SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs13466514 | snp | G/T | | | missense | Fbxo31 | Mm_Celera | 8:121554413 | GCAGCAGACTGTAGA[G/T]ATTGACCTGCAGCGC | 76454 |
rs32626055 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxo31 | GRCm38.p3 | 8:121563017 | TTCACAGACCGCCGG[A/G]AGGGCTGAGCATCCA | 76454 |
rs32628328 | snp | A/T | 0.5 | 0 | intron-variant | Fbxo31 | GRCm38.p3 | 8:121577514 | CTCTCTCTCTCTCTC[A/T]CACACACACACAATA | 76454 |
rs32648739 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Fbxo31 | GRCm38.p3 | 8:121568227 | GGCTGTCCACCCCCA[G/T]GGGGAAGATCCAGTC | 76454 |
rs32914340 | snp | A/C | 0.32 | 0.24 | intron-variant | Fbxo31 | Mm_Celera | 8:121567099 | GAGGCAGGCGGATTT[A/C]TGAGTTCGAGGCCAG | 76454 |
rs32937067 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fbxo31 | GRCm38.p3 | 8:121565474 | AGGATGAGGCTGCGG[C/T]ACTCATCACTCCTGG | 76454 |
rs45651134 | snp | C/G | 0.336735 | 0.234472 | intron-variant | Fbxo31 | Mm_Celera | 8:121573202 | TCTCCAGGACACAGT[C/G]TCAGGAAGCCCAGTC | 76454 |
rs45729966 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Fbxo31 | Mm_Celera | 8:121570870 | TTGGCAGTTTTTCTC[G/T]TTCCGTGTTCCATAT | 76454 |
rs45756124 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Fbxo31 | Mm_Celera | 8:121574517 | TCGTTCCTCCAGGAC[C/G]TGGACAGACCCTGTC | 76454 |
rs45762176 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fbxo31 | Mm_Celera | 8:121562788 | GTGAAAGGGCAAGAG[A/G]TCAGGTGCTGGGCCT | 76454 |
rs45771022 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime | Fbxo31 | Mm_Celera | 8:121550439 | CTGAGTGATGGCGGT[A/G]ATGTCCTGACACTGG | 76454 |
rs45813140 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Fbxo31 | Mm_Celera | 8:121573053 | AAACCCAGAATAGCA[C/T]TCCTAGAGAACATCA | 76454 |
rs45852125 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fbxo31 | Mm_Celera | 8:121564158 | TAGGCTGACAGGCAC[A/G]TGGCGCTGAGCCCAG | 76454 |
rs45934898 | snp | A/T | 0.32 | 0.24 | intron-variant | Fbxo31 | Mm_Celera | 8:121561753 | GTGACCGTGTGCTGC[A/T]GGAACTGGGACGACA | 76454 |
rs45940760 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Fbxo31 | Mm_Celera | 8:121573319 | AGGAGGCTTTCCTGG[A/G]CCCTTCAGAGGTCAT | 76454 |
rs46038207 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Fbxo31 | Mm_Celera | 8:121554616 | AGTGACTCGAGGTGG[C/T]CTGAGGGAGCGCAGA | 76454 |
rs46065753 | snp | C/T | 0.231111 | 0.249285 | utr-variant-3-prime | Fbxo31 | Mm_Celera | 8:121551307 | GGAAGCTCAGGCAGA[C/T]GCTCCCAAAGGCTGG | 76454 |
rs46085051 | snp | A/G | 0.32 | 0.24 | intron-variant | Fbxo31 | Mm_Celera | 8:121566084 | GAGCACTGAAATCCC[A/G]GGCAGCACCAAAGTA | 76454 |
rs46158312 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Fbxo31 | Mm_Celera | 8:121565722 | GATGGGCAGCACGGA[A/G]CAGAGGCAGCCGCTC | 76454 |
rs46227201 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fbxo31 | Mm_Celera | 8:121558487 | CTAGCCATCATAAAC[A/G]GCTCCAACAGACACC | 76454 |
rs46228198 | snp | A/T | | | intron-variant | Fbxo31 | Mm_Celera | 8:121571778 | CTCCCGACTTGATGA[A/T]AATGCACTGAACCTC | 76454 |
rs46313887 | snp | A/G | 0.32 | 0.24 | downstream-variant-500B | Fbxo31 | Mm_Celera | 8:121548992 | TTTCTGTCCTAGAAC[A/G]GCACTATTGCCCTCC | 76454 |
rs46357140 | snp | G/T | 0.244898 | 0.249948 | downstream-variant-500B | Fbxo31 | Mm_Celera | 8:121549099 | ATCCTTCATCCTTAT[G/T]TGGAAAAACCAAAGG | 76454 |
rs46378027 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Fbxo31 | Mm_Celera | 8:121562410 | GTCCCTCCTTGTCCT[C/T]GGTCCTGCACCTGCC | 76454 |
rs46501829 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxo31 | Mm_Celera | 8:121561809 | AGTTACACACAAACC[C/T]TGGGAAGAAGCCAGC | 76454 |
