SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6336113 | snp | A/G | 0.5 | 0 | intron-variant | Plcg2 | Mm_Celera | 8:117511611 | ctccatggcctctgc[A/G]tcagctcctgcctcc | 234779 |
rs6336591 | snp | A/G | 0.5 | 0 | intron-variant | Plcg2 | Mm_Celera | 8:117511682 | aacagactgtgattc[A/G]ggntatataagccaa | 234779 |
rs6336594 | snp | A/G | 0.5 | 0 | intron-variant | Plcg2 | Mm_Celera | 8:117511685 | agactgtgattcngg[A/G]tatataagccaaaga | 234779 |
rs6337314 | snp | A/G | 0.5 | 0 | intron-variant | Plcg2 | Mm_Celera | 8:117511857 | TGCCCCTTCTGTATC[A/G]GAGCAGCNGAACAAC | 234779 |
rs6337732 | snp | C/T | 0.5 | 0 | intron-variant | Plcg2 | Mm_Celera | 8:117511865 | CTGTATCNGAGCAGC[C/T]GAACAACGGATGCNG | 234779 |
rs6337773 | snp | A/T | 0.5 | 0 | intron-variant | Plcg2 | Mm_Celera | 8:117511879 | CNGAACAACGGATGC[A/T]GTTGGCGTTTTGGTT | 234779 |
rs6360944 | snp | A/T | 0.5 | 0 | intron-variant | Plcg2 | Mm_Celera | 8:117598732 | ACACAGATTCTAATT[A/T]AAAAAATCTTCCAAA | 234779 |
rs6374408 | snp | A/G | 0.375 | 0.216506 | intron-variant | Plcg2 | Mm_Celera | 8:117598862 | TGCCGCTGCCTCGTA[A/G]CTTTGTGTAGGAAAA | 234779 |
rs13480011 | snp | A/G | 0.303361 | 0.244239 | intron-variant | Plcg2 | Mm_Celera | 8:117545016 | TTAAAACTCAGTAGC[A/G]AGCTGACAGACAGTT | 234779 |
rs31562224 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Plcg2 | Mm_Celera | 8:117546016 | AAGATACATTACAGG[A/G]AGACACAGCAAAAGG | 234779 |
rs31562227 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117546089 | AATATAAGGGCCACT[A/G]TAGCATTGAACTTGA | 234779 |
rs31562230 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Plcg2 | Mm_Celera | 8:117546839 | TACCACTGTGTGCTC[A/G]TGGTTGCCAGCATAC | 234779 |
rs31562233 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117546877 | CCGTGGAAGCAGGAG[A/G]CATGAACGCTCTCTT | 234779 |
rs31563106 | snp | C/T | 0.32 | 0.24 | intron-variant | Plcg2 | Mm_Celera | 8:117546892 | GCATGAACGCTCTCT[C/T]CTGTTGGCTCTTAGT | 234779 |
rs31563109 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117546927 | TCTCTAGAACTGCGG[A/G]GTCACTTTCTCACCA | 234779 |
rs31563112 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117547029 | CATGCATTCACACAT[A/G]TGTACTCTTGCCCGT | 234779 |
rs31563925 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117547577 | AGAGGTGGCCGGAAT[A/G]TCATCCCCGGTAGCT | 234779 |
rs31563928 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117547591 | TATCATCCCCGGTAG[C/T]TGACGTAACTTTGAC | 234779 |
rs31563931 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117547853 | ACAGGCTTCTCCCCT[C/G]TAGGTACCGGATCCT | 234779 |
rs31564714 | snp | C/T | 0.18 | 0.24 | intron-variant | Plcg2 | Mm_Celera | 8:117548089 | AAGGAGGTGGGAGCA[C/T]GTGTGTGCACGTGTG | 234779 |
rs31564717 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117548225 | AGAGAGAGCCATGCT[C/T]TAGGTGTGAAGGATA | 234779 |
rs31564720 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117548713 | CTACAAGCAGGAAGC[C/T]CAGCCACGAGCCCCA | 234779 |
rs31564722 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117551143 | AAGGGAACCCTCCAT[A/G]TACACACACAATCAT | 234779 |
rs31565535 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117551480 | TGTGCCGTTTGTGTC[A/G]TGTTGGTGCCTGTAC | 234779 |
rs31565537 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117551532 | TGAGGTCTGGATGGC[A/G]CATTTTGGGCAGACG | 234779 |
rs31565540 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117552298 | GTTTCTACACTTAGT[C/T]TAAACTCCATTAGGA | 234779 |
rs31565543 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117552707 | GAGTTGGATGAACCC[A/G]GGACTGTGGAGTCTG | 234779 |
rs31566275 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117552744 | CAACTCTAGGTTCTT[A/T]TCCTAGCCTTAGGTC | 234779 |
rs31566278 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Plcg2 | Mm_Celera | 8:117552890 | TCAGCTTTGCAGATG[A/G]TCATGTCTTAACGGC | 234779 |
rs31566281 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Plcg2 | Mm_Celera | 8:117552910 | GTCTTAACGGCACAC[C/T]CTCATAGATGGAGAG | 234779 |
rs31566375 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117538692 | TACAGAGCTGGCCCA[A/C]TGCCTCACTGTCACA | 234779 |
rs31566377 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117538928 | TCGGAGCAAGGCTTT[C/T]GTGTGGGGCACTCGA | 234779 |
rs31566380 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117538989 | CCTCTAGAGCTTTCT[C/T]CTCCCTCATCCTGAA | 234779 |
rs31566383 | snp | C/T | 0.32 | 0.24 | intron-variant | Plcg2 | Mm_Celera | 8:117539153 | TCCAAGTACAGCGAC[C/T]TGAGTGTAGGTCCCC | 234779 |
rs31566565 | snp | C/T | 0.32 | 0.24 | synonymous-codon | Plcg2 | Mm_Celera | 8:117556048 | AGCCAAGGCTGTCCG[C/T]CACAAGGCAGAATGT | 234779 |
rs31566568 | snp | C/T | 0.32 | 0.24 | intron-variant | Plcg2 | Mm_Celera | 8:117556200 | AGATCATACTTCATG[C/T]CTGCTAATGCATGCT | 234779 |
rs31566571 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117556413 | ATGAAGGTAGTTAAC[A/G]TGGTCACTGAGAGAT | 234779 |
rs31566934 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Plcg2 | Mm_Celera | 8:117580346 | CGCCTATGAGGTGTG[C/T]GGACTCCTCAGTGAA | 234779 |
rs31566937 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Plcg2 | Mm_Celera | 8:117581002 | CAAAACATCAAAAGC[C/T]CTCTTAAATAACCTA | 234779 |
rs31566940 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Plcg2 | Mm_Celera | 8:117581342 | TGATGAAGCATGGGC[C/T]TATTTCTGCTGATAC | 234779 |
rs31566943 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Plcg2 | Mm_Celera | 8:117581490 | GCTTAGGTAGCTATC[A/G]TGCACATCTTATTGG | 234779 |
rs31566975 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117562680 | AGTGGGAACTGGTTA[C/T]GGTTCTGAGGAACAC | 234779 |
rs31566978 | snp | A/G | 0.32 | 0.24 | intron-variant | Plcg2 | Mm_Celera | 8:117562898 | GGGTCTGCAAGGGAT[A/G]TGGAAGGGGAGGCGC | 234779 |
rs31566981 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Plcg2 | Mm_Celera | 8:117562980 | CAAGCCACACTTGTG[C/T]GGATTCCGTTGCATT | 234779 |
rs31567214 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117553046 | GGAAGTGTCAGTCAC[A/G]GATGTGAAGGGCTTG | 234779 |
rs31567217 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117553078 | TGATGCAGCCTCCAG[C/G]CCTGGGAAGTGTGAC | 234779 |
rs31567220 | snp | A/G | 0.32 | 0.24 | intron-variant | Plcg2 | Mm_Celera | 8:117553168 | GATGGATGGAGAACT[A/G]GTTCCTAGCCCTCAA | 234779 |
rs31567222 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117553357 | GAGTGCTGACTCACG[C/G]TCCAGCAACAGGGAG | 234779 |
rs31567416 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117539840 | TATCTTCTGGCCTTA[C/T]ACTTTGAGACACTAA | 234779 |
rs31567419 | snp | A/C | 0.32 | 0.24 | intron-variant | Plcg2 | Mm_Celera | 8:117540041 | TAGCTGGAACTTGAC[A/C]TTGGCAGTGCTCTGT | 234779 |
rs31567422 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117540642 | TGCTCAGCACTAAAG[A/T]ATTTTTTATTGGCAT | 234779 |
rs31567484 | snp | C/T | 0.32 | 0.24 | intron-variant | Plcg2 | Mm_Celera | 8:117557154 | ATAAACTTACATATC[C/T]GGAGATGGGATTTCT | 234779 |
rs31567487 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117557401 | ATGATTGAGAGGTAC[A/G]CAACCCACTGGCATC | 234779 |
rs31567490 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Plcg2 | Mm_Celera | 8:117557431 | CATCCTCCTTTGTTC[C/T]AGGGTCTTCGGGAAT | 234779 |
rs31567493 | snp | C/G/T | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117557533 | GTGGCTAAGAACTCT[C/G/T]CAGTGCTCCACATAA | 234779 |
rs31567706 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Plcg2 | Mm_Celera | 8:117581522 | GGTTCTGGACCCAAG[A/G]CCTCAGGATGGCGTG | 234779 |
rs31567709 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Plcg2 | Mm_Celera | 8:117582038 | AAAAGTGACATCTGG[C/T]TGGGCAATAGATTGG | 234779 |
rs31567712 | snp | A/C | 0.165289 | 0.235211 | intron-variant | Plcg2 | Mm_Celera | 8:117582133 | CTGCTAAGAGGAACA[A/C]AGACACATACTAGTT | 234779 |
rs31567864 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117563310 | CTCACTTCCTGAGGG[C/T]ATGGTGAAGCAGCCC | 234779 |
rs31567867 | snp | C/T | 0.32 | 0.24 | intron-variant | Plcg2 | Mm_Celera | 8:117563369 | TGGGGGTCCAGACCC[C/T]GAAGAATGTGCAGTT | 234779 |
rs31567870 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Plcg2 | Mm_Celera | 8:117563426 | CCTAAACAGCTGCAA[A/G]TAGCAGGGCCCTTGA | 234779 |
rs31567873 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Plcg2 | Mm_Celera | 8:117563608 | TTGTGAGGTTAGCCG[C/T]GTTTGGAGGCACACA | 234779 |
rs31568244 | snp | A/G | 0.32 | 0.24 | intron-variant | Plcg2 | Mm_Celera | 8:117554634 | TACTATGAGTTTTAG[A/G]AATTGTGTCCCAAGA | 234779 |
rs31568246 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Plcg2 | Mm_Celera | 8:117555064 | AGTTGAAGCGAGTGG[C/T]ATTTGGGGCTGTTGG | 234779 |
rs31568249 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117555116 | ACAAGCAGAATTAGT[C/T]ACTGGCATGGGTGGT | 234779 |
rs31568251 | snp | A/G/T | 0.132653 | 0.220748 | intron-variant | Plcg2 | GRCm38.p3 | 8:117555196 | TGCTATGATAGAGTA[A/G/T]TCTGGGTCTTATCCC | 234779 |
rs31568305 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Plcg2 | Mm_Celera | 8:117540698 | GCGTAACCCATTATG[A/G]CATGTTCATACATGA | 234779 |
rs31568308 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Plcg2 | Mm_Celera | 8:117540839 | TGACTAGTGGGTTTA[A/G]TTAGGGTTAGTTACA | 234779 |
rs31568310 | snp | A/C | 0.32 | 0.24 | intron-variant | Plcg2 | Mm_Celera | 8:117540897 | GTGGCTACACCACTA[A/C]AGAAAATGTCTCTTA | 234779 |
rs31568313 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Plcg2 | Mm_Celera | 8:117541620 | AGCTGACTCTGATTT[A/C]AGTTCGATAGCAAGG | 234779 |
rs31568356 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117557577 | TAGTGTTGAGCCTTG[A/G]CCTTTGGCGTGAAGA | 234779 |
rs31568358 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117557579 | GTGTTGAGCCTTGAC[C/T]TTTGGCGTGAAGAGG | 234779 |
rs31568361 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117557667 | TGAATCTTTCTGTGA[A/C]TATCTGCAAGCATAT | 234779 |
rs31568435 | snp | C/G | 0.197531 | 0.244432 | intron-variant | Plcg2 | Mm_Celera | 8:117582264 | CAAAGCCTTGCTTTT[C/G]TCTGCCTTTTTTCCT | 234779 |
rs31568438 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Plcg2 | Mm_Celera | 8:117582615 | CCAGCTCATCTTTGG[C/T]TCTATCCTTCCCAGA | 234779 |
rs31568441 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Plcg2 | Mm_Celera | 8:117582809 | ACAAACACTTTGACC[A/G]TAAGGTAGAAACTGG | 234779 |
