SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs4231997 | snp | A/G | 0.21875 | 0.248039 | downstream-variant-500B | Fbxo15 | GRCm38.p3 | 18:84981754 | AAATGCAAGAATCTC[A/G]GTGATTTAGGCTGGG | 50764 |
rs4231998 | snp | A/G | 0.21875 | 0.248039 | downstream-variant-500B | Fbxo15 | GRCm38.p3 | 18:84981640 | TCTTGGTCTCTCTGT[A/G]TTGTTATTGGGGAGT | 50764 |
rs4231999 | snp | C/T | 0.21875 | 0.248039 | downstream-variant-500B | Fbxo15 | GRCm38.p3 | 18:84981635 | GTCTCTCTGTGTTGT[C/T]ATTGGGGAGTTAGCT | 50764 |
rs4232000 | snp | C/T | 0.483892 | 0.0882862 | downstream-variant-500B | Fbxo15 | GRCm38.p3 | 18:84981549 | TCACTGAGGCATGCT[C/T]TATTAAAAATGTCAA | 50764 |
rs4232001 | snp | A/T | 0.21875 | 0.248039 | downstream-variant-500B | Fbxo15 | Mm_Celera | 18:84981544 | GAGGCATGCTTTATT[A/T]AAAATGTCAACTTCT | 50764 |
rs4232002 | snp | A/G | 0.21875 | 0.248039 | downstream-variant-500B | Fbxo15 | GRCm38.p3 | 18:84981519 | ACTTCTAAACACTGT[A/G]GTCACAAACCATAAT | 50764 |
rs4232003 | snp | A/T | 0.21875 | 0.248039 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | Fbxo15 | Mm_Celera | 18:84981404 | AACAGCTTACTAATA[A/T]CAAGACTCCCTACTG | 50764 |
rs6278094 | snp | A/T | 0.32 | 0.24 | intron-variant | Fbxo15 | Mm_Celera | 18:84959702 | TTACATATGGATACC[A/T]TAAGCTACACNCCTA | 50764 |
rs6278116 | snp | G/T | 0.32 | 0.24 | intron-variant | Fbxo15 | Mm_Celera | 18:84959713 | TACCNTAAGCTACAC[G/T]CCTAGACTACAGGAA | 50764 |
rs6279692 | snp | A/G | 0.391111 | 0.206368 | missense, nc-transcript-variant | Fbxo15 | Mm_Celera | 18:84960089 | CATTCGAATCTTTCC[A/G]TAAATGACAACTCTG | 50764 |
rs13464065 | snp | C/T | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | Fbxo15, Timm21 | Mm_Celera | 18:84951414 | AAGTGGTACCTAACA[C/T]CTCTTATAGATTATT | 50764 |
rs29540865 | snp | C/T | 0.401235 | 0.199068 | intron-variant, upstream-variant-2KB | Fbxo15, Timm21 | Mm_Celera | 18:84952713 | ACCTTTCCGGAGCAC[C/T]AAGCCAAGTTGTTTT | 50764 |
rs29543967 | snp | C/T | 0.304688 | 0.243945 | intron-variant | Fbxo15 | Mm_Celera | 18:84946461 | ACTTAAAATGTGGTA[C/T]CAGGAAGACAAGCTC | 50764 |
rs29547557 | snp | A/G | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Fbxo15 | Mm_Celera | 18:84954132 | ACAAAAAAATGCCAC[A/G]AAGTAGCCATGCCAT | 50764 |
rs29555844 | snp | C/T | 0.429688 | 0.173817 | intron-variant | Fbxo15 | Mm_Celera | 18:84978026 | CTCCATGGAAGCATT[C/T]CCTGTACCCTCCATT | 50764 |
rs29564292 | snp | G/T | 0.49827 | 0.0293608 | intron-variant | Fbxo15 | Mm_Celera | 18:84958264 | TCATTTTTCTCCCCC[G/T]GTCTCAGAATGCCAT | 50764 |
rs29571448 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Fbxo15 | Mm_Celera | 18:84970650 | AACAGAGGAAATAGT[C/T]CAGTTGTGCCTTTGA | 50764 |
rs29571948 | snp | A/C | 0.456747 | 0.140554 | intron-variant | Fbxo15 | Mm_Celera | 18:84968400 | AGGAGAATATGAGGC[A/C]GTCTCGATGTCTAGA | 50764 |
rs29574334 | snp | C/T | 0.375 | 0.216506 | intron-variant | Fbxo15 | Mm_Celera | 18:84946565 | GATGATTCATGCTTG[C/T]AAATATAGCGCCAGA | 50764 |
rs29575084 | snp | A/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Fbxo15, Timm21 | Mm_Celera | 18:84953334 | ACAGGGTATGTCAAC[A/T]GCTTAAGCTATCCCT | 50764 |
