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 |
rs12984708 | snp | A/G | 0.5 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:534612 | GCCCGCCCTGTCCAG[A/G]CCTCGCCCACGATCC | 997 |
rs12984899 | snp | A/G | 0 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:540503 | GTGGCCAGGCCCCCC[A/G]GGTTTAGAATCCGGA | 997 |
rs12984900 | snp | C/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:540504 | TGGCCAGGCCCCCCG[C/G]GTTTAGAATCCGGAG | 997 |
rs12984940 | snp | A/G | 0.375 | 0.216506 | intron-variant | CDC34 | GRCh38.p7 | 19:540554 | CCGGGTTTAGAATCC[A/G]GAGGCCGGGGTGGCC | 997 |
rs12984950 | snp | A/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:540564 | AATCCGGAGGCCGGG[A/G]TGGCCAGGCCCCCCG | 997 |
rs12985200 | snp | C/T | 0.031825 | 0.122064 | intron-variant | CDC34 | GRCh38.p7 | 19:532347 | ATCCCCAGTTCCCTT[C/T]AAGGCATCGTCCGGT | 997 |
rs12985201 | snp | A/G | 0 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:540602 | AATCCGGAGGCCGGG[A/G]TGGCCAGGCCCCCCG | 997 |
rs12985212 | snp | A/G | 0 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:540617 | GTGGCCAGGCCCCCC[A/G]GGTTTAGAATCCGGA | 997 |
rs12985216 | snp | C/G | 0 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:540618 | TGGCCAGGCCCCCCG[C/G]GTTTAGAATCCGGAG | 997 |
rs12985246 | snp | A/G | 0 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:540640 | AATCCGGAGGCCGGG[A/G]TGGCCAGGCCCCCCG | 997 |
rs12985264 | snp | A/G | 0.395818 | 0.203069 | intron-variant | CDC34 | GRCh38.p7 | 19:540678 | AATCCGGAGGCCGGG[A/G]TGGCCAGGCCCCCCA | 997 |
rs16989712 | snp | A/G | 0.202035 | 0.245356 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:530724 | CTCAGCTACTCGGGA[A/G]GCTGAGGCGGACACT | 997 |
rs16989717 | snp | C/G | 0.0150606 | 0.0854603 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:530807 | GCCTGGGCCACAGAA[C/G]GAGACTCTGTCTCAT | 997 |
rs16989721 | snp | A/T | 0.0111728 | 0.0739025 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:530916 | GCTTGGGGTGGGGGC[A/T]CCGTGGGGCTGGCGC | 997 |
rs16989724 | snp | C/T | 0.111928 | 0.208413 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:531115 | CCTCAGAGCCCTCCC[C/T]GACCTCGCCCACTTC | 997 |
rs16989726 | snp | C/G | 0.193028 | 0.243422 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:531157 | GCTGTCGGGGGAACC[C/G]AGGCAGCGCCGCGCC | 997 |
rs16989728 | snp | C/G | 0.00953873 | 0.0683987 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:531169 | ACCGAGGCAGCGCCG[C/G]GCCTGGAAGCCAGGT | 997 |
rs16989730 | snp | C/T | 0.00636936 | 0.0560724 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:531456 | CAGAGCAGCCCTGCC[C/T]GCCTCCTTGCGCACA | 997 |
rs16989733 | snp | C/T | 0.0158469 | 0.0875917 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:531473 | CCTCCTTGCGCACAG[C/T]GTCCGCGGTGCTGGT | 997 |
rs16989736 | snp | A/G | 0.0111728 | 0.0739025 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:531501 | GGTCGAGCAGGGGGC[A/G]ACGGCGGCGGCCTCG | 997 |
rs16989739 | snp | A/C | 0.0460142 | 0.144533 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:531530 | CGGGGATCGGAAGAG[A/C]CCGGGGCTGCGCGCT | 997 |
rs16989741 | snp | C/T | 0.021333 | 0.101051 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:531537 | CGGAAGAGCCCGGGG[C/T]TGCGCGCTCGAACCC | 997 |
rs16989743 | snp | A/C | 0.0178098 | 0.0926698 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:531546 | CCGGGGCTGCGCGCT[A/C]GAACCCTCCCTCCCG | 997 |
rs16989748 | snp | A/G | 0.02016 | 0.0983543 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:531547 | CGGGGCTGCGCGCTC[A/G]AACCCTCCCTCCCGG | 997 |
rs16989750 | snp | A/G | 0.106987 | 0.205054 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:531625 | CCCGGCGTCCCCTGC[A/G]GCCGGGCGCGCAGGC | 997 |
rs16989752 | snp | A/C | 0.00199481 | 0.0315187 | utr-variant-5-prime | CDC34 | GRCh38.p7 | 19:531736 | GGGCCCGGCCAAGGC[A/C]AGCGCCGGTGGGGCG | 997 |
rs16989755 | snp | C/G | 0.0162591 | 0.0886858 | utr-variant-5-prime | CDC34 | GRCh38.p7 | 19:531818 | GCAGAGGAGGAGGCA[C/G]GCGGCGGCCCCGGTG | 997 |
rs16989771 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | CDC34 | GRCh38.p7 | 19:532184 | CCAGCTCCCTGCCCC[A/G]CGGTCCTAGCGCTGT | 997 |
rs16989781 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, missense | CDC34 | GRCh38.p7 | 19:538797 | GCAGCCATGGTGGGC[A/G]GGCCCCGTGCGGCCT | 997 |
rs16989782 | snp | C/T | 0.0219753 | 0.102493 | intron-variant, synonymous-codon | CDC34 | GRCh38.p7 | 19:538867 | GTCACAGGGTAGCTG[C/T]CCTGGCCGTCCCTCT | 997 |
rs16989783 | snp | C/T | 0.0110494 | 0.0735024 | intron-variant, synonymous-codon | CDC34 | GRCh38.p7 | 19:538906 | TGTCCTCGGTGGCCC[C/T]GGTCCGGTCGTGTCA | 997 |
rs16989788 | snp | A/G | 0.5 | 0 | intron-variant, missense | CDC34 | GRCh38.p7 | 19:538961 | GGCCCGGTTCTTCCC[A/G]GCCACCTCCCTGAGG | 997 |
rs16989793 | snp | C/T | 0.0126979 | 0.078662 | intron-variant, missense | CDC34 | GRCh38.p7 | 19:538982 | CTCCCTGAGGCACCA[C/T]CTCCTTGAGATCCCA | 997 |
rs16990492 | snp | C/G | 0.00636936 | 0.0560724 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:529875 | TCCTCTTCCGGGGAC[C/G]AGACTCATGAAGCCG | 997 |
rs16990493 | snp | A/C | 0.0490535 | 0.14873 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:529938 | TGGCCCTGGTCCCAG[A/C]CTGGTTTTTGTTTTT | 997 |
rs16990494 | snp | A/G | 0.0376037 | 0.131863 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:530109 | CCCGCCACCACGCCC[A/G]GATAATTTTTTGTAT | 997 |
rs16990496 | snp | G/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:530140 | TTTTAGTAGAGACGG[G/T]GTTTCACCATATTAG | 997 |
rs16990498 | snp | A/C | 0.137867 | 0.223442 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:530556 | CGACGCAGACGGATC[A/C]CTTTATTAGTCCAAA | 997 |
rs16990500 | snp | G/T | 0.0402882 | 0.136092 | intron-variant | CDC34 | GRCh38.p7 | 19:532268 | ACGTTCCCCCACCCA[G/T]CTCTGCCCGGCCCCC | 997 |
rs16990502 | snp | C/T | 0.465996 | 0.12588 | intron-variant | CDC34 | GRCh38.p7 | 19:532337 | GTCCTCGAAAATCCC[C/T]AGTTCCCTTCAAGGC | 997 |
rs16990506 | snp | A/C | 0.0869089 | 0.189476 | intron-variant | CDC34 | GRCh38.p7 | 19:532364 | AGGCATCGTCCGGTC[A/C]CCTGTTAGGCTCTTG | 997 |
rs16990508 | snp | A/T | 0.0980852 | 0.198549 | intron-variant | CDC34 | GRCh38.p7 | 19:532575 | CAAAGAGGCCCCCCC[A/T]GACCCCGTAGCTGCT | 997 |
rs16990510 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | CDC34 | GRCh38.p7 | 19:532800 | CCTCGGGAAGGCCGA[A/G]GTAGGGGCGTGCCTC | 997 |
rs16990517 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | CDC34 | GRCh38.p7 | 19:533395 | TGAACCGCACCCGCT[C/T]AGCGGCTGTGAGGGC | 997 |
rs16990522 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | CDC34 | GRCh38.p7 | 19:534243 | GCCTTGCTCTGTGGC[C/T]GCGGCCAAGTCACTT | 997 |
rs16990530 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CDC34 | GRCh38.p7 | 19:534317 | CCCCCAAGACACCCC[A/G]CGTGCCCTCCCTGTC | 997 |
rs16990532 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC34 | GRCh38.p7 | 19:534319 | CCCAAGACACCCCGC[A/G]TGCCCTCCCTGTCCA | 997 |
rs16990537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:534395 | TCCGGGAGGGGCCTC[A/G]CCCACAATCCAAGAC | 997 |
rs16990539 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CDC34 | GRCh38.p7 | 19:535096 | GGTGGCATCACGCCC[C/T]AGGCTGCAGGCCAGA | 997 |
rs16990542 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CDC34 | GRCh38.p7 | 19:535131 | TCTGTCACCTGGCAC[A/G]TGGCTTCAGGCCTCC | 997 |
rs16990545 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | CDC34 | GRCh38.p7 | 19:535248 | AGGTTTCTGTGACCT[A/G]TGGGTCTGCCTGCCT | 997 |
rs16990550 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | CDC34 | GRCh38.p7 | 19:535366 | TTTGCTAACTGAGCA[A/G]TCATCTGTGCTAACC | 997 |
rs16990554 | snp | A/C/G | 0.00131836 | 0.0256409 | synonymous-codon | CDC34 | GRCh38.p7 | 19:535839 | TCTGCCCCTGCAGGC[A/C/G]CGCCTCAAGTTCCCC | 997 |
rs16990556 | snp | A/G | 0.00217253 | 0.0328905 | synonymous-codon | CDC34 | GRCh38.p7 | 19:536245 | TCTTCTTGTGCAGAC[A/G]GGGGACGTGTGTATC | 997 |
rs16990568 | snp | C/T | 0.000110936 | 0.00744687 | intron-variant | CDC34 | GRCh38.p7 | 19:536929 | CTGGGTGGGTCCAGG[C/T]GTCCCCGTGACCCTC | 997 |
rs16990571 | snp | A/G/T | 0.00307843 | 0.0391124 | intron-variant | CDC34 | GRCh38.p7 | 19:537171 | GGGCGGGGGCGTCAC[A/G/T]GGAGGAGAGACTCAG | 997 |
rs16990583 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | CDC34 | GRCh38.p7 | 19:538289 | GCTGTGCAGTCGCCT[A/C]CCGGCGCCTTCTGTA | 997 |
rs16990585 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:538292 | GTGCAGTCGCCTACC[A/G]GCGCCTTCTGTACCT | 997 |
rs16990590 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | CDC34 | GRCh38.p7 | 19:538416 | CCTTCTCTTGGGTGC[C/T]TGTGTTCACATGAAT | 997 |
rs16990594 | in-del | -/C | 0.0116955 | 0.0755709 | intron-variant | CDC34 | GRCh38.p7 | 19:538525 | TGTTACATAGAGGCC[-/C]TTCCTATCCATTTTT | 997 |
rs16990597 | snp | A/G | 0.261884 | 0.249717 | intron-variant | CDC34 | GRCh38.p7 | 19:538531 | ATAGAGGCCCTTCCT[A/G]TCCATTTTTTTTTTT | 997 |
rs16990600 | snp | G/T | 0.106633 | 0.204807 | intron-variant | CDC34 | GRCh38.p7 | 19:538599 | CTCACCTATTTTTGT[G/T]GGTATTTTGTATAAA | 997 |
rs16990605 | snp | A/G | 0.0110494 | 0.0735024 | intron-variant | CDC34 | GRCh38.p7 | 19:538671 | GCATGTGTCTTCCTC[A/G]CCCCAGGACCCAGGA | 997 |
rs16990608 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant, downstream-variant-500B | CDC34 | GRCh38.p7 | 19:539412 | CCACCCGTGCAGTGC[C/T]GTCCCCGGGGCACTG | 997 |
rs16990610 | snp | A/G | 0.0111728 | 0.0739025 | intron-variant, downstream-variant-500B | CDC34 | GRCh38.p7 | 19:539422 | AGTGCCGTCCCCGGG[A/G]CACTGTCAGTCACCC | 997 |
rs16990616 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | CDC34 | GRCh38.p7 | 19:539678 | GAGCCGTGCCTGGTC[A/G]GTGATAGGGGCTCGA | 997 |
rs16990622 | snp | A/G | 0.109108 | 0.206518 | intron-variant | CDC34 | GRCh38.p7 | 19:539753 | TGGGGTCAGCGTGCC[A/G]CCTGGCCCTGCTGTG | 997 |
rs16990625 | snp | C/T | 0.450859 | 0.148847 | intron-variant | CDC34 | GRCh38.p7 | 19:541095 | TCGGGGCGGGGCAGG[C/T]GGGTGTGACTGCACT | 997 |
rs16990626 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | CDC34 | GRCh38.p7 | 19:541124 | CTGCGCCCGTCCAGC[C/T]TCCCACCCGCACCTC | 997 |
rs16990628 | snp | C/T | 0.0110494 | 0.0735024 | intron-variant | CDC34 | GRCh38.p7 | 19:541128 | GCCCGTCCAGCCTCC[C/T]ACCCGCACCTCCTGC | 997 |
rs16990634 | snp | A/G | 0.392521 | 0.205397 | intron-variant | CDC34 | GRCh38.p7 | 19:541217 | TTGTCCTAAGTGGTC[A/G]CCACACGCCGTTTTA | 997 |
rs16990638 | snp | C/T | 0.334642 | 0.235236 | intron-variant | CDC34 | GRCh38.p7 | 19:541242 | GTTTTAAGAGAAACC[C/T]GAGCGTTGGGGTGAG | 997 |
rs16990648 | snp | A/G | 0.0257821 | 0.110573 | intron-variant | CDC34 | GRCh38.p7 | 19:541262 | GTTGGGGTGAGCGTC[A/G]GACCTGGGGGAGGGG | 997 |
rs16990650 | snp | A/C/G | 5.28956e-05 | 0.00514247 | missense, utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541520 | AGCTGCTTCGGGGAC[A/C/G]ATGAGGATGACTCTG | 997 |
rs16990654 | snp | A/G | 0.00597247 | 0.0543191 | utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541771 | CGGGGCTCGGTGGAC[A/G]GGCCCAGGGTGGGAG | 997 |
rs16990656 | snp | C/T | 0.0124219 | 0.0778244 | utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541836 | GAGCCCGACTTCTAC[C/T]GGGGTCCCCCAGCTT | 997 |
rs16990659 | snp | A/G | 0.0252325 | 0.109451 | utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541887 | AGGAGCCACGGGGGC[A/G]CTGCTGGGAACGTGG | 997 |
rs16990665 | in-del | -/G | 0.0475351 | 0.146656 | utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541959 | GTAGCGGTCCGAGGG[-/G]CCCGGTCCTGCCTGT | 997 |
rs16990672 | snp | A/G | 0.0240643 | 0.107019 | upstream-variant-2KB, utr-variant-3-prime | GZMM, CDC34 | GRCh38.p7 | 19:542077 | AATCTAAATAAAACT[A/G]CTTTATGAGAGGCCA | 997 |
rs16990676 | snp | C/G/T | 0.034553 | 0.126973 | upstream-variant-2KB, downstream-variant-500B | GZMM, CDC34 | GRCh38.p7 | 19:542242 | GTCCCGCGGCCTGTA[C/G/T]GTTCCCATGACTTGG | 997 |
rs16990680 | snp | A/G | 0.00597247 | 0.0543191 | upstream-variant-2KB, downstream-variant-500B | GZMM, CDC34 | GRCh38.p7 | 19:542257 | CGTTCCCATGACTTG[A/G]GTCAGACAGGCCTGG | 997 |
rs16990684 | snp | C/T | 0.00279162 | 0.0372561 | upstream-variant-2KB, downstream-variant-500B | GZMM, CDC34 | GRCh38.p7 | 19:542339 | CCTCCTCCCTGTGAC[C/T]AGGTGCATCTAGTGG | 997 |
rs16990690 | snp | A/C | 0.00597247 | 0.0543191 | upstream-variant-2KB, downstream-variant-500B | GZMM, CDC34 | GRCh38.p7 | 19:542465 | CAGATGCCCCCGATC[A/C]GCACTCCGGCGGCTC | 997 |
rs16990694 | snp | A/T | 0.0532157 | 0.154195 | upstream-variant-2KB, downstream-variant-500B | GZMM, CDC34 | GRCh38.p7 | 19:542563 | CGTCCTGGTGTCAGG[A/T]AGTCCCCAGCATCGT | 997 |
rs16990892 | in-del | -/ACCT | 0.0118339 | 0.076006 | intron-variant | CDC34 | GRCh38.p7 | 19:538307 | GCGCCTTCTGTACCT[-/ACCT]GCAGTCCACTTAGCT | 997 |
rs16990893 | in-del | -/C | 0.0471551 | 0.14613 | intron-variant, downstream-variant-500B | CDC34 | GRCh38.p7 | 19:539434 | GTCAGTCACCCCCCC[-/C]AGCCCATCGGAGAGC | 997 |
rs17425535 | snp | C/T | 0.127254 | 0.217792 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:531576 | GGCGGAGGCGCTCGG[C/T]GCCGTAGGCGGGACC | 997 |
rs17425542 | snp | A/G | 0.0158469 | 0.0875917 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:531594 | CGTAGGCGGGACCGG[A/G]GCCGGGACTCCACCT | 997 |
rs17425549 | snp | C/G | 0.0482946 | 0.147699 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:531598 | GGCGGGACCGGGGCC[C/G]GGACTCCACCTCCCG | 997 |
rs17425573 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CDC34 | GRCh38.p7 | 19:537718 | TGCAGTGCAGTGGTG[C/T]GATCTCGGCTCACTG | 997 |
rs17672563 | snp | C/T | 0.29789 | 0.24537 | intron-variant | CDC34 | GRCh38.p7 | 19:539871 | AGGTCCTGGTGTGCG[C/T]GGTGCAGCCCCTCAT | 997 |
rs17841729 | in-del | -/CGTCCCGTATCCACCCAGACCATCAGGTAGGCCGGGCTC | 0.0637604 | 0.166778 | intron-variant | CDC34 | GRCh38.p7 | 19:536432 | AGGTAGGCCGGGCTC[lengthTooLong]CCCCGCAGGCTGTGG | 997 |
rs17841731 | snp | A/C | 0.0652144 | 0.168387 | intron-variant | CDC34 | GRCh38.p7 | 19:532918 | CCAGCTGGTCTTGGC[A/C]TTTCTCAGAGTCCAC | 997 |
rs17841732 | snp | C/G | 0.337386 | 0.23423 | intron-variant | CDC34 | GRCh38.p7 | 19:532930 | GGCCTTTCTCAGAGT[C/G]CACTGAACAGGTGGC | 997 |
rs17841733 | snp | C/T | 0.0744748 | 0.178019 | intron-variant | CDC34 | GRCh38.p7 | 19:532948 | CTGAACAGGTGGCTT[C/T]TTGGGACCCAAACCC | 997 |
rs17841735 | snp | A/G | 0.0640965 | 0.167152 | intron-variant | CDC34 | GRCh38.p7 | 19:533314 | CCCCGGCCAGCTGCG[A/G]GCGTGGGGCCGAGGG | 997 |
rs17841736 | snp | G/T | 0.0110494 | 0.0735024 | intron-variant | CDC34 | GRCh38.p7 | 19:533653 | AAGGAGGGGATGGGG[G/T]TTTCTGGCTGCTGTG | 997 |
rs17841737 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | CDC34 | GRCh38.p7 | 19:533692 | ACCGGTTGCCAGGGA[C/T]TGTGGGCAGAGCTTC | 997 |
rs17841738 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | CDC34 | GRCh38.p7 | 19:533732 | CATTAGGGGATAATC[C/T]GGTTTTCCGGATTTC | 997 |
rs17841742 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | CDC34 | GRCh38.p7 | 19:534096 | AAAATAAGAGGCTCA[C/T]TGGGACTTGGTGGGG | 997 |
rs17841746 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | CDC34 | GRCh38.p7 | 19:535657 | CAGAAAAGGCTTCAG[A/G]CAGCCTTCTGGGGAC | 997 |
rs17841747 | snp | C/T | 0.000131954 | 0.00812156 | intron-variant | CDC34 | GRCh38.p7 | 19:535828 | GCCACCTGCCTTCTG[C/T]CCCTGCAGGCGCGCC | 997 |
rs17841748 | snp | A/C | 0.0341408 | 0.126114 | intron-variant | CDC34 | GRCh38.p7 | 19:536374 | CTGTGTCCACCCAGA[A/C]CATCAGGTAGGCCGG | 997 |
rs17841749 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | CDC34 | GRCh38.p7 | 19:536395 | GGTAGGCCGGGCTCC[A/G]TCCCGTATCCACCCA | 997 |
rs17841750 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | CDC34 | GRCh38.p7 | 19:536426 | GACCATCAGGTAGGC[C/T]GGGCTCCCCCGCAGG | 997 |
