SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6208502 | snp | A/G | 0.5 | 0 | intron-variant | Tnfaip3 | Mm_Celera | 10:19006695 | GGTCAAGACTCTGAA[A/G]CCTAAAATGATATTG | 21929 |
rs6208539 | snp | C/T | 0.5 | 0 | intron-variant | Tnfaip3 | Mm_Celera | 10:19006715 | AAATGATATTGATTC[C/T]AANCACCTCACAGAA | 21929 |
rs6208553 | snp | A/G | 0.5 | 0 | intron-variant | Tnfaip3 | Mm_Celera | 10:19006718 | TGATATTGATTCNAA[A/G]CACCTCACAGAAGGG | 21929 |
rs6208571 | snp | C/T | 0.5 | 0 | intron-variant | Tnfaip3 | Mm_Celera | 10:19006735 | ACCTCACAGAAGGGA[C/T]ATTTAATCCTCCGTG | 21929 |
rs6209065 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Tnfaip3 | Mm_Celera | 10:19006812 | ACAAAAAGCAAGGCC[C/T]GGAACTCCAAGATCC | 21929 |
rs6209614 | snp | A/G | 0.290657 | 0.246672 | synonymous-codon | Tnfaip3 | Mm_Celera | 10:19006915 | GTGCTGGCTGTCATA[A/G]CCNAGGACGATGGGA | 21929 |
rs6209623 | snp | A/T | 0.231111 | 0.249285 | synonymous-codon | Tnfaip3 | Mm_Celera | 10:19006918 | CTGGCTGTCATANCC[A/T]AGGACGATGGGATAT | 21929 |
rs6210115 | snp | A/G | 0.5 | 0 | synonymous-codon | Tnfaip3 | Mm_Celera | 10:19007008 | AGCAAAATTGGAACC[A/G]GATTCCAAACTTCTT | 21929 |
rs29315296 | snp | C/G | 0.375 | 0.216506 | utr-variant-5-prime, upstream-variant-2KB | Tnfaip3 | Mm_Celera | 10:19015224 | GCGCGCGCCGCAGCC[C/G]GGGATCGTGGTCCGG | 21929 |
rs29317324 | snp | A/G | 0.345679 | 0.230967 | utr-variant-3-prime | Tnfaip3 | Mm_Celera | 10:19001055 | TAAGTATAAATAACC[A/G]TTTCACATTAACAAT | 21929 |
rs29318501 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | Tnfaip3 | Mm_Celera | 10:19012547 | ATCACACCTCTCAGG[A/G]AAAAAAAAAAAAAAA | 21929 |
rs29327850 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tnfaip3 | Mm_Celera | 10:19007641 | TGGGTTTGATTCCCC[C/T]ACCTAAAATCACATG | 21929 |
rs29330459 | snp | C/T | 0.5 | 0 | intron-variant | Tnfaip3 | Mm_Celera | 10:19009837 | TTTCCCCCCACCCCC[C/T]CCCCCTTAAAAAATA | 21929 |
rs29330909 | snp | A/G | 0.48 | 0.0979796 | upstream-variant-2KB, intron-variant | Tnfaip3 | Mm_Celera | 10:19012751 | GGTACCACTCAGGAC[A/G]AAGAGTGGCCATATG | 21929 |
rs29334414 | snp | A/G | 0.5 | 0 | utr-variant-3-prime | Tnfaip3 | Mm_Celera | 10:19001170 | AAGAAGGACAAAGAC[A/G]TATGTAAGGGGAAAA | 21929 |
rs29338247 | snp | A/C | 0.5 | 0 | utr-variant-3-prime | Tnfaip3 | Mm_Celera | 10:19001176 | GACAAAGACATATGT[A/C]AGGGGAAAAGATAGG | 21929 |
rs29340638 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Tnfaip3 | Mm_Celera | 10:19008783 | GATAGGGCTGGTCTG[A/G]CTATGACTCAGTGGT | 21929 |
