SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs2178 | snp | C/T | 0.397994 | 0.201489 | intron-variant | TRIM22 | GRCh38.p7 | 11:5701938 | TATTGACCGTACTTG[C/T]TCTTTGCTTTTTTTT | 10346 |
rs2179 | snp | C/G | 0.388964 | 0.20782 | intron-variant | TRIM22 | GRCh38.p7 | 11:5701877 | GCTGCTACGTTGTTA[C/G]AGCAACCCCAGAAAA | 10346 |
rs8433 | snp | A/G | 0.0182019 | 0.0936463 | utr-variant-3-prime | TRIM22 | GRCh38.p7 | 11:5710408 | ACTTTGCTAGATAAC[A/G]TGGATATGAGTTGAC | 10346 |
rs885002 | snp | C/T | 0.211516 | 0.24702 | upstream-variant-2KB | TRIM22 | GRCh38.p7 | 11:5688953 | TACCCTGTTGTCTAT[C/T]GTATTCTTGTTTAAC | 10346 |
rs999295 | snp | C/T | 0.397846 | 0.203932 | intron-variant | TRIM22 | GRCh38.p7 | 11:5709018 | GTCAAGTGAAGGATA[C/T]GGGATAGGTGTGTCT | 10346 |
rs1063303 | snp | C/G | 0.49978 | 0.011893 | missense | TRIM22 | GRCh38.p7 | 11:5698520 | TCCAGCGGAGGTTGA[C/G]GGGATCGTCAGTAGA | 10346 |
rs1140277 | snp | C/G | | | utr-variant-3-prime | TRIM22 | GRCh38.p7 | 11:5710090 | ttttaacattatatt[C/G]tctacaaagacctta | 10346 |
rs1140278 | snp | C/G | | | utr-variant-3-prime | TRIM22 | GRCh38.p7 | 11:5710092 | ttaacattatattct[C/G]tacaaagaccttatt | 10346 |
rs1498553 | snp | C/T | 0.499923 | 0.00618962 | upstream-variant-2KB | TRIM22 | GRCh38.p7 | 11:5687798 | ATGTTCAAAGCCAGA[C/T]GAGAATAAAAGGATG | 10346 |
rs1498554 | snp | A/G | 0.0372196 | 0.131242 | upstream-variant-2KB | TRIM22 | GRCh38.p7 | 11:5688227 | CAAGAAGGAGTCAAC[A/G]TTATAGCTCACGCCT | 10346 |
rs1498555 | snp | G/T | 0.492137 | 0.0622048 | intron-variant | TRIM22 | GRCh38.p7 | 11:5691767 | TATCTCGATCTTATC[G/T]CTGAGCATTTTGTAC | 10346 |
rs1498556 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | TRIM22 | GRCh38.p7 | 11:5691927 | TTGTCAAGTCTAGTA[C/T]AGGACCCAATAAATA | 10346 |
rs1995162 | snp | A/G | 0.261884 | 0.249717 | intron-variant | TRIM22 | GRCh38.p7 | 11:5691030 | GAGAGGCCGCAGGAC[A/G]GGCAGACTGCTGCTC | 10346 |
rs2133260 | snp | C/G | 0.49645 | 0.0419827 | intron-variant | TRIM22 | GRCh38.p7 | 11:5700796 | ATCCAGCTAATTTTT[C/G]TATTTTTAATAGAGA | 10346 |
rs2133261 | snp | A/C | 0.494057 | 0.0541878 | intron-variant | TRIM22 | GRCh38.p7 | 11:5700870 | CTCAGATGCACCCGG[A/C]CGAGAAACTTCCTCT | 10346 |
rs2133262 | snp | C/G | 0.507018 | 0.0716108 | intron-variant | TRIM22 | GRCh38.p7 | 11:5700906 | CCTAGTTTGCTGAGA[C/G]TTTTTATCATGAATG | 10346 |
