SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6507 | snp | C/T | 0.262974 | 0.249663 | synonymous-codon | CDC34 | GRCh38.p7 | 19:532066 | CTGGGAGGTGGCCAT[C/T]TTCGGGCCCCCCAAC | 997 |
rs7150 | snp | C/T | 0.464947 | 0.127663 | utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541685 | TTTGGCTTTTTCTCC[C/T]TCCCCATGTCTGTTC | 997 |
rs7528 | snp | C/T | 0.0611083 | 0.163768 | utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541917 | GGCGGGGGGCCGTTT[C/T]CTGACACTACCAGCC | 997 |
rs7529 | snp | A/T | 0.185788 | 0.241613 | utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:542009 | AGCCACGTCCAGCAC[A/T]GAGTGGACGGATTCA | 997 |
rs892201 | snp | C/T | 0.195837 | 0.244062 | intron-variant | CDC34 | GRCh38.p7 | 19:536536 | CGGGGCCTGCGGCAC[C/T]GTGTGTCGGTGCAGA | 997 |
rs892202 | snp | A/C | 0.18968 | 0.248073 | intron-variant | CDC34 | GRCh38.p7 | 19:536610 | TAGAGGTGTCCCGCC[A/C]TCCTCAGTCCTGGGG | 997 |
rs892203 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | CDC34 | GRCh38.p7 | 19:536742 | TCCTGGAGTGTAGTC[C/T]AGGCAGGACGTGCGG | 997 |
rs892204 | snp | A/G | 0.190519 | 0.242821 | intron-variant | CDC34 | GRCh38.p7 | 19:536900 | AGGCCATGAGGCCAG[A/G]TGAAGGTCACCTGCT | 997 |
rs1108113 | snp | C/T | 0.477937 | 0.102688 | intron-variant | CDC34 | GRCh38.p7 | 19:536681 | GCCACGTGTGCCGCC[C/T]GGGCCTCGTCCCCAG | 997 |
rs1108114 | snp | A/G | 0.464947 | 0.127663 | intron-variant | CDC34 | GRCh38.p7 | 19:536878 | TGGGGGCCTGAGACA[A/G]AAGCAGAGGCCATGA | 997 |
rs1108115 | snp | A/G | 0.4776 | 0.103433 | intron-variant | CDC34 | GRCh38.p7 | 19:536510 | CTGTACCTGCACGGT[A/G]GGTGCTTTCACGGGG | 997 |
rs1313710 | snp | A/G | 0 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:540780 | CCGGGTTTAGAATCC[A/G]GAGGCTGGGATGGCC | 997 |
rs1313711 | snp | C/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:540804 | GATGGCCAGGCCCCC[C/G]GGTTTAGAATCCGGA | 997 |
rs1313712 | snp | A/G | 0.429305 | 0.174212 | intron-variant | CDC34 | GRCh38.p7 | 19:540817 | CCCGGTTTAGAATCC[A/G]GAGGCCGGGGTGGCC | 997 |
rs1313713 | snp | C/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:540841 | GGTGGCCAGGCCCCC[C/G]GGTTTAGAATCCTGC | 997 |
rs1982084 | snp | C/T | 0.375 | 0.216506 | intron-variant | CDC34 | GRCh38.p7 | 19:540080 | GCCGGGGTGGCCAGG[C/T]CCCCCAGGTTTAGAA | 997 |
rs2011204 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | CDC34 | GRCh38.p7 | 19:537694 | AGAGTTATACTCTCT[C/T]GCCTAGGCTGCAGTG | 997 |
rs2011210 | snp | C/G | 0.441705 | 0.160466 | intron-variant | CDC34 | GRCh38.p7 | 19:537645 | aaaaaaaaaggccgg[C/G]cgcggtggctcacgc | 997 |
rs2011211 | snp | C/T | 0.0955749 | 0.196603 | intron-variant | CDC34 | GRCh38.p7 | 19:537598 | ACCTCGTGATCCATC[C/T]GCCTCGGCCTCCCAA | 997 |
rs2011225 | snp | C/T | 0.464947 | 0.127663 | intron-variant | CDC34 | GRCh38.p7 | 19:537421 | GCAGTGGCGCGATCT[C/T]GGCTCACTGCAAGCT | 997 |
