| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs264307705 | snp | C/T | | | synonymous-codon, nc-transcript-variant | Fbxw10 | Mm_Celera | 11:62875077 | GACCAGCCTCGGGGA[C/T]GAGCATTCCAGGTCT | 213980 |
| rs264391016 | snp | C/T | | | intron-variant | Fbxw10 | Mm_Celera | 11:62856241 | CTGGTAGCTCCGCAG[C/T]TCTGGTTATTCATGC | 213980 |
| rs264472344 | snp | A/C | | | intron-variant | Fbxw10 | Mm_Celera | 11:62848349 | AAAAAAAAAAAAAAA[A/C]CAGACTGTGGTCCTC | 213980 |
| rs264499309 | snp | A/G | | | intron-variant | Fbxw10 | Mm_Celera | 11:62851934 | AGACTGTGATTCCAG[A/G]CCTGAAGACCTTCCC | 213980 |
| rs264552718 | in-del | -/TT | | | intron-variant | Fbxw10 | Mm_Celera | 11:62851177 | CAATAGGCATTGGGC[-/TT]TCTTTTTTTTTTTCC | 213980 |
| rs264650599 | in-del | -/A | | | intron-variant | Fbxw10 | Mm_Celera | 11:62863239 | CAGAGCTACAATGAG[-/A]AAAAAATAGGATTTG | 213980 |
| rs264719418 | snp | A/T | | | intron-variant | Fbxw10 | Mm_Celera | 11:62854782 | CACCACAGAGAGAGC[A/T]CTTAGCTTTGTATTT | 213980 |
| rs264746283 | snp | C/G | | | intron-variant | Fbxw10 | Mm_Celera | 11:62867033 | CTTGGGGAAGTAGGA[C/G]TTTTTGCTCACATAT | 213980 |
| rs264762609 | snp | C/T | | | upstream-variant-2KB | Fbxw10 | Mm_Celera | 11:62846842 | AATAGACTCTAACAG[C/T]CACAAATGTAAGAAG | 213980 |
| rs264824875 | snp | G/T | | | intron-variant | Fbxw10 | Mm_Celera | 11:62850048 | GGAGAAGGAGAAGAA[G/T]TATTGAAGAGTTTTA | 213980 |
| rs264834513 | snp | C/T | | | synonymous-codon, nc-transcript-variant | Fbxw10 | Mm_Celera | 11:62857709 | CAACTTGTGGAATGC[C/T]TACCAGAACCAGGAA | 213980 |
| rs264970243 | snp | C/T | | | intron-variant | Fbxw10 | Mm_Celera | 11:62859151 | TTCGAAGTGGTTTCA[C/T]CTTCCTGTTTGCTGG | 213980 |
| rs265087866 | snp | A/G | | | intron-variant | Fbxw10 | Mm_Celera | 11:62856019 | AAGTCTATTCAGTTG[A/G]CAACAAAAAGATACT | 213980 |
| rs265191466 | snp | A/G | | | intron-variant | Fbxw10 | Mm_Celera | 11:62858457 | TCCTATCAATCATTA[A/G]TTAAGAAAACGCCCT | 213980 |
| rs265345477 | snp | C/T | | | intron-variant | Fbxw10 | Mm_Celera | 11:62859725 | GCCTTGCCTTCTGAA[C/T]GGCACTGAATTTCGT | 213980 |
| rs265366037 | snp | A/G | | | intron-variant | Fbxw10 | Mm_Celera | 11:62860790 | GGATCCATCCTTTCA[A/G]CCACTCATATTAAAG | 213980 |
| rs265453366 | snp | C/T | | | intron-variant | Fbxw10 | Mm_Celera | 11:62868159 | AGGCATTAGAAATTG[C/T]TTTATTCTATTCAGC | 213980 |
| rs265463605 | snp | C/T | | | intron-variant | Fbxw10 | Mm_Celera | 11:62862514 | TAATCTTACCAATGC[C/T]AACAGTGACAAGACC | 213980 |
