 |
rs34579939 | in-del | -/AC | | | intron-variant | CDC27 | GRCh38.p7 | 17:47144873 | TATATCACACACACA[-/AC]CACACACACACATAA | 996 |
rs34596516 | in-del | -/CA | | | intron-variant | CDC27 | GRCh38.p7 | 17:47177879 | ACACACACACACACA[-/CA]TATCTCCAAAGAGCT | 996 |
rs34628696 | in-del | -/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47172283 | TATAAGAAACCAAGG[-/G]AAATAATACAATGAA | 996 |
rs34804720 | in-del | -/A | | | intron-variant | CDC27 | GRCh38.p7 | 17:47146610 | AAGGGTACTTCCTCA[-/A]TGGTGGGACAAGATT | 996 |
rs34885804 | in-del | -/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47144018 | AGACATTAATATTTT[-/T]ACTTGATTTATGACC | 996 |
rs34953511 | in-del | -/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47167034 | TAACTTTTTTATTTT[-/T]AGTAGAGACAAGGTT | 996 |
rs35001684 | in-del | -/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47177925 | ATTAATGTATTTTTT[-/T]CCTCATAGTCTAACA | 996 |
rs35003451 | in-del | -/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47185035 | TGGGTTAGTCCCCAG[-/G]TGCACTAATTTAAAA | 996 |
rs35087240 | in-del | -/A | | | intron-variant | CDC27 | GRCh38.p7 | 17:47145885 | TGGGCGACAACAGCG[-/A]AAACTCTGTCTCAAA | 996 |
rs35138348 | in-del | -/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47147785 | TGTGCCTGTAGTCCC[-/C]AGCTACTCAGGAGGC | 996 |
rs35160918 | in-del | -/CA/CACA | | | intron-variant | CDC27 | GRCh38.p7 | 17:47144871 | ACACACACACACACA[-/CA/CACA]TAAATCCTTTTAATC | 996 |
rs35234493 | in-del | -/A | 0.405082 | 0.196086 | intron-variant | CDC27 | GRCh38.p7 | 17:47163226 | AAAAGACAAAAAAAA[-/A]GTCTATACTGGAGAT | 996 |
rs35238829 | snp | A/G | 0.103082 | 0.202275 | intron-variant | CDC27 | GRCh38.p7 | 17:47186760 | CATTAAAACTTTAAA[A/G]AAAAAAAAATGCAGA | 996 |
rs35248358 | in-del | -/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47156480 | TGAGTTGGAGTCTTG[-/G]TCTGTCGCCCAGGAT | 996 |
rs35350670 | in-del | -/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47176862 | TTATTCCACATCTTT[-/T]AGTAGAATTCTGGAT | 996 |
rs35393637 | in-del | -/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47155497 | TGATCTGCCCACCTC[-/C]AGCCTCCCAAAGTGC | 996 |
rs35413371 | in-del | -/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47162210 | ATCAGCAACGAAGCC[-/C]ATAATTCATGTACTT | 996 |
rs35427044 | in-del | -/G | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47189180 | ACCGTCATCCTCGAG[-/G]CTCAGGCCCACTTTC | 996 |
rs35468341 | in-del | -/G | | | frameshift-variant, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47142324 | CCAATTTTGTAATTT[-/G]CCAGGCTATCATTTA | 996 |
rs35561621 | in-del | -/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47124715 | CTCACATCTATCTGC[-/G]TTCTCCATTTAATCT | 996 |
rs35570204 | in-del | -/T | 0.499995 | 0.00159744 | intron-variant | CDC27 | GRCh38.p7 | 17:47121742 | CTGGCATATATATAC[-/T]TTTTTTTTTTTTTTG | 996 |
rs35617754 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47121495 | TAGGCTGGAGTGCAG[A/T]GGCACAATCATAGCT | 996 |
rs35730575 | in-del | -/A | | | intron-variant | CDC27 | GRCh38.p7 | 17:47174232 | GTACCCCAAACACAA[-/A]CTAAAGAAGCAGTGG | 996 |
rs35766560 | in-del | -/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47134322 | TTTTTTTTTTTTTTT[-/T]AATTCAACGTCTTGC | 996 |
rs35785123 | in-del | -/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47145225 | GGGCCACCTTGCAGG[-/G]AAAAAAGAATGCAAA | 996 |
rs35788312 | in-del | -/A | 0.499897 | 0.00718776 | intron-variant | CDC27 | GRCh38.p7 | 17:47130877 | CAAAAAAAAAAAAAA[-/A]TTAAATTAAAAAAGT | 996 |
rs35845296 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | CDC27 | GRCh38.p7 | 17:47135164 | CCTAACAATGCTATT[C/T]CCACATTTCTGTTTT | 996 |
rs35856124 | in-del | -/A | | | intron-variant | CDC27 | GRCh38.p7 | 17:47187716 | GGCAAAAAAAAAAAA[-/A]TCATTAACTATTAAA | 996 |
rs35938440 | in-del | -/A | | | intron-variant | CDC27 | GRCh38.p7 | 17:47124017 | AAAGTTTTGACCAAG[-/A]CGTTTTTACTTATTT | 996 |
rs35940111 | in-del | -/G | | | upstream-variant-2KB, utr-variant-5-prime | CDC27 | GRCh38.p7 | 17:47189326 | CGAGCGGGACACGGG[-/G]AATACCCGAAGTGGA | 996 |
rs35962181 | in-del | -/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47172701 | TCTGTCCCTCCTTTT[-/T]ACATTAGGAAATGCC | 996 |
rs36028247 | in-del | -/T | 0 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47126811 | AAAAAATTTTTTTTT[-/T]GAGACAGAGTCTCCC | 996 |
rs36061147 | in-del | -/A | | | intron-variant | CDC27 | GRCh38.p7 | 17:47145272 | CACTGTGTTGAAAAG[-/A]AAAATGTTGAGAATT | 996 |
rs36096371 | in-del | -/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47174092 | AGTGAGATTCTGTTT[-/T]AAATAAATAAATAAA | 996 |
rs55717332 | in-del | -/TATATA | | | intron-variant | CDC27 | GRCh38.p7 | 17:47133132 | ATATATATATATATA[-/TATATA]ATATATATGTATTTT | 996 |
rs55841275 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47135532 | ATCATTATACTTGTG[C/T]TATAGATGAAGAAAA | 996 |
rs56205214 | in-del | -/GAAGGAAGGAAG | | | intron-variant | CDC27 | GRCh38.p7 | 17:47175101 | AAGGAAGGAAGTAAG[-/GAAGGAAGGAAG]TTGTAGCAGCACTAC | 996 |
rs57433865 | in-del | -/A | | | intron-variant | CDC27 | GRCh38.p7 | 17:47137003 | CATTTCATAAGAAAA[-/A]CATTTTAGTTAGAAG | 996 |
rs57622200 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47175037 | AGAGAGAAAGAGAGA[A/C/G]AGAGGAAGGAAGGAA | 996 |
rs57778121 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47188717 | TCATACAAGACAAAA[A/T]AAAAAAAACCTCCGT | 996 |
rs57868315 | in-del | -/T | 0 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47123422 | TTTTTTTTTTTTTTT[-/T]CTTTCTGAGACAGAA | 996 |
rs58151287 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47180917 | GTCTAAATCCATGTT[C/T]TTCACCATAGAATAC | 996 |
rs58182973 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47127217 | TCAGTGAGCTATGAT[C/T]GCACCACTGCACTCC | 996 |
rs58631604 | in-del | -/T | 0 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47125264 | TTTTTTTTTTTTTTT[-/T]GAGATGGCGTTTCAC | 996 |
rs58733658 | snp | A/G | 0.375 | 0.216506 | intron-variant | CDC27 | GRCh38.p7 | 17:47175033 | AGAAAGAGAGAAAGA[A/G]AGAGAGAGGAAGGAA | 996 |
rs58792671 | snp | G/T | 0.029116 | 0.117091 | intron-variant | CDC27 | GRCh38.p7 | 17:47185104 | ACCAGCTAGCTATTC[G/T]TAAATATAAAATATT | 996 |
rs59064809 | in-del | -/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47175006 | GGAAAGGAAAGGAGA[-/G]GAGAGAAAGAAAGAA | 996 |
rs59080750 | snp | A/G | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47175005 | CAGGAAAGGAAAGGA[A/G]AGAGAGAAAGAAAGA | 996 |
rs59470054 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47155825 | AGGTGTGGTGGCATG[C/T]GCCTGCAGTCCCAGC | 996 |
rs59790354 | in-del | -/ACA/ACACAC/ACACACAC/ACACACACAC/C | 0.625 | 0.125 | intron-variant | CDC27 | GRCh38.p7 | 17:47124210 | CACACACACACACAC[lengthTooLong]CCCTCTTCGTGAAAT | 996 |
rs59821284 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47155823 | CCAGGTGTGGTGGCA[C/T]GTGCCTGCAGTCCCA | 996 |
rs60087127 | in-del | -/CTATCTA/CTATCTAT/CTATCTATCTAT | 0 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47124286 | TATCTATCTATCTAT[lengthTooLong]TCATTTTTATTTATT | 996 |
rs60574276 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47180762 | CTTTAAATAAACCAT[C/T]TCATTGAATTTTTAA | 996 |
rs61502164 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47180780 | ATTGAATTTTTAATT[C/T]TAAGGGGCAATGATT | 996 |
rs61749925 | snp | C/T | 0.00749812 | 0.0607687 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47154771 | ACTTGGGGTTTCTAA[C/T]GGCAAAATCCCAAAA | 996 |
rs62075598 | snp | A/C | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47135526 | TTATATATCATTATA[A/C]TTGTGTTATAGATGA | 996 |
rs62075599 | snp | A/C | 0.46875 | 0.121031 | intron-variant | CDC27 | GRCh38.p7 | 17:47135547 | TTATAGATGAAGAAA[A/C]GGTATTAAACACTAT | 996 |
rs62075600 | snp | A/G | 0.444444 | 0.157135 | intron-variant | CDC27 | GRCh38.p7 | 17:47135561 | AAGGTATTAAACACT[A/G]TGCTAATGATAGTGA | 996 |
rs62075601 | snp | A/G | 0.444444 | 0.157135 | intron-variant | CDC27 | GRCh38.p7 | 17:47135584 | GATAGTGAAAGTGAA[A/G]ACAAAAGAAAGGCTA | 996 |
rs62075602 | snp | A/C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47135638 | TTGCTCAGTATTTAG[A/C/T]TACCTAAATACGTCA | 996 |
rs62075603 | snp | A/C | 0.375 | 0.216506 | intron-variant | CDC27 | GRCh38.p7 | 17:47135661 | ATACGTCAGCATTTA[A/C]ACTCCTCCTAGTAAA | 996 |
rs62075604 | snp | C/T | 0.375 | 0.216506 | intron-variant | CDC27 | GRCh38.p7 | 17:47135666 | TCAGCATTTAAACTC[C/T]TCCTAGTAAAAGCTT | 996 |
rs62075605 | snp | G/T | 0.444444 | 0.157135 | intron-variant | CDC27 | GRCh38.p7 | 17:47135681 | CTCCTAGTAAAAGCT[G/T]GCCAATCTGAATAAT | 996 |
rs62075606 | snp | G/T | 0 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47135722 | ACACAATTTTTGATA[G/T]GGTTAAGTTTTTTAA | 996 |
rs62075607 | snp | A/G | 0.375 | 0.216506 | intron-variant | CDC27 | GRCh38.p7 | 17:47135744 | GTTTTTTAAGAATGC[A/G]ACTCCTGCAAAATAG | 996 |
rs62075608 | snp | A/G | 0 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47135770 | AATAGCTGAACAGAC[A/G]ATACACATTTAAAAA | 996 |
rs62075609 | snp | A/G | 0 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47135825 | ACTTGGGAAAAAATC[A/G]AAAACAACACAAGTC | 996 |
rs62075610 | snp | A/C | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47135831 | GAAAAAATCAAAAAC[A/C]ACACAAGTCTTATTA | 996 |
rs62075611 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136558 | GGTGTTGAGGCAGAA[A/G]TAGGACCAAACTTTT | 996 |
rs62075612 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136567 | GCAGAAATAGGACCA[A/C]ACTTTTTCATATCTT | 996 |
rs62075613 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136576 | GGACCAAACTTTTTC[A/C]TATCTTATTCAGTTG | 996 |
rs62075614 | snp | C/T | 0 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47136627 | GTAATTTCCTATGTG[C/T]CTACTTATACACAAG | 996 |
rs62075615 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136640 | TGTCTACTTATACAC[A/G]AGTACAAAAAAGTAA | 996 |
rs62075616 | snp | C/G | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47136910 | ATCTGCAAAAGTTTG[C/G]TAGAAGGCTGAAACT | 996 |
rs62075617 | snp | A/C | 0.5 | 0 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137157 | TACCACTTACCATGC[A/C]TTATAATGTCTAGGA | 996 |
rs62075618 | snp | C/T | 0.498877 | 0.0236694 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137161 | ACTTACCATGCATTA[C/T]AATGTCTAGGATTGA | 996 |
rs62075619 | snp | C/T | 0.5 | 0 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137178 | ATGTCTAGGATTGAC[C/T]CTGATAGCATTTCGA | 996 |
rs62075620 | snp | G/T | | | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137303 | CTCTCTGGAAGAATT[G/T]AATTGCAATATCATG | 996 |
rs62075621 | snp | C/T | 0 | 0 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137307 | CTGGAAGAATTTAAT[C/T]GCAATATCATGTTCC | 996 |
rs62075622 | snp | A/G | 0.499869 | 0.00809448 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137316 | TTTAATTGCAATATC[A/G]TGTTCCCGTTGCAGA | 996 |
rs62075623 | snp | A/C/T | 1.6659e-05 | 0.00288604 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137333 | GTTCCCGTTGCAGAC[A/C/T]GAAACAGTTCCCTGC | 996 |
rs62075657 | snp | G/T | | | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47138766 | TTTATCCATGTCTGT[G/T]AAGTCTTTTGACAGA | 996 |
rs62075658 | snp | G/T | | | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47138775 | GTCTGTTAAGTCTTT[G/T]GACAGAACTGAAAGA | 996 |
rs62075659 | snp | A/C/G | 0.000711563 | 0.0188487 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47138844 | GATCTCCATGCCTTC[A/C/G]ACTCTATAATTCTCA | 996 |
rs62077260 | snp | A/G | 0.5 | 0 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47138850 | CATGCCTTCAACTCT[A/G]TAATTCTCAATCCTT | 996 |
