SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6355273 | snp | A/T | 0.5 | 0 | intron-variant | Usp54 | Mm_Celera | 14:20592931 | aagtttaaggtcaga[A/T]taggctacttaagaA | 78787 |
rs6356835 | snp | A/G | 0.5 | 0 | intron-variant | Usp54 | Mm_Celera | 14:20593293 | cacgcctttaatccc[A/G]gcaccctggagggag | 78787 |
rs13469163 | snp | C/G | | | synonymous-codon, intron-variant | Usp54, 1810062O18Rik | Mm_Celera | 14:20552150 | CCTTGATCCTAAACT[C/G]TACCCTCCCCAACCA | 78787 |
rs13469164 | snp | A/G | | | missense, intron-variant | Usp54, 1810062O18Rik | Mm_Celera | 14:20561269 | CCTCCTCTTTCCATG[A/G]GCTCGGGGCTTCCTG | 78787 |
rs30104213 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Usp54, 1810062O18Rik | GRCm38.p3 | 14:20554530 | CCAGTAGTGAATACC[A/C]AAATTTAAGTATATT | 78787 |
rs30223962 | snp | C/T | 0.5 | 0 | intron-variant | Usp54, 1810062O18Rik | GRCm38.p3 | 14:20554973 | GTTTATCTGTCCCTG[C/T]AGTAGACTAAATGCT | 78787 |
rs30241060 | snp | A/T | 0.5 | 0 | intron-variant | Usp54 | Mm_Celera | 14:20616501 | AATTATGAAAATACA[A/T]TGACAGTAACACTAA | 78787 |
rs30250577 | snp | G/T | 0.465374 | 0.126941 | intron-variant | Usp54, 1810062O18Rik | GRCm38.p3 | 14:20566202 | ATTGCTATTAAGAAG[G/T]CTTTAGAACAACTAA | 78787 |
rs30258551 | snp | A/C/G | 0.492188 | 0.0620098 | intron-variant | Usp54 | GRCm38.p3 | 14:20587536 | TGTCCAGAGGTAGCC[A/C/G]AGGCAGACTCCCCCA | 78787 |
rs30259414 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Usp54 | GRCm38.p3 | 14:20580871 | CTTAAGCAAGCAGAC[A/G]TAGTTCATGCCTTAG | 78787 |
rs30318421 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Usp54, 1810062O18Rik | GRCm38.p3 | 14:20558276 | GGATGTATCAAAAAA[A/T]ATTTTTTAATAAATG | 78787 |
rs30323748 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Usp54 | Mm_Celera | 14:20616304 | AAAAAAAAAAAAAAA[A/C]GAAAAGAAAAGAAAA | 78787 |
rs30352927 | snp | C/G | 0.375 | 0.216506 | intron-variant | Usp54 | GRCm38.p3 | 14:20574389 | GGAGAAGGAGAAGGA[C/G]AAGAACAAGAACAAG | 78787 |
rs30485432 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Usp54 | GRCm38.p3 | 14:20581327 | CTATCTTGTTTCTTT[A/G]TATCCTTCTCAATTA | 78787 |
rs30496677 | snp | G/T | 0.465374 | 0.126941 | intron-variant | Usp54 | GRCm38.p3 | 14:20587758 | CTTGTTCCTTTAACC[G/T]TACTATTCCTCATGG | 78787 |
rs30544939 | snp | A/G | 0.32 | 0.24 | intron-variant | Usp54 | Mm_Celera | 14:20600970 | GCAACCCAGCACTGA[A/G]GAGCTGAAAGAGGGG | 78787 |
rs30588791 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Usp54 | GRCm38.p3 | 14:20600837 | TTAGTTCCCTACAGA[A/G]CCTGAGAGCCTAAGT | 78787 |
rs30689654 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Usp54 | Mm_Celera | 14:20585881 | AGTCACAAAGTATGT[A/C]TGCCTTACCAACACT | 78787 |
rs30689655 | snp | G/T | 0.132653 | 0.220748 | missense, upstream-variant-2KB | Usp54 | GRCm38.p3 | 14:20583354 | TAGCATGTCTTGGTG[G/T]ATGGCAGGAACTGAG | 78787 |
rs30689656 | snp | C/T | 0.132653 | 0.220748 | intron-variant, upstream-variant-2KB | Usp54 | Mm_Celera | 14:20583219 | CAAGTTGGCATTTCT[C/T]TCTTACTGTAATAGA | 78787 |