rs29343045 | snp | A/C | 0.5 | 0 | upstream-variant-2KB | Tnfaip3 | Mm_Celera | 10:19015703 | AACCCAAAAAACCAC[A/C]CAGACACACAGGACC | 21929 |
rs29344058 | snp | C/T | 0.495 | 0.0497494 | intron-variant | Tnfaip3 | Mm_Celera | 10:19009661 | ACTCCCTTCCTCATC[C/T]ACCACAGTCTCAGAT | 21929 |
rs29345620 | snp | G/T | 0.429688 | 0.173817 | missense | Tnfaip3 | Mm_Celera | 10:19003739 | GGGGAACCAGCTTTC[G/T]CAGAGGCAGTAACAG | 21929 |
rs29353577 | snp | A/G | 0.484429 | 0.0868505 | missense | Tnfaip3 | Mm_Celera | 10:19002963 | GCCCGGGCACATTTC[A/G]GCCTTGAGGCTACCT | 21929 |
rs29360722 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Tnfaip3 | Mm_Celera | 10:19011361 | CAGACACATTTACAG[C/T]TGTCATTCATTCCTT | 21929 |
rs29362665 | snp | C/T | 0.487535 | 0.077957 | missense, intron-variant | Tnfaip3 | Mm_Celera | 10:19011855 | CTCCCATATACCTGC[C/T]GGCAGGAAACCCCAG | 21929 |
rs29367527 | snp | C/T | 0.487535 | 0.077957 | upstream-variant-2KB, intron-variant | Tnfaip3 | Mm_Celera | 10:19012923 | AAGACAGCAATGATT[C/T]AGAGCACCTAGGAAG | 21929 |
rs29370349 | snp | A/C | 0.5 | 0 | upstream-variant-2KB, intron-variant | Tnfaip3 | Mm_Celera | 10:19012655 | AGAGACACCCCTCCC[A/C]CTTCCTTTACCCTAA | 21929 |
rs29370352 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tnfaip3 | GRCm38.p3 | 10:19005741 | GAAGTTCTGAAGGGG[A/G]AAAAAAAAAAAGAAG | 21929 |
rs29373516 | snp | C/T | 0.487535 | 0.077957 | upstream-variant-2KB, intron-variant | Tnfaip3 | Mm_Celera | 10:19012692 | AAACACAATCAAAGG[C/T]GGAAGACATGAAATT | 21929 |
rs29377951 | snp | A/G | 0.465374 | 0.126941 | upstream-variant-2KB, intron-variant | Tnfaip3 | Mm_Celera | 10:19012967 | CTTAATACCAGTCGG[A/G]CACCTTGCTATCCTC | 21929 |
rs45713242 | snp | C/T | 0.336735 | 0.234472 | upstream-variant-2KB | Tnfaip3 | Mm_Celera | 10:19017208 | AATAGATGCAGGCTC[C/T]ACCCTCAGGAAACCT | 21929 |
rs45728041 | snp | C/G | 0.32 | 0.24 | intron-variant | Tnfaip3 | Mm_Celera | 10:19011167 | TACAAGCCTTCATGC[C/G]CTCTGTACCCTAACA | 21929 |
rs45778943 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime | Tnfaip3 | Mm_Celera | 10:19002536 | TCTCAGCTCACCAGG[A/G]CAAAGTCTCGGTTAC | 21929 |
rs45911865 | snp | A/G | 0.32 | 0.24 | intron-variant | Tnfaip3 | Mm_Celera | 10:19009033 | GTATAAAACTAGTCC[A/G]CTCTTCATTCTTGTT | 21929 |
rs46060127 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tnfaip3 | Mm_Celera | 10:19003799 | ATCCCATCCGGGTTA[C/T]GTTGCACACACAGAC | 21929 |
rs46066651 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tnfaip3 | Mm_Celera | 10:19010512 | GAATGCAGTCACTGA[C/T]ACAAGAAAATGTCAC | 21929 |