rs17841751 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | CDC34 | GRCh38.p7 | 19:536468 | AGGCCTGATTCGGGA[A/C]CTGCCAGCTGGCGGT | 997 |
rs17841752 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | CDC34 | GRCh38.p7 | 19:536527 | GTGCTTTCACGGGGC[C/T]TGCGGCACTGTGTGT | 997 |
rs17841754 | snp | A/G | 0.0475351 | 0.146656 | intron-variant | CDC34 | GRCh38.p7 | 19:536545 | CGGCACTGTGTGTCG[A/G]TGCAGACTCCCACCA | 997 |
rs17841755 | snp | C/T | 0.0114282 | 0.0747228 | intron-variant | CDC34 | GRCh38.p7 | 19:536566 | ACTCCCACCAGGACC[C/T]CAGGCCGGCCCCACC | 997 |
rs17841758 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CDC34 | GRCh38.p7 | 19:536756 | CCAGGCAGGACGTGC[A/G]GGTGTGAGGGCAGCC | 997 |
rs17841759 | snp | C/T | 0.0118339 | 0.076006 | intron-variant | CDC34 | GRCh38.p7 | 19:536858 | AGGTCCAGCCCCTGC[C/T]GTTCTGGGGGCCTGA | 997 |
rs17841760 | snp | C/T | 0.0111728 | 0.0739025 | intron-variant | CDC34 | GRCh38.p7 | 19:537748 | GCAGCCTCCACTACT[C/T]GGGTTGGAGCAGTTC | 997 |
rs17841761 | snp | A/G | 0.0112991 | 0.0743093 | intron-variant | CDC34 | GRCh38.p7 | 19:537928 | TCCCAAAGTGCTGGG[A/G]TGACAGGCGTGAGCC | 997 |
rs17841762 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CDC34 | GRCh38.p7 | 19:538034 | ATGAAGAAATGGGGT[C/T]GTGCTGTGTGTGCCC | 997 |
rs17841765 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | CDC34 | GRCh38.p7 | 19:538229 | GCCTTACTCATGTCT[A/G]GAGTGCGTCCCTGCA | 997 |
rs17841766 | snp | C/G | 0.0614824 | 0.164198 | intron-variant | CDC34 | GRCh38.p7 | 19:538230 | CCTTACTCATGTCTG[C/G]AGTGCGTCCCTGCAG | 997 |
rs17841775 | in-del | -/T | 0.0118339 | 0.076006 | intron-variant | CDC34 | GRCh38.p7 | 19:533466 | GGACGCCCGTGGGTT[-/T]CTGCATCTGGAATCC | 997 |
rs28558712 | snp | C/G/T | 5.38826e-05 | 0.00519027 | intron-variant | CDC34 | GRCh38.p7 | 19:536369 | ACCCCCTGTGTCCAC[C/G/T]CAGAACATCAGGTAG | 997 |
rs28575072 | snp | A/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:536376 | GTGTCCACCCAGAAC[A/G]TCAGGTAGGCCGGGC | 997 |
rs28687356 | snp | C/T | 0.00119296 | 0.0243938 | intron-variant | CDC34 | GRCh38.p7 | 19:535974 | CTCCGGGACCCAGGG[C/T]GCTGGGAGCCTCACG | 997 |
rs28731438 | snp | A/G | 4.97236e-05 | 0.00498591 | intron-variant | CDC34 | GRCh38.p7 | 19:535970 | CATCCTCCGGGACCC[A/G]GGGTGCTGGGAGCCT | 997 |
rs34509095 | in-del | -/T | | | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:530844 | TGTCCTACCCGAGTC[-/T]TTTTTTTTTTTTTTT | 997 |
rs34534471 | in-del | -/A | | | intron-variant | CDC34 | GRCh38.p7 | 19:534459 | ACAGGGAGGGCACTC[-/A]GGGGGTCTTGGATCG | 997 |
rs34635182 | in-del | -/A | 0.461481 | 0.133325 | intron-variant | CDC34 | GRCh38.p7 | 19:538536 | TGAGAAAAAAAAAAA[-/A]TGGATAGGAAGGGCC | 997 |
rs35184527 | in-del | -/G | | | intron-variant, downstream-variant-500B | CDC34 | GRCh38.p7 | 19:539507 | AGGCGTCTGGCCTCA[-/G]GGGACGTCCCTGGGT | 997 |
rs35573985 | snp | C/G/T | 4.83983e-05 | 0.00491907 | synonymous-codon, utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541390 | GGCCAGCGTGGTGGG[C/G/T]ACCTTCACGCCGTCA | 997 |
rs36028188 | in-del | -/CG | | | intron-variant | CDC34 | GRCh38.p7 | 19:535591 | AGGTGGCCGGGACCC[-/CG]GGCCCAGCACAACTG | 997 |
rs36138952 | snp | A/G | 0.5 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:536046 | CTCCCAGCGCCCCGG[A/G]TCCCGGAAGGACGAG | 997 |
rs36167898 | snp | A/C | 0.48 | 0.0979796 | intron-variant | CDC34 | GRCh38.p7 | 19:534777 | GAGGTCTGGACAGGG[A/C]GGGCACTCGGGGGTC | 997 |
rs36194358 | snp | C/T | 0.4021 | 0.198407 | intron-variant | CDC34 | GRCh38.p7 | 19:534419 | TCTGGACAGGGAGGG[C/T]ACTCGGGGGTCTTGG | 997 |
rs41443449 | snp | A/G | 0.194245 | 0.243704 | intron-variant | CDC34 | GRCh38.p7 | 19:538024 | CTGTGCTTTAATGAA[A/G]AAATGGGGTCGTGCT | 997 |
rs57007979 | snp | A/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:534667 | CCAGACCTCGCCCAC[A/G]ATCCAAGACCCCCGA | 997 |
rs57351326 | snp | A/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:534595 | ATCCAAGACCCCCGA[A/G]TGCCCGCCCTGTCCA | 997 |
rs58582208 | snp | G/T | | | intron-variant | CDC34 | GRCh38.p7 | 19:534733 | GACCCCCGAGTGCCC[G/T]CCCTGTCCAGACCTC | 997 |
rs59035058 | in-del | -/TCCGGGGCGCTGGGAGCCTCACGTCCTCGTCCTTCCGGGA | | | intron-variant | CDC34 | GRCh38.p7 | 19:536085 | CTCGTCCTTCCGGGA[lengthTooLong]CCCGAGGCGCTGGGA | 997 |
rs59682509 | snp | A/T | | | intron-variant | CDC34 | GRCh38.p7 | 19:534594 | GATCCAAGACCCCCG[A/T]GTGCCCGCCCTGTCC | 997 |
rs59769036 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CDC34 | GRCh38.p7 | 19:537647 | GTGAGCCACCGCGGC[C/T]GGCCTTTTTTTTTTT | 997 |
rs59908696 | snp | A/G | 0.46875 | 0.121031 | intron-variant | CDC34 | GRCh38.p7 | 19:534553 | CCAAGACCCCCGAGT[A/G]CCCTCCCTGTCAAGG | 997 |
rs59935289 | snp | A/G | 0.267364 | 0.249396 | intron-variant | CDC34 | GRCh38.p7 | 19:534700 | GCCCTCCCTGTCCAG[A/G]CCTCGCCCACGATCC | 997 |
rs59951398 | snp | A/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:534685 | CCAAGACCCCCGAGT[A/G]CCCTCCCTGTCCAGA | 997 |
rs60780048 | in-del | -/AA | | | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:530843 | AAAAAAAAAAAAAAA[-/AA]GACTCGGGTAGGACA | 997 |
rs61644328 | snp | A/C | 0.267364 | 0.249396 | intron-variant | CDC34 | GRCh38.p7 | 19:534697 | AGTGCCCTCCCTGTC[A/C]AGACCTCGCCCACGA | 997 |
rs62132563 | snp | C/T | 0.4021 | 0.198407 | intron-variant | CDC34 | GRCh38.p7 | 19:534426 | CCCCGAGTACCCTCC[C/T]TGTCCAGACCTCGCC | 997 |
rs62132564 | snp | A/G | 0.377187 | 0.215229 | intron-variant | CDC34 | GRCh38.p7 | 19:534434 | ACCCTCCCTGTCCAG[A/G]CCTCGCCCACGATCC | 997 |
rs66609379 | multinucleotide-polymorphism | AG/TA | 0 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:534593 | ATCCAAGACCCCCTG[AG/TA]TGCCCTCCCTGTCCA | 997 |
rs71171995 | in-del | -/TCCCGAGTACCCTCCCTGTCCAGACCTCGCCCACGATCCAAGACCCCCTGAGTGCCCTCCCTGTCCAGACCTCACCCACGATCCAAGAC | 0 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:534499 | CCCACGATCCAAGAC[lengthTooLong]CCCCTGTATGCCCTC | 997 |
rs71171997 | in-del | -/GGGCGCTGGGAGCCTCACATCCTCGTCCTTCCGGGACCCG | 0 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:536089 | TCCTTCCGGGACCCG[lengthTooLong]AGGCGCTGGGAGCCT | 997 |
rs71335256 | snp | A/G | 0.5 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:534755 | CCAGACCTCGCCCAC[A/G]ATCCAAGACCCCCGA | 997 |
rs71335257 | snp | C/T | 0.5 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:534925 | CTCCCTGTCCAGGCT[C/T]CCACCACGATCGCTC | 997 |
rs72363216 | in-del | -/T | 0.397994 | 0.201489 | intron-variant | CDC34 | GRCh38.p7 | 19:534857 | CGATCCAAGACCCCC[-/T]GAGTGCCCTCCCTGT | 997 |
rs72972105 | snp | A/G | 0.0558544 | 0.157504 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:529785 | ACCGCTCGGCCCAGA[A/G]CTCTTTCTTGGATCC | 997 |
rs72972115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:535591 | GCAGTTGTGCTGGGC[C/T]GGGTCCCGGCCACCT | 997 |
rs73489739 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | CDC34 | GRCh38.p7 | 19:540881 | GGAGAGGCTCAGGCC[A/G]TTTTTGCGTTTCCCA | 997 |
rs73919634 | snp | A/T | 0.497695 | 0.0338674 | intron-variant | CDC34 | GRCh38.p7 | 19:534506 | ATCCAAGACCCCCTG[A/T]GTGCCCTCCCTGTCC | 997 |
rs74450144 | snp | C/G | 0.5 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:537632 | GCAGGGATTACAGGC[C/G]TGAGCCACCGCGGCC | 997 |
rs74543696 | snp | A/G | 0 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:540223 | AATCCGGAGGCCGGG[A/G]TGGCCAGGCCCCCCG | 997 |
rs74727479 | snp | A/G | 0 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:540402 | CCGGGTTTAGAATCC[A/G]GAGGCCGGGGTGGCC | 997 |
rs74861405 | snp | A/G | 0.5 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:536108 | CGCTGGGAGCCTCAT[A/G]TCCTCGTCCTTCCGG | 997 |
rs74973191 | snp | C/T | 0 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:534471 | CCCTGAGTGCCCTCC[C/T]TGTCCAGACCTCACC | 997 |
rs75370815 | snp | A/G | 0 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:540213 | CCGGGTTTAGAATCC[A/G]GAGGCCGGGGTGGCC | 997 |
rs75466060 | snp | A/T | | | intron-variant | CDC34 | GRCh38.p7 | 19:538536 | GGCCCTTCCTATCCA[A/T]TTTTTTTTTTTCTCA | 997 |
rs75476778 | snp | C/T | 0.0498117 | 0.149749 | intron-variant | CDC34 | GRCh38.p7 | 19:536128 | CGTCCTTCCGGGACC[C/T]GGGGCGCTGGGAGCC | 997 |
rs75654008 | snp | A/G | 0.000396504 | 0.0140746 | intron-variant | CDC34 | GRCh38.p7 | 19:535932 | CTACGAGGTGAGCGC[A/G]GCCCCCACGGGCCTC | 997 |
rs75965912 | snp | C/T | 0.5 | 0 | intron-variant, downstream-variant-500B | CDC34 | GRCh38.p7 | 19:539353 | GGCACCGTCACCCCC[C/T]CAGCCCGTCCACCCT | 997 |
rs76270394 | snp | A/G | 0 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:540200 | GTGGCCAGGCCCCCC[A/G]GGTTTAGAATCCGGA | 997 |
rs76301282 | snp | G/T | 0.46875 | 0.121031 | intron-variant | CDC34 | GRCh38.p7 | 19:534866 | ACCCCCTGAGTGCCC[G/T]CCCTGTCCAGACCTC | 997 |
rs76419259 | snp | C/G | 0.5 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:540201 | TGGCCAGGCCCCCCG[C/G]GTTTAGAATCCGGAG | 997 |
rs76720850 | snp | A/C/G | 2.7485e-05 | 0.00370698 | missense, synonymous-codon | CDC34 | GRCh38.p7 | 19:541382 | GCGGAGCGTGACGGC[A/C/G]TGAAGGTGCCCACCA | 997 |
rs76904038 | snp | A/G | 0.444444 | 0.157135 | intron-variant | CDC34 | GRCh38.p7 | 19:534617 | CCCTGTCCAGACCTC[A/G]CCCACGATCCAAGAC | 997 |
rs77062538 | snp | C/T | 0 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:540181 | TTAGAATCCGGAGGC[C/T]GGGGTGGCCAGGCCC | 997 |
rs77150325 | snp | C/G | 0 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:540390 | TGGCCAGGCCCCCCG[C/G]GTTTAGAATCCGGAG | 997 |
rs77236521 | snp | A/G | 0 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:534568 | ACCCTCCCTGTCAAG[A/G]CCTCGCCCACGATCC | 997 |
rs77994788 | snp | A/G | 0.258288 | 0.249863 | intron-variant | CDC34 | GRCh38.p7 | 19:534656 | GCCCTCCCTGTCCAG[A/G]CCTCGCCCACGATCC | 997 |
rs78001795 | snp | A/G | 0.375 | 0.216506 | intron-variant | CDC34 | GRCh38.p7 | 19:534573 | CCCTGTCAAGGCCTC[A/G]CCCACGATCCAAGAC | 997 |
rs78090242 | snp | C/T | 0.5 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:534516 | CCCTGAGTGCCCTCC[C/T]TGTCCAGACCTCGCC | 997 |
rs78239552 | snp | A/G | 0 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:540185 | AATCCGGAGGCCGGG[A/G]TGGCCAGGCCCCCCG | 997 |
rs78339074 | snp | A/G | 0 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:540389 | GTGGCCAGGCCCCCC[A/G]GGTTTAGAATCCGGA | 997 |
rs78367623 | snp | A/G | 0.375 | 0.216506 | intron-variant | CDC34 | GRCh38.p7 | 19:534888 | CCAGACCTCGCCCAC[A/G]ATCCAAGACCCCCTG | 997 |
rs78582371 | snp | A/G/T | 0.0399052 | 0.1355 | intron-variant | CDC34 | GRCh38.p7 | 19:540917 | CCTGTGCTGGTTCCC[A/G/T]TCTCCAGGGATGGTC | 997 |
rs78714304 | snp | A/G | 0.5 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:534524 | GCCCTCCCTGTCCAG[A/G]CCTCGCCCACAATCC | 997 |
rs79369390 | snp | A/G | 0.42 | 0.183303 | intron-variant | CDC34 | GRCh38.p7 | 19:534623 | CCAGACCTCGCCCAC[A/G]ATCCAAGACCCCCGA | 997 |
rs79401086 | snp | A/G | 0 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:540137 | CCGGGTTTAGAATCC[A/G]GAGGCCGGGGTGGCC | 997 |
rs79530593 | snp | A/G | 0 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:540412 | AATCCGGAGGCCGGG[A/G]TGGCCAGGCCCCCCG | 997 |
rs79755074 | snp | A/G | 0 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:534479 | GCCCTCCCTGTCCAG[A/G]CCTCACCCACGATCC | 997 |
rs79944544 | snp | A/C | 0.375 | 0.216506 | intron-variant | CDC34 | GRCh38.p7 | 19:534653 | AGTGCCCTCCCTGTC[A/C]AGACCTCGCCCACGA | 997 |
rs80126079 | in-del | -/TT | | | intron-variant | CDC34 | GRCh38.p7 | 19:538546 | ATCCATTTTTTTTTT[-/TT]CTCAGAGTGATATTG | 997 |
rs80154033 | snp | G/T | 0.5 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:537366 | TTTCCTCTTTTTTTT[G/T]GTTTGAGACAGAGTC | 997 |
rs80285476 | snp | C/T | 0 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:540219 | TTAGAATCCGGAGGC[C/T]GGGGTGGCCAGGCCC | 997 |
rs111457578 | snp | C/T | 0.5 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:540687 | GCCGGGGTGGCCAGG[C/T]CCCCCACGTTTAGAA | 997 |
rs111668322 | snp | C/T | | | intron-variant | CDC34 | GRCh38.p7 | 19:534648 | CCCCGAGTGCCCTCC[C/T]TGTCCAGACCTCGCC | 997 |
rs111745919 | snp | A/G | 0 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:540541 | GTGGCCAGGCCCCCC[A/G]GGTTTAGAATCCGGA | 997 |
rs111872830 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CDC34 | GRCh38.p7 | 19:536678 | CGTGCCACGTGTGCC[A/G]CCTGGGCCTCGTCCC | 997 |
rs111938151 | snp | A/G | 0.444444 | 0.157135 | intron-variant | CDC34 | GRCh38.p7 | 19:540827 | AATCCGGAGGCCGGG[A/G]TGGCCAGGCCCCCGG | 997 |
rs111982875 | snp | C/T | 0.5 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:540823 | TTAGAATCCGGAGGC[C/T]GGGGTGGCCAGGCCC | 997 |
rs111994293 | snp | C/T | 0.5 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:536126 | CTCGTCCTTCCGGGA[C/T]CCGGGGCGCTGGGAG | 997 |
rs112129774 | snp | C/T | 0.5 | 0 | intron-variant, missense | CDC34 | GRCh38.p7 | 19:538970 | CTTCCCGGCCACCTC[C/T]CTGAGGCACCACCTC | 997 |
rs112231897 | snp | C/T | 0.5 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:540535 | GCCGGGGTGGCCAGG[C/T]CCCCCGGGTTTAGAA | 997 |
rs112259175 | snp | A/G | 0.5 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:540592 | CCGGGTTTAGAATCC[A/G]GAGGCCGGGGTGGCC | 997 |
rs112405171 | snp | C/T | 0.5 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:536086 | CTCGTCCTTCCGGGA[C/T]CCGAGGCGCTGGGAG | 997 |
rs112514898 | snp | C/T | 0.5 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:540573 | GCCGGGGTGGCCAGG[C/T]CCCCCGGGTTTAGAA | 997 |
rs112529655 | snp | A/C | | | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:531637 | TGCGGCCGGGCGCGC[A/C]GGCGCAAGTCGGACC | 997 |
rs112639513 | snp | C/T | | | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:530300 | ACAATGCCACTGGCA[C/T]AGTCCGAGGGCAGGG | 997 |
rs112640920 | snp | A/G | 0 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:540579 | GTGGCCAGGCCCCCC[A/G]GGTTTAGAATCCGGA | 997 |
rs112672295 | snp | A/G | 0.497695 | 0.0338674 | intron-variant | CDC34 | GRCh38.p7 | 19:534507 | TCCAAGACCCCCTGA[A/G]TGCCCTCCCTGTCCA | 997 |
rs112689202 | snp | A/G | 0 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:540465 | GTGGCCAGGCCCCCC[A/G]GGTTTAGAATCCGGA | 997 |
rs112805632 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | CDC34 | GRCh38.p7 | 19:536113 | GGAGCCTCATGTCCT[C/T]GTCCTTCCGGGACCC | 997 |
rs112901204 | snp | C/T | 0.5 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:534455 | CCCACGATCCAAGAC[C/T]CCCTGAGTGCCCTCC | 997 |
rs113037139 | snp | C/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:533293 | TGCAGGGCCCGGCCC[C/G]CTCTGCCCCGGCCAG | 997 |
rs113206606 | snp | A/G | 0.5 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:535833 | CTGCCTTCTGCCCCT[A/G]CAGGCGCGCCTCAAG | 997 |
rs113408534 | snp | C/T | 0.5 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:540459 | GCCGGGGTGGCCAGG[C/T]CCCCCGGGTTTAGAA | 997 |
rs113438781 | snp | A/G | 0.5 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:540478 | CCGGGTTTAGAATCC[A/G]GAGGCCGGGGTGGCC | 997 |
rs113439740 | snp | C/T | 0.5 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:534411 | CCCACAATCCAAGAC[C/T]CCCGAGTACCCTCCC | 997 |
rs113544950 | snp | A/G | 0.5 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:534464 | CAAGACCCCCTGAGT[A/G]CCCTCCCTGTCCAGA | 997 |
rs113550888 | snp | C/T | 0.5 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:540497 | GCCGGGGTGGCCAGG[C/T]CCCCCGGGTTTAGAA | 997 |
rs113645017 | snp | C/T | 0.5 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:538083 | AACATGTGTCTGTGC[C/T]TTAATGAAGAAATGG | 997 |
rs113654410 | snp | A/G | 0.5 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:540516 | CCGGGTTTAGAATCC[A/G]GAGGCCGGGGTGGCC | 997 |
