SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs4230910 | snp | A/G | 0.40625 | 0.270633 | intron-variant | Pacsin2 | Mm_Celera | 15:83398339 | tagagaatgagggaa[A/G]ccacagtcaggtgct | 23970 |
rs4230911 | snp | C/G | 0.21875 | 0.248039 | intron-variant | Pacsin2 | Mm_Celera | 15:83398373 | gacagtctgaagcag[C/G]cccacatcctacacc | 23970 |
rs4230912 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Pacsin2 | Mm_Celera | 15:83398381 | gaagcagccccacat[C/T]ctacacctgggatta | 23970 |
rs4230913 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Pacsin2 | Mm_Celera | 15:83398406 | ggattaaagtgaaaa[C/T]atagatagtatttct | 23970 |
rs4230914 | snp | A/C | 0.21875 | 0.248039 | intron-variant | Pacsin2 | Mm_Celera | 15:83398438 | tgttttttaaagaaa[A/C]taaaattctcactac | 23970 |
rs4230915 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Pacsin2 | Mm_Celera | 15:83398454 | taaaattctcactac[A/G]GCCCGAAACTGCTGA | 23970 |
rs4230916 | snp | A/C | 0.21875 | 0.248039 | intron-variant | Pacsin2 | Mm_Celera | 15:83398460 | tctcactacGGCCCG[A/C]AACTGCTGAATATTT | 23970 |
rs4230917 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Pacsin2 | Mm_Celera | 15:83398462 | tcactacGGCCCGAA[A/G]CTGCTGAATATTTCA | 23970 |
rs6204958 | snp | G/T | 0.5 | 0 | intron-variant | Pacsin2 | Mm_Celera | 15:83446912 | GGAGAGCTACTGACT[G/T]GTGGGAACGACGGCA | 23970 |
rs31622312 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Pacsin2 | Mm_Celera | 15:83380347 | GGATGAGGGGCTGCC[A/G]GGTGCAGAACACTAC | 23970 |
rs31627964 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Pacsin2 | Mm_Celera | 15:83395216 | GCATAAACCATGCAC[A/T]GCACCACTCCTCTGA | 23970 |
rs31654048 | snp | C/T | 0.375 | 0.216506 | intron-variant | Pacsin2 | Mm_Celera | 15:83384325 | CAGCCCAGGCTCTGT[C/T]TACTGTCAGGCCAGA | 23970 |
rs31705776 | snp | A/C | 0.408163 | 0.193609 | intron-variant | Pacsin2 | Mm_Celera | 15:83380845 | AGCTCCCCATTCTCG[A/C]TGACTTTGGAGGGTC | 23970 |
rs31705778 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Pacsin2 | Mm_Celera | 15:83381048 | AGAGCCTCTAAAGCA[C/T]AGTAGCTGAGCAGGA | 23970 |
rs31705780 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pacsin2 | Mm_Celera | 15:83381169 | TATCTAAGCATGGAG[A/G]CCTCTACAGCATACA | 23970 |
rs31705782 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Pacsin2 | Mm_Celera | 15:83382015 | TGGCCCCTGCTCTCC[A/G]GTTTCCCAGCAAACT | 23970 |
rs31706574 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Pacsin2 | Mm_Celera | 15:83382065 | TAAAGGTTATGGTGG[C/T]TGGCACCCATATAAC | 23970 |
rs31706576 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Pacsin2 | Mm_Celera | 15:83382854 | AATGTCCTCAAAGGG[C/T]TTCTGTTTTCCCAAC | 23970 |
rs31706578 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Pacsin2 | Mm_Celera | 15:83382882 | AACAAGAAGCTGTCA[C/T]CAACTGTTGAAGTAC | 23970 |
rs31706580 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Pacsin2 | Mm_Celera | 15:83383330 | CTACAGTCTTGGGCC[A/G]TGGATCTCAGCCCAA | 23970 |
rs31706582 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pacsin2 | Mm_Celera | 15:83383596 | AAGCTTGGTGATCCA[C/T]GAGTTAGTCACAAAA | 23970 |
