SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs13466799 | snp | A/T | 0.5 | 0 | synonymous-codon | Ubl7 | GRCm38.p3 | 9:57929787 | AAGCCTCCGGGCCCT[A/T]CAGGCCACTGGAGGT | 69459 |
rs29595679 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon | Ubl7 | GRCm38.p3 | 9:57921681 | CCTGGTTCTGCACTC[C/T]GTAGCAGGCAGCACC | 69459 |
rs29650289 | snp | A/C | 0.375 | 0.216506 | intron-variant | Ubl7 | Mm_Celera | 9:57915783 | GAGACAAAGCCCATT[A/C]ATTGTCCAGACACAC | 69459 |
rs29687185 | snp | A/T | 0.5 | 0 | upstream-variant-2KB | Ubl7 | GRCm38.p3 | 9:57909896 | TTATGAACTTTTTTT[A/T]AAAAAAAGATTTATT | 69459 |
rs29694583 | snp | A/C | 0.375 | 0.216506 | intron-variant | Ubl7 | Mm_Celera | 9:57915796 | TTCATTGTCCAGACA[A/C]ACAAGAGATCACACA | 69459 |
rs29737283 | snp | C/G | 0.375 | 0.216506 | upstream-variant-2KB | Ubl7 | GRCm38.p3 | 9:57910843 | AAGCTACAACCTACT[C/G]GCTTCTAGGACCTCA | 69459 |
rs29738194 | snp | C/T | 0.5 | 0 | intron-variant | Ubl7 | Mm_Celera | 9:57918291 | TGGTGAAAGTTTATT[C/T]AGAGCTTTCACGTGC | 69459 |
rs29783094 | snp | G/T | 0.375 | 0.216506 | intron-variant | Ubl7 | Mm_Celera | 9:57913897 | CTGGGATCAAAGGCG[G/T]GCACCACTACGCCCG | 69459 |
rs29786628 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ubl7 | Mm_Celera | 9:57915190 | AAGTAGCTCTCGGAG[A/G]AACTCTACAAAACCT | 69459 |
rs29791171 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ubl7 | Mm_Celera | 9:57915855 | TACCTCTTCTACGTC[A/G]AGCTTTTACCTCTCT | 69459 |
rs29840371 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Ubl7 | GRCm38.p3 | 9:57918026 | ATGACATGGTTGCTG[C/T]GCTGACCTCCGGGCA | 69459 |
rs29842813 | snp | C/T | 0.5 | 0 | intron-variant | Ubl7 | Mm_Celera | 9:57912193 | GGTTGGGTGATCTTG[C/T]TTGAACCTCACAACA | 69459 |
rs29987569 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ubl7 | Mm_Celera | 9:57923404 | TAGTTTGACAGGTGA[A/G]CCTTCCCAGAAAGGG | 69459 |
rs30033630 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | Ubl7 | GRCm38.p3 | 9:57909186 | CTCTTAGCCGCTGAG[C/T]TCTCTCCAGCCCCCA | 69459 |
rs30066215 | snp | G/T | 0.5 | 0 | missense | Ubl7 | GRCm38.p3 | 9:57929714 | CTGTCTTTCCACAGA[G/T]CCAGTGGCAGCCTCA | 69459 |
rs30089768 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Ubl7 | Mm_Celera | 9:57915401 | TTTTTTTTTTTTTGG[G/T]TTTTCGAGACAGGGT | 69459 |
rs30120896 | snp | A/C | 0.375 | 0.216506 | intron-variant | Ubl7 | Mm_Celera | 9:57913907 | AGGCGTGCACCACTA[A/C]GCCCGGCAAAATGTA | 69459 |
rs30139663 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ubl7 | GRCm38.p3 | 9:57913011 | GTTACACTGAACTAC[A/G]TTATTATTTAAGACT | 69459 |
rs30242935 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ubl7 | Mm_Celera | 9:57916161 | TTTCGTTTGTTTTTC[C/T]CGCCATCAGTATGTT | 69459 |