rs113709830 | snp | C/G | 0.5 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:540694 | TGGCCAGGCCCCCCA[C/G]GTTTAGAATCCGGAG | 997 |
rs113776545 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | CDC34 | GRCh38.p7 | 19:539437 | GCACTGTCAGTCACC[C/G]CCCCAGCCCATCGGA | 997 |
rs113939486 | in-del | -/C | 0.5 | 0 | intron-variant | CDC34 | GRCh38.p7 | 19:534300 | GTCAAACAGAGGACA[-/C]CCCCCCAAGACACCC | 997 |
rs114582274 | snp | C/T | 0.00716087 | 0.0594067 | intron-variant | CDC34 | GRCh38.p7 | 19:536935 | GGGTCCAGGCGTCCC[C/T]GTGACCCTCAGGGCC | 997 |
rs115103796 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | CDC34 | GRCh38.p7 | 19:534420 | CAAGACCCCCGAGTA[C/T]CCTCCCTGTCCAGAC | 997 |
rs115296819 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | CDC34 | GRCh38.p7 | 19:536178 | GTCCTCATCCTCCGG[A/G]ACCTGGGGCACTGGG | 997 |
rs116075349 | snp | A/T | 0.00795532 | 0.062565 | intron-variant, downstream-variant-500B | CDC34 | GRCh38.p7 | 19:539203 | GGATGTTGGTCTTGC[A/T]GAACAGGACCTCCAG | 997 |
rs116932400 | snp | A/G | 0.00013188 | 0.00811929 | synonymous-codon | CDC34 | GRCh38.p7 | 19:535893 | AGCCTTTCGGTTCCT[A/G]ACCAAGATGTGGCAC | 997 |
rs117103061 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CDC34 | GRCh38.p7 | 19:532437 | GCGTGGGGCTCTTGC[C/T]CACCTCCTCCTTGGC | 997 |
rs137932806 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | CDC34 | GRCh38.p7 | 19:536014 | TTCCGGGACCCGGGG[C/T]GCTGGGAGCCTCACG | 997 |
rs138167005 | snp | A/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:533129 | CCAGACGTGACCTTT[A/G]ACTTCTTTTAGCGTT | 997 |
rs139014138 | snp | C/T | 0.00195711 | 0.0312206 | synonymous-codon | CDC34 | GRCh38.p7 | 19:537046 | GATCTCCCTCCTGAA[C/T]GAGCCCAACACCTTC | 997 |
rs139519432 | in-del | -/TACC | 0.0115144 | 0.0749975 | intron-variant | CDC34 | GRCh38.p7 | 19:538302 | TACCGGCGCCTTCTG[-/TACC]TACCTGCAGTCCACT | 997 |
rs139785602 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CDC34 | GRCh38.p7 | 19:538655 | ATATTGCACACATAA[C/T]GCATGTGTCTTCCTC | 997 |
rs139926290 | snp | C/T | 0.00066516 | 0.0182246 | synonymous-codon, utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541462 | CTCAGACCTCTTCTA[C/T]GACGACTACTACGAG | 997 |
rs139963220 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | CDC34 | GRCh38.p7 | 19:539083 | GGACTCTGCTGTGGT[C/T]GCCGTTTCTGCCTGT | 997 |
rs140384237 | snp | A/G | 1.80781e-05 | 0.00300645 | missense, utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541536 | ATGAGGATGACTCTG[A/G]CACGGAGGAGTCCTG | 997 |
rs140398542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:535077 | GTGGCCCAGGAGGGC[C/T]GTGGGTGGCATCACG | 997 |
rs140810113 | snp | C/T | 0.000155102 | 0.00880494 | synonymous-codon | CDC34 | GRCh38.p7 | 19:536296 | GGACGACCCCCAGAG[C/T]GGGGAGCTGCCCTCA | 997 |
rs141012488 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | CDC34 | GRCh38.p7 | 19:537229 | CCACGGCCGCCCAGC[A/C]CCACCTTCCTGGTGA | 997 |
rs141634653 | snp | C/T | 0.000102354 | 0.00715308 | synonymous-codon, utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541465 | AGACCTCTTCTACGA[C/T]GACTACTACGAGGAC | 997 |
rs141921412 | snp | A/C/T | 0.000488161 | 0.0156158 | synonymous-codon, utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541438 | CAAGGCGCCGGCGCC[A/C/T]GACGAGGGCTCAGAC | 997 |
rs142107576 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CDC34 | GRCh38.p7 | 19:538387 | CTCATGCCCCAGAGC[C/T]GAGCCCCACAGCCCC | 997 |
rs142231793 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | CDC34 | GRCh38.p7 | 19:540842 | GTGGCCAGGCCCCCG[A/G]GTTTAGAATCCTGCT | 997 |
rs142363739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon | CDC34 | GRCh38.p7 | 19:538951 | CTGGCTCCTTGGCCC[A/G]GTTCTTCCCGGCCAC | 997 |
rs143039634 | snp | A/G | 0.000120262 | 0.00775349 | synonymous-codon, missense | CDC34 | GRCh38.p7 | 19:541369 | GACCAAGGTGGACGC[A/G]GAGCGTGACGGCGTG | 997 |
rs143052486 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, missense | CDC34 | GRCh38.p7 | 19:538731 | GCTGGTACCTGGTGT[C/T]GTGGGGTCATCTCGG | 997 |
rs143064307 | snp | C/T | | | intron-variant | CDC34 | GRCh38.p7 | 19:540749 | TTAGAATCCGGAGGC[C/T]GGGATGGCCAGGCCC | 997 |
rs143937615 | snp | A/G | 0.000526639 | 0.0162186 | missense | CDC34 | GRCh38.p7 | 19:531947 | ATGGCTCGGCCGCTA[A/G]TGCCCAGCTCGCAGA | 997 |
rs144217837 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CDC34 | GRCh38.p7 | 19:536689 | TGCCGCCTGGGCCTC[A/G]TCCCCAGGTACAAGC | 997 |
rs144601967 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | CDC34 | GRCh38.p7 | 19:533003 | CCTCTGGCGGTTTAA[-/T]TCCAAGCAGTTTCTG | 997 |
rs144633844 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, downstream-variant-500B | GZMM, CDC34 | GRCh38.p7 | 19:542461 | ACCACAGATGCCCCC[A/G]ATCAGCACTCCGGCG | 997 |
rs145222487 | snp | C/T | 1.66305e-05 | 0.00288357 | synonymous-codon | CDC34 | GRCh38.p7 | 19:537016 | CTCTCCCCACAGGAC[C/T]ATTCTCCTGAGTGTG | 997 |
rs146070014 | snp | A/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:540023 | CCAGGTTTAGAATCC[A/G]GAGGCCGGGGTGGCC | 997 |
rs146221392 | snp | A/C/G | 0.000564544 | 0.0167919 | synonymous-codon, utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541540 | GGATGACTCTGGCAC[A/C/G]GAGGAGTCCTGACAC | 997 |
rs146359513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:538499 | ACGGCCTTAATGGTT[C/T]CTGCTCTTCCTGTTA | 997 |
rs146385161 | snp | C/T | 0.00131492 | 0.0256073 | synonymous-codon | CDC34 | GRCh38.p7 | 19:536335 | GAACCCCACGCAGAA[C/T]GTCAGGTAAGCCGGC | 997 |
rs146527192 | snp | A/G | 6.03761e-05 | 0.00549404 | missense | CDC34 | GRCh38.p7 | 19:536279 | ATCCTCCACCCGCCG[A/G]TGGACGACCCCCAGA | 997 |
rs146546301 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | CDC34 | GRCh38.p7 | 19:536782 | CAGCCCCGGGTCTGA[C/T]GGAGGGGTCTGCACC | 997 |
rs146636351 | snp | A/C | 0.000153988 | 0.00877328 | synonymous-codon | CDC34 | GRCh38.p7 | 19:537040 | GAGTGTGATCTCCCT[A/C]CTGAACGAGCCCAAC | 997 |
rs146663310 | snp | A/G | 9.89006e-05 | 0.00703139 | missense | CDC34 | GRCh38.p7 | 19:535855 | CGCCTCAAGTTCCCC[A/G]TCGACTACCCATACT | 997 |
rs147105441 | snp | C/T | 7.30353e-05 | 0.00604254 | missense, utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541428 | GCGTGAAGACCAAGG[C/T]GCCGGCGCCCGACGA | 997 |
rs147136672 | snp | A/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:536054 | TCCGGGACCCGGGGC[A/G]CTGGGAGCCTCACGT | 997 |
rs147363174 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | CDC34 | GRCh38.p7 | 19:533519 | AGTTTGGGTCTCGAG[A/G]TTGCCAAATGGTTTT | 997 |
rs147613525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:539876 | CTGGTGTGCGCGGTG[C/T]AGCCCCTCATAGGGC | 997 |
rs147651045 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CDC34 | GRCh38.p7 | 19:537981 | GTGTTTTCATAGATT[C/T]TTCCAGGCTTTTCAG | 997 |
rs148173026 | snp | A/G | 0.000901973 | 0.0212173 | synonymous-codon, utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541429 | CGTGAAGACCAAGGC[A/G]CCGGCGCCCGACGAG | 997 |
rs148476389 | in-del | -/CTCACGTCCTCGTCCTTCCGGGACCCGAGGCGCTGGGAGC | | | intron-variant | CDC34 | GRCh38.p7 | 19:536103 | GAGGCGCTGGGAGCC[lengthTooLong]TCATGTCCTCGTCCT | 997 |
rs148639611 | snp | A/G | 4.87151e-05 | 0.0049351 | missense | CDC34 | GRCh38.p7 | 19:532034 | GTGACACTGGTGGAC[A/G]AGGGCGATCTATACA | 997 |
rs148705017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon | CDC34 | GRCh38.p7 | 19:538915 | TGGCCCCGGTCCGGT[C/T]GTGTCACCTGGCCCA | 997 |
rs149323266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:533350 | TGCCTCCCGCACGAT[A/G]TGTGTCTGCTCTCCG | 997 |
rs149530313 | in-del | -/CTC | | | intron-variant | CDC34 | GRCh38.p7 | 19:536630 | CAGTCCTGGGGCCTT[-/CTC]CTTACCCAGCCGTCT | 997 |
rs149885611 | snp | C/T | 0.00318978 | 0.0398085 | utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541853 | GGGTCCCCCAGCTTC[C/T]GGACTGGCCGCACCC | 997 |
rs150067991 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:530656 | AACATGGTGAAACCC[C/T]ATCTCTACTTAAAAT | 997 |
rs150311005 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:538248 | TGCGTCCCTGCAGGC[A/T]CTTGGCCTGGTGAGC | 997 |
rs150670250 | snp | C/T | 1.70857e-05 | 0.00292276 | synonymous-codon, utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541456 | CGAGGGCTCAGACCT[C/T]TTCTACGACGACTAC | 997 |
rs150686262 | snp | A/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:540753 | AATCCGGAGGCTGGG[A/G]TGGCCAGGCCCCCGG | 997 |
rs151212892 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CDC34 | GRCh38.p7 | 19:540861 | TAGAATCCTGCTGAG[A/G]CCACGGAGAGGCTCA | 997 |
rs181081343 | snp | C/T | | | intron-variant | CDC34 | GRCh38.p7 | 19:540274 | GGGTGGCCAGGCCCC[C/T]CGGTTTAGAATCCGG | 997 |
rs181247487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:534094 | CCAAAATAAGAGGCT[C/T]ATTGGGACTTGGTGG | 997 |
rs181829016 | snp | C/T | 0.00138408 | 0.0262702 | intron-variant | CDC34 | GRCh38.p7 | 19:537159 | TCCGGTGAGGGCGGG[C/T]GGGGGCGTCACGGGA | 997 |
rs181912431 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:530322 | AGGGCAGGGCCACCC[A/G]TCACGGGCACGACTC | 997 |
rs182430342 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB, downstream-variant-500B | GZMM, CDC34 | GRCh38.p7 | 19:542574 | CAGGAAGTCCCCAGC[A/G]TCGTTTTATTACATG | 997 |
rs183007797 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, downstream-variant-500B | GZMM, CDC34 | GRCh38.p7 | 19:542232 | GAGCAGCCGGGTCCC[A/G]CGGCCTGTACGTTCC | 997 |
rs183289861 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | CDC34 | GRCh38.p7 | 19:538583 | ATTTCCTCACAGAGG[C/T]CTCACCTATTTTTGT | 997 |
rs183386877 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CDC34 | GRCh38.p7 | 19:534936 | GGCTTCCACCACGAT[C/T]GCTCTGGGGGTGCTG | 997 |
rs183392182 | snp | A/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:540730 | GGTGGCCAGGCCCCC[A/G]GGTTTAGAATCCGGA | 997 |
rs183600625 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CDC34 | GRCh38.p7 | 19:532329 | CTGCTGCAGTCCTCG[A/G]AAATCCCCAGTTCCC | 997 |
rs183774154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:533827 | GGTGCTGCCACCCAC[A/G]AGGACTCTCCCTTCC | 997 |
rs183928612 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | CDC34 | GRCh38.p7 | 19:535635 | GCTGGGATCAGCTCG[A/G]GTGACTCAGAAAAGG | 997 |
rs184317422 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CDC34 | GRCh38.p7 | 19:536752 | TAGTCTAGGCAGGAC[A/G]TGCGGGTGTGAGGGC | 997 |
rs184453203 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CDC34 | GRCh38.p7 | 19:539854 | GGGGGCAGGTTCCTC[A/G]TAGGTCCTGGTGTGC | 997 |
rs184774019 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CDC34 | GRCh38.p7 | 19:532937 | CTCAGAGTCCACTGA[A/G]CAGGTGGCTTCTTGG | 997 |
rs185151998 | snp | C/T | 0.00716266 | 0.059414 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:531208 | CCCGCCTCGCTCCCG[C/T]CCCTTCCTCCCTTCC | 997 |
rs185289998 | snp | A/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:534200 | AAGTCTTGGGGAACC[A/G]CAGGACAGTTCTGAG | 997 |
rs185529285 | snp | A/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:540033 | AATCCGGAGGCCGGG[A/G]TGGCCAGGCCCCCCA | 997 |
rs185922759 | snp | A/C/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:540275 | GGTGGCCAGGCCCCC[A/C/G]GGTTTAGAATCCGGA | 997 |
rs186039083 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:538038 | AGAAATGGGGTCGTG[A/C]TGTGTGTGCCCAGTG | 997 |
rs186064309 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CDC34 | GRCh38.p7 | 19:537416 | GGAGTGCAGTGGCGC[A/G]ATCTCGGCTCACTGC | 997 |
rs186090936 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | CDC34 | GRCh38.p7 | 19:534592 | ACGATCCAAGACCCC[C/T]GAGTGCCCGCCCTGT | 997 |
rs186317644 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:537787 | CATCCTGCCAAGCAG[C/G]TGGGATTACAGGTGC | 997 |
rs186829055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:533110 | GTTTTCTTGATCTCA[C/T]GATCCAGACGTGACC | 997 |
rs186941064 | snp | A/C | 0.00358779 | 0.0422022 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:530512 | CTGGGCGCGGTGGCT[A/C]ATGCCTATAATCCCA | 997 |
rs187195189 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | CDC34 | GRCh38.p7 | 19:540778 | CCCCGGGTTTAGAAT[A/C]CAGAGGCTGGGATGG | 997 |
rs188080894 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:535224 | TGCTGACAGGGAAGG[A/T]GTCCTGCCAGGTTTC | 997 |
rs188443728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CDC34 | GRCh38.p7 | 19:539488 | GGCGTCCGCTGGGTC[C/T]CGCCACCCAGGGACG | 997 |
rs188596409 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CDC34 | GRCh38.p7 | 19:532788 | TGTAACCTGCGCCCT[C/T]GGGAAGGCCGAAGTA | 997 |
rs188820235 | snp | A/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:540298 | AATCCGGAGGCCGGG[A/G]TGGCCAGGCCCCCCG | 997 |
rs188852614 | snp | C/T | | | intron-variant | CDC34 | GRCh38.p7 | 19:540009 | GGGTGGCCAGGCCCC[C/T]AGGTTTAGAATCCGG | 997 |
rs189087066 | snp | C/T | 0.00318978 | 0.0398085 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:530249 | ACCGTGCCCGGCCTG[C/T]ATGTTGATGCAGCTG | 997 |
rs189188049 | snp | A/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:540061 | CCACGTTTAGAATCC[A/G]GAGGCCGGGGTGGCC | 997 |
rs189477909 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CDC34 | GRCh38.p7 | 19:536820 | CCTCCCTGGTCTTGG[C/T]GTGGGAGGGAGGAGA | 997 |
rs189573880 | snp | A/C | | | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:531289 | ACGGGGAAACGGAGA[A/C]GGGGACGCGGGGTCG | 997 |
rs189762426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:534090 | GTGCCCAAAATAAGA[A/G]GCTCATTGGGACTTG | 997 |
rs190017499 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CDC34 | GRCh38.p7 | 19:536400 | GCCGGGCTCCGTCCC[A/G]TATCCACCCAGACCA | 997 |
rs190119425 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CDC34 | GRCh38.p7 | 19:534234 | GAAGTTCCAGCCTTG[C/T]TCTGTGGCCGCGGCC | 997 |
rs191159521 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC34 | GRCh38.p7 | 19:538554 | TTTTTTTTTCTCAGA[A/G]TGATATTGCATAGAT | 997 |
rs191172540 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:537977 | GTTAGTGTTTTCATA[C/G]ATTCTTCCAGGCTTT | 997 |
rs191244510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:533740 | GATAATCCGGTTTTC[C/T]GGATTTCCCAGGGAG | 997 |
rs191319752 | snp | A/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:534799 | CCAGACCTCGCCCAT[A/G]ATCCAAGACCCCCGA | 997 |
rs191638856 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CDC34 | GRCh38.p7 | 19:539819 | GGGACATTCTTGACG[C/T]GTGTCCTGGAGGTGG | 997 |
rs191669169 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:534915 | CCTGAGTGCCCTCCC[G/T]GTCCAGGCTTCCACC | 997 |
rs191797639 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | GZMM, CDC34 | GRCh38.p7 | 19:542524 | GGGGAGCCGTGGCCC[C/T]GGGCACACAGGGCAG | 997 |
rs191879677 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CDC34 | GRCh38.p7 | 19:536544 | GCGGCACCGTGTGTC[C/G]GTGCAGACTCCCACC | 997 |
rs191947256 | snp | A/C | 0.00535465 | 0.0514651 | utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541599 | CACTAGGGCCGGACC[A/C]GTGGCTCCTTAGACG | 997 |
rs192084718 | snp | A/G | 0.039522 | 0.134904 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:530771 | GCGGAGGTTGCAGTG[A/G]GATTGTGCCACTGCA | 997 |
rs192497408 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CDC34 | GRCh38.p7 | 19:535314 | CATACTGACTCATCC[A/C]CTCCCACGGCCTGGG | 997 |
rs192543890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, missense | CDC34 | GRCh38.p7 | 19:538907 | GTCCTCGGTGGCCCC[A/G]GTCCGGTCGTGTCAC | 997 |
rs192590370 | snp | A/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:540010 | GGTGGCCAGGCCCCC[A/G]GGTTTAGAATCCGGA | 997 |
rs193121977 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | CDC34 | GRCh38.p7 | 19:532928 | TTGGCCTTTCTCAGA[C/G]TCCACTGAACAGGTG | 997 |