rs31707234 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Pacsin2 | Mm_Celera | 15:83383766 | GAGCCCACAGACTCC[A/G]TGACTTCCTGGAGGG | 23970 |
rs31707236 | snp | A/G | 0.304688 | 0.243945 | intron-variant | Pacsin2 | Mm_Celera | 15:83383768 | GCCCACAGACTCCGT[A/G]ACTTCCTGGAGGGAG | 23970 |
rs31707238 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pacsin2 | Mm_Celera | 15:83383795 | GGAGAGCCCTGGCCA[A/G]GCTTTTCCACAGTTC | 23970 |
rs31707240 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Pacsin2 | Mm_Celera | 15:83383830 | TGTTGGTATAGCAGG[C/T]GCTCTGAAGGAGGCA | 23970 |
rs31707242 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pacsin2 | Mm_Celera | 15:83384479 | AAGGCTGGTGGTACT[C/T]TTGGCCACTACCTTC | 23970 |
rs31707854 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Pacsin2, LOC105246001 | Mm_Celera | 15:83385172 | ATTCCTCAAAGCAAC[A/G]GCACAGCAGCCCCTG | 23970 |
rs31707856 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Pacsin2, LOC105246001 | Mm_Celera | 15:83385691 | ATACAACAGCTGAAG[A/G]ATGTGAGCTCTGCTG | 23970 |
rs31707858 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Pacsin2, LOC105246001 | Mm_Celera | 15:83385763 | AGAGTGGCCCAGTGA[C/T]CAGATGTCCAGGAAG | 23970 |
rs31707860 | snp | A/G | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Pacsin2, LOC105246001 | Mm_Celera | 15:83386167 | GTGGCTGCTTCCATC[A/G]TCTTAAAGAGACAAG | 23970 |
rs31708324 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pacsin2, LOC105246001 | Mm_Celera | 15:83386959 | ACCCCAGTATTCAGA[C/T]GGGCTACTGATTGGC | 23970 |
rs31708326 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pacsin2, LOC105246001 | Mm_Celera | 15:83386974 | TGGGCTACTGATTGG[C/T]TTATAAGGGCTCTAA | 23970 |
rs31708328 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pacsin2, LOC105246001 | Mm_Celera | 15:83387685 | AATGTCTCTTTCAGT[A/G]TTCATCAGAGAGGAG | 23970 |
rs31708330 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pacsin2, LOC105246001 | Mm_Celera | 15:83387832 | ATTCCTGCGGTTCTA[A/G]CAATGCCTTCTGGTG | 23970 |
rs31708332 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Pacsin2, LOC105246001 | Mm_Celera | 15:83387899 | ACTGCTATCTAGCAC[A/G]GAGGCCCAGATCCCT | 23970 |
rs31708634 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Pacsin2, LOC105246001 | Mm_Celera | 15:83388440 | GTTCTGACGAAGCCA[A/T]GTTCGTGTCATCTCA | 23970 |
rs31708636 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon, intron-variant | Pacsin2, LOC105246001 | Mm_Celera | 15:83388638 | CTTCTCCTCTTTGCA[C/T]GCTGTGTGGTGCGCC | 23970 |
rs31708638 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pacsin2, LOC105246001 | Mm_Celera | 15:83388699 | CTTTCTCAGTGTAGC[A/G]GGTTGCAAGTTCAGA | 23970 |
rs31708640 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pacsin2, LOC105246001 | Mm_Celera | 15:83389330 | TTCCCAAGGACTTGT[A/G]TGACAAAGCATGATA | 23970 |
rs31708642 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Pacsin2, LOC105246001 | Mm_Celera | 15:83389653 | CCAAGTATCAGCAGC[A/G]GTGCCTGGCTCCCTG | 23970 |
