SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6281847 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Ubap2 | Mm_Celera | 4:41227902 | AAAatgaaaatcaca[C/T]ggtgctgagcatggt | 68926 |
rs6282388 | snp | A/T | 0.304688 | 0.243945 | intron-variant | Ubap2 | Mm_Celera | 4:41228015 | gtcagtcagaccatg[A/T]ctaaaacaGTATACA | 68926 |
rs6283468 | snp | A/G | 0.5 | 0 | intron-variant | Ubap2 | Mm_Celera | 4:41228200 | TACCAGAAAAGGCAA[A/G]GACAGACTTCTGTTT | 68926 |
rs6287286 | snp | A/G | 0.290657 | 0.246672 | synonymous-codon | Ubap2 | GRCm38.p3 | 4:41195626 | TGTCTTGTTGTAGAC[A/G]GAACCAGTCATATCA | 68926 |
rs6287854 | snp | C/T | 0.5 | 0 | intron-variant | Ubap2 | Mm_Celera | 4:41195726 | TCCAGGTTCCAGTCC[C/T]GGAGAGGAGCTGACA | 68926 |
rs6288890 | snp | C/T | 0.5 | 0 | intron-variant | Ubap2 | Mm_Celera | 4:41195913 | TCTCTGAGCATGTGC[C/T]GCTCAGTACTGGGAG | 68926 |
rs6355768 | snp | C/T | 0.5 | 0 | intron-variant | Ubap2 | Mm_Celera | 4:41198966 | AGGAAAATAAGATAA[C/T]ACATTTGGTACGAGC | 68926 |
rs6357155 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Ubap2 | Mm_Celera | 4:41232539 | ccccAAGACAGCCAT[A/G]TTGGATGCAGTCATC | 68926 |
rs6357204 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Ubap2 | Mm_Celera | 4:41232568 | TCGCTGTATTTTCTT[C/T]TAGGTGACATATTAT | 68926 |
rs6357210 | snp | A/G | 0.207612 | 0.24638 | synonymous-codon | Ubap2 | GRCm38.p3 | 4:41199254 | CATCTGGAGCTCATC[A/G]TAACCGTAAATCTGC | 68926 |
rs6358173 | snp | C/T | 0.207612 | 0.24638 | intron-variant | Ubap2 | Mm_Celera | 4:41232723 | AACTTATTTTCTATG[C/T]CTGTGCGTTGTAAGG | 68926 |
rs13473043 | snp | A/G | | | stop-gained | Ubap2 | Mm_Celera | 4:41196394 | TCTGCCACCTGGCTA[A/G]AGCTATACCGGCCTC | 68926 |
rs13473044 | snp | A/T | | | synonymous-codon | Ubap2 | Mm_Celera | 4:41196403 | GAATCCTGGTCTGCC[A/T]CCTGGCTACAGCTAT | 68926 |
rs13477666 | snp | A/G | 0.194824 | 0.243835 | intron-variant | Ubap2 | Mm_Celera | 4:41273576 | TTAGCATGCCCATTA[A/G]TAGGAGAAAAAAAAA | 68926 |
rs28303198 | snp | A/G | 0.231111 | 0.249285 | upstream-variant-2KB | Ubap2 | Mm_Celera | 4:41277192 | AGCCCTCAACAAACA[A/G]AATTATGTTCAAACC | 68926 |
rs28303199 | snp | C/G | 0.124444 | 0.216185 | upstream-variant-2KB | Ubap2 | Mm_Celera | 4:41275752 | ACCCAGAACGTCCTC[C/G]GCTGAAGGCCACGAG | 68926 |
rs28303200 | snp | A/G | 0.124444 | 0.216185 | upstream-variant-2KB, utr-variant-5-prime | Ubap2 | Mm_Celera | 4:41275270 | GCGGCGGAGATGGTG[A/G]CATTGCTTGTGGTCA | 68926 |
rs28303201 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ubap2 | Mm_Celera | 4:41275010 | TCAGGGCCCTGGGAG[A/G]CAGGATGAAGGGGAC | 68926 |
rs28303203 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ubap2 | Mm_Celera | 4:41273109 | CTAAACCTTTGCCCA[A/G]TAAGACAAATCTCAT | 68926 |
rs28303204 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ubap2 | Mm_Celera | 4:41273057 | AGGAAAAATCAGGCA[A/G]GAACATAATGACAGC | 68926 |
rs28303205 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Ubap2 | Mm_Celera | 4:41271658 | CATCTGTGGGCCTAT[A/C]GAGTTCAAGGCTGAC | 68926 |
rs28303206 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ubap2 | Mm_Celera | 4:41269219 | CTTCCTTTACCTCCT[A/G]TACAAAGACACTCCA | 68926 |
rs28303207 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ubap2 | Mm_Celera | 4:41268889 | ACACATTTAAAAAAC[A/G]AACAGGAGGGCTGGT | 68926 |
rs28303208 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Ubap2 | Mm_Celera | 4:41268808 | CAGCTCCAACTCCTA[C/G]GCCTTCTTCTCACAG | 68926 |
rs28303209 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ubap2 | Mm_Celera | 4:41268627 | GGACAGCATAGACTA[C/T]ATAAAGAAACTGTCT | 68926 |