rs30689657 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Usp54 | Mm_Celera | 14:20581403 | CTTTTTCTTGGGAGA[C/T]TTTCTATGTAGGAAT | 78787 |
rs30689658 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Usp54 | Mm_Celera | 14:20581238 | AGGTAGACTTAAAAA[A/C]ATGACATTGACAATC | 78787 |
rs30689659 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Usp54 | Mm_Celera | 14:20581148 | ATTCAAAACCACGGA[A/G]TGAAACGACCAGGTG | 78787 |
rs30689660 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp54 | Mm_Celera | 14:20580911 | TTCTCAAAACTTTTC[A/G]TTTCAGTAGTTACTC | 78787 |
rs30689661 | snp | A/G | 0.5 | 0 | intron-variant | Usp54 | GRCm38.p3 | 14:20580860 | TCCTCAAAGCCCTTA[A/G]GCAAGCAGACATAGT | 78787 |
rs30689662 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp54 | Mm_Celera | 14:20580135 | CACAAAGACTGGCAC[A/G]TTTTAGGGAACCACT | 78787 |
rs30689663 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Usp54 | Mm_Celera | 14:20578676 | AGGTTGTCAGTAATG[A/G]AATGTGACCATTTTG | 78787 |
rs30690794 | snp | C/G | 0.336735 | 0.234472 | intron-variant | Usp54 | Mm_Celera | 14:20578609 | CTCAAATGCATGAGA[C/G]TTAACAAATTTATTT | 78787 |
rs30690795 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Usp54 | GRCm38.p3 | 14:20578066 | TGAGTTTCATTTTAT[C/T]TTACTGAAGCACTGT | 78787 |
rs30690796 | snp | C/T | 0.32 | 0.24 | intron-variant | Usp54 | Mm_Celera | 14:20577954 | GAGAGCTGGGTAATA[C/T]TTAAAGGCAAAAGAA | 78787 |
rs30690797 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Usp54 | Mm_Celera | 14:20577919 | CCTTGCAAAAACAAG[C/T]AGGCACTGAGCTCCA | 78787 |
rs30690798 | snp | A/G | 0.492188 | 0.0620098 | synonymous-codon | Usp54 | GRCm38.p3 | 14:20576487 | CCTGTAGACATTCAC[A/G]CTGTCAGGCGGGGCA | 78787 |
rs30690799 | snp | A/C | 0.5 | 0 | intron-variant | Usp54 | GRCm38.p3 | 14:20575708 | AGGTTAAGAACACGG[A/C]TTCCACGGCAACTCA | 78787 |
rs30690800 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Usp54, 1810062O18Rik | Mm_Celera | 14:20565916 | TAGTCGGGAAACGCC[A/G]TAGCCAGTAGCAGTT | 78787 |
rs30690801 | snp | A/G | 0.32 | 0.24 | intron-variant | Usp54, 1810062O18Rik | Mm_Celera | 14:20565878 | GGCCATCTGCATGAC[A/G]ACACTAGTTCCTATT | 78787 |
rs30690802 | snp | A/G | 0.32 | 0.24 | intron-variant | Usp54, 1810062O18Rik | Mm_Celera | 14:20565263 | CATGAAAGCCAGGAG[A/G]CCAAACACATTAATT | 78787 |
rs30690803 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Usp54, 1810062O18Rik | Mm_Celera | 14:20564563 | ACAACAACATGAAGG[A/G]TACAATCAGATTCCA | 78787 |
rs30691635 | snp | A/G | 0.124444 | 0.216185 | upstream-variant-2KB | Usp54 | Mm_Celera | 14:20644622 | CCTGAGGACTCAGCT[A/G]TGTGGCAGAGCAAGT | 78787 |
rs30691636 | snp | A/G | 0.124444 | 0.216185 | upstream-variant-2KB | Usp54 | Mm_Celera | 14:20644591 | AAAGAACTAATAAAT[A/G]ATGACCATAGATGGG | 78787 |
rs30691637 | snp | A/G | 0.32 | 0.24 | upstream-variant-2KB | Usp54 | Mm_Celera | 14:20644530 | AAGGAGGTGGATCTT[A/G]GAAGTGTTTGGAAAG | 78787 |
rs30691638 | snp | G/T | 0.32 | 0.24 | upstream-variant-2KB | Usp54 | Mm_Celera | 14:20644468 | TTTGTGCAGTATAAC[G/T]GGGCCTTGATAGAGA | 78787 |
