| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs4227796 | snp | A/G | 0.244898 | 0.249948 | utr-variant-3-prime | Fbxo9 | Mm_Celera | 9:78081578 | TTTCACATTTTGAGT[A/G]TGATGCAAAGCCACT | 71538 |
| rs4227797 | snp | A/C | 0.244898 | 0.249948 | utr-variant-3-prime | Fbxo9 | Mm_Celera | 9:78081797 | CCAGGAATCAACTAT[A/C]Cttttaaataaaaaa | 71538 |
| rs4227798 | snp | A/C | 0.244898 | 0.249948 | utr-variant-3-prime | Fbxo9 | Mm_Celera | 9:78081798 | CAGGAATCAACTATC[A/C]ttttaaataaaaaaa | 71538 |
| rs30194666 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Fbxo9 | Mm_Celera | 9:78092841 | TTGTGTGTGTGTGTG[A/T]GAGAGAGAGAGAGAG | 71538 |
| rs30280018 | snp | A/G | 0.5 | 0 | intron-variant | Fbxo9 | Mm_Celera | 9:78090465 | AAATGGAATCAGTGT[A/G]TTAAAGGGACAGACT | 71538 |
| rs33693271 | snp | A/G | 0.5 | 0 | intron-variant | Fbxo9 | Mm_Celera | 9:78099955 | GGAGAGGCAGAGGCA[A/G]CGGGATCAGATGTCC | 71538 |
| rs33757893 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Fbxo9 | Mm_Celera | 9:78102045 | CAACAGCAAAAAAAA[A/T]AAAATAAAATCATTT | 71538 |
| rs46123833 | snp | A/G | 0.18 | 0.24 | intron-variant | Fbxo9 | Mm_Celera | 9:78094624 | GCTATTTTGTAAATA[A/G]TGCATTTGGATTTTA | 71538 |
| rs46134558 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Fbxo9 | Mm_Celera | 9:78089618 | TACATCCTACCACAC[A/G]GCTCCAAAAACTGGA | 71538 |
| rs46136017 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Fbxo9 | Mm_Celera | 9:78087797 | CAGGTCGAGTGCTAG[C/T]GTAAAAACCAACCAC | 71538 |
| rs46191631 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Fbxo9 | Mm_Celera | 9:78088870 | GACTTGAACCCACAC[G/T]AAGCAAGCACTCCGT | 71538 |
| rs46497281 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Fbxo9 | Mm_Celera | 9:78083599 | TGGGCTGTGAGGACA[C/T]AGCCGGGCTTGGTAG | 71538 |
| rs46576562 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Fbxo9 | Mm_Celera | 9:78087075 | TAGATTAAAAAATAC[C/T]GAGGACCGTTTTGTG | 71538 |
| rs46592744 | snp | A/C | | | intron-variant | Fbxo9 | Mm_Celera | 9:78106376 | TCGAAGGCAGAGAGC[A/C]CATCTTTGTCACAGC | 71538 |
| rs47059575 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Fbxo9 | Mm_Celera | 9:78097408 | TTGACTGAATCCTTA[C/T]GCACCTCCCATAAAA | 71538 |
| rs47097098 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fbxo9 | Mm_Celera | 9:78084759 | GGTCACCCTGAGTAC[C/T]ACATGTAAACCTATG | 71538 |
| rs47127448 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Fbxo9 | Mm_Celera | 9:78091177 | GGTAGGGTGGATGGA[G/T]ATGTCAAAAAGTACA | 71538 |
| rs47273371 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Fbxo9 | Mm_Celera | 9:78085278 | ATCAGAGGAGGCAGG[A/G]AAGCCAGTGCCCTGG | 71538 |
| rs47332469 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Fbxo9 | Mm_Celera | 9:78097865 | TATGCTTCTAGACAA[C/T]GCTATTTTAGAGGTT | 71538 |
