SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs7516 | snp | A/G | 0.198922 | 0.244726 | synonymous-codon | TNK2 | GRCh38.p7 | 3:195868183 | CAACCTGTTCCTCCC[A/G]CCCCAGGGTGGGGGC | 10188 |
rs733119 | snp | A/C | 0.403684 | 0.197183 | intron-variant, downstream-variant-500B | TNK2 | GRCh38.p7 | 3:195866527 | TCCATATTTCTGTTT[A/C]AAGTAACATTTAAAA | 10188 |
rs745497 | snp | C/T | 0.481473 | 0.0944461 | intron-variant | TNK2 | GRCh38.p7 | 3:195890936 | GTGAGGAGTCAGATC[C/T]TGAGACCTCAGGTGG | 10188 |
rs880803 | snp | A/G | 0.030278 | 0.119257 | intron-variant | TNK2 | GRCh38.p7 | 3:195878779 | CAGGTCTGGAGCCTC[A/G]GAACAAGTGGATGTG | 10188 |
rs880804 | snp | A/G | 0.181978 | 0.240568 | intron-variant | TNK2 | GRCh38.p7 | 3:195878918 | GGTGGGAGGCACGGG[A/G]AGTGGGGGGAGGCAC | 10188 |
rs880805 | snp | A/C | 0.181978 | 0.240568 | intron-variant | TNK2 | GRCh38.p7 | 3:195878919 | GTGGGAGGCACGGGA[A/C]GTGGGGGGAGGCACG | 10188 |
rs881753 | snp | C/T | 0.499996 | 0.00139776 | intron-variant | TNK2 | GRCh38.p7 | 3:195879899 | GGTAAGGTATGAATA[C/T]AGTTGCCTTTAAACA | 10188 |
rs1056726 | snp | C/T | 0.15925 | 0.232947 | synonymous-codon | TNK2 | GRCh38.p7 | 3:195868534 | CACGCTCATCGACTT[C/T]GGTGAGGAGCCCGTG | 10188 |
rs1056749 | snp | C/T | 0.307452 | 0.243309 | synonymous-codon | TNK2 | GRCh38.p7 | 3:195867934 | GTGGCCTGGACCTGC[C/T]TCCCCTCCCCGGGTG | 10188 |
rs1871529 | snp | C/T | 0.470715 | 0.117409 | intron-variant | TNK2 | GRCh38.p7 | 3:195906746 | gctcagtttaccata[C/T]gtcattatatctcaa | 10188 |
rs2241413 | snp | A/G | 0.492823 | 0.0594727 | intron-variant | TNK2 | GRCh38.p7 | 3:195872214 | TCCAGGGCCCTCAGC[A/G]CGGCACGCGTGGGCG | 10188 |
rs2278033 | snp | A/G | 0.462541 | 0.13163 | intron-variant | TNK2 | GRCh38.p7 | 3:195870417 | GGTCCTAGGCTTTCC[A/G]TCCTGGGGTCAGGTG | 10188 |
rs2278034 | snp | A/G | 0.499574 | 0.0145909 | intron-variant | TNK2 | GRCh38.p7 | 3:195870036 | TTCACAGGCCACCCT[A/G]AGGCTGCTGTTCTGT | 10188 |
rs2344654 | snp | C/T | 0.387642 | 0.208697 | downstream-variant-500B | TNK2 | GRCh38.p7 | 3:195862899 | CGTCCACTTCCCCAG[C/T]GCAGAGACGCCTGTA | 10188 |
rs2432529 | snp | C/T | 0.48178 | 0.0936921 | intron-variant | TNK2 | GRCh38.p7 | 3:195880472 | CCTCTCCGAGGGTCA[C/T]TGCTGAGTTAGGTGA | 10188 |
rs2550258 | snp | G/T | | | | | GRCh38.p7 | 3:195880888 | TGTCCTCTCCAAGGG[G/T]CATTGCTGGGGGGCG | 10188 |
rs2550259 | snp | G/T | | | | | GRCh38.p7 | 3:195880475 | TGTCCTCTCCGAGGG[G/T]CACTGCTGAGTTAGG | 10188 |
rs2550260 | snp | A/T | | | | | GRCh38.p7 | 3:195880457 | CTGCTGAGTTAGGTG[A/T]TACAGGGATATATGC | 10188 |
rs2550284 | snp | A/G | | | | | GRCh38.p7 | 3:195888753 | GGGAAGCTACCGAGA[A/G]CCGCCTGGACCCACG | 10188 |
rs2620623 | snp | A/G | | | intron-variant | TNK2 | GRCh38.p7 | 3:195880893 | TGCTGTGTCCTCTCC[A/G]AGGGGCATTGCTGGG | 10188 |
rs2620624 | snp | G/T | | | intron-variant | TNK2 | GRCh38.p7 | 3:195880755 | GGTGTTACAGGGATA[G/T]ATGCTGTGTCCTCTC | 10188 |
rs2620625 | snp | C/T | | | intron-variant | TNK2 | GRCh38.p7 | 3:195880639 | TATGCTGTGTCCTCT[C/T]CAAGGGGCATTGCTG | 10188 |
rs2620626 | snp | C/T | 0 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195880536 | GATGCTGTGTCCTCT[C/T]CAAGGGGCATTGCTG | 10188 |
rs3747669 | snp | A/G | 0.447727 | 0.152984 | synonymous-codon, utr-variant-5-prime | TNK2 | GRCh38.p7 | 3:195888505 | GGTGACGTTGAGGTC[A/G]TCTCGGAGCCGCAGG | 10188 |
rs3747670 | snp | C/T | | | intron-variant | TNK2 | GRCh38.p7 | 3:195888640 | CTCAGGGACAAGGGT[C/T]GTGGGGGGACAACAG | 10188 |
rs3747671 | snp | A/G | 0.46855 | 0.121392 | intron-variant | TNK2 | GRCh38.p7 | 3:195908386 | GGGATGAAAGGCCAA[A/G]AGAACGAGGGCAGTG | 10188 |
rs3747672 | snp | A/G | 0.481165 | 0.0951993 | intron-variant, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195885163 | CAGGCTGCCCCACTG[A/G]CAGTTTGGCAAAACC | 10188 |
rs3747673 | snp | C/T | 0.0165453 | 0.0894365 | missense, upstream-variant-2KB, utr-variant-5-prime | TNK2 | GRCh38.p7 | 3:195884973 | TCTCAGAGCACCTTC[C/T]GGAAGACCTCGCCCG | 10188 |
rs3749333 | snp | A/G | 0.000175151 | 0.00935653 | missense | TNK2 | GRCh38.p7 | 3:195867848 | AGCCGGGGTGGCAGC[A/G]GGGAGCTGCCAGGTG | 10188 |
rs3749334 | snp | A/G | 0.000925398 | 0.0214905 | missense | TNK2 | GRCh38.p7 | 3:195867924 | CCCGCGGAGGCACCC[A/G]GGGAGGGGAAGCAGG | 10188 |
rs3761718 | snp | A/G | 0.0746199 | 0.178162 | synonymous-codon, utr-variant-5-prime | TNK2 | GRCh38.p7 | 3:195879148 | GGCATGGGAGAAGGT[A/G]CGTGTCTTCAGGCTC | 10188 |
rs3890033 | snp | C/T | 0.490782 | 0.0672626 | intron-variant | TNK2 | GRCh38.p7 | 3:195864656 | TCAGTAAGAACCACC[C/T]GAGACAGTGACAGAC | 10188 |
rs3890034 | snp | A/G | 0.215144 | 0.247558 | intron-variant | TNK2 | GRCh38.p7 | 3:195864692 | ACAGCGAGTGCCTGC[A/G]TCCCAGATGCAAATC | 10188 |
rs3892583 | snp | C/T | 0.410568 | 0.191619 | intron-variant | TNK2 | GRCh38.p7 | 3:195864924 | AACCACCCGAGACAG[C/T]GACAGACAGGTGACA | 10188 |
rs3893768 | snp | C/T | 0.213333 | 0.247296 | intron-variant | TNK2 | GRCh38.p7 | 3:195865411 | AGAGTGCCTGCGTCC[C/T]GGGTGCAAATCAGTT | 10188 |
rs4082351 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TNK2 | GRCh38.p7 | 3:195907188 | CTGAAGCCAGACAGT[G/T]AGAGCCACTCTGGCC | 10188 |
rs4560328 | snp | A/G | 0.219648 | 0.248151 | intron-variant | TNK2 | GRCh38.p7 | 3:195902819 | CAGTGGCGCAATCTC[A/G]GCTCGCTGCAACCTC | 10188 |
rs4927788 | snp | A/G | 0.29278 | 0.246313 | intron-variant, upstream-variant-2KB | TNK2, MIR6829 | GRCh38.p7 | 3:195884369 | GAGCATGGGCTGGAC[A/G]TGGTGGCTCACACCT | 10188 |
rs4927789 | snp | C/G | 0 | 0 | intron-variant, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195892795 | CCAACTGCCCGCCCG[C/G]CCGCCCTCCCTCTTG | 10188 |
rs4927790 | snp | G/T | 0.382279 | 0.212137 | intron-variant | TNK2 | GRCh38.p7 | 3:195901130 | GGGAGCCAGAGAAAT[G/T]TCCGGTGCTTCAAGA | 10188 |
rs4927791 | snp | C/T | 0.382279 | 0.212137 | intron-variant | TNK2 | GRCh38.p7 | 3:195901133 | AGCCAGAGAAATGTC[C/T]GGTGCTTCAAGACAT | 10188 |
rs6421308 | snp | A/G | 0.472147 | 0.114677 | intron-variant | TNK2 | GRCh38.p7 | 3:195901401 | ATTGGCAGACACAGT[A/G]TACAGGGGACAGAGA | 10188 |
rs6583266 | snp | A/G | 0.332106 | 0.236133 | intron-variant | TNK2 | GRCh38.p7 | 3:195870678 | CCGGATCCACCCTCC[A/G]TCCCTGCACCAACTG | 10188 |
rs6762607 | snp | A/G | 0.132409 | 0.220618 | intron-variant | TNK2 | GRCh38.p7 | 3:195895170 | CCGCCGCAGGGGGCA[A/G]GGCTGAGCCCGGCTC | 10188 |
rs6771909 | snp | A/G | 0.158302 | 0.232576 | intron-variant, upstream-variant-2KB | TNK2, MIR6829 | GRCh38.p7 | 3:195882937 | GGAGTAACTCTCTTG[A/G]CACTGAGCACCAGCA | 10188 |
rs6773526 | snp | A/G | 0.266546 | 0.249452 | utr-variant-3-prime | TNK2 | GRCh38.p7 | 3:195864004 | GGACAGCGCTGGTGC[A/G]GGAGGGATGGGCAGG | 10188 |
rs6773702 | snp | A/G | 0.211212 | 0.246973 | downstream-variant-500B | TNK2 | GRCh38.p7 | 3:195862891 | ACTGGTGATACAGGC[A/G]TCTCTGCACTGGGGA | 10188 |
rs6782052 | snp | A/G | 0.328148 | 0.237472 | intron-variant | TNK2 | GRCh38.p7 | 3:195905950 | aaaggcttatatcca[A/G]aatatatcaagaact | 10188 |
rs6784831 | snp | C/T | 0.187369 | 0.242028 | intron-variant | TNK2 | GRCh38.p7 | 3:195903941 | aatcaatggtattta[C/T]atatactagcaacaa | 10188 |
rs6785122 | snp | A/G | 0.313814 | 0.241719 | intron-variant | TNK2 | GRCh38.p7 | 3:195906567 | aaagtagaccagcct[A/G]ttacctggggtaggg | 10188 |
rs6791922 | snp | C/T | 0.299411 | 0.245069 | intron-variant | TNK2 | GRCh38.p7 | 3:195906075 | acatgagaagatgcc[C/T]gacaacatgagtcat | 10188 |
rs6793113 | snp | C/T | 0.0391387 | 0.134304 | intron-variant | TNK2 | GRCh38.p7 | 3:195874200 | CGCTCAGTAACTGGG[C/T]GAGAATGCCGCTGAG | 10188 |
rs6796626 | snp | A/C | 0.328616 | 0.237317 | intron-variant | TNK2 | GRCh38.p7 | 3:195905949 | aaaaggcttatatcc[A/C]gaatatatcaagaac | 10188 |
rs6799624 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNK2 | GRCh38.p7 | 3:195905991 | caacacgaaaaaccc[C/T]acacaattaaaaatg | 10188 |
rs7340710 | snp | C/T | 0.301932 | 0.244547 | intron-variant | TNK2 | GRCh38.p7 | 3:195903315 | aaagtattgggatta[C/T]aggcgtgagccaccg | 10188 |
rs7355913 | snp | A/G | 0.302435 | 0.244439 | intron-variant | TNK2 | GRCh38.p7 | 3:195905259 | ggctggaatgcagtg[A/G]cgcaatcttggctca | 10188 |
rs7634904 | snp | A/G | 0.325091 | 0.238456 | intron-variant | TNK2 | GRCh38.p7 | 3:195902911 | cataccatcacaccc[A/G]gctaatttttgtatt | 10188 |
rs7636635 | snp | C/T | 0.423413 | 0.180077 | intron-variant | TNK2 | GRCh38.p7 | 3:195875916 | GAAATCTCAGCACCA[C/T]GTTCCCGTCCGGGCC | 10188 |
rs9325405 | snp | G/T | 0.409721 | 0.192325 | intron-variant | TNK2 | GRCh38.p7 | 3:195870957 | GTGGGTTCTGGTGTG[G/T]GGGGACTCGCTGTGT | 10188 |
rs9798824 | snp | C/G | | | intron-variant | TNK2 | GRCh38.p7 | 3:195881222 | ACAGCGTCTATCCCT[C/G]TAACACCCGCCCCCA | 10188 |
rs9809360 | snp | A/G | | | upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195910487 | GCTCAGGGCCACTCA[A/G]CCCTTGTTACTGTCC | 10188 |
rs9812133 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | TNK2 | GRCh38.p7 | 3:195870921 | CCGCTGTGTGGGTTC[A/C/T]GGTGTGTGGGGGCCC | 10188 |
rs9812155 | snp | C/T | 0.32 | 0.24 | intron-variant | TNK2 | GRCh38.p7 | 3:195870964 | CTGGTGTGTGGGGAC[C/T]CGCTGTGTGGGGTTC | 10188 |
rs9815549 | snp | G/T | 0.275899 | 0.248655 | intron-variant | TNK2 | GRCh38.p7 | 3:195876781 | GCACACCCACAACCC[G/T]CCCAGGAGCAGCCGC | 10188 |
rs9824499 | snp | C/T | 0.480064 | 0.0978296 | intron-variant | TNK2 | GRCh38.p7 | 3:195880587 | CCCAGCAATGCCCCT[C/T]GGAGAGGACACAGCA | 10188 |
rs9829709 | snp | A/G | 0.483708 | 0.088773 | intron-variant | TNK2 | GRCh38.p7 | 3:195889802 | CTGTCTGCGTAAGGT[A/G]TGTCAGAGCTGAGGG | 10188 |
rs9832143 | snp | A/G | | | intron-variant | TNK2 | GRCh38.p7 | 3:195880781 | ACACCCCCCCCAGCA[A/G]TGCCCCTTGGAGAGG | 10188 |
rs9832273 | snp | A/T | | | intron-variant | TNK2 | GRCh38.p7 | 3:195880860 | AGGACACAGCATCTA[A/T]CCCTGTAACACCCGC | 10188 |
rs9833567 | snp | G/T | 0.367708 | 0.220556 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | TNK2 | GRCh38.p7 | 3:195895909 | CCTGCCCCGCAGCTC[G/T]GCCCTGCGCTCAGCC | 10188 |
rs9836713 | snp | A/T | 0.5 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195880758 | AGGACACAGCATCTA[A/T]CCCTGTAACACCCCC | 10188 |
rs9839985 | snp | A/G | 0.237593 | 0.249692 | intron-variant | TNK2 | GRCh38.p7 | 3:195891624 | TCTCCACCCGGCCAC[A/G]GCCACCGCTGCCCTG | 10188 |
rs9842474 | snp | G/T | 0 | 0 | intron-variant, downstream-variant-500B | TNK2, MIR6829 | GRCh38.p7 | 3:195881897 | TTCCTAGATGGATGG[G/T]GAGCGAATGGGTGCA | 10188 |
rs9846297 | snp | A/G | 0.362523 | 0.223246 | intron-variant, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195893167 | TCCGCTGGGCCCTGC[A/G]ATGACTCCTCAGAGA | 10188 |
rs9853696 | snp | C/G | 0 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195875052 | CGCCCACGCACGCTC[C/G]GAGGCACAGGAAGCT | 10188 |
rs9853700 | snp | A/G | 0 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195875061 | ACGCTCCGAGGCACA[A/G]GAAACTCCCCCTCGG | 10188 |
rs9853880 | snp | A/G | 0 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195875181 | ATGGCGCCCACGCAC[A/G]CTCGGAGGCACAGGA | 10188 |
rs9854951 | snp | C/G | 0.245631 | 0.249962 | intron-variant | TNK2 | GRCh38.p7 | 3:195891664 | CAAAGTGACCCCCCC[C/G]CTCCAGGGCTCAGCC | 10188 |
rs9860453 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNK2 | GRCh38.p7 | 3:195870922 | CGCTGTGTGGGTTCT[A/G]GTGTGTGGGGGCCCG | 10188 |
rs9860456 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TNK2 | GRCh38.p7 | 3:195870930 | GGGTTCTGGTGTGTG[G/T]GGGCCCGCTGTGTGG | 10188 |
rs9860487 | snp | A/G | 0.5 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195870992 | TTCTGGTGTGTGGGG[A/G]CCCGCTGTGTGGGTT | 10188 |
rs9863553 | snp | A/G | 0.260976 | 0.249759 | intron-variant | TNK2 | GRCh38.p7 | 3:195892383 | GCCCAACCAGTCCCC[A/G]GCAGTCCAGCCCCTG | 10188 |
rs9866046 | snp | A/G | 0.312837 | 0.241974 | intron-variant | TNK2 | GRCh38.p7 | 3:195902213 | gacacttgactgacc[A/G]cctgcaatcctcaaa | 10188 |
rs9868797 | snp | C/G | | | intron-variant | TNK2 | GRCh38.p7 | 3:195875230 | CGCCCACGCACGCTC[C/G]GAGGCACAGGAAGCT | 10188 |
rs9868818 | snp | A/C/G | 0.31014 | 0.242659 | intron-variant | TNK2 | GRCh38.p7 | 3:195875283 | ACGCTCCGAGGCACA[A/C/G]GAAGCTCCCCTCGGG | 10188 |
rs9871110 | snp | A/G | 0.483053 | 0.0904792 | intron-variant | TNK2 | GRCh38.p7 | 3:195898455 | CTGCCTGCTGTTACT[A/G]TGGGCCCTTCCCTCA | 10188 |
rs9875284 | snp | C/T | 0.5 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195870994 | CTGGTGTGTGGGGGC[C/T]CGCTGTGTGGGTTCT | 10188 |
rs9876028 | snp | A/G | 0 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195875093 | ATGGCGCCCACGCAC[A/G]CTCCGAGGCACAAGA | 10188 |
rs9876157 | snp | A/G | 0.5 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195875137 | ATGGCGCCCACGCAC[A/G]CTCCGAGGCACAAGA | 10188 |
rs9876295 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TNK2 | GRCh38.p7 | 3:195875198 | TCCGAGGCACAAGAA[A/G]CTCCCCCTCGGGATG | 10188 |
rs9880526 | snp | A/G | 0.299411 | 0.245069 | upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195910228 | CGGAGCACTCCTGAA[A/G]GAGGGAGGGTTTGTC | 10188 |
rs10048932 | snp | A/C | | | intron-variant | TNK2 | GRCh38.p7 | 3:195903259 | gttagccaggatggt[A/C]tcaatctcctgacct | 10188 |
rs10579442 | in-del | -/CT | 0.268424 | 0.24932 | intron-variant | TNK2 | GRCh38.p7 | 3:195867281 | TGGGCACACCCACCC[-/CT]GTCAGCACCACTAGG | 10188 |
rs10626163 | in-del | -/GAG | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195892681 | TGGCAGGGAGCAGAG[-/GAG]CTTTCCTCACGCTGG | 10188 |
rs10626380 | in-del | -/GAG | 0.483199 | 0.0901004 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195892678 | GTCTGGCAGGGAGCA[-/GAG]GAGCTTTCCTCACGC | 10188 |
rs10707803 | in-del | -/C | 0.475525 | 0.107882 | intron-variant | TNK2 | GRCh38.p7 | 3:195881636 | TCTATCCTTGTAACA[-/C]CCCCCCCCCAGCAAC | 10188 |
rs10881557 | snp | G/T | 0.302435 | 0.244439 | intron-variant | TNK2 | GRCh38.p7 | 3:195904184 | gatcacctgagccca[G/T]gaagtcgaggttgca | 10188 |
rs10881558 | snp | A/T | 0.329084 | 0.237162 | intron-variant | TNK2 | GRCh38.p7 | 3:195904591 | tcacaagatgagaaa[A/T]gtcctggagatggat | 10188 |
rs11185487 | snp | A/G | 0.487324 | 0.0785968 | intron-variant | TNK2 | GRCh38.p7 | 3:195876763 | ACGGAAGGGCGGGGC[A/G]GGGCACACCCACAAC | 10188 |
rs11185498 | snp | C/T | 0.314787 | 0.241459 | intron-variant | TNK2 | GRCh38.p7 | 3:195901944 | CTGACGCTGAGTGAA[C/T]GCATGGATTCTGTGA | 10188 |
rs11457784 | in-del | -/C | 0.0652144 | 0.168387 | intron-variant | TNK2 | GRCh38.p7 | 3:195865699 | ATCAGTTAAGAACGA[-/C]CCCGAGACAGTATGG | 10188 |
rs11540613 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | TNK2 | GRCh38.p7 | 3:195868716 | AGGTTGGTTCTGTGA[C/T]GGAAAGGGAGAGCCC | 10188 |
rs11706425 | snp | G/T | | | intron-variant | TNK2 | GRCh38.p7 | 3:195870901 | GGGTTCCAGTGTGTG[G/T]GGGCCCGCTGTGTGG | 10188 |
rs11708930 | snp | C/G | 0.5 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195880516 | CCCTGTAACACCCCC[C/G]CCCCCAGCAATGCCC | 10188 |
rs11713323 | snp | C/T | 0.350982 | 0.228698 | intron-variant | TNK2 | GRCh38.p7 | 3:195887657 | AGAACATCATGACTT[C/T]TAGATGCTACAACCC | 10188 |
rs11714255 | snp | C/G | | | intron-variant | TNK2 | GRCh38.p7 | 3:195869216 | AGCGAGGCCAAGGCA[C/G]AAGCCAGGGCCACAC | 10188 |
rs11714769 | snp | A/G | 0.277778 | 0.248452 | intron-variant | TNK2 | GRCh38.p7 | 3:195874577 | TCCGAGGCACAAGAA[A/G]CTCCCCCTCGGGATG | 10188 |
rs11714830 | snp | A/G | 0 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195874751 | ACGCTCCGAGGCACA[A/G]GAAGCTCCCCTCGGG | 10188 |
rs11717090 | snp | A/G | 0.313326 | 0.241847 | intron-variant | TNK2 | GRCh38.p7 | 3:195906825 | CGAAGCACAAGGTGG[A/G]GGCTAATCCCGGGCT | 10188 |
rs11719343 | snp | A/T | 0.32885 | 0.23724 | intron-variant | TNK2 | GRCh38.p7 | 3:195903662 | gcagaggttgcagtg[A/T]gccaagattgtgcca | 10188 |
rs11719529 | snp | G/T | 0 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195904283 | aaaaaaaaaaaaagg[G/T]gaaagcaatccaagt | 10188 |
rs11720557 | snp | A/C | 0.431177 | 0.172264 | intron-variant | TNK2 | GRCh38.p7 | 3:195901765 | TACAAATATGGAAAC[A/C]AGCTCTGGAGAGGTG | 10188 |
rs11720562 | snp | C/T | 0 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195874714 | AGGCACAAGAAACTC[C/T]CCCTCGGGATGGCGC | 10188 |
rs11918909 | snp | A/G | 0.0376037 | 0.131863 | intron-variant, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195886067 | GCAGTGGGGACCGGT[A/G]TCATTTCACTGAAGA | 10188 |
rs11922419 | snp | A/G | | | intron-variant | TNK2 | GRCh38.p7 | 3:195904179 | gggacgatcacctga[A/G]cccaggaagtcgagg | 10188 |
rs11922898 | snp | A/C | 0.48 | 0.0979796 | intron-variant | TNK2 | GRCh38.p7 | 3:195864846 | GCAAATCAGTAAGAA[A/C]CACCCGAGACAGTGA | 10188 |
rs11923784 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TNK2 | GRCh38.p7 | 3:195891544 | TTTAAGAGGACCAGG[C/T]GTCGTGGCTTTCCGG | 10188 |
rs11924461 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TNK2 | GRCh38.p7 | 3:195905629 | cataccttgcaccac[A/G]taacaaaaattaacc | 10188 |
rs11926590 | snp | A/G | | | intron-variant | TNK2 | GRCh38.p7 | 3:195877439 | AAAAGCTGCAGTGCA[A/G]GTGGAAGAGGCTCCC | 10188 |
rs11926661 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | TNK2 | GRCh38.p7 | 3:195907720 | TAGACTGGGCTGGGA[A/G]CTCCTGTCCTGACAG | 10188 |
rs11927966 | snp | A/T | | | intron-variant | TNK2 | GRCh38.p7 | 3:195904201 | aagtcgaggttgcag[A/T]gagccatgatcacac | 10188 |
rs12106975 | snp | C/G | 0.158302 | 0.232576 | intron-variant, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195886149 | GTGGCAGATCCAAGA[C/G]CCCTAAATCTCAGCA | 10188 |
rs12233585 | snp | A/G | 0.0830469 | 0.186082 | intron-variant | TNK2 | GRCh38.p7 | 3:195878229 | AAGCGATCCCAGGGC[A/G]GGGCCCAGCCCTGCA | 10188 |
rs12485493 | snp | A/G | 0.5 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195880958 | TGGAGAGGACACAGC[A/G]TCTATCCCTGTAACA | 10188 |
rs12486320 | snp | A/G | | | intron-variant | TNK2 | GRCh38.p7 | 3:195881516 | CCTTGGAGAGGACAC[A/G]GCATCTATCCCTGTA | 10188 |
rs12487782 | snp | C/T | 0.49753 | 0.0350569 | intron-variant | TNK2 | GRCh38.p7 | 3:195873356 | GAAGGCTCTCACAGG[C/T]TGTGAGGCTCCCGCG | 10188 |
rs12487966 | snp | A/C | 0.229723 | 0.249176 | intron-variant | TNK2 | GRCh38.p7 | 3:195880624 | CCTGTAACACCCCCC[A/C]AGCAATGCCCCTTGA | 10188 |