| rs265488607 | in-del | -/ACACACACAC | | | intron-variant | Fbxw10 | GRCm38.p3 | 11:62864269 | TTTGGCAGTGTCCCT[-/ACACACACAC]ACACACACACACACA | 213980 |
| rs265613042 | snp | G/T | | | intron-variant | Fbxw10 | Mm_Celera | 11:62863903 | TAGTAATGCCATTCA[G/T]AAAACTCCAAGCTGC | 213980 |
| rs265726475 | snp | C/T | | | intron-variant | Fbxw10 | GRCm38.p3 | 11:62866867 | CTGTGCAGTGGAAAG[C/T]AGAAACAGTGTTTGC | 213980 |
| rs265736435 | snp | C/T | | | intron-variant | Fbxw10 | Mm_Celera | 11:62861245 | GTCCGAGTACATAAG[C/T]TTTGGGCTGTGGTTG | 213980 |
| rs265819056 | in-del | -/ACACACACGG | | | intron-variant | Fbxw10 | Mm_Celera | 11:62873956 | CACACACACACACAC[-/ACACACACGG]GGGGGGGGGAGCGGG | 213980 |
| rs265916956 | in-del | -/C | | | intron-variant | Fbxw10 | Mm_Celera | 11:62866174 | TTTCTTTCTTTCTTT[-/C]CTTTCTTTCTTTCTT | 213980 |
| rs265923927 | snp | A/C | | | upstream-variant-2KB | Fbxw10 | Mm_Celera | 11:62845305 | TGTGGGAGGGCCAGT[A/C]TCACCATGGGTGGGG | 213980 |
| rs265957006 | in-del | -/TTGGC | | | intron-variant | Fbxw10 | Mm_Celera | 11:62857864 | TTCTCTAGGCCACCT[-/TTGGC]TTGAGAGGTAGTGCA | 213980 |
| rs265970954 | snp | C/T | | | intron-variant | Fbxw10 | Mm_Celera | 11:62871162 | CCTAGGCAAGCAGCC[C/T]GAGCCACACCCAGGA | 213980 |
| rs265980257 | snp | A/G | | | intron-variant | Fbxw10 | Mm_Celera | 11:62864612 | ATAAAAAAAAAGATT[A/G]GTTTTAGATATGATT | 213980 |
| rs266097194 | snp | A/G | | | intron-variant | Fbxw10 | Mm_Celera | 11:62867427 | CAGGTGAAGGTTTCT[A/G]GGGGAAAAGTCCCTA | 213980 |
| rs266154527 | snp | C/T | | | intron-variant | Fbxw10 | Mm_Celera | 11:62849114 | AGAGCAGCTGAGCCA[C/T]CTGTCCAGCCCCTCT | 213980 |
| rs266252516 | snp | A/G | | | intron-variant | Fbxw10 | Mm_Celera | 11:62868908 | TCATGGGAGAGGTGG[A/G]ATATAGCTTTGGGGT | 213980 |
| rs386870464 | in-del | -/A | | | intron-variant | Fbxw10 | Mm_Celera | 11:62874061 | AAATGAAAAAAAAAA[-/A]CATCAAAGTGAGACG | 213980 |
| rs386870648 | snp | A/G | | | intron-variant | Fbxw10 | GRCm38.p3 | 11:62850027 | GAAGGAGGAGGAGGA[A/G]GAGGAGGAGAAGGAG | 213980 |
| rs386952225 | in-del | -/TT | | | intron-variant | Fbxw10 | Mm_Celera | 11:62870939 | AATTAACTTTTTTTT[-/TT]AATAATTGAGACATA | 213980 |
| rs386956442 | in-del | -/GTCAGAG | | | intron-variant | Fbxw10 | Mm_Celera | 11:62848578 | GGTCAGAGGTCAGAG[-/GTCAGAG]ACCTACAAAGGTCTA | 213980 |
| rs386959163 | in-del | -/T | | | intron-variant | Fbxw10 | Mm_Celera | 11:62851190 | GCTCTTTTTTTTTTT[-/T]CCTCATTTAATCCTC | 213980 |
