SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs29829144 | snp | C/T | 0.48 | 0.0979796 | downstream-variant-500B | Pcgf1 | GRCm38.p3 | 6:83081114 | AGTGGATGTCACAAT[C/T]CATGTCAAGAGAGGA | 69837 |
rs30114911 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB | Pcgf1 | Mm_Celera | 6:83077501 | AGTCTCTCCCCTCTC[A/G]CTCGAATCTCCAGTT | 69837 |
rs30415058 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB | Pcgf1 | GRCm38.p3 | 6:83077268 | ACATACACTCCTTTC[C/T]GTGAGGTTCCTGTTA | 69837 |
rs30499014 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB | Pcgf1 | GRCm38.p3 | 6:83078025 | GAGGTCGGGTCCCAG[A/G]ACTCCCACACTCCGG | 69837 |
rs30519142 | snp | A/G | 0.495 | 0.0497494 | downstream-variant-500B | Pcgf1 | GRCm38.p3 | 6:83081139 | AGAGGACATGTGGCC[A/G]CAATAGGACTGAAGA | 69837 |
rs30555978 | snp | C/T | 0.32 | 0.24 | synonymous-codon | Pcgf1 | GRCm38.p3 | 6:83079698 | CCACTCTAAAGCCCA[C/T]TATTATCGATATGAT | 69837 |
rs30702836 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB | Pcgf1 | GRCm38.p3 | 6:83077371 | TTTGGTCGTTCCTCT[C/T]CACACTGCCTTTTTT | 69837 |
rs30750128 | snp | C/T | 0.188366 | 0.242283 | missense | Pcgf1 | Mm_Celera | 6:83080090 | GTGAGAGCTGAGGTC[C/T]GCCATCTCCGAAGGG | 69837 |
rs30753427 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB | Pcgf1 | Mm_Celera | 6:83076694 | GCTGGGATTAAAGGT[A/G]TGCGCCACCATGCCC | 69837 |
rs46990525 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon | Pcgf1 | Mm_Celera | 6:83079192 | CAAGATCCACGAGAC[A/G]CAGCCGTTGCTCAAT | 69837 |
rs47391575 | snp | A/C | | | utr-variant-5-prime | Pcgf1 | GRCm38.p3 | 6:83078418 | GGGCCAGATTGCGAT[A/C]GCGATGAGGCTTCGG | 69837 |
rs47887879 | snp | C/G | | | intron-variant | Pcgf1 | GRCm38.p3 | 6:83080351 | TGAGAGCGGTCTGCT[C/G]AGATAGCTTAGTCAA | 69837 |
rs47888091 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Pcgf1 | Mm_Celera | 6:83078915 | GGTCCGGGTGAAGAT[C/T]AAAGACCTGAATGAA | 69837 |
rs47918095 | snp | C/T | | | intron-variant | Pcgf1 | Mm_Celera | 6:83080516 | AGGGACAAGTCTCTG[C/T]CCAGCACTACTTCCC | 69837 |
rs48567396 | snp | A/T | 0.231111 | 0.249285 | missense | Pcgf1 | Mm_Celera | 6:83079179 | CCATGTGCAACATCA[A/T]GATCCACGAGACGCA | 69837 |
rs48604579 | snp | A/T | 0.142012 | 0.225474 | missense | Pcgf1 | Mm_Celera | 6:83079143 | GTATCGTGAAGTACC[A/T]GCAAACCAGCAAGTA | 69837 |
rs49142031 | snp | C/T | 0.124444 | 0.216185 | missense | Pcgf1 | Mm_Celera | 6:83079202 | GAGACGCAGCCGTTG[C/T]TCAATCTCAAACTGG | 69837 |