rs46178978 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tnfaip3 | Mm_Celera | 10:19009122 | AATACTATTCAGTCA[A/G]TAAGGCAATAAAGCT | 21929 |
rs46379585 | snp | G/T | 0.32 | 0.24 | intron-variant | Tnfaip3 | Mm_Celera | 10:19008730 | TTGCCGTCCAAGGCA[G/T]TATATACACCAGGAA | 21929 |
rs46395750 | snp | A/G | 0.244898 | 0.249948 | utr-variant-3-prime | Tnfaip3 | Mm_Celera | 10:19001641 | GAGGTAACAAGGAGA[A/G]AGAAGACAGCCATCC | 21929 |
rs46469537 | snp | A/T | | | intron-variant | Tnfaip3 | Mm_Celera | 10:19011241 | TGGCTGCAGAAGTTC[A/T]TATCTGCTGACCCAG | 21929 |
rs46522074 | snp | C/T | | | upstream-variant-2KB, intron-variant | Tnfaip3 | Mm_Celera | 10:19012167 | AGCAGAGTCCCGAGT[C/T]TAGACTGTCACTGAA | 21929 |
rs46694645 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tnfaip3 | Mm_Celera | 10:19009951 | GTGTGAATCCTTGCT[A/G]ATTCAAAGGCCAAGG | 21929 |
rs47067283 | snp | G/T | 0.32 | 0.24 | intron-variant | Tnfaip3 | Mm_Celera | 10:19008717 | TTCTACGGAAGCTTT[G/T]CCGTCCAAGGCATTA | 21929 |
rs47122066 | snp | A/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Tnfaip3 | Mm_Celera | 10:19014706 | GGATTTGGTGGCCTC[A/T]GAGAAACCCATCCCC | 21929 |
rs47135702 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tnfaip3 | Mm_Celera | 10:19010146 | GTAACAAAATGGGAC[A/G]TGGTAAAAACCACAA | 21929 |
rs47238509 | snp | A/C | 0.32 | 0.24 | upstream-variant-2KB | Tnfaip3 | Mm_Celera | 10:19017276 | AAAGCACACACCACG[A/C]AGAGAATATTAATCT | 21929 |
rs47309717 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Tnfaip3 | Mm_Celera | 10:19010561 | GTAAGTATTCCATGA[G/T]CGCACGTGCTCTCCT | 21929 |
rs47395513 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tnfaip3 | Mm_Celera | 10:19008367 | CTGTGAGGAGCAAGG[C/T]TAAGCAGCCCAAAGC | 21929 |
rs47448004 | snp | C/G | 0.48 | 0.0979796 | upstream-variant-2KB, intron-variant | Tnfaip3 | Mm_Celera | 10:19012824 | TATGGACATCTTTCC[C/G]TGTGGGTCAATGCTG | 21929 |
rs47501177 | snp | A/C | 0.124444 | 0.216185 | upstream-variant-2KB, intron-variant | Tnfaip3 | Mm_Celera | 10:19013758 | AACATGCAAATGTCA[A/C]TGTCTGGTAGCCTAC | 21929 |
rs47502324 | snp | A/G | 0.336735 | 0.234472 | utr-variant-3-prime | Tnfaip3 | Mm_Celera | 10:19001682 | CATGGCCAGGGACTA[A/G]CCAGGCCCCCAGGAC | 21929 |
rs47588361 | snp | A/G | 0.32 | 0.24 | synonymous-codon | Tnfaip3 | Mm_Celera | 10:19002932 | ACTGCGACAGGCCAG[A/G]ATGTTCTTGCAGGAG | 21929 |
