SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3023726 | snp | C/T | | | upstream-variant-2KB | Trim16 | GRCm38.p3 | 11:62818726 | CAGGAGTTAATTTCC[C/T]GACACCTCTGCAAGG | 94092 |
rs3687060 | snp | C/T | 0.5 | 0 | intron-variant | Trim16 | GRCm38.p3 | 11:62822091 | TAACCAGGGTATTTC[C/T]TTTGTTCCTGTACCA | 94092 |
rs3687065 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Trim16 | GRCm38.p3 | 11:62822100 | TATTTCCTTTGTTCC[A/T]GTACCAGAGGTAGAC | 94092 |
rs26955249 | snp | A/G | 0.444444 | 0.157135 | utr-variant-3-prime | Trim16 | GRCm38.p3 | 11:62842638 | CTCAGCTCCGCAAAG[A/G]ACCTCTTCAATGGCA | 94092 |
rs26955250 | snp | C/T | 0.489796 | 0.070696 | utr-variant-3-prime | Trim16 | GRCm38.p3 | 11:62842429 | TCACTGGTCGCCTCC[C/T]TTTCCCACTGAACAA | 94092 |
rs26955251 | snp | C/T | 0.244898 | 0.249948 | utr-variant-3-prime | Trim16 | Mm_Celera | 11:62842413 | CTGTGCAGGGCAGGG[C/T]TCACTGGTCGCCTCC | 94092 |
rs26955252 | snp | A/C | 0.497778 | 0.0332592 | utr-variant-3-prime | Trim16 | GRCm38.p3 | 11:62842276 | TTCATGATCTAGTGC[A/C]TTGCCTCTCCTTCCA | 94092 |
rs26955253 | snp | C/T | 0.489796 | 0.070696 | utr-variant-3-prime | Trim16 | GRCm38.p3 | 11:62842035 | TGGATTTCTATTGCC[C/T]TAGCCTGAAGTCCCT | 94092 |
rs26955254 | snp | G/T | 0.46875 | 0.121031 | utr-variant-3-prime | Trim16 | GRCm38.p3 | 11:62841895 | AGGAGCTATGCCTGT[G/T]TGTTTGTGCTAAGTT | 94092 |
rs26955255 | snp | A/G | 0.21875 | 0.248039 | utr-variant-3-prime | Trim16 | Mm_Celera | 11:62841865 | AGGTATTTGGGGACA[A/G]CGTTCACCTCTCGCA | 94092 |
rs26955256 | snp | C/T | 0.142012 | 0.225474 | utr-variant-3-prime | Trim16 | Mm_Celera | 11:62841819 | GACTTCATGGACTTG[C/T]CTATTTTCTTGCCCA | 94092 |
rs26955257 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime | Trim16 | GRCm38.p3 | 11:62841695 | GCAGCAGCGGCAGGA[C/T]CACCATTAATCAGCA | 94092 |
rs26955258 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon | Trim16 | Mm_Celera | 11:62840903 | GTCTAAGAAAGAAAA[C/T]GCCATCCGGATTGTG | 94092 |
rs26955259 | snp | A/C | 0.489796 | 0.070696 | missense | Trim16 | GRCm38.p3 | 11:62840849 | GATTCACAAGTTTGA[A/C]TGCAAGTTCTCAGAG | 94092 |
rs26955260 | snp | C/T | 0.391111 | 0.206368 | missense | Trim16 | GRCm38.p3 | 11:62840746 | AGACCCCGCTCAAGG[C/T]CAGCCCCTTCAGAAG | 94092 |
rs26955261 | snp | A/C | 0.473373 | 0.11227 | synonymous-codon | Trim16 | GRCm38.p3 | 11:62840396 | TATTTCCTCAGATGC[A/C]TGTGACATCACGTTT | 94092 |
rs26955262 | snp | A/C | 0.444444 | 0.157135 | missense | Trim16 | Mm_Celera | 11:62840392 | TCTGTATTTCCTCAG[A/C]TGCCTGTGACATCAC | 94092 |
rs26955263 | snp | C/G | 0.336735 | 0.234472 | intron-variant | Trim16 | Mm_Celera | 11:62840317 | ATGGGTAAATGAAAC[C/G]AAAAGATGGGTGTTT | 94092 |
rs26955264 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Trim16 | GRCm38.p3 | 11:62840046 | CTGCATTTGACAGCA[C/T]GTCTAAGGCTTTACC | 94092 |
rs26955265 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Trim16 | Mm_Celera | 11:62839859 | ATTCCAGCTAAGATT[C/T]GCCTCTGGCTTAGAT | 94092 |