rs30691639 | snp | C/G/T | 0.124444 | 0.216185 | utr-variant-5-prime | Usp54 | Mm_Celera | 14:20643015 | GTGTAGTGGCAGAGT[C/G/T]CGGAGAATCACTACA | 78787 |
rs30691640 | snp | C/T | 0.124444 | 0.216185 | utr-variant-5-prime | Usp54 | Mm_Celera | 14:20641831 | TGCATTCAGTTCTGT[C/T]AAGTAAAAACATATA | 78787 |
rs30691641 | snp | A/G | 0.142012 | 0.225474 | utr-variant-5-prime | Usp54 | Mm_Celera | 14:20641804 | CGAAGCCCTTGAGAA[A/G]TTTTCGTGAGGTGCA | 78787 |
rs30691642 | snp | C/T | 0.32 | 0.24 | utr-variant-5-prime | Usp54 | Mm_Celera | 14:20641569 | GCGAAAAAAGACAGA[C/T]CTAAGGTGTTTAGCT | 78787 |
rs30691643 | snp | A/G | 0.152778 | 0.230321 | utr-variant-5-prime | Usp54 | Mm_Celera | 14:20641204 | GTCTGCTCCCGCCGG[A/G]GACAGTTATTATGGC | 78787 |
rs30691974 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Usp54, 1810062O18Rik | Mm_Celera | 14:20564078 | TTCCTTATTTAGAAC[G/T]TATGCTCGATAGCAG | 78787 |
rs30691975 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Usp54, 1810062O18Rik | GRCm38.p3 | 14:20563333 | AAGGGTATTCAACCC[A/G]TCTATATGAGTGTTC | 78787 |
rs30691976 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Usp54, 1810062O18Rik | Mm_Celera | 14:20563240 | GGAGTGCTTCGAAAC[A/C]CAACCTGTTTTAGGC | 78787 |
rs30691977 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Usp54, 1810062O18Rik | Mm_Celera | 14:20562983 | ACAAAAAAAAAAATA[C/T]ATCCTGAGAGGAAAC | 78787 |
rs30691978 | snp | A/G | 0.32 | 0.24 | intron-variant | Usp54, 1810062O18Rik | Mm_Celera | 14:20562778 | GCTACCCTAGGGTCC[A/G]ATGGGGTAGCTCAGT | 78787 |
rs30691979 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Usp54, 1810062O18Rik | Mm_Celera | 14:20562481 | TATTCTTTACTACTC[A/G]CAAAGTCCCATTCCA | 78787 |
rs30691980 | snp | C/T | 0.444444 | 0.157135 | missense, nc-transcript-variant, downstream-variant-500B | Usp54, 1810062O18Rik | GRCm38.p3 | 14:20562012 | CTGTGGAATGCAGAG[C/T]GATTGACGCTGTCCA | 78787 |
rs30691981 | snp | C/T | 0.124444 | 0.216185 | missense, intron-variant, downstream-variant-500B | Usp54, 1810062O18Rik | Mm_Celera | 14:20561932 | TATCTTCAAGGGCAT[C/T]TAATGGCAGGCATTC | 78787 |
rs30691982 | snp | C/T | 0.32 | 0.24 | missense, intron-variant, downstream-variant-500B | Usp54, 1810062O18Rik | GRCm38.p3 | 14:20561641 | TCTGCATGGGGTCAG[C/T]AGCATGAAGCACAGG | 78787 |
rs30691983 | snp | G/T | 0.32 | 0.24 | synonymous-codon, intron-variant | Usp54, 1810062O18Rik | GRCm38.p3 | 14:20561423 | AGAAGAGCTCTTCCT[G/T]ACACCATTTGGCAAA | 78787 |
rs30692304 | snp | A/G | 0.244898 | 0.249948 | utr-variant-5-prime | Usp54 | Mm_Celera | 14:20641150 | CCCGGGCGAAGGCCA[A/G]CTGTTCTGATGGAGT | 78787 |
rs30692305 | snp | A/G | 0.124444 | 0.216185 | utr-variant-5-prime | Usp54 | Mm_Celera | 14:20641058 | GCCTGGCGACTGACG[A/G]CTGAGGACGTATCGC | 78787 |
rs30692306 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Usp54 | GRCm38.p3 | 14:20640610 | TTTTCTCCCGTTCTG[A/G]GTCCCCTTAACCTCC | 78787 |
rs30692307 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Usp54 | Mm_Celera | 14:20640298 | CAGAGTGTTGGTTCG[C/T]TGGATTATTTCTTTG | 78787 |
