SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6220003 | snp | A/C | 0.21875 | 0.248039 | intron-variant | Uchl3 | Mm_Celera | 14:101693664 | GACGAAATCCAGCTT[A/C]GCGGTTATGTTTGCT | 50933 |
rs6220962 | snp | A/T | 0.5 | 0 | intron-variant | Uchl3 | Mm_Celera | 14:101693793 | GGTTGAAACTCCACA[A/T]TATGCTAAACTCCTG | 50933 |
rs6398893 | snp | C/T | 0.5 | 0 | intron-variant | Uchl3 | Mm_Celera | 14:101676813 | AAGTGCTTTATAAAG[C/T]TGGAAANTTTTTCTG | 50933 |
rs6398909 | snp | A/T | 0.5 | 0 | intron-variant | Uchl3 | Mm_Celera | 14:101676820 | TTATAAAGNTGGAAA[A/T]TTTTTCTGCCCATTT | 50933 |
rs6399546 | snp | C/T | 0.32 | 0.24 | intron-variant | Uchl3 | Mm_Celera | 14:101676957 | GGTCCCTGGCTAGCT[C/T]CTCATCTCATGCACT | 50933 |
rs30295267 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Uchl3 | Mm_Celera | 14:101657857 | CTCTACCTTATTTAC[A/G]TATATATATATATAT | 50933 |
rs31072586 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Uchl3 | Mm_Celera | 14:101679562 | TAATTGCTGATGACT[C/T]TGCAATCCTTCATGT | 50933 |
rs31396227 | snp | A/G | 0.375 | 0.216506 | intron-variant | Uchl3 | Mm_Celera | 14:101690791 | TTTTTTTTTTAACTA[A/G]AAAAAGATGTTTTTG | 50933 |
rs45675336 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Uchl3 | Mm_Celera | 14:101669725 | GTCACTTCCAAGAGT[A/G]CTGCGGTGCCTTCTT | 50933 |
rs45721346 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Uchl3 | Mm_Celera | 14:101684097 | GTCTGCCCTGCTCTT[C/T]AGTCCCGGCTGGCTT | 50933 |
rs45786079 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Uchl3 | Mm_Celera | 14:101680961 | TGGACTCCTTGGGAA[C/G]CTCCTGTGCTTGATA | 50933 |
rs45798306 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Uchl3 | Mm_Celera | 14:101673029 | GGCAATATATTTTCC[A/G]TGTGTAAACTAAAGC | 50933 |
rs45803548 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Uchl3 | Mm_Celera | 14:101659589 | GACACTAATGGCCTT[C/T]AGCGATCGTTTTTAG | 50933 |
rs45820972 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Uchl3 | Mm_Celera | 14:101674848 | ATGAAGGCGAGAAAG[A/G]AAACCCCAAGTGGTC | 50933 |
rs45925592 | snp | C/T | 0.375 | 0.216506 | intron-variant | Uchl3 | Mm_Celera | 14:101657731 | GACATATAGTCCATC[C/T]GGTAAACAGCCAGTT | 50933 |
rs46069193 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Uchl3 | Mm_Celera | 14:101663571 | GAATTGAATTTTTAT[A/G]GCATATCATTTCATC | 50933 |
rs46070755 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Uchl3 | Mm_Celera | 14:101677026 | TTCCCTGAATGCAGG[A/G]AAGCCTTGCCTTTCT | 50933 |
rs46104643 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Uchl3 | Mm_Celera | 14:101681578 | AGAGGCAGGACCAGG[A/G]CTGAAGAATGCCTGG | 50933 |
rs46144088 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Uchl3 | Mm_Celera | 14:101679303 | AATAGACTACAGCTA[A/G]TTTAAAACATGGCTT | 50933 |
rs46177328 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Uchl3 | Mm_Celera | 14:101687934 | GCTTCCCAGAACGAA[C/T]GAGGCCCTGAGGAAA | 50933 |