| rs47547300 | snp | G/T | 0.260355 | 0.249785 | intron-variant | Fbxo9 | Mm_Celera | 9:78082811 | TTCTTCATTATGACT[G/T]TCAACATATTCCTAA | 71538 |
| rs47627454 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Fbxo9 | Mm_Celera | 9:78096704 | TCCAGCCTGTATTTA[A/G]TGATCTAATCCCTTC | 71538 |
| rs47949994 | snp | C/G | 0.46875 | 0.121031 | utr-variant-5-prime, upstream-variant-2KB | Fbxo9, Ick | Mm_Celera | 9:78109038 | GTGGTAACAGCCAAC[C/G]CAAGTCACGTCGAAC | 71538 |
| rs48200137 | snp | A/C | | | intron-variant | Fbxo9 | Mm_Celera | 9:78083235 | ACCCTGTCTCGAAAA[A/C]CCAAAAAAAAAAAAA | 71538 |
| rs48278365 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Fbxo9 | Mm_Celera | 9:78089904 | CTATTCAGAGACATT[A/G]CCGACATCAATCAGA | 71538 |
| rs48441426 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Fbxo9 | Mm_Celera | 9:78085801 | TGTGCATAAACGTCC[A/G]GCTCTTGTGGCAAAA | 71538 |
| rs48945416 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Fbxo9 | Mm_Celera | 9:78088349 | CTTTAAGTCAATGCA[C/T]CCAGACTATAATAGA | 71538 |
| rs49155075 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Fbxo9 | Mm_Celera | 9:78088689 | AGAGAGGGCTCTAGA[C/T]AGAGGGCCATGTAGA | 71538 |
| rs49240574 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxo9 | Mm_Celera | 9:78089249 | TCCACCAGAAGGTAG[A/G]GAGGTCCCAGCCACC | 71538 |
| rs49320811 | snp | A/G | 0.391111 | 0.206368 | downstream-variant-500B | Fbxo9 | Mm_Celera | 9:78081450 | TCTGTTGGCTATCCC[A/G]GGACCATTCATTAAA | 71538 |
| rs49366535 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxo9 | Mm_Celera | 9:78095652 | GATGCGCACAGTGGC[A/G]CCGAGTTCCTCCAGC | 71538 |
| rs49381139 | snp | C/T | 0.21875 | 0.248039 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | Fbxo9, Ick | Mm_Celera | 9:78108546 | GTCGCCGGTCGCCAG[C/T]GGAGGCCGAGCACCG | 71538 |
| rs49389142 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Fbxo9 | Mm_Celera | 9:78088064 | TTACGCTTTCAAAAA[A/T]TAACTCTGGGAGACA | 71538 |
| rs49491790 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Fbxo9 | Mm_Celera | 9:78094961 | GCACATTCTAACCTT[G/T]AAGTGCTGTTATTTG | 71538 |
| rs49774660 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Fbxo9 | Mm_Celera | 9:78086125 | GAGAACGAGCTTGCA[C/T]AGGCCTTGCAGGACA | 71538 |
| rs49848855 | snp | A/G | 0.277778 | 0.248452 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | Fbxo9, Ick | Mm_Celera | 9:78108585 | GCTGAGCGTCGGCCC[A/G]GCAGGAGACGTCTGG | 71538 |
| rs50240878 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Fbxo9 | Mm_Celera | 9:78085814 | CCAGCTCTTGTGGCA[A/G]AACCGTCTGGGGATT | 71538 |
| rs50311587 | snp | G/T | | | intron-variant | Fbxo9 | Mm_Celera | 9:78083230 | GAGAAACCCTGTCTC[G/T]AAAACCCAAAAAAAA | 71538 |
| rs50394358 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Fbxo9 | Mm_Celera | 9:78091692 | CTGTTCTCATCAGAA[C/T]CGCCCTCTGACATTA | 71538 |
