SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3668718 | snp | A/G | 0.489796 | 0.070696 | upstream-variant-2KB | Plrg1 | Mm_Celera | 3:83055198 | AAAAGAAACGAAAAA[A/G]TTGCTTGCTTAAAAC | 53317 |
rs3668806 | snp | A/G | 0.489796 | 0.070696 | upstream-variant-2KB | Plrg1 | Mm_Celera | 3:83055253 | CTGGAAGCAGGTACC[A/G]CCCCTAAACGTTAAG | 53317 |
rs3669327 | snp | C/G/T | 0.489796 | 0.070696 | upstream-variant-2KB | Plrg1 | GRCm38.p3 | 3:83055332 | AGACTCCGCCCAGCT[C/G/T]CGCCGAGACCCGCCC | 53317 |
rs3669383 | snp | A/G | 0.489796 | 0.070696 | upstream-variant-2KB | Plrg1 | Mm_Celera | 3:83055362 | CTTCTGCCTGGAGAC[A/G]TCGTTCGTCCCCGCC | 53317 |
rs3722937 | snp | C/T | 0.5 | 0 | intron-variant | Plrg1 | GRCm38.p3 | 3:83063702 | TTGGGTTTTGAACTC[C/T]AGAGTGATATCTGCT | 53317 |
rs6290175 | snp | C/T | 0.5 | 0 | intron-variant | Plrg1 | GRCm38.p3 | 3:83060782 | AGCGGGCCTTGGGCA[C/T]GGGCCTGAATTGTCT | 53317 |
rs6291169 | snp | C/T | 0.5 | 0 | intron-variant | Plrg1 | Mm_Celera | 3:83060899 | gttctgggaattgaa[C/T]ttctcatgctggaac | 53317 |
rs6292201 | snp | A/C | 0.5 | 0 | missense | Plrg1 | Mm_Celera | 3:83061104 | TCTGACCGTTCCCAG[A/C]CCACAGCAATGAATT | 53317 |
rs6292761 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Plrg1 | Mm_Celera | 3:83061215 | TGAGCTCTGTTTAAT[A/G]CAAATAGCAGCCAGG | 53317 |
rs6307305 | snp | A/C | 0.5 | 0 | intron-variant | Plrg1 | Mm_Celera | 3:83061542 | gcagaggggctctgg[A/C]gctcagtggccagcc | 53317 |
rs6309388 | snp | A/G | 0.5 | 0 | intron-variant | Plrg1 | Mm_Celera | 3:83061909 | cacgcacgcacgcac[A/G]catgcacTGAACTGT | 53317 |
rs6359037 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Plrg1 | Mm_Celera | 3:83070753 | TAACACAAGGTTTCT[A/G]TGGTGTGTTGAGTGT | 53317 |
rs6359590 | snp | C/T | 0.32699 | 0.23785 | intron-variant | Plrg1 | Mm_Celera | 3:83070900 | CCATGCAGCATGTTG[C/T]ATAGTTTAGACATCT | 53317 |
rs6360092 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Plrg1 | Mm_Celera | 3:83070973 | TGCCTGATGTTTGGT[C/T]GGATTTTAAATGTTA | 53317 |
rs6360540 | snp | C/T | 0.375 | 0.216506 | intron-variant | Plrg1 | Mm_Celera | 3:83071011 | TATAAATTAGAGACT[C/T]AGAGGGAATTagaga | 53317 |
rs6361091 | snp | A/G | 0.5 | 0 | intron-variant | Plrg1 | Mm_Celera | 3:83071111 | tgtgtgtgtgtgtgt[A/G]tNGCTGGTGTAATGT | 53317 |
rs6361093 | snp | A/T | 0.5 | 0 | intron-variant | Plrg1 | Mm_Celera | 3:83071113 | tgtgtgtgtgtgtnt[A/T]GCTGGTGTAATGTTC | 53317 |
rs13475307 | snp | C/G | 0.375 | 0.216506 | missense | Plrg1 | GRCm38.p3 | 3:83059371 | ACCCATCCATACCCA[C/G]CAGGACCCGGTAAGT | 53317 |
rs30006860 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Plrg1 | GRCm38.p3 | 3:83053681 | CATTCTACCTCACTG[A/G]TCATTGCTCAACAGG | 53317 |
rs30054176 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Plrg1 | GRCm38.p3 | 3:83064883 | GGGTTTGATCTTAGT[C/T]ATTCTGATTGCTATA | 53317 |