rs199984661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:532137 | CCCCCGCCCGGGTCC[C/T]GGAGCCCACGAGCGA | 997 |
rs200004159 | in-del | -/A | | | intron-variant | CDC34 | GRCh38.p7 | 19:540804 | ATGGCCAGGCCCCCC[-/A]GGTTTAGAATCCGGA | 997 |
rs200040937 | snp | C/T | | | intron-variant | CDC34 | GRCh38.p7 | 19:537901 | ACCTCAGGTGATCCA[C/T]CCGCCTCGGCCTCCC | 997 |
rs200041545 | in-del | -/TTG | 0.0356815 | 0.128715 | intron-variant | CDC34 | GRCh38.p7 | 19:533026 | AGTTTCTGGATGTTT[-/TTG]TTGTTGTTGGGAGCG | 997 |
rs200077543 | in-del | -/GGGGCGCTGG | | | intron-variant | CDC34 | GRCh38.p7 | 19:536129 | GTCCTTCCGGGACCC[-/GGGGCGCTGG]GAGCCTCACGTCCTC | 997 |
rs200139704 | snp | A/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:539986 | CCAGGTTTAGAATCC[A/G]GAGGCCGGGGTGGCC | 997 |
rs200149926 | snp | C/T | | | intron-variant | CDC34 | GRCh38.p7 | 19:534736 | CCCCGAGTGCCCTCC[C/T]TGTCCAGACCTCGCC | 997 |
rs200451047 | snp | A/G | | | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:529777 | TGGAAGTGACCGCTC[A/G]GCCCAGAGCTCTTTC | 997 |
rs200517034 | snp | A/C | 0.00020527 | 0.0101288 | missense | CDC34 | GRCh38.p7 | 19:536271 | GTATCTCCATCCTCC[A/C]CCCGCCGGTGGACGA | 997 |
rs200761288 | snp | A/C/G | 6.82156e-05 | 0.00583985 | missense, utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541463 | TCAGACCTCTTCTAC[A/C/G]ACGACTACTACGAGG | 997 |
rs200901382 | snp | A/G | 2.183e-05 | 0.00330371 | synonymous-codon, utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541399 | GAAGGTGCCCACCAC[A/G]CTGGCCGAGTACTGC | 997 |
rs201298448 | snp | A/G | 1.65343e-05 | 0.00287521 | intron-variant | CDC34 | GRCh38.p7 | 19:535943 | GCGCGGCCCCCACGG[A/G]CCTCAAGTCCTCATC | 997 |
rs201584025 | snp | A/G | 0.000724613 | 0.0190205 | missense, utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541442 | GCGCCGGCGCCCGAC[A/G]AGGGCTCAGACCTCT | 997 |
rs201685527 | in-del | -/A | | | intron-variant | CDC34 | GRCh38.p7 | 19:540275 | GTGGCCAGGCCCCCC[-/A]GGTTTAGAATCCGGA | 997 |
rs201715065 | snp | G/T | 3.53157e-05 | 0.00420198 | stop-gained, utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541523 | TGCTTCGGGGACGAT[G/T]AGGATGACTCTGGCA | 997 |
rs201928514 | in-del | -/TG | | | intron-variant | CDC34 | GRCh38.p7 | 19:534553 | CAAGACCCCCGAGTA[-/TG]CCCTCCCTGTCAAGG | 997 |
rs202107697 | snp | C/T | 0.000316634 | 0.0125784 | intron-variant | CDC34 | GRCh38.p7 | 19:537170 | CGGGCGGGGGCGTCA[C/T]GGGAGGAGAGACTCA | 997 |
rs202165115 | snp | C/T | | | intron-variant | CDC34 | GRCh38.p7 | 19:540840 | GGGTGGCCAGGCCCC[C/T]GGGTTTAGAATCCTG | 997 |
rs202229553 | snp | A/G | 8.25839e-05 | 0.00642535 | intron-variant | CDC34 | GRCh38.p7 | 19:535930 | ATCTACGAGGTGAGC[A/G]CGGCCCCCACGGGCC | 997 |
rs367570848 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | CDC34 | GRCh38.p7 | 19:532583 | CCCCCCCAGACCCCG[G/T]AGCTGCTATTGTTGG | 997 |
rs367784423 | snp | A/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:540147 | AATCCGGAGGCCGGG[A/G]TGGCCAGGCCCCCCG | 997 |
rs367825954 | snp | C/T | 0.00128549 | 0.0253198 | intron-variant | CDC34 | GRCh38.p7 | 19:536994 | CGGGCCGCCCCACTC[C/T]GACCCACTCTCCCCA | 997 |
rs368089180 | snp | C/T | 8.404e-05 | 0.00648174 | missense | CDC34 | GRCh38.p7 | 19:537135 | AGGATCGGGAGTACA[C/T]AGACATCATCCGGTG | 997 |
rs368248891 | snp | C/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:539974 | TGGCCAGGCCCCCCA[C/G]GTTTAGAATCCGGAG | 997 |
rs368421890 | snp | A/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:540109 | AATCCGGAGGCCGGG[A/G]TGGCCAGGCCCCCCA | 997 |
rs368428873 | snp | A/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:536736 | CGTGTGTCCTGGAGT[A/G]TAGTCTAGGCAGGAC | 997 |
rs368438131 | snp | C/T | 1.65987e-05 | 0.00288082 | synonymous-codon | CDC34 | GRCh38.p7 | 19:537052 | CCTCCTGAACGAGCC[C/T]AACACCTTCTCGCCC | 997 |
rs368574139 | snp | C/T | | | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:530726 | CAGCTACTCGGGAGG[C/T]TGAGGCGGACACTAG | 997 |
rs368575228 | snp | C/T | 3.90297e-05 | 0.00441739 | synonymous-codon | CDC34 | GRCh38.p7 | 19:532087 | GCCCCCCAACACCTA[C/T]TACGAGGGCGGCTAC | 997 |
rs368677686 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | CDC34 | GRCh38.p7 | 19:535908 | GACCAAGATGTGGCA[C/T]CCTAACATCTACGAG | 997 |
rs368818872 | snp | A/G | 0.000153988 | 0.00877327 | utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541590 | AGTTTACCTCACTAG[A/G]GCCGGACCCGTGGCT | 997 |
rs369177801 | snp | A/G | | | upstream-variant-2KB, downstream-variant-500B | GZMM, CDC34 | GRCh38.p7 | 19:542133 | GCAGCCTCCACGTCC[A/G]TGAGTGACTGCACAC | 997 |
rs369178332 | snp | A/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:540261 | AATCCGGAGGCCGGG[A/G]TGGCCAGGCCCCCCG | 997 |
rs369297199 | snp | A/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:540288 | CCCGGTTTAGAATCC[A/G]GAGGCCGGGGTGGCC | 997 |
rs369427490 | snp | A/G | 1.76571e-05 | 0.00297123 | synonymous-codon, utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541435 | GACCAAGGCGCCGGC[A/G]CCCGACGAGGGCTCA | 997 |
rs369453041 | snp | A/G | 5.04342e-05 | 0.00502141 | intron-variant | CDC34 | GRCh38.p7 | 19:536980 | AGGCTGGGGTGCCCC[A/G]GGCCGCCCCACTCCG | 997 |
rs369587037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:536613 | AGGTGTCCCGCCATC[C/T]TCAGTCCTGGGGCCT | 997 |
rs369737989 | snp | A/G | 3.39449e-05 | 0.00411962 | intron-variant | CDC34 | GRCh38.p7 | 19:536237 | ACCTGTCTTCTTCTT[A/G]TGCAGACGGGGGACG | 997 |
rs369824190 | snp | A/G | 0.000581468 | 0.017041 | intron-variant | CDC34 | GRCh38.p7 | 19:536199 | GGGCACTGGGAGCCC[A/G]TGCTGACCTCTGACC | 997 |
rs369872688 | snp | C/G | | | utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541598 | TCACTAGGGCCGGAC[C/G]CGTGGCTCCTTAGAC | 997 |
rs369947987 | snp | G/T | 0.000306701 | 0.0123797 | intron-variant | CDC34 | GRCh38.p7 | 19:541309 | AGTCCAGGCACGTGG[G/T]TGGCGCCCTCACCCA | 997 |
rs369990220 | snp | G/T | 0.000187769 | 0.00968759 | missense, utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541460 | GGCTCAGACCTCTTC[G/T]ACGACGACTACTACG | 997 |
rs370041184 | snp | A/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:538011 | GTTTAACGCATGTCT[A/G]TGCTTTAATGAAGAA | 997 |
rs370660202 | snp | C/T | | | intron-variant | CDC34 | GRCh38.p7 | 19:534545 | CCCACAATCCAAGAC[C/T]CCCGAGTACCCTCCC | 997 |
rs370722276 | snp | C/T | 0.000117419 | 0.00766132 | intron-variant | CDC34 | GRCh38.p7 | 19:536984 | TGGGGTGCCCCGGGC[C/T]GCCCCACTCCGACCC | 997 |
rs370729651 | snp | C/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:532478 | CCCCGGCTGCCTCCC[C/G]CTCCGCCCCTGCGAG | 997 |
rs370735978 | snp | A/G | 0.000265591 | 0.0115206 | utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541574 | CAGAATAAACTTGCC[A/G]AGTTTACCTCACTAG | 997 |
rs370944279 | snp | A/G | 4.59548e-05 | 0.00479326 | intron-variant | CDC34 | GRCh38.p7 | 19:536348 | AACGTCAGGTAAGCC[A/G]GCCCAACCCCCTGTG | 997 |
rs371106154 | snp | A/G | 0.000281789 | 0.0118666 | intron-variant | CDC34 | GRCh38.p7 | 19:532141 | CGCCCGGGTCCCGGA[A/G]CCCACGAGCGACCTC | 997 |
rs371228164 | snp | A/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:534641 | CCAAGACCCCCGAGT[A/G]CCCTCCCTGTCCAGA | 997 |
rs371610837 | snp | C/T | 1.66549e-05 | 0.00288568 | synonymous-codon | CDC34 | GRCh38.p7 | 19:537112 | GAAGTGGAAAGAGAG[C/T]AAGGGGAAGGATCGG | 997 |
rs371653474 | snp | A/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:540162 | GTGGCCAGGCCCCCC[A/G]GGTTTAGAATCCGGA | 997 |
rs371692795 | snp | A/G | 0.00013805 | 0.00830698 | intron-variant | CDC34 | GRCh38.p7 | 19:537156 | TCATCCGGTGAGGGC[A/G]GGCGGGGGCGTCACG | 997 |
rs371714665 | snp | A/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:541192 | CCTGGAGTTCCTCAC[A/G]CACAGGGCTTTGTCC | 997 |
rs371714733 | snp | G/T | | | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:530751 | CACTAGCTTGAACCC[G/T]GGAGGCGGAGGTTGC | 997 |
rs371748620 | snp | C/T | | | intron-variant | CDC34 | GRCh38.p7 | 19:534666 | TCCAGACCTCGCCCA[C/T]GATCCAAGACCCCCG | 997 |
rs372012440 | snp | C/T | 0.000165618 | 0.00909843 | intron-variant | CDC34 | GRCh38.p7 | 19:535962 | CAAGTCCTCATCCTC[C/T]GGGACCCAGGGTGCT | 997 |
rs372269784 | snp | G/T | 3.70693e-05 | 0.00430503 | missense | CDC34 | GRCh38.p7 | 19:541372 | CAAGGTGGACGCGGA[G/T]CGTGACGGCGTGAAG | 997 |
rs372336362 | snp | A/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:533680 | TGTGCCCACCAGACC[A/G]GTTGCCAGGGATTGT | 997 |
rs372655671 | snp | A/G | | | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:530601 | TCCTTTCAAAACCTA[A/G]CAACACACTTGAGGT | 997 |
rs372730157 | snp | C/T | | | intron-variant | CDC34 | GRCh38.p7 | 19:540654 | GGTGGCCAGGCCCCC[C/T]GGGTTTAGAATCCGG | 997 |
rs372864316 | snp | C/T | 3.59615e-05 | 0.00424022 | intron-variant | CDC34 | GRCh38.p7 | 19:536228 | CCTGTTCTGACCTGT[C/T]TTCTTCTTGTGCAGA | 997 |
rs373005303 | snp | C/T | | | intron-variant | CDC34 | GRCh38.p7 | 19:534829 | AGTGCCCTCCCTGTC[C/T]AGACCTCGCCCACGA | 997 |
rs373167298 | snp | A/G | 8.56201e-05 | 0.00654238 | intron-variant | CDC34 | GRCh38.p7 | 19:536962 | GGCCAGAGAAGAGCC[A/G]GAAGGCTGGGGTGCC | 997 |
rs373174282 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC34 | GRCh38.p7 | 19:539668 | CCAGAGCCCAGAGCC[A/G]TGCCTGGTCGGTGAT | 997 |
rs373322357 | snp | A/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:534529 | CCCTGTCCAGACCTC[A/G]CCCACAATCCAAGAC | 997 |
rs373877648 | snp | A/G/T | 0.000133803 | 0.00817832 | missense | CDC34 | GRCh38.p7 | 19:537126 | GCAAGGGGAAGGATC[A/G/T]GGAGTACACAGACAT | 997 |
rs373978979 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CDC34 | GRCh38.p7 | 19:535213 | ACAGGGGGCGATGCT[A/G]ACAGGGAAGGAGTCC | 997 |
rs373981582 | snp | A/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:537305 | GATGGAGGCCGGGCC[A/G]AGTGGCGGAGGGTCC | 997 |
rs374096503 | snp | A/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:540706 | CCACGTTTAGAATCC[A/G]GAGGCCGGGGTGGCC | 997 |
rs374183557 | snp | G/T | | | intron-variant, downstream-variant-500B | CDC34 | GRCh38.p7 | 19:539451 | CCCCCCAGCCCATCG[G/T]AGAGCTTGGAAAGCA | 997 |
rs374233988 | snp | A/G | 0.000650884 | 0.0180283 | intron-variant | CDC34 | GRCh38.p7 | 19:536995 | GGGCCGCCCCACTCC[A/G]ACCCACTCTCCCCAC | 997 |
rs374242233 | snp | C/G | 0.000155666 | 0.00882094 | intron-variant | CDC34 | GRCh38.p7 | 19:532146 | GGGTCCCGGAGCCCA[C/G]GAGCGACCTCGGGCG | 997 |
rs374337560 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B | GZMM, CDC34 | GRCh38.p7 | 19:542428 | GGGCGTTGATCTCAG[C/T]GTCTCAGGGCTCCCA | 997 |
rs374369696 | snp | C/T | 4.9597e-05 | 0.00497956 | synonymous-codon | CDC34 | GRCh38.p7 | 19:532033 | CGTGACACTGGTGGA[C/T]GAGGGCGATCTATAC | 997 |
rs374673100 | in-del | -/CCCCC | | | utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541733 | AGAGAAGAGGGGCTG[-/CCCCC]CCCCACCGCCACTCA | 997 |
rs374693104 | snp | C/T | | | intron-variant | CDC34 | GRCh38.p7 | 19:534622 | TCCAGACCTCGCCCA[C/T]GATCCAAGACCCCCG | 997 |
rs374799441 | snp | A/G/T | 8.38081e-05 | 0.00647286 | intron-variant | CDC34 | GRCh38.p7 | 19:536985 | GGGGTGCCCCGGGCC[A/G/T]CCCCACTCCGACCCA | 997 |
rs374872375 | snp | C/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:533912 | CCCAGGGCCGCTGCT[C/G]CCCAGCCACTGCCTG | 997 |
rs374905654 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | CDC34 | GRCh38.p7 | 19:535803 | AGGTCTTGGGGCTGG[A/G]CTGGACTGAGCCACC | 997 |
rs374959120 | snp | C/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:540805 | ATGGCCAGGCCCCCC[C/G]GTTTAGAATCCGGAG | 997 |
rs375119866 | snp | A/G | | | intron-variant, downstream-variant-500B | CDC34 | GRCh38.p7 | 19:539419 | TGCAGTGCCGTCCCC[A/G]GGGCACTGTCAGTCA | 997 |
rs375133735 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:530503 | TCAGGTGGGCTGGGC[A/G]CGGTGGCTCATGCCT | 997 |
rs375170465 | snp | A/G | 9.16784e-05 | 0.00676984 | intron-variant | CDC34 | GRCh38.p7 | 19:536930 | TGGGTGGGTCCAGGC[A/G]TCCCCGTGACCCTCA | 997 |
rs375186759 | snp | A/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:540668 | CCGGGTTTAGAATCC[A/G]GAGGCCGGGGTGGCC | 997 |
rs375224993 | snp | G/T | | | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:529954 | CTGGTTTTTGTTTTT[G/T]GTTTTTTTTTTTTTT | 997 |
rs375521090 | snp | A/G | 9.89038e-05 | 0.00703151 | missense | CDC34 | GRCh38.p7 | 19:535886 | CTCCACCAGCCTTTC[A/G]GTTCCTGACCAAGAT | 997 |
rs375626558 | snp | C/T | | | intron-variant | CDC34 | GRCh38.p7 | 19:541132 | GTCCAGCCTCCCACC[C/T]GCACCTCCTGCCCTT | 997 |
rs375818778 | snp | C/T | 3.54371e-05 | 0.00420919 | missense, utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541434 | AGACCAAGGCGCCGG[C/T]GCCCGACGAGGGCTC | 997 |
rs376164577 | snp | G/T | 1.84466e-05 | 0.00303693 | missense, utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541546 | CTCTGGCACGGAGGA[G/T]TCCTGACACCACCAG | 997 |
rs376456892 | in-del | -/C | | | intron-variant | CDC34 | GRCh38.p7 | 19:540232 | GCCGGGGTGGCCAGG[-/C]CCCCCGGGTTTAGAA | 997 |
rs376651637 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541792 | AGGGTGGGAGCGGCC[A/G]GCCCACCTGTCCCCT | 997 |
rs376691492 | snp | C/G | | | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:530332 | CACCCGTCACGGGCA[C/G]GACTCAGGGGAGGCT | 997 |
rs376709652 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B | GZMM, CDC34 | GRCh38.p7 | 19:542357 | GTGCATCTAGTGGGA[C/T]GGGAGCTGCCTCTGC | 997 |
rs376731647 | snp | A/C | 2.16055e-05 | 0.00328668 | synonymous-codon | CDC34 | GRCh38.p7 | 19:536339 | CCCACGCAGAACGTC[A/C]GGTAAGCCGGCCCAA | 997 |
rs376770367 | in-del | -/T | | | intron-variant | CDC34 | GRCh38.p7 | 19:533099 | AAACCAGGGCAGTTT[-/T]CTTGATCTCACGATC | 997 |
rs376816532 | snp | C/T | 0.000153988 | 0.00877328 | utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541572 | ACCAGAATAAACTTG[C/T]CGAGTTTACCTCACT | 997 |
rs376850117 | in-del | -/C | 0.229429 | 0.249152 | intron-variant | CDC34 | GRCh38.p7 | 19:540649 | GCCGGGGTGGCCAGG[-/C]CCCCCGGGTTTAGAA | 997 |
rs377054372 | snp | C/T | 0.000634607 | 0.0178017 | intron-variant | CDC34 | GRCh38.p7 | 19:536231 | GTTCTGACCTGTCTT[C/T]TTCTTGTGCAGACGG | 997 |
rs377074777 | snp | A/G | 0.000106502 | 0.00729655 | intron-variant | CDC34 | GRCh38.p7 | 19:537180 | CGTCACGGGAGGAGA[A/G]ACTCAGATCCGGCCT | 997 |
rs377081676 | snp | C/T | | | intron-variant | CDC34 | GRCh38.p7 | 19:539869 | GTAGGTCCTGGTGTG[C/T]GCGGTGCAGCCCCTC | 997 |
rs377091050 | multinucleotide-polymorphism | AA/GG | | | intron-variant | CDC34 | GRCh38.p7 | 19:535634 | AGCTGGGATCAGCTC[AA/GG]GTGACTCAGAAAAGG | 997 |
rs377164965 | snp | C/G/T | 0.0036145 | 0.0423861 | intron-variant | CDC34 | GRCh38.p7 | 19:541292 | GGGCCGGGCAGGGGC[C/G/T]GAGTCCAGGCACGTG | 997 |
rs377177218 | snp | C/G/T | 0.000103834 | 0.00720467 | missense, synonymous-codon, utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541441 | GGCGCCGGCGCCCGA[C/G/T]GAGGGCTCAGACCTC | 997 |
rs377498927 | snp | A/G | 0.00010214 | 0.00714559 | intron-variant | CDC34 | GRCh38.p7 | 19:536966 | AGAGAAGAGCCGGAA[A/G]GCTGGGGTGCCCCGG | 997 |
rs377515310 | snp | A/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:540767 | GATGGCCAGGCCCCC[A/G]GGTTTAGAATCCAGA | 997 |
rs377683521 | snp | A/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:541082 | CTTGGGTTGTGCTTC[A/G]GGGCGGGGCAGGCGG | 997 |
rs377686357 | snp | C/T | | | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:531206 | ATCCCGCCTCGCTCC[C/T]GCCCCTTCCTCCCTT | 997 |
rs386805628 | multinucleotide-polymorphism | CCA/TCG | | | intron-variant | CDC34 | GRCh38.p7 | 19:541260 | GCGTTGGGGTGAGCG[CCA/TCG]GACCTGGGGGAGGGG | 997 |
rs398033668 | in-del | -/T | 0 | 0 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:529969 | GGTTTTTTTTTTTTT[-/T]GAGACGGAGTCTCTG | 997 |
rs527418144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:536619 | CCCGCCATCCTCAGT[C/T]CTGGGGCCTTCTCCT | 997 |