rs30328809 | snp | A/T | 0.375 | 0.216506 | intron-variant | Ubl7 | GRCm38.p3 | 9:57914807 | CTCTATCCTTATTGG[A/T]TTAGATCCCCATTGG | 69459 |
rs30339062 | snp | C/T | 0.18 | 0.24 | intron-variant | Ubl7 | GRCm38.p3 | 9:57918119 | AGGATAGTGCTGAAG[C/T]GTGGACCAGGATGAA | 69459 |
rs30340915 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ubl7 | Mm_Celera | 9:57912614 | GGGTTGACTTTTAAC[C/T]GTTAATGCCTTATTG | 69459 |
rs30374531 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ubl7 | GRCm38.p3 | 9:57929530 | ACAACAAACTCATTT[A/G]TTTTCTTCACATTCA | 69459 |
rs30388072 | snp | C/G | 0.375 | 0.216506 | intron-variant | Ubl7 | Mm_Celera | 9:57919816 | ATTGGAAGGGCCTTC[C/G]GGGAGCTGGAGGAAT | 69459 |
rs33621849 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ubl7 | GRCm38.p3 | 9:57914846 | GATGTGACGTTGTTA[C/T]TGTTAACACCACTAA | 69459 |
rs33665875 | snp | G/T | 0.33241 | 0.236027 | intron-variant | Ubl7 | Mm_Celera | 9:57919557 | AGCCTGTCTCAGTCA[G/T]GCATTGGTTGTAGAT | 69459 |
rs33702713 | snp | A/T | 0.375 | 0.216506 | intron-variant | Ubl7 | GRCm38.p3 | 9:57912595 | GAGAGATGAGTAGGG[A/T]GGTGGGTTGACTTTT | 69459 |
rs33743328 | snp | A/G | 0.32 | 0.24 | intron-variant | Ubl7 | Mm_Celera | 9:57918534 | TTCCAGAGTACTGTG[A/G]TTCAGTTCCCAGCAC | 69459 |
rs36252428 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Ubl7 | Mm_Celera | 9:57918316 | ACGTGCCTTGCACTT[C/G]CTTAGTCTGTACTGG | 69459 |
rs36271901 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Ubl7 | Mm_Celera | 9:57922064 | CTTGAGGGAGATGGT[C/G]CTAGGAACTAGCTTC | 69459 |
rs36281848 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ubl7 | Mm_Celera | 9:57923844 | CATGCAGTGTCATGG[C/T]GTAGAGCACCCTGAG | 69459 |
rs36373395 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Ubl7 | Mm_Celera | 9:57917400 | CTTAACCAAATTCAG[C/T]TTAGAACACTGTTAG | 69459 |
rs36376219 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ubl7 | Mm_Celera | 9:57917773 | CATCAGTATCTCTGC[C/T]CAGGGCCTCAATATG | 69459 |
rs36385443 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ubl7 | Mm_Celera | 9:57921887 | GGGGAGAGAAGAGAT[A/G]GGAATTTGGAGCATA | 69459 |
rs36512685 | snp | A/G | 0.152778 | 0.230321 | upstream-variant-2KB | Ubl7 | Mm_Celera | 9:57910474 | CATTGTTGCATGTTC[A/G]CGGTGGGCCAGAAAC | 69459 |
rs36615845 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Ubl7 | Mm_Celera | 9:57918096 | ATGCTATGACCTAGA[G/T]TACCCTGAGGATAGT | 69459 |
rs36631932 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ubl7 | Mm_Celera | 9:57928660 | GAAAGGTTTACTTAA[C/T]AGGTTTCTTTGTGAC | 69459 |
rs36683315 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Ubl7 | Mm_Celera | 9:57928120 | GTATAAACAAATATT[G/T]AGAAGGCAGTTTAGT | 69459 |
rs36757255 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ubl7 | Mm_Celera | 9:57919450 | GTTGTTTAGCATAGG[A/G]ACTGACAGTACATTG | 69459 |
