SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6205970 | snp | A/C | 0.5 | 0 | intron-variant | Bptf | Mm_Celera | 11:107066551 | ACATGTAGCCATGTT[A/C]CAATCAGAGTCCTTG | 207165 |
rs6206016 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Bptf | Mm_Celera | 11:107066587 | GCAGAACAGTGGCCA[C/T]GAGTCCTGGGACAGG | 207165 |
rs6207001 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Bptf | Mm_Celera | 11:107066756 | TTTCTGGCTGTGACA[C/T]TGGATAGAGAAGAGA | 207165 |
rs6228103 | snp | C/T | 0.304688 | 0.243945 | synonymous-codon | Bptf | GRCm38.p3 | 11:107061804 | AGTCGATGGAATGAT[C/T]CCCAGGACCTTCTGC | 207165 |
rs6228599 | snp | A/G | 0.5 | 0 | intron-variant | Bptf | Mm_Celera | 11:107061851 | CTTAGAAAGAGATGA[A/G]GAAGACATGAACCAC | 207165 |
rs6244003 | snp | A/C | 0.207612 | 0.24638 | intron-variant | Bptf | Mm_Celera | 11:107062405 | CAAAGAGCAGCTATG[A/C]CAACGACTGTCCAGC | 207165 |
rs6244602 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Bptf | Mm_Celera | 11:107062527 | TCCACTCATTCACCC[C/T]GGCTCTACCTGAATT | 207165 |
rs6273566 | snp | C/G | 0.5 | 0 | intron-variant | Bptf | Mm_Celera | 11:107110226 | AGGGTCTCACACATG[C/G]TAGGCAAACACTACT | 207165 |
rs6286876 | snp | C/T | 0.5 | 0 | intron-variant | Bptf | Mm_Celera | 11:107110419 | CAGACTATGATCCTG[C/T]GTGTGTCAGGATCTC | 207165 |
rs6286915 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Bptf | Mm_Celera | 11:107110439 | GTCAGGATCTCCTGG[A/G]GAACTTTAATCACTA | 207165 |
rs13464189 | snp | A/G | 0.142012 | 0.225474 | missense | Bptf | Mm_Celera | 11:107099728 | AGCACAAAGGTCCAG[A/G]TAGCAGAGCTAATAG | 207165 |
rs13481215 | snp | G/T | 0.314099 | 0.241643 | upstream-variant-2KB | Bptf | Mm_Celera | 11:107133182 | CTAATTGCCAACTAA[G/T]TTATTATGTATTCAC | 207165 |
rs27010311 | snp | A/G | 0.142012 | 0.225474 | upstream-variant-2KB | Bptf | Mm_Celera | 11:107133122 | CCCACTAACTAACTG[A/G]CTTATTACAATATAG | 207165 |
rs27010312 | snp | C/T | 0.132653 | 0.220748 | upstream-variant-2KB | Bptf | Mm_Celera | 11:107132967 | TGCACCAAATGTTGC[C/T]AAATTGAGGTGGCTC | 207165 |
rs27010313 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Bptf | Mm_Celera | 11:107113183 | AACAAGCTAAGAACA[C/T]AGCCACTGCTTTCTG | 207165 |
rs27010314 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Bptf | Mm_Celera | 11:107113082 | AACCAAAGTGGTACA[G/T]GGAACTAGAGAAAAA | 207165 |
rs27010315 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Bptf | Mm_Celera | 11:107112580 | CTATATGTGGCACTG[A/C]ACTGGAGTGGGACAG | 207165 |
rs27010316 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Bptf | Mm_Celera | 11:107111680 | TATGGAACCTTGCTC[C/T]CACAAACACACCAGT | 207165 |
rs27010317 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Bptf | GRCm38.p3 | 11:107111433 | TTGGCTCACCAGAGC[C/T]GCACAGAAGTCCTCA | 207165 |
rs27010318 | snp | G/T | 0.231111 | 0.249285 | synonymous-codon | Bptf | GRCm38.p3 | 11:107111361 | AGACGTGTCCTCTTC[G/T]CGAAGAACTGCTTTC | 207165 |
rs27010319 | snp | C/G | 0.124444 | 0.216185 | synonymous-codon | Bptf | Mm_Celera | 11:107111040 | GCACGTCTCACAGCA[C/G]AGCAGATCCCCAAGT | 207165 |
rs27010320 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon | Bptf | GRCm38.p3 | 11:107110911 | CTTTTGGACTTCAGC[A/G]ACACAGTCAGTCACA | 207165 |
rs27010321 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Bptf | Mm_Celera | 11:107110025 | GAGCCTCAAAATGCA[A/G]AAGCTCACAATACCA | 207165 |
rs27010322 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Bptf | Mm_Celera | 11:107109970 | CACTGAAGTTCATGC[A/G]TCAGAGTTTTCTCTT | 207165 |
rs27010323 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Bptf | Mm_Celera | 11:107109934 | AGCATCAATGATGGA[A/G]CCATTCTGCCCTCCA | 207165 |
