SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs14090 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TBK1 | GRCh38.p7 | 12:64501773 | TCTACCATTTACAAA[C/T]GTGTCAAGTCAGTCT | 29110 |
rs4075093 | snp | A/T | 0.443195 | 0.158668 | intron-variant | TBK1 | GRCh38.p7 | 12:64483446 | AAATACATTAATAAA[A/T]CTAGGTATTTTCAAA | 29110 |
rs4075094 | snp | A/T | 0.227959 | 0.249026 | intron-variant | TBK1 | GRCh38.p7 | 12:64483273 | TGTACATAGGAAATG[A/T]ATATATTTATGAGGT | 29110 |
rs6581568 | snp | A/G | 0.44306 | 0.158832 | intron-variant | TBK1 | GRCh38.p7 | 12:64487773 | TTCTTTGTTTTTACA[A/G]TCTTTAAAAGTGTAA | 29110 |
rs6581569 | snp | A/G | 0.285519 | 0.247464 | intron-variant | TBK1 | GRCh38.p7 | 12:64492779 | ccaggttggagtgca[A/G]tggcgtaatctcggc | 29110 |
rs6581570 | snp | A/G | 0.322245 | 0.239334 | intron-variant | TBK1 | GRCh38.p7 | 12:64497491 | AAAGGGTGTTGATTT[A/G]AGTATTGTATCATCG | 29110 |
rs6581571 | snp | A/C | 0.335559 | 0.234904 | intron-variant | TBK1 | GRCh38.p7 | 12:64498356 | GTTGCTTTTTAAGAT[A/C]CCAGCACTTTGGTGC | 29110 |
rs7137215 | snp | A/G | 0.441295 | 0.160954 | downstream-variant-500B | TBK1 | GRCh38.p7 | 12:64502407 | GCAACCTCGGCCTCC[A/G]AGGTTCAAGCAATTC | 29110 |
rs7137380 | snp | A/T | | | intron-variant | TBK1 | GRCh38.p7 | 12:64472651 | CATCTGTTCTCAGTG[A/T]CTATGGTATTAGTGC | 29110 |
rs7295843 | snp | A/T | 0.440884 | 0.161442 | intron-variant | TBK1 | GRCh38.p7 | 12:64495927 | AAGGTTGATTGTGTT[A/T]AAAAAAAAAAAAAAA | 29110 |
rs7298226 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TBK1 | GRCh38.p7 | 12:64456088 | TGTTTTAATGATTTT[C/T]GTGGTCATTTAAGGC | 29110 |
rs7298599 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | TBK1 | GRCh38.p7 | 12:64478928 | TCACTAATAAAGGAA[A/G]CATGTGACTCATAAG | 29110 |
rs7298692 | snp | A/G | 0.442926 | 0.158996 | intron-variant | TBK1 | GRCh38.p7 | 12:64456270 | GTGATTTCACTGACA[A/G]AAGTTCAGTGTAATG | 29110 |
rs7303577 | snp | A/C | 0.229723 | 0.249176 | intron-variant | TBK1 | GRCh38.p7 | 12:64480322 | TATGAATAATTTCCC[A/C]AGATCTTCATTAGGA | 29110 |
rs7316037 | snp | A/G | 0.335788 | 0.23482 | intron-variant | TBK1 | GRCh38.p7 | 12:64453031 | ACTTTCGTTTTGGAC[A/G]GTGTAAGGAAGTAGG | 29110 |
rs7397683 | snp | C/T | 0.473634 | 0.111748 | intron-variant | TBK1 | GRCh38.p7 | 12:64499227 | TTTTTGTATTTTTAG[C/T]AGAGCTGGGGTTTCA | 29110 |
rs7486100 | snp | A/T | 0.49931 | 0.0185663 | synonymous-codon, nc-transcript-variant | TBK1 | GRCh38.p7 | 12:64482007 | TCATAAGATTTATAT[A/T]CATAGCTATAATACG | 29110 |
rs7487627 | snp | A/G | 0.474272 | 0.110462 | intron-variant | TBK1 | GRCh38.p7 | 12:64486123 | TGCTTGATTTTTATT[A/G]TAATACATTTGTTTC | 29110 |
rs7957676 | snp | C/G | 0.00755907 | 0.0610114 | downstream-variant-500B | TBK1 | GRCh38.p7 | 12:64502227 | TCTAGGGACAATTTT[C/G]TGTCTCTTCTAAACC | 29110 |
