SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3023701 | snp | C/T | | | intron-variant, utr-variant-3-prime | Fbxl13 | Mm_Celera | 5:21514960 | GAAACAATGTGTCAA[C/T]CAGACCTGGGGCTGT | 320118 |
rs3654056 | snp | A/C | 0.5 | 0 | intron-variant | Fbxl13 | Mm_Celera | 5:21598997 | AGTACAGGCAGATGT[A/C]CCGCACTGAGATTCG | 320118 |
rs3657499 | snp | A/G | 0.5 | 0 | intron-variant | Fbxl13 | Mm_Celera | 5:21602720 | ATAAAGCAAGCCAGA[A/G]CTGATGCTATAACTT | 320118 |
rs3657521 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Fbxl13 | Mm_Celera | 5:21602730 | CCAGAACTGATGCTA[C/T]AACTTGAGTAGTCTA | 320118 |
rs3657544 | snp | A/G | 0.5 | 0 | intron-variant | Fbxl13 | Mm_Celera | 5:21602738 | GATGCTATAACTTGA[A/G]TAGTCTAGCATCTCC | 320118 |
rs3657545 | snp | A/G | 0.5 | 0 | intron-variant | Fbxl13 | Mm_Celera | 5:21602740 | TGCTATAACTTGAGT[A/G]GTCTAGCATCTCCAA | 320118 |
rs3657612 | snp | A/T | 0.290657 | 0.246672 | intron-variant | Fbxl13 | Mm_Celera | 5:21602765 | CTCCAACCAAGAGAG[A/T]GTGCTTCCCATGTAA | 320118 |
rs3658220 | snp | C/T | 0.5 | 0 | intron-variant | Fbxl13 | Mm_Celera | 5:21602867 | CTGTGTAACACATTA[C/T]GGTACAGGGGTGGGG | 320118 |
rs3658792 | snp | C/T | 0.5 | 0 | intron-variant | Fbxl13 | Mm_Celera | 5:21602923 | CCAGGTAAGCTATTG[C/T]CTAGAGATCACCTCC | 320118 |
rs3658909 | snp | C/G | 0.5 | 0 | intron-variant | Fbxl13 | Mm_Celera | 5:21602989 | GGAGGGGTAAATGCA[C/G]CCCAAGCAACATTAT | 320118 |
rs3659517 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Fbxl13 | GRCm38.p3 | 5:21603105 | GACTAGAAACTATCA[C/T]ACAACAACTGAGTGA | 320118 |
rs3660015 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Fbxl13 | GRCm38.p3 | 5:21603131 | AGTGAACTGGGAACT[A/G]GAGAGGAAAAGAAGT | 320118 |
rs3692738 | snp | A/G | 0.5 | 0 | intron-variant | Fbxl13 | Mm_Celera | 5:21505669 | TCTTATTCTCCCAAA[A/G]TCAGCCAAATGCATG | 320118 |
rs3693353 | snp | A/G | 0.5 | 0 | intron-variant | Fbxl13 | Mm_Celera | 5:21505754 | CTAAGTTTATCTCCA[A/G]AGAAGCTTCCTCCTG | 320118 |
rs3694691 | snp | C/G | 0.5 | 0 | intron-variant | Fbxl13 | Mm_Celera | 5:21505993 | GCTCACATGACCTCA[C/G]AGAGACTGAGGCAAC | 320118 |
rs3694710 | snp | A/G | 0.5 | 0 | intron-variant | Fbxl13 | Mm_Celera | 5:21506006 | CACAGAGACTGAGGC[A/G]ACAAGCACAGAATCT | 320118 |
rs3695252 | snp | A/G | 0.5 | 0 | intron-variant | Fbxl13 | Mm_Celera | 5:21506085 | TTTTGTGTTTTCGTG[A/G]GATTCCTGAGTTTTT | 320118 |
rs3695820 | snp | C/T | 0.5 | 0 | intron-variant | Fbxl13 | Mm_Celera | 5:21506153 | GCTCTTTTCCTTTTG[C/T]TTGTCCTAACCAACT | 320118 |
rs3695851 | snp | A/G | 0.5 | 0 | intron-variant | Fbxl13 | Mm_Celera | 5:21506172 | TCCTAACCAACTCCA[A/G]TGTGATAGTTTTGGT | 320118 |
rs3695866 | snp | G/T | 0.5 | 0 | intron-variant | Fbxl13 | Mm_Celera | 5:21506184 | CCAATGTGATAGTTT[G/T]GGTTTGATTACATTT | 320118 |
rs3700027 | snp | A/T | 0.489796 | 0.070696 | intron-variant | Fbxl13 | GRCm38.p3 | 5:21630512 | CAGGATTTAACTACA[A/T]TCTACTTCCTGGTGC | 320118 |