rs50360436 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon | Pcgf1 | Mm_Celera | 6:83080585 | TGAGGTTCTCCCAGA[C/T]CACATGACAATGAAA | 69837 |
rs50665575 | snp | A/G | 0.124444 | 0.216185 | downstream-variant-500B | Pcgf1 | Mm_Celera | 6:83081088 | ATGCTGCAGTATATG[A/G]TGCCAGCCCCAGTGG | 69837 |
rs51777924 | snp | C/T | 0.124444 | 0.216185 | downstream-variant-500B | Pcgf1 | Mm_Celera | 6:83080955 | AAGAAAGGTCTCCTC[C/T]ATCTACCAAATGCCC | 69837 |
rs51949726 | snp | A/C | 0.124444 | 0.216185 | synonymous-codon | Pcgf1 | Mm_Celera | 6:83078957 | CTGCCTGTGCGCGGG[A/C]TACTTCGTGGATGCC | 69837 |
rs211798674 | snp | G/T | | | upstream-variant-2KB | Pcgf1 | Mm_Celera | 6:83077583 | CCGTAGGGACCCAGT[G/T]ATGACAGTGTACCAG | 69837 |
rs211968191 | snp | G/T | | | upstream-variant-2KB | Pcgf1 | Mm_Celera | 6:83076635 | TTTTAACAGTTTTTT[G/T]TTTTTTTCGAGACAG | 69837 |
rs213069733 | snp | A/G | | | synonymous-codon | Pcgf1 | Mm_Celera | 6:83080137 | AATGCTAAATCCACA[A/G]CATGTAAGTAAGCCC | 69837 |
rs214558160 | snp | A/G | | | intron-variant | Pcgf1 | Mm_Celera | 6:83079994 | CCCTTTGAAGGAGCC[A/G]TTTCTCCCAGCAACC | 69837 |
rs214736410 | snp | C/T | | | upstream-variant-2KB | Pcgf1 | Mm_Celera | 6:83078015 | GGTCGGAGGCGAGGT[C/T]GGGTCCCAGGACTCC | 69837 |
rs215335326 | snp | A/T | | | downstream-variant-500B | Pcgf1 | Mm_Celera | 6:83081271 | ATCTGAGCCCAGGAC[A/T]GAAGGGTCAGCTAGC | 69837 |
rs215438628 | in-del | -/TTTT | | | upstream-variant-2KB | Pcgf1 | Mm_Celera | 6:83077380 | CCTCTTCACACTGCC[-/TTTT]TTTTTTTTCTATTTC | 69837 |
rs216593406 | in-del | -/TT | | | upstream-variant-2KB | Pcgf1 | Mm_Celera | 6:83076613 | CCTAAGCTTGTGCCA[-/TT]TTTTTTTTTAACAGT | 69837 |
rs216620415 | snp | A/G | | | synonymous-codon | Pcgf1 | Mm_Celera | 6:83080068 | GAACAAGTATGTTCG[A/G]TGTTCTGTGAGAGCT | 69837 |
rs216698175 | snp | A/G | | | upstream-variant-2KB | Pcgf1 | Mm_Celera | 6:83078051 | TCCGGAGCTGTAGCG[A/G]CGGGCGATAGCCCGG | 69837 |
rs216907187 | snp | C/T | | | upstream-variant-2KB | Pcgf1 | Mm_Celera | 6:83076424 | CAAACTCAAGAGATC[C/T]ACTGCCTCTGCCCTG | 69837 |
rs218915032 | in-del | -/A | | | intron-variant | Pcgf1 | Mm_Celera | 6:83078684 | CTGGTCTCCCGAGGG[-/A]AAAAAAGAGAGTCAG | 69837 |
rs219910164 | in-del | -/TTTTTTTTTTTTTT | | | upstream-variant-2KB | Pcgf1 | Mm_Celera | 6:83076713 | GCCACCATGCCCTGC[-/TTTTTTTTTTTTTT]TTTTTTTTTTTTCTT | 69837 |
rs220254318 | in-del | -/TCCCCCG | | | intron-variant | Pcgf1 | Mm_Celera | 6:83078766 | GAAGGGGGAGCTCAC[-/TCCCCCG]TCTCTTCTCGGGGGC | 69837 |
