| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs247893656 | snp | A/C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45075637 | TATTTTAAATGAGAA[A/C/T]CCCCCCCCCCAGACT | 269529 |
| rs247907600 | in-del | -/GTGTGTGTGAGA | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45046522 | TGTGTGTGTGTGTGT[-/GTGTGTGTGAGA]GACATGTGCTACAGC | 269529 |
| rs247913006 | snp | G/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45074554 | CTTTTCTATTTCAAG[G/T]GCAAACAAGGGAGCA | 269529 |
| rs247913157 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45074007 | GCTGAGCTTGGCACA[C/T]AGCAAACACACAGCA | 269529 |
| rs247937520 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45037070 | TGTGTGTGTGTGTAT[A/G]TATATATATATATAT | 269529 |
| rs247972815 | snp | A/G | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45046773 | ACTTGGAAACCCTTG[A/G]CTGTCCCTGGGACTC | 269529 |
| rs248012491 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45082343 | GGCCCATTAAAGGAA[C/T]ACGTTTCTCTCTCAT | 269529 |
| rs248022751 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45072162 | AACAGCCATGGTGGT[A/G]CACACATCTGCAATC | 269529 |
| rs248036278 | snp | G/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45072361 | ATCACTAAGAAGGAA[G/T]GATCTAGGGCAGCTC | 269529 |
| rs248071570 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45079973 | AGGGTGATCTCACAC[A/G]CATGGAGTTAAACTA | 269529 |
| rs248102156 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45071800 | TAGGGAGGCGAGAGT[C/T]AGAACAGCAAGCAGG | 269529 |
| rs248132356 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45079394 | ACTACACAGTTAGTT[C/T]TTGTCTCAAAAAGCA | 269529 |
| rs248179716 | in-del | -/A | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45056010 | CTGTGCTTCTTAGTC[-/A]ACGTTCCAGAATCTC | 269529 |
| rs248258983 | snp | A/G | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45049056 | AATGACAGGCCTGTG[A/G]AAGCTGCCTCCACAC | 269529 |
| rs248260561 | snp | A/G | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45057373 | CTGCAAGGCCTGCTC[A/G]CCCTTCAGAGCCCTC | 269529 |
| rs248283869 | in-del | -/CTC | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45047332 | CAACACTTAGAAAAA[-/CTC]CTAAGGAAAAGTGCA | 269529 |
| rs248311338 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45064694 | CCTTCCTTTGATCAG[C/T]TGCCTTATTACAGTG | 269529 |
| rs248351013 | snp | C/T | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45056617 | CCTATGATAACTGTG[C/T]GAAGAGAAAAATCCT | 269529 |
| rs248457379 | in-del | -/CAGGTGCCAAGAGTCA | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45052969 | GTCTCTCCTGCCTCT[-/CAGGTGCCAAGAGTCA]CAGCTATGGGCTACG | 269529 |
| rs248523266 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45070651 | CGCAGAGCCCCGTGT[A/G]ACAAGCAAATAAGAC | 269529 |
| rs248564326 | in-del | -/TTGGG | | | utr-variant-3-prime | Fbxo10 | Mm_Celera | 4:45035077 | CGTGGGCACGTCGGA[-/TTGGG]TTGGGTAGGGTGGGG | 269529 |
| rs248657799 | snp | C/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45038015 | GCTCCATGAGGACTT[C/G]AGGTTTCTGACAACA | 269529 |
| rs248667008 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45073866 | GAATTGCTACTTTAC[C/T]GGTGACATTAAACAT | 269529 |
| rs248696832 | snp | C/T | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45047618 | GCTCTGGCACCTCTC[C/T]TCTTGCTGTTCTTGT | 269529 |
| rs248805869 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45042833 | ATCTTTGGGCCACAG[C/T]GAGCGCAGTTGACCA | 269529 |
| rs248851054 | snp | C/T | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45050961 | TGGCAAGTATGCGTG[C/T]TATCAACTGATCCAT | 269529 |
| rs248871773 | snp | C/T | | | upstream-variant-2KB | Fbxo10 | GRCm38.p3 | 4:45086244 | CGACTGGTTGCTCCT[C/T]TCTTCTTACCCTCAT | 269529 |
| rs248926233 | in-del | -/TGTA | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45046526 | GTGTGTGTGTGTGTG[-/TGTA]TGTGAGAGACATGTG | 269529 |
| rs248927031 | snp | C/T | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45055609 | GCCACATAACTCCTG[C/T]CAAACATCTCCTGGG | 269529 |
| rs248931637 | in-del | -/AAGC | | | intron-variant | Fbxo10 | Mm_Celera | 4:45069960 | AAGGAAAGAAAGAGA[-/AAGC]AAGCAAGCAAGCAAA | 269529 |
| rs248966095 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45064140 | AGACATGGAGCTATA[A/G]GAGCTGGAGTTTGTC | 269529 |
| rs248971871 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45042555 | GCTGGGATTAAAGGC[A/G]TGTGCCACCACACCC | 269529 |
| rs248979078 | snp | A/T | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45053300 | CACATATACCCGCAC[A/T]CCCGTGCACACACAT | 269529 |
| rs249018735 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45078883 | CCTGAAAACTATAGA[C/T]ACTAAGTGAGGCCGC | 269529 |
| rs249035720 | snp | C/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45080932 | GGAAGGGCGATGGAG[C/G]CCTTAAATTCAGATA | 269529 |
| rs249044020 | snp | A/G | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45050786 | GTGTGCATACCATAT[A/G]CATGCAGGCGTATTC | 269529 |
| rs249070142 | in-del | -/TTTGTTTG | | | intron-variant | Fbxo10 | Mm_Celera | 4:45068791 | ATCTTTCCAGTCCAT[-/TTTGTTTG]TTTGTTTGTTTGTTT | 269529 |
| rs249081558 | snp | G/T | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45050049 | CTCTTTTGAGATCTC[G/T]GAGGGGGCTGGCTAG | 269529 |
| rs249116549 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45075386 | TTTTTAATGTTTGTT[C/T]ATTTTGGAGGGAGGC | 269529 |
| rs249166444 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45084220 | CTCCTGCATCCCAGG[C/T]GAAGGCTAGCAAACC | 269529 |
| rs249191173 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45037543 | TTGGTTGTGGGCAGC[A/G]CCATCCTAAGGGCTG | 269529 |
| rs249224554 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45074817 | TTTACAAAGGAGCTG[A/G]CTATGGTGCCTGGGC | 269529 |
| rs249247412 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45083218 | CGTGAGCACACGCGC[A/G]CGCGCACACACACAC | 269529 |
| rs249262383 | in-del | -/TTCTTT | | | intron-variant | Fbxo10 | Mm_Celera | 4:45075332 | AGAGAGACAAAGAGA[-/TTCTTT]TTCTTTTTCTTTTCT | 269529 |
| rs249402358 | snp | A/G | | | intron-variant, nc-transcript-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45061104 | CCCTCATCTGCCCAA[A/G]GGCACCACAGCTACT | 269529 |
| rs249436192 | in-del | -/CA | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45050329 | TGACTAAGGATAATC[-/CA]CAGAGGGCTTTAGAA | 269529 |
| rs249489284 | snp | A/G | | | intron-variant, nc-transcript-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45060557 | GCTGCTGCTGGTGCC[A/G]CCTTACGGCTCCTCT | 269529 |
| rs249642537 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45078139 | CACCTCCTAAACCTC[C/T]CCAAACAGTGCCACC | 269529 |
| rs249642619 | snp | G/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45070032 | GCATGCATGCATCCA[G/T]ATGTGCATGTGTGCA | 269529 |
| rs249662807 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45080722 | GAAACAGTCGCCTGG[A/G]AACACATGGATGCTT | 269529 |
| rs249701175 | snp | G/T | | | utr-variant-3-prime | Fbxo10 | Mm_Celera | 4:45035878 | TTCCGAGCACACACC[G/T]GGGCTTGGGCCTGAG | 269529 |
| rs249730734 | snp | A/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45077376 | AACAAGTGGGATCTC[A/T]TGAAACTAACAGGCT | 269529 |
| rs249746355 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | Fbxo10, Polr1e | Mm_Celera | 4:45034607 | CAGAGCTGGCCCTGC[A/G]TGCAGACCCAAGCCC | 269529 |
| rs249841470 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45043481 | AAAGGAAACGTTAGT[A/G]AAGTCAGTGGGGCAG | 269529 |
| rs249843412 | snp | A/G | | | intron-variant, nc-transcript-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45061489 | GAAGGTGACCGCTCT[A/G]TGCTAATGAGTACTG | 269529 |
| rs249861257 | snp | C/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45067582 | GTGACCCCTTTGAGG[C/G]TTGAACAACCCAACC | 269529 |
| rs249877316 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45042648 | AAATCCTCCACTTGG[A/G]CTGGTGAGATGGCTC | 269529 |
| rs249881865 | snp | A/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45070285 | TCCTTCAAGCACTGT[A/T]GTACTCTCCCCGCGC | 269529 |
| rs249899182 | in-del | -/TTTTTTTTTT | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45050900 | AGGCCCCCATGCCTA[-/TTTTTTTTTT]TTTTTTTATGCTGGG | 269529 |
| rs249918327 | in-del | -/A | | | intron-variant | Fbxo10 | Mm_Celera | 4:45067690 | CTATGAAGTGGCAAC[-/A]AAAATAATGCTATGG | 269529 |
| rs249926405 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45069313 | CTTCACATTAGTCCA[C/T]GGGGATCCATGCAGC | 269529 |
| rs249952293 | snp | A/G | | | intron-variant, nc-transcript-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45060218 | CTTTCCCCGTCTGTA[A/G]CATGAGGCTTGCTAG | 269529 |
| rs250004339 | snp | A/G | | | utr-variant-3-prime | Fbxo10 | Mm_Celera | 4:45034892 | CACTTGGAGCCAGGG[A/G]AGAGTCACGTGGAGA | 269529 |
| rs250016831 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45068503 | AACCTTGAACTCTTG[A/G]GCTCAGCTGATCCTC | 269529 |
| rs250021858 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45070513 | AGCCAGAAACACTGT[A/G]CTGCTGTGTGTAGTC | 269529 |
| rs250104805 | snp | C/T | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45052228 | ACATACATACAGATA[C/T]AGAGACAGACACACA | 269529 |
| rs250282285 | in-del | -/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45042412 | GTTTTGTTTTGTTTT[-/G]TTCTTTCTTTCTTTC | 269529 |
