SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3665532 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Ubr2 | Mm_Celera | 17:46975359 | CCACATTCACGCAGT[A/G]CCCAAAGTGACCAGA | 224826 |
rs4136738 | snp | A/T | 0.5 | 0 | intron-variant | Ubr2 | Mm_Celera | 17:46959863 | CTCTCTCTCTCTCTC[A/T]CACACACACACACAC | 224826 |
rs6171964 | snp | A/G | 0.5 | 0 | intron-variant | Ubr2 | Mm_Celera | 17:46971863 | ATGGGCCAATTCCTT[A/G]GAAGACATGAACTGT | 224826 |
rs6215528 | snp | C/T | 0.5 | 0 | intron-variant | Ubr2 | Mm_Celera | 17:46935185 | taagagcactggctg[C/T]tcttccagaggtcct | 224826 |
rs6215986 | snp | C/T | 0.5 | 0 | intron-variant | Ubr2 | Mm_Celera | 17:46935212 | tcctgagttcaattc[C/T]cagcaagnacatngt | 224826 |
rs6216004 | snp | C/T | 0.5 | 0 | intron-variant | Ubr2 | Mm_Celera | 17:46935220 | tcaattcncagcaag[C/T]acatngtggctcaca | 224826 |
rs6216007 | snp | A/G | 0.5 | 0 | intron-variant | Ubr2 | Mm_Celera | 17:46935225 | tcncagcaagnacat[A/G]gtggctcacaaccat | 224826 |
rs6216083 | snp | C/T | 0.5 | 0 | intron-variant | Ubr2 | Mm_Celera | 17:46935261 | agaggatatgtttaa[C/T]gctctcttctggcac | 224826 |
rs6230459 | snp | C/T | 0.304688 | 0.243945 | intron-variant | Ubr2 | Mm_Celera | 17:46935536 | GAGAAAGGAGAAGAA[C/T]TTGGTAAATATGTGG | 224826 |
rs6230505 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Ubr2 | Mm_Celera | 17:46935555 | GTAAATATGTGGTCA[C/T]NTTATAAGCACACAA | 224826 |
rs6230506 | snp | A/G | 0.5 | 0 | intron-variant | Ubr2 | Mm_Celera | 17:46935556 | TAAATATGTGGTCAN[A/G]TTATAAGCACACAAG | 224826 |
rs6231580 | snp | A/G | 0.5 | 0 | intron-variant | Ubr2 | Mm_Celera | 17:46935700 | CTGAGGGTCAGGGGG[A/G]TGAATCCCCCGCTTG | 224826 |
rs6333004 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Ubr2 | Mm_Celera | 17:46954092 | AGGAGCGTCAGAATC[C/T]GGGGCGGTCATGTCA | 224826 |
rs6333039 | snp | A/C | 0.5 | 0 | intron-variant | Ubr2 | Mm_Celera | 17:46954109 | GGGCGGTCATGTCAG[A/C]AGGAGGTCAAGCATC | 224826 |
rs6333505 | snp | C/T | 0.5 | 0 | intron-variant | Ubr2 | Mm_Celera | 17:46954191 | GAACTGGCTTAAACA[C/T]AGGCAGCATAACTAA | 224826 |
rs6333946 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Ubr2 | Mm_Celera | 17:46954216 | AACTAATCCTCACAG[C/T]GGATTTGGAGTCCTA | 224826 |
rs13469533 | snp | A/G | | | synonymous-codon | Ubr2 | GRCm38.p3 | 17:46932473 | CCTTGACGACTATGG[A/G]GAGACCGACCAGGGA | 224826 |
rs13469535 | snp | C/T | | | synonymous-codon | Ubr2 | GRCm38.p3 | 17:46934101 | ACACACCTACTCCTG[C/T]GGCTCCGGGGCCGGC | 224826 |
rs29499096 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ubr2 | Mm_Celera | 17:46937305 | CCAGTCAGACCCAGT[A/G]GCTCACTCTCTCTTC | 224826 |
rs33192590 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Ubr2 | Mm_Celera | 17:46987096 | GCCTTTAATCCCAGC[A/C]CTTAGGAAGCAGAGA | 224826 |
rs33242763 | snp | A/C/T | 0.188366 | 0.242283 | synonymous-codon | Ubr2 | GRCm38.p3 | 17:46976088 | TGTGAGGAGCATTCG[A/C/T]GCCTACAACAGGGTT | 224826 |