rs3711484 | snp | A/C | 0.489796 | 0.070696 | intron-variant, downstream-variant-500B | Fbxl13 | Mm_Celera | 5:21514445 | GAATGGTGAGAGTGG[A/C]CCCCAAAAATACAGG | 320118 |
rs3725277 | snp | A/G | 0.5 | 0 | intron-variant | Fbxl13 | GRCm38.p3 | 5:21598530 | AAATTATGTTTAGAA[A/G]TAAGAAAATGGGACA | 320118 |
rs3725346 | snp | C/T | 0.5 | 0 | intron-variant | Fbxl13 | Mm_Celera | 5:21598564 | CCAATATAGGGACCC[C/T]GAGAAAAGAAAAAGC | 320118 |
rs6166155 | snp | C/T | 0.5 | 0 | intron-variant | Fbxl13 | Mm_Celera | 5:21632904 | GAGTCACTGCCTTTG[C/T]ATCCACACATGtgtg | 320118 |
rs6207640 | snp | A/G | 0.5 | 0 | intron-variant | Fbxl13 | Mm_Celera | 5:21540637 | AGCAGCTGCTCAGAA[A/G]CNCAGGCATGAAGCC | 320118 |
rs6207642 | snp | A/G | 0.5 | 0 | intron-variant | Fbxl13 | Mm_Celera | 5:21540639 | CAGCTGCTCAGAANC[A/G]CAGGCATGAAGCCTG | 320118 |
rs6220367 | snp | C/T | 0.5 | 0 | intron-variant | Fbxl13 | Mm_Celera | 5:21540662 | GAAGCCTGCAGTGTT[C/T]TTTACAAAGCTACAT | 320118 |
rs6220457 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Fbxl13 | Mm_Celera | 5:21540713 | TGTACTTGGTGAGTG[C/T]TCCCTTCTCACTCCC | 320118 |
rs6344045 | snp | A/G | 0.46281 | 0.131194 | intron-variant | Fbxl13, Lrrc17 | Mm_Celera | 5:21553857 | TCAGTCTTTGGCTTT[A/G]TGGAGTCGCTTGGTC | 320118 |
rs6344697 | snp | A/G | 0.46281 | 0.131194 | intron-variant | Fbxl13, Lrrc17 | Mm_Celera | 5:21553987 | CGTGCACACTGCTGA[A/G]TGGCTCGTGAATCTG | 320118 |
rs6345260 | snp | A/G | 0.42 | 0.183303 | intron-variant | Fbxl13, Lrrc17 | Mm_Celera | 5:21554079 | ACATCCAAGCTCTTT[A/G]AGTGGATGGTCACCC | 320118 |
rs6346387 | snp | A/C | 0.5 | 0 | intron-variant | Fbxl13, Lrrc17 | Mm_Celera | 5:21554281 | CAGATTCAAAGAATG[A/C]AATTTTTGTATTCAT | 320118 |
rs6346477 | snp | A/G | 0.455 | 0.143091 | intron-variant | Fbxl13, Lrrc17 | Mm_Celera | 5:21554332 | AGGCAAGAACTGAAA[A/G]TCAACGTACATTAAA | 320118 |
rs6346961 | snp | C/G | 0.336735 | 0.234472 | intron-variant | Fbxl13, Lrrc17 | Mm_Celera | 5:21554367 | TTTCTAACACCTAAT[C/G]GGGTAGCGCTAACAC | 320118 |
rs6353489 | snp | A/C | 0.5 | 0 | intron-variant | Fbxl13 | Mm_Celera | 5:21635094 | AAAAACAAGAAAAAA[A/C]AAAAACAAAAAACCT | 320118 |
rs6358681 | snp | C/T | 0.48 | 0.0979796 | intron-variant, synonymous-codon | Fbxl13, Lrrc17 | Mm_Celera | 5:21560933 | CTTACCACCCTCTTG[C/T]TGCAGCACAACCAGA | 320118 |
rs13478132 | snp | C/T | 0.490869 | 0.0669478 | intron-variant | Fbxl13 | GRCm38.p3 | 5:21494675 | AAGACTGGGGAATGA[C/T]GTGAAAAAAAAAGGA | 320118 |
rs13478133 | snp | A/G | 0.498866 | 0.0237825 | intron-variant | Fbxl13 | GRCm38.p3 | 5:21614246 | CAGAAACTGCAGGTC[A/G]TCCCCTTGGGTTTCT | 320118 |
rs29194121 | snp | A/T | 0.5 | 0 | intron-variant | Fbxl13 | Mm_Celera | 5:21538342 | TGGATACAGAAAATG[A/T]GAAACATTTGCACAA | 320118 |
rs29501538 | snp | A/T | 0.375 | 0.216506 | intron-variant | Fbxl13 | GRCm38.p3 | 5:21643634 | GGCAAGTAAGACTTT[A/T]CAAACCATTACAAAC | 320118 |