rs28303210 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Ubap2 | Mm_Celera | 4:41268564 | CTCAGGAGGTGGAGG[C/G]AAAAGATCTCTCTGA | 68926 |
rs28303211 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ubap2 | Mm_Celera | 4:41267563 | AAGGCCAGTCTGGTA[C/T]ACAAGAATCCCAGGC | 68926 |
rs28303212 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ubap2 | Mm_Celera | 4:41267544 | GAGGAACCTCTGTAA[A/G]TTCAAGGCCAGTCTG | 68926 |
rs28303213 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ubap2 | Mm_Celera | 4:41265683 | CAGTCTCCTCAAAAA[A/G]AAAGCTCTGCAGTTT | 68926 |
rs28303214 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Ubap2 | GRCm38.p3 | 4:41263540 | CACAAGGGGTTCATA[C/G]CTCTAACCTCAGCAT | 68926 |
rs28303215 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Ubap2 | GRCm38.p3 | 4:41263460 | TAGTTTTATGTCAAA[A/T]CCAAGACCACCTCTA | 68926 |
rs28303216 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ubap2 | Mm_Celera | 4:41262695 | GGTCACTCTGCTCTG[A/G]CAAAATGGCTGAAAC | 68926 |
rs28303217 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ubap2 | Mm_Celera | 4:41262616 | TGCCTGATGTGAACA[C/T]GACTGAGACATCTAT | 68926 |
rs28303218 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ubap2 | Mm_Celera | 4:41261114 | CCTGATAATTAAGAA[A/G]CTATCTTCCTGTCTG | 68926 |
rs28303219 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ubap2 | Mm_Celera | 4:41260480 | TTCCTCTGTGTAGTG[A/G]GTAACCAAGAACACA | 68926 |
rs28303220 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Ubap2 | Mm_Celera | 4:41259790 | CTACATGTACGCCAC[C/G]GTGCATGCAAGCACT | 68926 |
rs28303221 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ubap2 | Mm_Celera | 4:41259607 | AAAGCAAACTTCAAA[A/G]GAATCCTAGCATTCA | 68926 |
rs28303222 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ubap2 | Mm_Celera | 4:41259342 | GGCTGGAGTGAGAGC[C/T]CAGGAGTTAAAAGAA | 68926 |
rs28303223 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ubap2 | Mm_Celera | 4:41259130 | ACTGTCTATAAACCC[A/G]TGCCTCTAAGTCTTG | 68926 |
rs28303224 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ubap2 | Mm_Celera | 4:41259061 | GGCCAGCCTCTACTT[C/T]AGACCCTATCTTCAA | 68926 |
rs28303225 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ubap2 | Mm_Celera | 4:41258609 | TCTCAAACAAAAAAG[C/T]CCACATTACACACAG | 68926 |
rs28303226 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Ubap2 | Mm_Celera | 4:41258467 | CCACTGAGCCACATA[G/T]CCCAGCCTTTAAACC | 68926 |
rs28303227 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Ubap2 | Mm_Celera | 4:41258173 | CCACTCCTACGCAGC[G/T]TTCTCAGCTCTGAAC | 68926 |
rs28303228 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ubap2 | Mm_Celera | 4:41258094 | CAGCCCACATTCTCT[C/T]CAGCTACCAAAGGGC | 68926 |
rs28303229 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ubap2 | Mm_Celera | 4:41257802 | GACAGCAAGAAGAAA[C/T]CACCACTGCCAATCT | 68926 |
rs28303230 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ubap2 | Mm_Celera | 4:41257781 | TGGTTTATAAAGTCT[A/G]CAACAGACAGCAAGA | 68926 |
rs28303231 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Ubap2 | Mm_Celera | 4:41257640 | AAATACCCAGCAAGG[A/C]CTCCCTACATTTTTG | 68926 |
rs28303232 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ubap2 | Mm_Celera | 4:41257406 | CACTAAGCTCCACAG[C/T]CTTTCTTTTTCTTTC | 68926 |
rs28303233 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ubap2 | Mm_Celera | 4:41257225 | CAAAAAGGATTCAAA[C/T]CCATCTGGTCCCTAG | 68926 |
rs28303234 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ubap2 | Mm_Celera | 4:41257186 | TGCTTCCATTTTACA[A/G]AGTCACCGTTTGTTA | 68926 |