rs2291841 | snp | A/C | 0.267091 | 0.249415 | utr-variant-5-prime | TRIM22 | GRCh38.p7 | 11:5689666 | ACAGCAGATGCTAGA[A/C]CATAATGTAGCATTA | 10346 |
rs2291842 | snp | C/T | 0.377664 | 0.214968 | synonymous-codon | TRIM22 | GRCh38.p7 | 11:5698437 | GGTGAATGTGCTGGA[C/T]AACCTGGCAGCAGCT | 10346 |
rs2291843 | snp | A/G | 0.00814003 | 0.0632752 | missense | TRIM22 | GRCh38.p7 | 11:5698489 | AGGCAGGATGCCAGC[A/G]CGCTCATCTCAGATC | 10346 |
rs2291844 | snp | C/T | 0.463234 | 0.130503 | intron-variant | TRIM22 | GRCh38.p7 | 11:5698605 | ACACAGAGGCCGATT[C/T]TCCTTCCCTTCCCAG | 10346 |
rs2291845 | snp | C/T | 0.240478 | 0.249819 | intron-variant | TRIM22 | GRCh38.p7 | 11:5708350 | AGCGGGAGGTTTTTT[C/T]AGGTTAGGATATAGG | 10346 |
rs2343233 | snp | A/G | 0.461813 | 0.132798 | intron-variant | TRIM22 | GRCh38.p7 | 11:5701836 | GAGAGACTAAATCTC[A/G]GTTGTTTAAAAACCA | 10346 |
rs2880580 | snp | G/T | 0.494013 | 0.0543839 | intron-variant | TRIM22 | GRCh38.p7 | 11:5701177 | TCCTTTCTCATAATG[G/T]CTTTACTTGGCTCTG | 10346 |
rs3072123 | snp | A/G/T | | | upstream-variant-2KB | TRIM22 | GRCh38.p7 | 11:5688573 | TGGGTGTGTGTGTGT[A/G/T]TGTGTTGTGTGGTGT | 10346 |
rs3740991 | snp | C/T | | | intron-variant | TRIM22 | GRCh38.p7 | 11:5708716 | TTAAACCATGTAGTT[C/T]TTTTTTTTTTTTTTT | 10346 |
rs3740992 | snp | A/G | 0.139564 | 0.224285 | intron-variant | TRIM22 | GRCh38.p7 | 11:5708780 | GGAGTGCAATGGCGC[A/G]GTCTCGGCTCACTGC | 10346 |
rs4290258 | snp | A/G | 0.387642 | 0.208697 | intron-variant | TRIM22 | GRCh38.p7 | 11:5701718 | CAGAGCCCAAAATCA[A/G]TGTACCAGCAACCAC | 10346 |
rs4348934 | snp | A/C/G | | | intron-variant | TRIM22 | GRCh38.p7 | 11:5699494 | gcgccactgcagtcc[A/C/G]cagtccggcctgggc | 10346 |
rs4360724 | snp | A/G | 0.493925 | 0.054776 | intron-variant | TRIM22 | GRCh38.p7 | 11:5701200 | TGGCTCTGGATTAGG[A/G]TAATGCTGACCTCAT | 10346 |
rs4369439 | snp | A/G | 0.494013 | 0.0543839 | intron-variant | TRIM22 | GRCh38.p7 | 11:5701278 | TTTGGGGAGAATTTT[A/G]ATAATTTCCTTCTCC | 10346 |
rs4376934 | snp | A/G | 0.3748 | 0.216622 | intron-variant | TRIM22 | GRCh38.p7 | 11:5699466 | GAAGCGGAGCTTGCA[A/G]TGAACCGAGATTGCG | 10346 |
rs4525262 | snp | A/C | 0.493837 | 0.055168 | intron-variant | TRIM22 | GRCh38.p7 | 11:5701214 | GGTAATGCTGACCTC[A/C]TAGAATGTGTTACAA | 10346 |
rs4604919 | snp | C/T | 0.494143 | 0.0537956 | intron-variant | TRIM22 | GRCh38.p7 | 11:5701416 | TAAATTCTATTGTTG[C/T]GTAAGAAAACATTTT | 10346 |
