SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6208459 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | Fbxo28 | GRCm38.p3 | 1:182341840 | CGAGCAAGGATTCCG[C/T]AAACCCTAAGAAAGG | 67948 |
rs6314235 | snp | G/T | 0.5 | 0 | intron-variant | Fbxo28 | Mm_Celera | 1:182327168 | CTCTAGCATTGACCT[G/T]TCACTGCTGAATAGC | 67948 |
rs6314274 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Fbxo28 | Mm_Celera | 1:182327193 | AATAGCATCCCCTTA[C/T]ACACAGGCGTCATCC | 67948 |
rs6327746 | snp | A/T | 0.207612 | 0.24638 | intron-variant | Fbxo28 | Mm_Celera | 1:182327348 | AGGGATAAATAGTTC[A/T]TGCTTTCAAGTGTTT | 67948 |
rs6327785 | snp | C/T | 0.5 | 0 | intron-variant | Fbxo28 | Mm_Celera | 1:182327373 | GTGTTTGTATGCATA[C/T]ACATTTTAATTTCTC | 67948 |
rs6327849 | snp | C/T | 0.5 | 0 | intron-variant | Fbxo28 | Mm_Celera | 1:182327420 | GGCAAATTGCTTTAA[C/T]GTAATGTCTGTTTAA | 67948 |
rs6328836 | snp | C/T | 0.5 | 0 | intron-variant | Fbxo28 | Mm_Celera | 1:182327537 | tttatgtgcaccatg[C/T]gggtgcctgataccc | 67948 |
rs13461551 | snp | G/T | | | utr-variant-3-prime | Fbxo28 | Mm_Celera | 1:182313599 | AGCGATGCCCCTGCT[G/T]GAGAATGGTGGAGTC | 67948 |
rs13461552 | snp | A/T | 0.432133 | 0.171253 | utr-variant-3-prime | Fbxo28 | GRCm38.p3 | 1:182314667 | AGACCATAGTGGTAT[A/T]TGGAGTCTCCAAATC | 67948 |
rs13461553 | snp | C/T | 0.493827 | 0.0552116 | utr-variant-3-prime | Fbxo28 | GRCm38.p3 | 1:182313909 | CCCTGTCAGTGAGCT[C/T]ATCCCGGAGTCGGCG | 67948 |
rs13464512 | snp | C/T | 0.304688 | 0.243945 | utr-variant-3-prime | Fbxo28 | GRCm38.p3 | 1:182315603 | ACTGTCGTATTTTTA[C/T]TTTAATTATGTACTA | 67948 |
rs13470705 | snp | A/G | | | synonymous-codon | Fbxo28 | GRCm38.p3 | 1:182316990 | AGTAGGGACCTCCTC[A/G]GGGTCTGGGCAGAGT | 67948 |
rs30541116 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Fbxo28 | GRCm38.p3 | 1:182332178 | GCTGCCAATGTATGT[C/T]AACTTGCAACTCTAA | 67948 |
rs30560661 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fbxo28 | GRCm38.p3 | 1:182339133 | ACTGCTCCCTCCCGC[A/G]CTTGGCCAGTCTTAG | 67948 |
rs30563631 | snp | C/T | 0.375 | 0.216506 | intron-variant | Fbxo28 | GRCm38.p3 | 1:182329180 | GATTAAAGGTGTGCA[C/T]ACACCCCGACCCCCG | 67948 |
rs30657947 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB | Fbxo28 | GRCm38.p3 | 1:182342597 | TGGTAAGGTGTAGCA[C/T]GTAGTCTCAAAATAA | 67948 |
rs30749944 | snp | A/G | 0.432133 | 0.171253 | utr-variant-3-prime | Fbxo28 | GRCm38.p3 | 1:182315059 | GTATGCTGCTGCTTC[A/G]GAGTCTTAAGCGCTC | 67948 |
rs30769572 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxo28 | GRCm38.p3 | 1:182329583 | CAATATATTATCAGT[A/G]TACCTGTATCCAAGA | 67948 |
rs30802042 | snp | A/C | 0.5 | 0 | intron-variant | Fbxo28 | GRCm38.p3 | 1:182332246 | TATAGCACAGCACAG[A/C]ACACAGCACACAGCA | 67948 |
rs30803983 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxo28 | GRCm38.p3 | 1:182318776 | TGTCTATTGCAATGG[A/G]ACTTTATATCATGCG | 67948 |