rs29502011 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Fbxl13, Lrrc17 | Mm_Celera | 5:21546938 | ATTCTTTCTCTTTGC[A/G]GGCAGGGACATGGCT | 320118 |
rs29509972 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Fbxl13 | Mm_Celera | 5:21496413 | CCAAACCTCAGCTGT[C/T]TCCTGGCTCTCTCGG | 320118 |
rs29511550 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fbxl13, Lrrc17 | Mm_Celera | 5:21571523 | TGACTTTTGAGGGGG[A/G]TATTCATTAAGCCCC | 320118 |
rs29523689 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fbxl13, Lrrc17 | Mm_Celera | 5:21554508 | TGAAGAAGCCTTATG[C/T]ACCTTGCTAGTGGAC | 320118 |
rs29524306 | snp | C/G | 0.498615 | 0.0262793 | upstream-variant-2KB, intron-variant | Fbxl13, Armc10 | GRCm38.p3 | 5:21646789 | CCCTTCTAAAAGGAT[C/G]GCTTAAGTCGTGAAA | 320118 |
rs29525088 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fbxl13 | GRCm38.p3 | 5:21606793 | GAGGGTGCTGCTTAC[A/G]GGCTTGCTTTCTTAT | 320118 |
rs29526062 | snp | A/C | 0.375 | 0.216506 | intron-variant | Fbxl13, Lrrc17 | GRCm38.p3 | 5:21562670 | ACACACACACACACA[A/C]AAAAAAAAAATGCTA | 320118 |
rs29526513 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxl13 | Mm_Celera | 5:21491983 | GTAGTGCGCGCGCGC[A/G]CGCACACACACACAC | 320118 |
rs29530132 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Fbxl13 | Mm_Celera | 5:21607557 | ACCTCAAAGTCCACC[A/G]ACACAGTGACACACT | 320118 |
rs29530251 | snp | A/G | 0.5 | 0 | intron-variant | Fbxl13, Lrrc17 | Mm_Celera | 5:21547403 | AAAGCCTGACAACCC[A/G]ACTTCTAGCCTGATG | 320118 |
rs29530253 | snp | A/T | 0.5 | 0 | intron-variant | Fbxl13 | GRCm38.p3 | 5:21605895 | GAAGTGCCTTTATCC[A/T]CTGAGGCATCTTGCT | 320118 |
rs29531286 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fbxl13 | Mm_Celera | 5:21583957 | TGAGTTCAGTAAACA[A/G]AGCATGTGCGGGGAG | 320118 |
rs29542208 | snp | C/T | 0.375 | 0.216506 | intron-variant | Fbxl13 | Mm_Celera | 5:21609597 | AAATGCTATTTTTAA[C/T]GACTTTAAGGCTCTT | 320118 |
rs29543603 | snp | C/T | 0.5 | 0 | intron-variant | Fbxl13, Lrrc17 | Mm_Celera | 5:21546601 | TGTCCCCCTGTACTT[C/T]AGTTAAAGCTTAGCT | 320118 |
rs29545250 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Fbxl13 | GRCm38.p3 | 5:21495886 | AGCACATGTTCTCCA[A/G]AAGTGCTTGGCAGAG | 320118 |
rs29548034 | snp | C/T | 0.375 | 0.216506 | intron-variant | Fbxl13 | Mm_Celera | 5:21524694 | GCCGAACAGCTCAGG[C/T]TCAAGACCCGGAGCT | 320118 |
rs29559399 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Fbxl13 | Mm_Celera | 5:21605821 | CAACTTGCAGGAATC[A/C]GTTCTCATTCCACCA | 320118 |
rs29560432 | snp | A/G/T | 0.375 | 0.216506 | intron-variant | Fbxl13 | GRCm38.p3 | 5:21642843 | ATTACTGGAAGAAAA[A/G/T]AAACAACAGACAACA | 320118 |
rs29561991 | snp | A/G | 0.5 | 0 | intron-variant | Fbxl13, Lrrc17 | Mm_Celera | 5:21550485 | GAGCTGTGTGGCCAG[A/G]CTGCACTCTGCTGAC | 320118 |
rs29563431 | snp | C/T | 0.375 | 0.216506 | intron-variant | Fbxl13, Lrrc17 | Mm_Celera | 5:21554775 | ATAAGGGTCTTTGGA[C/T]TTTTATGTTTATATT | 320118 |
