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 |