rs12489282 | snp | A/G | 0.375 | 0.216506 | intron-variant | TNK2 | GRCh38.p7 | 3:195880885 | ACCCGCCCCCCAGCA[A/G]TGCCCCTTGGAGAGG | 10188 |
rs12490307 | snp | C/G | 0.289657 | 0.253848 | upstream-variant-2KB, intron-variant | TNK2 | GRCh38.p7 | 3:195896569 | GCTGCAAAGCCGGGA[C/G]ACTGTAGAAGGCAAG | 10188 |
rs12490642 | snp | C/T | 0.460252 | 0.135255 | intron-variant | TNK2 | GRCh38.p7 | 3:195889337 | TTCAAGAAATAAATC[C/T]CAATTTACATGTGAA | 10188 |
rs12491124 | snp | C/T | 0.214541 | 0.247473 | intron-variant | TNK2 | GRCh38.p7 | 3:195894836 | GGAAGGGAAGCTACC[C/T]CATCCATCAACACCG | 10188 |
rs12491213 | snp | C/T | 0.301429 | 0.244653 | intron-variant | TNK2 | GRCh38.p7 | 3:195895111 | CACATAAACACACCG[C/T]TCTCTGTCCCCTGGC | 10188 |
rs12494665 | snp | A/G | 0.313326 | 0.241847 | intron-variant | TNK2 | GRCh38.p7 | 3:195906677 | TTGAAGGTGGGGGTG[A/G]TTTCACGGGTATATA | 10188 |
rs12494741 | snp | A/G | 0.473543 | 0.111932 | intron-variant | TNK2 | GRCh38.p7 | 3:195876795 | CGCCCAGGAGCAGCC[A/G]CTCCCGGCCCCTCCC | 10188 |
rs12495000 | snp | A/G | 0.0377219 | 0.132053 | intron-variant | TNK2 | GRCh38.p7 | 3:195871886 | AAAATGGCAGGGACA[A/G]CATTCCCCTGGAGAA | 10188 |
rs12495019 | snp | C/G | | | intron-variant | TNK2 | GRCh38.p7 | 3:195871903 | ATTCCCCTGGAGAAC[C/G]CTCCCCGGAGAACCC | 10188 |
rs12496236 | snp | C/G | 0.5 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195875408 | CGCCCACGCACGCTC[C/G]GAGGCACAAGAAGCT | 10188 |
rs12496845 | snp | A/G | 0.48 | 0.0979796 | intron-variant | TNK2 | GRCh38.p7 | 3:195875376 | TCGGAGGCACAGGAA[A/G]CTCCCCCTCGGGATG | 10188 |
rs12497548 | snp | A/C | | | intron-variant | TNK2 | GRCh38.p7 | 3:195871932 | CCTCCCCTGGAGAAC[A/C]CTCCCCTGGAGAACA | 10188 |
rs12629675 | snp | C/G | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195886740 | AGAGGGGCTGTGAAG[C/G]CCTCACCGCACACAG | 10188 |
rs12632436 | snp | C/G/T | 0.112465 | 0.209395 | intron-variant | TNK2 | GRCh38.p7 | 3:195887804 | GTACATGTGTGTATG[C/G/T]CGTGCGTGTGCATGC | 10188 |
rs12634163 | snp | C/T | 0.112983 | 0.209108 | intron-variant | TNK2 | GRCh38.p7 | 3:195887766 | ACGCGTGTGCGCACG[C/T]GTGTGCGTCTGCGCG | 10188 |
rs12636406 | snp | G/T | 0 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195866026 | TGCCTCCTGCCATGG[G/T]GCTGGCTCCAGCCAT | 10188 |
rs13059257 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | TNK2 | GRCh38.p7 | 3:195908122 | CTTGTGTGTTGACTG[C/T]ACCATGCAGAGCATA | 10188 |
rs13060518 | snp | C/G | | | intron-variant | TNK2 | GRCh38.p7 | 3:195881061 | TTGAAGAGGACACAG[C/G]ATCTGTCCCTCTAAC | 10188 |
rs13060522 | snp | A/G | | | intron-variant | TNK2 | GRCh38.p7 | 3:195881066 | GAGGACACAGGATCT[A/G]TCCCTCTAACACCCC | 10188 |
rs13063157 | snp | A/C | | | intron-variant | TNK2 | GRCh38.p7 | 3:195871947 | CCTCCCCTGGAGAAC[A/C]TTCCCCTGGAGAACC | 10188 |
rs13066070 | snp | A/G | 0 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195874622 | TCCGAGGCACAAGAA[A/G]CTCCCCTCGGGATGG | 10188 |
rs13066245 | snp | G/T | 0.276461 | 0.248596 | intron-variant | TNK2 | GRCh38.p7 | 3:195874707 | CGCTCCGAGGCACAA[G/T]AAACTCTCCCTCGGG | 10188 |
rs13067149 | snp | A/G | 0 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195875226 | ATGGCGCCCACGCAC[A/G]CTCCGAGGCACAAGA | 10188 |
rs13067358 | snp | A/G | | | intron-variant | TNK2 | GRCh38.p7 | 3:195875359 | ATGGCGCCCACGCAC[A/G]CTCCGAGGCACAAGA | 10188 |
rs13068361 | snp | C/T | | | intron-variant | TNK2 | GRCh38.p7 | 3:195871948 | CTCCCCTGGAGAACA[C/T]TCCCCTGGAGAACCC | 10188 |
rs13070364 | snp | A/C | | | upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195909762 | gcgccccgagcccgc[A/C]tgcGCCTGCGCCTGC | 10188 |
rs13074460 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TNK2 | GRCh38.p7 | 3:195870933 | TTCTGGTGTGTGGGG[A/G]CCCGCTGTGTGGGTT | 10188 |
rs13082352 | snp | A/G | | | intron-variant | TNK2 | GRCh38.p7 | 3:195889808 | GCGTAAGGTGTGTCA[A/G]AGCTGAGGGCGTGGC | 10188 |
rs13084300 | snp | G/T | | | upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195909797 | CCCCGGGGTGGGGGG[G/T]GGGGGGGAGTCGGCC | 10188 |
rs13084520 | snp | A/G | 0.279195 | 0.248289 | upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195910568 | GATCAGACACATCGG[A/G]AACTGTGTAGGGCTG | 10188 |
rs13084875 | snp | C/T | 0.446771 | 0.154211 | intron-variant | TNK2 | GRCh38.p7 | 3:195869765 | GGAGATGGAGGAGGC[C/T]CCAGGCAGAGCCGGA | 10188 |
rs13087251 | snp | A/G | 0.339605 | 0.23339 | intron-variant | TNK2 | GRCh38.p7 | 3:195868761 | CAGGCAGGGTCTGGG[A/G]CACGAGGGGAGGTGG | 10188 |
rs13091201 | snp | C/T | | | intron-variant | TNK2 | GRCh38.p7 | 3:195870892 | GTGAGCTTGGGGTTC[C/T]AGTGTGTGTGGGCCC | 10188 |
rs13091355 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TNK2 | GRCh38.p7 | 3:195870935 | CTGGTGTGTGGGGGC[C/T]CGCTGTGTGGGTTCT | 10188 |
rs13091590 | snp | A/G | | | intron-variant | TNK2 | GRCh38.p7 | 3:195874706 | ACGCTCCGAGGCACA[A/G]GAAACTCTCCCTCGG | 10188 |
rs13096591 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195909796 | GCCCCGGGGTGGGGG[G/T]TGGGGGGGAGTCGGC | 10188 |
rs13097551 | snp | A/C | | | intron-variant | TNK2 | GRCh38.p7 | 3:195871977 | CCTCCCCTGGAGAAC[A/C]CTCCCCTGGAGAACC | 10188 |
rs13097552 | snp | C/T | | | intron-variant | TNK2 | GRCh38.p7 | 3:195871978 | CTCCCCTGGAGAACC[C/T]TCCCCTGGAGAACCC | 10188 |
rs13099718 | snp | A/G | | | intron-variant | TNK2 | GRCh38.p7 | 3:195870893 | TGAGCTTGGGGTTCC[A/G]GTGTGTGTGGGCCCG | 10188 |
rs13433937 | snp | C/T | 0.0608686 | 0.163491 | missense | TNK2 | GRCh38.p7 | 3:195864185 | CCAGACGCATCTCAG[C/T]GCCTAGAGAATGGGA | 10188 |
rs28448757 | snp | A/G | | | intron-variant, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195886568 | TGACCAGAGAAACCC[A/G]GAGATTAGAGAGGGT | 10188 |
rs28452384 | snp | A/G | | | intron-variant | TNK2 | GRCh38.p7 | 3:195880842 | CAGCAATGCCCCTTG[A/G]AGAGGACACAGCATC | 10188 |
rs28491933 | snp | C/G | | | intron-variant | TNK2 | GRCh38.p7 | 3:195874742 | CGCCCACGCACGCTC[C/G]GAGGCACAGGAAGCT | 10188 |
rs28641194 | snp | A/G | | | intron-variant | TNK2 | GRCh38.p7 | 3:195881049 | CAGCAATGCCCCTTG[A/G]AGAGGACACAGGATC | 10188 |
rs28706969 | snp | A/G | 0.488118 | 0.0761554 | intron-variant | TNK2 | GRCh38.p7 | 3:195874605 | ATGGCGCCCACGCAC[A/G]CTCCGAGGCACAAGA | 10188 |
rs28711904 | snp | C/T | | | intron-variant | TNK2 | GRCh38.p7 | 3:195887921 | GCACGTGCATGCGTG[C/T]GTGCACGTGTGTGCG | 10188 |
rs28719688 | snp | A/C | | | intron-variant | TNK2 | GRCh38.p7 | 3:195880577 | ACACCCGCCCCCCAG[A/C]AATGCCCCTCGGAGA | 10188 |
rs28733615 | snp | C/T | 0.0520825 | 0.152737 | intron-variant | TNK2 | GRCh38.p7 | 3:195887931 | GCGTGCGTGCACGTG[C/T]GTGCGCATGTGCGTG | 10188 |
rs34049168 | snp | A/G | 0.364401 | 0.222289 | intron-variant | TNK2 | GRCh38.p7 | 3:195868786 | AGGTGGCACGTGGGA[A/G]AGAAAGCCAAGTGTC | 10188 |
rs34091425 | in-del | -/GAG | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195892679 | TCTGGCAGGGAGCAG[-/GAG]AGCTTTCCTCACGCT | 10188 |
rs34094610 | in-del | -/G | | | frameshift-variant | TNK2 | GRCh38.p7 | 3:195868273 | TGGCTGGGCCCGGCA[-/G]GGGACCCCCGCGCCC | 10188 |
rs34116952 | in-del | -/A | 0 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195904100 | TCTACAGAAAATTCC[-/A]AAAAAAAAATTAGCC | 10188 |
rs34134349 | in-del | -/CT | 0.499396 | 0.0173617 | intron-variant | TNK2 | GRCh38.p7 | 3:195875658 | CGCCCTGTCCGCGCC[-/CT]CTCTCTCCCGCCATG | 10188 |
rs34189351 | snp | C/T | 0.00146332 | 0.0270096 | missense | TNK2 | GRCh38.p7 | 3:195870143 | AGATGCTGGGGGGGC[C/T]GGGAGGTGCTCAGTT | 10188 |
rs34221697 | snp | A/G | 0.0197687 | 0.0974348 | utr-variant-5-prime | TNK2 | GRCh38.p7 | 3:195908561 | GAAGAGGTTCCCGCC[A/G]GCCGCGGCCTGCCCT | 10188 |
rs34284754 | in-del | -/C | | | intron-variant | TNK2 | GRCh38.p7 | 3:195881757 | CGACCCCCAACAATG[-/C]CCCTTGGAGAGGACA | 10188 |
rs34335234 | in-del | -/G | | | intron-variant | TNK2 | GRCh38.p7 | 3:195900187 | GGGGTGCTGGGGCGC[-/G]GGGCTGCCACACAGG | 10188 |
rs34356305 | in-del | -/GT | | | intron-variant | TNK2 | GRCh38.p7 | 3:195887739 | CCTGTGTGTATGTGC[-/GT]GTGTGTGCACACGCG | 10188 |
rs34360390 | in-del | -/C | | | intron-variant | TNK2 | GRCh38.p7 | 3:195894962 | TCCTAAAAGACTGAA[-/C]CCCCAATCCTAGCAG | 10188 |
rs34382127 | snp | C/T | 0.411242 | 0.191052 | intron-variant | TNK2 | GRCh38.p7 | 3:195864989 | AACCACCCGAGACAG[C/T]GACAGACAGGTGACA | 10188 |
rs34436565 | in-del | -/A | | | intron-variant | TNK2 | GRCh38.p7 | 3:195878044 | CTGCAGCCCAGTGGG[-/A]AAAGGGTGGTGGAGG | 10188 |
rs34468408 | snp | A/C | 0.0217236 | 0.101931 | upstream-variant-2KB, intron-variant | TNK2 | GRCh38.p7 | 3:195897034 | CTCCCACCTCCACCT[A/C]CCTCTTCTCCAAGCC | 10188 |
rs34513179 | in-del | -/T | | | intron-variant, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195894427 | CCCCTTTTTTTTTTT[-/T]GAGAGTCTTGCTCTA | 10188 |
rs34526730 | in-del | -/C | | | intron-variant | TNK2 | GRCh38.p7 | 3:195881550 | CCCCCCCCAGCAATG[-/C]CCCTTGAAGAGGACA | 10188 |
rs34665404 | snp | C/G | 0.0268448 | 0.113076 | intron-variant | TNK2 | GRCh38.p7 | 3:195891663 | GCAAAGTGACCCCCC[C/G]CCTCCAGGGCTCAGC | 10188 |
rs34684285 | in-del | -/AG | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195892677 | GGTCTGGCAGGGAGC[-/AG]AGAGCTTTCCTCACG | 10188 |
rs34730376 | in-del | -/C | | | intron-variant | TNK2 | GRCh38.p7 | 3:195877072 | GGTACTTCCAGGGGA[-/C]CCCCCCCACCCTTAA | 10188 |
rs34833157 | in-del | -/C | | | intron-variant, nc-transcript-variant | TNK2, MIR6829 | GRCh38.p7 | 3:195882373 | AGCTGGAGGACCCTG[-/C]CCCTTCTCAGCAGCC | 10188 |
rs34867944 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNK2, MIR6829 | GRCh38.p7 | 3:195882806 | GAGGTTGCAGTGAGC[C/T]TAGATCATGCCATTG | 10188 |
rs34875772 | in-del | -/A | | | intron-variant, downstream-variant-500B | TNK2, MIR6829 | GRCh38.p7 | 3:195881941 | AGGCTTAGAACAGAC[-/A]AAGGGCAGGCCCAAG | 10188 |
rs34893900 | in-del | -/C | | | intron-variant | TNK2 | GRCh38.p7 | 3:195903857 | TAGAAAATCCAAAGG[-/C]AAGTTACAAAAAAGC | 10188 |
rs34999515 | snp | A/G | | | intron-variant | TNK2 | GRCh38.p7 | 3:195870962 | TTCTGGTGTGTGGGG[A/G]CTCGCTGTGTGGGGT | 10188 |
rs35027723 | in-del | -/C | | | intron-variant, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195893639 | CCAGCTGCTCTTACA[-/C]CCCCCTCGCTACGGC | 10188 |
rs35088312 | multinucleotide-polymorphism | AT/CC | | | intron-variant | TNK2 | GRCh38.p7 | 3:195872023 | ATTCCCCTGGAGAAC[AT/CC]TCCCCTGGAGAACCC | 10188 |
rs35122084 | in-del | -/C | | | intron-variant | TNK2 | GRCh38.p7 | 3:195903906 | TAGCAAGACTGCAGG[-/C]ATTCAAGCTCAAAAT | 10188 |
rs35186478 | in-del | -/A | | | intron-variant | TNK2 | GRCh38.p7 | 3:195904262 | TGAGACCTTGTCTTT[-/A]AAAAAAAAAAAAAAA | 10188 |
rs35213237 | in-del | -/G | | | intron-variant | TNK2 | GRCh38.p7 | 3:195901979 | TCTGAAGAAGGGACA[-/G]GGGGTTCCAGGAAAA | 10188 |
rs35224968 | in-del | -/G | | | intron-variant | TNK2 | GRCh38.p7 | 3:195871003 | GGGGGCCCGCTGTGT[-/G]GGGTTCTGGTGTGTG | 10188 |
rs35240998 | in-del | -/C | | | intron-variant, downstream-variant-500B | TNK2, MIR6829 | GRCh38.p7 | 3:195881872 | ACCCTGGCACGTGGG[-/C]CCTCAAGAATTCCTA | 10188 |
rs35259333 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | TNK2 | GRCh38.p7 | 3:195901864 | CAAGGATGCGGGCCC[A/G]TGGAGGTCCCCGCGG | 10188 |
rs35271355 | in-del | -/A | 0.32885 | 0.23724 | intron-variant | TNK2 | GRCh38.p7 | 3:195903009 | CCACCTCGGCCTCCC[-/A]AAAGTACTGGGATTA | 10188 |
rs35325260 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | TNK2 | GRCh38.p7 | 3:195881723 | CCTTGGAGAGGACAC[A/G]GGATCTATCCCTGAA | 10188 |
rs35441969 | snp | A/C | | | intron-variant | TNK2 | GRCh38.p7 | 3:195872037 | CCTCCCCTGGAGAAC[A/C]CTCCCCTGGAGAACA | 10188 |
rs35443697 | snp | A/G | 0.1652 | 0.235179 | intron-variant | TNK2 | GRCh38.p7 | 3:195888227 | CCAGCTTTAGGGAAG[A/G]CCTCACTCTCCTCAA | 10188 |
rs35515602 | in-del | -/G | | | frameshift-variant | TNK2 | GRCh38.p7 | 3:195878531 | TGACGTTGTAGATGT[-/G]CCTGGGGACAGTCCT | 10188 |
rs35538436 | in-del | -/T | | | intron-variant | TNK2 | GRCh38.p7 | 3:195868779 | GAGGGGAGGTGGCAC[-/T]GTGGGAGAGAAAGCC | 10188 |
rs35570456 | snp | C/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | TNK2, MIR6829 | GRCh38.p7 | 3:195882757 | CAGCTACTTGGAAGC[C/T]TGAGGCAGGAATATC | 10188 |
rs35572141 | in-del | -/GTGT | | | intron-variant | TNK2 | GRCh38.p7 | 3:195887836 | GGTGTGCGCACACAC[-/GTGT]GTGTGTGTGTGCGTG | 10188 |
rs35718959 | snp | C/T | | | intron-variant | TNK2 | GRCh38.p7 | 3:195903499 | AGGCGGGCAGGTCAC[C/T]TGAGGTCAGGAGTTT | 10188 |
rs35759128 | snp | A/G | 0.00434739 | 0.0464198 | missense | TNK2 | GRCh38.p7 | 3:195870138 | CTCCTAGATGCTGGG[A/G]GGGCCGGGAGGTGCT | 10188 |
rs35879039 | snp | C/T | 0.444533 | 0.157025 | intron-variant | TNK2 | GRCh38.p7 | 3:195871993 | CTCCCCTGGAGAACC[C/T]TCCCCTGGAGAACAT | 10188 |
rs35946216 | in-del | -/C | | | utr-variant-5-prime, intron-variant | TNK2 | GRCh38.p7 | 3:195895496 | GGCCGGGTGGTCGCG[-/C]CCCTCCTCCTGCCGG | 10188 |
rs35990866 | in-del | -/G | | | upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195909171 | CCTGGTGCTGCCCGC[-/G]GGGCCCCAGCCCCTC | 10188 |
rs35992567 | in-del | -/GA | 0.0221141 | 0.102801 | intron-variant | TNK2 | GRCh38.p7 | 3:195901689 | CGCCAGCTCTTCACT[-/GA]GAGTGTACCTTCACT | 10188 |
rs36080464 | multinucleotide-polymorphism | AA/GC | | | intron-variant | TNK2 | GRCh38.p7 | 3:195878918 | GGTGGGAGGCACGGG[AA/GC]GTGGGGGGAGGCACG | 10188 |
rs55636345 | snp | A/G/T | 1.65359e-05 | 0.00287536 | missense, synonymous-codon, upstream-variant-2KB, utr-variant-5-prime | TNK2, MIR6829 | GRCh38.p7 | 3:195883250 | CTCCCGGATGAAGTC[A/G/T]TCCATGGCTTCTGGC | 10188 |
rs55647828 | snp | C/G | 0.000488269 | 0.0156172 | missense, upstream-variant-2KB, utr-variant-5-prime | TNK2 | GRCh38.p7 | 3:195884903 | CGCAGGTCCTTCTCC[C/G]CAATGAGGCAGGTGA | 10188 |
rs55701110 | snp | A/G | 0.00259789 | 0.0359471 | synonymous-codon | TNK2 | GRCh38.p7 | 3:195879058 | CCTCACCTGACTGCC[A/G]TTGAGGCCGATCCAG | 10188 |
rs55715968 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TNK2 | GRCh38.p7 | 3:195899572 | CCTGACCTCATGATC[C/T]GCCCACCTCAGCCGC | 10188 |
rs55725156 | snp | C/T | 0.5 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195865241 | TCAGTAAGAACCACC[C/T]GAGACAGTGACAGAC | 10188 |
rs55734494 | snp | C/T | 0.000991072 | 0.0222386 | synonymous-codon | TNK2 | GRCh38.p7 | 3:195878587 | CTTGTCGATCTTATG[C/T]AGGATCTGAAGGTGA | 10188 |
rs55752178 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNK2 | GRCh38.p7 | 3:195871918 | GCTCCCCGGAGAACC[C/T]TCCCCTGGAGAACCC | 10188 |
rs55772932 | snp | C/G | 0.5 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195881020 | ACAGTGTCTATCCCT[C/G]TAACACCACCCGCCA | 10188 |
rs55781440 | snp | A/G | 0.48 | 0.0979796 | intron-variant | TNK2 | GRCh38.p7 | 3:195875331 | TCGGAGGCACAGGAA[A/G]CTCCCCCTCGGGATG | 10188 |
rs55800940 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant, upstream-variant-2KB | TNK2, MIR6829 | GRCh38.p7 | 3:195882773 | TGAGGCAGGAATATC[A/G]CGTGAACCCAGGAGG | 10188 |
rs55804249 | in-del | -/C | | | intron-variant | TNK2 | GRCh38.p7 | 3:195880827 | CTGTAACACCCCCCC[-/C]AGCAATGCCCCTTGG | 10188 |
rs55820842 | in-del | -/AG | 0 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195869631 | AGAGGGCAGAGTGTA[-/AG]GAGAGACGAAGGGAG | 10188 |
rs55842111 | snp | A/G | 0.0193296 | 0.0963907 | synonymous-codon | TNK2 | GRCh38.p7 | 3:195878578 | CTCCCCCTCCTTGTC[A/G]ATCTTATGCAGGATC | 10188 |
rs55854417 | snp | C/T | | | intron-variant | TNK2 | GRCh38.p7 | 3:195904219 | GCCATGATCACACCA[C/T]TGCTCTCCGGCCTGG | 10188 |
rs55855604 | snp | A/G | | | intron-variant | TNK2 | GRCh38.p7 | 3:195874611 | CCCACGCACGCTCCG[A/G]GGCACAAGAAGCTCC | 10188 |
rs55886945 | snp | C/G | 0.5 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195875363 | CGCCCACGCACGCTC[C/G]GAGGCACAGGAAACT | 10188 |
rs55920263 | snp | C/G | 0.227369 | 0.248974 | intron-variant | TNK2 | GRCh38.p7 | 3:195865947 | GTGCACAGGGCCACG[C/G]TGCTGGGACAAGGGC | 10188 |
rs55995666 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | TNK2 | GRCh38.p7 | 3:195889773 | AGCGGACCCACCGCA[C/T]AGCAAACCCATCCCT | 10188 |
rs56003471 | snp | A/G | 0.00695353 | 0.0585527 | synonymous-codon, upstream-variant-2KB, utr-variant-5-prime | TNK2 | GRCh38.p7 | 3:195884917 | CCCAATGAGGCAGGT[A/G]AGGCTCTGCAGGGGC | 10188 |
rs56036945 | snp | C/T | 6.59131e-05 | 0.0057404 | missense, utr-variant-5-prime, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195886999 | ATCCACGACTTGCGT[C/T]TGCACAAGGCCTTCC | 10188 |
rs56054753 | snp | A/G | 5.00404e-05 | 0.00500177 | synonymous-codon, upstream-variant-2KB, utr-variant-5-prime | TNK2 | GRCh38.p7 | 3:195884959 | TGGGCCCCCAGGGGC[A/G]GGCGAGGTCTTCCGG | 10188 |
rs56161912 | snp | A/G | 8.15982e-05 | 0.0063869 | missense, upstream-variant-2KB, utr-variant-5-prime | TNK2 | GRCh38.p7 | 3:195884813 | CACAGAGAGCTCACC[A/G]TCTTCCCTGAGGGCG | 10188 |
rs56190948 | snp | A/G | 0.00263487 | 0.0362007 | synonymous-codon, utr-variant-5-prime | TNK2 | GRCh38.p7 | 3:195888496 | GGACAGGCGGGTGAC[A/G]TTGAGGTCATCTCGG | 10188 |
rs56204861 | snp | A/C/G | 0.0134861 | 0.0810011 | intron-variant | TNK2 | GRCh38.p7 | 3:195871917 | CGCTCCCCGGAGAAC[A/C/G]CTCCCCTGGAGAACC | 10188 |
rs56230425 | in-del | -/CC | | | intron-variant | TNK2 | GRCh38.p7 | 3:195880520 | GTAACACCCCCCCCC[-/CC]AGCAATGCCCCTTGG | 10188 |
rs56251144 | snp | A/C | 0.444533 | 0.157025 | intron-variant | TNK2 | GRCh38.p7 | 3:195871992 | CCTCCCCTGGAGAAC[A/C]CTCCCCTGGAGAACA | 10188 |
rs56260729 | snp | A/G | 0.352712 | 0.227926 | missense | TNK2 | GRCh38.p7 | 3:195868079 | CTGGGAGAGGGGGCC[A/G]GGGAGCCGGCCGGAG | 10188 |
rs56261799 | snp | G/T | 0.426966 | 0.176587 | upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195910366 | GAAAACCCAGCGCTC[G/T]GATTCCCAGCGGCGG | 10188 |
rs56289265 | snp | A/G | 3.31038e-05 | 0.00406827 | synonymous-codon, upstream-variant-2KB, utr-variant-5-prime | TNK2, MIR6829 | GRCh38.p7 | 3:195883214 | GAGGTTTCGGTGGTC[A/G]AGCGAGTGCATGGCA | 10188 |
rs56311748 | snp | A/G | 0.243633 | 0.249919 | intron-variant | TNK2 | GRCh38.p7 | 3:195875417 | ACGCTCCGAGGCACA[A/G]GAAGCTCCCCCTCGG | 10188 |
rs56329545 | in-del | -/TC | | | intron-variant | TNK2 | GRCh38.p7 | 3:195875665 | TCCGCGCCCTCTCTC[-/TC]CCGCCATGAACAGGC | 10188 |
rs56401727 | snp | C/G | 0.218151 | 0.247963 | upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195909929 | GCCTTCCTGCGGTGC[C/G]GAGGAGCGGTGGCGC | 10188 |