rs62077261 | snp | G/T | 0.0016501 | 0.0286762 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47141966 | TAGCTTCTTTGCAGT[G/T]GTATGAACACAAAGC | 996 |
rs62077262 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47147260 | AAAAATTAGCTGGGC[A/G]TGGTGGCGCGCGCCT | 996 |
rs62077263 | snp | C/G | 0.444444 | 0.157135 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47156932 | GGGTTAATGGACTAA[C/G]AGCTGCTGGTCCTCC | 996 |
rs62077264 | snp | A/C | 0.5 | 0 | stop-gained, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47156994 | TGAACCTGTTTAGAT[A/C]ATATGGAAGTTCCTG | 996 |
rs62077265 | snp | C/T | | | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47171940 | ATCAACACAACATTT[C/T]GCAAGCAGGTATTTG | 996 |
rs62077266 | snp | C/T | 0.4838 | 0.08853 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47171950 | CATTTTGCAAGCAGG[C/T]ATTTGCATTGCGGTG | 996 |
rs62077268 | snp | C/T | | | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47171999 | TCAAGAGTCTATATG[C/T]TTTATATGCCTTTCC | 996 |
rs62077269 | snp | C/G/T | 0.00116129 | 0.0240689 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47172006 | TCTATATGCTTTATA[C/G/T]GCCTTTCCTGAGCGG | 996 |
rs62077270 | snp | G/T | | | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47172025 | TTTCCTGAGCGGTAA[G/T]AACAGGTTGCCAGTA | 996 |
rs62077271 | snp | C/T | 2.47087e-05 | 0.00351479 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47172033 | GCGGTAATAACAGGT[C/T]GCCAGTAAAAACAAG | 996 |
rs62077272 | snp | A/G | | | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47172042 | ACAGGTTGCCAGTAA[A/G]AACAAGGCTTCTTCT | 996 |
rs62077273 | snp | C/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47173920 | CAACATGGCGAAACC[C/T]CGTCTTCTACTAAAA | 996 |
rs62077274 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | CDC27 | GRCh38.p7 | 17:47179798 | AGGTACATAAATAAC[A/G]TGGATTAAACAGCTT | 996 |
rs62077275 | snp | A/G | | | missense, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47181585 | TAAAGGCGTTCTGCG[A/G]GGAAAACCGCATCTC | 996 |
rs62077276 | snp | A/G | | | missense, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47181588 | AGGCGTTCTGCGAGG[A/G]AAACCGCATCTCGGT | 996 |
rs62077278 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47183336 | ATGCCTTAGATACAG[A/T]AAAGGCTCAACAAAT | 996 |
rs62077279 | snp | C/T | | | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47189156 | ATTACCTGGACGGGT[C/T]CCTGCAGCACCGTCA | 996 |
rs62077280 | snp | C/T | | | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47189169 | GTTCCTGCAGCACCG[C/T]CATCCTCGAGGCTCA | 996 |
rs62077281 | snp | A/T | 0.5 | 0 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47189205 | ACTTTCTGCAGTGCC[A/T]CAGGCCCCCCCTGTA | 996 |
rs66518624 | snp | C/T | 0.109108 | 0.206518 | intron-variant | CDC27 | GRCh38.p7 | 17:47146039 | ATAATTTAAAAACCC[C/T]AATAAAAATTTTGAA | 996 |
rs67501653 | in-del | -/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47179335 | ACTGATATTGTCCAC[-/G]CAAGAAAACTGTTGC | 996 |
rs67551364 | snp | C/T | 0.109461 | 0.206758 | intron-variant | CDC27 | GRCh38.p7 | 17:47164372 | ATTTTAACTTAATTT[C/T]TTTAAACTTTACTTT | 996 |
rs67602179 | in-del | -/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47123413 | TACTTTTTTTTCTAC[-/T]TTTTTTTTTTTTTTT | 996 |
rs67861319 | snp | A/G | 0.318896 | 0.240319 | intron-variant | CDC27 | GRCh38.p7 | 17:47147591 | CAAAAACATAGAAGA[A/G]ACTGGATGAGGTGGC | 996 |
rs67963569 | in-del | -/T | 0.401747 | 0.198678 | intron-variant | CDC27 | GRCh38.p7 | 17:47131844 | AGGCTAATTTTTAAA[-/T]TTTTTTTGTAGAGAT | 996 |
rs68100136 | snp | C/T | 0.318174 | 0.240525 | intron-variant | CDC27 | GRCh38.p7 | 17:47124256 | ATCCTTGCTTTTGGT[C/T]ATCTATCTATCTATC | 996 |
rs71138586 | in-del | -/TATTATTATTAT | 0 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47132770 | TATTATTATTATTAT[-/TATTATTATTAT]ATTTTAAAGATAGCA | 996 |
rs71138587 | in-del | -/TATATATATATA | 0 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47133028 | ATATATATATATATA[-/TATATATATATA]CACACACACACACAC | 996 |
rs71138588 | in-del | -/CATACA | 0 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47133055 | ACACACACACACACA[-/CATACA]TACATATATACACAC | 996 |
rs71138589 | in-del | -/ATAT | 0 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47133127 | TATATATATATATAT[-/ATAT]ATATATAATATATAT | 996 |
rs71138590 | in-del | -/C/CAAAC | 0 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47147431 | AAACAAACAAACAAA[-/C/CAAAC]AAAAAAAACACTAGG | 996 |
rs71138591 | in-del | -/A | 0 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47149096 | AAAAAAAAAAAAAAA[-/A]GAAAAAGAAAGAAAT | 996 |
rs71138592 | in-del | -/AGGAAGGAAGGAAGGAAGGA | 0 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47175060 | GGAAGGAAGGAAGGA[-/AGGAAGGAAGGAAGGAAGGA]AGGAAGGAAGGAAGG | 996 |
rs71365043 | in-del | -/ATCT/ATCTATCT/ATCTATCTATCT/ATCTATCTATCTATCT | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47124256 | TCCTTGCTTTTGGTC[lengthTooLong]ATCTATCTATCTATC | 996 |
rs71365050 | in-del | -/G | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47181306 | AACAACAAAAACCCT[-/G]GGGGGAAAAAAAAAC | 996 |
rs71375392 | snp | A/C | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47119640 | GTAAAGGAGATAAAC[A/C]ATTTAAGACTGTTTA | 996 |
rs71375393 | snp | C/T | 0.0973687 | 0.197999 | intron-variant | CDC27 | GRCh38.p7 | 17:47133858 | GGTTCAAGCGATTTT[C/T]GTGCCTCAGCCTCCC | 996 |
rs71375394 | snp | C/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47134156 | CTCCCACCTTGGCCT[C/T]CCAAACGCTAGGATT | 996 |
rs71375395 | snp | C/G | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47155828 | TGTGGTGGCATGTGC[C/G]TGCAGTCCCAGCTAC | 996 |
rs71375396 | snp | A/G | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47155833 | TGGCATGTGCCTGCA[A/G]TCCCAGCTACTCAGG | 996 |
rs71375397 | snp | A/C | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47181032 | CAAGGCAGGTGGATC[A/C]CCTAAGCTCAGGAAT | 996 |
rs71375398 | snp | C/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47181083 | ATAGCAAAACCCTAT[C/T]TCTACCAAAAAAAAA | 996 |
rs71375399 | snp | C/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47181085 | AGCAAAACCCTATCT[C/T]TACCAAAAAAAAAAA | 996 |
rs72523723 | in-del | -/TTA | | | intron-variant | CDC27 | GRCh38.p7 | 17:47157588 | AGATAAAGCTGTAAA[-/TTA]TKWAAATAAACTACA | 996 |
rs72628347 | snp | A/G | 0.13875 | 0.223883 | intron-variant | CDC27 | GRCh38.p7 | 17:47132777 | ATTATTATTATTATT[A/G]TTATATTTTAAAGAT | 996 |
rs72628348 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | CDC27 | GRCh38.p7 | 17:47159463 | CACGTGCCAAGACGA[C/T]GCCCGTGCTCCTGGG | 996 |
rs72823438 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | CDC27 | GRCh38.p7 | 17:47184307 | AAAACCTTTTCCTTG[C/T]CAATCTCTTAATATA | 996 |
rs73308992 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | CDC27 | GRCh38.p7 | 17:47123223 | ATTAACTTTCATTTA[C/G]AGTGATTTTAAATTG | 996 |
rs73310804 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | CDC27 | GRCh38.p7 | 17:47131645 | AACATAATGTACATA[C/T]CTTTTCTCCTGTTAA | 996 |
rs73310808 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | CDC27 | GRCh38.p7 | 17:47135862 | AGAACTGAGTTCCTG[A/G]CCGGGTATGGTGGCT | 996 |
rs73310810 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136242 | CAAGTTGATTGTTAC[A/G]TTGGTCAGCAAAAGC | 996 |
rs73310814 | snp | C/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47136783 | TATCCAATAAGTGAA[C/T]TATGCTATTCCTTTC | 996 |
rs73317687 | snp | A/G | 0.0460142 | 0.144533 | intron-variant | CDC27 | GRCh38.p7 | 17:47163048 | CTCTAAATTTAGATC[A/G]AAGTTTTTATTAAAA | 996 |
rs73319503 | snp | A/G | 0.329018 | 0.237184 | stop-gained, intron-variant, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47169996 | CATCATGGCTTTTCT[A/G]CTTATTAAACACTCC | 996 |
rs73319510 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | CDC27 | GRCh38.p7 | 17:47179260 | GTCTTTCTCCAAATA[C/T]AGAAACTGCTACTAG | 996 |
rs73319513 | snp | C/G | 0.0333695 | 0.124785 | intron-variant | CDC27 | GRCh38.p7 | 17:47184767 | TCTTGTGCCGGGATT[C/G]GGGGGAAGAACAGAT | 996 |
rs73319515 | snp | G/T | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47189244 | GGCCCGGCCAGCCCC[G/T]GCTCATTTAAACTCA | 996 |
rs73985136 | snp | C/G | 0.5 | 0 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47117961 | TGGATTTTCCATATC[C/G]TTTAATGAATTGCAA | 996 |
rs74348171 | snp | A/G | 0.498227 | 0.0297225 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137153 | TCATTACCACTTACC[A/G]TGCATTATAATGTCT | 996 |
rs74390782 | snp | A/G | 0.49987 | 0.00805967 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137324 | CAATATCATGTTCCC[A/G]TTGCAGACTGAAACA | 996 |
rs74398156 | snp | A/C/T | 0.000952405 | 0.0218013 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47158287 | ATTCTGATCCTTTGG[A/C/T]AAGCCGATCTGTCTT | 996 |
rs74409560 | snp | A/C | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47173373 | TTAGTGCTGCAGCTA[A/C]AAAAAAAAAAAAAGA | 996 |
rs74412760 | snp | C/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47131817 | AGGACCACAGGTGTG[C/T]ACCACCATGCCAGGC | 996 |
rs74412898 | snp | C/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47135496 | GCACAACATATCTGC[C/T]TTATTTGAGTGGCTT | 996 |
rs74479251 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136444 | CCGTATCTGACAAAA[A/T]AACTACCACAGAGTT | 996 |
rs74480903 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136259 | TGGTCAGCAAAAGCT[A/G]GCACTATTTTTTTGG | 996 |
rs74492629 | snp | A/C | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47136867 | GCAACAAAGTAACAA[A/C]ACTAAACAAACAAAA | 996 |
rs74496366 | snp | A/C/G/T | 0.000743161 | 0.0192623 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47141998 | AAATAACCTTTCCCC[A/C/G/T]TTTCACGAAGAAGGC | 996 |
rs74501757 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136537 | ATAAATGTCAACAGT[A/G]AGTATGGTGTTGAGG | 996 |
rs74596521 | in-del | -/AACA | | | intron-variant | CDC27 | GRCh38.p7 | 17:47135709 | ATCCTCCTTTAAACA[-/AACA]CAATTTTTGATATGG | 996 |
rs74608601 | snp | A/G | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47131909 | CTCCTGACCTTAAGT[A/G]ATTCACCTGCCTCGG | 996 |
rs74628496 | snp | A/G | 0.5 | 0 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157050 | AATTACAGCTGAATC[A/G]ATATAAGACACTGAG | 996 |
rs74641214 | snp | A/T | 0.0414363 | 0.137845 | intron-variant | CDC27 | GRCh38.p7 | 17:47141493 | ATAAAACATATTCGA[A/T]GTCAAAAATTCACCC | 996 |
rs74648663 | snp | C/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47137068 | TAACCAAATTCATGA[C/T]AATAAAGAGCTATCT | 996 |
rs74710570 | snp | A/C/G | 0.00296233 | 0.0383722 | synonymous-codon, missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47154702 | TCCGGTGGATGGCAC[A/C/G]TCAATTACAGGAGGT | 996 |
rs74720779 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47189218 | CCTCAGGCCCCCCCT[A/G]TAGCGGCTCCGGCCC | 996 |
rs74725442 | snp | C/T | 0 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47136818 | TTCCCAAGCACTTTT[C/T]ATCCCAATCACCATT | 996 |
rs74727415 | snp | C/T | 0.444444 | 0.157135 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47142384 | GTTTTACTTTTTGTT[C/T]TTCTGTTTGGGATTT | 996 |
rs74759780 | snp | A/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47131842 | CCAGGCTAATTTTTA[A/T]ATTTTTTTTGTAGAG | 996 |
rs74771330 | snp | A/G | 0.5 | 0 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47141910 | GCACAGTACCCAACC[A/G]GTATTGTAGTGGTGA | 996 |
rs74809933 | snp | C/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47160246 | TTTTTTTTTTTTTTT[C/T]CCTGAGAGTCTGGCC | 996 |
rs74851674 | snp | C/T | 0 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47136803 | CTATTCCTTTCCAAT[C/T]TCCCAAGCACTTTTC | 996 |