rs31568594 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Plcg2 | Mm_Celera | 8:117524990 | CGGTAGCAGCCTAGC[C/T]TTGTGTTCCGGTGGC | 234779 |
rs31568597 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Plcg2 | GRCm38.p3 | 8:117536311 | TGTGAGCACATGTCC[A/G]GGCTGTGTGGAGCTG | 234779 |
rs31568599 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Plcg2 | Mm_Celera | 8:117536400 | GAGCTGGTGTGAGCA[C/T]GTGTCCAGGCTGTGT | 234779 |
rs31568601 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Plcg2 | Mm_Celera | 8:117536405 | GGTGTGAGCATGTGT[C/G]CAGGCTGTGTGGAGC | 234779 |
rs31568666 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Plcg2 | Mm_Celera | 8:117564288 | ATGAAGAAGCACAGG[A/G]TGTGCAGGCAACAGG | 234779 |
rs31568669 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Plcg2 | Mm_Celera | 8:117564421 | GGAATGAAGATCCAG[A/G]GAGTCAAATCTGCTT | 234779 |
rs31568672 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Plcg2 | Mm_Celera | 8:117564583 | TACTCCTGTTAGGTA[C/T]GTGTTTCTAGAGATG | 234779 |
rs31568936 | snp | G/T | 0.197531 | 0.244432 | intron-variant | Plcg2 | Mm_Celera | 8:117587925 | AAGAATGAAATTATA[G/T]CATTTACATGTGGAG | 234779 |
rs31568939 | snp | A/C/T | 0.277778 | 0.248452 | intron-variant | Plcg2 | Mm_Celera | 8:117589014 | GATCTGATCTGCTGC[A/C/T]GACTGTCAATGCAGC | 234779 |
rs31568942 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Plcg2 | Mm_Celera | 8:117589378 | GACCTGCTTGCCTTC[A/T]GCCTTCTGGTCTTGT | 234779 |
rs31569134 | snp | A/C | 0.165289 | 0.235211 | intron-variant | Plcg2 | Mm_Celera | 8:117582886 | ACAGCCTCAATGACG[A/C]TACTCCAGGAACCAC | 234779 |
rs31569137 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Plcg2 | Mm_Celera | 8:117582940 | ATAGCCATGTATGTG[A/G]CTAAGAAAATGGCCC | 234779 |
rs31569140 | snp | A/T | 0.165289 | 0.235211 | intron-variant | Plcg2 | Mm_Celera | 8:117583257 | AATATTTTATAATGA[A/T]TGGCTCACTAGAAGG | 234779 |
rs31569143 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Plcg2 | Mm_Celera | 8:117583294 | TCAGGAAGTGTGTCA[C/T]GTTCTGCAAGTCTGT | 234779 |
rs31569214 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117555348 | ACACAGCAGAGACAA[C/T]CCACTAAGATATGTT | 234779 |
rs31569217 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117555604 | GTTCTAAACCTGTCA[C/G]TTGACCAGTTCATCG | 234779 |
rs31569219 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117555809 | TTGGTTTCCTGTCCA[C/T]ACTCAGGAGAATTGG | 234779 |
rs31569222 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117555857 | GACTCTGGTCAGAGA[G/T]GGACTCACAGCTGTC | 234779 |
rs31569224 | snp | C/T | 0.32 | 0.24 | intron-variant | Plcg2 | Mm_Celera | 8:117557689 | CAAGCATATAAATAT[C/T]TGTTCATATACATTC | 234779 |
rs31569227 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117557809 | ACACCTTCCCACATA[C/T]ACCACTCTTTCTTCT | 234779 |
rs31569229 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117557931 | TCAGCCACAGGTGGA[A/G]TCTTGTTACCAAGCA | 234779 |
rs31569230 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Plcg2 | Mm_Celera | 8:117558237 | TCTGGGGTTGACGGT[A/G]ACCCAGAATGATTGA | 234779 |
rs31569232 | snp | C/T | 0.32 | 0.24 | intron-variant | Plcg2 | Mm_Celera | 8:117558295 | CTCCTGTCGTGCTGC[C/T]GAGGTGACATTTGAC | 234779 |
rs31569296 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Plcg2 | Mm_Celera | 8:117541843 | TTCTGGGTGTTGGCT[C/G]TATCTTGGACTGGGT | 234779 |
rs31569299 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Plcg2 | Mm_Celera | 8:117541963 | GCTGAGAGCCAGAGC[A/G]GCCCCAGGTAACGGA | 234779 |
rs31569302 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Plcg2 | Mm_Celera | 8:117541971 | CCAGAGCGGCCCCAG[A/G]TAACGGAGTAACAGC | 234779 |
rs31569395 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Plcg2 | Mm_Celera | 8:117564774 | TTACTCAATTGCTAA[A/G]TAGCTGCATTGGCTC | 234779 |
rs31569398 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Plcg2 | Mm_Celera | 8:117565815 | TCTCTGACGATGACA[A/G]AGGCCAGGTTGATAA | 234779 |
rs31569401 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Plcg2 | GRCm38.p3 | 8:117565847 | TGTGGAGACCCACAC[C/T]TGAGGCCGGGTTCTT | 234779 |
rs31569615 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117589389 | CTTCAGCCTTCTGGT[A/C]TTGTCCTTGGAGAAT | 234779 |
rs31569618 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117589472 | TCCTTAGCTCTAGGG[C/T]GATATTGCTTTGGGT | 234779 |
rs31569621 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117589506 | AAAGCTTAACTAGCT[C/T]TTCCTGATTGGCTAG | 234779 |
rs31569654 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Plcg2 | Mm_Celera | 8:117536451 | TCCAGGCTGTGTGGA[A/G]CTGGTGTGAGCACAT | 234779 |
rs31569657 | snp | C/T | 0.32 | 0.24 | intron-variant | Plcg2 | Mm_Celera | 8:117536594 | AGGGAACAGCTGCAG[C/T]GTGTCCCAGCAGGGA | 234779 |
rs31569660 | snp | A/G | 0.32 | 0.24 | intron-variant | Plcg2 | Mm_Celera | 8:117537468 | TGCCTGTCTTCCAGA[A/G]CAATGCCCGGCAGGC | 234779 |
rs31569663 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Plcg2 | Mm_Celera | 8:117537837 | GAGGAGGTTCAGGAC[C/T]CAGGCTCTGCTTCTG | 234779 |
rs31569716 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Plcg2 | Mm_Celera | 8:117583337 | GGATGTGTGGGTGAA[C/T]CTGGGTCAGCCTTGG | 234779 |
rs31569719 | snp | A/T | 0.165289 | 0.235211 | intron-variant | Plcg2 | Mm_Celera | 8:117583355 | GGGTCAGCCTTGGGA[A/T]CAGAGCTGTTATGGG | 234779 |
rs31569722 | snp | C/T | 0.165289 | 0.235211 | synonymous-codon | Plcg2 | Mm_Celera | 8:117583505 | CTGGGACGGGCCTGA[C/T]GGGAAGCCCATTATC | 234779 |
rs31570114 | snp | C/T | 0.32 | 0.24 | intron-variant | Plcg2 | Mm_Celera | 8:117565886 | CTTTTCTAACTCTGC[C/T]GGATGCTTGGCTCTT | 234779 |
rs31570117 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Plcg2 | Mm_Celera | 8:117566109 | GGGAGGCTTTTGAAT[C/G]CTGGGAGTCTGTAGC | 234779 |
rs31570120 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Plcg2 | Mm_Celera | 8:117566163 | AAACGTGATGGGTTC[C/T]ATTAGCATCTGCGTC | 234779 |
rs31570123 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Plcg2 | Mm_Celera | 8:117566204 | TTGTCCCCTTTTTGA[C/T]CCTTACTCTCCTCTT | 234779 |
rs31570135 | snp | C/T | 0.32 | 0.24 | intron-variant | Plcg2 | Mm_Celera | 8:117542134 | CTGCTCACCTCGGGT[C/T]GCACTTGGTGTGTTA | 234779 |
rs31570138 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Plcg2 | Mm_Celera | 8:117542679 | ATCCATTCATACGTC[A/G]TCTCCAGCATGTCGT | 234779 |
rs31570141 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Plcg2 | Mm_Celera | 8:117542689 | ACGTCGTCTCCAGCA[C/T]GTCGTCTCCAGGTGA | 234779 |
rs31570155 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117555864 | GTCAGAGATGGACTC[A/C]CAGCTGTCTTCTAGG | 234779 |
rs31570354 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117558337 | ACCTTGTCACAAAGG[C/T]TGGAACACCTACCAC | 234779 |
rs31570357 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117558405 | CCTGCAATGTATGAT[A/G]GGAGAGACTGGTCCT | 234779 |
rs31570360 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117559165 | CCCGATGCCAGCTCC[C/T]GGTGTATGGTGGCAG | 234779 |
rs31570363 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117559184 | GTATGGTGGCAGAAT[A/G]TGGTGACAGGGGTGA | 234779 |
rs31570384 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117589549 | TTAACCAGTAAGATT[C/T]GAGGCTCTTTCCTGC | 234779 |
rs31570387 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117589673 | GCATGTTCCCTCTAG[C/T]TGCTGCCCATCTTTG | 234779 |
rs31570390 | snp | C/T | 0.32 | 0.24 | synonymous-codon | Plcg2 | Mm_Celera | 8:117589887 | GGAGAAATGGTTCCA[C/T]AAGAAGGTGGAGAGT | 234779 |
rs31570393 | snp | A/T | 0.231111 | 0.249285 | synonymous-codon | Plcg2 | Mm_Celera | 8:117590158 | CCGGATCCGGTCTAC[A/T]ATGGAGAATGGGGTC | 234779 |
rs31570426 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117538213 | GCTGGTTGTGATATC[A/G]TGACAGGCAAAGAGG | 234779 |
rs31570525 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Plcg2 | Mm_Celera | 8:117584795 | TGCTGCAAGCATCTT[C/T]TCTCCTCAGGGAGCC | 234779 |
rs31570528 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Plcg2 | Mm_Celera | 8:117585156 | ACTCTGTCCTGTGCC[A/G]CCTGCAGCTTCCCCG | 234779 |
rs31570531 | snp | A/G | 0.165289 | 0.235211 | synonymous-codon | Plcg2 | Mm_Celera | 8:117585191 | CTTGTCTATCGAGGA[A/G]CACTGCAGTGTGGAG | 234779 |
rs31570746 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117566500 | TCTGCTTTAAAACCA[C/T]GTGAGCATGTTTCCG | 234779 |
rs31570749 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Plcg2 | Mm_Celera | 8:117566657 | GCCTCCACTATCAGG[C/T]TGTTCCTTTCCTCTG | 234779 |
rs31570752 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Plcg2 | Mm_Celera | 8:117566934 | TTTAGGCTTGCTTAG[C/T]GCCTCTCTCAGGAAC | 234779 |
rs31570804 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Plcg2 | Mm_Celera | 8:117543518 | CCTTCCCCTTTATCC[C/T]GTTTGGTATTTTTCT | 234779 |
rs31570806 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117543683 | ACAGTGCACAGAAAA[A/G]CCATGTCCTGTAAAC | 234779 |
rs31570809 | snp | C/T | 0.32 | 0.24 | intron-variant | Plcg2 | Mm_Celera | 8:117543827 | AGCCTTCCTTGGTGC[C/T]GATCACAACTGGATT | 234779 |
rs31570812 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117543867 | TTTCAGAAGCGGTGG[C/T]CTTCACCAAAGAACA | 234779 |
rs31571076 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117590387 | TTCTCATTTCCAGGA[A/C]CCCGTTCTCTTTGAC | 234779 |
rs31571079 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Plcg2 | Mm_Celera | 8:117590428 | CTTAGAAGTCTATGA[G/T]AACTATTCCCACTTG | 234779 |
rs31571082 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Plcg2 | Mm_Celera | 8:117591003 | TACCATCTGGACCAT[A/T]GCCACTCCTGTTCAA | 234779 |
rs31571156 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Plcg2 | Mm_Celera | 8:117559292 | GGATGAATGGCCATA[A/G]CATCCTTTGTTTAAA | 234779 |
rs31571159 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117559310 | TCCTTTGTTTAAATT[C/T]GCCTTTCTTTCTGAG | 234779 |
rs31571162 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117559677 | GAGAACTTGGCAGTG[A/G]ATGGTGTTAACTCTT | 234779 |
rs31571354 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Plcg2 | Mm_Celera | 8:117585856 | GGACATCAACATTTG[C/T]ATACTTGTGTTGTTA | 234779 |
rs31571357 | snp | C/G | 0.297521 | 0.245442 | intron-variant | Plcg2 | Mm_Celera | 8:117586058 | AGGTCCCCAAAAAGT[C/G]AGAGTTAGAATTTAG | 234779 |