rs2011226 | snp | A/G | 0.464841 | 0.127841 | intron-variant | CDC34 | GRCh38.p7 | 19:537414 | CTGGAGTGCAGTGGC[A/G]CGATCTCGGCTCACT | 997 |
rs2288951 | snp | A/G | 0.464841 | 0.127841 | intron-variant | CDC34 | GRCh38.p7 | 19:538487 | CTTTACGGGTTGACG[A/G]CCTTAATGGTTCCTG | 997 |
rs2288952 | snp | A/G | 0.375 | 0.216506 | intron-variant, synonymous-codon | CDC34 | GRCh38.p7 | 19:538930 | CGTGTCACCTGGCCC[A/G]GGTGGCTGGCTCCTT | 997 |
rs2288953 | snp | C/T | 0.433884 | 0.169371 | intron-variant, utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:538994 | CCACCTCCTTGAGAT[C/T]CCAGCACAGAAATAA | 997 |
rs2288954 | snp | C/G | 0.464841 | 0.127841 | intron-variant, downstream-variant-500B | CDC34 | GRCh38.p7 | 19:539174 | CAGGCTGCCGTGGAG[C/G]CCGGCTTGGTCAGGG | 997 |
rs2288955 | snp | A/G | 0.465892 | 0.126058 | intron-variant, downstream-variant-500B | CDC34 | GRCh38.p7 | 19:539222 | CAGGACCTCCAGACC[A/G]TCCTCCAGCTCATGC | 997 |
rs2288956 | snp | C/T | 0.298144 | 0.245321 | intron-variant, downstream-variant-500B | CDC34 | GRCh38.p7 | 19:539279 | GGTGCAGGTCAGTTC[C/T]CACCCTGGCCCTCCC | 997 |
rs2396295 | snp | A/G | 0.190833 | 0.242898 | intron-variant | CDC34 | GRCh38.p7 | 19:536437 | AGGCCGGGCTCCCCC[A/G]CAGGCTGTGGCGCCA | 997 |
rs3760879 | snp | C/T | 0.278399 | 0.248382 | upstream-variant-2KB, downstream-variant-500B | GZMM, CDC34 | GRCh38.p7 | 19:542494 | CACCCCGAGGGTGTG[C/T]CTGGACGGAGCTGGA | 997 |
rs3760880 | snp | A/C | 0.112631 | 0.208878 | upstream-variant-2KB, downstream-variant-500B | GZMM, CDC34 | GRCh38.p7 | 19:542473 | CGGAGCTGGAGCCGC[A/C]GGAGTGCTGATCGGG | 997 |
rs3810355 | snp | A/G | 0.00398564 | 0.0444627 | upstream-variant-2KB, downstream-variant-500B | GZMM, CDC34 | GRCh38.p7 | 19:542233 | GGGAACGTACAGGCC[A/G]CGGGACCCGGCTGCT | 997 |
rs3826891 | snp | C/T | 0.112983 | 0.209108 | upstream-variant-2KB, downstream-variant-500B | GZMM, CDC34 | GRCh38.p7 | 19:542395 | GCGGCTGTGGACCCG[C/T]GACGAAGCTTTGCTG | 997 |
rs3930362 | snp | C/G | 0 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:540049 | TGGCCAGGCCCCCCA[C/G]GTTTAGAATCCGGAG | 997 |
rs3930363 | snp | A/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:540099 | CCAGGTTTAGAATCC[A/G]GAGGCCGGGGTGGCC | 997 |
rs3930364 | snp | C/T | | | intron-variant | CDC34 | GRCh38.p7 | 19:540118 | GCCGGGGTGGCCAGG[C/T]CCCCCACGTTTAGAA | 997 |
rs3930365 | snp | C/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:540125 | TGGCCAGGCCCCCCA[C/G]GTTTAGAATCCGGAG | 997 |
rs4264506 | snp | C/T | 0.468949 | 0.12067 | intron-variant | CDC34 | GRCh38.p7 | 19:536088 | CGTCCTTCCGGGACC[C/T]GAGGCGCTGGGAGCC | 997 |
rs4541184 | snp | A/G | 0.5 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:536068 | CGCTGGGAGCCTCAC[A/G]TCCTCGTCCTTCCGG | 997 |
rs4919914 | snp | C/T | 0.465788 | 0.126237 | intron-variant | CDC34 | GRCh38.p7 | 19:532570 | GGAGACAAAGAGGCC[C/T]CCCCAGACCCCGTAG | 997 |
