SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6159272 | snp | A/C | 0.5 | 0 | intron-variant | Fbxo17 | Mm_Celera | 7:28723107 | TGCCAAGACAGAGGA[A/C]TCCATGTTTTATTTT | 50760 |
rs6160242 | snp | C/T | 0.5 | 0 | intron-variant | Fbxo17 | Mm_Celera | 7:28723225 | TTTGATTTTCTTAGA[C/T]TTTTCTGTTCAGTCA | 50760 |
rs30722697 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Fbxo17 | Mm_Celera | 7:28730273 | AATTCTTATTTTTTT[A/T]AAAAAAGGAATGAAA | 50760 |
rs30792218 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Fbxo17 | GRCm38.p3 | 7:28729271 | GAGTGTTCTCTGCTG[G/T]AGCCATCAGCAGCGT | 50760 |
rs30926822 | snp | A/C | 0.444444 | 0.157135 | upstream-variant-2KB | Fbxo17 | GRCm38.p3 | 7:28716418 | ACCCATCTCCCACCC[A/C]CTATGTAGCTATCCA | 50760 |
rs30961587 | snp | A/T | 0.5 | 0 | utr-variant-5-prime, nc-transcript-variant | Fbxo17 | Mm_Celera | 7:28724616 | TTCTCTTGAGTAAAT[A/T]CCTAGGAATGGAATT | 50760 |
rs30971173 | snp | C/T | 0.5 | 0 | intron-variant | Fbxo17 | GRCm38.p3 | 7:28729747 | ACAGCAGTGCATGTA[C/T]CCATGATTCCAGAAC | 50760 |
rs31007629 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Fbxo17 | GRCm38.p3 | 7:28726700 | GTTCCAGACACTTTT[C/G]TGTATGCGTTTTTGT | 50760 |
rs32152703 | snp | A/G | 0.48 | 0.0979796 | downstream-variant-500B | Fbxo17 | Mm_Celera | 7:28738460 | TATGTGCATGTGTGT[A/G]TCTCTGTATGGGTAT | 50760 |
rs33865292 | snp | C/T | 0.5 | 0 | intron-variant | Fbxo17 | GRCm38.p3 | 7:28729872 | CATTGAGCTGCACCT[C/T]AGACCTGCACTGGTG | 50760 |
rs33866627 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fbxo17 | GRCm38.p3 | 7:28729247 | GCAGCGTTTCGCTGT[C/T]GTCACCTAGGTTCTA | 50760 |
rs33895559 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Fbxo17 | GRCm38.p3 | 7:28735054 | ATTCCCTGCTCGGCT[G/T]CCTAATGTGTGGGGC | 50760 |
rs45637174 | snp | A/C | | | intron-variant | Fbxo17 | GRCm38.p3 | 7:28718420 | AAACCAGTAAGCAGC[A/C]ATCCTCCATGGCCTC | 50760 |
rs45641486 | snp | A/C | | | intron-variant | Fbxo17 | Mm_Celera | 7:28722264 | ACCCACACTTCCTTA[A/C]ACCTTCTATAGGTTC | 50760 |
rs45718094 | snp | A/G | | | intron-variant | Fbxo17 | GRCm38.p3 | 7:28717529 | CCACGTTTCATACAT[A/G]CTTTGTTTTTATGGA | 50760 |
rs45731965 | snp | G/T | | | intron-variant | Fbxo17 | Mm_Celera | 7:28731550 | AACATCACGGGCCCT[G/T]TTTCTAGGCAGCTTC | 50760 |
rs45827007 | snp | C/T | | | intron-variant | Fbxo17 | Mm_Celera | 7:28721395 | GCCATTCCTCAGGGG[C/T]CCGAGTGCATTTGCT | 50760 |
rs45854680 | snp | A/G | | | intron-variant | Fbxo17 | Mm_Celera | 7:28722353 | TCTTCAGGCCTCCAC[A/G]GTACTGCATACTTAT | 50760 |
