SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6208176 | snp | C/T | 0.5 | 0 | intron-variant | Tbl1x | Mm_Celera | X:77623581 | gggattatagacata[C/T]gctgcagctggcttt | 21372 |
rs6208227 | snp | C/T | 0.5 | 0 | intron-variant | Tbl1x | Mm_Celera | X:77596959 | cacatgcacacTCTC[C/T]CCACCAACAAAATAA | 21372 |
rs6210281 | snp | A/G | 0.5 | 0 | intron-variant | Tbl1x | Mm_Celera | X:77623937 | CTGTTTGGGAAAGAG[A/G]AAAGGAGTAAAAAAG | 21372 |
rs6223767 | snp | A/T | 0.5 | 0 | intron-variant | Tbl1x | Mm_Celera | X:77624178 | GAAAATTATTATAAT[A/T]ATGTTACACAAAGGA | 21372 |
rs6224471 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Tbl1x | Mm_Celera | X:77630908 | GTTGTGGGGAGGAAG[A/G]GAAGGCTGGGNGATA | 21372 |
rs6224878 | snp | A/G | 0.5 | 0 | intron-variant | Tbl1x | Mm_Celera | X:77630919 | GAAGNGAAGGCTGGG[A/G]GATACCTTATGCCCC | 21372 |
rs6224985 | snp | A/T | 0.207612 | 0.24638 | intron-variant | Tbl1x | Mm_Celera | X:77630978 | AGCTAAACAGTAAAA[A/T]ATACAATGAGTCtct | 21372 |
rs6225533 | snp | C/T | 0.5 | 0 | intron-variant | Tbl1x | Mm_Celera | X:77631084 | agctagactggccag[C/T]gagcttgagtgatct | 21372 |
rs6397750 | snp | G/T | 0.5 | 0 | intron-variant | Tbl1x | Mm_Celera | X:77581213 | ggattaaaggcatgt[G/T]ccactaccacccagc | 21372 |
rs29031234 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tbl1x | Mm_Celera | X:77626295 | AAGAACCATGTCACT[A/G]CATGTCTTTGCTGGG | 21372 |
rs29031235 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Tbl1x | Mm_Celera | X:77626020 | TCCTAACTACCTCAG[A/T]GTCATTATCTCACAT | 21372 |
rs29031236 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Tbl1x | Mm_Celera | X:77625563 | TGATCCATTCAAATG[A/G]ACTTCATTGTATTTG | 21372 |
rs29031237 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Tbl1x | GRCm38.p3 | X:77623224 | ATTTTTGTGTTTGTA[A/G]TGTCTACAATATGTG | 21372 |
rs29031238 | snp | A/C | 0.32 | 0.24 | intron-variant | Tbl1x | Mm_Celera | X:77622106 | CCTAGCTTGGACCTG[A/C]AGATCCGGGAAGCTA | 21372 |
rs29031239 | snp | C/T | 0.429688 | 0.173817 | intron-variant | Tbl1x | Mm_Celera | X:77621596 | TTAGGCTATGCCATG[C/T]TTCTGTCCACATATT | 21372 |
rs29031240 | snp | A/G | 0.32 | 0.24 | intron-variant | Tbl1x | Mm_Celera | X:77621334 | GTTAAAATATTGGTG[A/G]AACAAGGACAGAACC | 21372 |
rs29031241 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Tbl1x | Mm_Celera | X:77620891 | AGAGAAGAATTTCAT[C/G]ACTGAAAAGTTCGCT | 21372 |
rs29031242 | snp | C/G | 0.336735 | 0.234472 | intron-variant | Tbl1x | Mm_Celera | X:77620052 | GGCCCTAGGTTAAAT[C/G]AGTACTGAAGCTTTC | 21372 |
rs29031243 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Tbl1x | Mm_Celera | X:77618084 | CTTTCAGAATTTGGC[A/G]CCTGGTGCGTGCTAG | 21372 |
rs29031364 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tbl1x | Mm_Celera | X:77571164 | CAGTTGAGGAATGCC[A/G]TTCTACCTATTGTAT | 21372 |