rs4625503 | snp | A/G | 0.49995 | 0.00499176 | intron-variant | TRIM22 | GRCh38.p7 | 11:5691296 | ACTCTAAGGGGGTCC[A/G]CGTGAGAGGGTCGTG | 10346 |
rs4910574 | snp | C/T | 0.451359 | 0.148171 | intron-variant | TRIM22 | GRCh38.p7 | 11:5695492 | TTCTATTTTTATCAA[C/T]TGATTAAAAACCCAA | 10346 |
rs4910575 | snp | C/T | 0.396182 | 0.202807 | intron-variant | TRIM22 | GRCh38.p7 | 11:5703464 | AATCTTGGCTCACTG[C/T]AAGCTCTGCTTCCCG | 10346 |
rs4910835 | snp | A/G | 0.152667 | 0.230274 | intron-variant | TRIM22 | GRCh38.p7 | 11:5695633 | ttatatagttccaca[A/G]atttactagaaatta | 10346 |
rs4910836 | snp | C/T | 0.47709 | 0.104548 | intron-variant | TRIM22 | GRCh38.p7 | 11:5695737 | ATATGCAAATATTCA[C/T]GAATCATGCAAATAT | 10346 |
rs4910837 | snp | A/G | 0.477004 | 0.104734 | intron-variant | TRIM22 | GRCh38.p7 | 11:5695833 | TAGTGCATTTAACAT[A/G]GAAAATGTGTTTTGG | 10346 |
rs4910838 | snp | A/G | 0.496245 | 0.0431677 | intron-variant | TRIM22 | GRCh38.p7 | 11:5703447 | CTGGAGAGCAGTGGC[A/G]CAATCTTGGCTCACT | 10346 |
rs4910839 | snp | A/G | 0.212425 | 0.24716 | intron-variant | TRIM22 | GRCh38.p7 | 11:5703665 | gctgggactacaggc[A/G]tgagccaccgcgccc | 10346 |
rs5021595 | snp | C/T | 0.40853 | 0.193309 | intron-variant | TRIM22 | GRCh38.p7 | 11:5707668 | TACAAAAAAATTAGC[C/T]GGATGTGGTAGCAGG | 10346 |
rs5789424 | in-del | -/GT | 0.495596 | 0.0467178 | upstream-variant-2KB | TRIM22 | GRCh38.p7 | 11:5688560 | TGGGTGTGTGTGTGT[-/GT]ATGTGTTGTGTGGTG | 10346 |
rs6578678 | snp | C/T | 0.330714 | 0.236612 | intron-variant | TRIM22 | GRCh38.p7 | 11:5691295 | AACTCTAAGGGGGTC[C/T]GCGTGAGAGGGTCGT | 10346 |
rs6578679 | snp | C/G | 0.429538 | 0.173972 | intron-variant | TRIM22 | GRCh38.p7 | 11:5691617 | GTAGCACCCAATGAA[C/G]CTCTGGTATCCACTC | 10346 |
rs7112085 | snp | C/T | 0.433382 | 0.169915 | intron-variant | TRIM22 | GRCh38.p7 | 11:5692428 | TTACAAAATGACTTA[C/T]CTGAAACATATTGAC | 10346 |
rs7113258 | snp | A/T | 0.405255 | 0.195948 | utr-variant-3-prime | TRIM22 | GRCh38.p7 | 11:5710225 | GAGATGCTTGTACAT[A/T]ATTTTCCTAATACCT | 10346 |
rs7116081 | snp | A/G | 0.452227 | 0.146984 | intron-variant | TRIM22 | GRCh38.p7 | 11:5702837 | ATAATGTCTTTTAAC[A/G]TTTATGGCAAAGTAT | 10346 |
rs7129909 | snp | A/G | 0.427423 | 0.176128 | intron-variant | TRIM22 | GRCh38.p7 | 11:5689947 | GGAGGCTTTGAGAAG[A/G]ATAGATTGATTGTGT | 10346 |
rs7480654 | snp | C/T | 0.386313 | 0.209568 | intron-variant | TRIM22 | GRCh38.p7 | 11:5701609 | CAGGTACAACTGTAG[C/T]GGTAATCATTTCCTG | 10346 |