rs26955266 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim16 | Mm_Celera | 11:62839855 | CACCATTCCAGCTAA[A/G]ATTTGCCTCTGGCTT | 94092 |
rs26955267 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Trim16 | GRCm38.p3 | 11:62839404 | ATAAGGTTTCACCTC[C/T]CAGCTGAAGGGACTT | 94092 |
rs26955268 | snp | A/G | 0.32 | 0.24 | intron-variant | Trim16 | GRCm38.p3 | 11:62839132 | GCACGGCATTTCTAA[A/G]TGGTGCTTTGTGGTA | 94092 |
rs26955269 | snp | C/T | 0.124444 | 0.216185 | missense | Trim16 | Mm_Celera | 11:62837292 | GCAAGTATAGGACCT[C/T]GAAACCTGAGCCCAG | 94092 |
rs26955270 | snp | C/T | 0.18 | 0.24 | intron-variant | Trim16 | Mm_Celera | 11:62837050 | TGATGTCTGATGTGA[C/T]GCTGATGCTGATGTG | 94092 |
rs26955271 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim16 | Mm_Celera | 11:62836852 | CAGGGAAGGTGAGGC[A/G]CTTTCTGGAATGGTG | 94092 |
rs26955272 | snp | A/G | 0.5 | 0 | missense | Trim16 | GRCm38.p3 | 11:62836817 | CTAGAAAGCTATAAG[A/G]AAAAGCTCCAGGAAT | 94092 |
rs26955273 | snp | A/C | 0.231111 | 0.249285 | missense | Trim16 | Mm_Celera | 11:62836787 | ACAGATTCAACTCTG[A/C]ACTTGATCCAATTGC | 94092 |
rs26955274 | snp | G/T | 0.277778 | 0.248452 | synonymous-codon | Trim16 | Mm_Celera | 11:62836711 | GAAGACAGAGGACAC[G/T]GCCTCCCCTAGCATT | 94092 |
rs26955275 | snp | A/C | 0.35503 | 0.226867 | intron-variant | Trim16 | Mm_Celera | 11:62836575 | GTCTAGAAGCATAGA[A/C]CACGTTATGGTCACT | 94092 |
rs26955276 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Trim16 | Mm_Celera | 11:62836339 | ACTTCAAGAGATTCT[C/T]TTTCCCACTTGATTT | 94092 |
rs26955277 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Trim16 | Mm_Celera | 11:62836269 | AAGAAGGTTCTTATG[C/T]TCTGTGCCCAGTCTG | 94092 |
rs26955278 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Trim16 | Mm_Celera | 11:62836233 | TATGGAGAGAGAAAG[A/G]CTTTAAGGAATGGCA | 94092 |
rs26955279 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Trim16 | Mm_Celera | 11:62836025 | AACACTCTTCCCTGG[A/T]CCTACATTGGTTTTG | 94092 |
rs26955280 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Trim16 | Mm_Celera | 11:62835966 | TCCAGTCTGCTATTT[A/C]AAGTCTCATGACACC | 94092 |
rs26955281 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Trim16 | Mm_Celera | 11:62835899 | CAGAGCTGCGGTTTG[C/G]ACTTCCCTTCTGCAG | 94092 |
rs26955282 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trim16 | Mm_Celera | 11:62835795 | ATTGTTGGCATGAAC[C/T]GTAATTTACACTTGA | 94092 |
rs26955283 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Trim16 | Mm_Celera | 11:62834691 | GTATCACTGTACACA[A/C]GAGGCATAAACCGGT | 94092 |
rs26955284 | snp | C/G | 0.336735 | 0.234472 | intron-variant | Trim16 | GRCm38.p3 | 11:62834610 | ACTGGAGTTACTGTT[C/G]GTTTTCAGACAGGGC | 94092 |
rs26955285 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Trim16 | Mm_Celera | 11:62834466 | TCGTGGCTGGTTTAA[A/G]GAGCCACGGGGCTTT | 94092 |
