SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3660323 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Fbxw7, Gm35486 | GRCm38.p3 | 3:84820626 | TAGATGAGATGTGCT[C/T]CTCTGGACTGCCATT | 50754 |
rs3662600 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Fbxw7 | GRCm38.p3 | 3:84935908 | TGCCTCTGAGTCATC[C/T]CTGGGTCAGAATCAA | 50754 |
rs3676725 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxw7 | Mm_Celera | 3:84955905 | TTCAATTGTGGAAAT[A/G]TATTTAATGCTCCTG | 50754 |
rs3679772 | snp | C/T | 0.5 | 0 | intron-variant | Fbxw7, LOC105244479 | GRCm38.p3 | 3:84844338 | AACCTCCTGCCTCAT[C/T]CCACCACACCCATCT | 50754 |
rs3683473 | snp | A/G | 0.489796 | 0.070696 | missense | Fbxw7 | GRCm38.p3 | 3:84903756 | GAACTTGTGGGTGCA[A/G]ACCCTAGGCCTGGAG | 50754 |
rs3684554 | snp | A/G | 0.5 | 0 | synonymous-codon | Fbxw7 | GRCm38.p3 | 3:84903911 | GGAGGAAGAGGAGGA[A/G]GAGGAAGAGGAGGAG | 50754 |
rs3685204 | snp | A/C | 0.5 | 0 | intron-variant | Fbxw7, Gm35486 | Mm_Celera | 3:84815817 | GGTGACAAGTGGGAG[A/C]GGGTGGGTGCTTTGA | 50754 |
rs3685774 | snp | C/T | 0.5 | 0 | intron-variant | Fbxw7, Gm35486 | GRCm38.p3 | 3:84815902 | ACCAATAGGAGAAAG[C/T]GTCAGTTTGCAGGAG | 50754 |
rs3703424 | snp | A/T | 0.396694 | 0.202437 | intron-variant | Fbxw7 | Mm_Celera | 3:84959397 | ATACTGTGGATTTTT[A/T]TAATTTAAGTTAGTT | 50754 |
rs3720890 | snp | C/T | 0.5 | 0 | intron-variant | Fbxw7 | GRCm38.p3 | 3:84911851 | GTGGTAACACAGAGG[C/T]TCCTGTATGCTTCCT | 50754 |
rs3725481 | snp | A/C | 0.456747 | 0.140554 | intron-variant | Fbxw7 | GRCm38.p3 | 3:84931364 | CAGTGGTGCTGTGTG[A/C]CACTTTGTAGAAACA | 50754 |
rs4135478 | snp | A/C | 0.5 | 0 | intron-variant | Fbxw7, LOC105244479 | GRCm38.p3 | 3:84844497 | ATTATGTCCTACAAC[A/C]CCCTCGTCTACTTAG | 50754 |
rs4135496 | snp | A/C/G | 0.5 | 0 | intron-variant | Fbxw7, LOC105244479 | GRCm38.p3 | 3:84844503 | TCCTACAACACCCTC[A/C/G]TCTACTTAGATTATG | 50754 |
rs4136366 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fbxw7, LOC105244479 | GRCm38.p3 | 3:84847555 | GACTCAGATCTGCTC[C/T]CATTAGGAGGTCATG | 50754 |
rs4140281 | snp | A/G/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Fbxw7, Gm35486 | GRCm38.p3 | 3:84821704 | TTTGTATAATACAGT[A/G/T]CAATAGTGATCCCTT | 50754 |
rs6194580 | snp | C/T | 0.32 | 0.24 | intron-variant | Fbxw7 | Mm_Celera | 3:84959022 | ACGCCTGTTACACGG[C/T]ATGCATCTTCTAAAA | 50754 |
rs6195561 | snp | A/G | 0.5 | 0 | intron-variant | Fbxw7 | Mm_Celera | 3:84959197 | AGGAATGTGAGGTTA[A/G]TTTAGGANCTCCATC | 50754 |
rs6195566 | snp | A/G | 0.5 | 0 | intron-variant | Fbxw7 | Mm_Celera | 3:84959205 | GAGGTTANTTTAGGA[A/G]CTCCATCAGTGANTC | 50754 |
rs6195597 | snp | A/G | 0.5 | 0 | intron-variant | Fbxw7 | Mm_Celera | 3:84959218 | GANCTCCATCAGTGA[A/G]TCNCTGGGATTGGTA | 50754 |
rs6195598 | snp | A/G | 0.5 | 0 | intron-variant | Fbxw7 | Mm_Celera | 3:84959221 | CTCCATCAGTGANTC[A/G]CTGGGATTGGTAACT | 50754 |