rs33251727 | snp | A/G | 0.5 | 0 | intron-variant | Ubr2 | Mm_Celera | 17:46938053 | TCCTCCAGGAAAGAG[A/G]CGGGGTAACCAGAGG | 224826 |
rs33321092 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ubr2 | Mm_Celera | 17:46937462 | GTTTTCCTTTATAAG[A/G]TCATGGCATCTCTTC | 224826 |
rs33391907 | snp | C/T | 0.5 | 0 | intron-variant | Ubr2 | Mm_Celera | 17:46938083 | GCCGCACCTGAGATC[C/T]AGCCACTGCTTCTCC | 224826 |
rs33417652 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ubr2 | Mm_Celera | 17:46947258 | AGAACCACTGCACAG[C/T]CAGGAACAAACACAC | 224826 |
rs33473740 | snp | C/T | 0.495 | 0.0497494 | intron-variant | Ubr2 | Mm_Celera | 17:46970884 | GCTGTTATGTCACTG[C/T]TCTCAGGACCTATCA | 224826 |
rs33491773 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ubr2 | Mm_Celera | 17:46937920 | AAGGCTCACAACCAT[C/T]TGTATCTGTATGGCT | 224826 |
rs33534171 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Ubr2 | Mm_Celera | 17:46956908 | TTGTTCATATTAACC[C/T]GTTAAAGTTTTGTTT | 224826 |
rs33628992 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ubr2 | Mm_Celera | 17:46953265 | CCTATGGAGTCCAGG[A/G]GAGGCATCAGATCCC | 224826 |
rs33648033 | snp | C/T | 0.207612 | 0.24638 | intron-variant | Ubr2 | Mm_Celera | 17:46943546 | ACTCCTGCGCGCTCC[C/T]GGGATCTCTTCCCAG | 224826 |
rs33704785 | snp | A/C/T | 0.375 | 0.216506 | intron-variant | Ubr2 | Mm_Celera | 17:46939122 | CAGATTCCTGCCTCC[A/C/T]GGAGTGCTGGGGTTA | 224826 |
rs45646549 | snp | C/T | 0.124444 | 0.216185 | intron-variant, downstream-variant-500B | Ubr2 | Mm_Celera | 17:46967177 | ACGTGGGCGTTGTGA[C/T]ACAGGCTCTTACCTT | 224826 |
rs45653335 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Ubr2 | Mm_Celera | 17:46937040 | ACCCCTCACAGCAGG[A/C]GCTCTGGGTTCTGGA | 224826 |
rs45659814 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ubr2 | Mm_Celera | 17:46968676 | CCAGCCAGTGTTTTG[A/G]GTCTCCCAAAATTGT | 224826 |
rs45665385 | snp | G/T | 0.165289 | 0.235211 | intron-variant | Ubr2 | Mm_Celera | 17:46986201 | AGAAACTAAAATTGC[G/T]CTTTAATGCTCTCTT | 224826 |
rs45687764 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Ubr2 | Mm_Celera | 17:46963662 | AACACACTTAGCACC[G/T]CCCACTGCTCTGAGC | 224826 |
rs45696894 | snp | A/G | | | intron-variant | Ubr2 | Mm_Celera | 17:46999031 | GGGACCACAGGTCAC[A/G]GCAGGTCAGATTCCG | 224826 |
rs45697666 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ubr2 | Mm_Celera | 17:46984511 | TGCACACATCACATA[C/T]ATCTGTGTTAGAAAT | 224826 |
rs45719369 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Ubr2 | Mm_Celera | 17:46940683 | CACGCCCTAAGCTCT[A/C]AGCAGCTCATCAGCG | 224826 |
rs45721829 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Ubr2 | Mm_Celera | 17:46981022 | AGTCCAAGCTGTCAA[A/C]CGTCAGGTGCACCAT | 224826 |