rs26955286 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Trim16 | Mm_Celera | 11:62834424 | ACCAGATAGAGAAAG[C/T]CTGTGCAAAGACAGG | 94092 |
rs26955287 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Trim16 | GRCm38.p3 | 11:62834392 | GGAAGGTGGGTCAAG[C/T]TCTAGGTGCTGTATG | 94092 |
rs26955288 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Trim16 | Mm_Celera | 11:62834288 | TGGGACTGCCTTATT[A/G]TACAGGGAACTGTAA | 94092 |
rs26955289 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Trim16 | Mm_Celera | 11:62833874 | TACAGTCTGGTGTTC[C/T]TTCATCTTTGGGTTC | 94092 |
rs26955290 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Trim16 | Mm_Celera | 11:62832775 | TGTTCTCCCAGCATT[A/G]CATTCCAAGGTGTAG | 94092 |
rs26955291 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Trim16 | Mm_Celera | 11:62832306 | CTCCAGGACCCTTTC[C/T]AATATGTGTGTGTAT | 94092 |
rs26955292 | snp | A/T | 0.375 | 0.216506 | intron-variant | Trim16 | Mm_Celera | 11:62831671 | TTTTAGAATCTGTTT[A/T]AAAAGTGGTCAGAAG | 94092 |
rs26955293 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim16 | Mm_Celera | 11:62831559 | TAATTGTTCTTTGAT[A/G]AAGGACCTACATGTT | 94092 |
rs26955294 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Trim16 | Mm_Celera | 11:62831499 | ATGATCTCTGATGGA[C/T]GTGACCTTGAATTTT | 94092 |
rs26955295 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Trim16 | Mm_Celera | 11:62831409 | GGCCTGTTTAGGAAG[A/G]AGAGGCCACAGCAGA | 94092 |
rs26955296 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Trim16 | GRCm38.p3 | 11:62831201 | AATCTGCCATGGTGA[C/T]TTCCTTGGCCTGAGA | 94092 |
rs26955297 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Trim16 | Mm_Celera | 11:62831200 | GAATCTGCCATGGTG[A/G]TTTCCTTGGCCTGAG | 94092 |
rs26955298 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim16 | Mm_Celera | 11:62831160 | GTCAGATCTTGCCTT[A/G]ACTCTTCCTATTGAC | 94092 |
rs26955299 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Trim16 | Mm_Celera | 11:62831023 | GAGGATCACACAGGA[C/T]ATTACCTTGTTCTGG | 94092 |
rs26955300 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Trim16 | Mm_Celera | 11:62830773 | TCCTGTCTCTCTCCA[A/G]GGCCCTCATGGTTGC | 94092 |
rs26955301 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Trim16 | Mm_Celera | 11:62830693 | CACCTCTGACTCCCA[C/T]GTAAACCTGTCAATG | 94092 |
rs26955302 | snp | A/G | 0.165289 | 0.235211 | missense | Trim16 | Mm_Celera | 11:62820986 | CCCTGGATGCAGCCC[A/G]CAGGAACAAAGAGGT | 94092 |
rs26955303 | snp | C/T | 0.33241 | 0.236027 | missense, utr-variant-5-prime | Trim16 | GRCm38.p3 | 11:62820602 | TGTCAGCTATCCCAG[C/T]AGAAAAAGAAGATGC | 94092 |
rs26955304 | snp | C/T | 0.124444 | 0.216185 | utr-variant-5-prime | Trim16 | Mm_Celera | 11:62820337 | CTGGAGGAGCCTCGT[C/T]CTGTCTGAGTAACTG | 94092 |
rs26955305 | snp | A/C/T | 0.32 | 0.24 | upstream-variant-2KB | Trim16 | GRCm38.p3 | 11:62820094 | GGGACCGCTCAAAGC[A/C/T]GCAGAGGCTTACAAT | 94092 |