rs57229082 | in-del | -/C | | | intron-variant | TNK2 | GRCh38.p7 | 3:195875072 | CACAAGAAACTCCCC[-/C]TCGGGATGGCGCCCA | 10188 |
rs57254604 | in-del | -/TG | | | intron-variant | TNK2 | GRCh38.p7 | 3:195887746 | GTATGTGCGTGTGTG[-/TG]CACACGCGTGTGCGC | 10188 |
rs57282579 | snp | C/G | 0.5 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195874919 | CGCCCACGCACGCTC[C/G]GAGGCACAAGAAGCT | 10188 |
rs57419976 | snp | A/G | | | intron-variant | TNK2 | GRCh38.p7 | 3:195874976 | TCCGAGGCACAAGAA[A/G]CTCCCCTCGGGATGG | 10188 |
rs57692480 | in-del | -/CCCCACCCCCC | | | intron-variant, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195897825 | ACCCCCCCACCCCCC[-/CCCCACCCCCC]GCCCCCAGCTTCTTA | 10188 |
rs57820533 | snp | A/T | 0.163236 | 0.234461 | intron-variant, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195894415 | AGGCCGGCTCCTGGA[A/T]CCCCCACCCCCTTTT | 10188 |
rs57872314 | snp | C/T | 0.00116473 | 0.0241041 | missense | TNK2 | GRCh38.p7 | 3:195868010 | TGTGGGCGCGTGGGC[C/T]GAGGGGGGATGGGTA | 10188 |
rs58049606 | snp | A/G | 0.385932 | 0.209815 | intron-variant | TNK2 | GRCh38.p7 | 3:195901011 | GGGAAGTGAACATTC[A/G]GTCTACAAGATACAC | 10188 |
rs58113480 | in-del | -/GTGTGT | | | intron-variant | TNK2 | GRCh38.p7 | 3:195887970 | CGTGTGTGTGTGTGT[-/GTGTGT]ATGCCTGTGCGTGTG | 10188 |
rs58308269 | snp | C/T | 0.462363 | 0.131916 | intron-variant | TNK2 | GRCh38.p7 | 3:195888901 | ATCAACCTGTGCTCA[C/T]ATTCCTGCTCTAAGT | 10188 |
rs58321048 | snp | A/C | | | intron-variant | TNK2 | GRCh38.p7 | 3:195902629 | TCTCAAAAAAAAAAA[A/C]CAAAAAAAAACAAAC | 10188 |
rs58347397 | snp | A/G | 0 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195874843 | TCCGAGGCACAAGAA[A/G]CTCCCCTCGGGATGG | 10188 |
rs58431049 | in-del | -/TT | | | intron-variant | TNK2 | GRCh38.p7 | 3:195890473 | TTTTTTTTTTTTTTT[-/TT]GAGACAGAGTGAGAC | 10188 |
rs58467562 | snp | A/G | 0 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195875048 | ATGGCGCCCACGCAC[A/G]CTCGGAGGCACAGGA | 10188 |
rs58613248 | in-del | -/TG | | | intron-variant | TNK2 | GRCh38.p7 | 3:195887849 | ACGTGTGTGTGTGTG[-/TG]CGTGTCTGTGTGCGC | 10188 |
rs58874508 | in-del | -/T | | | intron-variant | TNK2 | GRCh38.p7 | 3:195871954 | TGGAGAACATTCCCC[-/T]GGAGAACCCTCCCCT | 10188 |
rs58890236 | in-del | -/C | 0 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195875383 | CACAAGAAACTCCCC[-/C]TCGGGATGGCGCCCA | 10188 |
rs58959832 | in-del | -/C | | | intron-variant | TNK2 | GRCh38.p7 | 3:195875205 | CACAAGAAACTCCCC[-/C]TCGGGATGGCGCCCA | 10188 |
rs59022470 | in-del | -/TGTGCACGTGCATGCGTG | | | intron-variant | TNK2 | GRCh38.p7 | 3:195887903 | GCACGTGCATGCGTG[-/TGTGCACGTGCATGCGTG]CGTGCACGTGTGTGC | 10188 |
rs59178606 | snp | A/G | 0.167484 | 0.23599 | intron-variant | TNK2 | GRCh38.p7 | 3:195898665 | GGGTCTTGCTCTGTT[A/G]CCCAGGCTGGAGTGC | 10188 |
rs59229384 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | TNK2 | GRCh38.p7 | 3:195906490 | AACTCCAAAATACTT[C/T]TGTTGAATGAAAGAC | 10188 |
rs59851848 | snp | C/G | 0.25634 | 0.24992 | intron-variant | TNK2 | GRCh38.p7 | 3:195888082 | TCCCTACAGATCTCT[C/G]CACATGGACCCCCCG | 10188 |
rs60002031 | snp | A/G | 0 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195881139 | AACACCCCCCCAGCA[A/G]TGCCCCTTGGAGAGG | 10188 |
rs60167945 | in-del | -/AA | | | intron-variant | TNK2 | GRCh38.p7 | 3:195902660 | ATAAAAAAAAAAAAA[-/AA]CACCTCTCAGCAAAG | 10188 |
rs60186332 | snp | G/T | 0.176219 | 0.238865 | intron-variant, downstream-variant-500B | TNK2 | GRCh38.p7 | 3:195866419 | TTGGCCAGGCTGGTC[G/T]CGAACTCCTGACCTC | 10188 |
rs60221201 | in-del | -/GT | 0.426047 | 0.177503 | intron-variant | TNK2 | GRCh38.p7 | 3:195887782 | TGCGCGCGTGTGTGT[-/GT]ACATGTGTGTATGCC | 10188 |
rs60377054 | in-del | -/T | | | intron-variant | TNK2 | GRCh38.p7 | 3:195871909 | TGGAGAACGCTCCCC[-/T]GGAGAACCCTCCCCT | 10188 |
rs60454220 | snp | A/G | 0 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195875020 | TCCGAGGCACAAGAA[A/G]CTCCCCCTCGGGATG | 10188 |
rs60500503 | snp | A/G | 0 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195874795 | ACGCTCCGAGGCACA[A/G]GAAGCTCCCCTCGGG | 10188 |
rs60565985 | in-del | -/GT | | | intron-variant | TNK2 | GRCh38.p7 | 3:195887854 | TGTGTGTGTGTGCGT[-/GT]CTGTGTGCGCAGGCG | 10188 |
rs60684695 | in-del | -/GC | | | intron-variant | TNK2 | GRCh38.p7 | 3:195880771 | ATCCCTGTAACACCC[-/GC]CCCCCAGCAATGCCC | 10188 |
rs60876752 | snp | A/G | | | intron-variant | TNK2 | GRCh38.p7 | 3:195875287 | TCCGAGGCACACGAA[A/G]CTCCCCTCGGGATGG | 10188 |
rs60933312 | snp | A/G | 0.277778 | 0.248452 | intron-variant | TNK2 | GRCh38.p7 | 3:195874826 | ATGGCGCCCACGCAC[A/G]CTCCGAGGCACAAGA | 10188 |
rs60997729 | snp | A/G | 0.375 | 0.216506 | intron-variant | TNK2 | GRCh38.p7 | 3:195875239 | ACGCTCCGAGGCACA[A/G]GAAGCTCCCCTCGGG | 10188 |
rs61007721 | in-del | -/TGTG | | | intron-variant | TNK2 | GRCh38.p7 | 3:195887847 | ACACGTGTGTGTGTG[-/TGTG]CGTGTCTGTGTGCGC | 10188 |
rs61058949 | snp | A/C | 0.314057 | 0.241654 | intron-variant | TNK2 | GRCh38.p7 | 3:195905808 | ATTAATCAAAATTTA[A/C]AACTTCTCTTCAAAA | 10188 |
rs61137304 | in-del | -/GT | 0.5 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195887956 | TGCGTGTGTGCCTGC[-/GT]GTGTGTGTGTGTGTG | 10188 |
rs61150851 | in-del | -/C | | | intron-variant | TNK2 | GRCh38.p7 | 3:195875334 | GAGGCACAAGAAACT[-/C]CCCCTCGGGATGGCG | 10188 |
rs61218216 | snp | C/G | 0.279461 | 0.248258 | intron-variant | TNK2 | GRCh38.p7 | 3:195906306 | TACCACATGACCCAG[C/G]CATTCCGGTCCTAGG | 10188 |
rs61220086 | snp | A/G | 0.5 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195874964 | GCCCACGCACACTCC[A/G]AGGCACAAGAAGCTC | 10188 |
rs61230253 | snp | A/G | 0.5 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195875154 | TCCGAGGCACAAGAA[A/G]CTCCCCTCGGGATGG | 10188 |
rs61248803 | snp | A/G | 0.148661 | 0.22854 | intron-variant | TNK2 | GRCh38.p7 | 3:195899552 | GGCCAGGATGGTCTC[A/G]ATCTCCTGACCTCAT | 10188 |
rs61378818 | snp | A/C | | | intron-variant | TNK2 | GRCh38.p7 | 3:195902630 | CTCAAAAAAAAAAAA[A/C]AAAAAAAAACAAACA | 10188 |
rs62283329 | snp | C/T | 0.0167194 | 0.0898897 | synonymous-codon | TNK2 | GRCh38.p7 | 3:195868090 | GGCCGGGGAGCCGGC[C/T]GGAGCCTGCAGTTGC | 10188 |
rs62283330 | snp | A/G | 0.25045 | 0.25 | intron-variant | TNK2 | GRCh38.p7 | 3:195869366 | TAGGCCAGGGCAGCC[A/G]CGGAAGCTCACAGCA | 10188 |
rs62283331 | snp | C/G | 0.5 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195873473 | AGGCGGGGGCGGTGA[C/G]AGCCCCGTGGGCAGT | 10188 |
rs62283332 | snp | G/T | 0.5 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195878354 | GGGCTGGGCCTGGAG[G/T]AAGAGGAAGGTCGTG | 10188 |
rs62283334 | snp | C/T | 0.261056 | 0.249755 | intron-variant, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195897613 | CTCAAGCAATCCTCC[C/T]GCCTCCATCTCCTGA | 10188 |
rs62283337 | snp | C/T | 0.5 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195907087 | AAGGCCTTTCTCCCA[C/T]TCATCTACCACAAGT | 10188 |
rs62283338 | snp | C/G | 0.271432 | 0.24908 | intron-variant | TNK2 | GRCh38.p7 | 3:195907433 | GGTCCATCTGACTCA[C/G]AGCCACACCTCGGGC | 10188 |
rs67488570 | in-del | -/GT | | | intron-variant | TNK2 | GRCh38.p7 | 3:195887836 | GGTGTGCGCACACAC[-/GT]GTGTGTGTGTGTGCG | 10188 |
rs67747403 | snp | A/G | 0.375 | 0.216506 | intron-variant | TNK2 | GRCh38.p7 | 3:195875372 | ACGCTCGGAGGCACA[A/G]GAAACTCCCCCTCGG | 10188 |
rs67947627 | in-del | -/G | | | intron-variant | TNK2 | GRCh38.p7 | 3:195870973 | GACTCGCTGTGTGGG[-/G]TTCTGGTGTGTGGGG | 10188 |
rs71180978 | in-del | -/TTCTGGTGTGTGGGGGCCCGCTGTGTGGG | 0 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195871034 | GGCCCGCTGTGTGGG[lengthTooLong]GTTCTGGTGTGTGGG | 10188 |
rs71180980 | in-del | -/GAGCCCCGTGGGCAGTGTCTGGGCAGGCGGGGGCGGTGA | 0 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195873511 | AGGCGGGGGCGGTGA[lengthTooLong]CAGCCCCGTGGGCAG | 10188 |
rs71180982 | in-del | -/C | 0.166832 | 0.235761 | intron-variant | TNK2 | GRCh38.p7 | 3:195875656 | CGCCCTGTCCGCGCC[-/C]TTCTCTCCCGCCATG | 10188 |
rs71180983 | in-del | -/C | 0.166832 | 0.235761 | intron-variant | TNK2 | GRCh38.p7 | 3:195875660 | CCCTGTCCGCGCCCT[-/C]CTCTCTCCCGCCATG | 10188 |
rs71274258 | in-del | -/T | 0.5 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195904280 | TGGATTGCTTTCACC[-/T]TTTTTTTTTTTTTTT | 10188 |
rs71321858 | snp | A/G | 0.5 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195875421 | TCCGAGGCACAAGAA[A/G]CTCCCCCTCGGGATG | 10188 |
rs71321859 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TNK2 | GRCh38.p7 | 3:195875691 | ACAGGCCGGAGTCCC[C/T]GTGGCCATGGGAGGG | 10188 |
rs71321860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNK2, MIR6829 | GRCh38.p7 | 3:195883645 | TTTTGAGACAGTCTC[A/G]CTCTTGTCGCCCAGG | 10188 |
rs71321861 | snp | A/G | 0.5 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195890819 | ATTCAGAACATAGCA[A/G]AAGTCCACTATTTGC | 10188 |
rs71321862 | snp | C/T | 0.0863743 | 0.189015 | utr-variant-5-prime, intron-variant | TNK2 | GRCh38.p7 | 3:195895427 | AGCATCCTCCAGAAG[C/T]GCAGGGCCGCTACTG | 10188 |
rs71321863 | snp | A/G | 0.02016 | 0.0983543 | upstream-variant-2KB, intron-variant | TNK2 | GRCh38.p7 | 3:195897522 | TTTGTTTGTTTGTTT[A/G]AGATAGGATCTCACT | 10188 |
rs71321864 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195909996 | ATGGAGGAGCGCCGG[A/G]ACAGGTCTCTCATTC | 10188 |
rs71617326 | snp | C/T | 0 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195875024 | AGGCACAAGAAACTC[C/T]CCCTCGGGATGGCGC | 10188 |
rs71617327 | snp | A/G | 0 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195875106 | ACGCTCCGAGGCACA[A/G]GAAGCTCCCCCTCGG | 10188 |
rs71637188 | in-del | -/AG | 0.421526 | 0.181876 | intron-variant | TNK2 | GRCh38.p7 | 3:195869630 | GAGAGGGCAGAGTGT[-/AG]TAGAGAGACGAAGGG | 10188 |
rs71637189 | in-del | -/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | TNK2, MIR6829 | GRCh38.p7 | 3:195883648 | GAGACAGTCTCACTC[-/T]TTGTCGCCCAGGCTG | 10188 |
rs71934963 | in-del | -/TG | | | intron-variant | TNK2 | GRCh38.p7 | 3:195887963 | GTGCCTGCGTGTGTG[-/TG]TGTGTGTGTGTATGC | 10188 |
rs73087325 | snp | C/T | 0.180064 | 0.240019 | intron-variant | TNK2 | GRCh38.p7 | 3:195873154 | TCAGGAGGGGCTCTA[C/T]CTGTGTCCAAAAGGG | 10188 |
rs73087332 | snp | C/T | 0.5 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195881675 | GAGAGGACACAGCAT[C/T]TATCCCTATAACACC | 10188 |
rs73087335 | snp | A/C/G | 0.109814 | 0.206997 | intron-variant | TNK2 | GRCh38.p7 | 3:195887956 | TGCGTGTGTGCCTGC[A/C/G]TGTGTGTGTGTGTGT | 10188 |
rs73087352 | snp | C/T | 0.303688 | 0.244167 | intron-variant | TNK2 | GRCh38.p7 | 3:195907373 | CAGCACCACTCCCTC[C/T]GCCCCCAGAGGAGAG | 10188 |
rs73087353 | snp | C/T | 0.151334 | 0.229706 | intron-variant | TNK2 | GRCh38.p7 | 3:195908138 | ACCATGCAGAGCATA[C/T]AGCATGGAGGCACCC | 10188 |
rs73087356 | snp | C/G | 0.304688 | 0.243945 | utr-variant-5-prime, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195908984 | TCCCACTGCCGCTCC[C/G]CCAGTTCGCCGGAAC | 10188 |
rs73205788 | snp | A/T | 0.039522 | 0.134904 | intron-variant | TNK2 | GRCh38.p7 | 3:195865720 | GACAGTATGGGACAG[A/T]CAGGTGACAGGGAGT | 10188 |
rs73205792 | snp | C/G/T | 0.0146672 | 0.084371 | intron-variant | TNK2 | GRCh38.p7 | 3:195874435 | CACCACTCGAGAAAA[C/G/T]ATGCTTGCTCCTGGG | 10188 |
rs73205793 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNK2 | GRCh38.p7 | 3:195877944 | GCAGAGGAGGAAGCA[C/T]GGGAGTCCAGAACTC | 10188 |
rs73205796 | snp | C/T | 0.273049 | 0.248935 | intron-variant, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195893166 | CTCCGCTGGGCCCTG[C/T]GATGACTCCTCAGAG | 10188 |
rs73205797 | snp | A/G | 0.050192 | 0.150256 | upstream-variant-2KB, intron-variant | TNK2 | GRCh38.p7 | 3:195896252 | TCTGAAGCAGCCACT[A/G]ACTCTTTAGTACCAG | 10188 |
rs73205799 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TNK2 | GRCh38.p7 | 3:195900377 | GGGAATGTCACTTGA[A/G]AGAGGAGGGGTGAGG | 10188 |
rs73891159 | snp | C/T | 0.195214 | 0.243923 | downstream-variant-500B | TNK2 | GRCh38.p7 | 3:195862919 | GGAAGTGGACGGCCG[C/T]GGTGGGTGATACCCA | 10188 |
rs73891160 | snp | C/G | 0.193028 | 0.243422 | intron-variant, downstream-variant-500B | TNK2 | GRCh38.p7 | 3:195866806 | GGAGCGGCCTGCGAG[C/G]TGTTGGGCTTCCTCC | 10188 |
rs73891162 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | TNK2 | GRCh38.p7 | 3:195868946 | CCGGTGAGCCCCGCC[C/T]CGCTCCGTCTAAGCT | 10188 |
rs73891165 | snp | A/G | 0.0252325 | 0.109451 | intron-variant, upstream-variant-2KB | TNK2, MIR6829 | GRCh38.p7 | 3:195882960 | CACCAGCAAAATCCA[A/G]AGACAGACCCGGACT | 10188 |
rs73891166 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195886869 | AAGTGCCGGCAGAAC[A/G]GCGAGATTCGACCTG | 10188 |
rs73891168 | snp | C/T | 0.0252325 | 0.109451 | intron-variant, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195892818 | CCCTCTTGCCTGCCT[C/T]TCTCTCTCCCTCTCT | 10188 |
rs73891170 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant, upstream-variant-2KB, missense | TNK2 | GRCh38.p7 | 3:195894335 | GATGTCCAGTAAGAA[C/T]AAGACCTGTAACTGG | 10188 |
rs73891171 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TNK2 | GRCh38.p7 | 3:195902212 | AGACACTTGACTGAC[C/T]GCCTGCAATCCTCAA | 10188 |
rs73891172 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | TNK2 | GRCh38.p7 | 3:195904747 | GAAAAACCAGTATCA[A/T]TTACAATAGCATAAA | 10188 |
rs73891174 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | TNK2 | GRCh38.p7 | 3:195908373 | CTTCCTCCCTCCAGG[A/G]ATGAAAGGCCAAAAG | 10188 |
rs73891175 | snp | C/T | 0.077417 | 0.180873 | utr-variant-5-prime | TNK2 | GRCh38.p7 | 3:195908584 | CCTGCCCTCAGGCAG[C/T]GGCTCCCAGAGCTCA | 10188 |
rs74394633 | snp | C/G | 0.5 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195899038 | GAGGCGGAGGTTGCA[C/G]TGAGCCAAGATCGTA | 10188 |
rs74435345 | snp | A/G | 0.176861 | 0.239062 | intron-variant, upstream-variant-2KB | TNK2, MIR6829 | GRCh38.p7 | 3:195883872 | TTGCTGTAGAAGGAA[A/G]ATGCTGTAAATGTAA | 10188 |
rs74436494 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TNK2 | GRCh38.p7 | 3:195889159 | CAAAGACCACTCCAC[C/G]GGCCACCACTCAAGT | 10188 |
rs74450868 | snp | C/T | 0.167158 | 0.235875 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | TNK2 | GRCh38.p7 | 3:195895682 | ACTCAGCCCTCAGCC[C/T]GCCTCCAGGGCCCCA | 10188 |
rs74555607 | snp | A/G | 0.152334 | 0.230133 | intron-variant | TNK2 | GRCh38.p7 | 3:195874450 | CATGCTTGCTCCTGG[A/G]GGAAGGAGAGTAAGA | 10188 |
rs74653172 | in-del | -/CC | | | intron-variant, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195897827 | CCCCCCACCCCCCCC[-/CC]ACCCCCCGCCCCCAG | 10188 |
rs74662466 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | TNK2 | GRCh38.p7 | 3:195901510 | CAGCTGGGGGGCCCA[C/G]GAGGTACAGCTGCTG | 10188 |
rs74749130 | snp | A/G | 0.188631 | 0.242351 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195892705 | ACGCTGGCTGCAGCC[A/G]GGATCCTCTGTCCTG | 10188 |
rs74858518 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TNK2 | GRCh38.p7 | 3:195901676 | GGAAGACACTATGCG[C/T]CAGCTCTTCACTGAG | 10188 |
rs74861414 | snp | C/G | 0.0345262 | 0.126772 | intron-variant, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195893937 | CTGGTCTAACTCCAG[C/G]AGGTGGGGAGAAGGA | 10188 |
rs74940023 | snp | A/G | 0.444444 | 0.157135 | intron-variant | TNK2 | GRCh38.p7 | 3:195874928 | ACGCTCCGAGGCACA[A/G]GAAGCTCCCCTCGGG | 10188 |
rs74988592 | snp | A/G | | | intron-variant, downstream-variant-500B | TNK2 | GRCh38.p7 | 3:195866479 | GTGCTGGGGATTACA[A/G]CCATGAGCCACGGTG | 10188 |
rs74994370 | snp | A/C | 0 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195902618 | GCAAGACTCCGTCTC[A/C]AAAAAAAAAAACAAA | 10188 |
rs75025075 | snp | G/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | TNK2, MIR6829 | GRCh38.p7 | 3:195883633 | TGGAATTTTTTTTTT[G/T]GAGACAGTCTCGCTC | 10188 |
rs75030861 | snp | A/G/T | 0.00028672 | 0.0119704 | synonymous-codon, missense | TNK2 | GRCh38.p7 | 3:195867912 | GGGACAGGGGCTCCC[A/G/T]CGGAGGCACCCGGGG | 10188 |
rs75037234 | snp | C/T | 0.031825 | 0.122064 | intron-variant | TNK2 | GRCh38.p7 | 3:195868944 | GGCCGGTGAGCCCCG[C/T]CTCGCTCCGTCTAAG | 10188 |
rs75070205 | snp | C/T | 0.188946 | 0.24243 | intron-variant | TNK2 | GRCh38.p7 | 3:195877550 | CTTCCTGGTCCTCAA[C/T]ACTGCCCCTGCCTCA | 10188 |
rs75103579 | snp | A/T | 0.0452528 | 0.143452 | intron-variant | TNK2 | GRCh38.p7 | 3:195898472 | GGGCCCTTCCCTCAG[A/T]CCTCGAGGGCCCAAT | 10188 |
rs75152364 | snp | G/T | | | intron-variant | TNK2 | GRCh38.p7 | 3:195904510 | GTCAGAAGGTAAAAT[G/T]GTGGTTCTCAGGGGC | 10188 |
rs75216796 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | TNK2 | GRCh38.p7 | 3:195887960 | TGTGTGCCTGCGTGT[A/G]TGTGTGTGTGTGTGT | 10188 |
rs75244312 | snp | A/G | 0.5 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195880986 | ACACCCGCCCCCAGC[A/G]ATGCCCCTTGGAGAG | 10188 |
rs75321560 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | TNK2 | GRCh38.p7 | 3:195891558 | GCGTCGTGGCTTTCC[A/G]GAAGCAAGCCCAGAG | 10188 |
rs75417972 | snp | C/T | 0.258843 | 0.249844 | intron-variant | TNK2 | GRCh38.p7 | 3:195906564 | CAGAAAGTAGACCAG[C/T]CTGTTACCTGGGGTA | 10188 |
rs75454932 | in-del | -/GCCGGGG | | | intron-variant, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195894185 | ACCCAGGGACCGGGG[-/GCCGGGG]AACAATTTAAGCAGG | 10188 |
rs75489217 | snp | C/G | 0.5 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195888053 | ATCAGCAAACCATCT[C/G]AGAGTTAGCGTTCTC | 10188 |
rs75541004 | snp | G/T | 0.0479149 | 0.147179 | intron-variant | TNK2 | GRCh38.p7 | 3:195887747 | TATGTGCGTGTGTGT[G/T]CACACGCGTGTGCGC | 10188 |
rs75648564 | snp | A/G | 0 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195874932 | TCCGAGGCACAGGAA[A/G]CTCCCCTCGGGATGG | 10188 |
rs75701106 | snp | C/G | 0 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195874653 | CGCCCACGCACACTC[C/G]GAGGCACAAGAAGCT | 10188 |
rs75861841 | snp | C/G | 0.23846 | 0.249734 | intron-variant | TNK2 | GRCh38.p7 | 3:195889505 | CGGACGCTTCAGACT[C/G]TGTTGTCCCTACACG | 10188 |
rs75977711 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TNK2 | GRCh38.p7 | 3:195870739 | ATTAAAGCCTGGAGG[A/C]ATGGGGCTGGGCTGG | 10188 |