rs6196658 | snp | C/T | 0.5 | 0 | intron-variant | Fbxw7 | Mm_Celera | 3:84959385 | AGATTGCCTTGAATA[C/T]TGTGGATTTTTNTAA | 50754 |
rs6197212 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Fbxw7 | Mm_Celera | 3:84959467 | ATCAAGAACATACCA[A/G]CACAGCTATCATAGA | 50754 |
rs6219499 | snp | G/T | 0.5 | 0 | intron-variant | Fbxw7 | Mm_Celera | 3:84837326 | CTAGAGGGCTTTGCA[G/T]TTTATTGAGCAGGGG | 50754 |
rs6236286 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Fbxw7 | Mm_Celera | 3:84916792 | TTGTCCATAGAGTGG[C/T]GCCATAAAACTGAGG | 50754 |
rs6236769 | snp | A/T | 0.359862 | 0.224567 | intron-variant | Fbxw7 | Mm_Celera | 3:84916838 | CTCTCAATGAAGACC[A/T]AATATTCTGTGTCTG | 50754 |
rs6237326 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Fbxw7 | Mm_Celera | 3:84916926 | CCCTTGGATGTATAA[C/T]AAGTGCATTAAGGAA | 50754 |
rs6250284 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Fbxw7 | Mm_Celera | 3:84917028 | GTAGTACCTGTCACA[C/T]AGTATCACTGAGAGT | 50754 |
rs6250361 | snp | A/C | 0.5 | 0 | intron-variant | Fbxw7 | Mm_Celera | 3:84917078 | GTAGCCAGGACGAGT[A/C]CTGAGAGTCTTCAGC | 50754 |
rs6250822 | snp | A/G | 0.5 | 0 | intron-variant | Fbxw7 | Mm_Celera | 3:84917134 | ATGTCAATTATTTCA[A/G]AGTTACAANTTTGTG | 50754 |
rs6250832 | snp | A/G | 0.5 | 0 | intron-variant | Fbxw7 | Mm_Celera | 3:84917143 | ATTTCANAGTTACAA[A/G]TTTGTGCTAAAGCTA | 50754 |
rs6250924 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Fbxw7 | Mm_Celera | 3:84917201 | GTTGGTTTCTAAGAG[A/G]TCATCTGGTGCATTG | 50754 |
rs6301246 | snp | A/G | 0.5 | 0 | intron-variant | Fbxw7 | GRCm38.p3 | 3:84932713 | ggggagagggaactt[A/G]tagagcccacctcca | 50754 |
rs6315181 | snp | C/T | 0.5 | 0 | intron-variant | Fbxw7 | Mm_Celera | 3:84933070 | aaaaggtggaagaag[C/T]tgaggaggagggtga | 50754 |
rs6315216 | snp | A/G | 0.5 | 0 | intron-variant | Fbxw7 | Mm_Celera | 3:84933096 | ggtgaccttatagga[A/G]gaccagcagtctcaa | 50754 |
rs6337012 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Fbxw7 | Mm_Celera | 3:84901466 | ATTCTTTTGAGCCTC[A/G]GTTGTCTAGTGTTTA | 50754 |
rs6387315 | snp | C/T | 0.5 | 0 | intron-variant | Fbxw7 | Mm_Celera | 3:84910460 | ttggagaaatcttgc[C/T]gatgaaaattggact | 50754 |
rs6388259 | snp | G/T | 0.5 | 0 | intron-variant | Fbxw7 | Mm_Celera | 3:84910585 | TATATAGTGTTCAGG[G/T]TTGGAAGGGGTTAGG | 50754 |
rs6389279 | snp | G/T | 0.5 | 0 | intron-variant | Fbxw7 | Mm_Celera | 3:84910788 | CTGAATCAACGTCCT[G/T]TTTTTGGTTTGTTTG | 50754 |
rs6394363 | snp | C/T | 0.5 | 0 | intron-variant | Fbxw7, LOC105244479 | Mm_Celera | 3:84865172 | GGTGGCtgtgaacag[C/T]gctgcagcaagcact | 50754 |
rs6395934 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Fbxw7, LOC105244479 | Mm_Celera | 3:84865441 | CAATAATCAAGTACC[A/G]TGGTATAGTTTATGG | 50754 |
rs6395982 | snp | C/T | 0.5 | 0 | intron-variant | Fbxw7, LOC105244479 | Mm_Celera | 3:84865475 | TTTTTAATATAACCA[C/T]ACAAAAATGTTTTGT | 50754 |
rs6396406 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Fbxw7, LOC105244479 | Mm_Celera | 3:84865515 | CATTCGCTAAAGGAG[C/T]GTCTCTAGATATATG | 50754 |