| rs250288186 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45041303 | ACCTCAAATAGTACG[A/G]GGGACTCAGGGAGTC | 269529 |
| rs250292106 | snp | C/T | | | intron-variant, nc-transcript-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45045691 | GACAAGGGCTGCCCA[C/T]GGCTGGTGCTCAGTA | 269529 |
| rs250386843 | snp | C/T | | | intron-variant, upstream-variant-2KB | Fbxo10, Gm30939 | Mm_Celera | 4:45045217 | CTAGTGTAAGAGACT[C/T]ACATCCGAAGGGTGG | 269529 |
| rs250422077 | snp | A/T | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45052888 | GGGCTCAAACTCAGG[A/T]CCTTGCACCTGTTAG | 269529 |
| rs250464908 | in-del | -/GAAGC | | | utr-variant-3-prime, downstream-variant-500B | Fbxo10, Polr1e | Mm_Celera | 4:45034663 | TCAGTACAGTCTAGT[-/GAAGC]CCTTTGGGAGCTGGC | 269529 |
| rs250468047 | in-del | -/AAAC | | | intron-variant | Fbxo10 | Mm_Celera | 4:45082747 | AAAAGAAAAAAAAAA[-/AAAC]AAAAACGAAACAAGC | 269529 |
| rs250469672 | in-del | -/CTGC | | | intron-variant | Fbxo10 | Mm_Celera | 4:45070337 | AGTTTTGTTGTCTGT[-/CTGC]CTGTCTATCTGTCTT | 269529 |
| rs250486653 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45074741 | AGGGCTTTGTGCACA[C/T]CAAACAAGCTGGCTA | 269529 |
| rs250502415 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45077752 | CACACACACAAAGAA[A/G]ACAATGGCGACTAAG | 269529 |
| rs250561286 | snp | A/G | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45047222 | CTACATGTTATGCTT[A/G]TGTAGCATCTTTAGC | 269529 |
| rs250651123 | snp | A/G | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45054530 | AGGCAACACACCCCA[A/G]GACCCTTAGGGAAAA | 269529 |
| rs250754189 | in-del | -/TTGGTTGGTTGG | | | intron-variant | Fbxo10 | Mm_Celera | 4:45068804 | ATTTTGTTTGTTTGT[-/TTGGTTGGTTGG]TTGGTTGGTTGGTTT | 269529 |
| rs250774754 | in-del | -/AGAT | | | intron-variant | Fbxo10 | Mm_Celera | 4:45080004 | AACGGCACTGTGTAG[-/AGAT]AGATGCACACACACA | 269529 |
| rs250795461 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45071973 | GTTCCCGTGGGCCCC[A/G]ACCAGAGCTACTAGC | 269529 |
| rs251088667 | snp | A/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45036873 | TGCAGGAAGGTGATT[A/T]AGTGCAGACTCGGCA | 269529 |
| rs251165564 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45036253 | ATTTCCTCTTAGGCC[C/T]TCAACTTCCTCTTCT | 269529 |
| rs251196622 | snp | A/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45082509 | GTCTTATACCACAGC[A/T]CCGCATCTGCATCAT | 269529 |
| rs251209175 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45065417 | CCCTGGTGTAATCCT[A/G]GCCATCTGCTGGGCT | 269529 |
| rs251326097 | snp | A/G | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45057615 | TACCTGTATATATAT[A/G]TGTGTGTGTACTTGC | 269529 |
| rs251383980 | snp | C/G | | | intron-variant, nc-transcript-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45059799 | TTATATGATTACCAT[C/G]CACAAGTCTCTCCTG | 269529 |
| rs251407254 | snp | C/G | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45056739 | TGAGACAAGGTTTCA[C/G]TAGCCCAGGCTGGCC | 269529 |
| rs251469548 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45082772 | ACAAGCCAGAACGAC[A/G]GACGAGTGACTGGTG | 269529 |
| rs251613754 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45074581 | AGCAAATGGTAAGTT[C/T]TTAAGGGCCAGATGC | 269529 |
| rs251716100 | in-del | -/GA | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45046530 | TGTGTGTGTGTGTGT[-/GA]GAGACATGTGCTACA | 269529 |
| rs251719308 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45038894 | CTGACCTCAAAGTGG[A/G]GAGGCCTCCTGGAAT | 269529 |
| rs251719667 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45073756 | GACAGTGTCCTTCTC[A/G]TCCTTCTTGTCACCT | 269529 |
| rs251758383 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45037920 | GGATGACTTCAAGTA[C/T]AGTGCTTGTCACACC | 269529 |
| rs251808993 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45037365 | GTATCCTCCCACATC[A/G]AAAGACCCCACAGGT | 269529 |
| rs251878244 | snp | A/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45064547 | ACTCAGGACATTTTG[A/T]GTTCACGCTCTCTGT | 269529 |
| rs251879053 | snp | A/G | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45057430 | GGATTGTTTCATAGC[A/G]CTCAGTATGACTTCT | 269529 |
| rs251932482 | snp | A/G | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45046972 | TAATAAAAGCTCTGC[A/G]CTCTAGGTGTTGTGG | 269529 |
| rs251994468 | snp | C/T | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45056386 | CCCTTCCCTTCCCTC[C/T]GCCCCCCACACCCAC | 269529 |
| rs251995278 | snp | C/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45075275 | AGATCACCTGAGGCA[C/G]GGAGAAATATGGCCA | 269529 |
| rs252027457 | in-del | -/GTGGTACA | | | intron-variant | Fbxo10 | Mm_Celera | 4:45043248 | GCATCAGGCATGAAT[-/GTGGTACA]CAGATATACATGCAG | 269529 |
| rs252051266 | snp | C/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45067378 | AAAGGAAGAAAGAGA[C/G]AGAGGAAGAGAGAAA | 269529 |
| rs252175970 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45069582 | TGTGGTCTCCCACCC[C/T]CCACTCCACTGGAGA | 269529 |
| rs252303832 | in-del | -/CCCTGAAATGC | | | intron-variant | Fbxo10 | Mm_Celera | 4:45065206 | CTATGGAATCTAGAT[-/CCCTGAAATGC]CCCTGGGATCTACCT | 269529 |
| rs252398948 | in-del | -/TGAAATGCCCG | | | intron-variant | Fbxo10 | Mm_Celera | 4:45065209 | TGGAATCTAGATCCC[-/TGAAATGCCCG]TGGGATCTACCTAAG | 269529 |
| rs252470337 | in-del | -/C | | | intron-variant | Fbxo10 | Mm_Celera | 4:45082060 | CCAGGACAGGCGACT[-/C]TGGAGAAGGAACAGC | 269529 |
| rs252505988 | snp | C/T | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45059433 | AAGTCTTAAATAAGT[C/T]CTCTGATACTCATGA | 269529 |
| rs252568194 | snp | A/G | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45056944 | AAGCTGAGTGTGGTG[A/G]CACACACTTTTAACT | 269529 |
| rs252661817 | snp | C/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45042408 | GTTTTGTTTTGTTTT[C/G]TTTTTTCTTTCTTTC | 269529 |
| rs252701193 | snp | A/G | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45050595 | TATCTCTTTTCTGAT[A/G]TGACCTGGAACTCAC | 269529 |
| rs252722839 | snp | C/T | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45052115 | ACACACATGCATGCA[C/T]ACACACACATACCCA | 269529 |
| rs252783916 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45040096 | CACCTAGCTTCGGGA[C/T]CCTCATTCCAGGGAC | 269529 |
| rs252818957 | snp | A/G | | | intron-variant, nc-transcript-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45059873 | CTTGTGCCTACAGGT[A/G]TGTTCTCTACCTGAG | 269529 |
| rs252881217 | snp | A/G | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45049038 | TACAAGATAATGTGT[A/G]CCAATGACAGGCCTG | 269529 |
| rs252987529 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45073605 | TGGAGCATCAGAAAC[C/T]GTCTAATTTGGACTG | 269529 |
| rs252992821 | snp | A/T | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45053778 | GAGGCCAGCTGTGAT[A/T]GCATAGTAAGACTGT | 269529 |
| rs253018810 | snp | G/T | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45053405 | ACACACATGATCTTG[G/T]TTGTTTAGTTTTTAA | 269529 |
| rs253025802 | in-del | -/ATATTA | | | intron-variant | Fbxo10 | Mm_Celera | 4:45037084 | TATATATATATATAT[-/ATATTA]TTTTTTTCATTTCCT | 269529 |
| rs253051233 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45081746 | TCTCTCTCCTCTGAG[A/G]GTGACAAGAAGGACC | 269529 |
| rs253052809 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45079152 | CCAAGGAAAGTAAGT[C/T]AAAGCCTCGAGACAC | 269529 |
| rs253112226 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45078575 | GAGAACAAACGCCTC[A/G]GCAAGGATGTGGGAG | 269529 |
| rs253158556 | snp | A/C | | | intron-variant | Fbxo10 | Mm_Celera | 4:45063308 | AGCCTTCAGATGAAG[A/C]TGTAGAACTCTCAGC | 269529 |
| rs253197064 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45079907 | AACTTACTGTGACCT[A/G]ATCACACCAGTGACA | 269529 |
| rs253242542 | in-del | -/A | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45053248 | TCAGTGAAGTGCATG[-/A]AAAAAAAGGAACCCG | 269529 |
| rs253283186 | in-del | -/C | | | intron-variant | Fbxo10 | Mm_Celera | 4:45074112 | CCAGCATCTTAGGAA[-/C]AAAAAAAAAAGTCTG | 269529 |
| rs253337501 | in-del | -/TGTGTGTGTGCA | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45049360 | TTTTCTCATTCTGTT[-/TGTGTGTGTGCA]TGTGTGTGTGCATGT | 269529 |
| rs253360685 | in-del | -/GTTT | | | intron-variant | Fbxo10 | Mm_Celera | 4:45072937 | AGGGAGTGTTTGGGG[-/GTTT]GTTTGTTTGTTTTGT | 269529 |
| rs253432410 | snp | C/T | | | intron-variant, nc-transcript-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45061204 | CCATAAGCCTGAAAC[C/T]TTGCCTATGCTGCTG | 269529 |
| rs253534449 | snp | G/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45072065 | CCTGCAAGGAGGACA[G/T]ACTGGCTTGCATTCT | 269529 |
| rs253576211 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45069755 | CCTCTCCGAGTCTAT[C/T]TCCCCAATCTCTCAC | 269529 |
| rs253578994 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45070298 | GTAGTACTCTCCCCG[C/T]GCTAGGATGAAGGTT | 269529 |
| rs253579017 | snp | A/C/G | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45078695 | ATATGTCTACCACAC[A/C/G]ACCCAGCTAGACCAC | 269529 |
| rs253630166 | snp | G/T | | | synonymous-codon, downstream-variant-500B | Fbxo10, Gm30939 | Mm_Celera | 4:45062206 | CACTCAAGGTGCGTC[G/T]CTCCTTCTTCCTGCG | 269529 |
| rs253630509 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45071584 | AGGCATAAGCCAGCG[C/T]GTCCAACCAAGAACC | 269529 |