rs527530911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:533327 | CGGGCGTGGGGCCGA[A/G]GGACCGATGCCTCCC | 997 |
rs527637452 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | CDC34 | GRCh38.p7 | 19:536402 | CGGGCTCCGTCCCGT[A/G]TCCACCCAGACCATC | 997 |
rs528359168 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:536172 | CTCCACGTCCTCATC[A/C]TCCGGGACCTGGGGC | 997 |
rs528567215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, missense | CDC34 | GRCh38.p7 | 19:538776 | GCTGGGCGGTCTCGG[C/T]TCTGAGCAGCCATGG | 997 |
rs528813518 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CDC34 | GRCh38.p7 | 19:537903 | CTCAGGTGATCCACC[C/T]GCCTCGGCCTCCCAA | 997 |
rs528972506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:534266 | AGTCACTTGCCTTAC[A/G]GGGCACCAGTGAGTT | 997 |
rs529084466 | snp | C/T | | | intron-variant | CDC34 | GRCh38.p7 | 19:540332 | TTAGAATCCGGAGGC[C/T]GGGGTGGCCAGGCCC | 997 |
rs529532980 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:537464 | TTCACGCCATTCTCC[G/T]GCCTCAGCCTCCCAA | 997 |
rs529619721 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541886 | GAGGAGCCACGGGGG[C/T]GCTGCTGGGAACGTG | 997 |
rs529699447 | snp | C/T | | | intron-variant | CDC34 | GRCh38.p7 | 19:538012 | TTTAACGCATGTCTG[C/T]GCTTTAATGAAGAAA | 997 |
rs529807175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:536464 | GCCAAGGCCTGATTC[A/G]GGACCTGCCAGCTGG | 997 |
rs529844893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:540088 | GGCCAGGCCCCCCAG[A/G]TTTAGAATCCGGAGG | 997 |
rs529993620 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | CDC34 | GRCh38.p7 | 19:539525 | AGGCCAGACGCCTGC[C/T]CTCCACGCGTCATGC | 997 |
rs529996528 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:533198 | GGGCCCTGTGTGAGC[C/G]GTGGGGAACGAGCAC | 997 |
rs530104711 | snp | A/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:540071 | AATCCGGAGGCCGGG[A/G]TGGCCAGGCCCCCCA | 997 |
rs530228467 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:531299 | GGAGACGGGGACGCG[A/G]GGTCGCGCCGGATGG | 997 |
rs530470854 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:530352 | CAGGGGAGGCTGGGC[C/T]GCCCCGTCCTCACCA | 997 |
rs530962958 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:534354 | GGGCCCGTCCACGAT[C/G]CAAGACCCCCAAAGT | 997 |
rs531058537 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | GZMM, CDC34 | GRCh38.p7 | 19:542391 | CATCCAGCAAAGCTT[C/T]GTCGCGGGTCCACAG | 997 |
rs531081404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:538392 | GCCCCAGAGCTGAGC[C/T]CCACAGCCCCTTCTC | 997 |
rs531094138 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:535222 | GATGCTGACAGGGAA[G/T]GAGTCCTGCCAGGTT | 997 |
rs531121143 | snp | A/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:533866 | CTGGGAGGGAGTTGG[A/G]GGAGCGTGGAAATAC | 997 |
rs531252469 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:534620 | TGTCCAGACCTCGCC[A/C]ACGATCCAAGACCCC | 997 |
rs531324534 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC34 | GRCh38.p7 | 19:537446 | CAAGCTCCGCCTCCC[A/G]GGTTCACGCCATTCT | 997 |
rs531327735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:533356 | CCGCACGATATGTGT[C/T]TGCTCTCCGAGCTAA | 997 |
rs531419496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:533759 | TTTCCCAGGGAGGGG[A/G]CCTCTAGACATCTGC | 997 |
rs531775710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:532773 | CCATCCCCTGCTTTA[C/T]GTAACCTGCGCCCTC | 997 |
rs531877075 | snp | A/G | 1.7195e-05 | 0.0029321 | missense, utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541493 | GACGGCGAGGTGGAG[A/G]AGGAGGCCGACAGCT | 997 |
rs532288607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:532358 | CCTTCAAGGCATCGT[C/T]CGGTCCCCTGTTAGG | 997 |
rs532291150 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | CDC34 | GRCh38.p7 | 19:536189 | CCGGGACCTGGGGCA[C/G]TGGGAGCCCGTGCTG | 997 |
rs532486883 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CDC34 | GRCh38.p7 | 19:535726 | ATACGGTGTCCCTCA[A/C]ACACACCCTCAGGCA | 997 |
rs532522609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CDC34 | GRCh38.p7 | 19:539126 | GTGCGTGTTGGCCTC[A/G]TGGCAGCCCAAGTCC | 997 |
rs532632831 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:530635 | GGGTTCGAGACCAGC[A/C]TGGCCAACATGGTGA | 997 |
rs532873435 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:529810 | GGATCCCTCCCTCCC[G/T]CTCCACTCCTGATGC | 997 |
rs533232200 | in-del | -/T | | | intron-variant | CDC34 | GRCh38.p7 | 19:534548 | CAATCCAAGACCCCC[-/T]GAGTACCCTCCCTGT | 997 |
rs533324617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:537554 | AGACGGGGTTTCAGC[A/G]TGTTAGCCAGGATGG | 997 |
rs533432350 | snp | C/T | | | intron-variant | CDC34 | GRCh38.p7 | 19:537500 | TGGGACTACAGGCGC[C/T]CGTCACCACGCCCGG | 997 |
rs533526325 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | GZMM, CDC34 | GRCh38.p7 | 19:542274 | TCAGACAGGCCTGGG[C/T]AGCATCCCCCAGCCT | 997 |
rs533730436 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | CDC34 | GRCh38.p7 | 19:532227 | CCCGAAGCCTCCTGG[C/G]TTGGGCTCGTTTCCC | 997 |
rs533744115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:536494 | GCGGTCCTGGGCCTC[A/G]CTGTACCTGCACGGT | 997 |
rs533826485 | snp | C/T | | | intron-variant | CDC34 | GRCh38.p7 | 19:540560 | TTAGAATCCGGAGGC[C/T]GGGGTGGCCAGGCCC | 997 |
rs533899194 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC34 | GRCh38.p7 | 19:532449 | TGCCCACCTCCTCCT[C/T]GGCGGGGGCTGGACC | 997 |
rs534707935 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | GZMM, CDC34 | GRCh38.p7 | 19:542457 | CAGGACCACAGATGC[A/C]CCCGATCAGCACTCC | 997 |
rs535149765 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC34 | GRCh38.p7 | 19:534387 | CCTGCCTGTCCGGGA[A/G]GGGCCTCGCCCACAA | 997 |
rs535735359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:533393 | TCTGAACCGCACCCG[C/T]TCAGCGGCTGTGAGG | 997 |
rs535747164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:537685 | TTTGGAGACAGAGTT[A/G]TACTCTCTTGCCTAG | 997 |
rs535777504 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | GZMM, CDC34 | GRCh38.p7 | 19:542129 | AGAGGCAGCCTCCAC[A/G]TCCATGAGTGACTGC | 997 |
rs536208913 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:530687 | ACAAAATTAGCCGGA[C/T]GTGGTGGCGGGCACC | 997 |
rs536218032 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC34 | GRCh38.p7 | 19:539748 | TCAAATGGGGTCAGC[A/G]TGCCGCCTGGCCCTG | 997 |
rs536294587 | snp | C/T | | | intron-variant | CDC34 | GRCh38.p7 | 19:538659 | TGCACACATAATGCA[C/T]GTGTCTTCCTCGCCC | 997 |
rs536378976 | snp | C/T | 0.00113499 | 0.0237951 | intron-variant | CDC34 | GRCh38.p7 | 19:536220 | ACCTCTGACCTGTTC[C/T]GACCTGTCTTCTTCT | 997 |
rs536402715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:532397 | CCCCGGAGGGGTGGC[C/T]GGGGGCCCTCCCTGT | 997 |
rs537189363 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | GZMM, CDC34 | GRCh38.p7 | 19:542503 | GTCCAGGCACACCCT[C/T]GGGGTGGGGAGCCGT | 997 |
rs537323814 | snp | A/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:539809 | CAGTCCTGGGGGGAC[A/G]TTCTTGACGCGTGTC | 997 |
rs537345099 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:530169 | AGCCACAATGGTCTC[G/T]ATCTCCTGACATTGT | 997 |
rs537362360 | snp | C/T | | | intron-variant, missense | CDC34 | GRCh38.p7 | 19:538760 | GGGGCAGCATCCTGG[C/T]GCTGGGCGGTCTCGG | 997 |
rs537408764 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC34 | GRCh38.p7 | 19:537280 | GCCCATTTACAGGGT[A/G]CCAGTCACAGATGGA | 997 |
rs537447531 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541703 | CCCATGTCTGTTCTG[A/G]GTTTTCACGTGCTTC | 997 |
rs537496597 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CDC34 | GRCh38.p7 | 19:532683 | CCAACAAAGGCCCGG[A/C]TGAGCCTTGGCAGCC | 997 |
rs537733016 | snp | C/T | | | utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541586 | GCCGAGTTTACCTCA[C/T]TAGGGCCGGACCCGT | 997 |
rs537773564 | snp | G/T | | | intron-variant | CDC34 | GRCh38.p7 | 19:540754 | ATCCGGAGGCTGGGA[G/T]GGCCAGGCCCCCGGG | 997 |
rs538055780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:539839 | CCTGGAGGTGGAGCC[A/G]GGGGCAGGTTCCTCG | 997 |
rs538330130 | snp | C/T | | | intron-variant | CDC34 | GRCh38.p7 | 19:535720 | GGCAGGATACGGTGT[C/T]CCTCACACACACCCT | 997 |
rs538351708 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:536004 | GTCCTCATCCTTCCG[C/G]GACCCGGGGCGCTGG | 997 |
rs538561765 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:533190 | AAAGCGAGGGGCCCT[G/T]TGTGAGCGGTGGGGA | 997 |
rs538608200 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:539029 | CACACTATTTTTATC[C/T]CTCAAAACTCCCTGT | 997 |
rs538758995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:535614 | GGCCACCTGGACTGT[A/G]TAGGAGCTGGGATCA | 997 |
rs538769877 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | CDC34 | GRCh38.p7 | 19:539324 | AGCCGCCACCTCTGC[A/G]GTGCCGTCCCCGGGG | 997 |
rs538772455 | snp | A/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:537218 | GGCCCCTGGTCCCAC[A/G]GCCGCCCAGCCCCAC | 997 |
rs538779222 | snp | A/G | | | utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541691 | TTTTTCTCCCTCCCC[A/G]TGTCTGTTCTGGGTT | 997 |
rs539136701 | snp | C/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:540695 | GGCCAGGCCCCCCAC[C/G]TTTAGAATCCGGAGG | 997 |
rs539154218 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:530072 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 997 |
rs539257114 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | GZMM, CDC34 | GRCh38.p7 | 19:542214 | TGTCCTGGGAGGCAC[A/G]GGGAGCAGCCGGGTC | 997 |
rs539349527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:538516 | TGCTCTTCCTGTTAC[A/G]TAGAGGCCCTTCCTA | 997 |
rs539755326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:538205 | ACTGACTGTTAGTCA[A/G]GGGTGTTGGCCTTAC | 997 |
rs539768512 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:533990 | GCCAGAGAGAGCCCT[C/T]CACAGCCGACTTGCT | 997 |
rs539920175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:537217 | CGGCCCCTGGTCCCA[C/T]GGCCGCCCAGCCCCA | 997 |
rs540203085 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC34 | GRCh38.p7 | 19:539892 | AGCCCCTCATAGGGC[C/T]GGGTGTACACGGTGC | 997 |
rs540354355 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC34 | GRCh38.p7 | 19:533333 | TGGGGCCGAGGGACC[A/G]ATGCCTCCCGCACGA | 997 |
rs540478067 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CDC34 | GRCh38.p7 | 19:539115 | TTTTCATCTGTGTGC[C/G]TGTTGGCCTCGTGGC | 997 |
rs540725912 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:529772 | AGCTCTGGAAGTGAC[A/C]GCTCGGCCCAGAGCT | 997 |
rs540737169 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:531253 | ACCCTAGGACAGACT[G/T]CGCGCCCGTCCCCTG | 997 |
rs540764604 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC34 | GRCh38.p7 | 19:534515 | CCCCTGAGTGCCCTC[C/T]CTGTCCAGACCTCGC | 997 |
rs540789004 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:530261 | CTGTATGTTGATGCA[G/T]CTGTGTGTACCCAGG | 997 |
rs540799993 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CDC34 | GRCh38.p7 | 19:535677 | CTTCTGGGGACTTGA[C/T]CCCAGGCCTGTGAGA | 997 |
rs540926894 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:531585 | GCTCGGCGCCGTAGG[C/T]GGGACCGGGGCCGGG | 997 |
rs540957756 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:536056 | CGGGACCCGGGGCGC[A/T]GGGAGCCTCACGTCC | 997 |
rs541031513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:537937 | GCTGGGATGACAGGC[A/G]TGAGCCACTGCACCT | 997 |
rs541148059 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC34 | GRCh38.p7 | 19:536449 | CCCACAGGCTGTGGC[A/G]CCAAGGCCTGATTCG | 997 |
rs541607767 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CDC34 | GRCh38.p7 | 19:541155 | CTGCCCTTCCCGAGC[C/T]CCCTCCTCTGTCATT | 997 |
rs541634763 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541770 | TCGGGGCTCGGTGGA[C/T]GGGCCCAGGGTGGGA | 997 |
rs541757471 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | GZMM, CDC34 | GRCh38.p7 | 19:542249 | GGCCTGTACGTTCCC[A/G]TGACTTGGGTCAGAC | 997 |
rs541832630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:539553 | TGCATCCCCATAAAA[A/G]GCACTGGGCTTGTGG | 997 |
rs541927965 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CDC34 | GRCh38.p7 | 19:533006 | CTGGCGGTTTAATTC[C/T]AAGCAGTTTCTGGAT | 997 |
rs541959264 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | CDC34 | GRCh38.p7 | 19:536396 | GTAGGCCGGGCTCCG[A/T]CCCGTATCCACCCAG | 997 |
rs542019154 | snp | C/G/T | 5.12346e-05 | 0.00506114 | missense, synonymous-codon, utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541459 | GGGCTCAGACCTCTT[C/G/T]TACGACGACTACTAC | 997 |
rs542020813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:536543 | TGCGGCACCGTGTGT[C/T]GGTGCAGACTCCCAC | 997 |
rs542020946 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CDC34 | GRCh38.p7 | 19:532332 | CTGCAGTCCTCGAAA[A/G]TCCCCAGTTCCCTTC | 997 |
rs542181239 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CDC34 | GRCh38.p7 | 19:537376 | TTTTTTGTTTGAGAC[A/G]GAGTCTCTCTCTGTC | 997 |
rs542222928 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:531070 | ATGGTGACTTCAACG[A/G]GGACCAGGGAAGCCC | 997 |
rs542973764 | snp | A/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:536134 | TCCGGGACCCGGGGC[A/G]CTGGGAGCCTCACGT | 997 |
rs543103521 | snp | A/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:536475 | ATTCGGGACCTGCCA[A/G]CTGGCGGTCCTGGGC | 997 |
rs543166895 | snp | C/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:534949 | ATCGCTCTGGGGGTG[C/G]TGCTCTCGTGCCTTG | 997 |
rs543560982 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC34 | GRCh38.p7 | 19:537618 | CGGCCTCCCAAAGTG[C/T]AGGGATTACAGGCGT | 997 |
rs543604407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:534256 | GCCGCGGCCAAGTCA[C/T]TTGCCTTACGGGGCA | 997 |
rs543768374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:533189 | CAAAGCGAGGGGCCC[C/T]GTGTGAGCGGTGGGG | 997 |
rs543966361 | snp | A/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:540585 | AGGCCCCCCGGGTTT[A/G]GAATCCGGAGGCCGG | 997 |
rs544178793 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant, downstream-variant-500B | CDC34 | GRCh38.p7 | 19:539156 | CCGCTGAGCTGTGTC[A/G]GGCAGGCTGCCGTGG | 997 |
rs544398196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:541117 | GACTGCACTGCGCCC[A/G]TCCAGCCTCCCACCC | 997 |
rs544441423 | snp | C/T | | | intron-variant | CDC34 | GRCh38.p7 | 19:535056 | AGGCTTCCTTGTTTA[C/T]CTGCTGTGGCCCAGG | 997 |
rs544696893 | in-del | -/C | 0.00478085 | 0.0486577 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:530200 | ATCCGCCCGCCTCGG[-/C]CCCCCCAAAGTGTTG | 997 |
rs544918262 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC34 | GRCh38.p7 | 19:532282 | AGCTCTGCCCGGCCC[C/T]CTCCTCGGACCGTCT | 997 |
rs544991914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:534593 | CGATCCAAGACCCCC[A/G]AGTGCCCGCCCTGTC | 997 |
rs545084224 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:530910 | GGCTCAGCTTGGGGT[A/G]GGGGCTCCGTGGGGC | 997 |
rs545537569 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541788 | GCCCAGGGTGGGAGC[G/T]GCCGGCCCACCTGTC | 997 |
rs545726688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:538339 | GCGTGGCTGTGTGTG[A/G]TGACCCACGGCTCTC | 997 |
rs545767042 | snp | C/T | | | intron-variant | CDC34 | GRCh38.p7 | 19:540257 | TTAGAATCCGGAGGC[C/T]GGGGTGGCCAGGCCC | 997 |
rs545950455 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC34 | GRCh38.p7 | 19:533741 | ATAATCCGGTTTTCC[A/G]GATTTCCCAGGGAGG | 997 |
rs546079836 | snp | C/G | | | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:530555 | CCGACGCAGACGGAT[C/G]CCTTTATTAGTCCAA | 997 |