rs29575606 | snp | C/T | 0.375 | 0.216506 | intron-variant | Fbxo15 | Mm_Celera | 18:84940086 | GATTAAAGGCGTGCA[C/T]CACCACGCCCGGCAG | 50764 |
rs29575958 | snp | G/T | 0.265928 | 0.249492 | intron-variant | Fbxo15 | Mm_Celera | 18:84944551 | CTACCTCCTGCTTTA[G/T]GGGTGGCTCCCCAAG | 50764 |
rs29580435 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fbxo15 | Mm_Celera | 18:84977179 | TGCATTTCCTTAGCC[A/G]TCTTCTGATTCATTT | 50764 |
rs29583699 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Fbxo15 | Mm_Celera | 18:84959369 | ACAGAACCACAAAAT[C/T]GTCCAGTCTCTAACC | 50764 |
rs29624915 | snp | C/T | 0.484429 | 0.0868505 | intron-variant, utr-variant-3-prime | Fbxo15, Timm21 | Mm_Celera | 18:84948558 | AAAACATACATACAA[C/T]TAAATACCATGTTTT | 50764 |
rs29625601 | snp | G/T | 0.375 | 0.216506 | intron-variant | Fbxo15 | Mm_Celera | 18:84962438 | GGGTTATAAATTTTG[G/T]GTTTGTAGAATTTAT | 50764 |
rs29670053 | snp | C/G | 0.197531 | 0.244432 | intron-variant, upstream-variant-2KB | Fbxo15 | Mm_Celera | 18:84954406 | ACCTACCTGCCTGGT[C/G]TTTAACTGGTTAGAC | 50764 |
rs29675256 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Fbxo15 | Mm_Celera | 18:84970953 | TAAGGTCTGTAATAA[A/G]ACTGAGAAGGTAATA | 50764 |
rs29676292 | snp | A/C | 0.197531 | 0.244432 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | Fbxo15, Timm21 | Mm_Celera | 18:84952035 | GTTCGCAGAGCAACT[A/C]AGTCAACGCATGCGC | 50764 |
rs29685103 | snp | G/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Fbxo15 | Mm_Celera | 18:84954242 | AAGCATTTACTACAC[G/T]CCCTTTGCAGAATGT | 50764 |
rs29720648 | snp | A/C/G | 0.444444 | 0.157135 | intron-variant | Fbxo15 | GRCm38.p3 | 18:84974342 | TCTTACCCTGCAGCC[A/C/G]CACCATATCGACTTG | 50764 |
rs29726025 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxo15 | Mm_Celera | 18:84978225 | TTAGTGGTGGGCTGC[A/G]TGCAGGTGGATGGTT | 50764 |
rs29726455 | snp | A/C | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Fbxo15, Timm21 | Mm_Celera | 18:84953171 | GATTAAAGGGTTGTG[A/C]CACCAACCCTACCCT | 50764 |
rs29733661 | snp | G/T | 0.33241 | 0.236027 | intron-variant | Fbxo15 | Mm_Celera | 18:84975197 | AATCTACTTTGACCT[G/T]CTGCTTCTGTGTGCA | 50764 |
rs29772250 | snp | A/G | 0.401235 | 0.199068 | intron-variant, upstream-variant-2KB | Fbxo15, Timm21 | Mm_Celera | 18:84952796 | TGTAAGGACCCTCAG[A/G]GTGACTTCTTTTCTC | 50764 |
rs29816331 | snp | C/T | 0.197531 | 0.244432 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | Fbxo15, Timm21 | Mm_Celera | 18:84951691 | CGCGTGCGCTGTGTC[C/T]AGGATGAAGAGGGCG | 50764 |
rs29818438 | snp | C/G | 0.387812 | 0.208586 | intron-variant | Fbxo15 | Mm_Celera | 18:84943429 | AAGAAGAGTGCTATA[C/G]CTGCCTACACCCTCA | 50764 |
rs29825727 | snp | C/T | 0.375 | 0.216506 | intron-variant | Fbxo15 | Mm_Celera | 18:84941393 | AGAATAAAGTCTTTC[C/T]CCCTTAAGTTGCTTT | 50764 |
rs29863817 | snp | C/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Fbxo15, Timm21 | Mm_Celera | 18:84952705 | TTTTGTGCACCTTTC[C/T]GGAGCACTAAGCCAA | 50764 |
rs29873358 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Fbxo15 | Mm_Celera | 18:84942394 | TTGGCAGCTGCTGAG[A/G]ATAAAAATGGATGCA | 50764 |