rs46531907 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxo31 | Mm_Celera | 8:121559335 | CTAGGGTACATAACT[C/T]GGCCTCATCGGGGAT | 76454 |
rs46551455 | snp | C/T | 0.142012 | 0.225474 | utr-variant-3-prime | Fbxo31 | Mm_Celera | 8:121549983 | GGCCCTCTGCTCTAA[C/T]GCCCATAGGTCCTGA | 76454 |
rs46693529 | snp | C/T | 0.32 | 0.24 | intron-variant | Fbxo31 | Mm_Celera | 8:121557999 | CCAGCTCAGGAGTGG[C/T]GATCATGCCTGGCAC | 76454 |
rs46694952 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Fbxo31 | Mm_Celera | 8:121569134 | TTAAACATAGGAAAT[C/T]GTTATCGTGGGCTGG | 76454 |
rs46861450 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Fbxo31 | Mm_Celera | 8:121567715 | GCCAACAGTGGGACC[A/C]AAGATTAAAGCGAGG | 76454 |
rs46886236 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Fbxo31 | Mm_Celera | 8:121573083 | AAGCTCCCGCACTGT[C/G]CATGAACACCTGAAC | 76454 |
rs46921065 | snp | C/T | 0.142012 | 0.225474 | utr-variant-3-prime | Fbxo31 | Mm_Celera | 8:121549513 | GAGTGACACAGGTGA[C/T]ATCAGGCACCAGGTA | 76454 |
rs46967071 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Fbxo31 | Mm_Celera | 8:121566798 | CACTGCCCTTTCTTT[C/T]TGTCAAAGGGTTACA | 76454 |
rs46997757 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Fbxo31 | Mm_Celera | 8:121567919 | GCCTTGCCACACGGC[A/G]GGACACGAGCTGTCT | 76454 |
rs47010720 | snp | A/G | 0.152778 | 0.230321 | utr-variant-3-prime | Fbxo31 | Mm_Celera | 8:121550610 | GCAAACCCACAAGGC[A/G]CCTTTTCTCCAAAAT | 76454 |
rs47035490 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Fbxo31 | Mm_Celera | 8:121573069 | TCCTAGAGAACATCA[A/C]GCTCCCGCACTGTCC | 76454 |
rs47042176 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Fbxo31 | Mm_Celera | 8:121572317 | TCTCCCTTGATGTAT[A/G]TCCCAGAAGTCCCTC | 76454 |
rs47115801 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Fbxo31 | Mm_Celera | 8:121553006 | CTTGCCTATTTGTGG[A/C]CCAGAAGCTACTGTG | 76454 |
rs47128531 | snp | A/C | 0.32 | 0.24 | intron-variant | Fbxo31 | Mm_Celera | 8:121566836 | TCCCATCTTCAGAGA[A/C]ATCTGTACCGAGTCA | 76454 |
rs47140872 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxo31 | Mm_Celera | 8:121560637 | CCATGGAGTCACAGA[C/T]GGCTACTGAGCACAG | 76454 |
rs47177638 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Fbxo31 | Mm_Celera | 8:121568393 | CATCGCTCCAGCACA[C/T]CACAGGGATTGGACC | 76454 |
rs47190505 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fbxo31 | Mm_Celera | 8:121558808 | CCTGGTCGCGGAGAC[C/T]GGAGACCGTAACCTG | 76454 |
rs47193556 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Fbxo31 | Mm_Celera | 8:121564094 | CCATTCTATACCTCA[A/C]GCTGTCCCAGAACTC | 76454 |
rs47253749 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Fbxo31 | Mm_Celera | 8:121573649 | AGACTCAAGCTCAGC[A/G]GTGAAGCAGCCTTAA | 76454 |
rs47281623 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Fbxo31 | Mm_Celera | 8:121561168 | GTACAGAGTAATGGG[A/G]GCACGCGTCTAGGAG | 76454 |
rs47295551 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Fbxo31 | Mm_Celera | 8:121553014 | TTTGTGGACCAGAAG[A/C]TACTGTGACAACTGA | 76454 |
rs47299251 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Fbxo31 | Mm_Celera | 8:121574545 | GTCCTTCTATTTCTC[G/T]AACAGTCTGTGTTTT | 76454 |
rs47311467 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Fbxo31 | Mm_Celera | 8:121572468 | TCACCAGCGACAGGG[C/T]GGACACTCAGGTCAC | 76454 |
rs47329792 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime | Fbxo31 | Mm_Celera | 8:121551205 | AGGTCCCTCGCCAGC[A/G]GGATGAGTTCTCAGC | 76454 |
rs47463107 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Fbxo31 | Mm_Celera | 8:121561048 | AAAGAACTACAAGGA[C/T]GCACAGGCTGCAGGC | 76454 |