| rs387002973 | in-del | -/T | | | intron-variant | Fbxw10 | Mm_Celera | 11:62856514 | AAAAGAATTTTTTTT[-/T]ATTTTTTGTCTTCCA | 213980 |
| rs387100025 | in-del | -/T | | | intron-variant | Fbxw10 | Mm_Celera | 11:62866219 | TTCTTTCTTTCCTTC[-/T]CTTCCTTCCTTCCTT | 213980 |
| rs387101819 | in-del | -/GTGTGTGTGTGT | | | intron-variant | Fbxw10 | Mm_Celera | 11:62860665 | TGTGTGTGTGTGTGT[-/GTGTGTGTGTGT]ACATGCTTGTGGGTG | 213980 |
| rs387131933 | in-del | -/A | | | intron-variant | Fbxw10 | Mm_Celera | 11:62864607 | GGGAAATAAAAAAAA[-/A]GATTAGTTTTAGATA | 213980 |
| rs387173642 | in-del | -/T | | | intron-variant | Fbxw10 | Mm_Celera | 11:62869004 | GTACTGGCATTTTTT[-/T]CTTGCAGACTCTCAC | 213980 |
| rs387248876 | in-del | -/GT | | | intron-variant | Fbxw10 | Mm_Celera | 11:62854573 | TGTGTGTGTGTGTGT[-/GT]TCTAAATATATTATT | 213980 |
| rs387281542 | in-del | -/A | | | intron-variant | Fbxw10 | Mm_Celera | 11:62875325 | TATACACGGAAAAAA[-/A]TATTTTATACAGAAT | 213980 |
| rs387283558 | in-del | -/C | | | intron-variant | Fbxw10 | Mm_Celera | 11:62872982 | ATGACGATCCTTAGC[-/C]TTATACTGTTCTTTC | 213980 |
| rs387284685 | in-del | -/AGA | | | intron-variant | Fbxw10 | GRCm38.p3 | 11:62850014 | GGAGGAGGAGGAGAA[-/AGA]GGAGGAGGAGGAGGA | 213980 |
| rs387304329 | snp | A/G | | | intron-variant | Fbxw10 | GRCm38.p3 | 11:62850037 | GAGGAGGAGGAGGAG[A/G]AGGAGAAGAATTATT | 213980 |
| rs387376951 | in-del | -/GAGAGAGAGA | | | intron-variant | Fbxw10 | GRCm38.p3 | 11:62875780 | GAGGGGAAGGGGAAG[-/GAGAGAGAGA]GAGAGAGAGAGAGAG | 213980 |
| rs387413340 | in-del | -/TT | | | intron-variant | Fbxw10 | Mm_Celera | 11:62860340 | ATTCTTTTTTTTTTT[-/TT]CCTAAATAGGGTTTC | 213980 |
| rs387465283 | in-del | -/AAG | | | intron-variant | Fbxw10 | Mm_Celera | 11:62863871 | ACTGGATATAAAAAG[-/AAG]GCTATAAAAGCAAGT | 213980 |
| rs387502532 | in-del | -/T | | | intron-variant | Fbxw10 | Mm_Celera | 11:62870880 | CTCTGGATTTTTTTT[-/T]CTTTAAAAATAATCT | 213980 |
| rs387518943 | in-del | -/A | | | intron-variant | Fbxw10 | Mm_Celera | 11:62873055 | ATAAAAAGAAAAAAA[-/A]CTCAATTCTCAGCAT | 213980 |
| rs387525980 | in-del | -/AGAGAG | | | intron-variant | Fbxw10 | GRCm38.p3 | 11:62875703 | GACACACAGAGAGAA[-/AGAGAG]AGAGAGAGAGAGAGA | 213980 |
| rs387629125 | in-del | -/TCTT | | | intron-variant | Fbxw10 | GRCm38.p3 | 11:62866383 | CTTCCTTCCTTCCTT[-/TCTT]CCTTCTCTCTCTCTC | 213980 |
| rs387637491 | in-del | -/A | | | intron-variant | Fbxw10 | Mm_Celera | 11:62850821 | GCTTAAAAAAAAAAA[-/A]GAAAAGCTTTTGTTG | 213980 |