rs28303235 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ubap2 | Mm_Celera | 4:41256852 | AACCCAGCATCAACT[C/T]CTGGCCTCTGTAAGC | 68926 |
rs28303236 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ubap2 | Mm_Celera | 4:41256475 | GAGACAATGAGCTCT[C/T]TCCTCCACCTGGTTT | 68926 |
rs28303237 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ubap2 | Mm_Celera | 4:41256030 | TCTGCGCCTGCGGCT[C/T]GCACCCAGCTGCTAG | 68926 |
rs28303238 | snp | C/G | 0.5 | 0 | intron-variant | Ubap2 | Mm_Celera | 4:41254359 | TCTTAAGGCTAAAGG[C/G]CCCAGGGAATAGAAT | 68926 |
rs28303239 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ubap2 | Mm_Celera | 4:41253957 | TTAGATCTGATTGTC[A/G]TAAGTTACAAGACAC | 68926 |
rs28303240 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Ubap2 | Mm_Celera | 4:41253594 | TGGTGATGTAGCTCA[G/T]TTGGTAGAGTGCCTG | 68926 |
rs28303241 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ubap2 | Mm_Celera | 4:41253248 | AATCCAAATAGGTCA[C/T]ATCACAATGACAAGT | 68926 |
rs28303242 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ubap2 | Mm_Celera | 4:41252621 | GTTACAGCAACATGG[C/T]TAAATACACCAAGTT | 68926 |
rs28303243 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ubap2 | Mm_Celera | 4:41251925 | CAGCACATGCCTTTA[A/G]CTGCAAAACCCGGGA | 68926 |
rs28303244 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ubap2 | Mm_Celera | 4:41250956 | TGTCTAACCTCAAAA[A/G]CCACAGTGATTTATG | 68926 |
rs28303245 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ubap2 | Mm_Celera | 4:41250788 | ACCAACAATAAAAAT[A/G]TATCAAGCCAGGGAT | 68926 |
rs28303246 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ubap2 | Mm_Celera | 4:41250390 | TCTTGGCATAGCAGT[C/T]CTTCTTGATCAGCTG | 68926 |
rs28303247 | snp | C/T | 0.32 | 0.24 | intron-variant | Ubap2 | Mm_Celera | 4:41249105 | CAACCATTCAGGACT[C/T]CAATTCCAGGAGATC | 68926 |
rs28303248 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ubap2 | Mm_Celera | 4:41248544 | CACAGCAGCTGACAA[C/T]ACCCCATTTCTTTTC | 68926 |
rs28303249 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ubap2 | Mm_Celera | 4:41248515 | AGGTTTGTATGGTGA[A/G]TCAACCAAGCAATCA | 68926 |
rs28303250 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ubap2 | Mm_Celera | 4:41247425 | GCCTGCCTGCACTTG[A/G]CATCATGGGACTGGT | 68926 |
rs28303251 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ubap2 | Mm_Celera | 4:41246375 | GTGGGCAAAGGCAGA[A/G]AGATGTTAGTAAGAG | 68926 |
rs28303252 | snp | C/G | 0.32 | 0.24 | intron-variant | Ubap2 | Mm_Celera | 4:41245892 | TATTAGACTCAATAG[C/G]AGACTACCTTGGAAC | 68926 |
rs28303253 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Ubap2 | Mm_Celera | 4:41245309 | ACAGCGATGCTATGT[A/T]TCAATAAGTCTCAGT | 68926 |
rs28303254 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Ubap2 | Mm_Celera | 4:41245250 | AGTCAACTTCTGGAC[G/T]CACAGCTGATAGACT | 68926 |
rs28303255 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ubap2 | Mm_Celera | 4:41245045 | TCTCAGTGCCTAGGT[A/G]TCATTTTCATGTTGA | 68926 |
rs28303256 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ubap2 | Mm_Celera | 4:41244328 | TGTTCTTACACTCAA[C/T]ATGTGCATATCGACA | 68926 |
rs28303257 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Ubap2 | Mm_Celera | 4:41244122 | TTCTAGCCCCGGCAG[C/G]TATTAATTGTACATG | 68926 |
rs28303258 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ubap2 | Mm_Celera | 4:41244070 | ATGATACCTCATGAC[C/T]GTCTCTAAGCCCAGG | 68926 |
rs28303259 | snp | C/T | 0.42 | 0.183303 | intron-variant | Ubap2 | Mm_Celera | 4:41243883 | CTCCCAGCAACCACA[C/T]GGTGACTCAACCATC | 68926 |