rs29882288 | snp | A/G | 0.375 | 0.216506 | intron-variant, utr-variant-3-prime, downstream-variant-500B | Fbxo15, Timm21 | Mm_Celera | 18:84947472 | TTGCTACATTTCATG[A/G]TTTTTTTTGTAAGAA | 50764 |
rs29882292 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Fbxo15 | Mm_Celera | 18:84942894 | AGAGTATCTAGACTT[A/G]GAAATGTTGGGTCCT | 50764 |
rs29911837 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fbxo15 | Mm_Celera | 18:84961950 | CACAAACTTCTCACC[A/G]GCCAGCTCTGTCACC | 50764 |
rs29926006 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fbxo15 | Mm_Celera | 18:84963473 | AAACAGTACATCATT[A/G]AGGAAAGTCAGGGCA | 50764 |
rs29968130 | snp | A/C | 0.49827 | 0.0293608 | intron-variant | Fbxo15 | Mm_Celera | 18:84962778 | GTCCCATGCTTGCAC[A/C]CTGCATATCAGACTG | 50764 |
rs29972766 | snp | G/T | 0.290657 | 0.246672 | intron-variant | Fbxo15 | Mm_Celera | 18:84978173 | GAATCTACATGGAGC[G/T]CGACATTAGTTTGAT | 50764 |
rs29979621 | snp | A/C | 0.401235 | 0.199068 | intron-variant, upstream-variant-2KB | Fbxo15, Timm21 | Mm_Celera | 18:84951919 | TGAACAGGGCCACAA[A/C]AGGCTAACGGACCAA | 50764 |
rs29982119 | snp | C/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Fbxo15 | Mm_Celera | 18:84954372 | TTGTACCATTTTCTC[C/T]TAATGGTGCCAAGAA | 50764 |
rs29982393 | snp | A/T | 0.345679 | 0.230967 | intron-variant | Fbxo15 | Mm_Celera | 18:84971941 | TTCTTAAACCATTGG[A/T]TCACATATTAGTTAC | 50764 |
rs30014573 | snp | C/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Fbxo15, Timm21 | Mm_Celera | 18:84953066 | TTTTTTTTTTTGAGG[C/T]AAGGTCTATGTAGCC | 50764 |
rs30015091 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxo15 | Mm_Celera | 18:84980737 | TCCCTAGGGTGGTTG[A/G]GTCACTCAGGAGATG | 50764 |
rs30028892 | snp | C/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Fbxo15 | Mm_Celera | 18:84954241 | AAAGCATTTACTACA[C/T]TCCCTTTGCAGAATG | 50764 |
rs30118321 | snp | C/G | 0.493827 | 0.0552116 | intron-variant | Fbxo15 | Mm_Celera | 18:84957932 | CCCTAGGATGCATAC[C/G]GTGTCCCCCATCCTC | 50764 |
rs30128342 | snp | G/T | 0.375 | 0.216506 | intron-variant | Fbxo15 | Mm_Celera | 18:84968350 | TGGTTCACATAGTTC[G/T]CTGAATAGAGTTTTT | 50764 |
rs30130147 | snp | A/G | 0.387812 | 0.208586 | intron-variant, upstream-variant-2KB | Fbxo15, Timm21 | Mm_Celera | 18:84952735 | AGTTGTTTTCTAGAT[A/G]GTCACATCTTGATAT | 50764 |
rs30131010 | snp | A/C/T | 0.432133 | 0.171253 | intron-variant, upstream-variant-2KB | Fbxo15 | GRCm38.p3 | 18:84954364 | AAAGAAGTTTGTACC[A/C/T]TTTTCTCTTAATGGT | 50764 |
rs30155324 | snp | G/T | 0.207612 | 0.24638 | intron-variant, upstream-variant-2KB | Fbxo15, Timm21 | Mm_Celera | 18:84951875 | CAGCGTTTCCGTTTC[G/T]TCTCAGGAAAACAGC | 50764 |
rs30161587 | snp | A/G | 0.32 | 0.24 | intron-variant | Fbxo15 | Mm_Celera | 18:84942910 | GAAATGTTGGGTCCT[A/G]GTTAAGTATGGTTCT | 50764 |
rs30163229 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxo15 | Mm_Celera | 18:84978341 | TGCAGTTCTGCTGGG[A/G]TGATCATAGGTCCGA | 50764 |