rs47516136 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxo31 | Mm_Celera | 8:121560959 | ACACTAATGTGGACA[C/T]CTTACTCTGAATGCA | 76454 |
rs47551771 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fbxo31 | Mm_Celera | 8:121562095 | GTCCCTCTGCAGACC[A/G]TCTGAGCCTGGGAGT | 76454 |
rs47572177 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Fbxo31 | Mm_Celera | 8:121567354 | TGATTTCCTTGACAG[C/T]GCAGACCCATTTCCA | 76454 |
rs47642543 | snp | A/G | 0.32 | 0.24 | intron-variant | Fbxo31 | Mm_Celera | 8:121562136 | TCCCTCTAGTCCAAA[A/G]GAAAGATGCGACTAA | 76454 |
rs47681672 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Fbxo31 | Mm_Celera | 8:121573386 | GGCTAGCCTTTCCCT[C/T]GCCACTGGGGACAGC | 76454 |
rs47850623 | snp | A/C | 0.32 | 0.24 | intron-variant | Fbxo31 | Mm_Celera | 8:121562501 | AGACAGGAGTCCCTG[A/C]ATACTCTAATACACT | 76454 |
rs47877391 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Fbxo31 | Mm_Celera | 8:121565175 | AGCTCCCATACTCAG[C/T]GTGCAGTACGCTCTG | 76454 |
rs47951877 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxo31 | Mm_Celera | 8:121566150 | GATGCCTTTAACCGT[C/T]ATGGACTTGAAAGGA | 76454 |
rs47977984 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Fbxo31 | Mm_Celera | 8:121566383 | ATGCAAAACCAAGGA[A/G]AACTCGCGCAAAGCA | 76454 |
rs48012524 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fbxo31 | Mm_Celera | 8:121560301 | GTAACATCTGGCCCT[A/G]AAAGGAAACCCCTGG | 76454 |
rs48022286 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Fbxo31 | Mm_Celera | 8:121566988 | GGTGAGCTCTGACCA[C/T]TCAGAGTGAGATGTA | 76454 |
rs48149866 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Fbxo31 | Mm_Celera | 8:121572370 | GGCACGGACAAGGGG[C/T]CAGCAAGAGAAACTG | 76454 |
rs48209690 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Fbxo31 | Mm_Celera | 8:121553421 | TCACCTGTAAGATGT[G/T]CATGGTGACGCCACC | 76454 |
rs48315235 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Fbxo31 | Mm_Celera | 8:121561119 | TCACCTCTGAACTCA[C/T]AAGCACAGACAGCAT | 76454 |
rs48329963 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxo31 | Mm_Celera | 8:121562975 | CACTCAGCAGCACCA[C/T]CCAGAAATGAGGAGG | 76454 |
rs48371389 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fbxo31 | Mm_Celera | 8:121564625 | GCCACAGCGCAGGGC[A/G]TGAGGTACGTACGGC | 76454 |
rs48436730 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Fbxo31 | Mm_Celera | 8:121564779 | AGGTGAGCGGCTGCC[A/G]TGTGATGTGACCTGA | 76454 |
rs48440281 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Fbxo31 | Mm_Celera | 8:121561842 | CCTCCCTTCCGCTCA[C/T]ACCAGCCAGAGAGCT | 76454 |
rs48453650 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Fbxo31 | Mm_Celera | 8:121562741 | AGAGCCCGCTGAGAG[C/T]CCAGCTGGCGCTACG | 76454 |
rs48498361 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fbxo31 | Mm_Celera | 8:121568002 | CACTTCAGCTCTGAC[A/G]ATCCCCAGAGACTGG | 76454 |
rs48527155 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Fbxo31 | Mm_Celera | 8:121564152 | GAGTGCTAGGCTGAC[A/T]GGCACGTGGCGCTGA | 76454 |
rs48586801 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Fbxo31 | Mm_Celera | 8:121573863 | CCACATGAGGCCTGT[C/G]TCACAAAAAGTGAAA | 76454 |
rs48601313 | snp | C/T | 0.231111 | 0.249285 | utr-variant-3-prime | Fbxo31 | Mm_Celera | 8:121551711 | GACTCCCTGGCAATC[C/T]TTGGTGGCTCCTAGC | 76454 |
rs48764747 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Fbxo31 | Mm_Celera | 8:121569970 | TTAGGGTAAATGAAA[C/T]GCCCTTGCATCCCTC | 76454 |
rs48780117 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxo31 | Mm_Celera | 8:121557939 | AGAGTCATCACCAGG[A/G]CGAGTCCCAGCTACA | 76454 |
