SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6191692 | snp | A/G | 0.5 | 0 | intron-variant | Nbeal1 | Mm_Celera | 1:60274971 | gatgtttctgttacc[A/G]taaaaacttatttct | 269198 |
rs6192272 | snp | G/T | 0.5 | 0 | intron-variant | Nbeal1 | Mm_Celera | 1:60275103 | aggaaaccaaggaca[G/T]tagcaagagcccata | 269198 |
rs6193769 | snp | A/G | 0.5 | 0 | intron-variant | Nbeal1 | Mm_Celera | 1:60275356 | tagctacttcaggat[A/G]tatactcaaatagga | 269198 |
rs6194349 | snp | C/T | 0.5 | 0 | intron-variant | Nbeal1 | Mm_Celera | 1:60275482 | ctgaaaatttcatga[C/T]tgcatttttctttac | 269198 |
rs6208396 | snp | C/T | 0.5 | 0 | intron-variant | Nbeal1 | Mm_Celera | 1:60275792 | ttcttttctccatat[C/T]cctttcagcatttgt | 269198 |
rs6208447 | snp | A/G | 0.5 | 0 | intron-variant | Nbeal1 | Mm_Celera | 1:60275820 | tgttgtgtgtggtat[A/G]ttgatctttgcaatt | 269198 |
rs6227920 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Nbeal1 | GRCm38.p3 | 1:60315883 | AAAGCACAGAGGTGC[A/G]ATTACAAAGGTCAGA | 269198 |
rs6228442 | snp | G/T | 0.5 | 0 | intron-variant | Nbeal1 | Mm_Celera | 1:60315965 | ATTCTAGTAAGCTAC[G/T]GTAACTTGGGGACTA | 269198 |
rs6229675 | snp | C/T | 0.5 | 0 | intron-variant | Nbeal1 | Mm_Celera | 1:60316217 | ttCCATGCAGAAACA[C/T]ACCTTTTCATTATTT | 269198 |
rs6282881 | snp | C/T | 0.5 | 0 | intron-variant, utr-variant-3-prime | Nbeal1 | Mm_Celera | 1:60280406 | ATCAATTGAGCTTTC[C/T]ATAAATAGAAATATA | 269198 |
rs6296662 | snp | C/T | 0.21875 | 0.248039 | intron-variant, utr-variant-3-prime | Nbeal1 | Mm_Celera | 1:60280635 | ATGATTTTCTAATCC[C/T]ACTTCATTTTGTTCT | 269198 |
rs6389697 | snp | C/T | 0.5 | 0 | intron-variant | Nbeal1 | Mm_Celera | 1:60291661 | aactggaggttcagg[C/T]ggccgtcagccttca | 269198 |
rs6390325 | snp | G/T | 0.207612 | 0.24638 | intron-variant | Nbeal1 | Mm_Celera | 1:60291805 | TTGGAAGATATTTCC[G/T]TTAAGTATTAACTTT | 269198 |
rs6390868 | snp | A/G | 0.49827 | 0.0293608 | synonymous-codon | Nbeal1 | GRCm38.p3 | 1:60291911 | GAGAGGGCCAGCTGC[A/G]GTGGAGGCACTCAAT | 269198 |
rs6391379 | snp | A/G | 0.207612 | 0.24638 | intron-variant | Nbeal1 | Mm_Celera | 1:60291966 | GGTACCAGCCGGAAT[A/G]CCTCCTCTCTCACAA | 269198 |
rs6391434 | snp | A/G | 0.5 | 0 | intron-variant | Nbeal1 | Mm_Celera | 1:60291991 | TCACAATACTTAAAC[A/G]GCATTAGTATTTGAC | 269198 |
rs45639424 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Nbeal1 | Mm_Celera | 1:60229485 | GCAAAGTCTAGCACA[A/G]CTCTTATTTATATGA | 269198 |
rs45668069 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nbeal1 | Mm_Celera | 1:60278566 | ATGCTAGTTTTTGAA[C/T]GTAGAATTCCTTTCC | 269198 |
rs45669792 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Nbeal1 | Mm_Celera | 1:60304691 | AATGTTAGCTCTCAT[G/T]TTTGAACTATAGATA | 269198 |
rs45677903 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Nbeal1 | GRCm38.p3 | 1:60199746 | GAGATGCTGAAATGT[C/T]ATAAATGACCATAGT | 269198 |