rs29031365 | snp | G/T | 0.5 | 0 | intron-variant | Tbl1x | Mm_Celera | X:77571069 | AGATTGGGATCCAAG[G/T]GAGGTCAAGCAGTAA | 21372 |
rs29031366 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tbl1x | Mm_Celera | X:77570955 | CTCAGGCAGGGCCTC[C/T]GTAGAGCAGGTATAA | 21372 |
rs29031367 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tbl1x | Mm_Celera | X:77570815 | GCTGCTCAGCCAACT[C/T]TAAGGTGTAGAGATG | 21372 |
rs29031368 | snp | C/G | 0.32 | 0.24 | intron-variant | Tbl1x | Mm_Celera | X:77570801 | TACCTGTAACAGCAG[C/G]TGCTCAGCCAACTCT | 21372 |
rs29031369 | snp | G/T | 0.32 | 0.24 | intron-variant | Tbl1x | Mm_Celera | X:77570699 | ATTGTTAGACATATT[G/T]TCACTTCCAAGTGTT | 21372 |
rs29031370 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tbl1x | Mm_Celera | X:77570452 | GTTGCAGATCTATAG[C/T]GCCCTATACTAGTCT | 21372 |
rs29031371 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Tbl1x | Mm_Celera | X:77570115 | TGAGGATGGAGTAAC[A/T]CAGGCTGGCTGGGTG | 21372 |
rs29031372 | snp | A/G | 0.32 | 0.24 | intron-variant | Tbl1x | Mm_Celera | X:77568807 | GCTTACTCACTCCGA[A/G]CCCACCCTGGGGAAT | 21372 |
rs29031373 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tbl1x | Mm_Celera | X:77568295 | CTGTTTAGTTTTAGA[C/T]GCTTTCAAGCTCTGA | 21372 |
rs29031394 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Tbl1x | Mm_Celera | X:77526237 | GATCTCTGCCTCTGA[A/G]TCCAAAACCTCAGCC | 21372 |
rs29031395 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tbl1x | Mm_Celera | X:77525839 | AGGCTGGTAATCATA[C/T]TTACTATGTCTAAGT | 21372 |
rs29031396 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Tbl1x | Mm_Celera | X:77525703 | TAATCATCTTTACAC[C/T]CCAGCCTTGAAATTC | 21372 |
rs29031397 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Tbl1x | Mm_Celera | X:77525305 | TGTATGACAATAAAT[A/C]CTGGAGGTTGTTGAA | 21372 |
rs29031398 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Tbl1x | Mm_Celera | X:77525062 | CTTTTGGTACACATA[C/G]GTGTGCACACATAAA | 21372 |
rs29031399 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tbl1x | Mm_Celera | X:77524009 | AAAGGAGATATGTAG[A/G]TGGTTCATAAAGATG | 21372 |
rs29031400 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tbl1x | Mm_Celera | X:77523983 | CCTCTTAGAATTTTT[A/G]ACTGCAGTATAAAGG | 21372 |
rs29031401 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Tbl1x | Mm_Celera | X:77521198 | TTCCCCTTAGAAGAT[C/G]AGGCTATTAAAATGA | 21372 |
rs29031402 | snp | C/T | 0.32 | 0.24 | intron-variant | Tbl1x | Mm_Celera | X:77521122 | ATACAGAATGAAATG[C/T]TTTGTCTGGTGACAC | 21372 |
rs29031403 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tbl1x | Mm_Celera | X:77520967 | ACCCTACTGGTTTGT[A/G]TTTCCTGTGTGTTGA | 21372 |
rs29031484 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Tbl1x | Mm_Celera | X:77618066 | ATACTAACTTATACC[C/G]TTCTTTCAGAATTTG | 21372 |