rs7482103 | snp | C/G | | | intron-variant | TRIM22 | GRCh38.p7 | 11:5708910 | ttaCACCCTGTATTT[C/G]TTAAGGGTCCTACTA | 10346 |
rs7927644 | snp | C/T | 0.489142 | 0.0728777 | intron-variant | TRIM22 | GRCh38.p7 | 11:5700488 | TAGTACAATGTTCAA[C/T]AGGGATGGTGAGAGG | 10346 |
rs7935494 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TRIM22 | GRCh38.p7 | 11:5689967 | ATTGATTGTGTCTGG[A/G]TGAGTTTAATTTGTA | 10346 |
rs7935564 | snp | A/G | 0.497837 | 0.0328141 | missense | TRIM22 | GRCh38.p7 | 11:5697287 | AGGCTGATAAAGGAG[A/G]ATCAAGAGGCTGAGA | 10346 |
rs7935903 | snp | A/G | 0.491157 | 0.065903 | intron-variant | TRIM22 | GRCh38.p7 | 11:5697512 | AGTTTAGGGGCTGGA[A/G]AGTAGACATATCATA | 10346 |
rs7935929 | snp | A/G | 0.491263 | 0.0655142 | intron-variant | TRIM22 | GRCh38.p7 | 11:5697587 | GTGAAAACGCTTCCT[A/G]TGAATCCTGTGTTCC | 10346 |
rs7936441 | snp | A/T | 0.299664 | 0.245017 | intron-variant | TRIM22 | GRCh38.p7 | 11:5705182 | CAACTTTACAGTAAT[A/T]ATTTTAAGATATATA | 10346 |
rs7936676 | snp | C/T | 0.492679 | 0.0600586 | intron-variant | TRIM22 | GRCh38.p7 | 11:5697482 | TAGGTCTCAATTTAA[C/T]TCCTTCCCTGTTGGA | 10346 |
rs7942160 | snp | A/G | 0.489142 | 0.0728777 | intron-variant | TRIM22 | GRCh38.p7 | 11:5700487 | CTAGTACAATGTTCA[A/G]CAGGGATGGTGAGAG | 10346 |
rs7943175 | snp | A/G | 0 | 0 | intron-variant | TRIM22 | GRCh38.p7 | 11:5691635 | CTGGTATCCACTCCT[A/G]TTTTAGAAGTTGCTA | 10346 |
rs7946891 | snp | G/T | 0.273587 | 0.248885 | intron-variant | TRIM22 | GRCh38.p7 | 11:5705581 | GGAGGTCAAGTCTTT[G/T]TTGGTATAAAGGGGG | 10346 |
rs7948996 | snp | G/T | 0.46137 | 0.133501 | downstream-variant-500B | TRIM22 | GRCh38.p7 | 11:5710992 | ATGCTGTTCAGATCT[G/T]TTTCTCGTAATGAAA | 10346 |
rs7949803 | snp | C/T | 0.0456336 | 0.143994 | upstream-variant-2KB | TRIM22 | GRCh38.p7 | 11:5688727 | tctcagtttcctgag[C/T]agctgggactacagg | 10346 |
rs7950181 | snp | C/G | 0.397813 | 0.201621 | intron-variant | TRIM22 | GRCh38.p7 | 11:5698730 | TAAGTGTATGAATGG[C/G]AAGGGAAATTCCCAT | 10346 |
rs7950219 | snp | C/G | 0.336702 | 0.234484 | intron-variant | TRIM22 | GRCh38.p7 | 11:5698790 | ATTTGAGCTTGGAGA[C/G]GATTCTTTGTaccat | 10346 |
rs7950912 | snp | C/T | 0.331874 | 0.236213 | intron-variant | TRIM22 | GRCh38.p7 | 11:5698618 | TTTTCCTTCCCTTCC[C/T]AGTCTCTAGGCTTTC | 10346 |
rs10664616 | in-del | -/TTT/TTTT | 0.446902 | 0.154045 | intron-variant | TRIM22 | GRCh38.p7 | 11:5695566 | AGGGTTTTTTTTTTT[-/TTT/TTTT]CAGGTGATAAAAATA | 10346 |
