SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3668317 | snp | C/T | 0.5 | 0 | intron-variant | Ube2o | Mm_Celera | 11:116563141 | ATGCATATAGGCAAA[C/T]ACTTTACACAAAATA | 217342 |
rs6189025 | snp | A/G | 0.5 | 0 | intron-variant | Ube2o | GRCm38.p3 | 11:116552032 | GGGCTGCAGTTCGGG[A/G]AGAAGGCTTGCTGTA | 217342 |
rs6189959 | snp | C/T | 0.5 | 0 | intron-variant | Ube2o | GRCm38.p3 | 11:116552187 | AGCCCATTCATTAAA[C/T]TGGCCATGGTCAATC | 217342 |
rs6293129 | snp | G/T | 0.489796 | 0.070696 | downstream-variant-500B | Ube2o | GRCm38.p3 | 11:116537268 | CTGGGCTACACCCAT[G/T]AGCTATCTCTGGGTC | 217342 |
rs6307028 | snp | A/G | 0.483471 | 0.0893938 | downstream-variant-500B | Ube2o | GRCm38.p3 | 11:116537448 | GCTAGATGCTGTGGT[A/G]TCAATTTCCCGGGAA | 217342 |
rs6307619 | snp | A/G | 0.483471 | 0.0893938 | downstream-variant-500B | Ube2o | GRCm38.p3 | 11:116537564 | CAGACTCCACGTGAC[A/G]AGAGATGAAGGCCAT | 217342 |
rs6382081 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2o | GRCm38.p3 | 11:116542179 | ACAGACCCTTTGCCC[A/G]TCTTGCACCCCAAGC | 217342 |
rs6382141 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Ube2o | GRCm38.p3 | 11:116542233 | AGGCTCTGGGCAGTC[A/G]GTCCGTTAGCATCTG | 217342 |
rs6383017 | snp | A/C | 0.415225 | 0.187619 | intron-variant | Ube2o | GRCm38.p3 | 11:116542347 | ATAAGGTCTGTGTGG[A/C]CTGCACCAGGAATGA | 217342 |
rs6383163 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Ube2o | GRCm38.p3 | 11:116542428 | TGTGGCCTGCTTCCC[A/C]CTGAATGGCTGCCGA | 217342 |
rs13468158 | snp | A/G | | | utr-variant-3-prime | Ube2o | Mm_Celera | 11:116537895 | CCTGTGCTGTGCCAG[A/G]ACCACCGGGGCAGCA | 217342 |
rs13468159 | snp | A/G | | | missense | Ube2o | Mm_Celera | 11:116539598 | ATGGCATTAATCCGT[A/G]TGGTGCAGTCCATGA | 217342 |
rs13481249 | snp | A/G | 0.481176 | 0.0951712 | synonymous-codon | Ube2o | GRCm38.p3 | 11:116541583 | TAGCTTCTTGATATC[A/G]TCCAAAAACTTCTTC | 217342 |
rs27002268 | snp | A/G | 0.188366 | 0.242283 | missense | Ube2o | GRCm38.p3 | 11:116539432 | GAGCTGCTGTCTTTA[A/G]GGGCCCCATTGGGCA | 217342 |
rs27002269 | snp | C/G | 0.487535 | 0.077957 | synonymous-codon | Ube2o | GRCm38.p3 | 11:116539065 | GTCCTCTGTGCTTTC[C/G]GGCATGCCCGCCTCC | 217342 |
rs27002270 | snp | G/T | 0.124444 | 0.216185 | utr-variant-3-prime | Ube2o | Mm_Celera | 11:116538898 | TCTTGCACTTCAGCA[G/T]CAAACTTGCCGCAGG | 217342 |
rs27002271 | snp | A/G | 0.493827 | 0.0552116 | utr-variant-3-prime | Ube2o | GRCm38.p3 | 11:116538258 | AGAGGCTGAGCCACC[A/G]GATGGGAGAGGCCCT | 217342 |
rs27029237 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Ube2o | Mm_Celera | 11:116576626 | GGGCCACCAGGGTGA[A/G]GTCAGGATGCCAGAA | 217342 |
rs27029238 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Ube2o | Mm_Celera | 11:116576436 | CCATCCCAACAGGAT[A/C]GGTGAAATGAAGAAG | 217342 |
rs27029239 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Ube2o | GRCm38.p3 | 11:116576355 | CAAGCCAAAACAAGT[A/G]CCTCCAGAAAGACTC | 217342 |