rs30692308 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Usp54 | Mm_Celera | 14:20640198 | TTTAGAGCAGCAATC[A/T]ATCACTATCCTACTC | 78787 |
rs30692309 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Usp54 | Mm_Celera | 14:20640080 | ACACCCTCTTCTTTC[A/G]GCTCACAAACGCTCC | 78787 |
rs30692310 | snp | A/T | 0.260355 | 0.249785 | intron-variant | Usp54 | Mm_Celera | 14:20638215 | GTGCAACATACTTGT[A/T]ATCTCAAGGACTTGA | 78787 |
rs30692311 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Usp54 | Mm_Celera | 14:20633892 | CAACATAGCACACCA[C/T]TAAGAATACTTTTTG | 78787 |
rs30692312 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp54 | Mm_Celera | 14:20633722 | AGGGAGGGAGGAAGG[A/G]AAACCCCAAAAGTAT | 78787 |
rs30692313 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Usp54 | Mm_Celera | 14:20632553 | TCTGGCCTTAACCTC[C/T]AGAGTGCTGGGATGT | 78787 |
rs30692864 | snp | C/T | 0.32 | 0.24 | intron-variant | Usp54, 1810062O18Rik | Mm_Celera | 14:20560806 | GACCTTGTTCTCTGG[C/T]TTTCAGTTTTTACAT | 78787 |
rs30692865 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Usp54, 1810062O18Rik | Mm_Celera | 14:20560678 | ATTTCAATTCTGACC[A/G]AGAAAAAAGCAATTG | 78787 |
rs30692866 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Usp54, 1810062O18Rik | Mm_Celera | 14:20560669 | TCCAACCCAATTTCA[A/G]TTCTGACCAAGAAAA | 78787 |
rs30692867 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Usp54, 1810062O18Rik | Mm_Celera | 14:20560313 | CCACCACGCCCGGCT[C/T]ACTATCAACTCTTGA | 78787 |
rs30692868 | snp | C/T | 0.32 | 0.24 | intron-variant | Usp54, 1810062O18Rik | Mm_Celera | 14:20559856 | CTGCTTCCACCTTTA[C/T]GTAGATCATTCGAAC | 78787 |
rs30692869 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp54, 1810062O18Rik | Mm_Celera | 14:20559819 | TAGTGAGACAATCTC[A/G]AAACTGAGCCATCTC | 78787 |
rs30692870 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp54, 1810062O18Rik | Mm_Celera | 14:20557201 | ACATACAGAGAGAGA[A/G]TGCTTAAGTATACTG | 78787 |
rs30692871 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Usp54, 1810062O18Rik | Mm_Celera | 14:20557090 | CCTGCCCTTGACCTA[C/T]ATTTGGTGCATATTT | 78787 |
rs30692872 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Usp54, 1810062O18Rik | Mm_Celera | 14:20557018 | TTAAATTATAATCAA[A/C]TATCAATACTGCTTT | 78787 |
rs30692873 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Usp54, 1810062O18Rik | Mm_Celera | 14:20556666 | TTTCAGAATCAAGCC[C/T]AATACTTGTAATCTA | 78787 |
rs30693124 | snp | G/T | 0.18 | 0.24 | intron-variant | Usp54 | Mm_Celera | 14:20632232 | ATTTCATTTCAAAAT[G/T]CTCTAACAGTGGTAT | 78787 |
rs30693125 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Usp54 | Mm_Celera | 14:20632147 | GTTTTACCATCTTTA[A/C]GTATTTACTGTCATG | 78787 |
rs30693126 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Usp54 | Mm_Celera | 14:20628058 | TACCCTTGTGGACTT[C/T]GAGCTAAGGCAGGGT | 78787 |
rs30693127 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Usp54 | Mm_Celera | 14:20622312 | ACTACACACACAGTC[A/C]ATGATGGCTAAAGGG | 78787 |
