SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs13463536 | snp | G/T | | | missense, intron-variant | Oasl2 | Mm_Celera | 5:114899849 | GGCGAGAAACCGGGA[G/T]GTCGTCATCAGCTTC | 23962 |
rs13463537 | snp | G/T | | | synonymous-codon | Oasl2 | GRCm38.p3 | 5:114906771 | GCAGGTCTGTTGCAC[G/T]ACTGTAGGCCCCAGC | 23962 |
rs13463538 | snp | C/G | | | missense | Oasl2 | Mm_Celera | 5:114911362 | CTCATTAGGGTAATC[C/G]ACTAGTCTGGCTGCT | 23962 |
rs13463539 | snp | G/T | | | utr-variant-3-prime | Oasl2 | Mm_Celera | 5:114912014 | TGCATGCTCCTGTTT[G/T]AAAACAACTACTATC | 23962 |
rs29508642 | snp | C/T | 0.375 | 0.216506 | intron-variant | Oasl2 | GRCm38.p3 | 5:114903577 | AAACTATTAAAGCCA[C/T]AAATCTAATGAGAAC | 23962 |
rs29509038 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Oasl2 | Mm_Celera | 5:114905987 | TATCTCCAATCCTAA[C/T]GGAAGGGCTTTGCTT | 23962 |
rs29538270 | snp | A/C | 0.5 | 0 | intron-variant | Oasl2 | Mm_Celera | 5:114908421 | AATGCCCCCCCCCCC[A/C]AAAAAAAAAAAAACA | 23962 |
rs29543138 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Oasl2 | GRCm38.p3 | 5:114906514 | AACAGTGGAGGCTGC[A/G]GAGGCCCGCCTCCAG | 23962 |
rs29543781 | snp | A/G | 0.375 | 0.216506 | utr-variant-5-prime, upstream-variant-2KB | Oasl2 | GRCm38.p3 | 5:114896944 | CACGTCACTCACTGA[A/G]GATAACTAGACAGAA | 23962 |
rs29564161 | snp | A/C | 0.5 | 0 | intron-variant | Oasl2 | Mm_Celera | 5:114902992 | ATGAGACTTCTAAGG[A/C]TCTTTTTCCCACCTC | 23962 |
rs29565274 | snp | A/G | 0.5 | 0 | synonymous-codon, intron-variant | Oasl2 | GRCm38.p3 | 5:114900014 | GATGGATATCCTCCC[A/G]GCTTACGATGCTTTG | 23962 |
rs29586070 | snp | A/T | 0.5 | 0 | intron-variant | Oasl2 | GRCm38.p3 | 5:114898041 | AAATTAGCCTTGCAA[A/T]GCTGAAGGACAGAGG | 23962 |
rs29668304 | snp | A/G | 0.5 | 0 | intron-variant | Oasl2 | GRCm38.p3 | 5:114904471 | TACACCCATGCACAC[A/G]AGGAGAGCTCCAACT | 23962 |
rs29733780 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Oasl2 | GRCm38.p3 | 5:114904208 | CATTGTGGGAAAGGA[A/G]GTAAGAGGAGCCTAA | 23962 |
rs29822904 | snp | A/C/G | 0.5 | 0 | missense, intron-variant | Oasl2 | GRCm38.p3 | 5:114899943 | AGAGAGGGCAAAAGG[A/C/G]CCCCTCGCTCCCTCA | 23962 |
rs32136794 | snp | A/G | | | utr-variant-3-prime | Oasl2 | Mm_Celera | 5:114911488 | TTAAAACCCTCTCCT[A/G]TAGCCGGGCAGTGGT | 23962 |
rs32136795 | snp | C/T | | | utr-variant-3-prime | Oasl2 | Mm_Celera | 5:114911863 | CATTCTGTGAGTCAC[C/T]GAATCTCAAAGAGCA | 23962 |
rs32136796 | snp | G/T | | | utr-variant-3-prime | Oasl2 | GRCm38.p3 | 5:114912044 | CTGGCCCATGCAGCA[G/T]GCCAAATCATCTTGT | 23962 |
rs32136797 | snp | G/T | | | utr-variant-3-prime | Oasl2 | Mm_Celera | 5:114912096 | CCATGTTAGACTCCC[G/T]TGGACGTAAATCTAT | 23962 |