rs27029240 | snp | A/G/T | 0.489796 | 0.070696 | intron-variant | Ube2o | GRCm38.p3 | 11:116573437 | AAGTGTCTCAGTCCC[A/G/T]TGGCCCAGCTGTAGA | 217342 |
rs27029241 | snp | A/C | 0.493827 | 0.0552116 | intron-variant | Ube2o | GRCm38.p3 | 11:116573010 | CCTCTAGCACCGCAT[A/C]CGCCAAGCCTGATGT | 217342 |
rs27029242 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2o | Mm_Celera | 11:116570256 | TGTGGTTGTCATCAC[A/G]GCTACCTAGTCAACA | 217342 |
rs27029243 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Ube2o | GRCm38.p3 | 11:116570255 | ATGTGGTTGTCATCA[A/C]GGCTACCTAGTCAAC | 217342 |
rs27029244 | snp | C/T | 0.32 | 0.24 | intron-variant | Ube2o | Mm_Celera | 11:116569912 | CAGGCCTTAACTAAA[C/T]TCATCAACTCTGTAC | 217342 |
rs27029245 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ube2o | Mm_Celera | 11:116569244 | CACGCTCGTCTCTTT[C/T]AAAGGCTAAAGTACT | 217342 |
rs27029246 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ube2o | Mm_Celera | 11:116569213 | CCAGCTGCCCTTCCA[A/G]CTGCCACTGCTGTCC | 217342 |
rs27029247 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Ube2o | Mm_Celera | 11:116568484 | AAAGGTGATTCCCCT[C/T]TTCGTTCTCATCAGC | 217342 |
rs27029248 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ube2o | Mm_Celera | 11:116568372 | GTCTGATGTCAAAAC[C/T]TTTCCCTAACAAACT | 217342 |
rs27029249 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Ube2o | Mm_Celera | 11:116568125 | CTCTCAGCAACACTC[G/T]CTTAAGCTGGGCGTG | 217342 |
rs27029250 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Ube2o | GRCm38.p3 | 11:116568108 | CTGGCCAGAACCAGC[A/G]TCTCTCAGCAACACT | 217342 |
rs27029251 | snp | C/T | 0.32 | 0.24 | intron-variant | Ube2o | Mm_Celera | 11:116568031 | AATAGTCAGAAGTGT[C/T]TGAGTGAACATGCAG | 217342 |
rs27029252 | snp | C/T | 0.32 | 0.24 | intron-variant | Ube2o | Mm_Celera | 11:116567847 | GAGCGAGCGAGCGAA[C/T]GTGCAACTGGAACAT | 217342 |
rs27029253 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ube2o | Mm_Celera | 11:116567800 | TGTCCTTACCTGCTT[C/T]ACCAGGCTCAGCCAA | 217342 |
rs27029254 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ube2o | Mm_Celera | 11:116567540 | CCCTAAGATAGCTCA[C/T]GGGCACTGCATAAGT | 217342 |
rs27029255 | snp | A/G | 0.33241 | 0.236027 | intron-variant | Ube2o | GRCm38.p3 | 11:116567454 | AGTTGCTGTTTCACA[A/G]TCGGAGTTATTTTGT | 217342 |
rs27029256 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2o | Mm_Celera | 11:116567302 | CACTGCTCACCCTCA[C/T]TCCAAGCTTCACTAC | 217342 |
rs27029257 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Ube2o | GRCm38.p3 | 11:116567263 | AGCCAAAGCTTTCCA[C/T]GTTTTGGTTTTCCTT | 217342 |
rs27029258 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Ube2o | GRCm38.p3 | 11:116566137 | GGAACCTGACCCCTT[G/T]GTACAGCTTGTTAGG | 217342 |
rs27029259 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Ube2o | GRCm38.p3 | 11:116565914 | AAGGAATCCCGGCAA[A/G]GGGTCAAGGAATGAC | 217342 |
rs27029260 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ube2o | Mm_Celera | 11:116565890 | GGGACACTTCAAACA[C/T]GCAGGAGGAAGGAAT | 217342 |