| rs50576379 | snp | A/G | | | intron-variant | Fbxo9 | Mm_Celera | 9:78083099 | AAAAAAAAGGCAGCC[A/G]AGTGTGGTGGCACAC | 71538 |
| rs50577216 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Fbxo9 | Mm_Celera | 9:78087636 | AAAAGCTAAGTTAAA[A/G]TCCTTAGAAGCAAAT | 71538 |
| rs50612733 | snp | A/C | 0.124444 | 0.216185 | downstream-variant-500B | Fbxo9 | Mm_Celera | 9:78081256 | GTGATTTATGTGACG[A/C]GCAAATGTTCATTTG | 71538 |
| rs50713711 | snp | C/G | | | intron-variant | Fbxo9 | Mm_Celera | 9:78083133 | TTTAATCCCAGCACT[C/G]GGGAGGCAGAAGCAG | 71538 |
| rs50747346 | snp | C/T | 0.408163 | 0.193609 | downstream-variant-500B | Fbxo9 | Mm_Celera | 9:78081174 | TCATGGTTTTATAAT[C/T]TGCTGTTACTGCTTC | 71538 |
| rs51103507 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime | Fbxo9 | Mm_Celera | 9:78081690 | TGACAGATCTGCTCA[A/G]AAACCTGCTTGAAAA | 71538 |
| rs51157437 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Fbxo9 | Mm_Celera | 9:78089216 | TGTATACAATCCCAG[A/C]GTCACATACGGCTGT | 71538 |
| rs51239647 | snp | A/T | 0.32 | 0.24 | intron-variant | Fbxo9 | Mm_Celera | 9:78083543 | GGTTTTACTCTGGAC[A/T]CACTGCATCAGATCA | 71538 |
| rs51248474 | snp | A/G | 0.21875 | 0.248039 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | Fbxo9, Ick | Mm_Celera | 9:78108437 | CACCAGGCAGCGGCA[A/G]TAACTGCGGGCCCGG | 71538 |
| rs51279440 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Fbxo9 | Mm_Celera | 9:78086909 | TATTTCTCAGCTGCA[G/T]ACCCACGTGCTGAAC | 71538 |
| rs51285581 | snp | A/G | 0.46281 | 0.131194 | intron-variant | Fbxo9 | Mm_Celera | 9:78097492 | CCAAATGGCTCATTT[A/G]GGTTTGAGCTACTAC | 71538 |
| rs51823600 | snp | A/G | 0.336735 | 0.234472 | downstream-variant-500B | Fbxo9 | Mm_Celera | 9:78081408 | AAGGTAAAGGCCAGC[A/G]ATGGCTGACGCAGTG | 71538 |
| rs51834718 | snp | C/G | 0.336735 | 0.234472 | intron-variant | Fbxo9 | Mm_Celera | 9:78085189 | CTGTGAACACTGTGA[C/G]TGGCTTCCTTATAGA | 71538 |
| rs51935037 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Fbxo9 | Mm_Celera | 9:78085742 | TACTGTATTCCCGTG[C/T]GTGAGGACCCTAGGG | 71538 |
| rs51944025 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Fbxo9 | Mm_Celera | 9:78094906 | AGGAAGCAGTCAGGG[C/T]GCCTGTATCTGTCTG | 71538 |
| rs52013061 | snp | A/G | 0.391111 | 0.206368 | synonymous-codon | Fbxo9 | Mm_Celera | 9:78082082 | CACTGCAGTCTCACC[A/G]GTTGCTCTGGAAACA | 71538 |
| rs52015424 | snp | C/T | | | intron-variant | Fbxo9 | Mm_Celera | 9:78106530 | ACTCGATATGTAGAC[C/T]AGGCTGGCCTTGAAT | 71538 |
| rs52398718 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Fbxo9 | Mm_Celera | 9:78090082 | TTACTTCAAACTAAA[A/G]TTCCTTTCTGGGTCA | 71538 |
| rs52484001 | snp | A/T | | | intron-variant | Fbxo9 | Mm_Celera | 9:78092864 | AGAGAGAGAGAGTGT[A/T]TGTGTGTGTGTACCT | 71538 |