rs31571360 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Plcg2 | Mm_Celera | 8:117586113 | TGGATGGGGAATAGC[A/G]CAGCTTATTAACCTA | 234779 |
rs31571362 | snp | C/T | 0.165289 | 0.235211 | synonymous-codon | Plcg2 | Mm_Celera | 8:117586523 | CAAGAAAGATGAGCA[C/T]AAGCCCCAGGGCGAG | 234779 |
rs31571455 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Plcg2 | Mm_Celera | 8:117567038 | ATCCAATGGAACCCT[A/G]TGACTATTGGAAGAC | 234779 |
rs31571458 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Plcg2 | Mm_Celera | 8:117567050 | CCTGTGACTATTGGA[A/G]GACTTCTTGAGGATG | 234779 |
rs31571461 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Plcg2 | Mm_Celera | 8:117567092 | GGCTATGTTGCTGGA[C/T]GGTGTGACTTGGGAC | 234779 |
rs31571755 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117543933 | ACTTCCTCTGGGTTC[C/T]AGTACCCTGCTTATC | 234779 |
rs31571758 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Plcg2 | Mm_Celera | 8:117544047 | GGAACAGAGACATCG[A/C]CAGTGGAGGGAGGAG | 234779 |
rs31571761 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117544776 | TACTGGATAGTGTGT[C/T]GAAATAAGGTACTTT | 234779 |
rs31571763 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117544801 | TACTTTTTGTCCTTA[A/G]CCATACATACTGCTG | 234779 |
rs31571924 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Plcg2 | GRCm38.p3 | 8:117591058 | CCTGGAGCTCCCATG[A/G]CCAGCTTCATTCTTT | 234779 |
rs31571927 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Plcg2 | Mm_Celera | 8:117591065 | CTCCCATGACCAGCT[C/T]CATTCTTTTCCTTCC | 234779 |
rs31571929 | snp | C/T | 0.32 | 0.24 | intron-variant | Plcg2 | Mm_Celera | 8:117591107 | GAATCTCCACTGGTC[C/T]GCCATGTGCCTCCGG | 234779 |
rs31571932 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Plcg2 | Mm_Celera | 8:117591135 | CGGAATCCTCTGCTT[C/T]GTCCTCCTCACAGCC | 234779 |
rs31572005 | snp | A/G/T | 0.336735 | 0.234472 | intron-variant | Plcg2 | Mm_Celera | 8:117560027 | TTGATTTTGGTTTTC[A/G/T]TATTCGAGACAAAAC | 234779 |
rs31572008 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Plcg2 | Mm_Celera | 8:117560082 | TGTCCCTGCATCATA[A/G]AGGTGACTCTGTCCG | 234779 |
rs31572011 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117561092 | GGGATACTTCAGAAG[A/G]AACTTTGATCCCAGA | 234779 |
rs31572235 | snp | A/T | 0.18 | 0.24 | intron-variant | Plcg2 | Mm_Celera | 8:117586726 | TTCAAATAATTTCAT[A/T]TTCCATATCATAAGT | 234779 |
rs31572238 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Plcg2 | Mm_Celera | 8:117586774 | TGTCATAGACCCTAG[A/G]TTCATAACACTCCCA | 234779 |
rs31572241 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Plcg2 | Mm_Celera | 8:117586849 | ACCTTGCAGAAACCT[C/T]TCCCAAATAGGAGTA | 234779 |
rs31572243 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Plcg2 | Mm_Celera | 8:117587037 | AGTTCACTGTGAGGC[A/G]GAGCATCCTGACAGG | 234779 |
rs31572324 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Plcg2 | Mm_Celera | 8:117567181 | GTTGGTCACCTTAGT[C/T]ACAGGAGCACATGGG | 234779 |
rs31572327 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117567192 | TAGTTACAGGAGCAC[A/G]TGGGTCCTTTGTAAA | 234779 |
rs31572330 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Plcg2 | Mm_Celera | 8:117567270 | GCGTTTTGTCCTCTT[A/G]CTCTAACTGCCCATT | 234779 |
rs31572333 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Plcg2 | Mm_Celera | 8:117567278 | TCCTCTTACTCTAAC[C/T]GCCCATTTTCCTAAT | 234779 |
rs31572716 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117544986 | TCCTCTGGGCAGTTC[A/G]TTTCTTCCTACGCTT | 234779 |
rs31572719 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Plcg2 | Mm_Celera | 8:117544997 | GTTCGTTTCTTCCTA[C/T]GCTTTAAAACTCAGT | 234779 |
rs31572723 | snp | A/T | 0.207612 | 0.24638 | intron-variant | Plcg2 | Mm_Celera | 8:117545041 | ACAGTTGCTTCTGGG[A/T]AGAATTTAACAATCT | 234779 |
rs31572815 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117591136 | GGAATCCTCTGCTTC[A/G]TCCTCCTCACAGCCT | 234779 |
rs31572818 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Plcg2 | Mm_Celera | 8:117591672 | CCTGAGGTCTGGGGC[G/T]TTGATCTCAGAGACC | 234779 |
rs31572821 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Plcg2 | Mm_Celera | 8:117591677 | GGTCTGGGGCTTTGA[A/T]CTCAGAGACCGGTTT | 234779 |
rs31572823 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117591764 | ATAGGGCTCACGATA[A/G]CAATCACGGCAGTAC | 234779 |
rs31572864 | snp | C/T | 0.32 | 0.24 | intron-variant | Plcg2 | Mm_Celera | 8:117561101 | CAGAAGGAACTTTGA[C/T]CCCAGAGTGCTCCAG | 234779 |
rs31572867 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Plcg2 | Mm_Celera | 8:117561176 | GCCTCTGACTAAGCC[C/T]GTTTCTCAGAGGAAA | 234779 |
rs31572870 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Plcg2 | Mm_Celera | 8:117561614 | CTTCTACAGCGTCAC[A/G]CTTACCTTGTAAGAA | 234779 |
rs31572873 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117561736 | GCTCACGGACAGGGT[C/T]ATCATTAAACCATGA | 234779 |
rs31573156 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Plcg2 | Mm_Celera | 8:117567519 | CATGTCAGTGTCATT[C/T]GTGGGATTCCCCTTG | 234779 |
rs31573159 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Plcg2 | Mm_Celera | 8:117567520 | ATGTCAGTGTCATTC[A/G]TGGGATTCCCCTTGC | 234779 |
rs31573162 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Plcg2 | Mm_Celera | 8:117568128 | GAGGGTGGACACCCG[A/G]CTATGTGCGCTCACC | 234779 |
rs31573166 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Plcg2 | Mm_Celera | 8:117587341 | CTCCTTCAGCCAGGC[C/T]AGCTCCCAGCTGTCT | 234779 |
rs31573169 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Plcg2 | Mm_Celera | 8:117587500 | ATAGCATTCACTAAC[A/G]TCCTTTTCCCATCAC | 234779 |
rs31573172 | snp | A/C | 0.165289 | 0.235211 | intron-variant | Plcg2 | Mm_Celera | 8:117587525 | CATCACATATATTAG[A/C]AGTCAACTTGCTGCT | 234779 |
rs31573546 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Plcg2 | Mm_Celera | 8:117562315 | GAGCCGTGTCCTGTT[C/T]GATTTGGCTGCCTTC | 234779 |
rs31573549 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Plcg2 | Mm_Celera | 8:117562377 | GAGTAAGGCTCTCAA[A/G]GGGCTTATCCCCACC | 234779 |
rs31573552 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Plcg2 | Mm_Celera | 8:117562433 | TACATCCTTCTTAAA[A/G]CCTTCTTTTTACTTT | 234779 |
rs31573646 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Plcg2 | Mm_Celera | 8:117591791 | GTACGTAGTACTCAC[A/G]CTAGTCCGTAGTACT | 234779 |
rs31573648 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117591864 | TAGCAATCACAAGGA[A/C]GAGTTCCTTTCTCCT | 234779 |
rs31573651 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Plcg2 | Mm_Celera | 8:117591897 | CCCTCTTTTATCCGC[G/T]AAAGAGAGAGTTCCA | 234779 |
rs31573655 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117545356 | CTGGCCGGTCCTTCA[G/T]GGGCTGGAATCGAGA | 234779 |
rs31573658 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Plcg2 | Mm_Celera | 8:117545489 | TGCATTGTACTAACA[C/G]TTATTTGTATCAGTG | 234779 |
rs31573661 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117545601 | GCTCAGGTTATTATC[C/T]CATTATTCCTTAGGT | 234779 |
rs31573915 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Plcg2 | Mm_Celera | 8:117579904 | CAACACGTGAGTTTC[C/T]GGATGAGCCCAGGCT | 234779 |
rs31573918 | snp | C/G | 0.165289 | 0.235211 | intron-variant | Plcg2 | Mm_Celera | 8:117579925 | AGCCCAGGCTGGCTC[C/G]GGCAGAGCTGGCTGT | 234779 |
rs31573921 | snp | A/T | 0.152778 | 0.230321 | intron-variant | Plcg2 | Mm_Celera | 8:117580238 | GCAACTTTACAGAGC[A/T]GATGTTTTATGACTT | 234779 |
rs31574095 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Plcg2 | Mm_Celera | 8:117587812 | TGAGTTATCCAAAGG[C/T]CTGTCTGTTCTAGTA | 234779 |
rs31574098 | snp | A/C/T | 0.165289 | 0.235211 | intron-variant | Plcg2 | Mm_Celera | 8:117587884 | CAAAATGTCACGCAT[A/C/T]CACAGTGGAGTCCGA | 234779 |
rs31574101 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Plcg2 | Mm_Celera | 8:117587895 | GCATCCACAGTGGAG[C/T]CCGATTCAGCCTCTA | 234779 |
rs31574355 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Plcg2 | Mm_Celera | 8:117562611 | GCCATTGTGACTCAG[G/T]GTGCACGCATGCGTA | 234779 |
rs31574454 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117592084 | CTGTTTTCATACCAG[C/T]TGCCTTTCCAAACTT | 234779 |
rs31574457 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117592136 | CCAAAATCTTTCTGA[A/G]CCTCACCCGTGTTCC | 234779 |
rs31574460 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117592172 | CCAGATGTTTCCCTG[C/T]GACACTGCTGTAGCT | 234779 |
rs31574463 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117592261 | GACCTCCTCATACTC[C/T]TGGGGTCTTGATAAA | 234779 |
rs31574544 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117545943 | CTTACATAGGAAGGA[C/T]GACTGATTTCACAAC | 234779 |
rs31574695 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117592613 | CCAGCTTGTTTTCCT[C/T]TTCTGGATGCAGGTG | 234779 |
rs31574698 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117592755 | CTTCAGGTAGGCGTG[C/T]GGGCACTGTTTGTAC | 234779 |
rs31574701 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Plcg2 | Mm_Celera | 8:117593763 | TTCTGGGTCCATGTT[C/T]CTGTAGCTTCCAGAT | 234779 |
rs31574794 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Plcg2 | Mm_Celera | 8:117600978 | CTGGTGGACTGCATG[C/T]GTTTGGTTCCCATGC | 234779 |
rs31574797 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Plcg2 | Mm_Celera | 8:117601003 | CCATGCAATACCAAC[C/T]CTCACCAGCAGATGG | 234779 |
rs31574800 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Plcg2 | Mm_Celera | 8:117601057 | TCTCTGGCTTCCTAA[A/C]GGGTCCTGCTTCCCT | 234779 |
rs31574803 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Plcg2 | Mm_Celera | 8:117601289 | CTTGACTGGTCTCCT[A/C]TTGTGGTGACTCTAA | 234779 |
rs31575106 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Plcg2 | Mm_Celera | 8:117604731 | AATATCAGCTTTGCC[A/T]TCTCAGTTGGTTCTC | 234779 |
rs31575109 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117605070 | GACTCTGTAATGAAA[A/T]CGCATTTTAAGCCAC | 234779 |
rs31575112 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117605103 | CACAGGTAGTGGCGG[C/T]GTGGCGCTAAACGGC | 234779 |
rs31575176 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Plcg2 | Mm_Celera | 8:117592284 | TTGATAAAAACATTG[C/T]TGCCTTTCTTCCAGA | 234779 |