| rs387777894 | in-del | -/GTGTGTGTGT | | | intron-variant | Fbxw10 | Mm_Celera | 11:62856127 | TGTGTGTGTGTGTGT[-/GTGTGTGTGT]AGGAGGGGGCAGAGA | 213980 |
| rs387792553 | in-del | -/AT | | | intron-variant | Fbxw10 | Mm_Celera | 11:62860490 | CATGTCTATATATAT[-/AT]CTATATATTTAAAAT | 213980 |
| rs387793832 | in-del | -/CCC | | | intron-variant | Fbxw10 | Mm_Celera | 11:62853511 | CATATTTGCAGCCAC[-/CCC]CCCCCCCCCGCTGTG | 213980 |
| rs387807411 | in-del | -/GAGAGA | | | intron-variant | Fbxw10 | Mm_Celera | 11:62875732 | AGAGAGAGAGAGAGA[-/GAGAGA]ATAGGTCAGCAGGAA | 213980 |
| rs387843217 | in-del | -/CA | | | intron-variant | Fbxw10 | Mm_Celera | 11:62864311 | ACACACACACACACA[-/CA]TACATTTCTACCATG | 213980 |
| rs387856432 | in-del | -/T | | | intron-variant | Fbxw10 | Mm_Celera | 11:62866650 | CTCTTTTCTTTTTTT[-/T]ATCCCTGGTGATGTT | 213980 |
| rs387899732 | snp | C/T | | | intron-variant | Fbxw10 | GRCm38.p3 | 11:62862055 | TCTTTTCTTTTCTTT[C/T]TTTCTTTCTTTCTTT | 213980 |
| rs578364442 | snp | A/G | | | intron-variant | Fbxw10 | GRCm38.p3 | 11:62851171 | CATTTAACAATAGGC[A/G]TTGGGCTCTTTTTTT | 213980 |
| rs578379516 | snp | C/G | | | intron-variant | Fbxw10 | GRCm38.p3 | 11:62866450 | TTTCTCTGTCTCTCT[C/G]TGTGTCTCTGTCGCT | 213980 |
| rs578414807 | snp | C/T | | | intron-variant | Fbxw10 | GRCm38.p3 | 11:62861992 | CAATGTGTATCCCCC[C/T]TTTCTTTTCTTTTCT | 213980 |
| rs578421572 | snp | C/T | | | intron-variant | Fbxw10 | GRCm38.p3 | 11:62876496 | ATGTCTGATGGTCTG[C/T]CCTTTTCAGCAACAA | 213980 |
| rs579119709 | snp | C/T | | | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | Fbxw10 | GRCm38.p3 | 11:62873392 | GCTGCAGGTGTCTCT[C/T]CTCTACCTCCGGGTC | 213980 |
| rs579357107 | snp | A/G | | | intron-variant | Fbxw10 | GRCm38.p3 | 11:62850013 | GAGGAGGAGGAGGAG[A/G]AGGAGGAGGAGGAGG | 213980 |
| rs579463238 | snp | C/T | | | intron-variant | Fbxw10 | GRCm38.p3 | 11:62857259 | CAAGCAGTATCTGAG[C/T]GCTGGACTCAAAGGC | 213980 |
| rs579518330 | snp | C/T | | | missense, nc-transcript-variant | Fbxw10 | GRCm38.p3 | 11:62874952 | TCCAGGATGGTGGCC[C/T]ACACGGACAGCAACA | 213980 |
| rs579739750 | snp | C/T | | | intron-variant | Fbxw10 | GRCm38.p3 | 11:62864689 | GATGTTGGGCCAATG[C/T]ATTTGTATGACTCCA | 213980 |
| rs579776278 | snp | C/T | | | intron-variant | Fbxw10 | GRCm38.p3 | 11:62866169 | TTTCTCTTTCTTTCT[C/T]TCTTTCTTTCTTTCT | 213980 |
| rs580043517 | snp | A/C | | | intron-variant | Fbxw10 | GRCm38.p3 | 11:62862389 | GCTTTCCAGTCAGTT[A/C]CAGATAGAGGAGTGG | 213980 |