rs7957827 | snp | C/T | 0.0803491 | 0.183626 | downstream-variant-500B | TBK1 | GRCh38.p7 | 12:64502345 | ttgagacaagagtct[C/T]gctctgttgctcagg | 29110 |
rs7963264 | snp | A/G | 0.046775 | 0.145601 | intron-variant | TBK1 | GRCh38.p7 | 12:64483922 | tgaggcacgagaatc[A/G]cttgaatccaggagg | 29110 |
rs7963729 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | TBK1 | GRCh38.p7 | 12:64491578 | cagtgagccgagatc[A/G]tgccacttgcactcc | 29110 |
rs7963791 | snp | A/G | 0.473634 | 0.111748 | intron-variant | TBK1 | GRCh38.p7 | 12:64491881 | TTTTCAGTGGAACAG[A/G]ATAGAAAATGTCAGA | 29110 |
rs7972334 | snp | C/T | 0.226484 | 0.248892 | intron-variant | TBK1 | GRCh38.p7 | 12:64481072 | TTTCCAAAATGAAAT[C/T]GTCATGTAACTAGAT | 29110 |
rs7975785 | snp | A/T | 0.44306 | 0.158832 | intron-variant | TBK1 | GRCh38.p7 | 12:64487616 | GTCAATTGCTGATCC[A/T]TGAAGCTTTTATTCC | 29110 |
rs9634288 | snp | A/G | 0.224116 | 0.248656 | intron-variant | TBK1 | GRCh38.p7 | 12:64492464 | GGCATGTGCCACCAC[A/G]CCCAGCTAATTTTGT | 29110 |
rs9788149 | snp | C/T | 0.138546 | 0.223781 | intron-variant | TBK1 | GRCh38.p7 | 12:64494736 | CATAACAGTAAGATA[C/T]TATTTTTGTCTTTCA | 29110 |
rs10128757 | snp | C/T | 0.455263 | 0.142713 | intron-variant | TBK1 | GRCh38.p7 | 12:64467594 | TAAAGTCAGTAAATA[C/T]TTGAAATACTTAAGA | 29110 |
rs10626258 | in-del | -/AT/ATAT | | | intron-variant | TBK1 | GRCh38.p7 | 12:64458512 | TATATATATATATAT[-/AT/ATAT]GGATCTCTATTATTT | 29110 |
rs10714405 | in-del | -/A | 0.498392 | 0.028309 | intron-variant | TBK1 | GRCh38.p7 | 12:64465501 | ATTATTCATAATAGC[-/A]AAAAAAAAAAAAGAT | 29110 |
rs10784409 | snp | C/T | | | intron-variant | TBK1 | GRCh38.p7 | 12:64454991 | CAATTTTTTTTTTTT[C/T]TTTTTTTTTTTTTTG | 29110 |
rs10784410 | snp | C/T | | | intron-variant | TBK1 | GRCh38.p7 | 12:64454992 | AAttttttttttttc[C/T]tttttttttttttgc | 29110 |
rs10784411 | snp | G/T | 0.221141 | 0.248329 | intron-variant | TBK1 | GRCh38.p7 | 12:64462147 | cctaaatcatgctgt[G/T]agactctccagtggc | 29110 |
rs10784412 | snp | A/G | 0.221141 | 0.248329 | intron-variant | TBK1 | GRCh38.p7 | 12:64472215 | TTCTCATTAAAATGT[A/G]TTTCTCAAAAGAGTC | 29110 |
rs10878173 | snp | C/G | 0.465996 | 0.12588 | intron-variant | TBK1 | GRCh38.p7 | 12:64472195 | ATACTTGTCTGCATT[C/G]TGATTTCTCATTAAA | 29110 |
rs10878175 | snp | C/G | 0.473359 | 0.112298 | intron-variant | TBK1 | GRCh38.p7 | 12:64473558 | agatgatatgatagg[C/G]tctacagcacagatg | 29110 |
rs10878176 | snp | C/G | 0.473359 | 0.112298 | intron-variant | TBK1 | GRCh38.p7 | 12:64476753 | tttgcctaagacaat[C/G]tatagaagagtatgt | 29110 |
rs10878177 | snp | A/C | 0.253264 | 0.249979 | intron-variant | TBK1 | GRCh38.p7 | 12:64489981 | TTATTTATAAAACAT[A/C]TTTTTAAAACTATGT | 29110 |
rs10878178 | snp | C/T | 0.453331 | 0.145452 | intron-variant | TBK1 | GRCh38.p7 | 12:64492171 | CATGATTTACCTGCT[C/T]ATAGGCCTAGTGGAC | 29110 |
rs10878179 | snp | A/G | 0.441705 | 0.160466 | intron-variant | TBK1 | GRCh38.p7 | 12:64494308 | ACTCTACCAAAAAAA[A/G]AAAAAGAAAAAAAAG | 29110 |