rs27029261 | snp | C/G | 0.32 | 0.24 | intron-variant | Ube2o | Mm_Celera | 11:116565515 | AGTATAAGGAAGACA[C/G]GAGACAACCTTTGAT | 217342 |
rs27029262 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Ube2o | GRCm38.p3 | 11:116565465 | CTCAAATACAAGCCA[C/T]CGTAGGCCACACCCA | 217342 |
rs27029263 | snp | G/T | 0.497041 | 0.0383476 | intron-variant | Ube2o | GRCm38.p3 | 11:116565449 | TCACTGCCTAACCTA[G/T]CTCAAATACAAGCCA | 217342 |
rs27029264 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Ube2o | GRCm38.p3 | 11:116565218 | CACTATCTGAGATGA[C/T]GGGAAACATGAGCCA | 217342 |
rs27029265 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Ube2o | GRCm38.p3 | 11:116564776 | AATGTGTCATTTCAG[C/T]TGGGGCGTGGTGGTG | 217342 |
rs27029266 | snp | C/G | 0.359862 | 0.224567 | intron-variant | Ube2o | GRCm38.p3 | 11:116564752 | GTTATCCAATCTCCA[C/G]GAAGTAAAAATGTGT | 217342 |
rs27029267 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ube2o | Mm_Celera | 11:116564633 | CCAGTACAGTCCCGC[A/G]CTATACCTCCAATCA | 217342 |
rs27046968 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Ube2o | GRCm38.p3 | 11:116564485 | AAGCCTAAAGGTGAG[A/T]TTTTGACAGTTTCCA | 217342 |
rs27046969 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Ube2o | GRCm38.p3 | 11:116564368 | ATGAACACATTCTTC[C/T]GGCATTTTTGGAATA | 217342 |
rs27046970 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Ube2o | GRCm38.p3 | 11:116564295 | CAGACATACACTAGA[A/G]ATGCGTGGAACATAT | 217342 |
rs27046971 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ube2o | GRCm38.p3 | 11:116563450 | GGTCTGGCTCAGACC[A/G]TTCCTTGGTTCCCAT | 217342 |
rs27046972 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Ube2o | GRCm38.p3 | 11:116562738 | CCATCTAGAAAGACC[A/C]AGGGAAGGTGTGCAG | 217342 |
rs27046973 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2o | GRCm38.p3 | 11:116562289 | CGGACATAGGTAGTC[A/G]ACGCTTTACACACTT | 217342 |
rs27046974 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ube2o | GRCm38.p3 | 11:116561096 | AATGTGTGCCCATGT[A/G]TGAGCATGTTTAATG | 217342 |
rs27046975 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Ube2o | GRCm38.p3 | 11:116559868 | AGGTGGGTTAGGTCG[A/G]ATGGGCTAGCTGAAA | 217342 |
rs27046976 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ube2o | GRCm38.p3 | 11:116559741 | GCTGCTGATGATTGG[C/T]TCAGATTGGCTTTCT | 217342 |
rs27046977 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Ube2o | GRCm38.p3 | 11:116559352 | CAGGATTCCCATGGC[C/T]AGAGCAGGACCTGTC | 217342 |
rs27046978 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2o | Mm_Celera | 11:116559342 | AATAGGCTGCCAGGA[C/T]TCCCATGGCTAGAGC | 217342 |
rs27046979 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ube2o | Mm_Celera | 11:116558613 | TTTCCTCTTCTCCAC[A/G]GCACTTTATGGCTTG | 217342 |
rs27046980 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Ube2o | GRCm38.p3 | 11:116558486 | ACATGGAGAAACTAG[C/T]TTGGGCAAGCATAGA | 217342 |
