SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6183903 | snp | A/G | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | Ube2n | Mm_Celera | 10:95545270 | GTGTTCTGTAAGAGT[A/G]CTCCCAGTCAGCCAA | 93765 |
rs6196828 | snp | A/G | 0.484429 | 0.0868505 | utr-variant-3-prime, nc-transcript-variant | Ube2n | Mm_Celera | 10:95545406 | GAATCGGAAGTTTTA[A/G]GACTACATAGGAGAG | 93765 |
rs6238179 | snp | G/T | 0.5 | 0 | upstream-variant-2KB, nc-transcript-variant | Ube2n | Mm_Celera | 10:95514706 | GCGACCCGCCTGCCC[G/T]GTCCGCAGGGAACCG | 93765 |
rs6252501 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, nc-transcript-variant | Ube2n | Mm_Celera | 10:95515030 | GCCACCAGGTCGGAG[A/G]GAAGGCTGTCGGAAG | 93765 |
rs6333426 | snp | A/G | 0.5 | 0 | intron-variant | Ube2n | Mm_Celera | 10:95538519 | aggccagcctgatct[A/G]cagagtgagttccag | 93765 |
rs6333554 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Ube2n | Mm_Celera | 10:95538591 | aaaaaCTTAAACCAG[A/G]AGTGGTGGTGCCTGC | 93765 |
rs6334571 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Ube2n | Mm_Celera | 10:95538764 | GTGTGCCAAGTTGTA[A/C]CNGCCATATTGTCTN | 93765 |
rs6334581 | snp | C/T | 0.5 | 0 | intron-variant | Ube2n | Mm_Celera | 10:95538766 | GTGCCAAGTTGTANC[C/T]GCCATATTGTCTNGC | 93765 |
rs6334594 | snp | C/T | 0.304688 | 0.243945 | intron-variant | Ube2n | Mm_Celera | 10:95538779 | NCNGCCATATTGTCT[C/T]GCTGGCCCATCAACT | 93765 |
rs29323075 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2n | Mm_Celera | 10:95524010 | GAAATCCGCCTGCCT[C/T]TGCCTCCCAAGTACT | 93765 |
rs29373060 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ube2n | Mm_Celera | 10:95523258 | CTGGCCTCTAACTCA[A/G]AAATCCGCCTGCCTC | 93765 |
rs29376264 | snp | C/T | 0.32 | 0.24 | intron-variant | Ube2n | Mm_Celera | 10:95523160 | TAAAACTTAACTTCC[C/T]TTTTTTTTTTTTTTT | 93765 |
rs45785692 | snp | C/T | 0.32 | 0.24 | intron-variant | Ube2n | Mm_Celera | 10:95520370 | AGTGTGGTGGGATCA[C/T]AGGCATACCAACAAA | 93765 |
rs45878586 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2n | Mm_Celera | 10:95524658 | TCTTTTACATTTCAT[C/T]CAACTTAGTTTATAA | 93765 |
rs45926513 | snp | C/T | | | intron-variant | Ube2n | Mm_Celera | 10:95520131 | AGATAGACACACCCT[C/T]CCCCATTTTTTTAAG | 93765 |
rs46107210 | snp | A/G | 0.32 | 0.24 | intron-variant | Ube2n | Mm_Celera | 10:95519284 | GTCTCCAGCTGTGAA[A/G]CATCCTTCTTGTTTT | 93765 |
rs46125424 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ube2n | Mm_Celera | 10:95517116 | AAAACAAGATAGTGG[C/T]AAACCCATGCTGTAA | 93765 |
rs46126557 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Ube2n | Mm_Celera | 10:95516948 | CAGTTGATATTGATA[C/T]TCTGCAGTAATATGA | 93765 |
rs46139230 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Ube2n | Mm_Celera | 10:95524569 | GAAGAAATTCCAGGC[G/T]TGTGACTGCCTGAAC | 93765 |
rs46167720 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Ube2n | Mm_Celera | 10:95518680 | CCCCATAATCCCCTC[C/T]TTTTCATTGTATAGC | 93765 |
