SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs2863 | snp | A/C | 0.0283406 | 0.115616 | utr-variant-3-prime, downstream-variant-500B | CDC23, KIF20A | GRCh38.p7 | 5:138187749 | AACATCATTCTGGAC[A/C]ATGGGAACCTTGAAA | 8697 |
rs2864 | snp | A/G | 0.416708 | 0.186302 | utr-variant-3-prime, downstream-variant-500B | CDC23, KIF20A | GRCh38.p7 | 5:138187741 | TTCCCATGGTCCAGA[A/G]TGATGTTTGATTCTT | 8697 |
rs1016647 | snp | C/T | 0.495891 | 0.0451408 | intron-variant | CDC23 | GRCh38.p7 | 5:138208708 | TAATCTTAAATTTTT[C/T]TGTTTCATTCTTGCT | 8697 |
rs1056698 | snp | C/T | 0.00249799 | 0.0352527 | synonymous-codon | CDC23 | GRCh38.p7 | 5:138198224 | TGAGATTGATAAATA[C/T]CGTGTAGAAACGTGC | 8697 |
rs1802292 | snp | A/T | 0.00953873 | 0.0683987 | utr-variant-3-prime | CDC23 | GRCh38.p7 | 5:138188797 | AGAATCCTGGCAGGA[A/T]CAGACATTATCTTGC | 8697 |
rs2057831 | snp | A/G | 0.453697 | 0.14494 | intron-variant | CDC23 | GRCh38.p7 | 5:138199444 | tccacaaacaaaaaa[A/G]agaAAGAAATAGTTT | 8697 |
rs2107682 | snp | C/T | 0.410905 | 0.191336 | intron-variant | CDC23 | GRCh38.p7 | 5:138207446 | CTTACAGATTTGACT[C/T]GAGGAAAATGTGAGT | 8697 |
rs2231468 | snp | A/G | 0.495927 | 0.0449436 | upstream-variant-2KB | CDC23 | GRCh38.p7 | 5:138214162 | GCCCGGCTAATTTTT[A/G]TGTATTTTTAGTAGA | 8697 |
rs2231469 | snp | C/T | 0.0134861 | 0.0810011 | upstream-variant-2KB | CDC23 | GRCh38.p7 | 5:138214083 | GTGATCCGCCCGCCT[C/T]GGCCTCCCACAGTGT | 8697 |
rs2231470 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | CDC23 | GRCh38.p7 | 5:138213889 | TTAACAATTATTGTT[A/G]AATAAATGTTACAGA | 8697 |
rs2231471 | snp | A/C/G/T | 0.000420104 | 0.014488 | missense | CDC23 | GRCh38.p7 | 5:138213287 | GTACCTCCATGGTCC[A/C/G/T]GGTGGCTGTGACGGC | 8697 |
rs2231472 | snp | C/T | 0.187495 | 0.24206 | intron-variant | CDC23 | GRCh38.p7 | 5:138213120 | GGAAGGGACGGGGCT[C/T]GGATCCTTGGCCTTG | 8697 |
rs2231473 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | CDC23 | GRCh38.p7 | 5:138202320 | CTCCAGCCTGGGCAA[C/T]AAAGCAAAGTGAGAC | 8697 |
rs2231474 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | CDC23 | GRCh38.p7 | 5:138202035 | AACAGCCAGGCAGGT[A/G]ATATGAATGGTCTGA | 8697 |
rs2231475 | snp | A/G | 1.68057e-05 | 0.00289872 | intron-variant | CDC23 | GRCh38.p7 | 5:138201059 | TGCTTCAAGCCTTTT[A/G]TAATTCTGTAGTAAT | 8697 |
rs2231476 | snp | A/G | 0.039522 | 0.134904 | intron-variant | CDC23 | GRCh38.p7 | 5:138198341 | ACTTGTATTAGCTAC[A/G]GGAAAAATAATTTAG | 8697 |
rs2231477 | snp | A/G | 0.0163267 | 0.0888639 | intron-variant | CDC23 | GRCh38.p7 | 5:138192259 | GCTTCGGTAAGCCTG[A/G]TCACTTGACAATGCG | 8697 |
rs2231478 | snp | C/G | 0.322113 | 0.239374 | intron-variant | CDC23 | GRCh38.p7 | 5:138192228 | TCTGATATGGGAAGG[C/G]CTAATAACTTTTTTT | 8697 |
rs2231479 | snp | A/G | 0.00736138 | 0.0602204 | synonymous-codon | CDC23 | GRCh38.p7 | 5:138189654 | TTCAACTTGTGCACA[A/G]AAGTGTTGTGCATTT | 8697 |