rs46211416 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Uchl3 | Mm_Celera | 14:101670161 | TTGTTTCTATGCATT[A/G]TACCTCTGAGATATA | 50933 |
rs46239105 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Uchl3 | Mm_Celera | 14:101680536 | TGTGTTGCACTGAGA[A/C]ATGTGGAGATGCAAT | 50933 |
rs46296008 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Uchl3 | Mm_Celera | 14:101676498 | AGGGGAAGGCTCACT[C/T]GCATTTATAACCCTT | 50933 |
rs46301234 | snp | A/G/T | 0.345679 | 0.230967 | intron-variant | Uchl3 | GRCm38.p3 | 14:101658201 | CTAGACCTGCATGTA[A/G/T]TTTTTTTGTCATTTG | 50933 |
rs46301740 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Uchl3 | Mm_Celera | 14:101685976 | CTTGGTGAATATCCA[G/T]CTTTCCACTCCATAG | 50933 |
rs46346460 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Uchl3 | Mm_Celera | 14:101693184 | CCTACTTGGATCATT[C/T]TTTGTGCATTAACAT | 50933 |
rs46437928 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Uchl3 | Mm_Celera | 14:101659526 | GTCGTCCCTGCTTTG[C/G]TTTGGCTTTAGAAAA | 50933 |
rs46602960 | snp | C/G | 0.396694 | 0.202437 | intron-variant | Uchl3 | Mm_Celera | 14:101659380 | TGTGTACTCTGAGAT[C/G]GTGGCTGTCTAATCT | 50933 |
rs46674353 | snp | A/G | 0.42 | 0.183303 | intron-variant | Uchl3 | Mm_Celera | 14:101659278 | TTAGCTCAAGCCAGC[A/G]CTATGACTCTTCTCC | 50933 |
rs46732391 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Uchl3 | Mm_Celera | 14:101687826 | TGGCCAGGCAGGCAC[G/T]CGGGAACTCGCTGCC | 50933 |
rs46733856 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Uchl3 | Mm_Celera | 14:101669518 | CTCTTAACGTTGTAG[A/G]CTGTTGGTTTGTATT | 50933 |
rs46898226 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Uchl3 | Mm_Celera | 14:101674898 | TTCAGTCATTGGCCA[A/G]AAAGAACCACCGGGT | 50933 |
rs46939169 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Uchl3 | Mm_Celera | 14:101672663 | TTCTGGTATACCTGT[C/T]CTCGCTGTAGAGATG | 50933 |
rs47010888 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Uchl3 | Mm_Celera | 14:101677445 | GAACCCAGTTGTTAG[C/T]CCTGCAAGGGAGGGT | 50933 |
rs47085339 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Uchl3 | Mm_Celera | 14:101670998 | CCTGTCTTCAGGCCT[C/T]CTCTAACTCTGGCTA | 50933 |
rs47087101 | snp | G/T | 0.32 | 0.24 | intron-variant | Uchl3 | Mm_Celera | 14:101665251 | TCTTATTGGCAAAAT[G/T]CTTAGCTATCTGTCT | 50933 |
rs47174677 | snp | A/G | 0.32 | 0.24 | intron-variant | Uchl3 | Mm_Celera | 14:101666298 | TCACAGGCAGGCAAT[A/G]AGTAAAATAACCGAT | 50933 |
rs47209238 | snp | C/G | 0.375 | 0.216506 | missense | Uchl3 | Mm_Celera | 14:101667017 | AACATTGAAAAAGTT[C/G]CTGGAGGAGTCTGTA | 50933 |
rs47312339 | snp | C/T | | | intron-variant | Uchl3 | Mm_Celera | 14:101666405 | ACTTTAAATCATTTT[C/T]TTAGGTTAGGCTGCA | 50933 |
rs47350603 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Uchl3 | Mm_Celera | 14:101668225 | CAAGTGAATAAAGTG[C/T]TAAGTATTGCTCTAA | 50933 |