rs220926579 | snp | A/C | | | intron-variant | Pcgf1 | Mm_Celera | 6:83080234 | GAAGAAAGCTCAGGC[A/C]GGAAGATCACTTCAA | 69837 |
rs221298934 | snp | A/G | | | upstream-variant-2KB | Pcgf1 | Mm_Celera | 6:83077168 | GTGGCCTGGGCCAGG[A/G]AGGTAAACCATAGCT | 69837 |
rs221768052 | snp | A/G | | | upstream-variant-2KB | Pcgf1 | Mm_Celera | 6:83078275 | GAGGGGGCGAGGGCG[A/G]GGTGTGCCGGAAAAC | 69837 |
rs222516684 | snp | A/C | | | upstream-variant-2KB | Pcgf1 | Mm_Celera | 6:83076945 | AGTTGCAAGTATTTA[A/C]AGTGTATACTGTAAT | 69837 |
rs222659634 | in-del | -/T | | | upstream-variant-2KB | Pcgf1 | Mm_Celera | 6:83076636 | TTTAACAGTTTTTTG[-/T]TTTTTTCGAGACAGG | 69837 |
rs223056221 | snp | A/C | | | intron-variant | Pcgf1 | Mm_Celera | 6:83080461 | GCAAACTTGTAATCG[A/C]AGCAGTGGAGCCGCA | 69837 |
rs226972895 | in-del | -/TCCTAAT | | | downstream-variant-500B | Pcgf1 | Mm_Celera | 6:83080904 | AGGCTTTGGCCTGGG[-/TCCTAAT]TCCTCTTAAGTCTCC | 69837 |
rs227031299 | snp | G/T | | | intron-variant | Pcgf1 | Mm_Celera | 6:83080019 | GCAACCCTTCCCTCA[G/T]ACACCTGTGCCCTCC | 69837 |
rs227134038 | snp | C/T | | | synonymous-codon | Pcgf1 | Mm_Celera | 6:83080624 | GCTGTCCCGCTGGTT[C/T]GGCAAGGTAAGCCGG | 69837 |
rs228993825 | snp | C/G | | | upstream-variant-2KB | Pcgf1 | Mm_Celera | 6:83077842 | GGTTCCCCGGGGGGT[C/G]TCTCCCTCTCCACCC | 69837 |
rs229468592 | snp | C/T | | | upstream-variant-2KB | Pcgf1 | Mm_Celera | 6:83077565 | TATTCTTTTAAAATT[C/T]CGCCGTAGGGACCCA | 69837 |
rs229568276 | snp | C/T | | | intron-variant | Pcgf1 | Mm_Celera | 6:83079428 | CTGCCCTTCACCCCT[C/T]CTTAGGTGAAGAGAA | 69837 |
rs230383006 | snp | A/C | | | intron-variant | Pcgf1 | Mm_Celera | 6:83079836 | GAGGGAGTGTCTGCT[A/C]CCCTGAAGAAAGTGT | 69837 |
rs232445226 | snp | A/G | | | upstream-variant-2KB | Pcgf1 | Mm_Celera | 6:83076794 | GGAACTCACTCTGTA[A/G]ACCAGGCTGGCCTTG | 69837 |
rs235129767 | snp | A/G | | | upstream-variant-2KB | Pcgf1 | Mm_Celera | 6:83076650 | GTTTTTTTCGAGACA[A/G]GGTTTCTCTATAGCC | 69837 |
rs235158202 | in-del | -/TTTT | | | upstream-variant-2KB | Pcgf1 | GRCm38.p3 | 6:83076612 | CCTAAGCTTGTGCCA[-/TTTT]TTTTTTTTTTTAACA | 69837 |
rs235454071 | snp | C/T | | | upstream-variant-2KB | Pcgf1 | Mm_Celera | 6:83076430 | CAAGAGATCTACTGC[C/T]TCTGCCCTGCCTGTT | 69837 |
rs236138530 | snp | A/G | | | intron-variant | Pcgf1 | Mm_Celera | 6:83080149 | ACAGCATGTAAGTAA[A/G]CCCATCATGTTACGG | 69837 |
rs236217670 | snp | C/T | | | upstream-variant-2KB | Pcgf1 | Mm_Celera | 6:83078068 | GGGCGATAGCCCGGC[C/T]TCGGGGTCCCAGGGC | 69837 |