rs45858718 | snp | A/G | | | intron-variant | Fbxo17 | GRCm38.p3 | 7:28719673 | TTCTGATTCTGTGTT[A/G]GCCCCTTACAAAGCC | 50760 |
rs45928386 | snp | C/T | | | intron-variant | Fbxo17 | Mm_Celera | 7:28725533 | ACCCCTGCGAGAGCA[C/T]GAGGCAAATTGTAGC | 50760 |
rs46033197 | snp | C/T | | | intron-variant | Fbxo17 | GRCm38.p3 | 7:28719792 | GGTGAACGCCTGTGA[C/T]CCTAGCACTCTGGAG | 50760 |
rs46053347 | snp | C/T | | | intron-variant | Fbxo17 | GRCm38.p3 | 7:28719783 | AGGTATGGAGGTGAA[C/T]GCCTGTGACCCTAGC | 50760 |
rs46057319 | snp | A/T | | | intron-variant | Fbxo17 | GRCm38.p3 | 7:28719663 | TTGCCCTCAATTCTG[A/T]TTCTGTGTTGGCCCC | 50760 |
rs46098067 | snp | C/T | | | intron-variant | Fbxo17 | GRCm38.p3 | 7:28731488 | GTGGGGTCATACTTA[C/T]ACCCTTTCCAAACAT | 50760 |
rs46109712 | snp | A/C | | | intron-variant | Fbxo17 | GRCm38.p3 | 7:28728119 | CTTGTGACTCGCAGA[A/C]TGATGGAGTTACGTG | 50760 |
rs46111936 | snp | A/G | | | intron-variant | Fbxo17 | Mm_Celera | 7:28721398 | ATTCCTCAGGGGTCC[A/G]AGTGCATTTGCTTTC | 50760 |
rs46210650 | snp | A/G | | | intron-variant | Fbxo17 | GRCm38.p3 | 7:28719921 | TAATTCCAGCCCTGG[A/G]AAAGAAGAGGCAGGC | 50760 |
rs46252341 | snp | C/T | | | intron-variant | Fbxo17 | GRCm38.p3 | 7:28717614 | TGGTGATTCTCAAGA[C/T]TCAGAGTTAAAGGCG | 50760 |
rs46351829 | snp | G/T | | | intron-variant | Fbxo17 | GRCm38.p3 | 7:28717593 | AGTGCCTGCCGCCAA[G/T]CCTCCTGGTGATTCT | 50760 |
rs46398307 | snp | A/G | | | intron-variant | Fbxo17 | Mm_Celera | 7:28720660 | GATGTGGTGGCACAC[A/G]CCTTTAATCCCAGCA | 50760 |
rs46404841 | snp | A/G | | | intron-variant | Fbxo17 | Mm_Celera | 7:28722712 | CAGATCTCTATAGGT[A/G]GAGGCCAGCCTGGTC | 50760 |
rs46426226 | snp | G/T | | | intron-variant | Fbxo17 | Mm_Celera | 7:28722105 | TTATGATAAGCAACT[G/T]AAGGAAGAAAGGGTT | 50760 |
rs46435771 | snp | A/G | | | intron-variant | Fbxo17 | Mm_Celera | 7:28722265 | CCCACACTTCCTTAA[A/G]CCTTCTATAGGTTCC | 50760 |
rs46448083 | snp | C/T | | | intron-variant | Fbxo17 | Mm_Celera | 7:28717694 | CACATCAAACACTTG[C/T]GCAACAATAACATCT | 50760 |
rs46459562 | snp | G/T | | | intron-variant | Fbxo17 | Mm_Celera | 7:28719728 | TTTTTTTGTTTTTTT[G/T]TTTTTAAATCCCCTA | 50760 |
rs46496375 | snp | A/T | | | intron-variant | Fbxo17 | Mm_Celera | 7:28719734 | TGTTTTTTTTTTTTT[A/T]AATCCCCTATCAAAA | 50760 |
rs46503098 | snp | A/T | | | intron-variant | Fbxo17 | Mm_Celera | 7:28724119 | TATCTCTCCTCCCCT[A/T]CATTTTGTGGCCCAT | 50760 |
rs46608353 | snp | C/G | | | intron-variant | Fbxo17 | GRCm38.p3 | 7:28723320 | GTCCTGGGCTGGATC[C/G]CCAGCACAGCAAAGT | 50760 |
rs46629972 | snp | G/T | | | intron-variant | Fbxo17 | Mm_Celera | 7:28725526 | AAATCACACCCCTGC[G/T]AGAGCACGAGGCAAA | 50760 |