rs29031485 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Tbl1x | Mm_Celera | X:77617829 | ATTTTAGAGTAGATC[A/G]TCTGTGTTTTACAGT | 21372 |
rs29031486 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Tbl1x | Mm_Celera | X:77617614 | ATTTAGGCTTCATCT[A/G]ACACATCTCCTTTTA | 21372 |
rs29031487 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Tbl1x | Mm_Celera | X:77617152 | AGCTGCACACTGTCT[A/T]AGAAGCACTGTGGTG | 21372 |
rs29031488 | snp | A/G | 0.32 | 0.24 | intron-variant | Tbl1x | Mm_Celera | X:77617111 | TCTTGAACTACACAC[A/G]AGTTAACTGAGTATT | 21372 |
rs29031489 | snp | C/G | 0.415225 | 0.187619 | intron-variant | Tbl1x | Mm_Celera | X:77616431 | TGCTAAGACTGGACA[C/G]AGCACCTGTGTAGTT | 21372 |
rs29031490 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Tbl1x | Mm_Celera | X:77616393 | TTAAACAAATGCTAA[A/G]GAGAACACATTAACA | 21372 |
rs29031491 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Tbl1x | Mm_Celera | X:77616363 | GAGACAGACGCTGAG[A/T]ATAAGAGCTACATAT | 21372 |
rs29031492 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Tbl1x | Mm_Celera | X:77615455 | TCTTTATGGGCATAC[C/G]ACTAGCCATTTTTCT | 21372 |
rs29031493 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Tbl1x | Mm_Celera | X:77615225 | GAATTTATCTCCAAC[A/T]TCCCATAGAATGGAG | 21372 |
rs29031568 | snp | A/G | 0.142012 | 0.225474 | downstream-variant-500B | Tbl1x | Mm_Celera | X:77663389 | ATCTGAGACAGTCTT[A/G]GATCAAATGGGTAGG | 21372 |
rs29031569 | snp | A/G | 0.152778 | 0.230321 | utr-variant-3-prime | Tbl1x | Mm_Celera | X:77662463 | TACCATTCCCAGCAC[A/G]TCCAGGATGCTGCCT | 21372 |
rs29031570 | snp | A/C | 0.391111 | 0.206368 | utr-variant-3-prime | Tbl1x | Mm_Celera | X:77661853 | GTTCATCTCTACAGA[A/C]GATCAGCTGTTAGAT | 21372 |
rs29031571 | snp | C/G | 0.231111 | 0.249285 | utr-variant-3-prime | Tbl1x | Mm_Celera | X:77661412 | ACTGACTTGTTGTTT[C/G]TTTAATTAGTAATGG | 21372 |
rs29031572 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime | Tbl1x | Mm_Celera | X:77661313 | TTGGCTATTTTTTAA[A/G]AACAAAATAAGGCAT | 21372 |
rs29031573 | snp | G/T | 0.124444 | 0.216185 | utr-variant-3-prime | Tbl1x | Mm_Celera | X:77661066 | GTGTAGCTACCGATG[G/T]GCACTTTTATCAAGA | 21372 |
rs29031634 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tbl1x | Mm_Celera | X:77568183 | TCCTTTGTTGCCCAG[A/G]CCCCATCCTGTGTAT | 21372 |
rs29031635 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tbl1x | Mm_Celera | X:77567956 | CCAGGCCCTGGCCTA[A/G]AATAAGTCTTAATTA | 21372 |
rs29031636 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tbl1x | Mm_Celera | X:77567909 | ATCTTTCTTTCTGGG[A/G]ATGCAAAGCTATTGG | 21372 |
rs29031637 | snp | C/T | 0.32 | 0.24 | intron-variant | Tbl1x | Mm_Celera | X:77567021 | GAATTATTGGGTGGG[C/T]CTACAATGTGGAAAA | 21372 |
rs29031638 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tbl1x | Mm_Celera | X:77566905 | CACATGTTGAGAAGG[A/G]CACATTTGGGGAACT | 21372 |