rs76007885 | snp | C/T | 0.189261 | 0.242509 | intron-variant | TNK2 | GRCh38.p7 | 3:195891168 | TCACAGCTGTAATCC[C/T]AGCACTTAGGCTGAG | 10188 |
rs76104732 | snp | A/G | 0.5 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195874887 | TCCGAGGCACAAGAA[A/G]CTCCCCCTCGGGATG | 10188 |
rs76106876 | snp | G/T | 0.0659589 | 0.169201 | utr-variant-3-prime | TNK2 | GRCh38.p7 | 3:195864010 | CGCTGGTGCAGGAGG[G/T]ATGGGCAGGGCAGGG | 10188 |
rs76153126 | snp | A/G | 0.167484 | 0.23599 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | TNK2 | GRCh38.p7 | 3:195895624 | GGGCTGACCCCCACC[A/G]AGAGCCGGGGCTCTG | 10188 |
rs76580747 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | TNK2 | GRCh38.p7 | 3:195904403 | AATGAACCTTGAATA[C/T]GCTAGGCCGAGGTGA | 10188 |
rs76674096 | snp | A/G | 0.5 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195874649 | ATGGCGCCCACGCAC[A/G]CTCCGAGGCACAAGA | 10188 |
rs76833542 | snp | C/T | 0.0513262 | 0.151752 | intron-variant | TNK2 | GRCh38.p7 | 3:195906925 | AGGCTCCAAAGGGCC[C/T]GAGGTTTCTTTACTC | 10188 |
rs76835790 | snp | A/C | 0 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195874972 | ACGCTCCGAGGCACA[A/C]GAAGCTCCCCTCGGG | 10188 |
rs76861300 | snp | C/G | 0.5 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195873498 | GGCAGTGTCTGGGCA[C/G]GCGGGGGCGGTGACA | 10188 |
rs77456141 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195893564 | ACTCCATCAAGCCCC[C/T]GTGGGGCCCTCATGT | 10188 |
rs77690405 | snp | A/G | 0.0524604 | 0.153226 | intron-variant | TNK2 | GRCh38.p7 | 3:195904009 | CATAACAGCATTACT[A/G]ACAACAGCCAAAAGG | 10188 |
rs77750212 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TNK2 | GRCh38.p7 | 3:195864300 | AAGCTGGCAGTCCCC[A/G]GCAAGGACTGTAAAA | 10188 |
rs77828245 | snp | A/G | 0.273318 | 0.24891 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | TNK2 | GRCh38.p7 | 3:195895745 | GTCCCCCGTATTCAC[A/G]GTAAGGGGCCATCCG | 10188 |
rs78025742 | snp | A/G | 0.147321 | 0.227941 | intron-variant | TNK2 | GRCh38.p7 | 3:195881506 | CAGCAACGCCCCTTG[A/G]AGAGGACACGGCATC | 10188 |
rs78025818 | snp | A/G | 0 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195875065 | TCGGAGGCACAGGAA[A/G]CTCCCCCTCGGGATG | 10188 |
rs78226512 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TNK2 | GRCh38.p7 | 3:195908423 | CTACGCTCTCGCCAG[A/G]GACCTGCAGCCTCTC | 10188 |
rs78292793 | snp | C/T | 0.118235 | 0.212457 | intron-variant | TNK2 | GRCh38.p7 | 3:195868830 | CCACTCCCAACTCCC[C/T]CCGAGGTCTGAGGTC | 10188 |
rs78304653 | snp | A/G | 0.00499351 | 0.0497174 | intron-variant, utr-variant-5-prime, missense | TNK2 | GRCh38.p7 | 3:195892511 | CAGCGGGACCCCCCC[A/G]AGCAGTCACTGGGGA | 10188 |
rs78461454 | snp | G/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | TNK2, MIR6829 | GRCh38.p7 | 3:195883634 | GGAATTTTTTTTTTT[G/T]AGACAGTCTCGCTCT | 10188 |
rs78539539 | snp | C/G | 0.0193772 | 0.0965046 | upstream-variant-2KB, intron-variant | TNK2 | GRCh38.p7 | 3:195896777 | CACCCCACGTGTACA[C/G]CCCCTCTGCTCTTCA | 10188 |
rs78596878 | snp | C/G | 0.5 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195869764 | GGGAGATGGAGGAGG[C/G]CCCAGGCAGAGCCGG | 10188 |
rs78621228 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TNK2 | GRCh38.p7 | 3:195899863 | TTTGTGAGGAACACT[G/T]GAGAACGGTGGCTGC | 10188 |
rs78741259 | snp | G/T | 0 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195890472 | TTTTTTTTTTTTTTT[G/T]TTGAGACAGAGTGAG | 10188 |
rs78765789 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | TNK2 | GRCh38.p7 | 3:195871434 | CCATGTGGACCTGCA[C/T]ACATCCCCAGGGCCT | 10188 |
rs79051401 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | TNK2 | GRCh38.p7 | 3:195901019 | AACATTCAGTCTACA[A/G]GATACACTGCTCATT | 10188 |
rs79057146 | snp | G/T | 0.165527 | 0.235296 | intron-variant | TNK2 | GRCh38.p7 | 3:195904228 | ACACCACTGCTCTCC[G/T]GCCTGGGAGACAGAG | 10188 |
rs79229020 | snp | C/T | 0.298144 | 0.245321 | intron-variant, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195894633 | GTCTCAGGTGATCTG[C/T]CCGCCTCGGCCTCCC | 10188 |
rs79264848 | snp | A/G | 0.5 | 0 | missense | TNK2 | GRCh38.p7 | 3:195878313 | TTGTCCGGTTCCTCA[A/G]AGTCCTGAAGGGCCC | 10188 |
rs79375363 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | TNK2 | GRCh38.p7 | 3:195887959 | GTGTGTGCCTGCGTG[C/T]GTGTGTGTGTGTGTG | 10188 |
rs79411036 | snp | A/T | 0.5 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195873488 | GAGCCCCGTGGGCAG[A/T]GTCTGGGCAGGCGGG | 10188 |
rs79414530 | snp | C/G | 0.0256215 | 0.110247 | upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195909905 | CCGACTCCCCCGGGC[C/G]CGGCCTGCGCCTTCC | 10188 |
rs79566675 | snp | A/G | 0.030665 | 0.119967 | intron-variant | TNK2 | GRCh38.p7 | 3:195870770 | CCACAGCATGCCAGG[A/G]GTGGGGCAGAGGGCA | 10188 |
rs79719455 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TNK2 | GRCh38.p7 | 3:195900135 | AGGGAGAGCCTGACA[C/T]TGGTCTTAAGGAAGG | 10188 |
rs79836672 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | TNK2 | GRCh38.p7 | 3:195872956 | AGGTGCGGGGGTGCC[A/G]GGGGACACCTAGGGC | 10188 |
rs79846907 | snp | C/T | 0.5 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195881009 | TTGGAGAGGACACAG[C/T]GTCTATCCCTCTAAC | 10188 |
rs80040883 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | TNK2 | GRCh38.p7 | 3:195877797 | AGGCAGGCCTGGGAG[C/G]GGGTGGTGGGCTCAG | 10188 |
rs80062149 | snp | C/T | 0.0108067 | 0.0727088 | intron-variant | TNK2 | GRCh38.p7 | 3:195870449 | CAGGGACTCCAACTA[C/T]ACCCTACAAGGGCAG | 10188 |
rs80062592 | snp | A/G | 0.46875 | 0.121031 | intron-variant | TNK2 | GRCh38.p7 | 3:195875462 | ACGCTCGGAGGCACA[A/G]GAAGCTCCCCCTCGG | 10188 |
rs80090804 | snp | C/T | 0.157642 | 0.232314 | upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195910763 | TAAATTATCTAACAC[C/T]GCCAGTAATGGCAGC | 10188 |
rs80167201 | snp | A/C | | | missense | TNK2 | GRCh38.p7 | 3:195867597 | AGCCCCGAGGAGCCT[A/C]CCCCCCTGCCTGTGC | 10188 |
rs80189052 | snp | A/T | 0.0505692 | 0.150756 | upstream-variant-2KB, intron-variant | TNK2 | GRCh38.p7 | 3:195896617 | CCTCCCTTCTTGCCC[A/T]GGCTGGATAAAGGAT | 10188 |
rs80298024 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | TNK2 | GRCh38.p7 | 3:195904120 | AAAATTAGCCAGGCA[C/T]GGTGGTACACACCTG | 10188 |
rs80317236 | snp | A/C | 0 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195902617 | AGCAAGACTCCGTCT[A/C]AAAAAAAAAAAACAA | 10188 |
rs111283176 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNK2 | GRCh38.p7 | 3:195880688 | CTCAGCAATGACCCT[C/T]GGAGAGGACACAGCA | 10188 |
rs111326019 | snp | A/G | | | intron-variant | TNK2 | GRCh38.p7 | 3:195880874 | AACCCTGTAACACCC[A/G]CCCCCCAGCAATGCC | 10188 |
rs111407333 | snp | C/T | 0.5 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195865306 | TCAGTAAGAACCACC[C/T]GAGACAGTGACAGAC | 10188 |
rs111447911 | snp | C/T | 0.5 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195872719 | CCTATGGTTTGCAAA[C/T]AAGGAGGCACGCTGG | 10188 |
rs111448861 | in-del | -/GG/T | 0 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195870956 | GTGGGTTCTGGTGTG[-/GG/T]GGGGGACTCGCTGTG | 10188 |
rs111476474 | snp | C/T | 0.148326 | 0.228391 | intron-variant | TNK2 | GRCh38.p7 | 3:195903265 | CAGGATGGTCTCAAT[C/T]TCCTGACCTCGTGAT | 10188 |
rs111478609 | snp | C/G | 0.115088 | 0.210473 | intron-variant | TNK2 | GRCh38.p7 | 3:195864527 | CAGTAAGAACCACCC[C/G]AGACAGCGACAGACA | 10188 |
rs111499644 | snp | A/G | 0.5 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195881038 | ACACCACCCGCCAGC[A/G]ATGCCCCTTGAAGAG | 10188 |
rs111519574 | snp | A/C/G | 0.00478085 | 0.0486577 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195892741 | GTCTTCTCTCCAGGG[A/C/G]AGTGGTCACAGTCCA | 10188 |
rs111596071 | snp | A/G | 0.0505692 | 0.150756 | intron-variant | TNK2 | GRCh38.p7 | 3:195898670 | TTGCTCTGTTGCCCA[A/G]GCTGGAGTGCAGTGG | 10188 |
rs111597116 | snp | C/G | 0.0256215 | 0.110247 | intron-variant | TNK2 | GRCh38.p7 | 3:195905174 | ACAAAACAGAATCCA[C/G]AATTAGACACACACA | 10188 |
rs111618622 | snp | C/G/T | 0.00135446 | 0.0259888 | missense | TNK2 | GRCh38.p7 | 3:195867593 | AGAGGCACAGGCAGG[C/G/T]GGGTAGGCTCCTCGG | 10188 |
rs111626462 | snp | A/G | 0.5 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195874515 | ATGGCGCCCACGCAC[A/G]CTCCGAGGCACAAGA | 10188 |
rs111695615 | snp | C/T | 0.5 | 0 | missense | TNK2 | GRCh38.p7 | 3:195867470 | CGGGCCCCTGGGTTG[C/T]TGTTGTTGGTGGAGA | 10188 |
rs111696826 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195894687 | AGCCACCGCGCCCGG[A/C]CCGGCCCGGCCCCCT | 10188 |
rs111776599 | snp | A/G | 0.5 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195875150 | ACACTCCGAGGCACA[A/G]GAAGCTCCCCTCGGG | 10188 |
rs111866199 | snp | A/G | 0.0569829 | 0.158885 | intron-variant, upstream-variant-2KB | TNK2, MIR6829 | GRCh38.p7 | 3:195883862 | AAAAGGTGTTTTGCT[A/G]TAGAAGGAAAATGCT | 10188 |
rs111872607 | snp | A/C/G | | | intron-variant | TNK2 | GRCh38.p7 | 3:195881320 | GAGGACACAGGATCT[A/C/G]TCCCTCTAACACCCC | 10188 |
rs111881029 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TNK2 | GRCh38.p7 | 3:195894905 | GATATTCATATTCAG[A/G]AGCCTAGTAAACGGG | 10188 |
rs111895498 | snp | C/T | | | intron-variant | TNK2 | GRCh38.p7 | 3:195864742 | CGCAGGCACTCGCTG[C/T]CACCTGTCTGTCACT | 10188 |
rs111938993 | snp | C/G | 0 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195901853 | ACTGCTTGGCACAAG[C/G]ATGCGGGCCCATGGA | 10188 |
rs112003856 | snp | A/G | | | intron-variant | TNK2 | GRCh38.p7 | 3:195874136 | ACGGGCTCCCCGGTG[A/G]CTGCCGCGGGCCAGA | 10188 |
rs112022404 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNK2 | GRCh38.p7 | 3:195871290 | TACATAGGAGACAGG[A/G]CCTCTCCCAGGTATG | 10188 |
rs112025939 | snp | C/T | 1.68193e-05 | 0.00289989 | synonymous-codon | TNK2 | GRCh38.p7 | 3:195872377 | GCTGATGTCCTGGGC[C/T]GACAGGCCGGCCACG | 10188 |
rs112035920 | snp | C/T | 0.0696718 | 0.173152 | intron-variant, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195887107 | CCCGAGAGAGGCTGC[C/T]GCCTGTGGTCCCCTT | 10188 |
rs112040958 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B | TNK2 | GRCh38.p7 | 3:195866671 | GGCTCCAATTCCCTC[C/T]TGTACTCATTTGAAA | 10188 |
rs112062037 | snp | C/G | | | intron-variant | TNK2 | GRCh38.p7 | 3:195867328 | CCCCTTGGGCCCTGC[C/G]CCGCTTCGCCCACAG | 10188 |
rs112088254 | snp | A/G | | | intron-variant | TNK2 | GRCh38.p7 | 3:195864478 | AGACAGCGACAGACA[A/G]GTGACACGGAGTGCC | 10188 |
rs112100534 | snp | A/G | 0.0501905 | 0.150254 | intron-variant | TNK2 | GRCh38.p7 | 3:195869096 | CATTAGTGCAGGCAC[A/G]GAGCCGCCTCCTGCC | 10188 |
rs112112461 | snp | A/G | 0 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195889981 | CTGAGAAGCAGGCAC[A/G]CACAGCCTGGGCCCA | 10188 |
rs112119526 | snp | A/C/T | 0.000300555 | 0.0122554 | intron-variant | TNK2 | GRCh38.p7 | 3:195872497 | AGATGGCACGGTGAA[A/C/T]GCCAGGCGTGGCGGG | 10188 |
rs112288459 | snp | C/T | 0.444444 | 0.157135 | intron-variant | TNK2 | GRCh38.p7 | 3:195873140 | GCCTCCCCGTCTCCT[C/T]AGGAGGGGCTCTACC | 10188 |
rs112290084 | snp | A/G | | | intron-variant | TNK2 | GRCh38.p7 | 3:195881463 | CCCCTTGGAGAGGAC[A/G]CAGGATCTGTCCCTC | 10188 |
rs112312452 | snp | A/C/T | 0.000448823 | 0.0149739 | intron-variant | TNK2 | GRCh38.p7 | 3:195867335 | GGCCCTGCCCCGCTT[A/C/T]GCCCACAGCCAGGCT | 10188 |
rs112323386 | snp | A/G | 0.444444 | 0.157135 | intron-variant | TNK2 | GRCh38.p7 | 3:195888289 | TCTCATCACACATCA[A/G]CACCTACTGATGTCC | 10188 |
rs112323520 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | TNK2 | GRCh38.p7 | 3:195901268 | TCGGGAATGGAGGCT[C/T]ATGGAGGCTCAGGAT | 10188 |
rs112362099 | snp | G/T | 0.0171299 | 0.090948 | utr-variant-3-prime | TNK2 | GRCh38.p7 | 3:195864149 | GCTCAGGTGATTCCT[G/T]CAGGCAGGCCCTCTG | 10188 |
rs112384084 | snp | C/T | 0.0303461 | 0.119382 | missense | TNK2 | GRCh38.p7 | 3:195867623 | GGGCTCTGGGCCTCA[C/T]GCAGGAAGCGCTGGT | 10188 |
rs112403128 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195864240 | TACAGAAGGTTCAGC[A/C/G]GGGCAGGCACCGGGG | 10188 |
rs112506771 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195885123 | CCACCTGGTGATCCC[C/T]GGCTTCGGCTTCCAG | 10188 |
rs112621440 | in-del | -/A | 0.0256215 | 0.110247 | intron-variant | TNK2 | GRCh38.p7 | 3:195904362 | CCCTTTAAAAAGAAG[-/A]AAATTCTGACATATG | 10188 |
rs112623814 | snp | A/G | 0.5 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195865284 | GTGCCTGCGTCCCAG[A/G]TGCAAATCAGTAAGA | 10188 |
rs112638966 | snp | G/T | 0.0240643 | 0.107019 | upstream-variant-2KB, intron-variant | TNK2 | GRCh38.p7 | 3:195896378 | CCAGACCCTGGAAGG[G/T]CACTAGGTGAGGCTC | 10188 |
rs112651299 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195908241 | TCTGCACAGACCTGG[A/C]AGCCACCCAGACGTC | 10188 |
rs112681454 | snp | A/G | 0.5 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195877415 | ATTGCACCGAAGGCC[A/G]CAGACTCCAAAAGCT | 10188 |
rs112740728 | snp | A/G/T | 0.00466222 | 0.0480567 | missense, synonymous-codon | TNK2 | GRCh38.p7 | 3:195868663 | CAGCCTCTTGAAGTC[A/G/T]CTGGACAAGGGGTCT | 10188 |
rs112789638 | snp | A/C | 0.0221141 | 0.102801 | intron-variant | TNK2 | GRCh38.p7 | 3:195902685 | AGCAAAGTAGGAATA[A/C]AAGAGAGCTTTTTGC | 10188 |
rs112799763 | snp | A/C | | | upstream-variant-2KB, intron-variant | TNK2 | GRCh38.p7 | 3:195895984 | CCCCCGCCCCGAGGC[A/C]CCCGCGGCCGGTTCC | 10188 |
rs112823008 | in-del | -/T | 0.5 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195871969 | TGGAGAACCCTCCCC[-/T]GGAGAACCCTCCCCT | 10188 |
rs112894240 | snp | G/T | | | intron-variant | TNK2 | GRCh38.p7 | 3:195875400 | CGGGATGGCGCCCAC[G/T]CACGCTCCGAGGCAC | 10188 |
rs112897657 | snp | C/T | 0.187369 | 0.242028 | intron-variant | TNK2 | GRCh38.p7 | 3:195903109 | GCAGTGGCGCCATCT[C/T]GGCTTACTGCAACCT | 10188 |
rs112907281 | snp | C/T | 0 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195869040 | GCTCCTGCGCCCTGG[C/T]GAGTTAGTGAGCCCT | 10188 |
rs112914538 | snp | G/T | | | intron-variant | TNK2 | GRCh38.p7 | 3:195874503 | GCTCCCCTCGGGATG[G/T]CGCCCACGCACACTC | 10188 |
rs112924872 | snp | A/C | 0 | 0 | downstream-variant-500B | TNK2 | GRCh38.p7 | 3:195863222 | GAGGCCTCCCGGTGT[A/C]CAGGCCTGCGCGCCC | 10188 |
rs112937233 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNK2 | GRCh38.p7 | 3:195899050 | GCAGTGAGCCAAGAT[C/T]GTACCACTGCACTCC | 10188 |
rs112937592 | snp | C/T | 0.5 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195872053 | CTCCCCTGGAGAACA[C/T]TCCCCTGGAGAACAT | 10188 |
rs112972972 | snp | A/G | 0.5 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195865087 | GAGTGCCTGCGTCCC[A/G]GGTGCAAATCAGTAA | 10188 |
rs113021491 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | TNK2 | GRCh38.p7 | 3:195903503 | GGGCAGGTCACCTGA[A/G]GTCAGGAGTTTGAGA | 10188 |
rs113028562 | snp | A/G | 0.209084 | 0.246629 | intron-variant | TNK2 | GRCh38.p7 | 3:195872077 | AGAACATTCCCCTGG[A/G]GAACCCCCACCAGGC | 10188 |
rs113034256 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | TNK2 | GRCh38.p7 | 3:195875540 | TGGGACTTCCAAGAG[A/G]ACCGTGTCACTTCTC | 10188 |
rs113053952 | snp | A/G | 0.5 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195881212 | TGGAGAGGACACAGC[A/G]TCTATCCCTGTAACA | 10188 |
rs113055553 | snp | A/C/T | | | intron-variant | TNK2 | GRCh38.p7 | 3:195874504 | CTCCCCTCGGGATGG[A/C/T]GCCCACGCACACTCC | 10188 |
rs113106902 | snp | A/G | 0.020301 | 0.0986831 | intron-variant | TNK2 | GRCh38.p7 | 3:195888612 | CTCCCAGCCTCTGTG[A/G]GGGGAGGAGTGGCTC | 10188 |
rs113120669 | snp | A/C/T | 0.000333821 | 0.0129154 | missense | TNK2 | GRCh38.p7 | 3:195867737 | ATGCAGGGACCAGCC[A/C/T]GCGGGCCAGGGGCCT | 10188 |
rs113158562 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195884645 | CGAGACTCCATCTCA[A/G]AAATAAATAAATAAA | 10188 |
rs113159815 | snp | C/T | 0.5 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195865176 | TCAGTAAGAACCACC[C/T]GAGACAGTGACAGAC | 10188 |
rs113201969 | snp | C/G | 0.0185938 | 0.0946107 | utr-variant-3-prime | TNK2 | GRCh38.p7 | 3:195864053 | CGCAGCCTTGGCCTT[C/G]CTCCATCCCCGGGAG | 10188 |
rs113229337 | snp | C/G | 0.5 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195881231 | ATCCCTGTAACACCC[C/G]CCCCCAGCGATGCCC | 10188 |
rs113278004 | snp | C/G/T | 0.00279162 | 0.0372561 | intron-variant | TNK2 | GRCh38.p7 | 3:195888096 | TGCACATGGACCCCC[C/G/T]GGTAGTCAGAATGAT | 10188 |
rs113282909 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | TNK2 | GRCh38.p7 | 3:195873840 | GGGGGGCGCGGGGCG[C/T]GGGGAGACGGGGCTG | 10188 |
rs113363119 | snp | C/T | 0 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195865702 | CAGTTAAGAACGACC[C/T]GAGACAGTATGGGAC | 10188 |
rs113375305 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | TNK2 | GRCh38.p7 | 3:195877724 | AGGCTGTGGGAGGAG[A/G]GTTAGGTATAGAGAG | 10188 |
rs113463068 | snp | A/T | | | intron-variant | TNK2 | GRCh38.p7 | 3:195888086 | TACAGATCTCTGCAC[A/T]TGGACCCCCCGGTAG | 10188 |
rs113498671 | snp | C/T | 1.66665e-05 | 0.00288669 | missense, upstream-variant-2KB, utr-variant-5-prime | TNK2 | GRCh38.p7 | 3:195884972 | GCGGGCGAGGTCTTC[C/T]GGAAGGTGCTCTGAG | 10188 |
rs113517950 | snp | C/T | 0.000606557 | 0.0174043 | intron-variant | TNK2 | GRCh38.p7 | 3:195870296 | CGTCCTGGAGGAAAC[C/T]GGGTGTAGTCTTGGG | 10188 |
rs113587710 | snp | C/T | 0.000275962 | 0.0117433 | intron-variant | TNK2 | GRCh38.p7 | 3:195878644 | GAGCGCCCAGCCCTT[C/T]ACTTCCCGCCTTCCC | 10188 |
rs113651392 | in-del | -/T | 0.5 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195899334 | AAATAGCCAAAATAA[-/T]TTTTTTTTTTTGAGA | 10188 |
rs113728103 | snp | A/G/T | 0.000155988 | 0.00883004 | missense | TNK2 | GRCh38.p7 | 3:195870140 | CCTAGATGCTGGGGG[A/G/T]GCCGGGAGGTGCTCA | 10188 |
rs113738773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195901831 | CATTCAGCCCATTCA[C/T]GACTGTACTGCTTGG | 10188 |
rs113752015 | snp | C/T | 0.5 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195864981 | TCAGTAAGAACCACC[C/T]GAGACAGCGACAGAC | 10188 |
rs113792845 | snp | A/G | | | intron-variant | TNK2 | GRCh38.p7 | 3:195869875 | GGAAGGAGGGAGGAG[A/G]GACGCCGGGGCGGAC | 10188 |
rs113853344 | snp | C/T | | | intron-variant | TNK2 | GRCh38.p7 | 3:195865211 | GACAGCGAGTGCCTG[C/T]GTCCCAGATGCAAAT | 10188 |
rs113863500 | snp | C/T | 0.5 | 0 | intron-variant | TNK2 | GRCh38.p7 | 3:195864566 | GGAGTGCCTGCATCC[C/T]AGATGCAAATCAGTA | 10188 |