rs2231480 | snp | C/T | 0.0076846 | 0.0615081 | synonymous-codon | CDC23 | GRCh38.p7 | 5:138189633 | TTGTGCATTTAATGA[C/T]GTGAGTATCAGTTCT | 8697 |
rs2231481 | snp | G/T | 0.030278 | 0.119257 | intron-variant | CDC23 | GRCh38.p7 | 5:138189500 | AGGCTGAGGCAGGAG[G/T]ATCGCTTGTGTCCAG | 8697 |
rs2906124 | snp | A/T | 0.453818 | 0.144769 | intron-variant | CDC23 | GRCh38.p7 | 5:138193146 | GTTGCCAGGGTGGTC[A/T]CAAACTCCTGAGCTC | 8697 |
rs2906125 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CDC23 | GRCh38.p7 | 5:138197388 | CTAACATGAAAAGAT[A/G]GCAAAGATATATCAT | 8697 |
rs2906126 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CDC23 | GRCh38.p7 | 5:138197389 | TAACATGAAAAGATG[A/G]CAAAGATATATCATT | 8697 |
rs2906127 | snp | A/G | 0.416545 | 0.186448 | intron-variant | CDC23 | GRCh38.p7 | 5:138203777 | aattagccgggcatg[A/G]tagtgagcacctgta | 8697 |
rs2906128 | snp | C/T | 0.417359 | 0.185718 | upstream-variant-2KB | CDC23 | GRCh38.p7 | 5:138214365 | AAAAAAAAGAAAAAA[C/T]GGAAGCTCAGAGAAG | 8697 |
rs2967782 | snp | C/G | 0.453575 | 0.145111 | intron-variant | CDC23 | GRCh38.p7 | 5:138193993 | GCGCTCTAAGTTTCC[C/G]TCTCACACAAGAATC | 8697 |
rs2967783 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | CDC23 | GRCh38.p7 | 5:138197243 | CCCGGGAGGCAGAGC[C/T]TTCAGTGAGCCAATG | 8697 |
rs2967784 | snp | C/T | 0.416545 | 0.186448 | intron-variant | CDC23 | GRCh38.p7 | 5:138203550 | cggagattaaagaga[C/T]atgacaactgattct | 8697 |
rs2967785 | snp | C/T | 0.452227 | 0.146984 | intron-variant | CDC23 | GRCh38.p7 | 5:138208024 | TGGAATGCAGTGGTG[C/T]GATATTGGCTGACTG | 8697 |
rs2967786 | snp | C/T | 0.434976 | 0.168179 | intron-variant | CDC23 | GRCh38.p7 | 5:138211986 | TAATCTTCTTGAAAA[C/T]GCAGCAATTATTAAC | 8697 |
rs2967787 | snp | A/G | 0.417359 | 0.185718 | intron-variant | CDC23 | GRCh38.p7 | 5:138212600 | GGATTACAGGCGTGA[A/G]CCACCGCGCCAGACC | 8697 |
rs3172747 | snp | C/T | 0.0215351 | 0.101508 | downstream-variant-500B, missense, nc-transcript-variant | CDC23, KIF20A | GRCh38.p7 | 5:138187256 | AGGAAAATCAGCAAC[C/T]AAACCAACAACCACC | 8697 |
rs4552585 | snp | C/T | 0.418169 | 0.184985 | intron-variant | CDC23 | GRCh38.p7 | 5:138197470 | GGCAAGCAAACAATA[C/T]AGACGTAACATGTAA | 8697 |
rs4552586 | snp | A/T | 0.277778 | 0.248452 | intron-variant | CDC23 | GRCh38.p7 | 5:138197499 | AATACATATTTATTT[A/T]TTTTTTTTTTTTTTT | 8697 |
rs4994127 | snp | A/G | 0.416055 | 0.186885 | intron-variant | CDC23 | GRCh38.p7 | 5:138197590 | caacctccacctccc[A/G]ggttcatgtgattct | 8697 |
rs6873026 | snp | A/G | | | intron-variant | CDC23 | GRCh38.p7 | 5:138205465 | catgattccacttat[A/G]taaggtacttagagt | 8697 |
rs6875526 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | CDC23 | GRCh38.p7 | 5:138193890 | ttgaacccaggaggc[A/G]gaggttgcggtgagc | 8697 |
rs10035677 | snp | A/G | 0 | 0 | intron-variant | CDC23 | GRCh38.p7 | 5:138195774 | ATATATTATATATGT[A/G]TATATATACATATAT | 8697 |