| rs253686879 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45041063 | TCCAGGTTTTTCTCA[C/T]GGACATGGCTGACTT | 269529 |
| rs253713510 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45036455 | TGAATGCATCAGGGC[A/G]TGGTGGCGAATGCTT | 269529 |
| rs253716389 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45070585 | GAGTAAATCCTTACT[A/G]GACTAACAGTGCTGA | 269529 |
| rs253748449 | in-del | -/A | | | intron-variant | Fbxo10 | Mm_Celera | 4:45063515 | AATAAATATTTTTTT[-/A]AAAAAACTATTTTCT | 269529 |
| rs253804466 | snp | C/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45067276 | CTCAGGAGGCAGAGA[C/G]AGAAGGACCTCTGTG | 269529 |
| rs253855751 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45070820 | CTCTAACCAAATCAA[C/T]GCCATCCATCACAAA | 269529 |
| rs253877184 | in-del | -/GA | | | upstream-variant-2KB | Fbxo10 | Mm_Celera | 4:45086097 | CCACGGGGGCGGGGG[-/GA]GATTTTATTTCTTGT | 269529 |
| rs253924383 | snp | C/T | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45052630 | CACCTATGTCTGCCT[C/T]CCTAGTCCTGAATTC | 269529 |
| rs253964561 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45063339 | TCTGCCTACACCATG[C/T]CTGCCTAGATGCTGC | 269529 |
| rs253987391 | snp | A/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45072752 | GACACTGTGTGCTTA[A/T]GTCAGGAGCTCTGAG | 269529 |
| rs254045805 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45081103 | TCCAGAGGGAATCTG[A/G]CTGGCAGGGATCTGA | 269529 |
| rs254109571 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45080351 | TTTTGTTTGTTTCTG[A/G]ATTGAGATCTTGCCA | 269529 |
| rs254147088 | snp | A/C | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45046073 | GAGCAGCAGAAGCCC[A/C]CACAAAAGTATGGAG | 269529 |
| rs254175885 | snp | A/G | | | intron-variant, upstream-variant-2KB | Fbxo10, Gm30939 | Mm_Celera | 4:45045464 | CTTCCACCTCTCAGG[A/G]TCTGGGTTACGAGTA | 269529 |
| rs254182555 | snp | C/G | | | intron-variant, nc-transcript-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45061034 | GCCTGGATTTGAGCT[C/G]TAACCTCACTAATTA | 269529 |
| rs254186443 | in-del | -/CAACTGT | | | intron-variant | Fbxo10 | Mm_Celera | 4:45042899 | CCAGATGAAGACTCA[-/CAACTGT]CTGTGCAGCTACAGT | 269529 |
| rs254256903 | snp | C/T | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45053210 | GACAAAACAAAATAG[C/T]TAACTGATGTGGAAA | 269529 |
| rs254292006 | snp | A/C | | | intron-variant | Fbxo10 | Mm_Celera | 4:45065234 | CCTAAGAGAGTTTGG[A/C]TCATACAGAGAGAGG | 269529 |
| rs254376591 | snp | A/G | | | intron-variant, nc-transcript-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45059644 | GGCGAAGGGGAGCGC[A/G]GAGGAGGGCCACTCT | 269529 |
| rs254400723 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45067909 | GTCGGTCTCACTTCC[C/T]CCTCCCATCAGCCAC | 269529 |
| rs254405419 | snp | A/C | | | intron-variant | Fbxo10 | Mm_Celera | 4:45073694 | CTACAAAATCCAGGG[A/C]ACCTTATCTGGAGAG | 269529 |
| rs254488479 | snp | C/G | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45055111 | CTCAGAGGAGCAGGC[C/G]CAAAGAGAAGATCCA | 269529 |
| rs254504930 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45070952 | ATCCCATCAGGGAAG[A/G]GGGAGCAGTGGACCC | 269529 |
| rs254548644 | in-del | -/GAGG | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45055088 | CTGAATGCTGAGAGA[-/GAGG]GGGGCCGCTCAGAGG | 269529 |
| rs254562347 | snp | C/G | | | utr-variant-3-prime | Fbxo10 | Mm_Celera | 4:45035192 | CCTGTGACGGGTGCT[C/G]AACTTCCCCTTGGGG | 269529 |
| rs254569731 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45038660 | GGATCTACTTCAGGC[C/T]TTGAGAACTAGACAG | 269529 |
| rs254667512 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45073413 | TTTTTAAAAAGATTA[C/T]TATAAATAGGTACAC | 269529 |
| rs254678557 | snp | C/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45082147 | GCGGATTTCTGAGTT[C/G]GAGGCCAGCCTGGTC | 269529 |
| rs254727231 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45081685 | CAGCTCTTCCAGTGA[C/T]ATCACACGGCGGTCA | 269529 |
| rs254760675 | snp | A/T | | | intron-variant, nc-transcript-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45046169 | TGAGATACTGGGCCC[A/T]CCTATGAAAAGCATG | 269529 |
| rs254788693 | snp | C/G | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45048281 | GAGAAGACAGGAGAC[C/G]GGGCAGGTGTTCCTG | 269529 |
| rs254803141 | in-del | -/A | | | intron-variant | Fbxo10 | Mm_Celera | 4:45077199 | TGTTGAGTCTTGTGG[-/A]AAAAAATTGTTCCTT | 269529 |
| rs254836519 | snp | A/C | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45055819 | AGCTTATCTCTCTTC[A/C]CACGGTAACCTCCAT | 269529 |
| rs254863702 | in-del | -/C | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45054375 | CGAATTAAGAAAATG[-/C]CTTAAAGACCTGCAT | 269529 |
| rs254950167 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45074025 | CAAACACACAGCAAA[C/T]GGAAGAGGTTCTCTC | 269529 |
| rs255037359 | in-del | -/ACCTCATACCCTGTCCTCTG | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45051854 | GAAGGAGAGAACCAA[-/ACCTCATACCCTGTCCTCTG]ACCTCATACCCAGGA | 269529 |
| rs255073406 | in-del | -/C | | | intron-variant | Fbxo10 | Mm_Celera | 4:45074065 | TTTCCTAAAGCAAAT[-/C]CCTCTTCCTCTTCGA | 269529 |
| rs255188624 | snp | C/T | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45046588 | CTGTCGGGAGTTGGT[C/T]CTGTCCTTCCACTAC | 269529 |
| rs255349026 | snp | A/G | | | upstream-variant-2KB | Fbxo10 | Mm_Celera | 4:45085086 | AATTATATGAAGTAC[A/G]TGAAAAGAGCTCTTT | 269529 |
| rs255375233 | in-del | -/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45067991 | ACAGGCCCAGCAGCT[-/G]GAACACTGGTGCAGG | 269529 |
| rs255404022 | snp | C/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45084468 | GCGGGCTCCCGAGAA[C/G]CCTCCTTCCTGCGCC | 269529 |
| rs255430667 | snp | G/T | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45052744 | TGCAATTTCAGGTCT[G/T]TCCCTTTCACTGGCC | 269529 |
| rs255442926 | snp | G/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45074881 | CCCCAGCGGGGTCTG[G/T]TCCTCCGTATTTTTA | 269529 |
| rs255444270 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45067063 | GTCTCCATCAGTCTC[C/T]GCCCCAGCTTTCAGG | 269529 |
| rs255493029 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45074335 | CTCTAAGGGCCTCTG[A/G]ACTCAGATCCTCAGG | 269529 |
| rs255552083 | snp | A/C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45077141 | TTCACCTTAGTCCTC[A/C/T]CTAAACTCTGGCCCT | 269529 |
| rs255624049 | snp | A/G | | | upstream-variant-2KB | Fbxo10 | Mm_Celera | 4:45086127 | TATAAACATTTAAAC[A/G]TCAAGACAGTGGCGT | 269529 |
| rs255708934 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45036126 | TAGAGACGGTGCTTG[C/T]GAGTGGCTGCGTCTC | 269529 |
| rs255755520 | snp | C/T | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45054093 | ATGTTAGGGTTACTA[C/T]TGCTGTGATGAAACA | 269529 |
| rs255785930 | snp | G/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45067753 | AAGGGGTTGCAGCGT[G/T]AGGAAGGTGAGAGCC | 269529 |
| rs255794809 | snp | C/T | | | intron-variant, nc-transcript-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45061854 | GTACAGGAATAAATA[C/T]TAAATTCTCAAGTCT | 269529 |
| rs255863438 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45083911 | GGGCCGAAGAATTCA[C/T]CTCTACTTTTATTTA | 269529 |
| rs255945334 | snp | A/C | | | intron-variant, nc-transcript-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45060439 | ATAACACAACGGAGC[A/C]CCTCAGGAATCAGAT | 269529 |
| rs255982235 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45069199 | ACAGACTGAGGCCAG[C/T]CAGTCCTTCTCCCTT | 269529 |
| rs256139783 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45069473 | AGTGTGACGTCTGTA[A/G]GAACTGGAAAAACAA | 269529 |
| rs256171977 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45076133 | CCCAGCACTGGGGAG[A/G]CAGAGGCATGATAGT | 269529 |
| rs256189380 | in-del | -/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45080055 | ACGGCCATCCACAGG[-/T]CAAGATGGCAGCCTC | 269529 |
| rs256463051 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45043042 | CACACCGGGCAGGGA[C/T]GCTGCTCCTGCACTC | 269529 |
| rs256498620 | snp | A/G | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45051171 | ACAAAACCAAACTCC[A/G]TATGTTCCCATGTCT | 269529 |
| rs256513892 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45067583 | TGACCCCTTTGAGGC[C/T]TGAACAACCCAACCC | 269529 |
| rs256529337 | snp | C/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45081727 | TGGGTGCAGCACTCA[C/G]AGCTCTCTCTCCTCT | 269529 |
| rs256582170 | snp | C/T | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45050390 | AAGGATGGCCACCGC[C/T]TTTCTAAATTCACGA | 269529 |
| rs256583570 | snp | C/T | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45050474 | CATATACTAGTCACA[C/T]ATGCAAGGGTTTTGT | 269529 |
| rs256622764 | snp | C/G | | | intron-variant, utr-variant-3-prime | Fbxo10, Polr1e | Mm_Celera | 4:45033999 | GCTCAGCAGGTGACC[C/G]CAATGAAGGAGTGTC | 269529 |
| rs256628877 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45075657 | CCCCCCAGACTCATA[C/T]ATTTGCTTAGTGGGC | 269529 |
| rs256666059 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45075182 | CTTAGCCAGGGCAAG[A/G]TATCACACAGGATAG | 269529 |
| rs256688050 | snp | A/G | | | synonymous-codon, intron-variant | Fbxo10, Gm30939 | GRCm38.p3 | 4:45058599 | TGAGCCCCCCAGGAC[A/G]GGGCGTGGGCCCTGC | 269529 |
| rs256705458 | snp | C/T | | | upstream-variant-2KB | Fbxo10 | Mm_Celera | 4:45084753 | GTGGGCGGGAACTGC[C/T]GGAGGCTCCTAGGGG | 269529 |
