SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3693662 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxl2 | Mm_Celera | 9:114025757 | AGACTCTCTGCTCCC[A/G]ACACTCATGGGTCAG | 72179 |
rs3694903 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Fbxl2 | Mm_Celera | 9:114025967 | ACTCTCAAGAAATCA[C/G]GGCGTAACCTTGCCC | 72179 |
rs6258277 | snp | A/G | 0.5 | 0 | intron-variant | Ubp1, Fbxl2 | Mm_Celera | 9:113964322 | catgtgtgcgtgtgc[A/G]tgcatgtAAGCTTTC | 72179 |
rs6292514 | snp | C/T | 0.5 | 0 | intron-variant | Ubp1, Fbxl2 | Mm_Celera | 9:113966071 | CTGCTGTTGTGCCTG[C/T]GTCCCGGCCTCCTCC | 72179 |
rs6293023 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ubp1, Fbxl2 | Mm_Celera | 9:113966139 | CAGCTCTTTCTACAC[C/T]GTTGTCCTATCTCAA | 72179 |
rs6293705 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Ubp1, Fbxl2 | Mm_Celera | 9:113966321 | AACCACTGACTGGCT[A/G]CATAGAAAGGCTCTA | 72179 |
rs6294297 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Ubp1, Fbxl2 | Mm_Celera | 9:113966430 | TCTTCAGACATGACA[A/G]TGACTTTTTAAAAGC | 72179 |
rs6308267 | snp | A/C | 0.5 | 0 | intron-variant | Ubp1, Fbxl2 | Mm_Celera | 9:113973219 | TTTACTATTAGAAGT[A/C]CAACTCACCTGTGCT | 72179 |
rs6308712 | snp | A/G | 0.5 | 0 | intron-variant | Ubp1, Fbxl2 | Mm_Celera | 9:113973294 | TATAATCTTTAAGTC[A/G]GTCTTCACAGGACCT | 72179 |
rs6310366 | snp | C/T | 0.359862 | 0.224567 | intron-variant, missense, nc-transcript-variant | Ubp1, Fbxl2 | Mm_Celera | 9:113973625 | AAGGACACTGTGCCC[C/T]GATTAGAAGCTCTCA | 72179 |
rs13462514 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | Ubp1, Fbxl2 | Mm_Celera | 9:113975825 | TGAACCTTATGCTGG[A/C]CTGGGGAGGAGATAG | 72179 |
rs29639885 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Fbxl2 | Mm_Celera | 9:113999011 | GTGAAAGGTATTTCT[A/C]ACCAGGCAGTGGTGG | 72179 |
rs29645077 | snp | A/T | 0.375 | 0.216506 | intron-variant | Fbxl2 | Mm_Celera | 9:113980764 | GTTCCTACATGTACA[A/T]TTGGGGTAATTTAGG | 72179 |
rs29645227 | snp | C/T | 0.32 | 0.24 | intron-variant | Fbxl2 | GRCm38.p3 | 9:114005499 | GGTTGTCGCAGAGGC[C/T]GTCTATGTCTTTCAT | 72179 |
rs29647559 | snp | A/C | 0.375 | 0.216506 | intron-variant | Fbxl2 | Mm_Celera | 9:114010093 | GTACGGAAGCAGCCC[A/C]GGTGCCTGGATCACT | 72179 |
rs29689098 | snp | G/T | 0.375 | 0.216506 | intron-variant | Fbxl2 | GRCm38.p3 | 9:113999584 | ACAATAGAGAGACTG[G/T]CTTTTTTTTTTTTTT | 72179 |
rs29739480 | snp | A/T | 0.444444 | 0.157135 | upstream-variant-2KB | Fbxl2 | Mm_Celera | 9:114027895 | ATTTGTTGGGTTTTT[A/T]AAATGTGGCTGAATA | 72179 |
rs29745223 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Fbxl2 | Mm_Celera | 9:114008596 | TTGACCCGGTGCCTG[A/C]CAGGAACTGAACTCC | 72179 |
rs29786798 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Fbxl2 | Mm_Celera | 9:114000233 | GGAGACTGAGCACAC[A/G]CAAGTCTCAGTGCTG | 72179 |
rs29790685 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fbxl2 | Mm_Celera | 9:114025571 | TCAGTAAAATACGGT[A/G]GACAGGGATGGAGAA | 72179 |