rs46733075 | snp | A/G | | | intron-variant | Fbxo17 | GRCm38.p3 | 7:28721826 | TCCACATCCAGCTCT[A/G]ATTCATCCTTTTAAA | 50760 |
rs46761855 | snp | G/T | | | intron-variant | Fbxo17 | GRCm38.p3 | 7:28725912 | CTCCTGTTTAGGACT[G/T]ACATGGTCACAATCA | 50760 |
rs46799591 | snp | A/T | | | intron-variant | Fbxo17 | GRCm38.p3 | 7:28724932 | GGAATCACGTAGTCA[A/T]TGGAACCATGATTGT | 50760 |
rs46814713 | snp | C/T | | | intron-variant | Fbxo17 | GRCm38.p3 | 7:28726348 | AAGTTCAAGGCCAGC[C/T]TTGGCTGCCTAGAAC | 50760 |
rs46821102 | snp | C/G | | | intron-variant | Fbxo17 | GRCm38.p3 | 7:28718475 | CCTGCCCTGATTTCT[C/G]GATAATGAACTACAG | 50760 |
rs46847514 | snp | C/T | | | intron-variant | Fbxo17 | Mm_Celera | 7:28726925 | TTAAAGGCCTAATAT[C/T]AGTTCAATAAATGGT | 50760 |
rs47018732 | snp | C/T | | | intron-variant | Fbxo17 | GRCm38.p3 | 7:28728477 | TACCCCTCTTCTTTT[C/T]CTGTGTAACACGCGT | 50760 |
rs47085366 | snp | A/G | | | intron-variant | Fbxo17 | Mm_Celera | 7:28718833 | AAGATGAGCACGCAG[A/G]TAAACCCAGGAAGAG | 50760 |
rs47119686 | snp | G/T | | | intron-variant | Fbxo17 | Mm_Celera | 7:28735146 | GGAGTGGGTGTAAGG[G/T]ACGCATCAAGCACCA | 50760 |
rs47140108 | snp | A/G | | | intron-variant | Fbxo17 | GRCm38.p3 | 7:28727726 | TGTTGGGAATGCTAA[A/G]CCAGCTGGCCAATCC | 50760 |
rs47155272 | snp | A/T | | | intron-variant | Fbxo17 | Mm_Celera | 7:28727199 | AATTGATGTAATTAT[A/T]AAAAAAAAAAAAAAG | 50760 |
rs47166122 | snp | A/G | | | intron-variant | Fbxo17 | GRCm38.p3 | 7:28728757 | GATCTGTCTACCTCT[A/G]CCTCAGGAGCACTGA | 50760 |
rs47189159 | snp | A/C | | | intron-variant | Fbxo17 | Mm_Celera | 7:28721495 | CTTTAGGAGTCCAGA[A/C]ATTTTTTTATTTTTA | 50760 |
rs47246382 | snp | A/C | | | intron-variant | Fbxo17 | Mm_Celera | 7:28718245 | ACTTGGGAAGAGGGT[A/C]CCACAACTGAACAGA | 50760 |
rs47290511 | snp | A/G | | | intron-variant | Fbxo17 | GRCm38.p3 | 7:28724856 | AGCTGTTTGTTTGGA[A/G]GGAAGAAGCCAGATT | 50760 |
rs47292433 | snp | A/G | | | intron-variant | Fbxo17 | GRCm38.p3 | 7:28725139 | CAAACAGGCTGGCAA[A/G]GTGTTTCAGTGTAGC | 50760 |
rs47295645 | snp | C/G | | | intron-variant | Fbxo17 | Mm_Celera | 7:28726949 | AAATGGTTCATTGAC[C/G]TGTTCTACAGCAGTT | 50760 |
rs47300855 | snp | G/T | | | intron-variant | Fbxo17 | GRCm38.p3 | 7:28724979 | TGAAGAGTAACAGGA[G/T]CGACTCAGTGGTTGG | 50760 |
rs47302944 | snp | A/C | | | intron-variant | Fbxo17 | GRCm38.p3 | 7:28727709 | TTTTATGTTGGTCCC[A/C]GTGTTGGGAATGCTA | 50760 |
rs47325198 | snp | A/G | | | intron-variant | Fbxo17 | Mm_Celera | 7:28717879 | TGGATCACTCTGGCT[A/G]GCAGCCCCTTTGCAG | 50760 |