rs30063371 | snp | C/T | 0.32 | 0.24 | intron-variant | Plrg1 | GRCm38.p3 | 3:83065129 | GGTTACTGAAGATTT[C/T]CCCTCTCTTCCCCGC | 53317 |
rs30156990 | snp | G/T | 0.375 | 0.216506 | intron-variant | Plrg1 | GRCm38.p3 | 3:83060599 | TGAACCTGTAAGGCA[G/T]CCCCAATTAAATGTC | 53317 |
rs30211063 | snp | C/T | 0.32 | 0.24 | intron-variant | Plrg1 | Mm_Celera | 3:83059010 | ACAAGATTACAGTGG[C/T]GTCTACAGGGAAAAC | 53317 |
rs30254522 | snp | A/G | 0.32 | 0.24 | upstream-variant-2KB | Plrg1 | GRCm38.p3 | 3:83055201 | AGAAACGAAAAAGTT[A/G]CTTGCTTAAAACCTC | 53317 |
rs30304621 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Plrg1 | GRCm38.p3 | 3:83062861 | CCCAATGCAGGTTCC[C/T]GCAGCTGCTATGAGT | 53317 |
rs30404680 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Plrg1 | Mm_Celera | 3:83071566 | TCTTCCTGCCTCTGC[C/T]TCTCCGATGCTGGGA | 53317 |
rs30456943 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Plrg1 | Mm_Celera | 3:83070369 | GCTAATTAGTGTGTA[A/G]CACACTAAAGAAAAC | 53317 |
rs30459114 | snp | A/C | 0.401235 | 0.199068 | intron-variant | Plrg1 | Mm_Celera | 3:83069154 | CCTCCGACCGACTCG[A/C]GTTCTAGTTTCTCTT | 53317 |
rs30504586 | snp | C/G | 0.375 | 0.216506 | intron-variant | Plrg1 | Mm_Celera | 3:83068635 | TAGCAAGGAAAATAA[C/G]TTTATGGTTGGGGCC | 53317 |
rs30512111 | snp | C/T | 0.375 | 0.216506 | intron-variant | Plrg1 | GRCm38.p3 | 3:83056242 | GAGGTCTAAACCTCA[C/T]CGACCCTGGAAACCC | 53317 |
rs30555426 | snp | C/T | 0.375 | 0.216506 | intron-variant | Plrg1 | Mm_Celera | 3:83068615 | CACAATTGCCAATTA[C/T]GAAGTAGCAAGGAAA | 53317 |
rs30605134 | snp | A/T | 0.359862 | 0.224567 | utr-variant-3-prime | Plrg1 | Mm_Celera | 3:83072222 | TGAGGATATCCGGTC[A/T]TTCATGAAAGCTCAC | 53317 |
rs30609657 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Plrg1 | GRCm38.p3 | 3:83062289 | TCTCCATGACGTCAG[A/G]CCAGCAGTCCACCCA | 53317 |
rs30645833 | snp | A/G | 0.5 | 0 | intron-variant | Plrg1 | GRCm38.p3 | 3:83065684 | AAGATTCCTCTGTTG[A/G]GAATTCTCTCAGAAC | 53317 |
rs30648741 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Plrg1 | Mm_Celera | 3:83059167 | GTCAGTGGGAGGGGC[A/G]CCTTGACTTATTAGC | 53317 |
rs30698484 | snp | G/T | 0.5 | 0 | intron-variant | Plrg1 | Mm_Celera | 3:83058495 | AATGCATTTTAGAAT[G/T]TTGTAGTTGTTAAAA | 53317 |
rs30704567 | snp | A/G | 0.5 | 0 | intron-variant | Plrg1 | Mm_Celera | 3:83058297 | TATCTATACAATTTA[A/G]CTATATTCAGACATT | 53317 |
rs30743066 | snp | C/G | 0.345679 | 0.230967 | intron-variant | Plrg1 | Mm_Celera | 3:83068945 | CCTTTTCCTATCATG[C/G]TAACTTTACTTTACA | 53317 |
rs30747673 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Plrg1 | Mm_Celera | 3:83070580 | TTCCCATTAATTCCT[A/G]TCAATCTTTGTTCTA | 53317 |
rs30758739 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB | Plrg1 | GRCm38.p3 | 3:83054951 | TAAATCACAAAACCT[C/T]AACACTTTAGCGTCA | 53317 |