rs30995308 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Fbxo28 | GRCm38.p3 | 1:182318140 | AACTTGTCATGGAGA[A/G]TCCGCAGCATAGGCT | 67948 |
rs31040037 | snp | C/T | 0.375 | 0.216506 | intron-variant | Fbxo28 | GRCm38.p3 | 1:182331460 | GAGGCTCTGAAGGAA[C/T]AAAAGGCAAGACTGC | 67948 |
rs31056370 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fbxo28 | GRCm38.p3 | 1:182329386 | CCTCTTTTTTAAAAA[C/T]TTGAGACAGGGTTTC | 67948 |
rs31125475 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxo28 | GRCm38.p3 | 1:182320025 | GTTCAAGACATTCAC[A/G]TAGTCTATATAGAAA | 67948 |
rs31156117 | snp | C/T | 0.5 | 0 | intron-variant | Fbxo28 | GRCm38.p3 | 1:182340601 | ATAATAAGTAAACCA[C/T]TCCGACTGCAGGAGG | 67948 |
rs31164431 | snp | A/T | 0.32 | 0.24 | intron-variant | Fbxo28 | GRCm38.p3 | 1:182339532 | GCGGGGAGGGAGGGG[A/T]GCCATAGGGACTCCT | 67948 |
rs31184563 | snp | C/T | 0.33241 | 0.236027 | utr-variant-3-prime | Fbxo28 | GRCm38.p3 | 1:182316574 | CTGTCAAGAATGGGT[C/T]TGTTTAAAATCCGTA | 67948 |
rs31303280 | snp | A/C | 0.5 | 0 | intron-variant | Fbxo28 | Mm_Celera | 1:182332319 | GCACACAGAACACAG[A/C]ACACAGCACACAGCA | 67948 |
rs31375233 | snp | C/T | 0.33241 | 0.236027 | utr-variant-3-prime | Fbxo28 | GRCm38.p3 | 1:182314196 | ATAGCGCATACATCT[C/T]GAAACTACTGAATTA | 67948 |
rs31378731 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fbxo28 | GRCm38.p3 | 1:182327834 | AGCCGCCCAAGCCAC[A/G]CTTGTGACATTATGT | 67948 |
rs31402579 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Fbxo28 | GRCm38.p3 | 1:182329647 | CCTCTCAGTTTTTGC[C/T]TCTTGCCCTGGCTAC | 67948 |
rs31404814 | snp | C/G | 0.489796 | 0.070696 | intron-variant | Fbxo28 | GRCm38.p3 | 1:182320013 | GAACCTGCATCCGTT[C/G]AAGACATTCACATAG | 67948 |
rs31439636 | snp | A/T | 0.375 | 0.216506 | intron-variant | Fbxo28 | GRCm38.p3 | 1:182331237 | AGTTGGTTATTACTG[A/T]AACAATCTGAAGGTA | 67948 |
rs31489389 | snp | A/G | 0.32 | 0.24 | upstream-variant-2KB | Fbxo28 | GRCm38.p3 | 1:182342792 | GTAGTATTATTTCAT[A/G]CATAAAAATACACAC | 67948 |
rs31507956 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxo28 | GRCm38.p3 | 1:182331957 | GCCACAGAAGCCAAC[A/G]TGCAAACACACGAAG | 67948 |
rs31526550 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Fbxo28 | GRCm38.p3 | 1:182322017 | CAAAACTGTGACAGC[A/G]TGCGGCAGAGCTGCA | 67948 |
rs31531180 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Fbxo28 | GRCm38.p3 | 1:182329761 | ATAAAGAGTTGAAAC[G/T]TATATATGAAAAATC | 67948 |
rs31576832 | snp | A/G | 0.5 | 0 | intron-variant | Fbxo28 | GRCm38.p3 | 1:182317441 | ATGGATCTAGAGGGC[A/G]TAATATATCCAAAAC | 67948 |
rs31578201 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB | Fbxo28 | GRCm38.p3 | 1:182342321 | GCACCAACAACTGGC[C/T]GGTTTACAACTGCTT | 67948 |
rs31617600 | snp | C/T | 0.359862 | 0.224567 | synonymous-codon | Fbxo28 | GRCm38.p3 | 1:182317209 | GACCTGCTGCTGCAG[C/T]TTGGTAACCTCTTGT | 67948 |
