SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3697592 | snp | A/T | 0.5 | 0 | intron-variant | Pparg | Mm_Celera | 6:115469200 | CAATGTAAACTAGAT[A/T]AAAAAAAAAAATTAC | 19016 |
rs3698220 | snp | A/G | 0.5 | 0 | intron-variant | Pparg | Mm_Celera | 6:115469306 | TGCTAGGGCTCTCTT[A/G]GCTTTGTATAGAAAT | 19016 |
rs3698385 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Pparg | Mm_Celera | 6:115469385 | AAGGCTGTCAGTGAT[C/T]CAGAGTGTTAATAAC | 19016 |
rs3699371 | snp | C/G | 0.415225 | 0.187619 | intron-variant | Pparg | Mm_Celera | 6:115469494 | ATGCCTAAGTGGATC[C/G]TTTGAAGTATGGGAA | 19016 |
rs6211345 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Pparg | Mm_Celera | 6:115464041 | TAGATGAAAATTATC[A/G]TTGAATCCAGTTTTC | 19016 |
rs6211421 | snp | C/T | 0.5 | 0 | intron-variant | Pparg | Mm_Celera | 6:115464085 | GCTTCTGATAGGAAG[C/T]TGAGAATCAACNTCA | 19016 |
rs6211793 | snp | A/G | 0.5 | 0 | intron-variant | Pparg | Mm_Celera | 6:115464097 | AAGNTGAGAATCAAC[A/G]TCAAATTACATTAAA | 19016 |
rs6340867 | snp | A/G | 0.5 | 0 | intron-variant | Pparg | Mm_Celera | 6:115366658 | taccactttgtctgg[A/G]ttcctagagaggctg | 19016 |
rs6341382 | snp | A/T | 0.5 | 0 | intron-variant | Pparg | Mm_Celera | 6:115366801 | ctgagccatttctct[A/T]gccccATCTTATTCT | 19016 |
rs6341821 | snp | A/T | 0.5 | 0 | intron-variant | Pparg | Mm_Celera | 6:115366854 | TATATTTAACTACTT[A/T]AAAAAAAAACCTATA | 19016 |
rs6341880 | snp | C/T | 0.5 | 0 | intron-variant | Pparg | Mm_Celera | 6:115366884 | AGACTTATCTGGAAT[C/T]CTAANATGGAGATAA | 19016 |
rs6341892 | snp | A/T | 0.5 | 0 | intron-variant | Pparg | Mm_Celera | 6:115366889 | TATCTGGAATNCTAA[A/T]ATGGAGATAAAATGA | 19016 |
rs6342353 | snp | A/G | 0.5 | 0 | intron-variant | Pparg | Mm_Celera | 6:115366950 | AGTTCAGATTGGCAT[A/G]GACCTGGNAGTGAGG | 19016 |
rs6342369 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Pparg | Mm_Celera | 6:115366958 | TTGGCATNGACCTGG[A/G]AGTGAGGAGTCCTTT | 19016 |
rs6350947 | snp | C/G/T | 0.456747 | 0.140554 | intron-variant | Pparg | Mm_Celera | 6:115418086 | CTCTCAGTGTGTTTT[C/G/T]GGGTATTGTAAACAA | 19016 |
rs8236549 | snp | A/G | 0.4032 | 0.19756 | synonymous-codon | Pparg | GRCm38.p3 | 6:115473037 | AAGGTTAATGAAACC[A/G]GGGATATTTTTGGCA | 19016 |
rs8236550 | snp | A/G | 0.470416 | 0.117969 | synonymous-codon | Pparg | GRCm38.p3 | 6:115473055 | CACTTGGTCATTCAA[A/G]TCAAGGTTAATGAAA | 19016 |
rs8239553 | snp | A/T | 0.21875 | 0.248039 | upstream-variant-2KB | Pparg | Mm_Celera | 6:115360545 | TTCGCCTTCATAACA[A/T]TCTGAGATtaaaaat | 19016 |
rs8239554 | in-del | -/T | 0.5 | 0 | upstream-variant-2KB | Pparg | Mm_Celera | 6:115360572 | aaataaaaataaaac[-/T]nagattaaaaataaa | 19016 |
rs8239555 | in-del | -/G | 0.5 | 0 | upstream-variant-2KB | Pparg | Mm_Celera | 6:115360573 | aataaaaataaaacn[-/G]agattaaaaataaaa | 19016 |
rs8239556 | in-del | -/A | 0.444444 | 0.157135 | upstream-variant-2KB | Pparg | Mm_Celera | 6:115360592 | ttaaaaataaaaann[-/A]nannngaaaAAAGGG | 19016 |
rs8239557 | in-del | -/A | 0.444444 | 0.157135 | upstream-variant-2KB | Pparg | Mm_Celera | 6:115360593 | taaaaataaaaannn[-/A]annngaaaAAAGGGA | 19016 |
rs8239558 | snp | A/T | 0.5 | 0 | upstream-variant-2KB | Pparg | Mm_Celera | 6:115360619 | AGGGAGATCCTAAAT[A/T]CACTTAATTCatata | 19016 |
rs8254771 | snp | A/G | 0.35503 | 0.226867 | upstream-variant-2KB | Pparg | Mm_Celera | 6:115360159 | CTGAAAGAGTGCAAG[A/G]AAAGGAACTGTCTAT | 19016 |
rs8254772 | snp | A/C | 0.124444 | 0.216185 | upstream-variant-2KB | Pparg | Mm_Celera | 6:115360200 | TCAGGCTCCCGAGGC[A/C]AGAAGCTCCAATAGT | 19016 |