| rs256718789 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45083900 | ACAGCAACCTCGGGC[C/T]GAAGAATTCATCTCT | 269529 |
| rs256739055 | snp | A/C | | | utr-variant-3-prime | Fbxo10 | Mm_Celera | 4:45035825 | GGTCTAGGATCTTCC[A/C]AGGCCTAACTTCCAC | 269529 |
| rs256758160 | snp | A/G | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45053374 | CACACACATATACCC[A/G]CACACCCATGAGCGC | 269529 |
| rs256776138 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45075784 | TATCTCCCTCCCCCC[C/T]ACTCCCTCTTGTCTG | 269529 |
| rs256987792 | in-del | -/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45071505 | AGACAGGGTTTCTCT[-/G]TCTCCAAAAGAGCAC | 269529 |
| rs257057457 | snp | A/C | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45045759 | TCTAACCTAGGGCCA[A/C]ATACATGCTGAGCAA | 269529 |
| rs257155666 | in-del | -/AAT | | | intron-variant | Fbxo10 | Mm_Celera | 4:45075635 | GTATTTTAAATGAGA[-/AAT]ACCCCCCCCCCCAGA | 269529 |
| rs257221603 | snp | A/G | | | utr-variant-3-prime | Fbxo10 | Mm_Celera | 4:45035079 | TGGGCACGTCGGATT[A/G]GGTTGGGTAGGGTGG | 269529 |
| rs257242983 | snp | C/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45069039 | GAAAAAAGACAAAGA[C/G]CACATTTCACAAAGA | 269529 |
| rs257253476 | snp | A/C | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45051749 | TGGTCAAAGGATAAT[A/C]AAAAACTACCAGGGG | 269529 |
| rs257257863 | snp | A/G | | | intron-variant, upstream-variant-2KB | Fbxo10, Gm30939 | Mm_Celera | 4:45044333 | GACATCATTAGATAC[A/G]TCCAGAAAGGGGAAG | 269529 |
| rs257342528 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45043170 | CATTGGATGGGGTGG[A/G]AGAGATGGGCCAGTG | 269529 |
| rs257388779 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45069561 | GAGAGGTGAGGGCAA[C/T]GTTTCTGTGGTCTCC | 269529 |
| rs257389341 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45075978 | CTTTGGCCATGTGCC[C/T]TTTTACAGCAACAGA | 269529 |
| rs257419375 | snp | C/T | | | upstream-variant-2KB | Fbxo10 | Mm_Celera | 4:45084949 | TGATGTGTGTAGTAC[C/T]TGTTGCACCAACTAC | 269529 |
| rs257488143 | in-del | -/TTTTTTTTTTTT | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45083531 | AATCACCCTACTGTA[-/TTTTTTTTTTTT]TTTTTTTTTTTTTTT | 269529 |
| rs257494621 | snp | A/G/T | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45074415 | AGGTCAGCAGGTTTC[A/G/T]GGTTCCTGACCGTCT | 269529 |
| rs257519894 | snp | A/G | | | utr-variant-3-prime | Fbxo10 | Mm_Celera | 4:45035681 | AAACACTCCAATTGC[A/G]CTTCCCTTTCTCCTG | 269529 |
| rs257571009 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45043246 | GGGCATCAGGCATGA[A/G]TGTGGTACACAGATA | 269529 |
| rs257687065 | snp | A/G | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45051462 | CAAAAATGGGCAAGA[A/G]CCAACTTGCAGTACT | 269529 |
| rs257708954 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45063047 | TGACAACCCTGTAAT[C/T]CCAGCCCCACAGTGA | 269529 |
| rs257775223 | in-del | -/CTG | | | intron-variant | Fbxo10 | Mm_Celera | 4:45036210 | CTCCTGAATCACTGA[-/CTG]CTGCTGTTGAGGCTA | 269529 |
| rs257827390 | snp | G/T | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45049526 | CCTCAGGGATCTGCC[G/T]GATTCTGCCTCCCCA | 269529 |
| rs257857656 | snp | C/T | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45058114 | AGTAAGACTCTTTCC[C/T]GCTCTGGGTCTCTAT | 269529 |
| rs257914374 | snp | C/G | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45055989 | CAGATCTGACCATGA[C/G]AGCTCTCTGTGCTTC | 269529 |
| rs257966920 | snp | A/G | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45055872 | CTCAGGCTAGAGACC[A/G]AAGCCTCAAGGTCCT | 269529 |
| rs258044414 | snp | A/C | | | intron-variant | Fbxo10 | Mm_Celera | 4:45063822 | GTCAGGAAGACAAGA[A/C]AAGTCACTAGTACCG | 269529 |
| rs258050866 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45064468 | TGGCTTTGTTTGGGG[A/G]GGATTAGGAGGTGTG | 269529 |
| rs258064417 | snp | C/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45065725 | ACCAGAAAAGCAATG[C/G]AAGCAAGGGCATCCC | 269529 |
| rs258085463 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45082252 | CCCCCCCCAAAAAAA[A/G]AGAGGCGGCTCATCC | 269529 |
| rs258099156 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45064731 | CACAGCAAGAGAAAA[A/G]CAATTAATACCACTG | 269529 |
| rs258114358 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45081597 | GACTGGCAGGGATCC[A/G]ACTAACTGACAGGGA | 269529 |
| rs258269170 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45040846 | AGGAGCTCTGGGTGG[A/G]GCACAGAGGGCACCC | 269529 |
| rs258275319 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45068166 | CTGGGAAATTTTGGG[C/T]AAAAACATCTGTAAT | 269529 |
| rs258279266 | in-del | -/GC | | | intron-variant | Fbxo10 | Mm_Celera | 4:45039298 | GATATGGGGTCACTA[-/GC]ACAACCTTATCCCCG | 269529 |
| rs258364347 | in-del | -/A | | | intron-variant | Fbxo10 | Mm_Celera | 4:45082738 | TGCAACTGGAAAAAG[-/A]AAAAAAAAAAAAAAC | 269529 |
| rs258370841 | in-del | -/C | | | intron-variant | Fbxo10 | Mm_Celera | 4:45036606 | GGGAACCCAACCACT[-/C]TTCTGACCTCTGCAG | 269529 |
| rs258376188 | in-del | -/G | | | upstream-variant-2KB | Fbxo10 | Mm_Celera | 4:45084696 | AGCGGGGCTCGGCGA[-/G]TGGAGGGCGAGCGTG | 269529 |
| rs258388187 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45037270 | GGACTTGCCGGAGAG[C/T]GAGAGCAAGCAGGCA | 269529 |
| rs258396597 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45038336 | CTCAGAGCATTCCAG[A/G]AAGTTTACAACATTG | 269529 |
| rs258401910 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45078997 | ACAATGTACCTGCAG[A/G]ACCAGCTGAATGGAC | 269529 |
| rs258432362 | snp | C/G | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45047782 | AGTCTTCCACGAGCT[C/G]CCCTGGCCCTCAAAG | 269529 |
| rs258454134 | in-del | -/C | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45056065 | CCCCAACTCCTCCTG[-/C]CCTTTATCCCCCCCA | 269529 |
| rs258516696 | snp | G/T | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45047147 | AACAGCAACACAGAC[G/T]TGTCAGCCTCCATTC | 269529 |
| rs258564483 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45072484 | TCTCGGCGGAACAAC[A/G]CTAACAGGTTAATGA | 269529 |
| rs258565234 | snp | C/T | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45055584 | AGAAGCTAACCACCA[C/T]GCGTTTCTGGCCACA | 269529 |
| rs258629774 | snp | C/T | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45050998 | AGACCCATAGTCAAG[C/T]ACTGTATGTCATTTT | 269529 |
| rs258642746 | snp | G/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45072581 | TAAAAGAGAGTAAAA[G/T]GCAAGCCACAAAGCC | 269529 |
| rs258696241 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45039463 | GGATTAAAGGCGTGC[A/G]CCACCATGCCCGGCT | 269529 |
| rs258711267 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45040374 | CTCACAAGCAATGTT[C/T]CAGGCCAACTACAAC | 269529 |
| rs258739699 | in-del | -/AA | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45057555 | TATAGCTCTGTCTTT[-/AA]AAAAAAAATTAAGAT | 269529 |
| rs258744114 | snp | A/G | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45049187 | AGGTTTATCAGAGCA[A/G]GATGCTTAGGAGAGT | 269529 |
| rs258818653 | snp | G/T | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45058267 | CAAAAGCAAGGCTCA[G/T]GCTCTTGGCAGTGAC | 269529 |
| rs258821987 | snp | A/G | | | synonymous-codon | Fbxo10 | Mm_Celera | 4:45041981 | GATGCCTCTGTCCCC[A/G]TTGGCGTGGATCACA | 269529 |
| rs258839592 | snp | C/T | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45049423 | ACTGCAGGTGTCACT[C/T]GTCAAGAGCACCCAC | 269529 |
| rs258874377 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45073910 | TCTGGTCTCTGGCTG[C/T]TCTTCCTCATCTATA | 269529 |
| rs258893220 | snp | A/G | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45048664 | TACCAAGACGGACAC[A/G]GCCAGGACAAAACAC | 269529 |
| rs258902530 | snp | G/T | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45057281 | ACTGGACACTCTCTC[G/T]CGGTTTAGAAGTACA | 269529 |
| rs258915540 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45082088 | AGCGAGCCGGACAGT[A/G]GTGGCGCACGCCTTT | 269529 |
| rs258950015 | snp | A/C | | | intron-variant | Fbxo10 | Mm_Celera | 4:45083814 | ATCATGGACTCCTAG[A/C]TTGCTATTTTAACAA | 269529 |
| rs259010184 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45082257 | CCCAAAAAAAGAGAG[A/G]CGGCTCATCCATTAA | 269529 |
| rs259084483 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45080227 | AAAAAAATGTTCAAA[A/G]CAAAGATAGTGAAAT | 269529 |
| rs259293270 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45072105 | TCTGCCTTCACAGGC[A/G]GCTGAACTCTGCTTT | 269529 |
| rs259352119 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45065845 | GACTGGGTGTAGTCA[C/T]CCATATCTCTAATCC | 269529 |
| rs259416493 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45072228 | CTGGGGCCAGTCTGA[A/G]CTGTACAGCAAGACC | 269529 |
| rs259576418 | snp | A/C | | | upstream-variant-2KB | Fbxo10 | Mm_Celera | 4:45085846 | CATGCTTAGACGTCG[A/C]TTACGTTTGGCAAAC | 269529 |
| rs259601298 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45065862 | CATATCTCTAATCCA[A/G]CCACTTGGGAGTATC | 269529 |
| rs259613683 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45078341 | CCACTTTGACATTTT[A/G]TTTCGACCGGTCAGA | 269529 |
| rs259676478 | snp | A/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45073402 | TGCAGTTACTTTTTT[A/T]AAAAAGATTATTATA | 269529 |
| rs259763888 | snp | A/G | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45054916 | TTTGGCCCAGACCAT[A/G]AGCTAGGAGTGAGAA | 269529 |