rs36780969 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ubl7 | Mm_Celera | 9:57928471 | AAGTGTTGTCTTCAG[C/T]GATAAGGTTTTATTG | 69459 |
rs36818254 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Ubl7 | Mm_Celera | 9:57928607 | GCACTGCTGTTTTGT[A/G]TAATCTATAGCTTCT | 69459 |
rs36848285 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Ubl7 | Mm_Celera | 9:57928246 | GAGCAGGCCTCAAAG[C/G]CAATCATAGAACAGT | 69459 |
rs36857021 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Ubl7 | Mm_Celera | 9:57919915 | ACAGAGACTGTTCTA[G/T]TGTGGTGGTCTGTAT | 69459 |
rs36860306 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Ubl7 | Mm_Celera | 9:57921277 | ACTGAGCCTTTCTGA[C/T]CCTTCTAAGGTCAGA | 69459 |
rs36880817 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ubl7 | Mm_Celera | 9:57924661 | TCAGACAGTTGTAAA[C/T]GTATCAGACAAGTGG | 69459 |
rs36900353 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ubl7 | Mm_Celera | 9:57920140 | TAAGTACAAGAAAAG[A/G]TTTGAAGAAATATGA | 69459 |
rs36935000 | snp | A/G | 0.244898 | 0.249948 | synonymous-codon | Ubl7 | Mm_Celera | 9:57912840 | ATCTGTTCCAGACCC[A/G]GAGCTGATCGGTGAG | 69459 |
rs36956578 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ubl7 | Mm_Celera | 9:57928355 | GGTAAGACCCTTCTC[C/T]TACAGTAGCCTGCAT | 69459 |
rs37035503 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ubl7 | Mm_Celera | 9:57924340 | CTCACTCCTGCCTAT[A/G]TCTGTTTGTCTTCCT | 69459 |
rs37081480 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Ubl7 | Mm_Celera | 9:57918271 | AGAAGTTGCTATTTG[G/T]CATATGGTGAAAGTT | 69459 |
rs37134158 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ubl7 | Mm_Celera | 9:57924677 | GTATCAGACAAGTGG[C/T]ACATCTTCCTGAAAG | 69459 |
rs37219510 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ubl7 | Mm_Celera | 9:57919263 | CAGTTATGGTAATGA[C/T]AGATAGAGCCTGGGT | 69459 |
rs37264428 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ubl7 | Mm_Celera | 9:57928382 | GCATAGAAACTTGTG[A/G]GATTATTAAAAAGCT | 69459 |
rs37363460 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Ubl7 | Mm_Celera | 9:57916581 | ATACACTTTCGTAGT[C/T]CTACAATAACAGGCC | 69459 |
rs37467747 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Ubl7 | Mm_Celera | 9:57925367 | ATCTTTGAACACTAC[A/T]TGGTAAACTGAGTCA | 69459 |
rs37473931 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ubl7 | Mm_Celera | 9:57924532 | AGGAGCCATTATATA[C/T]AGTCGTTCTAAATTT | 69459 |
rs37475553 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Ubl7 | Mm_Celera | 9:57922778 | GGTAACTCCCCTTTT[G/T]ACTTACTTGCCTTTA | 69459 |
rs37476414 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ubl7 | Mm_Celera | 9:57923690 | ATCTGAACTGAGAGA[A/G]GTTTAAGCTGATTGG | 69459 |