rs546148893 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CDC34 | GRCh38.p7 | 19:536562 | GCAGACTCCCACCAG[A/G]ACCCCAGGCCGGCCC | 997 |
rs546187952 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CDC34 | GRCh38.p7 | 19:541042 | TTGCCGGCATCGTTA[G/T]TTTCTCCCAGCTCCT | 997 |
rs546349151 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | CDC34 | GRCh38.p7 | 19:533464 | TGGGACGCCCGTGGG[-/T]TTCTGCATCTGGAAT | 997 |
rs546756616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:539654 | GGTAGCAGCCAGCCC[C/T]AGAGCCCAGAGCCGT | 997 |
rs546919945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:536176 | ACGTCCTCATCCTCC[A/G]GGACCTGGGGCACTG | 997 |
rs546962256 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CDC34 | GRCh38.p7 | 19:534313 | ACACCCCCCAAGACA[A/C]CCCGCGTGCCCTCCC | 997 |
rs546996790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:533906 | TGAGTGCCCAGGGCC[A/G]CTGCTGCCCAGCCAC | 997 |
rs547222172 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:535277 | CTGACCCCCCAAGAC[C/G]GGACACCTGAGGGCA | 997 |
rs547222393 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:529949 | CCAGACTGGTTTTTG[G/T]TTTTGGTTTTTTTTT | 997 |
rs547288357 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, downstream-variant-500B | GZMM, CDC34 | GRCh38.p7 | 19:542549 | GGGCAGGCACCTCAC[A/G]TCCTGGTGTCAGGAA | 997 |
rs547306064 | snp | C/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:540466 | TGGCCAGGCCCCCCG[C/G]GTTTAGAATCCGGAG | 997 |
rs547627869 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, downstream-variant-500B | GZMM, CDC34 | GRCh38.p7 | 19:542460 | GACCACAGATGCCCC[C/T]GATCAGCACTCCGGC | 997 |
rs547821044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:537501 | GGGACTACAGGCGCC[C/T]GTCACCACGCCCGGC | 997 |
rs547865848 | snp | G/T | | | intron-variant, downstream-variant-500B | CDC34 | GRCh38.p7 | 19:539296 | ACCCTGGCCCTCCCC[G/T]GCGTCTCCCCACAGC | 997 |
rs548379087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:532858 | GCCTCCCGGCTCGGG[C/T]CCGCGTCCCGGACCC | 997 |
rs548698367 | snp | C/G | 0.0314385 | 0.121371 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:531640 | GGCCGGGCGCGCAGG[C/G]GCAAGTCGGACCTGG | 997 |
rs548802366 | snp | C/T | | | intron-variant | CDC34 | GRCh38.p7 | 19:534343 | CTGTCCAGGAGGGGC[C/T]CGTCCACGATCCAAG | 997 |
rs549379010 | snp | A/G | 1.66244e-05 | 0.00288304 | missense | CDC34 | GRCh38.p7 | 19:537099 | CCGTGATGTACAGGA[A/G]GTGGAAAGAGAGCAA | 997 |
rs549451229 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:529889 | CCAGACTCATGAAGC[C/T]GGGGCCAGGTGTTGG | 997 |
rs549493422 | snp | G/T | | | intron-variant | CDC34 | GRCh38.p7 | 19:535061 | TCCTTGTTTACCTGC[G/T]GTGGCCCAGGAGGGC | 997 |
rs549609062 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | CDC34 | GRCh38.p7 | 19:534365 | CGATCCAAGACCCCC[A/T]AAGTGCCCTGCCTGT | 997 |
rs549649192 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CDC34 | GRCh38.p7 | 19:533787 | TGCCACAGGGTCAGT[C/T]CTCAGAAGCCAGTGT | 997 |
rs549728138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:533364 | TATGTGTCTGCTCTC[C/T]GAGCTAATTAGTGTC | 997 |
rs549951764 | snp | C/T | 0.00557099 | 0.0524829 | intron-variant | CDC34 | GRCh38.p7 | 19:541246 | TAAGAGAAACCTGAG[C/T]GTTGGGGTGAGCGTC | 997 |
rs550012804 | snp | A/G | 0.000103341 | 0.00718749 | missense, utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541496 | GGCGAGGTGGAGGAG[A/G]AGGCCGACAGCTGCT | 997 |
rs550014565 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CDC34 | GRCh38.p7 | 19:536722 | TGGGCCGTGTTGCCC[A/G]TGTGTCCTGGAGTGT | 997 |
rs550579219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, missense | CDC34 | GRCh38.p7 | 19:538911 | TCGGTGGCCCCGGTC[C/T]GGTCGTGTCACCTGG | 997 |
rs550648439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:539719 | TGCGGCTGCAGCCTC[A/G]TTCCTGTTTTCTGTC | 997 |
rs550679751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:535397 | CTCCCCACACCCTGG[C/T]TGCCAAGGCCCTGGA | 997 |
rs550809348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:539908 | GGGTGTACACGGTGC[C/T]CTCCAGGAAGTTTGA | 997 |
rs550838680 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:530654 | CCAACATGGTGAAAC[C/T]CCATCTCTACTTAAA | 997 |
rs550928825 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:529840 | CTGTTTTCCTTTCCC[C/G]AGACAGGTTTGCCTG | 997 |
rs551199712 | snp | C/T | | | intron-variant | CDC34 | GRCh38.p7 | 19:540522 | TTAGAATCCGGAGGC[C/T]GGGGTGGCCAGGCCC | 997 |
rs551566109 | in-del | -/T | | | intron-variant | CDC34 | GRCh38.p7 | 19:534680 | CGATCCAAGACCCCC[-/T]GAGTGCCCTCCCTGT | 997 |
rs551664238 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:538003 | GCTTTTCAGTTTAAC[G/T]CATGTCTGTGCTTTA | 997 |
rs551772306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:541218 | TGTCCTAAGTGGTCG[C/T]CACACGCCGTTTTAA | 997 |
rs551932521 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:534053 | AGCCTGGGTTTGCTC[C/T]GGGGAAAAGACATTC | 997 |
rs551967354 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC34 | GRCh38.p7 | 19:537563 | TTCAGCGTGTTAGCC[A/G]GGATGGTCTCGATCT | 997 |
rs552021466 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | GZMM, CDC34 | GRCh38.p7 | 19:542316 | GCGGCCAGAAAGCCC[C/G]CAGAGTTCCTCCTCC | 997 |
rs552161530 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime | CDC34 | GRCh38.p7 | 19:531898 | GGTCGCGCGGCCCCG[A/C]GCTGCTCCGACCCCG | 997 |
rs552257053 | snp | A/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:540427 | GTGGCCAGGCCCCCC[A/G]GGTTTAGAATCCGGA | 997 |
rs552664066 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:530720 | TAATCTCAGCTACTC[A/G]GGAGGCTGAGGCGGA | 997 |
rs552686527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:538624 | TATAAACAGAATCTT[A/G]AAAACAACTTTTAAA | 997 |
rs552896179 | snp | A/C | 0.00398564 | 0.0444627 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:531477 | CTTGCGCACAGCGTC[A/C]GCGGTGCTGGTCGAG | 997 |
rs553149201 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | CDC34 | GRCh38.p7 | 19:535594 | GTTGTGCTGGGCCGG[A/C/G]TCCCGGCCACCTGGA | 997 |
rs553679275 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, downstream-variant-500B | GZMM, CDC34 | GRCh38.p7 | 19:542148 | ATGAGTGACTGCACA[C/T]GGCCAGTCCCACTGG | 997 |
rs553693388 | snp | C/T | | | utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541841 | CGACTTCTACCGGGG[C/T]CCCCCAGCTTCCGGA | 997 |
rs553740681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:537690 | AGACAGAGTTATACT[C/T]TCTTGCCTAGGCTGC | 997 |
rs553925045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:537397 | TCTCTCTGTCACCCA[A/G]GCTGGAGTGCAGTGG | 997 |
rs553929381 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC34 | GRCh38.p7 | 19:533104 | AGGGCAGTTTTCTTG[A/G]TCTCACGATCCAGAC | 997 |
rs553933865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:541281 | CTGGGGGAGGGGGGC[C/T]GGGCAGGGGCCGAGT | 997 |
rs554131287 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:540978 | CTTCCTTTGCTCCTG[C/G]GCTGAGGAAGGCTTT | 997 |
rs554591668 | snp | G/T | 3.55802e-05 | 0.00421768 | intron-variant | CDC34 | GRCh38.p7 | 19:536229 | CTGTTCTGACCTGTC[G/T]TCTTCTTGTGCAGAC | 997 |
rs554624523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:536015 | TCCGGGACCCGGGGC[A/G]CTGGGAGCCTCACGT | 997 |
rs554753992 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC34 | GRCh38.p7 | 19:532218 | TGGGCGGGCCCCGAA[A/G]CCTCCTGGCTTGGGC | 997 |
rs555005329 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:538269 | CCTGGTGAGCTCTGG[C/G]TACAGCTGTGCAGTC | 997 |
rs555026631 | snp | C/T | | | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:529752 | CCTCGGCCTCGGCCC[C/T]GGACAGCTCTGGAAG | 997 |
rs555065937 | snp | G/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, downstream-variant-500B | GZMM, CDC34 | GRCh38.p7 | 19:542514 | CCCTCGGGGTGGGGA[G/T]CCGTGGCCCTGGGCA | 997 |
rs555165542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:538575 | TTGCATAGATTTCCT[C/T]ACAGAGGCCTCACCT | 997 |
rs555203289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CDC34 | GRCh38.p7 | 19:539417 | CGTGCAGTGCCGTCC[C/T]CGGGGCACTGTCAGT | 997 |
rs555423478 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:530205 | GCCCGCCTCGGCCCC[C/G]CAAAGTGTTGGGATC | 997 |
rs555627646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:534085 | TAGAGGTGCCCAAAA[C/T]AAGAGGCTCATTGGG | 997 |
rs555718367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:533605 | CCGCAGCCCCACCTC[A/G]AAGCCAGGCCTGTGA | 997 |
rs555822496 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC34 | GRCh38.p7 | 19:537304 | AGATGGAGGCCGGGC[C/T]GAGTGGCGGAGGGTC | 997 |
rs556080802 | snp | C/T | | | utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541628 | CGACAGACTACCTCA[C/T]GGAGGTTTTGTGCTG | 997 |
rs556199614 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:539845 | GGTGGAGCCGGGGGC[A/G]GGTTCCTCGTAGGTC | 997 |
rs556361125 | snp | C/T | 6.3803e-05 | 0.00564778 | intron-variant | CDC34 | GRCh38.p7 | 19:536378 | GTCCACCCAGAACAT[C/T]AGGTAGGCCGGGCTC | 997 |
rs556391590 | snp | A/G | 0.000104217 | 0.00721788 | missense, utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541439 | AAGGCGCCGGCGCCC[A/G]ACGAGGGCTCAGACC | 997 |
rs556458993 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541712 | GTTCTGGGTTTTCAC[C/G]TGCTTCAGAGAAGAG | 997 |
rs556718389 | in-del | -/CT | 0.0580162 | 0.160132 | intron-variant | CDC34 | GRCh38.p7 | 19:540817 | CCGGTTTAGAATCCG[-/CT]GAGGCCGGGGTGGCC | 997 |
rs556733110 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:530914 | CAGCTTGGGGTGGGG[A/G]CTCCGTGGGGCTGGC | 997 |
rs556738390 | snp | C/T | | | intron-variant | CDC34 | GRCh38.p7 | 19:535722 | CAGGATACGGTGTCC[C/T]TCACACACACCCTCA | 997 |
rs556970853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:536007 | CTCATCCTTCCGGGA[C/T]CCGGGGCGCTGGGAG | 997 |
rs556983533 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CDC34 | GRCh38.p7 | 19:539354 | GCACCGTCACCCCCC[A/C]AGCCCGTCCACCCTG | 997 |
rs557022232 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CDC34 | GRCh38.p7 | 19:539059 | TGGGCCAACACACAT[A/G]TGCCATGTGGACTCT | 997 |
rs557132777 | snp | A/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:540238 | GTGGCCAGGCCCCCC[A/G]GGTTTAGAATCCGGA | 997 |
rs557393893 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | GZMM, CDC34 | GRCh38.p7 | 19:542225 | GCACGGGGAGCAGCC[A/G]GGTCCCGCGGCCTGT | 997 |
rs557439429 | snp | C/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:540542 | TGGCCAGGCCCCCCG[C/G]GTTTAGAATCCGGAG | 997 |
rs557956974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:537729 | GGTGCGATCTCGGCT[C/T]ACTGCAGCCTCCACT | 997 |
rs558085690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:533538 | CCAAATGGTTTTAGC[A/G]GCTCCTCCGCCAGCC | 997 |
rs558174517 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541688 | GGCTTTTTCTCCCTC[C/T]CCATGTCTGTTCTGG | 997 |
rs558182313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:533179 | GCCAGAGGGACAAAG[C/T]GAGGGGCCCTGTGTG | 997 |
rs558211066 | snp | C/G/T | 0.000421812 | 0.0145175 | intron-variant | CDC34 | GRCh38.p7 | 19:541331 | CCTCACCCACCCTGT[C/G/T]CCCCCAGGAAGCAGG | 997 |
rs558283840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:536506 | CTCGCTGTACCTGCA[C/T]GGTAGGTGCTTTCAC | 997 |
rs558566019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:532477 | ACCCCGGCTGCCTCC[C/T]CCTCCGCCCCTGCGA | 997 |
rs558603779 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CDC34 | GRCh38.p7 | 19:532256 | CCTTCTATGGCCACG[C/T]TCCCCCACCCAGCTC | 997 |
rs558916156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:534572 | TCCCTGTCAAGGCCT[C/T]GCCCACGATCCAAGA | 997 |
rs559138397 | snp | C/G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:530283 | GTACCCAGGGCATAG[C/G/T]AACAATGCCACTGGC | 997 |
rs559232149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CDC34 | GRCh38.p7 | 19:539097 | TCGCCGTTTCTGCCT[A/G]TTTTTTCATCTGTGT | 997 |
rs559329187 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC34 | GRCh38.p7 | 19:538294 | GCAGTCGCCTACCGG[C/T]GCCTTCTGTACCTGC | 997 |
rs559938686 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541898 | GGGCGCTGCTGGGAA[C/T]GTGGGCGGGGGGCCG | 997 |
rs560111118 | snp | C/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:531670 | GCCGCGGAGCGCAGG[C/G]GCAGTCGGGGCCAGG | 997 |
rs560126811 | in-del | -/T | | | intron-variant | CDC34 | GRCh38.p7 | 19:534724 | CGATCCAAGACCCCC[-/T]GAGTGCCCTCCCTGT | 997 |
rs560143767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:536171 | CCTCCACGTCCTCAT[C/T]CTCCGGGACCTGGGG | 997 |
rs560172612 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CDC34 | GRCh38.p7 | 19:532336 | AGTCCTCGAAAATCC[C/T]CAGTTCCCTTCAAGG | 997 |
rs560198662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:541191 | CCCTGGAGTTCCTCA[C/T]GCACAGGGCTTTGTC | 997 |
rs560889794 | snp | C/T | | | intron-variant | CDC34 | GRCh38.p7 | 19:534842 | TCCAGACCTCGCCCA[C/T]GATCCAAGACCCCCT | 997 |
rs560959388 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:531109 | CCCACCCCTCAGAGC[A/C]CTCCCCGACCTCGCC | 997 |
rs561124783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:536154 | GAGCCTCACGTCCTC[A/G]TCCTCCACGTCCTCA | 997 |
rs561204965 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | CDC34 | GRCh38.p7 | 19:539585 | CTGGGCTTGGGGCTG[G/T]CTGTCTGCTCCCTGG | 997 |
rs561336514 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC34 | GRCh38.p7 | 19:538485 | TTCTTTACGGGTTGA[C/T]GGCCTTAATGGTTCC | 997 |
rs561339443 | snp | C/T | | | intron-variant | CDC34 | GRCh38.p7 | 19:535002 | CCCTGACCCAGACAA[C/T]CTCTGTGTCTGGCAC | 997 |
rs561343033 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:537823 | ACCACGCCGAGCTAA[G/T]TTTTGTAATTTTTAG | 997 |
rs561380001 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:537459 | CCGGGTTCACGCCAT[A/T]CTCCTGCCTCAGCCT | 997 |
rs561380610 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:530510 | GGCTGGGCGCGGTGG[C/T]TCATGCCTATAATCC | 997 |
rs561463145 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CDC34 | GRCh38.p7 | 19:535232 | GGGAAGGAGTCCTGC[C/T]AGGTTTCTGTGACCT | 997 |
rs561497941 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, missense | CDC34 | GRCh38.p7 | 19:538767 | CATCCTGGTGCTGGG[C/T]GGTCTCGGCTCTGAG | 997 |
rs561522177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:535636 | CTGGGATCAGCTCGG[A/G]TGACTCAGAAAAGGC | 997 |
rs561707140 | snp | C/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:540314 | TGGCCAGGCCCCCCG[C/G]GTTTAGAATCCGGAG | 997 |
rs561791042 | snp | A/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:533329 | GGCGTGGGGCCGAGG[A/G]ACCGATGCCTCCCGC | 997 |
rs561933346 | snp | C/T | | | intron-variant | CDC34 | GRCh38.p7 | 19:540067 | TTAGAATCCGGAGGC[C/T]GGGGTGGCCAGGCCC | 997 |
rs562214633 | snp | C/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541867 | CCGGACTGGCCGCAC[C/G]CCGGAGGAGCCACGG | 997 |
rs562248714 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CDC34 | GRCh38.p7 | 19:533497 | TGCGTCCCCACACAG[A/G]GAACAGAGTTTGGGT | 997 |
rs562261225 | snp | C/T | | | intron-variant | CDC34 | GRCh38.p7 | 19:535814 | CTGGGCTGGACTGAG[C/T]CACCTGCCTTCTGCC | 997 |
rs562321325 | snp | A/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:540655 | GTGGCCAGGCCCCCC[A/G]GGTTTAGAATCCGGA | 997 |
rs562542475 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant, downstream-variant-500B | CDC34 | GRCh38.p7 | 19:539490 | CGTCCGCTGGGTCCC[A/G]CCACCCAGGGACGTC | 997 |
rs562671332 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CDC34 | GRCh38.p7 | 19:536608 | CCTAGAGGTGTCCCG[A/C]CATCCTCAGTCCTGG | 997 |
rs562734508 | snp | A/G/T | 0.000540248 | 0.016427 | intron-variant | CDC34 | GRCh38.p7 | 19:536936 | GGTCCAGGCGTCCCC[A/G/T]TGACCCTCAGGGCCA | 997 |