rs48816661 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Fbxo31 | Mm_Celera | 8:121568382 | ACTGGTGAGCGCATC[A/G]CTCCAGCACATCACA | 76454 |
rs48849361 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Fbxo31 | Mm_Celera | 8:121573920 | AGCACCGCACCTCGG[A/C]GGTCAAGGCCAACTA | 76454 |
rs48862774 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Fbxo31 | Mm_Celera | 8:121570717 | GCTCACTGCCACTCC[A/G]AATCAGGCTCAGCCC | 76454 |
rs48883910 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Fbxo31 | Mm_Celera | 8:121570656 | CACCAGACCCTGGTC[A/G]GCGGCTAGGTGGGAC | 76454 |
rs48895727 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fbxo31 | Mm_Celera | 8:121566068 | AATGAGAGCATTTGC[C/G]GAGCACTGAAATCCC | 76454 |
rs48900997 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Fbxo31 | Mm_Celera | 8:121566545 | AGCTCTGCTGTCTGC[G/T]CTGCTATGGTCCAGT | 76454 |
rs48994280 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxo31 | Mm_Celera | 8:121560732 | TCAGGGAGAGGGACA[A/G]CCCAGCCTTTGGACA | 76454 |
rs49025243 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxo31 | Mm_Celera | 8:121566682 | AGGTCTCCTTAATGC[A/G]CAGTATGGCTGGACC | 76454 |
rs49212682 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Fbxo31 | Mm_Celera | 8:121562167 | CCGTCCTGTCTCATC[A/C]TAGTCACTGGGTCAC | 76454 |
rs49246151 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Fbxo31 | Mm_Celera | 8:121571321 | AGGAAATGGTGCAGC[A/T]CTTTCATAGACACGA | 76454 |
rs49271936 | snp | C/G | 0.336735 | 0.234472 | intron-variant | Fbxo31 | Mm_Celera | 8:121570850 | ACTTTATTTAGCGCT[C/G]CAGGTTGGCAGTTTT | 76454 |
rs49430401 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Fbxo31 | Mm_Celera | 8:121565129 | AGCCATCAGGCCCAG[C/G]TTAGGAGTGTTTGCA | 76454 |
rs49508924 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Fbxo31 | Mm_Celera | 8:121573124 | TGACAGACAGACCAG[C/T]CGAAATGCACGCACA | 76454 |
rs49573897 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Fbxo31 | Mm_Celera | 8:121570609 | ACCTTCCCACAAGTC[A/G]TCAAAAGCAGCTGCC | 76454 |
rs49573990 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Fbxo31 | Mm_Celera | 8:121560989 | ACCAACCACCAGCCA[C/T]ACCCTCAGCAGCTAC | 76454 |
rs49587777 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Fbxo31 | Mm_Celera | 8:121570640 | CTTAGCTTAGCTCTC[A/G]CACCAGACCCTGGTC | 76454 |
rs49673284 | snp | G/T | 0.231111 | 0.249285 | synonymous-codon | Fbxo31 | Mm_Celera | 8:121554365 | GAGCTCGTTGAAGTT[G/T]CGGAGGTTCTCCACG | 76454 |
rs49675014 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Fbxo31 | Mm_Celera | 8:121561729 | AAACAACTGCCTTCA[C/T]AAACATTAGTGACCG | 76454 |
rs49702288 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxo31 | Mm_Celera | 8:121552699 | TCCAGGTTCCTGATC[A/G]AATTTGCTAAGCACG | 76454 |
rs49817237 | snp | A/G | 0.244898 | 0.249948 | synonymous-codon, intron-variant | Fbxo31 | GRCm38.p3 | 8:121566303 | GTCCCGGCAAGACAC[A/G]CCTGTGATCTCCAGC | 76454 |
rs49881456 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Fbxo31 | Mm_Celera | 8:121562205 | AGTCCCCGGTGCATG[G/T]TAAGAATCAGGAGAT | 76454 |
rs49949773 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime | Fbxo31 | Mm_Celera | 8:121550357 | TCAAAGGGACACAAG[A/G]TGAGTCAGGACCAAG | 76454 |
rs49952196 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Fbxo31 | Mm_Celera | 8:121571986 | TTTAGAGATGAGCAT[G/T]TGTGGGCCTTCTGGA | 76454 |
rs50082757 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Fbxo31 | Mm_Celera | 8:121566225 | GGCCACTGCCACTTA[C/T]GGAGCCCTGGCTCAA | 76454 |
rs50131585 | snp | A/T | 0.408163 | 0.193609 | intron-variant | Fbxo31 | Mm_Celera | 8:121571208 | AGTGAATGACAGACA[A/T]GCCGAGAAACTTCTC | 76454 |