rs113885720 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNK2 | GRCh38.p7 | 3:195865111 | TCAGTAAGAACCACC[C/T]GAGACAGTGACAGAC | 10188 |
rs113996846 | snp | C/G/T | 0.00874735 | 0.0655527 | intron-variant | TNK2 | GRCh38.p7 | 3:195869638 | CAGAGTGTAGAGAGA[C/G/T]GAAGGGAGAGAAGTG | 10188 |
rs114233225 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | TNK2 | GRCh38.p7 | 3:195908051 | ACAGGGTTACAAGAT[A/G]AGGTTCTGTTAATCC | 10188 |
rs114272733 | snp | A/G | 0.0176565 | 0.0922849 | synonymous-codon | TNK2 | GRCh38.p7 | 3:195867987 | GGGGGGCTGGAGACA[A/G]CTGGACGTGTGGGCG | 10188 |
rs114434313 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | TNK2 | GRCh38.p7 | 3:195871751 | CTTCTCTCAGGACCC[C/T]TGCATCTGAGCAGCA | 10188 |
rs114439325 | snp | A/G | 0.0171721 | 0.0910559 | intron-variant | TNK2 | GRCh38.p7 | 3:195872492 | GACAGAGATGGCACG[A/G]TGAACGCCAGGCGTG | 10188 |
rs114491239 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | TNK2 | GRCh38.p7 | 3:195875693 | AGGCCGGAGTCCCCG[C/T]GGCCATGGGAGGGCC | 10188 |
rs114493331 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TNK2 | GRCh38.p7 | 3:195898499 | CAATCCTGGCTGGCA[C/T]GCACGCCCTCTGGGC | 10188 |
rs114532920 | snp | A/C | 0.0498117 | 0.149749 | upstream-variant-2KB, intron-variant | TNK2 | GRCh38.p7 | 3:195896332 | AGACAGATGCTGTGA[A/C]CTCTCCTCCCCACGC | 10188 |
rs114615072 | snp | A/C/G | 0.0245654 | 0.10824 | intron-variant | TNK2 | GRCh38.p7 | 3:195870374 | CGTCTCAGCTGGGGG[A/C/G]TGTCCTGGAGAGAAG | 10188 |
rs114671815 | snp | A/G | 0.0232847 | 0.105357 | utr-variant-3-prime | TNK2 | GRCh38.p7 | 3:195863786 | TGGCCAACACATCCC[A/G]CCTGCCCAGGTCCAG | 10188 |
rs114691067 | snp | C/G | 0.0444908 | 0.142359 | intron-variant | TNK2 | GRCh38.p7 | 3:195903364 | CACTCTTAATGGTGA[C/G]AGACTAAATGCATCC | 10188 |
rs114780640 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | TNK2 | GRCh38.p7 | 3:195901200 | ACCTTGAAGAGCCCG[A/G]GACCCTCAAAGGGGA | 10188 |
rs114861726 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | TNK2 | GRCh38.p7 | 3:195900845 | TCTTCCAGGGCTGGG[C/T]AGAGGCTGCCCGGCT | 10188 |
rs114951929 | snp | A/G | 0.0652144 | 0.168387 | intron-variant | TNK2 | GRCh38.p7 | 3:195864852 | CAGTAAGAAACACCC[A/G]AGACAGTGACAGACA | 10188 |
rs114974453 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | TNK2 | GRCh38.p7 | 3:195869854 | CCAGGATCTGAGCTC[G/T]GCCGTGGAAGGAGGG | 10188 |
rs115004961 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | TNK2 | GRCh38.p7 | 3:195870632 | CCACATGGCCAGGAG[C/G]TGCGGGAGAGGCTGG | 10188 |
rs115008136 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195893428 | CAAGTTCCCAAACCC[A/G]CTCAAAACAAACAAA | 10188 |
rs115141314 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195886920 | CCCAGGACCAGAAGC[A/G]GAGGGGGGCGTTCGA | 10188 |
rs115498547 | snp | C/T | 0.000407138 | 0.014262 | intron-variant | TNK2 | GRCh38.p7 | 3:195870355 | TCCACAGAACCTGAC[C/T]GCACGTCTCAGCTGG | 10188 |
rs115540288 | snp | C/T | 0.0524604 | 0.153226 | intron-variant | TNK2 | GRCh38.p7 | 3:195900699 | CACATGCCCAGGTGC[C/T]GAGGCCAGGACACGA | 10188 |
rs115588506 | snp | A/C/G | 0.00182347 | 0.0301431 | intron-variant | TNK2 | GRCh38.p7 | 3:195888613 | TCCCAGCCTCTGTGG[A/C/G]GGGAGGAGTGGCTCA | 10188 |
rs115716054 | snp | A/G/T | 0.00279258 | 0.0372817 | intron-variant, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195893652 | CACCCCCCTCGCTAC[A/G/T]GCCCCCAGACACACC | 10188 |
rs115717686 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | TNK2 | GRCh38.p7 | 3:195864250 | TCAGCGGGGCAGGCA[C/G]CGGGGGTCACACTGG | 10188 |
rs115824214 | snp | C/T | 0.0146672 | 0.084371 | intron-variant, upstream-variant-2KB | TNK2, MIR6829 | GRCh38.p7 | 3:195883592 | AGATAACCAGTATGA[C/T]GAGAGAATATTCAAA | 10188 |
rs115904739 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | TNK2 | GRCh38.p7 | 3:195871828 | TGAACCTGTTTCACA[A/G]ATGAAGTGTCTCAGA | 10188 |
rs116071536 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | TNK2 | GRCh38.p7 | 3:195869049 | CCCTGGCGAGTTAGT[A/G]AGCCCTCATCCCCGC | 10188 |
rs116082540 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | TNK2 | GRCh38.p7 | 3:195864886 | GACAGCAAGTGCCTG[C/T]GTCCCGGGTGCAAAT | 10188 |
rs116083597 | snp | C/T | 0.0236746 | 0.106192 | upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195910824 | GGACCACCCCCCTGT[C/T]GCCTGGCTTCAGGAA | 10188 |
rs116140673 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TNK2 | GRCh38.p7 | 3:195880061 | CATAAGGGTTGCCCA[C/T]AGCCACCGCTTGGGA | 10188 |
rs116164316 | snp | C/T | 0.0124221 | 0.077825 | intron-variant | TNK2 | GRCh38.p7 | 3:195878617 | AGGAGGTGCAGAGTT[C/T]GACGACAAACAGAGC | 10188 |
rs116205407 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | TNK2 | GRCh38.p7 | 3:195891088 | ATATAACAGGTTATA[C/T]ATTTCTATTAACTTT | 10188 |
rs116515338 | snp | G/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195910238 | CTGAAGGAGGGAGGG[G/T]TTGTCTCAGGCCTGA | 10188 |
rs116515392 | snp | C/T | 0.00325258 | 0.0401959 | intron-variant | TNK2 | GRCh38.p7 | 3:195892400 | CAGTCCAGCCCCTGC[C/T]CCCCACTCACTGTGT | 10188 |
rs116571703 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | TNK2, MIR6829 | GRCh38.p7 | 3:195884001 | TGAGTGGACGGAGAA[C/T]GAGGAGCCCTCTGAG | 10188 |
rs116603602 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | TNK2 | GRCh38.p7 | 3:195889200 | CCACAGCAAGCGGAA[C/G]ACAGGAGGGAGGGGT | 10188 |
rs116668398 | snp | A/G/T | 0.00874735 | 0.0655527 | intron-variant | TNK2 | GRCh38.p7 | 3:195880041 | GATGACCATGCGTCC[A/G/T]GGATCATAAGGGTTG | 10188 |
rs116818829 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | TNK2 | GRCh38.p7 | 3:195888768 | ACCGCCTGGACCCAC[A/G]TCCCCTATTCCTGCC | 10188 |
rs116823120 | snp | C/T | 0.037299 | 0.131815 | intron-variant, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195886397 | GGGGAGGAAAGACCA[C/T]GGCTGGCTCACTTCC | 10188 |
rs117052745 | snp | G/T | | | intron-variant | TNK2 | GRCh38.p7 | 3:195877715 | ACTCCCGAGAGGCTG[G/T]GGGAGGAGGGTTAGG | 10188 |
rs117220947 | snp | C/T | 0.130008 | 0.219321 | intron-variant | TNK2 | GRCh38.p7 | 3:195881681 | ACACAGCATTTATCC[C/T]TATAACACCCCCCCG | 10188 |
rs117348498 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | TNK2 | GRCh38.p7 | 3:195877805 | CTGGGAGGGGGTGGT[A/G]GGCTCAGCAGGAAGG | 10188 |
rs117443655 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | TNK2 | GRCh38.p7 | 3:195889910 | TGGGGACCAAGCCAT[A/C]CCCCTCCCCCACTCA | 10188 |
rs117543169 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TNK2 | GRCh38.p7 | 3:195907156 | GTGTATGTGTTTAAA[A/G]CAGACCGTTCTCTCC | 10188 |
rs117648511 | snp | C/T | 0.00292304 | 0.0381179 | intron-variant | TNK2 | GRCh38.p7 | 3:195870259 | CGTGTGGAGGGGTGG[C/T]AGAATCTCATCAGAG | 10188 |
rs117834992 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TNK2 | GRCh38.p7 | 3:195888004 | TGCATGCGTGTGTGC[A/G]TGTGAGAGAGCAAGA | 10188 |
rs118011638 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | TNK2 | GRCh38.p7 | 3:195903389 | GCATCCCCTGGAAGA[C/T]CAGAAACAAGGTATC | 10188 |
rs118076211 | snp | C/T | 0.00225112 | 0.0334738 | intron-variant, downstream-variant-500B | TNK2, MIR6829 | GRCh38.p7 | 3:195882031 | AGGGACTCTGTGAGC[C/T]GGCAGCACCTGCCCC | 10188 |
rs118077641 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TNK2 | GRCh38.p7 | 3:195871661 | TACAGCTGTGGCTCC[A/G]GGGACCTTTCCACCA | 10188 |
rs137926717 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TNK2 | GRCh38.p7 | 3:195889113 | CTAAGTTCCTCCCAG[C/T]GCCTGACCACCCCAG | 10188 |
rs137950708 | snp | A/G | 0.00358779 | 0.0422022 | utr-variant-3-prime | TNK2 | GRCh38.p7 | 3:195863561 | TGGGCCCTGGTCCCC[A/G]CCAGAGAATGGTCTG | 10188 |
rs138014809 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195904493 | GGAGCCAAATTCATA[C/G]AGTCAGAAGGTAAAA | 10188 |
rs138081236 | snp | A/C | 3.56646e-05 | 0.00422268 | synonymous-codon, intron-variant | TNK2 | GRCh38.p7 | 3:195895249 | CTTCCCCATTACCTG[A/C]GGTCCCTCCTCGCCC | 10188 |
rs138187175 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | TNK2 | GRCh38.p7 | 3:195879321 | GGCGCCGTGTGAAGC[A/G]GGCAGGACCCCTTGA | 10188 |
rs138222609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195880324 | GAGTCTTTCCCTGGC[A/G]AACTTCCCTGATGTT | 10188 |
rs138236865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195869744 | AGTATGATAGGCAGA[A/G]GACCGGGAGATGGAG | 10188 |
rs138330429 | snp | C/T | 0.000488887 | 0.015627 | missense | TNK2 | GRCh38.p7 | 3:195867632 | GCCTCACGCAGGAAG[C/T]GCTGGTAGCGCTCCA | 10188 |
rs138351820 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195906368 | CACACAAAGACTAAC[A/C]AACACGTTCACAGCA | 10188 |
rs138533223 | snp | A/G | 0.000181511 | 0.00952483 | utr-variant-3-prime | TNK2 | GRCh38.p7 | 3:195864157 | GATTCCTTCAGGCAG[A/G]CCCTCTGGCTCTCCA | 10188 |
rs138574167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195865931 | GGAGAAACTCCGCAC[C/T]GTGCACAGGGCCACG | 10188 |
rs138584671 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNK2 | GRCh38.p7 | 3:195889819 | GTCAGAGCTGAGGGC[A/G]TGGCCAGGCTAGCCC | 10188 |
rs138590895 | snp | C/T | 0.00041978 | 0.0144815 | missense, upstream-variant-2KB, utr-variant-5-prime | TNK2 | GRCh38.p7 | 3:195884829 | TCTTCCCTGAGGGCG[C/T]GTCCCACTCGCCCCT | 10188 |
rs138613497 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195893295 | CGGCAGCCTGCCAGA[C/G]TGGGGCAGTCCAGCC | 10188 |
rs138643153 | snp | C/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195910059 | AAGTCACTTCCACCC[C/G]GTCTCAGTTGTTCCA | 10188 |
rs138841002 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TNK2 | GRCh38.p7 | 3:195902163 | TGGTGGCAGTTGAGA[C/G]CTGACCCAAGAAAAT | 10188 |
rs138860026 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TNK2 | GRCh38.p7 | 3:195872947 | AGTTCTGAGAGGTGC[A/G]GGGGTGCCGGGGGAC | 10188 |
rs138888577 | snp | A/G | | | intron-variant | TNK2 | GRCh38.p7 | 3:195876137 | CTCTGTATGCGGAAC[A/G]AAAGTGCTGCCAGCC | 10188 |
rs138902635 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | TNK2 | GRCh38.p7 | 3:195864038 | GGGCTCCCAGCCTCC[C/T]GCAGCCTTGGCCTTG | 10188 |
rs139091372 | snp | A/G | | | intron-variant | TNK2 | GRCh38.p7 | 3:195881557 | CAGCAATGCCCCTTG[A/G]AGAGGACACAGCATC | 10188 |
rs139128052 | snp | A/G | 1.73869e-05 | 0.00294842 | missense | TNK2 | GRCh38.p7 | 3:195872436 | CCACACACAGCGTCC[A/G]TGTGTTCTGGCCACG | 10188 |
rs139132927 | snp | A/C | | | intron-variant | TNK2 | GRCh38.p7 | 3:195900871 | CGGCTCGTCATCCTG[A/C]CTGCTGCCAGCTCAG | 10188 |
rs139172714 | in-del | -/C | | | intron-variant | TNK2 | GRCh38.p7 | 3:195891663 | CAAAGTGACCCCCCC[-/C]CCTCCAGGGCTCAGC | 10188 |
rs139268974 | snp | A/G/T | 0.00336027 | 0.0408521 | synonymous-codon | TNK2 | GRCh38.p7 | 3:195868144 | CTGGAAGATCTCTGC[A/G/T]GTCTGTGCGGAGCTG | 10188 |
rs139343303 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195894695 | CGCCCGGCCCGGCCC[A/G]GCCCCCTTTCTCCTC | 10188 |
rs139410247 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | TNK2 | GRCh38.p7 | 3:195887582 | TGTCTAACTTGACAC[A/G]TTATTACCTATTTAG | 10188 |
rs139419149 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195910205 | CACCTCTCTTTCCCC[A/G]GGGCCAACGGAGCAC | 10188 |
rs139421236 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNK2 | GRCh38.p7 | 3:195871466 | AGCCAGCAGGTTCAC[A/G]TCTCCAGGACTCTGG | 10188 |
rs139465714 | in-del | -/T | | | intron-variant, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195885945 | CCTCTGCCCTGTGCT[-/T]CCTCCCAGTAACTAG | 10188 |
rs139466729 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon | TNK2 | GRCh38.p7 | 3:195868543 | CTCACCGAAGTCGAT[A/G]AGCGTGACCTCAGCC | 10188 |
rs139571237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195864574 | TGCATCCTAGATGCA[A/G]ATCAGTAAGAACCAC | 10188 |
rs139623696 | snp | G/T | 0.000153988 | 0.00877328 | missense | TNK2 | GRCh38.p7 | 3:195867695 | TGGGTGCTGCTGACC[G/T]TCTTGCCATCCCGGA | 10188 |
rs139696100 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | TNK2 | GRCh38.p7 | 3:195890596 | GCTGGGATCACAGGC[A/G]CCCGGCTAATTTTTG | 10188 |
rs139797100 | snp | C/T | 0.000231085 | 0.0107466 | missense | TNK2 | GRCh38.p7 | 3:195868158 | CGGTCTGTGCGGAGC[C/T]GGGCGGCTTGCCCCC | 10188 |
rs139833457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195894998 | CCTGGACTCCCTTGG[A/G]GCATGGAAGAAAGCC | 10188 |
rs139869381 | snp | A/G | 5.49808e-05 | 0.00524284 | synonymous-codon | TNK2 | GRCh38.p7 | 3:195872467 | CCACCAGTAGTTCTC[A/G]GCCCTGCGCGACAGA | 10188 |
rs139901896 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TNK2 | GRCh38.p7 | 3:195900700 | ACATGCCCAGGTGCC[A/G]AGGCCAGGACACGAG | 10188 |
rs139953860 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TNK2 | GRCh38.p7 | 3:195890915 | GATGCTGCCTTCACG[A/G]TGTTTCCACCTGAGG | 10188 |
rs140110931 | snp | A/G | 0.130351 | 0.219509 | intron-variant | TNK2 | GRCh38.p7 | 3:195881683 | ACAGCATTTATCCCT[A/G]TAACACCCCCCCGCC | 10188 |
rs140132025 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195887278 | CCAAAAACTTGAAGC[A/G]ATGGGCTTCTCCCAG | 10188 |
rs140221068 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNK2 | GRCh38.p7 | 3:195898033 | GCAGCTCCACCAGGA[A/G]GCTGCACAGGTACCA | 10188 |
rs140240456 | snp | C/T | 0.0115144 | 0.0749975 | downstream-variant-500B | TNK2 | GRCh38.p7 | 3:195862961 | GTACACTCCTCAGTG[C/T]CTTTTCAATTTTGAA | 10188 |
rs140260778 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195877116 | GAATGCTCCCCGGAG[C/T]GCCACGCTTGCAATC | 10188 |
rs140281383 | snp | G/T | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195893747 | GGAGCCCCTGTTTCT[G/T]GCACACTGCTCTCTT | 10188 |
rs140384949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195888360 | CCACCCGTGCACCGA[A/G]TGGTCCTGAGGACAG | 10188 |
rs140431873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195878910 | CGGGGCGTGGTGGGA[A/G]GCACGGGAAGTGGGG | 10188 |
rs140571564 | snp | C/G | | | intron-variant | TNK2 | GRCh38.p7 | 3:195865614 | ATGCCTGCGTCCCAG[C/G]TGCAAATCAGTAAGA | 10188 |
rs140597247 | snp | C/T | | | intron-variant | TNK2 | GRCh38.p7 | 3:195876220 | CAAATCTAGACACAG[C/T]ACGAAACATCTAGGT | 10188 |
rs140707536 | snp | A/T | 8.97062e-05 | 0.00669665 | missense | TNK2 | GRCh38.p7 | 3:195866892 | GGGCTCACTCACTTG[A/T]GGTGGGCAGGGCCCC | 10188 |
rs140753891 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | TNK2 | GRCh38.p7 | 3:195889462 | CACAGCCACCCGGCT[A/C]CCCAGGAGTTGCCAG | 10188 |
rs140768562 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | TNK2 | GRCh38.p7 | 3:195863755 | GTCCCACCGGGTGCC[A/G]GTCCGCCTCTCCCTG | 10188 |
rs140843768 | snp | C/T | 0.0316786 | 0.121802 | intron-variant, utr-variant-5-prime, synonymous-codon | TNK2 | GRCh38.p7 | 3:195892510 | GCAGCGGGACCCCCC[C/T]GAGCAGTCACTGGGG | 10188 |
rs140979568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNK2, MIR6829 | GRCh38.p7 | 3:195883550 | TCCTGGGGGAATGCC[A/G]GGCTTAAATACCAAC | 10188 |
rs141030162 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195905974 | AAGAACTCTTCAGAA[C/G]TCAACACGAAAAACC | 10188 |
rs141068207 | snp | A/T | 0.0170251 | 0.090679 | intron-variant | TNK2 | GRCh38.p7 | 3:195898272 | TCCCAACGGTGACAA[A/T]GAGATCAGGAGTCAG | 10188 |
rs141093172 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TNK2 | GRCh38.p7 | 3:195896798 | CTGCTCTTCACTTGT[C/G]TCTTTATATCTCCAC | 10188 |
rs141121252 | snp | A/G | 0.000159661 | 0.00893336 | synonymous-codon | TNK2 | GRCh38.p7 | 3:195868291 | GACCCCCGCGCCCAC[A/G]AGGGTGCTGTTGATG | 10188 |
rs141234146 | snp | C/T | 0.00557276 | 0.0524912 | intron-variant | TNK2 | GRCh38.p7 | 3:195876561 | ACCGACACCCAGGCC[C/T]GCTCCCAAGCCTCAC | 10188 |
rs141255935 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195875798 | CCTCCGCATGAACCT[G/T]CTACCTCCTGCTGCC | 10188 |
rs141305197 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TNK2 | GRCh38.p7 | 3:195906535 | AGTAAATGCTGCAAA[C/G]TCAGACACAGTGACA | 10188 |
rs141375696 | snp | A/C/T | 3.36492e-05 | 0.00410167 | synonymous-codon | TNK2 | GRCh38.p7 | 3:195872380 | GATGTCCTGGGCCGA[A/C/T]AGGCCGGCCACGGAG | 10188 |
rs141404332 | snp | A/G/T | 0.000445206 | 0.0149134 | synonymous-codon, missense | TNK2 | GRCh38.p7 | 3:195878463 | CCAGCAGGAAGTCCC[A/G/T]CAGGGCCACAAACGT | 10188 |
rs141437423 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNK2 | GRCh38.p7 | 3:195869608 | ACAAAGGAGGGAGAC[A/G]GCCGGACGAGAGGGC | 10188 |
rs141507655 | in-del | -/CCCCCCCC | | | intron-variant | TNK2 | GRCh38.p7 | 3:195895085 | ATCACTAAGTCACCA[-/CCCCCCCC]CCGCCACACCCACAT | 10188 |
rs141507877 | in-del | -/CCGGGGG | 0.259951 | 0.249802 | intron-variant, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195894179 | AAGGAGACCCAGGGA[-/CCGGGGG]CCGGGGAACAATTTA | 10188 |
rs141713554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195908096 | CCCTTCTGTGGGACG[C/T]GTTTTGAGGACTTGT | 10188 |
rs141733252 | snp | A/C | 0.0232847 | 0.105357 | intron-variant | TNK2 | GRCh38.p7 | 3:195902956 | GGTTTCACCATGTTG[A/C]CCAGGCTGGTCTTGA | 10188 |
rs141749567 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNK2 | GRCh38.p7 | 3:195900338 | GCCCTGCTATGCCTC[A/G]TCCCCTCCAACTCCA | 10188 |
rs141775390 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNK2 | GRCh38.p7 | 3:195904376 | GAAAATTCTGACATA[C/T]GCTGCAATGTAAATG | 10188 |
rs141775487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | TNK2 | GRCh38.p7 | 3:195866789 | CTGTGTCTCCCTGGC[C/T]GGGAGCGGCCTGCGA | 10188 |
rs141795099 | snp | C/T | | | intron-variant | TNK2 | GRCh38.p7 | 3:195903306 | CGGCCTCCCAAAGTA[C/T]TGGGATTACAGGCGT | 10188 |
rs141804984 | in-del | -/GCTGTGTGGGTTCTGGTGTGTGGGGGCCC | | | intron-variant | TNK2 | GRCh38.p7 | 3:195870996 | GTGTGTGGGGGCCCG[lengthTooLong]CTGTGTGGGTTCTGG | 10188 |
rs141910942 | in-del | -/C | 0.209084 | 0.246629 | intron-variant | TNK2 | GRCh38.p7 | 3:195872074 | GGAGAACATTCCCCT[-/C]GGAGAACCCCCACCA | 10188 |
rs142018067 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | TNK2 | GRCh38.p7 | 3:195890377 | CAACTCAATTCATGA[A/C]GGTGTTTATGATCAT | 10188 |
rs142118912 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | TNK2, MIR6829 | GRCh38.p7 | 3:195883707 | GCAACCTCTGCCTCC[C/T]GGGTTCAAGTGATTC | 10188 |
rs142180599 | in-del | -/CCGGGGC | 0.00795532 | 0.062565 | intron-variant | TNK2 | GRCh38.p7 | 3:195872876 | AGTTCCCTGGCAAGG[-/CCGGGGC]CCCAGTCCTCTTCTG | 10188 |