rs6396906 | snp | G/T | 0.5 | 0 | intron-variant | Fbxw7, LOC105244479 | Mm_Celera | 3:84865599 | TCTATAGCAATTATA[G/T]CACATGCTTACATGA | 50754 |
rs6396937 | snp | C/T | 0.495868 | 0.0452663 | intron-variant | Fbxw7, LOC105244479 | Mm_Celera | 3:84865625 | CATGAGCAGCAGTTA[C/T]AGTATTCTGTTTAGC | 50754 |
rs29980244 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Fbxw7, LOC105244479 | Mm_Celera | 3:84869493 | TTAAAGGAATCAATG[A/G]AATGCTCATGAATAG | 50754 |
rs30008104 | snp | A/G | 0.5 | 0 | synonymous-codon | Fbxw7 | GRCm38.p3 | 3:84954904 | GGACCATGGTTCTGA[A/G]GTTCGTTCCTTTTCT | 50754 |
rs30008384 | snp | C/G | 0.5 | 0 | intron-variant | Fbxw7 | GRCm38.p3 | 3:84823907 | TCTCTCATTTACCTA[C/G]GAACACACAATCACA | 50754 |
rs30019266 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Fbxw7 | GRCm38.p3 | 3:84898493 | GACAGGAGATGGAGC[A/G]CCTGCACTTGCTGGT | 50754 |
rs30029362 | snp | A/C | 0.5 | 0 | intron-variant | Fbxw7, LOC105244479 | GRCm38.p3 | 3:84858060 | TTGCCAACAGCAAGC[A/C]ATCTTCTGGAGGCAT | 50754 |
rs30060998 | snp | C/T | 0.5 | 0 | intron-variant | Fbxw7 | GRCm38.p3 | 3:84961600 | AGCAGAAAGAAACTA[C/T]ATGCCACACTGGGCA | 50754 |
rs30062970 | snp | C/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Fbxw7, LOC105244479 | Mm_Celera | 3:84887982 | TTAGTTACTGTTCTG[C/T]TGCTATGATAAAGCA | 50754 |
rs30083033 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Fbxw7 | Mm_Celera | 3:84973278 | CTTTGTCACTTTTGG[C/T]CTGACGTGTCACACA | 50754 |
rs30104031 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fbxw7, LOC105244479 | GRCm38.p3 | 3:84872912 | AGGAGCTGTCACTAG[A/G]GGTTGGGCTCTGAGG | 50754 |
rs30105302 | snp | C/T | 0.375 | 0.216506 | intron-variant | Fbxw7, LOC105244479 | Mm_Celera | 3:84858081 | CTGGAGGCATTTTCT[C/T]TGTTGAGGCTCCCTC | 50754 |
rs30105569 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Fbxw7, LOC105244479 | GRCm38.p3 | 3:84862700 | TGCTGGGTGCATACA[C/T]GTGGCAGTCAGAGGA | 50754 |
rs30105957 | snp | G/T | 0.375 | 0.216506 | intron-variant | Fbxw7 | GRCm38.p3 | 3:84897618 | AAACCTCTTTTTCTC[G/T]ATTGCACTCACCCCA | 50754 |
rs30108139 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Fbxw7, LOC105244479 | GRCm38.p3 | 3:84856934 | TTATTGGCTGAGGCA[C/T]ATTAGTAGCTTTGTC | 50754 |
rs30109627 | snp | A/G | 0.5 | 0 | intron-variant | Fbxw7 | GRCm38.p3 | 3:84893845 | GACTGTCCACAGAAC[A/G]GGTCATCTTATCCAC | 50754 |
rs30112528 | snp | G/T | 0.5 | 0 | intron-variant | Fbxw7 | Mm_Celera | 3:84955782 | TTTTGATTTAGTTAT[G/T]TTTATTCTGTGAAAC | 50754 |
rs30113353 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Fbxw7, LOC105244479 | GRCm38.p3 | 3:84882934 | GAGATGAGCCATCCC[A/C]TGGGAGCAAGGGCAC | 50754 |
rs30116080 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxw7, LOC105244479 | Mm_Celera | 3:84850134 | AATGGGGCTTCTGAG[A/G]GAGGCTATTCAGAAC | 50754 |