| rs107768941 | snp | A/G | | | intron-variant | Fbxo9 | Mm_Celera | 9:78107135 | GGAGACACTTTCTCA[A/G]GTGAGGCGTGCCTTC | 71538 |
| rs211756983 | in-del | -/T | | | intron-variant | Fbxo9 | Mm_Celera | 9:78104638 | TCAATTCTGCACCTC[-/T]AGGTGACCCAGGCTT | 71538 |
| rs211789157 | snp | A/C | | | upstream-variant-2KB, intron-variant | Fbxo9, Ick | Mm_Celera | 9:78110831 | GCCATGGACTTTTGA[A/C]AAGGTTGGAGCAGGT | 71538 |
| rs211911074 | snp | C/G | | | intron-variant | Fbxo9 | Mm_Celera | 9:78086386 | CTACATGAGAAGGAA[C/G]CAGACACCACCACAC | 71538 |
| rs211971318 | snp | C/T | | | intron-variant | Fbxo9 | Mm_Celera | 9:78093383 | CCTGCCATACTCATC[C/T]CTGAGGAGACACAGG | 71538 |
| rs212011716 | snp | A/G | | | intron-variant | Fbxo9 | Mm_Celera | 9:78103234 | ACCTCTCTCTACCTT[A/G]TATTCCTCTAATTCA | 71538 |
| rs212030638 | snp | A/G | | | intron-variant | Fbxo9 | Mm_Celera | 9:78094077 | AAAATACCAATTCAC[A/G]TGAAATTTAAAAAGA | 71538 |
| rs212055249 | snp | A/T | | | intron-variant | Fbxo9 | Mm_Celera | 9:78101917 | TCATCTTCTGAGGCA[A/T]GCAGATCTCTGAGTT | 71538 |
| rs212267779 | in-del | -/CACTGCA | | | intron-variant | Fbxo9 | Mm_Celera | 9:78095620 | CAGCCTCATCAGGAC[-/CACTGCA]CACTCTGGCTGATGC | 71538 |
| rs212425653 | snp | A/G | | | intron-variant | Fbxo9 | Mm_Celera | 9:78087041 | TTTAGGTTTTTGAGT[A/G]CGGTTCCTGTCATAA | 71538 |
| rs212536791 | snp | C/T | | | intron-variant | Fbxo9 | Mm_Celera | 9:78087992 | AGGAGGAGCCAGCAT[C/T]CCACTGCTGGCCTCT | 71538 |
| rs212550113 | snp | A/T | | | intron-variant | Fbxo9 | Mm_Celera | 9:78095529 | GGATTCTTATATTTT[A/T]ATTTAAGAAAAATGT | 71538 |
| rs212585597 | snp | G/T | | | intron-variant | Fbxo9 | Mm_Celera | 9:78096781 | TTTTCTAATAAAAAT[G/T]CCCTTAATTTGTCAC | 71538 |
| rs212619674 | snp | G/T | | | intron-variant | Fbxo9 | Mm_Celera | 9:78105774 | CCCCAAAGGATCCCC[G/T]TGTAAACAGAGGTCC | 71538 |
| rs212657050 | snp | A/G | | | intron-variant | Fbxo9 | Mm_Celera | 9:78105013 | CTGGCGTGGTTTAAC[A/G]TGGAATAAAGGTGGG | 71538 |
| rs212767550 | snp | C/T | | | intron-variant | Fbxo9 | Mm_Celera | 9:78089383 | TCCCAGCTCCATCCA[C/T]CACTGTCTCTCAGAA | 71538 |
| rs212822498 | snp | A/C | | | intron-variant | Fbxo9 | Mm_Celera | 9:78088697 | CTCTAGATAGAGGGC[A/C]ATGTAGAGGACAAAA | 71538 |
| rs212952122 | snp | C/T | | | intron-variant | Fbxo9 | Mm_Celera | 9:78098494 | CATTTCTCTCACTCA[C/T]TTTGTCTGCCCTTAG | 71538 |
| rs212986419 | in-del | -/ATTATG | | | downstream-variant-500B | Fbxo9 | Mm_Celera | 9:78081016 | ATAGCAGATATTTAC[-/ATTATG]ATTAATAGTAGTAGC | 71538 |
| rs212991592 | snp | C/T | | | intron-variant | Fbxo9 | Mm_Celera | 9:78107092 | ATTAAGAAAATGCCC[C/T]GCAGGCTTGACTGCA | 71538 |
| rs213021227 | snp | C/T | | | intron-variant | Fbxo9 | Mm_Celera | 9:78098906 | TGCATCCTCTGCATC[C/T]GGAGCCGACTACCAT | 71538 |
| rs213086300 | snp | C/T | | | intron-variant | Fbxo9 | Mm_Celera | 9:78091048 | TAAGAGTTGGCTTGG[C/T]CATAGTGTCTGTTCA | 71538 |