rs30800039 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Plrg1 | Mm_Celera | 3:83070341 | TTGCCCTGTGTGTGT[A/G]CACATTTGTTGGGCT | 53317 |
rs30844984 | snp | A/G | 0.375 | 0.216506 | intron-variant | Plrg1 | Mm_Celera | 3:83067991 | CAAAACAATTGCTTG[A/G]TTTCAGATTTGGGAC | 53317 |
rs30846486 | snp | C/T | 0.5 | 0 | intron-variant | Plrg1 | GRCm38.p3 | 3:83056624 | GAGCTTTCTCATCTT[C/T]GTTGTTGATTGCTGT | 53317 |
rs30896571 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Plrg1 | Mm_Celera | 3:83067438 | TCTATAGCTTGTTTC[C/T]CTGTTGTTCAGCATG | 53317 |
rs30901221 | snp | C/T | 0.5 | 0 | intron-variant | Plrg1 | Mm_Celera | 3:83069904 | CTTAGGACGGCCTTT[C/T]AGTTCCCATCTGCTG | 53317 |
rs30944310 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Plrg1 | Mm_Celera | 3:83067676 | GATGTCTAACTGTAA[A/G]CAGACACACAGACAG | 53317 |
rs30957859 | snp | A/C | 0.5 | 0 | intron-variant | Plrg1 | GRCm38.p3 | 3:83063298 | AGCTGGGTAGGCCCA[A/C]TGATGCCTTTTCTGC | 53317 |
rs31133168 | snp | C/T | 0.375 | 0.216506 | intron-variant | Plrg1 | Mm_Celera | 3:83068584 | CAGATATTTGTGTTA[C/T]GATTCATAACAGTAG | 53317 |
rs31137510 | snp | C/T | 0.265928 | 0.249492 | intron-variant | Plrg1 | GRCm38.p3 | 3:83056561 | AATATCTACTGAACA[C/T]ATTGTAGGCATTACT | 53317 |
rs31147645 | snp | A/T | 0.375 | 0.216506 | intron-variant | Plrg1 | GRCm38.p3 | 3:83059567 | TTGGACAGAGGACAA[A/T]AAGCCTTATGTTTGC | 53317 |
rs31176187 | snp | C/T | 0.375 | 0.216506 | intron-variant | Plrg1 | Mm_Celera | 3:83067574 | AGTGCAACTTTCTCC[C/T]CACAGTTAGTGAGCT | 53317 |
rs31188585 | snp | A/G | 0.375 | 0.216506 | intron-variant | Plrg1 | GRCm38.p3 | 3:83060181 | TTAAAGGCCTGTGCC[A/G]CCACGCCCGGCTCCA | 53317 |
rs31195885 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Plrg1 | Mm_Celera | 3:83069907 | AGGACGGCCTTTCAG[C/T]TCCCATCTGCTGCTG | 53317 |
rs31196867 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Plrg1 | Mm_Celera | 3:83067650 | AGGGATGTGGCCACT[A/G]GGAATGGGTAGATGT | 53317 |
rs31236432 | snp | C/G | 0.375 | 0.216506 | intron-variant | Plrg1 | GRCm38.p3 | 3:83056433 | TTCTCCCCCCACCAA[C/G]TCATCCCATTGCCTA | 53317 |
rs31247214 | snp | A/G | 0.197531 | 0.244432 | synonymous-codon | Plrg1 | Mm_Celera | 3:83068078 | TGTGATCGTGAGCAC[A/G]AGGAGTCCTTATTTG | 53317 |
rs31283076 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Plrg1 | Mm_Celera | 3:83069122 | CGGCCATTCTGCAGC[C/T]GCCGCAAGCACCTCC | 53317 |
rs31288187 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Plrg1 | Mm_Celera | 3:83056575 | ACATTGTAGGCATTA[C/T]TCAGTTACTTTTCTA | 53317 |
rs31289424 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Plrg1 | Mm_Celera | 3:83065109 | TATCCCTCTATCAGA[G/T]GTAGGGTTACTGAAG | 53317 |
rs31330827 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Plrg1 | Mm_Celera | 3:83068251 | AACCCTTCTGCCTTT[A/G]TCTTTAGGTGATACG | 53317 |
rs31336175 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | Plrg1 | GRCm38.p3 | 3:83053668 | TTGTACCAGGCCACA[C/T]TCTACCTCACTGATC | 53317 |
