SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6180863 | snp | C/G | 0.5 | 0 | intron-variant | Ubr5 | Mm_Celera | 15:38026180 | CTGAAATTAAAACTT[C/G]GACTATTATTAACTG | 70790 |
rs6351141 | snp | A/G | 0.5 | 0 | intron-variant | Ubr5 | Mm_Celera | 15:38054293 | cgaaaccacacgcct[A/G]tgcaaatatatccat | 70790 |
rs13459147 | snp | A/G | 0.375 | 0.216506 | synonymous-codon, nc-transcript-variant | Ubr5 | GRCm38.p3 | 15:37976176 | GGATTTAGAGGACAC[A/G]GATGATGGTGATGAC | 70790 |
rs13467730 | snp | C/T | | | synonymous-codon, nc-transcript-variant | Ubr5 | GRCm38.p3 | 15:37986094 | CATGGAAGATGTTGG[C/T]GCAGAGCCTGGATCG | 70790 |
rs13467731 | snp | A/C | 0.244898 | 0.249948 | synonymous-codon, nc-transcript-variant | Ubr5 | GRCm38.p3 | 15:37984062 | TAAGGATGAACCAGG[A/C]GAGGGCAGTGGTGTA | 70790 |
rs13467732 | snp | C/T | 0.396694 | 0.202437 | synonymous-codon, nc-transcript-variant | Ubr5 | GRCm38.p3 | 15:37986166 | GGGCATGGTTATCTC[C/T]CATGACATGCTGCTG | 70790 |
rs31555584 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ubr5 | Mm_Celera | 15:37979445 | AAATACCAAATACCT[C/T]CTATAACCTAATAAG | 70790 |
rs31562958 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Ubr5 | Mm_Celera | 15:37969799 | AACCAGGAACATAGC[C/T]GGACTCATCCACTCA | 70790 |
rs31573869 | snp | C/G | 0.375 | 0.216506 | intron-variant | Ubr5 | Mm_Celera | 15:38008891 | ATGAAGATAAATTAA[C/G]TTATTAGAAAATTTT | 70790 |
rs31579525 | snp | C/G | 0.375 | 0.216506 | intron-variant | Ubr5 | Mm_Celera | 15:37988788 | CCCCCAGAAAAATAA[C/G]ATGACTTTCCAAAAT | 70790 |
rs31609525 | snp | A/C | 0.304688 | 0.243945 | intron-variant | Ubr5 | Mm_Celera | 15:38061224 | AGGGGTAAAATAGAA[A/C]CAGCAAGAACAGCTA | 70790 |
rs31614518 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Ubr5 | Mm_Celera | 15:38060872 | TAGAAACTGAAAGCA[C/T]AGTACTCTAATGAGC | 70790 |
rs31633842 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Ubr5 | Mm_Celera | 15:37972510 | CGCATTAACACTGCA[A/G]GAATGATGAATGAAA | 70790 |
rs31670713 | snp | C/T | 0.429688 | 0.173817 | intron-variant | Ubr5 | Mm_Celera | 15:37986848 | TCTTCTGTTCCTCCA[C/T]TGATATAGTCCAACT | 70790 |
rs31684584 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ubr5 | Mm_Celera | 15:38003424 | TTAAGATCTACTATG[A/G]TTAGATTCACAAACC | 70790 |
rs31691936 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Ubr5 | Mm_Celera | 15:37972337 | AGCCTTAGCCTCATT[G/T]TGCAGAAGGAAACCC | 70790 |
rs31762267 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ubr5 | Mm_Celera | 15:37981726 | CTCTTTCTCTGGGGT[A/G]TGTGCAGTATGTCGT | 70790 |
rs31817479 | snp | C/T | 0.32 | 0.24 | intron-variant | Ubr5 | Mm_Celera | 15:37992266 | ATTTAGAATTGATGA[C/T]TGGACTGGAGTGACC | 70790 |
rs31835652 | snp | A/G | 0.46875 | 0.121031 | intron-variant, upstream-variant-2KB | Ubr5 | Mm_Celera | 15:38012060 | CCTTTGAACTCAGGA[A/G]CTATTGAGTCACATG | 70790 |