| rs213205475 | snp | A/G | | | intron-variant | Fbxo9 | Mm_Celera | 9:78099990 | TCATCCTTATGTGAG[A/G]GCAGCCTGGGTTTCA | 71538 |
| rs213214357 | snp | G/T | | | intron-variant | Fbxo9 | Mm_Celera | 9:78098974 | AGGGACTTGACCAGT[G/T]AGACACTTAAAATGT | 71538 |
| rs213271220 | snp | C/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | Fbxo9, Ick | Mm_Celera | 9:78108300 | GGTTACCATGCTGGC[C/G]GGCGGCCGGCCCAGT | 71538 |
| rs213440805 | snp | C/G | | | intron-variant | Fbxo9 | Mm_Celera | 9:78083650 | CTGAAGTCATCCACA[C/G]AGTGGAAATGTGATG | 71538 |
| rs213511274 | in-del | -/TTT | | | intron-variant | Fbxo9 | Mm_Celera | 9:78084304 | CTAGTTTAGGCATTC[-/TTT]TTTTTTTTTAAGTTT | 71538 |
| rs213524316 | snp | C/G | | | intron-variant | Fbxo9 | Mm_Celera | 9:78101127 | AGCAGGACCCTGAGG[C/G]TTCATATCTTTCACA | 71538 |
| rs213568016 | snp | A/T | | | intron-variant | Fbxo9 | Mm_Celera | 9:78082420 | GCCATCTTTTGATAC[A/T]TATGCAGCTAGAGAC | 71538 |
| rs213645856 | snp | G/T | | | upstream-variant-2KB, intron-variant | Fbxo9, Ick | Mm_Celera | 9:78110189 | AACTCGCCAGTCCTA[G/T]TTTTCCTAGTTCTTG | 71538 |
| rs213735881 | snp | G/T | | | intron-variant | Fbxo9 | Mm_Celera | 9:78092248 | GAGAGAGAGATGCTA[G/T]CAGCCTAAAATAACT | 71538 |
| rs213774732 | snp | C/T | | | missense | Fbxo9 | Mm_Celera | 9:78101577 | GTGTCTGCAGCTGCT[C/T]TCAGCATAGAGCTTC | 71538 |
| rs213798620 | snp | G/T | | | intron-variant | Fbxo9 | Mm_Celera | 9:78091897 | GGGAGAAGAGCACTT[G/T]CGGCTCTTGCAGAGG | 71538 |
| rs213864392 | snp | C/T | | | intron-variant | Fbxo9 | Mm_Celera | 9:78085474 | ACTAGACAAAGGAAT[C/T]TAGAGAAAGTTGCAA | 71538 |
| rs214035712 | snp | C/T | | | upstream-variant-2KB, intron-variant | Fbxo9, Ick | Mm_Celera | 9:78110704 | AGGTTGGAAACAGCA[C/T]TAATCTCTGCATATA | 71538 |
| rs214076877 | snp | A/C | | | intron-variant | Fbxo9 | Mm_Celera | 9:78104037 | CAAACCAACCAAAAA[A/C]CATTAACAAATCAAA | 71538 |
| rs214114803 | snp | A/G | | | intron-variant | Fbxo9 | Mm_Celera | 9:78103449 | TGGACCAAAACAACA[A/G]TTGGGTGAGTAAAAT | 71538 |
| rs214275389 | snp | A/G | | | synonymous-codon | Fbxo9 | Mm_Celera | 9:78087570 | TTTCAAGCAAGCCAG[A/G]CGCCAGATTTCAGGG | 71538 |
| rs214287679 | snp | A/G | | | intron-variant | Fbxo9 | Mm_Celera | 9:78095361 | ACAGCGCAGAGACGC[A/G]GGCAGAGCACATTAA | 71538 |
| rs214304832 | snp | C/T | | | intron-variant | Fbxo9 | Mm_Celera | 9:78098695 | GGGGATTCTGGAGGG[C/T]GGTGCTGGTTTTTGT | 71538 |
| rs214349745 | snp | C/T | | | intron-variant | Fbxo9 | Mm_Celera | 9:78094283 | CAAGAAACTAAACAG[C/T]GCTCAAAAGAGATAG | 71538 |
| rs214523395 | snp | A/G | | | intron-variant | Fbxo9 | Mm_Celera | 9:78089876 | CTGACTTTATGAATC[A/G]CTGCAGTCCAGACTA | 71538 |
| rs214593740 | snp | A/G | | | intron-variant | Fbxo9 | Mm_Celera | 9:78086062 | GAGCACCTAGAACGC[A/G]GCGTCCCAGTGCCCC | 71538 |