rs31575179 | snp | C/T | 0.32 | 0.24 | intron-variant | Plcg2 | Mm_Celera | 8:117592485 | CTGTCTTTGGAGGTG[C/T]GCAAGGTCAGGGAAG | 234779 |
rs31575181 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Plcg2 | Mm_Celera | 8:117592581 | TCCTGCCGGCTCTCC[A/G]TCTGGGAGGACCCTC | 234779 |
rs31575436 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Plcg2 | Mm_Celera | 8:117601338 | GAGCCCTCTTGTCTC[A/G]CATTCCAGACTGGAT | 234779 |
rs31575439 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Plcg2 | Mm_Celera | 8:117601366 | GATGGGTGCTGATTC[A/G]CCACGGAGGTCTTCC | 234779 |
rs31575442 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Plcg2 | Mm_Celera | 8:117601421 | GCTCTAGCAATGACA[A/C]AAGCTTGTTTGTGGT | 234779 |
rs31575474 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Plcg2 | Mm_Celera | 8:117594372 | TAGCCTCGCCCTGGG[C/T]TCCCAGGACAGGGGC | 234779 |
rs31575476 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117596208 | GGCTGTGGCTGATTG[C/G]TGTAGCTGCTAGCAT | 234779 |
rs31575479 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon | Plcg2 | Mm_Celera | 8:117596376 | CTACTACGAGAAGCA[C/T]GCGCTCTATCGCAAG | 234779 |
rs31575482 | snp | G/T | 0.32 | 0.24 | intron-variant | Plcg2 | Mm_Celera | 8:117596453 | ATATGGTAGGTTGAC[G/T]CCCTTGGGCTTGTTA | 234779 |
rs31575745 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Plcg2 | Mm_Celera | 8:117605277 | GTGCACTTGTTTTCT[C/T]AGCTTGATTCCAGGC | 234779 |
rs31575748 | snp | A/C | 0.32 | 0.24 | intron-variant | Plcg2 | Mm_Celera | 8:117605666 | TTAGCATGTGTGGTA[A/C]CAGGGACGTGGCGGG | 234779 |
rs31575751 | snp | G/T | 0.32 | 0.24 | intron-variant | Plcg2 | Mm_Celera | 8:117605694 | GGGGCATTCTGTGTA[G/T]AGATGAGCCGTGATT | 234779 |
rs31575884 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Plcg2 | Mm_Celera | 8:117619705 | GTGATAGGATAATAG[A/G]TAGTGTAGATATTCC | 234779 |
rs31575887 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Plcg2 | Mm_Celera | 8:117619748 | GCCAACACAGGGATG[A/G]AGGATGGTGTAAGGA | 234779 |
rs31575890 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Plcg2 | Mm_Celera | 8:117619771 | TGTAAGGAAATGGGG[C/T]GTGTCTAATCTGTGC | 234779 |
rs31575893 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117620155 | TATTGTCTTTCGTAA[A/G]TTGTGTCTGTTACCT | 234779 |
rs31575915 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Plcg2 | Mm_Celera | 8:117612131 | TGACTTGTCCTTACA[A/G]TTTCTGCTCAAGGCT | 234779 |
rs31575918 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Plcg2 | Mm_Celera | 8:117612336 | ATGGTCCACACGTGA[A/T]GGTCAGAGGACAGGG | 234779 |
rs31575921 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Plcg2 | Mm_Celera | 8:117612683 | CAGTAGATTCTAATT[C/T]CTTAAGGCTTACACC | 234779 |
rs31575934 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Plcg2 | Mm_Celera | 8:117592596 | ATCTGGGAGGACCCT[C/T]ACCAGCTTGTTTTCC | 234779 |
rs31575937 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117592605 | GACCCTCACCAGCTT[A/G]TTTTCCTCTTCTGGA | 234779 |
rs31576156 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Plcg2 | Mm_Celera | 8:117627419 | CTGCTGGATGTCACT[A/G]TGACCTCCGGATGCG | 234779 |
rs31576159 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Plcg2 | Mm_Celera | 8:117627452 | AGCCATCAAGACTTT[C/T]CCAAACAAGGGATTG | 234779 |
rs31576162 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Plcg2 | Mm_Celera | 8:117627495 | CCCTGATGGAGTTTT[C/T]TCATGAAGTGTTTGT | 234779 |
rs31576165 | snp | A/G | 0.32 | 0.24 | intron-variant | Plcg2 | Mm_Celera | 8:117631689 | TTCAGCCCAGGAAGG[A/G]ATATCAAGAACAGAG | 234779 |
rs31576168 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117631708 | TCAAGAACAGAGACA[A/G]GGCAGAAGCCAGGCC | 234779 |
rs31576171 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Plcg2 | Mm_Celera | 8:117631717 | GAGACAGGGCAGAAG[C/T]CAGGCCTTGTAATCA | 234779 |
rs31576255 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Plcg2 | Mm_Celera | 8:117601676 | CCTCTCAAGTTCATT[A/T]AAAAAAATCAGGAGA | 234779 |
rs31576258 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117601728 | TTTCACCTAACCCCT[C/T]GGCATCAAAGCCATA | 234779 |
rs31576261 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Plcg2 | Mm_Celera | 8:117601754 | CCATACGACAGCAGG[A/T]GAGGAACGGCCCCCC | 234779 |
rs31576405 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117596479 | TGTTAGTCATATCAC[A/G]GTCTACATTTTAGAG | 234779 |
rs31576407 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117596855 | CCCAGCGAGAGCAAC[A/G]CTGAATGATGAATGA | 234779 |
rs31576409 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117596921 | CCTGGTGGGCCATGG[G/T]AAGGCACTGGCTCTT | 234779 |
rs31576412 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117596957 | CGTACACTGCAGGGT[C/T]CTGAGTGCACAGAAG | 234779 |
rs31576494 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon | Plcg2 | Mm_Celera | 8:117634435 | GAATCAGCTGCAGCT[A/G]TACCAGGAGAAGTGC | 234779 |
rs31576497 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Plcg2 | Mm_Celera | 8:117634533 | GGAGCTTCTAGGAGC[A/G]ACCTAGAGGCTTCCT | 234779 |
rs31576500 | snp | A/G | 0.32 | 0.24 | downstream-variant-500B | Plcg2 | Mm_Celera | 8:117635150 | GCCGTTAAGCGTTCT[A/G]TACCTGATCTGTACA | 234779 |
rs31576503 | snp | C/T | 0.32 | 0.24 | downstream-variant-500B | Plcg2 | Mm_Celera | 8:117635182 | TAAACAGGAGTTCCT[C/T]TGTGGTGAGCAAGCT | 234779 |
rs31576574 | snp | C/T | 0.32 | 0.24 | intron-variant | Plcg2 | Mm_Celera | 8:117605988 | CTCCCTTTTCCCTTC[C/T]TGTGACTCTGGTAGG | 234779 |
rs31576577 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117606090 | GTCAGACTCAATTCT[C/T]ACCTTTGTAGCTGAT | 234779 |
rs31576580 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Plcg2 | Mm_Celera | 8:117606096 | CTCAATTCTCACCTT[C/T]GTAGCTGATGCCCTG | 234779 |
rs31576583 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117606376 | GTGCAGACACCAGTA[C/T]GGGGCAGATCAGGGT | 234779 |
rs31576664 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Plcg2 | Mm_Celera | 8:117612733 | ATGGTTTCCTGGTGC[C/G]GGATTCTTTCCTAAC | 234779 |
rs31576667 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Plcg2 | Mm_Celera | 8:117612845 | TGGCCTGTGCCCATG[C/T]GCGCCCGGAGCTGGT | 234779 |
rs31576670 | snp | A/G | 0.391111 | 0.206368 | synonymous-codon | Plcg2 | Mm_Celera | 8:117612950 | TTCGCTCAATGGGCG[A/G]ACAGGCTACGTCCTG | 234779 |
rs31576673 | snp | C/T | 0.132653 | 0.220748 | synonymous-codon | Plcg2 | Mm_Celera | 8:117612971 | CTACGTCCTGCAGCC[C/T]GAGAGCATGCGCTCT | 234779 |
rs31576686 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117620183 | CCTGCAGCCAGTCCT[C/T]GTTAATTGCCTATTA | 234779 |
rs31576689 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Plcg2 | Mm_Celera | 8:117620216 | TAGCCTTTCTTGCTG[C/T]CTTTCCTCAGTGATA | 234779 |
rs31576692 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Plcg2 | Mm_Celera | 8:117620504 | CCTCAATAAAAAGAC[A/G]CATTTCAAGGTCCGC | 234779 |
rs31576875 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Plcg2 | Mm_Celera | 8:117627657 | AGGAGTGTTTTAGCA[C/T]TATGATATTACGTGT | 234779 |
rs31576878 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Plcg2 | Mm_Celera | 8:117627784 | TCTCTCTTTTTTTTT[C/T]CTGCACGTGATATTT | 234779 |
rs31576881 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Plcg2 | Mm_Celera | 8:117627868 | AAAGTCCTTCTCTGG[C/T]GTGTGATTTTTCAAA | 234779 |
rs31576984 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Plcg2 | Mm_Celera | 8:117601810 | CCTCACAGAGGCCGC[C/T]TGCCCTCACTGATTG | 234779 |
rs31576987 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117601896 | CACTCTGGGCGTCTC[A/C]GCTGCAGGCGCTCCC | 234779 |
rs31576990 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117601906 | GTCTCAGCTGCAGGC[A/G]CTCCCTCACTGTCAT | 234779 |
rs31576993 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117602159 | CTGGCAAGGGGCTGT[A/G]GGTAAACGGCAGCTG | 234779 |
rs31577044 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Plcg2 | Mm_Celera | 8:117631829 | CAGACAGAGATACCT[C/T]ATTTCAGTATGGAGA | 234779 |
rs31577047 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117631892 | AGCCACAGCACTCAC[A/G]AAGTCCCGACTCACC | 234779 |
rs31577050 | snp | A/C/T | 0.260355 | 0.249785 | intron-variant | Plcg2 | GRCm38.p3 | 8:117631914 | CGACTCACCGCAGTT[A/C/T]GAGAAAGCTACGATG | 234779 |
rs31577053 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117631981 | TAAGGAAAGAATCCG[G/T]TCCAGAGCATCACAG | 234779 |
rs31577416 | snp | A/C | 0.32 | 0.24 | downstream-variant-500B | Plcg2 | Mm_Celera | 8:117635229 | AGGTAACTGACTTCC[A/C]CGGAAGGTGAGCTGA | 234779 |
rs31577419 | snp | A/G | 0.124444 | 0.216185 | downstream-variant-500B | Plcg2 | Mm_Celera | 8:117635288 | AAAAAAAAAGATTTC[A/G]GCTAAGAGGCAAATG | 234779 |
rs31577422 | snp | A/G | 0.152778 | 0.230321 | downstream-variant-500B | Plcg2 | Mm_Celera | 8:117635416 | TCTAGACAAAGCTAC[A/G]TGGAATCTGCAGAAA | 234779 |
rs31577435 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117596977 | GTGCACAGAAGGCCG[A/G]ATATGGTCATGATAT | 234779 |
rs31577438 | snp | A/G | 0.32 | 0.24 | intron-variant | Plcg2 | Mm_Celera | 8:117597028 | TCCTTGATTTCCTGA[A/G]AGGAGACAGATTCTG | 234779 |
rs31577441 | snp | A/G | 0.32 | 0.24 | intron-variant | Plcg2 | Mm_Celera | 8:117597655 | AAACCTAGGAGACAG[A/G]AGTGAACGAATAATG | 234779 |
rs31577445 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Plcg2 | Mm_Celera | 8:117620525 | CAAGGTCCGCTGCAC[A/G]TGGACCCTGATTGTA | 234779 |
rs31577448 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117620565 | TGGGCTCCAGAGAGA[G/T]TGATCAATGCAGCCA | 234779 |
rs31577451 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117620747 | AGGAATTAAACCACA[A/G]TAGTATCAATCACTC | 234779 |
rs31577536 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117613131 | TGTGGTTCACCTGGG[A/G]TCATTCTGGGCTGAA | 234779 |
rs31577539 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Plcg2 | Mm_Celera | 8:117613650 | TGGGAGGTAGCTTAG[C/T]TTTTGGAGTGTTTAT | 234779 |
rs31577542 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Plcg2 | Mm_Celera | 8:117614071 | AGTCAGACTTTAGGG[C/T]CCCGAAAAAAATCCA | 234779 |
rs31577576 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117606942 | CAAGACACTGCCTGC[A/C]AGAAGGTGGGAGTCC | 234779 |
rs31577579 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117606962 | GGTGGGAGTCCCCAT[C/T]AGCATGTGACTATAG | 234779 |