rs45678370 | snp | A/T | | | intron-variant | Nbeal1 | Mm_Celera | 1:60198264 | ATGTCTTGGAAAAAA[A/T]ATATATATATATAAT | 269198 |
rs45702041 | snp | C/T | 0.231111 | 0.249285 | intron-variant, utr-variant-3-prime | Nbeal1 | Mm_Celera | 1:60280750 | CTGCCTTTTAGTACA[C/T]ATAGTGTGAAAATAT | 269198 |
rs45704153 | snp | A/G | | | intron-variant | Nbeal1 | GRCm38.p3 | 1:60215909 | CTGTTGTGTAAGAAT[A/G]TAGTAAAGGCAAACA | 269198 |
rs45704932 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Nbeal1 | Mm_Celera | 1:60283520 | TTCAAAAATTTCTGT[A/G]GTCAACATATCTTAT | 269198 |
rs45714232 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Nbeal1 | Mm_Celera | 1:60276166 | TTAAGCGTACAGTTC[A/C]ATGTAAGTTGGAGTG | 269198 |
rs45724544 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Nbeal1 | Mm_Celera | 1:60244269 | ACCTGCTTTTGATAA[G/T]CGAGTGCTTTAGATT | 269198 |
rs45728147 | snp | C/T | 0.231111 | 0.249285 | intron-variant, downstream-variant-500B | Nbeal1 | Mm_Celera | 1:60281032 | ACAGTGTAGTACTTA[C/T]GTTTAATTCTTTTGC | 269198 |
rs45793032 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Nbeal1 | Mm_Celera | 1:60289533 | TTAATCCCACTCCAC[A/G]TTACTTTTTGAAACA | 269198 |
rs45800298 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nbeal1 | Mm_Celera | 1:60286633 | GGTTAGCTCAGAAGC[A/G]TTTCTGTAAATCTCT | 269198 |
rs45812419 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Nbeal1 | Mm_Celera | 1:60295855 | TCATTTAACTCTGAA[A/G]TGTTTTCTTAAATTA | 269198 |
rs45820826 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nbeal1 | Mm_Celera | 1:60230044 | AACTTTTGGCATTAA[A/G]GATTGCCTTCTCCAG | 269198 |
rs45821161 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime | Nbeal1 | Mm_Celera | 1:60332533 | TGTCTTTTCAGTTGA[A/G]TCTTAAAGAACTTTT | 269198 |
rs45823265 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nbeal1 | Mm_Celera | 1:60284138 | GGTATGCTCAGAGTC[A/G]AGCCATTTTCCTCTC | 269198 |
rs45832105 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Nbeal1 | GRCm38.p3 | 1:60292735 | ATTTAATGTTTTCAG[A/G]AAATTACTTTCTGGT | 269198 |
rs45833017 | snp | C/T | 0.32 | 0.24 | intron-variant | Nbeal1 | Mm_Celera | 1:60214579 | TTTCTGTCCACCAGA[C/T]CAAGCAAGGTGTTCA | 269198 |
rs45853778 | snp | C/T | | | intron-variant | Nbeal1 | Mm_Celera | 1:60295336 | TAAAATTCATGGCTG[C/T]CCTTATGGAGACCGA | 269198 |
rs45865886 | snp | C/T | | | intron-variant | Nbeal1 | GRCm38.p3 | 1:60314334 | TCTCTGATGACATTG[C/T]AAATAGTAGCAATTC | 269198 |
rs45877678 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nbeal1 | Mm_Celera | 1:60266642 | ACAATGGCAGTTGGG[C/T]CTATTTTCAACTTTA | 269198 |
rs45886330 | snp | A/G | | | intron-variant | Nbeal1 | Mm_Celera | 1:60295186 | CTTTTTAATTTTGAT[A/G]TCTTGTTTCACGAAT | 269198 |
rs45898902 | snp | A/T | 0.32 | 0.24 | intron-variant | Nbeal1 | Mm_Celera | 1:60270922 | CATGCTTTTAAATCC[A/T]TTTGGGTATATAGTA | 269198 |