rs31621782 | snp | C/T | 0.5 | 0 | intron-variant | Fbxo28 | GRCm38.p3 | 1:182319544 | CAGGCGTGGGGTGCA[C/T]ATCAGTAACCTCACC | 67948 |
rs31650301 | snp | A/C | 0.32 | 0.24 | intron-variant | Fbxo28 | GRCm38.p3 | 1:182339633 | CACATGAAAGAGATG[A/C]TGATTATTAATAATT | 67948 |
rs31670162 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fbxo28 | GRCm38.p3 | 1:182330244 | GAGCAGTAAAATGAT[A/G]CACCTGAAAGTTTTA | 67948 |
rs31723926 | snp | C/T | 0.401235 | 0.199068 | utr-variant-3-prime | Fbxo28 | GRCm38.p3 | 1:182316135 | TTAAATCAATGTCGG[C/T]GCAGCTCTAACAGTG | 67948 |
rs31725171 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Fbxo28 | GRCm38.p3 | 1:182319100 | AATGAGGTAGAGTAT[C/T]GAGCTGACCTAATGG | 67948 |
rs31736289 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fbxo28 | GRCm38.p3 | 1:182330287 | TCCTTTTTATCAAAA[A/G]CCAACCAACCAACCT | 67948 |
rs31772031 | snp | A/G | 0.5 | 0 | intron-variant | Fbxo28 | Mm_Celera | 1:182332313 | AACACAGCACACAGA[A/G]CACAGCACACAGCAC | 67948 |
rs31812083 | snp | A/G | 0.32 | 0.24 | intron-variant | Fbxo28 | GRCm38.p3 | 1:182339454 | ACCCAGTGACATCAG[A/G]TTAAGAAAGGACCTC | 67948 |
rs31855585 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Fbxo28 | GRCm38.p3 | 1:182331225 | ACTCCCAAGGTCAGT[C/T]GGTTATTACTGAAAC | 67948 |
rs31868775 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxo28 | GRCm38.p3 | 1:182320855 | GTCATGGGTTTTAGA[A/G]GGCTGGTTGCTTTGA | 67948 |
rs31915505 | snp | A/C | 0.345679 | 0.230967 | intron-variant | Fbxo28 | GRCm38.p3 | 1:182318843 | CTCAACCCTCCTTGA[A/C]TCATACATGGTCCTC | 67948 |
rs31931887 | snp | C/T | 0.5 | 0 | intron-variant | Fbxo28 | GRCm38.p3 | 1:182319501 | TAAAAACCCAGTGAG[C/T]GGGGATGACAAGATT | 67948 |
rs31959242 | snp | C/T | 0.32 | 0.24 | intron-variant | Fbxo28 | GRCm38.p3 | 1:182321716 | AACAACCAAAACAAA[C/T]GTATATTGTTAATGT | 67948 |
rs32043043 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Fbxo28 | GRCm38.p3 | 1:182321852 | CTCTTTGCATATAAG[A/T]TTCCATTAGGAAAGG | 67948 |
rs32054157 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB | Fbxo28 | GRCm38.p3 | 1:182342673 | ATACAGAAATTCAGG[A/G]AACAGGCTTATAATC | 67948 |
rs32096944 | snp | A/T | 0.5 | 0 | intron-variant | Fbxo28 | Mm_Celera | 1:182340646 | CATTTGAAAAAAAAA[A/T]GCAAACAAGCGGGAG | 67948 |
rs32097844 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fbxo28 | GRCm38.p3 | 1:182329183 | TAAAGGTGTGCATAC[A/G]CCCCGACCCCCGGCC | 67948 |
rs32122570 | snp | C/T | 0.375 | 0.216506 | intron-variant | Fbxo28 | Mm_Celera | 1:182318145 | GTCATGGAGAGTCCG[C/T]AGCATAGGCTTTTGC | 67948 |
rs32145532 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Fbxo28 | GRCm38.p3 | 1:182331386 | GTCAGAGTCACTAAC[A/G]AGAACCAAGTAAACC | 67948 |
rs32163651 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxo28 | Mm_Celera | 1:182331880 | ACAAAAACAGAAGAG[A/G]AAAAAAGCAAAACAA | 67948 |
