SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs4214369 | snp | C/T | 0.48 | 0.0979796 | upstream-variant-2KB | Usp16 | Mm_Celera | 16:87454226 | CGTTCTCTTTGCCCC[C/T]TCCTTGCCCCCGACT | 74112 |
rs4214370 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Usp16 | Mm_Celera | 16:87455232 | TAGGGCCGGCGGGCG[A/C]CGGGAAGGGTGGCTG | 74112 |
rs4214371 | snp | C/T | 0.5 | 0 | intron-variant | Usp16 | Mm_Celera | 16:87455742 | CAAGTTTCCCTCTGC[C/T]GTCTCAAGGGAAGCT | 74112 |
rs4214372 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Usp16 | Mm_Celera | 16:87456397 | TCTTAAATCTTCATT[A/G]AAACCTGGTGGTGAT | 74112 |
rs4214373 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Usp16 | Mm_Celera | 16:87456721 | TGATATACAAATGAC[A/G]CTATCTGAAGATGAA | 74112 |
rs4214374 | snp | A/G | 0.375 | 0.216506 | intron-variant | Usp16 | Mm_Celera | 16:87456909 | GGCCGCAAGCTCAGT[A/G]TATAGTAGTTGAGGA | 74112 |
rs4214375 | snp | A/G | 0.499055 | 0.0217186 | intron-variant | Usp16 | Mm_Celera | 16:87466823 | AATAGGATGTGAGAA[A/G]TGATCTAGCCATATG | 74112 |
rs4214376 | snp | C/T | 0.32 | 0.24 | intron-variant | Usp16 | Mm_Celera | 16:87467408 | TTTTGTGTTGGTCAT[C/T]TACTGCTGGGCATGG | 74112 |
rs4214377 | snp | A/C | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Usp16 | Mm_Celera | 16:87468581 | GCCCAGAGACAGCAC[A/C]ACCCACAAGGGGACC | 74112 |
rs4214378 | snp | A/G | 0.5 | 0 | missense, utr-variant-5-prime, upstream-variant-2KB | Usp16 | GRCm38.p3 | 16:87469747 | AAAATGAACAAGAGA[A/G]AGAGAAATCGGAAAA | 74112 |
rs4214379 | snp | C/T | 0.46281 | 0.131194 | intron-variant, upstream-variant-2KB | Usp16 | Mm_Celera | 16:87469918 | GTTGATTTTTATCTT[C/T]CCTGTGTGAATTCTG | 74112 |
rs4214380 | snp | C/T | 0.471655 | 0.115624 | intron-variant | Usp16 | Mm_Celera | 16:87471616 | CATATTGGATGTTTA[C/T]ATTGGTCAGCTCTGT | 74112 |
rs4214381 | snp | C/T | 0.46281 | 0.131194 | intron-variant | Usp16 | Mm_Celera | 16:87471709 | CTTTATTCCCATTTG[C/T]AGGAACCTTTAGAAG | 74112 |
rs4214382 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Usp16 | Mm_Celera | 16:87477483 | CCAGCCCAACCCTGA[A/C]ACAGCAGGACAGGAA | 74112 |
rs4214383 | snp | C/T | 0.5 | 0 | intron-variant | Usp16 | Mm_Celera | 16:87480489 | GTGTCTGGAATTCAA[C/T]CTAGGACTTTGTACA | 74112 |
rs4214384 | snp | C/T | 0.453686 | 0.144955 | intron-variant | Usp16 | Mm_Celera | 16:87481483 | GAACTTAAAAATCTC[C/T]GACCTAATCTGGTAT | 74112 |
rs4214385 | snp | C/T | 0.32 | 0.24 | intron-variant | Usp16 | Mm_Celera | 16:87482122 | CTGGCTGTCCTGGAA[C/T]TCACTTTGTAGACCA | 74112 |
rs4214386 | snp | G/T | 0.375 | 0.216506 | intron-variant | Usp16 | Mm_Celera | 16:87482198 | GCTGGGATTAAAGGC[G/T]CGCGCCACCACGCCC | 74112 |
rs4214387 | snp | A/G | 0.499055 | 0.0217186 | downstream-variant-500B, synonymous-codon | Cct8, Usp16 | Mm_Celera | 16:87483201 | ACTGAACTCACAAGC[A/G]TATCTCCTATTTTAT | 74112 |
rs13462631 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon, utr-variant-5-prime | Usp16 | Mm_Celera | 16:87472099 | AACACGTTTTAAAGG[A/G]TACCAGCAACAAGAC | 74112 |