rs236379641 | snp | G/T | | | synonymous-codon | Pcgf1 | Mm_Celera | 6:83080077 | TGTTCGGTGTTCTGT[G/T]AGAGCTGAGGTCCGC | 69837 |
rs237852030 | snp | A/G | | | downstream-variant-500B | Pcgf1 | Mm_Celera | 6:83081209 | TATTCTGTATAGCTG[A/G]AAAATAGAAACAAGA | 69837 |
rs240150502 | snp | C/T | | | intron-variant | Pcgf1 | Mm_Celera | 6:83078661 | TGCGCGTTGTGTCTC[C/T]GACAGCGTCTGGTCT | 69837 |
rs240389709 | snp | A/C | | | upstream-variant-2KB | Pcgf1 | Mm_Celera | 6:83077437 | CATTTGTCAATCATG[A/C]CCACACAAGAGTCCC | 69837 |
rs241513406 | in-del | -/GAA | | | downstream-variant-500B | Pcgf1 | Mm_Celera | 6:83081156 | AATAGGACTGAAGAG[-/GAA]GAAGAGTAATATTTA | 69837 |
rs242588644 | snp | G/T | | | upstream-variant-2KB | Pcgf1 | Mm_Celera | 6:83077575 | AAATTCCGCCGTAGG[G/T]ACCCAGTGATGACAG | 69837 |
rs242683968 | snp | A/G | | | upstream-variant-2KB | Pcgf1 | Mm_Celera | 6:83077084 | ATGCTGTGGGAAGAA[A/G]GGTCTAAAGAGGGAA | 69837 |
rs243071409 | in-del | -/A | | | intron-variant | Pcgf1 | Mm_Celera | 6:83078625 | TCTGGCCGAGTTGCC[-/A]AAACGCTGGACTTGG | 69837 |
rs243178790 | snp | A/G | | | upstream-variant-2KB | Pcgf1 | Mm_Celera | 6:83077252 | ACTTATGGGGTAACA[A/G]ACATACACTCCTTTC | 69837 |
rs244474935 | snp | G/T | | | intron-variant | Pcgf1 | Mm_Celera | 6:83080471 | AATCGCAGCAGTGGA[G/T]CCGCACAGAGGAAGA | 69837 |
rs244510406 | snp | A/T | | | synonymous-codon | Pcgf1 | Mm_Celera | 6:83080582 | CAATGAGGTTCTCCC[A/T]GATCACATGACAATG | 69837 |
rs244770456 | snp | A/T | | | utr-variant-5-prime | Pcgf1 | Mm_Celera | 6:83078397 | TAAGATGGCGTCTCC[A/T]CAGGGGGGCCAGATT | 69837 |
rs246150417 | snp | A/G | | | upstream-variant-2KB | Pcgf1 | Mm_Celera | 6:83078301 | AAAACTAGCCAATCC[A/G]GAGAATGTGAGGCCC | 69837 |
rs246926475 | snp | C/T | | | downstream-variant-500B | Pcgf1 | Mm_Celera | 6:83080949 | ACTGGAAAGAAAGGT[C/T]TCCTCCATCTACCAA | 69837 |
rs246968972 | snp | A/C | | | intron-variant | Pcgf1 | Mm_Celera | 6:83080020 | CAACCCTTCCCTCAG[A/C]CACCTGTGCCCTCCC | 69837 |
rs247222815 | snp | C/T | | | upstream-variant-2KB | Pcgf1 | Mm_Celera | 6:83076463 | AATTAAAGGTGTGTG[C/T]CACCATACTTGGCTC | 69837 |
rs250342680 | snp | C/G | | | upstream-variant-2KB | Pcgf1 | Mm_Celera | 6:83077949 | TGGGACGCAGCTCCG[C/G]AACGCGGACGCCGCA | 69837 |
rs251398143 | snp | C/T | | | downstream-variant-500B | Pcgf1 | Mm_Celera | 6:83081263 | TAGAGCAGATCTGAG[C/T]CCAGGACAGAAGGGT | 69837 |
rs251577842 | snp | A/G | | | upstream-variant-2KB | Pcgf1 | Mm_Celera | 6:83076816 | CTGGCCTTGAACTCA[A/G]AAAACCGGCTGCCTC | 69837 |
