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 |