rs26955306 | snp | A/C/T | 0.31405 | 0.280505 | upstream-variant-2KB | Trim16 | Mm_Celera | 11:62820083 | ATATGGCTTGTGGGA[A/C/T]CGCTCAAAGCCGCAG | 94092 |
rs26955307 | snp | G/T | 0.46875 | 0.121031 | upstream-variant-2KB | Trim16 | Mm_Celera | 11:62820063 | AGAGAGAGATCCACC[G/T]CAAAATATGGCTTGT | 94092 |
rs26955308 | snp | C/T | 0.42 | 0.183303 | upstream-variant-2KB | Trim16 | GRCm38.p3 | 11:62819904 | GTGGTGGTGGTAGGA[C/T]GAAGCTGGTGGCTCA | 94092 |
rs26955309 | snp | C/T | 0.132653 | 0.220748 | upstream-variant-2KB | Trim16 | Mm_Celera | 11:62818858 | TAGCAACTGTCTCTT[C/T]GTGGAGATCACAGAG | 94092 |
rs26955310 | snp | A/G | 0.473373 | 0.11227 | upstream-variant-2KB | Trim16 | GRCm38.p3 | 11:62818281 | AAGTTCTGCCAAGAA[A/G]TATCCCCGGGTCTGT | 94092 |
rs29384328 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Trim16 | GRCm38.p3 | 11:62822428 | GGAAGCTTCTGGAAC[A/G]CCATCTTATTAGAGA | 94092 |
rs29389867 | snp | A/G | 0.375 | 0.216506 | intron-variant | Trim16 | GRCm38.p3 | 11:62826326 | ACTCCCTGAGGCTTC[A/G]TGGGGAAACAGCCAG | 94092 |
rs29394088 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB | Trim16 | GRCm38.p3 | 11:62818958 | CCGATGGCCCCTTCC[C/T]GTGCCCATTCTCAGC | 94092 |
rs29394510 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Trim16 | GRCm38.p3 | 11:62831414 | GTTTAGGAAGGGGAG[A/G]CCACAGCAGAGGTCT | 94092 |
rs29400225 | snp | A/C/T | 0.5 | 0 | upstream-variant-2KB | Trim16 | GRCm38.p3 | 11:62819687 | CGTGTTCCAGGTTCA[A/C/T]TGTGAGGTCCTCTCT | 94092 |
rs29402533 | snp | C/T | 0.444444 | 0.157135 | synonymous-codon | Trim16 | GRCm38.p3 | 11:62820973 | GACAGTACTGTCTCC[C/T]TGGATGCAGCCCGCA | 94092 |
rs29406487 | snp | A/G | 0.375 | 0.216506 | intron-variant | Trim16 | Mm_Celera | 11:62825608 | GTGCAACCCTGTGCT[A/G]TCCAGCTCTAAGGCA | 94092 |
rs29407851 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Trim16 | GRCm38.p3 | 11:62833269 | ATGGGGGGCTCCTGC[C/T]CCCTAGAAACACTGC | 94092 |
rs29408427 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Trim16 | GRCm38.p3 | 11:62829765 | TCACACTAGCCTAGA[A/G]CTCACCATATAGAGC | 94092 |
rs29410056 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Trim16 | GRCm38.p3 | 11:62823255 | AGAGCAGCAAGTGTT[C/T]TTAATGGCTGAACCA | 94092 |
rs29410516 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB | Trim16 | GRCm38.p3 | 11:62819138 | CAGCTGAGCTGAGCA[C/T]GGAAGGGGAGAAGCA | 94092 |
rs29411025 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Trim16 | GRCm38.p3 | 11:62823300 | AGCTTTAAAAAGATT[A/T]ATTTATTTTATTTTA | 94092 |
rs29411819 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Trim16 | GRCm38.p3 | 11:62821049 | GTGGGAGGAGGTGTC[C/T]CCAGGGAGAGGTCAC | 94092 |
rs29416903 | snp | A/G | 0.375 | 0.216506 | intron-variant | Trim16 | GRCm38.p3 | 11:62833486 | TCAGAAAACTCAAAT[A/G]TTTATATTATGATTC | 94092 |
rs29417267 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Trim16 | GRCm38.p3 | 11:62829866 | TCAAGATCATATATG[C/T]TTTCTTAACTAGGAG | 94092 |