rs5826697 | in-del | -/T | 0.227959 | 0.249026 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:529956 | GGTTTTTGTTTTTGG[-/T]TTTTTTTTTTTTTGA | 997 |
rs5826698 | in-del | -/T | 0.5 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:536038 | CTCACGTCCTCGTCC[-/T]TCCGGGACCCGGGGC | 997 |
rs5826701 | snp | C/T | 0 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:540042 | GCCGGGGTGGCCAGG[C/T]CCCCCACGTTTAGAA | 997 |
rs6510823 | snp | C/G | 0.29046 | 0.246704 | intron-variant | CDC34 | GRCh38.p7 | 19:533872 | GGGAGTTGGGGGAGC[C/G]TGGAAATACAGAACC | 997 |
rs6510824 | snp | C/T | 0.321053 | 0.23969 | intron-variant | CDC34 | GRCh38.p7 | 19:533986 | GGCCGCCAGAGAGAG[C/T]CCTCCACAGCCGACT | 997 |
rs6510825 | snp | A/G | 0.321292 | 0.23962 | intron-variant | CDC34 | GRCh38.p7 | 19:534062 | TTGCTCCGGGGAAAA[A/G]ACATTCTTAGAGGTG | 997 |
rs7249135 | snp | G/T | 0.0399052 | 0.1355 | intron-variant | CDC34 | GRCh38.p7 | 19:536585 | GCCGGCCCCACCGTC[G/T]GGAACCACCTAGAGG | 997 |
rs7249253 | snp | G/T | 0.493793 | 0.055364 | intron-variant | CDC34 | GRCh38.p7 | 19:534601 | GACCCCCGAGTGCCC[G/T]CCCTGTCCAGACCTC | 997 |
rs7251904 | snp | A/G | 0.46875 | 0.121031 | intron-variant | CDC34 | GRCh38.p7 | 19:534729 | CCAAGACCCCCGAGT[A/G]CCCTCCCTGTCCAGA | 997 |
rs7252421 | snp | A/G | 0 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:540743 | CCGGGTTTAGAATCC[A/G]GAGGCTGGGATGGCC | 997 |
rs7254191 | snp | A/G | 0.0337553 | 0.125452 | intron-variant, missense | CDC34 | GRCh38.p7 | 19:538740 | TGGTGTCGTGGGGTC[A/G]TCTCGGGGCAGCATC | 997 |
rs7254483 | snp | A/T | 0.0573587 | 0.15934 | intron-variant, missense | CDC34 | GRCh38.p7 | 19:538974 | CCGGCCACCTCCCTG[A/T]GGCACCACCTCCTTG | 997 |
rs7255072 | snp | A/G | 0.466308 | 0.125343 | intron-variant, downstream-variant-500B | CDC34 | GRCh38.p7 | 19:539250 | TGCTGGCGGTGTGCC[A/G]GCGGCACCTCCACGG | 997 |
rs7255299 | snp | A/G | 0 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:540790 | AATCCAGAGGCTGGG[A/G]TGGCCAGGCCCCCCG | 997 |
rs7256060 | snp | C/T | 0.273318 | 0.24891 | intron-variant | CDC34 | GRCh38.p7 | 19:534798 | TCCAGACCTCGCCCA[C/T]GATCCAAGACCCCCG | 997 |
rs7256168 | snp | G/T | 0.5 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:534821 | GACCCCCGAGTGCCC[G/T]CCCTGTCCAGACCTC | 997 |
rs7259097 | snp | C/T | 0 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:540786 | TTAGAATCCAGAGGC[C/T]GGGATGGCCAGGCCC | 997 |
rs7259421 | snp | C/T | 0.492386 | 0.0612297 | intron-variant | CDC34 | GRCh38.p7 | 19:535004 | CTGACCCAGACAACC[C/T]CTGTGTCTGGCACTG | 997 |
rs7508345 | snp | A/C/G | 0.000148877 | 0.0086265 | intron-variant | CDC34 | GRCh38.p7 | 19:535949 | CCCCCACGGGCCTCA[A/C/G]GTCCTCATCCTCCGG | 997 |
rs8104513 | snp | A/G | 0.0399052 | 0.1355 | intron-variant | CDC34 | GRCh38.p7 | 19:538098 | CTTAATGAAGAAATG[A/G]GGTCGTGCTGTGTGT | 997 |