rs11175395 | snp | A/G | | | intron-variant | TBK1 | GRCh38.p7 | 12:64452974 | GGAACTTTGTCCATA[A/G]GCCATGTCGTCAAAC | 29110 |
rs11175396 | snp | A/C | 0.0352966 | 0.128072 | intron-variant | TBK1 | GRCh38.p7 | 12:64453302 | TATTTTTCTTATTAT[A/C]CTGAAGGTACATACA | 29110 |
rs11175397 | snp | C/G | 0.0352966 | 0.128072 | intron-variant | TBK1 | GRCh38.p7 | 12:64455174 | TATTTTTTGTGGAGA[C/G]GGGGTTTTGCCGTGT | 29110 |
rs11175398 | snp | A/G | 0.448066 | 0.152544 | intron-variant | TBK1 | GRCh38.p7 | 12:64457198 | GACGATGAGATAAGC[A/G]TACATGGGGGAGGGG | 29110 |
rs11175399 | snp | C/G/T | 0 | 0 | intron-variant | TBK1 | GRCh38.p7 | 12:64459003 | ACATAGGATTATGAA[C/G/T]CAGTTAAATGGCCTT | 29110 |
rs11175400 | snp | A/T | | | intron-variant | TBK1 | GRCh38.p7 | 12:64460828 | acagagggagactcc[A/T]tctcaaaaaaaaaaa | 29110 |
rs11175402 | snp | G/T | 0.449345 | 0.150869 | intron-variant | TBK1 | GRCh38.p7 | 12:64463865 | AATGTTAGTTTTTTT[G/T]TTTTGTTTTTTTTTT | 29110 |
rs11175403 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | TBK1 | GRCh38.p7 | 12:64464105 | ttgacctcgtgatcc[A/G]cccacctcagcctcc | 29110 |
rs11175406 | snp | C/T | 0.33533 | 0.234987 | intron-variant | TBK1 | GRCh38.p7 | 12:64475968 | GGCTGAACTAATTTG[C/T]ATTCCCACCAATAGT | 29110 |
rs11175407 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | TBK1 | GRCh38.p7 | 12:64476185 | TTTTTTGAGATGGAG[C/T]CTCGCTCTGTTGCCC | 29110 |
rs11175408 | snp | C/T | 0.473174 | 0.112665 | intron-variant | TBK1 | GRCh38.p7 | 12:64477790 | TTGTCATAGATGGCT[C/T]TTATTATTTTGAGAT | 29110 |
rs11175410 | snp | A/G | 0.137867 | 0.223442 | intron-variant | TBK1 | GRCh38.p7 | 12:64484649 | CCCAGCTGCATGGGA[A/G]GCTGAGGTAGGAGGA | 29110 |
rs11175411 | snp | C/T | 0.335788 | 0.23482 | intron-variant | TBK1 | GRCh38.p7 | 12:64485385 | TTTAGACATTGTGTT[C/T]GCTCTATAAAGGATA | 29110 |
rs11175412 | snp | C/T | 0.473451 | 0.112115 | intron-variant | TBK1 | GRCh38.p7 | 12:64488038 | TAACCAGTATGTATA[C/T]ATGCAAATATCCCAA | 29110 |
rs11175413 | snp | C/T | 0.473359 | 0.112298 | intron-variant | TBK1 | GRCh38.p7 | 12:64488860 | AGTTGGGTGTGGTGG[C/T]GCACGCCTGTAGTCC | 29110 |
rs11175414 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | TBK1 | GRCh38.p7 | 12:64491128 | GTATTATAGAAGTGC[A/G]CAGGTTTATATATTA | 29110 |
rs11175415 | snp | A/G | | | intron-variant | TBK1 | GRCh38.p7 | 12:64494323 | AAAAAAGAAAAAAAA[A/G]AAAAAATTAGCAAGA | 29110 |
rs11175416 | snp | C/G/T | 0.0209646 | 0.10038 | intron-variant | TBK1 | GRCh38.p7 | 12:64496729 | CGTCTTAATTTTAAC[C/G/T]GCATTCAATAGGCAT | 29110 |
rs11175417 | snp | C/G | 0.473543 | 0.111932 | intron-variant | TBK1 | GRCh38.p7 | 12:64501017 | GCCTGCCTCGGCCTC[C/G]CAAAGTGCTGGGATT | 29110 |
rs11175418 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | TBK1 | GRCh38.p7 | 12:64501051 | ggcgtgagccactgc[A/G]ccggccCCAATTCTA | 29110 |