| rs580116097 | snp | C/T | | | upstream-variant-2KB | Fbxw10 | GRCm38.p3 | 11:62845758 | GGCTTCCACCTCCTC[C/T]TCCTCTGTCTTCTCT | 213980 |
| rs580269803 | snp | C/T | | | intron-variant | Fbxw10 | GRCm38.p3 | 11:62856891 | GATGACGATGGATGA[C/T]ATAGGCTGCTCTGTG | 213980 |
| rs580311033 | snp | C/T | | | synonymous-codon, nc-transcript-variant | Fbxw10 | GRCm38.p3 | 11:62875119 | GCACAGCCTGAAGGA[C/T]TCTGTGTCTAGTAAA | 213980 |
| rs580373095 | snp | C/T | | | intron-variant | Fbxw10 | GRCm38.p3 | 11:62856236 | AAGGCCTGGTAGCTC[C/T]GCAGTTCTGGTTATT | 213980 |
| rs580820247 | snp | C/T | | | upstream-variant-2KB | Fbxw10 | GRCm38.p3 | 11:62846385 | ACGCAGTCTTTTTGG[C/T]GTTGTGTGCACAGTG | 213980 |
| rs580836940 | snp | A/T | | | intron-variant | Fbxw10 | GRCm38.p3 | 11:62849703 | GGCCCTTCCTGCAGC[A/T]CCTTCTATGCATCTT | 213980 |
| rs580919649 | snp | C/T | | | intron-variant | Fbxw10 | GRCm38.p3 | 11:62866430 | TCTCTCTCTCTGTCT[C/T]TCTGTTTCTCTGTCT | 213980 |
| rs581119708 | snp | C/G | | | intron-variant | Fbxw10 | GRCm38.p3 | 11:62875704 | ACACACAGAGAGAAA[C/G]AGAGAGAGAGAGAGA | 213980 |
| rs581451976 | snp | C/T | | | synonymous-codon, nc-transcript-variant | Fbxw10 | GRCm38.p3 | 11:62876685 | GCTCTGGAAAGTCCC[C/T]ATGACACCTGACCGA | 213980 |
| rs581475393 | snp | G/T | | | synonymous-codon, nc-transcript-variant | Fbxw10 | GRCm38.p3 | 11:62875164 | GTCCCGGGTTCACCT[G/T]AAACAAACCAAGAAC | 213980 |
| rs581566197 | snp | C/T | | | intron-variant | Fbxw10 | GRCm38.p3 | 11:62866302 | CTTTCTTTCTTTCTT[C/T]CTTTCTTTCTTTCTT | 213980 |
| rs581580798 | snp | C/T | | | intron-variant | Fbxw10 | GRCm38.p3 | 11:62858755 | GATCTAGATATGCCA[C/T]AAAAGACTATTTGTG | 213980 |
| rs581763924 | snp | A/G | | | intron-variant | Fbxw10 | GRCm38.p3 | 11:62850015 | GGAGGAGGAGGAGAA[A/G]GAGGAGGAGGAGGAG | 213980 |
| rs581978361 | snp | C/T | | | intron-variant | Fbxw10 | GRCm38.p3 | 11:62854540 | TGTCTGTGCATGTGT[C/T]TCTCCGAGTGTGTGT | 213980 |
| rs582064737 | snp | A/G | | | intron-variant | Fbxw10 | GRCm38.p3 | 11:62850040 | GAGGAGGAGGAGAAG[A/G]AGAAGAATTATTGAA | 213980 |
| rs582263567 | snp | A/G | | | intron-variant, downstream-variant-500B | Fbxw10 | GRCm38.p3 | 11:62873578 | TGGGTCATTCTATTC[A/G]GTCTTTTCCTTTCTC | 213980 |
| rs582308171 | snp | A/T | | | intron-variant | Fbxw10 | GRCm38.p3 | 11:62860600 | TTCATATATTTTAGT[A/T]TTAGAGATTTATTTA | 213980 |
| rs582672319 | snp | G/T | | | intron-variant | Fbxw10 | GRCm38.p3 | 11:62871517 | CTGCTTCATCCTCCT[G/T]AGTGTGCTGTATTTC | 213980 |
