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 |