SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6156395 | snp | G/T | 0.5 | 0 | intron-variant | Fbxl7 | Mm_Celera | 15:26872237 | atagatagatagata[G/T]atattctgganagga | 448987 |
rs6156411 | snp | A/G | 0.5 | 0 | intron-variant | Fbxl7 | Mm_Celera | 15:26872248 | gatanatattctgga[A/G]aggangtagggaagg | 448987 |
rs6156823 | snp | C/T | 0.5 | 0 | intron-variant | Fbxl7 | Mm_Celera | 15:26872253 | atattctgganagga[C/T]gtagggaaggggaac | 448987 |
rs6162379 | snp | C/T | 0.5 | 0 | intron-variant | Fbxl7 | Mm_Celera | 15:26760906 | cagatataTGCTAGA[C/T]AGCATATTCATTTGA | 448987 |
rs6162476 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26760949 | AGTAGGATTTTCATA[A/G]ATATTGAAGTCCCTT | 448987 |
rs6163401 | snp | G/T | 0.5 | 0 | intron-variant | Fbxl7 | Mm_Celera | 15:26761105 | ATTCCTTTTCTTATG[G/T]GTGCTNCCGTGCAGG | 448987 |
rs6163413 | snp | A/G | 0.495 | 0.0497494 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26761111 | TTTCTTATGTGTGCT[A/G]CCGTGCAGGGTCAGA | 448987 |
rs6170607 | snp | A/G | 0.5 | 0 | intron-variant | Fbxl7 | Mm_Celera | 15:26872460 | cattctattcacaat[A/G]gctaggaaatgaaaa | 448987 |
rs6171206 | snp | A/G | 0.5 | 0 | intron-variant | Fbxl7 | Mm_Celera | 15:26872596 | ACAAATTTGAAAAGG[A/G]CCCAGGAGGGAAGGA | 448987 |
rs6171775 | snp | A/G | 0.5 | 0 | intron-variant | Fbxl7 | Mm_Celera | 15:26872695 | ATAATCTGACCATAC[A/G]ANAGATACTTTAACA | 448987 |
rs6187426 | snp | G/T | 0.5 | 0 | intron-variant | Fbxl7 | Mm_Celera | 15:26650360 | TTGCTTCCAATGTCT[G/T]NTTCCTTGTGTACAT | 448987 |
rs6187427 | snp | G/T | 0.5 | 0 | intron-variant | Fbxl7 | Mm_Celera | 15:26650361 | TGCTTCCAATGTCTN[G/T]TTCCTTGTGTACATT | 448987 |
rs6187537 | snp | A/T | 0.5 | 0 | intron-variant | Fbxl7 | Mm_Celera | 15:26650425 | TAAGATAGTTACATA[A/T]TTTTAAATCCCAATT | 448987 |
rs6187935 | snp | A/G | 0.5 | 0 | intron-variant | Fbxl7 | Mm_Celera | 15:26650456 | CTCTTTCTTCTAGAG[A/G]CAATCATTTAAAAGT | 448987 |
rs6190000 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Fbxl7 | Mm_Celera | 15:26650883 | GTATCTAATAGACCA[C/G]TAAAATTCCTCTAGA | 448987 |
rs6208354 | snp | C/G | 0.207612 | 0.24638 | synonymous-codon | Fbxl7 | Mm_Celera | 15:26543306 | CAGGGATTCCAGGCC[C/G]GTGTCGGAGACCAGG | 448987 |
rs6228033 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Fbxl7 | Mm_Celera | 15:26876236 | CCATTCCAGAAAGGA[C/T]GTTTAATGCAATAAA | 448987 |
rs6228485 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Fbxl7 | Mm_Celera | 15:26876270 | ACTATTTTCTAGGTC[C/T]TGTTCAAAGCTCCAG | 448987 |
rs6228534 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Fbxl7 | Mm_Celera | 15:26876294 | GCTCCAGATGAATCT[A/G]GATAGTTATATAGAA | 448987 |
rs6241630 | snp | A/G | 0.207612 | 0.24638 | intron-variant | Fbxl7 | Mm_Celera | 15:26876374 | GACAGGGACAGATGC[A/G]CAGCACCATCGCCTT | 448987 |
rs6241750 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Fbxl7 | Mm_Celera | 15:26876440 | ATCCTTCCTGAGAAC[C/T]TGGACTTGCTTTAGC | 448987 |
rs6242706 | snp | A/G | 0.5 | 0 | intron-variant | Fbxl7 | Mm_Celera | 15:26876556 | GCGGCTCTAAGTTTC[A/G]AACTAAGAGAAAAAA | 448987 |
rs6253277 | snp | A/C | 0.5 | 0 | intron-variant | Fbxl7 | Mm_Celera | 15:26694397 | acagggacagtaagg[A/C]atatttgggggggtg | 448987 |
rs6253860 | snp | A/G/T | 0.5 | 0 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26694523 | AAATTAACTTTAAAA[A/G/T]AGAATAAAAGCAAGA | 448987 |
rs6266712 | snp | A/G | 0.5 | 0 | intron-variant | Fbxl7 | Mm_Celera | 15:26694602 | aatgttttatataGT[A/G]TAACATTATTGTAAT | 448987 |
rs6267398 | snp | C/T | 0.5 | 0 | intron-variant | Fbxl7 | Mm_Celera | 15:26694762 | TTCATAAGAACTGCC[C/T]ACCTCAACACNGAAA | 448987 |
rs6267419 | snp | C/T | 0.5 | 0 | intron-variant | Fbxl7 | Mm_Celera | 15:26694773 | TGCCNACCTCAACAC[C/T]GAAAAACAGGGTGTT | 448987 |
rs6267972 | snp | C/G | 0.5 | 0 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26694855 | CTCAATTAATAAACT[C/G]TACATAGATGATTCT | 448987 |
rs6329292 | snp | A/C | 0.207612 | 0.24638 | intron-variant | Fbxl7 | Mm_Celera | 15:26634716 | ATGTGGACTTAAATT[A/C]TTTCTTGATGTGCCT | 448987 |
rs6329942 | snp | A/C | 0.207612 | 0.24638 | intron-variant | Fbxl7 | Mm_Celera | 15:26634859 | AAAATACACTGAGAA[A/C]TTTGCTGGACAAGGG | 448987 |
rs6336482 | snp | A/G | 0.5 | 0 | intron-variant | Fbxl7 | Mm_Celera | 15:26822194 | ATTTTCTACCTGACT[A/G]CTTCCTATAGAACTG | 448987 |
rs6342757 | snp | G/T | 0.5 | 0 | intron-variant | Fbxl7 | Mm_Celera | 15:26634915 | GCCCAGTGGTAATCT[G/T]TCTNATTCCATGGTG | 448987 |
rs6342759 | snp | C/T | 0.5 | 0 | intron-variant | Fbxl7 | Mm_Celera | 15:26634919 | AGTGGTAATCTNTCT[C/T]ATTCCATGGTGACTT | 448987 |
rs6342805 | snp | G/T | 0.5 | 0 | intron-variant | Fbxl7 | Mm_Celera | 15:26634942 | GGTGACTTTAAAAAT[G/T]AGTCCTAAATATATT | 448987 |
rs6343249 | snp | A/G | 0.207612 | 0.24638 | intron-variant | Fbxl7 | Mm_Celera | 15:26634983 | TGCATGGGGAAATGT[A/G]TGATTATCTGACACA | 448987 |
rs6343321 | snp | C/T | 0.5 | 0 | intron-variant | Fbxl7 | Mm_Celera | 15:26635019 | TGGCCAATGGGATTG[C/T]ATNGATGCATCGAGT | 448987 |
rs6343335 | snp | C/G | 0.5 | 0 | intron-variant | Fbxl7 | Mm_Celera | 15:26635022 | CCAATGGGATTGNAT[C/G]GATGCATCGAGTTAT | 448987 |
rs6343360 | snp | C/T | 0.5 | 0 | intron-variant | Fbxl7 | Mm_Celera | 15:26635039 | ATGCATCGAGTTATA[C/T]GAGGTCTGCTGCATA | 448987 |
rs6350700 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Fbxl7 | Mm_Celera | 15:26822467 | AGGTGCTATGGAAAA[C/T]ACCTCCCTGTAAATC | 448987 |
rs6350783 | snp | A/G | 0.304688 | 0.243945 | intron-variant | Fbxl7 | Mm_Celera | 15:26822523 | CAAGCAAGACTATCT[A/G]TGTGTAAGTATAGCT | 448987 |
rs6351286 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Fbxl7 | Mm_Celera | 15:26822606 | AGCTGTAACTAGGCT[C/T]GAAAACAAAGTTCTC | 448987 |
rs6351442 | snp | A/G | 0.455 | 0.143091 | intron-variant | Fbxl7 | Mm_Celera | 15:26551282 | TTACTTGCCTAACAC[A/G]GTGGGTTTTTACTTC | 448987 |
rs6351879 | snp | A/T | 0.5 | 0 | intron-variant | Fbxl7 | Mm_Celera | 15:26551349 | ATGCTTCTGATTTTT[A/T]NAAACCTCTCTGACA | 448987 |
rs6351883 | snp | A/T | 0.5 | 0 | intron-variant | Fbxl7 | Mm_Celera | 15:26551350 | TGCTTCTGATTTTTN[A/T]AAACCTCTCTGACAA | 448987 |
rs6351923 | snp | G/T | 0.5 | 0 | intron-variant | Fbxl7 | Mm_Celera | 15:26551370 | CTCTCTGACAAATCT[G/T]ACATATTCCAACCTC | 448987 |
rs6352447 | snp | A/G | 0.481176 | 0.0951712 | intron-variant | Fbxl7 | Mm_Celera | 15:26551479 | TGGGTCCCGTCTGGC[A/G]CCAAAGTTTGACTCT | 448987 |
rs6365119 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Fbxl7 | Mm_Celera | 15:26896350 | TTTTTTTGGTGGTGA[A/G]ACGAACACGCAGCAG | 448987 |
rs6377987 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | Fbxl7 | Mm_Celera | 15:26896413 | AGCTTAGTGATATGT[C/T]TATCTTTATATATAC | 448987 |
rs6378853 | snp | A/T | 0.432133 | 0.171253 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26604880 | ACTGCTGTTTTTTTT[A/T]AAAATACATCTCATA | 448987 |
rs6384972 | snp | C/T | 0.207612 | 0.24638 | intron-variant | Fbxl7 | Mm_Celera | 15:26631554 | AAGTCAGGTTGTGAG[C/T]GTGCATGCTCATGTC | 448987 |
rs6393134 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26605203 | AGCAGAGGATGGCCT[A/G]GTCAATCATCAATGG | 448987 |
rs6393613 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26605262 | TCTATGGCCCAGTGT[G/T]GGGGGAATGCCAGGG | 448987 |
rs6394212 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxl7 | Mm_Celera | 15:26605383 | GAAATGTAAATAAAG[A/G]AAATATCCAATAAAA | 448987 |
rs6394224 | snp | C/T | 0.5 | 0 | intron-variant | Fbxl7 | Mm_Celera | 15:26605390 | aaataaagnaaatat[C/T]caataaaaaaaaaaC | 448987 |
rs6404806 | snp | C/T | 0.5 | 0 | intron-variant | Fbxl7 | Mm_Celera | 15:26825594 | atgctctctttttca[C/T]ttgtagttctcaaga | 448987 |
rs6406006 | snp | C/T | 0.5 | 0 | intron-variant | Fbxl7 | Mm_Celera | 15:26825844 | CCTAATGACAAGTCA[C/T]AAATATNCATATGTT | 448987 |
rs6406024 | snp | A/T | 0.5 | 0 | intron-variant | Fbxl7 | Mm_Celera | 15:26825851 | ACAAGTCANAAATAT[A/T]CATATGTTGACTGTT | 448987 |
rs13461930 | snp | A/G | | | intron-variant | Fbxl7 | Mm_Celera | 15:26707746 | GGCCAAAAGGAATCT[A/G]GTCCTCAGAGCTCCA | 448987 |
rs13466157 | snp | A/G | | | intron-variant | Fbxl7 | Mm_Celera | 15:26654760 | AGTAAGGCATGAGCA[A/G]TGCAGATATGCAGAG | 448987 |
rs13482490 | snp | A/G | 0.495868 | 0.0452663 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26775871 | GTCCTCAGCAGCTCA[A/G]CTGGACCAGCAGCTA | 448987 |
rs13482491 | snp | A/G | 0.312175 | 0.242145 | upstream-variant-2KB | Fbxl7 | GRCm38.p3 | 15:26897531 | GTTGGCCTACTCGTC[A/G]TGAACGTTTGAGAAC | 448987 |
rs31538355 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Fbxl7 | Mm_Celera | 15:26551756 | GCCTGGGTTTTACTC[C/T]CTGTGGCTGACCATT | 448987 |
rs31551225 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26603534 | TCAAGAGAGCATTGT[A/G]TAGCTAGCTACGCAG | 448987 |
rs31559080 | snp | C/T | 0.375 | 0.216506 | intron-variant | Fbxl7 | Mm_Celera | 15:26690762 | ACACACACACACATA[C/T]ATATATATATGTATA | 448987 |
rs31560090 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26594995 | TCAGTGTTGCAAAGG[A/G]ACAGGGTGAGCATGA | 448987 |
rs31572623 | snp | A/C/T | 0.493827 | 0.0552116 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26776310 | AGGGAATAAAGAATG[A/C/T]CCATCCCAGATCATA | 448987 |
rs31575373 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26704159 | AGAGAATTGTGGGAA[A/G]GAATGGACAGTCCCG | 448987 |
rs31579440 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26708636 | TTAATCAACTGTAAG[A/G]GTGAAAGGATCAGAA | 448987 |
rs31580082 | snp | A/C | 0.387812 | 0.208586 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26627380 | GCTTACCACACAAAG[A/C]TAAAACTATCAAATT | 448987 |
rs31581310 | snp | G/T | 0.359862 | 0.224567 | intron-variant | Fbxl7 | Mm_Celera | 15:26792663 | GCTGTGAAACCAAGA[G/T]ACTGTGTTTTAAGAG | 448987 |
rs31581858 | snp | C/G | 0.498615 | 0.0262793 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26808383 | TGTCTCTTCAGATGC[C/G]TACTGATTTCCAAGT | 448987 |
rs31584950 | snp | C/T | 0.5 | 0 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26779404 | CTCCCCAACAACCCT[C/T]TCTGTGTCTCCTCTT | 448987 |
rs31592001 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26593498 | AATGGTTTAATGCAG[A/G]ACAATCCTTTATCAC | 448987 |
rs31592307 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26695272 | ATGGCGTCCCTAAGA[A/G]GGCTGACAAATGATG | 448987 |
rs31594705 | snp | A/G | 0.5 | 0 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26681106 | GGGCACCTGTCCTCC[A/G]GTCCGGACGGTGGCT | 448987 |
rs31595560 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26785097 | AAAGAGCTTCCTGTG[C/T]TATGGAAGAAGGGAG | 448987 |
rs31596954 | snp | A/T | 0.401235 | 0.199068 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26801217 | ATTTCATAGCATCAT[A/T]CCCTTCATCCTATGT | 448987 |
rs31608073 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Fbxl7 | Mm_Celera | 15:26556365 | CACTTGTTGCTCTTC[C/T]AAAGGAACCGGGTTC | 448987 |
rs31611545 | snp | C/G | 0.32 | 0.24 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26869017 | AGGTGTACACACACA[C/G]AGAGTGATGTAAAAG | 448987 |
rs31615351 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Fbxl7 | Mm_Celera | 15:26758037 | AGTGACTTTCATCTT[C/T]CCAATTTAAAGACTA | 448987 |
rs31622129 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26758217 | CAAAGTGAAGAGCAA[A/G]TTTGGGGATGAGGTC | 448987 |
rs31627305 | snp | A/C | 0.456747 | 0.140554 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26594936 | GAATATTCCAGACAA[A/C]TGGTCCCCATGAAAC | 448987 |
rs31627845 | snp | A/G | 0.5 | 0 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26769959 | ACCACGCTAAAAGAG[A/G]AAGAACTCTTCTGCT | 448987 |
rs31628082 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26727063 | AATAAATAACATTGT[C/T]CTTTAAGGTCTTGAT | 448987 |
rs31636578 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Fbxl7 | Mm_Celera | 15:26896241 | CTTCCATTAAATAGG[A/G]AAAAAAAAAAGATAG | 448987 |
rs31641748 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26784345 | GTGTGGCCAGAAAGG[A/G]AGGCCTAAGATTAAA | 448987 |
rs31644711 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Fbxl7 | Mm_Celera | 15:26627160 | ACTTTGAGATTAAGG[C/T]AGCATATAAAATGTG | 448987 |
rs31650114 | snp | C/T | 0.5 | 0 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26704862 | GGACAGAAAGGGCCT[C/T]TCTCATGGTCAGCAA | 448987 |
rs31653410 | snp | C/T | 0.375 | 0.216506 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26746252 | TGCAAGCTCTGTCCA[C/T]GCAAGCATGAGCTGA | 448987 |
rs31665752 | snp | C/T | 0.375 | 0.216506 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26764781 | ATTTGAGGGCTGGGC[C/T]CAGCCCAGGAGAATG | 448987 |
rs31666478 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26719537 | GAGTTAACTGTTACT[C/T]CTGTGCAAGAGCAGG | 448987 |
rs31668322 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26747567 | ATTGGTTAATCCCCA[C/T]TGATGCCTACTTTCT | 448987 |
rs31677693 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26601044 | GAGATTCCAGAGTCT[A/G]CAAGGATAGTGCCAA | 448987 |
rs31681483 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fbxl7 | Mm_Celera | 15:26548901 | GATTAGGGGGAAAAA[A/G]GGGGTGGGCCTCGGG | 448987 |
rs31682420 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26652145 | TCTTTGCAATCATGG[A/G]AAGCTTTGACACCAA | 448987 |
rs31683042 | snp | G/T | 0.465374 | 0.126941 | intron-variant | Fbxl7 | Mm_Celera | 15:26658680 | AGGATGTAGAAGATG[G/T]CACTAAAAGAAGGAG | 448987 |
rs31685170 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26721335 | AAAGGGCACACTGTA[A/G]AAAATATTCTACCTA | 448987 |
rs31685716 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fbxl7 | Mm_Celera | 15:26774059 | TACTCCCCTACCCAC[C/T]CACTCCTACTTCTTG | 448987 |
rs31687305 | snp | A/G | 0.492188 | 0.0620098 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26694136 | CAAAAATGTCTCTGA[A/G]ATGAATAGAAGCATG | 448987 |
rs31689284 | snp | C/T | 0.5 | 0 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26607382 | ATTGATTTATCTTTG[C/T]TTATCTTCAGAAGGA | 448987 |
rs31702692 | snp | C/G | 0.432133 | 0.171253 | intron-variant | Fbxl7 | Mm_Celera | 15:26558373 | TTTATAGTTCCAAAA[C/G]TCAATTTTATATCCC | 448987 |
rs31708099 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Fbxl7 | Mm_Celera | 15:26767688 | TAAACTGCTAAGCAC[A/G]TAAGTTCTGTATATT | 448987 |
rs31713950 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26779915 | ATATCAAGACAGATC[A/G]TTCCTTAAGACTTAA | 448987 |
rs31714826 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fbxl7 | Mm_Celera | 15:26548161 | TAAGAGATCCTAAAA[C/T]ACAACACAAAAATCT | 448987 |
rs31714943 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26693106 | ATCCTCCCTTGCTTG[C/T]TATTTCCCAGGAGCA | 448987 |
rs31716582 | snp | C/T | 0.492188 | 0.0620098 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26716889 | AATAAAACAAAGAGA[C/T]ACACAGGATAAACGA | 448987 |
rs31716999 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26628537 | AAATAGGCCCTGCAA[A/G]AAGACAGCCCTACCT | 448987 |
rs31718070 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26704512 | GCTGGGGACACACAT[A/G]AATGAAGTCCCACTC | 448987 |
rs31718913 | snp | G/T | 0.5 | 0 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26587943 | ATATGACCACAGCCA[G/T]CTAGCTATCCTGCGC | 448987 |
rs31733818 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26764149 | GCTTATACTCTAAGC[C/T]ATCAGAATTTATAAA | 448987 |
rs31736595 | snp | A/G | 0.455 | 0.143091 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26776218 | TTCCTAGTTCATGAC[A/G]ATCACAGTCCTACAT | 448987 |
rs31739039 | snp | C/T | 0.455 | 0.143091 | intron-variant | Fbxl7 | Mm_Celera | 15:26776962 | TAGTAGTCAAGTTAC[C/T]CACATTTTGTATCTT | 448987 |
rs31749318 | snp | A/C/T | 0.5 | 0 | intron-variant, nc-transcript-variant | Fbxl7, LOC105245899 | GRCm38.p3 | 15:26729875 | AGGCTGCTCCTGTGA[A/C/T]GTTCCAGGCAGCACA | 448987 |
rs31756440 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26627812 | AAGAAATTACATTTT[C/T]TCAAACACAGCCATT | 448987 |
rs31757258 | snp | A/C/G | 0.484429 | 0.0868505 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26698086 | TGCTACAAGACTGCT[A/C/G]TGACCATATTTATTT | 448987 |
rs31758663 | snp | A/C | 0.484429 | 0.0868505 | intron-variant | Fbxl7 | Mm_Celera | 15:26781095 | ATTCTCTTCCTCTGG[A/C]TCTCCATGTTTGGTT | 448987 |
rs31760602 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26740485 | ACTACCAGGCATTGT[A/G]GCAAAGAAGGAACTG | 448987 |
rs31762137 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26717009 | GTATCCTCTCAAATC[A/G]ATGCATGCATAGGAT | 448987 |
rs31762141 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fbxl7 | Mm_Celera | 15:26549425 | TCAAGAGCTCCGGGG[C/T]ACTGGTTAGTTCATA | 448987 |
rs31762227 | snp | A/C | 0.375 | 0.216506 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26607173 | ATCCTGGAACTGGGA[A/C]TTCACAAGGGGAAAG | 448987 |