rs29031639 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Tbl1x | Mm_Celera | X:77566413 | AGTGGTCTTCATTTT[G/T]TTTTACTTAATCTAT | 21372 |
rs29031640 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tbl1x | Mm_Celera | X:77564868 | GCTTTTCAGTTTTCA[A/G]AATTTCCTAAAGTCT | 21372 |
rs29031641 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Tbl1x | Mm_Celera | X:77564832 | CCCTGTTCTTTGTTA[A/C]CATACCTAACTTCTG | 21372 |
rs29031642 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tbl1x | Mm_Celera | X:77564201 | GAATCTCATTTATGC[C/T]GGGCTGGCTGCAAAC | 21372 |
rs29031643 | snp | G/T | 0.49827 | 0.0293608 | intron-variant | Tbl1x | Mm_Celera | X:77564172 | TCCTTAGCATTCTTT[G/T]TCAGGTGGAGGAAGA | 21372 |
rs29031684 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tbl1x | Mm_Celera | X:77614874 | AGATAGTCAGCAGTT[A/G]CATGTTTGTATTCAG | 21372 |
rs29031685 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tbl1x | Mm_Celera | X:77613891 | GGCAGTGCTTCTATA[A/G]TAACTTCTTAAGAGT | 21372 |
rs29031686 | snp | A/T | 0.207612 | 0.24638 | intron-variant | Tbl1x | Mm_Celera | X:77613580 | CTGATGTGGTAGCCA[A/T]CATTTCCTGATGTAG | 21372 |
rs29031687 | snp | A/G | 0.32 | 0.24 | intron-variant | Tbl1x | Mm_Celera | X:77612305 | ATCAATTAATTTAAG[A/G]CAGTCATCTGCTGGG | 21372 |
rs29031688 | snp | C/T | 0.32 | 0.24 | intron-variant | Tbl1x | Mm_Celera | X:77611841 | CACACCACAAACTCT[C/T]TCTATTTGTGCTAAT | 21372 |
rs29031689 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Tbl1x | Mm_Celera | X:77611793 | AGAAAAGTGATAAGG[A/G]CAGACAGACAGTATT | 21372 |
rs29031690 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tbl1x | Mm_Celera | X:77610645 | CAGCCATGATGAATG[A/G]AAAATTATTCAAGGG | 21372 |
rs29031691 | snp | C/T | 0.32 | 0.24 | intron-variant | Tbl1x | Mm_Celera | X:77609942 | ATTGTGCTGGCTTGA[C/T]GTTTTTGTTCCTTGT | 21372 |
rs29031692 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tbl1x | Mm_Celera | X:77609261 | CAACAGATTGGCAAG[C/T]CCTAGAGAATCAGCT | 21372 |
rs29031693 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Tbl1x | Mm_Celera | X:77608700 | GATCTGTGTTGTTGT[A/C]ATCCTCTTGGGCTTT | 21372 |
rs29031774 | snp | C/T | 0.32 | 0.24 | upstream-variant-2KB | Tbl1x | Mm_Celera | X:77509268 | CTGAAGCTGTAATGA[C/T]GTCAACTTGTTATTT | 21372 |
rs29031775 | snp | C/T | 0.32 | 0.24 | upstream-variant-2KB | Tbl1x | Mm_Celera | X:77509126 | CAGGAATGCTTTTAA[C/T]CAACTTCAGTTTGGA | 21372 |
rs29031844 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Tbl1x | Mm_Celera | X:77661032 | CATGGCACTTGCCAG[C/T]TACATCTTTCTCACA | 21372 |
rs29031845 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon | Tbl1x | Mm_Celera | X:77659738 | TTTAGATCTCCGAAA[A/G]TAAACACAAAATGTA | 21372 |
rs29031846 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tbl1x | Mm_Celera | X:77659304 | TGTCATGAGAAGATA[A/G]TTTTCAGACAAGCCT | 21372 |