rs13462632 | snp | A/G | | | missense | Usp16 | Mm_Celera | 16:87479444 | GCTCCTGAATGTCCT[A/G]GGGATTTCAATGGTG | 74112 |
rs13462633 | snp | C/T | | | missense | Usp16 | Mm_Celera | 16:87479535 | ATTTGAATGCTGCTG[C/T]TGATCCTGATGAAAT | 74112 |
rs13462634 | snp | A/G | | | missense | Usp16 | Mm_Celera | 16:87479685 | GTTCCATTCAACATT[A/G]CTTATATCAGTTCAC | 74112 |
rs13473679 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime, intron-variant, downstream-variant-500B | Cct8, Usp16 | Mm_Celera | 16:87483975 | TGAGGAACTTGTCAT[C/T]GGTTAAGAGTTGTGT | 74112 |
rs45632812 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Usp16 | Mm_Celera | 16:87466114 | AGAGTCAGGTTGCAG[A/G]ATTTTGAAGCAAGCA | 74112 |
rs45641466 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon | Usp16 | Mm_Celera | 16:87476827 | AAGGAGCGATCTTCC[A/G]TCAGGGACAAGCAAG | 74112 |
rs45726497 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp16 | Mm_Celera | 16:87472856 | TCCTGAAGTGGTGGT[A/G]TGCCCTAAGAAGCGG | 74112 |
rs45760528 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp16 | Mm_Celera | 16:87478370 | AGGCAGTCTTGGAGT[A/G]TGTCCTTTTGTGATT | 74112 |
rs45814863 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Usp16 | Mm_Celera | 16:87478500 | GACGTGAAAGTTTCA[C/T]ACTTCTAGACGGTGT | 74112 |
rs45873321 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Usp16 | Mm_Celera | 16:87462622 | CTACTGTGTGTCATC[A/T]GCCTCCTGGTATGGT | 74112 |
rs45889717 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Usp16 | Mm_Celera | 16:87474754 | GCAAGGAGTGTGCCT[C/T]TGCCAGGGCTATTTA | 74112 |
rs45954910 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Usp16 | Mm_Celera | 16:87482542 | GGGGTTTTAAAGTAC[A/C]ACCTAAATGTTAGCC | 74112 |
rs45982691 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Usp16 | Mm_Celera | 16:87460416 | ATCTCTGTTTATTGA[A/G]CAGGAAGCCAGTTGC | 74112 |
rs45983513 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Usp16 | Mm_Celera | 16:87471967 | GCAGCAGTTTGTGTG[A/G]TAATGAAATCTACCT | 74112 |
rs46028003 | snp | C/T | 0.32 | 0.24 | intron-variant | Usp16 | Mm_Celera | 16:87472869 | GTGTGCCCTAAGAAG[C/T]GGTGTTGAATAGGCT | 74112 |
rs46097695 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Usp16 | Mm_Celera | 16:87462641 | TCCTGGTATGGTTGA[C/T]GTACTAAAGCTCAGG | 74112 |
rs46196120 | snp | A/G | 0.124444 | 0.216185 | missense | Usp16 | Mm_Celera | 16:87479211 | CGGAAGACAATGAAC[A/G]TGAAGCTGACACAGC | 74112 |
rs46241312 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Usp16 | Mm_Celera | 16:87464120 | TACTTAAAAAGACCA[C/T]CATGTGTTAGGAACA | 74112 |
rs46249808 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime, intron-variant, downstream-variant-500B | Cct8, Usp16 | GRCm38.p3 | 16:87483552 | TTGTTATTTACTGTA[C/T]CCACTACTGGCAACA | 74112 |
rs46288692 | snp | A/T | 0.132653 | 0.220748 | upstream-variant-2KB | Usp16 | Mm_Celera | 16:87454207 | TCATCTGGGTCCTGA[A/T]TCCCGTTCTCTTTGC | 74112 |