rs45732287 | snp | A/G | 0.444444 | 0.157135 | synonymous-codon | Ubr2 | GRCm38.p3 | 17:46976064 | GATAACGGTCATCAG[A/G]TTCTCTTCTGTGAGG | 224826 |
rs45732792 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ubr2 | Mm_Celera | 17:46959372 | CCCCTGGCACTTGCA[C/T]GCAGCACCAGCACTC | 224826 |
rs45734751 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ubr2 | Mm_Celera | 17:46993819 | GCGTGCGAGGAGCCC[A/G]TGAGCACACATGCGA | 224826 |
rs45742808 | snp | A/G | 0.132653 | 0.220748 | intron-variant, downstream-variant-500B | Ubr2 | Mm_Celera | 17:46967180 | TGGGCGTTGTGACAC[A/G]GGCTCTTACCTTATG | 224826 |
rs45764767 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Ubr2 | Mm_Celera | 17:46936301 | GCTCAGAATGAGTGA[C/G]GAGGTAGACAGAGAT | 224826 |
rs45765434 | snp | C/T | 0.32 | 0.24 | intron-variant | Ubr2 | Mm_Celera | 17:46936260 | ATGATGGTAGTGTCT[C/T]GGAGTTCCCATTCCT | 224826 |
rs45778602 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ubr2 | Mm_Celera | 17:46981228 | CTGTGAAGTTTCTTA[A/G]AATTCCAGCTGGATA | 224826 |
rs45781772 | snp | G/T | 0.35503 | 0.226867 | intron-variant | Ubr2 | Mm_Celera | 17:46999237 | GGTGTGACTGGCCTT[G/T]TATCTTTTGGGCATA | 224826 |
rs45781907 | snp | C/G | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Ubr2 | Mm_Celera | 17:46973626 | TAGGAGGTTTTCATA[C/G]ATTGTTCAAGTCTCA | 224826 |
rs45786590 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Ubr2 | Mm_Celera | 17:46966003 | TCTCTAGCTCAGCTC[C/T]GCTCCCTAGTCACTG | 224826 |
rs45792955 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ubr2 | Mm_Celera | 17:46975566 | TTGTGCAAGGACAAC[C/T]GAGGTCAGAACTTAG | 224826 |
rs45798622 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ubr2 | Mm_Celera | 17:46942121 | CCTAGCTCCTTGCTA[C/T]ACATTTTCCAGATCT | 224826 |
rs45848780 | snp | A/T | 0.408163 | 0.193609 | intron-variant | Ubr2 | Mm_Celera | 17:46935831 | TCTAAACTGCCTAAG[A/T]TTATGTTCTCGCTGG | 224826 |
rs45878074 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ubr2 | Mm_Celera | 17:46995033 | CAAAGTACCTTTGCG[C/T]GTACTTTGTGGTAAA | 224826 |
rs45892096 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Ubr2 | Mm_Celera | 17:46989078 | ACCTTTCGAGCTTGG[C/T]GTGGGAAGCTCAGAG | 224826 |
rs45909590 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Ubr2 | Mm_Celera | 17:46999098 | ATGTACTAGATGAAC[C/T]CAACTGGAAGGACAT | 224826 |
rs45932239 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ubr2 | Mm_Celera | 17:47001132 | TCAGCCTTAACATAT[A/G]TGCTCCCTACATCAC | 224826 |
rs45946894 | snp | A/C/G | 0.297521 | 0.245442 | intron-variant | Ubr2 | GRCm38.p3 | 17:46992348 | CTTTCTTAACTCTTC[A/C/G]AGTTCCAAGCAGCAT | 224826 |
rs45949739 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Ubr2 | Mm_Celera | 17:46999913 | GTCCTGAGGCTTTAC[A/C]CACTAAGCTACCTCA | 224826 |
rs45959167 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Ubr2 | Mm_Celera | 17:46985902 | ACGTGATACTGGACG[C/T]ATGAAGGCAAATGTC | 224826 |