rs47623531 | snp | A/C | 0.231111 | 0.249285 | upstream-variant-2KB, intron-variant | Tnfaip3 | Mm_Celera | 10:19012891 | AGAGCACTTGGCTAT[A/C]CATCCTAATTTCCTA | 21929 |
rs47647136 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB, intron-variant | Tnfaip3 | Mm_Celera | 10:19013117 | TAAATTCTCTTGTTC[C/T]CTGCTTGAAAGGGAG | 21929 |
rs47651564 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon | Tnfaip3 | Mm_Celera | 10:19005631 | CAAGTACTCCTTTAG[A/G]AGCTTTTCCTTCATC | 21929 |
rs47767441 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tnfaip3 | Mm_Celera | 10:19003847 | AATGGGTCCCAGCAC[A/G]GATGAGCACAGCCTT | 21929 |
rs47787330 | snp | A/G | 0.132653 | 0.220748 | intron-variant, upstream-variant-2KB | Tnfaip3 | Mm_Celera | 10:19015036 | CTGCAAAGCCAGCGC[A/G]AGGCAGCTCCACACT | 21929 |
rs47937073 | snp | A/G | 0.32 | 0.24 | intron-variant | Tnfaip3 | Mm_Celera | 10:19008497 | ATTCTTCTATGTAGT[A/G]CCTGGTGCCAGCAGT | 21929 |
rs48034959 | snp | C/T | 0.124444 | 0.216185 | utr-variant-5-prime, intron-variant | Tnfaip3 | Mm_Celera | 10:19011920 | AAAGATCTTAGTCAC[C/T]TCTACTCCCAGGATA | 21929 |
rs48255854 | snp | C/G | 0.124444 | 0.216185 | utr-variant-3-prime | Tnfaip3 | Mm_Celera | 10:19000974 | GTTCTTTAAAACAAT[C/G]TGAAGTCCAAAAAAG | 21929 |
rs48257697 | snp | A/G | 0.231111 | 0.249285 | upstream-variant-2KB, intron-variant | Tnfaip3 | Mm_Celera | 10:19012356 | ATGTATAAATACTTG[A/G]TTCAGAGAGTTTAGG | 21929 |
rs48299315 | snp | C/G | 0.124444 | 0.216185 | intron-variant, utr-variant-5-prime | Tnfaip3 | Mm_Celera | 10:19014526 | CCTAAAGTGGAGTCC[C/G]CAACAAGCAGGCCAG | 21929 |
rs48433971 | snp | A/G | 0.124444 | 0.216185 | intron-variant, utr-variant-5-prime | Tnfaip3 | Mm_Celera | 10:19014560 | ATCATTTCTGCATGC[A/G]TACTCTTCTTAAACT | 21929 |
rs48563191 | snp | C/T | 0.32 | 0.24 | synonymous-codon | Tnfaip3 | Mm_Celera | 10:19004458 | CTGATTTCACTCACG[C/T]TTATTTTCTCTGTAT | 21929 |
rs48815221 | snp | C/G | 0.132653 | 0.220748 | missense | Tnfaip3 | Mm_Celera | 10:19005008 | GGGCTCCAGTTTGAG[C/G]AGCCAAGTCCCACGC | 21929 |
rs48869085 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tnfaip3 | Mm_Celera | 10:19006623 | TCTGAAAATCTCAAA[C/T]CCTCGAATCTGACTT | 21929 |
rs49031241 | snp | A/G | 0.132653 | 0.220748 | utr-variant-3-prime | Tnfaip3 | Mm_Celera | 10:19001358 | GGCAGAAACTTCCTC[A/G]TCCTCACGGCTATTG | 21929 |
rs49050951 | snp | A/C | 0.32 | 0.24 | intron-variant | Tnfaip3 | Mm_Celera | 10:19011202 | CGTACTTAGAAAACA[A/C]CTTAAAATCAAATAT | 21929 |
rs49088375 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Tnfaip3 | Mm_Celera | 10:19010716 | AATAGTCATCAGTGG[A/T]AAAGTTCTTTATGTA | 21929 |