rs11286924 | in-del | -/T | 0.221439 | 0.248363 | intron-variant | TBK1 | GRCh38.p7 | 12:64472660 | TCAGTGACTATGGTA[-/T]TAGTGCAGAGTGTCC | 29110 |
rs11358053 | in-del | -/T | | | intron-variant | TBK1 | GRCh38.p7 | 12:64454673 | CTAGAAACTCAGATC[-/T]TTTTTTTTTTTTTTT | 29110 |
rs11447930 | in-del | -/T | | | intron-variant | TBK1 | GRCh38.p7 | 12:64469793 | GTACTTTTTTTTTTT[-/T]CCCCAACCCCACTTT | 29110 |
rs11531252 | snp | A/G | 0.0498117 | 0.149749 | intron-variant | TBK1 | GRCh38.p7 | 12:64465238 | CAACAAAGCAAGACT[A/G]TCTCAAAAAAAAAAA | 29110 |
rs11538420 | snp | A/C/T | 0.00207268 | 0.0321254 | missense, synonymous-codon, nc-transcript-variant | TBK1 | GRCh38.p7 | 12:64460236 | TAATAACATAAGCTT[A/C/T]CTTCGTCCAGTGGAT | 29110 |
rs11610527 | snp | A/T | | | intron-variant | TBK1 | GRCh38.p7 | 12:64471566 | ccatgttggccaggc[A/T]agtctcaaactcctg | 29110 |
rs11614161 | snp | A/G | 0.282632 | 0.247861 | intron-variant | TBK1 | GRCh38.p7 | 12:64497498 | GTTGATTTAAGTATT[A/G]TATCATCGATAGTTT | 29110 |
rs11829120 | snp | A/C | 0.226188 | 0.248863 | intron-variant | TBK1 | GRCh38.p7 | 12:64476730 | tttggggtattcatc[A/C]tgaattatttgccta | 29110 |
rs11829350 | snp | C/G | 0.079617 | 0.182947 | intron-variant | TBK1 | GRCh38.p7 | 12:64471793 | TAACACATCAGGACA[C/G]AGCCAGTGGGCACAA | 29110 |
rs11829573 | snp | C/T | 0.0792508 | 0.182605 | intron-variant | TBK1 | GRCh38.p7 | 12:64473440 | ttaaaatgggagata[C/T]taaagcatgtttgta | 29110 |
rs11829815 | snp | A/G | 0.0803491 | 0.183626 | intron-variant | TBK1 | GRCh38.p7 | 12:64477680 | tggctgagacttcta[A/G]tactatgttgaatag | 29110 |
rs11829882 | snp | A/C | | | intron-variant | TBK1 | GRCh38.p7 | 12:64472249 | TTCCCACCCCCATCT[A/C]CAGCACCCCCCCACC | 29110 |
rs11832740 | snp | G/T | 0.0807149 | 0.183963 | intron-variant | TBK1 | GRCh38.p7 | 12:64478146 | TATTTGGCCCTATCt[G/T]ttgttttgtttgttt | 29110 |
rs11833571 | snp | A/G | 0.0818113 | 0.184966 | intron-variant | TBK1 | GRCh38.p7 | 12:64453422 | TCGTGAGTGAAATGT[A/G]ATGACTGGCAAATGT | 29110 |
rs11836852 | snp | A/C | 0.334871 | 0.235153 | intron-variant | TBK1 | GRCh38.p7 | 12:64458405 | TATTAAATTGCTTTT[A/C]GTTACTAAAGTATGA | 29110 |
rs11837054 | snp | A/G | 0.0807149 | 0.183963 | intron-variant | TBK1 | GRCh38.p7 | 12:64481769 | TTTGATTTGCTGGTA[A/G]ATACTATGATTTTTT | 29110 |
rs11837890 | snp | G/T | 0.228253 | 0.249052 | intron-variant | TBK1 | GRCh38.p7 | 12:64470203 | GACCAATACCCCCTT[G/T]TTATAATAAATATTT | 29110 |
rs12296451 | snp | A/G | 0 | 0 | intron-variant | TBK1 | GRCh38.p7 | 12:64501072 | cCCAATTCTATCTTA[A/G]CTTATAAATCCCACC | 29110 |
rs12296600 | snp | A/G | | | intron-variant | TBK1 | GRCh38.p7 | 12:64494316 | aaaaaaaaaaaaaga[A/G]aaaaaagaaaaaatt | 29110 |
rs12310146 | snp | A/G | | | intron-variant | TBK1 | GRCh38.p7 | 12:64494314 | ccaaaaaaaaaaaaa[A/G]aaaaaaaagaaaaaa | 29110 |