rs30122513 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Fbxw7 | Mm_Celera | 3:84958446 | ATCCAAAATTTTTAA[C/T]TCTGAAATATTGGTA | 50754 |
rs30125185 | snp | C/T | 0.304688 | 0.243945 | intron-variant | Fbxw7 | GRCm38.p3 | 3:84941636 | TATACTGTGCTTGTA[C/T]TTAAATGTCCTATGT | 50754 |
rs30153823 | snp | A/C | 0.444444 | 0.157135 | upstream-variant-2KB, utr-variant-3-prime | Fbxw7, Gm35486 | GRCm38.p3 | 3:84814034 | GGTTTCACCCCACGC[A/C]AAGGGAAGGGTGGGA | 50754 |
rs30156104 | snp | A/T | 0.5 | 0 | intron-variant | Fbxw7, LOC105244479 | GRCm38.p3 | 3:84869480 | TTTTTTTTTTTTTTT[A/T]AAGGAATCAATGAAA | 50754 |
rs30158367 | snp | G/T | 0.42 | 0.183303 | intron-variant | Fbxw7 | GRCm38.p3 | 3:84911620 | ATCTCATGTTTCATC[G/T]GTGCGCTCACCCTGG | 50754 |
rs30164438 | snp | G/T | 0.5 | 0 | intron-variant | Fbxw7 | Mm_Celera | 3:84932450 | AGCAATCATGGGGGT[G/T]GGGGGGAAAGGGAGG | 50754 |
rs30170188 | snp | C/T | 0.495868 | 0.0452663 | intron-variant | Fbxw7 | Mm_Celera | 3:84832687 | TGCACGAGTAGAGTA[C/T]CTAGTGATTTATTAA | 50754 |
rs30177800 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | Dear1, Fbxw7 | GRCm38.p3 | 3:84966305 | AAGCAAAATTGATAT[C/T]CCTCCCCCCCCCCGG | 50754 |
rs30200011 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fbxw7, Gm35486 | Mm_Celera | 3:84815983 | GACACTTGCACCTTT[C/T]TGGACACTAAACTGA | 50754 |
rs30204073 | snp | C/G/T | 0.5 | 0 | intron-variant | Fbxw7, LOC105244479 | GRCm38.p3 | 3:84857954 | CTTGCTCAGTCTGCT[C/G/T]TCTTATAGAACTTAG | 50754 |
rs30212627 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Fbxw7 | GRCm38.p3 | 3:84836862 | TCTCCTGTCTCACCC[A/G]TACTTTTCAGGCACA | 50754 |
rs30255388 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fbxw7 | GRCm38.p3 | 3:84837122 | CACCATTCGTAGCTT[C/T]ACCTGGCATAGTGCA | 50754 |
rs30256123 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Fbxw7 | GRCm38.p3 | 3:84889199 | CACTTAAAGCATTCC[A/T]TGGCTTCCCAAACCC | 50754 |
rs30256883 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fbxw7 | Mm_Celera | 3:84832674 | ATCAGAGGTTACATG[C/T]ACGAGTAGAGTATCT | 50754 |
rs30258376 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxw7 | GRCm38.p3 | 3:84837154 | CTGTTTAAATGAAGG[A/G]AAGAGGACTTGTTTT | 50754 |
rs30260340 | snp | A/G | 0.493827 | 0.0552116 | intron-variant, upstream-variant-2KB | Fbxw7, LOC105244479 | Mm_Celera | 3:84887485 | AATAACATCCAGCAA[A/G]GTTTATATTTTTCAT | 50754 |
rs30308026 | snp | G/T | 0.375 | 0.216506 | intron-variant | Fbxw7 | Mm_Celera | 3:84839395 | TTATTTATTTATGAT[G/T]TTATGATAGTTTCAG | 50754 |
rs30309443 | snp | A/T | 0.5 | 0 | intron-variant, nc-transcript-variant | Fbxw7, LOC105244479 | Mm_Celera | 3:84853794 | TTACATACTCAAACT[A/T]CAGTGCATTTTCATG | 50754 |
rs30358552 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fbxw7 | Mm_Celera | 3:84908394 | TAAAGTTTCTGCTTA[C/T]ATGCTCTGTAATCCT | 50754 |
rs30401400 | snp | C/T | 0.408163 | 0.193609 | utr-variant-5-prime, intron-variant | Dear1, Fbxw7 | Mm_Celera | 3:84965462 | CTGTAAGCAGTGTCC[C/T]GCTCATTATGGTTGA | 50754 |