rs49113174 | snp | G/T | 0.124444 | 0.216185 | upstream-variant-2KB | Tnfaip3 | Mm_Celera | 10:19016970 | TTCTATTTAAAACCT[G/T]CCAGTATTTGTCTTC | 21929 |
rs49130946 | snp | A/G | 0.32 | 0.24 | intron-variant | Tnfaip3 | Mm_Celera | 10:19009258 | TGAACAGAAAAGATC[A/G]CTAGAGCCTAGTGTC | 21929 |
rs49220928 | snp | C/T | 0.231111 | 0.249285 | upstream-variant-2KB | Tnfaip3 | Mm_Celera | 10:19016394 | GTGACATTGAAACTC[C/T]GTGACAAAGAAACCT | 21929 |
rs49323836 | snp | C/T | 0.408163 | 0.193609 | upstream-variant-2KB | Tnfaip3 | Mm_Celera | 10:19015785 | TCAGAAAGAGCCCTC[C/T]GCAGGGTCCCGAAGG | 21929 |
rs49335580 | snp | C/T | 0.124444 | 0.216185 | missense | Tnfaip3 | Mm_Celera | 10:19004840 | CTGGCATTAATCTGC[C/T]GGGCGTGGCAACGCT | 21929 |
rs49500378 | snp | C/G | 0.260355 | 0.249785 | upstream-variant-2KB | Tnfaip3 | Mm_Celera | 10:19016526 | GTGTGAGGCTCTTCC[C/G]GGAAAGGAGCCGGGA | 21929 |
rs49573411 | snp | A/T | 0.231111 | 0.249285 | synonymous-codon | Tnfaip3 | Mm_Celera | 10:19004884 | ATGCTGCACATTCAA[A/T]GTAAAAGGGCACCCA | 21929 |
rs49734777 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tnfaip3 | Mm_Celera | 10:19005777 | GTGAGTAAAACATTA[C/T]CCTGCTAAATGATGG | 21929 |
rs49909006 | snp | A/C | 0.35503 | 0.226867 | intron-variant | Tnfaip3 | Mm_Celera | 10:19003368 | GGTTTCAGTCTATGG[A/C]TGACTGTATTAGCTT | 21929 |
rs49958163 | snp | A/C | 0.32 | 0.24 | upstream-variant-2KB, intron-variant | Tnfaip3 | Mm_Celera | 10:19013225 | GCAACTAGAATTAGG[A/C]AGGAACATAGAATGA | 21929 |
rs49962611 | snp | C/T | 0.32 | 0.24 | intron-variant | Tnfaip3 | Mm_Celera | 10:19007938 | ATAGAATCGCCTACC[C/T]AGGAATCAGCTGTCC | 21929 |
rs49976630 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB | Tnfaip3 | Mm_Celera | 10:19017401 | TCTAGGTTTGCTGAG[C/T]TGGGAATTCAATAAA | 21929 |
rs49990684 | snp | C/T | 0.231111 | 0.249285 | upstream-variant-2KB, intron-variant | Tnfaip3 | Mm_Celera | 10:19012630 | GCTGTCCTTCCAGGT[C/T]CCAATGCTCAGAGAC | 21929 |
rs50134143 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tnfaip3 | Mm_Celera | 10:19003427 | TCATGCAATGTATCC[A/G]CCTCAGGAGCCAATA | 21929 |
rs50199471 | snp | C/T | 0.32 | 0.24 | intron-variant | Tnfaip3 | Mm_Celera | 10:19011010 | GATTCTGATTTTCAA[C/T]GCTCTACTTTCCTTC | 21929 |
rs50202859 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tnfaip3 | Mm_Celera | 10:19005403 | AGCTCCCAGAACCCA[C/T]TTCCACAATGCAGTC | 21929 |