rs29832047 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fbxl2 | Mm_Celera | 9:113999464 | GCATGGCCTGCATGC[A/G]CCCTCCTTTCCACTG | 72179 |
rs29835857 | snp | C/T | 0.375 | 0.216506 | intron-variant | Fbxl2 | Mm_Celera | 9:113998753 | AAGACAGCATCTGTA[C/T]ATTGTAGGATGGATT | 72179 |
rs29840069 | snp | C/T | 0.375 | 0.216506 | intron-variant | Fbxl2 | Mm_Celera | 9:114000616 | GAGAAGGATGGGAAA[C/T]GGTCACGTTTGCATG | 72179 |
rs29842461 | snp | C/T | 0.32 | 0.24 | intron-variant | Fbxl2 | Mm_Celera | 9:114004657 | CCCCACAAAGTCACA[C/T]TGCCCATACACTCAC | 72179 |
rs29871232 | snp | A/C | 0.32 | 0.24 | intron-variant | Fbxl2 | Mm_Celera | 9:114014347 | CCAGGATCACCCCCA[A/C]CCCCAATCTCACCCC | 72179 |
rs29878027 | snp | C/T | 0.375 | 0.216506 | intron-variant | Fbxl2 | Mm_Celera | 9:113992469 | GTACTCATACACACA[C/T]ACACACAGGAGCTAG | 72179 |
rs29880402 | snp | G/T | 0.375 | 0.216506 | intron-variant | Fbxl2 | Mm_Celera | 9:114015593 | CCTGACTAAGACAGA[G/T]GGAAAGGATGGATGC | 72179 |
rs29882956 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB | Fbxl2 | GRCm38.p3 | 9:114028137 | ACATTAGCTGGGGCT[A/G]GCTTACAGTTTTAGA | 72179 |
rs29883217 | snp | C/T | 0.375 | 0.216506 | intron-variant | Fbxl2 | Mm_Celera | 9:113998840 | CCCAGGGCAACTGCT[C/T]TGAATGGCAGGAATG | 72179 |
rs29889463 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Fbxl2 | Mm_Celera | 9:114001175 | TGGGGCCGGCACACA[C/T]TGCTACCCGGCTAAC | 72179 |
rs29918399 | snp | C/T | 0.375 | 0.216506 | intron-variant | Fbxl2 | Mm_Celera | 9:113994475 | TGTCCATCAGGCAGC[C/T]GTGCTGGGTGCCAAG | 72179 |
rs29932552 | snp | G/T | 0.375 | 0.216506 | intron-variant | Fbxl2 | Mm_Celera | 9:113997303 | AGGACCCCCACTGCA[G/T]CAGATGCCACAGCTG | 72179 |
rs29945534 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fbxl2 | Mm_Celera | 9:114004544 | CTTATTGATTATTTG[A/G]GAGTTTTACATAATG | 72179 |
rs29989422 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Fbxl2 | Mm_Celera | 9:114002536 | GAAGCACACAAGCTC[A/G]GAAAGAGGAGAGAAG | 72179 |
rs30022235 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fbxl2 | Mm_Celera | 9:114000193 | CTTCTAAGAAACTAG[A/G]GAGATGGGGAGGGCG | 72179 |
rs30035176 | snp | A/C/G | 0.375 | 0.216506 | intron-variant | Fbxl2 | GRCm38.p3 | 9:114000263 | GATCTGATGCACACC[A/C/G]CGACACTCCACATGT | 72179 |
rs30080839 | snp | C/T | 0.375 | 0.216506 | intron-variant | Fbxl2 | Mm_Celera | 9:113994546 | GAGAGAAGCAACTCC[C/T]GGGGCTTGTCTGCTG | 72179 |
rs30090023 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fbxl2 | Mm_Celera | 9:114003526 | AAGGCAAGATGATGA[A/G]ATGGTGTCAATATTT | 72179 |
rs30145644 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fbxl2 | Mm_Celera | 9:114025281 | CCTTTGCCAAAGGGA[A/G]GGATACAGAGTCAGG | 72179 |
rs30172805 | snp | G/T | 0.5 | 0 | intron-variant | Ubp1, Fbxl2 | Mm_Celera | 9:113972503 | GGGGGCTGGAGAGAC[G/T]GCTCAGCAGTTAAGA | 72179 |
rs30174771 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fbxl2 | Mm_Celera | 9:114002591 | GTTATTCTGCTGATG[C/T]TGTGAACCCACAGGT | 72179 |