rs12311964 | snp | A/C | 0.279195 | 0.248289 | intron-variant | TBK1 | GRCh38.p7 | 12:64472516 | AAGTGTATAACTTTC[A/C]TGAAGGCAGATGGCA | 29110 |
rs12313449 | snp | A/G | 0.473726 | 0.111565 | upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant | TBK1, XPOT | GRCh38.p7 | 12:64450349 | AGACAGGGTCTCACT[A/G]TGTTACCCAGTCTGG | 29110 |
rs12319677 | snp | A/G | 0.454904 | 0.143228 | intron-variant | TBK1 | GRCh38.p7 | 12:64469330 | TCATCTTAGCCTACC[A/G]AGAACACCAAGCAGA | 29110 |
rs12367468 | snp | C/T | 0.443195 | 0.158668 | intron-variant | TBK1 | GRCh38.p7 | 12:64475338 | gggtatgttgtgtag[C/T]gctgaggtttggact | 29110 |
rs12367640 | snp | A/G | 0 | 0 | upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant | TBK1, XPOT | GRCh38.p7 | 12:64450932 | AAGGCCTGTGGCTCA[A/G]TTAATCACTCCCACA | 29110 |
rs12423601 | snp | G/T | | | intron-variant | TBK1 | GRCh38.p7 | 12:64476532 | tttgtttttttcttg[G/T]tgattcgtttaagtt | 29110 |
rs12426606 | snp | A/T | 0.0193772 | 0.0965046 | intron-variant | TBK1 | GRCh38.p7 | 12:64458535 | TATATATATATATGG[A/T]TCTCTATTATTTGTA | 29110 |
rs12819714 | snp | A/T | 0 | 0 | intron-variant | TBK1 | GRCh38.p7 | 12:64490422 | GAAAGAATTTTTCCC[A/T]TCTTTAGAAACTTCT | 29110 |
rs12819770 | snp | A/T | 0 | 0 | intron-variant | TBK1 | GRCh38.p7 | 12:64490500 | TCAAATGACTACTGT[A/T]ATTTAAACCTCTCTC | 29110 |
rs12819953 | snp | C/T | 0 | 0 | intron-variant | TBK1 | GRCh38.p7 | 12:64490508 | CTACTGTAATTTAAA[C/T]CTCTCTCGCTGCCTC | 29110 |
rs12820141 | snp | C/G | | | intron-variant | TBK1 | GRCh38.p7 | 12:64490567 | GCTCTTGTGTTCTTG[C/G]TGTGGCAGTTAAAGC | 29110 |
rs12820485 | snp | A/G | 0 | 0 | intron-variant | TBK1 | GRCh38.p7 | 12:64490569 | TCTTGTGTTCTTGCT[A/G]TGGCAGTTAAAGCAA | 29110 |
rs12826520 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | TBK1 | GRCh38.p7 | 12:64482238 | AATTAGCTTGTTTCT[C/T]AAACTGTAAGTTTTA | 29110 |
rs17853341 | snp | A/C | 0 | 0 | missense, nc-transcript-variant | TBK1 | GRCh38.p7 | 12:64495763 | CAGTTCAAAAAAGAC[A/C]AAGCAGAACGTAGTA | 29110 |
rs17857028 | snp | A/G | 1.6636e-05 | 0.00288405 | missense, nc-transcript-variant | TBK1 | GRCh38.p7 | 12:64484472 | AGCCGGGAACCTCTG[A/G]ATACCATAGGATTAA | 29110 |
rs34144451 | in-del | -/T | | | intron-variant | TBK1 | GRCh38.p7 | 12:64481070 | GTTTCCAAAATGAAA[-/T]TTGTCATGTAACTAG | 29110 |
rs34148587 | in-del | -/C | | | intron-variant | TBK1 | GRCh38.p7 | 12:64466612 | CCAAAGTAATTCAAG[-/C]AAATCATATGCTTAA | 29110 |
rs34194131 | in-del | -/TA | 0.441158 | 0.161117 | utr-variant-3-prime, nc-transcript-variant | TBK1 | GRCh38.p7 | 12:64502051 | AACTGTTTTAAGCTG[-/TA]TATTTCTTTAATTCT | 29110 |
rs34331722 | in-del | -/A | | | intron-variant | TBK1 | GRCh38.p7 | 12:64453454 | TATTCCTTATTTGTG[-/A]AAAGGGAATCTTATT | 29110 |
rs34350141 | in-del | -/G | | | intron-variant | TBK1 | GRCh38.p7 | 12:64485235 | TGGACTCATTGTGTT[-/G]GGTGTATATTTAAGG | 29110 |