rs31337719 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Plrg1 | Mm_Celera | 3:83069086 | TCTGCTGCTCCCCCT[A/G]AGCCGTACCAGAGGC | 53317 |
rs31342695 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Plrg1 | Mm_Celera | 3:83071475 | TATTTTATATTTAGA[A/G]ACAAGGTATCACATG | 53317 |
rs31380738 | snp | C/G | 0.304688 | 0.243945 | utr-variant-5-prime | Plrg1 | Mm_Celera | 3:83055570 | TCCGGAAAGAGCTGC[C/G]GAATAGTGGCGGCGT | 53317 |
rs31381264 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Plrg1 | Mm_Celera | 3:83069399 | AACTACAGATTTTAA[A/G]ATAAAAAGATTCATT | 53317 |
rs31387203 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Plrg1 | Mm_Celera | 3:83059143 | TACTGTGAAGAACAG[C/T]TGGAACAGGTCGTCA | 53317 |
rs31435483 | snp | A/T | 0.359862 | 0.224567 | intron-variant | Plrg1 | Mm_Celera | 3:83072104 | TTGTTTACTGTTCTG[A/T]TTTTAGACAGAAGAA | 53317 |
rs31519174 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Plrg1 | Mm_Celera | 3:83064955 | GACTAAGGATATTGA[A/C]CTTTTCTTTAAGTGC | 53317 |
rs31539423 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Plrg1 | Mm_Celera | 3:83071706 | CTATAGTACCATCAG[C/T]TTCATCCTCTGGATA | 53317 |
rs31600952 | snp | C/G | 0.375 | 0.216506 | upstream-variant-2KB | Plrg1 | Mm_Celera | 3:83054865 | TAAGATCGCAAATAG[C/G]AACTACATCAATACA | 53317 |
rs31665336 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Plrg1 | Mm_Celera | 3:83070742 | GTGTCTGGAGGTAAC[A/G]CAAGGTTTCTATGGT | 53317 |
rs31685566 | snp | A/C/G | 0.336735 | 0.234472 | intron-variant | Plrg1 | Mm_Celera | 3:83066208 | GGGTGAAGTAGGAAC[A/C/G]GGAGAGCCTGCCTGA | 53317 |
rs31725764 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Plrg1 | GRCm38.p3 | 3:83066290 | TGGGGCTGATGGATT[C/T]TAATAGACACAGCTT | 53317 |
rs36326107 | snp | C/T | 0.46281 | 0.131194 | intron-variant | Plrg1 | GRCm38.p3 | 3:83071723 | TCATCCTCTGGATAG[C/T]GATCTGACCTGCTCA | 53317 |
rs36389465 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Plrg1 | GRCm38.p3 | 3:83071928 | AAATGGAAATCCAAC[C/T]GAACCCATGTATCCC | 53317 |
rs36472124 | snp | A/G | 0.336735 | 0.234472 | downstream-variant-500B | Plrg1 | Mm_Celera | 3:83072365 | AAAGAATTCAGGCAT[A/G]TTGAGGATTGTTGTT | 53317 |
rs36496277 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Plrg1 | GRCm38.p3 | 3:83069148 | CCTCCACCTCCGACC[A/G]ACTCGCGTTCTAGTT | 53317 |
rs36518002 | snp | C/T | 0.244898 | 0.249948 | synonymous-codon | Plrg1 | Mm_Celera | 3:83066741 | TGGAAATCAGTGGTT[C/T]GTTACAGGATCTGCT | 53317 |
rs36542990 | snp | C/T | 0.336735 | 0.234472 | synonymous-codon | Plrg1 | Mm_Celera | 3:83071197 | CCTTGCAGCTGACAA[C/T]GGCACCATGCACCTT | 53317 |
rs36865045 | snp | A/C | 0.165289 | 0.235211 | upstream-variant-2KB | Plrg1 | GRCm38.p3 | 3:83054472 | TTAAGGTCTTTCTTA[A/C]ATTTCCTTAGTGTTT | 53317 |