rs8107361 | snp | A/G | 0.190833 | 0.242898 | intron-variant | CDC34 | GRCh38.p7 | 19:538160 | CTGTGCTTTAATGAA[A/G]AAATGGGGTCGTGCT | 997 |
rs10402948 | snp | C/T | 0.184203 | 0.241186 | intron-variant, downstream-variant-500B | CDC34 | GRCh38.p7 | 19:539266 | GCGGCACCTCCACGG[C/T]GCAGGTCAGTTCCCA | 997 |
rs10406729 | snp | C/T | 0.5 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:536107 | GCGCTGGGAGCCTCA[C/T]GTCCTCGTCCTTCCG | 997 |
rs10409849 | snp | C/G | 0.499992 | 0.00199679 | intron-variant | CDC34 | GRCh38.p7 | 19:535621 | TGGACTGTGTAGGAG[C/G]TGGGATCAGCTCGGG | 997 |
rs10415110 | snp | A/G | 0.106278 | 0.204558 | intron-variant | CDC34 | GRCh38.p7 | 19:535535 | GACCTGGGCTGCCAC[A/G]GGCCTGGAGCCACGC | 997 |
rs10415326 | snp | A/G | 0.232067 | 0.249356 | intron-variant | CDC34 | GRCh38.p7 | 19:535634 | AGCTGGGATCAGCTC[A/G]GGTGACTCAGAAAAG | 997 |
rs10419323 | snp | A/G | 0.11228 | 0.208646 | intron-variant | CDC34 | GRCh38.p7 | 19:539903 | GGGCCGGGTGTACAC[A/G]GTGCCCTCCAGGAAG | 997 |
rs10421502 | snp | A/T | 0.106633 | 0.204807 | intron-variant | CDC34 | GRCh38.p7 | 19:538169 | AATGAAGAAATGGGG[A/T]CGTGCTGTGTGTGCC | 997 |
rs10426138 | snp | A/G | 0.5 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:536090 | TCCTTCCGGGACCCG[A/G]GGCGCTGGGAGCCTC | 997 |
rs10853978 | snp | C/T | 0.476574 | 0.105661 | intron-variant | CDC34 | GRCh38.p7 | 19:539593 | GGGGCTGTCTGTCTG[C/T]TCCCTGGTGCCCTCC | 997 |
rs10853979 | snp | A/C | 0.464841 | 0.127841 | intron-variant | CDC34 | GRCh38.p7 | 19:539812 | TCCTGGGGGGACATT[A/C]TTGACGCGTGTCCTG | 997 |
rs10853980 | snp | C/T | 0.464841 | 0.127841 | intron-variant | CDC34 | GRCh38.p7 | 19:539817 | GGGGGACATTCTTGA[C/T]GCGTGTCCTGGAGGT | 997 |
rs11557524 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541912 | ACGTGGGCGGGGGGC[C/T]GTTTCCTGACACTAC | 997 |
rs11557525 | snp | A/C/T | 0.000830146 | 0.0203578 | synonymous-codon | CDC34 | GRCh38.p7 | 19:537034 | TCTCCTGAGTGTGAT[A/C/T]TCCCTCCTGAACGAG | 997 |
rs11667548 | snp | C/G | 0.0387552 | 0.1337 | intron-variant | CDC34 | GRCh38.p7 | 19:539730 | CCTCGTTCCTGTTTT[C/G]TGTCAAATGGGGTCA | 997 |
rs11878756 | snp | A/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:534439 | CCCTGTCCAGACCTC[A/G]CCCACGATCCAAGAC | 997 |
rs11881685 | snp | C/G | 0.0532157 | 0.154195 | intron-variant | CDC34 | GRCh38.p7 | 19:535528 | TATGCCTGACCTGGG[C/G]TGCCACGGGCCTGGA | 997 |
rs11881961 | snp | A/G | 0.5 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:534401 | AGGGGCCTCGCCCAC[A/G]ATCCAAGACCCCCGA | 997 |
rs11881969 | snp | A/G | 0.18 | 0.24 | intron-variant | CDC34 | GRCh38.p7 | 19:534484 | CCCTGTCCAGACCTC[A/G]CCCACGATCCAAGAC | 997 |
rs11883123 | snp | C/T | 0.16976 | 0.236773 | intron-variant | CDC34 | GRCh38.p7 | 19:537453 | cgcctcccgggttca[C/T]gccattctcctgcct | 997 |
rs12461965 | snp | C/T | 0.17138 | 0.237316 | intron-variant | CDC34 | GRCh38.p7 | 19:533133 | ACGTGACCTTTGACT[C/T]CTTTTAGCGTTCAGG | 997 |