rs50267098 | snp | C/G | 0.124444 | 0.216185 | utr-variant-3-prime | Tnfaip3 | Mm_Celera | 10:19001401 | CAGTGTTCCTATCCA[C/G]TACCCAAGGGCACAG | 21929 |
rs50322462 | snp | G/T | 0.32 | 0.24 | intron-variant | Tnfaip3 | Mm_Celera | 10:19009197 | AATCCATATTCAGGG[G/T]CACTGCTCCTTCATC | 21929 |
rs50420722 | snp | C/T | 0.336735 | 0.234472 | utr-variant-3-prime | Tnfaip3 | Mm_Celera | 10:19002174 | TTTCCTGCAGAACCT[C/T]GGGAGCCAAGTCGGC | 21929 |
rs50521502 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Tnfaip3 | Mm_Celera | 10:19002229 | GATGTGCTCCGCCTA[C/T]GTCCTGTTTTTCCCT | 21929 |
rs50675677 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Tnfaip3 | Mm_Celera | 10:19011398 | GTTTCCATAGGCACC[C/T]GTCTAATGCCATTTA | 21929 |
rs50817131 | snp | C/T | 0.244898 | 0.249948 | utr-variant-3-prime | Tnfaip3 | Mm_Celera | 10:19001713 | ATGGTGGAAAGCAAA[C/T]ATGTTATCTCAAGAA | 21929 |
rs51191413 | snp | A/G | 0.244898 | 0.249948 | downstream-variant-500B | Tnfaip3 | Mm_Celera | 10:19000802 | ATTATTTTTCAGAAG[A/G]TATCATTCTTTCCAT | 21929 |
rs51222427 | snp | A/G | 0.35503 | 0.226867 | utr-variant-3-prime | Tnfaip3 | Mm_Celera | 10:19002493 | CAGGCTGACCCTGAC[A/G]TCATGCACTGCCGGT | 21929 |
rs51275777 | snp | A/T | 0.142012 | 0.225474 | upstream-variant-2KB, intron-variant | Tnfaip3 | Mm_Celera | 10:19012675 | CTTTACCCTAAAAGA[A/T]CAAACACAATCAAAG | 21929 |
rs51296623 | snp | A/G | 0.32 | 0.24 | intron-variant | Tnfaip3 | Mm_Celera | 10:19011071 | TCTGGCCAGTGAAGG[A/G]CAAGTTATAGATGAT | 21929 |
rs51535663 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon | Tnfaip3 | Mm_Celera | 10:19005559 | TGCTTACTTTGCAGC[A/G]TTGATCAGGTGAGTC | 21929 |
rs51547343 | snp | G/T | 0.32 | 0.24 | missense, intron-variant | Tnfaip3 | Mm_Celera | 10:19011832 | CCGTTAGGCTGCCTT[G/T]AACACTGCTCCCATA | 21929 |
rs51567411 | snp | C/T | 0.142012 | 0.225474 | utr-variant-3-prime | Tnfaip3 | Mm_Celera | 10:19002669 | CAGGGGTCTGGATCA[C/T]AGTACCACTGTGAAT | 21929 |
rs51590044 | snp | A/G | 0.124444 | 0.216185 | upstream-variant-2KB, intron-variant | Tnfaip3 | Mm_Celera | 10:19013807 | ACTCTCACTAGCACT[A/G]CCTGTTTAAAACAGA | 21929 |
rs51804357 | snp | C/T | 0.32 | 0.24 | intron-variant | Tnfaip3 | Mm_Celera | 10:19008988 | TTCCTTTTCATGCCC[C/T]AAAGAGTAAACATTT | 21929 |
rs51881929 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Tnfaip3 | Mm_Celera | 10:19014786 | CAAGGTCTACGTGCC[C/T]ATGAACACGCTGCAC | 21929 |
rs211700843 | snp | C/T | | | utr-variant-3-prime | Tnfaip3 | Mm_Celera | 10:19002636 | CACTGTCCCAGGGCC[C/T]ACCCTTCCTGTGGCA | 21929 |