rs32136798 | snp | C/T | | | utr-variant-3-prime | Oasl2 | GRCm38.p3 | 5:114912118 | TAAATCTATCTCCCT[C/T]GTCTAATCAGACTCG | 23962 |
rs32136799 | snp | C/T | | | downstream-variant-500B | Oasl2 | Mm_Celera | 5:114912278 | GGTCTGAGGCCATTT[C/T]AGAGTCCACCTACTT | 23962 |
rs32136800 | snp | C/T | | | downstream-variant-500B | Oasl2 | GRCm38.p3 | 5:114912314 | TGCCCCTAACCCACA[C/T]ATTATTCTCTGGAGA | 23962 |
rs32136801 | snp | A/G | | | downstream-variant-500B | Oasl2 | Mm_Celera | 5:114912365 | CAACCTCATGCTGGC[A/G]CGTAGTCATGGCCTC | 23962 |
rs32136802 | snp | A/G | | | downstream-variant-500B | Oasl2 | Mm_Celera | 5:114912469 | TTTCAGTCTTGGAAC[A/G]TGGGGCCCCGGTACA | 23962 |
rs32138052 | snp | A/T | | | upstream-variant-2KB | Oasl2 | Mm_Celera | 5:114895368 | AAACCTTTAAAAAAA[A/T]TTGTAATGGAAATCA | 23962 |
rs32138053 | snp | A/G | | | upstream-variant-2KB | Oasl2 | GRCm38.p3 | 5:114895426 | ACCTTGTTAAGGACC[A/G]AGAGATCAAGCAGAC | 23962 |
rs32139324 | snp | C/T | | | upstream-variant-2KB | Oasl2 | GRCm38.p3 | 5:114895470 | CCCAAAGGCCATCTC[C/T]GGGGTCCTGAGGTGA | 23962 |
rs32139325 | snp | G/T | | | upstream-variant-2KB | Oasl2 | Mm_Celera | 5:114895517 | ACAGACAGCATCCCC[G/T]TCAAGCTGTGGTCCC | 23962 |
rs32139326 | snp | C/T | | | upstream-variant-2KB | Oasl2 | GRCm38.p3 | 5:114895777 | ATCTTCAGTTTCCAC[C/T]AGACTACTTACAACG | 23962 |
rs32139327 | snp | A/G | | | upstream-variant-2KB | Oasl2 | Mm_Celera | 5:114895783 | AGTTTCCACCAGACT[A/G]CTTACAACGTCATCT | 23962 |
rs32139328 | snp | C/T | | | upstream-variant-2KB | Oasl2 | Mm_Celera | 5:114896896 | TAGTCAGGAACCTAA[C/T]CCTACACCCAAGGCT | 23962 |
rs32139329 | snp | A/G/T | 0.625 | 0.125 | utr-variant-5-prime, upstream-variant-2KB | Oasl2 | GRCm38.p3 | 5:114896963 | AACTAGACAGAAAAC[A/G/T]TCGTGAGACTACCTC | 23962 |
rs32139330 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB | Oasl2 | Mm_Celera | 5:114897136 | ATGATGAGCAGCCTC[C/G]GGGAGACTAGCTGAG | 23962 |
rs32139331 | snp | C/T | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | Oasl2 | GRCm38.p3 | 5:114897425 | TGCATCCTTAACTCC[C/T]GTTCCCTTCTGCCTT | 23962 |
rs32139332 | snp | A/T | | | utr-variant-5-prime, intron-variant, splice-donor-variant, upstream-variant-2KB | Oasl2 | GRCm38.p3 | 5:114897449 | CTGCCTTGAAGAAGG[A/T]AAACTGGATCTCCCT | 23962 |
rs32139333 | snp | A/G | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | Oasl2 | Mm_Celera | 5:114897496 | TTCTTGTCAAAGCTT[A/G]GTTTCTGTTTCCAGT | 23962 |
rs32140114 | snp | C/T | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | Oasl2 | Mm_Celera | 5:114897570 | CAACTCTCCATCCCA[C/T]TGTCTCCTCCAGAGA | 23962 |
rs32140115 | snp | A/G | | | synonymous-codon, upstream-variant-2KB | Oasl2 | GRCm38.p3 | 5:114897673 | AGCTGAAATGGACCC[A/G]TTCCCCGACCTGTAT | 23962 |