rs30177727 | snp | A/T | 0.32 | 0.24 | intron-variant | Fbxl2 | Mm_Celera | 9:113991586 | AGTCCATGGGGCTCA[A/T]CAGGGGCCACGGAAT | 72179 |
rs30178264 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fbxl2 | Mm_Celera | 9:114025375 | CACTCCAGAAGGCTC[A/G]GAACCAAAGCATTCC | 72179 |
rs30185064 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Fbxl2 | Mm_Celera | 9:113998314 | ACTCACAACTACACT[C/G]TGAGACAGGCTTTGT | 72179 |
rs30226687 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fbxl2 | Mm_Celera | 9:114006074 | GCTGGCCCAAGAGCC[C/T]GAGGCCACACACACA | 72179 |
rs30236024 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Fbxl2 | Mm_Celera | 9:114004291 | TCGAAGTAACAGCCA[C/T]GTGGAGTTAAATGTC | 72179 |
rs30285642 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Fbxl2 | Mm_Celera | 9:114017055 | TAGCTCCTCGCCCAG[A/G]GCCATCACTACGCAA | 72179 |
rs30287427 | snp | G/T | 0.375 | 0.216506 | upstream-variant-2KB | Fbxl2 | GRCm38.p3 | 9:114027438 | GGGATATATATGACC[G/T]TGTCTTGAAAAACCA | 72179 |
rs30330032 | snp | A/C | 0.375 | 0.216506 | intron-variant | Fbxl2 | Mm_Celera | 9:114016046 | ACCTTTAAAAAAAAA[A/C]CCAAAAAACCAAAAA | 72179 |
rs30332701 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fbxl2 | Mm_Celera | 9:113998712 | CTATATGGTAAGACG[A/G]CCCCTGAGCCATCTC | 72179 |
rs30372262 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fbxl2 | Mm_Celera | 9:114025339 | CAGCACCTAAGCCAA[A/G]GCTGAGAACTAGACG | 72179 |
rs30374203 | snp | A/G | 0.32 | 0.24 | intron-variant | Fbxl2 | Mm_Celera | 9:113991779 | GTACCCAAAGGCTGC[A/G]CACAACCATCTATAA | 72179 |
rs30378777 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Fbxl2 | Mm_Celera | 9:114008696 | CCTGCCCGCCACCCC[A/C]GCCGGCATGACTGGT | 72179 |
rs30422746 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxl2 | Mm_Celera | 9:113998972 | AGCAGTGTTTTCCTG[A/G]TAAACCAGAGTTTCC | 72179 |
rs30423608 | snp | A/T | 0.444444 | 0.157135 | upstream-variant-2KB | Fbxl2 | GRCm38.p3 | 9:114028200 | GGGCAGCGTGCAGGC[A/T]GGAGCCGAGAGTTCT | 72179 |
rs30430646 | snp | G/T | 0.32 | 0.24 | intron-variant | Fbxl2 | GRCm38.p3 | 9:114004739 | TCCCCACCCCACCCC[G/T]CCAGAAGCCACCAAC | 72179 |
rs30440176 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fbxl2 | Mm_Celera | 9:114007638 | GGCATGCATGCATGC[A/G]TGCTTGTGTATGCGT | 72179 |
rs30471656 | snp | C/T | 0.375 | 0.216506 | intron-variant | Fbxl2 | Mm_Celera | 9:114002865 | GAGCAGCTGGCAGCC[C/T]CTCTCCCCACCTGCT | 72179 |
rs30484732 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fbxl2 | Mm_Celera | 9:113999816 | TCTTAACTGCTAATG[A/G]ATGAGGGAGGACCCA | 72179 |
rs30509377 | snp | G/T | 0.375 | 0.216506 | intron-variant | Fbxl2 | Mm_Celera | 9:114002717 | ATGTGTGTATGCCTG[G/T]GTGAGTTTGTGTTCC | 72179 |
rs30512124 | snp | C/T | 0.375 | 0.216506 | intron-variant | Fbxl2 | Mm_Celera | 9:113996702 | AAACAAACATAGTGG[C/T]ACACACAGGTTTGTG | 72179 |