rs31766637 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Fbxl7 | Mm_Celera | 15:26776679 | TTATGCAATCTCTGT[C/T]CTGTCCAATTTTAAT | 448987 |
rs31779731 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26704880 | TCATGGTCAGCAAAT[A/G]GCCTCTCACTGAGAG | 448987 |
rs31781774 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26720775 | ATCGAATCTAGCATC[C/T]ACCTTATATGAGCAT | 448987 |
rs31783170 | snp | C/G | 0.465374 | 0.126941 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26776368 | GGTGTAGGAGATTGA[C/G]TCGTGGCACCAGTGG | 448987 |
rs31786066 | snp | A/G | 0.5 | 0 | intron-variant | Fbxl7 | Mm_Celera | 15:26606287 | AGAAAGAGAGAAAGA[A/G]AGAAAGAGAGAAAGA | 448987 |
rs31786290 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26771034 | TGCTCTAAAATCAGA[C/T]TTTGTGATAGGCATT | 448987 |
rs31786401 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26604315 | TCTCGGCCATGGTGG[C/T]AGAGCATTTGAAAAG | 448987 |
rs31795213 | snp | A/G | 0.5 | 0 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26588363 | GACAGCTATCTGACA[A/G]CATCGACTCAAAGGC | 448987 |
rs31796118 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26599037 | GAAACTCCCAAGTGG[C/T]CCACTTTATTTTATT | 448987 |
rs31798806 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26757428 | AGAGAGGTATTCCAA[C/T]ATTACCAATGCACAG | 448987 |
rs31806665 | snp | C/T | 0.5 | 0 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26701289 | ACATTTTCTAAGAAA[C/T]AGGATTAAGAACAGT | 448987 |
rs31806668 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26698981 | TGCAACGTGCAAGAG[A/G]GCAGGTGACCAGTTT | 448987 |
rs31808027 | snp | A/C/T | 0.456747 | 0.140554 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26583842 | TTCACTCTTTATGAA[A/C/T]AGTAACCAAAATTAA | 448987 |
rs31812117 | snp | G/T | 0.375 | 0.216506 | intron-variant | Fbxl7 | Mm_Celera | 15:26691533 | ATATATTGATGGCAG[G/T]GGGGCCATCCACTAG | 448987 |
rs31813576 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxl7 | Mm_Celera | 15:26687513 | TGTGTGTGTGTGTGT[A/G]TATATATATATATAA | 448987 |
rs31813595 | snp | C/G | 0.48 | 0.0979796 | intron-variant, nc-transcript-variant | Fbxl7, LOC105245899 | GRCm38.p3 | 15:26730061 | AATGTTCTGTGTTGG[C/G]AGTGATGTCACTTAG | 448987 |
rs31823292 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26594908 | ACCAGGACAGAAGAA[A/G]TGACAGGACATGGAA | 448987 |
rs31825135 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26594428 | AGGGCAATAATTAAT[A/G]GAAGCCAAAAGCTAT | 448987 |
rs31826698 | snp | A/C/G | 0.48 | 0.0979796 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26783378 | CAACTCTACTCCATC[A/C/G]TGGCTTAATCTGGGC | 448987 |
rs31827155 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26760082 | GTTGTCTTCAAGCTC[A/G]TAGCATTCTTGACCT | 448987 |
rs31830144 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26555933 | TAAATAGCTCTTCTT[A/G]GTAAAATCTACCTAC | 448987 |
rs31831062 | snp | C/T | 0.5 | 0 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26726475 | GACATGAGGACAAGT[C/T]AACTTGGAACAGTGG | 448987 |
rs31831106 | snp | G/T | 0.432133 | 0.171253 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26620027 | AGAAACTCTTTTAGC[G/T]TCTCAAAATTTTGCT | 448987 |
rs31832611 | snp | A/C | 0.408163 | 0.193609 | intron-variant | Fbxl7 | Mm_Celera | 15:26787767 | TTTGTAGTCTTTTAC[A/C]CTGGTATTATTTTCA | 448987 |
rs31838912 | snp | A/G | 0 | 0 | intron-variant | Fbxl7 | Mm_Celera | 15:26687491 | TGTGTGTGTGTGTGT[A/G]TGTGTGTGTATATAT | 448987 |
rs31843451 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26700585 | GGTACACTTAATATA[C/T]GGATGTGAAGCAATA | 448987 |
rs31846324 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26713714 | AAACAAGCAAAATGC[A/G]CATTACTAGTTTCAT | 448987 |
rs31846691 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fbxl7 | Mm_Celera | 15:26720616 | TAATGCAGAAGACTT[A/G]TTCTAGTGTGCAGAC | 448987 |
rs31847586 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26841396 | AAAAAACAGGAGAAA[A/T]CATAATAATAAAAGT | 448987 |
rs31848533 | snp | A/G | 0.5 | 0 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26811701 | GAGTAAAGGAAGTAA[A/G]CAGGTCGAGGGAAAG | 448987 |
rs31852596 | snp | A/G | 0.32 | 0.24 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26601004 | ACGTTCGCCATTTCC[A/G]CTGCAACCAATTCTG | 448987 |
rs31856728 | snp | A/T | 0.456747 | 0.140554 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26783646 | CTAGATTGCTTAAGG[A/T]CCTCCTTCATGGAAT | 448987 |
rs31858825 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26593897 | AGCATTTCATGCAGA[C/T]GTGCCAAATAATTTT | 448987 |
rs31861726 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26628386 | ATCCAAACAGCATCT[C/T]GCTGCATTCCCCCTT | 448987 |
rs31865505 | snp | A/G | 0.5 | 0 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26782986 | GACACAACACCTAAA[A/G]CTTATTAGCCAGCCA | 448987 |
rs31868847 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26715970 | CAGGCTAAGATCATT[C/T]TAGTCTTATAGGAGT | 448987 |
rs31870066 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Fbxl7 | Mm_Celera | 15:26747641 | AAAGGAGAGGATTAA[A/G]TGAAGAAACCTGGCA | 448987 |
rs31872192 | snp | A/G/T | 0.401235 | 0.199068 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26602021 | GAAAAGCTGTTTCAG[A/G/T]GCTGTGTTTCCAAAA | 448987 |
rs31873907 | snp | G/T | 0.465374 | 0.126941 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26742047 | AAGAACCTTTCAAAG[G/T]TAAATCCCACTTTGA | 448987 |
rs31875298 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26873803 | TCTAAATTAACCCCA[C/T]ATTGTCTGCTTAAAT | 448987 |
rs31876212 | snp | A/G | 0.32 | 0.24 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26688632 | CATACTCCCTTACTT[A/G]CACCTGGAAACGTGC | 448987 |
rs31877813 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26858716 | TTTCTCCTCAACCAA[C/T]GTTTTCCCACTGGCT | 448987 |
rs31879731 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26766164 | TCTGAGTTGATAAAG[C/T]TTCATCTCCTGGGCT | 448987 |
rs31880149 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26741944 | AGTGCCCAGTTTAGG[A/G]AAAGCACTGTTTAGC | 448987 |
rs31880906 | snp | A/G | 0.486111 | 0.0821678 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26615485 | ATCATGTGTGTGTTC[A/G]TTTTTCTAGATCTTC | 448987 |
rs31881074 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Fbxl7 | Mm_Celera | 15:26607237 | CAAACATCTTTGCTT[C/T]TTTTCTGTTTCTCTC | 448987 |
rs31885585 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26702402 | AGAACTTAATAGAGC[A/G]GAGTGCCAGGGAGTA | 448987 |
rs31889852 | snp | C/T | 0.42 | 0.183303 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26601003 | GACGTTCGCCATTTC[C/T]ACTGCAACCAATTCT | 448987 |
rs31898785 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Fbxl7 | Mm_Celera | 15:26818940 | GACTTGACAGAACAG[A/G]GTATGCCCAACTCTC | 448987 |
rs31898914 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26835097 | ACAAAAAAAAAAAAA[A/C]CCCACACAACTGGAC | 448987 |
rs31899556 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26745967 | GCAGTGGTGGCGCAC[A/G]CCTTTAATCCCAGCA | 448987 |
rs31899822 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26827701 | CATAGGCATAATCAA[C/T]AGTTTTACTTTTCGA | 448987 |
rs31905161 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Fbxl7 | Mm_Celera | 15:26608962 | CAAAATACCCATGGG[A/T]GGAGATACAGAAACA | 448987 |
rs31909689 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26601943 | ATTTCTCCAGGAAAC[A/G]GCAAGGGATGTGTAT | 448987 |
rs31910403 | snp | A/T | 0.492188 | 0.0620098 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26716810 | TCTAACAGTGATTTT[A/T]AAAAAAATGTCATAA | 448987 |
rs31911984 | snp | A/T | 0.375 | 0.216506 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26714081 | GTTGCTGGGAATTGA[A/T]CTCAGGACCTCTGGA | 448987 |
rs31914773 | snp | C/T | 0.375 | 0.216506 | intron-variant | Fbxl7 | Mm_Celera | 15:26690760 | ACACACACACACACA[C/T]ATATATATATATGTA | 448987 |
rs31916938 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26826370 | GTCCAAAGTCACTTC[A/T]CAGATTCAAAGAAGC | 448987 |
rs31918488 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26697895 | TTGAGTGAAGGCTAC[A/G]AATGAAAAGGGTTTT | 448987 |
rs31918491 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26588997 | TTTGGGGGACTATTA[C/T]ACAACATTCCATAGA | 448987 |
rs31919470 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Fbxl7 | Mm_Celera | 15:26608912 | TCCCCCTGCTCACCA[A/T]CCCACCCACTCCCGC | 448987 |
rs31922151 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Fbxl7 | Mm_Celera | 15:26787604 | TTCTTTTTTTATTTT[A/T]TTTTAATTTTTTTTT | 448987 |
rs31923839 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26610308 | TCTGTCTGCATGTAT[C/G]CCTGCATGCCAAGAG | 448987 |
rs31924999 | snp | A/G | 0.495 | 0.0497494 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26755099 | TTCCAGTTAGCATCA[A/G]TGGCCATCCAAGCAT | 448987 |
rs31926882 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26693220 | TGCACATGTCACTGT[A/G]TAGTCCTTCAAGACA | 448987 |
rs31926940 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxl7 | Mm_Celera | 15:26842748 | TGTGTGTGTGTGTGT[A/G]TATATATATATATAT | 448987 |
rs31931518 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26588250 | GATTTCTAGGCTAAC[A/G]GCATAGATTTGTGAT | 448987 |
rs31934723 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Fbxl7 | Mm_Celera | 15:26780959 | TTTTACATCTAATGG[A/G]ATTTCCAAAGACTGA | 448987 |
rs31943747 | snp | C/T | 0.375 | 0.216506 | intron-variant | Fbxl7 | Mm_Celera | 15:26552312 | ACAGATAAACATATA[C/T]ACATAATTAAATAAA | 448987 |
rs31946479 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Fbxl7 | Mm_Celera | 15:26548477 | GTCAACGCTCATGAC[C/T]GGATGCACCACGGGC | 448987 |
rs31948872 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26784480 | TACAAAGTGAAAAGA[A/T]GAAAAAGAAGCCGAC | 448987 |
rs31950616 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26702071 | GCAGGCAATGACTGC[A/G]ACAAAATAAAGTAAA | 448987 |
rs31955465 | snp | A/G | 0.32 | 0.24 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26602812 | TAGATAGCATCTGAG[A/G]GCTATAGCAGAGATT | 448987 |
rs31958605 | snp | A/C | 0.375 | 0.216506 | intron-variant | Fbxl7 | Mm_Celera | 15:26843631 | TACAGTTGCCCGGAT[A/C]AGCTTGTTAAAATTA | 448987 |
rs31958635 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Fbxl7 | Mm_Celera | 15:26815700 | AAATACATAAAAATA[G/T]AATATTAATTATTAG | 448987 |
rs31959054 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Fbxl7 | Mm_Celera | 15:26556374 | CTCTTCTAAAGGAAC[C/G]GGGTTCAATTCCTGG | 448987 |
rs31960718 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26775481 | TGGCAGACTAGCAGA[A/G]TAGATACGGGCTGCC | 448987 |
rs31965604 | snp | A/C/G | 0.54 | 0.18 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26598962 | TTTTGCTTCTTATAT[A/C/G]TGCTGCATATTCTGG | 448987 |
rs31967374 | snp | A/T | 0.375 | 0.216506 | intron-variant | Fbxl7 | Mm_Celera | 15:26551666 | CAAAGGAAAGACAAA[A/T]GGGGGCGTCATCTGA | 448987 |
rs31974908 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Fbxl7 | Mm_Celera | 15:26608898 | TATCTCATCCCCTCT[C/G]CCCCTGCTCACCAAC | 448987 |
rs31976501 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26713782 | ATAAAAAAATAACAA[A/G]ATAAGAGATGACTAT | 448987 |
rs31987038 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fbxl7 | Mm_Celera | 15:26602505 | AACCTCTAAGTCTGA[C/T]TTTTCACCATTTGTG | 448987 |
rs31987110 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26620012 | TTCACAGACTGGGCT[A/G]GAAACTCTTTTAGCT | 448987 |
rs31988498 | snp | A/G/T | 0.429688 | 0.173817 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26719558 | CAAGAGCAGGCTTAC[A/G/T]AGCCCTGTGGTATTT | 448987 |
rs31999501 | snp | A/T | 0.49827 | 0.0293608 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26694017 | TGCTCACTTATGAAT[A/T]CATGTATATGCATAT | 448987 |
rs32002346 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26603201 | CATAGGAACCAATTA[C/T]AGACTATGGAAAAAC | 448987 |
rs32003963 | snp | A/C | 0.375 | 0.216506 | intron-variant | Fbxl7 | Mm_Celera | 15:26796845 | GAGAGCTGCTCAGTG[A/C]TTCTGACATTCACCC | 448987 |
rs32004041 | snp | A/C | 0.493827 | 0.0552116 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26766609 | AATAAATCAGTCTTG[A/C]AACTTTTCTCTCTTT | 448987 |
rs32005360 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26721699 | GATATAGTATGGATT[A/G]TAGGAGTAAATATTG | 448987 |
rs32013264 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26780185 | CAGAAACTACTAAGA[C/T]GTCTTAAGAATGAGC | 448987 |
rs32015123 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26595125 | GGCTTGAAGCAGATA[A/G]TGTGTGTCAAAATTC | 448987 |
rs32019614 | snp | A/C | 0.5 | 0 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26700243 | CATGTTTGTCTAGCT[A/C]AACTTAAGCCCTTGT | 448987 |
rs32024204 | snp | G/T | 0.475309 | 0.108333 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26703993 | TTCTGCACCTGCTAA[G/T]ACTCAGCCTATCTGG | 448987 |
rs32031205 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Fbxl7 | Mm_Celera | 15:26629229 | AGTTCTATTTTCTAA[A/G]CTGTTCAAGTTGCTA | 448987 |
rs32032999 | snp | A/C | 0.456747 | 0.140554 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26792649 | AGTGGGGCTCTTATG[A/C]TGTGAAACCAAGATA | 448987 |
rs32035728 | snp | A/T | 0.456747 | 0.140554 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26785686 | CAACATGACTGGAAG[A/T]AATTATGTTGGGACT | 448987 |
rs32036404 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26628444 | AGTTGCAAAAACCAT[A/G]ATAAAATGTCTCCTA | 448987 |
rs32041386 | snp | G/T | 0.493827 | 0.0552116 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26719985 | TCTCTGCCACTCTAT[G/T]TCCTCTGCTGGGGCA | 448987 |
rs32042927 | snp | C/G | 0.401235 | 0.199068 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26602066 | ACCCGAACAGAGCTC[C/G]TCTGCAAAGAGGCAA | 448987 |
rs32046432 | snp | A/C | 0.375 | 0.216506 | intron-variant | Fbxl7 | Mm_Celera | 15:26705485 | CCTGAGAATGTTTGC[A/C]CAATGTGCACATGCT | 448987 |
rs32055681 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26703206 | TCCAAGTGAGGAGAG[C/T]TTGTCTCTTATGAGC | 448987 |
rs32056330 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26622037 | TGAGCAAAACCCAGT[C/T]AAGCTGCCTTCACAA | 448987 |
rs32056508 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26589200 | TTGAAGTGAGTCATG[A/G]CTTCGTAGGAGACAT | 448987 |
rs32058828 | snp | C/T | 0.5 | 0 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26727536 | GGCTTATTGCTAAGC[C/T]CCCAAACAGGGTCTC | 448987 |
rs32068658 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26775972 | ATTCAGTTCTCAGAG[C/T]ATGCAACAGCCTTTC | 448987 |
rs32069391 | snp | A/T | 0.415225 | 0.187619 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26691720 | GAGAGAGATTTGAGT[A/T]TTGGAAGGAGTGCTT | 448987 |
rs32069413 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26780377 | AAAATATTCCCTCTC[C/T]GAAGACTACATAGAT | 448987 |
rs32069568 | snp | A/G | 0.5 | 0 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26561752 | GGTAAAAGTAACAAC[A/G]TAGTTGTAGTCATTA | 448987 |
rs32076278 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26717601 | ACCGTACTCGACATA[A/G]CGATGGACACACAGT | 448987 |
rs32080862 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26551645 | AAAAGAGCTGTAAAA[A/T]TAACCCAAAGGAAAG | 448987 |
rs32084696 | snp | C/G | 0.5 | 0 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26881384 | AGGTAGGGAAAGCCA[C/G]CTCTAGCAGGTTGTT | 448987 |
rs32085341 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26726252 | TAAAGAATCTCCTAC[C/T]ACAGGCTTTCCCTGT | 448987 |
rs32087676 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26691613 | CCTATTCTAGAAAAT[A/G]TTGGAAATGTCTCCT | 448987 |
rs32088851 | snp | A/T | 0.475309 | 0.108333 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26768686 | CATTTAATATTTTCC[A/T]GAAGGTCATATAAAC | 448987 |
rs32089993 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26589229 | ATGCAGAGTTTATAG[A/G]AAATATTTGCAGAAG | 448987 |
rs32096669 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26754599 | TGTGAGATGCTAGGC[C/T]CTGTGAGCCCCTTAC | 448987 |
rs32097446 | snp | G/T | 0.304688 | 0.243945 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26775963 | TATGATGTAATTCAG[G/T]TCTCAGAGTATGCAA | 448987 |
rs32102937 | snp | A/T | 0.375 | 0.216506 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26765019 | TTTTGTCTCTCTTCC[A/T]TCACCTGTGAATGTA | 448987 |
rs32103221 | snp | G/T | 0.495 | 0.0497494 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26588871 | CCACCATGTTAGGTT[G/T]TGGCTAATTCGAAAA | 448987 |
rs32104030 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26697808 | TTCCACTCAGAACAG[A/G]TTTCCATGCATAAAA | 448987 |