rs32140116 | snp | A/C | | | intron-variant | Oasl2 | Mm_Celera | 5:114898148 | CCTGTCTAAGAAATA[A/C]TACTTGGCCAGGCGT | 23962 |
rs32140117 | snp | A/G | 0.5 | 0 | intron-variant | Oasl2 | GRCm38.p3 | 5:114898384 | TACTACTTTACTTCT[A/G]AGTGAAGGAAACCTA | 23962 |
rs32140118 | snp | A/G | | | intron-variant | Oasl2 | Mm_Celera | 5:114898477 | CCATTGGGATTCTAA[A/G]GGCTGCCTGTGTAAG | 23962 |
rs32140119 | snp | A/G | | | intron-variant | Oasl2 | GRCm38.p3 | 5:114898848 | ACTCTGAGCCATGGT[A/G]GCAGAGGTTAAGACG | 23962 |
rs32140120 | snp | C/T | | | intron-variant | Oasl2 | GRCm38.p3 | 5:114899026 | TGGTTCCTGCAAATT[C/T]CTGCCTGACCTAGGT | 23962 |
rs32140121 | snp | C/G/T | | | intron-variant | Oasl2 | GRCm38.p3 | 5:114899276 | AGGAGCTGAGGTTTA[C/G/T]ACTCTCTCATCTTCT | 23962 |
rs32140122 | snp | C/T | | | intron-variant | Oasl2 | GRCm38.p3 | 5:114899336 | AGCAGAAAAAGGATT[C/T]TGTTTCATTATAGCA | 23962 |
rs32140123 | snp | C/T | | | missense, intron-variant | Oasl2 | Mm_Celera | 5:114899767 | CGGGAAAGGGGACAA[C/T]GCTGAACCACAGATC | 23962 |
rs32141034 | snp | A/G | | | missense, intron-variant | Oasl2 | Mm_Celera | 5:114899826 | TGCTTTTCCAGTTTC[A/G]AAGAGCAGGCGAGAA | 23962 |
rs32141035 | snp | A/T | | | missense, intron-variant | Oasl2 | Mm_Celera | 5:114899913 | CTGGCCTACAACATC[A/T]TTGTCCTTACCCACA | 23962 |
rs32141036 | snp | A/T | | | intron-variant | Oasl2 | Mm_Celera | 5:114900044 | GGGTAAATCCAGTGG[A/T]AGTTTCAGTTTAAAG | 23962 |
rs32141037 | snp | A/G | | | intron-variant | Oasl2 | Mm_Celera | 5:114900299 | AGGTCTTTAGGGTCC[A/G]ACAGAACTGTATTAG | 23962 |
rs32141038 | snp | C/T | | | missense, utr-variant-5-prime | Oasl2 | Mm_Celera | 5:114901305 | ATAAGAAGTAAGGGC[C/T]ACCCTGGTGACTTCT | 23962 |
rs32141039 | snp | C/T | | | intron-variant | Oasl2 | GRCm38.p3 | 5:114901450 | GGAGCAGAGGGTACG[C/T]ACGCATCTGTAGCCC | 23962 |
rs32141040 | snp | G/T | | | intron-variant | Oasl2 | GRCm38.p3 | 5:114901578 | GAGAGATCGAGTGGG[G/T]ATACAAGAAGTGGGT | 23962 |
rs32141041 | snp | A/G | | | intron-variant | Oasl2 | Mm_Celera | 5:114901627 | TGAGTGACCTGCAGG[A/G]CCCTGGACCATCTAA | 23962 |
rs32141042 | snp | C/T | | | intron-variant | Oasl2 | GRCm38.p3 | 5:114901660 | ACCCAGCATCCCTGT[C/T]GGTGAGAGCGTCTGC | 23962 |
rs32141043 | snp | A/G | | | intron-variant | Oasl2 | GRCm38.p3 | 5:114901726 | CAAGTGCGATTAAGT[A/G]CTCACTCAGATGAGG | 23962 |
rs32141994 | snp | C/T | | | intron-variant | Oasl2 | GRCm38.p3 | 5:114901798 | TAACAATAATAAAGC[C/T]ACCATTGTGTCAGAC | 23962 |
rs32141995 | snp | G/T | | | intron-variant | Oasl2 | Mm_Celera | 5:114902120 | TTAGCATTTCTTTCT[G/T]GCTATCTGACTAATT | 23962 |