rs30165151 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxo15 | Mm_Celera | 18:84938135 | GTTCTGACCATGGTG[A/G]TTTGTCCTCAGAGTT | 50764 |
rs30166488 | snp | A/C/T | 0.46875 | 0.121031 | intron-variant | Fbxo15 | GRCm38.p3 | 18:84942430 | AGGCCTCCTGGAGCC[A/C/T]AGGTTTAAGAAGGTT | 50764 |
rs30167322 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Fbxo15 | Mm_Celera | 18:84942808 | ACTTAGAAAACTGAG[A/G]CTGGATGGGTTTCAA | 50764 |
rs30180477 | snp | C/T | 0.375 | 0.216506 | intron-variant | Fbxo15 | Mm_Celera | 18:84936698 | TCCTGTTGCCCCTCA[C/T]GTGTCCCCTCTTCAA | 50764 |
rs30253593 | snp | C/T | 0.375 | 0.216506 | intron-variant | Fbxo15 | Mm_Celera | 18:84944670 | ATTCTGGGTCATATG[C/T]TAGGCCTTGAACTTA | 50764 |
rs30255613 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fbxo15 | Mm_Celera | 18:84946296 | AGGCATGGTGCAGGA[A/G]GAGCTGAGAGTTCTA | 50764 |
rs30258656 | snp | C/T | 0.375 | 0.216506 | intron-variant | Fbxo15 | Mm_Celera | 18:84946598 | GACTAAGGCAAGCAG[C/T]TGAAAAGTTTATGGC | 50764 |
rs30303209 | snp | C/T | 0.375 | 0.216506 | intron-variant | Fbxo15 | Mm_Celera | 18:84968961 | GGACAGCCAGGGCTT[C/T]GAAGAGAAACCCTGT | 50764 |
rs36247343 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Fbxo15 | Mm_Celera | 18:84968321 | GTACTTATACACACT[A/G]CATGCTCAGAGGGTG | 50764 |
rs36259882 | snp | A/T | 0.260355 | 0.249785 | intron-variant, nc-transcript-variant | Fbxo15 | Mm_Celera | 18:84964696 | TCCATGGTGAGGCCT[A/T]CCTTACTGAAACAAT | 50764 |
rs36265505 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Fbxo15 | Mm_Celera | 18:84975982 | AGGAAGAAGGTGGGC[G/T]TCCCATTCAGAAGCC | 50764 |
rs36273805 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Fbxo15 | Mm_Celera | 18:84946473 | GTACCAGGAAGACAA[G/T]CTCTGCTGATATTTT | 50764 |
rs36293834 | snp | C/G | 0.244898 | 0.249948 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | Fbxo15, Timm21 | Mm_Celera | 18:84951672 | GCTTCTGCGCCGATC[C/G]CTGCGCGTGCGCTGT | 50764 |
rs36299727 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Fbxo15 | Mm_Celera | 18:84969160 | TAACAGCAATGAGAC[C/T]TCTGCTTAGCATAAA | 50764 |
rs36304686 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Fbxo15 | Mm_Celera | 18:84973983 | CGTATCGGCTCCCCT[G/T]CTTAAGAATTTATCA | 50764 |
rs36307544 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fbxo15 | Mm_Celera | 18:84938247 | CCATGAACATAGTTC[C/G]CAGATGGGCTGCAGC | 50764 |
rs36308720 | snp | G/T | 0.124444 | 0.216185 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | Fbxo15, Timm21 | Mm_Celera | 18:84951463 | ATTAAAATGCCCTAT[G/T]TAACCGTCTTGCGGA | 50764 |
rs36310712 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fbxo15 | Mm_Celera | 18:84967397 | TTGGCTATACCTGAG[A/G]TGCCGGATTATGCTG | 50764 |
rs36313003 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Fbxo15 | Mm_Celera | 18:84974951 | AGTGAGGAACATTAC[A/T]GAAGACCAAGTTTGT | 50764 |
rs36316281 | snp | A/C | 0.152778 | 0.230321 | intron-variant | Fbxo15 | Mm_Celera | 18:84967841 | GTAATGAGGTTGTTA[A/C]AACCTGCAGGAGCTG | 50764 |
rs36319900 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxo15 | Mm_Celera | 18:84981035 | GAGGGTTTTGGAGTG[C/T]ATTATTTCCAGTCTG | 50764 |