rs74875648 | snp | A/C | 0 | 0 | stop-gained, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47158250 | CAGAGGAAAGGATTT[A/C]AACTAAGGCTCTTTT | 996 |
rs74885171 | snp | G/T | | | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47138740 | TTTGGTTAACATACC[G/T]CTGGCGAATTTTTAT | 996 |
rs74885629 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47170395 | TAGAGACAGGGTCTC[A/T]CTATGTTGACCAGGC | 996 |
rs74905672 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CDC27 | GRCh38.p7 | 17:47152810 | TGAAACTTTGTGTTA[C/T]TTCCAAAACATTACA | 996 |
rs74912710 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | CDC27 | GRCh38.p7 | 17:47177271 | AAAAAAAATGTTTAA[A/G]AAGTACTAATATTAA | 996 |
rs74925848 | snp | G/T | 0.5 | 0 | CDC27 | 17 | allele_origin=G(somatic)/T(germline) | 17:47157038 | AGTATCAGGTGAAAT[G/T]ACAGCTGAATCAATA | 996 |
rs75008516 | snp | G/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47135729 | TTTTGATATGGTTAA[G/T]TTTTTTAAGAATGCA | 996 |
rs75012977 | snp | A/G | 0.000195606 | 0.0098876 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47142254 | TTTTTGTAGATTAAA[A/G]GCCTGAATCTGAGGT | 996 |
rs75028330 | snp | G/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47178820 | TTTCCGTTTTTTTTT[G/T]GAGACGGAGTCTCGC | 996 |
rs75029365 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136216 | GCTATCGGAAGAGAC[A/G]GCAGCATTGGCAAGT | 996 |
rs75040309 | snp | C/G | 0.5 | 0 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47142428 | CATTTTTAATTTTTT[C/G]CTATTCTCCTGTAAA | 996 |
rs75066641 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136540 | AATGTCAACAGTAAG[G/T]ATGGTGTTGAGGCAG | 996 |
rs75122004 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | CDC27 | GRCh38.p7 | 17:47174656 | ACATAGAAAGATTTC[C/T]AGAATGTACTGCTAA | 996 |
rs75133586 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47181641 | CCATATAGCAGCCTG[C/G]AAATGGAGGAAAAAG | 996 |
rs75160620 | snp | G/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47121757 | TTTTTTTTTTTTTTT[G/T]AGACAGAGTTTCATT | 996 |
rs75175938 | snp | A/G | 0.5 | 0 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157266 | CGTAAGAACTGTCTC[A/G]GGCTGTCTGTGAGAT | 996 |
rs75184508 | snp | G/T | 0.5 | 0 | CDC27 | 17 | allele_origin=G(somatic)/T(germline) | 17:47157037 | CAGTATCAGGTGAAA[G/T]TACAGCTGAATCAAT | 996 |
rs75187507 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47159108 | GATTTAAATGCTTTA[A/T]ATATAGCATAAATGA | 996 |
rs75204938 | snp | A/C | | | stop-gained, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157120 | AAATTCAATCTGTTT[A/C]ATTCCTGAAACAGAA | 996 |
rs75239352 | snp | A/C/G | 0.147868 | 0.228187 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47170015 | ATTAAACACTCCACC[A/C/G]GATAAGATTTGTTCC | 996 |
rs75241171 | snp | A/G | 0.5 | 0 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157068 | ATAAGACACTGAGGA[A/G]TCTGTATTCAAGGAG | 996 |
rs75257202 | snp | A/G | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47135490 | AAAAAAGCACAACAT[A/G]TCTGCTTTATTTGAG | 996 |
rs75266218 | snp | A/G | 0 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47136743 | AAAGCAGCAACTAGT[A/G]AATTTTTTCAATTTT | 996 |
rs75284424 | snp | C/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47135512 | TTATTTGAGTGGCTT[C/T]ATATATCATTATACT | 996 |
rs75353677 | snp | A/T | 0.497306 | 0.0366003 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157341 | GTTGCTAAAGTTCTG[A/T]AAAGATGTGAATTTA | 996 |
rs75372133 | snp | C/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47133112 | ACAAATATACATATA[C/T]ATATATATATATATA | 996 |
rs75382094 | snp | A/C | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47136872 | AAAGTAACAAAACTA[A/C]ACAAACAAAAAACAA | 996 |
rs75400273 | snp | C/T | 0.217551 | 0.247885 | intron-variant | CDC27 | GRCh38.p7 | 17:47165665 | CAAAGAGTTTTAATT[C/T]TGATAAAATTTATCA | 996 |
rs75409257 | snp | A/G | 0 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47136819 | TCCCAAGCACTTTTC[A/G]TCCCAATCACCATTT | 996 |
rs75418255 | in-del | -/T | 0.318415 | 0.240457 | intron-variant | CDC27 | GRCh38.p7 | 17:47175174 | AAGGTCTTTTGAGTG[-/T]TAAGTCCAAAATAAT | 996 |
rs75494554 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136337 | ATTAACAACATATTC[A/G]CAAATCAAAAAATGT | 996 |
rs75549443 | snp | C/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47136355 | AATCAAAAAATGTTT[C/T]AGTAATATAATGCTT | 996 |
rs75580209 | snp | C/T | 1.73072e-05 | 0.00294165 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47142271 | CCTGAATCTGAGGTG[C/T]GATTGTGGATATTTT | 996 |
rs75637741 | snp | A/G | 0.00171818 | 0.0292599 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137257 | CCTAATAGAGTATAG[A/G]CATAAGCGTAATTTG | 996 |
rs75655423 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136715 | GTAACTCAATAAACC[A/G]GAACACTGTCAAAAA | 996 |
rs75661039 | snp | A/T | 0.499997 | 0.00130509 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137238 | AGTTAAGACAAACTC[A/T]TGCCCTAATAGAGTA | 996 |
rs75729335 | snp | G/T | | | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47141860 | ATACTTACTTGCATG[G/T]ACTCTGAAAGTTCAA | 996 |
rs75731161 | snp | A/G | 0.000263752 | 0.0114807 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137216 | CTAATGCTTTGTCCA[A/G]TTCTTCAGTTAAGAC | 996 |
rs75841851 | snp | A/T | 0 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47135788 | ACACATTTAAAAAAA[A/T]AACAACACAAGGATC | 996 |
rs75843203 | snp | A/G | 0.00914312 | 0.0669923 | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47189996 | AAAGTTTAAAATGGA[A/G]TTTGAAGGATGGGTA | 996 |
rs75856059 | snp | G/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47145910 | CTCAAAAAAAAAAAA[G/T]TCAACCATGTGATTA | 996 |
rs75894512 | snp | A/G | 0.00252232 | 0.0354232 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47141944 | GGTAGATGGCTCAAA[A/G]TATTTATAGCTTCTT | 996 |
rs75901699 | snp | C/T | 0.499137 | 0.0207489 | intron-variant | CDC27 | GRCh38.p7 | 17:47131865 | TTGTAGAGATGGGGT[C/T]TCGCTATGTTGCCCA | 996 |
rs75932008 | snp | A/T | | | splice-donor-variant | CDC27 | GRCh38.p7 | 17:47143881 | AGAAATCTTTAAATT[A/T]CCTTGGTTGTGGAGC | 996 |
rs75964898 | snp | A/G | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47131841 | GCCAGGCTAATTTTT[A/G]AATTTTTTTTGTAGA | 996 |
rs75967626 | snp | C/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47133052 | ACACACACACACACA[C/T]ACATACATATACACA | 996 |
rs75978496 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136488 | TATACCTTATCTTGA[C/T]ATTTAAACTATTAAG | 996 |
rs75990396 | snp | C/G | 0.0520463 | 0.15269 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157279 | TCAGGCTGTCTGTGA[C/G]ATAAACTATGATTAG | 996 |
rs76000968 | snp | C/T | 0.21303 | 0.247251 | intron-variant | CDC27 | GRCh38.p7 | 17:47124322 | GGAGTCTCGCTCTGT[C/T]GCCCAGGCTGGAGTG | 996 |
rs76012916 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CDC27 | GRCh38.p7 | 17:47135383 | GGATGGTTTATATTA[C/T]GGAGACTTCTCATGG | 996 |
rs76158881 | snp | A/G | | | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47154753 | ATAGGATCCATCTCC[A/G]GGACTTGGGGTTTCT | 996 |
rs76179380 | snp | G/T | 0.00180174 | 0.0299603 | intron-variant | CDC27 | GRCh38.p7 | 17:47123844 | AAAATGTCATTATTT[G/T]CTATGAAAGTCACTG | 996 |
rs76190542 | snp | A/C | | | stop-gained, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47158217 | CTACCTATTTCACAT[A/C]ATGATTCAAAGGGAG | 996 |
rs76209083 | snp | C/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47160248 | TTTTTTTTTTTTTTC[C/T]TGAGAGTCTGGCCCT | 996 |
rs76210350 | snp | A/T | 0.0185938 | 0.0946107 | intron-variant | CDC27 | GRCh38.p7 | 17:47126065 | TCTTACTTTTACCTT[A/T]AAGACTTAAGATTTA | 996 |
rs76213328 | snp | G/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47128787 | TTTTTTTTTTTTTTT[G/T]TGAGATGAAGTCTCG | 996 |
rs76217022 | snp | G/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47135845 | CAACACAAGTCTTAT[G/T]AAGAACTGAGTTCCT | 996 |
rs76250140 | snp | A/G | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47136917 | AAAGTTTGGTAGAAG[A/G]CTGAAACTGTTGAGT | 996 |
rs76284911 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136253 | TTACATTGGTCAGCA[A/G]AAGCTAGCACTATTT | 996 |
rs76285115 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47137100 | ACAAGAAAAATTAGT[A/G]AGTACCAGCACCATC | 996 |
rs76316064 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136714 | AGTAACTCAATAAAC[C/T]AGAACACTGTCAAAA | 996 |
rs76328350 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136388 | GATTTAGAAGCAAAT[A/C]GAATGATACAACTCA | 996 |
rs76334365 | snp | A/G | 0.5 | 0 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47142255 | TTTTGTAGATTAAAG[A/G]CCTGAATCTGAGGTG | 996 |
rs76359747 | snp | G/T | 0.0112993 | 0.0743099 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157260 | TGTTTCCGTAAGAAC[G/T]GTCTCAGGCTGTCTG | 996 |
rs76364895 | in-del | -/A | | | intron-variant | CDC27 | GRCh38.p7 | 17:47186761 | ATTAAAACTTTAAAG[-/A]AAAAAAAATGCAGAA | 996 |
rs76368015 | snp | G/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47136500 | TGATATTTAAACTAT[G/T]AAGTCAGTCCAGAAA | 996 |
rs76383230 | snp | A/G | | | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47154743 | AGTTTTGTAAATAGG[A/G]TCCATCTCCAGGACT | 996 |
rs76387305 | snp | G/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47120161 | TCTATCATCTCTGAA[G/T]GTTAAAGGTGATCCC | 996 |
rs76389918 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47170397 | GAGACAGGGTCTCAC[A/T]ATGTTGACCAGGCTG | 996 |
rs76419572 | snp | A/G | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47131802 | GCCTCCCAAGTAGCC[A/G]GGACCACAGGTGTGC | 996 |
rs76437119 | snp | C/G | 0.153055 | 0.230438 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47151828 | GTGGACCAGAACTTT[C/G]TGTTTGTGCAAGAAT | 996 |
rs76456882 | snp | C/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47131912 | CTGACCTTAAGTGAT[C/T]CACCTGCCTCGGCCT | 996 |
rs76466763 | snp | C/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47131801 | AGCCTCCCAAGTAGC[C/T]AGGACCACAGGTGTG | 996 |
rs76485121 | snp | C/G | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47136397 | GCAAATAGAATGATA[C/G]AACTCAACTGCTATA | 996 |
rs76499169 | snp | A/C | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47137087 | AAAGAGCTATCTAAC[A/C]AGAAAAATTAGTAAG | 996 |
rs76505635 | snp | G/T | 0.217551 | 0.247885 | intron-variant | CDC27 | GRCh38.p7 | 17:47165611 | TATTTTCTCCCAGGC[G/T]GTGACTTGTGTGTAT | 996 |
rs76561718 | snp | A/G | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47135685 | TAGTAAAAGCTTGCC[A/G]ATCTGAATAATCCTC | 996 |
rs76564584 | snp | C/T | 0.00716266 | 0.059414 | utr-variant-3-prime, downstream-variant-500B | CDC27 | GRCh38.p7 | 17:47117867 | TGTTTTTCTGTGCCT[C/T]CTTATTAAAATACAG | 996 |
rs76575872 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136959 | GTATTCTATTATCAT[G/T]AGTTAATTTAAGAGT | 996 |
rs76587210 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47132964 | TTTTTTGTAGAGATG[C/G]GGTTTTGCCATGTTG | 996 |
rs76598828 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136518 | GTCAGTCCAGAAAAA[C/T]ACAATAAATGTCAAC | 996 |
rs76621174 | snp | C/T | 0.190833 | 0.242898 | intron-variant | CDC27 | GRCh38.p7 | 17:47132654 | CACTGCATCCTTGAA[C/T]TTCCGGGTTCAAAGA | 996 |
rs76624491 | snp | C/T | | | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157232 | ATAAGACACTTACAA[C/T]TGTGTCCTGGGGTGT | 996 |
rs76637433 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136317 | TGCAAAATGAGACAT[A/G]ATCCATTAACAACAT | 996 |
rs76673485 | snp | A/G | 0.499137 | 0.0207489 | intron-variant | CDC27 | GRCh38.p7 | 17:47131868 | TAGAGATGGGGTCTC[A/G]CTATGTTGCCCAGGC | 996 |