rs47366731 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Uchl3 | Mm_Celera | 14:101693768 | CAGTTATCTAACTCT[C/T]AATAAGGTTGGTTGA | 50933 |
rs47582818 | snp | A/T | 0.32 | 0.24 | intron-variant | Uchl3 | Mm_Celera | 14:101666317 | AAAATAACCGATGTG[A/T]GAATGCCTTGTCTTT | 50933 |
rs47727409 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Uchl3 | Mm_Celera | 14:101676627 | TGTAAGTCCAATTTT[A/G]CCAAAAAGTTTGAAA | 50933 |
rs47734324 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Uchl3 | Mm_Celera | 14:101661817 | TTCCATGCATACATG[C/T]GGTTTCCACCAGTGC | 50933 |
rs47761288 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Uchl3 | Mm_Celera | 14:101681090 | AAGTCATGAAGAAAG[A/T]CCTCTGGGCATAGGC | 50933 |
rs47992740 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Uchl3 | Mm_Celera | 14:101668959 | AGCTCTGCCGGGTCT[A/G]TCTCTGCTCCTTTGG | 50933 |
rs48002377 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Uchl3 | Mm_Celera | 14:101690288 | GTGCATTGTGTACAT[A/G]CTGTGCCCACAGAGA | 50933 |
rs48026603 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Uchl3 | Mm_Celera | 14:101675398 | TAAGAAAGTTTTTTT[C/T]TTCAAAGATCTTCTA | 50933 |
rs48046500 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Uchl3 | Mm_Celera | 14:101692801 | AGTTACAGACATGGC[A/G]CTGTAATCCCTCTCT | 50933 |
rs48073139 | snp | C/G | 0.32 | 0.24 | intron-variant | Uchl3 | Mm_Celera | 14:101666271 | TGAGCAGTACGGCCA[C/G]ACCCTTGTATCTCAC | 50933 |
rs48176140 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Uchl3 | Mm_Celera | 14:101674818 | CAACAACGGACAAAC[A/G]TTTGCAAGTCGTACA | 50933 |
rs48207459 | snp | C/G | 0.32 | 0.24 | intron-variant | Uchl3 | Mm_Celera | 14:101659701 | GGGTTCTTGAATGTG[C/G]AGTCTCTTCTTGCTT | 50933 |
rs48257424 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Uchl3 | Mm_Celera | 14:101666341 | TGTCTTTCTCACACC[A/G]TTGCCGTCAGACAGT | 50933 |
rs48283719 | snp | C/T | 0.32 | 0.24 | intron-variant | Uchl3 | Mm_Celera | 14:101663859 | CTGAGCCATATGTGC[C/T]ATTTTGTGTAACTTT | 50933 |
rs48296317 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Uchl3 | Mm_Celera | 14:101669649 | GTTAAAACTAGTGAT[A/G]AGGACCAATAGAAGA | 50933 |
rs48346798 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Uchl3 | Mm_Celera | 14:101668972 | CTGTCTCTGCTCCTT[C/T]GGTTGCCTCTTTTGA | 50933 |
rs48405265 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Uchl3 | Mm_Celera | 14:101659026 | GAGCGTGGTTGTACT[C/T]CTCTATGGTATTTCC | 50933 |
rs48484621 | snp | A/C | 0.345679 | 0.230967 | intron-variant | Uchl3 | Mm_Celera | 14:101663249 | ATGTGTCTTTTTAAC[A/C]TTTTCGTGTTTGTTT | 50933 |
rs48532467 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Uchl3 | Mm_Celera | 14:101677244 | CTTAACATCATTCAT[C/T]GGACATTGTGGTCTA | 50933 |
rs48534318 | snp | C/T | 0.375 | 0.216506 | intron-variant | Uchl3 | Mm_Celera | 14:101667090 | GACGTCAGTACCTTC[C/T]TTCTATCCAACCTCA | 50933 |