rs30402900 | snp | G/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Fbxw7, LOC105244479 | Mm_Celera | 3:84862865 | AATCCCAGCACTTGG[G/T]AGGCAGAGGCAGGCG | 50754 |
rs30406254 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Fbxw7, LOC105244479 | GRCm38.p3 | 3:84883310 | TCTCAACACCATCAA[C/T]AGTCTGAAGCACGAT | 50754 |
rs30407595 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Fbxw7, LOC105244479 | Mm_Celera | 3:84869064 | CGTAGTTCCTCTTCT[C/T]TAAGTGTTATTAGAC | 50754 |
rs30452348 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Fbxw7, LOC105244479 | Mm_Celera | 3:84858248 | ACTTTTAAATGTTTA[C/G]TTCAGTCATTCCAGT | 50754 |
rs30456924 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Fbxw7 | GRCm38.p3 | 3:84924567 | CTGCAGGATCGAGGT[C/T]GACCTGAGTGGTTCG | 50754 |
rs30457371 | snp | C/T | 0.5 | 0 | intron-variant | Fbxw7 | GRCm38.p3 | 3:84968854 | ACTTGTATGGACAGC[C/T]GTTCACATCTCTGCT | 50754 |
rs30463346 | snp | A/T | 0.444444 | 0.157135 | intron-variant, nc-transcript-variant | Fbxw7, LOC105244479 | GRCm38.p3 | 3:84850996 | AGAAAGCCACCCCAA[A/T]GGGTACACATATACA | 50754 |
rs30463742 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | Fbxw7 | GRCm38.p3 | 3:84934814 | AGGACGGTTTGAACT[C/T]TCTCTTAAGTCTCTG | 50754 |
rs30471439 | snp | A/T | 0.5 | 0 | intron-variant | Fbxw7, LOC105244479 | GRCm38.p3 | 3:84859846 | TCAAACAAGTTGGTT[A/T]GTAAATGGTTAAAGG | 50754 |
rs30511052 | snp | A/G | 0.429688 | 0.173817 | intron-variant | Fbxw7 | Mm_Celera | 3:84929877 | TCTGAATTTAGAAAT[A/G]TGATATCTCCCCAAA | 50754 |
rs30512779 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fbxw7 | Mm_Celera | 3:84825022 | CTGGAAATACAAAGC[C/T]TTGGAAAATCGTAAA | 50754 |
rs30554945 | snp | C/T | 0.391111 | 0.206368 | intron-variant, nc-transcript-variant | Fbxw7, LOC105244479 | GRCm38.p3 | 3:84884465 | TTAACACTTTCCAAA[C/T]GCTAGTGGAATCAGA | 50754 |
rs30555679 | snp | G/T | 0.487535 | 0.077957 | downstream-variant-500B | Fbxw7 | GRCm38.p3 | 3:84979625 | GCCTTAGATGAAGTC[G/T]CGGGATGGCAGGATT | 50754 |
rs30556451 | snp | A/G | 0.42 | 0.183303 | intron-variant | Fbxw7 | Mm_Celera | 3:84943825 | TAAGTTTGAATTTTA[A/G]CTACATCTAATATGT | 50754 |
rs30559142 | snp | A/T | 0.484429 | 0.0868505 | intron-variant | Fbxw7 | GRCm38.p3 | 3:84949557 | GCATACTTCACTTGC[A/T]TCATCCACAGTAGAC | 50754 |
rs30561828 | snp | G/T | 0.375 | 0.216506 | intron-variant | Fbxw7 | GRCm38.p3 | 3:84839384 | TATTTATTTATTTAT[G/T]ATGTTATGATAGTTT | 50754 |
rs30594434 | snp | C/T | 0.375 | 0.216506 | intron-variant | Fbxw7 | Mm_Celera | 3:84899905 | TCTTATGCAGCAAGG[C/T]TTATTCTAGTGCTTC | 50754 |
rs30601856 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Fbxw7 | GRCm38.p3 | 3:84889776 | AATAACCTGCACCAG[C/T]TAAGCCTCTGGACCA | 50754 |
rs30609107 | snp | C/T | 0.375 | 0.216506 | intron-variant | Fbxw7, LOC105244479 | GRCm38.p3 | 3:84859862 | GTAAATGGTTAAAGG[C/T]GCTTGCTGCCAAGTC | 50754 |