rs32111514 | snp | C/G | 0.493827 | 0.0552116 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26864281 | CACATCATGGAAACC[C/G]ACTGTGGGAGACTAT | 448987 |
rs32114325 | snp | C/T | 0.387812 | 0.208586 | missense | Fbxl7 | GRCm38.p3 | 15:26543736 | GTCATATCAAGGTAT[C/T]GGATGGAAATCTGTT | 448987 |
rs32115650 | snp | A/C | 0.387812 | 0.208586 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26615239 | TATCTCTCTGTCTCA[A/C]ATAAGCAAGAAAACA | 448987 |
rs32116057 | snp | A/G | 0.429688 | 0.173817 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26615503 | TTTCTAGATCTTCAA[A/G]AGGAAAACTGAAAGA | 448987 |
rs32118313 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26611369 | AACCTCCCAATTAGA[C/T]AGAAAAACATATTGA | 448987 |
rs32118360 | snp | A/T | 0.475309 | 0.108333 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26769227 | ATTTAAATACAACTG[A/T]TTCTCATTGATGGTT | 448987 |
rs32119152 | snp | C/T | 0.375 | 0.216506 | intron-variant | Fbxl7 | Mm_Celera | 15:26746248 | ATGGTGCAAGCTCTG[C/T]CCACGCAAGCATGAG | 448987 |
rs32127385 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26841461 | AAACAGTAATGTCTC[A/G]TAAAGTCTGAGCAAA | 448987 |
rs32129186 | snp | C/T | 0.5 | 0 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26594584 | CAGTGTCCACATAGA[C/T]TGGAAGACCAAATTG | 448987 |
rs32131388 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26698460 | CAAAAGACAAGGCCC[A/G]TGACCCTTTTCCATT | 448987 |
rs32132280 | snp | G/T | 0.5 | 0 | utr-variant-3-prime | Fbxl7 | GRCm38.p3 | 15:26542753 | AAGAGAGTATGGAAC[G/T]CTGGGGTGTAGCTTG | 448987 |
rs32132797 | snp | A/G | 0.492188 | 0.0620098 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26696206 | GTGACATGTGTTTAT[A/G]CAGCACCTGAAGCTA | 448987 |
rs32133539 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26866548 | TGAATCTGTGTTCCC[A/G]CGTGAATCAGGAAAC | 448987 |
rs32133979 | snp | C/T | 0.429688 | 0.173817 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26627859 | AAAACACCCTTCAGC[C/T]AAAACTCAATATCTA | 448987 |
rs32140108 | snp | A/G | 0.5 | 0 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26726457 | GCGAGGCCTTTCACC[A/G]AGGACATGAGGACAA | 448987 |
rs32144340 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26604371 | TCCACCAAAGCAGGA[A/G]TGCTGACAAACACGG | 448987 |
rs32145688 | snp | G/T | 0.465374 | 0.126941 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26589305 | TTAAAGAACTGGTCT[G/T]CTAACTCGCGCATAG | 448987 |
rs32150126 | snp | C/G | 0.444444 | 0.157135 | intron-variant, nc-transcript-variant | Fbxl7, LOC105245899 | GRCm38.p3 | 15:26737130 | CTGTAAATCCTAATC[C/G]CCATGCCTTTGTTCT | 448987 |
rs32155139 | snp | G/T | 0.46875 | 0.121031 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26786181 | CCAAGACCACACACA[G/T]GTCAGGCCATAGCCA | 448987 |
rs32156800 | snp | G/T | 0.475309 | 0.108333 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26759029 | ATCTGTTCCCCGAAT[G/T]TTGATTTACATTTAG | 448987 |
rs32159915 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26622287 | AGCAGTGTGATCAAC[C/T]TCCCTCCTGACAGCT | 448987 |
rs32162679 | snp | A/T | 0.465374 | 0.126941 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26755327 | GTTTATCCAACACGC[A/T]CAGAGAAAACCACCA | 448987 |
rs32164936 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26752183 | AGGCCTCCAGTGTCA[A/G]GGTATTTTTAGGTTG | 448987 |
rs32172151 | snp | C/T | 0.32 | 0.24 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26690425 | GCAGAAAGAGTGTGC[C/T]AGAGCGGATGGCTGA | 448987 |
rs32178156 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26602303 | GTCTTAATCAATGGC[C/T]GTGTGCTTCCTTGAA | 448987 |
rs32179496 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26726312 | TTCTAATGCAGGGTG[A/G]CTCTGGACTGCAATT | 448987 |
rs32187314 | snp | A/C | 0.401235 | 0.199068 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26595140 | GTGTGTGTCAAAATT[A/C]CCAAAGACCTACTGT | 448987 |
rs32189174 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26598706 | AAGTAAGGTCATGGA[C/T]ACACATGCCAAGGTT | 448987 |
rs32190933 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Fbxl7 | Mm_Celera | 15:26556482 | CCTGATACGCACACA[A/G]CACACAGATATACAT | 448987 |
rs32191767 | snp | C/T | 0.32 | 0.24 | intron-variant | Fbxl7 | Mm_Celera | 15:26637946 | CCCAATTGATCTTTT[C/T]TTATAAGAAAGCACT | 448987 |
rs32193345 | snp | A/G | 0.5 | 0 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26766822 | ATTATTTGGGCTTTC[A/G]GGAGAGGCAAACACT | 448987 |
rs32194805 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Fbxl7 | Mm_Celera | 15:26600990 | TTTCCTGTGCATAGA[C/T]GTTCGCCATTTCCAC | 448987 |
rs32195152 | snp | A/C | 0.415225 | 0.187619 | intron-variant | Fbxl7 | Mm_Celera | 15:26691249 | ACAGATTCCTAAAAG[A/C]TGTGTTAGTTTGTTC | 448987 |
rs32199345 | snp | A/C | 0.49827 | 0.0293608 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26698386 | AAAATGTATCACGTG[A/C]TTTAGTAGCTTGGAG | 448987 |
rs32203971 | snp | A/C | 0.375 | 0.216506 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26628447 | TGCAAAAACCATAAT[A/C]AAATGTCTCCTAACA | 448987 |
rs32206358 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26745834 | ATGAATCCCACATGG[C/T]ACTGTTATGATTCCA | 448987 |
rs32212684 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26600965 | GAAAGGTCAGGGACG[A/G]AAATCTTTATTTCCT | 448987 |
rs32215357 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26627899 | TTTAGTGCAGCCTAC[C/T]GAGTTTTGATGAAAG | 448987 |
rs32217927 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26636335 | GAGATGCTTGGACGA[C/T]ATGGTCTAACTGCAG | 448987 |
rs32219001 | snp | C/T | 0.375 | 0.216506 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26783374 | AAGTCAACTCTACTC[C/T]ATCATGGCTTAATCT | 448987 |
rs32220125 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Fbxl7 | Mm_Celera | 15:26714118 | GTCAGTGCTCTTAAG[C/G]ACTGATCCATCCCTC | 448987 |
rs32221505 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26768811 | AATCTTGTTTAAGTT[A/G]TGTGTCAGAATATTC | 448987 |
rs32222138 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26720489 | TTTTGTTTTAGTTTT[A/G]TATATTTGTTAATTC | 448987 |
rs32223258 | snp | C/T | 0.429688 | 0.173817 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26604406 | ATTTTACGTCCAATG[C/T]TACGCATACTAAACT | 448987 |
rs32224104 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26593892 | CCAGAAGCATTTCAT[A/G]CAGACGTGCCAAATA | 448987 |
rs32224342 | snp | G/T | 0.49827 | 0.0293608 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26701794 | CAGGTTAGATGCATT[G/T]TGTTACATGACAAAA | 448987 |
rs32226992 | snp | A/G | 0.5 | 0 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26589527 | ATGTGGTTCTCCAAT[A/G]TTTCTATGCTTTATG | 448987 |
rs32230894 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26705629 | TTTCTGTAAATGAAC[C/T]GACTATAGCACAGTT | 448987 |
rs32235600 | snp | A/G | 0.5 | 0 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26702144 | AAAGGCGGAGAGAGC[A/G]ACATTAAAGGAAAGT | 448987 |
rs32236420 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26745953 | TGGGCATTAGCGAGG[C/T]AGTGGTGGCGCACAC | 448987 |
rs32236558 | snp | A/T | 0.493827 | 0.0552116 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26796403 | TTTTCCTTAAAAATC[A/T]TTGAAGATCAATCTA | 448987 |
rs32237157 | snp | A/C | 0.375 | 0.216506 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26852065 | ATGATGCCCCCCCCC[A/C]AAAAAAAAAAACTCA | 448987 |
rs32240500 | snp | C/T | 0.375 | 0.216506 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26740629 | CTCCAGTTTGCCTTC[C/T]TCTTTTTTGTTTGTT | 448987 |
rs32246727 | snp | G/T | 0.415225 | 0.187619 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26656283 | AATTGTAAAATGGGT[G/T]CCATTCAACTTATGA | 448987 |
rs32252888 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26627606 | TCTATTACAACAGCA[C/T]GTTTGAAGATGCAAA | 448987 |
rs32252921 | snp | A/G | 0.5 | 0 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26765880 | AAGGGAAGAAGAGAT[A/G]AAATAAGCCTCGGGA | 448987 |
rs32253307 | snp | A/G | 0.5 | 0 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26594755 | TAAGATCTTCAGTTT[A/G]GGGTCAGTCTTAGCC | 448987 |
rs32256877 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26691022 | TAAAAAAATATTTTC[A/C]ATAAAAAATGATGAA | 448987 |
rs32257547 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fbxl7 | Mm_Celera | 15:26551671 | GAAAGACAAAAGGGG[A/G]CGTCATCTGACCATG | 448987 |
rs32265866 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26624126 | CAGGCCCCATTCAGT[A/G]GGTGGGGAAGTTGAA | 448987 |
rs32270288 | snp | C/G/T | 0.444444 | 0.157135 | upstream-variant-2KB | Fbxl7 | GRCm38.p3 | 15:26896074 | AGTTTTGAAAGCTTC[C/G/T]GAGACACGACTTTTT | 448987 |
rs32273492 | snp | C/T | 0.5 | 0 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26754432 | TAATAAGGATAAGCA[C/T]AATTGTACACAAAAA | 448987 |
rs32274733 | snp | G/T | 0.375 | 0.216506 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26615427 | GAGGGTACCCAACTG[G/T]GAGGGTAGGTCCTCC | 448987 |
rs32276557 | snp | G/T | 0.455 | 0.143091 | intron-variant | Fbxl7 | Mm_Celera | 15:26776796 | AGAAAATAGAACATA[G/T]TTTAGCAAAGATAAT | 448987 |
rs32290519 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Fbxl7 | Mm_Celera | 15:26885258 | CATAGGACCAAGGGC[A/C]TCTCCTCCCATTGAT | 448987 |
rs32292835 | snp | A/T | 0.33241 | 0.236027 | intron-variant | Fbxl7 | Mm_Celera | 15:26830917 | AAAGGAACAGGGCAG[A/T]CTATGTTAGAGTAGC | 448987 |
rs32293918 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26823484 | AGCTCAGTTTGTACT[A/C]AAAAACAAAAACAAA | 448987 |
rs32294362 | snp | G/T | 0.498615 | 0.0262793 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26875909 | AATGCCCAGAAATCA[G/T]AGTCAGCCACAAACT | 448987 |
rs32297025 | snp | A/T | 0.432133 | 0.171253 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26762376 | GCCAATGAGGAGCGC[A/T]CCATAGATTTACAAT | 448987 |
rs32299095 | snp | G/T | 0.484429 | 0.0868505 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26710659 | CAGAAGATTGAGTGT[G/T]CGTTTAGCCTCGCAG | 448987 |
rs32301409 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26594731 | CCTCAGCAGAGTTCA[C/T]TCTCTAATTAAGATC | 448987 |
rs32301585 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26695620 | ATTGTTTTTACACAA[C/T]GTTATAAATATTTCC | 448987 |
rs32306669 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26750259 | GACCAGGCTGACCTC[A/G]AACTCAGAAATCTGC | 448987 |
rs32307112 | snp | A/T | 0.455 | 0.143091 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26824113 | AAGGAGATAAGATTA[A/T]CAGTTGTATGCCTTG | 448987 |
rs32308116 | snp | A/C | 0.5 | 0 | intron-variant | Fbxl7 | Mm_Celera | 15:26780989 | AATCCAGATTTCAGA[A/C]CCTCCAAAGCCCCCG | 448987 |
rs32308737 | snp | A/T | 0.486111 | 0.0821678 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26607410 | GGAGGGAGATATTTT[A/T]AAACCAAATATATAA | 448987 |
rs32310234 | snp | A/T | 0.5 | 0 | intron-variant | Fbxl7 | Mm_Celera | 15:26608953 | TAGGGGGAACAAAAT[A/T]CCCATGGGTGGAGAT | 448987 |
rs32317178 | snp | C/T | 0.375 | 0.216506 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26625330 | TATTTATGTGTTTGT[C/T]TGTCTGTCTGTCTGT | 448987 |
rs32318454 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | Fbxl7 | Mm_Celera | 15:26701983 | AGCAATCTCAGACAG[C/T]CCACTCTTCTTTTGC | 448987 |
rs32320658 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26603049 | TTTGTGGTGAAACTT[A/G]TGTTTTGTTGCAGCA | 448987 |
rs32321262 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26622218 | ACTTTGAAAGTGAGA[A/G]ATCAGAAAGGAGTGA | 448987 |
rs32326003 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26780862 | GATTTCCTATGCAGT[C/T]GTGACACTTTCAGTG | 448987 |
rs32332891 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26718079 | CCAGTCAGAGTATAT[C/T]CAGCCAAGGTCCTTC | 448987 |
rs32337659 | snp | A/C | 0.493827 | 0.0552116 | intron-variant, nc-transcript-variant | Fbxl7, LOC105245899 | GRCm38.p3 | 15:26735626 | TAGCTTTCGGTCTTA[A/C]CTAATCATCTTGGTT | 448987 |
rs32346083 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Fbxl7 | Mm_Celera | 15:26787564 | TTCTTTACCCCTCCC[A/C]ACTCAGATAGCACAG | 448987 |
rs32349973 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxl7 | Mm_Celera | 15:26645448 | CATATATATGTGTAT[A/G]TATATATATATATAT | 448987 |
rs32352055 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Fbxl7 | Mm_Celera | 15:26714117 | AGTCAGTGCTCTTAA[C/G]GACTGATCCATCCCT | 448987 |
rs32353818 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26608551 | CACAGAAGGCGGATG[A/G]CTAAGTGAAAAGCTC | 448987 |
rs32354417 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26610245 | AATTCTTTGTTGTTG[C/T]TGAGTGGAATTTTTA | 448987 |
rs32358290 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26691651 | GCTTGGGGGTTAAGG[A/G]GACTGGAGATCCCTT | 448987 |
rs32359208 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26702463 | GTGTTCAGGGAGGGT[A/G]TGTGCAGGTAGGCTG | 448987 |
rs32359770 | snp | A/G | 0.444444 | 0.157135 | intron-variant, nc-transcript-variant | Fbxl7, LOC105245899 | GRCm38.p3 | 15:26729795 | GGTCCCTCCAATATC[A/G]ATCACTGATCAAGAA | 448987 |
rs32360078 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fbxl7 | Mm_Celera | 15:26690773 | CATATATATATATAT[A/G]TATATATATATATAC | 448987 |
rs32362423 | snp | A/C | 0.465374 | 0.126941 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26608527 | ATGGCTGTGCATCTG[A/C]GAACGTGGCACAGAA | 448987 |
rs32363781 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fbxl7 | Mm_Celera | 15:26878490 | CACATAGGAAATACA[A/G]CATGACAGAGGCAGG | 448987 |
rs32363983 | snp | C/G | 0.375 | 0.216506 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26652427 | TCTCTCTCTCTCTCT[C/G]TGTGTGTGTGTGTGT | 448987 |
rs32364346 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26594125 | CTTTGCCCTGGAACA[C/T]AAGAAATAATTTGCT | 448987 |
rs32364794 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26603283 | GAAGCCTGTAATGTT[C/T]TTCGAGCTCAACTAT | 448987 |
rs32376590 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26610883 | CTTTGTAGGGAAAAT[A/G]GAAGTGTTTTTATTT | 448987 |
rs32378778 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26767984 | ACATGTAGACATGAA[C/T]GCTGACACTGATCAC | 448987 |
rs32379695 | snp | C/T | 0.5 | 0 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26710156 | CCAATAAAAATTTGG[C/T]TTTATCCACATATTT | 448987 |
rs32382087 | snp | A/T | 0.493827 | 0.0552116 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26693363 | CACGCTGTAGTGAAA[A/T]GGGACTGGCAGGAAA | 448987 |
rs32382324 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26710671 | TGTTCGTTTAGCCTC[A/G]CAGTGAGACAGGAAG | 448987 |
rs32385558 | snp | A/G | 0.5 | 0 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26780469 | GAGGAGTGAGGGAGA[A/G]CTAATTGTCTTGGAG | 448987 |
rs32386912 | snp | A/G | 0.5 | 0 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26795156 | AATTCTCCTCTGTCT[A/G]GACAGTGCATAACTT | 448987 |
rs32388313 | snp | C/G | 0.375 | 0.216506 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26607395 | TGCTTATCTTCAGAA[C/G]GAGGGAGATATTTTT | 448987 |
rs32389677 | snp | A/C | 0.495 | 0.0497494 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26777459 | GTAAAATGTTATCTT[A/C]ATTTCTTCATAGCTT | 448987 |
rs32391496 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Fbxl7 | Mm_Celera | 15:26862329 | AAAGCCTGGAGCAAC[C/T]GCCATCCTGCAGTGA | 448987 |
rs32397495 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26624127 | AGGCCCCATTCAGTG[A/G]GTGGGGAAGTTGAAG | 448987 |
rs32397768 | snp | A/C | 0.484429 | 0.0868505 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26701824 | AGTGATGAGACAAAA[A/C]CCCTCAAATTCTAGA | 448987 |
rs32400868 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Fbxl7 | Mm_Celera | 15:26550434 | ATGAACTAACCAGTA[A/C]CCCCAAGAGCTCGTG | 448987 |
rs32400984 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26598904 | AATATTTGCTGCATG[A/G]ATTATTAACAGATGC | 448987 |
rs32403452 | snp | G/T | 0.375 | 0.216506 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26623075 | GGAAGAGCAGCATCT[G/T]CTCTTAAACAATGAG | 448987 |
rs32405837 | snp | C/T | 0.5 | 0 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26768864 | ATGAGAGAGGTTACA[C/T]TTTATGATGGGATCA | 448987 |
rs32405974 | snp | A/G | 0.455 | 0.143091 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26776598 | ATCCAAACTATTTTT[A/G]TTTTCCAAATGCATC | 448987 |
rs32417872 | snp | C/G | 0.375 | 0.216506 | intron-variant | Fbxl7 | Mm_Celera | 15:26545222 | TATATTTGGTCCAGG[C/G]AATGGTACTATTAGG | 448987 |
rs32423617 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26661241 | ATTCCTAAAACAGAG[C/T]TGTTCATTTGAGGCT | 448987 |
rs32427130 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26607161 | AATAAGTTTATAATC[C/T]TGGAACTGGGAATTC | 448987 |