| rs259765768 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45063876 | TAGTCTCTACCCTCT[C/T]CAGTCAGACTCTAAG | 269529 |
| rs259826114 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45077498 | CCTCGCCAGAATACA[C/T]GAAGAACTCAGAAAA | 269529 |
| rs259882682 | in-del | -/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45079851 | AGAGACTATGTTTGC[-/T]AAACGTCCTTGGTAA | 269529 |
| rs259897800 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45073216 | CAAACCTCACTCCTA[A/G]GGTCTGGCAGTAATA | 269529 |
| rs259905195 | snp | C/G | | | intron-variant, nc-transcript-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45059618 | CGGTGAGATGGAACT[C/G]ATACAACTTTGGCGA | 269529 |
| rs260038601 | snp | C/T | | | intron-variant, nc-transcript-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45061412 | TAACAGGGCCACGTC[C/T]AGCCAATGCATAGGC | 269529 |
| rs260076667 | snp | A/G | | | intron-variant, nc-transcript-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45060911 | TACTTCCAGGTCTGT[A/G]GACCAGCACGGGGAC | 269529 |
| rs260114849 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45037784 | TTTGCACATCAACAA[A/G]GAAAGAAACCATGTG | 269529 |
| rs260146621 | snp | G/T | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45053076 | AGTCCAGCACTGGAG[G/T]GACAGGGCAGGAAAG | 269529 |
| rs260185478 | snp | C/G | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45052577 | GGCTCACCTCAGCCT[C/G]GCTGTGTAGCCAGCA | 269529 |
| rs260263215 | snp | G/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45065446 | CTGGCTGCATCACTG[G/T]CTGCCACCTTGCTTT | 269529 |
| rs260270743 | snp | A/G | | | intron-variant, nc-transcript-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45060144 | CTGATGGCTCACCAC[A/G]GCTCTGCCTCTTCCA | 269529 |
| rs260351543 | snp | C/T | | | intron-variant, nc-transcript-variant, upstream-variant-2KB | Fbxo10, Gm30939 | Mm_Celera | 4:45045623 | TCTACACTGTCAGTC[C/T]CTGAGAGTAGAGCTG | 269529 |
| rs260358369 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45063470 | TTCACAGCAGTAAAA[C/T]TCTAACTAATACATG | 269529 |
| rs260362555 | in-del | -/A | | | intron-variant, nc-transcript-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45060854 | AGTCAGCACTTACTC[-/A]AGGCACAGAAGGTCT | 269529 |
| rs260424936 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45071670 | CAAGACCCCCGAGAA[C/T]GCGTGTGAACTCCAA | 269529 |
| rs260463783 | snp | C/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45070411 | CTTGAGCCCAGCACG[C/G]CCACTTAGACTGACA | 269529 |
| rs260470220 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45039319 | CTTATCCCCGGGGAA[A/G]CCAACGCTTTACTTT | 269529 |
| rs260498944 | snp | A/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45078064 | AAGCAGAAAGCAGAG[A/T]GCAGGAACCTTAAAT | 269529 |
| rs260622561 | snp | C/T | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45046745 | CCACCTTCTGAAATC[C/T]CATAATCTAGACACT | 269529 |
| rs260653803 | in-del | -/C | | | intron-variant | Fbxo10 | Mm_Celera | 4:45074375 | AACCCATTTCTCCTG[-/C]CCCCATGAGCCTTTA | 269529 |
| rs260713305 | snp | G/T | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45054801 | ACACAGGAACCTGAA[G/T]ACTTTAACGGATGCC | 269529 |
| rs260725121 | snp | C/T | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45054351 | GGCTGGACCCTCCCT[C/T]GTCGATCACGAATTA | 269529 |
| rs260790708 | snp | G/T | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45053547 | AACAAGGTAGCACAA[G/T]ACAACTCAAACATAT | 269529 |
| rs260831572 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45079598 | TGCAAGTCTCCTACC[A/G]CTACACAAACAAATG | 269529 |
| rs260861470 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45078915 | CAGACCTAGACGGAC[A/G]GACGGACTCTGCACG | 269529 |
| rs261024314 | snp | C/T | | | intron-variant, upstream-variant-2KB | Fbxo10, Gm30939 | Mm_Celera | 4:45045170 | CCCTCAGCCTCAGCC[C/T]TGCCCTCTGACCTCA | 269529 |
| rs261128726 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45069899 | GAAAGGCAATAAAGA[C/T]GAAGTTCCTATCCTC | 269529 |
| rs261196236 | snp | G/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45077319 | GCTTCAGGATATACT[G/T]ACGTAAAGATTTTCT | 269529 |
| rs261208043 | in-del | -/CATGAGG | | | intron-variant | Fbxo10 | Mm_Celera | 4:45067782 | CCGCTGTTCTGAAGA[-/CATGAGG]CGATACCTCTGGAAA | 269529 |
| rs261309804 | snp | G/T | | | intron-variant, nc-transcript-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45060000 | GACCAGGACAGGTTA[G/T]GGCCCAGCCACAGGC | 269529 |
| rs261434316 | snp | A/G | | | upstream-variant-2KB | Fbxo10 | Mm_Celera | 4:45085273 | CTGATTTATGTGCAC[A/G]CAGGGGGCCCTGGAA | 269529 |
| rs261437663 | snp | C/T | | | utr-variant-3-prime | Fbxo10 | Mm_Celera | 4:45035624 | CATGTACTGTCTGAG[C/T]CTCCGCGGCTCTTCA | 269529 |
| rs261438857 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45062990 | GAGTTCTGGGATGGA[A/G]AGATGGCTCAGACAT | 269529 |
| rs261526786 | snp | A/C | | | intron-variant, nc-transcript-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45060731 | CCATCGTGGATTTAG[A/C]ACTCGAATACGTGAA | 269529 |
| rs261823551 | snp | A/G/T | | | intron-variant, upstream-variant-2KB | Fbxo10, Gm30939 | Mm_Celera | 4:45045257 | CTTCTGCCTCATCCC[A/G/T]GTGAATGGCAAGGCA | 269529 |
| rs261840274 | snp | A/C | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45059456 | ACTCATGAAATGCTA[A/C]GTGAGAATTACTGTC | 269529 |
| rs261846722 | snp | A/T | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45052928 | CTAACATTGAGACAC[A/T]CACCCCAGCCTTATC | 269529 |
| rs261918349 | snp | A/G | | | utr-variant-3-prime | Fbxo10 | Mm_Celera | 4:45034903 | AGGGGAGAGTCACGT[A/G]GAGACGGCAGTGTCT | 269529 |
| rs261923089 | snp | A/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45077459 | GGAAAATCTCTGCCA[A/T]ATACATCTGACAGAG | 269529 |
| rs261972922 | snp | C/T | | | upstream-variant-2KB | Fbxo10 | Mm_Celera | 4:45086482 | CCACAGGTAACCCAA[C/T]AGCTATCATCCTTTT | 269529 |
| rs262051620 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45084265 | ATTCTCTCAGACACT[C/T]GCAAAGCCCTGGGGC | 269529 |
| rs262104368 | in-del | -/G | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45053453 | ACTGTGACTCTTTCT[-/G]GGTGTAGTCAGTAGT | 269529 |
| rs262141085 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45065934 | AACACTCTCCTTTTG[A/G]CATAAGCTGACCATA | 269529 |
| rs262199810 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45075546 | CCATCTTGCTAGCCT[A/G]GGATTTTTTTTCTTT | 269529 |
| rs262229917 | in-del | -/GA | | | intron-variant | Fbxo10 | Mm_Celera | 4:45067374 | AAGAAAGGAAGAAAG[-/GA]AGACAGAGGAAGAGA | 269529 |
| rs262307209 | snp | A/C | | | intron-variant | Fbxo10 | Mm_Celera | 4:45076220 | ATGGGTGTGGGGCAG[A/C]CCACTGCAGCAGGCA | 269529 |
| rs262307798 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45082025 | GCTGACAGGAGAATC[C/T]GTAGCTCGTTCACAC | 269529 |
| rs262336841 | snp | C/T | | | upstream-variant-2KB | Fbxo10 | Mm_Celera | 4:45085409 | CTCCAACCCTGTATC[C/T]CACCATCCCGAGGTC | 269529 |
| rs262379177 | snp | C/T | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45050953 | TGCCTGCATGGCAAG[C/T]ATGCGTGTTATCAAC | 269529 |
| rs262399218 | snp | A/G | | | intron-variant, nc-transcript-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45059298 | ATGTCACTCAGAGGA[A/G]CTGAGAAGTAGGTCC | 269529 |
| rs262431645 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45083658 | CCTGACTCATTCGGT[A/G]GGAACAACAGGTTCA | 269529 |
| rs262467715 | in-del | -/AGGCG | | | intron-variant | Fbxo10 | Mm_Celera | 4:45082052 | CACAAAGCCCAGGAC[-/AGGCG]AGGCGACTTGGAGAA | 269529 |
| rs262488689 | snp | A/G | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45056687 | CATAAATACCCACAT[A/G]CTTTACTAAGTAGCC | 269529 |
| rs262489041 | snp | C/T | | | intron-variant, nc-transcript-variant | Fbxo10, Gm30939 | GRCm38.p3 | 4:45060109 | AGACAGGGGATGCTG[C/T]CGGTGGTTGGGGGTA | 269529 |
| rs262633998 | snp | A/G | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45056454 | TTGAATTTGTGATAT[A/G]CCTTAACCTCCTGAG | 269529 |
| rs262677456 | in-del | -/A | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45052930 | AACATTGAGACACAC[-/A]CCCCAGCCTTATCTG | 269529 |
| rs262731272 | snp | C/G/T | | | intron-variant | Fbxo10, Gm30939 | GRCm38.p3 | 4:45050184 | TGCCAGCACCCCTCA[C/G/T]GTCTCTCTGGCAACA | 269529 |
| rs262736433 | snp | C/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45067566 | AGGAAGCCTATGGGT[C/G]GTGACCCCTTTGAGG | 269529 |
| rs262787540 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45074711 | ATCTTTGTCACAGCA[C/T]TGGGGATTGAACCCA | 269529 |
| rs262898187 | in-del | -/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45038594 | TTACTGTTTCTCAGA[-/G]GCCATTCACACAATG | 269529 |
| rs262936163 | snp | C/G | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45049948 | CTCTCTACCCATGTG[C/G]CCTGGCTGCACTTGT | 269529 |
| rs262958170 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45079848 | AAAGAGAGACTATGT[C/T]TGCAAACGTCCTTGG | 269529 |
| rs263069274 | in-del | -/AAAAC | | | intron-variant | Fbxo10 | Mm_Celera | 4:45080291 | TAAAAACCATCATTA[-/AAAAC]AAAACAAAACAAAAC | 269529 |
| rs263111476 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45041264 | AGTGGGGTGGTGGTC[A/G]TGCCCCAAAGATCCA | 269529 |
| rs263151285 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45042899 | CCAGATGAAGACTCA[C/T]AACTGTCTGTGCAGC | 269529 |