rs10676047 | in-del | -/TG | | | upstream-variant-2KB | TRIM22 | GRCh38.p7 | 11:5688562 | TCTTTTTTTTTGGGT[-/TG]GTGTGTGTGTATGTG | 10346 |
rs10742775 | snp | G/T | 0.409552 | 0.192466 | intron-variant | TRIM22 | GRCh38.p7 | 11:5703112 | TACATGGGAATATTG[G/T]GTGATGCTGAGGTTT | 10346 |
rs10769180 | snp | C/T | 0.381113 | 0.21286 | intron-variant | TRIM22 | GRCh38.p7 | 11:5698021 | TAGAGGGATTTAAGA[C/T]ACAGAAAGGCAAAGT | 10346 |
rs10769181 | snp | A/C | 0.455858 | 0.141853 | intron-variant | TRIM22 | GRCh38.p7 | 11:5700390 | AAAGTGCTAGGATTA[A/C]AGGCGTGAGCCACCG | 10346 |
rs10769182 | snp | C/T | 0.496416 | 0.0421803 | intron-variant | TRIM22 | GRCh38.p7 | 11:5701571 | GAATGCCATTTAAAT[C/T]AGTTGCTATATAGTG | 10346 |
rs10769183 | snp | A/C | 0.494057 | 0.0541878 | intron-variant | TRIM22 | GRCh38.p7 | 11:5701577 | CATTTAAATCAGTTG[A/C]TATATAGTGTGCTGT | 10346 |
rs10769184 | snp | A/C | 0.49423 | 0.0534032 | intron-variant | TRIM22 | GRCh38.p7 | 11:5701631 | CATTTCCTGTGGCTG[A/C]TGTAAGAAATTGTCA | 10346 |
rs10769185 | snp | A/T | 0.496382 | 0.0423778 | intron-variant | TRIM22 | GRCh38.p7 | 11:5703562 | GGCTAATTTTTTGTA[A/T]TTTTAGTAGAGACGG | 10346 |
rs10769188 | snp | A/C | 0.451608 | 0.147832 | intron-variant | TRIM22 | GRCh38.p7 | 11:5705937 | ATACACAGTGAGTAC[A/C]TGGAGGCCAGACAAA | 10346 |
rs10838543 | snp | C/T | 0.496668 | 0.0406796 | synonymous-codon | TRIM22 | GRCh38.p7 | 11:5696532 | TGTCTGTGAGCACCA[C/T]GGAAAAAAACTCCAG | 10346 |
rs10838544 | snp | A/G | 0.496245 | 0.0431677 | intron-variant | TRIM22 | GRCh38.p7 | 11:5696871 | TTTTAGCAAGGAAAA[A/G]TTGAATGAATGGAGA | 10346 |
rs10838545 | snp | C/T | 0.472052 | 0.11486 | intron-variant | TRIM22 | GRCh38.p7 | 11:5696929 | CCCCTCCAAGAAGAA[C/T]AGTATTTTTGGGAAC | 10346 |
rs10838546 | snp | A/C | 0.495927 | 0.0449436 | intron-variant | TRIM22 | GRCh38.p7 | 11:5696983 | GTGGCAATGAAAGGA[A/C]GTCTTTCCTTACTGC | 10346 |
rs10838548 | snp | A/G | 0.499703 | 0.0121769 | intron-variant | TRIM22 | GRCh38.p7 | 11:5697865 | TGTGCCACCATGCCC[A/G]GCTAATTTTTTGTAT | 10346 |
rs10838549 | snp | A/C | 0.498754 | 0.0249289 | intron-variant | TRIM22 | GRCh38.p7 | 11:5697998 | ATGAGCCACTGTGCC[A/C]GGCCAGGTAGAGGGA | 10346 |
rs10838553 | snp | A/G | 0.488965 | 0.0734569 | intron-variant | TRIM22 | GRCh38.p7 | 11:5700186 | AGAATGTGGTGGCAC[A/G]ATCTCACCTCACTGC | 10346 |