rs142197396 | snp | A/C | 0.0360663 | 0.129354 | intron-variant | TNK2 | GRCh38.p7 | 3:195889906 | CGGCTGGGGACCAAG[A/C]CATCCCCCTCCCCCA | 10188 |
rs142207704 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNK2 | GRCh38.p7 | 3:195888170 | GGACATACACTCTAC[A/G]TGAGAACAATCACAA | 10188 |
rs142308594 | snp | A/G | 0.000527296 | 0.0162287 | synonymous-codon, utr-variant-5-prime | TNK2 | GRCh38.p7 | 3:195888469 | GTCCTCATTCTTGAC[A/G]TACTCAAAGTGGGAC | 10188 |
rs142416449 | snp | A/C/G | 0.000132869 | 0.00814975 | missense, utr-variant-5-prime | TNK2 | GRCh38.p7 | 3:195888432 | CCCACCTACCAGGCC[A/C/G]ACCCATGCCGATCTT | 10188 |
rs142476959 | snp | A/G | 0.00157375 | 0.0280071 | synonymous-codon | TNK2 | GRCh38.p7 | 3:195878521 | GCACTGGACCATGAC[A/G]TTGTAGATGTCCTGG | 10188 |
rs142511086 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNK2 | GRCh38.p7 | 3:195869127 | ATCAGGGGCTATAAG[A/G]ACTATCCTTGGAGAG | 10188 |
rs142515837 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNK2 | GRCh38.p7 | 3:195870698 | TGCACCAACTGTCAG[C/T]ATCTGAGACTTAGTC | 10188 |
rs142527530 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TNK2 | GRCh38.p7 | 3:195903102 | TCGGAATGCAGTGGC[A/G]CCATCTCGGCTTACT | 10188 |
rs142547410 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | TNK2 | GRCh38.p7 | 3:195871735 | ACAGTGAGTGGGAAA[A/G]CTTCTCTCAGGACCC | 10188 |
rs142696733 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TNK2 | GRCh38.p7 | 3:195891810 | CTCAAAGCCATGCCC[A/G]GGGTGGTCAGGGCTG | 10188 |
rs142714540 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195910175 | GCACCCCAAAGGCCC[A/G]GAAACCCGGACCATC | 10188 |
rs142813738 | in-del | -/GA | | | intron-variant | TNK2 | GRCh38.p7 | 3:195869636 | GCAGAGTGTAGAGAG[-/GA]ACGAAGGGAGAGAAG | 10188 |
rs142868475 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNK2 | GRCh38.p7 | 3:195869927 | CGAGGAGGCCCACCT[C/T]GGCGGATACAGCTGC | 10188 |
rs142882209 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195895024 | AAGCCCAACGGGCAG[C/G]TTTTTGGGGTCCCAG | 10188 |
rs142904090 | snp | C/G | | | intron-variant | TNK2 | GRCh38.p7 | 3:195869879 | GGAGGGAGGAGGGAC[C/G]CCGGGGCGGACGGGC | 10188 |
rs142918561 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | TNK2 | GRCh38.p7 | 3:195878081 | GGGCAGGGAAAGGCA[A/C]TAGGAAGACGGAGGC | 10188 |
rs143026587 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TNK2 | GRCh38.p7 | 3:195894956 | TCAGTTCTCCTAAAA[C/G]ACTGAACCCCAATCC | 10188 |
rs143060720 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | TNK2 | GRCh38.p7 | 3:195901379 | ACCAGAGAAGAGGCC[C/T]TGCTTCATTGGCAGA | 10188 |
rs143079228 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | TNK2 | GRCh38.p7 | 3:195865507 | CAGTAAGAACCACCC[A/G]AGACTGGGACAGACA | 10188 |
rs143166115 | snp | A/G | 0.000425969 | 0.0145878 | missense | TNK2 | GRCh38.p7 | 3:195868233 | GCCGCGCCTGCTCAG[A/G]CACAAAGGCGTAGTT | 10188 |
rs143180132 | in-del | -/T | 0.00438332 | 0.0466095 | intron-variant | TNK2 | GRCh38.p7 | 3:195877516 | TGCGAGCACAGGGGA[-/T]TTCCTCCACTTCACT | 10188 |
rs143205499 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TNK2 | GRCh38.p7 | 3:195897177 | CTCACCCCTCTGTGC[A/G]CAGAGCCCAGGCTTC | 10188 |
rs143332010 | snp | C/G | 0.0170251 | 0.090679 | intron-variant | TNK2 | GRCh38.p7 | 3:195898824 | CTGCGGCTGGGCCCG[C/G]TGGCTCACGTCTGTA | 10188 |
rs143348369 | snp | C/T | 0.00171354 | 0.0292204 | intron-variant, missense | TNK2 | GRCh38.p7 | 3:195867197 | GCAGCCCTCTGCACG[C/T]TCCAGCCGTGGCACT | 10188 |
rs143433872 | snp | C/T | 0.00819329 | 0.0634785 | intron-variant, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195885589 | AGGTTGAACCGTGAG[C/T]GTGTGTGTGGTTCAG | 10188 |
rs143469229 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNK2 | GRCh38.p7 | 3:195877006 | ACGGCTTTCCAGCTC[A/G]TGGAGGTGGACACGG | 10188 |
rs143501780 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNK2 | GRCh38.p7 | 3:195898171 | AACCACACCCCACCA[C/T]GGACCCCCAACCAAG | 10188 |
rs143508144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195900814 | CTCCCAGCAGCTAGC[C/T]ACTCCCAGAGAGAGC | 10188 |
rs143587665 | snp | G/T | 3.32497e-05 | 0.00407722 | missense, downstream-variant-500B, utr-variant-5-prime, intron-variant | TNK2, MIR6829 | GRCh38.p7 | 3:195882293 | GTGCTTACGTAGCCG[G/T]TCCAACAACGATCCC | 10188 |
rs143787673 | snp | A/C | 0.00199213 | 0.0314975 | missense | TNK2 | GRCh38.p7 | 3:195868688 | GGGTCTTGGTCCTCG[A/C]TCACAGGGTCATAGG | 10188 |
rs143850445 | snp | C/G/T | 8.86775e-05 | 0.00665821 | missense | TNK2 | GRCh38.p7 | 3:195867663 | GGTAGGATGGTCGCT[C/G/T]GGGCAGCAAGTAATA | 10188 |
rs144006896 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | TNK2 | GRCh38.p7 | 3:195864860 | AACACCCGAGACAGT[C/G]ACAGACAGGTGACAG | 10188 |
rs144082002 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | TNK2 | GRCh38.p7 | 3:195866096 | CATATATATATTTAC[A/G]TAATATATAAAGTGT | 10188 |
rs144093599 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNK2 | GRCh38.p7 | 3:195904843 | AACACTGCTGAGAGA[C/T]AGTAAACAAAACCTA | 10188 |
rs144161756 | snp | A/C/T | 0.0138187 | 0.0819672 | synonymous-codon | TNK2 | GRCh38.p7 | 3:195868426 | CCGGGGCAGTGCCCG[A/C/T]GTGGGGCTCTGAGGC | 10188 |
rs144183552 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TNK2 | GRCh38.p7 | 3:195870887 | GCCCTGTGAGCTTGG[G/T]GTTCCAGTGTGTGTG | 10188 |
rs144307708 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | TNK2 | GRCh38.p7 | 3:195903281 | TCCTGACCTCGTGAT[C/G]TGCACATCTCGGCCT | 10188 |
rs144307971 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | TNK2 | GRCh38.p7 | 3:195900170 | TTCTCATCGGACTGC[A/G]AAGGGGTGCTGGGGC | 10188 |
rs144411046 | snp | A/G | 0.0341408 | 0.126114 | intron-variant, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195894649 | CCGCCTCGGCCTCCC[A/G]AAGTGCTGAGATGAC | 10188 |
rs144447654 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TNK2 | GRCh38.p7 | 3:195891262 | AAATAGAAAATTAGC[C/T]GGGCCTGGTGGCACA | 10188 |
rs144573163 | snp | A/G | 0.000186293 | 0.00964944 | missense | TNK2 | GRCh38.p7 | 3:195867740 | CAGGGACCAGCCCGC[A/G]GGCCAGGGGCCTGGA | 10188 |
rs144587664 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195874397 | GCCGAGGCAAGAGCC[A/C]CCATGGCTGCTGGGA | 10188 |
rs144603034 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195893060 | TGACTCAAACAGCAC[A/G]TATGAAGCAGGGCTG | 10188 |
rs144607338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195890845 | TTTGCAAAAATGTCA[A/G]TGAAGGCAACCCCCT | 10188 |
rs144684574 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNK2 | GRCh38.p7 | 3:195889794 | ACCCATCCCTGTCTG[C/T]GTAAGGTGTGTCAGA | 10188 |
rs144721682 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | TNK2 | GRCh38.p7 | 3:195888017 | GCGTGTGAGAGAGCA[A/C]GAAAGAGAGCGTGAG | 10188 |
rs144738391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | TNK2 | GRCh38.p7 | 3:195866652 | AGCCTCCTTCAACCA[A/G]AGAGGCTCCAATTCC | 10188 |
rs144776074 | snp | C/T | | | intron-variant | TNK2 | GRCh38.p7 | 3:195890121 | AACTCTCAGTTCAAA[C/T]CCTGGCTCTTCCACC | 10188 |
rs144814844 | snp | A/G | 0.000283359 | 0.0118996 | missense, upstream-variant-2KB, utr-variant-5-prime | TNK2 | GRCh38.p7 | 3:195884963 | CCCCCAGGGGCGGGC[A/G]AGGTCTTCCGGAAGG | 10188 |
rs144960537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195901199 | GACCTTGAAGAGCCC[A/G]GGACCCTCAAAGGGG | 10188 |
rs144981601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195876131 | CACCCGCTCTGTATG[C/T]GGAACAAAAGTGCTG | 10188 |
rs144986514 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195874492 | GTGTGCAAGAAGCTC[C/T]CCTCGGGATGGCGCC | 10188 |
rs145039321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195907178 | GTTCTCTCCACTGAA[A/G]CCAGACAGTGAGAGC | 10188 |
rs145057853 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | TNK2 | GRCh38.p7 | 3:195872941 | TCCAGGAGTTCTGAG[A/G]GGTGCGGGGGTGCCG | 10188 |
rs145141263 | snp | A/G | 0.0115144 | 0.0749975 | upstream-variant-2KB, intron-variant | TNK2 | GRCh38.p7 | 3:195896772 | GAATCCACCCCACGT[A/G]TACACCCCCTCTGCT | 10188 |
rs145156595 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | TNK2 | GRCh38.p7 | 3:195871562 | GGGGCCACAGGGGGG[G/T]CATGGGAGAAGCTCT | 10188 |
rs145183858 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | TNK2 | GRCh38.p7 | 3:195887974 | TGTGTGTGTGTGTGT[A/G]TATGCCTGTGCGTGT | 10188 |
rs145232843 | in-del | -/GTGTGT | | | intron-variant | TNK2 | GRCh38.p7 | 3:195887956 | TGCGTGTGTGCCTGC[-/GTGTGT]GTGTGTGTGTGTGTA | 10188 |
rs145238871 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | TNK2 | GRCh38.p7 | 3:195863314 | GGAGCCTCGCTTGGG[A/G]CCTGGAGCTTGCTGA | 10188 |
rs145486009 | snp | A/G | 1.64749e-05 | 0.00287005 | synonymous-codon | TNK2 | GRCh38.p7 | 3:195878276 | GATGACGGTGATGAC[A/G]TCATTCATCTGGATG | 10188 |
rs145536913 | snp | A/C/G | 0.000870513 | 0.0208457 | missense, synonymous-codon | TNK2 | GRCh38.p7 | 3:195868687 | GGGGTCTTGGTCCTC[A/C/G]CTCACAGGGTCATAG | 10188 |
rs145550791 | snp | A/G | 0.000153988 | 0.00877328 | missense, upstream-variant-2KB, utr-variant-5-prime | TNK2 | GRCh38.p7 | 3:195884996 | CTCTGAGAGTGATGA[A/G]GTGGGAACTCAGCCT | 10188 |
rs145559327 | snp | A/C | 0.000153988 | 0.00877328 | missense | TNK2 | GRCh38.p7 | 3:195879076 | GAGGCCGATCCAGGG[A/C]TCCTGGCCGTAGGTG | 10188 |
rs145573083 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TNK2 | GRCh38.p7 | 3:195891705 | GGCTCCTAGTCTCCC[A/G]CAGGGAGAGCAGTCT | 10188 |
rs145592276 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TNK2 | GRCh38.p7 | 3:195905362 | CCGCCACCACGCCTG[A/G]CTAATTTTTTGTATT | 10188 |
rs145626266 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | TNK2 | GRCh38.p7 | 3:195906356 | AAAGTGTACATCCAC[A/C]CAAAGACTAACAAAC | 10188 |
rs145704966 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TNK2 | GRCh38.p7 | 3:195903889 | TGCTAGAATAAGTCA[A/G]TTTAGCAAGACTGCA | 10188 |
rs145745099 | snp | G/T | | | intron-variant | TNK2 | GRCh38.p7 | 3:195865205 | ACAGGTGACAGCGAG[G/T]GCCTGCGTCCCAGAT | 10188 |
rs145846055 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TNK2 | GRCh38.p7 | 3:195906257 | ACCACTTTGGAAAAC[A/G]GTCTGGCAGTTTCTT | 10188 |
rs145862992 | snp | A/G/T | 0.000407706 | 0.0142724 | missense, synonymous-codon | TNK2 | GRCh38.p7 | 3:195866951 | CTCCAGGTTCCAGTC[A/G/T]AACATCTCCAGCACT | 10188 |
rs145954545 | snp | C/G | 3.59034e-05 | 0.00423679 | missense | TNK2 | GRCh38.p7 | 3:195872461 | GCCACGCCACCAGTA[C/G]TTCTCGGCCCTGCGC | 10188 |
rs145961208 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195886201 | TGCCTCCACCATCCC[A/G]ACACTACTCATCCTT | 10188 |
rs146083230 | snp | C/T | 5.62588e-05 | 0.00530342 | intron-variant | TNK2 | GRCh38.p7 | 3:195870281 | TCATCAGAGCCCCTT[C/T]GTCCTGGAGGAAACC | 10188 |
rs146174264 | snp | C/T | | | intron-variant, upstream-variant-2KB | TNK2, MIR6829 | GRCh38.p7 | 3:195883961 | TGCACTGAGTGACAG[C/T]GGCTTCCCCGGGAGA | 10188 |
rs146218821 | in-del | -/G | | | intron-variant | TNK2 | GRCh38.p7 | 3:195888648 | CAAGGGTTGTGGGGG[-/G]ACAACAGGGGCCTGC | 10188 |
rs146238089 | snp | C/T | 0.00351418 | 0.0417701 | intron-variant, downstream-variant-500B | TNK2 | GRCh38.p7 | 3:195866851 | CTGGGACAGCCCTCC[C/T]GGGGCACGGAGCGGG | 10188 |
rs146286287 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | TNK2 | GRCh38.p7 | 3:195903046 | TGAGCCACCGCACCC[A/G]GCCAGCTAACACCAC | 10188 |
rs146294741 | in-del | -/GCACGTGCATGCGTGTGT | | | intron-variant | TNK2 | GRCh38.p7 | 3:195887888 | TGAGCGCGTGCGTAC[-/GCACGTGCATGCGTGTGT]GCACGTGCATGCGTG | 10188 |
rs146324750 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | TNK2 | GRCh38.p7 | 3:195902369 | ACGCCTGTAATCCCA[A/G]CACTGTGGGAGGCCG | 10188 |
rs146324948 | snp | A/G | 0.00102737 | 0.0226414 | synonymous-codon, downstream-variant-500B, intron-variant | TNK2, MIR6829 | GRCh38.p7 | 3:195882086 | ATGTTCCTGCATGAC[A/G]TAATGGTCGTCATTC | 10188 |
rs146405223 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195887496 | CACGTTATTACCTAT[C/T]TAGCTATTTTAACTA | 10188 |
rs146442175 | snp | C/G | 0.000179984 | 0.00948471 | missense, intron-variant | TNK2 | GRCh38.p7 | 3:195869502 | CCCCACTTACTCTGA[C/G]TGAAGAAGGCAGGCT | 10188 |
rs146623412 | snp | C/T | 1.79236e-05 | 0.00299357 | missense | TNK2 | GRCh38.p7 | 3:195868268 | TGGCCCTGGCTGGGC[C/T]CGGCAGGGACCCCCG | 10188 |
rs146624046 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195875592 | GAGGCTCAGTGTGGC[C/T]GAGGCACCAGCAGTC | 10188 |
rs146640916 | snp | A/G | 0.000171603 | 0.00926132 | synonymous-codon | TNK2 | GRCh38.p7 | 3:195866984 | GTGGCACTCCCCTCT[A/G]GGCCGCAGACCCAGC | 10188 |
rs146648972 | snp | A/G | 0.000197687 | 0.00994004 | synonymous-codon | TNK2 | GRCh38.p7 | 3:195878267 | CCTTCCCTCGATGAC[A/G]GTGATGACATCATTC | 10188 |
rs146670915 | snp | A/C | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | TNK2 | GRCh38.p7 | 3:195897304 | ACTGGTCTGGGGAGG[A/C]GGCTGGCCAGGGCCC | 10188 |
rs146742433 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | TNK2 | GRCh38.p7 | 3:195900868 | GCCCGGCTCGTCATC[C/G]TGCCTGCTGCCAGCT | 10188 |
rs146748807 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TNK2 | GRCh38.p7 | 3:195871810 | TTCCCCTTATTGGGG[A/G]GGTGAACCTGTTTCA | 10188 |
rs146864403 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | TNK2, MIR6829 | GRCh38.p7 | 3:195881943 | GGCTTAGAACAGACA[A/G]GGGCAGGCCCAAGCA | 10188 |
rs146905259 | snp | C/G | 0.0310518 | 0.120672 | intron-variant | TNK2 | GRCh38.p7 | 3:195869337 | GGGGCGGGCTCGAGG[C/G]GGGGCAGGCATGCTA | 10188 |
rs146962404 | in-del | -/C | | | intron-variant | TNK2 | GRCh38.p7 | 3:195878135 | AGGGTTCAGGCCCAA[-/C]CCGCCAGCCTGTATG | 10188 |
rs146975438 | in-del | -/GGGTTCTGGTGTGTGGGGGCCCGCTGTGT | | | intron-variant | TNK2 | GRCh38.p7 | 3:195870974 | GGGACTCGCTGTGTG[lengthTooLong]GGGTTCTGGTGTGTG | 10188 |
rs146983496 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TNK2 | GRCh38.p7 | 3:195879676 | CGTTCTGGGCACCCC[C/T]GGTTGAGGGGGAAGT | 10188 |
rs146993278 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TNK2, MIR6829 | GRCh38.p7 | 3:195883583 | AAAAGTAAGAGATAA[A/C]CAGTATGATGAGAGA | 10188 |
rs147053694 | snp | A/T | 0.000530124 | 0.0162721 | missense | TNK2 | GRCh38.p7 | 3:195868676 | TCGCTGGACAAGGGG[A/T]CTTGGTCCTCGCTCA | 10188 |
rs147097664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195868879 | TCTCAGCGCACCTCC[A/G]ACCACTCCATCAGGA | 10188 |
rs147116325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195901636 | GGAGAATATGAAGGG[A/G]CAGAAGTCATAGCCT | 10188 |
rs147134893 | snp | A/C | 0.025641 | 0.110417 | intron-variant | TNK2 | GRCh38.p7 | 3:195877073 | GTACTTCCAGGGGAC[A/C]CCCCCACCCTTAATC | 10188 |
rs147211568 | snp | A/G | 1.77259e-05 | 0.00297702 | synonymous-codon | TNK2 | GRCh38.p7 | 3:195867664 | GTAGGATGGTCGCTC[A/G]GGCAGCAAGTAATAG | 10188 |
rs147242417 | in-del | -/T | 0.2776 | 0.248472 | intron-variant | TNK2 | GRCh38.p7 | 3:195898661 | GACTGGGTCTTGCTC[-/T]TGTTGCCCAGGCTGG | 10188 |
rs147317510 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNK2 | GRCh38.p7 | 3:195866145 | TTTAAATGTCTATAT[A/G]TTTTGTTAAACTATA | 10188 |
rs147391024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195905183 | AATCCAGAATTAGAC[A/G]CACACAAACAATTGA | 10188 |
rs147494854 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TNK2 | GRCh38.p7 | 3:195890846 | TTGCAAAAATGTCAG[A/T]GAAGGCAACCCCCTC | 10188 |
rs147508229 | snp | A/G | | | intron-variant | TNK2 | GRCh38.p7 | 3:195902118 | AGGAAAAACCACCAC[A/G]GAACTTTGGAAGCTG | 10188 |
rs147576388 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNK2 | GRCh38.p7 | 3:195871566 | CCACAGGGGGGTCAT[A/G]GGAGAAGCTCTCCTC | 10188 |
rs147620284 | snp | C/T | 0.0170251 | 0.090679 | intron-variant, upstream-variant-2KB | TNK2, MIR6829 | GRCh38.p7 | 3:195883675 | GCTGGAATGCAGTGA[C/T]GTGATCTCAGCTCAC | 10188 |
rs147683114 | snp | A/G | 0.00100629 | 0.0224083 | synonymous-codon, utr-variant-5-prime | TNK2 | GRCh38.p7 | 3:195879130 | GAACATCCAGGTGTC[A/G]CTGGCATGGGAGAAG | 10188 |
rs147724137 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNK2 | GRCh38.p7 | 3:195869074 | CCCCGCCCCTGTCAC[A/G]GCACACCATTAGTGC | 10188 |
rs147776988 | snp | A/C | 0.376989 | 0.215346 | intron-variant | TNK2 | GRCh38.p7 | 3:195872022 | ATTCCCCTGGAGAAC[A/C]CTCCCCTGGAGAACC | 10188 |
rs147786918 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNK2 | GRCh38.p7 | 3:195903292 | TGATCTGCACATCTC[A/G]GCCTCCCAAAGTATT | 10188 |
rs147892155 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TNK2 | GRCh38.p7 | 3:195888022 | TGAGAGAGCAAGAAA[A/G]AGAGCGTGAGCACGA | 10188 |
rs148016583 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195885735 | GGACAGGGAGGAGCC[A/G]AAGGTCAAGGGACAG | 10188 |
rs148060819 | snp | A/C/T | 8.31696e-05 | 0.00644816 | synonymous-codon, upstream-variant-2KB, utr-variant-5-prime | TNK2, MIR6829 | GRCh38.p7 | 3:195883169 | CACCATCTTCATGGG[A/C/T]GGCGTGAGCACCACC | 10188 |
rs148092490 | snp | A/C | 0.210909 | 0.246925 | intron-variant | TNK2 | GRCh38.p7 | 3:195872052 | CCTCCCCTGGAGAAC[A/C]CTCCCCTGGAGAACA | 10188 |
rs148176734 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | TNK2 | GRCh38.p7 | 3:195890146 | TCCACCTCGGCGACC[A/G]GGCCAGGCAGCTGGG | 10188 |
rs148253032 | snp | C/T | 0.00476339 | 0.0485696 | intron-variant | TNK2 | GRCh38.p7 | 3:195876548 | AAGCTCTGCCACCAC[C/T]GACACCCAGGCCCGC | 10188 |
rs148272120 | snp | C/T | 0.00499348 | 0.0497172 | synonymous-codon, intron-variant | TNK2 | GRCh38.p7 | 3:195869531 | CTGAGGTGGGCGAGG[C/T]GGAGGCTCCCCTGCA | 10188 |
rs148305404 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TNK2 | GRCh38.p7 | 3:195903547 | CATAGTGAAACCCCA[G/T]CTCTACTAAGGATAC | 10188 |
rs148323328 | snp | C/T | 0.0135386 | 0.0811717 | missense | TNK2 | GRCh38.p7 | 3:195867585 | GCAGCAGCAGAGGCA[C/T]AGGCAGGGGGGTAGG | 10188 |
rs148366432 | snp | A/G | 0.0056801 | 0.0529886 | intron-variant | TNK2 | GRCh38.p7 | 3:195869591 | ACGGAGCAGGACAGA[A/G]GACAAAGGAGGGAGA | 10188 |
rs148423089 | snp | G/T | 0.00227842 | 0.0336757 | missense | TNK2 | GRCh38.p7 | 3:195867767 | TGGATCACCTGGGGG[G/T]TGGCGTACTTGGGGT | 10188 |
rs148475313 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TNK2 | GRCh38.p7 | 3:195903080 | TTTTTTTTCTTTTGT[A/G]ACAGAGTCGGAATGC | 10188 |