| rs263205997 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45080740 | CACATGGATGCTTTG[C/T]CAAGAATCACCCGAA | 269529 |
| rs263220084 | snp | C/G | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45048065 | GTAAAGCAGCCTGCA[C/G]CAGCTGGTTCTCGCC | 269529 |
| rs263275675 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45038633 | AGAGAATTAGTAACA[C/T]TGCCACCCATCGGAT | 269529 |
| rs263304303 | snp | A/C/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45073051 | TGGAAAAGTCAATAA[A/C/G]TAGACACAAGGACCT | 269529 |
| rs263322621 | snp | A/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45080997 | ACGAGCGGTGACCCC[A/T]GAAGGATAGAAGAAG | 269529 |
| rs263355658 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45072650 | CCTTAAATGTTGCAG[C/T]TGGACACACCATGGT | 269529 |
| rs263371889 | in-del | -/C | | | intron-variant, nc-transcript-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45061607 | TTCTGCCTCCCCCAT[-/C]CCCACATGCTGCTCA | 269529 |
| rs263433217 | snp | A/C | | | intron-variant | Fbxo10 | Mm_Celera | 4:45070935 | TGACAGGCACACCTG[A/C]GATCCCATCAGGGAA | 269529 |
| rs263449218 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45078776 | CTCATGTTCACTGCT[A/G]CCCTGCTGACAACAC | 269529 |
| rs263480672 | snp | A/G | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45047886 | ACATGATTGGTGCCT[A/G]TCACAGTCTGCCCAT | 269529 |
| rs263574773 | snp | A/C | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45054208 | GAAAGTCAAACAGGA[A/C]AGGAGCCTGGAGACA | 269529 |
| rs263588238 | snp | A/G | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45053519 | GGAATTTGTGTGTTA[A/G]GAAGTCTCTTCAAAC | 269529 |
| rs263671626 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45040136 | TGACTGGGGTGGTCC[A/G]TGGCACTAGAGGACT | 269529 |
| rs263698645 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45066399 | GCCCATAAATTGCTT[A/G]TAAGAAATATGCAAA | 269529 |
| rs263790103 | snp | G/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45064399 | AGAATGTGGTAGTTT[G/T]AATGAGATTGGGTCC | 269529 |
| rs263883562 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45064082 | GTGGTATTGTTGCAG[A/G]CAGTAAAGCAGGAAG | 269529 |
| rs263900143 | snp | A/C | | | intron-variant | Fbxo10 | Mm_Celera | 4:45072013 | AGCTGCTTTGAGTCG[A/C]TGCACAAAAGGTTCT | 269529 |
| rs263958152 | snp | A/C | | | intron-variant | Fbxo10 | Mm_Celera | 4:45039933 | ATGATTTTTGTTGGT[A/C]TCTGTGACTGTTTCA | 269529 |
| rs264022777 | in-del | -/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45075550 | CTTGCTAGCCTAGGA[-/T]TTTTTTTCTTTATTC | 269529 |
| rs264024211 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45036309 | GCCTTCCTCCCACCA[C/T]CGCCACCACAGCAGC | 269529 |
| rs264058796 | in-del | -/CAA | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45053490 | AGGCTACTAATACTC[-/CAA]CAAGAGTGTCAGGAA | 269529 |
| rs264073333 | snp | A/T | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45045994 | GGGGGGAGTTAGGGC[A/T]GGCTTCCCTCAGGAA | 269529 |
| rs264125236 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45070703 | GCCATGTCTAAGACC[A/G]TGTGGTAGGCCTCAC | 269529 |
| rs264214398 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45037462 | ATACCTAGGAAACAG[A/G]CCTATCTCTGAGTGT | 269529 |
| rs264237753 | snp | A/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45076085 | CTCCTTGTTGTCTTT[A/T]TGCAAACAATTATTT | 269529 |
| rs264295662 | snp | C/T | | | utr-variant-3-prime | Fbxo10 | Mm_Celera | 4:45035780 | TAGTCCCCAGGCAGC[C/T]GAGGGTTTCAGGTGT | 269529 |
| rs264313928 | snp | C/T | | | intron-variant, upstream-variant-2KB | Fbxo10, Gm30939 | Mm_Celera | 4:45045345 | CTCTGCAACCCTATC[C/T]CATATATTCCCCCCT | 269529 |
| rs264317905 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | Fbxo10, Polr1e | Mm_Celera | 4:45034779 | GGCAGGACAGGGTAT[A/G]TAAGGACCCAGAGTT | 269529 |
| rs264386988 | snp | A/C | | | intron-variant | Fbxo10 | Mm_Celera | 4:45070257 | GCCTCCAAAGGACAA[A/C]GTGCACATAACATCC | 269529 |
| rs264424619 | in-del | -/ACAT | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45052208 | CCTCACACACACACC[-/ACAT]ACATACATACATACA | 269529 |
| rs264445900 | snp | G/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45068750 | AGGACCTCTGAAGGA[G/T]CAGTCAGTGCTCTTA | 269529 |
| rs264484715 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45075638 | ATTTTAAATGAGAAC[C/T]CCCCCCCCCAGACTC | 269529 |
| rs264558544 | snp | A/G | | | upstream-variant-2KB | Fbxo10 | Mm_Celera | 4:45085957 | AAGCCTGAGTTCCTG[A/G]ATTTGTGCTATCAAA | 269529 |
| rs264577024 | snp | A/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45063515 | AATAAATATTTTTTT[A/T]AAAAAACTATTTTCT | 269529 |
| rs264682318 | snp | A/G | | | intron-variant, nc-transcript-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45060224 | CCGTCTGTAGCATGA[A/G]GCTTGCTAGTTTATA | 269529 |
| rs264692652 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45068852 | GTTTCTCTGTGTAGC[C/T]CTGGCTATCCTGGAC | 269529 |
| rs264721459 | snp | C/T | | | utr-variant-3-prime | Fbxo10 | Mm_Celera | 4:45035899 | TGGGCCTGAGGCAGG[C/T]CTTCTTGCTTACAGG | 269529 |
| rs264733289 | snp | A/G | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45053469 | GGTGTAGTCAGTAGT[A/G]TGCAAAGGCTACTAA | 269529 |
| rs264910135 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45040507 | CATTACCCAGGGACC[A/G]CCTCCGTAGCCCACT | 269529 |
| rs264944741 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45066920 | GCTTTCTCAACGTTA[A/G]GATAGCAGCCTGTTA | 269529 |
| rs265062037 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45075745 | TTGAGGTTTCAAAAG[C/T]CCATACCAGACAGAA | 269529 |
| rs265071853 | snp | C/T | | | upstream-variant-2KB | Fbxo10 | Mm_Celera | 4:45084781 | GGGCCTGGAAGCGGG[C/T]GGATCCTTCCCATCA | 269529 |
| rs265107982 | snp | A/C | | | intron-variant | Fbxo10 | Mm_Celera | 4:45082243 | CCCCCACCCCCCCCC[A/C]CAAAAAAAGAGAGGC | 269529 |
| rs265131763 | snp | C/T | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45051265 | TTGTTTTTAGATTCA[C/T]CTGTTATATAGGGAA | 269529 |
| rs265154588 | snp | C/T | | | intron-variant, nc-transcript-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45059560 | TCAGCAGTACAGTGC[C/T]TGCCTAGCACGCAGG | 269529 |
| rs265185672 | snp | C/T | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45057207 | ATGCCTATTAGCTTA[C/T]TGAGCACTTCTGCTA | 269529 |
| rs265215545 | in-del | -/G | | | upstream-variant-2KB | Fbxo10 | Mm_Celera | 4:45086086 | GTCCAAAGGTGCCAC[-/G]GGGGGCGGGGGGATT | 269529 |
| rs265240289 | in-del | -/C | | | intron-variant | Fbxo10 | Mm_Celera | 4:45077434 | CAGCCTACAGAATAT[-/C]GGGGGTGGGGGAAAA | 269529 |
| rs265284243 | snp | A/G | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45049494 | CTGTAAGTAGGTGAG[A/G]CCGGCTGGCCAGCGA | 269529 |
| rs265332924 | in-del | -/AA | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45047119 | TTTGCTTTTTTTTTT[-/AA]AAAAAAAAAAAAAAC | 269529 |
| rs265339138 | snp | C/T | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45055444 | AGCTCCACACTCCCA[C/T]CTACATAAAACCCTG | 269529 |
| rs265375378 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45080519 | ATACCAAACACGCTT[C/T]GCTTTCAGTAGAGCA | 269529 |
| rs265385274 | in-del | -/A | | | intron-variant | Fbxo10 | Mm_Celera | 4:45079306 | GATTCCAGCACATAG[-/A]AGCTTGAGGCAGGAG | 269529 |
| rs265416533 | snp | C/T | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45050276 | TTACCCCTTTGCGCC[C/T]CATGTCTTCACTTGG | 269529 |
| rs265531118 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45039698 | GTATGGGGCTAGAAG[C/T]GTTAGCTCAGCGGTT | 269529 |
| rs265549371 | in-del | -/CAAT | | | utr-variant-3-prime | Fbxo10 | Mm_Celera | 4:45034869 | GGGTGGTGAGCAACA[-/CAAT]CAATCACTTGGAGCC | 269529 |
| rs265554588 | snp | A/T | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45048644 | TGAGTACTGCCTCAC[A/T]GCTGTACCAAGACGG | 269529 |
| rs265589581 | snp | C/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45073383 | ATGAAGATGAAGCTG[C/G]TCCTGCAGTTACTTT | 269529 |
| rs265593537 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45081606 | GGATCCGACTAACTG[A/G]CAGGGATCTGGTCCC | 269529 |
| rs265619330 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45071860 | GCACAGGCGTAAGGC[A/G]GGTGTGAGGACAAGC | 269529 |
| rs265642344 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45079568 | ATCTGAGGTCCATCC[C/T]GGGAACCCACCTTAT | 269529 |
| rs265645033 | in-del | -/CATGCGTGCA | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45048769 | GTGTGTGTGTGTGTG[-/CATGCGTGCA]TGCGTGTGTGTGTGT | 269529 |
| rs265742412 | in-del | -/TTTG | | | intron-variant | Fbxo10 | Mm_Celera | 4:45068618 | TTTTGTTGTTGTTTC[-/TTTG]TTTAAGATGTATTTA | 269529 |
| rs265743785 | snp | C/T | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45053277 | CGAGAGAGCTCAGTC[C/T]TCAGATGCACATATA | 269529 |
| rs265793694 | snp | A/G | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45046894 | CACCAAGGCGCATGC[A/G]TCATGGGGCAAGTCT | 269529 |
| rs265827213 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45064706 | CAGCTGCCTTATTAC[A/G]GTGCCTTACCACAGC | 269529 |
| rs265835441 | in-del | -/TTT | | | intron-variant | Fbxo10 | Mm_Celera | 4:45038923 | TCGGTTGTGGAACTC[-/TTT]TTTTTTTTTTTTTTA | 269529 |
| rs265850341 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45072426 | AGCTTCCCCACCCAC[A/G]CCGTGAAGCATACAG | 269529 |