rs27010324 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Bptf | Mm_Celera | 11:107109810 | GGGTGACAACAGATC[A/G]TGCAAGTGCCTATCG | 207165 |
rs27010325 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Bptf | Mm_Celera | 11:107109769 | AGGACCCAACTATCA[A/C]GATGAATGCCAAGCA | 207165 |
rs27010326 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Bptf | Mm_Celera | 11:107107195 | AATGTGAAAAGCAAA[A/T]AAAGGCCAAGCCCAG | 207165 |
rs27010327 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Bptf | Mm_Celera | 11:107107182 | CGTGATCGCTGCCAA[C/T]GTGAAAAGCAAAAAA | 207165 |
rs27010328 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Bptf | Mm_Celera | 11:107107135 | TTCAGGGTCGAGGAA[A/G]GAGGATTCCAAAAGC | 207165 |
rs27010329 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Bptf | Mm_Celera | 11:107106469 | GCTCAAGAAAAGACA[G/T]AGGTGCTAGCTGAAA | 207165 |
rs27010330 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Bptf | Mm_Celera | 11:107104315 | TACTCTACTACAAGG[A/G]ACACTTAACCTGAAA | 207165 |
rs27010331 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Bptf | Mm_Celera | 11:107103509 | AACATACTAACTCGT[C/T]GGCCAGGCCTGTGCA | 207165 |
rs27010332 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Bptf | Mm_Celera | 11:107103088 | GGAAGCTTTGGTTCT[C/T]CAGGCTCACTGGAAC | 207165 |
rs27010333 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Bptf | Mm_Celera | 11:107102698 | CTGCTCACAGCAGCC[A/G]TACTTCTCAGTTCTC | 207165 |
rs27010334 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Bptf | Mm_Celera | 11:107102524 | CACAACAAACTCACT[A/G]CTTCAGGCAGAAGTC | 207165 |
rs27010335 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Bptf | Mm_Celera | 11:107102497 | ATTCTGATCTCTGAG[A/G]ACTTTCTCCTCCACA | 207165 |
rs27010336 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Bptf | Mm_Celera | 11:107102158 | ACTCCATGCATCCAG[A/G]TTCACACTGCTAGCT | 207165 |
rs27010337 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Bptf | Mm_Celera | 11:107102082 | GTGACCCTTAAACCT[C/T]GGAGTACAAATTGTC | 207165 |
rs27010338 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Bptf | Mm_Celera | 11:107101497 | CTGTTTCACTTCCCA[C/T]GGACCCTCTTCTGGC | 207165 |
rs27010339 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Bptf | Mm_Celera | 11:107101407 | ACAGACAGTTTCAAG[C/T]GCTCAGTGAGTTCTA | 207165 |
rs27010340 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Bptf | Mm_Celera | 11:107101365 | CGACGTCAGCCTTCT[C/T]AGCTCTTAAACACAA | 207165 |
rs27010341 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Bptf | Mm_Celera | 11:107101258 | AGGACAGCGTCCAAC[A/C]AAGAGCAGCTGTCAA | 207165 |
rs27010342 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Bptf | Mm_Celera | 11:107101008 | ACTTTGGTATGACTG[C/T]TGTGGAAGTGATGGA | 207165 |
rs27010343 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Bptf | Mm_Celera | 11:107100971 | GGTGCACACTTGGCA[G/T]CATTTTCCGCATGCT | 207165 |
rs27010344 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Bptf | Mm_Celera | 11:107100148 | GTCCCTTGATACAGA[A/G]GGCACGGCCATGACA | 207165 |
rs27010345 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Bptf | Mm_Celera | 11:107100115 | CAGCCTGGGAAAGAT[A/C]TGGTCTGAATGGGCT | 207165 |
rs27010346 | snp | A/G | 0.132653 | 0.220748 | synonymous-codon | Bptf | GRCm38.p3 | 11:107099693 | CAGTTCTGCTTCCCA[A/G]TATCCTTTGTCTAGG | 207165 |
rs27010347 | snp | C/T | 0.132653 | 0.220748 | synonymous-codon | Bptf | GRCm38.p3 | 11:107099576 | CTCACCATTAGCTGC[C/T]GCTAGGAAGGACTTG | 207165 |
rs27010348 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Bptf | Mm_Celera | 11:107099429 | GCTTACTGTGGCGTA[A/G]CTAGGATCCCTGCAG | 207165 |