rs46217267 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ube2n | Mm_Celera | 10:95516222 | AATCTTGCACTGCCC[A/G]GTTTGCCAGCTAAGT | 93765 |
rs46226080 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ube2n | Mm_Celera | 10:95539252 | AGTGTAGATTCCAGT[A/G]AAATCTTAGATCAGT | 93765 |
rs46276408 | snp | A/G | 0.48 | 0.0979796 | utr-variant-3-prime, nc-transcript-variant | Ube2n | Mm_Celera | 10:95544239 | TTACACATTACCCAC[A/G]GTGGCCTGGTGGGCA | 93765 |
rs46385066 | snp | C/T | 0.32 | 0.24 | utr-variant-3-prime, nc-transcript-variant | Ube2n | Mm_Celera | 10:95544674 | CCAGCCTACCTGTTT[C/T]TGTATGTGTGGTTCT | 93765 |
rs46395657 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ube2n | Mm_Celera | 10:95525185 | CTATGCAGTTTCTAT[A/G]TTATTGATCACTGGT | 93765 |
rs46430617 | snp | G/T | 0.32 | 0.24 | intron-variant | Ube2n | Mm_Celera | 10:95516118 | ACATAACACCATTAA[G/T]TCTTCATAGTGTTAT | 93765 |
rs46517631 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ube2n | Mm_Celera | 10:95516097 | TCTTGATTTCCTAAA[A/G]TCTTTACATAACACC | 93765 |
rs46519773 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime, nc-transcript-variant | Ube2n | Mm_Celera | 10:95544749 | ACATTCACTTAACAA[A/G]AGCATATTAACATTT | 93765 |
rs46540926 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2n | Mm_Celera | 10:95541081 | AGTTTCACGTTTTAT[A/G]TGAAAATTATGCCAT | 93765 |
rs46563955 | snp | A/G | 0.32 | 0.24 | intron-variant | Ube2n | Mm_Celera | 10:95520487 | ATAGTTGACTTACTT[A/G]ATTAAAATCTAGCAA | 93765 |
rs46588797 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2n | Mm_Celera | 10:95525503 | AAGATAGGAGTAAGA[C/T]GTTCTTGTGAGGTTT | 93765 |
rs46689046 | snp | A/C | 0.32 | 0.24 | intron-variant | Ube2n | Mm_Celera | 10:95516715 | TATGAATCTTAGAAC[A/C]TTTCCAAGTAGGTTT | 93765 |
rs46805758 | snp | A/G | 0.48 | 0.0979796 | downstream-variant-500B | Ube2n | Mm_Celera | 10:95546117 | AAGCTTGATTTTGGA[A/G]GATCTTTGTTTCTGT | 93765 |
rs46916653 | snp | A/G | 0.32 | 0.24 | intron-variant | Ube2n | Mm_Celera | 10:95540456 | CCCTTGACTACAAAG[A/G]ATGACCAAATTTTAG | 93765 |
rs47033932 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Ube2n | Mm_Celera | 10:95531188 | CCCTTGGTGCTAACT[A/C]CTGACATTCTTTCTA | 93765 |
rs47157657 | snp | C/T | 0.32 | 0.24 | intron-variant | Ube2n | Mm_Celera | 10:95537807 | CCCTGTCAGTGCTTT[C/T]TCTCCCTCTCTACAT | 93765 |
rs47220918 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2n | Mm_Celera | 10:95524689 | CACAGAAAGATTTAC[A/G]TTTTCTGGCCTGCTC | 93765 |
rs47274247 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Ube2n | Mm_Celera | 10:95531146 | TGCTCGTGTCCAGTA[C/G]AAGCTGCTGCTATTC | 93765 |
rs47325190 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Ube2n | Mm_Celera | 10:95522868 | TGCCTGCATTTTTAT[G/T]TCTTGTGGACCAGTG | 93765 |
rs47355014 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ube2n | Mm_Celera | 10:95516340 | ATTTGTACAAAGTAA[A/G]TGGAGGGCCTCTTTG | 93765 |