rs27046981 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ube2o | Mm_Celera | 11:116558263 | TCTAACATTAACACA[A/G]TGGTGTCCAAGCCCA | 217342 |
rs27046982 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2o | GRCm38.p3 | 11:116558055 | CCCTAGAAGGATGAG[A/G]ACAGAGTGCATCTCA | 217342 |
rs27046983 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ube2o | GRCm38.p3 | 11:116558016 | ACTGTGTCTGGAGTG[A/G]CCCTGTACCCACGGA | 217342 |
rs27046984 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2o | GRCm38.p3 | 11:116555588 | TTAACAGACTGGCCT[A/G]TAGGTCAAGGTGTTA | 217342 |
rs27046985 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Ube2o | GRCm38.p3 | 11:116554885 | GCTGCTAATCAGAAT[C/T]CCAGTAAGTGCTTTA | 217342 |
rs27046986 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Ube2o | GRCm38.p3 | 11:116554592 | ATGAGCTCTGATCTC[A/G]TTAGCGCATCATAAC | 217342 |
rs27046987 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2o | GRCm38.p3 | 11:116554461 | TACCCTGGAGGAACA[A/G]GTACAACACAGACCC | 217342 |
rs27046988 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2o | GRCm38.p3 | 11:116552840 | GAGCTAGGCCACATA[A/G]AGACAGGCCAGGACT | 217342 |
rs27046989 | snp | C/G | 0.5 | 0 | intron-variant | Ube2o | GRCm38.p3 | 11:116552658 | GGGGTGTATCCACGA[C/G]CAGGTCTTTCATTTA | 217342 |
rs27046990 | snp | A/G | 0.32 | 0.24 | intron-variant | Ube2o | Mm_Celera | 11:116547575 | AGGTCTGACACGGAC[A/G]TTTGTGATGTGTGAG | 217342 |
rs27046991 | snp | G/T | 0.497778 | 0.0332592 | intron-variant | Ube2o | GRCm38.p3 | 11:116546697 | GACATGCACAACAGA[G/T]CACTGGCCCTCAGAG | 217342 |
rs27046992 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Ube2o | GRCm38.p3 | 11:116546621 | ACCATCTTGCACCTA[C/T]AGCTCAGCCTCTGCC | 217342 |
rs27046993 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Ube2o | Mm_Celera | 11:116546610 | CCCTAAAACACACCA[C/T]CTTGCACCTACAGCT | 217342 |
rs27046994 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Ube2o | GRCm38.p3 | 11:116546573 | GGACTCAGTCAGCAC[C/T]AAACACCAAGACTAA | 217342 |
rs27046995 | snp | A/G | 0.391111 | 0.206368 | synonymous-codon, upstream-variant-2KB | Ube2o | GRCm38.p3 | 11:116545957 | TGGGTAGAAGCCATA[A/G]GAGTCATCAAAGAAG | 217342 |
rs27046996 | snp | A/C | 0.391111 | 0.206368 | synonymous-codon, upstream-variant-2KB | Ube2o | GRCm38.p3 | 11:116545888 | TACAGGCTTGACCCC[A/C]GAGAGCCACTGGACA | 217342 |
rs27046997 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Ube2o | Mm_Celera | 11:116545825 | CCCTCACCCCATTTA[C/T]GTGCTTACCTCCTCC | 217342 |
rs27046998 | snp | C/T | 0.426035 | 0.177515 | intron-variant, upstream-variant-2KB | Ube2o | GRCm38.p3 | 11:116545718 | GGTCCATGAGTAGAG[C/T]CTAGGCTGCTCCAAT | 217342 |
rs27046999 | snp | C/T | 0.391111 | 0.206368 | intron-variant, upstream-variant-2KB | Ube2o | GRCm38.p3 | 11:116545671 | AACCCATGAGTAGAG[C/T]CTAGGCTGCTCCAAT | 217342 |
rs27047000 | snp | C/G | 0.426035 | 0.177515 | intron-variant, upstream-variant-2KB | Ube2o | GRCm38.p3 | 11:116545503 | ACACAAGCCAGTCAG[C/G]CATTCATCAGATGGA | 217342 |