rs10838554 | snp | C/T | 0.489142 | 0.0728777 | intron-variant | TRIM22 | GRCh38.p7 | 11:5700260 | CCCAGGACTAGCGCA[C/T]ACCGCCACACCTGGC | 10346 |
rs10838556 | snp | C/T | 0.488726 | 0.0742286 | intron-variant | TRIM22 | GRCh38.p7 | 11:5700410 | GTGAGCCACCGCGCC[C/T]GGCCAGCAGTTTGTA | 10346 |
rs10838557 | snp | C/T | | | intron-variant | TRIM22 | GRCh38.p7 | 11:5700605 | TTTTTTTTTTTTTTT[C/T]CAGATTTGTAATGAA | 10346 |
rs10838561 | snp | A/G | 0.386884 | 0.209196 | intron-variant | TRIM22 | GRCh38.p7 | 11:5703344 | AGGATTATGGCCTCC[A/G]GCTGCATCCATGTTG | 10346 |
rs10838568 | snp | G/T | 0.460702 | 0.134554 | intron-variant | TRIM22 | GRCh38.p7 | 11:5705890 | TCATACTGAAAAATG[G/T]ATGAGATCACCTACA | 10346 |
rs11038719 | snp | C/T | 0 | 0 | upstream-variant-2KB | TRIM22 | GRCh38.p7 | 11:5687958 | AAACACATTCACTCA[C/T]TGAGCGCTCACTCCC | 10346 |
rs11038733 | snp | C/G | | | intron-variant | TRIM22 | GRCh38.p7 | 11:5691727 | ACAGAGCTAAGGCAA[C/G]GAGTTGGTAATTTCT | 10346 |
rs11038736 | snp | C/T | 0 | 0 | intron-variant | TRIM22 | GRCh38.p7 | 11:5692662 | TTTAAAAGATGTTGG[C/T]TAGGCCAGGCACCTG | 10346 |
rs11038738 | snp | A/G | 0.421684 | 0.181726 | intron-variant | TRIM22 | GRCh38.p7 | 11:5693000 | CCTGCCTCAGCCTCC[A/G]GAGTAGCGGGGACTA | 10346 |
rs11038741 | snp | C/T | 0.423257 | 0.180228 | intron-variant | TRIM22 | GRCh38.p7 | 11:5693954 | TCTTCTAGCTTCTAA[C/T]AGTTTCCTGGAAACC | 10346 |
rs11038746 | snp | A/G | 0.496416 | 0.0421803 | intron-variant | TRIM22 | GRCh38.p7 | 11:5696921 | TTTCATTGCCCCTCC[A/G]AGAAGAACAGTATTT | 10346 |
rs11038751 | snp | C/T | 0.357024 | 0.225933 | intron-variant | TRIM22 | GRCh38.p7 | 11:5697828 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 10346 |
rs11038753 | snp | A/G | 0.264848 | 0.249559 | intron-variant | TRIM22 | GRCh38.p7 | 11:5698558 | CAGGTAAGACTTGGG[A/G]TGGAGCACCTACGTA | 10346 |
rs11038758 | snp | C/T | | | intron-variant | TRIM22 | GRCh38.p7 | 11:5699246 | GTTGTATGTTGTGGC[C/T]GGGCGCGGTGGCTCA | 10346 |
rs11038759 | snp | C/T | 0.499994 | 0.00179711 | intron-variant | TRIM22 | GRCh38.p7 | 11:5700056 | TTGGCATTTTCTACA[C/T]GGAGAATCATGTCAT | 10346 |
rs11038760 | snp | A/C | 0.488786 | 0.0740357 | intron-variant | TRIM22 | GRCh38.p7 | 11:5700400 | GATTAAAGGCGTGAG[A/C]CACCGCGCCTGGCCA | 10346 |
rs11038769 | snp | A/G | 0.142272 | 0.225598 | intron-variant | TRIM22 | GRCh38.p7 | 11:5704370 | ATTCAGACTTTCACT[A/G]TTAATTATGTTATTA | 10346 |