rs27010349 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Bptf | Mm_Celera | 11:107099388 | ACCAGGGCAAGAAAC[A/G]GCCCACTAAAGCACA | 207165 |
rs27010350 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Bptf | Mm_Celera | 11:107098391 | TATGATTACAAAATG[C/T]TGGAAGCTATACAAT | 207165 |
rs27010351 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Bptf | Mm_Celera | 11:107097181 | AACTTGGGCAGAGTG[C/T]CACCATGGCATGGCA | 207165 |
rs27010352 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Bptf | Mm_Celera | 11:107097114 | AGACCTTCCTTTCTG[A/G]AGCTCTGTAACTATT | 207165 |
rs27010353 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Bptf | Mm_Celera | 11:107096685 | GTGAAAGGCTTCAAG[C/T]GAGACTGGACACACA | 207165 |
rs27010354 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Bptf | Mm_Celera | 11:107095996 | AACAAATGCCACTAA[C/T]GAATTTGCATGTTTG | 207165 |
rs27010355 | snp | C/T | 0.132653 | 0.220748 | missense | Bptf | Mm_Celera | 11:107095772 | CTGTCAGCGTCCTTG[C/T]CTGCGGAAGGGTCCT | 207165 |
rs27010356 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Bptf | Mm_Celera | 11:107095586 | ACATGGGAGAGACTC[A/T]CTTAAATATCCTTAG | 207165 |
rs27010357 | snp | A/T | 0.132653 | 0.220748 | intron-variant, missense | Bptf | Mm_Celera | 11:107095171 | CACAGAGTTACCTTT[A/T]TCCCCAACTTCTGTT | 207165 |
rs27010358 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Bptf | Mm_Celera | 11:107094163 | TCACAAACTCGGAGG[C/T]CCTCAAAAGCTTGAA | 207165 |
rs27010359 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Bptf | Mm_Celera | 11:107094110 | TGCAGGCTTCAGCAA[C/T]GCTCAACGCTGGTTG | 207165 |
rs27010360 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Bptf | Mm_Celera | 11:107093983 | ACAGCAGCCAACTGC[A/G]CTCTGCTTCACTGGA | 207165 |
rs27010361 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Bptf | Mm_Celera | 11:107093960 | TTCCTACAGATGGCC[A/G]AAGCACCACAGCAGC | 207165 |
rs27010362 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Bptf | Mm_Celera | 11:107092865 | GAACGGTTATTACAT[C/T]TGACTGATATCCACC | 207165 |
rs27010363 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Bptf | Mm_Celera | 11:107092784 | CTAGGCACAGAAAAG[C/T]AACCGTTACTTGCTG | 207165 |
rs27010364 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Bptf | Mm_Celera | 11:107092623 | AAATCAAGTGAGAAG[C/T]TCCATACCATGGAGG | 207165 |
rs27010365 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Bptf | Mm_Celera | 11:107089185 | TGTCCGGAGTTACTA[A/C]GCCACAGAAAAGCAT | 207165 |
rs27010366 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Bptf | Mm_Celera | 11:107089078 | TCCAGGAGAAAGCTG[C/G]CATGGAAGGAGAAAG | 207165 |
rs27010367 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Bptf | Mm_Celera | 11:107089060 | CACTGACAGCAAACT[G/T]TTTCCAGGAGAAAGC | 207165 |
rs27024468 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Bptf | Mm_Celera | 11:107087790 | GACATCAGCGCTACC[C/T]GCTACACGTGCTTGC | 207165 |
rs27024469 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Bptf | Mm_Celera | 11:107087689 | GCTTACACCTGTAAT[C/T]CCTAGGACAGGAAGA | 207165 |
rs27024470 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Bptf | Mm_Celera | 11:107087271 | AACAGATTTGGAGAG[A/G]ATTCTGCACTCTCAG | 207165 |
rs27024471 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Bptf | Mm_Celera | 11:107087224 | GAGCTTATGGTCTCA[C/T]ATTTCTAAAGTGTTC | 207165 |
rs27024472 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Bptf | Mm_Celera | 11:107087040 | AGAGTGAAATACACC[A/G]TTAGTCTCTCGGTCC | 207165 |
rs27024473 | snp | A/G | 0.197531 | 0.244432 | intron-variant, synonymous-codon | Bptf | Mm_Celera | 11:107086857 | GCTGGAGGCAGTGGT[A/G]GCACTAGTGTTACTG | 207165 |