rs10036450 | snp | A/G | 0.231482 | 0.249313 | intron-variant | CDC23 | GRCh38.p7 | 5:138196675 | aacctccgcctccag[A/G]gttcacaccattctc | 8697 |
rs10042337 | snp | A/C | 0 | 0 | upstream-variant-2KB | CDC23 | GRCh38.p7 | 5:138215163 | ctgggcttaaatgat[A/C]ctctcgccttgccct | 8697 |
rs10061084 | snp | C/T | | | intron-variant | CDC23 | GRCh38.p7 | 5:138210416 | ctgtagtcccagcta[C/T]tcaggaggctgagga | 8697 |
rs10064166 | snp | G/T | 0 | 0 | intron-variant | CDC23 | GRCh38.p7 | 5:138197896 | AGCTTTCACATTCTA[G/T]GGTATGTATTTGTTA | 8697 |
rs11742723 | snp | C/T | | | intron-variant | CDC23 | GRCh38.p7 | 5:138211045 | ggaaaataaattatt[C/T]taccaaaaaaacatc | 8697 |
rs11743620 | snp | A/T | 0.231189 | 0.249291 | intron-variant | CDC23 | GRCh38.p7 | 5:138202850 | aaagattgcttcaga[A/T]aaaaattaacaatga | 8697 |
rs11746039 | snp | A/C | | | intron-variant | CDC23 | GRCh38.p7 | 5:138196867 | ttacaggtgtgagcc[A/C]ccgcgcctggccTTT | 8697 |
rs11950139 | snp | A/T | 0 | 0 | intron-variant | CDC23 | GRCh38.p7 | 5:138193628 | aGAGGTATGATTCTG[A/T]CTCAAAAAAAAAAAA | 8697 |
rs11959165 | snp | A/T | | | intron-variant | CDC23 | GRCh38.p7 | 5:138210850 | CTCTACTTCTCAATA[A/T]ATATGCTTTATTTAC | 8697 |
rs13162536 | snp | A/G | | | intron-variant | CDC23 | GRCh38.p7 | 5:138197179 | ggcgtggtggcaggc[A/G]cctgtagtcccagct | 8697 |
rs13162540 | snp | A/C/G | | | intron-variant | CDC23 | GRCh38.p7 | 5:138197195 | cctgtagtcccagct[A/C/G]ctcgggaggctgagg | 8697 |
rs13167206 | snp | A/C | | | intron-variant | CDC23 | GRCh38.p7 | 5:138190408 | ggttgcagtgagcca[A/C]gatcataccactaca | 8697 |
rs13167208 | snp | A/G | | | intron-variant | CDC23 | GRCh38.p7 | 5:138190413 | cagtgagccaagatc[A/G]taccactacactcca | 8697 |
rs13167345 | snp | A/G | | | intron-variant | CDC23 | GRCh38.p7 | 5:138190502 | ggcactgtggctcac[A/G]cctgtaatcccagca | 8697 |
rs13167466 | snp | A/G | | | intron-variant | CDC23 | GRCh38.p7 | 5:138190397 | tggaaggtggaggtt[A/G]cagtgagccaagatc | 8697 |
rs13167607 | snp | A/G | | | intron-variant | CDC23 | GRCh38.p7 | 5:138190486 | aaaaaaaaaaaagct[A/G]ggcactgtggctcac | 8697 |
rs13167919 | snp | C/G | 0.0569829 | 0.158885 | intron-variant | CDC23 | GRCh38.p7 | 5:138190647 | GCAAGCGCCTGTAAT[C/G]CCAGCTACTCGGGAG | 8697 |
rs13187409 | snp | A/T | | | intron-variant | CDC23 | GRCh38.p7 | 5:138190494 | aaaagctgggcactg[A/T]ggctcacacctgtaa | 8697 |
rs17171780 | snp | C/G | 0.100588 | 0.200439 | intron-variant | CDC23 | GRCh38.p7 | 5:138205127 | ACCATGCCGCCCGGG[C/G]TTCCTTTTATATTTT | 8697 |
rs17228297 | snp | C/T | 3.29603e-05 | 0.00405944 | intron-variant | CDC23 | GRCh38.p7 | 5:138213080 | TCGAGCTGATCTAGT[C/T]TGTGTGGGTGTTCCA | 8697 |
rs17228304 | snp | C/G | 0.000313472 | 0.0125155 | missense | CDC23 | GRCh38.p7 | 5:138212993 | CCTCCGCCTATTACA[C/G]AGGTAAGGACATGTT | 8697 |
rs17228311 | snp | A/C | 0.00112311 | 0.0236706 | intron-variant | CDC23 | GRCh38.p7 | 5:138212968 | CATGTTTACAGTGAG[A/C]GCTCCCCATCAACCC | 8697 |