rs29424254 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Trim16 | GRCm38.p3 | 11:62831391 | CATGTAAATTTCTCA[G/T]TGGGCCTGTTTAGGA | 94092 |
rs29426089 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Trim16 | GRCm38.p3 | 11:62831410 | GCCTGTTTAGGAAGG[A/G]GAGACCACAGCAGAG | 94092 |
rs29426293 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Trim16 | GRCm38.p3 | 11:62838328 | TGTCCTTTCTGTTGC[C/T]GTGATAAACCACTCT | 94092 |
rs29427658 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Trim16 | Mm_Celera | 11:62822470 | AGACCCTCAAATTGC[A/G]ACATTGTAACTTTAA | 94092 |
rs29429399 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Trim16 | GRCm38.p3 | 11:62833192 | CTGCTTGGGTTGCTG[A/C]AGTCACCAACACTTT | 94092 |
rs29433066 | snp | C/G | 0.375 | 0.216506 | intron-variant | Trim16 | GRCm38.p3 | 11:62839577 | TCCTATTGCAATGTT[C/G]CTTTGCTGGGAATGG | 94092 |
rs29434720 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Trim16 | GRCm38.p3 | 11:62833229 | CCTTAGTGAGGACTG[C/T]CTGCTAGAAAGAAAT | 94092 |
rs29436807 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Trim16 | Mm_Celera | 11:62828317 | CCCAGTGTAGTCTCT[C/T]TTGTTTCACATATAT | 94092 |
rs29436888 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Trim16 | Mm_Celera | 11:62821983 | GCTCAAGGCAGTTCC[C/T]TCTTTGCACTGTTGG | 94092 |
rs29439914 | snp | C/G | 0.375 | 0.216506 | missense, intron-variant | Trim16 | GRCm38.p3 | 11:62820676 | CATGACCCCGCAGAG[C/G]TCGGGGCTCCTGGTG | 94092 |
rs29441671 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Trim16 | GRCm38.p3 | 11:62839257 | AGGCTATACATTAAC[C/T]AGTCTACGTTAGTCA | 94092 |
rs29443543 | snp | G/T | 0.375 | 0.216506 | intron-variant | Trim16 | Mm_Celera | 11:62825358 | TTCCATAGTTTGTTT[G/T]CCAAGAGTCAGGAGT | 94092 |
rs29446824 | snp | A/G | 0.32 | 0.24 | intron-variant | Trim16 | GRCm38.p3 | 11:62823888 | AGTATAGGCCACCTC[A/G]TGTACCATGGAGACT | 94092 |
rs29448470 | snp | C/G | 0.444444 | 0.157135 | upstream-variant-2KB | Trim16 | GRCm38.p3 | 11:62819905 | TGGTGGTGGTAGGAT[C/G]AAGCTGGTGGCTCAT | 94092 |
rs29448581 | snp | A/G | 0.375 | 0.216506 | intron-variant | Trim16 | GRCm38.p3 | 11:62825626 | CAGCTCTAAGGCAGG[A/G]TGCACCAGGGTCTGG | 94092 |
rs29448893 | snp | A/C | 0.5 | 0 | intron-variant | Trim16 | GRCm38.p3 | 11:62821863 | GATCCTGGATGAGAC[A/C]TTGGGGGTGGACCCC | 94092 |
rs29456129 | snp | C/T | 0.5 | 0 | intron-variant | Trim16 | GRCm38.p3 | 11:62831921 | CCTGGTTTCAGAAAG[C/T]TAACACAAGCTTGCT | 94092 |
rs29458187 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Trim16 | GRCm38.p3 | 11:62839232 | AACAGCAATGAGCAT[G/T]ATATATGTGAGGCTA | 94092 |
rs29460103 | snp | C/G/T | 0.444444 | 0.157135 | intron-variant | Trim16 | GRCm38.p3 | 11:62822009 | GTTGGTTGGCACACC[C/G/T]AGAGCCTTTCTGTGG | 94092 |
rs29467617 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB | Trim16 | GRCm38.p3 | 11:62818924 | TATGTGGAAGGGGAC[A/G]GTGCCTTCCCTCTTC | 94092 |