| rs582876591 | snp | A/G | | | intron-variant | Fbxw10 | GRCm38.p3 | 11:62856319 | GAGATGGTAAAAATC[A/G]GTGTTAGGTAAAATT | 213980 |
| rs582997881 | snp | A/G | | | synonymous-codon, nc-transcript-variant | Fbxw10 | GRCm38.p3 | 11:62874957 | GATGGTGGCCCACAC[A/G]GACAGCAACATTCTC | 213980 |
| rs583065764 | snp | C/T | | | intron-variant | Fbxw10 | GRCm38.p3 | 11:62857862 | GGCTTCTCTAGGCCA[C/T]CTTTGAGAGGTAGTG | 213980 |
| rs583167779 | snp | A/G | | | intron-variant | Fbxw10 | GRCm38.p3 | 11:62856892 | ATGACGATGGATGAC[A/G]TAGGCTGCTCTGTGA | 213980 |
| rs583382285 | snp | A/G | | | upstream-variant-2KB | Fbxw10 | GRCm38.p3 | 11:62846612 | TTACAAAGCTATGGT[A/G]AGACCTTCTGCTACA | 213980 |
| rs583414436 | snp | A/C | | | intron-variant | Fbxw10 | GRCm38.p3 | 11:62875469 | ATGACATCTAAAGAG[A/C]AAAACATGTGGGTTA | 213980 |
| rs583458406 | snp | A/G | | | intron-variant | Fbxw10 | GRCm38.p3 | 11:62865857 | GCGTTATGACATGGT[A/G]TCACAGGGCTGGTAA | 213980 |
| rs583676580 | snp | C/T | | | upstream-variant-2KB | Fbxw10 | GRCm38.p3 | 11:62845851 | TAGCCTTTATTTGAC[C/T]AGTTAGAATGGGGAA | 213980 |
| rs583738018 | snp | A/T | | | upstream-variant-2KB | Fbxw10 | GRCm38.p3 | 11:62845073 | TTATAAAAAGGAAGC[A/T]AGTACCGTCCTATAA | 213980 |
| rs583767719 | snp | A/C | | | missense, nc-transcript-variant | Fbxw10 | GRCm38.p3 | 11:62875160 | CAAAGTCCCGGGTTC[A/C]CCTGAAACAAACCAA | 213980 |
| rs583993841 | snp | C/T | | | intron-variant | Fbxw10 | GRCm38.p3 | 11:62866212 | TTCTTTCTTTCTTTC[C/T]TTCCTTCCTTCCTTC | 213980 |
| rs584138413 | snp | C/T | | | intron-variant | Fbxw10 | GRCm38.p3 | 11:62876492 | CAGGATGTCTGATGG[C/T]CTGCCCTTTTCAGCA | 213980 |
| rs584233876 | snp | C/T | | | intron-variant | Fbxw10 | GRCm38.p3 | 11:62860877 | CCTCTGAGTGATCTC[C/T]TCCTCCTTGTTTCTT | 213980 |
| rs584259999 | snp | A/G | | | intron-variant | Fbxw10 | GRCm38.p3 | 11:62860318 | TTTTTTTCTGTTTTT[A/G]AAAAATATTCTTTTT | 213980 |
| rs584734202 | snp | C/T | | | intron-variant | Fbxw10 | GRCm38.p3 | 11:62866372 | CTTCCTTCCTCCTTC[C/T]TTCCTTCCTTTCTTC | 213980 |
| rs584782016 | snp | C/G | | | intron-variant | Fbxw10 | GRCm38.p3 | 11:62866442 | TCTCTCTGTTTCTCT[C/G]TCTCTCTGTGTGTCT | 213980 |
| rs584990664 | snp | G/T | | | synonymous-codon, nc-transcript-variant | Fbxw10 | GRCm38.p3 | 11:62876694 | AGTCCCTATGACACC[G/T]GACCGATTCCTTCTG | 213980 |
| rs585015233 | snp | C/T | | | intron-variant | Fbxw10 | GRCm38.p3 | 11:62862390 | CTTTCCAGTCAGTTA[C/T]AGATAGAGGAGTGGT | 213980 |