rs31708805 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Pacsin2 | Mm_Celera | 15:83399167 | TCCAGGGCATCTCCT[C/G]AAAGACAGCAATGAC | 23970 |
rs31708807 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Pacsin2 | Mm_Celera | 15:83399260 | CTTTATTAAACGTGA[C/G]CCACTTATAGAGAGG | 23970 |
rs31708809 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pacsin2 | Mm_Celera | 15:83399629 | ACTCCTCAGCTTCCA[C/T]ACTGCAAGAAGGCAA | 23970 |
rs31708811 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Pacsin2 | Mm_Celera | 15:83399692 | GACCCCTTGCTGCAG[C/T]CTACAAAATCTTTGG | 23970 |
rs31708813 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Pacsin2 | Mm_Celera | 15:83399725 | ACATCCAGGGCTTGA[A/C]TATTTTATCACAAGC | 23970 |
rs31708814 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Pacsin2, LOC105246001 | Mm_Celera | 15:83390160 | AGGAAAAAGATGATT[G/T]TTGAACTAATCCTTT | 23970 |
rs31708816 | snp | C/T | 0.18 | 0.24 | intron-variant | Pacsin2, LOC105246001 | Mm_Celera | 15:83390378 | CCTCCCTGAGAGACA[C/T]ACACACTAGGGTCAG | 23970 |
rs31708818 | snp | A/C | 0.132653 | 0.220748 | intron-variant, nc-transcript-variant | Pacsin2, LOC105246001 | Mm_Celera | 15:83391752 | CTCAAGGTGAGCTTA[A/C]CTTTATTCACTCCCA | 23970 |
rs31708820 | snp | C/T | 0.132653 | 0.220748 | intron-variant, nc-transcript-variant | Pacsin2, LOC105246001 | Mm_Celera | 15:83391760 | GAGCTTACCTTTATT[C/T]ACTCCCATGAGCAGT | 23970 |
rs31708822 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon, downstream-variant-500B | Pacsin2, LOC105246001 | Mm_Celera | 15:83392565 | TGCATACGCCTTCTC[A/G]ATGCGTGCCCGCTCA | 23970 |
rs31708880 | snp | C/T | 0.124444 | 0.216185 | downstream-variant-500B | Pacsin2 | Mm_Celera | 15:83375119 | TGAGAAAGGACCGTG[C/T]AGGAGTGGTCATTTC | 23970 |
rs31708882 | snp | C/T | 0.124444 | 0.216185 | downstream-variant-500B | Pacsin2 | Mm_Celera | 15:83375137 | GAGTGGTCATTTCAT[C/T]CTACTTCTAGCCCCC | 23970 |
rs31708905 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Pacsin2 | Mm_Celera | 15:83400249 | GCCCTAAGATGGCCC[A/G]TGGCTGAACTTACGC | 23970 |
rs31708907 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Pacsin2 | Mm_Celera | 15:83400468 | GAAAGCAATTTACTG[C/T]TCAGCAAAGGAGAGG | 23970 |
rs31708909 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pacsin2 | Mm_Celera | 15:83400769 | ACAGCCTTCTCGCTT[A/G]GAACCCAGGACAGAA | 23970 |
rs31708911 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Pacsin2 | Mm_Celera | 15:83400872 | CAGTTTTTCAGACAC[A/G]GTAACTCAGCAAACA | 23970 |
rs31708913 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Pacsin2 | Mm_Celera | 15:83401161 | AGAATGGAAACAAAG[G/T]TGCAGAGTTCTTTCC | 23970 |
rs31709055 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pacsin2 | Mm_Celera | 15:83401178 | GCAGAGTTCTTTCCA[C/T]GAGGGTAAAATATGG | 23970 |
rs31709057 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pacsin2 | Mm_Celera | 15:83401190 | CCATGAGGGTAAAAT[A/G]TGGTTAAGAGTTTAC | 23970 |