rs45987320 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Ubr2 | Mm_Celera | 17:46968539 | GAAAAAAGCATGGGT[G/T]TGTGTAAGCACAAGT | 224826 |
rs45989289 | snp | A/T | 0.444444 | 0.157135 | synonymous-codon | Ubr2 | Mm_Celera | 17:46964768 | TCACTTGAAATGTGC[A/T]ACGGACTCGATGACG | 224826 |
rs45997469 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ubr2 | Mm_Celera | 17:46963270 | TTTACACCACTCATC[A/G]AAAACATATGTTAAA | 224826 |
rs46003270 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Ubr2 | Mm_Celera | 17:46935725 | CGCTTGTAACCCGTG[A/C]CAGCTTGGAGAACTA | 224826 |
rs46010338 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Ubr2 | Mm_Celera | 17:46959033 | ATGGTGGGATGCTGA[A/C]AACACAGCTGTTTTT | 224826 |
rs46021061 | snp | C/T | | | intron-variant | Ubr2 | Mm_Celera | 17:46984162 | TAATTCTATTTTTAA[C/T]TTCTAGAGAAATTGT | 224826 |
rs46042875 | snp | C/T | 0.391111 | 0.206368 | intron-variant, upstream-variant-2KB | Ubr2 | Mm_Celera | 17:46973460 | CCACCTGAACTAGAC[C/T]GTGACTCAGATGACC | 224826 |
rs46047339 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Ubr2 | Mm_Celera | 17:46942346 | TGAACAGATGAAGGC[A/C]TCATGGCCAGGCAAG | 224826 |
rs46061598 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ubr2 | Mm_Celera | 17:46938812 | TTGCCATTCTCCCTC[A/G]ATTTTCTGACATGCG | 224826 |
rs46064550 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Ubr2 | Mm_Celera | 17:47000412 | GAACTGCAGCTAGCA[C/T]AGAGACGGTTGGGTT | 224826 |
rs46068542 | snp | A/G | | | intron-variant | Ubr2 | Mm_Celera | 17:46944959 | TATACCTCGGAACAA[A/G]CAGACACCAGGCAAC | 224826 |
rs46073637 | snp | A/G | | | intron-variant | Ubr2 | Mm_Celera | 17:47008312 | GTTTAATCCTATATA[A/G]ATCTATATAGGAACG | 224826 |
rs46094289 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ubr2 | Mm_Celera | 17:46998488 | AGGAAATCACTGGAG[C/T]CTGATCCCAGATATC | 224826 |
rs46096283 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Ubr2 | Mm_Celera | 17:46960814 | TAAGCCTGCTGAGAC[A/C]GTCCAAGCATGGCAG | 224826 |
rs46106057 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Ubr2 | Mm_Celera | 17:46994430 | TTGACAAGTAAATGC[G/T]ACTGAACGAGAATTG | 224826 |
rs46109762 | snp | A/C/G | 0.165289 | 0.235211 | intron-variant | Ubr2 | Mm_Celera | 17:46993706 | TAACAACAACAACAA[A/C/G]GATTCTACCAGTGAC | 224826 |
rs46121163 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ubr2 | Mm_Celera | 17:47004923 | TATGTTGTATTACTA[A/G]TTGTGGCTTCCACAG | 224826 |
rs46131777 | snp | A/G | | | intron-variant | Ubr2 | Mm_Celera | 17:46998801 | GGAGGCGAGAACAAG[A/G]GCGCAAATAAAAACA | 224826 |
rs46140093 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ubr2 | Mm_Celera | 17:46958219 | GTATGAGCACTGCAC[A/G]ACAGTCACAGCAGGA | 224826 |
rs46151711 | snp | C/T | | | intron-variant | Ubr2 | Mm_Celera | 17:46945487 | AAGGAGCACCCGCTG[C/T]TCTTGCAGAGGACCT | 224826 |