rs37604603 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ubl7 | Mm_Celera | 9:57919626 | GCCTTACGGGCCGAC[C/T]GTGGTTACAGCTACA | 69459 |
rs37823573 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Ubl7 | Mm_Celera | 9:57920761 | CATGTGAAGTGTGGC[A/T]CAATGAAGCAGTGTG | 69459 |
rs37846903 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Ubl7 | Mm_Celera | 9:57923571 | GGCCGGGTTGAACTG[A/C]TAGACTTCAAGAAGA | 69459 |
rs37869399 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ubl7 | Mm_Celera | 9:57924845 | CAATGGAAGCTTCAC[A/G]GCACTCAGAGTCACG | 69459 |
rs37984702 | snp | A/C | 0.32 | 0.24 | intron-variant | Ubl7 | Mm_Celera | 9:57927703 | TACATTATTTAACTT[A/C]TTATTATGTGTATGT | 69459 |
rs38122820 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ubl7 | Mm_Celera | 9:57920601 | TGTGCCATTCCTCAC[A/G]CGGTCAGGCTAGAAA | 69459 |
rs38199475 | snp | G/T | 0.165289 | 0.235211 | intron-variant | Ubl7 | Mm_Celera | 9:57919945 | TACAACCCTCCTATA[G/T]AAGCACTCAAATGGA | 69459 |
rs38248517 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Ubl7 | Mm_Celera | 9:57928805 | TGCTTTCATAGAGCC[G/T]ACATTCTTCTTCATT | 69459 |
rs38341023 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Ubl7 | Mm_Celera | 9:57927086 | TCCACTACACCTCAT[G/T]GTAAACACAACTTAA | 69459 |
rs38408270 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ubl7 | Mm_Celera | 9:57923940 | AGATTTATCTGGTAG[C/T]TCTTGGTAGTTCTTG | 69459 |
rs38698755 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ubl7 | Mm_Celera | 9:57928447 | TTATTTCTCTGTTTC[A/G]TGCTACCAAAGTGTT | 69459 |
rs38704086 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ubl7 | GRCm38.p3 | 9:57916613 | AGGAAGGAGGTTACT[C/T]ACTGAAAGCCAGCCT | 69459 |
rs38777151 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ubl7 | Mm_Celera | 9:57928136 | AGAAGGCAGTTTAGT[A/G]CAGTGCCAATTTTTC | 69459 |
rs38803920 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Ubl7 | GRCm38.p3 | 9:57920275 | CACCTAATGGCTCTC[A/C]ATCGTCCTTTGTGGC | 69459 |
rs38829547 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ubl7 | Mm_Celera | 9:57924355 | GTCTGTTTGTCTTCC[C/T]ACCACCTTCTCTTCA | 69459 |
rs39402260 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Ubl7 | GRCm38.p3 | 9:57924886 | TTGTAATGGCAGAAG[A/G]TTGTAAACAGTCAAC | 69459 |
rs39494567 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ubl7 | Mm_Celera | 9:57923998 | TACATGGAGAGTCAG[C/T]GTCTCAGCATTGTAT | 69459 |
rs39859246 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ubl7 | Mm_Celera | 9:57924205 | CATTGCTGAGATGGA[C/T]ACCTGTTTATCTCCA | 69459 |
rs46629730 | snp | C/T | | | intron-variant | Ubl7 | Mm_Celera | 9:57917079 | ACTTTTTTATGTATG[C/T]ATATGTTTATTTATT | 69459 |
rs46990103 | snp | C/T | | | intron-variant | Ubl7 | Mm_Celera | 9:57917221 | AAGCAATTTGATGTT[C/T]CTTCAAAGCACTGCC | 69459 |