rs30522911 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fbxl2 | Mm_Celera | 9:113999532 | TGGTATGGATCTGTG[A/G]GTTCAAAGCCATCCA | 72179 |
rs33670765 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ubp1, Fbxl2 | Mm_Celera | 9:113961580 | TCCCAGGAGATGATG[C/T]ATAACAAACCCTTTT | 72179 |
rs33681260 | snp | C/T | 0 | 0 | intron-variant | Fbxl2 | Mm_Celera | 9:114003883 | GTTCAGATATTGGAG[C/T]CTCAAATAATGTGGT | 72179 |
rs33693974 | snp | A/G | 0.5 | 0 | intron-variant | Fbxl2 | Mm_Celera | 9:113999283 | ACATATCCTGCTTCC[A/G]GCCAAGCTAGTATTC | 72179 |
rs33701964 | snp | A/G/T | 0.375 | 0.216506 | intron-variant | Fbxl2 | GRCm38.p3 | 9:114001675 | CCAGAATTAAAAAAA[A/G/T]AAATAAATAAATAAA | 72179 |
rs33739952 | snp | G/T | 0.375 | 0.216506 | intron-variant | Fbxl2 | Mm_Celera | 9:113987144 | AGTTCAGGAGCAGTT[G/T]ATAAACTGATGGAGA | 72179 |
rs45707974 | snp | C/T | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Fbxl2 | Mm_Celera | 9:114018143 | TCAGAACAGAAATGC[C/T]TACTGTCCTGCAGAA | 72179 |
rs45715793 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ubp1, Fbxl2 | Mm_Celera | 9:113974445 | TATGTCACCCAGGCA[A/G]CTAATTGTACCATTC | 72179 |
rs45720670 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Fbxl2 | Mm_Celera | 9:114013077 | ACTCTGCTCATGTGT[A/C]GATTCAACTCTATCT | 72179 |
rs45765459 | snp | A/C | 0.244898 | 0.249948 | utr-variant-3-prime, nc-transcript-variant, intron-variant | Ubp1, Fbxl2 | Mm_Celera | 9:113975968 | CGAGCCGAGCCGAGC[A/C]GAGCAGATGAGCAGA | 72179 |
rs45770007 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Fbxl2 | Mm_Celera | 9:113983006 | CTGTCAATCACTGAG[C/T]TGGCTGTCCTTGTAA | 72179 |
rs45771154 | snp | A/G | 0.277778 | 0.248452 | upstream-variant-2KB | Fbxl2 | Mm_Celera | 9:114027524 | CGTTTTAAATGATCA[A/G]TGAATCCGATCACAG | 72179 |
rs45814546 | snp | A/G | 0.32 | 0.24 | intron-variant | Fbxl2 | Mm_Celera | 9:114023613 | TACTTCAGTTGGGAA[A/G]GCTTTGATGTGGAGG | 72179 |
rs45839012 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Ubp1, Fbxl2 | Mm_Celera | 9:113958949 | ACAGAGGTAATGCAG[A/T]GCAGCCTTTGGCTTT | 72179 |
rs45858510 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl2 | Mm_Celera | 9:113985160 | TGACAGAAGTGCAAA[A/G]GTCATCGTGGTCATC | 72179 |
rs45880088 | snp | C/T | | | intron-variant | Fbxl2 | Mm_Celera | 9:113994620 | GTGTTGAAGAGAGGG[C/T]GTACTGGCTAGTTTT | 72179 |
rs46041189 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Ubp1, Fbxl2 | Mm_Celera | 9:113967751 | GCTAGCATTCTTTTT[G/T]CTTGTGTATGGAGCC | 72179 |
rs46084491 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Ubp1, Fbxl2 | Mm_Celera | 9:113964454 | AGGCACTGGGAATCT[C/T]GAGTTTATACGGGCT | 72179 |
rs46182589 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl2 | Mm_Celera | 9:114017119 | GTTTTGAGAGACATT[A/G]GCGACAGTTTGGAAA | 72179 |
rs46208652 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Ubp1, Fbxl2 | Mm_Celera | 9:113962919 | CTTACTGTGATCACC[G/T]TTATGCCTGGAGGCC | 72179 |