rs31577582 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117607409 | TGCCAGAGTTCTAAC[A/G]TGGGGCAGGAAGGGT | 234779 |
rs31577714 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Plcg2 | Mm_Celera | 8:117628098 | CTGACAGTGGAATAA[A/C]TAGAACAAGAACAAA | 234779 |
rs31577717 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Plcg2 | Mm_Celera | 8:117628505 | ACCATCATCAGGGAA[C/T]AAGCTGGTGGTCCCT | 234779 |
rs31577720 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Plcg2 | Mm_Celera | 8:117628528 | TGGTCCCTGGCAGGG[A/G]CATTTAGAAAACTGG | 234779 |
rs31577723 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Plcg2 | Mm_Celera | 8:117628626 | AGGTAGTGAGATCTA[C/T]GGGAAACCCAGCTTG | 234779 |
rs31577826 | snp | A/G | 0.32 | 0.24 | intron-variant | Plcg2 | Mm_Celera | 8:117602205 | TCTCTCTGATGGCAA[A/G]CCCGTCAGTCACCTG | 234779 |
rs31577829 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Plcg2 | Mm_Celera | 8:117602442 | TGGCACTTGGCAGCC[A/G]CTATGTGCACAGTAT | 234779 |
rs31577832 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117602461 | TGTGCACAGTATCAC[A/G]TATCCTTACTCTGCT | 234779 |
rs31578006 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Plcg2 | Mm_Celera | 8:117631994 | CGGTCCAGAGCATCA[C/T]AGCAGGAGATGAAGC | 234779 |
rs31578009 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Plcg2 | Mm_Celera | 8:117632032 | GCTGATGCAGGAGAG[C/T]TAGCCGAGTCACTGG | 234779 |
rs31578012 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Plcg2 | Mm_Celera | 8:117632033 | CTGATGCAGGAGAGT[C/T]AGCCGAGTCACTGGC | 234779 |
rs31578185 | snp | A/T | 0.231111 | 0.249285 | downstream-variant-500B | Plcg2 | Mm_Celera | 8:117635470 | GACATTTTTTCTTTG[A/T]CTCATGGCTAGTGAT | 234779 |
rs31578188 | snp | A/G | 0.391111 | 0.206368 | downstream-variant-500B | Plcg2 | Mm_Celera | 8:117635588 | GAGGCTGCTGCCAAG[A/G]TCCTCTGGGGCCACA | 234779 |
rs31578191 | snp | C/T | 0.32 | 0.24 | downstream-variant-500B | Plcg2 | Mm_Celera | 8:117635609 | TGGGGCCACAGCCAA[C/T]AGCATCATTGCTGGT | 234779 |
rs31578214 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Plcg2 | Mm_Celera | 8:117620748 | GGAATTAAACCACAA[C/T]AGTATCAATCACTCT | 234779 |
rs31578217 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117620981 | TCTAGTTGGCAGATG[C/T]TTTAACTTTACTATG | 234779 |
rs31578220 | snp | C/T | 0.32 | 0.24 | intron-variant | Plcg2 | Mm_Celera | 8:117621272 | AGTCCTGGTGAGTCA[C/T]GGGCCCTGACCAGTT | 234779 |
rs31578223 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Plcg2 | Mm_Celera | 8:117621346 | TGAGCTGAAACCCTT[C/T]CCAGGACCAGTCAAG | 234779 |
rs31578274 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117597690 | AGGAGATGAGGAAAG[A/G]CTGACAGCAGTGACT | 234779 |
rs31578277 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117597707 | TGACAGCAGTGACTC[A/G]GGGTAGAGGGACAGG | 234779 |
rs31578280 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117597779 | TGCTGCATATGCCTG[C/T]CAGTTTCCCTGGTAT | 234779 |
rs31578283 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117598659 | GGTTAATCGAATTCC[A/G]TCCAGATGGAACTGA | 234779 |
rs31578305 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Plcg2 | Mm_Celera | 8:117614741 | TTAGGTGCAGACCAA[G/T]TCAGCTGGCCTTCTC | 234779 |
rs31578308 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Plcg2 | Mm_Celera | 8:117614879 | AGGCCAAGGGGTCCA[G/T]CAGCTCACACGTGTT | 234779 |
rs31578311 | snp | A/G | 0.132653 | 0.220748 | synonymous-codon | Plcg2 | Mm_Celera | 8:117615246 | CCCTGTCTGGGCTCC[A/G]ACTCAGGAGAAGGTG | 234779 |
rs31578445 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Plcg2 | Mm_Celera | 8:117607915 | GGATGTATGGACCAA[C/T]CTAGACAACATCTCT | 234779 |
rs31578448 | snp | A/C/T | 0.260355 | 0.249785 | intron-variant | Plcg2 | Mm_Celera | 8:117607935 | ACAACATCTCTAAAG[A/C/T]GCTCAGCGTAGGATG | 234779 |
rs31578451 | snp | A/C/G | 0.244898 | 0.249948 | intron-variant | Plcg2 | GRCm38.p3 | 8:117607998 | TCTTGTAAAAGCATT[A/C/G]TGTCAGCCATTGCCC | 234779 |
rs31578476 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Plcg2 | Mm_Celera | 8:117628655 | TGGTGGCTTTCCAGC[C/T]AAAGGCACACATAGC | 234779 |
rs31578479 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Plcg2 | Mm_Celera | 8:117628708 | GGAGAAAAGCCATGA[C/T]ACATTGGTGGCTTTG | 234779 |
rs31578482 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Plcg2 | Mm_Celera | 8:117628932 | TAGAGTTTGGCCATG[C/T]CAGGTCCAAAGAGAG | 234779 |
rs31578625 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117602486 | TCTGCTTGTTCAGGC[C/T]AAAGAAGCAAATTAG | 234779 |
rs31578628 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117602525 | TGCTACTGCCGGGTA[A/C]GGATTTGGTTATGTT | 234779 |
rs31578631 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117602557 | AGAAAGATCTCAGGC[C/T]GTGTGGAAGGCAGGC | 234779 |
rs31578635 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117632161 | AATGCTAAGCTTCGA[A/G]AGCCTTGGGTTGGGG | 234779 |
rs31578638 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117632286 | GCCTGGGTGACAGTA[C/T]ATCCATTTATTACGA | 234779 |
rs31578641 | snp | A/G | 0.32 | 0.24 | intron-variant | Plcg2 | Mm_Celera | 8:117632316 | ACATGATTTACTGAA[A/G]CATTTGAGCCCCGCC | 234779 |
rs31578926 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Plcg2 | Mm_Celera | 8:117621427 | CTGGAGTGGGCTGTA[C/T]AGTCTGCGGGGAGAG | 234779 |
rs31578929 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Plcg2 | Mm_Celera | 8:117622034 | ATTCAAATGGTAACA[A/T]GTAAATGTGGTGGGA | 234779 |
rs31578932 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117622107 | TTAGACTAGGCTCTC[A/G]TAGCTGGTAACCTGT | 234779 |
rs31578966 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117598681 | TGGAACTGAGTCTCG[A/C]TAGAGTCCCGAGTTT | 234779 |
rs31578969 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117598707 | AGTTTCGGTGAACCA[C/T]CTTTGGGCCACACAG | 234779 |
rs31578972 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117598719 | CCACCTTTGGGCCAC[A/G]CAGATTCTAATTAAA | 234779 |
rs31578974 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Plcg2 | Mm_Celera | 8:117615391 | AAATCCGGTAAGGAG[C/T]GTTGGCAAGGATGTT | 234779 |
rs31578977 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117615506 | ACAACAAAGCCATTC[A/G]GAAGGGTACTAAGCA | 234779 |
rs31578980 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Plcg2 | Mm_Celera | 8:117615572 | CCTTTCAACTTTGGC[A/C]TCTTTGAGGAAACCA | 234779 |
rs31578983 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Plcg2 | Mm_Celera | 8:117615608 | GTTAGACTATCTTCA[A/G]CCTGGCGCTGTTTGC | 234779 |
rs31579065 | snp | A/G | 0.32 | 0.24 | intron-variant | Plcg2 | Mm_Celera | 8:117629089 | GAAGAAAGGTCTACC[A/G]TGCAGCTATAGAGAG | 234779 |
rs31579068 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Plcg2 | Mm_Celera | 8:117629103 | CATGCAGCTATAGAG[A/T]GGATGGCGGGCAGTG | 234779 |
rs31579071 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Plcg2 | Mm_Celera | 8:117629130 | AGTGGAGCTGGAAGA[C/T]GGAAGTCAGAGGCAC | 234779 |
rs31579194 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117608123 | GTGCGTGTGTGGAGC[A/G]GAGTCCTCCCTCCCC | 234779 |
rs31579197 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117608913 | AACAGCATGGTGGAG[A/G]ATCTAAAGAGGGTAG | 234779 |
rs31579200 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117608952 | GGAGATTGTCTTCAG[A/G]ACAGAAAAACACCCA | 234779 |
rs31579203 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon | Plcg2 | Mm_Celera | 8:117609191 | CGCCATTGAGCTCTC[A/G]GACTTGGTTGTATAC | 234779 |
rs31579204 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117632386 | CTGTGCATTGATGGT[A/G]CGCTGGTCACCCAGG | 234779 |
rs31579207 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117632451 | TCGTGCCTGCAGATG[A/T]CCCATGCTTTCTGCT | 234779 |
rs31579210 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Plcg2 | Mm_Celera | 8:117632556 | GCCATAGTTATTCTT[C/T]TGGTGGAGGTCTTTC | 234779 |
rs31579213 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Plcg2 | Mm_Celera | 8:117632630 | ATTCTTGAGAGGAAA[A/G]AAAAAAAGCAGCCTG | 234779 |
rs31579484 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117602578 | GAAGGCAGGCGTGTG[A/G]TTCTAAGTTAGGGGT | 234779 |
rs31579487 | snp | G/T | 0.32 | 0.24 | intron-variant | Plcg2 | Mm_Celera | 8:117602646 | GAGAGGCACAGAGGA[G/T]CAGCTGCCAGGGCTC | 234779 |
rs31579490 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117602777 | GGGGCAGTTCTGGGT[C/T]GTGGAGCTTCCCTGG | 234779 |
rs31579493 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117603114 | GAGTCTGGGCAAGTG[C/T]CTACACTGAGCTGCA | 234779 |
rs31579515 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Plcg2 | Mm_Celera | 8:117625013 | CCTGTGGTCTTCTTT[A/G]GGCTGTAAGAATTAA | 234779 |
rs31579518 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Plcg2 | Mm_Celera | 8:117625134 | ACAGCCATTGTGGTA[A/G]TCCAGGGAGTGAAAA | 234779 |
rs31579521 | snp | A/G | 0.32 | 0.24 | intron-variant | Plcg2 | Mm_Celera | 8:117625447 | CGGTAGGTGGTCAAC[A/G]ACCCAGTCAGCCAAG | 234779 |
rs31579523 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Plcg2 | Mm_Celera | 8:117625474 | CAAGGGTACCACCAC[C/T]CTCTAATGTAAGATA | 234779 |
rs31579556 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Plcg2 | Mm_Celera | 8:117615778 | GCATCCCAAACTTAC[C/T]GTCTCGCACTAGACT | 234779 |
rs31579559 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117616820 | CCTTCCTCCCCGGAT[C/T]TCACATGTAACCCAA | 234779 |
rs31579562 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Plcg2 | Mm_Celera | 8:117616871 | TGGATTTCTTCCTCA[G/T]CCACGGCATTGCCAG | 234779 |
rs31579625 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117598815 | GTTCGATGCCCTCCT[C/T]GCGAGGCCAGCGCTA | 234779 |
rs31579630 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117599189 | GGCCCAGCCCGGATG[G/T]TTAGGTTTGGGACAT | 234779 |
rs31579633 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117599253 | ACCTCCATCCTCCTC[A/C]CAGAGTTACGGACTC | 234779 |
rs31579674 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Plcg2 | Mm_Celera | 8:117629157 | GCACCTTGGGAGCTA[C/G]CTCGTGGAGCCCTGG | 234779 |
rs31579677 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117629774 | GATTGTTGAAGTGAC[A/C]GGCTGGGCCACTCTT | 234779 |