| rs265856035 | in-del | -/A | | | intron-variant | Fbxo10 | Mm_Celera | 4:45065354 | TATCAGCTAATTACT[-/A]TTGTTTCCCTAAGAA | 269529 |
| rs265939073 | in-del | -/TCTTTT | | | intron-variant | Fbxo10, Gm30939 | Mm_Celera | 4:45058128 | CGCTCTGGGTCTCTA[-/TCTTTT]TTTTTTTTTCTGGGA | 269529 |
| rs265977147 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45062759 | CTGGGTGAGTCTGTG[C/T]TGCAGTTCCAGAGAT | 269529 |
| rs266015637 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45038071 | AGTGCAGTCCTAATT[A/G]AAATAGTTTAGCTCA | 269529 |
| rs266042653 | snp | C/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45077008 | TCCTGCAGAAGCCAT[C/T]AACTACCAATGGCTC | 269529 |
| rs266079695 | snp | C/T | | | utr-variant-3-prime | Fbxo10 | GRCm38.p3 | 4:45035169 | GAATGTGTGTGTTCA[C/T]ACAGAATCCTGTGAC | 269529 |
| rs266116986 | in-del | -/T | | | intron-variant | Fbxo10 | Mm_Celera | 4:45072971 | TTTTGTTTTGTTTTG[-/T]TTTTGCTTGTTTTTG | 269529 |
| rs266128102 | snp | A/G | | | intron-variant | Fbxo10 | Mm_Celera | 4:45069729 | CCTGGGGCTGAAAGC[A/G]AGTCCCCAAACCTCT | 269529 |
| rs266183301 | snp | A/C | | | intron-variant | Fbxo10 | Mm_Celera | 4:45075066 | CTTTAGCCTCTCACG[A/C]AGCTGAGGTTACTGG | 269529 |
| rs266213999 | snp | A/G | | | intron-variant, upstream-variant-2KB | Fbxo10, Gm30939 | Mm_Celera | 4:45044708 | CTGCCCCAGGAAGGT[A/G]TCCTCACCATAGATG | 269529 |
| rs578401226 | snp | A/G | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45079320 | GAAGCTTGAGGCAGG[A/G]GGACTGCTGTGTGCT | 269529 |
| rs578415030 | snp | A/G | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45039159 | GTGGAACTCTTTGCC[A/G]GAGAAAAAATATTGT | 269529 |
| rs578420466 | snp | G/T | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45072954 | TTGTTTGTTTGTTTT[G/T]TTTTTGTTTTGTTTT | 269529 |
| rs578448266 | snp | A/C | | | intron-variant | Fbxo10, Gm30939 | GRCm38.p3 | 4:45052083 | CACACACACACACAT[A/C]CATATACACACATTC | 269529 |
| rs578591803 | snp | C/T | | | intron-variant | Fbxo10, Gm30939 | GRCm38.p3 | 4:45053478 | AGTAGTATGCAAAGG[C/T]TACTAATACTCCAAC | 269529 |
| rs578593124 | snp | C/G | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45071214 | GACTTATTTTTCTCT[C/G]GATTTGTGTGTGTGT | 269529 |
| rs578822420 | snp | A/G | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45042758 | GTAATGAGATCTGAC[A/G]CCCTCTTCTGGCACA | 269529 |
| rs578823977 | snp | G/T | | | upstream-variant-2KB | Fbxo10 | GRCm38.p3 | 4:45084686 | AGGGCGGGGCGAGCG[G/T]GGCTCGGCGATGGAG | 269529 |
| rs578866005 | snp | C/T | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45077620 | GGGCAGCAAAATGGC[C/T]ATTATATCTTACAAC | 269529 |
| rs579024792 | snp | A/G | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45064224 | AGGTAATTTGCTTTT[A/G]CAATGGATTACAATT | 269529 |
| rs579200303 | snp | A/G | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45042505 | GACCAGGCTGGCCTC[A/G]AACTCAGAAATCCAC | 269529 |
| rs579206707 | snp | A/G | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45076906 | AGGCATGGGTGTGGG[A/G]CAGCCCACTGCAGCA | 269529 |
| rs579250180 | snp | A/G | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45066315 | TTTACAAGACTGCAC[A/G]AGCTGCTTCTCACTT | 269529 |
| rs579413542 | snp | A/G | | | intron-variant | Fbxo10, Gm30939 | GRCm38.p3 | 4:45047300 | ACAGTGATATGGAAC[A/G]ACCTGGGACCACACA | 269529 |
| rs579416856 | snp | C/T | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45080041 | CATGTGACAAAGAGA[C/T]GGCCATCCACAGGTC | 269529 |
| rs579430908 | snp | C/T | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45037714 | TGGTGTGCCACATGC[C/T]CAAACTGTGAGGTGA | 269529 |
| rs579434677 | snp | C/T | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45071218 | TATTTTTCTCTGGAT[C/T]TGTGTGTGTGTGTGT | 269529 |
| rs579480405 | snp | A/C | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45078440 | TGAGTTCAAGGCCAG[A/C]CTGGTCTACAGAGCG | 269529 |
| rs579589564 | snp | C/T | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45081276 | AGGGTTCTGACTGAC[C/T]GGCAGGGATCTGACT | 269529 |
| rs579592984 | snp | G/T | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45039856 | TGTTCTGTTTGTGAT[G/T]CACTGAATACATAGT | 269529 |
| rs579626558 | snp | A/G | | | intron-variant | Fbxo10, Gm30939 | GRCm38.p3 | 4:45055535 | TTTCCCTTATTGTCA[A/G]AATCCCTGAAAATCA | 269529 |
| rs579771429 | snp | A/T | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45073401 | CTGCAGTTACTTTTT[A/T]TAAAAAGATTATTAT | 269529 |
| rs579794269 | snp | A/G | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45039786 | TGGACGACAGCCCCC[A/G]CTGAATACACCTTTT | 269529 |
| rs579808576 | snp | C/T | | | intron-variant | Fbxo10, Gm30939 | GRCm38.p3 | 4:45056076 | TCCTGCCTTTATCCC[C/T]CCCACTATGGCTGCT | 269529 |
| rs579816816 | snp | C/G | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45081482 | CGACTGACTGGCAGG[C/G]ATCAGACTGACTGGC | 269529 |
| rs579972623 | snp | C/T | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45081192 | TGACTGGCAGGGATC[C/T]GACTGACTGGCAGGG | 269529 |
| rs580202517 | snp | A/G | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45067359 | CAGGAAGGAAGGAAG[A/G]AAGAAAGGAAGAAAG | 269529 |
| rs580282686 | snp | A/C | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45077750 | CACACACACACAAAG[A/C]AAACAATGGCGACTA | 269529 |
| rs580309784 | snp | G/T | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45078170 | GACTGTCCTCACGTA[G/T]TCAAAGGCCTGAGAT | 269529 |
| rs580386101 | snp | A/G | | | intron-variant, nc-transcript-variant | Fbxo10, Gm30939 | GRCm38.p3 | 4:45045665 | CTGTATCGCTACACG[A/G]CCAGTTCCGAGACAA | 269529 |
| rs580485503 | snp | G/T | | | intron-variant | Fbxo10, Gm30939 | GRCm38.p3 | 4:45054361 | TCCCTTGTCGATCAC[G/T]AATTAAGAAAATGCC | 269529 |
| rs580647056 | snp | A/G | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45039823 | TGTTATATTTTGATG[A/G]TTTATAGTGATGTTA | 269529 |
| rs580677881 | snp | C/T | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45070201 | TCTGCAGACCACGTG[C/T]TCTGCCAGCCCGACA | 269529 |
| rs580747600 | snp | A/G | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45083214 | CTCACGTGAGCACAC[A/G]CGCGCGCGCACACAC | 269529 |
| rs580938208 | snp | A/G | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45076216 | AGGCATGGGTGTGGG[A/G]CAGCCCACTGCAGCA | 269529 |
| rs580991012 | snp | C/G | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45042403 | TTTCTGTTTTGTTTT[C/G]TTTTGTTTTTTCTTT | 269529 |
| rs581082126 | snp | A/G | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45063215 | AGGAGGTGTGGCCTT[A/G]TTAGAGTAGGTGTGT | 269529 |
| rs581088327 | snp | C/T | | | upstream-variant-2KB | Fbxo10 | GRCm38.p3 | 4:45085691 | GCAAGTGCTACCCCC[C/T]TGTACCCCCTGTACC | 269529 |
| rs581198172 | snp | C/T | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45081562 | TGACTGGCAGGGATC[C/T]GACTGACTGGCAGGG | 269529 |
| rs581220242 | snp | C/G | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45042490 | GGAACGCACTTTGTA[C/G]ACCAGGCTGGCCTCA | 269529 |
| rs581224354 | snp | C/T | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45076384 | GCCCACTGCAGCAGG[C/T]ATGGGTGTGGGGCAG | 269529 |
| rs581398176 | snp | G/T | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45071215 | ACTTATTTTTCTCTG[G/T]ATTTGTGTGTGTGTG | 269529 |
| rs581502875 | snp | A/G | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45078897 | ATACTAAGTGAGGCC[A/G]CACAGACCTAGACGG | 269529 |
| rs581590894 | snp | C/G/T | | | intron-variant | Fbxo10, Gm30939 | GRCm38.p3 | 4:45052022 | ACACAGACACACACA[C/G/T]ACACACACACCACAT | 269529 |
| rs581654418 | snp | A/G | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45067391 | GACAGAGGAAGAGAG[A/G]AAGGAAGGAAGGAAG | 269529 |
| rs581706756 | snp | G/T | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45072955 | TGTTTGTTTGTTTTG[G/T]TTTTGTTTTGTTTTG | 269529 |
| rs581812166 | snp | A/T | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45039443 | CCTCTGCCTCCCAAG[A/T]GCTGGGATTAAAGGC | 269529 |
| rs581868507 | snp | C/T | | | intron-variant | Fbxo10, Gm30939 | GRCm38.p3 | 4:45052251 | GACACACACAATGTG[C/T]AGTAATAATAATAAA | 269529 |
| rs581876052 | snp | A/G | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45042519 | CAAACTCAGAAATCC[A/G]CCTGCCTCTGCCTCC | 269529 |
| rs582000599 | snp | A/C | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45077429 | AGAGGCAGCCTACAG[A/C]ATATCGGGGGTGGGG | 269529 |
| rs582039945 | snp | A/G | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45067351 | CAGACAGACAGGAAG[A/G]AAGGAAGAAAGAAAG | 269529 |
| rs582172238 | snp | C/T | | | intron-variant, upstream-variant-2KB | Fbxo10, Gm30939 | GRCm38.p3 | 4:45044198 | ACGTCCTAGTTGTGA[C/T]CCTGAGTGAGTGCCT | 269529 |
| rs582258793 | snp | A/G | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45064229 | ATTTGCTTTTACAAT[A/G]GATTACAATTAAGAG | 269529 |
| rs582465352 | snp | A/G | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45078167 | ACCGACTGTCCTCAC[A/G]TAGTCAAAGGCCTGA | 269529 |
| rs582583877 | snp | C/T | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45073652 | AGGCCTGAAGACTTA[C/T]GCCTTTCAAGTTAAA | 269529 |
| rs582677738 | snp | C/T | | | intron-variant | Fbxo10, Gm30939 | GRCm38.p3 | 4:45053984 | GGTTGTGAGCCACCA[C/T]GTGGTTGCTGGGATT | 269529 |
| rs582691717 | snp | C/T | | | intron-variant | Fbxo10, Gm30939 | GRCm38.p3 | 4:45056024 | TCACGTTCCAGAATC[C/T]CACCCTCTGCAGCCC | 269529 |