rs27047001 | snp | A/G | 0.391111 | 0.206368 | intron-variant, upstream-variant-2KB | Ube2o | GRCm38.p3 | 11:116545478 | CAAATAGCTGCCCGA[A/G]CCCTTCCTAACACAA | 217342 |
rs27047002 | snp | A/G | 0.495868 | 0.0452663 | intron-variant, upstream-variant-2KB | Ube2o | Mm_Celera | 11:116545271 | ATTTATAGGCAGACC[A/G]ATACATGCTAGGGGT | 217342 |
rs27047003 | snp | C/T | 0.48 | 0.0979796 | intron-variant, upstream-variant-2KB | Ube2o | GRCm38.p3 | 11:116545270 | CATTTATAGGCAGAC[C/T]AATACATGCTAGGGG | 217342 |
rs27047004 | snp | C/T | 0.432133 | 0.171253 | intron-variant, upstream-variant-2KB | Ube2o | GRCm38.p3 | 11:116545239 | GCACTTCTGAGAGCT[C/T]CGTGGGATGCCTGGT | 217342 |
rs27047005 | snp | G/T | 0.48 | 0.0979796 | synonymous-codon, upstream-variant-2KB | Ube2o | GRCm38.p3 | 11:116544707 | CCCTATTTCACTCCC[G/T]GCTCTGGCTTCCCCT | 217342 |
rs27047006 | snp | C/G | 0.391111 | 0.206368 | synonymous-codon, upstream-variant-2KB | Ube2o | GRCm38.p3 | 11:116544629 | CTGAAGCTCCTCCGA[C/G]CCCTCATCCTGCATC | 217342 |
rs27047007 | snp | A/G | 0.48 | 0.0979796 | synonymous-codon, upstream-variant-2KB | Ube2o | GRCm38.p3 | 11:116544425 | GTTTTTGATGGACAA[A/G]GGAATGCTCTTTTTA | 217342 |
rs27047008 | snp | A/G | 0.48 | 0.0979796 | synonymous-codon, missense | Ube2o | GRCm38.p3 | 11:116543936 | CACAGGGAAAAGGTC[A/G]TTGGAGCGGATGTTG | 217342 |
rs27047009 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Ube2o | GRCm38.p3 | 11:116543752 | GGAAATCAGGAGGGC[A/C]GTGACTAACTGAAGA | 217342 |
rs27047010 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2o | GRCm38.p3 | 11:116543540 | TTCTCCAATGAGCTG[C/T]GGCAAAAGCAGGGCT | 217342 |
rs27047011 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon | Ube2o | Mm_Celera | 11:116543453 | CGTGTTACCAATGCG[A/G]ATGACAATGTCAGTT | 217342 |
rs27047012 | snp | A/G | 0.487535 | 0.077957 | synonymous-codon | Ube2o | GRCm38.p3 | 11:116543420 | TACCTCATCCTCCTT[A/G]GGTAGAGCCCCATCC | 217342 |
rs27047013 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ube2o | Mm_Celera | 11:116543373 | ACTGCAGCCACCACC[C/T]AGACAGAAGCTGCAG | 217342 |
rs27047014 | snp | A/C | 0.487535 | 0.077957 | intron-variant | Ube2o | GRCm38.p3 | 11:116543223 | GACTGTGTGGGCTCT[A/C]AGCTGCAATGGAGGG | 217342 |
rs27047015 | snp | A/C | 0.432133 | 0.171253 | intron-variant | Ube2o | GRCm38.p3 | 11:116543141 | TGACCTTTCTCAACA[A/C]CTCCAGCCTTTCCTC | 217342 |
rs27047016 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Ube2o | GRCm38.p3 | 11:116543120 | CCCCTTGTGTCCAGA[C/T]TGTCTTGACCTTTCT | 217342 |
rs27047017 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Ube2o | GRCm38.p3 | 11:116543023 | CAAGTCTGCAGCAAT[C/T]CTCTCCCCACAGGTA | 217342 |
rs27047018 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ube2o | Mm_Celera | 11:116542753 | ACAGAGGAGGCCGGG[A/G]TTCTACGTGGCCAGT | 217342 |
rs27047019 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ube2o | Mm_Celera | 11:116542619 | ACTGTCCTAGAAACA[A/G]CAGCAGGGAGCACCC | 217342 |