rs76715333 | snp | C/T | 0.5 | 0 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47138865 | ATAATTCTCAATCCT[C/T]CTAACCTCTGAGAAT | 996 |
rs76718177 | in-del | -/AT | | | intron-variant | CDC27 | GRCh38.p7 | 17:47135729 | TTTGATATGGTTAAG[-/AT]TTTTTTAAGAATGCA | 996 |
rs76772202 | snp | A/C/G/T | 4.99275e-05 | 0.00499616 | intron-variant | CDC27 | GRCh38.p7 | 17:47138736 | GTATTTTGGTTAACA[A/C/G/T]ACCTCTGGCGAATTT | 996 |
rs76774563 | snp | A/C | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47154088 | AGCGAGACCCTGTCT[A/C]AAAAAAAAAAAAAAA | 996 |
rs76782714 | snp | G/T | 0.469276 | 0.120074 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47171969 | TGCATTGCGGTGTAG[G/T]ACAACTGTGTCCTTT | 996 |
rs76836152 | snp | A/G | 0 | 0 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47138806 | GCAACATCTTTTTGA[A/G]GATGCCAAAGTGTTG | 996 |
rs76836956 | snp | A/G/T | 0.000223023 | 0.0105577 | missense, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47143937 | TCTTCGAGGCAGTGC[A/G/T]TTTGGGGGAGATGTA | 996 |
rs76894625 | snp | A/C/T | 1.72943e-05 | 0.00294055 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47142269 | GGCCTGAATCTGAGG[A/C/T]GTGATTGTGGATATT | 996 |
rs76926116 | snp | C/T | 0.499997 | 0.00128859 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137239 | GTTAAGACAAACTCA[C/T]GCCCTAATAGAGTAT | 996 |
rs76954024 | in-del | -/TAGT | 0.318415 | 0.240457 | intron-variant | CDC27 | GRCh38.p7 | 17:47174602 | AAATCAATCGTGTAC[-/TAGT]TAAATTATGCTATGT | 996 |
rs76957166 | snp | A/G | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47131835 | CACCATGCCAGGCTA[A/G]TTTTTAAATTTTTTT | 996 |
rs76989110 | snp | C/T | 0.444444 | 0.157135 | intron-variant | CDC27 | GRCh38.p7 | 17:47136267 | AAAAGCTAGCACTAT[C/T]TTTTTGGCCATCTTT | 996 |
rs76989964 | snp | A/G | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47131794 | GTGCTTCAGCCTCCC[A/G]AGTAGCCAGGACCAC | 996 |
rs76995821 | snp | C/T | 0.5 | 0 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47141917 | ACCCAACCAGTATTG[C/T]AGTGGTGAGAAGGTA | 996 |
rs77008868 | snp | C/T | 0 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47136816 | ATTTCCCAAGCACTT[C/T]TCATCCCAATCACCA | 996 |
rs77025218 | snp | G/T | 0.0236746 | 0.106192 | downstream-variant-500B | CDC27 | GRCh38.p7 | 17:47117443 | GTCTGAATAAAACCC[G/T]TCAGCTCTTTGTACT | 996 |
rs77034041 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47158306 | CCGATCTGTCTTGCT[A/G]TGGAGAGAAACAAGT | 996 |
rs77095606 | snp | A/C | | | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157111 | GAAGATTCTAAATTC[A/C]ATCTGTTTAATTCCT | 996 |
rs77104082 | snp | A/G | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47131818 | GGACCACAGGTGTGC[A/G]CCACCATGCCAGGCT | 996 |
rs77109718 | snp | A/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47131914 | GACCTTAAGTGATTC[A/T]CCTGCCTCGGCCTCC | 996 |
rs77113847 | snp | A/G | | | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47169985 | AGTAACAATATCATC[A/G]TGGCTTTTCTGCTTA | 996 |
rs77144621 | snp | A/G | 0.184203 | 0.241186 | intron-variant | CDC27 | GRCh38.p7 | 17:47168245 | GGGAGGTTGCGGGGT[A/G]GGGATGAAAAGTCCC | 996 |
rs77146736 | snp | C/T | 0 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47136840 | ATCACCATTTCGGTG[C/T]TCGAAGAAAAAGCAA | 996 |
rs77277197 | snp | C/G | 2.36214e-05 | 0.00343659 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47154780 | TTCTAATGGCAAAAT[C/G]CCAAAACTGAGAAGA | 996 |
rs77283122 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136684 | CTAAATAAAAGGGTA[C/T]ACTAAGTTCTTAATA | 996 |
rs77291892 | snp | A/G | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47131830 | TGCACCACCATGCCA[A/G]GCTAATTTTTAAATT | 996 |
rs77309811 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47183308 | TACATCTAAATTATA[C/T]TAAGTGATTAATATG | 996 |
rs77320707 | snp | G/T | | | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47158254 | GGAAAGGATTTAAAC[G/T]AAGGCTCTTTTGGTA | 996 |
rs77358063 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136184 | AACTGAGTTCTTAAA[A/G]TATTACAGAGAACAT | 996 |
rs77397554 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136534 | ACAATAAATGTCAAC[A/G]GTAAGTATGGTGTTG | 996 |
rs77428610 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136708 | CTTAATAGTAACTCA[A/G]TAAACCAGAACACTG | 996 |
rs77440865 | snp | C/T | 0.000642956 | 0.0179183 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47143920 | GTAAAGAGTCGTGAA[C/T]TTCTTCGAGGCAGTG | 996 |
rs77445213 | snp | C/T | 0 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47136832 | TCATCCCAATCACCA[C/T]TTCGGTGTTCGAAGA | 996 |
rs77467652 | snp | A/C/G/T | 1.68465e-05 | 0.00290223 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47158232 | AATGATTCAAAGGGA[A/C/G/T]ACCAGAGGAAAGGAT | 996 |
rs77510601 | snp | C/T | 0.5 | 0 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47142277 | TCTGAGGTGTGATTG[C/T]GGATATTTTCCCTTC | 996 |
rs77532061 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47137024 | TAGTTAGAAGTTATT[C/G]ACCAGTATGTACCAT | 996 |
rs77550690 | snp | G/T | 0.5 | 0 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47142348 | TCATTTATGTTAGGT[G/T]GAGTTATTCCTCCTT | 996 |
rs77556970 | snp | C/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47131904 | TCCAACTCCTGACCT[C/T]AAGTGATTCACCTGC | 996 |
rs77600149 | snp | C/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47123403 | TACTTTTTTTTCTAC[C/T]TTTTTTTTTTTTTTT | 996 |
rs77609498 | snp | C/G | 0.000180567 | 0.00950006 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47142357 | TTAGGTTGAGTTATT[C/G]CTCCTTTATTAGTTT | 996 |
rs77618938 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47170396 | AGAGACAGGGTCTCA[A/C]TATGTTGACCAGGCT | 996 |
rs77651484 | snp | C/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47131825 | AGGTGTGCACCACCA[C/T]GCCAGGCTAATTTTT | 996 |
rs77657363 | snp | A/C | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47135513 | TATTTGAGTGGCTTT[A/C]TATATCATTATACTT | 996 |
rs77659049 | snp | C/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47137007 | TTCATAAGAAAACAT[C/T]TTAGTTAGAAGTTAT | 996 |
rs77673482 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136215 | AGCTATCGGAAGAGA[A/C]AGCAGCATTGGCAAG | 996 |
rs77685276 | snp | A/G | 0.499979 | 0.00324668 | stop-gained, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137192 | CTCTGATAGCATTTC[A/G]AAAACAAGCTAATGC | 996 |
rs77714652 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | CDC27 | GRCh38.p7 | 17:47184711 | ATACTGCTTCCATCC[C/T]GCTTTGCTCAATCAA | 996 |
rs77718787 | snp | A/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47136302 | CAATGTAACTACTAC[A/T]GCAAAATGAGACATA | 996 |
rs77719517 | snp | C/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47131807 | CCAAGTAGCCAGGAC[C/T]ACAGGTGTGCACCAC | 996 |
rs77722052 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | CDC27 | GRCh38.p7 | 17:47137625 | GGTTGAATAATGTGA[C/T]TCTACCTTCTTGTTT | 996 |
rs77739281 | snp | A/C | 0.000319415 | 0.0126335 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47143952 | GTTTGGGGGAGATGT[A/C]ATAGTGGGGCTCAAT | 996 |
rs77807516 | snp | C/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47131908 | ACTCCTGACCTTAAG[C/T]GATTCACCTGCCTCG | 996 |
rs77819908 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136650 | TACACAAGTACAAAA[A/G]AGTAAAATAGAGATA | 996 |
rs77870608 | snp | A/G | | | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47142021 | AAGAAGGCTCATCAA[A/G]CCTTCTAGGAGAAAA | 996 |
rs77871715 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47137363 | CAGCACACCAGGCCT[C/T]AAAAAAATGGGAACA | 996 |
rs77891297 | snp | G/T | | | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47138803 | AGAGCAACATCTTTT[G/T]GAAGATGCCAAAGTG | 996 |
rs77900013 | snp | C/G/T | 0.00288171 | 0.0378491 | splice-acceptor-variant | CDC27 | GRCh38.p7 | 17:47157125 | CAATCTGTTTAATTC[C/G/T]TGAAACAGAAAATTT | 996 |
rs77904232 | snp | A/T | | | splice-acceptor-variant | CDC27 | GRCh38.p7 | 17:47158305 | GCCGATCTGTCTTGC[A/T]GTGGAGAGAAACAAG | 996 |
rs77979510 | snp | A/G | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47136349 | TTCACAAATCAAAAA[A/G]TGTTTTAGTAATATA | 996 |
rs77981119 | snp | C/T | 0 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47123420 | TTTTTTTTTTTTTTT[C/T]TTCTTTCTGAGACAG | 996 |
rs78002830 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47137026 | GTTAGAAGTTATTGA[C/G]CAGTATGTACCATCC | 996 |
rs78019952 | snp | G/T | | | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47154708 | GGATGGCACATCAAT[G/T]ACAGGAGGTGTATTA | 996 |
rs78043820 | snp | C/T | | | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157115 | ATTCTAAATTCAATC[C/T]GTTTAATTCCTGAAA | 996 |
rs78046362 | snp | A/C | 0.375 | 0.216506 | intron-variant | CDC27 | GRCh38.p7 | 17:47136824 | AGCACTTTTCATCCC[A/C]ATCACCATTTCGGTG | 996 |
rs78061427 | snp | A/G | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47131855 | TAAATTTTTTTTGTA[A/G]AGATGGGGTCTCGCT | 996 |
rs78063747 | snp | C/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47131783 | AAGTGATCCTTGTGC[C/T]TCAGCCTCCCAAGTA | 996 |
rs78070990 | snp | C/G | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47143332 | TGCAAATGATAACAT[C/G]TGACATAACCATAGT | 996 |
rs78072949 | snp | A/G | 0.0212764 | 0.100923 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157064 | CAATATAAGACACTG[A/G]GGAATCTGTATTCAA | 996 |
rs78080061 | snp | A/C | 0.5 | 0 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47142320 | AGAGTCCAATTTTGT[A/C]ATTTCCAGGCTATCA | 996 |
rs78095535 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | CDC27 | GRCh38.p7 | 17:47180479 | CTACTTCCAAGCATT[A/G]CTCTTTGTCCTTTTG | 996 |
rs78096182 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47132093 | AAGGGCAATTCTGTG[A/T]TTTTTTATGCTAAGC | 996 |
rs78096575 | snp | A/G | 0.185788 | 0.241613 | intron-variant | CDC27 | GRCh38.p7 | 17:47148806 | AATTCTTGGCCAGGC[A/G]TAGTGGCTCATGCCT | 996 |
rs78108688 | snp | C/T | 0.0849745 | 0.187794 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157291 | TGAGATAAACTATGA[C/T]TAGGTACTTGTGTTG | 996 |
rs78111769 | snp | C/T | | | splice-acceptor-variant, intron-variant | CDC27 | GRCh38.p7 | 17:47170043 | TCCCCTTCTGCAAGC[C/T]TTTAAAATACAAATT | 996 |
rs78120523 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | CDC27 | GRCh38.p7 | 17:47164805 | CTGAGCGACAGAGCG[C/T]AAGATTCCATTTCAA | 996 |
rs78165862 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47175176 | AGGTCTTTTGAGTGT[A/T]AGTCCAAAATAATTA | 996 |
rs78168854 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136221 | CGGAAGAGACAGCAG[C/T]ATTGGCAAGTTGATT | 996 |
rs78297144 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136314 | TACTGCAAAATGAGA[C/T]ATAATCCATTAACAA | 996 |
rs78317389 | snp | A/C | 0 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47173374 | TAGTGCTGCAGCTAC[A/C]AAAAAAAAAAAAGAA | 996 |
rs78332669 | snp | A/G | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47137064 | TAAGTAACCAAATTC[A/G]TGATAATAAAGAGCT | 996 |
rs78349431 | snp | C/G | | | splice-donor-variant | CDC27 | GRCh38.p7 | 17:47154671 | TTTACATGGAAAATA[C/G]CTTTTTTGAAGGGGC | 996 |
rs78395997 | snp | A/C | 0.451745 | 0.147645 | CDC27 | 17 | allele_origin=A(germline)/C(somatic) | 17:47157344 | GCTAAAGTTCTGTAA[A/C]GATGTGAATTTAAAT | 996 |
rs78399615 | snp | C/T | 0.5 | 0 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47142426 | TTCATTTTTAATTTT[C/T]TGCTATTCTCCTGTA | 996 |
rs78493795 | snp | G/T | 0.499794 | 0.010153 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157054 | ACAGCTGAATCAATA[G/T]AAGACACTGAGGAAT | 996 |
rs78501339 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47189256 | CCCTGCTCATTTAAA[C/G]TCACCAGCGACCGTT | 996 |