rs48541869 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Uchl3 | Mm_Celera | 14:101677324 | GAAAAACTTACTTGG[A/G]ACTACTCTCAAATTA | 50933 |
rs48573942 | snp | A/T | 0.42 | 0.183303 | missense | Uchl3 | Mm_Celera | 14:101667061 | AAGAGAGAGCCAAAT[A/T]CCTGGAGAACTATGA | 50933 |
rs48641455 | snp | A/G/T | 0.231111 | 0.249285 | intron-variant | Uchl3 | GRCm38.p3 | 14:101674684 | GAATGCTGGCAGGTG[A/G/T]TTCAAAGATGATAGA | 50933 |
rs48657657 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Uchl3 | Mm_Celera | 14:101681816 | GCCAGAAGATCATGA[A/G]CCAGCTAGCCTGGTA | 50933 |
rs48748344 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Uchl3 | Mm_Celera | 14:101673428 | TCTTTGGGTAGGAGC[C/T]TGTAAACTCTCAGAA | 50933 |
rs48799135 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Uchl3 | Mm_Celera | 14:101686695 | TGGTGTGTGCCGTAC[A/G]TCCACAGAGACTTGT | 50933 |
rs48809360 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Uchl3 | Mm_Celera | 14:101668937 | TCTGGGCCACATGGT[C/G]TTCAGCAGCTCTGCC | 50933 |
rs48839010 | snp | C/G/T | 0.297521 | 0.245442 | intron-variant | Uchl3 | GRCm38.p3 | 14:101668024 | CTGACTGGAGCAGTT[C/G/T]GAAGTTTAGCTAGCT | 50933 |
rs48885254 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Uchl3 | Mm_Celera | 14:101673185 | TTGAGAAAGTTTAAC[C/G]TGAATGGCAATGGGA | 50933 |
rs48968651 | snp | C/T | 0.375 | 0.216506 | intron-variant | Uchl3 | Mm_Celera | 14:101667180 | TTTGGGGAAGCATCA[C/T]TGTCTTATCCGTAAG | 50933 |
rs49055682 | snp | A/C | | | intron-variant | Uchl3 | Mm_Celera | 14:101682658 | TAGGAATACACATAC[A/C]CACACACACACACTA | 50933 |
rs49121142 | snp | C/T | 0.32 | 0.24 | intron-variant | Uchl3 | Mm_Celera | 14:101661603 | CAGTGTGTGTGTCTC[C/T]TTCTGGTCATTTACA | 50933 |
rs49129259 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Uchl3 | Mm_Celera | 14:101684319 | AATGTGAGTGCTGAC[A/T]TGCTGAACTTTTCTT | 50933 |
rs49279565 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Uchl3 | Mm_Celera | 14:101681793 | GATGGGAGGCAGACA[C/T]CCGAGAAGCCAGAAG | 50933 |
rs49413381 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Uchl3 | Mm_Celera | 14:101672767 | GTATTACTGTCTATC[A/G]TCAAATGCCATTTCC | 50933 |
rs49543784 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Uchl3 | Mm_Celera | 14:101686101 | TCTTTATCCTTCAAC[A/G]CTCCGATTTCACTTA | 50933 |
rs49696399 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Uchl3 | Mm_Celera | 14:101675037 | TTACATATTTAATTT[C/G]AGTCTTTTAGAATAA | 50933 |
rs49806819 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Uchl3 | Mm_Celera | 14:101687872 | TTCCTGGGATGCTTG[C/T]GAGCGATTGAATGAT | 50933 |
rs49865968 | snp | G/T | 0.375 | 0.216506 | synonymous-codon | Uchl3 | Mm_Celera | 14:101666619 | CAATGCCTGTGGAAC[G/T]ATTGGACTAATCCAT | 50933 |
rs49903330 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Uchl3 | Mm_Celera | 14:101675112 | CACACTTCCAGGTGA[A/G]TGAATCACAATTTAC | 50933 |