rs31874191 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ubr5 | Mm_Celera | 15:37983309 | TTTCTCTGTGTAGCC[C/T]TGGCTGTCCTGGAAC | 70790 |
rs31882908 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ubr5 | Mm_Celera | 15:38056589 | TTGGCGACAGAAAGC[C/T]GCAGCTACTCAGTAG | 70790 |
rs31885995 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | Ubr5 | Mm_Celera | 15:37971957 | AAGGCATCAGTTACA[C/T]TACTACCACTCAGTG | 70790 |
rs31902169 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Ubr5 | Mm_Celera | 15:38065011 | TTAGTCACAGCAAAG[A/G]TGTGGAGGTGCAGGT | 70790 |
rs31933035 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Ubr5 | Mm_Celera | 15:37982166 | TTTCTAAGGGTTACC[A/G]ATGGTTGCACATGGC | 70790 |
rs31953878 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Ubr5 | Mm_Celera | 15:38067801 | CAGCTGTTCCTGGAG[A/G]TGTTTGCTGTGAGAG | 70790 |
rs31955194 | snp | C/G | 0.492188 | 0.0620098 | utr-variant-3-prime, downstream-variant-500B | Ubr5 | Mm_Celera | 15:37967581 | CCACCTGCACTGAAA[C/G]AGGGGTACAAAGAAA | 70790 |
rs31960254 | snp | C/T | 0.429688 | 0.173817 | intron-variant | Ubr5 | Mm_Celera | 15:37981713 | TGCCAGGGCCTTTCT[C/T]TTTCTCTGGGGTGTG | 70790 |
rs31979366 | snp | A/G/T | 0.492188 | 0.0620098 | intron-variant | Ubr5 | Mm_Celera | 15:37974125 | AATTGTGATCGCAAC[A/G/T]AAAAAAGAAAATATA | 70790 |
rs31990219 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Ubr5 | Mm_Celera | 15:37969561 | TAAATATAAAATACT[A/C]TGAAAGATCTATCCT | 70790 |
rs32025512 | snp | A/G | 0.375 | 0.216506 | intron-variant, downstream-variant-500B | Ubr5 | Mm_Celera | 15:37991075 | TGAAGTAAAAAAAAG[A/G]TGTATGGATATTGGA | 70790 |
rs32049798 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ubr5 | Mm_Celera | 15:37983269 | GGTTTTTTGTTTTTG[C/T]TTGTTCATTTTTTTC | 70790 |
rs32058825 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ubr5 | Mm_Celera | 15:38066352 | TCTGAGGCCAGCCCA[A/G]AACACTTGAGACTCT | 70790 |
rs32075273 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ubr5 | Mm_Celera | 15:37980370 | CATAAACACAACTAG[C/T]ATACAGGTTTCACAC | 70790 |
rs32079302 | snp | A/C | 0.375 | 0.216506 | intron-variant | Ubr5 | Mm_Celera | 15:38070556 | ATGAATGAGGACAGC[A/C]TGGTCTACAGAGTGA | 70790 |
rs32082972 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ubr5 | Mm_Celera | 15:37974217 | TTTGGTTCTACAAAT[A/G]TGATCAAATATCGTG | 70790 |
rs32118176 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Ubr5 | Mm_Celera | 15:37974366 | TGTCAAAAATGATTT[A/T]CAGCAGTCAGTGTGA | 70790 |
rs32132193 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ubr5 | Mm_Celera | 15:38006881 | AATGCAATACCTATA[C/T]ACTTGAAAGAAAATC | 70790 |
rs32133088 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Ubr5 | Mm_Celera | 15:37976833 | AAATAGACATGAGAG[C/G]GCATGTATGCAGGAG | 70790 |
rs32144470 | snp | C/T | 0.492188 | 0.0620098 | intron-variant | Ubr5 | Mm_Celera | 15:37996237 | CACACATGTGTGGTG[C/T]CGACCTAAAAGTGAT | 70790 |