rs251812818 | in-del | -/TTTTTTTTTTTTTTTTTTTT | | | upstream-variant-2KB | Pcgf1 | GRCm38.p3 | 6:83076712 | GCCACCATGCCCTGC[-/TTTTTTTTTTTTTTTTTTTT]TTTTTTTTTTTTTTT | 69837 |
rs252400799 | in-del | -/TTT | | | upstream-variant-2KB | Pcgf1 | Mm_Celera | 6:83077381 | CCTCTTCACACTGCC[-/TTT]TTTTTCTATTTCCAT | 69837 |
rs252696910 | snp | A/G | | | intron-variant | Pcgf1 | Mm_Celera | 6:83080357 | CGGTCTGCTCAGATA[A/G]CTTAGTCAAGTATTT | 69837 |
rs253578135 | snp | A/G | | | upstream-variant-2KB | Pcgf1 | Mm_Celera | 6:83078039 | GGACTCCCACACTCC[A/G]GAGCTGTAGCGGCGG | 69837 |
rs253612414 | snp | A/T | | | upstream-variant-2KB | Pcgf1 | Mm_Celera | 6:83076903 | CTTTTAACAGTTTTC[A/T]TGAGGTCTAATTTAT | 69837 |
rs254932116 | snp | A/G | | | intron-variant | Pcgf1 | Mm_Celera | 6:83079970 | GGTGAGAGGGGTTGA[A/G]GGGAGGGCCCCTTTG | 69837 |
rs258476346 | in-del | -/AGGACTGCACTGTATAGAG | | | upstream-variant-2KB | Pcgf1 | Mm_Celera | 6:83077972 | ACGCCGCAGCGGAGC[-/AGGACTGCACTGTATAGAG]AGGACCCCGGGTCGG | 69837 |
rs259389593 | snp | A/G | | | intron-variant | Pcgf1 | Mm_Celera | 6:83079370 | AATCAAAAAAATACA[A/G]AGATAAAGAGGTCAA | 69837 |
rs260789951 | snp | C/T | | | upstream-variant-2KB | Pcgf1 | Mm_Celera | 6:83078109 | TCTTAGCACAAGCTA[C/T]CGAAGTTGATCCAGA | 69837 |
rs261398120 | in-del | -/C | | | intron-variant | Pcgf1 | Mm_Celera | 6:83080533 | AGCACTACTTCCCTG[-/C]CCCATCTCCCTCTTA | 69837 |
rs261619618 | snp | C/T | | | upstream-variant-2KB | Pcgf1 | Mm_Celera | 6:83077158 | AGGTGACTAGGTGGC[C/T]TGGGCCAGGAAGGTA | 69837 |
rs262165470 | snp | G/T | | | intron-variant | Pcgf1 | Mm_Celera | 6:83080474 | CGCAGCAGTGGAGCC[G/T]CACAGAGGAAGAGAC | 69837 |
rs262543313 | snp | G/T | | | intron-variant | Pcgf1 | Mm_Celera | 6:83080164 | GCCCATCATGTTACG[G/T]GGAAAACAAGGGACT | 69837 |
rs264937860 | snp | A/C | | | intron-variant | Pcgf1 | Mm_Celera | 6:83079768 | GCAGGTCAGAGGTTG[A/C]GTGAAGTGATACTAC | 69837 |
rs387211535 | in-del | -/TT | | | upstream-variant-2KB | Pcgf1 | Mm_Celera | 6:83076623 | GCCATTTTTTTTTTT[-/TT]AACAGTTTTTTGTTT | 69837 |
rs387726345 | in-del | -/T | | | upstream-variant-2KB | Pcgf1 | Mm_Celera | 6:83076642 | AGTTTTTTGTTTTTT[-/T]CGAGACAGGGTTTCT | 69837 |
rs580424539 | snp | C/G | | | upstream-variant-2KB | Pcgf1 | GRCm38.p3 | 6:83076597 | CCTGCACTCCTGATC[C/G]CCTAAGCTTGTGCCA | 69837 |
rs581592593 | snp | A/C | | | downstream-variant-500B | Pcgf1 | GRCm38.p3 | 6:83081166 | AAGAGGAAGAAGAGT[A/C]ATATTTAAGGAAAAA | 69837 |