rs562765177 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CDC34 | GRCh38.p7 | 19:532789 | GTAACCTGCGCCCTC[C/G]GGAAGGCCGAAGTAG | 997 |
rs562925528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:532316 | GGACCTTCAGCCTCT[A/G]CTGCAGTCCTCGAAA | 997 |
rs563053670 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CDC34 | GRCh38.p7 | 19:540864 | AATCCTGCTGAGGCC[A/G]CGGAGAGGCTCAGGC | 997 |
rs563159717 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:529866 | GCCTGCTGGTCCTCT[A/T]CCGGGGACCAGACTC | 997 |
rs563267401 | in-del | -/A | 0.434543 | 0.168653 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:530825 | GACTCTGTCTCATTT[-/A]AAAAAAAAAAAAAAA | 997 |
rs563285959 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:530350 | CTCAGGGGAGGCTGG[C/G]CTGCCCCGTCCTCAC | 997 |
rs563290392 | snp | A/G | | | intron-variant, downstream-variant-500B | CDC34 | GRCh38.p7 | 19:539177 | GCTGCCGTGGAGCCC[A/G]GCTTGGTCAGGGATG | 997 |
rs563322844 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC34 | GRCh38.p7 | 19:535215 | AGGGGGCGATGCTGA[C/T]AGGGAAGGAGTCCTG | 997 |
rs563397914 | snp | C/T | | | intron-variant | CDC34 | GRCh38.p7 | 19:540408 | TTAGAATCCGGAGGC[C/T]GGGGTGGCCAGGCCC | 997 |
rs563530119 | snp | G/T | | | intron-variant | CDC34 | GRCh38.p7 | 19:538112 | GGGGTCGTGCTGTGT[G/T]TGCCCAGTGACTGAC | 997 |
rs563776588 | snp | A/G | 0.00013704 | 0.00827655 | missense, utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541487 | TACGAGGACGGCGAG[A/G]TGGAGGAGGAGGCCG | 997 |
rs564153358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:533756 | GGATTTCCCAGGGAG[A/G]GGGCCTCTAGACATC | 997 |
rs564165909 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC34 | GRCh38.p7 | 19:532350 | CCCAGTTCCCTTCAA[A/G]GCATCGTCCGGTCCC | 997 |
rs564209470 | snp | A/G | 1.66277e-05 | 0.00288333 | missense | CDC34 | GRCh38.p7 | 19:537017 | TCTCCCCACAGGACC[A/G]TTCTCCTGAGTGTGA | 997 |
rs564308353 | snp | A/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:540630 | CCGGGTTTAGAATCC[A/G]GAGGCCGGGGTGGCC | 997 |
rs564310622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:532764 | CCCTGGGCTCCATCC[C/T]CTGCTTTATGTAACC | 997 |
rs564349423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:536573 | CCAGGACCCCAGGCC[A/G]GCCCCACCGTCTGGA | 997 |
rs564528210 | snp | C/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:540428 | TGGCCAGGCCCCCCG[C/G]GTTTAGAATCCGGAG | 997 |
rs565142831 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:541081 | CCTTGGGTTGTGCTT[C/G]GGGGCGGGGCAGGCG | 997 |
rs565150109 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CDC34 | GRCh38.p7 | 19:536436 | TAGGCCGGGCTCCCC[C/T]ACAGGCTGTGGCGCC | 997 |
rs565181219 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:539902 | AGGGCCGGGTGTACA[A/C]GGTGCCCTCCAGGAA | 997 |
rs565236947 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, missense | CDC34 | GRCh38.p7 | 19:538802 | CATGGTGGGCGGGCC[C/T]CGTGCGGCCTCCTGG | 997 |
rs565330797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:536081 | ACGTCCTCGTCCTTC[C/T]GGGACCCGAGGCGCT | 997 |
rs565346557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CDC34 | GRCh38.p7 | 19:539125 | TGTGCGTGTTGGCCT[C/T]GTGGCAGCCCAAGTC | 997 |
rs565504757 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CDC34 | GRCh38.p7 | 19:535716 | CTTGGGCAGGATACG[G/T]TGTCCCTCACACACA | 997 |
rs565534043 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:531592 | GCCGTAGGCGGGACC[C/G]GGGCCGGGACTCCAC | 997 |
rs565812139 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CDC34 | GRCh38.p7 | 19:538185 | CGTGCTGTGTGTGCC[C/T]AGTGACTGACTGTTA | 997 |
rs565993068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CDC34 | GRCh38.p7 | 19:539472 | TTGGAAAGCAAAGCT[C/T]GGCGTCCGCTGGGTC | 997 |
rs566018444 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541667 | CTCCTCTGGTTGTTT[C/T]GTTTTGGCTTTTTCT | 997 |
rs566367360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:537528 | CGGCTAATTTTTTGT[A/G]TTTTTAGTAGAGACG | 997 |
rs566386511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:540707 | CACGTTTAGAATCCG[A/G]AGGCCGGGGTGGCCA | 997 |
rs566540549 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC34 | GRCh38.p7 | 19:532448 | TTGCCCACCTCCTCC[C/T]TGGCGGGGGCTGGAC | 997 |
rs566555388 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:531471 | CGCCTCCTTGCGCAC[A/G]GCGTCCGCGGTGCTG | 997 |
rs566578638 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CDC34 | GRCh38.p7 | 19:536480 | GGACCTGCCAGCTGG[C/T]GGTCCTGGGCCTCGC | 997 |
rs567078703 | snp | C/T | | | intron-variant | CDC34 | GRCh38.p7 | 19:532440 | TGGGGCTCTTGCCCA[C/T]CTCCTCCTTGGCGGG | 997 |
rs567133305 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:539806 | TTCCAGTCCTGGGGG[C/G]ACATTCTTGACGCGT | 997 |
rs567142738 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | CDC34 | GRCh38.p7 | 19:532600 | GCTGCTATTGTTGGG[A/G]AGCTGGGCCCGTGAG | 997 |
rs567226541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:535540 | GGGCTGCCACGGGCC[C/T]GGAGCCACGCGGGCA | 997 |
rs567309356 | snp | A/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:534345 | GTCCAGGAGGGGCCC[A/G]TCCACGATCCAAGAC | 997 |
rs567696390 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, downstream-variant-500B | GZMM, CDC34 | GRCh38.p7 | 19:542438 | CTCAGCGTCTCAGGG[C/T]TCCCAGGACCACAGA | 997 |
rs567734162 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | CDC34 | GRCh38.p7 | 19:534366 | GATCCAAGACCCCCA[A/G]AGTGCCCTGCCTGTC | 997 |
rs567844469 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:529913 | GTGTTGGGGCACCTG[C/T]GGGACAGAGTGGCCC | 997 |
rs567996314 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CDC34 | GRCh38.p7 | 19:533374 | CTCTCCGAGCTAATT[A/T]GTGTCTGAACCGCAC | 997 |
rs568244921 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, downstream-variant-500B | GZMM, CDC34 | GRCh38.p7 | 19:542091 | TACTTTATGAGAGGC[C/G]AGAGAAGCTGTGCTT | 997 |
rs568383315 | snp | A/G | 6.65912e-05 | 0.00576985 | synonymous-codon | CDC34 | GRCh38.p7 | 19:537109 | CAGGAAGTGGAAAGA[A/G]AGCAAGGGGAAGGAT | 997 |
rs568560296 | snp | A/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:537719 | GCAGTGCAGTGGTGC[A/G]ATCTCGGCTCACTGC | 997 |
rs568742634 | snp | A/C/G | 5.25592e-05 | 0.00512609 | missense, utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541514 | GCCGACAGCTGCTTC[A/C/G]GGGACGATGAGGATG | 997 |
rs568919686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CDC34 | GRCh38.p7 | 19:539410 | TGCCACCCGTGCAGT[A/G]CCGTCCCCGGGGCAC | 997 |
rs568931811 | snp | A/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:540526 | AATCCGGAGGCCGGG[A/G]TGGCCAGGCCCCCCG | 997 |
rs568942384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:536208 | GAGCCCGTGCTGACC[C/T]CTGACCTGTTCTGAC | 997 |
rs568952451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:532366 | GCATCGTCCGGTCCC[C/T]TGTTAGGCTCTTGGC | 997 |
rs569064607 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:532176 | GCCGGGAACCAGCTC[A/C]CTGCCCCGCGGTCCT | 997 |
rs569104921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:536463 | CGCCAAGGCCTGATT[C/T]GGGACCTGCCAGCTG | 997 |
rs569216076 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:531264 | GACTTCGCGCCCGTC[C/T]CCTGCACAGACGGGG | 997 |
rs569270011 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:535464 | GGGGAGCCTGGAGCC[C/G]CTGCCAGTCCATTCT | 997 |
rs569625410 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | CDC34 | GRCh38.p7 | 19:538541 | TTCCTATCCATTTTT[G/T]TTTTTTCTCAGAGTG | 997 |
rs569697329 | snp | A/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:540086 | GTGGCCAGGCCCCCC[A/G]GGTTTAGAATCCGGA | 997 |
rs569823925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:535024 | GTCTGGCACTGGGGC[C/T]CAGCAGGAAAACAGT | 997 |
rs570112334 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541689 | GCTTTTTCTCCCTCC[C/T]CATGTCTGTTCTGGG | 997 |
rs570174099 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:542000 | AGGTCCTGGAGCCAC[A/G]TCCAGCACAGAGTGG | 997 |
rs570191489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:534054 | GCCTGGGTTTGCTCC[A/G]GGGAAAAGACATTCT | 997 |
rs570228092 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CDC34 | GRCh38.p7 | 19:534351 | GAGGGGCCCGTCCAC[A/G]ATCCAAGACCCCCAA | 997 |
rs570299798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:538014 | TAACGCATGTCTGTG[C/T]TTTAATGAAGAAATG | 997 |
rs570349789 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:532935 | TTCTCAGAGTCCACT[G/T]AACAGGTGGCTTCTT | 997 |
rs570462349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:532539 | CCTTTCAGCTGCCCT[C/T]CCCGCCCTCCCCGGA | 997 |
rs570784670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:541226 | GTGGTCGCCACACGC[C/T]GTTTTAAGAGAAACC | 997 |
rs570894238 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CDC34 | GRCh38.p7 | 19:535117 | GCAGGCCAGACAGCT[C/G]TGTCACCTGGCACGT | 997 |
rs570932928 | snp | A/T | | | intron-variant | CDC34 | GRCh38.p7 | 19:534447 | AGACCTCGCCCACGA[A/T]CCAAGACCCCCTGAG | 997 |
rs571098145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:536507 | TCGCTGTACCTGCAC[A/G]GTAGGTGCTTTCACG | 997 |
rs571173625 | snp | A/G | 0.000167595 | 0.00915257 | synonymous-codon | CDC34 | GRCh38.p7 | 19:532045 | GGACGAGGGCGATCT[A/G]TACAACTGGGAGGTG | 997 |
rs571210789 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:531503 | TCGAGCAGGGGGCGA[C/G]GGCGGCGGCCTCGGG | 997 |
rs571296965 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B | CDC34 | GRCh38.p7 | 19:539323 | CAGCCGCCACCTCTG[C/T]GGTGCCGTCCCCGGG | 997 |
rs571591865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:534414 | ACAATCCAAGACCCC[C/T]GAGTACCCTCCCTGT | 997 |
rs571654837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:538512 | TTCCTGCTCTTCCTG[C/T]TACATAGAGGCCCTT | 997 |
rs571730598 | snp | C/T | 3.31978e-05 | 0.00407404 | synonymous-codon | CDC34 | GRCh38.p7 | 19:537067 | CAACACCTTCTCGCC[C/T]GCAAACGTGGACGCC | 997 |
rs571732917 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:529986 | AGACGGAGTCTCTGT[C/T]GCCCAGGCTGGAGCG | 997 |
rs571895688 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:530564 | ACGGATCCCTTTATT[A/C]GTCCAAACTGCATCC | 997 |
rs572034401 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541775 | GCTCGGTGGACGGGC[C/T]CAGGGTGGGAGCGGC | 997 |
rs572155946 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | GZMM, CDC34 | GRCh38.p7 | 19:542202 | ATCTGGGAGGCCTGT[C/T]CTGGGAGGCACGGGG | 997 |
rs572183534 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CDC34 | GRCh38.p7 | 19:532682 | TCCAACAAAGGCCCG[G/T]ATGAGCCTTGGCAGC | 997 |
rs572301458 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC34 | GRCh38.p7 | 19:540996 | TGAGGAAGGCTTTTG[C/T]CCCCCAGTGGGGCAG | 997 |
rs572348607 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CDC34 | GRCh38.p7 | 19:534126 | GTTTGGTACAGATGA[A/G]GCCTTGGCTGTTGTC | 997 |
rs572889436 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CDC34 | GRCh38.p7 | 19:532981 | AGTTCTGGGCCGTTT[C/T]TTCTGCCCTCTGGCG | 997 |
rs572913817 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:531578 | CGGAGGCGCTCGGCG[C/T]CGTAGGCGGGACCGG | 997 |
rs572980331 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:532220 | GGCGGGCCCCGAAGC[C/T]TCCTGGCTTGGGCTC | 997 |
rs573018261 | snp | C/T | | | intron-variant | CDC34 | GRCh38.p7 | 19:540294 | TTAGAATCCGGAGGC[C/T]GGGGTGGCCAGGCCC | 997 |
rs573340187 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CDC34 | GRCh38.p7 | 19:539111 | TGTTTTTTCATCTGT[A/G/T]TGCGTGTTGGCCTCG | 997 |
rs573473659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CDC34 | GRCh38.p7 | 19:539436 | GGCACTGTCAGTCAC[C/T]CCCCCAGCCCATCGG | 997 |
rs573543261 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | CDC34 | GRCh38.p7 | 19:535112 | AGGCTGCAGGCCAGA[C/G]AGCTCTGTCACCTGG | 997 |
rs573554406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:536035 | GAGCCTCACGTCCTC[A/G]TCCTCCGGGACCCGG | 997 |
rs573797233 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:529724 | GGCCCAGAGGCCCTT[A/C]CGGGTGAGGACGCCT | 997 |
rs574113657 | snp | C/T | | | utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:542013 | ACGTCCAGCACAGAG[C/T]GGACGGATTCACCGT | 997 |
rs574123726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:533623 | GCCAGGCCTGTGAGG[C/T]GGCTGCTGTTCTGGA | 997 |
rs574415290 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | CDC34 | GRCh38.p7 | 19:540005 | GCCGGGGTGGCCAGG[A/C]CCCCAGGTTTAGAAT | 997 |
rs574481306 | snp | A/G | | | intron-variant, downstream-variant-500B | CDC34 | GRCh38.p7 | 19:539168 | GTCGGGCAGGCTGCC[A/G]TGGAGCCCGGCTTGG | 997 |
rs574611087 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | CDC34 | GRCh38.p7 | 19:539847 | TGGAGCCGGGGGCAG[G/T]TTCCTCGTAGGTCCT | 997 |
rs574694402 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541756 | GCCACTCACGTCACT[C/T]GGGGCTCGGTGGACG | 997 |
rs574765920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:537334 | CCAGCCAGGTTCAAG[C/T]CCAGCTTCTTGCCCC | 997 |
rs574803051 | snp | A/T | 1.73228e-05 | 0.00294297 | intron-variant | CDC34 | GRCh38.p7 | 19:536955 | CCCTCAGGGCCAGAG[A/T]AGAGCCGGAAGGCTG | 997 |
rs575040991 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC34 | GRCh38.p7 | 19:532580 | AGGCCCCCCCAGACC[C/T]CGTAGCTGCTATTGT | 997 |
rs575169224 | in-del | -/GACA | 0.0023933 | 0.0345097 | utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541614 | CGTGGCTCCTTAGAC[-/GACA]GACTACCTCACGGAG | 997 |
rs575306670 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:530993 | TTTCCCAGTTTCTCT[G/T]GGGGGCAGGAGCACC | 997 |
rs575307516 | snp | A/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:540251 | CCGGGTTTAGAATCC[A/G]GAGGCCGGGGTGGCC | 997 |
rs575307726 | snp | C/T | | | intron-variant | CDC34 | GRCh38.p7 | 19:540611 | GCCGGGGTGGCCAGG[C/T]CCCCCGGGTTTAGAA | 997 |
rs575346279 | snp | C/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:540011 | GTGGCCAGGCCCCCA[C/G]GTTTAGAATCCGGAG | 997 |
rs575417260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:536010 | ATCCTTCCGGGACCC[A/G]GGGCGCTGGGAGCCT | 997 |
rs575590641 | snp | A/G | 0.00636936 | 0.0560724 | utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541827 | AGGGGAGCTGAGCCC[A/G]ACTTCTACCGGGGTC | 997 |
rs575716107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:537762 | TCGGGTTGGAGCAGT[C/T]CTCCCCCTTCATCCT | 997 |
rs575989648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CDC34 | GRCh38.p7 | 19:539063 | CCAACACACATGTGC[C/T]ATGTGGACTCTGCTG | 997 |
rs576201874 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:534251 | CTGTGGCCGCGGCCA[A/T]GTCACTTGCCTTACG | 997 |
rs576456652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:533547 | TTTAGCAGCTCCTCC[A/G]CCAGCCCCTTCTGTC | 997 |
rs576472281 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:533186 | GGACAAAGCGAGGGG[C/G]CCTGTGTGAGCGGTG | 997 |
rs576491328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:537251 | TCCTGGTGAGGGTGG[C/T]GGAGCTTCCTGGTGC | 997 |
rs576836011 | snp | C/T | | | intron-variant | CDC34 | GRCh38.p7 | 19:537686 | TTGGAGACAGAGTTA[C/T]ACTCTCTTGCCTAGG | 997 |
rs576911337 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, downstream-variant-500B | CDC34 | GRCh38.p7 | 19:539479 | GCAAAGCTTGGCGTC[C/T]GCTGGGTCCCGCCAC | 997 |
rs577049383 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | CDC34 | GRCh38.p7 | 19:536584 | GGCCGGCCCCACCGT[C/T]TGGAACCACCTAGAG | 997 |
rs577291421 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:530310 | TGGCACAGTCCGAGG[A/G]CAGGGCCACCCGTCA | 997 |
rs577455586 | snp | C/G | 0.00279162 | 0.0372561 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:530880 | CAGGCTGGGAGGAGG[C/G]CACAGCCAGGCTCGG | 997 |