rs78505871 | snp | C/T | 0.141934 | 0.225437 | intron-variant | CDC27 | GRCh38.p7 | 17:47174947 | GGCAACAGCGAAACT[C/T]GGTCGAAACAGGACT | 996 |
rs78578806 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47183305 | CAGTACATCTAAATT[A/G]TATTAAGTGATTAAT | 996 |
rs78639269 | snp | C/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47131806 | CCCAAGTAGCCAGGA[C/T]CACAGGTGTGCACCA | 996 |
rs78801909 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136389 | ATTTAGAAGCAAATA[A/G]AATGATACAACTCAA | 996 |
rs78805567 | snp | A/G | 0 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47136737 | TGTCAAAAAGCAGCA[A/G]CTAGTAAATTTTTTC | 996 |
rs78831743 | snp | A/G | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47136514 | TTAAGTCAGTCCAGA[A/G]AAATACAATAAATGT | 996 |
rs78879455 | snp | A/G | 0.218151 | 0.247963 | intron-variant | CDC27 | GRCh38.p7 | 17:47145879 | TGCAGCCTGGGCGAC[A/G]ACAGCGAAACTCTGT | 996 |
rs78943400 | snp | A/G | 0.191461 | 0.24305 | intron-variant | CDC27 | GRCh38.p7 | 17:47166540 | TTACCAATCTTTCCA[A/G]GGACCAGCTTTGGTT | 996 |
rs78962518 | snp | A/G | 0 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47136801 | TGCTATTCCTTTCCA[A/G]TTTCCCAAGCACTTT | 996 |
rs78974535 | snp | C/T | 0.499137 | 0.0207489 | intron-variant | CDC27 | GRCh38.p7 | 17:47131870 | GAGATGGGGTCTCGC[C/T]ATGTTGCCCAGGCTG | 996 |
rs79048040 | snp | A/G | 0.0879971 | 0.190408 | intron-variant | CDC27 | GRCh38.p7 | 17:47182889 | TCTCCAGCCTATCAC[A/G]GTGGTGTGAGCCTTT | 996 |
rs79107865 | snp | C/T | 0.5 | 0 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47142301 | TCCCTTCTGAAATGA[C/T]GGAAGAGTCCAATTT | 996 |
rs79161705 | snp | C/G | 0 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47135611 | GCTATCTATTTTGTA[C/G]TTAGAATAAAGTTGC | 996 |
rs79201963 | snp | C/T | | | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47141873 | TGTACTCTGAAAGTT[C/T]AAAATAGGCCCTTCC | 996 |
rs79223295 | snp | A/T | 0.444444 | 0.157135 | intron-variant | CDC27 | GRCh38.p7 | 17:47129284 | ATTAACAGCTTGGAA[A/T]AATGTCTCAGATCAA | 996 |
rs79255400 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136456 | AAAAAACTACCACAG[A/G]GTTATGGCTTCAGAA | 996 |
rs79259606 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136952 | GGATCTGGTATTCTA[C/T]TATCATTAGTTAATT | 996 |
rs79260965 | snp | G/T | | | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137240 | TTAAGACAAACTCAT[G/T]CCCTAATAGAGTATA | 996 |
rs79285536 | snp | G/T | 0.5 | 0 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137226 | GTCCAATTCTTCAGT[G/T]AAGACAAACTCATGC | 996 |
rs79328205 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47176296 | ATTTCATTATTCATT[A/C]TGTTGTTCAGAGTCA | 996 |
rs79329544 | snp | A/G | 0 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47135610 | GGCTATCTATTTTGT[A/G]CTTAGAATAAAGTTG | 996 |
rs79348596 | snp | A/T | | | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47170027 | ACCAGATAAGATTTG[A/T]TCCCCTTCTGCAAGC | 996 |
rs79400513 | snp | C/T | 0.217551 | 0.247885 | intron-variant | CDC27 | GRCh38.p7 | 17:47134018 | AGCCTACCAAAGTGC[C/T]GGGATTGCAGGTGTG | 996 |
rs79415072 | snp | A/G | | | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47141889 | AAAATAGGCCCTTCC[A/G]ATTTGGCACAGTACC | 996 |
rs79429845 | snp | A/G | 0.0625067 | 0.165367 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47154713 | GCACATCAATTACAG[A/G]AGGTGTATTAGTGTA | 996 |
rs79431868 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47168936 | TGACAACAGATAACA[A/T]TTACACATGTGAAGC | 996 |
rs79452779 | snp | A/C | | | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47154785 | ATGGCAAAATCCCAA[A/C]ACTGAGAAGAGGTTG | 996 |
rs79454290 | snp | C/T | | | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47143951 | CGTTTGGGGGAGATG[C/T]AATAGTGGGGCTCAA | 996 |
rs79454648 | snp | A/G | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47131804 | CTCCCAAGTAGCCAG[A/G]ACCACAGGTGTGCAC | 996 |
rs79468554 | snp | A/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47131829 | GTGCACCACCATGCC[A/T]GGCTAATTTTTAAAT | 996 |
rs79479079 | snp | A/G | | | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47154747 | TTGTAAATAGGATCC[A/G]TCTCCAGGACTTGGG | 996 |
rs79487913 | snp | C/G | | | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47141930 | TGTAGTGGTGAGAAG[C/G]TAGATGGCTCAAAAT | 996 |
rs79511188 | snp | A/C | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47131926 | TTCACCTGCCTCGGC[A/C]TCCTAAAGCGCTGGC | 996 |
rs79580708 | snp | A/C/T | 8.55287e-05 | 0.00653899 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47189217 | GCCTCAGGCCCCCCC[A/C/T]GTAGCGGCTCCGGCC | 996 |
rs79590719 | snp | A/G | 0.109831 | 0.207009 | intron-variant | CDC27 | GRCh38.p7 | 17:47137133 | TACGACTTTGTCTTT[A/G]TACTTCATTACCACT | 996 |
rs79621013 | snp | A/C | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47135710 | ATCCTCCTTTAAACA[A/C]AATTTTTGATATGGT | 996 |
rs79624051 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136519 | TCAGTCCAGAAAAAT[A/G]CAATAAATGTCAACA | 996 |
rs79777815 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136254 | TACATTGGTCAGCAA[A/T]AGCTAGCACTATTTT | 996 |
rs79778866 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136489 | ATACCTTATCTTGAT[A/G]TTTAAACTATTAAGT | 996 |
rs79803437 | snp | A/T | 0 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47172530 | ACCAGATTGAAAAAA[A/T]TCCACTTGTTTTGCT | 996 |
rs79810536 | snp | C/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47131813 | AGCCAGGACCACAGG[C/T]GTGCACCACCATGCC | 996 |
rs79860768 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47132851 | CACGGCTCACTGCAG[A/C]CTTGACCTCCCAGGC | 996 |
rs79861125 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136427 | AATAACCCCAAAGAT[A/C]ACCGTATCTGACAAA | 996 |
rs79881964 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47137099 | AACAAGAAAAATTAG[C/T]AAGTACCAGCACCAT | 996 |
rs79909660 | snp | A/G | 0.00131355 | 0.0255939 | intron-variant | CDC27 | GRCh38.p7 | 17:47132248 | ATTAATGTTTAGAAA[A/G]CTACTTACTACTCCA | 996 |
rs79929872 | snp | A/C | 0.5 | 0 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47142280 | GAGGTGTGATTGTGG[A/C]TATTTTCCCTTCTGA | 996 |
rs79936417 | snp | A/C | | | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47158269 | TAAGGCTCTTTTGGT[A/C]ACATTCTGATCCTTT | 996 |
rs79942001 | snp | C/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47131789 | TCCTTGTGCTTCAGC[C/T]TCCCAAGTAGCCAGG | 996 |
rs79953954 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136481 | TCAGAATTATACCTT[A/C]TCTTGATATTTAAAC | 996 |
rs79972073 | snp | G/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47137032 | AGTTATTGACCAGTA[G/T]GTACCATCCCTAAGT | 996 |
rs79983326 | snp | C/T | 0.215747 | 0.247642 | intron-variant | CDC27 | GRCh38.p7 | 17:47134129 | GTTTCAAACTCTTAG[C/T]CTCAAACAATCCTCC | 996 |
rs79991719 | snp | C/G/T | 0.666667 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47136658 | TACAAAAAAGTAAAA[C/G/T]AGAGATACTGCTAAA | 996 |
rs79998271 | snp | C/T | 1.64893e-05 | 0.0028713 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47151857 | ATTGGAGTTACCTCT[C/T]GGCTATTTCCACTCT | 996 |
rs80029043 | snp | A/C | | | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47141875 | TACTCTGAAAGTTCA[A/C]AATAGGCCCTTCCAA | 996 |
rs80120716 | snp | A/G | | | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47143932 | GAACTTCTTCGAGGC[A/G]GTGCGTTTGGGGGAG | 996 |
rs80157017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47188544 | ACCTCCTCCCCTGGT[A/G]TTGGTGCTTGCGCCT | 996 |
rs80179289 | snp | A/C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136415 | CTCAACTGCTATAAT[A/C/G]ACCCCAAAGATAACC | 996 |
rs80196260 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47144896 | ACACACACACACATA[A/C]ATCCTTTTAATCTGC | 996 |
rs80199507 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136463 | TACCACAGAGTTATG[A/G]CTTCAGAATTATACC | 996 |
rs80202554 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136953 | GATCTGGTATTCTAT[G/T]ATCATTAGTTAATTT | 996 |
rs80219523 | snp | C/T | 0.061519 | 0.16424 | intron-variant | CDC27 | GRCh38.p7 | 17:47137134 | ACGACTTTGTCTTTG[C/T]ACTTCATTACCACTT | 996 |
rs80351303 | snp | A/G | 0.444444 | 0.157135 | intron-variant | CDC27 | GRCh38.p7 | 17:47136284 | TTTTGGCCATCTTTC[A/G]GGCAATGTAACTACT | 996 |
rs111227623 | snp | A/C/T | 1.66101e-05 | 0.0028818 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47138796 | AACTGAAAGAGCAAC[A/C/T]TCTTTTTGAAGATGC | 996 |
rs111247437 | in-del | -/A | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47136324 | GAGACATAATCCATT[-/A]AACAACATATTCACA | 996 |
rs111256526 | in-del | -/A | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47146956 | TAGTTCCAGCTACCC[-/A]GGAGCCTGAAGTGGG | 996 |
rs111322439 | snp | A/G | 0.000729927 | 0.0190901 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137295 | TTGGATAGCTCTCTG[A/G]AAGAATTTAATTGCA | 996 |
rs111393154 | snp | C/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47167305 | CTAAAAATAAAAGAA[C/T]ATGATGCTCTTTAGG | 996 |
rs111414808 | snp | A/G | 6.60164e-05 | 0.0057449 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47151895 | GACAGACTTTGTTCC[A/G]GTTTGGCCGATTCTG | 996 |
rs111474812 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47149527 | AAAAAAAAAAAAAAA[A/G]AAAGAAATGTTAAAA | 996 |
rs111476024 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CDC27 | GRCh38.p7 | 17:47174267 | CAGCCATAAATCTAA[A/G]AAGCACAGAATATGT | 996 |
rs111540357 | snp | A/G | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47177554 | GCCTGGGTGACAGAG[A/G]GAGACCCTATCTGAA | 996 |
rs111547798 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CDC27 | GRCh38.p7 | 17:47159535 | CACCTTGCAAGGGAC[A/G]GCGTAGGGCTTGCCA | 996 |
rs111564733 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | CDC27 | GRCh38.p7 | 17:47126605 | TTGAAGCAAGTAAAC[A/G]CTGATTTATGTGGCC | 996 |
rs111571062 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CDC27 | GRCh38.p7 | 17:47162301 | TCATCTAAACCATCA[A/G]TAGATTCCTAATTAA | 996 |
rs111624338 | snp | A/G | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47136986 | GAGTTTGTTAAAGAC[A/G]TACATTTCATAAGAA | 996 |
rs111634577 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | CDC27 | GRCh38.p7 | 17:47182415 | AATAAAATATCTCTG[A/T]AACTCCCTGTGTGTT | 996 |
rs111686468 | snp | C/T | 0.0618563 | 0.164627 | intron-variant | CDC27 | GRCh38.p7 | 17:47145795 | AATCCCAGCCACTCG[C/T]GGGTTCAAGTGTAAT | 996 |
rs111716323 | snp | A/C/G | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47136883 | ACTAAACAAACAAAA[A/C/G]ACAACTACAGTATCT | 996 |
rs111718069 | snp | C/G | 0 | 0 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47188912 | TCGGACGGGAAAGGC[C/G]GTTATTTTCGCCGAA | 996 |
rs111732517 | snp | C/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47122750 | ACGATCTTGGCTCAC[C/T]GCAACCTCCACCTCC | 996 |
rs111785717 | snp | C/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47180319 | CATTGGGACCTTAAA[C/T]TCCTGCTGCCCAGAT | 996 |
rs111797798 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CDC27 | GRCh38.p7 | 17:47133681 | CGACTCAGGTGATCC[A/G]CCCGCCTCGGCCTCG | 996 |
rs111846025 | snp | G/T | 0 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47136748 | AGCAACTAGTAAATT[G/T]TTTCAATTTTTTTTC | 996 |
rs111851549 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | CDC27 | GRCh38.p7 | 17:47159930 | TGCCTCCACGAGCTC[C/G]GTGGCCTCGGTCCCG | 996 |
rs111881998 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47147660 | GGACTGCTTCAGGCC[A/C]GGAGGTCAAGATCTG | 996 |
rs111886110 | snp | A/G | | | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47169951 | ATGAAAGAGTAAAGC[A/G]AGCTGAATCACCAAA | 996 |