rs32427335 | snp | C/T | 0.5 | 0 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26684973 | GCCCCAGTGGCTCCC[C/T]CTCTCTTCCTGCTGT | 448987 |
rs32427342 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26605778 | ACTTTCTAAATAACT[A/C]GGTGGGGCTTCTGTG | 448987 |
rs32428158 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26702484 | AGGTAGGCTGTGTTC[A/G]GGGAGGGAGTGTCCA | 448987 |
rs32431485 | snp | A/T | 0.46875 | 0.121031 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26780725 | TGTGAAGTGTTTCAG[A/T]TCTACCTAAAGTTAT | 448987 |
rs32434893 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxl7 | Mm_Celera | 15:26811126 | CTTAGATAGCATGTG[A/G]TTCACATACATACAT | 448987 |
rs32437277 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26627782 | AAATGAAACATATAT[C/T]ACACTTTAATCTAAA | 448987 |
rs32443671 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26781164 | GCTCTAATTTCTCTT[A/G]TTTTATAGGCTGAGT | 448987 |
rs32444031 | snp | C/T | 0.455 | 0.143091 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26791725 | GATTGGCATAGAGAG[C/T]CTCTTACCAACTCAG | 448987 |
rs32448922 | snp | G/T | 0.32 | 0.24 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26622749 | TTGCTATGGGCATAG[G/T]CTTTAAGACCCTCAT | 448987 |
rs32449073 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Fbxl7 | Mm_Celera | 15:26619805 | ACTTTTAAGTCACCC[A/G]ACATAGCTTATAGGT | 448987 |
rs32449413 | snp | A/C | 0.5 | 0 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26623276 | TTCTCTATGTGCATA[A/C]GTGTGCGTGCCTGCA | 448987 |
rs32449569 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26700129 | AACTGCTACACTGTC[A/G]GCATGAGATTTCTGG | 448987 |
rs32449573 | snp | C/T | 0.375 | 0.216506 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26624321 | TGACTTTTCCCCATT[C/T]GAGCCCTGGGTTCAT | 448987 |
rs32452769 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26784405 | GGGGAGAGGAAATCG[A/T]AGGTACTCCTGATTT | 448987 |
rs32452976 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26608253 | AAGTGGTAACATGTT[A/G]TGGGTCTATGTTGAT | 448987 |
rs32460197 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Fbxl7 | Mm_Celera | 15:26549842 | AAACTCCATCATAAG[C/T]CATAAAATGCAGTGC | 448987 |
rs32466952 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fbxl7 | Mm_Celera | 15:26690719 | AATGGTGTTTTCAAA[A/G]ATTTTATATATACAC | 448987 |
rs32467014 | snp | C/T | 0.42 | 0.183303 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26618285 | TGCCTCTGAATGTAG[C/T]TCATGTCTTCAAGAT | 448987 |
rs32467278 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fbxl7 | Mm_Celera | 15:26554762 | ACTCTCCCCTGGCTT[C/T]ACTTTTCCTCACTCT | 448987 |
rs32471365 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Fbxl7 | Mm_Celera | 15:26584896 | GGGCAACTACTATCA[C/G]TAGTACAGGACCATC | 448987 |
rs32471769 | snp | A/G | 0.48 | 0.0979796 | intron-variant, nc-transcript-variant | Fbxl7, LOC105245899 | GRCm38.p3 | 15:26730002 | CTGGGAAGGGGCTAA[A/G]GCTAGGGAGCATTCT | 448987 |
rs32473535 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26721767 | TGTGAACATATATAT[A/G]ATGAAACTACTTAGT | 448987 |
rs32477660 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Fbxl7 | Mm_Celera | 15:26549075 | CAGCTATAGTAATTA[C/T]CAGTGATTTGAAAAT | 448987 |
rs32480209 | snp | A/G | 0.5 | 0 | intron-variant | Fbxl7 | Mm_Celera | 15:26885348 | TTTCTTTGGTTGGTG[A/G]TTTAGTCCCTGGGAG | 448987 |
rs32480641 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Fbxl7 | Mm_Celera | 15:26703292 | TTGGATCAAGTTCTC[A/G]ATCGCTGGACACAAA | 448987 |
rs32481626 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26622090 | CCTGGGCCAGTGCTC[C/T]ACCTTCTAGAGGGTA | 448987 |
rs32483813 | snp | A/G | 0.5 | 0 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26871718 | TGCCTCTGCCTCCCG[A/G]GTACTGGGATTAAAG | 448987 |
rs32485282 | snp | C/T | 0.5 | 0 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26767285 | GTAGGCTACAATTTG[C/T]TCGCTCTCAGAAATT | 448987 |
rs32490753 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26779897 | AGAGAGAAATAAATT[A/G]ACATATCAAGACAGA | 448987 |
rs32491365 | snp | C/T | 0.375 | 0.216506 | intron-variant | Fbxl7 | Mm_Celera | 15:26828620 | GCGGTCCACAGAATA[C/T]ATTTCTATATAAAAT | 448987 |
rs32494431 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26601870 | AACTGTGGTGAGACT[C/T]TCCAAATGGACACAT | 448987 |
rs32495249 | snp | C/T | 0.492188 | 0.0620098 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26750770 | CTAGGGATATTCTTG[C/T]TAATAAATATGAGGC | 448987 |
rs32497302 | snp | G/T | 0.359862 | 0.224567 | intron-variant | Fbxl7 | Mm_Celera | 15:26693011 | CATAAAAATAAACAC[G/T]CAAAATTTGACCCAA | 448987 |
rs32506033 | snp | G/T | 0.475309 | 0.108333 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26624995 | TTAATAATAAACAGT[G/T]TCCTAGATTGGAGCA | 448987 |
rs32510880 | snp | G/T | 0.484429 | 0.0868505 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26715677 | TTTTTTCTTTTTAAC[G/T]TATGTTTAAGCACAT | 448987 |
rs32511366 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26751994 | AATCCTTATAATGGT[C/T]CTTTGGTTGCATGCA | 448987 |
rs32515891 | snp | A/T | 0.498615 | 0.0262793 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26747300 | CACAGCTGGATCTTC[A/T]TAGTTTTGGAACAAA | 448987 |
rs32518308 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26862585 | TTCTGACTAGTTCCC[A/G]TGAAGGTGAGCTAGT | 448987 |
rs32524177 | snp | A/T | 0.387812 | 0.208586 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26614927 | TATCTTATGTAAAGA[A/T]GTTGTGTTGTTCATG | 448987 |
rs32524587 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Fbxl7 | Mm_Celera | 15:26666456 | TCAAAGAGAAGCCAC[C/T]TCTGTTAACATGCAC | 448987 |
rs32525281 | snp | A/G | 0.5 | 0 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26774553 | CCCCACCCTGGAATC[A/G]ATCCCATAATCAGCT | 448987 |
rs32525727 | snp | A/G | 0.5 | 0 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26726751 | TGAGCCAGGAGAAGG[A/G]GCCCAGTCCAAAAAC | 448987 |
rs32526261 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26588835 | TGTATCTTATTTGTC[A/G]TGCTTTTTGATTTCC | 448987 |
rs32526975 | snp | A/T | 0.32 | 0.24 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26869002 | TGTGCACATGTATAT[A/T]GGTGTACACACACAG | 448987 |
rs32529053 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26663483 | TTCCATAAACACATG[C/T]GTGTATAAACATATG | 448987 |
rs33858492 | snp | A/C | 0.475309 | 0.108333 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26588597 | AGGAATGTTCTTCTG[A/C]GCTTCTGGGCAAATA | 448987 |
rs36241051 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Fbxl7 | Mm_Celera | 15:26591236 | TCCTGGGATCTTTTT[C/T]CCTGGTTTCCATGTG | 448987 |
rs36241419 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26703034 | AGAAGTTGTGATAAT[A/G]ATCTAGCTGAGAGAT | 448987 |
rs36241729 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26707267 | ATGTTCTAGCTCTTG[C/T]AGAGGATCCAAATGG | 448987 |
rs36242244 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26613343 | AGACCTGCACATTGA[G/T]GAGAGAGGATTGGCC | 448987 |
rs36242809 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26590956 | AGGAGGTAGAGGCTG[A/G]CATAGATAGACTCAT | 448987 |
rs36244035 | snp | A/T | 0.375 | 0.216506 | intron-variant | Fbxl7 | Mm_Celera | 15:26642506 | GTGATAGTGGTTTTA[A/T]ACATCTAGTTACCTT | 448987 |
rs36244424 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26624500 | TTTTTCTGTCTCCAG[C/T]CTTTTAAACACGCTG | 448987 |
rs36245181 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Fbxl7 | Mm_Celera | 15:26601354 | TTACAATCCATTGCA[A/G]TTTGGCGTTCTGTGA | 448987 |
rs36245679 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26578736 | CTTTCTTGCACAAGG[C/T]CACAGACAACCATGA | 448987 |
rs36255358 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26611749 | AGGATCTAAGCCATG[C/T]TCACAAAGCCAATTT | 448987 |
rs36256753 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26705969 | AGAAGTGAAAGAGTC[C/T]ACACATAGACCCAAG | 448987 |
rs36257216 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26649553 | TCACTCATGCAATGC[C/T]ATCAGTTATTCTCAA | 448987 |
rs36258642 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26795919 | TAATTAATTTCTTCA[A/C]ACACATCCAAGTTCC | 448987 |
rs36263239 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26693975 | TTTGAGGCAAAATAT[A/G]TCAATCCCTGCTCTG | 448987 |
rs36266088 | snp | A/C | 0.32 | 0.24 | intron-variant | Fbxl7 | Mm_Celera | 15:26591729 | AATGTACTGAAATGG[A/C]AACCATGAGTTTGAG | 448987 |
rs36267230 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26799721 | ACTTGAAACTAATCT[C/G]TTCTCTCTTGAAAAT | 448987 |
rs36267297 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26793224 | GGATTTCTTACCCCT[A/C]GAGAACCACTTTTTA | 448987 |
rs36267464 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26740495 | ATTGTAGCAAAGAAG[A/G]AACTGTAGAAAGAGA | 448987 |
rs36268015 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26616252 | AATATAGATATGGAT[G/T]TCACCTTGCTGATAG | 448987 |
rs36268525 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26611787 | AAGGAAAATAAGTGA[A/G]TGAGCATACCTCATA | 448987 |
rs36268659 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26562231 | GGTATGGGTCAGTTT[A/C]TAGGGACACAGTTTG | 448987 |
rs36272881 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26621181 | AGAGACCATGATGAG[C/T]TCAGAGGTCTGTGAT | 448987 |
rs36273281 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26575649 | TTAGCACAAGAGTGT[A/G]GATTTGGAGTTAAAC | 448987 |
rs36274660 | snp | G/T | 0.375 | 0.216506 | intron-variant, nc-transcript-variant | Fbxl7, LOC105245899 | Mm_Celera | 15:26735899 | TCTTCATATGAGAAA[G/T]TACCCAAATACCCAT | 448987 |
rs36274753 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26553869 | TTCAAAGTTTTGGAG[A/G]GATTAAGGATTCCTC | 448987 |
rs36275085 | snp | C/T | 0.32 | 0.24 | intron-variant | Fbxl7 | Mm_Celera | 15:26641922 | CTATGATAAGGAAGA[C/T]TCCACTGTGGTTGCA | 448987 |
rs36278927 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26612607 | GGTTAGCAGACAGAC[A/G]TAAAATATCACTAAT | 448987 |
rs36279426 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26809644 | AGCAAATAAATCATG[C/G]AACAGTCTCTGCACA | 448987 |
rs36282116 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26556793 | TTAAGGGCAAATTAA[C/G]TACCACATAATCACA | 448987 |
rs36282829 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26607358 | AAGTCTTGTTTTCTA[A/G]CAGATTCTATTGATT | 448987 |
rs36283395 | snp | A/T | 0.486111 | 0.0821678 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26601635 | TACTGAGAATGTGAG[A/T]TGCAAACCACTGCCG | 448987 |
rs36283687 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26800053 | AGTTGCATTTGATAA[C/G]TAAGCTGAAGAATTG | 448987 |
rs36284292 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26620236 | TTGGTTACTGAGGCC[C/G]CAGAGCGGTGCTTCC | 448987 |
rs36287507 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26744900 | GAACAGATGGATCTA[C/T]AGTCAGCTACACATT | 448987 |
rs36289070 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26574987 | TTTATATGTTGGTGA[C/T]GTTTCCCAGTTGAAC | 448987 |
rs36290149 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26719394 | AGAAGAGCCATGATC[A/G]CTGACATCACATAAG | 448987 |
rs36291211 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Fbxl7 | Mm_Celera | 15:26557166 | GAGATGCAGAAACCA[C/T]GTAGAGCCAAGCTCA | 448987 |
rs36294404 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Fbxl7 | Mm_Celera | 15:26692470 | CCCAACTGTCTGGAC[A/T]ACTTGTAAGCATCAA | 448987 |
rs36295594 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26749293 | AGAGAAGTAAGGTTG[C/T]CAATAGAGGATCAAG | 448987 |
rs36296007 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26719417 | CACATAAGGACCCTC[A/G]GGACATCTAACTTTG | 448987 |
rs36297308 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26718218 | CCACCACTGGCTTCC[A/C]TTGCTTTCCAACCTA | 448987 |
rs36298055 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26617064 | CCCTACAGACCACAT[A/G]GTAACATTTGATTGG | 448987 |
rs36300562 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26795478 | AACCATTAAGATTTA[A/G]AGCATCATAGAATTG | 448987 |
rs36304452 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26796560 | CAGCATCTCATTTCC[A/G]ACTATGCACGGGCTG | 448987 |
rs36304681 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26789969 | GCTCGTAAATAAGGA[A/C]CTCTCAGAATGAAAC | 448987 |
rs36306457 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Fbxl7 | Mm_Celera | 15:26596204 | GCTCTGCTTCTGGCG[A/T]GTTTAGGGTTTATTA | 448987 |
rs36311786 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26594334 | GGAATGGTGAAAGGG[C/T]TTTGTTTTCCTCTCA | 448987 |
rs36311804 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26759864 | ACTGACAGGTCACAG[C/T]GCACCTTTTAAATCT | 448987 |
rs36314442 | snp | C/T | 0.124444 | 0.216185 | downstream-variant-500B | Fbxl7 | Mm_Celera | 15:26540173 | TAAAATGCAAAGCTA[C/T]GAATTCCACAATCTC | 448987 |
rs36315648 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26635185 | CCAAGCACATTCTCT[C/G]AGCAAAGAGGTGATG | 448987 |
rs36317540 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26614210 | CTATATTACCAGAAA[C/T]TGAAAATAGACTACT | 448987 |
rs36318001 | snp | C/G | 0.231111 | 0.249285 | utr-variant-3-prime | Fbxl7 | Mm_Celera | 15:26541330 | GTAACAAATGTAGCA[C/G]GCTTGGCTTGCAGCA | 448987 |
rs36320440 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Fbxl7 | Mm_Celera | 15:26653907 | AATTGGAATTTACTT[A/T]AAAAAAAAATGTAGT | 448987 |
rs36321926 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26749473 | GACTTTGCTACATGA[A/G]ATCTAGCCTCAAGGA | 448987 |
rs36322238 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26560025 | CAAAAGAAATCAAGG[C/T]TCAGTTTCAAAGTCT | 448987 |
rs36324111 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26622274 | AGACGTGTTTGCCAG[C/T]AGTGTGATCAACTTC | 448987 |
rs36324377 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26712785 | TCAAGAAGGGTTCTT[A/G]CCATTACTAATGAGA | 448987 |
rs36324412 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26789709 | TCATTTCCAAGTAAG[A/T]GGCTAGAACACAAAA | 448987 |
rs36328152 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26621194 | AGCTCAGAGGTCTGT[G/T]ATTGAGAGAAACTAA | 448987 |
rs36328158 | snp | A/T | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | Fbxl7, LOC105245899 | Mm_Celera | 15:26736899 | AAGAATGCCATTGCC[A/T]AAATATAATCAAATG | 448987 |
rs36328168 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26801764 | TAGGAAGTACTGGAT[C/T]CTGAAGGTAATGAAC | 448987 |
rs36328772 | snp | A/C | 0.408163 | 0.193609 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26617846 | CGAGGATGGGTAGAA[A/C]ATGTGATTTCAGGTC | 448987 |
rs36331134 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26561446 | TAACCACTATTTCAA[G/T]TAAAAGCTCCACGAG | 448987 |
rs36331924 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26596012 | TGTTAGGTAAACCAC[A/T]GACTGAGGATTAAAT | 448987 |
rs36332690 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26595721 | TGTTTCTCAGTGAAA[A/T]TCTTCAACCCAGCTC | 448987 |
rs36336866 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Fbxl7 | Mm_Celera | 15:26555519 | GAAACAGATGACTCA[C/T]GGAGCTATCAAGATA | 448987 |
rs36337219 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26797929 | CCTGATTGGCTGAGT[A/C]TGATCTCACCTCAAG | 448987 |
rs36338503 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26583971 | CAAGGCAAACTTCCA[C/G]CTTTCTGAAAATGGA | 448987 |
rs36341888 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26623863 | GTTAAACCAATTTGA[A/G]ATTAGTGTTTCTTAG | 448987 |
rs36341890 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26595181 | GTCTGAAAGAATGAG[A/G]TCCCATATACAGATA | 448987 |
rs36342049 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26638707 | ATTAGAACTCTTTAC[A/T]TTTTAAGACCTACAG | 448987 |
rs36342280 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26595574 | GCTAATCCAAGCGCC[A/G]TTCAAGGTGGGTTAA | 448987 |
rs36343452 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26711928 | CTGAGTTGTGGTCTT[C/T]CTAAAATCCAACAGA | 448987 |
rs36345051 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26636822 | AATAATGGTACTTTT[C/T]AGGAAAGCATGAAGT | 448987 |
rs36346043 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26544007 | GTTATTTGTCAATTT[A/G]GCTGAATTTTGAGTT | 448987 |
rs36347239 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26553487 | CAACTCCAAAGTTGC[A/T]CTGTTTCTAGGGCGA | 448987 |
rs36351220 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26592917 | GGACGTTTTTGGACC[G/T]TTTATAACTTTGCAT | 448987 |
rs36352206 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26708531 | GCATTAGAAAGAAGA[A/T]TTGTGGACAAATTGC | 448987 |
rs36356309 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26791427 | AACTTCACAGCACAG[A/G]ACAGTGCAAAGTCTC | 448987 |