rs31709059 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Pacsin2 | Mm_Celera | 15:83401225 | ATGGCTGGAGTCAAA[A/G]CTCAAGTGTCAGGAC | 23970 |
rs31709061 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Pacsin2 | Mm_Celera | 15:83401267 | ATGCAGGAGGTGCAG[A/G]GTTCCATTCCTAGTG | 23970 |
rs31709063 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pacsin2 | Mm_Celera | 15:83401437 | ATGCTCTATCAAGAT[C/T]CAGGCCCTTTGTACA | 23970 |
rs31709074 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon, downstream-variant-500B | Pacsin2, LOC105246001 | Mm_Celera | 15:83392571 | CGCCTTCTCGATGCG[C/T]GCCCGCTCATGCAGA | 23970 |
rs31709075 | snp | A/G | 0.142012 | 0.225474 | intron-variant, downstream-variant-500B | Pacsin2, LOC105246001 | Mm_Celera | 15:83392765 | TGCGGCAGAGCCACA[A/G]GTCTGCAAGGTCAGG | 23970 |
rs31709077 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pacsin2 | Mm_Celera | 15:83394001 | ACACATCCTATCACT[A/G]TAAGCTGCATCACAA | 23970 |
rs31709079 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Pacsin2 | Mm_Celera | 15:83394109 | TTAGTGTTCCCATCT[C/T]ATGAAGAGTTATGAC | 23970 |
rs31709081 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pacsin2 | Mm_Celera | 15:83394462 | GCTGGCTTGGAAGAC[A/G]CAAGGAATGACGGAC | 23970 |
rs31709083 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pacsin2 | Mm_Celera | 15:83394597 | GGCCTCTTTCTTCCA[C/T]CACATTCCCGAGGAA | 23970 |
rs31709084 | snp | C/T | 0.231111 | 0.249285 | downstream-variant-500B | Pacsin2 | GRCm38.p3 | 15:83375238 | CAGCTTCTAAAACCT[C/T]TTTTTCTATTAACTC | 23970 |
rs31709086 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime, downstream-variant-500B | Pacsin2 | Mm_Celera | 15:83375799 | GAGGTTCTTTGTGCG[A/G]GCAGGACCAGCTGGG | 23970 |
rs31709088 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime, downstream-variant-500B | Pacsin2 | Mm_Celera | 15:83376114 | TGAGGGTGGATGCAA[A/G]GCAAAGGGACTGTCA | 23970 |
rs31709090 | snp | A/T | 0.124444 | 0.216185 | utr-variant-3-prime | Pacsin2 | Mm_Celera | 15:83376599 | ATGAGCTTGGAGCCC[A/T]GGCCAATGAGAATCA | 23970 |
rs31709092 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pacsin2 | Mm_Celera | 15:83377848 | GAAGGATCCACAGAA[A/G]GTCTCCAGGGCAGAG | 23970 |
rs31709154 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pacsin2 | Mm_Celera | 15:83378703 | GTAACTGACAGCACA[C/T]GGGATGCCTACAAAG | 23970 |
rs31709156 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Pacsin2 | Mm_Celera | 15:83378738 | TAACAGTGGGTGACC[A/G]ACAGTGAAGGAAGGG | 23970 |
rs31709158 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Pacsin2 | Mm_Celera | 15:83379349 | GAGAAGCTGCAGGCT[A/G]CGAATATCCCAGAGT | 23970 |
rs31709160 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Pacsin2 | Mm_Celera | 15:83379538 | AGAGGCCCGACACTG[C/T]CCCACCAGGTCTGGA | 23970 |
rs31709162 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Pacsin2 | Mm_Celera | 15:83380346 | GGGATGAGGGGCTGC[C/T]GGGTGCAGAACACTA | 23970 |
rs31709175 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Pacsin2 | Mm_Celera | 15:83394889 | GAAATGAGCTGTGTC[C/T]GCCTCTGACACTAGC | 23970 |