rs111963153 | snp | C/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47173510 | GGTTTCTTTTCACCT[C/T]ATAAGTTTTTAAAAA | 996 |
rs112006064 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | CDC27 | GRCh38.p7 | 17:47168014 | AGGGCGAGGCATGGG[C/G]AAAGAGAGGTGCGGA | 996 |
rs112016766 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | CDC27 | GRCh38.p7 | 17:47156471 | AATTTTTTTTGAGTT[A/G]GAGTCTTGGTCTGTC | 996 |
rs112025751 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | CDC27 | GRCh38.p7 | 17:47161796 | ATCTCATTGTTTGAG[G/T]ATTATCCTAAGCTTC | 996 |
rs112039926 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | CDC27 | GRCh38.p7 | 17:47174824 | AGCCGGGTGTGGTGG[C/T]GTGCACCTGTGATCC | 996 |
rs112067488 | snp | A/G | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47136990 | TTGTTAAAGACGTAC[A/G]TTTCATAAGAAAACA | 996 |
rs112101478 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47190934 | GCTAGGGCTGAAAGA[C/T]TCAAGATGGCTTCAC | 996 |
rs112106760 | snp | A/C | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47146637 | GATTAGTCCAGACTA[A/C]GGCTACTTTTGTCTG | 996 |
rs112110518 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CDC27 | GRCh38.p7 | 17:47136049 | CGGGAGGCTGAGGCA[A/G]GAGAATGGCGTGAAC | 996 |
rs112119468 | snp | A/G | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47137000 | CGTACATTTCATAAG[A/G]AAACATTTTAGTTAG | 996 |
rs112120512 | snp | C/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47146543 | AGCTCATACTTTCAA[C/T]AGGCAGAGTGAAGAA | 996 |
rs112142979 | snp | G/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47136653 | ACAAGTACAAAAAAG[G/T]AAAATAGAGATACTG | 996 |
rs112150744 | in-del | -/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47134475 | CACCATGCCTAATTG[-/T]TTTTTTTTTGTTTTG | 996 |
rs112187822 | snp | C/T | 0.5 | 0 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47151863 | GTTACCTCTCGGCTA[C/T]TTCCACTCTGTGAGA | 996 |
rs112216339 | snp | A/G | 0.487749 | 0.0772993 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157083 | ATCTGTATTCAAGGA[A/G]TACTTTGAATTGGAA | 996 |
rs112216853 | snp | C/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47136509 | AACTATTAAGTCAGT[C/T]CAGAAAAATACAATA | 996 |
rs112217389 | snp | A/G | 0.5 | 0 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47129444 | GTGAAATTTGCATAG[A/G]GGGTTCTTGGGATCA | 996 |
rs112230628 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | CDC27 | GRCh38.p7 | 17:47170493 | CTGGCCAATTTGTTT[C/T]TTGTAAAAAAAATTT | 996 |
rs112309517 | snp | C/T | 0.0618563 | 0.164627 | intron-variant | CDC27 | GRCh38.p7 | 17:47133702 | CTCGGCCTCGGCCTC[C/T]CAAAGTGGTGGGATT | 996 |
rs112355622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47175281 | AAACCAGATAGACGC[C/T]TCTTCTTCACGCTGA | 996 |
rs112357254 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CDC27 | GRCh38.p7 | 17:47164163 | ACAGTATTCAGTAAG[A/G]TAACATGCTGTACAG | 996 |
rs112358095 | snp | A/G | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47149686 | TCAGCTGGGCATGGT[A/G]GCTCATGCCTGTAAT | 996 |
rs112367102 | snp | A/C | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47136403 | AGAATGATACAACTC[A/C]ACTGCTATAATAACC | 996 |
rs112410015 | snp | C/G | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47136874 | AGTAACAAAACTAAA[C/G]AAACAAAAAACAACT | 996 |
rs112467863 | in-del | -/G | 0.5 | 0 | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47190191 | GTGGTGGGAAGAGTA[-/G]GGGGGTCGGAAATTC | 996 |
rs112488600 | snp | C/G/T | 1.6486e-05 | 0.00287102 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47169972 | AATCACCAAACTCAG[C/G/T]AACAATATCATCATG | 996 |
rs112513055 | snp | A/G | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47136995 | AAAGACGTACATTTC[A/G]TAAGAAAACATTTTA | 996 |
rs112530322 | snp | C/G/T | 3.76607e-05 | 0.00433926 | intron-variant | CDC27 | GRCh38.p7 | 17:47137144 | CTTTGTACTTCATTA[C/G/T]CACTTACCATGCATT | 996 |
rs112543557 | snp | C/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47147257 | TACAAAAATTAGCTG[C/G]GCATGGTGGCGCGCG | 996 |
rs112543578 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47119171 | AATACAATAGCATAC[A/G]TGTTAGAATCCAAGT | 996 |
rs112546992 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | CDC27 | GRCh38.p7 | 17:47135264 | AGCATGCTCCTATAC[G/T]TATAGACCTCAAAAT | 996 |
rs112607142 | snp | A/G | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47182039 | TCTAGTAGAGCACTC[A/G]TAACATGGTTATTTG | 996 |
rs112611936 | snp | A/G | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47149523 | TTAAAAAAAAAAAAA[A/G]AAAAAAAGAAATGTT | 996 |
rs112627286 | snp | A/G | 0.5 | 0 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137234 | CTTCAGTTAAGACAA[A/G]CTCATGCCCTAATAG | 996 |
rs112652231 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47130729 | AAAAATACAAAAAAT[C/T]AGCCAGGCGTGGTGT | 996 |
rs112692466 | snp | A/C/T | 5.10263e-05 | 0.00505084 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47189211 | TGCAGTGCCTCAGGC[A/C/T]CCCCCTGTAGCGGCT | 996 |
rs112698940 | snp | C/T | 0.000154945 | 0.00880048 | intron-variant | CDC27 | GRCh38.p7 | 17:47143994 | TGTACTAAAAAAAAA[C/T]TATAAAGGAAGACAT | 996 |
rs112707781 | snp | A/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47129244 | ATGAGTATTTCATGA[A/T]GACATAAAAATCACA | 996 |
rs112729209 | in-del | -/A | 0.361263 | 0.223876 | intron-variant | CDC27 | GRCh38.p7 | 17:47147428 | AAACAAAAAAAAAAA[-/A]CACTAGGCATAGAAA | 996 |
rs112746270 | snp | A/G | | | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47151918 | CGATTCTGGCAACAG[A/G]CTGTAAAACACGAAA | 996 |
rs112763614 | snp | A/G | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47149681 | AAATTTCAGCTGGGC[A/G]TGGTAGCTCATGCCT | 996 |
rs112775729 | snp | C/G | 0 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47161250 | AGGCTGGTCTCAAAC[C/G]TGGGATTACAGGTGT | 996 |
rs112775935 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47134785 | GGCCTTAATTGTTTT[C/T]TTTTTTTTTTTTTTT | 996 |
rs112799227 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | CDC27 | GRCh38.p7 | 17:47159742 | GGTCTGCTTCTGCAC[A/C]GGCATAATCTTCAAA | 996 |
rs112848754 | in-del | -/A | 0.499953 | 0.00483515 | frameshift-variant, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157041 | ATCAGGTGAAATTAC[-/A]GCTGAATCAATATAA | 996 |
rs112853746 | snp | A/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47136498 | CTTGATATTTAAACT[A/T]TTAAGTCAGTCCAGA | 996 |
rs112886976 | snp | A/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47121934 | TAGTAGAGACGAGGT[A/T]TCACCATGTTGGTCA | 996 |
rs112931476 | snp | A/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47182269 | AGGAATAACTTTTAA[A/T]TTTTTGAATATATGT | 996 |
rs112935092 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47132605 | GGGTCTCACTCTGTC[A/G]CCCAGGCTGGAGTGC | 996 |
rs112942510 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47135237 | CCTTGTCCCCCACTT[A/T]CTGTTATCAAAAGCA | 996 |
rs112979490 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47118564 | GTCATGGCAAAAACC[A/G]CAATTACTTATGCAC | 996 |
rs113018878 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CDC27 | GRCh38.p7 | 17:47138560 | TTTTTCTATTTGTGA[A/C]TCTGCACCACACATT | 996 |
rs113063013 | snp | C/G | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47145414 | AAATTGATCAGTGTA[C/G]GTGTTTGAGTGTTAT | 996 |
rs113085535 | snp | A/G | | | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47129417 | TTCATTTGCAAATAA[A/G]ACTGAGGCTCTGTGA | 996 |
rs113088130 | in-del | -/G | 9.9681e-05 | 0.00705908 | frameshift-variant, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47141924 | CAGTATTGTAGTGGT[-/G]AGAAGGTAGATGGCT | 996 |
rs113176853 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47145885 | CTGGGCGACAACAGC[A/G]AAACTCTGTCTCAAA | 996 |
rs113188393 | snp | C/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47147507 | TAATATAAGAAACAC[C/T]TAGAAATAACAAAGT | 996 |
rs113193445 | in-del | -/CTAC | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47123399 | CTTCTACTTTTTTTT[-/CTAC]TTTTTTTTTTTTTTT | 996 |
rs113194736 | snp | C/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47136223 | GAAGAGACAGCAGCA[C/T]TGGCAAGTTGATTGT | 996 |
rs113206140 | snp | G/T | | | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47156965 | ATAAACTTCGACCAG[G/T]TTTTGGTTTATTTTG | 996 |
rs113208517 | snp | A/C | 0 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47136753 | CTAGTAAATTTTTTC[A/C]ATTTTTTTTCCTATT | 996 |
rs113227981 | snp | A/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47186919 | CATAGTTTTTTTTTT[A/T]ATAAAGACAGTATCT | 996 |
rs113228467 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47160352 | CATGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 996 |
rs113361962 | in-del | -/TAAATGA | 6.88196e-05 | 0.00586558 | intron-variant | CDC27 | GRCh38.p7 | 17:47151965 | TTATGGGCTGCACTG[-/TAAATGA]TAAATGATAAAAGAC | 996 |
rs113394136 | in-del | -/AC | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47122675 | TAACTATATATATAC[-/AC]TTATTTATTTATTTT | 996 |
rs113412341 | snp | A/C | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47167397 | CCAGTGTTTGTACAT[A/C]ACTCCTCTCAAATAA | 996 |
rs113425487 | snp | A/C | 0.126564 | 0.217402 | intron-variant | CDC27 | GRCh38.p7 | 17:47126982 | TATTTTCAGTAGAGA[A/C]AGGGTTTCACCATGT | 996 |
rs113481420 | snp | C/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47142969 | GCATGAGCCACCGTG[C/T]CCGGCCTTTGTTTTG | 996 |
rs113496501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47148907 | AACATGGTGAAAGCC[A/G]ATCTCTACTAAAAAT | 996 |
rs113520197 | snp | A/G | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47176505 | AAAGACCACAAATAA[A/G]AGAGGGCTGGAAGAA | 996 |
rs113554121 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CDC27 | GRCh38.p7 | 17:47159702 | TGGCAACAAACGCCT[C/T]GAACCTGGTGCCCTG | 996 |
rs113576081 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CDC27 | GRCh38.p7 | 17:47172208 | TTAATTCAAATTTGA[A/G]TTATGGAGAAACGGT | 996 |
rs113580361 | in-del | -/AG/G | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47149091 | CAAAAAAAAAAAAAA[-/AG/G]AAAAAGAAAAAGAAA | 996 |
rs113608268 | snp | A/C | 0.5 | 0 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157338 | ACAGTTGCTAAAGTT[A/C]TGTAAAGATGTGAAT | 996 |
rs113629026 | snp | G/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47132615 | CTGTCACCCAGGCTG[G/T]AGTGCAGTGGGCCAA | 996 |
rs113637376 | snp | A/G | 0 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47144231 | CACCTTGTGATCATA[A/G]GTCAATAATCCTTAA | 996 |
rs113664998 | snp | C/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47128224 | TTGGTAGAGATGGGG[C/T]TTCACCCTGTTGGCC | 996 |
rs113666698 | in-del | -/A | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47137071 | CAAATTCATGATAAT[-/A]AAAGAGCTATCTAAC | 996 |
rs113668271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47128143 | TCAAGTGATTCTCGT[A/G]CCTCAGCCTCCCAAG | 996 |
rs113690642 | snp | G/T | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47189289 | CGGGGGATGGGGGAG[G/T]CCGAGCGATTGCCGA | 996 |
rs113715411 | snp | A/G | 0 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47167677 | CAGTAACAATCATCA[A/G]TACAGAAGACTTCTG | 996 |
rs113744718 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | CDC27 | GRCh38.p7 | 17:47139760 | TGTCTGCTAGGAATC[A/G]TAGGCCCTACCTATT | 996 |
rs113766653 | snp | C/T | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47177881 | ACACACACACACACA[C/T]ATCTCCAAAGAGCTA | 996 |
rs113864462 | in-del | -/AGTC | 0.5 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47136415 | TCAACTGCTATAATA[-/AGTC]AACCCCAAAGATAAC | 996 |