rs45903149 | snp | A/G | | | intron-variant | Nbeal1 | Mm_Celera | 1:60184591 | CTATCCTGGAACTTT[A/G]CTATGTAGACTAGGC | 269198 |
rs45906253 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Nbeal1 | GRCm38.p3 | 1:60227855 | AGAATAATTATGAGC[C/T]AGTCTTACTACTCAT | 269198 |
rs45917268 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Nbeal1 | Mm_Celera | 1:60186395 | TATTTTAATACATGT[A/G]TGCATGGAACTATTA | 269198 |
rs45932448 | snp | C/G | | | intron-variant | Nbeal1 | Mm_Celera | 1:60295371 | TAGGCCAGTGAAATG[C/G]CTCAGTGGGTAAAGG | 269198 |
rs45943194 | snp | A/G | 0.32 | 0.24 | intron-variant | Nbeal1 | Mm_Celera | 1:60203187 | AGTCTGTTCTGGCAC[A/G]CTAATGATACCAGAA | 269198 |
rs45944966 | snp | A/T | 0.32 | 0.24 | intron-variant | Nbeal1 | Mm_Celera | 1:60242760 | TAAAAAAAATTAGGG[A/T]TTGTAAAAGGAAGTT | 269198 |
rs45948270 | snp | A/G | 0.32 | 0.24 | intron-variant | Nbeal1 | Mm_Celera | 1:60225926 | TAAGAGACTTTGTAT[A/G]ACAACTTACAGCTAG | 269198 |
rs45957984 | snp | A/T | 0.32 | 0.24 | intron-variant | Nbeal1 | Mm_Celera | 1:60248320 | TATGTGATGTAAAGG[A/T]GATGAGAGTGATTAT | 269198 |
rs45979775 | snp | A/T | 0.408163 | 0.193609 | intron-variant | Nbeal1 | GRCm38.p3 | 1:60287617 | CATACAGAGCTGTCT[A/T]ACTTCGAGAGGTGAT | 269198 |
rs45987810 | snp | A/G | 0.32 | 0.24 | intron-variant | Nbeal1 | Mm_Celera | 1:60204597 | TAGCAGTAATTTGCA[A/G]GCAGTACCATGACAG | 269198 |
rs45989801 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nbeal1 | Mm_Celera | 1:60282098 | TAGCATATAAATATA[C/T]GTACACTAAGCTATC | 269198 |
rs46046770 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Nbeal1 | Mm_Celera | 1:60246155 | CAGATCTGAAAATTA[G/T]TCTTTAGTACTTTGT | 269198 |
rs46047820 | snp | C/G/T | 0.124444 | 0.216185 | synonymous-codon | Nbeal1 | GRCm38.p3 | 1:60235148 | GCAGAGCAGAACTAC[C/G/T]TGTGTGAATGCAAAC | 269198 |
rs46058376 | snp | G/T | | | intron-variant | Nbeal1 | GRCm38.p3 | 1:60253620 | ACTGTCGTGATAGTA[G/T]GCAGTTAAAGAAGTA | 269198 |
rs46079863 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Nbeal1 | GRCm38.p3 | 1:60287794 | CAGGAGCAAGCAAAC[G/T]TAGGTTTTCAGAGAA | 269198 |
rs46087635 | snp | A/G | 0.32 | 0.24 | intron-variant | Nbeal1 | Mm_Celera | 1:60271064 | TTTTTCAAATAGCCC[A/G]TCCGTTGTGTATATA | 269198 |
rs46092626 | snp | A/C | 0.32 | 0.24 | synonymous-codon | Nbeal1 | Mm_Celera | 1:60268034 | AGAATACTGCAATTC[A/C]GAAGAGTGGCAAGTT | 269198 |
rs46103323 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Nbeal1 | GRCm38.p3 | 1:60312689 | TTGATGTTTTATAAG[G/T]CTTCGTCTGTGGCTC | 269198 |
rs46127759 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Nbeal1 | Mm_Celera | 1:60297245 | GTTAACGCTATAACT[A/G]AAAGAGTAACCTTGT | 269198 |
rs46130933 | snp | C/T | | | intron-variant | Nbeal1 | Mm_Celera | 1:60301865 | TTATATGTCTTTCTT[C/T]CTTAAAAAAGTATTT | 269198 |