rs47340813 | snp | C/T | | | intron-variant | Fbxo17 | GRCm38.p3 | 7:28721621 | GAGGTTCTGTACCCA[C/T]AGGTTGAGACCCCCT | 50760 |
rs47442303 | snp | C/T | | | intron-variant | Fbxo17 | GRCm38.p3 | 7:28727680 | AAGAGGAGTCTGGGT[C/T]ACAGGATGATGGCTT | 50760 |
rs47466152 | snp | C/T | | | intron-variant | Fbxo17 | GRCm38.p3 | 7:28720189 | TTCCATGAGAATTTC[C/T]AAACATGTCCCAGAA | 50760 |
rs47470829 | snp | A/T | | | intron-variant | Fbxo17 | Mm_Celera | 7:28718051 | ATAACACAAATCTGA[A/T]TTTAGTGGtttgttt | 50760 |
rs47560976 | snp | C/T | | | intron-variant | Fbxo17 | GRCm38.p3 | 7:28720174 | GGAAAACAGCATCTG[C/T]TCCATGAGAATTTCC | 50760 |
rs47600007 | snp | C/T | | | upstream-variant-2KB | Fbxo17 | GRCm38.p3 | 7:28715090 | CCCTAAAGCTCCCCA[C/T]CCTGCGTGAGCCACA | 50760 |
rs47618554 | snp | A/G | | | intron-variant | Fbxo17 | GRCm38.p3 | 7:28720157 | CCTCAGTTTCCCTTG[A/G]TGGAAAACAGCATCT | 50760 |
rs47635873 | snp | C/T | | | intron-variant | Fbxo17 | GRCm38.p3 | 7:28726506 | TTTCCTCTGATTGCA[C/T]ACACATGCTTTAGCA | 50760 |
rs47652879 | snp | A/G | | | intron-variant | Fbxo17 | Mm_Celera | 7:28731507 | CTTTCCAAACATCAC[A/G]TGTTCTCTCAAGTGT | 50760 |
rs47673089 | snp | A/C | | | intron-variant | Fbxo17 | GRCm38.p3 | 7:28728567 | GCAGTTGTGACCCAC[A/C]ATGTAGGTGCTGGGA | 50760 |
rs47726433 | snp | C/T | | | intron-variant | Fbxo17 | Mm_Celera | 7:28731555 | CACGGGCCCTGTTTC[C/T]AGGCAGCTTCTAGAA | 50760 |
rs47733284 | snp | A/G | | | intron-variant | Fbxo17 | GRCm38.p3 | 7:28727961 | GTCTTCCCACCCTCC[A/G]ACCCCCACCTAGCCA | 50760 |
rs47742587 | snp | A/G | | | utr-variant-5-prime, nc-transcript-variant | Fbxo17 | GRCm38.p3 | 7:28724700 | TCATAACAGCTCCAA[A/G]TGGGGAGCAGCTCAA | 50760 |
rs47790353 | snp | C/T | | | intron-variant | Fbxo17 | GRCm38.p3 | 7:28730613 | AAAGTCAAGAATCTA[C/T]AAAAATAGCCGGGCA | 50760 |
rs47796562 | snp | A/G | | | intron-variant | Fbxo17 | GRCm38.p3 | 7:28723655 | AGAGTACTGTCTACT[A/G]ACATGTACCTTAAAT | 50760 |
rs47812464 | snp | C/T | | | intron-variant | Fbxo17 | Mm_Celera | 7:28722532 | GTGGCTCACAACCAT[C/T]CGTAACAAGATCTAA | 50760 |
rs47854444 | snp | A/T | | | intron-variant | Fbxo17 | GRCm38.p3 | 7:28717567 | CTACCGGGTCGATGG[A/T]GGCAGGAAAAAGTGC | 50760 |
rs47927419 | snp | C/T | | | intron-variant | Fbxo17 | GRCm38.p3 | 7:28717409 | TGTACTCAGAGATCC[C/T]CCTGCCTCTTCCTCT | 50760 |
rs48041578 | snp | A/G | | | intron-variant | Fbxo17 | Mm_Celera | 7:28718059 | AATCTGATTTTAGTG[A/G]tttgttttgttttgt | 50760 |
rs48055845 | snp | A/T | | | intron-variant | Fbxo17 | GRCm38.p3 | 7:28725026 | GGCCGATCTCTTGAG[A/T]TCAAGGGCACAGACC | 50760 |
rs48216743 | snp | A/G | | | intron-variant | Fbxo17 | GRCm38.p3 | 7:28730595 | GAGTAAGATGCCAAT[A/G]GGAAAGTCAAGAATC | 50760 |