rs46323175 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Usp16 | Mm_Celera | 16:87460892 | GTCATTCAGTAGTTA[C/G]TTGCTCTTACATACT | 74112 |
rs46448765 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime, intron-variant, downstream-variant-500B | Cct8, Usp16 | GRCm38.p3 | 16:87483651 | CGCATAAACTCTGGC[C/T]CAGCCACTATTGAAA | 74112 |
rs46515382 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Usp16 | Mm_Celera | 16:87473865 | ACCTCCTAAGAGGTA[A/T]CTGTGCCTCCTCAGC | 74112 |
rs46545878 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp16 | Mm_Celera | 16:87471264 | TGTGACTCAAGTGCT[A/G]TAGCCAAATGCATTT | 74112 |
rs46550550 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Usp16 | Mm_Celera | 16:87476177 | ATTTACAAAAGGACA[C/T]CTATACAACATGCTA | 74112 |
rs46606944 | snp | G/T | 0.231111 | 0.249285 | missense | Usp16 | Mm_Celera | 16:87479231 | GCTGACACAGCACTT[G/T]CGGGAGAAGTGGAAG | 74112 |
rs46628235 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Usp16 | Mm_Celera | 16:87463767 | GCTCTTGTCTAGTTG[C/T]TTCCACAGTCCCACT | 74112 |
rs46638003 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Usp16 | Mm_Celera | 16:87475228 | TGTTCTTAACCGCCC[C/T]CTTCAAAGTCTCTTA | 74112 |
rs46716273 | snp | C/T | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Usp16 | Mm_Celera | 16:87469208 | TTTCTAATGGTTAGG[C/T]TATTAGCTGCTTCCT | 74112 |
rs46746719 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB | Usp16 | Mm_Celera | 16:87454069 | ACATGATTCTCCATT[A/G]ATATACACTCGCGGT | 74112 |
rs46776877 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp16 | Mm_Celera | 16:87481110 | AAGTTTGTCAAAGTG[A/G]AGAAATTTAGACAGT | 74112 |
rs46813876 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Usp16 | Mm_Celera | 16:87463454 | TTAAAAATTGATGCA[A/G]TACCGTGGCTAGACT | 74112 |
rs46834532 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Usp16 | Mm_Celera | 16:87473972 | TATACACTTCATGTA[A/T]TTTGAAAATTATGTG | 74112 |
rs47043655 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Usp16 | Mm_Celera | 16:87466847 | CCATATGTGATAAAG[A/G]GCCTGGACTAAGGTC | 74112 |
rs47056955 | snp | C/G | 0.375 | 0.216506 | intron-variant | Usp16 | Mm_Celera | 16:87459895 | TCGGGTCCTCAGTCT[C/G]GCACAGCAGGTTGGC | 74112 |
rs47068795 | snp | A/G | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Usp16 | Mm_Celera | 16:87470057 | CATCAGGGAAACACA[A/G]GGTAGCCTGGTTCAG | 74112 |
rs47101892 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Usp16 | Mm_Celera | 16:87457546 | GGTTTTATAGAGACG[C/T]CCTGCCTATCCTCAG | 74112 |
rs47154578 | snp | C/T | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Usp16 | Mm_Celera | 16:87470115 | AAGTGATGAGAGTTA[C/T]TGCTGGGATTATTTC | 74112 |
rs47362232 | snp | A/G | 0.32 | 0.24 | intron-variant | Usp16 | Mm_Celera | 16:87480845 | TTAGAGCTTTAGGTC[A/G]TCCTTCTATAACAGA | 74112 |
rs47424621 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Usp16 | Mm_Celera | 16:87477637 | TCAAGACAGTCACCA[A/T]CGGTCTGAAAGGACA | 74112 |