rs17228325 | snp | C/T | 0.0696718 | 0.173152 | intron-variant | CDC23 | GRCh38.p7 | 5:138210953 | TGAAAAATCTGTGAA[C/T]TCTGTTAGTTCAGAG | 8697 |
rs17228332 | snp | C/G | 0.0189856 | 0.0955633 | intron-variant | CDC23 | GRCh38.p7 | 5:138210714 | TGGTTTGTTGAATAG[C/G]TTTCAGTTTGCTGTG | 8697 |
rs17228339 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CDC23 | GRCh38.p7 | 5:138210184 | CTGTTACCCAGGCTG[A/G]AGTGCAGTGGCTCAA | 8697 |
rs17228353 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | CDC23 | GRCh38.p7 | 5:138207883 | GAAGTGATGTGGCGC[A/G]ATCTTGGCTCACTGC | 8697 |
rs17228360 | snp | A/C | 0.0121208 | 0.0768991 | intron-variant | CDC23 | GRCh38.p7 | 5:138207867 | ATCTTGGCTCACTGC[A/C]GCAAGGCTCAGCCTC | 8697 |
rs17228367 | in-del | -/T | 0.0116955 | 0.0755709 | intron-variant | CDC23 | GRCh38.p7 | 5:138207632 | TATCTAATTTTTTTT[-/T]AACATAGAGAATTAC | 8697 |
rs17228374 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC23 | GRCh38.p7 | 5:138204939 | CAACAGAGCAAGACC[C/G]TGTCACCAAAAAAAA | 8697 |
rs17228381 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | CDC23 | GRCh38.p7 | 5:138203952 | ATGGCATTTGATACT[A/G]TATTCAATCTATTAT | 8697 |
rs17228395 | snp | C/T | 0.027392 | 0.113779 | intron-variant | CDC23 | GRCh38.p7 | 5:138203634 | GTGAGCCACTGCACC[C/T]GGCCGAATTCCAATC | 8697 |
rs17228408 | in-del | -/ATAA | 0.00676609 | 0.0577691 | intron-variant | CDC23 | GRCh38.p7 | 5:138202276 | TAAATAAATAAATAA[-/ATAA]TGACCAAAAGTCGAT | 8697 |
rs17228422 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | CDC23 | GRCh38.p7 | 5:138201803 | TCAAATAAAAACTGT[A/G]TGGGTCTAACAGAAT | 8697 |
rs17228428 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | CDC23 | GRCh38.p7 | 5:138200973 | CCTCTGGTGTCTTTT[C/T]GCTGTTTTGGAAGTA | 8697 |
rs17228435 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CDC23 | GRCh38.p7 | 5:138200414 | CCAGGCACGGTGGCT[C/T]ATGCCTGTAATCCTA | 8697 |
rs17228442 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | CDC23 | GRCh38.p7 | 5:138199813 | TGCCTACTAGACTTT[C/T]ATTATTGAAGGTTTG | 8697 |
rs17228449 | in-del | -/ATT | 0.030665 | 0.119967 | intron-variant | CDC23 | GRCh38.p7 | 5:138199809 | TACTAGACTTTCATT[-/ATT]GAAGGTTTGTTAAAC | 8697 |
rs17228456 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC23 | GRCh38.p7 | 5:138197901 | AAAGGTAACAAATAC[A/G]TACCATAGAATGTGA | 8697 |
rs17228463 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | CDC23 | GRCh38.p7 | 5:138195954 | AGTGATGGCAAGAAT[C/T]TCCTACTTGTTTAGT | 8697 |
rs17228470 | snp | A/T | 0.0310518 | 0.120672 | intron-variant | CDC23 | GRCh38.p7 | 5:138195257 | CTGTACCTTTCCCCC[A/T]TTAAGTTACTTGTGT | 8697 |
rs17228477 | snp | A/C | 0.0535932 | 0.154675 | intron-variant | CDC23 | GRCh38.p7 | 5:138195179 | GCAAGGTTTAATGGG[A/C]TGCTTGCTTTACAAA | 8697 |