rs31579680 | snp | G/T | 0.260355 | 0.249785 | intron-variant | Plcg2 | Mm_Celera | 8:117629973 | CAGGGAAATGCTGTT[G/T]TCACGGGGATTGTTG | 234779 |
rs31579683 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117630383 | ATACAAAATACTATA[A/C]GGTGTCAACAATATA | 234779 |
rs31579876 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117632660 | GTAATAAATTGATGC[C/T]CATTCGTGTGGAAGT | 234779 |
rs31579879 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117632694 | TATATAGATGGGCTA[C/T]GGTGGGAAGCCAAGC | 234779 |
rs31579882 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117632703 | GGGCTATGGTGGGAA[A/G]CCAAGCCAGAAGACC | 234779 |
rs31579976 | snp | C/T | 0.18 | 0.24 | intron-variant | Plcg2 | Mm_Celera | 8:117609251 | TTTGGGTGAGTCTCC[C/T]GGGGAAGACCCTTCC | 234779 |
rs31579979 | snp | A/C | 0.32 | 0.24 | intron-variant | Plcg2 | Mm_Celera | 8:117609354 | AACGGATCCAGGCAG[A/C]AGCCCTGTCCATGTT | 234779 |
rs31579982 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117609474 | TTGGACTGCACAAGA[C/T]CCTCTTTGTAATGCT | 234779 |
rs31580246 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117625638 | TCCATGTTCCTTCTG[C/T]GGTAGAAAGACCCGG | 234779 |
rs31580249 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117625737 | GGGTCTTAAAGCACT[C/T]CTCTTCAGAATGAAT | 234779 |
rs31580252 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Plcg2 | Mm_Celera | 8:117625799 | CAAGATGCTTAGAGA[A/G]TATATTCCTTATGGT | 234779 |
rs31580265 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Plcg2 | Mm_Celera | 8:117617036 | GATGTTTGGAAGCCT[A/G]GGCTCTATTCAGTGC | 234779 |
rs31580268 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Plcg2 | Mm_Celera | 8:117617347 | TGAGGGCCCAGACAC[C/T]AGAGGAAGAGTCTGG | 234779 |
rs31580271 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Plcg2 | Mm_Celera | 8:117617488 | TTTAAAGTCAGCACC[C/T]GAGCGGCTGGACGCT | 234779 |
rs31580276 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117599277 | CGGACTCAGTTTGCT[C/T]TGAAGGGCCTGCGTC | 234779 |
rs31580279 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117599345 | ACTGGCTCACAAGAG[C/T]GTCAGGCAGATGACA | 234779 |
rs31580282 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117599433 | GAACCCAGGACCTCT[C/T]ATATGCCAGGGTGAG | 234779 |
rs31580286 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117630416 | AACGATATAACGATA[G/T]AGAAGGCTTAGTTTC | 234779 |
rs31580289 | snp | C/G/T | 0.132653 | 0.220748 | intron-variant | Plcg2 | GRCm38.p3 | 8:117630456 | TGGCAGTGAAAAGCT[C/G/T]GGGAAGTAAAAGCTA | 234779 |
rs31580292 | snp | A/C | 0.32 | 0.24 | intron-variant | Plcg2 | Mm_Celera | 8:117630500 | TTCAGGTCACAGACA[A/C]GACTTTGAGCCTGCT | 234779 |
rs31580336 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117603164 | ATTGTCATACCTGGG[A/C]TGGATGCCGGATGCC | 234779 |
rs31580339 | snp | C/G/T | 0.142012 | 0.225474 | intron-variant | Plcg2 | Mm_Celera | 8:117603492 | ATGCTGAACCATCTC[C/G/T]TCAGCTCTAAGGAGC | 234779 |
rs31580342 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117603530 | TCACTGCAGGCCATT[C/T]GGCCCCACACACTCT | 234779 |
rs31580745 | snp | C/G | 0.32 | 0.24 | intron-variant | Plcg2 | Mm_Celera | 8:117633062 | GCTGCCGAGGTGAGA[C/G]TGCAGCAAGCATAGG | 234779 |
rs31580748 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117633080 | CAGCAAGCATAGGAT[G/T]GTAGTTCCTGAAGCA | 234779 |
rs31580751 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117633088 | ATAGGATTGTAGTTC[C/T]TGAAGCAGCGGCTGG | 234779 |
rs31580915 | snp | A/G | 0.32 | 0.24 | intron-variant | Plcg2 | Mm_Celera | 8:117609577 | GTGTATGTGTGTGGT[A/G]GTTACTCCCCGCACA | 234779 |
rs31580918 | snp | G/T | 0.260355 | 0.249785 | intron-variant | Plcg2 | Mm_Celera | 8:117610330 | CATCCAGAAGTATGG[G/T]TGACTGTCTCCTCTG | 234779 |
rs31580921 | snp | A/C | 0.32 | 0.24 | synonymous-codon | Plcg2 | Mm_Celera | 8:117610758 | CTTCCGAGAAATCCG[A/C]TCTTTTGTGGAGACG | 234779 |
rs31581105 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117599755 | TGGCCGTGTGGATAC[A/G]CCCAGTTCCTACAAG | 234779 |
rs31581108 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117599889 | CCATGCCTGTGCCTC[C/T]CTCTCACCACGAGCC | 234779 |
rs31581111 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117600408 | TTACAACTTCTGGGA[C/T]GGACTTAGTATCTAG | 234779 |
rs31581114 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117617520 | ATTTGCTATGTGCTT[C/T]TTCAGATTAGCCCAG | 234779 |
rs31581117 | snp | A/G | 0.32 | 0.24 | intron-variant | Plcg2 | Mm_Celera | 8:117617790 | TCGCTTGGAGACTGA[A/G]AAGAAAAACCCAGCA | 234779 |
rs31581120 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Plcg2 | Mm_Celera | 8:117617878 | AATCACAGCACGGCT[C/G]TTCTCCCTCGCCTTG | 234779 |
rs31581123 | snp | A/G/T | 0.336735 | 0.234472 | intron-variant | Plcg2 | GRCm38.p3 | 8:117618068 | GGGAGACAAACTTAC[A/G/T]GTACTCAGCTACCTT | 234779 |
rs31581135 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Plcg2 | Mm_Celera | 8:117630687 | AGGTAAAACGGCAAG[A/G]ATATGTTTTCATAGT | 234779 |
rs31581138 | snp | G/T | 0.32 | 0.24 | intron-variant | Plcg2 | Mm_Celera | 8:117630889 | ACCTTTAAACATGGC[G/T]ACCTCCCTGAGTCAT | 234779 |
rs31581141 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Plcg2 | Mm_Celera | 8:117631170 | AATAAAAATAAACCC[C/T]GAAAGAAAAAATATT | 234779 |
rs31581145 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Plcg2 | Mm_Celera | 8:117626219 | CAGATCACACATATA[G/T]AGAGAAAAGAAATCA | 234779 |
rs31581148 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Plcg2 | Mm_Celera | 8:117626562 | TGGCCATGAGCTCAG[C/T]ATTCCTCCAATACTT | 234779 |
rs31581151 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Plcg2 | Mm_Celera | 8:117626682 | AGTGGGGCTGGATAA[C/T]TGAGCAGGGTTGGTA | 234779 |
rs31581255 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117603631 | GCCCTGGAAGCTTTG[A/C]CATCTCTTAGTGTTG | 234779 |
rs31581258 | snp | A/G | 0.32 | 0.24 | intron-variant | Plcg2 | Mm_Celera | 8:117603683 | GAGGAACGAGTTCTT[A/G]GTCATCTGACAATAA | 234779 |
rs31581261 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Plcg2 | Mm_Celera | 8:117603734 | CTCCCCTTGAAATGC[C/T]GTCATCATAGATCAT | 234779 |
rs31581624 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117633213 | TGTTAACATGAGACA[A/C]CGGAAAGTATGCAGG | 234779 |
rs31581627 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117633214 | GTTAACATGAGACAA[C/G]GGAAAGTATGCAGGG | 234779 |
rs31581630 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Plcg2 | Mm_Celera | 8:117633794 | GCCTTTTAAGTCCCT[C/T]AATGAATGATACTAA | 234779 |
rs31581632 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117633874 | CGTGAACACGTGCCT[A/G]CATAGACACCCATGA | 234779 |
rs31581874 | snp | A/C | 0.142012 | 0.225474 | synonymous-codon | Plcg2 | Mm_Celera | 8:117610842 | GAAGGGCCTGACCCG[A/C]GTCTACCCCAAGGGA | 234779 |
rs31581877 | snp | C/T | 0.244898 | 0.249948 | synonymous-codon | Plcg2 | Mm_Celera | 8:117610845 | GGGCCTGACCCGAGT[C/T]TACCCCAAGGGACAG | 234779 |
rs31581880 | snp | C/T | 0.336735 | 0.234472 | synonymous-codon | Plcg2 | Mm_Celera | 8:117610905 | CCGTCTGTGGCTGTG[C/T]GGCTCCCAGATGGTG | 234779 |
rs31581883 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Plcg2 | Mm_Celera | 8:117611030 | AGCTAGTGGGATGTG[A/G]TTGTTTCTGAACAAG | 234779 |
rs31581976 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Plcg2 | Mm_Celera | 8:117618395 | TTGGCTTTAGTCCAC[G/T]AGTGGCTTCCCAGAG | 234779 |
rs31581979 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Plcg2 | Mm_Celera | 8:117618700 | AAGTCACAAACTACA[C/T]TAATCTAGACCAGTA | 234779 |
rs31581982 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117618846 | AATTTCAGCACAGCA[C/G]TATTTAATGAACTCA | 234779 |
rs31582004 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117600630 | ATTTCGCCTCCATAA[A/T]TTCCATCTTTTCTTG | 234779 |
rs31582007 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117600928 | TGTCGAGAGTTTAGT[C/T]TTTCTCCTGGTTGAG | 234779 |
rs31582014 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Plcg2 | Mm_Celera | 8:117631232 | CTAGTAAAATGCATG[C/T]CACACTTATACAGGC | 234779 |
rs31582017 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117631295 | GAGAATTTTGAAAAC[G/T]GAGGCTTGGGACAAC | 234779 |
rs31582020 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117631361 | AGCACCTGATAGCTT[C/T]GAGTGGTCCTGCGCC | 234779 |
rs31582023 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117631379 | GTGGTCCTGCGCCAT[C/T]GGAATCTATTTTGAA | 234779 |
rs31582104 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Plcg2 | Mm_Celera | 8:117626748 | AGAAGAGGCTTTGCC[A/G]AGTCAGACTCCCTGC | 234779 |
rs31582107 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117626899 | TCCATCTGCAGGCAG[G/T]TCACAGGAAAACCAG | 234779 |
rs31582110 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Plcg2 | Mm_Celera | 8:117626926 | CCAGTCAGCACTTGC[A/G]GCTGCGGAAGGCAGT | 234779 |
rs31582113 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117626939 | GCGGCTGCGGAAGGC[A/C]GTCCGAGAACACTTA | 234779 |
rs31582234 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117603786 | AGCACTCAGAGCTGA[A/G]CAGGCTAAGCCCTCC | 234779 |
rs31582237 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Plcg2 | Mm_Celera | 8:117603940 | CTCCGTAGTCTGTGG[C/T]GAAGGCTTTGGGGGA | 234779 |
rs31582240 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117604295 | TAGCATGAGGAAGGG[A/G]CAGTGCTTTGCTGGA | 234779 |
rs31582243 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Plcg2 | Mm_Celera | 8:117604578 | TACCAAGAGATGGGC[A/G]CAGGAAGGCACAGCC | 234779 |
rs31582495 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117634037 | CGATGATGGATGATG[A/G]TAAAGCAGAGGCCAG | 234779 |
rs31582498 | snp | C/G | 0.336735 | 0.234472 | intron-variant | Plcg2 | Mm_Celera | 8:117634132 | TTAAATTAGGCCCTG[C/G]CCTCCAGGAGCTGAC | 234779 |
rs31582501 | snp | C/G | 0.32 | 0.24 | intron-variant | Plcg2 | Mm_Celera | 8:117634171 | AAAACCTCTGCCCTC[C/G]GTTCTTCCAGGCACT | 234779 |
rs31582686 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Plcg2 | Mm_Celera | 8:117611162 | TGACCACGAGTGACA[G/T]AGAGGTATTATGACC | 234779 |
rs31582689 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Plcg2 | Mm_Celera | 8:117611206 | AAGGGAATGTAATAA[C/G]TTATTGAACTAGTAA | 234779 |
rs31582692 | snp | C/G/T | 0.244898 | 0.249948 | intron-variant | Plcg2 | Mm_Celera | 8:117612047 | TAGAGCATGGGCACA[C/G/T]TCCTTCAGCATAGGT | 234779 |