rs32141996 | snp | C/T | | | intron-variant | Oasl2 | Mm_Celera | 5:114902268 | CGTCATCTGTATTCC[C/T]GCAGCCCATACCTGG | 23962 |
rs32141997 | snp | A/T | | | intron-variant | Oasl2 | Mm_Celera | 5:114902312 | GGAGTTACCATGCCA[A/T]CTCACCGCAGTTTTG | 23962 |
rs32141998 | snp | A/G | | | intron-variant | Oasl2 | Mm_Celera | 5:114902321 | ATGCCAACTCACCGC[A/G]GTTTTGGTCCACCCT | 23962 |
rs32141999 | snp | C/G | | | intron-variant | Oasl2 | GRCm38.p3 | 5:114902351 | TTTAAACACACACAC[C/G]AGCTGTTGTCCTTGA | 23962 |
rs32142000 | snp | G/T | | | intron-variant | Oasl2 | Mm_Celera | 5:114902373 | TGTCCTTGAGTCGAT[G/T]GTGAGAGCTCCGTCC | 23962 |
rs32142001 | snp | A/G | 0.48 | 0.0979796 | missense | Oasl2 | GRCm38.p3 | 5:114904989 | TCCTCGTAAACTACC[A/G]CGACATCTGCATCTA | 23962 |
rs32142002 | snp | A/G | | | intron-variant | Oasl2 | Mm_Celera | 5:114905094 | GAGTCTATCAACCAC[A/G]TGACTTACGGCTCTG | 23962 |
rs32142003 | snp | C/T | | | intron-variant | Oasl2 | GRCm38.p3 | 5:114905102 | CAACCACGTGACTTA[C/T]GGCTCTGAGGCCTAG | 23962 |
rs32142964 | snp | A/G | 0.375 | 0.216506 | intron-variant | Oasl2 | GRCm38.p3 | 5:114905264 | TAGACCCCTAGAAAC[A/G]AAACCCAGCATGGAG | 23962 |
rs32142965 | snp | C/T | | | intron-variant | Oasl2 | GRCm38.p3 | 5:114905703 | CTTTCAGTCTCTGTC[C/T]GTGAGTGGTTCAACC | 23962 |
rs32142966 | snp | A/G | | | intron-variant | Oasl2 | GRCm38.p3 | 5:114905751 | TTCCAGTCAAGTTCC[A/G]ATTTATCGCTTCAAG | 23962 |
rs32142967 | snp | C/T | | | intron-variant | Oasl2 | GRCm38.p3 | 5:114906561 | ATCTTAAACATCCCG[C/T]GACAATTTGCCCTTA | 23962 |
rs32142968 | snp | C/T | | | synonymous-codon | Oasl2 | GRCm38.p3 | 5:114906747 | TGCAGAAGCTGCTTT[C/T]TGCCTGCTGCAGGTC | 23962 |
rs32142969 | snp | C/G | | | missense | Oasl2 | Mm_Celera | 5:114906770 | TGCAGGTCTGTTGCA[C/G]GACTGTAGGCCCCAG | 23962 |
rs32142971 | snp | C/T | | | synonymous-codon | Oasl2 | Mm_Celera | 5:114906786 | GACTGTAGGCCCCAG[C/T]GAGCGCTGGAATGTA | 23962 |
rs32142972 | snp | A/C | | | intron-variant | Oasl2 | Mm_Celera | 5:114906870 | ATCACGCTCTTCCCA[A/C]GGCATCCCAGCAAGG | 23962 |
rs32142973 | snp | C/T | | | intron-variant | Oasl2 | GRCm38.p3 | 5:114906930 | GGAAGAGCTCAAGAA[C/T]TGCTAAGTCTGCTGC | 23962 |
rs32143934 | snp | C/G | | | intron-variant | Oasl2 | GRCm38.p3 | 5:114906970 | AAGTCCTTTTATTTC[C/G]AGTCTTGACTCTGAT | 23962 |
rs32143935 | snp | A/C | | | intron-variant | Oasl2 | Mm_Celera | 5:114907254 | TTCTATGATTTAAGC[A/C]TGGGACCCGAATCTC | 23962 |
rs32143936 | snp | G/T | | | intron-variant | Oasl2 | GRCm38.p3 | 5:114907285 | CTTTCTTCAAGGATA[G/T]GCACCAACTGTACCT | 23962 |
rs32143937 | snp | G/T | | | intron-variant | Oasl2 | GRCm38.p3 | 5:114907567 | AGACAATCTGCCCTG[G/T]TCTATAGTCACCTCA | 23962 |