rs36357502 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26753377 | TACTAGAATATTGAA[A/G]AATAGAGTAACCAGA | 448987 |
rs36362276 | snp | C/G | 0.489796 | 0.070696 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26591768 | GCATTAACAAATCTA[C/G]ACTGCTTTTCTGGCT | 448987 |
rs36362535 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26694313 | GAATCTGAGGACTGC[A/G]AATCAGTGTATGGTG | 448987 |
rs36362548 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Fbxl7 | Mm_Celera | 15:26553422 | CAGGGGCAAATTCAC[A/C]GCATGTTCCCGTTCT | 448987 |
rs36365059 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26634412 | GGGGTGCTCACTTTT[G/T]GCTGAGAGTGATACT | 448987 |
rs36365198 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26716669 | TTTTCATGTGCACCT[C/T]GGAATAAACTAAGAT | 448987 |
rs36365409 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26585026 | TCTGGCTATTATAAG[C/T]TATGAGTGTCCTGTT | 448987 |
rs36367388 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26592148 | CTACATCTCTATGAG[A/G]GTATTAGGATTCAAT | 448987 |
rs36367443 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26577396 | CAGAAATTTACAAAG[C/T]GCTGTGCTGTGCACC | 448987 |
rs36368224 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26576293 | ACATGGGCAGAGACT[C/G]TGCAGACTGGAACTG | 448987 |
rs36373807 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26575974 | CGCTCCTCGACAATG[C/T]TTCTAATTCTTGGGC | 448987 |
rs36374292 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26741555 | TGCATGGTAGCAGTT[C/G]TCTAATCCAACAGTG | 448987 |
rs36374840 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26636623 | TTTCCTGTATTGGTT[A/G]CTGCTATCACATGCT | 448987 |
rs36377523 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26696983 | CACTTGTGAATGGTA[C/T]AGGTTCCACCTGACA | 448987 |
rs36378615 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26649616 | TCCCCTTTATCCAGC[C/T]TAAATCCCAAATAGC | 448987 |
rs36379128 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26658145 | ATGAGGAGAATAACA[A/C]GGGCTCCTTTGTAGG | 448987 |
rs36379219 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26813729 | CTCTATAAGTACAGA[C/T]AGGGAATTAATAAAT | 448987 |
rs36379743 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26701540 | TGAAAAACACTGTCA[A/G]TAAATAATAGTATGT | 448987 |
rs36380929 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26585616 | CCTAGCGTCCATCCA[A/G]CTTCAACTACAAGTG | 448987 |
rs36381297 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26657835 | GTAAAATACAATACA[C/G]TTCACTAGACATTTG | 448987 |
rs36383463 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26692548 | TGATTAAAACCATCA[C/T]TATCATTTGTTATCT | 448987 |
rs36385340 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26814217 | CAGCTTCATTCCTGG[A/C]TAAGAACCAGATACT | 448987 |
rs36386797 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26803090 | CACACTTCAGAGGCA[A/G]GTGCTTTCCTGTGTG | 448987 |
rs36387003 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26798679 | GGGATTTGTAGCAAC[A/C]GCAAATGGAGCAAGA | 448987 |
rs36387702 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26596314 | CCTTAAAATATCATT[C/T]GAATGTACTGTGCTA | 448987 |
rs36392836 | snp | G/T | 0.426035 | 0.177515 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26688721 | GCAACCATCAGCATG[G/T]TGGAGATTCCACTAA | 448987 |
rs36393411 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26586266 | ATGAGGTCTACAACC[A/G]TGAGCTCTTTAGACG | 448987 |
rs36398796 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26775074 | GTGCATTATTCTCAT[A/G]GCAAGGAAACATGAA | 448987 |
rs36399617 | snp | C/T | 0.132653 | 0.220748 | intron-variant, nc-transcript-variant | Fbxl7, LOC105245899 | Mm_Celera | 15:26736060 | AACTGAAGAAAATGC[C/T]CACAGAGAAGTGGAC | 448987 |
rs36402746 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26545173 | CCCCCTAACATTGCT[C/T]ATAGCCCTTAGATGG | 448987 |
rs36404070 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26717564 | TGGGATAATCTCCCT[A/G]AAGGTGATGGCAGGG | 448987 |
rs36404160 | snp | A/C/G | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26558186 | ATAGTCATCTGTGGA[A/C/G]TAAAGTAAAAGTTTG | 448987 |
rs36405548 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26625990 | ACCGTTTCCTGGATT[A/G]ATGCGATGTTAGTCA | 448987 |
rs36406285 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26755592 | ACTTAATACTTGAAA[C/T]TGTAAGGAGTCTACA | 448987 |
rs36406726 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26776531 | AAAGCAGGCACCCAC[A/G]ACATTTTTGTTTCAC | 448987 |
rs36407630 | snp | A/G | 0.18 | 0.24 | intron-variant | Fbxl7 | Mm_Celera | 15:26596550 | AATAGGGCTGAATAC[A/G]GCATAACTTAAAGGC | 448987 |
rs36407677 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26620620 | TTCACACCAAGGCAA[C/T]GAATCCTCATCCTTT | 448987 |
rs36408014 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26702037 | TATAGCTACCAATGC[A/C]TGACCTCACAGCTCC | 448987 |
rs36408392 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26626582 | GTAATTTTAAGTTGC[A/G]TTAGCTTTTTCATTT | 448987 |
rs36409558 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26584532 | CCCAAAGACATGATT[A/C]ACTTTAGCTCAAAAA | 448987 |
rs36409672 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26789689 | TCAGTCACACACTAA[A/G]CCACTCATTTCCAAG | 448987 |
rs36412534 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26595297 | CTCAGTAACTGTAAC[C/T]GACTTTACTCTTTTC | 448987 |
rs36413333 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26597787 | AACTCTTGGGTCCTC[A/G]CCATCTACAGTCAGC | 448987 |
rs36415063 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26719562 | AGCAGGCTTACGAGC[C/G]CTGTGGTATTTAGAA | 448987 |
rs36416476 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26793667 | GTTACCAAGAGACAG[C/T]AGTAATAAATTATGT | 448987 |
rs36416756 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26563681 | TCAAGGAAAACAGTC[A/G]AGTTTTTATAGTGTG | 448987 |
rs36416893 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26592035 | TTGTCTTGACTCTGC[A/C]GATACACAGTCTAGG | 448987 |
rs36417070 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26544108 | AGTCACACTTTATTT[C/T]CTTTGTTTTAAAATG | 448987 |
rs36417781 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26556708 | CCAAGGCTACTGCTC[A/G]ACCAGAAGACACTCT | 448987 |
rs36418111 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26628229 | AATGAGGTTAACATC[A/G]TCATGAAAGCACTAA | 448987 |
rs36419797 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26567620 | TACTGGGTATACTTC[A/C]AAGTCCTTTTGACGT | 448987 |
rs36421406 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26715398 | CCCAACTTCTGAAAC[G/T]TGCATTATGAAAACC | 448987 |
rs36424576 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Fbxl7 | Mm_Celera | 15:26797346 | CTATCTCATAGCAGA[C/T]AGATAGTTCAGAGGG | 448987 |
rs36425435 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26584931 | AAGGCGGCTTCAGAT[C/T]TAGCAAAGGGATGGC | 448987 |
rs36425823 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26562061 | GGAAACTTCATGTTC[C/T]GTAAATTACCCCTTT | 448987 |
rs36426246 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26707095 | TGAAACCGGCTTTCC[C/T]TTCCAGAATCAATGC | 448987 |
rs36427164 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26599463 | TGACACAATCCTCAC[A/G]AGGTCCCTATGTCCA | 448987 |
rs36427596 | snp | A/C/G | 0.132653 | 0.220748 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26770786 | AAAAGCAAACCTGTC[A/C/G]AATCTCTGGCTTCTG | 448987 |
rs36428676 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26792962 | TGGGTCTGTGTGGAG[A/C]TGGCAATGGGCGCCT | 448987 |
rs36428703 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26775391 | CTCAAGATGCTCTTT[A/C]CCCTGAAACATGAAT | 448987 |
rs36430586 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26814454 | AACCCCAGCCACATG[G/T]ATCACAGGTACTTTA | 448987 |
rs36432911 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26696602 | TGTGGTCTTTGCAAA[A/T]ATCCCATTTTAGACA | 448987 |
rs36432945 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26793901 | CATGAGAACATACTC[C/G]GATGAGTGCTTCTGA | 448987 |
rs36435774 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26639783 | TTAGGTTTCTCAAAC[C/T]GTCTTTGCTCTGAAG | 448987 |
rs36435917 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26548055 | AAGCTCTTCTCCAGC[A/G]TTAACAATTCTGAGT | 448987 |
rs36436471 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26588791 | AACCCCATAGCTGGT[C/T]AAGACACATTTATGA | 448987 |
rs36436723 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26543878 | GAAAGGGCACTTGGT[A/T]CCAGAGAGCCATAAC | 448987 |
rs36441517 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26559357 | CCTTGCTTGCAACAT[A/G]TCCAAAAGAAGATCA | 448987 |
rs36442162 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26585056 | TTGATATGCTGACAC[A/G]TTTGCATAAATTCTG | 448987 |
rs36444967 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26615053 | AATGTGGTGTCAAAA[C/T]AATGTTTCTCAGAAT | 448987 |
rs36445342 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26574990 | ATATGTTGGTGACGT[A/T]TCCCAGTTGAACACA | 448987 |
rs36446229 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26578906 | GAAGAATAAAGTACC[C/T]AGATCAGCAGAACTG | 448987 |
rs36449598 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26586981 | CCATGCTTTTCAATT[C/T]CATCCTATAACCAAA | 448987 |
rs36449605 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26758564 | ATGGCCAACTTCAAC[A/G]TTCATTAGTAGGGTA | 448987 |
rs36450246 | snp | A/G/T | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | Fbxl7, LOC105245899 | GRCm38.p3 | 15:26736552 | GTGCTGTGATGGGTC[A/G/T]TCATTTTCCTTAGCC | 448987 |
rs36454706 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26803943 | ATTGAGAGTGTGTAA[C/G]AGAGACCCATCCTGG | 448987 |
rs36456750 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26795422 | GGTACTCACTCAACA[C/T]TCACTGTGTGCCAGC | 448987 |
rs36458582 | snp | C/T | 0.132653 | 0.220748 | intron-variant, nc-transcript-variant | Fbxl7, LOC105245899 | Mm_Celera | 15:26733780 | AAAATTACACTGATA[C/T]ACTTGTTAATCAATT | 448987 |
rs36458597 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26637756 | CATGGTGAACACAGT[C/T]GTGGATGAAACATGG | 448987 |
rs36460158 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26774606 | GGCCACCCACGGGAA[C/T]AAGATCAACCTAACA | 448987 |
rs36460452 | snp | C/G/T | 0.132653 | 0.220748 | intron-variant, nc-transcript-variant | Fbxl7, LOC105245899 | GRCm38.p3 | 15:26732793 | GGCACAGACCTGTAT[C/G/T]ACCCAGATGATTGAC | 448987 |
rs36461252 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26621313 | GTGGAGCTACAACCT[A/T]CACGTGTCCGTTCAT | 448987 |
rs36461497 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26758185 | CCAGAATGTAGAACA[C/G]AGTTAGCAACTGACT | 448987 |
rs36463225 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26641111 | CATACTCAGATGGCC[C/G]TGAGCCCCATGTGGG | 448987 |
rs36464547 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26623817 | ACACCAGCTCTCCAG[C/G]CTGCCACCTCACTTT | 448987 |
rs36465265 | snp | G/T | 0.459184 | 0.136902 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26626933 | ACATACATTTCATGG[G/T]CTCTAAGAAGCAGTT | 448987 |
rs36465318 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26585383 | ATGTATTCTTGGAGC[A/T]GATCTAACCCAAGGG | 448987 |
rs36470497 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26590236 | TGTGCAAAGCAGACC[C/T]GTACAGCCACGCTCT | 448987 |
rs36475452 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26580262 | CTGAAAATATGTTCA[C/T]TTTTGATATGTGGCA | 448987 |
rs36475823 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26622470 | GGTGATGATGAGGCT[C/T]CATGTTATGCAAAGA | 448987 |
rs36476396 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26793174 | CTGCTATTAAATTCT[A/G]AGAGGATATATCTAC | 448987 |
rs36479822 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26551805 | CAGGGGCATCACTGT[A/G]GCTTTTACTATGGCT | 448987 |
rs36480047 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26560876 | ACAACAGCTATTGGT[C/T]AGGGAAGCTTGTTTT | 448987 |
rs36480827 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26792733 | TGAATACTAGCACAC[C/T]AGGACTAATGACTAG | 448987 |
rs36481065 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26655614 | AACCCATGACATGGT[G/T]CAGTTTTCTGTCTTT | 448987 |
rs36481703 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26576864 | GCGTTACATAGTCTC[A/G]AATTTCAAGGTTTGT | 448987 |
rs36482104 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26590507 | AAAACTTGACAATTG[C/T]ATATTCTGTGTCAGG | 448987 |
rs36484468 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26625051 | CAGTTTCAGGCTTTG[C/G]AGACCATTCTTTCCC | 448987 |
rs36486495 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26803247 | TGACGAATTCAGGCA[A/G]TTGGAGGTAGTTTAA | 448987 |
rs36487059 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26742229 | TACTCTCAGGTTTGC[C/T]GGGATAGCAGGCTGA | 448987 |
rs36488005 | snp | A/G | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | Fbxl7, LOC105245899 | Mm_Celera | 15:26734375 | GTCCAAGCTTAAAGT[A/G]ATATAGAGGCATTCT | 448987 |
rs36488389 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26653455 | GTAGAGGGAATATTT[C/T]AAAGGGAAAGATGAA | 448987 |
rs36489217 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26653512 | ACCCTTTGATGACTC[A/T]ATTGTGGAGAAAAGA | 448987 |
rs36490989 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26750356 | CTTAATGTACAACGC[A/C]GATCCTCACACTTCT | 448987 |
rs36491016 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26590637 | AAGGCTATCACTTAA[C/T]CTCAGCAGCAATTAT | 448987 |
rs36492795 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26662358 | GAGACATATGGCCAG[A/T]TTCTGCCTTTGGCTG | 448987 |
rs36492893 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26704417 | ATGAAGCACTAAGAA[A/G]GGAAGAAAGTAGATG | 448987 |
rs36493515 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Fbxl7 | Mm_Celera | 15:26593364 | AGATATTTAGTAACA[A/G]ACTCTGTAGATGAAA | 448987 |
rs36493543 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26591401 | GTGTAGATTCTTGAA[A/G]CCAGGGATGGTTTGC | 448987 |
rs36493582 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26815822 | CATGGGAGAGAACAC[A/G]AATGTGGTCAACAAG | 448987 |
rs36499524 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26703846 | AGACAAGCATCCTCA[C/T]TTAGATTCAGATCCT | 448987 |
rs36502166 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26799173 | TACAAGGTGGTAGGT[A/G]TTGGAGGTAAAATTT | 448987 |
rs36502792 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26573759 | CTCTAGGCATAGTAA[A/T]CAGAAGGTTCAGATA | 448987 |
rs36502884 | snp | A/G | 0.32 | 0.24 | intron-variant | Fbxl7 | Mm_Celera | 15:26772649 | CTCCCTGTCTTATAT[A/G]ACTGTTAAGTTATAC | 448987 |
rs36503087 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26625977 | GACAGGATTCTTCAC[C/T]GTTTCCTGGATTAAT | 448987 |
rs36503130 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26589097 | CTAATTACTGCTGTG[A/T]CTGATCCATGTGCTA | 448987 |
rs36503950 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26814426 | TGGTGATCCTCATAT[C/T]CCATAGCCAATCAAC | 448987 |
rs36504174 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26758968 | CTCATTGATTATTAG[C/T]TGGGATTGCTGTGGA | 448987 |
rs36504567 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26656922 | GAGGCACATGCCAAG[G/T]TTGGAAGGTAATTGA | 448987 |
rs36505640 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26574932 | TTTGACACATCTATT[A/T]CTGTGACAGATATCA | 448987 |
rs36508359 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26561384 | TATAGCTGCCATTAC[A/G]TCGCTCACACTCTTG | 448987 |
rs36508424 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26624687 | TACAGCTGTGGGACC[C/T]TCTGGAGCCTCAAGC | 448987 |
rs36508853 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26595552 | TGACTTCCTTGTCTG[A/G]GTGTGTGCTAATCCA | 448987 |
rs36509543 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26561729 | CAGACGTTTGTTCAC[A/G]TCTCTCAGGTAAAAG | 448987 |
rs36509711 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26755819 | GGAATTGCCAATTTC[A/T]TCTGGCCTGATTTGG | 448987 |
rs36510779 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26655527 | CGGATGTGCTTACTT[A/T]TTGAACAAGTTCATC | 448987 |
rs36511889 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26771358 | TAAACCTTTCCATAT[A/G]TGTAGGAATGATGCT | 448987 |
rs36513603 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26653016 | CACCTTTGAAAGATG[A/G]GAAAGATTCAGCTTA | 448987 |
rs36514362 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26775274 | GGCAGCTTCTCTTCA[C/T]CAAGCACACTGCTCC | 448987 |
rs36516281 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26705943 | GTGGTTTTTCAAGAT[C/T]GGGTTGTCCCAGAAG | 448987 |
rs36516806 | snp | A/T | 0.408163 | 0.193609 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26597257 | TCCTGGGATCATTAT[A/T]TTTTAGAGCATACAG | 448987 |