rs36320945 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Fbxo15 | Mm_Celera | 18:84966586 | CTCATATCTCAGCAA[C/G]AAGAGGAATGACTTG | 50764 |
rs36325953 | snp | C/G | 0.32 | 0.24 | intron-variant, downstream-variant-500B | Fbxo15, Timm21 | Mm_Celera | 18:84947084 | TACATTTACTCAATA[C/G]CACCAGGTCCATTCT | 50764 |
rs36333770 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Fbxo15 | Mm_Celera | 18:84978352 | TGGGATGATCATAGG[C/T]CCGAGTAAGTTGTAC | 50764 |
rs36337509 | snp | C/G | 0.35503 | 0.226867 | intron-variant | Fbxo15 | Mm_Celera | 18:84965293 | GTCCCAGTTTTTGTC[C/G]AAGTTGGTGAGGGAT | 50764 |
rs36342003 | snp | C/G | 0.408163 | 0.193609 | intron-variant, upstream-variant-2KB | Fbxo15 | Mm_Celera | 18:84954510 | CTGAGATTCTTGGAG[C/G]CAGGCTTTCATAAAT | 50764 |
rs36342854 | snp | A/C | 0.231111 | 0.249285 | intron-variant, downstream-variant-500B | Fbxo15, Timm21 | Mm_Celera | 18:84946884 | CACTTGTATGATCAA[A/C]ACTTCCAAGAGGAAG | 50764 |
rs36345974 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fbxo15 | Mm_Celera | 18:84939897 | TTAAACTCTATGGCA[A/G]TTTTAAAAAGGCAAG | 50764 |
rs36346929 | snp | A/T | 0.32 | 0.24 | intron-variant | Fbxo15, Timm21 | Mm_Celera | 18:84949537 | TTCCTAGCAGGTGAC[A/T]TGTGACAGTGGGTCC | 50764 |
rs36355214 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Fbxo15 | Mm_Celera | 18:84955618 | TGTGCTTGGAGATGA[A/G]TTGGCATCTTTAATG | 50764 |
rs36355648 | snp | A/G | 0.142012 | 0.225474 | intron-variant, upstream-variant-2KB | Fbxo15, Timm21 | Mm_Celera | 18:84953255 | CTTATGGATGTAACC[A/G]TCATGTACATTTTGC | 50764 |
rs36361725 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Fbxo15 | Mm_Celera | 18:84961623 | CCATAGCCAACAGAA[A/G]AATGTTTTTACAGCT | 50764 |
rs36362554 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fbxo15 | Mm_Celera | 18:84938895 | TGAATGTTGAGAGCA[C/T]TGTATAAGTGACCAT | 50764 |
rs36362809 | snp | A/T | 0.260355 | 0.249785 | intron-variant | Fbxo15 | Mm_Celera | 18:84972823 | TCATGCCATGTGAGG[A/T]ACTGGAAGCAGTGGT | 50764 |
rs36375298 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Fbxo15 | Mm_Celera | 18:84942334 | ACTTCACTGGTCTCC[A/G]GGGTGTAGGAGAATA | 50764 |
rs36375380 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Fbxo15 | Mm_Celera | 18:84967395 | CATTGGCTATACCTG[A/C]GATGCCGGATTATGC | 50764 |
rs36378303 | snp | A/G | 0.336735 | 0.234472 | intron-variant, upstream-variant-2KB | Fbxo15 | Mm_Celera | 18:84954575 | AGGCTGCTGTGTTCC[A/G]TGAAAGCTGAGCATC | 50764 |
rs36384355 | snp | C/T | 0.5 | 0 | intron-variant | Fbxo15 | Mm_Celera | 18:84961676 | AAGAGGTCTACCTAG[C/T]TGCTTCTTTCTTTGT | 50764 |
rs36385137 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxo15 | Mm_Celera | 18:84937266 | ACTCATAAAATGTCA[C/T]GTTTCTAGATCTCAC | 50764 |
rs36386425 | snp | G/T | 0.459184 | 0.136902 | intron-variant, upstream-variant-2KB | Fbxo15 | Mm_Celera | 18:84955467 | GGGCCTGTGAAGGGT[G/T]TGGTGATAAGTGATA | 50764 |
rs36390359 | snp | C/T | 0.32 | 0.24 | intron-variant, synonymous-codon, upstream-variant-2KB | Fbxo15, Timm21 | GRCm38.p3 | 18:84951148 | GACAGTTCTAGGTTG[C/T]ACTGTTATCTTCTGC | 50764 |