rs8254773 | snp | A/G | 0.124444 | 0.216185 | upstream-variant-2KB | Pparg | Mm_Celera | 6:115360201 | CAGGCTCCCGAGGCA[A/G]GAAGCTCCAATAGTC | 19016 |
rs8254774 | snp | G/T | 0.444444 | 0.157135 | upstream-variant-2KB | Pparg | Mm_Celera | 6:115360376 | GAACACTTTGTGTTC[G/T]TCCAGAGGACCCTTG | 19016 |
rs8254775 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB | Pparg | Mm_Celera | 6:115360388 | TTCTTCCAGAGGACC[C/T]TTGTTCGGTTCCCAG | 19016 |
rs8254776 | snp | A/C | 0.132653 | 0.220748 | upstream-variant-2KB | Pparg | Mm_Celera | 6:115360444 | CAGGGGAGCCCACAC[A/C]TCTCCCTCCGTTCAC | 19016 |
rs8254777 | snp | A/T | 0.391111 | 0.206368 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | Pparg | Mm_Celera | 6:115361271 | CTGAGGAGAAGTCAC[A/T]CTCTGACAGGAGCCT | 19016 |
rs8254778 | snp | A/G | 0.444444 | 0.157135 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | Pparg | Mm_Celera | 6:115361295 | GGAGCCTGTGAGACC[A/G]ACAGCCTGACGGGGT | 19016 |
rs8254779 | in-del | -/A | 0.142012 | 0.225474 | frameshift-variant | Pparg | Mm_Celera | 6:115473164 | ACTCCCTGGTCATGA[-/A]TCCTTGGCCCTCTGA | 19016 |
rs8254780 | snp | A/G | 0.336735 | 0.234472 | synonymous-codon | Pparg | GRCm38.p3 | 6:115473001 | TGTGATCTCTTGCAC[A/G]GCTTCTACGGATCGA | 19016 |
rs8254781 | snp | C/T | 0.336735 | 0.234472 | synonymous-codon | Pparg | GRCm38.p3 | 6:115472953 | AATTCGGATGGCCAC[C/T]TCTTTGCTCTGCTCC | 19016 |
rs8254782 | snp | A/G | 0.444444 | 0.157135 | synonymous-codon | Pparg | GRCm38.p3 | 6:115490033 | AGAGGACTCTGGGTG[A/G]TTCAGCTTGAGCTGC | 19016 |
rs29969982 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Pparg | GRCm38.p3 | 6:115422832 | TCAGATTTGCTTCAC[A/G]GGAACAAAATTCTCC | 19016 |
rs30014734 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pparg | GRCm38.p3 | 6:115466553 | GTCACTAAAGAAGTC[C/T]TAGGAACATTATACA | 19016 |
rs45639557 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115382887 | AGTTTTGTGTGTGTC[A/G]GACTGTGCAGAATGT | 19016 |
rs45654618 | snp | A/T | 0.408163 | 0.193609 | intron-variant | Pparg | Mm_Celera | 6:115387630 | TAACTTTAATTACAT[A/T]TAGGTATGCATGTGG | 19016 |
rs45687356 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115464460 | ATGACTTCGAGTGGA[A/G]TCAGCTAGTAGCTAT | 19016 |
rs45693233 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Pparg | Mm_Celera | 6:115440075 | ATACCAAAGTATGTT[C/T]ACTTTTCAAACTACT | 19016 |
rs45700899 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Pparg | Mm_Celera | 6:115391560 | AACTTCATTTTTCAT[G/T]CTAATTATTGTTACA | 19016 |
rs45722776 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115385772 | GGTAATTCGTACTCA[A/G]ATCAGAGGTATGAGG | 19016 |
rs45722938 | snp | A/G | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115476896 | GCCAGCTTGCTGAGA[A/G]AGATGACCTAGTTCT | 19016 |
rs45735678 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Pparg | Mm_Celera | 6:115378890 | CTAGTTTTATAATAT[C/T]TGTGTTACCAGAGAA | 19016 |
rs45749774 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115387167 | AAAAGAGTGTCTGTT[G/T]ATTAAAGATATCTGA | 19016 |
rs45763130 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Pparg | GRCm38.p3 | 6:115402837 | GAGCAGTTAGATGTC[A/G]TTTTTTTAATTTAAT | 19016 |
rs45771868 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115469006 | ATCAGAAAATCTCAT[G/T]CCCAGAGCCTTGGCC | 19016 |
rs45775174 | snp | A/C | | | intron-variant | Pparg | Mm_Celera | 6:115414008 | CTGGTTTATTTAAAT[A/C]ATTTAACAATTCTTT | 19016 |