rs36516829 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26798567 | TTGTCACGCCATGGT[A/G]CATCACAGAGGCCTT | 448987 |
rs36519502 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26641250 | TTATACATACACAGA[G/T]GAGGCACAACAGAGA | 448987 |
rs36520461 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Fbxl7 | Mm_Celera | 15:26571757 | TCTCATGTCACTGAA[C/T]GGAATTGCAGTTCAT | 448987 |
rs36520572 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26580131 | CAATATTTATGCTTA[C/T]GAGACACATTGAGAT | 448987 |
rs36523207 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26612058 | GTAATTTATAATTAA[A/T]CTTTGCTATAACAGT | 448987 |
rs36523303 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26771659 | CAGTGAAGGTTAGCT[A/G]AATGGATTAACCAGA | 448987 |
rs36526604 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26601917 | GAAGGACTGTGAACC[A/G]CTCTGGCAGCATTTC | 448987 |
rs36526745 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26705330 | AACTGTGCAGTAACA[C/T]GTGTGCAGAGATAAT | 448987 |
rs36529765 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26578523 | GGTTGTGGTAGTCAA[C/T]TTTCATTATCAGTTT | 448987 |
rs36536009 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26555197 | TCAGGCTGACTTTCC[A/G]AAAGGTACAGAATTC | 448987 |
rs36536422 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26803721 | CTGCTGTTAACAACA[C/T]TGTAGCATAGAGCTC | 448987 |
rs36536838 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26744808 | ACAACAGTGAATCTA[C/T]TAAAATTCCTGTCTA | 448987 |
rs36537826 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26773574 | AAGATATCTCTGGAT[A/G]AGATGGAAGCTCCTC | 448987 |
rs36539165 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26628786 | TCAAGAATGCTTAAA[A/C]CTACTAGGTCCCAAA | 448987 |
rs36539832 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Fbxl7 | Mm_Celera | 15:26608703 | TTCTGAGCTTTATCT[A/G]CACAGAAGCATTTTC | 448987 |
rs36541108 | snp | C/T | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | Fbxl7, LOC105245899 | Mm_Celera | 15:26736022 | AGGAAACTGGAGCCA[C/T]GAAGGTAATCAAAAG | 448987 |
rs36545937 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26599374 | ACTTAAGAACCCTTC[C/G]CTATGAATGGCTAGG | 448987 |
rs36546271 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26717271 | AAGGCAAGGAGAAGC[A/G]AGATAAGCCCAGGGA | 448987 |
rs36546420 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26601130 | CATGGCCACAGGTCT[A/G]GCCAGCTTTGATGTT | 448987 |
rs36550207 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26603736 | ACACCCTTGCATGCC[G/T]TGTCACACATTGTGT | 448987 |
rs36551428 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26741542 | AAACACTATAGGATG[C/T]ATGGTAGCAGTTCTC | 448987 |
rs36553104 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26585202 | GTGAAACTGTCAGCC[A/G]AGTATATCAAAATGA | 448987 |
rs36554818 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26772171 | GCTCTCGTGCTCCAC[A/G]GCCACACTTCCTTAG | 448987 |
rs36554862 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26632045 | TTGGCAATATAGCTG[A/G]TCTAGGTAGCCATGT | 448987 |
rs36558901 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26806070 | GATAAATGCCTCCTC[G/T]TTCTGATGACAAAGG | 448987 |
rs36561097 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26792855 | GGGATAACACGTGCC[C/T]GCGGATATTCTCGAT | 448987 |
rs36561461 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Fbxl7 | Mm_Celera | 15:26650988 | AGTGTAAGGACAGAA[G/T]GCACTTGCTGCCTGT | 448987 |
rs36561584 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26589122 | GTGCTAGATGCTTTC[C/T]TTGTGATCAAATATC | 448987 |
rs36562963 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26559494 | TGTCGCAGTGGTACG[A/G]CTTTCAATTATTCCT | 448987 |
rs36566460 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26620115 | TATTTATGACTCAGG[A/G]AAGAAATCTCCACAA | 448987 |
rs36568857 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26547855 | GTGGGTATGCATCTG[C/T]CCTTTCTCAAGAATG | 448987 |
rs36570967 | snp | A/C/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26592618 | GAGTTGCCAGACAAC[A/C/G]GCACTGAAACAGAGA | 448987 |
rs36571441 | snp | G/T | 0.152778 | 0.230321 | intron-variant | Fbxl7 | Mm_Celera | 15:26700586 | GTACACTTAATATAC[G/T]GATGTGAAGCAATAT | 448987 |
rs36572339 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26653207 | TGGTTTATAGGATAG[C/T]TCTTCACCAATACTT | 448987 |
rs36574030 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26624713 | CAAGCCTTTCATTTG[C/T]AGCAGTATAATTAGA | 448987 |
rs36577334 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26799970 | TTAATATATGTTAAA[A/G]TGTTCGTCCACTCTA | 448987 |
rs36581563 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26635811 | ATGAAATTACACCAG[C/T]GTTCTCAGTTCCATG | 448987 |
rs36583528 | snp | G/T | 0.124444 | 0.216185 | utr-variant-3-prime | Fbxl7 | Mm_Celera | 15:26542423 | GTTTGAAAATGGGCC[G/T]AAGGCTAATCCCTCA | 448987 |
rs36585623 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26793846 | AAGAATTGTGACAAA[G/T]AGCATGAGATAGATT | 448987 |
rs36588227 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26592872 | GAATGCAGGTGAAAA[C/G]GATGGATACTGGAAA | 448987 |
rs36589149 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26692524 | CAAATAATTACTGAA[A/C]GGTTCTTGTGATTAA | 448987 |
rs36590338 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26764864 | AGACAGCAGTTGAGA[C/T]AGTCTTCAAGGCTGA | 448987 |
rs36591786 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26806594 | GCTGTTCAGTGAGCG[C/T]TTATGAAGACCAAAG | 448987 |
rs36595200 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26613784 | AAAAATCTATTCAAA[A/C]TGAAGTATAGTCTTC | 448987 |
rs36595512 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26632139 | TCCATGTCCTGGAGA[A/G]TCTGACTTGCTCATG | 448987 |
rs36600593 | snp | A/C | 0.497778 | 0.0332592 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26592667 | TGGGCCATCAACATG[A/C]GGTCACACCCACCAT | 448987 |
rs36602163 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26789902 | GAATAAGTAAGAATG[C/T]GTTGGGAGCACACCC | 448987 |
rs36604094 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26621111 | ACCAGGAAGTAAGTA[C/T]GAGATTACATACGCT | 448987 |
rs36604821 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26573251 | CCAACTTTTCAACCT[A/G]AGGCAGGAACTAAGA | 448987 |
rs36606122 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26627299 | AAATCCAAGAAAGGA[C/T]CACAGCCTAACATCA | 448987 |
rs36608465 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26587457 | TAATAGTTACAGTAG[G/T]GCATTAGAACTTTGC | 448987 |
rs36609417 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26801257 | GCCATAAACCCAGTA[C/T]CTTTTTCATGACTCT | 448987 |
rs36609426 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26558015 | TGGAGCAATCATACA[A/G]CATAAGAACAATGAA | 448987 |
rs36610014 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26712034 | ATAGTGCACTTTGTG[G/T]AATAGACATACAAAA | 448987 |
rs36610804 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26618257 | CCAGAGATGCCTCCT[C/T]CTTTAGGCCTCGTGC | 448987 |
rs36611248 | snp | C/G | 0.165289 | 0.235211 | intron-variant | Fbxl7 | Mm_Celera | 15:26626309 | ATGGTTGGTCTTATG[C/G]CGTCACAGACTTCTG | 448987 |
rs36614307 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26622132 | GTTAAAGGCTGGCAG[A/T]TAAGGCACTTGATAG | 448987 |
rs36615524 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Fbxl7 | Mm_Celera | 15:26554482 | TTAGGAATCCCAAAA[C/T]AACCTCTCACTTATC | 448987 |
rs36618473 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26559466 | CATCTGCATCTCTTT[C/T]TTGTATGTAAAATGT | 448987 |
rs36619606 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26790103 | CAGTGGTCCTCGATG[C/G]AGGAAGGGTTTTCTA | 448987 |
rs36620273 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26706666 | ACAGAAAAGCAGTTC[C/T]CTCAGCCTATTTGTC | 448987 |
rs36622181 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26548121 | ATTAGCATCTCAGGC[A/G]TCTGCACTTCCATTG | 448987 |
rs36624263 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26636835 | TTTAGGAAAGCATGA[A/C]GTTCTGTGTTCCACG | 448987 |
rs36629711 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26797943 | TCTGATCTCACCTCA[A/G]GTATCAACAGGTAAT | 448987 |
rs36633412 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fbxl7 | Mm_Celera | 15:26593305 | CTTTCTTTCTCCTTT[C/T]TATTTTTAATTCTTA | 448987 |
rs36636490 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26656548 | ATCTTTACTCATGAG[C/G]ATCACAATATTTGGA | 448987 |
rs36637535 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26564983 | GGGAGCAAGAGCAAT[G/T]CACACATTTAACGTT | 448987 |
rs36643595 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Fbxl7 | Mm_Celera | 15:26561861 | CCCACATTACTTTAA[C/T]AATCTAATTTTATGT | 448987 |
rs36645588 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Fbxl7 | Mm_Celera | 15:26755955 | AGTCAGTTTAGTTGT[A/G]TCTAATTAGTTCACT | 448987 |
rs36649235 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26789810 | GCAGAACCAAAACGC[A/T]CTTAGAACATATGAA | 448987 |
rs36651972 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26709305 | AAGCAAGAAGTGAGG[C/T]AACAAGAGACAAGTA | 448987 |
rs36655257 | snp | A/C | 0.497041 | 0.0383476 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26626233 | TAATTGGGCTGGTAT[A/C]CAGTCTTTAAAAATG | 448987 |
rs36657616 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26641076 | TTGGTAACTACCACA[A/G]CAACCTTCAGGAATT | 448987 |
rs36657996 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26813289 | ATACATGCTCATGTG[C/T]CGCGCATACCAATGA | 448987 |
rs36662266 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26750821 | CAGAGAAAATACAAT[A/G]GGATACGCAATGTTC | 448987 |
rs36663825 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26747844 | GAGCAGCAGAACCTT[C/T]GCCCCTGGACTCCAG | 448987 |
rs36664934 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26557311 | ACCCTATCACAAACA[C/T]GGTGAAATGCTATAA | 448987 |
rs36666981 | snp | A/G | 0.32 | 0.24 | intron-variant | Fbxl7 | Mm_Celera | 15:26644151 | TTGTATCACACTCAG[A/G]AAAACGAGTGAGGTT | 448987 |
rs36668758 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26771580 | CCCTGGTGGGCAGGA[A/C]TGGCACGTTTCATGT | 448987 |
rs36670528 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26775100 | ATGAAAGAATGTTCC[A/G]GTCACTCATTAACCT | 448987 |
rs36670909 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26750337 | CCTGGCTTACAGGGA[A/G]GATCTTAATGTACAA | 448987 |
rs36671117 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26806376 | TTTGCTTCTCTACGG[G/T]CACTGGATGAAGGTA | 448987 |
rs36671769 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26611853 | CATCATTTACATAAG[C/T]CATTCATTCATCTCC | 448987 |
rs36672747 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26626808 | CTCCAGTACTTTCTC[C/T]CATCAGTCTTGCCAC | 448987 |
rs36673136 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26796917 | TTGAGCTCTTCTCAC[A/G]TTTCTCCTTACATTT | 448987 |
rs36674674 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26775488 | CTAGCAGAGTAGATA[C/T]GGGCTGCCACCTCCA | 448987 |
rs36675787 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26584306 | TGGCAGATATTATAA[A/G]ATTGGTTTTGATTAA | 448987 |
rs36678216 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26616865 | CACTTGACCAACGTT[C/T]TTAACCATTTTGGCA | 448987 |
rs36679461 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26583497 | TTCCAATGAAAATAC[C/T]TGGTTTAGCTCATCA | 448987 |
rs36680380 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26595079 | GTCCAGAGGGGAACA[C/T]TTTCTGCTGACAGAA | 448987 |
rs36681357 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26670291 | TGACTAATGAATCCA[C/T]TCTGAATTTCTGAGG | 448987 |
rs36686837 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26569974 | CCAAGAATCTGAGAA[A/T]GCAAGACAGGCCACA | 448987 |
rs36686898 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Fbxl7, LOC105245899 | Mm_Celera | 15:26738120 | AACAGCCTGATATTG[A/G]TGAGGTATAAATCCT | 448987 |
rs36691512 | snp | G/T | 0.32 | 0.24 | intron-variant | Fbxl7 | Mm_Celera | 15:26642623 | TCATTTTGCCAGACT[G/T]AGGAAATACACAGTT | 448987 |
rs36693885 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26794198 | TGAACCCTGCCCATC[A/G]TATGAAGATCAATAA | 448987 |
rs36697094 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26794502 | CTACATTAATAAGTG[C/T]TCAGATAATTATAAT | 448987 |
rs36697682 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26636424 | CTGCAAGCTGTTCTG[C/T]AGCCAGTAATATCTT | 448987 |
rs36698414 | snp | A/C | 0.124444 | 0.216185 | utr-variant-3-prime | Fbxl7 | Mm_Celera | 15:26540946 | CCAGATCATTTGGCA[A/C]GTCCCAGTGTCAAGG | 448987 |
rs36698448 | snp | G/T | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | Fbxl7, LOC105245899 | Mm_Celera | 15:26736275 | AAATAAGAAGGTAAG[G/T]GAAAGTAATGGCTGA | 448987 |
rs36698703 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fbxl7 | Mm_Celera | 15:26641684 | AAGTTAATGGTCTTG[C/T]GTCCAGTCATACCTG | 448987 |
rs36698961 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26796368 | GACTCCAGAGTTTTC[A/G]CAAAGCACCTTCCCG | 448987 |
rs36701456 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26709115 | TGAGCAAAACAAAAC[C/T]GTAATTCATGGCTCA | 448987 |
rs36702036 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26546315 | ATTGTGCCGTTTAAT[C/T]ATAAGATTGCATATT | 448987 |
rs36704053 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26601725 | AGTACAAGCTACTGC[A/G]TGACGGATGTCTACT | 448987 |
rs36708783 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26692685 | TAGATACTCAGAAAT[G/T]TCACCTAAACAACAT | 448987 |
rs36710073 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Fbxl7 | Mm_Celera | 15:26803452 | GCTATAATAGTGGTT[C/T]TTATAAACAAAACTC | 448987 |
rs36710667 | snp | C/T | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | Fbxl7, LOC105245899 | Mm_Celera | 15:26735608 | CATGCTATTACCATG[C/T]TGTAGCTTTCGGTCT | 448987 |
rs36714905 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26614143 | GACGTGGACTGATGT[C/G]TTCTCTCGCTTTGCT | 448987 |
rs36714991 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26775288 | ATCAAGCACACTGCT[C/T]CCAGTTGGAATTGAG | 448987 |
rs36715590 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Fbxl7 | Mm_Celera | 15:26629969 | TTGAATTAATGTTCA[C/G]ATTTTTATACACTCA | 448987 |
rs36716523 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26567865 | AACCTAATGCCGGAA[C/T]GATATGCTTAGATAT | 448987 |
rs36717308 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Fbxl7 | Mm_Celera | 15:26617878 | CAGCTCTCTTTAATA[G/T]TATTATTCTTGGTAC | 448987 |
rs36717568 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26708508 | TTTCCATGGCCACCA[C/T]GTGAGAAGCATTAGA | 448987 |
rs36720481 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26627250 | ATAGCAATAAAAAAA[C/T]TGAAAAACAGCTTCT | 448987 |
rs36723016 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Fbxl7 | Mm_Celera | 15:26557095 | GGAATGATGGGCTGA[C/G]ACAGAGCTCAGCAGA | 448987 |
rs36723608 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26617496 | ATATATGATATGAAG[A/T]TATATAAGACATAAA | 448987 |
rs36724365 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Fbxl7 | Mm_Celera | 15:26541312 | TGTGTATAAGCTTGG[C/T]CTGTAACAAATGTAG | 448987 |
rs36725789 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26794237 | CACAGCTACTGTCAT[C/T]ATTAAAAAATAACTG | 448987 |
rs36727661 | snp | C/T | 0.18 | 0.24 | intron-variant | Fbxl7 | Mm_Celera | 15:26594740 | AGTTCACTCTCTAAT[C/T]AAGATCTTCAGTTTG | 448987 |
rs36732193 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26792559 | ATTCTCATCTTTGGA[C/T]CTTTTGTTTTCTCTA | 448987 |
rs36734642 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26758393 | GACATGTGAAAGCCA[A/G]ATGTGTAAAACTAGA | 448987 |
rs36734988 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Fbxl7 | Mm_Celera | 15:26572941 | ATAATTCATAAACAA[C/T]CATTAGAAACATTAC | 448987 |
rs36735517 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26617194 | ATGGCTATGAAATCA[G/T]GAACTCACACCCTTG | 448987 |
rs36737363 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26807803 | GTTTCAACACCTATC[C/T]ACTTATCACAGTTGT | 448987 |
rs36738667 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Fbxl7 | Mm_Celera | 15:26636747 | ACACACTTGGGAGTA[C/T]CTGGGATTACTACTT | 448987 |
rs36740149 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26625063 | TTGCAGACCATTCTT[G/T]CCCATCTATTCCCTT | 448987 |
rs36740869 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Fbxl7 | Mm_Celera | 15:26615394 | TGGCTGGGAAGATCC[C/T]GGACTCAGATCTCTA | 448987 |
rs36742031 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26584116 | GAAAGCATGAGAAGA[A/T]GTGGCAATAGCCAGA | 448987 |
rs36746413 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26762016 | ATGCTCCCACTGAGA[C/T]GACTTATGAGCACGA | 448987 |