rs29563574 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Fbxl13 | Mm_Celera | 5:21525716 | TTTCTCTTATACACA[C/T]ACAACACCATGGAAC | 320118 |
rs29565103 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Fbxl13 | Mm_Celera | 5:21525918 | GCAAATTTTGACAAC[C/T]TTGAGTCCAGGGGCT | 320118 |
rs29566680 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Fbxl13 | Mm_Celera | 5:21533750 | CCCTAACAACTTCAT[A/T]CTGATTATGTTTGCA | 320118 |
rs29567014 | snp | C/T | 0.5 | 0 | intron-variant | Fbxl13, Lrrc17 | Mm_Celera | 5:21546555 | TGAGCTCAGGTGGCA[C/T]AGGTATCTTTGCTTA | 320118 |
rs29567375 | snp | C/T | 0.455 | 0.143091 | intron-variant | Fbxl13 | Mm_Celera | 5:21535228 | AACAGAAATGTGTTG[C/T]AATGTGCTTAGAAGC | 320118 |
rs29573823 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Fbxl13 | Mm_Celera | 5:21524828 | CATGTGGCTCATTCA[C/T]TGCACATGTGCACAA | 320118 |
rs29578833 | snp | C/T | 0.5 | 0 | intron-variant | Fbxl13 | Mm_Celera | 5:21603863 | AACAAGGCCACACCT[C/T]CAAATGGTGCCACTC | 320118 |
rs29579794 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxl13 | Mm_Celera | 5:21491985 | AGTGCGCGCGCGCGC[A/G]CACACACACACACAC | 320118 |
rs29585178 | snp | G/T | 0.48 | 0.0979796 | intron-variant, upstream-variant-2KB | Fbxl13, Lrrc17 | Mm_Celera | 5:21543232 | ACATTTACGGTCCTT[G/T]ATGTGGGACTTCTAT | 320118 |
rs29585820 | snp | A/T | 0.359862 | 0.224567 | intron-variant | Fbxl13, Lrrc17 | Mm_Celera | 5:21543925 | GATGTTCGGCAGTTT[A/T]ACAGCTGCAGTCTCT | 320118 |
rs29627888 | snp | A/G | 0.265928 | 0.249492 | intron-variant | Fbxl13 | Mm_Celera | 5:21596654 | AAAGTTGATGTCAAT[A/G]ATACTGTCTTCAAAT | 320118 |
rs29628304 | snp | A/G | 0.5 | 0 | intron-variant | Fbxl13 | GRCm38.p3 | 5:21601379 | TTTCCACTCTTCCTC[A/G]ATATGGTTCAGGAAC | 320118 |
rs29630595 | snp | A/G | 0.444444 | 0.157135 | intron-variant, utr-variant-5-prime | Fbxl13 | Mm_Celera | 5:21527864 | CTCTGGGTCTGGAGA[A/G]AAGCTCTCAGCTTTG | 320118 |
rs29634732 | snp | G/T | 0.375 | 0.216506 | intron-variant | Fbxl13 | Mm_Celera | 5:21640465 | TTTTAAATTAATTTA[G/T]TCTCTCATACATCCC | 320118 |
rs29635617 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fbxl13, Lrrc17 | Mm_Celera | 5:21574090 | CACACTTACCTTATT[A/G]CCTTTTTGCAACATC | 320118 |
rs29675759 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fbxl13, Lrrc17 | Mm_Celera | 5:21573883 | ACACCATCGCTTACC[A/G]AATTCAACCAGATGT | 320118 |
rs29675793 | snp | C/T | 0.375 | 0.216506 | intron-variant | Fbxl13 | Mm_Celera | 5:21596687 | CCTAGCAATACAAAT[C/T]AATGTATTCAAACTA | 320118 |
rs29678931 | snp | C/T | 0.493827 | 0.0552116 | upstream-variant-2KB, intron-variant | Fbxl13, Armc10 | GRCm38.p3 | 5:21646852 | CCAACCAATACCTGC[C/T]TGCCTCAAAGGTAGA | 320118 |
rs29679182 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Fbxl13 | Mm_Celera | 5:21537029 | GTTAAGAATATGCTT[C/T]GTGGAACATTGTCTT | 320118 |
rs29679820 | snp | G/T | 0.5 | 0 | intron-variant | Fbxl13, Lrrc17 | Mm_Celera | 5:21547352 | AGCTGTCCCCACCTG[G/T]GAAAAGGCTCGGCAG | 320118 |