rs46271361 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Ubp1, Fbxl2 | Mm_Celera | 9:113962219 | GCCGAGGAGTGAGTG[A/G]TACCTAGTAAGATAA | 72179 |
rs46278176 | snp | A/G | | | intron-variant | Fbxl2 | Mm_Celera | 9:113994235 | GTTCATGGATTCAAA[A/G]CACAGGAGCTCACTG | 72179 |
rs46297478 | snp | A/G | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | Ubp1, Fbxl2 | Mm_Celera | 9:113958799 | GCCGTGTGCAGCTCC[A/G]TGATTGAACTCATGT | 72179 |
rs46331502 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Fbxl2 | Mm_Celera | 9:114017951 | CTTGCAACTGGAGGC[C/T]GGAGCCAAACCCGAG | 72179 |
rs46345149 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl2 | Mm_Celera | 9:114017889 | ACTGGGAAGTCAGGT[A/G]GTCTACGTCCCTTTC | 72179 |
rs46348654 | snp | C/T | 0.32 | 0.24 | intron-variant | Ubp1, Fbxl2 | Mm_Celera | 9:113969060 | TCAGAAACAGGGTTA[C/T]CCACAGCCCAGCGAC | 72179 |
rs46362484 | snp | A/G | 0.124444 | 0.216185 | intron-variant, downstream-variant-500B | Ubp1, Fbxl2 | Mm_Celera | 9:113970395 | ACTTTCTTTGTCCTC[A/G]CTATGCATGCTGTAG | 72179 |
rs46381195 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Fbxl2 | Mm_Celera | 9:114001823 | CAGCAAACCATAGGC[A/T]CACATTATTAGAGTG | 72179 |
rs46460962 | snp | C/G | 0.124444 | 0.216185 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant, intron-variant | Ubp1, Fbxl2 | Mm_Celera | 9:113976721 | AGGCTTTAACAGCTT[C/G]TTTTATTCATACTGG | 72179 |
rs46473671 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Fbxl2 | Mm_Celera | 9:113985747 | GGGTTAATTCTCATT[A/C]GGCCTGAAACAGTTT | 72179 |
rs46510405 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl2 | Mm_Celera | 9:113983071 | ATGACGCCTGCACCT[A/G]GATTGCCCTCGGTGT | 72179 |
rs46535123 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl2 | Mm_Celera | 9:114016318 | CCACAGCTAGGTCGG[C/T]TGCGGGTGCCACGGG | 72179 |
rs46562824 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime, nc-transcript-variant, intron-variant | Ubp1, Fbxl2 | Mm_Celera | 9:113976962 | CTTTCCTTTTTGGAT[C/T]TCATGATTTATGGAA | 72179 |
rs46567271 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Fbxl2 | Mm_Celera | 9:114013099 | ACTCTATCTGCATGC[A/T]TAGGAAAGGCCACAG | 72179 |
rs46586277 | snp | C/T | 0.231111 | 0.249285 | intron-variant, downstream-variant-500B | Ubp1, Fbxl2 | Mm_Celera | 9:113970394 | AACTTTCTTTGTCCT[C/T]GCTATGCATGCTGTA | 72179 |
rs46590036 | snp | C/G | 0.32 | 0.24 | utr-variant-3-prime, nc-transcript-variant, intron-variant | Ubp1, Fbxl2 | Mm_Celera | 9:113975606 | AGAGAGAGAGAGAGC[C/G]TGTGCGAGCGAGCGA | 72179 |
rs46657591 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Ubp1, Fbxl2 | Mm_Celera | 9:113967302 | CTCATAGTAAGGTCA[G/T]TCTTCCCCACACACA | 72179 |
rs46672628 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Ubp1, Fbxl2 | Mm_Celera | 9:113959582 | GCCGAAATTGTTTTT[C/G]ATGTCCATGTCTTGA | 72179 |
rs46679539 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime, nc-transcript-variant, intron-variant | Ubp1, Fbxl2 | Mm_Celera | 9:113975878 | CTGTACTGGGTGACA[C/T]GGCCGTATGGGTCAG | 72179 |