rs32175204 | snp | C/G | 0.498615 | 0.0262793 | intron-variant | Ubr5 | Mm_Celera | 15:37980465 | GACTGCCATTTTTTC[C/G]CAGCTACAACTTGCT | 70790 |
rs32224441 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Ubr5 | Mm_Celera | 15:37978240 | GGAGCCTGCATTCCC[A/C]AGGAAACTCAAGGCT | 70790 |
rs32237462 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ubr5 | Mm_Celera | 15:38000036 | ATTTATAGATCATCA[C/T]AGCACATAATAAACC | 70790 |
rs32258710 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ubr5 | Mm_Celera | 15:38076905 | CTGGCCTCGAACTCA[A/G]AAATCCGCCTGCCTC | 70790 |
rs32262003 | snp | A/G | 0.345679 | 0.230967 | downstream-variant-500B | Ubr5 | Mm_Celera | 15:37966830 | TATCAAAGGCCAGGA[A/G]TCCTAAACAGGCACT | 70790 |
rs32264063 | snp | A/T | 0.5 | 0 | intron-variant | Ubr5 | Mm_Celera | 15:37980145 | TGTATGAGCCTTTTT[A/T]AAAAAGGGGGTTTGA | 70790 |
rs32276554 | snp | A/C | 0.32 | 0.24 | intron-variant | Ubr5 | Mm_Celera | 15:38015986 | AAAAATGTGGGAAAA[A/C]AGATACATTCTATTG | 70790 |
rs32291057 | snp | A/T | 0.375 | 0.216506 | intron-variant | Ubr5 | Mm_Celera | 15:38001752 | ACTACTACAGGCAAG[A/T]GGTCAGGGCTAGGTT | 70790 |
rs32295218 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | Ubr5 | Mm_Celera | 15:38079277 | CCTGATAGTAGGATC[C/T]TGGAAGTGACTGTGT | 70790 |
rs32296186 | snp | C/T | 0.455 | 0.143091 | intron-variant | Ubr5 | Mm_Celera | 15:37969719 | TTTTCTAAGACATAA[C/T]TGTGTAAGAAACATC | 70790 |
rs32306863 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Ubr5 | Mm_Celera | 15:37973900 | AATATTTCATATGCT[C/T]TTAATAGTCCCCATA | 70790 |
rs32317067 | snp | C/G | 0.492188 | 0.0620098 | intron-variant | Ubr5 | Mm_Celera | 15:38009062 | CTTAAAGCCCTATAT[C/G]AAGTGTGTTATTTTT | 70790 |
rs32323727 | snp | G/T | 0.375 | 0.216506 | intron-variant | Ubr5 | Mm_Celera | 15:37998995 | CAGACAGGCTCTTGC[G/T]ATGTTGCCCAGACTG | 70790 |
rs32342673 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ubr5 | Mm_Celera | 15:37972309 | CTGAATACCTCAGGT[A/G]CATTAATTGTTCAGC | 70790 |
rs32343574 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ubr5 | Mm_Celera | 15:37981942 | GTGTGTGTGTGTGTG[C/T]GCGTGTGCGTGTGTC | 70790 |
rs32346176 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Ubr5 | Mm_Celera | 15:37983253 | TGCTGTTGTTGTTTT[C/G]GGTTTTTTGTTTTTG | 70790 |
rs32369215 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Ubr5 | Mm_Celera | 15:38002028 | AGTAGAGAGGTGTTC[A/C]AATTCCAAAAGTTTG | 70790 |
rs32377723 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Ubr5 | Mm_Celera | 15:37971984 | AGTGACTAATTTCAG[A/C]AGCATTCTCTAACAT | 70790 |
rs32379402 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ubr5 | Mm_Celera | 15:38009603 | TTTTTATTAAACACC[A/G]AATAAAACAAAAGAG | 70790 |
rs32391277 | snp | C/G | 0.375 | 0.216506 | intron-variant | Ubr5 | Mm_Celera | 15:37988631 | AATATCTCAAAGCAA[C/G]TATTTATAATACTAT | 70790 |
rs32392586 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ubr5 | Mm_Celera | 15:37979409 | GAGAGGCTAGCTTTG[C/T]CTTGTGAACAGAACA | 70790 |