rs113884850 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CDC27 | GRCh38.p7 | 17:47150294 | ATGTTGAAGCCCTAA[A/G]CCCCAGTACATGTCA | 996 |
rs113893418 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | CDC27 | GRCh38.p7 | 17:47159032 | GCTGGAATTACAGGC[A/G]TGATCCACCACGCTT | 996 |
rs113916812 | snp | C/T | 0 | 0 | intron-variant | CDC27 | GRCh38.p7 | 17:47136763 | TTTTCAATTTTTTTT[C/T]CTATTATCCAATAAG | 996 |
rs114218405 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | CDC27 | GRCh38.p7 | 17:47137424 | TCTAAAACCAAATCT[A/G]TGACTAAAATCAAGC | 996 |
rs114423133 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | CDC27 | GRCh38.p7 | 17:47179132 | CCGACTATAAATCTC[A/G]AGAGAAAGACAAATG | 996 |
rs114471521 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CDC27 | GRCh38.p7 | 17:47187156 | GGACAATGCTGCTAT[A/G]AAAAAGAAGCAAATT | 996 |
rs114543601 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | CDC27 | GRCh38.p7 | 17:47159574 | CCCCCAGTAGCCTCT[C/G]CGCACGGGGACAATC | 996 |
rs114805714 | snp | C/T | 0.029116 | 0.117091 | intron-variant | CDC27 | GRCh38.p7 | 17:47135259 | TCAAAAGCATGCTCC[C/T]ATACTTATAGACCTC | 996 |
rs114808103 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | CDC27 | GRCh38.p7 | 17:47158833 | CATTGATGCCCAGGC[A/G]GGTCTTGAACTCATG | 996 |
rs114870776 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | CDC27 | GRCh38.p7 | 17:47163530 | ACATAGGGAGACCCC[A/G]TATCTACCAAAACCA | 996 |
rs115199788 | snp | A/C | | | splice-donor-variant | CDC27 | GRCh38.p7 | 17:47181561 | TGAATAGATTTCAAA[A/C]CTTCTGCATAAAGGC | 996 |
rs115232104 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | CDC27 | GRCh38.p7 | 17:47174222 | AAAAGATAACAGTAC[C/T]CCAAACACAACTAAA | 996 |
rs115325064 | snp | C/T | 0.0912534 | 0.193131 | intron-variant | CDC27 | GRCh38.p7 | 17:47148399 | CGGAGAGGAGAAAGA[C/T]TGGAAACAAAAATGA | 996 |
rs115376036 | snp | G/T | 0.0263992 | 0.111815 | intron-variant | CDC27 | GRCh38.p7 | 17:47175461 | CATGAACTCTGATGT[G/T]GTGTGAATTTAAGGG | 996 |
rs115606582 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | CDC27 | GRCh38.p7 | 17:47152371 | ACTTGGTAACAGTTC[C/T]AAAGGAGTTCAGAGG | 996 |
rs115629862 | snp | C/T | 0.0422008 | 0.138995 | intron-variant | CDC27 | GRCh38.p7 | 17:47165499 | TGTCCATTCAATTGT[C/T]TTACTTATTTTCTAA | 996 |
rs115761301 | snp | C/T | 0.217551 | 0.247885 | intron-variant | CDC27 | GRCh38.p7 | 17:47134409 | GAACTCTTAGGCTCA[C/T]GCAATCCTCCCACCT | 996 |
rs115767870 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CDC27 | GRCh38.p7 | 17:47127932 | GCTGGTCTCAAGTTC[C/T]GTGGACTCATGTGAT | 996 |
rs115821458 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CDC27 | GRCh38.p7 | 17:47186698 | GGTAGTAATTTGAGA[C/T]GGAGTTTTAATTTAG | 996 |
rs115831653 | snp | A/G | 0.00398564 | 0.0444627 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47118855 | AGGCCAAGCTTGGGC[A/G]GAAACTGTCCCCCAA | 996 |
rs115927691 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | CDC27 | GRCh38.p7 | 17:47139623 | GTAACATAAAATCTA[A/T]TTTTGAACAATTTTT | 996 |
rs115931975 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | CDC27 | GRCh38.p7 | 17:47147122 | AAAACACTAGGCAGC[C/T]GGGCGCGGTGGCTCA | 996 |
rs116001448 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | CDC27 | GRCh38.p7 | 17:47134088 | ATTTTTTGTGGAGAC[A/G]AGGTCTCACTATGTT | 996 |
rs116052093 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | CDC27 | GRCh38.p7 | 17:47163329 | AATTCTGGTATATAA[C/T]GGCTAAAATGAAAAG | 996 |
rs116181606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47183737 | ACAAGGTAGGGGCTA[C/T]GTCTGTTTTTGCTCA | 996 |
rs116224080 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | CDC27 | GRCh38.p7 | 17:47130946 | GCTGCAGAACTTTAA[C/T]AAATATCATGGTCAT | 996 |
rs116340610 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | CDC27 | GRCh38.p7 | 17:47161973 | TCTAACTTCAACCTT[A/C]CCTTTCCTTTGCCTG | 996 |
rs116541638 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | CDC27 | GRCh38.p7 | 17:47131972 | CACTGCAACTGGCCA[C/G]GAGATATCTTACTTG | 996 |
rs116565422 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | CDC27 | GRCh38.p7 | 17:47150111 | CTAAGAGAGGAGCAC[A/G]AAAGTATACTATTGT | 996 |
rs116570203 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | CDC27 | GRCh38.p7 | 17:47161375 | AAATGAAGAAAGGGC[A/G]TACAAAAAAACATTT | 996 |
rs116653366 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | CDC27 | GRCh38.p7 | 17:47164711 | AATCCCAGCTACTCC[A/G]GAGGCTGAGGCACGA | 996 |
rs116666314 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | CDC27 | GRCh38.p7 | 17:47184760 | CAGTGTCTCTTGTGC[C/T]GGGATTGGGGGGAAG | 996 |
rs117083077 | snp | A/G | 0.0663309 | 0.169604 | intron-variant | CDC27 | GRCh38.p7 | 17:47133685 | TCAGGTGATCCGCCC[A/G]CCTCGGCCTCGGCCT | 996 |
rs117489563 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CDC27 | GRCh38.p7 | 17:47128026 | TATCACTGGTTTGGT[A/G]TATTTCTTTCTATTT | 996 |
rs117594331 | snp | A/G | 0.0622301 | 0.165053 | intron-variant | CDC27 | GRCh38.p7 | 17:47147123 | AAACACTAGGCAGCC[A/G]GGCGCGGTGGCTCAC | 996 |
rs117745151 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CDC27 | GRCh38.p7 | 17:47180912 | ATAGAGTCTAAATCC[A/G]TGTTCTTCACCATAG | 996 |
rs117757076 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47148384 | ATCCAAAATGAAACA[C/T]GGAGAGGAGAAAGAT | 996 |
rs117778193 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | CDC27 | GRCh38.p7 | 17:47147555 | AAAACATTAAAAAAA[C/T]ACAAATACATCCTAT | 996 |
rs117791230 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CDC27 | GRCh38.p7 | 17:47146100 | TAAACATACTGATGC[A/G]TTGGGAGGGTGAGCC | 996 |
rs117855810 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CDC27 | GRCh38.p7 | 17:47160776 | CATCTGTTTATGTGC[A/G]GAATGTCAGTATAAC | 996 |
rs117908176 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | CDC27 | GRCh38.p7 | 17:47184552 | ATAAGAGGCAAGGGC[A/G]GGGGGAAAAAAGAAG | 996 |
rs117953218 | snp | C/T | 0.0941369 | 0.195465 | intron-variant | CDC27 | GRCh38.p7 | 17:47166708 | TTGAAACTGTTCTTT[C/T]ATAACAAACATTTAG | 996 |
rs118042836 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47166429 | CATACACATCCTTTC[A/T]CTGTCCTCAGGGTAG | 996 |
rs118058271 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47138148 | ACCAGGATGAGTTAT[A/T]TTTAGGATTCAAGAT | 996 |
rs118125119 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | CDC27 | GRCh38.p7 | 17:47184969 | GCCAAAAAGAACAAC[A/G]CTCCTCTCCCTCTCC | 996 |
rs118142526 | snp | G/T | 0.0232847 | 0.105357 | intron-variant | CDC27 | GRCh38.p7 | 17:47135866 | CTGAGTTCCTGGCCG[G/T]GTATGGTGGCTCATG | 996 |
rs118162583 | snp | A/T | | | downstream-variant-500B | CDC27 | GRCh38.p7 | 17:47117485 | ACCAAAAAAAAAAAA[A/T]TTTCAAATTAGAGTA | 996 |
rs137873918 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CDC27 | GRCh38.p7 | 17:47157794 | CAATGCTGAAAAATG[A/G]TCCTTTATGTATCCT | 996 |
rs137875512 | in-del | -/TT | 0.477937 | 0.102688 | intron-variant | CDC27 | GRCh38.p7 | 17:47123403 | TACTTTTTTTTCTAC[-/TT]TTTTTTTTTTTTTTT | 996 |
rs137909789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47154915 | CAGTGAGGATCTGAG[A/G]GGCAGATTAAAAATA | 996 |
rs137915267 | in-del | -/AGGAA | | | intron-variant | CDC27 | GRCh38.p7 | 17:47174991 | GGACAGGACAGGACA[-/AGGAA]GGAAAGGAAAGGAGA | 996 |
rs137920268 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CDC27 | GRCh38.p7 | 17:47127789 | CTCACTGCAACCTCC[A/G]CCTCCTGAGCTCAAG | 996 |
rs137957553 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CDC27 | GRCh38.p7 | 17:47146823 | TAATCCCAACAACTC[A/G]GGTGGGTGAGGTGGG | 996 |
rs137988196 | in-del | -/CAAAA | | | intron-variant | CDC27 | GRCh38.p7 | 17:47180946 | CAGACTCTTTTCTTA[-/CAAAA]AAAAAAAAAAAAAAA | 996 |
rs138020641 | snp | A/C/T | 0.513637 | 0.0814503 | synonymous-codon, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137277 | AGCGTAATTTGGATC[A/C/T]ACTTGGATAGCTCTC | 996 |
rs138027159 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CDC27 | GRCh38.p7 | 17:47153203 | ATGCAGACCTACATG[C/T]GTGACTTTTCTGGGA | 996 |
rs138180554 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47120434 | TTCCTTGGCAATCAA[A/G]TCACTGTTATAGGCA | 996 |
rs138199294 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | CDC27 | GRCh38.p7 | 17:47179820 | AAACAGCTTTATGTG[C/G]ACTAATCTGGGAATC | 996 |
rs138213658 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | CDC27 | GRCh38.p7 | 17:47185898 | TACTCCCAATTAATG[A/C]CCCAACATTTAGCAA | 996 |
rs138263010 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CDC27 | GRCh38.p7 | 17:47176582 | GAGGAGAAAAAAGAT[A/G]GCCAAATTGTGCAGG | 996 |
rs138264973 | in-del | -/C | | | frameshift-variant, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47137251 | CATGCCCTAATAGAG[-/C]GTATAGGCATAAGCG | 996 |
rs138328731 | in-del | -/AC | 0.492582 | 0.0604491 | intron-variant | CDC27 | GRCh38.p7 | 17:47177858 | TTTATATGTGTGTGT[-/AC]ACACACACACACACA | 996 |
rs138356815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47163827 | TGGAGTACAATGGCA[C/T]GATCTCAGCTCACTG | 996 |
rs138361104 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47136410 | TACAACTCAACTGCT[A/G]TAATAACCCCAAAGA | 996 |
rs138411024 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CDC27 | GRCh38.p7 | 17:47162056 | AAGTCAAGTTCATCT[C/T]TTCTCCCCAAAATCT | 996 |
rs138477571 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | CDC27 | GRCh38.p7 | 17:47150110 | ACTAAGAGAGGAGCA[C/T]GAAAGTATACTATTG | 996 |
rs138510120 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CDC27 | GRCh38.p7 | 17:47167198 | CATTTCCAAATGTTT[C/T]GAGATTTTCTTATCC | 996 |
rs138546665 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CDC27 | GRCh38.p7 | 17:47129013 | CTGACTCAGGTGATC[C/T]GCCCGCCTTGGTCTC | 996 |
rs138623180 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | CDC27 | GRCh38.p7 | 17:47180691 | AGAAACAAAACATAC[A/C]TTATCAGTGGTGTTT | 996 |
rs138754636 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47175888 | TAGTATGACATGTGG[A/C]TTAAAGTACCGACTC | 996 |
rs138789655 | snp | G/T | 0.00253032 | 0.035479 | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47154760 | CCATCTCCAGGACTT[G/T]GGGTTTCTAATGGCA | 996 |
rs138805201 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | CDC27 | GRCh38.p7 | 17:47141798 | CATGGGCATTTATTT[G/T]AATGAAATTGAAATT | 996 |
rs138810713 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47146439 | ATTACATTATAGTAC[C/T]ATAGTGAAGAAACTA | 996 |
rs138897254 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CDC27 | GRCh38.p7 | 17:47149340 | ACATGGTGAAACCCC[A/G]TTTCTACTAAAAATA | 996 |
rs139005122 | snp | C/T | 3.35441e-05 | 0.00409523 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47138842 | TAGATCTCCATGCCT[C/T]CAACTCTATAATTCT | 996 |
rs139089029 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | CDC27 | GRCh38.p7 | 17:47178126 | TTTCCAAAACAGCAA[A/G]TCTCAACTCACTAGT | 996 |
rs139228002 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CDC27 | GRCh38.p7 | 17:47162384 | TAATACTAACCATAG[C/T]CTGCCTATTTATCTT | 996 |
rs139292996 | in-del | -/AC | 0.0341408 | 0.126114 | intron-variant | CDC27 | GRCh38.p7 | 17:47122673 | TCTAACTATATATAT[-/AC]ACTTATTTATTTATT | 996 |
rs139300176 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | CDC27 | GRCh38.p7 | 17:47166941 | CTCACTGTAACCTCT[A/G]CCTCCCAGGTTCAAG | 996 |
rs139364321 | snp | C/T | 0.00268957 | 0.0365725 | intron-variant | CDC27 | GRCh38.p7 | 17:47169891 | ATGGAAATGCTTTTC[C/T]GACAGTTTGAATCAT | 996 |
rs139390207 | in-del | -/AAAC | | | intron-variant | CDC27 | GRCh38.p7 | 17:47135705 | AATAATCCTCCTTTA[-/AAAC]AACACAATTTTTGAT | 996 |