rs31582796 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117631380 | TGGTCCTGCGCCATC[C/G]GAATCTATTTTGAAT | 234779 |
rs31582799 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Plcg2 | Mm_Celera | 8:117631426 | GATTATTATAGCCAC[C/T]GTGGAGATCTGTGAC | 234779 |
rs31582802 | snp | G/T | 0.32 | 0.24 | intron-variant | Plcg2 | Mm_Celera | 8:117631630 | AATACCCCAGGGACA[G/T]GAAGAGTCACCTGTC | 234779 |
rs31582855 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Plcg2 | Mm_Celera | 8:117618963 | TCAAATCCACTTAAA[A/G]TGCACAATTGGGGAT | 234779 |
rs31582858 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Plcg2 | Mm_Celera | 8:117619320 | AAGACGCCCTGAAAC[A/C]GGGAGTTGTTACTTT | 234779 |
rs31582861 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Plcg2 | Mm_Celera | 8:117619553 | TATTGTGTAAAGGTG[A/G]GAAGCTGGGGCTGGT | 234779 |
rs31582876 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117627050 | TTCAAAGAGAACTGC[A/G]CTCAGCTATGCTTGG | 234779 |
rs31582879 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Plcg2 | Mm_Celera | 8:117627166 | GAGGTTTTGAATGGA[C/T]AACGTCCCCTCCTGC | 234779 |
rs31582882 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Plcg2 | Mm_Celera | 8:117627364 | CAGGCCACACGTGCA[A/G]TATGTTAGGCTTCCC | 234779 |
rs31583104 | snp | G/T | 0.32 | 0.24 | intron-variant | Plcg2 | Mm_Celera | 8:117634197 | GCACTCATGGGAGAC[G/T]CTAGGTGTGTCTCCC | 234779 |
rs31583106 | snp | A/C | 0.231111 | 0.249285 | synonymous-codon | Plcg2 | Mm_Celera | 8:117634378 | CCAGAACCTGCGCGG[A/C]GCCAACCGTGATGCC | 234779 |
rs31583109 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon | Plcg2 | Mm_Celera | 8:117634411 | GGTGAAGGAGTTCAA[C/T]GTTAACGAGAATCAG | 234779 |
rs45640093 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Plcg2 | Mm_Celera | 8:117505884 | ACCTTGCCTTAAAAA[C/T]GAAGTACTGTGAGAA | 234779 |
rs45753234 | snp | C/G/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Plcg2 | GRCm38.p3 | 8:117504756 | GAAGTTCTTGTGAAA[C/G/T]GACAGCAACCCCAGT | 234779 |
rs45821960 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117513052 | GGTACCAGTGTGTGT[C/G]ATATGTCCGCCTCCT | 234779 |
rs45881908 | snp | C/T | 0.32 | 0.24 | intron-variant | Plcg2 | Mm_Celera | 8:117513194 | CCGGGCTGTTCTGGG[C/T]TTACAGGAGTGGTGT | 234779 |
rs46008226 | snp | G/T | 0.459184 | 0.136902 | intron-variant | Plcg2 | Mm_Celera | 8:117507133 | AGCACATTTAATCAT[G/T]TGTTAGCATCAGCAT | 234779 |
rs46372453 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117509791 | GTGGGAAGACTGGAT[A/G]GAGGATGAGTGGGAA | 234779 |
rs46439235 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117508736 | AGCTTGGCCTTTCCA[C/T]GTTTGCATAGCTTTA | 234779 |
rs46452198 | snp | G/T | | | upstream-variant-2KB | Plcg2 | Mm_Celera | 8:117497157 | CTCAAACTCAAGAGA[G/T]TCACCAGCCTCTGCC | 234779 |
rs46457734 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Plcg2 | Mm_Celera | 8:117512868 | ATGTGCCACCACACA[C/T]ACCTTCTGGGACTTC | 234779 |
rs46839607 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Plcg2 | Mm_Celera | 8:117512371 | GCGTGAGCAGGGGTT[A/G]CACCCCAGAGACAAC | 234779 |
rs46844241 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Plcg2 | Mm_Celera | 8:117508624 | GGAGATAGCTCTGCC[A/T]GGTACCTAACAGAGC | 234779 |
rs47437891 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117512296 | AGCCAGCTCCGAAAG[G/T]TAGTAGTCTTTGGTG | 234779 |
rs47570829 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117509528 | GTAGGAATTACACCC[A/G]TGATGAGGAGGATTA | 234779 |
rs47792757 | snp | A/C | 0.35503 | 0.226867 | intron-variant, upstream-variant-2KB | Plcg2 | Mm_Celera | 8:117505027 | GGCTGTGCCTTCTCT[A/C]GTCACCTTATACTGG | 234779 |
rs47889577 | snp | A/T | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Plcg2 | Mm_Celera | 8:117506491 | CACGGGCCTGGCTGC[A/T]CCGTGGCAGTTTAAC | 234779 |
rs48046795 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117513754 | CTCTGAGATACAAGA[A/T]GTACCAGGCCTGGTA | 234779 |
rs48443620 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117513126 | GGATGTGAGGCTGTG[C/T]GCTGACGGGCAGCCT | 234779 |
rs48516932 | snp | C/T | 0.336735 | 0.234472 | intron-variant, upstream-variant-2KB | Plcg2 | Mm_Celera | 8:117505950 | GACCCTCTCTTCACC[C/T]GTATCCTGCATAAGC | 234779 |
rs48560464 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117513024 | AGGTGGCTGAAACAC[C/T]AGGTCACTAGCAGGT | 234779 |
rs48795187 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117508764 | TTATCTGTATTGGTT[G/T]CCACTGCACGTGCTA | 234779 |
rs49221341 | snp | A/T | 0.132653 | 0.220748 | intron-variant, utr-variant-5-prime | Plcg2 | Mm_Celera | 8:117506570 | AGTGGGTTTTTGCAG[A/T]CTTCTTAAAAAGTAA | 234779 |
rs49345075 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Plcg2 | Mm_Celera | 8:117507531 | TTGTGTGCAGGTTTT[A/T]AAAATTTATCCTGGT | 234779 |
rs49477176 | snp | G/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117508259 | AGCCCTCCTGCATAG[G/T]TCTTAATAATTTTTT | 234779 |
rs49641701 | snp | C/G/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Plcg2 | Mm_Celera | 8:117506279 | AGAGGCAATTACTTT[C/G/T]CCCAGGTGACTCTGG | 234779 |
rs49665328 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117507979 | GCACTGCCACTGACT[C/T]CTGTGCTTGTCCATT | 234779 |
rs49697209 | snp | C/T | 0.18 | 0.24 | intron-variant | Plcg2 | Mm_Celera | 8:117508909 | AAGACTCACTGCTAG[C/T]AGAAGAGCTGCCTTG | 234779 |
rs49879635 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117508418 | GGCGTGCGCCACCAC[A/G]ACAGGCAAAAAACCT | 234779 |
rs49894217 | snp | A/G | 0.244898 | 0.249948 | intron-variant, upstream-variant-2KB | Plcg2 | Mm_Celera | 8:117506547 | TGCCATTTGTCAGGA[A/G]CTGCAGCAGTGGGTT | 234779 |
rs49976751 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117513021 | GATAGGTGGCTGAAA[C/T]ACTAGGTCACTAGCA | 234779 |
rs50041518 | snp | C/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117503890 | ACAAGAAGAGAGGGT[C/G]GAGATTTGGTTATTC | 234779 |
rs50202452 | snp | A/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117513930 | TAACTGGGCGAGAAC[A/T]TACCCTTGGTTCTCC | 234779 |
rs50240413 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117512210 | TGCAAGTGTCCGCCA[A/G]GACATAGGCATTTGT | 234779 |
rs50568969 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Plcg2 | Mm_Celera | 8:117512055 | TACTTGTGCCTTGGC[G/T]TACAGATGAGACTGG | 234779 |
rs50743268 | snp | C/T | 0.244898 | 0.249948 | intron-variant, upstream-variant-2KB | Plcg2 | Mm_Celera | 8:117505941 | TTCACCTCTGACCCT[C/T]TCTTCACCTGTATCC | 234779 |
rs50942185 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117507556 | CCTGGTATATGTGTG[C/T]GCACCTTCGTGAGTT | 234779 |
rs50964972 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Plcg2 | Mm_Celera | 8:117512938 | CCAGGGTATCATGGG[A/G]CTGACTTTGTGAATG | 234779 |
rs50998946 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117512911 | GGTATTGACAGCAGA[A/G]CATATTTGTCCCCAG | 234779 |
rs51138033 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117543743 | CCACTGGTTGGCTGA[A/G]GTGTGTGGAGGGGCT | 234779 |
rs51157226 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Plcg2 | Mm_Celera | 8:117513107 | TCCTGCCAGAGCTGG[C/T]CTAGGATGTGAGGCT | 234779 |
rs51490653 | snp | A/C | | | intron-variant | Plcg2 | Mm_Celera | 8:117514444 | AGAAAGACAAAAGAC[A/C]CCGTAAATGCAAGGT | 234779 |
rs51727991 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117503169 | GCATTACCACAGCTG[A/G]CTTGTGCCCTTGTTT | 234779 |
rs51869336 | snp | C/T | | | intron-variant | Plcg2 | GRCm38.p3 | 8:117513930 | AACTGGGCGAGAACT[C/T]ACCCTTGGTTCTCCA | 234779 |
rs52117699 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Plcg2 | Mm_Celera | 8:117508565 | TGTGTGTGTGTATGA[C/T]ACAACCTGTTACTGC | 234779 |
rs52123192 | snp | A/T | | | upstream-variant-2KB | Plcg2 | Mm_Celera | 8:117497180 | CCTCTGCCTCTTGAG[A/T]GCTAGGATTAAAGGC | 234779 |
rs52468622 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Plcg2 | Mm_Celera | 8:117509463 | TCAGTGTGTGAGTAA[A/G]CATAGCCTGGGTGAG | 234779 |
rs211699313 | snp | G/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117591579 | CCCAGCTTTTTTTGC[G/T]TCCTTCCTTCCTTTC | 234779 |
rs211699693 | snp | C/T | | | synonymous-codon | Plcg2 | Mm_Celera | 8:117585200 | CGAGGAGCACTGCAG[C/T]GTGGAGCAGCAACGT | 234779 |
rs211710658 | snp | G/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117522468 | acggaggtcagaaga[G/T]ccttggaactggagt | 234779 |
rs211722532 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117632819 | CCATAGAATTATTTT[C/T]GTTGCTGCTTCATAC | 234779 |
rs211735614 | snp | G/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117547924 | TACATATGTGTAGAT[G/T]TATATGTGTTGGTGA | 234779 |
rs211740738 | snp | C/T | | | intron-variant, upstream-variant-2KB | Plcg2 | Mm_Celera | 8:117505967 | TATCCTGCATAAGCG[C/T]TGACCTAGCTTGTTC | 234779 |
rs211741658 | snp | C/T | | | upstream-variant-2KB | Plcg2 | Mm_Celera | 8:117497795 | ATTAAAGGTATGGAC[C/T]GTTAAGCGGAAAAAT | 234779 |
rs211747154 | in-del | -/A | | | intron-variant | Plcg2 | Mm_Celera | 8:117565735 | TTGTGCTGCCGTGGG[-/A]AGAGCAAGGGGGCAA | 234779 |
rs211777028 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117591281 | ATATATGTGCACGGT[A/G]TGTATATGATGCCCA | 234779 |
rs211777848 | in-del | -/AA | | | intron-variant | Plcg2 | Mm_Celera | 8:117512008 | GTCAAGCAAATACGC[-/AA]AGAGGACCTGAGCTT | 234779 |
rs211794197 | snp | A/C | | | intron-variant | Plcg2 | Mm_Celera | 8:117627258 | CTGAGCCTGTATTTA[A/C]TCGTACATCTGTCAC | 234779 |
rs211808281 | snp | G/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117512131 | GAGCTTGCCACATAG[G/T]CCACGTTGGCTGGTC | 234779 |
rs211812142 | snp | C/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117535951 | GAAGAATAGATTGTG[C/G]GTAAGAGAAGCAACC | 234779 |
rs211831494 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117579207 | ACTGCTGTGAGTAGA[C/T]ACCACCACCAAGGCA | 234779 |
rs211863711 | in-del | -/TGGTGA | | | intron-variant | Plcg2 | Mm_Celera | 8:117509166 | TGGTGGTGGTGGTGG[-/TGGTGA]TGATGATGATGATGG | 234779 |
rs211867567 | snp | A/C | | | intron-variant | Plcg2 | Mm_Celera | 8:117541390 | TTCTCAGCACCTGAC[A/C]GGCTAAGGGTCTCTG | 234779 |
rs211868362 | snp | A/C | | | intron-variant | Plcg2 | Mm_Celera | 8:117541965 | TGAGAGCCAGAGCGG[A/C]CCCAGGTAACGGAGT | 234779 |