rs12608630 | snp | C/T | 0.42443 | 0.179092 | intron-variant | CDC34 | GRCh38.p7 | 19:541260 | GCGTTGGGGTGAGCG[C/T]CGGACCTGGGGGAGG | 997 |
rs12609463 | snp | A/G | 0.183886 | 0.241099 | intron-variant | CDC34 | GRCh38.p7 | 19:541133 | TCCAGCCTCCCACCC[A/G]CACCTCCTGCCCTTC | 997 |
rs12972025 | snp | C/T | 0.331874 | 0.236213 | intron-variant | CDC34 | GRCh38.p7 | 19:534350 | GGAGGGGCCCGTCCA[C/T]GATCCAAGACCCCCA | 997 |
rs12972728 | snp | A/C | 0.46875 | 0.121031 | intron-variant | CDC34 | GRCh38.p7 | 19:534609 | AGTGCCCGCCCTGTC[A/C]AGACCTCGCCCACGA | 997 |
rs12972984 | snp | A/C | 0.277778 | 0.248452 | intron-variant | CDC34 | GRCh38.p7 | 19:534741 | AGTGCCCTCCCTGTC[A/C]AGACCTCGCCCACGA | 997 |
rs12973414 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CDC34 | GRCh38.p7 | 19:536147 | GCGCTGGGAGCCTCA[C/T]GTCCTCGTCCTCCAC | 997 |
rs12976021 | snp | C/T | 0.465158 | 0.127307 | intron-variant | CDC34 | GRCh38.p7 | 19:534263 | CCAAGTCACTTGCCT[C/T]ACGGGGCACCAGTGA | 997 |
rs12978637 | snp | A/G | 0.5 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:534462 | TCCAAGACCCCCTGA[A/G]TGCCCTCCCTGTCCA | 997 |
rs12978802 | snp | C/T | 0 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:540636 | TTAGAATCCGGAGGC[C/T]GGGGTGGCCAGGCCC | 997 |
rs12978882 | snp | A/G | 0.277778 | 0.248452 | intron-variant | CDC34 | GRCh38.p7 | 19:534744 | GCCCTCCCTGTCCAG[A/G]CCTCGCCCACGATCC | 997 |
rs12978889 | snp | A/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:534579 | CAAGGCCTCGCCCAC[A/G]ATCCAAGACCCCCGA | 997 |
rs12979110 | snp | A/C | 0.242488 | 0.249887 | intron-variant | CDC34 | GRCh38.p7 | 19:533552 | CAGCTCCTCCGCCAG[A/C]CCCTTCTGTCTGCTT | 997 |
rs12979642 | snp | A/G | 0.5 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:534843 | CCAGACCTCGCCCAC[A/G]ATCCAAGACCCCCTG | 997 |
rs12979793 | snp | A/G | 0.5 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:536130 | TCCTTCCGGGACCCG[A/G]GGCGCTGGGAGCCTC | 997 |
rs12983064 | snp | A/G | 0.152778 | 0.230321 | intron-variant, synonymous-codon | CDC34 | GRCh38.p7 | 19:538687 | CCCCAGGACCCAGGA[A/G]CATCCAGGGCACCTT | 997 |
rs12983594 | snp | C/G | 0.444444 | 0.157135 | intron-variant | CDC34 | GRCh38.p7 | 19:540087 | TGGCCAGGCCCCCCA[C/G]GTTTAGAATCCGGAG | 997 |
rs12984199 | snp | A/T | 0.5 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:534461 | ATCCAAGACCCCCTG[A/T]GTGCCCTCCCTGTCC | 997 |
rs12984443 | snp | A/G | 0.42 | 0.183303 | intron-variant | CDC34 | GRCh38.p7 | 19:534535 | CCAGACCTCGCCCAC[A/G]ATCCAAGACCCCCGA | 997 |
rs12984468 | snp | A/C | 0 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:534565 | AGTACCCTCCCTGTC[A/C]AGGCCTCGCCCACGA | 997 |
rs12984645 | snp | A/G | 0.445328 | 0.156035 | intron-variant | CDC34 | GRCh38.p7 | 19:533201 | CCCTGTGTGAGCGGT[A/G]GGGAACGAGCACCCT | 997 |