rs30693128 | snp | C/T | 0.132653 | 0.220748 | intron-variant, upstream-variant-2KB | Usp54 | Mm_Celera | 14:20620737 | TAATGAAAGAAAACA[C/T]GCAAATGACAAAGAA | 78787 |
rs30693129 | snp | A/G | 0.132653 | 0.220748 | intron-variant, upstream-variant-2KB | Usp54 | Mm_Celera | 14:20620690 | GAGGTACAAAAAGAG[A/G]ACAAAATCTTTAAGC | 78787 |
rs30693130 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Usp54 | Mm_Celera | 14:20616864 | GGAAACTTGTAATAA[C/T]GGTAGCAACTACTCA | 78787 |
rs30693131 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp54 | Mm_Celera | 14:20610617 | CACTCAACTCCACAC[A/G]AAATGCTGGCTTCTA | 78787 |
rs30693132 | snp | A/C/G | 0.124444 | 0.216185 | intron-variant | Usp54 | GRCm38.p3 | 14:20610611 | CAAAAACACTCAACT[A/C/G]CACACGAAATGCTGG | 78787 |
rs30693133 | snp | A/G | 0.32 | 0.24 | intron-variant | Usp54 | Mm_Celera | 14:20610555 | CAGAAAACAGCAAAG[A/G]CAAGAGAGGCAGTTG | 78787 |
rs30693724 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Usp54, 1810062O18Rik | Mm_Celera | 14:20556598 | TGTAAGAACAGTCAG[C/T]TGAAGATCGTCATCC | 78787 |
rs30693725 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp54, 1810062O18Rik | Mm_Celera | 14:20556444 | ACATGGCTTTCTCTC[A/G]TTAAGTAATTAACAT | 78787 |
rs30693726 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Usp54, 1810062O18Rik | Mm_Celera | 14:20556380 | CCTAGGAGGAAAACA[G/T]AAAAGCAAGGTGAAG | 78787 |
rs30693727 | snp | C/T | 0.32 | 0.24 | intron-variant | Usp54, 1810062O18Rik | Mm_Celera | 14:20556123 | GGTGAAACAGCAGCT[C/T]GCACTCCTTGCAGCC | 78787 |
rs30694034 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp54 | Mm_Celera | 14:20610461 | GCAGAAAGGAGTCAC[A/G]GGCTCTGAACGCAGC | 78787 |
rs30694035 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Usp54 | Mm_Celera | 14:20610148 | TCAATACCTGTTGAT[G/T]AATGTAGAACCAGGA | 78787 |
rs30694036 | snp | A/C | 0.32 | 0.24 | intron-variant | Usp54 | Mm_Celera | 14:20609853 | GTTTTATATAGTATC[A/C]GTCATGTATCATATG | 78787 |
rs30694037 | snp | C/G | 0.32 | 0.24 | intron-variant | Usp54 | GRCm38.p3 | 14:20609788 | CAAGTAAAGTATTTA[C/G]TTAGACATTGTATGG | 78787 |
rs30694038 | snp | A/G | 0.32 | 0.24 | intron-variant | Usp54 | Mm_Celera | 14:20609713 | ATTAGCTGGTTGCAT[A/G]ACTCTTCTTCCCTTC | 78787 |
rs30694039 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Usp54 | Mm_Celera | 14:20609680 | GGTGTGTCCAGTGGA[A/G]AGCTGAGGTGCAGGA | 78787 |
rs30694040 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Usp54 | Mm_Celera | 14:20608466 | CATGTCCTCAATATC[C/T]AGTCCAAAAGACAAG | 78787 |
rs30694041 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Usp54 | Mm_Celera | 14:20608185 | AACTTTGAAGATGAA[A/T]GCTGAACTAGTCTAA | 78787 |
rs30694042 | snp | A/G | 0.32 | 0.24 | utr-variant-5-prime | Usp54 | GRCm38.p3 | 14:20607489 | TGACCAATGCAGAGA[A/G]AAGTCTTTAAGTACT | 78787 |
rs30694043 | snp | A/G | 0.32 | 0.24 | utr-variant-5-prime | Usp54 | GRCm38.p3 | 14:20607341 | CCAGAAAATTGTTCC[A/G]ATTAAAGGCTGAGTT | 78787 |