rs49931286 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Uchl3 | Mm_Celera | 14:101677161 | AGATCTAACTAGATG[C/T]CGTTCTCCCATCTGA | 50933 |
rs49985439 | snp | A/G | 0.375 | 0.216506 | synonymous-codon | Uchl3 | Mm_Celera | 14:101665853 | GGTACCAAGACCAGT[A/G]TGCGCAGTGTTACTC | 50933 |
rs50532660 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Uchl3 | Mm_Celera | 14:101687137 | CTTACGCTGTGCTAT[A/G]TACTGTTTGGCCCAG | 50933 |
rs50533343 | snp | A/G/T | 0.124444 | 0.216185 | intron-variant | Uchl3 | Mm_Celera | 14:101692288 | TGCACCTAGGGCCTC[A/G/T]TATACTCTTGGCAAG | 50933 |
rs50588313 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Uchl3 | Mm_Celera | 14:101680064 | GCTGTTACATTATGG[A/G]GAACAAGACAGTATA | 50933 |
rs50624631 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Uchl3 | Mm_Celera | 14:101676095 | TATAATAGTATTTCA[A/G]TCTTTCATTGGTTAA | 50933 |
rs50635222 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Uchl3 | Mm_Celera | 14:101673274 | TCTAGTGTTTATCAA[A/G]TTGGGCTGATGAATT | 50933 |
rs50717794 | snp | C/T | 0.32 | 0.24 | intron-variant | Uchl3 | Mm_Celera | 14:101658962 | AACCTTAAGTTGCTT[C/T]GCCAGGGGTTTGATC | 50933 |
rs50757812 | snp | A/G | 0.5 | 0 | intron-variant | Uchl3 | Mm_Celera | 14:101659413 | TCTGTAATCCTTCTG[A/G]TTGTGTAGATTGTCT | 50933 |
rs50796892 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Uchl3 | Mm_Celera | 14:101681882 | CAAAAGAGGTGAAAC[A/G]TGGACCAAGGTGAAG | 50933 |
rs50892322 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Uchl3 | Mm_Celera | 14:101657607 | TAACTCTTAGTCTGA[A/G]CAAGGACTGTTTTAT | 50933 |
rs51106964 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Uchl3 | Mm_Celera | 14:101664389 | CAGTTCAGACTGGAT[C/T]GGCCTTCCCATTCTT | 50933 |
rs51139671 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Uchl3 | Mm_Celera | 14:101668186 | GTCTTCGGTCTCTGT[A/G]AGATGCTCACTTTAT | 50933 |
rs51163130 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Uchl3 | Mm_Celera | 14:101678158 | GACAAGTGTATATTT[C/T]ATTAAGGAGTCATAA | 50933 |
rs51240567 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Uchl3 | Mm_Celera | 14:101672713 | CTCTGATCTCGCCTT[C/T]AGTCCTTTTCCAGGG | 50933 |
rs51294909 | snp | A/G | 0.32 | 0.24 | intron-variant | Uchl3 | Mm_Celera | 14:101667534 | GCTAGTAATTCCACC[A/G]GTGAAAGGGACTGTC | 50933 |
rs51315461 | snp | C/T | | | intron-variant | Uchl3 | Mm_Celera | 14:101673698 | TTTTGGGTTTTTTTG[C/T]TTGCTTTGTTTTGTT | 50933 |
rs51439702 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Uchl3 | Mm_Celera | 14:101670143 | GCCACTGTTAGAGCC[A/G]CATTGTTTCTATGCA | 50933 |
rs51495806 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Uchl3 | Mm_Celera | 14:101666364 | CAGACAGTTACTGCT[C/T]TTTCTCAGGCTTTTG | 50933 |
rs51509103 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Uchl3 | Mm_Celera | 14:101672170 | ACTAGAGCTTTTTTA[C/T]GTGAGGTCCCTTGTT | 50933 |