rs17228484 | snp | C/G | 0.0260105 | 0.111035 | intron-variant | CDC23 | GRCh38.p7 | 5:138194248 | TGCCCATGCTGGTCT[C/G]GAACTCCTGACCTTA | 8697 |
rs17228498 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | CDC23 | GRCh38.p7 | 5:138193593 | TTCCTTTTTTTTTAA[A/G]ATGTTGTTTTGCTCT | 8697 |
rs17228505 | snp | A/C | 0.0238061 | 0.106472 | intron-variant | CDC23 | GRCh38.p7 | 5:138193571 | TTTTGCTCTATTACC[A/C]AAGCTGGAGTGCAGT | 8697 |
rs17228512 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | CDC23 | GRCh38.p7 | 5:138191994 | GTACTGGTTCCTCAA[A/G]AGAGAACTTCAGTTT | 8697 |
rs17228519 | snp | C/T | 0.00291355 | 0.0380564 | intron-variant | CDC23 | GRCh38.p7 | 5:138191951 | TGCTCAGACTGCCTG[C/T]TCTTCTTTCTCAGAC | 8697 |
rs17228526 | snp | C/T | 0 | 0 | intron-variant | CDC23 | GRCh38.p7 | 5:138191408 | ATGGTGGGTCCTGCA[C/T]GGTCTAGAGCCTCCC | 8697 |
rs17228533 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC23 | GRCh38.p7 | 5:138191207 | GGAGTTCAAGACCTG[A/G]GAGGTGGAGGTTGCA | 8697 |
rs17228540 | snp | A/C/T | 0.00319074 | 0.0398324 | intron-variant | CDC23 | GRCh38.p7 | 5:138190059 | TAACAGTAACTATCA[A/C/T]ATCTAATACTATTCT | 8697 |
rs17228547 | snp | C/T | 0.0142736 | 0.0832652 | utr-variant-3-prime, downstream-variant-500B | CDC23, KIF20A | GRCh38.p7 | 5:138187838 | TTAGAATATCTAATA[C/T]GACTTGAATTCATTT | 8697 |
rs17234695 | in-del | -/G | 0.417359 | 0.185718 | intron-variant | CDC23 | GRCh38.p7 | 5:138212797 | TTGAAAGACTTGGTG[-/G]TGCTCTTATTTAAAG | 8697 |
rs17234716 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | CDC23 | GRCh38.p7 | 5:138212313 | AATAAATAAATAAAG[G/T]TTTTACAATACCTAC | 8697 |
rs17234723 | snp | A/C | 0.0118339 | 0.076006 | intron-variant | CDC23 | GRCh38.p7 | 5:138210082 | ATTACAGGTGCATGC[A/C]ACAACACCTGGCTAA | 8697 |
rs17234730 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | CDC23 | GRCh38.p7 | 5:138210027 | GAGGTTTCACCATGT[A/T]GGCCAGGCTGGTCTC | 8697 |
rs17234737 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | CDC23 | GRCh38.p7 | 5:138210026 | AGGTTTCACCATGTT[A/G]GCCAGGCTGGTCTCG | 8697 |
rs17234758 | in-del | -/GTTTCT | 0.00358779 | 0.0422022 | intron-variant | CDC23 | GRCh38.p7 | 5:138205493 | ACTATTCTATTTTCT[-/GTTTCT]ATGATCTGGACTACT | 8697 |
rs17234765 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | CDC23 | GRCh38.p7 | 5:138205241 | TTTCACATACAATCT[A/G]TACCTGTGTAGAAGC | 8697 |
rs17234772 | snp | A/T | 0.0141837 | 0.08301 | intron-variant | CDC23 | GRCh38.p7 | 5:138205169 | CTGAAGTTTGGGATA[A/T]AATAAAGTTCCTTAA | 8697 |
rs17234793 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | CDC23 | GRCh38.p7 | 5:138203469 | ATTTATAAATCTTCC[C/T]TCCCTGTTTCTTTTT | 8697 |
rs17234800 | snp | G/T | 0.0463947 | 0.145069 | intron-variant | CDC23 | GRCh38.p7 | 5:138203181 | CCTTTCCATTTCCCC[G/T]TCCTTTCCTTTCCCT | 8697 |
rs17234807 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | CDC23 | GRCh38.p7 | 5:138203088 | CTTCATTTTGGATAT[G/T]TCTGATGTTTTTTCA | 8697 |