rs32143938 | snp | G/T | | | intron-variant | Oasl2 | GRCm38.p3 | 5:114907597 | AGAGACAGAGTCTAA[G/T]AATTTACCTCTAGCT | 23962 |
rs32143939 | snp | A/G | | | intron-variant | Oasl2 | Mm_Celera | 5:114907651 | ATTTGGTGGATCATC[A/G]TCACTGTTTTAGTCA | 23962 |
rs32143940 | snp | A/G | | | intron-variant | Oasl2 | Mm_Celera | 5:114908112 | AGTGAGTCTTCTACA[A/G]CTCACTGCAGACAGT | 23962 |
rs32143941 | snp | C/T | | | intron-variant | Oasl2 | Mm_Celera | 5:114908138 | ACAGTAAGTCCACTG[C/T]ACAGCCTTGCCCCAT | 23962 |
rs32143942 | snp | A/C | | | intron-variant | Oasl2 | Mm_Celera | 5:114908148 | CACTGTACAGCCTTG[A/C]CCCATAGGCCACCAC | 23962 |
rs32143943 | snp | G/T | | | intron-variant | Oasl2 | Mm_Celera | 5:114908259 | CTTGCTAAACCCACA[G/T]AAATCCTGTCCCTTG | 23962 |
rs32144534 | snp | G/T | | | intron-variant | Oasl2 | Mm_Celera | 5:114908306 | CTTCGGGAAAAGTTG[G/T]GATTTGTCCTCAAAA | 23962 |
rs32144535 | snp | A/G | | | intron-variant | Oasl2 | Mm_Celera | 5:114908359 | AAGGTAGACAGATAG[A/G]GTCTGAAAGGGACCT | 23962 |
rs32144536 | snp | C/T | | | intron-variant | Oasl2 | Mm_Celera | 5:114908380 | AAAGGGACCTGCCAT[C/T]TGGCCATCAAGTGCC | 23962 |
rs32144537 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Oasl2 | Mm_Celera | 5:114908473 | AGGACCCTTTGGGAA[A/G]CAAGGAAAAATGAAA | 23962 |
rs32144538 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Oasl2 | Mm_Celera | 5:114908937 | ATTTTCCAGAGACCA[A/G]CTCTCAGCCTCTTAC | 23962 |
rs32144539 | snp | C/T | | | intron-variant | Oasl2 | Mm_Celera | 5:114908999 | TGTGTGGTCCCTCTG[C/T]GTGTTCTCACTTCAC | 23962 |
rs32144540 | snp | A/T | | | intron-variant | Oasl2 | Mm_Celera | 5:114909166 | TGATTATAGCAGCTC[A/T]AAGGACCAGTGCCAG | 23962 |
rs32144541 | snp | C/T | | | intron-variant | Oasl2 | Mm_Celera | 5:114910364 | TCATTTAGAATCCAT[C/T]TGTTGGGCTGGAGAG | 23962 |
rs32144542 | snp | A/T | | | intron-variant | Oasl2 | Mm_Celera | 5:114910716 | GGCGTGAGTTAGTGG[A/T]ACTCTGAGCCTAGGG | 23962 |
rs32144543 | snp | G/T | | | intron-variant | Oasl2 | Mm_Celera | 5:114910786 | TTATGTCTCCCAGGT[G/T]GTCTTGGTAGATGAT | 23962 |
rs32145414 | snp | A/G | | | synonymous-codon | Oasl2 | Mm_Celera | 5:114911085 | CAGGAAGACCCTAGC[A/G]GATTATGGGATATTC | 23962 |
rs32145415 | snp | C/T | | | synonymous-codon | Oasl2 | Mm_Celera | 5:114911166 | CTTTGTGAAGTATCC[C/T]GGTGGCCAGAGCAAG | 23962 |
rs32145416 | snp | A/G | | | missense | Oasl2 | Mm_Celera | 5:114911188 | CAGAGCAAGCCTTTC[A/G]CCATCGACCCTGATG | 23962 |
rs32145417 | snp | A/G | | | missense | Oasl2 | Mm_Celera | 5:114911311 | GATGATGAGAGCCTT[A/G]AAGAGCTTGAGATCA | 23962 |
rs32145418 | snp | C/T | | | utr-variant-3-prime | Oasl2 | Mm_Celera | 5:114911460 | CTTAAATATCAACAT[C/T]CCCTTCTCTTGCTTA | 23962 |