rs577476668 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:531593 | CCGTAGGCGGGACCG[A/G]GGCCGGGACTCCACC | 997 |
rs577616744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:538642 | AACAACTTTTAAAAT[A/G]TTGCACACATAATGC | 997 |
rs577638325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:535597 | GTGCTGGGCCGGGTC[C/T]CGGCCACCTGGACTG | 997 |
rs577678329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:535206 | GGTGACCACAGGGGG[C/T]GATGCTGACAGGGAA | 997 |
rs578178652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC34 | GRCh38.p7 | 19:538326 | GTCCACTTAGCTTGC[A/G]TGGCTGTGTGTGGTG | 997 |
rs578255597 | in-del | -/C | 0.221439 | 0.248363 | intron-variant | CDC34 | GRCh38.p7 | 19:540805 | TGGCCAGGCCCCCCG[-/C]GTTTAGAATCCGGAG | 997 |
rs745378933 | snp | C/T | 1.65987e-05 | 0.00288082 | missense | CDC34 | GRCh38.p7 | 19:537060 | ACGAGCCCAACACCT[C/T]CTCGCCCGCAAACGT | 997 |
rs745482817 | snp | A/G | 0.000152864 | 0.00874121 | utr-variant-5-prime | CDC34 | GRCh38.p7 | 19:531889 | ACTCGCGGTGGTCGC[A/G]CGGCCCCGCGCTGCT | 997 |
rs745626145 | snp | A/G | 1.71413e-05 | 0.00292752 | missense, utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541484 | TACTACGAGGACGGC[A/G]AGGTGGAGGAGGAGG | 997 |
rs745639684 | snp | C/T | 3.71948e-05 | 0.00431231 | intron-variant | CDC34 | GRCh38.p7 | 19:536223 | TCTGACCTGTTCTGA[C/T]CTGTCTTCTTCTTGT | 997 |
rs745773741 | snp | A/G | 4.31016e-05 | 0.00464208 | synonymous-codon | CDC34 | GRCh38.p7 | 19:536275 | CTCCATCCTCCACCC[A/G]CCGGTGGACGACCCC | 997 |
rs745789869 | snp | A/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:535568 | GCAGCCAGTGCCCAC[A/G]TTCCCCAGCAGTTGT | 997 |
rs746097237 | snp | C/T | | | intron-variant | CDC34 | GRCh38.p7 | 19:536755 | TCTAGGCAGGACGTG[C/T]GGGTGTGAGGGCAGC | 997 |
rs746240753 | snp | A/G | 4.10787e-05 | 0.00453185 | missense | CDC34 | GRCh38.p7 | 19:532097 | ACCTACTACGAGGGC[A/G]GCTACTTCAAGGTGA | 997 |
rs746366208 | in-del | -/GGA | 3.43083e-05 | 0.00414161 | cds-indel | CDC34 | GRCh38.p7 | 19:541489 | CGAGGACGGCGAGGT[-/GGA]GGAGGAGGCCGACAG | 997 |
rs746373006 | snp | A/G | 9.12263e-05 | 0.00675314 | utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541594 | TACCTCACTAGGGCC[A/G]GACCCGTGGCTCCTT | 997 |
rs746478944 | snp | C/T | 3.36922e-05 | 0.00410426 | intron-variant | CDC34 | GRCh38.p7 | 19:536979 | AAGGCTGGGGTGCCC[C/T]GGGCCGCCCCACTCC | 997 |
rs746570745 | in-del | -/C | | | intron-variant | CDC34 | GRCh38.p7 | 19:540042 | GCCGGGGTGGCCAGG[-/C]CCCCCACGTTTAGAA | 997 |
rs746590575 | in-del | -/TGGTTGTTT | | | cds-indel | CDC34 | GRCh38.p7 | 19:541658 | GGTCCCCGTCTCCTC[-/TGGTTGTTT]CGTTTTGGCTTTTTC | 997 |
rs746640795 | snp | C/T | 1.66067e-05 | 0.00288151 | synonymous-codon | CDC34 | GRCh38.p7 | 19:537037 | CCTGAGTGTGATCTC[C/T]CTCCTGAACGAGCCC | 997 |
rs747007644 | snp | C/G/T | 0.000410168 | 0.0143151 | synonymous-codon, utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541405 | GCCCACCACGCTGGC[C/G/T]GAGTACTGCGTGAAG | 997 |
rs747062741 | snp | C/T | 8.12073e-05 | 0.00637158 | synonymous-codon | CDC34 | GRCh38.p7 | 19:536266 | CGTGTGTATCTCCAT[C/T]CTCCACCCGCCGGTG | 997 |
rs747065062 | snp | C/T | 3.82621e-05 | 0.00437374 | intron-variant | CDC34 | GRCh38.p7 | 19:536219 | GACCTCTGACCTGTT[C/T]TGACCTGTCTTCTTC | 997 |
rs747137440 | snp | A/T | | | intron-variant | CDC34 | GRCh38.p7 | 19:532932 | CCTTTCTCAGAGTCC[A/T]CTGAACAGGTGGCTT | 997 |
rs747285861 | snp | C/G | 0.000158869 | 0.00891118 | missense | CDC34 | GRCh38.p7 | 19:531951 | CTCGGCCGCTAGTGC[C/G]CAGCTCGCAGAAGGC | 997 |
rs747570195 | snp | C/G | 2.0371e-05 | 0.0031914 | utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541573 | CCAGAATAAACTTGC[C/G]GAGTTTACCTCACTA | 997 |
rs747732809 | snp | C/G | 4.15654e-05 | 0.00455861 | intron-variant | CDC34 | GRCh38.p7 | 19:536387 | GAACATCAGGTAGGC[C/G]GGGCTCCGTCCCGTA | 997 |
rs748081730 | snp | A/C/T | 0.000188377 | 0.00970325 | intron-variant | CDC34 | GRCh38.p7 | 19:541322 | GGGTGGCGCCCTCAC[A/C/T]CACCCTGTCCCCCCA | 997 |
rs748214921 | snp | A/T | | | intron-variant | CDC34 | GRCh38.p7 | 19:533579 | GCTTGGGGGAGCAGC[A/T]GGCTGAGGAGCCGCA | 997 |
rs748241028 | snp | C/T | 2.39134e-05 | 0.00345777 | missense, utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541391 | GACGGCGTGAAGGTG[C/T]CCACCACGCTGGCCG | 997 |
rs748408800 | in-del | -/CTA | 3.41425e-05 | 0.0041316 | cds-indel | CDC34 | GRCh38.p7 | 19:541459 | GGGCTCAGACCTCTT[-/CTA]CGACGACTACTACGA | 997 |
rs748418076 | snp | C/T | 3.31972e-05 | 0.004074 | synonymous-codon | CDC34 | GRCh38.p7 | 19:537073 | CTTCTCGCCCGCAAA[C/T]GTGGACGCCTCCGTG | 997 |
rs748664768 | snp | C/T | 5.24664e-05 | 0.00512156 | intron-variant | CDC34 | GRCh38.p7 | 19:537165 | GAGGGCGGGCGGGGG[C/T]GTCACGGGAGGAGAG | 997 |
rs748687986 | snp | C/T | 4.03951e-05 | 0.00449398 | synonymous-codon | CDC34 | GRCh38.p7 | 19:532051 | GGGCGATCTATACAA[C/T]TGGGAGGTGGCCATC | 997 |
rs748875983 | snp | A/G | 1.71973e-05 | 0.0029323 | missense, utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541494 | ACGGCGAGGTGGAGG[A/G]GGAGGCCGACAGCTG | 997 |
rs748895553 | snp | C/G | 0.00567737 | 0.052976 | missense | CDC34 | GRCh38.p7 | 19:531939 | CCGCCGCCATGGCTC[C/G]GCCGCTAGTGCCCAG | 997 |
rs749435711 | in-del | -/CTT | 1.65982e-05 | 0.00288077 | cds-indel | CDC34 | GRCh38.p7 | 19:537058 | GAACGAGCCCAACAC[-/CTT]CTCGCCCGCAAACGT | 997 |
rs749448774 | snp | C/T | | | intron-variant, downstream-variant-500B | CDC34 | GRCh38.p7 | 19:539418 | GTGCAGTGCCGTCCC[C/T]GGGGCACTGTCAGTC | 997 |
rs749454138 | in-del | -/GG | 5.18202e-05 | 0.00508993 | frameshift-variant | CDC34 | GRCh38.p7 | 19:532029 | CCGCGTGACACTGGT[-/GG]GGACGAGGGCGATCT | 997 |
rs749482311 | snp | A/C/G | 0.000119055 | 0.00771448 | intron-variant | CDC34 | GRCh38.p7 | 19:541335 | ACCCACCCTGTCCCC[A/C/G]CAGGAAGCAGGTCCT | 997 |
rs749678365 | snp | C/T | 9.91883e-05 | 0.00704161 | intron-variant | CDC34 | GRCh38.p7 | 19:535940 | TGAGCGCGGCCCCCA[C/T]GGGCCTCAAGTCCTC | 997 |
rs749706583 | snp | C/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:533826 | GGGTGCTGCCACCCA[C/G]GAGGACTCTCCCTTC | 997 |
rs750160188 | in-del | -/CCGGGGCGCTGGGAGCCTCACGTCCTCGTCCTTCCGGGAT | | | intron-variant | CDC34 | GRCh38.p7 | 19:536046 | CTCGTCCTCCGGGAC[lengthTooLong]CCGGGGCGCTGGGAG | 997 |
rs750241253 | snp | C/T | 5.10517e-05 | 0.00505205 | intron-variant | CDC34 | GRCh38.p7 | 19:541258 | GAGCGTTGGGGTGAG[C/T]GTCGGACCTGGGGGA | 997 |
rs750279936 | in-del | -/C | 1.70127e-05 | 0.00291652 | intron-variant | CDC34 | GRCh38.p7 | 19:536967 | AGAAGAGCCGGAAGG[-/C]CTGGGGTGCCCCGGG | 997 |
rs750297342 | snp | C/G | 4.2936e-05 | 0.00463316 | missense | CDC34 | GRCh38.p7 | 19:532043 | GTGGACGAGGGCGAT[C/G]TATACAACTGGGAGG | 997 |
rs750335335 | snp | C/T | 3.64153e-05 | 0.00426689 | missense, utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541539 | AGGATGACTCTGGCA[C/T]GGAGGAGTCCTGACA | 997 |
rs750346736 | in-del | -/GACA | | | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:530733 | CGGGAGGCTGAGGCG[-/GACA]GACACTAGCTTGAAC | 997 |
rs750580693 | snp | C/T | 2.45035e-05 | 0.00350016 | intron-variant | CDC34 | GRCh38.p7 | 19:536357 | TAAGCCGGCCCAACC[C/T]CCTGTGTCCACCCAG | 997 |
rs750842772 | snp | C/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:533428 | CAGCCTGGTCTGCTG[C/G]GGGCGATTCCTGAGC | 997 |
rs750860829 | snp | A/C/G/T | 0.000111164 | 0.00745471 | synonymous-codon, utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541423 | GTACTGCGTGAAGAC[A/C/G/T]AAGGCGCCGGCGCCC | 997 |
rs751118881 | snp | C/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:533545 | GTTTTAGCAGCTCCT[C/G]CGCCAGCCCCTTCTG | 997 |
rs751125999 | snp | C/G/T | 3.31418e-05 | 0.00407063 | intron-variant | CDC34 | GRCh38.p7 | 19:535967 | CCTCATCCTCCGGGA[C/G/T]CCAGGGTGCTGGGAG | 997 |
rs751143469 | snp | A/G | | | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:530723 | TCTCAGCTACTCGGG[A/G]GGCTGAGGCGGACAC | 997 |
rs751336520 | in-del | -/A | 3.19025e-05 | 0.00399377 | intron-variant | CDC34 | GRCh38.p7 | 19:536378 | TCCACCCAGAACATC[-/A]AGGTAGGCCGGGCTC | 997 |
rs751346098 | snp | C/T | 3.66643e-05 | 0.00428145 | intron-variant | CDC34 | GRCh38.p7 | 19:537194 | AGACTCAGATCCGGC[C/T]TGCACCCCGGCCCCT | 997 |
rs751471096 | snp | A/G | 1.71012e-05 | 0.00292409 | intron-variant | CDC34 | GRCh38.p7 | 19:537150 | CAGACATCATCCGGT[A/G]AGGGCGGGCGGGGGC | 997 |
rs751512779 | snp | A/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:536821 | CTCCCTGGTCTTGGC[A/G]TGGGAGGGAGGAGAC | 997 |
rs751546350 | snp | C/G | 3.59028e-05 | 0.00423676 | missense, utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541533 | ACGATGAGGATGACT[C/G]TGGCACGGAGGAGTC | 997 |
rs751549589 | snp | A/G | 0.000284914 | 0.0119321 | synonymous-codon | CDC34 | GRCh38.p7 | 19:532036 | GACACTGGTGGACGA[A/G]GGCGATCTATACAAC | 997 |
rs751635636 | snp | A/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:538281 | TGGGTACAGCTGTGC[A/G]GTCGCCTACCGGCGC | 997 |
rs751666566 | snp | A/G | 1.70644e-05 | 0.00292094 | missense, utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541470 | TCTTCTACGACGACT[A/G]CTACGAGGACGGCGA | 997 |
rs751704155 | snp | C/T | 4.5819e-05 | 0.00478617 | intron-variant | CDC34 | GRCh38.p7 | 19:536347 | GAACGTCAGGTAAGC[C/T]GGCCCAACCCCCTGT | 997 |
rs752021910 | snp | C/G | 1.82537e-05 | 0.00302101 | intron-variant | CDC34 | GRCh38.p7 | 19:536932 | GGTGGGTCCAGGCGT[C/G]CCCGTGACCCTCAGG | 997 |
rs752149119 | snp | C/T | 1.64963e-05 | 0.00287192 | synonymous-codon | CDC34 | GRCh38.p7 | 19:535911 | CAAGATGTGGCACCC[C/T]AACATCTACGAGGTG | 997 |
rs752260990 | in-del | -/TCT | 0.000145879 | 0.00853921 | intron-variant | CDC34 | GRCh38.p7 | 19:536227 | ACCTGTTCTGACCTG[-/TCT]TCTTCTTGTGCAGAC | 997 |
rs752271754 | snp | C/T | 1.64999e-05 | 0.00287222 | intron-variant | CDC34 | GRCh38.p7 | 19:535817 | GGCTGGACTGAGCCA[C/T]CTGCCTTCTGCCCCT | 997 |
rs752271966 | snp | C/T | 0.000234869 | 0.0108342 | synonymous-codon, missense | CDC34 | GRCh38.p7 | 19:541366 | GGGGACCAAGGTGGA[C/T]GCGGAGCGTGACGGC | 997 |
rs752387358 | snp | A/G | 3.32231e-05 | 0.00407559 | synonymous-codon | CDC34 | GRCh38.p7 | 19:537031 | CATTCTCCTGAGTGT[A/G]ATCTCCCTCCTGAAC | 997 |
rs752753399 | in-del | -/TGGCCAGGCCCCCGGGTTTAGAATCCGGAGGCTGGGA | | | intron-variant | CDC34 | GRCh38.p7 | 19:540717 | ATCCGGAGGCCGGGG[lengthTooLong]TGGCCAGGCCCCCGG | 997 |
rs752767197 | snp | C/T | | | intron-variant | CDC34 | GRCh38.p7 | 19:535511 | CCCTGGCCTGGGTCC[C/T]ATATGCCTGACCTGG | 997 |
rs753053260 | snp | A/G | 2.03147e-05 | 0.00318699 | missense | CDC34 | GRCh38.p7 | 19:536331 | GGTGGAACCCCACGC[A/G]GAACGTCAGGTAAGC | 997 |
rs753136045 | snp | C/T | | | intron-variant | CDC34 | GRCh38.p7 | 19:537955 | AGCCACTGCACCTGG[C/T]CTGGTGGTTAGTGTT | 997 |
rs753330216 | snp | A/G | 2.24414e-05 | 0.00334966 | intron-variant | CDC34 | GRCh38.p7 | 19:541268 | GTGAGCGTCGGACCT[A/G]GGGGAGGGGGGCCGG | 997 |
rs753354056 | snp | A/G | 0.000595947 | 0.0172516 | intron-variant, missense | CDC34 | GRCh38.p7 | 19:538748 | TGGGGTCATCTCGGG[A/G]CAGCATCCTGGTGCT | 997 |
rs753545182 | snp | C/T | | | intron-variant | CDC34 | GRCh38.p7 | 19:540156 | GCCGGGGTGGCCAGG[C/T]CCCCCGGGTTTAGAA | 997 |
rs753556081 | snp | A/G | 1.65083e-05 | 0.00287296 | intron-variant | CDC34 | GRCh38.p7 | 19:535795 | GCTGGGGCAGGTCTT[A/G]GGGCTGGGCTGGACT | 997 |
rs753572989 | in-del | -/TGA | | | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:529969 | GGTTTTTTTTTTTTT[-/TGA]GACGGAGTCTCTGTC | 997 |
rs753634855 | snp | C/T | 1.64855e-05 | 0.00287097 | synonymous-codon | CDC34 | GRCh38.p7 | 19:535890 | ACCAGCCTTTCGGTT[C/T]CTGACCAAGATGTGG | 997 |
rs753743468 | snp | C/G | 6.983e-05 | 0.00590848 | intron-variant | CDC34 | GRCh38.p7 | 19:536950 | CGTGACCCTCAGGGC[C/G]AGAGAAGAGCCGGAA | 997 |
rs753847628 | snp | G/T | | | intron-variant | CDC34 | GRCh38.p7 | 19:536167 | TCGTCCTCCACGTCC[G/T]CATCCTCCGGGACCT | 997 |
rs754037059 | snp | C/T | | | utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541975 | GGGCCCGGTCCTGCC[C/T]GTCAGCTCCAGGTCC | 997 |
rs754170025 | snp | A/G | 0.000116029 | 0.00761586 | intron-variant | CDC34 | GRCh38.p7 | 19:535973 | CCTCCGGGACCCAGG[A/G]TGCTGGGAGCCTCAC | 997 |
rs754515437 | snp | A/G | 0.000808081 | 0.0200845 | intron-variant | CDC34 | GRCh38.p7 | 19:541276 | CGGACCTGGGGGAGG[A/G]GGGCCGGGCAGGGGC | 997 |
rs754528124 | snp | C/G | 1.91999e-05 | 0.00309832 | utr-variant-3-prime | CDC34 | GRCh38.p7 | 19:541558 | GGAGTCCTGACACCA[C/G]CAGAATAAACTTGCC | 997 |
rs754537445 | snp | A/G | 3.90267e-05 | 0.00441722 | synonymous-codon | CDC34 | GRCh38.p7 | 19:532057 | TCTATACAACTGGGA[A/G]GTGGCCATCTTCGGG | 997 |
rs754636917 | snp | C/G | 3.3012e-05 | 0.00406262 | intron-variant | CDC34 | GRCh38.p7 | 19:535804 | GGTCTTGGGGCTGGG[C/G]TGGACTGAGCCACCT | 997 |
rs755422135 | snp | A/G | | | intron-variant, downstream-variant-500B | CDC34 | GRCh38.p7 | 19:539253 | TGGCGGTGTGCCGGC[A/G]GCACCTCCACGGTGC | 997 |
rs755467249 | snp | C/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:540656 | TGGCCAGGCCCCCCG[C/G]GTTTAGAATCCGGAG | 997 |
rs755516208 | snp | A/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:533844 | GGACTCTCCCTTCCC[A/G]CTGTGCCTGGGAGGG | 997 |
rs755579686 | snp | C/T | 2.97818e-05 | 0.00385876 | synonymous-codon | CDC34 | GRCh38.p7 | 19:536251 | TGTGCAGACGGGGGA[C/T]GTGTGTATCTCCATC | 997 |
rs755597506 | snp | C/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:532681 | CTCCAACAAAGGCCC[C/G]GATGAGCCTTGGCAG | 997 |
rs755679497 | snp | A/G | 1.7348e-05 | 0.00294512 | intron-variant | CDC34 | GRCh38.p7 | 19:537160 | CCGGTGAGGGCGGGC[A/G]GGGGCGTCACGGGAG | 997 |
rs755819680 | snp | G/T | 0.000169233 | 0.00919718 | missense | CDC34 | GRCh38.p7 | 19:532044 | TGGACGAGGGCGATC[G/T]ATACAACTGGGAGGT | 997 |
rs755840165 | snp | C/T | | | intron-variant | CDC34 | GRCh38.p7 | 19:537513 | GCCCGTCACCACGCC[C/T]GGCTAATTTTTTGTA | 997 |
rs755931291 | in-del | -/TGGCCAGGCCCCCCGGTTTAGAATCCGGAGGCCGGGG | | | intron-variant | CDC34 | GRCh38.p7 | 19:540791 | ATCCAGAGGCTGGGA[lengthTooLong]TGGCCAGGCCCCCGG | 997 |
rs755938695 | snp | G/T | | | intron-variant | CDC34 | GRCh38.p7 | 19:538661 | CACACATAATGCATG[G/T]GTCTTCCTCGCCCCA | 997 |
rs755976168 | snp | C/G | 2.49038e-05 | 0.00352864 | intron-variant | CDC34 | GRCh38.p7 | 19:536358 | AAGCCGGCCCAACCC[C/G]CTGTGTCCACCCAGA | 997 |
rs756091430 | in-del | -/GCCCCGGGCC | 1.69284e-05 | 0.00290928 | intron-variant | CDC34 | GRCh38.p7 | 19:536975 | CCGGAAGGCTGGGGT[-/GCCCCGGGCC]GCCCCACTCCGACCC | 997 |
rs756204841 | snp | C/G | 1.78232e-05 | 0.00298518 | intron-variant | CDC34 | GRCh38.p7 | 19:536940 | CAGGCGTCCCCGTGA[C/G]CCTCAGGGCCAGAGA | 997 |
rs756306140 | snp | A/G | 3.69235e-05 | 0.00429656 | intron-variant | CDC34 | GRCh38.p7 | 19:541301 | AGGGGCCGAGTCCAG[A/G]CACGTGGGTGGCGCC | 997 |
rs756344339 | in-del | -/ACGGAG | | | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:531282 | TGCACAGACGGGGAA[-/ACGGAG]ACGGGGACGCGGGGT | 997 |
rs756462163 | snp | A/G | 3.46159e-05 | 0.00416014 | missense | CDC34 | GRCh38.p7 | 19:541374 | AGGTGGACGCGGAGC[A/G]TGACGGCGTGAAGGT | 997 |
rs756640551 | snp | A/G | | | upstream-variant-2KB | CDC34 | GRCh38.p7 | 19:531660 | GTCGGACCTGGCCGC[A/G]GAGCGCAGGCGCAGT | 997 |
rs756906659 | snp | C/T | 6.90226e-05 | 0.00587423 | intron-variant | CDC34 | GRCh38.p7 | 19:537155 | ATCATCCGGTGAGGG[C/T]GGGCGGGGGCGTCAC | 997 |
rs756910510 | snp | A/G | | | intron-variant, synonymous-codon | CDC34 | GRCh38.p7 | 19:538705 | TCCAGGGCACCTTCC[A/G]TCCTGCACTCGCTGG | 997 |
rs756935173 | snp | C/G | | | intron-variant | CDC34 | GRCh38.p7 | 19:535687 | CTTGACCCCAGGCCT[C/G]TGAGAGTCCCTGCCT | 997 |
rs757085561 | in-del | -/CTG | 5.70239e-05 | 0.00533935 | intron-variant | CDC34 | GRCh38.p7 | 19:536911 | CCAGGTGAAGGTCAC[-/CTG]CTGGGTGGGTCCAGG | 997 |