rs48311075 | snp | C/T | | | intron-variant | Fbxo17 | GRCm38.p3 | 7:28731603 | CCTCAGCAAAACATC[C/T]TCCCATGTCTGCTTC | 50760 |
rs48316363 | snp | A/G | | | intron-variant | Fbxo17 | GRCm38.p3 | 7:28730587 | TAGGGATGGAGTAAG[A/G]TGCCAATAGGAAAGT | 50760 |
rs48329947 | snp | C/G | | | intron-variant | Fbxo17 | Mm_Celera | 7:28735167 | TCAAGCACCATACAC[C/G]TTCTTGTCCTGAAAA | 50760 |
rs48384996 | snp | C/T | | | intron-variant | Fbxo17 | GRCm38.p3 | 7:28730635 | AGCCGGGCATGATGG[C/T]TCACACCTTGAATCC | 50760 |
rs48385219 | snp | A/G | | | intron-variant | Fbxo17 | GRCm38.p3 | 7:28720244 | CCAGTCAGCACATCT[A/G]GTAAGGGACACTCAC | 50760 |
rs48390323 | snp | C/T | | | intron-variant | Fbxo17 | GRCm38.p3 | 7:28726006 | CAAATGTGGTGCACT[C/T]ATTACATCCGTGCAG | 50760 |
rs48401201 | snp | C/T | | | intron-variant | Fbxo17 | GRCm38.p3 | 7:28731039 | AATATGAGAATCCGA[C/T]TCCCAGGTAGCACTG | 50760 |
rs48475717 | snp | C/T | | | intron-variant | Fbxo17 | GRCm38.p3 | 7:28728128 | CGCAGACTGATGGAG[C/T]TACGTGTCAGAGAGC | 50760 |
rs48517878 | snp | A/C | | | intron-variant | Fbxo17 | Mm_Celera | 7:28731126 | AATCTTCTAGCCCAC[A/C]ACCCACCAGAGGCAG | 50760 |
rs48544267 | snp | G/T | | | intron-variant | Fbxo17 | GRCm38.p3 | 7:28730888 | TACAAAAATGGTATG[G/T]TAATGGCTAATACTT | 50760 |
rs48605835 | snp | C/T | | | intron-variant | Fbxo17 | GRCm38.p3 | 7:28725643 | GTGTTTTCAAAGAAA[C/T]CAAAACTCTTATTAC | 50760 |
rs48655038 | snp | A/G | | | intron-variant | Fbxo17 | Mm_Celera | 7:28726985 | CCGTGATCCTAGAAA[A/G]CTTAAGGCTAGGGCA | 50760 |
rs48699883 | snp | A/G | | | intron-variant | Fbxo17 | GRCm38.p3 | 7:28727924 | TTCATACCCCAGGCA[A/G]CAACCAAGGCTATAA | 50760 |
rs48796647 | snp | A/T | | | intron-variant | Fbxo17 | Mm_Celera | 7:28717725 | TACTTTTTATTTAAA[A/T]TCAAATTTAAAAAAA | 50760 |
rs48819328 | snp | C/T | | | intron-variant | Fbxo17 | GRCm38.p3 | 7:28731480 | CACTGTCTGTGGGGT[C/T]ATACTTACACCCTTT | 50760 |
rs48866524 | snp | A/G | | | intron-variant | Fbxo17 | Mm_Celera | 7:28721893 | TTAATCCCAGCACTC[A/G]GGAGGCAGAGGCAGG | 50760 |
rs48896473 | snp | C/T | | | intron-variant | Fbxo17 | GRCm38.p3 | 7:28721813 | GTGAGAGTGAGCTTC[C/T]ACATCCAGCTCTGAT | 50760 |
rs49027329 | snp | A/G | | | intron-variant | Fbxo17 | GRCm38.p3 | 7:28722780 | gataccctgtcttga[A/G]aaacaaacaaacaaa | 50760 |
rs49076006 | snp | C/T | | | intron-variant | Fbxo17 | Mm_Celera | 7:28717967 | GCTGTGTTTATTCCT[C/T]TCCGTGTAACGTTTG | 50760 |
rs49127769 | snp | C/T | | | intron-variant | Fbxo17 | GRCm38.p3 | 7:28720079 | TCCCATGAGTCTGTG[C/T]TCTGCCCTTGCTTTA | 50760 |