rs32405417 | snp | A/T | 0.375 | 0.216506 | intron-variant | Ubr5 | Mm_Celera | 15:38061555 | ACATAAAAGAAAAAG[A/T]ATTATAGATTATAAA | 70790 |
rs32418379 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Ubr5 | Mm_Celera | 15:37985725 | CCAAAAACTCTCTTT[A/T]AAAAAAAATTACTGC | 70790 |
rs32470754 | snp | A/G | 0.492188 | 0.0620098 | intron-variant | Ubr5 | Mm_Celera | 15:37995681 | TGCTCCAGCCATGGT[A/G]TCCTGGGTTCTTTTA | 70790 |
rs32473543 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ubr5 | Mm_Celera | 15:38052042 | ACACTTCCCCGAGGC[C/T]GTGTCCAGCTCAGAC | 70790 |
rs32477894 | snp | A/G | 0.49827 | 0.0293608 | intron-variant, upstream-variant-2KB | Ubr5 | Mm_Celera | 15:38012763 | CCTATCAACCTGGTA[A/G]CCTTCCTAATGCCAA | 70790 |
rs32482444 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Ubr5 | Mm_Celera | 15:37979251 | CCAAAGTTCTTTGAG[C/T]GTACTGTAGTCTCCT | 70790 |
rs32494980 | snp | A/T | 0.5 | 0 | intron-variant | Ubr5 | Mm_Celera | 15:37978377 | AATTCAAGACATGGC[A/T]AAGGCTCCCTGATAT | 70790 |
rs32496783 | snp | A/T | 0.375 | 0.216506 | intron-variant | Ubr5 | Mm_Celera | 15:38051221 | TAAATTTCTCTTCTC[A/T]AAAAAAAAAAAAAAA | 70790 |
rs32506308 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Ubr5 | Mm_Celera | 15:37969468 | CATAGTGCCAATGAT[A/G]CCCAGTAAGTGTCTA | 70790 |
rs32533169 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ubr5 | Mm_Celera | 15:38068346 | AAGACTAGGAGCAGC[A/G]GAGTCCCAGCAAGTT | 70790 |
rs32540156 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ubr5 | Mm_Celera | 15:37983399 | TGCTGGGATTAAAGG[C/T]GTGCGCCACTAAGCC | 70790 |
rs33170264 | snp | C/G | 0.277778 | 0.248452 | intron-variant | Ubr5 | Mm_Celera | 15:38068847 | CTAAGAGAGACTACT[C/G]TGAAAGAAGACACAA | 70790 |
rs33170266 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ubr5 | Mm_Celera | 15:38068658 | GAAGTGGTCTTTCCA[C/T]GCCAAAAAAAAACCC | 70790 |
rs33170268 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Ubr5 | Mm_Celera | 15:38068437 | GCCTGAGCACCACGG[A/G]CAACCCTCTCCTATA | 70790 |
rs33170271 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Ubr5 | Mm_Celera | 15:38067879 | CTCAGCAAGCAACTG[A/C]ACAGGCTCCCTTACC | 70790 |
rs33170604 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ubr5 | Mm_Celera | 15:38050496 | TGGCTCAGCTCTGCG[A/G]GTTCTCATCGTGCGA | 70790 |
rs33170606 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ubr5 | Mm_Celera | 15:38050418 | CAACTGTCCCAGGCA[C/T]GCAGAAAATGCTCAC | 70790 |
rs33170608 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Ubr5 | Mm_Celera | 15:38050302 | CTACACTCAAAGCGG[C/T]CAAGAAAAATGACAG | 70790 |
rs33170610 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Ubr5 | Mm_Celera | 15:38050136 | CGCACATGCAGAATG[C/T]AGGAGGCAAAAAGAG | 70790 |
rs33170612 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ubr5 | Mm_Celera | 15:38049268 | CTAAATTCCAGTTTG[C/T]TCAATTATATAGCAC | 70790 |