rs32198698 | snp | A/G | 0.387812 | 0.208586 | utr-variant-3-prime | Fbxo28 | GRCm38.p3 | 1:182314557 | GGTTTGATGCAAACA[A/G]AGGAAGATCCTGCCA | 67948 |
rs32251015 | snp | C/T | 0.375 | 0.216506 | intron-variant | Fbxo28 | GRCm38.p3 | 1:182330302 | GCCAACCAACCAACC[C/T]CAGGACAATTCAAAC | 67948 |
rs32309025 | snp | A/C/T | 0.444444 | 0.157135 | intron-variant | Fbxo28 | Mm_Celera | 1:182331893 | AGGAAAAAAGCAAAA[A/C/T]AAAAAAAAAAAAAAC | 67948 |
rs32321582 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fbxo28 | Mm_Celera | 1:182328321 | CTTACTGAAAACCAA[A/G]TAAGTATACAAGGGT | 67948 |
rs32370177 | snp | C/G | 0.456747 | 0.140554 | synonymous-codon | Fbxo28 | GRCm38.p3 | 1:182317167 | AATCTCACGCCTGAG[C/G]ACAGTCACGCCAGCG | 67948 |
rs32387791 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fbxo28 | GRCm38.p3 | 1:182322248 | CCCCTTCAGTTCCAT[A/G]TGAGTACTGTATGCA | 67948 |
rs32388021 | snp | A/G | 0.32 | 0.24 | intron-variant | Fbxo28 | GRCm38.p3 | 1:182326404 | TCTCCTAAAATAACA[A/G]TAAAAGTCACTGGCA | 67948 |
rs32392251 | snp | A/G | 0.401235 | 0.199068 | utr-variant-3-prime | Fbxo28 | GRCm38.p3 | 1:182316003 | TCTGTCTTAGCCAGT[A/G]CACCTGAACCCTACA | 67948 |
rs32472972 | snp | C/T | 0.32 | 0.24 | intron-variant | Fbxo28 | GRCm38.p3 | 1:182322010 | GCAAAACCAAAACTG[C/T]GACAGCATGCGGCAG | 67948 |
rs32494917 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Fbxo28 | GRCm38.p3 | 1:182329573 | TAACCTCTAACAATA[C/T]ATTATCAGTGTACCT | 67948 |
rs32523535 | snp | A/G | 0.32 | 0.24 | intron-variant | Fbxo28 | GRCm38.p3 | 1:182339593 | CCAGGAAAAGGCTTA[A/G]GATACAATATGCAGC | 67948 |
rs32554355 | snp | C/T | 0.375 | 0.216506 | intron-variant | Fbxo28 | GRCm38.p3 | 1:182330271 | TTTAAGTTTAAAACA[C/T]TCCTTTTTATCAAAA | 67948 |
rs32557686 | snp | G/T | 0.33241 | 0.236027 | intron-variant | Fbxo28 | GRCm38.p3 | 1:182330183 | GTTTGGGCCAAGCAG[G/T]ACCACCGACTTAAGT | 67948 |
rs32573530 | snp | A/C | 0.32 | 0.24 | intron-variant | Fbxo28 | GRCm38.p3 | 1:182326438 | ATGAAAGCAGTAGTA[A/C]AGGGTAAACTGTTAG | 67948 |
rs32578744 | snp | A/G | 0.32 | 0.24 | intron-variant | Fbxo28 | GRCm38.p3 | 1:182339531 | AGCGGGGAGGGAGGG[A/G]TGCCATAGGGACTCC | 67948 |
rs32664927 | snp | A/C | 0.375 | 0.216506 | utr-variant-3-prime | Fbxo28 | Mm_Celera | 1:182316656 | GGAGCAAGGTTAGCC[A/C]CCAAACACGATAGAA | 67948 |
rs32694801 | snp | G/T | 0.375 | 0.216506 | intron-variant | Fbxo28 | GRCm38.p3 | 1:182333538 | TAGTTAGGAATGACT[G/T]ACTGGGAGCTGCCAC | 67948 |
rs32755900 | snp | A/G/T | 0.375 | 0.216506 | intron-variant | Fbxo28 | GRCm38.p3 | 1:182328884 | TCTCTCTAGTCCCCC[A/G/T]CACCACACCTCCTTT | 67948 |
rs32763715 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fbxo28 | GRCm38.p3 | 1:182329834 | AAGCTGCACCCCCCC[C/T]CCCAAGTGTGACTCA | 67948 |
rs32764797 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Fbxo28 | GRCm38.p3 | 1:182331786 | CAGAGGAAACAGAAA[A/G]GTAGAAAAACCAATG | 67948 |