rs47405602 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2n | Mm_Celera | 10:95527962 | TCAGTCACCCGAAAA[C/T]CTTGTAGAATGCTTG | 93765 |
rs47414120 | snp | C/T | 0.231111 | 0.249285 | utr-variant-3-prime, nc-transcript-variant | Ube2n | Mm_Celera | 10:95544603 | GAGCTGAGTAGCAGT[C/T]ACCACTGGATGACAT | 93765 |
rs47453870 | snp | C/T | 0.32 | 0.24 | intron-variant | Ube2n | Mm_Celera | 10:95539950 | GCAGAGCACAGGAGT[C/T]CCTTGCCAGGCTTTG | 93765 |
rs47580125 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Ube2n | Mm_Celera | 10:95531040 | TCTTCAGGAGAGCCA[A/C]AGAGGTAGCTAGTAA | 93765 |
rs47601180 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Ube2n | Mm_Celera | 10:95517033 | AAATGCTTTACAGCA[A/G]AAAATTCAAGTGCTC | 93765 |
rs47634498 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Ube2n | Mm_Celera | 10:95541967 | TACTAGAAAACTTGG[A/C]AACTGTTCTTTTTTT | 93765 |
rs47637532 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2n | Mm_Celera | 10:95527190 | TTTGTTTGTTTAAAC[C/T]AGGGTAGCCCAGATT | 93765 |
rs47753514 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Ube2n | Mm_Celera | 10:95517016 | TTGTTATAAGCTTAC[A/G]GAAATGCTTTACAGC | 93765 |
rs47808844 | snp | C/T | 0.124444 | 0.216185 | downstream-variant-500B | Ube2n | Mm_Celera | 10:95545941 | AGGCTAAGTAATCAG[C/T]TCAAGGCCAGCACAG | 93765 |
rs47994467 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ube2n | Mm_Celera | 10:95536400 | GTTATTCCATATCTT[C/T]CTATATTACTTAGAG | 93765 |
rs48022222 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Ube2n | Mm_Celera | 10:95528464 | TTCTTCGTCTGAGTT[G/T]TAGGGATCCAGCAGT | 93765 |
rs48129662 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2n | Mm_Celera | 10:95516053 | ATTTTGATAAATACA[C/T]AAGGAACCACGGGGG | 93765 |
rs48259696 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime, nc-transcript-variant | Ube2n | Mm_Celera | 10:95543783 | GTCGTATACATGTAA[A/G]TGCTAACCTTATGGT | 93765 |
rs48278857 | snp | C/T | 0.32 | 0.24 | intron-variant | Ube2n | Mm_Celera | 10:95516749 | GGCATTGGAAGATCC[C/T]GAATATAGTTTAGTT | 93765 |
rs48297842 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2n | Mm_Celera | 10:95531133 | TGTGTAGTCTTGATG[C/T]TCGTGTCCAGTAGAA | 93765 |
rs48315432 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Ube2n | Mm_Celera | 10:95520931 | TTCTGCTCTGCAACT[G/T]TGTAAAGCTTGAGCT | 93765 |
rs48355931 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Ube2n | Mm_Celera | 10:95516302 | TTATAGCATTGTTCC[A/G]CTCTTCCAAAGTTTT | 93765 |
rs48360297 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2n | Mm_Celera | 10:95532895 | CTAAGCTAGGACTTT[C/T]CCACTAAGGCCAAAA | 93765 |
rs48389186 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2n | Mm_Celera | 10:95529616 | ACTAGCTTCTAGGGT[A/G]CGATTATTTGCAGTG | 93765 |
rs48580489 | snp | A/C | 0.32 | 0.24 | intron-variant | Ube2n | Mm_Celera | 10:95531433 | TGAGGTGGCAAGGAG[A/C]GATCCATAAAAGTTT | 93765 |