rs46132300 | snp | A/G | 0.32 | 0.24 | intron-variant | Nbeal1 | Mm_Celera | 1:60216829 | TAGAAATTGATCCTT[A/G]GAGTTGATTTAGTAA | 269198 |
rs46139808 | snp | C/G/T | 0.124444 | 0.216185 | intron-variant | Nbeal1 | GRCm38.p3 | 1:60228149 | GTCAGGTAACTGTGA[C/G/T]TAGGCAGTGCTGCAT | 269198 |
rs46140031 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Nbeal1 | Mm_Celera | 1:60246815 | AGAGTAACTTTATAT[A/G]AAAATCTTTTTTGCC | 269198 |
rs46140292 | snp | C/G | 0.32 | 0.24 | intron-variant | Nbeal1 | Mm_Celera | 1:60273243 | AAGCCTCTCTGCCTT[C/G]TCAGTTTTCTGGCAC | 269198 |
rs46145623 | snp | C/T | 0.32 | 0.24 | intron-variant | Nbeal1 | Mm_Celera | 1:60210730 | GGGACTATAAAGTGG[C/T]TTATGGACTTGTTTA | 269198 |
rs46154873 | snp | G/T | | | intron-variant | Nbeal1 | GRCm38.p3 | 1:60190699 | AACTTACTATTCCAT[G/T]ACTTGAATAATTGTA | 269198 |
rs46161485 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Nbeal1 | Mm_Celera | 1:60209320 | AAGCCCTGGCTCCAG[A/T]ATAGTTAAGCTCCAG | 269198 |
rs46164687 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nbeal1 | Mm_Celera | 1:60287549 | ATTTATTTAAGGTTG[A/G]TTTTGTGTGTAGATT | 269198 |
rs46173785 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nbeal1 | Mm_Celera | 1:60214119 | CATAGTTGAGAACTC[C/T]AGGGTTAGGCCCTGC | 269198 |
rs46178077 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Nbeal1 | Mm_Celera | 1:60205631 | TAATCTTTTTATCAC[C/T]ATGGCTGTCTAAGCA | 269198 |
rs46183725 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Nbeal1 | Mm_Celera | 1:60234398 | TATAGCTTAGTCTGA[A/C]GAAAACAGTTCTATA | 269198 |
rs46184954 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Nbeal1 | Mm_Celera | 1:60182925 | CTGTGTGGTTATGTT[C/T]TCAGATCACACAGCC | 269198 |
rs46194799 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Nbeal1 | Mm_Celera | 1:60225473 | GACAGAGGGCATTCA[G/T]TTGTCGCATGCCCTG | 269198 |
rs46200549 | snp | C/T | | | intron-variant | Nbeal1 | GRCm38.p3 | 1:60310428 | CTGGCCTAGAACTCG[C/T]TATGCAGATCAGGCT | 269198 |
rs46216395 | snp | C/T | 0.32 | 0.24 | synonymous-codon | Nbeal1 | Mm_Celera | 1:60236431 | CTCAGGTGTGCTGGT[C/T]GTGGCAGTGTGCACA | 269198 |
rs46223354 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Nbeal1 | GRCm38.p3 | 1:60192114 | GTTCTCTCTCGTGTA[C/T]TTGCATCGTTCAGTA | 269198 |
rs46241311 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Nbeal1 | Mm_Celera | 1:60294910 | TAGTCAATATCAGTG[A/G]TTCAGTGGTAGAACT | 269198 |
rs46244451 | snp | G/T | 0.32 | 0.24 | intron-variant | Nbeal1 | Mm_Celera | 1:60263916 | TCAGGGTAAGGCTGC[G/T]CATCTCTTGCTGGCT | 269198 |
rs46248794 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Nbeal1 | Mm_Celera | 1:60273536 | ATTTTAAGAAGTGTT[C/G]CAGTTCAGTGGTGAC | 269198 |
rs46250203 | snp | C/T | 0.32 | 0.24 | intron-variant | Nbeal1 | Mm_Celera | 1:60210847 | TTAGAGCTTTTGAAG[C/T]CCACTTTACTTATCT | 269198 |
rs46250739 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nbeal1 | Mm_Celera | 1:60264598 | GCTGTTGCAAACAGA[A/G]TGAAATATAAGTAGA | 269198 |