rs29681337 | snp | C/G | 0.5 | 0 | intron-variant | Fbxl13, Lrrc17 | Mm_Celera | 5:21546750 | AGCACACAGCCGTCT[C/G]TAACTTGGGCTCTTG | 320118 |
rs29683816 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fbxl13, Lrrc17 | Mm_Celera | 5:21554772 | GGTATAAGGGTCTTT[A/G]GACTTTTATGTTTAT | 320118 |
rs29683934 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxl13, Lrrc17 | Mm_Celera | 5:21568735 | GCAACTTATTAAAGC[A/G]AGCTTGTAACTGCTG | 320118 |
rs29684171 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Fbxl13, Lrrc17 | Mm_Celera | 5:21549521 | ATAAGTTAAACTACA[C/T]GTAAGCTTGATTGCA | 320118 |
rs29684393 | snp | A/G | 0.277778 | 0.248452 | upstream-variant-2KB, intron-variant | Fbxl13, Armc10 | Mm_Celera | 5:21646263 | GCTGCCCGGCAGGTG[A/G]ACTGGTTCGGGGCTC | 320118 |
rs29720347 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Fbxl13, Lrrc17 | Mm_Celera | 5:21568460 | CGGTGGTGGTGCACG[C/T]CTTTAGTCCTAGCAC | 320118 |
rs29727663 | snp | A/C | 0.375 | 0.216506 | intron-variant | Fbxl13, Lrrc17 | Mm_Celera | 5:21561754 | CATCATCCTCAGTTA[A/C]CTGGGAGGCTGGAAG | 320118 |
rs29728065 | snp | A/G | 0.265928 | 0.249492 | intron-variant, utr-variant-5-prime | Fbxl13 | Mm_Celera | 5:21528521 | ATAACTGCATCTCTG[A/G]GTCAGTCTGCTCAGT | 320118 |
rs29729517 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxl13 | Mm_Celera | 5:21605818 | GGACAACTTGCAGGA[A/G]TCCGTTCTCATTCCA | 320118 |
rs29729936 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fbxl13, Lrrc17 | Mm_Celera | 5:21572633 | ATCCATGGAGTAAGT[A/G]TGGTGTGCCTGAGCA | 320118 |
rs29732100 | snp | G/T | 0.375 | 0.216506 | intron-variant | Fbxl13 | Mm_Celera | 5:21612239 | AAAACAGGTTTTTTT[G/T]TGGGGGGGGGTGTTG | 320118 |
rs29733136 | snp | C/T | 0.375 | 0.216506 | intron-variant | Fbxl13, Lrrc17 | Mm_Celera | 5:21564245 | CTTCCAATGAGGGAA[C/T]TCAGCCTTTCCCAAA | 320118 |
rs29733766 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Fbxl13 | GRCm38.p3 | 5:21613841 | AGAGACCACTGCTAC[A/T]CACTAGTTTTCCATT | 320118 |
rs29773556 | snp | C/G | 0.277778 | 0.248452 | intron-variant, synonymous-codon | Fbxl13, Lrrc17 | GRCm38.p3 | 5:21561001 | GCTCCTGAGCTACCT[C/G]CGGCTCTATGACAAC | 320118 |
rs29773892 | snp | A/G | 0.207612 | 0.24638 | intron-variant | Fbxl13, Lrrc17 | Mm_Celera | 5:21564316 | AACTTGAGTCCCTCT[A/G]ATTGCTAGTGACTAT | 320118 |
rs29775520 | snp | C/T | 0.492188 | 0.0620098 | intron-variant | Fbxl13 | GRCm38.p3 | 5:21628893 | CACTCCTTAGTAGAT[C/T]GAAGCTCTGTGGCTG | 320118 |
rs29775522 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Fbxl13 | Mm_Celera | 5:21533716 | ATAAGGATGCTTGTC[A/G]TACTAGATTAGGGCC | 320118 |
rs29777809 | snp | G/T | 0.5 | 0 | intron-variant | Fbxl13, Lrrc17 | GRCm38.p3 | 5:21566254 | TGTTGACAACCAAAA[G/T]CCTACTAAATGGGAA | 320118 |
rs29779292 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fbxl13 | GRCm38.p3 | 5:21642822 | ATCACTCAGTGTGTA[A/G]AGGTAATTACTGGAA | 320118 |