rs33171124 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Ubr5 | Mm_Celera | 15:38067347 | AAAACTACCTGATAG[A/C]AAACAATGTAACTCC | 70790 |
rs33171126 | snp | C/G/T | 0.21875 | 0.248039 | intron-variant | Ubr5 | Mm_Celera | 15:38067114 | TCTCACATGCAGTGA[C/G/T]CCTCCTATCATCTGC | 70790 |
rs33171128 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Ubr5 | Mm_Celera | 15:38066982 | ATTATTGTCTACAGG[A/C]CGGGCCAACTGCCCA | 70790 |
rs33171130 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ubr5 | Mm_Celera | 15:38066598 | TCCATCAACCCGTTA[C/T]TTAAGCTATTCACTA | 70790 |
rs33171132 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Ubr5 | Mm_Celera | 15:38066526 | TGTAGCCCAGGCTGA[C/T]AAAGGTGCTTCTTTC | 70790 |
rs33171165 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Ubr5 | Mm_Celera | 15:38028869 | GCTCCTCAGCAATGT[A/C]TTTCTCAGCTCAGGA | 70790 |
rs33171167 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Ubr5 | Mm_Celera | 15:38028006 | TTACTATCTTATTGT[C/G]TCCCTCATTCAATTT | 70790 |
rs33171169 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Ubr5 | Mm_Celera | 15:38027735 | GAAGATGGCGTGCAA[A/G]CATGTAGAGCAGGAG | 70790 |
rs33171171 | snp | A/C | 0.277778 | 0.248452 | intron-variant | Ubr5 | Mm_Celera | 15:38027556 | CTAAAAAGCTTTAAA[A/C]TGTTTTACAATAGCA | 70790 |
rs33171173 | snp | G/T | 0.152778 | 0.230321 | intron-variant | Ubr5 | Mm_Celera | 15:38025439 | AACCTTGGCATCAGG[G/T]GTTTATAGGTCAGGT | 70790 |
rs33171394 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Ubr5 | Mm_Celera | 15:38049221 | CTTTCCTAACAACAT[A/G]TTCCCTTGGTTCTGG | 70790 |
rs33171396 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Ubr5 | Mm_Celera | 15:38049143 | AATGAAAACTGCTAA[C/T]TTCATTCTCACTACT | 70790 |
rs33171398 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ubr5 | Mm_Celera | 15:38047187 | GTTTTAATTTATTCA[A/G]TAAGCAGATTCTGCC | 70790 |
rs33171400 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Ubr5 | Mm_Celera | 15:38046763 | AACAAACCTCATCAA[C/T]TTAACTAAAAACCAA | 70790 |
rs33171402 | snp | C/G | 0.165289 | 0.235211 | intron-variant | Ubr5 | Mm_Celera | 15:38043605 | CTGATGCTCTGGAAA[C/G]AGACCCTGCCTCAAA | 70790 |
rs33171626 | snp | C/T | 0.152778 | 0.230321 | downstream-variant-500B | Ubr5 | Mm_Celera | 15:37967218 | TTAACTTTCTTATAG[C/T]TCACATGTATATAAA | 70790 |
rs33171628 | snp | A/G | 0.244898 | 0.249948 | downstream-variant-500B | Ubr5 | Mm_Celera | 15:37966958 | TCTCAGTCCACAAAT[A/G]TAAGGGTATTGGTCC | 70790 |
rs33171630 | snp | A/G | 0.32 | 0.24 | downstream-variant-500B | Ubr5 | Mm_Celera | 15:37966858 | ACTGAAAAGACAGGT[A/G]TCGTTAATTGTTTTT | 70790 |
rs33171636 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ubr5 | Mm_Celera | 15:37992968 | GTGATAGAAAAGGGA[C/T]CTAAGACAATACATC | 70790 |
rs33171638 | snp | A/G | 0.396694 | 0.202437 | synonymous-codon, nc-transcript-variant | Ubr5 | Mm_Celera | 15:37988293 | AGCAACATCAGGAGC[A/G]GATGGACCTGGCTTT | 70790 |