rs48735146 | snp | A/G | | | intron-variant | Ube2n | Mm_Celera | 10:95528303 | GTTCAGGAGATTGAA[A/G]ATAGGTCCTCAAGTT | 93765 |
rs48763802 | snp | C/T | 0.32 | 0.24 | intron-variant | Ube2n | Mm_Celera | 10:95539125 | TCAGGTTTTTCTATT[C/T]TCACAACCTATGCTA | 93765 |
rs48795608 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2n | Mm_Celera | 10:95531583 | TTGCTATTACTTTAC[C/T]GTGCAGTCTTACACT | 93765 |
rs48849255 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2n | Mm_Celera | 10:95519393 | GGTCACGCATGTGCC[A/G]TCAGCATACCACTTC | 93765 |
rs48905479 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ube2n | Mm_Celera | 10:95515974 | GGATGATCTGTGAAA[C/T]AGTTTGCCTCTCAGC | 93765 |
rs48996449 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Ube2n | Mm_Celera | 10:95520751 | TTCCTTTCCTATATG[A/G]TGAGGGTTTCTGCTT | 93765 |
rs49004977 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2n | Mm_Celera | 10:95521159 | GATTTAGGAAGTATA[A/G]CTATTGTAGCTAAGA | 93765 |
rs49017429 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Ube2n | Mm_Celera | 10:95516399 | GCAGTCACAAATGTC[G/T]GTGAGGCTGGGGTGT | 93765 |
rs49132751 | snp | A/G | 0.32 | 0.24 | intron-variant | Ube2n | Mm_Celera | 10:95528416 | AGGCATGTGTGTGCA[A/G]TGGCATGCATGTGGA | 93765 |
rs49263848 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime, nc-transcript-variant | Ube2n | Mm_Celera | 10:95543353 | GTCACAGTGAAGAGG[A/G]CAGTTGCATGTCACA | 93765 |
rs49310490 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Ube2n | Mm_Celera | 10:95528593 | TTGATACTTAATTAT[G/T]TGTGTGTGGTGTACC | 93765 |
rs49395258 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ube2n | Mm_Celera | 10:95531811 | ACATCTAACAAGCAG[C/T]TCCCCTGGTTGTCAT | 93765 |
rs49406769 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ube2n | Mm_Celera | 10:95519930 | GAGAGATTTCTTTTA[C/T]CCATTTTTATCATAA | 93765 |
rs49439662 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2n | Mm_Celera | 10:95516160 | ACTAAATTTTTAACA[C/T]TTTTTGGCATCTGTT | 93765 |
rs49536148 | snp | A/T | 0.32 | 0.24 | utr-variant-3-prime, nc-transcript-variant | Ube2n | Mm_Celera | 10:95544497 | TGGTTGGTTCAGAGC[A/T]GTTAAATGATAGTAT | 93765 |
rs49548104 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2n | Mm_Celera | 10:95528753 | CTGGCTGGCTTCCTT[C/T]ACACCCTCCTCCTGT | 93765 |
rs49608676 | snp | A/G | 0.48 | 0.0979796 | utr-variant-3-prime, nc-transcript-variant | Ube2n | Mm_Celera | 10:95543375 | CATGTCACATATGGC[A/G]TTTGAGCTTCAGGTG | 93765 |
rs49654836 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Ube2n | Mm_Celera | 10:95524931 | TGGGTAGACTTGGGT[A/T]CCAACTCCATCTGCT | 93765 |
rs49660827 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Ube2n | Mm_Celera | 10:95516920 | AGTTCTGTAAAATGC[C/T]CAGTAAACTGAACAG | 93765 |
rs49722737 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Ube2n | Mm_Celera | 10:95516446 | CTTGAATTAGAAAAA[C/G]AAGCCCTTTCATAGG | 93765 |