rs45777353 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Pparg | Mm_Celera | 6:115453906 | TTCAAGTTTCCAAAG[G/T]AGACACCCTGTGCAT | 19016 |
rs45781199 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115418887 | GAGAACAAGATAGAT[A/G]CATACTTACAGGAAA | 19016 |
rs45787490 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115373963 | TGGATGCAGTATTGA[A/G]ACTCAAACCCAGACC | 19016 |
rs45792435 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115441166 | CCTAGCCAAGTAAGC[G/T]TCACTTATCCAAACC | 19016 |
rs45792522 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115461547 | AAGTCACTGAACAGA[C/T]AGAAATGTTCCTGTA | 19016 |
rs45794401 | snp | A/G | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Pparg | Mm_Celera | 6:115365367 | TTTTCTGTTTTTGTG[A/G]GTCCTTCACAGACAA | 19016 |
rs45804653 | snp | A/G | 0.18 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115433413 | TAATTGGAGGTTATT[A/G]TTTTTGTTAGTGTAG | 19016 |
rs45806952 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115472724 | TGATAAATAGGAAGA[A/G]CCTCTCTCCTGTTTA | 19016 |
rs45807727 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115371335 | GCTAGGTAAACTGTT[C/T]GCCACTGAGCCACCA | 19016 |
rs45822703 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115388584 | TTACCTGCGTAACTT[C/G]TGATTTGGGGTAGTG | 19016 |
rs45826663 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Pparg | Mm_Celera | 6:115436815 | CAGGAAAAGATACAG[C/T]AACCTCAGGAATCTG | 19016 |
rs45826745 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115412182 | AGATAACTTTGGAAG[C/T]ACCAGTTGAATTCAT | 19016 |
rs45826789 | snp | G/T | 0.396694 | 0.202437 | intron-variant | Pparg | Mm_Celera | 6:115372226 | TGTTTCTGTCATGTA[G/T]TATTAAAGTATAGGG | 19016 |
rs45853449 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115397029 | TGTTAGGAGTCTGTA[C/T]ACCTATAAATCAGCA | 19016 |
rs45866169 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115376610 | GTGGTAGGGAGTTCC[A/G]GTTTTGAGAAAAGCT | 19016 |
rs45885522 | snp | C/G | 0.277778 | 0.248452 | intron-variant | Pparg | Mm_Celera | 6:115419715 | CACAAGTTAAATGTT[C/G]CTTTTGAAAGGAAGG | 19016 |
rs45887332 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Pparg | Mm_Celera | 6:115397830 | GCAGGTGGTTAGTCA[A/G]TGCTTACCCTGTGAG | 19016 |
rs45897754 | snp | A/C | 0.197531 | 0.244432 | intron-variant | Pparg | Mm_Celera | 6:115478595 | GTTCATATACTGTTA[A/C]TGATATCCAATGCCC | 19016 |
rs45911251 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Pparg | Mm_Celera | 6:115412728 | AGAGATGATGAAGGT[C/T]TTAGAACCCTAAGCA | 19016 |
rs45911754 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Pparg | Mm_Celera | 6:115485874 | TTGCATTTCATTCCC[C/T]GAGCCAGGTTCCAGC | 19016 |
rs45942963 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115424680 | GTTGAGCAATGGAAA[C/T]GCATCTTAGAAACAT | 19016 |
rs45944314 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115394328 | ATAATATATTCCTGG[C/T]TCACGGTTTTGTTTT | 19016 |
rs45956838 | snp | A/G | 0.124444 | 0.216185 | downstream-variant-500B | Pparg | Mm_Celera | 6:115490824 | CAAACTTCTCCCACG[A/G]CTCTGAGTTTTCACG | 19016 |
rs45957498 | snp | A/G | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Pparg | Mm_Celera | 6:115421617 | AAGATAAATACTTAA[A/G]AAAAACTTTGGCCAA | 19016 |
rs45982368 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Pparg | Mm_Celera | 6:115375552 | TTCATTTATTTCCAA[C/T]TTTAAAATTATAGTA | 19016 |
rs45996004 | snp | C/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Pparg | Mm_Celera | 6:115420020 | CATTGGTATTGAAAA[C/T]GGGATAATATAGGTA | 19016 |