rs148510577 | snp | C/T | 0.000429951 | 0.0146557 | synonymous-codon, downstream-variant-500B, intron-variant | TNK2, MIR6829 | GRCh38.p7 | 3:195882110 | GTCATTCTGAGGTAG[C/T]GCTCGCATCAGCCCA | 10188 |
rs148561701 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNK2 | GRCh38.p7 | 3:195877885 | ACCCAGGTGGATGGC[C/T]GAGTCCCTGTGCCAG | 10188 |
rs148613845 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | TNK2 | GRCh38.p7 | 3:195904984 | GTAGAAATTGACTAA[C/T]TAATTCTAAAATGTA | 10188 |
rs148743046 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | TNK2 | GRCh38.p7 | 3:195900188 | GGGGTGCTGGGGCGC[A/G]GGCTGCCACACAGGG | 10188 |
rs148791867 | snp | A/G | 8.23716e-05 | 0.00641709 | missense | TNK2 | GRCh38.p7 | 3:195878304 | ATGTGCAGCTTGTCC[A/G]GTTCCTCAAAGTCCT | 10188 |
rs148845181 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TNK2 | GRCh38.p7 | 3:195868852 | TCTGAGGTCAGCCAC[C/T]GGCGGCCAGGTTCTC | 10188 |
rs148868919 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | TNK2 | GRCh38.p7 | 3:195891797 | CTCCTGAAAACAGCT[C/G]AAAGCCATGCCCGGG | 10188 |
rs148932803 | snp | C/T | 0.000148693 | 0.00862115 | missense, downstream-variant-500B, intron-variant | TNK2, MIR6829 | GRCh38.p7 | 3:195882198 | TCACGGTGAATAAAG[C/T]GCTTGGACTCCAGGT | 10188 |
rs148940647 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | TNK2 | GRCh38.p7 | 3:195906316 | CCCAGCCATTCCGGT[A/C]CTAGGGATTTACCTA | 10188 |
rs149005549 | snp | C/T | 0.376989 | 0.215346 | intron-variant | TNK2 | GRCh38.p7 | 3:195872023 | TTCCCCTGGAGAACC[C/T]TCCCCTGGAGAACCC | 10188 |
rs149054383 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TNK2 | GRCh38.p7 | 3:195901221 | TCAAAGGGGAAGGGG[C/T]GTGCCTGGTCCAAGG | 10188 |
rs149059305 | snp | A/C | | | intron-variant | TNK2 | GRCh38.p7 | 3:195902644 | ACAAAAAAAAACAAA[A/C]ATAAAAAAAAAAAAA | 10188 |
rs149178487 | snp | A/G | 1.68216e-05 | 0.00290009 | intron-variant, missense | TNK2 | GRCh38.p7 | 3:195867182 | ACCTTCAGATACTGG[A/G]CAGCCCTCTGCACGC | 10188 |
rs149214349 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TNK2 | GRCh38.p7 | 3:195903487 | TTTGGCAGGCCGAGG[C/T]GGGCAGGTCACCTGA | 10188 |
rs149257266 | snp | A/G | 0.00651696 | 0.0567099 | synonymous-codon, upstream-variant-2KB, utr-variant-5-prime | TNK2 | GRCh38.p7 | 3:195884863 | CACCACGCCAAAGGA[A/G]CCATCACCCAGCTTC | 10188 |
rs149295036 | snp | A/G | 3.62575e-05 | 0.00425763 | missense | TNK2 | GRCh38.p7 | 3:195867717 | CATCCCGGACGATGG[A/G]CAGGATGCAGGGACC | 10188 |
rs149338288 | snp | A/G | | | intron-variant, downstream-variant-500B | TNK2 | GRCh38.p7 | 3:195866570 | AGAAAGAGGTGTGCA[A/G]ATCATGGGGTCCTAA | 10188 |
rs149542127 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195904497 | CCAAATTCATAGAGT[C/G]AGAAGGTAAAATGGT | 10188 |
rs149552240 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TNK2 | GRCh38.p7 | 3:195900093 | GCCATCTCAGAACCA[A/G]AACAACTCAGCCAGT | 10188 |
rs149663605 | snp | C/T | 0.0307296 | 0.120085 | synonymous-codon | TNK2 | GRCh38.p7 | 3:195868642 | CAGGCCTGGCTTCCG[C/T]AGGCCCAGCCTCTTG | 10188 |
rs149697992 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TNK2 | GRCh38.p7 | 3:195877196 | CCCAGGCCTCTCTTT[C/G]TAGAACCTTCTGCAT | 10188 |
rs149853438 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TNK2 | GRCh38.p7 | 3:195906145 | CAGACATGAGAGTGT[C/G]TAAAATTAGAGACTG | 10188 |
rs149876988 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | TNK2 | GRCh38.p7 | 3:195900969 | GTGGAGTGTGGAAAG[A/G]AGGAGTGGAGAGGAG | 10188 |
rs149991483 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TNK2 | GRCh38.p7 | 3:195887608 | TTTAGCTATTTTAAC[C/T]TGAAAGCCCTAATAC | 10188 |
rs150105233 | snp | A/G | 0.0189856 | 0.0955633 | utr-variant-3-prime | TNK2 | GRCh38.p7 | 3:195864008 | AGCGCTGGTGCAGGA[A/G]GGATGGGCAGGGCAG | 10188 |
rs150187481 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | TNK2 | GRCh38.p7 | 3:195901904 | GACCCACATTGGACT[C/T]GCTGAGTGGATACCA | 10188 |
rs150238977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195898329 | CATCACGCTCCAGCT[A/G]GGCAACTTTTGAGCA | 10188 |
rs150245181 | snp | A/G | 0.00134125 | 0.0258617 | missense | TNK2 | GRCh38.p7 | 3:195868641 | GCAGGCCTGGCTTCC[A/G]CAGGCCCAGCCTCTT | 10188 |
rs150315065 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195894030 | ATGGCAGGTGTGGAT[A/G]GAGTGGGGGCTGAGG | 10188 |
rs150367002 | snp | A/G | | | intron-variant | TNK2 | GRCh38.p7 | 3:195888666 | AACAGGGGCCTGCCC[A/G]AGTGACCTGGGCTCA | 10188 |
rs150404773 | snp | A/G | 0.00104985 | 0.0228872 | synonymous-codon, utr-variant-5-prime | TNK2 | GRCh38.p7 | 3:195888544 | TTGCAGCTGCACCTC[A/G]GACAGCAGCTCCAGC | 10188 |
rs150556045 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNK2 | GRCh38.p7 | 3:195873329 | GGCTCCCGCAAGACA[C/T]TCCTGACTCCCGAAG | 10188 |
rs150586085 | in-del | -/G | | | intron-variant | TNK2 | GRCh38.p7 | 3:195876177 | CCAAACGAGCCCCTG[-/G]GGAAAGACCAGTCAT | 10188 |
rs150628608 | snp | A/G | 0.034089 | 0.126025 | utr-variant-5-prime, intron-variant | TNK2 | GRCh38.p7 | 3:195895436 | CAGAAGTGCAGGGCC[A/G]CTACTGCGTCTCAGC | 10188 |
rs150680308 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TNK2 | GRCh38.p7 | 3:195890543 | GCAAACTCAGCCTCC[C/T]GGGTTCAGGCAATTC | 10188 |
rs150715337 | snp | C/T | 0.000220281 | 0.0104925 | synonymous-codon, upstream-variant-2KB, utr-variant-5-prime | TNK2 | GRCh38.p7 | 3:195884890 | CTTCTCCAGGAGGCG[C/T]AGGTCCTTCTCCCCA | 10188 |
rs150767247 | snp | A/G | 0.000522162 | 0.0161496 | synonymous-codon | TNK2 | GRCh38.p7 | 3:195872392 | CGACAGGCCGGCCAC[A/G]GAGGTCACCACGTTG | 10188 |
rs150800532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195876696 | GGAGCCCCCAGAGCC[C/T]CACCAGCAGCAGCCA | 10188 |
rs150843767 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TNK2 | GRCh38.p7 | 3:195864535 | ACCACCCCAGACAGC[A/G]ACAGACAGGTGACAC | 10188 |
rs150954634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195898230 | CCAGACACACCGGTC[A/G]GGCTGCTTCAACCGC | 10188 |
rs150996995 | snp | C/T | 0.0070988 | 0.0591524 | synonymous-codon | TNK2 | GRCh38.p7 | 3:195868441 | CGTGGGGCTCTGAGG[C/T]GGGGTCTCGTCCAGC | 10188 |
rs150999632 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | TNK2 | GRCh38.p7 | 3:195892249 | GCCAAGAAGAAGGAA[C/T]GCAGCAGCCGCAGGA | 10188 |
rs151076362 | snp | C/T | 0.00268948 | 0.0365719 | intron-variant, upstream-variant-2KB | TNK2, MIR6829 | GRCh38.p7 | 3:195883141 | CTGCCCGCCCCCTCC[C/T]GCCCGCAGTACTCAC | 10188 |
rs151094251 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNK2 | GRCh38.p7 | 3:195905488 | AGAGGAGTGAGCCAC[C/T]GTGCCCAGCCAGCAA | 10188 |
rs151229374 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNK2 | GRCh38.p7 | 3:195888269 | CCTTTATAACTGCCA[A/G]CTGTTCTCATCACAC | 10188 |
rs151330438 | snp | A/C/T | 0.000551599 | 0.0165983 | synonymous-codon, missense | TNK2 | GRCh38.p7 | 3:195878569 | GGGCAGCCGCTCCCC[A/C/T]TCCTTGTCGATCTTA | 10188 |
rs180675895 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | TNK2 | GRCh38.p7 | 3:195896474 | ACTGCCGGCGAGGCC[A/C]CCGAACGCCTGCTTC | 10188 |
rs180686960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195904913 | TCAATACTGCTAACC[A/G]ATCAATTCTCCCCAA | 10188 |
rs180688260 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195874456 | TGCTCCTGGGGGAAG[C/G]AGAGTAAGAGTGCGG | 10188 |
rs180857284 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | TNK2 | GRCh38.p7 | 3:195866579 | TGTGCAAATCATGGG[C/G]TCCTAAAAAGTGCCA | 10188 |
rs180873370 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195884424 | AAAGTGGGCAGATCA[G/T]CTGAGGTCAGGAGTT | 10188 |
rs180926125 | snp | A/G | | | intron-variant | TNK2 | GRCh38.p7 | 3:195899870 | GGAACACTGGAGAAC[A/G]GTGGCTGCTTCTTCC | 10188 |
rs181170393 | snp | C/T | | | utr-variant-3-prime | TNK2 | GRCh38.p7 | 3:195864063 | GCCTTGCTCCATCCC[C/T]GGGAGCAGCAGGAGC | 10188 |
rs181278571 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TNK2 | GRCh38.p7 | 3:195871358 | GAGCTGCCACCTAAC[A/G]TTCCCTCTGCAGTCC | 10188 |
rs181308066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195888755 | GAAGCTACCGAGAAC[C/T]GCCTGGACCCACGTC | 10188 |
rs181377833 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNK2 | GRCh38.p7 | 3:195889409 | GTAAAATATTCAGAA[A/G]GCACACTGAGCCACG | 10188 |
rs181406275 | snp | A/G | 0.174932 | 0.238463 | intron-variant | TNK2 | GRCh38.p7 | 3:195881546 | AACACCCCCCCCAGC[A/G]ATGCCCCTTGAAGAG | 10188 |
rs181533746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195900404 | GAGGATCTGACTAAA[C/T]AGCGTGACCCAGTCC | 10188 |
rs181582565 | snp | A/C/T | 0.0001367 | 0.00826638 | synonymous-codon, missense | TNK2 | GRCh38.p7 | 3:195868114 | CAGTTGCCTCATGCA[A/C/T]TCCTGCTGTAGCGCC | 10188 |
rs181590467 | snp | A/C | 0.000479731 | 0.0154802 | intron-variant, utr-variant-5-prime | TNK2 | GRCh38.p7 | 3:195885493 | TTCTCTGGCCTGACC[A/C]TTTGGTGCTGTCTGT | 10188 |
rs181613245 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | TNK2 | GRCh38.p7 | 3:195905303 | CTCCCGGGTTCATGC[A/G]ATTCTCCTGACTCAG | 10188 |
rs181706423 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNK2 | GRCh38.p7 | 3:195899488 | TGCGCCACCACGCCC[A/G]GCTAATTTTTATATT | 10188 |
rs181794570 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195893961 | AGAAGGACACCCCCA[A/G]CTTCAGTCCCTCTTC | 10188 |
rs181875951 | snp | A/G | 0.000115499 | 0.00759844 | synonymous-codon | TNK2 | GRCh38.p7 | 3:195879115 | CCACAGTGTCACCCC[A/G]AACATCCAGGTGTCG | 10188 |
rs182008143 | snp | C/T | | | intron-variant | TNK2 | GRCh38.p7 | 3:195873975 | GAGAGGACAGTACCC[C/T]GAGACGAGACGAGTC | 10188 |
rs182011958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195865927 | ATGTGGAGAAACTCC[A/G]CACCGTGCACAGGGC | 10188 |
rs182263574 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | TNK2 | GRCh38.p7 | 3:195874284 | CTGGCCTCTCCCTTC[C/T]GCCAACACTGCCCAG | 10188 |
rs182355191 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, intron-variant | TNK2 | GRCh38.p7 | 3:195869519 | GAAGAAGGCAGGCTG[A/G]GGTGGGCGAGGTGGA | 10188 |
rs182400288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195906314 | GACCCAGCCATTCCG[A/G]TCCTAGGGATTTACC | 10188 |
rs182508602 | snp | C/T | 1.82907e-05 | 0.00302408 | intron-variant | TNK2 | GRCh38.p7 | 3:195895237 | CTATCCCCTAGCCTT[C/T]CCCATTACCTGCGGT | 10188 |
rs182584560 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195887205 | GAGCCTCAACTGACC[A/G]ACGGTCTCTGCACTC | 10188 |
rs182598393 | snp | A/C/T | 0.00199481 | 0.0315187 | intron-variant | TNK2 | GRCh38.p7 | 3:195907039 | ACAGCTTGTAAGCGA[A/C/T]ATAACCAGATCAAAA | 10188 |
rs182599822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195869723 | GGATGAGGAACACGG[C/T]GGTCCAGTATGATAG | 10188 |
rs182654931 | snp | G/T | | | intron-variant, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195886661 | GACACTGGCCCCAAC[G/T]CTCAGACACAGCAGG | 10188 |
rs182666660 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | TNK2 | GRCh38.p7 | 3:195889836 | GGCCAGGCTAGCCCC[A/G]GACCCATGCTCAATC | 10188 |
rs182718314 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TNK2 | GRCh38.p7 | 3:195881703 | ACCCCCCCGCCAGCA[A/G]TGCCCCTTGGAGAGG | 10188 |
rs182810036 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNK2 | GRCh38.p7 | 3:195890599 | GGGATCACAGGCGCC[C/T]GGCTAATTTTTGTAT | 10188 |
rs182938028 | snp | C/T | | | intron-variant | TNK2 | GRCh38.p7 | 3:195871963 | TTCCCCTGGAGAACC[C/T]TCCCCTGGAGAACCC | 10188 |
rs183164702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | TNK2, MIR6829 | GRCh38.p7 | 3:195881847 | TATCCCTGTGATTTC[C/T]AGCACCCAGACCCTG | 10188 |
rs183171527 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TNK2 | GRCh38.p7 | 3:195901739 | CTTACTACCCCAGAT[C/T]ATCCCCACTTTACAA | 10188 |
rs183219484 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TNK2, MIR6829 | GRCh38.p7 | 3:195882971 | TCCAGAGACAGACCC[A/G]GACTGGACCGCAGCA | 10188 |
rs183261046 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNK2 | GRCh38.p7 | 3:195900551 | CCGGAGTGTCAACGC[C/T]GACACAAAGAGACAG | 10188 |
rs183289084 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TNK2 | GRCh38.p7 | 3:195872590 | CAGGCCTCAGGACCA[A/G]GCTGTGTGCCACCGG | 10188 |
rs183420019 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195875978 | CGGACATTCTGTTCA[A/T]AACGCCCGCCCGCTC | 10188 |
rs183429318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195885788 | AAAGCTGGCCACGTC[A/G]GTCTGACTCGGCCTC | 10188 |
rs183439612 | snp | G/T | | | intron-variant | TNK2 | GRCh38.p7 | 3:195902512 | AACCCCAGCTACTCA[G/T]GAGGCTGAGGCAGGA | 10188 |
rs183484345 | snp | A/C/G | 0.00100925 | 0.0224412 | intron-variant | TNK2 | GRCh38.p7 | 3:195876632 | AGCAGCTCCAGGCAC[A/C/G]GAGGGCAGGTGCTGT | 10188 |
rs183492056 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | TNK2 | GRCh38.p7 | 3:195891292 | ATGCCTGTAATCTCA[A/G]CTACTCAGGAGGCTG | 10188 |
rs183513544 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195897650 | GGGATTACAGGCGTG[C/T]ACTATCACACCCAGC | 10188 |
rs183525724 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TNK2 | GRCh38.p7 | 3:195896683 | TGCCTCACCTCCCCC[C/T]GTAAATCTCTGGCGT | 10188 |
rs183748278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195875613 | ACCAGCAGTCCAGAG[A/G]GGACTGAGGCCAGCC | 10188 |
rs184148301 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | TNK2 | GRCh38.p7 | 3:195873677 | CCCAGCCAGGCCGGG[A/G]AGAGAGGACGGAGGA | 10188 |
rs184160281 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | TNK2 | GRCh38.p7 | 3:195871014 | GTGTGGGTTCTGGTG[C/T]GTGGGGGCCCGCTGT | 10188 |
rs184180644 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TNK2 | GRCh38.p7 | 3:195869204 | GGTCTGGGAGGCAGC[A/G]AGGCCAAGGCAGAAG | 10188 |
rs184192036 | snp | G/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195910545 | AAACAGTTCACGGTA[G/T]GTGGCAAGATCAGAC | 10188 |
rs184239210 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | TNK2 | GRCh38.p7 | 3:195897300 | TCACACTGGTCTGGG[A/G]AGGAGGCTGGCCAGG | 10188 |
rs184306018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195888129 | GAACAGACTCAATTC[A/G]ATGCTTATGAAGGAG | 10188 |
rs184395551 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNK2 | GRCh38.p7 | 3:195902878 | CCTCGGCCTCCCAAG[C/T]AGCTGGAATTACATG | 10188 |
rs184402933 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TNK2 | GRCh38.p7 | 3:195864308 | AGTCCCCGGCAAGGA[C/T]TGTAAAATTTATCAT | 10188 |
rs184412835 | snp | A/G | 0.000446395 | 0.0149331 | missense, upstream-variant-2KB, utr-variant-5-prime | TNK2, MIR6829 | GRCh38.p7 | 3:195883240 | TGGCATTGACCTCCC[A/G]GATGAAGTCGTCCAT | 10188 |
rs184696640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195898932 | AAACCCCATCTCTAC[C/T]AAAAAATATAAAAAT | 10188 |
rs184828117 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195877383 | GGTCTCCTCCACCCA[A/C]CCCCAAGAGGCACAG | 10188 |
rs184851273 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195903793 | CAACAGGCATAAAGA[A/T]CAGAAAGGAGGAAGT | 10188 |
rs184925346 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNK2 | GRCh38.p7 | 3:195908449 | CTCTCACTTCCAAGC[A/G]CACCAACTCCAGCTA | 10188 |
rs185046001 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | TNK2 | GRCh38.p7 | 3:195863588 | TCTGGCACCCTTTCT[A/C]CGCTTCCTGAGCCAC | 10188 |
rs185062811 | snp | C/T | | | intron-variant | TNK2 | GRCh38.p7 | 3:195874049 | GCTCCCCAGCACGCA[C/T]ACAGCCTCCCACGGC | 10188 |
rs185181101 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195894517 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 10188 |
rs185193031 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195880686 | AACTCAGCAATGACC[C/G]TCGGAGAGGACACAG | 10188 |
rs185199731 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TNK2 | GRCh38.p7 | 3:195899953 | GTTGCCCTCTCCCAG[C/T]CCCGGCTTTGCCTCC | 10188 |
rs185396154 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | TNK2 | GRCh38.p7 | 3:195871506 | CAGGAGAAGGAAAAC[A/C]ACTGCTCGTGTGCAG | 10188 |
rs185436697 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNK2 | GRCh38.p7 | 3:195889224 | GAGGGGTGGGGCCTG[C/T]GGTGGGCTCGCAGAC | 10188 |
rs185496525 | snp | A/G | 0.00118074 | 0.0242688 | intron-variant, utr-variant-5-prime, missense | TNK2 | GRCh38.p7 | 3:195892500 | GCATCTCCACGCAGC[A/G]GGACCCCCCCGAGCA | 10188 |
rs185504108 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195866041 | TGCTGGCTCCAGCCA[A/C/T]GTGACCTCAGTTCAC | 10188 |
rs185593095 | snp | A/T | | | intron-variant | TNK2 | GRCh38.p7 | 3:195873449 | GAGCCCCGTGGGCAG[A/T]GTCTGGGCAGGCGGG | 10188 |
rs185614367 | snp | A/G | | | intron-variant, upstream-variant-2KB | TNK2, MIR6829 | GRCh38.p7 | 3:195884234 | GGGAGGAAGAGGCTC[A/G]GCTTCCTCTGAGTGG | 10188 |
rs185733253 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TNK2 | GRCh38.p7 | 3:195896508 | GCTGTACAGAAGCTC[C/T]TCGGCATCTTACTGC | 10188 |
rs185734671 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TNK2 | GRCh38.p7 | 3:195887738 | ACCTGTGTGTATGTG[C/T]GTGTGTGTGCACACG | 10188 |
rs185748699 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TNK2 | GRCh38.p7 | 3:195868914 | GGAACCTGCTCTGCC[C/T]GGCAGCCCCATGTGG | 10188 |
rs185880732 | snp | A/G | | | intron-variant | TNK2 | GRCh38.p7 | 3:195870900 | GGGGTTCCAGTGTGT[A/G]TGGGCCCGCTGTGTG | 10188 |
rs185977458 | snp | A/G | 0.000161199 | 0.00897628 | intron-variant, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195885530 | CCTCACCAGGGAGTC[A/G]GCTGCCCTTCATCCT | 10188 |
rs185983893 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNK2 | GRCh38.p7 | 3:195905357 | GGTGCCCGCCACCAC[A/G]CCTGGCTAATTTTTT | 10188 |
rs186209346 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TNK2 | GRCh38.p7 | 3:195889868 | CCAAAGAGGAACAGG[C/T]GAGAGAAAAAAGGCC | 10188 |
rs186336923 | snp | C/G | | | intron-variant | TNK2 | GRCh38.p7 | 3:195901235 | GCGTGCCTGGTCCAA[C/G]GTACCAGGAAGCTGT | 10188 |
rs186338726 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TNK2 | GRCh38.p7 | 3:195900423 | GTGACCCAGTCCACA[A/C]TGAACCTGAGGCTGA | 10188 |
rs186354097 | snp | A/T | 3.88071e-05 | 0.00440477 | intron-variant, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195885063 | CCGGGGGCCAGATGG[A/T]ATCCAACACCCCAGG | 10188 |