rs49857855 | snp | A/T | 0.426035 | 0.177515 | intron-variant | Ube2n | Mm_Celera | 10:95535894 | AAAAAGACTTCACCT[A/T]TTGGAGTGAACTAAT | 93765 |
rs49886591 | snp | A/T | 0.426035 | 0.177515 | intron-variant | Ube2n | Mm_Celera | 10:95516225 | CTTGCACTGCCCAGT[A/T]TGCCAGCTAAGTGCT | 93765 |
rs49927166 | snp | A/G | 0.32 | 0.24 | intron-variant | Ube2n | Mm_Celera | 10:95535829 | TTTAAGGACATTTAC[A/G]TTAATGCCAACCTTA | 93765 |
rs49962629 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2n | Mm_Celera | 10:95520161 | GCATACACTTGCTTG[A/G]TCACTTGTGCACATA | 93765 |
rs50044957 | snp | A/G | 0.32 | 0.24 | intron-variant | Ube2n | Mm_Celera | 10:95518558 | CAGTCATGGGGCTTC[A/G]CTGGTATTTTGTTGT | 93765 |
rs50129934 | snp | A/G | 0.444444 | 0.157135 | downstream-variant-500B | Ube2n | Mm_Celera | 10:95546078 | ATGTATGGGTGTTAG[A/G]AAACGGCAATTCACC | 93765 |
rs50260080 | snp | C/T | 0.32 | 0.24 | intron-variant | Ube2n | Mm_Celera | 10:95541096 | GTGAAAATTATGCCA[C/T]TGGGAGATTGTGTTA | 93765 |
rs50407162 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2n | Mm_Celera | 10:95515924 | GGAGACTGTTCTCTT[C/T]TCCGAGGCAAGGGCC | 93765 |
rs50521812 | snp | A/G/T | 0.375 | 0.216506 | intron-variant | Ube2n | GRCm38.p3 | 10:95526669 | AGTGCACCCGAATGC[A/G/T]GCTGCTTGTGGAGCC | 93765 |
rs50578713 | snp | C/T | 0.32 | 0.24 | intron-variant | Ube2n | Mm_Celera | 10:95518508 | ACAGTGTTGGCTTTG[C/T]TGTCCCTTGGACAAT | 93765 |
rs50604930 | snp | A/G | 0.32 | 0.24 | intron-variant | Ube2n | Mm_Celera | 10:95540423 | CCAGAGATTTTTGAG[A/G]ATTCTAGACCTCGTC | 93765 |
rs50665538 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ube2n | Mm_Celera | 10:95531065 | TAGTAAGAGGTTTAG[A/G]ATTGGACAGCAGTGA | 93765 |
rs50752300 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ube2n | Mm_Celera | 10:95521272 | CTACTCAAAAGCTGC[A/G]CTATGCAGAGGGAAT | 93765 |
rs50812200 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime, nc-transcript-variant | Ube2n | Mm_Celera | 10:95545105 | AGTTAGCCTTGGTTC[A/G]CTCAGATCATAGGCA | 93765 |
rs50883070 | snp | A/G | 0.32 | 0.24 | intron-variant | Ube2n | Mm_Celera | 10:95532907 | TTTTCCACTAAGGCC[A/G]AAACTTTGTAAGCAA | 93765 |
rs51062244 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Ube2n | Mm_Celera | 10:95532295 | TCCAGTGGAGTGTTA[A/C]TAATACTAAGTTAGA | 93765 |
rs51086170 | snp | C/T | 0.32 | 0.24 | intron-variant | Ube2n | Mm_Celera | 10:95519907 | CTACGAAAAAGTAGC[C/T]CCAAAGTGAGAGATT | 93765 |
rs51098461 | snp | A/G | 0.32 | 0.24 | intron-variant | Ube2n | Mm_Celera | 10:95520549 | TAATGTTTGTCTAGA[A/G]TTTTTAAAAGCCCTG | 93765 |
rs51161449 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2n | Mm_Celera | 10:95524642 | TGTCTCCACTTACAA[A/G]TCTTTTACATTTCAT | 93765 |
rs51173604 | snp | A/G | 0.32 | 0.24 | intron-variant | Ube2n | Mm_Celera | 10:95531528 | TGTGAAGCAGCCAAA[A/G]GAATAATGGATGGAA | 93765 |