rs47452927 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp16 | Mm_Celera | 16:87465311 | GTTGTGTGTGCAGAG[A/G]CCCAGCAGTGCCTCC | 74112 |
rs47506675 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Usp16 | Mm_Celera | 16:87477746 | GGTCAAGTTCTCGGG[C/T]TTTTTTTCCTCTAAG | 74112 |
rs47550444 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Usp16 | Mm_Celera | 16:87464551 | GATGTGCCACAGTGG[A/C]GGTCAGAAGACAGAG | 74112 |
rs47676738 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp16 | Mm_Celera | 16:87477743 | GTAGGTCAAGTTCTC[A/G]GGCTTTTTTTCCTCT | 74112 |
rs47780274 | snp | C/G | 0.231111 | 0.249285 | downstream-variant-500B, missense | Cct8, Usp16 | Mm_Celera | 16:87482980 | ACTGCAAGCTGTCAC[C/G]TCTCCAATCTTGTTC | 74112 |
rs47847183 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Usp16 | Mm_Celera | 16:87471551 | CCACTGAGCTGTTAG[C/G]TGCCCAGAGCTGAAG | 74112 |
rs47848765 | snp | A/G | 0.32 | 0.24 | intron-variant | Usp16 | Mm_Celera | 16:87481323 | ATATTACTACAACTT[A/G]GAAATTCTCCAGGAT | 74112 |
rs47886574 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB | Usp16 | Mm_Celera | 16:87454139 | AGGCTCCCTCAGTCC[C/T]GGTTCACAAGTACAC | 74112 |
rs48043790 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Usp16 | Mm_Celera | 16:87462470 | AGGTTGTAGTTTTCT[C/G]CAAGGCAGCTCCCTT | 74112 |
rs48051604 | snp | A/G | | | missense | Usp16 | Mm_Celera | 16:87461986 | TGTGCAGACACCTTA[A/G]AAAAGGGTTGGAACA | 74112 |
rs48092111 | snp | A/T | 0.32 | 0.24 | intron-variant | Usp16 | Mm_Celera | 16:87474195 | TCAGTACTGGCTGTC[A/T]TCAGATGTTAGCGCT | 74112 |
rs48149036 | snp | C/T | 0.32 | 0.24 | intron-variant | Usp16 | Mm_Celera | 16:87461246 | CTGTAGTGTGTGTTA[C/T]GGAAGGAATGCAGAG | 74112 |
rs48161285 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime, intron-variant, downstream-variant-500B | Cct8, Usp16 | GRCm38.p3 | 16:87483598 | CTAGTGCTGAGATTA[A/G]GATTGGGAGCAATGT | 74112 |
rs48166878 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp16 | Mm_Celera | 16:87472241 | CCAGTCCCAGAGGCC[A/G]CTGTGCTTTTAAACA | 74112 |
rs48171831 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Usp16 | Mm_Celera | 16:87478910 | ACTACTATTTCCACA[G/T]TAGTCCAATGTAATG | 74112 |
rs48305780 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Usp16 | Mm_Celera | 16:87464708 | TGGTGAGGTTCTGGC[A/G]TTGAGGCTGTGATTG | 74112 |
rs48360020 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon | Usp16 | Mm_Celera | 16:87466337 | TAGAAAACAAGCTGG[C/T]GTAAGAACTTCAAAA | 74112 |
rs48369222 | snp | C/T | 0.32 | 0.24 | synonymous-codon | Usp16 | Mm_Celera | 16:87479677 | TGATGAGTGTTCCAT[C/T]CAACATTGCTTATAT | 74112 |
rs48387595 | snp | G/T | 0.32 | 0.24 | intron-variant | Usp16 | Mm_Celera | 16:87464628 | CGCTAGCTATCTTTT[G/T]GAAGTTATAAGGATG | 74112 |
rs48445205 | snp | C/T | 0.32 | 0.24 | intron-variant | Usp16 | Mm_Celera | 16:87464573 | AAGACAGAGGGAATA[C/T]GCTCTCTCTAGTAGG | 74112 |