rs139417683 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CDC27 | GRCh38.p7 | 17:47155525 | TGCTGGGATTACAGG[C/T]ATGAGCCCCCATGCC | 996 |
rs139430554 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47165573 | GTCTAGATACAATCT[C/G]TGTTGTTTATGGGAT | 996 |
rs139483708 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47139962 | TCAAAATTCTCAGCT[G/T]CCAGAAAAGGTCTAG | 996 |
rs139584150 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47170245 | GCTTTGTTACCCAGG[C/T]TAGAGTGCAGTAGTA | 996 |
rs139708916 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | CDC27 | GRCh38.p7 | 17:47164762 | GTGGAGACTGCAGTG[A/G]GCTGAGATTGTGCAA | 996 |
rs139751753 | snp | G/T | 0.076894 | 0.180373 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157347 | AAAGTTCTGTAAAGA[G/T]GTGAATTTAAATGTT | 996 |
rs139771107 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, utr-variant-5-prime | CDC27 | GRCh38.p7 | 17:47188804 | TCATCTTTTAGGCAA[C/G]AGAGCGCTTGGGGTG | 996 |
rs139794316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47134475 | CACCATGCCTAATTG[C/T]TTTTTTTTTGTTTTG | 996 |
rs139863906 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CDC27 | GRCh38.p7 | 17:47129586 | AAAGGTGAGAACCAA[C/T]GTGACTCAAAACCAA | 996 |
rs139980206 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | CDC27 | GRCh38.p7 | 17:47182113 | CAGTGGTTCTCAACC[A/G]CTTTATGTGATATAC | 996 |
rs140127638 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47166551 | TCCAAGGACCAGCTT[C/T]GGTTTCTATGATTTT | 996 |
rs140138003 | in-del | -/A | 0.00636936 | 0.0560724 | intron-variant | CDC27 | GRCh38.p7 | 17:47151366 | TAAAATGTTAGCTAT[-/A]ATCTATTGAGTCCTT | 996 |
rs140171160 | snp | A/G | | | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157323 | GCAAGAGTTGGGCAG[A/G]CAGTTGCTAAAGTTC | 996 |
rs140191083 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47128354 | ATTTTAAAAGATTTT[A/G]CTTCATGGTTTCTGA | 996 |
rs140193420 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CDC27 | GRCh38.p7 | 17:47148113 | TGAGGCAGGAGAATC[A/G]CTTGAACCCAGGAGG | 996 |
rs140288772 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CDC27 | GRCh38.p7 | 17:47157565 | ATATATCATAAAAGT[C/T]TACCAGTAAGATAAA | 996 |
rs140330371 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | CDC27 | GRCh38.p7 | 17:47179044 | CAACCTCAGGTGATC[C/T]GCCCACCTCAGCCTC | 996 |
rs140377977 | snp | C/T | 0.039315 | 0.13554 | intron-variant | CDC27 | GRCh38.p7 | 17:47185462 | TGCTGGGATTACAGG[C/T]GTGAGGCACCGCGCC | 996 |
rs140495002 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47148292 | CAAAACAAAAAACCC[A/G]ACAACACTGGGTGTG | 996 |
rs140525375 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47137478 | AAATGGAGGAGCTTC[A/T]GTAGATACTCAATTC | 996 |
rs140572618 | in-del | -/A | 0.472147 | 0.114677 | intron-variant | CDC27 | GRCh38.p7 | 17:47149510 | GTGAGACTCTGTCTT[-/A]AAAAAAAAAAAAAAA | 996 |
rs140609650 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47179711 | TAAATATGGTTAAAC[C/T]GAATGGTGAGGTTCT | 996 |
rs140624034 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47137485 | GGAGCTTCAGTAGAT[A/T]CTCAATTCTAATTAT | 996 |
rs140682760 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CDC27 | GRCh38.p7 | 17:47182944 | GCTGGGAAGACTGCT[C/T]GAGTCCAGGAGTTCA | 996 |
rs140737545 | snp | C/T | 0.0239918 | 0.106866 | missense, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47141945 | GTAGATGGCTCAAAA[C/T]ATTTATAGCTTCTTT | 996 |
rs140772863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47155860 | CAGGAGTCTGAGGTG[A/G]GAGGATCGCTTGAGC | 996 |
rs140890673 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CDC27 | GRCh38.p7 | 17:47132631 | AGTGCAGTGGGCCAA[C/T]CATAGCTCACTGCAT | 996 |
rs140967083 | snp | C/T | 0.00676609 | 0.0577691 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47118854 | TAGGCCAAGCTTGGG[C/T]GGAAACTGTCCCCCA | 996 |
rs140968521 | snp | C/G/T | 0.00755907 | 0.0610114 | intron-variant | CDC27 | GRCh38.p7 | 17:47158486 | AAGCGCACAGAACAT[C/G/T]AATCAAAAGAAATGC | 996 |
rs141037843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47135324 | ATTAGGTTAATATGC[A/G]GGTATTTCTCCTGAA | 996 |
rs141232928 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CDC27 | GRCh38.p7 | 17:47177356 | CCGAGGTGGACAGAT[C/T]ACTTGAGGCTAGGAG | 996 |
rs141296251 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC27 | GRCh38.p7 | 17:47190114 | TAGGTGAAGAGATCA[G/T]GGAAAAGCTCAATAG | 996 |
rs141297048 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CDC27 | GRCh38.p7 | 17:47141230 | GATATTTTATTAATA[C/T]ATAGGTTTCTAAAAG | 996 |
rs141303249 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47183995 | TGCAAATAATTACCA[A/C]CAAATTACTCCTTTA | 996 |
rs141358574 | snp | C/G | 0.000399281 | 0.0141238 | missense, utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47120978 | AGTTGTGTGTCATCC[C/G]CATCTGTCATGCTGC | 996 |
rs141428277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47153047 | TCAAAATAAAACTTC[A/G]TAAGCCTTCCTCCGC | 996 |
rs141472199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47136006 | AATTAGCCGGGCATG[A/G]TGGCAGGCACCTGTA | 996 |
rs141490869 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47131962 | AGGCATGAGCCACTG[C/T]AACTGGCCAGGAGAT | 996 |
rs141501349 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47150143 | AGGTTCTGTGCTATA[C/T]ATGAAATTGTCTATT | 996 |
rs141572435 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47119928 | AACCAAAGGTAACCA[C/T]ACATTCTTACACTCT | 996 |
rs141622390 | in-del | -/T | | | downstream-variant-500B | CDC27 | GRCh38.p7 | 17:47117486 | CCAAAAAAAAAAAAA[-/T]TTTCAAATTAGAGTA | 996 |
rs141669888 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CDC27 | GRCh38.p7 | 17:47125973 | AACATTTCATGCAAC[C/T]AGCATGCCTATCCCC | 996 |
rs141680566 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | CDC27 | GRCh38.p7 | 17:47149815 | CAAAAATTAGCCGGG[C/T]GTGGTGGCACATGCC | 996 |
rs141784185 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CDC27 | GRCh38.p7 | 17:47146292 | GAATCCTTAAATTTG[C/T]AGCCAGTTGGTCAGA | 996 |
rs141829250 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | CDC27 | GRCh38.p7 | 17:47138596 | ACTTTCTCTTCCTCT[A/C]TGAGTCCCTGACTAG | 996 |
rs141857120 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CDC27 | GRCh38.p7 | 17:47174165 | TGAAGTGTTGTGACA[C/T]GGGTGGTTTCTTAGG | 996 |
rs141869467 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | CDC27 | GRCh38.p7 | 17:47167015 | GTGCACCACCATGCC[C/T]GGCTAACTTTTTTAT | 996 |
rs141980406 | snp | A/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47165216 | GTTTATCTATTTACT[A/T]ACTGAATTTTGGGTT | 996 |
rs142007102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47129050 | TGCTGGGATTACAGG[C/T]GTAAGCCACTGCGCC | 996 |
rs142137881 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47166211 | CATGAGTAGAGGAGT[A/G]TTTCTTCTTGTTCTG | 996 |
rs142213616 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | CDC27 | GRCh38.p7 | 17:47131788 | ATCCTTGTGCTTCAG[C/T]CTCCCAAGTAGCCAG | 996 |
rs142246099 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | CDC27 | GRCh38.p7 | 17:47159717 | CGAACCTGGTGCCCT[A/G]GCTGGCACGGGTCTG | 996 |
rs142265178 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CDC27 | GRCh38.p7 | 17:47126658 | TAAAATGGCTTTAAG[A/G]ATAATGAATAAAGTC | 996 |
rs142278808 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47120693 | ACAGAAAAGAAAGTT[C/G]CCCACCCTACCCCCC | 996 |
rs142317880 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CDC27 | GRCh38.p7 | 17:47123692 | GCTGGGATTACAGGC[A/G]TGAGGCACCATGCCT | 996 |
rs142449611 | snp | A/C | | | intron-variant | CDC27 | GRCh38.p7 | 17:47188259 | TGAAGTCTCCCAGAC[A/C]TGGTCCATTACCAAG | 996 |
rs142457434 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47128116 | GCTCACTGCAACCTC[A/T]GCCTCCTGGGTTCAA | 996 |
rs142643102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47177009 | AAACAGATGCTGAAC[A/G]TTTTACTCTGGTTCA | 996 |
rs142654054 | in-del | -/TTA | | | intron-variant | CDC27 | GRCh38.p7 | 17:47157587 | AAGATAAAGCTGTAA[-/TTA]ATGAAAATAAACTAC | 996 |
rs142728727 | snp | C/G/T | 0.0047834 | 0.0487097 | intron-variant | CDC27 | GRCh38.p7 | 17:47179984 | ATAGAAGACAGTGGC[C/G/T]GAGTACAGTGGCTCA | 996 |
rs142785535 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | CDC27 | GRCh38.p7 | 17:47146734 | AATAAAACTTTAAAA[C/T]ACCTAAAGGAATGCA | 996 |
rs142832566 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47131937 | CGGCCTCCTAAAGCG[C/T]TGGCATTACAGGCAT | 996 |
rs142853734 | snp | A/G | 0.143723 | 0.226286 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47171962 | AGGTATTTGCATTGC[A/G]GTGTAGTACAACTGT | 996 |
rs142967495 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | CDC27 | GRCh38.p7 | 17:47147763 | ATAATCAGCCACATG[G/T]GGTGGCATGTGCCTG | 996 |
rs142987740 | snp | A/G | | | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157343 | TGCTAAAGTTCTGTA[A/G]AGATGTGAATTTAAA | 996 |
rs143085986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47158524 | ACAAACTATCGTTGC[C/T]TTCTTGAATATTACT | 996 |
rs143101832 | in-del | -/AA | | | intron-variant | CDC27 | GRCh38.p7 | 17:47178554 | ATAAATAAAAATAAG[-/AA]AAAAAAAAAAAAACC | 996 |
rs143110715 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | CDC27 | GRCh38.p7 | 17:47121428 | TCAAAAGGTTTATGG[C/G]GTCAGTCTATCAGTC | 996 |
rs143181804 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | CDC27 | GRCh38.p7 | 17:47162616 | AAAGGAAGTAGACAA[A/T]CATTGATTAAGCAAA | 996 |
rs143232583 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47184004 | TTACCACCAAATTAC[A/T]CCTTTATGAAATCTG | 996 |
rs143254184 | snp | C/T | | | intron-variant | CDC27 | GRCh38.p7 | 17:47131930 | CCTGCCTCGGCCTCC[C/T]AAAGCGCTGGCATTA | 996 |
rs143321579 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC27 | GRCh38.p7 | 17:47179275 | TAGAAACTGCTACTA[A/G]TGACATAGGAGGCCC | 996 |
rs143337546 | in-del | -/C | 0.0460142 | 0.144533 | utr-variant-3-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47120702 | AAGTTCCCCACCCTA[-/C]CCCCCCATAAATTGT | 996 |
rs143453365 | snp | C/G | | | missense, utr-variant-5-prime, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47157340 | AGTTGCTAAAGTTCT[C/G]TAAAGATGTGAATTT | 996 |
rs143595952 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CDC27 | GRCh38.p7 | 17:47186481 | ATAATTGCTAAATCT[A/G]TATAAAATCTCTTTG | 996 |
rs143635967 | snp | C/T | 0.318656 | 0.240388 | intron-variant | CDC27 | GRCh38.p7 | 17:47145851 | GCAGTGAGCCAAGAT[C/T]GTGCCATTGCATTGC | 996 |
rs143738475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47140825 | TGTACTATTCAAAAT[C/T]AAATTATATGAATAG | 996 |
rs143754152 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CDC27 | GRCh38.p7 | 17:47148273 | CTGCAATAAAAAAAC[A/G]AAACAAAACAAAAAA | 996 |
rs143786623 | snp | G/T | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CDC27 | GRCh38.p7 | 17:47189257 | CCTGCTCATTTAAAC[G/T]CACCAGCGACCGTTA | 996 |
rs143903780 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CDC27 | GRCh38.p7 | 17:47133969 | TTGGCCAGGCTGGTC[G/T]TGAACTCCTGGCCTT | 996 |
rs144071321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47165610 | ATATTTTCTCCCAGG[C/T]TGTGACTTGTGTGTA | 996 |
rs144155421 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CDC27 | GRCh38.p7 | 17:47181939 | CCTTATAAACTGCTC[A/G]TCCCTAAAGATCCAG | 996 |
rs144215858 | snp | A/G | | | intron-variant | CDC27 | GRCh38.p7 | 17:47179084 | CTCTTATATCATTCT[A/G]CTGTTCCTTCTTTCT | 996 |
rs144338717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47155770 | AGCTTGGGCAACACA[A/G]CAAGACCCCATCTCT | 996 |
rs144346344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC27 | GRCh38.p7 | 17:47139848 | ATCAATTTTTTTCCT[C/T]ATCACATTCACAGCT | 996 |