rs46002291 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Pparg | Mm_Celera | 6:115434259 | ATTAACCTAAAACAA[A/G]AAGTCATTGAAAATT | 19016 |
rs46009770 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Pparg | Mm_Celera | 6:115487367 | ACAAGCAGGATATAA[C/T]GATGTGAGTAGGTTT | 19016 |
rs46012115 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Pparg | Mm_Celera | 6:115390374 | AATTCAATTGACAAG[A/G]TCTAGTTTTGCTAGT | 19016 |
rs46016286 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115414926 | GTATTAATTGTCCTG[A/G]TACTAAGTTTTATCA | 19016 |
rs46027909 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115396255 | AGCAGCCCGGTGATA[C/T]TGAATAACCTTCTCC | 19016 |
rs46055300 | snp | A/G | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115443454 | ACATTAATGAGTGTG[A/G]ATTGTATAATCATTC | 19016 |
rs46076755 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Pparg | Mm_Celera | 6:115397977 | GGATTCACTCAGAGT[C/T]TAAACGGTCAGTCAG | 19016 |
rs46096787 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115380918 | CTTGCAGAGTATTTA[C/T]ATCTTAATGTCTTCT | 19016 |
rs46096866 | snp | A/G | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115395245 | CCTGAGATACAACTC[A/G]GAAGCTAGATGGAGC | 19016 |
rs46097543 | snp | A/G | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115461072 | TTTTTTTAAATGGCA[A/G]TTGTTTAAAGATTTC | 19016 |
rs46124349 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115376493 | ATTACCTAATAGATA[A/G]TAGGCACTCAAATAT | 19016 |
rs46127268 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Pparg | Mm_Celera | 6:115455351 | AGGGAAGCTCAGAAT[A/G]CAAGTGCTAACATGT | 19016 |
rs46146082 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115462801 | TAGGAGTTGTCTCTC[A/G]ATTCATGTTTAAATG | 19016 |
rs46160271 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115367372 | TGCTGGGGTGAAGAA[C/G]TGGAAAGAACTCCTT | 19016 |
rs46196029 | snp | G/T | 0.18 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115479489 | GTTCCCCTTCAGTTC[G/T]TGAGTATACGTGCCA | 19016 |
rs46196758 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Pparg | Mm_Celera | 6:115459563 | GATTGGTCTGTGAAG[C/T]AGTAGATGATTCTGG | 19016 |
rs46223269 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115398890 | TTAATATCACAACAC[C/T]GGGGAGCAGACTTCC | 19016 |
rs46223975 | snp | G/T | 0.497778 | 0.0332592 | intron-variant | Pparg | Mm_Celera | 6:115390269 | ATCATTTTGTATGAG[G/T]CGAGTATTAACAATG | 19016 |
rs46239196 | snp | A/T | 0.473373 | 0.11227 | intron-variant | Pparg | Mm_Celera | 6:115390036 | AATCCAAGAACATGT[A/T]GTGTGGGCTCCTTTT | 19016 |
rs46265991 | snp | C/G | 0.277778 | 0.248452 | intron-variant | Pparg | Mm_Celera | 6:115454812 | GTCCTACTCTATGTT[C/G]ATTTGGCCCTGTTGC | 19016 |
rs46274689 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115419586 | ACACAATCCTAGGAG[C/G]AGATGCTACCAGATT | 19016 |
rs46301931 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Pparg | Mm_Celera | 6:115483824 | CAGACCCTTCGATAG[C/T]TTACTTTACTCTGTT | 19016 |
rs46302523 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Pparg | Mm_Celera | 6:115388737 | GAGTAGTGTGTTGTC[C/T]TAGTAGGTACAGCAC | 19016 |
rs46306894 | snp | G/T | 0.18 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115485104 | AGCCTTTCAGGGAAT[G/T]TCCTAGCAGGCCCTG | 19016 |
rs46312450 | snp | C/T | 0.489796 | 0.070696 | intron-variant, upstream-variant-2KB | Pparg | Mm_Celera | 6:115451709 | CCTTTGCTATATTAT[C/T]CTTGACTTCAGAGAA | 19016 |