rs46152993 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ubr2 | Mm_Celera | 17:46982032 | TCGTACATCTCTAGG[C/T]TGTATGTAAAGGTTG | 224826 |
rs46155298 | snp | C/T | | | intron-variant | Ubr2 | Mm_Celera | 17:46984322 | GATTTCCTCAGTTAG[C/T]ATGTGTTCCATGGCT | 224826 |
rs46157406 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Ubr2 | Mm_Celera | 17:46933579 | GTTTAAAAAATGACA[C/T]ACAACAGTTACTAAG | 224826 |
rs46160703 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Ubr2 | Mm_Celera | 17:46991687 | AAAGCGTTAGGGATG[A/G]GTAAAATCAAGTGTA | 224826 |
rs46161447 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Ubr2 | Mm_Celera | 17:47005507 | CTTAGCATCACTATA[A/T]AAAGCAAGAAAATTT | 224826 |
rs46177883 | snp | A/G | 0.32 | 0.24 | synonymous-codon | Ubr2 | Mm_Celera | 17:46959498 | GGTGAAGGTCTGCAC[A/G]TGCCCTTCCACGGCG | 224826 |
rs46178666 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Ubr2 | Mm_Celera | 17:46975263 | CACACAAAGGACCTG[C/T]AACCTCTCAGCAGCA | 224826 |
rs46188038 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ubr2 | Mm_Celera | 17:46977339 | TCAGTCATGTCTGAA[A/G]TCACTTGTGGGCTGC | 224826 |
rs46202860 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Ubr2 | Mm_Celera | 17:46940655 | GCGCGTTCTAAGGCT[A/G]TGCTGCCACAGCCAC | 224826 |
rs46209951 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Ubr2 | Mm_Celera | 17:46986322 | ATAGCCCAGCATTTT[A/T]AATCACTGAACAGAA | 224826 |
rs46213538 | snp | C/G/T | 0.32 | 0.24 | intron-variant | Ubr2 | GRCm38.p3 | 17:46966478 | GAAGGACCAGAAGTA[C/G/T]GACGGGACCAGTGGA | 224826 |
rs46224938 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Ubr2 | Mm_Celera | 17:46938110 | CTCCTGGCTCTAAGC[A/G]GCCTCTGGTCCTGGG | 224826 |
rs46239139 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Ubr2 | Mm_Celera | 17:46952509 | TGGCCAACAGAGACG[A/G]AGCTGTATTTTGATC | 224826 |
rs46247642 | snp | C/G | | | intron-variant | Ubr2 | Mm_Celera | 17:46988142 | CCTCTCCAGTCTGAG[C/G]CAGCCCGGTTACAAA | 224826 |
rs46254699 | snp | A/T | | | intron-variant | Ubr2 | Mm_Celera | 17:46988028 | CCCCCTAAGTTCACT[A/T]ACATAGAAAAGAGTT | 224826 |
rs46269920 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Ubr2 | Mm_Celera | 17:46985116 | AAACTCTTTTTAGAA[A/C]AGAACAGTTGCATAA | 224826 |
rs46269974 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Ubr2 | Mm_Celera | 17:46969106 | AATGGCTATGTCCAT[A/T]TAAAACTGTAAAAGG | 224826 |
rs46280106 | snp | C/T | 0.32 | 0.24 | intron-variant | Ubr2 | Mm_Celera | 17:46955477 | TCTCCAGCACTACAG[C/T]AACTTGTACAGGGAC | 224826 |
rs46292394 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ubr2 | Mm_Celera | 17:46996652 | CCTTGCTGTCCAATC[A/G]TGCTCCCGAGCTTCT | 224826 |
rs46314472 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ubr2 | Mm_Celera | 17:46962994 | GAGGAAACAACCGTT[C/T]CCAATGTGCAGACAT | 224826 |