rs36751453 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26743525 | TATGTCTCCATGGAA[A/G]GTGTTCTACAGTTGA | 448987 |
rs36752232 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26797306 | AAGCAATGTGGTAAC[C/T]GGAACATGTAGAGAA | 448987 |
rs36753034 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26638766 | TGCATTTTATAGCTC[A/G]AATGTGAAAAAGTGA | 448987 |
rs36754025 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26750395 | AAATTTGTTTGCCAG[C/T]AGTTAGTGTTATATT | 448987 |
rs36754995 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26792809 | GTGATGGTAGCATTC[A/C]TTTATAAGTTGTCAA | 448987 |
rs36755605 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26601737 | TGCGTGACGGATGTC[A/T]ACTGAAGCACGCACA | 448987 |
rs36759077 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26624769 | ACGGCCCTGGGGAGC[A/G]AACTAAGGCTTGCAG | 448987 |
rs36761534 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26720318 | ACATGGATTACTGTC[A/C]CTTCATCTGATTTTC | 448987 |
rs36763853 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26789885 | TGTCTTGGCATAAAC[A/G]TGAATAAGTAAGAAT | 448987 |
rs36763876 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26619381 | ACGGGGAATTGAAAA[A/G]CCTTTGCATTTCTAT | 448987 |
rs36764304 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26550098 | GCTGATAGTCAGGTC[A/G]TGCAGCAAGCCCACT | 448987 |
rs36765026 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26750048 | TCTCAATATATAAAG[A/C]ATGAAAATGTCAGAG | 448987 |
rs36768384 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26597306 | AGGCATGAATGGCTA[C/T]GGTAAGAATGAGGAC | 448987 |
rs36769412 | snp | A/T | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Fbxl7, LOC105245899 | Mm_Celera | 15:26739274 | TAACTTGTTGCTTTA[A/T]GAATCCACAAAATGT | 448987 |
rs36772380 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Fbxl7 | Mm_Celera | 15:26608611 | TGATGTTGACGTAGA[C/T]TCAAGCACAATGCCT | 448987 |
rs36776009 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26612592 | TGTGTCCTGTAAAAT[C/G]GTTAGCAGACAGACA | 448987 |
rs36776221 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26756572 | CAAAGAGTTGATAAA[A/G]TTAATTTCTGAAAAA | 448987 |
rs36777971 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26745913 | GTGTAGCACTGTTTT[C/T]GGAGTTTAAGTAGAA | 448987 |
rs36778192 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime | Fbxl7 | Mm_Celera | 15:26542936 | TGACCTCTTTTGCTC[A/G]TGAGAAATTAAAAAT | 448987 |
rs36781685 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26617041 | GTGCTATGAATTGGT[C/T]GTTTGATCCCTACAG | 448987 |
rs36784915 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26595605 | TGAAGAGATGGGCAT[A/G]TCCTATCTTCCATAA | 448987 |
rs36787979 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Fbxl7 | Mm_Celera | 15:26565314 | CAAATAAAGGGACTT[C/T]GTACATTTATGTACT | 448987 |
rs36788227 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26579869 | TCTTCCTTTCTGTTG[A/G]CAAAGTAATCTATTT | 448987 |
rs36789984 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26801307 | AAAATTTTCCTGCTG[A/G]ATTTTGGATTAAACT | 448987 |
rs36791333 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26564296 | TTAATTTAGGCTGAT[A/G]TGCTCACACCAAGGT | 448987 |
rs36792064 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26715570 | CAATTTTAAAAAGGC[A/G]GAATATTTTTTTAGT | 448987 |
rs36795093 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26611718 | CCATCTGGATTTTGT[C/T]TACTGTGATGTCTTC | 448987 |
rs36795595 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26578325 | TCTTAGATTTAGTTT[C/T]CTTACCAGATATTTT | 448987 |
rs36797199 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime | Fbxl7 | Mm_Celera | 15:26540526 | GTCATACAGCACGAC[A/G]TGATGTGAACATTAG | 448987 |
rs36797364 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26610644 | ATGTGTGATTGCTGT[G/T]ATTAAAATGTTATGA | 448987 |
rs36798233 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26565607 | TGGGCCCAGTTTCTG[A/G]TTGACCATCCTAGTT | 448987 |
rs36799321 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Fbxl7 | Mm_Celera | 15:26592180 | ATGGAGGATTTATCT[C/T]ATTGAACTAACTCAA | 448987 |
rs36802082 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26739461 | TCTCCCACGCCAAAA[C/T]AGTGCTCAGAAGAGG | 448987 |
rs36802570 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26557566 | AGTTGAACAGGAGAT[A/G]AAAATGAGAAATGGC | 448987 |
rs36802892 | snp | A/G | 0.32 | 0.24 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26597216 | TTCGCAAATTTAGCT[A/G]TACTCTTCCTTCAAG | 448987 |
rs36805219 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Fbxl7 | Mm_Celera | 15:26548592 | CTGAGTTAGGGAAAA[A/T]CATGAATCTCAGTGA | 448987 |
rs36805928 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26753531 | GTGAGATTGGGATGA[A/C]ATTAGCTCTTCCCAC | 448987 |
rs36807060 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Fbxl7 | Mm_Celera | 15:26564863 | GACTGCAGACACTCT[A/G]CCATCTCTATCTTTA | 448987 |
rs36807094 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26593395 | ACTGAACCATGGGCC[C/T]GGCATGACCATTAGC | 448987 |
rs36808182 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26587699 | CCAGGGAGAGTGATG[A/T]CATAATACTTCTAAC | 448987 |
rs36812054 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Fbxl7 | Mm_Celera | 15:26620722 | CAGAATAGGTGCTTC[A/G]GGGAGAAGGAAGACA | 448987 |
rs36813451 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26739574 | CTGTGAGTGAACCTA[A/T]GAGATCAGCATCAGG | 448987 |
rs36815957 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26790704 | TAAGGTTAGAGTTAG[G/T]CTGATCTTTCACTAC | 448987 |
rs36816443 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26587911 | GGGAAGCTTATAATT[A/C]GCCTGAGCTTTGAGA | 448987 |
rs36816484 | snp | A/C/T | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26700282 | ATAGGAGAAAACTTC[A/C/T]TTTTTTGTGAAGTTA | 448987 |
rs36817576 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26604145 | AATTTCAAGGAACCA[C/T]ATTTGAAAACATTAG | 448987 |
rs36819913 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26563405 | TAACTCGGGTGTTAG[G/T]GAATGAGACCTTATT | 448987 |
rs36821707 | snp | G/T | 0.497778 | 0.0332592 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26626946 | GGTCTCTAAGAAGCA[G/T]TTACACCTTTTGAAG | 448987 |
rs36821744 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26617936 | TCTCAGGGTCTGTGA[G/T]GACCTAAGCAAAGAG | 448987 |
rs36821887 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26806259 | CGTGTAAAGCAGGGT[A/G]TATGACACTGGATAT | 448987 |
rs36822960 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26718537 | TGTTAAATCTCTCTG[C/T]TTTATAGCTAATCAC | 448987 |
rs36823660 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26708764 | ACTGGTGGCTGTGTC[A/T]CTGTGTTGTGTTTAA | 448987 |
rs36830445 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26773255 | GCTCAATATAAAGTG[A/C]TCAGCACATAGAGTT | 448987 |
rs36835754 | snp | C/T | 0.231111 | 0.249285 | utr-variant-3-prime | Fbxl7 | Mm_Celera | 15:26542598 | CTTTGCACACTGATA[C/T]GAAGTGTTAATAGGA | 448987 |
rs36837455 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26758365 | ATAGGGAAATATACT[C/T]GGCAAACTGATGGAC | 448987 |
rs36838681 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26771405 | TGAACAATTCTCCTC[A/G]TATACTGAGCCTAAG | 448987 |
rs36845166 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26620318 | ACTTAGCTTTTAAAT[A/G]GCGGATCTCAGTCAC | 448987 |
rs36847002 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26773439 | TACTACAAACCATAG[A/G]CCATAGGCTATCACT | 448987 |
rs36847715 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26777765 | GTCATATCTGGACAT[C/T]CCTGGACACTAAACT | 448987 |
rs36848742 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26704078 | AGAGAAATGGGAAGC[A/G]AGTGAGAGGTATGAG | 448987 |
rs36851014 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26629327 | CTAGCCGATAAAATA[C/G]CTGAACACTCCATTA | 448987 |
rs36852889 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26749352 | GAATAAACAGGGAGC[A/G]ATGTAGATAGGCATC | 448987 |
rs36853641 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26566612 | TGGCTCACAGCCTCA[A/G]CTTATTTAGGGAATA | 448987 |
rs36855758 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Fbxl7 | Mm_Celera | 15:26795728 | GCTGCTGCTGCTGCC[A/G]CTGCCTCCACCACTG | 448987 |
rs36856029 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26620901 | GCCAACTGTGAGAAA[A/G]GTTATGAAAGCCAAT | 448987 |
rs36856343 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26591181 | TTAGTTTGTTCAAGA[A/T]GCTGCCGCCCCTTCA | 448987 |
rs36856978 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26547886 | CCAGGCAGTCTGATC[C/T]ATCGGTCGATGGCTA | 448987 |
rs36858695 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26586919 | ACAAATCAACAGGGA[A/C]TATGCAACATGATTG | 448987 |
rs36863687 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Fbxl7 | Mm_Celera | 15:26614636 | AAGAAGTGATTGAGC[A/G]TTCCCAGGAAGAAAA | 448987 |
rs36864022 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxl7 | Mm_Celera | 15:26645203 | ATTATGCTTCTTGGA[A/G]TTCCAATCAATTTAC | 448987 |
rs36864328 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26776623 | TGCATCTACTAAAGA[A/G]AAGTTAGAGCTTTGT | 448987 |
rs36866490 | snp | A/G | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | Fbxl7, LOC105245899 | Mm_Celera | 15:26736605 | TGGAGCATTGAGCAC[A/G]GCTGCGTCTATCACA | 448987 |
rs36867154 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26561889 | TGTTAAAACCCATTA[A/G]TTGAATAATGCTTGA | 448987 |
rs36871341 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26544995 | ATGGGATATTTGTGT[C/T]ACTACTAATCTGCTG | 448987 |
rs36873492 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Fbxl7 | Mm_Celera | 15:26551939 | GTTCTGGAGTATAAG[A/G]ATACAATTAAGGTGT | 448987 |
rs36874356 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26596167 | GGTGTTGTAGATGGC[A/G]AAGCAGAAAGCTGAA | 448987 |
rs36875225 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26587787 | CTTGTCAACGTTGGA[A/G]ATGCTCACGTGTTCT | 448987 |
rs36880352 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26581857 | CCATTTTGCCTCCTA[C/T]TTTTTGGGTATTGAG | 448987 |
rs36882536 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Fbxl7 | Mm_Celera | 15:26739513 | AGTAAAACACAAGAT[A/G]TCATTGATATGCTGT | 448987 |
rs36883117 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26650773 | CTTCCATAAGATTTT[C/T]ATATTTCATGGCCAC | 448987 |
rs36883139 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26555764 | AAGGACGGACCTCTA[C/T]GCCAACACTGCAAAA | 448987 |
rs36885730 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26744845 | AGCTCTGGTGAAATT[G/T]ACAATAGATTTGATA | 448987 |
rs36886059 | snp | A/G | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | Fbxl7, LOC105245899 | Mm_Celera | 15:26736657 | AGGAGAAGTGTCAGC[A/G]TGTTCTAGTGAGGGC | 448987 |
rs36887570 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26659801 | CAATAAAGACACAGA[C/T]ATCACTTCACTCTGG | 448987 |
rs36889492 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26581568 | CACAGAACATTCCAA[C/T]AGTTCAAGCTGATAG | 448987 |
rs36892262 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26656455 | ATTCCTATTCTGTGC[C/T]TTTCAATCTGTAAAA | 448987 |
rs36893690 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26740339 | GGCACAGCCTTCTTA[C/G]ACTTGGTGCCAATGG | 448987 |
rs36895345 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26561399 | ATCGCTCACACTCTT[A/G]TAAGTAATCCCACAC | 448987 |
rs36895459 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26745382 | ACGTACACACACACA[C/G]AGTTTACAATAATAA | 448987 |
rs36895468 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Fbxl7 | Mm_Celera | 15:26608621 | GTAGATTCAAGCACA[A/G]TGCCTTCCTACAAGG | 448987 |
rs36895581 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26569701 | ATTAGGTACACATTG[A/C]TAGTCCTAGGTGGTG | 448987 |
rs36895947 | snp | C/T | 0.375 | 0.216506 | intron-variant | Fbxl7 | Mm_Celera | 15:26648660 | AAATATTTGAGGTCA[C/T]TACGCTAGAACTGAC | 448987 |
rs36896313 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26720716 | TGCACTTCTGGGAAA[C/T]GGCAACAAAACAAGC | 448987 |
rs36897027 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26586443 | TTGTGGAAATAGAAA[C/T]GAACAGTAGCAAACC | 448987 |
rs36898361 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26796096 | TGGATAAGTCCTTGA[C/T]GAGCCCTTCTGATAC | 448987 |
rs36898472 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26771799 | CACTCTCAAGTTTCT[C/T]TTACAACACACCCTC | 448987 |
rs36900373 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26561397 | ACATCGCTCACACTC[C/T]TGTAAGTAATCCCAC | 448987 |
rs36903101 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Fbxl7 | Mm_Celera | 15:26593681 | CAATGTAATCTAGTT[C/T]TCTTAGAGTGCTGCA | 448987 |
rs36907394 | snp | A/C | 0.32 | 0.24 | intron-variant | Fbxl7 | Mm_Celera | 15:26617803 | AAACATATACCTATG[A/C]AAGAAAAAGAACCAG | 448987 |
rs36908198 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxl7 | Mm_Celera | 15:26707955 | AGCTCTGCCCTGCCC[A/G]AGCTCTAGTAACTTA | 448987 |
rs36909266 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26605923 | AAGCTATGCATAGTG[A/G]CATACACTGGCAATG | 448987 |
rs36909545 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26560112 | TTTGTAGTTGCAATG[A/G]AGTTTGCTCTTCTGG | 448987 |
rs36910827 | snp | A/T | 0.297521 | 0.245442 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26772377 | TGACTCCAATGTCTG[A/T]CCACTGCAACCTGTC | 448987 |
rs36918602 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26741381 | TAAAACAGTCACATG[C/T]TCGTTCTTCTTGGTT | 448987 |
rs36920511 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26614092 | GTTACACTTCCAGCC[G/T]AGGTGTGCAGTTCTT | 448987 |
rs36928854 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26553516 | GAAACCTTACCAGGA[C/T]GGGATTTTTTTCCCT | 448987 |
rs36931952 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26616433 | TGTCATAAGCTACAC[A/G]AAAATTCCAGGTACA | 448987 |
rs36934385 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26799699 | TGGAATTGTTCTTGA[A/G]CATAGCACTTGAAAC | 448987 |
rs36935614 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26807818 | TACTTATCACAGTTG[A/T]CTTTCAATGTCAATG | 448987 |
rs36936775 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26792065 | AATAAACACCATATG[C/T]TCTACCTCTGATTCA | 448987 |
rs36938297 | snp | A/C | 0.493827 | 0.0552116 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26617828 | AACCAGTCGGCACAG[A/C]TCCGAGGATGGGTAG | 448987 |
rs36940369 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26795954 | AGCTACTGTGCTCAT[G/T]GACCATTAAAAAAAA | 448987 |
rs36941153 | snp | C/T | 0.124444 | 0.216185 | downstream-variant-500B | Fbxl7 | Mm_Celera | 15:26540288 | TATGGTCCATGGAGA[C/T]AAAAGAACCTTGGAT | 448987 |
rs36947014 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26775156 | CCAACATTAGCACAC[C/T]CAGAACTGGTAGCTT | 448987 |
rs36948198 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26581221 | ATACAAAAGGAAATA[A/C]TGTATTTGTGAGAAA | 448987 |
rs36949848 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26584102 | ATTTGTAAGGTTTAG[A/C]AAGCATGAGAAGAAG | 448987 |
rs36950897 | snp | A/G/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26565854 | TTTGTGTACCACTTT[A/G/T]CTCCATAGGAAGAGA | 448987 |
rs36955293 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26553488 | AACTCCAAAGTTGCA[A/C]TGTTTCTAGGGCGAA | 448987 |
rs36961217 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26660704 | GCAACCAATATCCAG[C/T]TTGTGCCAGTCACCA | 448987 |
rs36963632 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime | Fbxl7 | Mm_Celera | 15:26542682 | AGATAGTTTAAGGAG[A/G]AGCTTTAGAGAGCCT | 448987 |
rs36964242 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26600779 | AGTCAAAGAGGATGG[A/G]AAAACTAATTTGCCT | 448987 |
rs36965505 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26776178 | ATGCTTCAATTATGA[C/T]GGTGACTTAGGCCTT | 448987 |
rs36966692 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26752593 | CACCCTGTCTGCTTA[A/C]CCCAAGCTCTCTGGT | 448987 |
rs36967128 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26776160 | GGCTCCAGCATGCTT[C/T]GAATGCTTCAATTAT | 448987 |
rs36968773 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26626339 | GCCCATGTTCACTTG[A/G]ACTCTATACTTTGGA | 448987 |
rs36970156 | snp | C/G | 0.46281 | 0.131194 | intron-variant | Fbxl7 | Mm_Celera | 15:26688630 | ATACTCCCTTACTCA[C/G]TGCACCTGGAAACGT | 448987 |
rs36972569 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26805117 | GTTTATTAATTTCCA[A/G]CTTAAATCTTTGCCT | 448987 |
rs36973402 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26584440 | TCATCACACCTGGCC[A/G]TTTTACATACCTATA | 448987 |