rs31709177 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pacsin2 | Mm_Celera | 15:83394976 | GCAACTCCTTCTTGC[C/T]ACCCacaaatattta | 23970 |
rs31709179 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Pacsin2 | Mm_Celera | 15:83395002 | ATTTAATAAACATCT[C/G]CTGTGTGCCAAGGGC | 23970 |
rs31709181 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pacsin2 | Mm_Celera | 15:83395015 | ctcctgtgtgccaag[A/G]gctatgtaaggcAGA | 23970 |
rs31709183 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pacsin2 | Mm_Celera | 15:83395862 | ACAAGACAGCAATGC[A/G]TATGATCAGTAAGGA | 23970 |
rs31709185 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Pacsin2 | Mm_Celera | 15:83401597 | CACAACCAAGAACAT[A/T]AGAGTACAAACCATC | 23970 |
rs31709187 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Pacsin2 | Mm_Celera | 15:83401602 | CCAAGAACATTAGAG[C/T]ACAAACCATCAATTC | 23970 |
rs31709189 | snp | A/G | 0.444444 | 0.157135 | synonymous-codon | Pacsin2 | Mm_Celera | 15:83401882 | CTCCCAGAAGCTGTC[A/G]CTGGACACTTCCACT | 23970 |
rs31709191 | snp | A/C/T | 0.444444 | 0.157135 | intron-variant | Pacsin2 | Mm_Celera | 15:83402287 | AAATAAGGCTGAGGG[A/C/T]GCTTCACTCACCTGG | 23970 |
rs31709193 | snp | A/C | 0.5 | 0 | intron-variant | Pacsin2 | Mm_Celera | 15:83404772 | TAAGCTAAATAAAAC[A/C]GGTAATTAGTGACAA | 23970 |
rs31709265 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pacsin2 | Mm_Celera | 15:83396753 | TGTGCGCACACTCCA[C/T]TACTGTTTGGCCTTG | 23970 |
rs31709267 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pacsin2 | Mm_Celera | 15:83397209 | GCTGAGACGGTTCAG[C/T]AGCAAGAGCGTTTCC | 23970 |
rs31709269 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Pacsin2 | Mm_Celera | 15:83397454 | TTTGAGTGTAATTTT[C/T]AACTCTAAATGTTGT | 23970 |
rs31709271 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Pacsin2 | Mm_Celera | 15:83398728 | CCTCTTTTGTGGCAA[A/G]AATTCCTACTAGTGC | 23970 |
rs31709325 | snp | A/G | 0.5 | 0 | intron-variant | Pacsin2 | Mm_Celera | 15:83406900 | GCCTGATGATGTCAC[A/G]TATGTATTTAGTTAC | 23970 |
rs31709327 | snp | A/G | 0.5 | 0 | intron-variant | Pacsin2 | Mm_Celera | 15:83406977 | GGCAGCCATGTTTGT[A/G]TCAAATTCAGCAAGC | 23970 |
rs31709329 | snp | A/T | 0.5 | 0 | intron-variant | Pacsin2 | Mm_Celera | 15:83407864 | ATCACCGCTCTTTGT[A/T]AAAAACGGACTGGGT | 23970 |
rs31709331 | snp | A/T | 0.5 | 0 | intron-variant | Pacsin2 | Mm_Celera | 15:83408081 | AAGAGCTTCAATACA[A/T]GTTCCAGCAGCTGAG | 23970 |
rs31709333 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pacsin2 | Mm_Celera | 15:83408939 | CAGCATGCAGAAGCT[C/T]AGAGGTTAACAGATG | 23970 |
rs31709415 | snp | A/G | 0.375 | 0.216506 | intron-variant | Pacsin2 | Mm_Celera | 15:83409230 | TGCCAAGCACTAGCC[A/G]CAGAGGGCAGCAGTG | 23970 |
rs31709417 | snp | G/T | 0.5 | 0 | intron-variant | Pacsin2 | Mm_Celera | 15:83409633 | GTGAGATCAAGTATG[G/T]CCTCAGAAGACTCCA | 23970 |
rs31709419 | snp | C/T | 0.375 | 0.216506 | intron-variant | Pacsin2 | Mm_Celera | 15:83411709 | CTTGAGCACACAAAC[C/T]ACCTGGTTCAGGCCT | 23970 |