rs46260801 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Nbeal1 | Mm_Celera | 1:60272697 | TGGGAGTAGAACACG[G/T]AACCTCTGAAAGTGC | 269198 |
rs46261491 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nbeal1 | Mm_Celera | 1:60216193 | AAATGCTCATCCTGA[C/T]TTAATTTTGTGCTTT | 269198 |
rs46273399 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nbeal1 | Mm_Celera | 1:60287988 | GTACAAAAGGTGCAC[A/G]TTTAAAAAGGTGCTT | 269198 |
rs46307702 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Nbeal1 | Mm_Celera | 1:60186452 | CTGTCTACACCTATC[C/T]ATCTTACCTATCTCC | 269198 |
rs46317630 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Nbeal1 | Mm_Celera | 1:60226099 | TTTATATTGTGTGCT[C/T]GTGTATTTAAGATGT | 269198 |
rs46330071 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Nbeal1 | Mm_Celera | 1:60286855 | TATGCCCACTGTATA[C/T]TTTGATCTTTCAAAT | 269198 |
rs46345326 | snp | C/T | 0.231111 | 0.249285 | intron-variant, utr-variant-3-prime | Nbeal1 | Mm_Celera | 1:60280628 | GAAAGAAATGATTTT[C/T]TAATCCCACTTCATT | 269198 |
rs46408186 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nbeal1 | Mm_Celera | 1:60283448 | ATTAAATACTGAAAA[A/G]TAAAGTTACAGCAAG | 269198 |
rs46427246 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Nbeal1 | Mm_Celera | 1:60237850 | GACTAGTAGGACAAA[G/T]TAGGGTGTTTGTCAA | 269198 |
rs46427330 | snp | C/T | 0.32 | 0.24 | intron-variant | Nbeal1 | Mm_Celera | 1:60330881 | CATTTCTCTGGATTA[C/T]CTTAAACAGATGCGA | 269198 |
rs46428514 | snp | C/T | 0.231111 | 0.249285 | intron-variant, downstream-variant-500B | Nbeal1 | Mm_Celera | 1:60281196 | TTATTAATAATTGTC[C/T]CATTCTAAGAGGTTA | 269198 |
rs46438914 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nbeal1 | Mm_Celera | 1:60182141 | ATTGACAATATTGGC[C/T]TGCTATTAAAAACTT | 269198 |
rs46442253 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Nbeal1 | Mm_Celera | 1:60264905 | AGATGCCACGCAGCT[C/T]CTAGACTGTCTGTCA | 269198 |
rs46444832 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Nbeal1 | Mm_Celera | 1:60278333 | GGCTTGAGGGTTTCA[C/G]AGTAAACTTAGTTAC | 269198 |
rs46454950 | snp | C/G | 0.32 | 0.24 | intron-variant | Nbeal1 | Mm_Celera | 1:60269014 | TAATCCCCAAGAAAC[C/G]TCTCCAGCCCTGTAA | 269198 |
rs46458730 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nbeal1 | Mm_Celera | 1:60276227 | GAGCCCAGTGGCAGG[A/G]CAGAATTGAAATCTA | 269198 |
rs46484067 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nbeal1 | Mm_Celera | 1:60204290 | ATTCCTTATTTCTCA[A/G]AAAAATTTTTTCCCA | 269198 |
rs46484614 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nbeal1 | Mm_Celera | 1:60230269 | AAGTCTATTTTTGAA[A/G]GTAAATTAAAGCATA | 269198 |
rs46484621 | snp | G/T | 0.32 | 0.24 | intron-variant | Nbeal1 | Mm_Celera | 1:60225501 | CTGGTGTAGGAACTA[G/T]GCAAACATCTAAATC | 269198 |