rs36974915 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26629731 | GTAGTCATTCCTATT[A/T]TTAGGCACATCCTTT | 448987 |
rs36976908 | snp | A/C | 0.459184 | 0.136902 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26595902 | TCATGTGGTATGTTG[A/C]GAGATTGTAATGGCT | 448987 |
rs36977085 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26746274 | ATGAGCTGAACATTC[A/C]AAAATGAAAGTAAAA | 448987 |
rs36978471 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26595021 | CATGACAGCAATGAT[C/G]TGGACTCCACAATGG | 448987 |
rs36978948 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26591613 | CCTACAATAGGTCCT[G/T]GTTTTATCTTGAGGA | 448987 |
rs36978997 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26777308 | TTCCTCACAGCATGT[C/T]TGTTCTGCTTAAAGA | 448987 |
rs36980140 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26558198 | GGAATAAAGTAAAAG[A/T]TTGTAGATTCTTTAA | 448987 |
rs36981324 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26775366 | CTTCTATCTATAGGT[A/C]TCTCCCATTCTCAAG | 448987 |
rs36985451 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26745939 | TAGAAACTTAAGGTT[G/T]GGCATTAGCGAGGTA | 448987 |
rs36989804 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime | Fbxl7 | Mm_Celera | 15:26542286 | GTGGACTTACCGAGC[A/G]CCCATGGAAACTCCT | 448987 |
rs36991298 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26616791 | AGATGGACACCTCTT[C/T]TTCAGAGAAGGGCAG | 448987 |
rs36992570 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Fbxl7 | Mm_Celera | 15:26608662 | TCATGATCGAGTTAT[A/T]TCTGGTCTTTTGAAA | 448987 |
rs36995414 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Fbxl7 | Mm_Celera | 15:26696460 | TAAGTCTATGAATAA[G/T]ATTTTCAGAGAGAAG | 448987 |
rs36998331 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26620148 | TACTGAGAAAATCCC[A/G]AAAGTATTCAATATT | 448987 |
rs37002348 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26793385 | TTTCACTGTCTAAAG[C/T]GGTTCTATTTTATAA | 448987 |
rs37003220 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26652479 | TGAGCTATAGAAGAG[A/G]ATTCCTTAGAATCAA | 448987 |
rs37003287 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26601342 | TCTTAGGTTTATTTA[C/T]AATCCATTGCAATTT | 448987 |
rs37004839 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26758670 | TTGGCTTGATAGTGG[A/T]ACAATTCACCCAACA | 448987 |
rs37010380 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26816283 | ACTTTTCTCTTGGCA[C/G]GAAAATTCAGAAGAC | 448987 |
rs37013179 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26753597 | ATCATAAATTTATAA[C/T]CTTCTTATGAAGCTC | 448987 |
rs37021930 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26575732 | AAGTCTTTAAGGCTT[A/G]ATGTATGAATCTGCA | 448987 |
rs37026978 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26620971 | TCAAGCAGCAGCACC[C/T]GAGCTTCACCAGAGT | 448987 |
rs37027285 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Fbxl7 | Mm_Celera | 15:26603072 | TTGCAGCAAAGAAGC[A/G]GGTGGAATTTAGAAA | 448987 |
rs37027755 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26613912 | AGCAAGCGAGATGGC[A/G]TTGGACAGAGTGAAG | 448987 |
rs37029670 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26810761 | CCTACTCAATAAAAG[C/T]GGGCATCCCTAGAGG | 448987 |
rs37029852 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26620713 | GACCATATGCAGAAT[A/G]GGTGCTTCGGGGAGA | 448987 |
rs37032305 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Fbxl7 | Mm_Celera | 15:26541719 | TCTCTGTGCCTGGCA[C/T]CTTGAATGAACAATA | 448987 |
rs37032594 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26771816 | TACAACACACCCTCA[C/T]TTTTTTATGGATGCC | 448987 |
rs37034363 | snp | A/C | 0.124444 | 0.216185 | utr-variant-3-prime | Fbxl7 | Mm_Celera | 15:26542296 | CGAGCGCCCATGGAA[A/C]CTCCTGAACGCACAA | 448987 |
rs37036619 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26711734 | GTTGGCCTAGAAATG[C/T]AGAATGTAGCAGACT | 448987 |
rs37036937 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26601621 | TCAAGCAGGTCTGTT[A/C]CTGAGAATGTGAGTT | 448987 |
rs37037744 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26565777 | ACTGCAGTCTCCTTA[C/T]ATGTGTGTGACAGGG | 448987 |
rs37038326 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26653480 | GATGAAACTGCAACA[A/G]GCTACTAATCTGCAA | 448987 |
rs37044830 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26797012 | AGGAGACAAGCTCCA[A/G]AACTCCTAAAAGGTA | 448987 |
rs37045003 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26777324 | TGTTCTGCTTAAAGA[A/G]CATGCTTCTTTTCTT | 448987 |
rs37045130 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26556801 | AAATTAAGTACCACA[C/T]AATCACATTTGGGTC | 448987 |
rs37045278 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26756309 | GTTTTTTTTTTTTCC[A/G]TTAACTATCACACAC | 448987 |
rs37045427 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26624080 | GATGCTTTTGAATCA[C/T]GGAAGCATTTATTGA | 448987 |
rs37046384 | snp | C/T | 0.32 | 0.24 | intron-variant | Fbxl7 | Mm_Celera | 15:26618192 | ATGCTGGCCAAACGT[C/T]CCCTTAGAGACTGCA | 448987 |
rs37047135 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26556640 | AGACTTTTCACAACG[G/T]ACTAAAGTATTTTCC | 448987 |
rs37048365 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26592771 | TTCTACCTTAATTAT[A/G]TGAACAAGACCTTAT | 448987 |
rs37049002 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26797915 | TACCGTAGCTGCCAC[C/G]TGATTGGCTGAGTCT | 448987 |
rs37053629 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26562465 | GGTGCATTTTGTTTT[C/T]GAGAATTTTCCCATG | 448987 |
rs37055364 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26613296 | ACGAGAAGTTACGTA[G/T]TCTGCACCCTCAGAA | 448987 |
rs37055998 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26641156 | ACTCAAAATGCCCCA[A/G]AGAAAGGATCCCGCT | 448987 |
rs37056223 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26564257 | AACATTTCATCTGTG[C/T]ACCTTTTCTCTTTGC | 448987 |
rs37059325 | snp | C/T | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | Fbxl7, LOC105245899 | Mm_Celera | 15:26733628 | TCACTCAAATATAAG[C/T]TTCAATATCCTCATT | 448987 |
rs37061084 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26601650 | TTGCAAACCACTGCC[A/G]GACAGGAAAAGAACG | 448987 |
rs37062470 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26559445 | TTTTTCAATGTTGAC[C/T]TCTAGCATCTGCATC | 448987 |
rs37063082 | snp | C/T | 0.444444 | 0.157135 | intron-variant, nc-transcript-variant | Fbxl7, LOC105245899 | GRCm38.p3 | 15:26730338 | TCTCTTTATCAACCG[C/T]TCCATCTCTTGGCAT | 448987 |
rs37063236 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26798294 | CACCGCTAGTGATCA[C/T]GAGAGTAGTTGTTAA | 448987 |
rs37066045 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26775911 | TGCTGCTGGAAGGGA[A/C]GCATAGCTCACTTAC | 448987 |
rs37070194 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26696261 | CCCTGAGAAATAAGC[A/G]ATTTAACCAGGCATG | 448987 |
rs37077771 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26716426 | TTGTTGGTCACCTAC[C/T]GTTGTGCTAACATAA | 448987 |
rs37078132 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26560747 | GCAGTTATGTTGCCC[A/G]TAGAATTTATGAAAA | 448987 |
rs37078975 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26755389 | TATTTCAAGGGGCCA[A/G]ACCAGGCGGCTGTTT | 448987 |
rs37079804 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26811791 | TATCGTAGGCAGCTA[C/T]AGTAACCAGCACTGT | 448987 |
rs37080018 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26706839 | GTGAAATTCCTCAGT[A/G]TCCATCATTATTGAA | 448987 |
rs37080402 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26595749 | CTCTTTCTTCACCTT[C/T]GATGGTATATATGGA | 448987 |
rs37080955 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26555583 | ATAGCTTCCACTTCA[A/C]ACAGGAACCACCTAT | 448987 |
rs37082635 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Fbxl7 | Mm_Celera | 15:26699318 | CTTATATGTTTACCA[A/G]GGTATTAAAATGTAT | 448987 |
rs37085002 | snp | A/C | 0.124444 | 0.216185 | utr-variant-3-prime | Fbxl7 | Mm_Celera | 15:26541138 | CCTGTGAACAGCCAT[A/C]TGTCCTGATGATGGT | 448987 |
rs37087008 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26756113 | ATTAACATTTTTAGT[A/G]AAGGAATACTACTTT | 448987 |
rs37087120 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26653572 | CCACGTATTTACTTT[A/C]TACTGCAAATGTCCT | 448987 |
rs37087981 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26797266 | GAGTTCGGTCTAAAG[A/T]GTTTTACCAACAAAC | 448987 |
rs37088590 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26799402 | TCCAGTATGACTTCT[A/G]GACCCTGACAAAGCA | 448987 |
rs37089207 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26586834 | CCACATAAATTAACC[A/G]GCAACATAAATGGGA | 448987 |
rs37090332 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26805493 | GTACTTTCTCTAGGG[A/G]CTACTCATTTCTAAA | 448987 |
rs37091327 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26560852 | TCATGTCTCTCCAGG[A/G]AAACTTACACAACAG | 448987 |
rs37094159 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Fbxl7 | Mm_Celera | 15:26695663 | TAGTGCATATGAGCA[C/T]GAAGTGAAGGTCCAT | 448987 |
rs37094248 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26558433 | TGGTGCCTCTTATGC[A/G]CATGCTTTTTAGTAG | 448987 |
rs37094678 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26546814 | AGTTAGCGTTGAAAG[C/T]TGACCTTTCCTTTTG | 448987 |
rs37097263 | snp | C/T | 0.495868 | 0.0452663 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26596571 | ACTTAAAGGCAGGTT[C/T]TGTATCAGGATCCAT | 448987 |
rs37100762 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26555228 | TTTGAGAGCTTTCAG[A/G]AGGCTATAATCATAA | 448987 |
rs37100795 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26587735 | ACTGCAAAGGCCTGT[A/G]ACTCTTGTCTGGTTA | 448987 |
rs37106320 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26562166 | AGAGACATTAAATGT[C/T]ATGGAACCTCTACTG | 448987 |
rs37106815 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26791408 | TGAGTAAAGCTGATA[A/G]TCTAACTTCACAGCA | 448987 |
rs37107338 | snp | C/T | 0.32 | 0.24 | intron-variant | Fbxl7 | Mm_Celera | 15:26648454 | GTTGTTTCACATTCC[C/T]AGCAAGGTTGGTGAC | 448987 |
rs37109513 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26799141 | GTGAAGCAATGGAGA[C/T]AGGAGCCTGTTTGCT | 448987 |
rs37115056 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26640541 | CCACATGTACAGAAC[A/C]ACATGATTGACCTGA | 448987 |
rs37115798 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Fbxl7 | Mm_Celera | 15:26589204 | AGTGAGTCATGGCTT[A/C]GTAGGAGACATGCAG | 448987 |
rs37116456 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26682069 | GGTTCTTATTTCATG[C/T]AACTGTGTAAACTCT | 448987 |
rs37116628 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26741648 | ACCACATAGCTGAAG[G/T]TATAGTTTCATGTTG | 448987 |
rs37118167 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26639818 | GGATAATCAGAATAG[C/G]AATCGAATATTATAC | 448987 |
rs37118683 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26561342 | ATTAACTATTTCTCC[A/G]GAGGGTGAGAGCTTC | 448987 |
rs37120692 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Fbxl7 | Mm_Celera | 15:26699167 | CGCACTGAAATGAAG[A/C]CCCTCAGTGATGGTA | 448987 |
rs37120824 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime | Fbxl7 | Mm_Celera | 15:26542711 | CTTCTTCAACGCTTA[A/G]TGTTGCAGCTGCTTC | 448987 |
rs37122614 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26716065 | GTAATTCCTTGGTCA[A/T]GCATTTACAATCCTT | 448987 |
rs37123324 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26801830 | ACATCACAGTCAGAA[A/G]TAGAAAGTGGTGCAC | 448987 |
rs37128283 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26626698 | AGTTTAAAAAAACCT[C/T]AACAGATTTATTAGG | 448987 |
rs37130437 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26749973 | AGATGTCAGTGGGAG[A/G]AGCTTGAAATTGAGG | 448987 |
rs37131160 | snp | A/G | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | Fbxl7, LOC105245899 | Mm_Celera | 15:26736649 | TCCAGGTAAGGAGAA[A/G]TGTCAGCATGTTCTA | 448987 |
rs37131833 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26650959 | CACACTAATCTCTAA[G/T]TGCAAGAGAGGAAAG | 448987 |
rs37137390 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26766580 | GAAGCAATTCTCAAG[C/T]CAAAAAAGTAATGAA | 448987 |
rs37147351 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26574212 | TGACACTGGCATGTT[A/G]ATAGCTTTGAACTAT | 448987 |
rs37149611 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26803994 | GGGATGCCATGTCAC[A/T]GACCCGGGTTATCAG | 448987 |
rs37152508 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26798192 | ATCAAAAGGAACTGT[A/G]GCTTGATTGACTCAA | 448987 |
rs37153792 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26796737 | AGCTTACAGCTGACA[C/T]AGTTTCCTACCACAG | 448987 |
rs37154667 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26615575 | GTTGATGCAGCAATT[G/T]CATTCCATCTGCCAC | 448987 |
rs37158904 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26796751 | ATAGTTTCCTACCAC[A/C]GAGATGTGGGAACTA | 448987 |
rs37159963 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26545105 | ACCTGTCCTTTTTCT[C/T]TGCCTGTATCCCCAG | 448987 |
rs37160007 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26710811 | GCAGGGGTTCTCCAC[A/G]TGAATAGCTGCTTTC | 448987 |
rs37161756 | snp | A/G | 0.231111 | 0.249285 | intron-variant, nc-transcript-variant | Fbxl7, LOC105245899 | Mm_Celera | 15:26734416 | AGTAACCAGAAGGGA[A/G]AGCAACTTACATACC | 448987 |
rs37162043 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26697344 | GCCCACTTGGTTTTC[A/G]ACATTTACTTGTCTG | 448987 |
rs37162122 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26752556 | TCAGCCTCCATGTTA[A/G]GCAGCTCCTCGTTCC | 448987 |
rs37162697 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26559183 | TTTATGTTTGAACTT[A/T]GCTTCCCCAAAGCTA | 448987 |
rs37164404 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26790347 | TACACCTCTCACCTT[A/G]TACAAACACATGAAT | 448987 |
rs37164695 | snp | A/G | 0.32 | 0.24 | intron-variant | Fbxl7 | Mm_Celera | 15:26565004 | ATTTAACGTTGGAGC[A/G]AGCAAAAGATAAACC | 448987 |
rs37166663 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26800433 | CACCTGTGTGGAATA[C/G]AGGCTTTCTCCCAAC | 448987 |
rs37169480 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26790125 | GGTTTTCTATTCATG[A/C]GAATGCTTAGCATAA | 448987 |
rs37170467 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26633593 | ATCCTTCAAAGCTGC[A/C]TCTATACATGATCTA | 448987 |
rs37171354 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26713023 | AACTGTGTTGGGGAG[A/T]CAATATTCACAGATT | 448987 |
rs37172746 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26818186 | TGTCCTCTTTCCAAA[A/T]ACATGGCTACATCCA | 448987 |
rs37172824 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26772937 | TAAATTACAGCAGAG[C/T]GGATACAGTGATATG | 448987 |
rs37173397 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26555914 | ATCAACTTGTTTTCA[A/G]TCTTAAATAGCTCTT | 448987 |
rs37174469 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26758915 | CTCAGTATAATTTTG[C/T]TGAGATCTCGTCATG | 448987 |
rs37174706 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26583985 | AGCTTTCTGAAAATG[G/T]AGCATACCTCTGAGT | 448987 |
rs37178944 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26592202 | CTAACTCAAAGGCCC[A/G]TTTCTACACACCATA | 448987 |
rs37179602 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26613104 | TCTGCAGTTTACAGC[A/G]AGGAGCCAAGATCTC | 448987 |
rs37181240 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Fbxl7 | Mm_Celera | 15:26802898 | GCACATGTTCCTGGT[C/G]GTTAGAGTTGAAGTT | 448987 |
rs37181674 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26746428 | CTTTGAAGGTTCAAG[A/G]ACACTCAAATTTCCC | 448987 |
rs37183732 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26705019 | TTTGAAACACGATTT[A/G]TAAAGTCTACATTTC | 448987 |
rs37189502 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26557366 | TCTCTTCACATGAAT[C/T]ATAGTACAAACATGT | 448987 |
rs37191307 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Fbxl7 | Mm_Celera | 15:26708361 | GTAGGCCATGGTTTC[A/T]GTAATTGACACTTAA | 448987 |
rs37191607 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26703506 | CCAAGAGTGTGTTAT[A/T]AAGCACTGAGTAATT | 448987 |
rs37191890 | snp | A/G | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | Fbxl7, LOC105245899 | Mm_Celera | 15:26736847 | TTGTGACAGTAGTTA[A/G]GAAATAATGACCCAG | 448987 |
rs37192804 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Fbxl7 | GRCm38.p3 | 15:26598117 | GCAGAACAATGGATG[C/T]GGTCTTATTCCTAGC | 448987 |
rs37194922 | snp | C/G | 0.124444 | 0.216185 | utr-variant-3-prime | Fbxl7 | Mm_Celera | 15:26542185 | TGAGCATCCAACAAG[C/G]CAAAGAACGTTCAGA | 448987 |
rs37196342 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fbxl7 | Mm_Celera | 15:26591059 | GAGCTCCTCTGCTTG[A/G]GATTCTTAGAAAAAA | 448987 |