rs27024474 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Bptf | Mm_Celera | 11:107086323 | ATCTCTAACCGGAAA[A/C]GTCCCTACGTGTGTC | 207165 |
rs27024475 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Bptf | Mm_Celera | 11:107086049 | TCACGAGTAAGGATA[G/T]GCACAGTTTCCCATG | 207165 |
rs27024476 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Bptf | Mm_Celera | 11:107085179 | GTCCTACCTTCAAAG[C/T]AGCCCTTGCTCTTTG | 207165 |
rs27024477 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Bptf | Mm_Celera | 11:107084608 | TGAGGTCAGTTACTA[A/C]TGAAGCATTAGGTAC | 207165 |
rs27024478 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Bptf | Mm_Celera | 11:107084414 | AGAGGCCCTCTCATA[A/G]CACACACATTACACA | 207165 |
rs27024479 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Bptf | Mm_Celera | 11:107084169 | GTACGTTATCTTCTC[A/G]TGGACTCTGTGTGTG | 207165 |
rs27024480 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Bptf | Mm_Celera | 11:107084084 | TCCACACAATATGCC[A/G]CTGATTAGATCAAGC | 207165 |
rs27024481 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Bptf | Mm_Celera | 11:107083965 | GAAGGCTGTAAACAG[G/T]CTTGATTCTCCTGTC | 207165 |
rs27024482 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Bptf | Mm_Celera | 11:107083770 | GCTCTGGCTGAGCCC[A/G]TGTAGGATTCTGCTT | 207165 |
rs27024483 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Bptf | Mm_Celera | 11:107083295 | ACCCCAGCTACTCAT[C/T]ACAGTATATTTTCCA | 207165 |
rs27024484 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Bptf | Mm_Celera | 11:107083175 | ATTATCCTCTTAACA[C/T]GAGAATCTCTCAACA | 207165 |
rs27024485 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Bptf | Mm_Celera | 11:107082809 | AAGTCCGACAAGCAG[A/G]CAGACAATGTCCTTC | 207165 |
rs27024486 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Bptf | Mm_Celera | 11:107082450 | TTGGAAGGGCAACTG[G/T]CTCTCCAATGCACAA | 207165 |
rs27024487 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Bptf | Mm_Celera | 11:107082448 | CATTGGAAGGGCAAC[A/T]GTCTCTCCAATGCAC | 207165 |
rs27024488 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Bptf | Mm_Celera | 11:107082332 | TTAAAGACTCAAGGG[A/T]GTAGTCCACATGTGT | 207165 |
rs27024489 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Bptf | Mm_Celera | 11:107082258 | ATGTTGCTCTTGGTA[C/T]TCACTACAAGAAAGA | 207165 |
rs27024490 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Bptf | Mm_Celera | 11:107081669 | CAAACAGGTGACATC[C/T]ATGACTAAGAGACTG | 207165 |
rs27024491 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon | Bptf | GRCm38.p3 | 11:107081443 | TGAATTGGTCGAGTA[C/T]TGATTGTGGTAGACT | 207165 |
rs27024492 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon | Bptf | GRCm38.p3 | 11:107081254 | AAGGAAGGATGAAGG[A/G]ATGTTGCTCTCTAGC | 207165 |
rs27024493 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Bptf | Mm_Celera | 11:107081135 | CTCACTGGTATTAAC[A/G]CTTTAAGGGACACAC | 207165 |
rs27024494 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Bptf | Mm_Celera | 11:107080880 | GAAGGAAGAAATCAC[A/G]TCACTCGGGTGCTCT | 207165 |
rs27024495 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Bptf | Mm_Celera | 11:107080602 | CTGTACCCTATGAAT[C/T]ATTGTAGACAGGAAA | 207165 |
rs27024496 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Bptf | Mm_Celera | 11:107079102 | GCCAGCCGTTCACAT[C/T]CATTTCCTGCACAGC | 207165 |
rs27024497 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Bptf | Mm_Celera | 11:107079077 | GGAAAGAAGCCACCA[A/C]CGTCTATCTGCCAGC | 207165 |
rs27024498 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Bptf | Mm_Celera | 11:107079053 | AGGAGGGACCAATAC[A/T]GTCCCTAAGGAAAGA | 207165 |