rs186400192 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | TNK2 | GRCh38.p7 | 3:195895720 | CAACTGGGGCCTTGG[A/G]GATTCACGAGTCCCC | 10188 |
rs186414107 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | TNK2 | GRCh38.p7 | 3:195874318 | CAGGCACAGAAGCCT[A/C]CTTTGGGACCCACTT | 10188 |
rs186467747 | snp | A/G | | | intron-variant | TNK2 | GRCh38.p7 | 3:195881617 | CCTTGAAGAGGACAC[A/G]GCATCTATCCTTGTA | 10188 |
rs186600762 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNK2 | GRCh38.p7 | 3:195904992 | TGACTAACTAATTCT[A/G]AAATGTATATGGAAG | 10188 |
rs186783613 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195902249 | AGGAACTGGCAGCCC[C/G]GGAAACCTCTGGAAG | 10188 |
rs186800421 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, utr-variant-5-prime, missense | TNK2 | GRCh38.p7 | 3:195892625 | GGGGTGGGCCCCTCC[A/G]CTCTGCTGCAAGCCC | 10188 |
rs187135760 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TNK2 | GRCh38.p7 | 3:195890630 | TTTTAGTGGAGACAG[C/G]GTTCCTCCATGTTGG | 10188 |
rs187148888 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNK2 | GRCh38.p7 | 3:195869298 | AGCCAGGGCCACACT[C/T]GTGAGCAGAAGCCCA | 10188 |
rs187172444 | snp | A/C/G | 0.000137618 | 0.00829419 | intron-variant | TNK2 | GRCh38.p7 | 3:195872263 | TCAGCATCCATCCCC[A/C/G]CCCAGTACTCACTCG | 10188 |
rs187219526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195889434 | GCCACGAATCTCATT[C/T]CCTCCCCAGCTGCAC | 10188 |
rs187380252 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195885897 | CCTTATCCGTCTGGG[A/C]TAGGGTGCCTCAAAT | 10188 |
rs187404883 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | TNK2 | GRCh38.p7 | 3:195871954 | TGGAGAACATTCCCC[C/T]GGAGAACCCTCCCCT | 10188 |
rs187551868 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | TNK2 | GRCh38.p7 | 3:195897427 | CCTGGCAGCTGAGGT[A/C]CTGAGGGCAGGCAAG | 10188 |
rs187621506 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195887518 | TTTTAACTAAGTCAG[G/T]GTCTAACTTGACACA | 10188 |
rs187630512 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TNK2 | GRCh38.p7 | 3:195907640 | AGTAGGTCTGGCACT[C/G]AGGCCACGAGGGAGT | 10188 |
rs187630894 | snp | A/G | 0.000433745 | 0.0147202 | intron-variant | TNK2 | GRCh38.p7 | 3:195870360 | AGAACCTGACCGCAC[A/G]TCTCAGCTGGGGGGT | 10188 |
rs187715056 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | TNK2, MIR6829 | GRCh38.p7 | 3:195881862 | CAGCACCCAGACCCT[A/G]GCACGTGGGCCCTCA | 10188 |
rs187745976 | snp | C/T | 0.0037383 | 0.0430718 | intron-variant | TNK2 | GRCh38.p7 | 3:195876493 | GCAGCCAAACAAACA[C/T]GGAGATATTCAGGGA | 10188 |
rs187788403 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TNK2 | GRCh38.p7 | 3:195902555 | CCCAGGAGGCAGAAG[G/T]TGCAGTGAGCCGAGA | 10188 |
rs187792283 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195881787 | ACAGCATCTATCCCC[G/T]TATCACCCCACCCAG | 10188 |
rs187966747 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | TNK2 | GRCh38.p7 | 3:195863748 | CTAGGAGGTCCCACC[A/G]GGTGCCGGTCCGCCT | 10188 |
rs187976227 | snp | C/T | 0.00199481 | 0.0315187 | downstream-variant-500B | TNK2 | GRCh38.p7 | 3:195862945 | ACCCAGTCATTTCAC[C/T]GTACACTCCTCAGTG | 10188 |
rs188053709 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195886762 | CGCACACAGGCTGCT[C/T]ACGTGTCCGTATCTG | 10188 |
rs188086250 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | TNK2, MIR6829 | GRCh38.p7 | 3:195883041 | TACTCCATCAGGTTG[A/G]GGGACCAAAGTAGGA | 10188 |
rs188330742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195906513 | TGAAAGACGCGATTC[C/T]GTTTACAGTAAATGC | 10188 |
rs188351152 | snp | A/G | 0.00186841 | 0.0305076 | intron-variant | TNK2 | GRCh38.p7 | 3:195876729 | GGGAACCAGCGGCTG[A/G]GGCCAACGGGGGCCT | 10188 |
rs188362416 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNK2 | GRCh38.p7 | 3:195873735 | ACAGCCTTGTAAGGT[A/G]ACGAGGCCTGGCTGG | 10188 |
rs188393783 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195893037 | GGGACTTTAGGGTGG[C/T]GGCTATGTGACTCAA | 10188 |
rs188477027 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TNK2 | GRCh38.p7 | 3:195875918 | AATCTCAGCACCACG[C/T]TCCCGTCCGGGCCGA | 10188 |
rs188619868 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNK2 | GRCh38.p7 | 3:195871133 | AGAAGGGCTGCAGAG[A/G]CCAGGGGCCTGGAAT | 10188 |
rs188770971 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TNK2 | GRCh38.p7 | 3:195896984 | TCTACCGTATTCTCA[A/G]GAATATATGCCAACC | 10188 |
rs188834087 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TNK2 | GRCh38.p7 | 3:195891437 | CTAACACTTCAACTG[C/T]ACTTACTATATGCGA | 10188 |
rs189108222 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | TNK2 | GRCh38.p7 | 3:195872805 | GACCTGGGACCCAAC[C/G]CCAGCTTTCAGGTCT | 10188 |
rs189123845 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNK2 | GRCh38.p7 | 3:195889387 | GAAAAGGTAATATAT[A/G]CACGTGGTAAAATAT | 10188 |
rs189301416 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TNK2 | GRCh38.p7 | 3:195899662 | TAAATTATCCATCAC[G/T]TTCCTATCCTTAAAG | 10188 |
rs189317160 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNK2 | GRCh38.p7 | 3:195879308 | AGTGGGTCTCAGGGG[C/T]GCCGTGTGAAGCGGG | 10188 |
rs189326195 | snp | A/G | 0.0126979 | 0.078662 | intron-variant, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195884423 | TAAAGTGGGCAGATC[A/G]TCTGAGGTCAGGAGT | 10188 |
rs189438782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195905302 | CCTCCCGGGTTCATG[C/T]GATTCTCCTGACTCA | 10188 |
rs189547767 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TNK2 | GRCh38.p7 | 3:195903294 | ATCTGCACATCTCGG[C/G]CTCCCAAAGTATTGG | 10188 |
rs189556323 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | TNK2 | GRCh38.p7 | 3:195864851 | TCAGTAAGAAACACC[C/T]GAGACAGTGACAGAC | 10188 |
rs189562053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNK2, MIR6829 | GRCh38.p7 | 3:195883398 | TCCAACTCGGCTCAA[C/T]GATCCCTGCCTGTGA | 10188 |
rs189626146 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | TNK2 | GRCh38.p7 | 3:195866106 | TTTACATAATATATA[A/C]AGTGTGTTTATATAT | 10188 |
rs189644488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195903988 | GTTTAAACAACGGTA[C/T]CATCTCATAACAGCA | 10188 |
rs189685204 | snp | A/G | | | intron-variant, utr-variant-5-prime | TNK2 | GRCh38.p7 | 3:195885429 | CGCATCGATGGAGCC[A/G]CAGGGGCCCTCCACA | 10188 |
rs189772417 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | TNK2 | GRCh38.p7 | 3:195890507 | CCAGGCTGGAGTACA[A/G]TGGTATGATCTTGGC | 10188 |
rs189913252 | snp | C/G/T | 0.00358779 | 0.0422022 | intron-variant | TNK2 | GRCh38.p7 | 3:195894986 | CTAGCAGTACTTCCT[C/G/T]GACTCCCTTGGGGCA | 10188 |
rs190025073 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TNK2 | GRCh38.p7 | 3:195896473 | GACTGCCGGCGAGGC[A/C]CCCGAACGCCTGCTT | 10188 |
rs190043911 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | TNK2 | GRCh38.p7 | 3:195874355 | GGGAAAGGAGACATC[A/T]AGCCCACCTCCCTTA | 10188 |
rs190103989 | snp | A/G | | | upstream-variant-2KB, intron-variant | TNK2 | GRCh38.p7 | 3:195896549 | ACATACTAGTCTTGG[A/G]AGTAGCTGCAAAGCC | 10188 |
rs190154381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195877676 | CAGGCGCTAGAACTG[C/T]GGGGGCTCAGGTGGA | 10188 |
rs190155521 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNK2 | GRCh38.p7 | 3:195874065 | ACAGCCTCCCACGGC[A/G]GCCCGTAGAGGAGGA | 10188 |
rs190221775 | snp | A/G | 0.0509478 | 0.151255 | upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195909106 | GCGCTCCTGCACCCC[A/G]GCCCGGGCCTCGCCG | 10188 |
rs190389389 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TNK2 | GRCh38.p7 | 3:195899009 | GCTGAGGCAGGAGAA[C/T]GGCGTGAACCCGGGA | 10188 |
rs190403344 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | TNK2 | GRCh38.p7 | 3:195869202 | CAGGTCTGGGAGGCA[G/T]CGAGGCCAAGGCAGA | 10188 |
rs190440974 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195885725 | AGGCCAGGGTGGACA[C/G]GGAGGAGCCGAAGGT | 10188 |
rs190441585 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TNK2 | GRCh38.p7 | 3:195887754 | GTGTGTGTGCACACG[C/T]GTGTGCGCACGTGTG | 10188 |
rs190447348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195905441 | CCTGACCTCATGATC[C/T]GCCCGCCTCAGCCTC | 10188 |
rs190642022 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TNK2 | GRCh38.p7 | 3:195890851 | AAAATGTCAGTGAAG[C/G]CAACCCCCTCTCATT | 10188 |
rs190693922 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TNK2 | GRCh38.p7 | 3:195900163 | AGGTGCCTTCTCATC[A/G]GACTGCGAAGGGGTG | 10188 |
rs190754997 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | TNK2, MIR6829 | GRCh38.p7 | 3:195881835 | TCCCACAGCATGTAT[A/C]CCTGTGATTTCCAGC | 10188 |
rs190789783 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195901697 | CTTCACTGAGAGTGT[A/C]CCTTCACTGGCTGAC | 10188 |
rs190800551 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195886227 | TCCTTCCCTAAAACC[C/T]GGGCAAAGGACCAGG | 10188 |
rs191051661 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | TNK2 | GRCh38.p7 | 3:195906255 | CAACCACTTTGGAAA[A/C]CAGTCTGGCAGTTTC | 10188 |
rs191054009 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TNK2 | GRCh38.p7 | 3:195875548 | CCAAGAGGACCGTGT[C/T]ACTTCTCGCAGCCCA | 10188 |
rs191213366 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | TNK2 | GRCh38.p7 | 3:195869338 | GGGCGGGCTCGAGGG[A/G]GGGCAGGCATGCTAG | 10188 |
rs191238985 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNK2 | GRCh38.p7 | 3:195873547 | GGGCACGCGGGGGCG[A/G]TGACAGCCCAGAGCT | 10188 |
rs191272776 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, missense | TNK2 | GRCh38.p7 | 3:195892647 | TGCAAGCCCCGCTGG[C/G]TTTCCACAGCTGGCC | 10188 |
rs191292079 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNK2 | GRCh38.p7 | 3:195876549 | AGCTCTGCCACCACC[A/G]ACACCCAGGCCCGCT | 10188 |
rs191322875 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TNK2 | GRCh38.p7 | 3:195897504 | TCTTCACCCCACATG[A/T]TTTTTGTTTGTTTGT | 10188 |
rs191543483 | snp | G/T | 0.0111196 | 0.0737302 | upstream-variant-2KB, intron-variant | TNK2 | GRCh38.p7 | 3:195897237 | AACCTCATCCCAGAG[G/T]AACCTGCACCAGGCA | 10188 |
rs191683167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195869703 | ACGGGAGGCCGCAGG[C/T]GGCAGGATGAGGAAC | 10188 |
rs191690543 | snp | C/T | 4.95471e-05 | 0.00497705 | intron-variant, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195886946 | TTCGAGGCTGCCCCC[C/T]TCCCACCTCCTCACC | 10188 |
rs191768701 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TNK2 | GRCh38.p7 | 3:195875931 | CGTTCCCGTCCGGGC[C/T]GAAGGTAGTCCAGAA | 10188 |
rs191769282 | snp | C/T | | | intron-variant | TNK2 | GRCh38.p7 | 3:195881651 | CCCCCCCCCCAGCAA[C/T]GCCCTTTGGAGAGGA | 10188 |
rs191848748 | snp | A/C | | | intron-variant | TNK2 | GRCh38.p7 | 3:195871962 | ATTCCCCTGGAGAAC[A/C]CTCCCCTGGAGAACC | 10188 |
rs191887962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195900495 | TCTGTATCAAGTCTT[A/G]AAAGTACTGTGAAAC | 10188 |
rs192112485 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | TNK2 | GRCh38.p7 | 3:195887615 | ATTTTAACTTGAAAG[A/C]CCTAATACGTTTCTA | 10188 |
rs192120757 | snp | C/G | | | intron-variant | TNK2 | GRCh38.p7 | 3:195908388 | GATGAAAGGCCAAAA[C/G]AACGAGGGCAGTGTG | 10188 |
rs192128886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195870855 | TGGGTTCTTTTTAGG[C/T]AAAACACATGGGCTG | 10188 |
rs192156623 | snp | C/T | | | intron-variant | TNK2 | GRCh38.p7 | 3:195889460 | TGCACAGCCACCCGG[C/T]TCCCCAGGAGTTGCC | 10188 |
rs192196366 | snp | C/G | 0.000940881 | 0.0216692 | utr-variant-3-prime | TNK2 | GRCh38.p7 | 3:195864135 | TGGTGGACGGACAGG[C/G]TCAGGTGATTCCTTC | 10188 |
rs192201096 | snp | C/T | 0.000800197 | 0.0199865 | intron-variant, upstream-variant-2KB | TNK2, MIR6829 | GRCh38.p7 | 3:195883113 | CCACACATATGGGAC[C/T]GGAGCCCTCTCCCTG | 10188 |
rs192250841 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime | TNK2 | GRCh38.p7 | 3:195863419 | CAGGTACTGAATGCC[A/G]GAGCAGCAACTTCGC | 10188 |
rs192267941 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNK2 | GRCh38.p7 | 3:195902434 | ACCAGCCTGGCCAAC[A/G]TGGTGAAACCCCATC | 10188 |
rs192597285 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TNK2, MIR6829 | GRCh38.p7 | 3:195884042 | TGCACCGCACGTGAT[C/G]TGAGCAGTAAGGACA | 10188 |
rs192603144 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195903347 | GCCCGGCCAGCTAAC[A/C]CCACTCTTAATGGTG | 10188 |
rs192615515 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | TNK2 | GRCh38.p7 | 3:195906613 | GGGGATGGAGGGGTT[C/T]CACAAGAAAACTTCT | 10188 |
rs192696984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TNK2, MIR6829 | GRCh38.p7 | 3:195882375 | CTGGAGGACCCTGCC[C/T]CTTCTCAGCAGCCCA | 10188 |
rs192739633 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | TNK2 | GRCh38.p7 | 3:195870985 | TGTGGGGTTCTGGTG[C/T]GTGGGGGCCCGCTGT | 10188 |
rs192744668 | snp | G/T | 0.0256215 | 0.110247 | upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195909895 | CCCGCTCTCCCCGAC[G/T]CCCCCGGGCCCGGCC | 10188 |
rs192760937 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNK2 | GRCh38.p7 | 3:195877318 | GGGCCTGGGAAGGCT[C/T]GGGGTGTCGGGGCCA | 10188 |
rs192974057 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNK2 | GRCh38.p7 | 3:195898679 | TGCCCAGGCTGGAGT[G/T]CAGTGGTGTGACCAT | 10188 |
rs193040512 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | TNK2 | GRCh38.p7 | 3:195873212 | AGTAGGGCTGCCAGT[A/C]CCCCTCTGACCTCAG | 10188 |
rs193162359 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNK2 | GRCh38.p7 | 3:195902770 | TTTGTTTTGTCTTGT[A/G]AGACAGTTTTGCTCT | 10188 |
rs199517894 | snp | A/G | | | intron-variant | TNK2 | GRCh38.p7 | 3:195881567 | CCTTGAAGAGGACAC[A/G]GCATCTATCCCTGTA | 10188 |
rs199549073 | snp | C/T | 0.00114596 | 0.0239096 | missense | TNK2 | GRCh38.p7 | 3:195868353 | CCACGTCGTCATAGG[C/T]GGGCGGGGGGGGCAG | 10188 |
rs199580567 | snp | C/T | | | intron-variant | TNK2 | GRCh38.p7 | 3:195871436 | ATGTGGACCTGCATA[C/T]ATCCCCAGGGCCTGA | 10188 |
rs199583041 | snp | A/C/T | | | intron-variant | TNK2 | GRCh38.p7 | 3:195902646 | AAAAAAAAACAAACA[A/C/T]AAAAAAAAAAAAAAA | 10188 |
rs199585638 | snp | A/G | 7.00955e-05 | 0.0059197 | intron-variant, nc-transcript-variant | TNK2, MIR6829 | GRCh38.p7 | 3:195882339 | GTCACCTGAGGCCAC[A/G]GAGGAGGCAGGAGGA | 10188 |
rs199599216 | snp | A/G | | | intron-variant | TNK2 | GRCh38.p7 | 3:195887853 | GTGTGTGTGTGTGCG[A/G]GTCTGTGTGCGCAGG | 10188 |
rs199636920 | snp | A/C/G | 0.0073341 | 0.0601195 | missense, synonymous-codon | TNK2 | GRCh38.p7 | 3:195870129 | TTTTCACCCCTCCTA[A/C/G]ATGCTGGGGGGGCCG | 10188 |
rs199645713 | snp | A/G | | | intron-variant | TNK2 | GRCh38.p7 | 3:195875665 | TCCGCGCCCTCTCTC[A/G]CCCGCCATGAACAGG | 10188 |
rs199680214 | snp | C/T | 0.00116398 | 0.0240963 | missense | TNK2 | GRCh38.p7 | 3:195868220 | AGGGGAGGGGGCGGC[C/T]GCGCCTGCTCAGGCA | 10188 |
rs199684133 | snp | A/C/G | 0.000127105 | 0.00797097 | missense, synonymous-codon | TNK2 | GRCh38.p7 | 3:195868246 | AGGCACAAAGGCGTA[A/C/G]TTGGTCTGGCCCTGG | 10188 |
rs199694736 | snp | A/T | 0.000371903 | 0.0136313 | missense | TNK2 | GRCh38.p7 | 3:195868491 | CCAGCTGCGCCAGGG[A/T]GGGCGCGCAGGGCCG | 10188 |
rs199697262 | snp | A/G | 0.00299551 | 0.0385848 | intron-variant | TNK2 | GRCh38.p7 | 3:195879229 | ACCCTACCTGCGTCC[A/G]CCCCAGGGACTTAAA | 10188 |
rs199724610 | snp | C/T | 0.00121201 | 0.0245873 | missense, downstream-variant-500B, utr-variant-5-prime, intron-variant | TNK2, MIR6829 | GRCh38.p7 | 3:195882291 | TGGTGCTTACGTAGC[C/T]GGTCCAACAACGATC | 10188 |
rs199747325 | snp | C/T | 0.00199803 | 0.031544 | missense, utr-variant-5-prime, upstream-variant-2KB | TNK2 | GRCh38.p7 | 3:195886994 | TACTCATCCACGACT[C/T]GCGTTTGCACAAGGC | 10188 |
rs199747568 | snp | A/G | 0.000230335 | 0.0107291 | missense | TNK2 | GRCh38.p7 | 3:195868067 | TCACCCCCCGGGCTG[A/G]GAGAGGGGGCCGGGG | 10188 |
rs199790167 | snp | C/G | 0.00023108 | 0.0107465 | intron-variant | TNK2 | GRCh38.p7 | 3:195869462 | AGAGAGGGGGCGGGG[C/G]CGGGGGCCAAGGCAT | 10188 |
rs199821504 | snp | A/C/G | 1.72665e-05 | 0.00293819 | missense, stop-gained, upstream-variant-2KB, utr-variant-5-prime | TNK2 | GRCh38.p7 | 3:195885018 | ACTCAGCCTCCAGTC[A/C/G]CTTTCCACTGAACAC | 10188 |
rs199906205 | snp | C/G | 0.00199805 | 0.0315442 | intron-variant | TNK2 | GRCh38.p7 | 3:195872265 | AGCATCCATCCCCGC[C/G]CAGTACTCACTCGTC | 10188 |
rs199917038 | snp | G/T | | | intron-variant | TNK2 | GRCh38.p7 | 3:195907995 | GGCTCGTGCCGTACC[G/T]AAGCCACTAGCTGTC | 10188 |
rs199918564 | snp | A/G | 6.72442e-05 | 0.00579807 | synonymous-codon, intron-variant | TNK2 | GRCh38.p7 | 3:195895372 | CCCCGCAGCGGCACC[A/G]GCAGCGTCACTGCCC | 10188 |
rs199949969 | snp | A/G | 2.80312e-05 | 0.00374364 | missense | TNK2 | GRCh38.p7 | 3:195867899 | CTCGAGCCTTGAGGG[A/G]ACAGGGGCTCCCGCG | 10188 |
rs199977969 | snp | A/G | 5.35705e-05 | 0.00517517 | intron-variant, downstream-variant-500B | TNK2 | GRCh38.p7 | 3:195866843 | GGCAGGCTCTGGGAC[A/G]GCCCTCCTGGGGCAC | 10188 |
rs200006490 | in-del | -/C | | | intron-variant | TNK2 | GRCh38.p7 | 3:195874580 | GAGGCACAAGAAGCT[-/C]CCCCTCGGGATGGCG | 10188 |
rs200026055 | snp | C/T | 0.000190164 | 0.00974915 | missense | TNK2 | GRCh38.p7 | 3:195867836 | GGTGAGCTTGAGAGC[C/T]GGGGTGGCAGCGGGG | 10188 |
rs200034892 | snp | C/T | 1.68046e-05 | 0.00289862 | synonymous-codon | TNK2 | GRCh38.p7 | 3:195872353 | GATGAAGCTGTTCTG[C/T]AGGGGCTGGCTGATG | 10188 |
rs200040970 | snp | A/G | 0.00199807 | 0.0315443 | synonymous-codon, utr-variant-5-prime | TNK2 | GRCh38.p7 | 3:195888565 | CAGCTCCAGCAGCCA[A/G]CCTGTGCCCTCCTCT | 10188 |
rs200078114 | snp | A/G | 0.00191342 | 0.0308715 | missense | TNK2 | GRCh38.p7 | 3:195867563 | GGGGCTGGGGTGCTG[A/G]GTGGGGGCAGCAGCA | 10188 |
rs200100429 | snp | C/T | 0.000205751 | 0.0101407 | synonymous-codon | TNK2 | GRCh38.p7 | 3:195867011 | CAGCCCGAAGAGCTG[C/T]TCCACCTGGGGGTAA | 10188 |
rs200103256 | snp | A/G | 0.000899642 | 0.0211899 | synonymous-codon | TNK2 | GRCh38.p7 | 3:195868498 | CGCCAGGGAGGGCGC[A/G]CAGGGCCGTAGGGCC | 10188 |
rs200104049 | snp | C/T | 1.65206e-05 | 0.00287403 | missense | TNK2 | GRCh38.p7 | 3:195879084 | TCCAGGGCTCCTGGC[C/T]GTAGGTGAACATTTC | 10188 |
rs200111079 | snp | C/T | 0.000586217 | 0.0171104 | intron-variant | TNK2 | GRCh38.p7 | 3:195867033 | TGGGGGTAAGGGTGG[C/T]GCCATGGACACGCGG | 10188 |