rs36918017 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Plrg1 | Mm_Celera | 3:83069930 | TGCTGCTGTTGCCTC[A/G]TGCTCTGTGGAATGA | 53317 |
rs36966635 | snp | A/G | 0.336735 | 0.234472 | downstream-variant-500B | Plrg1 | Mm_Celera | 3:83072745 | TAATTTGGGACTAAA[A/G]GATTGAAGATTCTTT | 53317 |
rs36984378 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Plrg1 | GRCm38.p3 | 3:83066296 | TGATGGATTCTAATA[A/G]ACACAGCTCTCAGTA | 53317 |
rs37000219 | snp | C/T | 0.459184 | 0.136902 | upstream-variant-2KB | Plrg1 | GRCm38.p3 | 3:83054539 | TTTCCTTGCAACGTG[C/T]ACAAACATTAGCCAC | 53317 |
rs37004865 | snp | A/G | 0.142012 | 0.225474 | synonymous-codon | Plrg1 | Mm_Celera | 3:83071371 | TAAAGTTTACAGAGA[A/G]GATGAGACTGCGGTA | 53317 |
rs37415112 | snp | C/T | 0.231111 | 0.249285 | upstream-variant-2KB | Plrg1 | Mm_Celera | 3:83055524 | AATACGCATGTGCGG[C/T]TAGCGTCACGTCCGG | 53317 |
rs37582551 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Plrg1 | Mm_Celera | 3:83071948 | CCATGTATCCCTGGT[C/T]AAACTTGGATAATGC | 53317 |
rs38047789 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Plrg1 | Mm_Celera | 3:83071790 | GTGATAAAGCATTAC[G/T]TTTTAAGTACAGTTC | 53317 |
rs38090194 | snp | C/G/T | 0.244898 | 0.249948 | downstream-variant-500B | Plrg1 | Mm_Celera | 3:83072714 | GAGTACTTTGAAGAT[C/G/T]TAAAACAATGGCTGA | 53317 |
rs38155850 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Plrg1 | Mm_Celera | 3:83071992 | GCTGTTTCTAAAATT[C/T]TTCAAGAGCCACTCA | 53317 |
rs38468735 | snp | A/C | 0.459184 | 0.136902 | upstream-variant-2KB | Plrg1 | GRCm38.p3 | 3:83054368 | CAGTAGACTGCCCTT[A/C]TGAGCCTTGCATAAG | 53317 |
rs38631341 | snp | C/T | 0.132653 | 0.220748 | synonymous-codon | Plrg1 | Mm_Celera | 3:83056857 | TGATAATGGAAAACC[C/T]GTGCCTTTGGATGAA | 53317 |
rs38632636 | snp | A/T | 0.260355 | 0.249785 | intron-variant | Plrg1 | Mm_Celera | 3:83066436 | GGAGAGTGGTGTCTT[A/T]TGCAATGATTTTGAG | 53317 |
rs38795996 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Plrg1 | Mm_Celera | 3:83068742 | GGCTGCCCATTGGCT[A/G]TTTAAGTCTCTAGTC | 53317 |
rs38850166 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Plrg1 | Mm_Celera | 3:83070167 | ACATCAGCACTGCGG[G/T]TCCCAGAGAAGGCAG | 53317 |
rs40201863 | snp | A/C | 0.165289 | 0.235211 | intron-variant | Plrg1 | Mm_Celera | 3:83066926 | CTGTTAGTTCTGTGT[A/C]GCTTACTGAAGGAAG | 53317 |
rs40243818 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Plrg1 | Mm_Celera | 3:83066977 | GATGGAAGCATAGTT[C/T]TCTGTAGAGGTGCGG | 53317 |
rs45699337 | snp | G/T | | | intron-variant | Plrg1 | Mm_Celera | 3:83057411 | TGCTCTCATGCTCCC[G/T]ACTCTTATGGCCAAG | 53317 |
rs45699366 | snp | A/G | | | upstream-variant-2KB | Plrg1 | GRCm38.p3 | 3:83053991 | CATCTTATTCTTTTC[A/G]TTTGTTTTGGTTTTA | 53317 |
rs45809539 | snp | G/T | | | intron-variant | Plrg1 | GRCm38.p3 | 3:83060260 | GTGTGTGCACTCTCG[G/T]GCACCTCACAGCCCT | 53317 |