rs47166475 | snp | A/G | | | intron-variant | Ubl7 | Mm_Celera | 9:57920410 | TTGGGATCCAGTTGA[A/G]TTGCTTGCTTTGAGA | 69459 |
rs47385487 | snp | A/G | | | intron-variant | Ubl7 | Mm_Celera | 9:57926871 | AAGTCTCTGGGTCAC[A/G]CCTTTCCAGAGCGCA | 69459 |
rs47551599 | snp | A/G | | | intron-variant | Ubl7 | GRCm38.p3 | 9:57926136 | TCCTAGATTAACAGA[A/G]TTTAAGCAGGCCAAG | 69459 |
rs47954041 | snp | A/G | | | intron-variant | Ubl7 | Mm_Celera | 9:57926832 | TGAGAAAGCAAGCAC[A/G]TCAGTAGCAAGGAAT | 69459 |
rs48187129 | snp | C/T | | | intron-variant | Ubl7 | GRCm38.p3 | 9:57928101 | AAAGGAACATAGTAT[C/T]TGTGTATAAACAAAT | 69459 |
rs48679044 | snp | A/T | | | intron-variant | Ubl7 | Mm_Celera | 9:57917022 | TCTTTCCTTTCCTTC[A/T]AGAAACTAGGATTAG | 69459 |
rs48899914 | snp | A/C | | | intron-variant | Ubl7 | Mm_Celera | 9:57920013 | GTGTTAGCTGGTGTG[A/C]TAAGCCATCCTTGTT | 69459 |
rs49108905 | snp | C/T | | | intron-variant | Ubl7 | GRCm38.p3 | 9:57919188 | ATTCTTAGAGGGTGA[C/T]GAGGGAAGGGACTCT | 69459 |
rs49433962 | snp | C/T | | | intron-variant | Ubl7 | Mm_Celera | 9:57927936 | CCAGAGCTTTCACTT[C/T]CACTTCTTCCGAAAT | 69459 |
rs49870439 | snp | A/T | | | intron-variant | Ubl7 | Mm_Celera | 9:57926979 | AAGGTAAAATAAACC[A/T]TTTTCTTCCCAAGTT | 69459 |
rs49994968 | snp | A/G | | | intron-variant | Ubl7 | Mm_Celera | 9:57927117 | GCTAGGTGTGATGAC[A/G]TGTATCTATAATCTT | 69459 |
rs50860114 | snp | C/T | | | intron-variant | Ubl7 | Mm_Celera | 9:57926227 | AGGACATCTATCTTA[C/T]GTCTTATTTTTGAAG | 69459 |
rs51586146 | snp | A/T | | | intron-variant | Ubl7 | GRCm38.p3 | 9:57914880 | TAGATATATATATAT[A/T]TTTTTTTTTACTTAA | 69459 |
rs51774177 | snp | G/T | | | intron-variant | Ubl7 | Mm_Celera | 9:57920468 | TGGATCTTGCCAGTG[G/T]TCCACTGTGTTAAGA | 69459 |
rs52115761 | snp | A/G | | | intron-variant | Ubl7 | Mm_Celera | 9:57916918 | TGTATGTATGTATGT[A/G]TGTATATATATATAT | 69459 |
rs52146160 | snp | A/G | | | intron-variant | Ubl7 | Mm_Celera | 9:57916904 | TATATATATATATAT[A/G]TATGTATGTATGTGT | 69459 |
rs52302037 | snp | A/G | | | intron-variant | Ubl7 | Mm_Celera | 9:57916924 | TATGTATGTGTGTAT[A/G]TATATATATGTATGT | 69459 |
rs52343301 | snp | C/G | | | intron-variant | Ubl7 | GRCm38.p3 | 9:57920923 | AGAGAGAGAGAGAGA[C/G]AGAGAGAGAGAGAGA | 69459 |
rs52499091 | snp | C/G | | | intron-variant | Ubl7 | Mm_Celera | 9:57920789 | GTGGAGAGAGAGAGA[C/G]AGAGAGAGAGAGAGA | 69459 |
rs52586550 | snp | A/T | | | intron-variant | Ubl7 | Mm_Celera | 9:57927272 | CAAAATGAAAATACA[A/T]TAAAAAATAAACAAA | 69459 |
rs211904399 | snp | C/T | | | intron-variant | Ubl7 | Mm_Celera | 9:57929606 | CATCAGTAGCTTTGC[C/T]GTGTGTCTTCTCTTT | 69459 |
rs212079410 | snp | A/G | | | intron-variant | Ubl7 | Mm_Celera | 9:57926228 | GGACATCTATCTTAC[A/G]TCTTATTTTTGAAGT | 69459 |