rs29031847 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tbl1x | Mm_Celera | X:77658999 | TTAAAAACATCCTTC[C/T]CTTTGTCCCTGAATG | 21372 |
rs29031848 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tbl1x | Mm_Celera | X:77658811 | TGGCTCCGTAAGTGG[C/T]GCCTCTGGTCTACTA | 21372 |
rs29031849 | snp | C/T | 0.32 | 0.24 | intron-variant | Tbl1x | Mm_Celera | X:77658152 | GGGGTCCTTCGTGCT[C/T]ACTCAAGTGCTTTGA | 21372 |
rs29031850 | snp | A/T | 0.32 | 0.24 | intron-variant | Tbl1x | Mm_Celera | X:77658092 | AATACCACAGTACAA[A/T]TGCGTATGTTCATTC | 21372 |
rs29031851 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tbl1x | Mm_Celera | X:77657310 | ACAATGTATACTACA[C/T]TTTGTTTTTCTATGT | 21372 |
rs29031852 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Tbl1x | Mm_Celera | X:77656849 | TAGCATATTTTTACT[A/C]GGTGATTCACAACAC | 21372 |
rs29031853 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tbl1x | Mm_Celera | X:77656656 | GATCAGGAGGAATTG[A/G]AGCCAGCCTGGCCTG | 21372 |
rs29031914 | snp | C/G | 0.32 | 0.24 | intron-variant | Tbl1x | Mm_Celera | X:77564028 | GACAGTGAATCTTAA[C/G]TGATGACTTGGGTTA | 21372 |
rs29031915 | snp | C/T | 0.32 | 0.24 | intron-variant | Tbl1x | Mm_Celera | X:77563916 | CACATCCTACTAAGT[C/T]CACATGGTACATTTT | 21372 |
rs29031916 | snp | A/G | 0.32 | 0.24 | intron-variant | Tbl1x | Mm_Celera | X:77563618 | TGTCATGGGTAAAAT[A/G]TCTGACTTTTAACTG | 21372 |
rs29031917 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Tbl1x | Mm_Celera | X:77563590 | GGTGTTGCTATGGTT[G/T]TAGTTCATGACTTGT | 21372 |
rs29031918 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Tbl1x | Mm_Celera | X:77563373 | TGTGTGTCCCATATA[A/C]TTCGTTATTTACACC | 21372 |
rs29031919 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Tbl1x | Mm_Celera | X:77563328 | CTTGCCTAGCTAAAT[A/C]TCTAGCCCTTTCCCT | 21372 |
rs29031920 | snp | A/G | 0.32 | 0.24 | intron-variant | Tbl1x | Mm_Celera | X:77563210 | GTTGACAGCTGATAC[A/G]TACATTGTGGTCTAG | 21372 |
rs29031921 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tbl1x | Mm_Celera | X:77563173 | TGATGGGCTATTAAG[C/T]AGAGCTACATAGCTT | 21372 |
rs29031922 | snp | A/G | 0.32 | 0.24 | intron-variant | Tbl1x | Mm_Celera | X:77563015 | GGCCTAGATACCACA[A/G]CAAGGATAATAGAGA | 21372 |
rs29031923 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tbl1x | Mm_Celera | X:77562774 | TGCTTCTTAGTGTAT[C/T]TTGGACATATTAGCA | 21372 |
rs29031934 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tbl1x | Mm_Celera | X:77608688 | GAGGCATGAGTTGAT[C/T]TGTGTTGTTGTCATC | 21372 |
rs29031935 | snp | A/G | 0.32 | 0.24 | intron-variant | Tbl1x | Mm_Celera | X:77607078 | ACTTCTGAGCTTCAA[A/G]TCCATCCCTTTGCAC | 21372 |
rs29031936 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tbl1x | Mm_Celera | X:77607030 | TTGCTCCTTTAGAAG[C/T]CACTTCAACTTTGCA | 21372 |