rs28303260 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ubap2 | Mm_Celera | 4:41243726 | TAGCTTCAAATTAGA[C/T]AGACAGACAAACAAG | 68926 |
rs28303261 | snp | A/C | 0.32 | 0.24 | intron-variant | Ubap2 | Mm_Celera | 4:41243112 | CAAACTGACAAGTCT[A/C]TGGAGTTCAAAGGAA | 68926 |
rs28303262 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ubap2 | Mm_Celera | 4:41243082 | CAAGGAAGCACAATC[C/T]ACATCAGTGACAGGC | 68926 |
rs28303263 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ubap2 | Mm_Celera | 4:41242962 | TGGGCTTAACATCAA[A/G]CATCTCTACCTGCTA | 68926 |
rs28303264 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ubap2 | Mm_Celera | 4:41242930 | CACGCAGGTTAGGAT[A/G]ATCAAATTCAGATCC | 68926 |
rs28303265 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ubap2 | Mm_Celera | 4:41242127 | ACCACCACAGCCTGG[C/T]CTATAAAATCCAACC | 68926 |
rs28303266 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ubap2 | Mm_Celera | 4:41242025 | GTCTCTCTAGATAGT[C/T]GTGGCTGCCCTGGAA | 68926 |
rs28303267 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Ubap2 | Mm_Celera | 4:41241110 | AATAGACACCCAAAC[G/T]TTGTCCTTTGACCTA | 68926 |
rs28303268 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ubap2 | Mm_Celera | 4:41240962 | GTAAGTTGTCAGGAT[A/G]CAGGAGCATGTATCT | 68926 |
rs28303269 | snp | A/G | 0.32 | 0.24 | intron-variant | Ubap2 | Mm_Celera | 4:41240920 | TCTAACCATACAACC[A/G]TGACACCTGACACCT | 68926 |
rs28303270 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ubap2 | Mm_Celera | 4:41240497 | ACAGAACCCAGGGCT[C/T]TAGCAAGGTAGGTGG | 68926 |
rs28303271 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ubap2 | Mm_Celera | 4:41240131 | AATGAAGATTAGAAA[A/G]AGGGATGTCAACAAA | 68926 |
rs28303272 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Ubap2 | GRCm38.p3 | 4:41239838 | TGCCTTCATGCACTG[A/T]TAGACACAGACACAC | 68926 |
rs28303273 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Ubap2 | GRCm38.p3 | 4:41239757 | GACATGCTTGTCTTC[A/G]TGTGTGTGTGTGTGT | 68926 |
rs28303274 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Ubap2 | Mm_Celera | 4:41239611 | GTCTCTACCAAGGCG[G/T]ATGGGCTGGCATAAT | 68926 |
rs28303275 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ubap2 | Mm_Celera | 4:41239123 | GCTCTCTATTCCTAC[A/G]CACTGCTGTGATGGC | 68926 |
rs28303276 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Ubap2 | Mm_Celera | 4:41239026 | CTATATTAATACAGT[G/T]CCTCCTACTGTCTTT | 68926 |
rs28303277 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Ubap2 | Mm_Celera | 4:41238581 | ATTCCAGCAGCTGTG[C/G]CCTATTTTGCCCAAT | 68926 |
rs28303278 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ubap2 | Mm_Celera | 4:41238549 | ATTTCATGTAGGTGG[A/G]TGATTGTATTATACA | 68926 |
rs28303279 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ubap2 | Mm_Celera | 4:41238425 | AACTGAACCACAGCC[C/T]AGCTCCATTCAACTT | 68926 |
rs28303280 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Ubap2 | Mm_Celera | 4:41238053 | CAGGCCTCTATTTCC[C/T]CAGCAGTGGGATTAA | 68926 |
rs28303281 | snp | A/T | 0.32 | 0.24 | intron-variant | Ubap2 | Mm_Celera | 4:41237974 | ACAGATTTCACTGTG[A/T]ATGCCTGAATGGCCT | 68926 |
rs28303282 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Ubap2 | Mm_Celera | 4:41237658 | AGTCTTATTACCTGT[C/G]TGGCTGGGAAGTCAC | 68926 |
rs28303283 | snp | A/G | 0.32 | 0.24 | intron-variant | Ubap2 | Mm_Celera | 4:41237544 | CAGATTGCACAGCTA[A/G]CACTCTTAGTTGCTG | 68926 |
rs28303284 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Ubap2 | Mm_Celera | 4:41237455 | CTTTGTCTCTGCCCC[G/T]TCTGAGCTGGGTTCA | 68926 |