| rs582805772 | snp | A/C | | | intron-variant | Fbxo10, Gm30939 | GRCm38.p3 | 4:45055230 | TGACCCCTGAACGAC[A/C]ACAGGGGAGTGCCCA | 269529 |
| rs582818072 | snp | A/G | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45037834 | ATACAGGTGAACTCA[A/G]ACGGGGCCTTTCATC | 269529 |
| rs582827638 | snp | A/T | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45071314 | GAGAGAGAGAGAGAG[A/T]GAGTAAATATATGTC | 269529 |
| rs582869229 | snp | C/G | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45075649 | GAACCCCCCCCCCCA[C/G]ACTCATATATTTGCT | 269529 |
| rs582981870 | snp | A/G | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45039869 | ATGCACTGAATACAT[A/G]GTTTCAGAGTTGTAA | 269529 |
| rs583041435 | snp | A/T | | | intron-variant | Fbxo10, Gm30939 | GRCm38.p3 | 4:45046533 | GTGTGTGTGTGTGAG[A/T]GACATGTGCTACAGC | 269529 |
| rs583053264 | snp | A/G | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45081341 | GGCAGGGATCTGACT[A/G]ACTGGCAGGGATCTG | 269529 |
| rs583208044 | snp | A/G | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45078535 | AAGAAAAAAAGAAAA[A/G]AAAAAAAAAGAAAAG | 269529 |
| rs583218859 | snp | A/T | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45078337 | AAAACCACTTTGACA[A/T]TTTGTTTCGACCGGT | 269529 |
| rs583294913 | snp | A/G | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45067434 | AGAGAGAGGAAGAGA[A/G]GAAGGAAGGAAGGAA | 269529 |
| rs583386044 | snp | A/C | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45067360 | AGGAAGGAAGGAAGA[A/C]AGAAAGGAAGAAAGA | 269529 |
| rs583468122 | snp | G/T | | | intron-variant | Fbxo10, Gm30939 | GRCm38.p3 | 4:45048078 | CACCAGCTGGTTCTC[G/T]CCTCCTACCCTGGGA | 269529 |
| rs583490880 | snp | A/G | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45067355 | CAGACAGGAAGGAAG[A/G]AAGAAAGAAAGGAAG | 269529 |
| rs583564146 | snp | C/T | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45039796 | CCCCCGCTGAATACA[C/T]CTTTTTAGAATTGTT | 269529 |
| rs583808913 | snp | A/G | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45082066 | ACAGGCGACTTGGAG[A/G]AGGAACAGCGAGCCG | 269529 |
| rs583908688 | snp | A/C/T | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45081486 | TGACTGGCAGGCATC[A/C/T]GACTGACTGGCAGGG | 269529 |
| rs584073215 | snp | A/G | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45039830 | TTTTGATGATTTATA[A/G]TGATGTTACCTGTTC | 269529 |
| rs584151609 | snp | A/G | | | intron-variant | Fbxo10, Gm30939 | GRCm38.p3 | 4:45052034 | ACAGACACACACACC[A/G]CATACACATACATAT | 269529 |
| rs584182515 | snp | G/T | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45042523 | CTCAGAAATCCACCT[G/T]CCTCTGCCTCCCGAG | 269529 |
| rs584194831 | snp | A/G | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45063333 | CTCAGCTCTGCCTAC[A/G]CCATGTCTGCCTAGA | 269529 |
| rs584269992 | snp | A/G | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45083220 | TGAGCACACGCGCGC[A/G]CGCACACACACACAC | 269529 |
| rs584300509 | snp | G/T | | | intron-variant, nc-transcript-variant | Fbxo10, Gm30939 | GRCm38.p3 | 4:45060801 | CAGGCCGTCTCCCGA[G/T]GAGCTTCAGCTGTGC | 269529 |
| rs584342232 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | Fbxo10, Polr1e | GRCm38.p3 | 4:45034654 | CTGTCACACTCAGTA[C/T]AGTCTAGTGAAGCCC | 269529 |
| rs584373246 | snp | C/T | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45079310 | CCAGCACATAGAAGC[C/T]TGAGGCAGGAGGACT | 269529 |
| rs584539131 | snp | A/C/G | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45071216 | CTTATTTTTCTCTGG[A/C/G]TTTGTGTGTGTGTGT | 269529 |
| rs584600308 | snp | C/T | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45071176 | CTAAGTCTTCGGTGC[C/T]ATCAGATATGGCATT | 269529 |
| rs584676942 | snp | C/T | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45079735 | ATGGTGGCTCACAAC[C/T]AACTGTAATGGGATC | 269529 |
| rs584709584 | snp | C/T | | | intron-variant | Fbxo10, Gm30939 | GRCm38.p3 | 4:45053166 | GCAGGAAACAACCAT[C/T]AGTTAAGAAAAAAAA | 269529 |
| rs584899625 | snp | C/T | | | intron-variant | Fbxo10, Gm30939 | GRCm38.p3 | 4:45051994 | ACACACACACACACA[C/T]ACACATACACACACA | 269529 |
| rs584906269 | snp | A/T | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45078742 | AGGCCCCCCAGAGCC[A/T]ACTGGAGACATCTGC | 269529 |
| rs584959065 | snp | A/G | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45076246 | AGGCATGGGTGTGGG[A/G]CAGCCCACTGCAGCA | 269529 |
| rs585071690 | snp | C/T | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45042431 | TTTCTTTCTTTCTTT[C/T]TTTTTTTTGAGACAG | 269529 |
| rs585299922 | snp | A/C | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45067356 | AGACAGGAAGGAAGG[A/C]AGAAAGAAAGGAAGA | 269529 |
| rs585311159 | snp | C/T | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45042504 | AGACCAGGCTGGCCT[C/T]AAACTCAGAAATCCA | 269529 |
| rs585317338 | snp | C/T | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45076864 | GCCCACTGCAGCAGG[C/T]ATGGGTGTGGGGCAG | 269529 |
| rs585458914 | snp | A/G | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45039777 | CACTAGCCTTGGACG[A/G]CAGCCCCCGCTGAAT | 269529 |
| rs585551877 | snp | A/C | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45067352 | AGACAGACAGGAAGG[A/C]AGGAAGAAAGAAAGG | 269529 |
| rs585640722 | snp | C/T | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45077709 | CTTCTGACCTCCACA[C/T]GTGTGTCTACACACA | 269529 |
| rs585694723 | snp | A/G | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45073653 | GGCCTGAAGACTTAC[A/G]CCTTTCAAGTTAAAA | 269529 |
| rs585790657 | snp | G/T | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45072991 | GCTTGTTTTTGGTTT[G/T]GTTTTGTTTTGAGGC | 269529 |
| rs585840149 | snp | C/T | | | intron-variant | Fbxo10, Gm30939 | GRCm38.p3 | 4:45055504 | ATGGCGACTTCCAAA[C/T]GCATGTTATTTTTTT | 269529 |
| rs585961816 | snp | C/T | | | intron-variant | Fbxo10, Gm30939 | GRCm38.p3 | 4:45056068 | CCAACTCCTCCTGCC[C/T]TTATCCCCCCCACTA | 269529 |
| rs585965399 | snp | C/T | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45081467 | TGACTGGCAGGGATC[C/T]GACTGACTGGCAGGC | 269529 |
| rs586075846 | snp | A/G | | | intron-variant, upstream-variant-2KB | Fbxo10, Gm30939 | GRCm38.p3 | 4:45044617 | AGGCCTAGAGGAGAT[A/G]AGACCTTGTCAGAAC | 269529 |
| rs586076044 | snp | A/G | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45080018 | GAGATAGATGCACAC[A/G]CACAAGGCATGTGAC | 269529 |
| rs586083064 | snp | G/T | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45039815 | TTTAGAATTGTTATA[G/T]TTTGATGATTTATAG | 269529 |
| rs586122385 | snp | A/G | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45068691 | GCACCAGAAGTGGGC[A/G]TCAGATCTTGTGAGC | 269529 |
| rs586192090 | snp | A/T | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45081265 | GACTGACTGGCAGGG[A/T]TCTGACTGACCGGCA | 269529 |
| rs586230765 | snp | C/T | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45078417 | GGAGGCAGAGGCAGG[C/T]GGATTTCTGAGTTCA | 269529 |
| rs586326152 | snp | A/T | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45038980 | ATTTATTTATTTATT[A/T]ATTATATGTAAGTAC | 269529 |
| rs586336175 | snp | A/C | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45072918 | AAACATGAAAGGCTA[A/C]GGAAGGGAGTGTTTG | 269529 |
| rs586378504 | snp | A/G | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45065164 | AAAAAAAAAAAAAAA[A/G]GTGAGGACAGGTGCA | 269529 |
| rs586419986 | snp | C/T | | | intron-variant, nc-transcript-variant | Fbxo10, Gm30939 | GRCm38.p3 | 4:45045663 | TCCTGTATCGCTACA[C/T]GACCAGTTCCGAGAC | 269529 |
| rs586598617 | snp | C/T | | | intron-variant | Fbxo10, Gm30939 | GRCm38.p3 | 4:45047095 | TCCTCTCAGGATGGC[C/T]GTTTTTGTTTTTGCT | 269529 |
| rs586620650 | snp | C/G | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45039911 | TTTTTGTGCTTTACT[C/G]TGCCAAATGATTTTT | 269529 |
| rs586801524 | snp | C/T | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45081505 | TGACTGGCAGGGATC[C/T]GACTGACTGGCAGGG | 269529 |
| rs586984717 | snp | A/G | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45078540 | AAAAAGAAAAAAAAA[A/G]AAAAGAAAAGAAAAC | 269529 |
| rs587019396 | snp | C/T | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45075787 | CTCCCTCCCCCCCAC[C/T]CCCTCTTGTCTGTCT | 269529 |
| rs587186694 | snp | C/G/T | | | intron-variant | Fbxo10, Gm30939 | GRCm38.p3 | 4:45052012 | ACATACACACACACA[C/G/T]ACACACACAGACACA | 269529 |
| rs587334502 | snp | C/T | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45039852 | TACCTGTTCTGTTTG[C/T]GATGCACTGAATACA | 269529 |
| rs587357456 | snp | A/G | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45042440 | TTCTTTTTTTTTTTT[A/G]AGACAGGGTTTCTCT | 269529 |
| rs587363511 | snp | A/C | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45076310 | ATGGGTGTGGGACAG[A/C]CCACTGCAGCAGGCA | 269529 |
| rs587384815 | snp | A/C | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45082238 | TCCCACCCCCACCCC[A/C]CCCCCCAAAAAAAGA | 269529 |
| rs587540874 | snp | A/G | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45067388 | AGAGACAGAGGAAGA[A/G]AGAAAGGAAGGAAGG | 269529 |
| rs587579173 | snp | A/G | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45078891 | CTATAGATACTAAGT[A/G]AGGCCGCACAGACCT | 269529 |
| rs864297719 | snp | A/C/G | | | intron-variant | Fbxo10 | GRCm38.p3 | 4:45067364 | AGGAAGGAAGAAAGA[A/C/G]AGGAAGAAAGAGACA | 269529 |