rs48619885 | snp | G/T | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Usp16 | Mm_Celera | 16:87469630 | TAACATTTGGCATGG[G/T]TATATTCTGTACTTT | 74112 |
rs48704635 | snp | G/T | 0.32 | 0.24 | intron-variant | Usp16 | Mm_Celera | 16:87464224 | TCTGACGGATGTGGC[G/T]GATTGGAGTGTTTGT | 74112 |
rs48724201 | snp | A/G | 0.244898 | 0.249948 | intron-variant, upstream-variant-2KB | Usp16 | Mm_Celera | 16:87469598 | AAAAGTTTTATTGTG[A/G]ATTTATAGATGTCAC | 74112 |
rs48837218 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Usp16 | Mm_Celera | 16:87480407 | TTTCTTATGAAGGGA[A/G]ATATGCCAAGTACCT | 74112 |
rs48865359 | snp | C/G | 0.231111 | 0.249285 | upstream-variant-2KB | Usp16 | Mm_Celera | 16:87454366 | CGATGCCTTTGAGTA[C/G]TTTTTCTCTTATTCA | 74112 |
rs49069264 | snp | A/T | 0.32 | 0.24 | intron-variant | Usp16 | Mm_Celera | 16:87464913 | TGAATCTGCTGAAAG[A/T]GTTTAAGAGCGAGAA | 74112 |
rs49080292 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Usp16 | Mm_Celera | 16:87463961 | ACTCATGGAATAGCA[C/T]GAACCAACTTCTGCA | 74112 |
rs49475957 | snp | C/T | 0.32 | 0.24 | intron-variant | Usp16 | Mm_Celera | 16:87478968 | AAGAATTTTTTTGTC[C/T]TAATTTATTTGAACT | 74112 |
rs49664769 | snp | C/T | 0.345679 | 0.230967 | upstream-variant-2KB | Usp16 | Mm_Celera | 16:87454266 | ACTTTTTTTTTTTTT[C/T]AATCGTGCTATGTCC | 74112 |
rs49670094 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Usp16 | Mm_Celera | 16:87465011 | CTAGCACCTCCTGTG[C/T]CTTTCCTTGTAGAGT | 74112 |
rs49693651 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Usp16 | Mm_Celera | 16:87472558 | AACACTTTTGTTAAT[C/T]ACCAGGATATATAGT | 74112 |
rs49836675 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | Usp16 | Mm_Celera | 16:87454899 | CTCCACAGTTAACAC[C/T]GCAGTGAACACGTGG | 74112 |
rs49922577 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Usp16 | Mm_Celera | 16:87473495 | TAGTTTGACTTATCC[G/T]TAGCTGGTTATTAAT | 74112 |
rs49933651 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Usp16 | Mm_Celera | 16:87474406 | ATTGTGTTAATTTTG[C/T]TCTCAGTGGTAGACT | 74112 |
rs49948599 | snp | A/C/G | 0.124444 | 0.216185 | intron-variant | Usp16 | GRCm38.p3 | 16:87476435 | TTTCATATTTCCTCA[A/C/G]CCTGTGATGATTGTT | 74112 |
rs50068623 | snp | A/G | 0.32 | 0.24 | synonymous-codon | Usp16 | Mm_Celera | 16:87458732 | AGACACGGTGGCCTC[A/G]GAGTCTGCAGGTATG | 74112 |
rs50139393 | snp | C/T | 0.375 | 0.216506 | intron-variant | Usp16 | Mm_Celera | 16:87455765 | GGGAAGCTGCAGTCC[C/T]TAAACCAGATCTTCT | 74112 |
rs50240858 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Usp16 | Mm_Celera | 16:87466864 | CCTGGACTAAGGTCA[C/T]TAAAGGTCAAAGGCT | 74112 |
rs50258199 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Usp16 | Mm_Celera | 16:87476202 | ATGCTATGGCATGCA[G/T]CCAGTAACACTCACT | 74112 |
rs50405771 | snp | A/G | 0.375 | 0.216506 | intron-variant | Usp16 | Mm_Celera | 16:87461087 | CAAAAGTTTTGCATC[A/G]TTAAAGTTTTTTCCT | 74112 |