rs32769372 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB | Fbxo28 | GRCm38.p3 | 1:182342627 | ACCCACTTCTCATGT[A/G]ATGCATTAATCACAA | 67948 |
rs32786706 | snp | C/T | 0.32 | 0.24 | intron-variant | Fbxo28 | GRCm38.p3 | 1:182326102 | ATCACATGAATGATA[C/T]ATATTAATAACTGCA | 67948 |
rs32801033 | snp | C/T | 0.32 | 0.24 | downstream-variant-500B | Fbxo28 | GRCm38.p3 | 1:182312855 | CTTACCTGGGTTCCA[C/T]TCCCCCCATTCAGGT | 67948 |
rs32804689 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Fbxo28 | GRCm38.p3 | 1:182329262 | TTGCATGTGCGTCTG[C/T]GTGGAATTCCTTAGA | 67948 |
rs33889043 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Fbxo28 | GRCm38.p3 | 1:182323078 | CCCTCCCCACCCCCC[A/C]AAAAAAAACCCAACA | 67948 |
rs45654375 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Fbxo28 | GRCm38.p3 | 1:182333359 | ACAGTCAATTCAAAC[A/G]TGTCTGGTGTAAAAT | 67948 |
rs45703422 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime | Fbxo28 | Mm_Celera | 1:182313137 | TTGTTGCTCATGAGC[A/G]TTAAGTAAACAGACA | 67948 |
rs45755216 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxo28 | Mm_Celera | 1:182318658 | GGCCTTAGCCAAGCG[C/T]GCTCTCAGCTTTCCT | 67948 |
rs45788253 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fbxo28 | Mm_Celera | 1:182332152 | CCATGGCAAACCATT[C/T]AATGATCACTGCTGC | 67948 |
rs45801259 | snp | A/G | | | intron-variant | Fbxo28 | GRCm38.p3 | 1:182333480 | ATGTCTATGTACTAT[A/G]TTCAGGCTGCTGCCT | 67948 |
rs45924630 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Fbxo28 | Mm_Celera | 1:182320579 | CCTGGCTTCATCAAA[G/T]TTTTTATTTTCTCTT | 67948 |
rs46109059 | snp | C/T | | | intron-variant | Fbxo28 | GRCm38.p3 | 1:182338082 | AGTCAGAGACATGCC[C/T]AATTCTAAGCAAAAG | 67948 |
rs46143538 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Fbxo28 | Mm_Celera | 1:182318160 | CAGCATAGGCTTTTG[C/G]ACTTCCTACTATACT | 67948 |
rs46173860 | snp | C/G | 0.124444 | 0.216185 | utr-variant-3-prime | Fbxo28 | Mm_Celera | 1:182316799 | CGCCTGGAAGCCTAA[C/G]GACACCATGTTGCTC | 67948 |
rs46247608 | snp | C/G | 0.124444 | 0.216185 | utr-variant-3-prime | Fbxo28 | Mm_Celera | 1:182316525 | TTTCTTTCAAGTGAA[C/G]AGGACATTTTATGTA | 67948 |
rs46323415 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Fbxo28 | Mm_Celera | 1:182325605 | TCCAAGCACTGAAAG[C/G]ACTTTTGCCAGTGTC | 67948 |
rs46470813 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Fbxo28 | Mm_Celera | 1:182314004 | GTGCATGCAGTAGTG[C/T]GATCCCAAGGTGCCA | 67948 |
rs46487420 | snp | G/T | 0.277778 | 0.248452 | utr-variant-3-prime | Fbxo28 | GRCm38.p3 | 1:182314445 | AAGCAGGGCTCGGCC[G/T]GACAGGGCCTGTTCT | 67948 |
rs46610287 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxo28 | Mm_Celera | 1:182327074 | GTGCCTTTACTTTGA[A/G]CACTGGAGTAAACAG | 67948 |
rs46634414 | snp | A/G | | | intron-variant | Fbxo28 | GRCm38.p3 | 1:182337311 | GGTTTGCAACTCATC[A/G]AACTGCCTGCCTCTG | 67948 |