| rs585158560 | snp | C/T | | | intron-variant | Fbxw10 | GRCm38.p3 | 11:62849717 | CACCTTCTATGCATC[C/T]TTACGCAAAGAGTGC | 213980 |
| rs585195957 | snp | A/G | | | missense, nc-transcript-variant | Fbxw10 | GRCm38.p3 | 11:62875007 | TCAAGTGGCAGTACA[A/G]CTCAGACAAGAACAA | 213980 |
| rs585359963 | snp | A/G | | | intron-variant | Fbxw10 | GRCm38.p3 | 11:62858824 | TATGTATATATGTAT[A/G]TATTTGAGGCTGGGT | 213980 |
| rs585868240 | snp | C/T | | | intron-variant | Fbxw10 | GRCm38.p3 | 11:62850870 | GGCATCCTACATCAA[C/T]AGTTTGACTTAAGAT | 213980 |
| rs585898470 | snp | A/G | | | intron-variant | Fbxw10 | GRCm38.p3 | 11:62874048 | AGTTTGCTTTGTACA[A/G]ATGAAAAAAAAAACA | 213980 |
| rs585907344 | snp | C/T | | | intron-variant | Fbxw10 | GRCm38.p3 | 11:62871930 | ACATGTCACAAAACA[C/T]GGCATTCTTATCAGC | 213980 |
| rs586015506 | snp | A/G | | | intron-variant | Fbxw10 | GRCm38.p3 | 11:62856339 | TAGGTAAAATTTCTT[A/G]TATTACTAGCTGTGG | 213980 |
| rs586247440 | snp | A/G | | | intron-variant | Fbxw10 | GRCm38.p3 | 11:62848030 | CCGGCACTGAACAGT[A/G]TCCTGCCTGCCTTGG | 213980 |
| rs586454552 | snp | A/G/T | | | intron-variant | Fbxw10 | GRCm38.p3 | 11:62862111 | TTTTTTTTTTTTTTT[A/G/T]AGAGAGTGTCACTGC | 213980 |
| rs586564643 | snp | A/T | | | upstream-variant-2KB | Fbxw10 | GRCm38.p3 | 11:62845641 | TATTGATAAGCTATA[A/T]GCCTAGATTGGGCAG | 213980 |
| rs586642674 | snp | C/T | | | intron-variant | Fbxw10 | GRCm38.p3 | 11:62866148 | TAGAACAGACTAGGA[C/T]TTCTTTTTCTCTTTC | 213980 |
| rs586677927 | snp | C/T | | | intron-variant | Fbxw10 | GRCm38.p3 | 11:62858277 | CTGAGAAAACCAAGG[C/T]AGGAACTCAAAGTAG | 213980 |
| rs586849868 | snp | G/T | | | intron-variant | Fbxw10 | GRCm38.p3 | 11:62866426 | TCTCTCTCTCTCTCT[G/T]TCTCTCTGTTTCTCT | 213980 |
| rs587034829 | snp | C/T | | | intron-variant | Fbxw10 | GRCm38.p3 | 11:62857237 | CAGCTGCGAGCACGA[C/T]AAGGGTCAAGCAGTA | 213980 |
| rs587143166 | snp | A/T | | | intron-variant | Fbxw10 | GRCm38.p3 | 11:62875473 | CATCTAAAGAGCAAA[A/T]CATGTGGGTTATGAT | 213980 |
| rs587226891 | snp | C/T | | | missense, nc-transcript-variant | Fbxw10 | GRCm38.p3 | 11:62875163 | AGTCCCGGGTTCACC[C/T]GAAACAAACCAAGAA | 213980 |
| rs587379519 | snp | C/T | | | upstream-variant-2KB | Fbxw10 | GRCm38.p3 | 11:62846307 | TAGCAGTGGTGACAG[C/T]GACAACAGAGAGACA | 213980 |
| rs587532820 | snp | C/T | | | intron-variant | Fbxw10 | GRCm38.p3 | 11:62866278 | CTTTCTTTCTTTCTT[C/T]CTTTCTTTCTTTCTT | 213980 |