rs211873339 | snp | G/T | | | intron-variant, upstream-variant-2KB | Plcg2 | Mm_Celera | 8:117505474 | CCTCAACACTGCTAT[G/T]TATGTATTTATTTAT | 234779 |
rs211877552 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117548807 | TTACTGTGTGCCTGA[A/G]GCAGAAATCCCCACC | 234779 |
rs211906204 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117585687 | GGAAGCTGTGTGAGC[A/G]TTGGGGTTCCAGTGG | 234779 |
rs211907302 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117573250 | ATTTCTTCAGCCCAC[C/T]GATGACTTAGCAAAC | 234779 |
rs211950445 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117620427 | CTGTTGAGATGGAGC[C/T]CTGCAACTGCTGTTT | 234779 |
rs211964396 | snp | A/C | | | intron-variant | Plcg2 | Mm_Celera | 8:117633166 | GAAGAACCTGCTCCT[A/C]CCCCACCCCGCCCTT | 234779 |
rs211968619 | in-del | -/CATA | | | intron-variant | Plcg2 | Mm_Celera | 8:117596035 | GTTTAGCTTGTGGGT[-/CATA]CATAGTATGGCACCT | 234779 |
rs211972779 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117579631 | GAGCCATTTGTACTG[A/G]AACCTCGAGAAACCG | 234779 |
rs212008893 | snp | C/T | | | synonymous-codon | Plcg2 | Mm_Celera | 8:117607105 | AAACCAGAAAGCCTT[C/T]GTCTTTATCCTGGAG | 234779 |
rs212016784 | in-del | -/ATGTGTTTG | | | upstream-variant-2KB | Plcg2 | Mm_Celera | 8:117496598 | AGAGGCCCGTGTTTC[-/ATGTGTTTG]ATGTCATCATGATCT | 234779 |
rs212023312 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117525062 | GTCTACCCGCATCTC[A/G]TGGGGCTTTGAAGTG | 234779 |
rs212023454 | snp | C/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117531338 | CATAACAGCGGCTAC[C/G]TTTTAGGGGGTTTTA | 234779 |
rs212030090 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117568127 | TGAGGGTGGACACCC[A/G]ACTATGTGCGCTCAC | 234779 |
rs212048043 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117573679 | TCTCTTCCGGATGCG[C/T]CTCTTCCCTCTCTGG | 234779 |
rs212066786 | snp | A/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117614479 | CCACTGCCTTACATA[A/T]ATGTGCTTGGTTTTA | 234779 |
rs212067257 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117536749 | TGAATTTCTGTGCAC[C/T]GTGGATATGCAGGCT | 234779 |
rs212094005 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117530878 | ATTACAGTGTTTGAA[C/T]CCCTCTCTCAAGTGA | 234779 |
rs212094443 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117620831 | CATTTATCAGTTGTG[C/T]CTTTGTAAGTACGTG | 234779 |
rs212113903 | snp | A/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117578310 | TTTATTATTATTATT[A/T]TTTAAATGCTAGGAG | 234779 |
rs212128576 | in-del | -/AG | | | intron-variant | Plcg2 | Mm_Celera | 8:117581892 | GAGAGGGAGAGGGAA[-/AG]AGAGAGAGAGACTTC | 234779 |
rs212145364 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117498955 | TCGAAGGGAAGGTGG[A/G]TTGTATCCGGACCTA | 234779 |
rs212156085 | in-del | -/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117600751 | GGCTTTGAACTTTTG[-/T]TCCTCCGGCCTTAGC | 234779 |
rs212156525 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117534285 | TTCCTGGGTACTACA[A/G]TTACCCTGGCTGTAT | 234779 |
rs212160152 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117625830 | ATGATGGCTTACCAA[C/T]CCCACCCCCCACCCC | 234779 |
rs212163141 | snp | C/T | | | upstream-variant-2KB | Plcg2 | Mm_Celera | 8:117496545 | CGGTGCTTTTAACCA[C/T]TGAGCCATCTCTCCA | 234779 |
rs212183781 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117612504 | TGGAACACACGTGGA[A/G]GTCTGAGGACAGCTG | 234779 |
rs212184859 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117577656 | TGACCCATGCAGAAG[A/G]CATCTGCTCGCCCCT | 234779 |
rs212219939 | in-del | -/AGGT | | | intron-variant | Plcg2 | Mm_Celera | 8:117568720 | GAGTGAGTTACCCTG[-/AGGT]AGCAGGTTATAGGGT | 234779 |
rs212223912 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117529228 | TTTCTGCACCATACC[C/T]CCCCGACTTGAACAG | 234779 |
rs212239827 | snp | A/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117618779 | CTAGAGCAGCCAACA[A/T]ACCAAACACTGCCTA | 234779 |
rs212249976 | in-del | -/GTT | | | intron-variant | Plcg2 | Mm_Celera | 8:117529496 | TTGGGGTAATGTCTC[-/GTT]TTTTTTTTTTCCCCT | 234779 |
rs212263510 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117572354 | TCTCTGGTCCAGCCT[C/T]TATTTATTTATGAAT | 234779 |
rs212286788 | snp | C/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117534968 | TGGTAGCTCATATAT[C/G]TCCTAGCTCTTGAGA | 234779 |
rs212286888 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117528596 | CCCTGTCTCTCTTCC[A/G]TTTTCTTTTCTCCTC | 234779 |
rs212298189 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117571839 | TGTCAGTGTGTATGT[A/G]TGTAGTGTATATGTG | 234779 |
rs212320251 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117598389 | ACTCCTCAAGCCCTT[C/T]CCGTTTACTCTTTGT | 234779 |
rs212321915 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117605758 | CTGATGTGGGTGCAC[A/G]GTAGCTTCCAGGGAT | 234779 |
rs212327473 | snp | C/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117561467 | GTGCCTAAAGCCAGC[C/G]AGCATGTTGAGGATA | 234779 |
rs212342765 | snp | A/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117540706 | CATTATGACATGTTC[A/T]TACATGAATTTACTG | 234779 |
rs212346520 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117618310 | GCCTTCCTTCACTTC[C/T]TTTCTCCACGTGAAA | 234779 |
rs212365014 | snp | A/C | | | intron-variant | Plcg2 | Mm_Celera | 8:117511668 | CCTTGGCTTTCCCTA[A/C]CAGACTGTGATTCGG | 234779 |
rs212370807 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117584453 | CGAGACAAATCACAG[C/T]CAGCTGCTATGGATA | 234779 |
rs212376409 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117524033 | AAGCAAGCAGACACC[A/G]TGAGTTCACCATAGT | 234779 |
rs212399049 | snp | A/C | | | intron-variant | Plcg2 | Mm_Celera | 8:117554331 | AGAGTCCTGTCTCAG[A/C]CCCATCCCATGTAGC | 234779 |
rs212439059 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117517473 | CGCCAGGCATCTCCC[C/T]TTGGGAACTTCATCA | 234779 |
rs212457354 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117598901 | TTGCTTTTTGCCTCC[A/G]GCTGCTCCATCTCCA | 234779 |
rs212464443 | snp | C/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117553961 | TCTCTGCCTCTATCA[C/G]CACCTTCTCTTATAA | 234779 |
rs212493862 | snp | A/G | | | upstream-variant-2KB | Plcg2 | Mm_Celera | 8:117497289 | GGACAGGGTTTCTCT[A/G]TGTGGCTTTGGCTGC | 234779 |
rs212505834 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117615875 | GCCAAAGTGGGTCAC[A/G]TATGAACCCGTTAAT | 234779 |
rs212509306 | snp | A/C | | | intron-variant | Plcg2 | Mm_Celera | 8:117538487 | GAGACCTTGCTGTCT[A/C]CTTGAGGATGGTTTC | 234779 |
rs212533808 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117524453 | CAGGTGTGCCTGTGT[C/T]TCAACTGATGTTGGC | 234779 |
rs212541879 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117569405 | AAACTTTTTATTACA[A/G]CTTAAAAAAACAAAA | 234779 |
rs212541922 | in-del | -/C | | | intron-variant | Plcg2 | Mm_Celera | 8:117575047 | CTGGTGCCAGATCAT[-/C]CCCAGGGGCCACACC | 234779 |
rs212543717 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117575291 | TGGGTACCATGCTGG[C/T]GTCTGGCGAGAAGAT | 234779 |
rs212544339 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117581412 | GTTCTGCTTCGTCTT[C/T]ACTCCTGACACCCTC | 234779 |
rs212554534 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117622393 | AAAGCACATGATATA[C/T]ATGTAGGCACAGAGA | 234779 |
rs212556459 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117531793 | TGCGCCACCACGCCC[A/G]GCTTTTAGGACAGCT | 234779 |
rs212569737 | snp | A/C | | | intron-variant | Plcg2 | Mm_Celera | 8:117567398 | ATGGGATGCAGGGGG[A/C]AAGGATAGATGGATG | 234779 |
rs212597952 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117517905 | AAGGTGGGCCACACC[C/T]CAGCACTGAAAGGGA | 234779 |
rs212599116 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117502088 | CTTCCCAAGCCATAG[A/G]CAGGGAACAGGTGGA | 234779 |
rs212607825 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117574760 | AGTCAGAGACACACC[C/T]GCGCCCATTGCTAGG | 234779 |
rs212617173 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117613493 | CAGAGATCTGCCTAC[C/T]TCTGCCTCCTGAGTG | 234779 |
rs212630825 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117527016 | GACAAGAAGAGGAGC[A/G]TTATGGGAGTGAGTG | 234779 |
rs212655954 | in-del | -/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117545318 | CAACAAAGAAAACAA[-/G]TGCCCAGACCAAGAC | 234779 |
rs212670966 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117570149 | CCTCTTAGGTCACAG[A/G]GCCCAAGAGACCACC | 234779 |
rs212684989 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117565250 | AGGGAGGCAAGTAGG[A/G]AGAAGGTCAGTTCAG | 234779 |
rs212692779 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117526413 | GGATGGAGGAGTGTC[C/T]GTGCTCTCAGCGATT | 234779 |
rs212692891 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117532432 | ACTTTGTAGATCAGG[C/T]TGGCCTCGAACTCAG | 234779 |
rs212699614 | in-del | -/GATAGG | | | intron-variant | Plcg2 | Mm_Celera | 8:117544946 | ACCTCTATTTCCATT[-/GATAGG]CCTTACACAGCGACT | 234779 |
rs212707195 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117515300 | CTTCACAAAGAACCG[A/G]TCCTGCTCAGAGCTG | 234779 |
rs212722188 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117595016 | GGTTTAATGTAATCA[C/T]ACTTGTCTATGTTTA | 234779 |
rs212728507 | snp | A/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117609936 | CTCTTCTCCTTTCCT[A/T]TCCTTTCTTTTCTTT | 234779 |
rs212728918 | snp | A/C | | | intron-variant | Plcg2 | Mm_Celera | 8:117601988 | AGAGTATGTGTAGAA[A/C]CCCCCGTGAGAACTC | 234779 |
rs212748927 | snp | A/G | | | intron-variant | Plcg2 | GRCm38.p3 | 8:117562108 | CTACCTGGAGAAAAG[A/G]GGTGGAGGCAGGCAG | 234779 |
rs212766170 | snp | A/G | | | intron-variant | Plcg2 | GRCm38.p3 | 8:117527295 | AAGGAGTTTGGGAAC[A/G]CCACCATTCCCGCCT | 234779 |
rs212770454 | snp | C/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117508355 | AGACCAGACTGGCCT[C/G]GAACTCAGAAATCCG | 234779 |
rs212790803 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117601651 | TTAAACCACTGAGCC[A/G]TCTCTCCAGCCTCTC | 234779 |
rs212802942 | snp | A/C | | | intron-variant | Plcg2 | Mm_Celera | 8:117552397 | CGAGGCCAGTCGGTT[A/C]CACATCAAGATCCTA | 234779 |
rs212825228 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117558644 | CCCCTCCCTCTTTCC[C/T]CTTCCTCTCTTCCTC | 234779 |
rs212839013 | in-del | -/A | | | intron-variant | Plcg2 | Mm_Celera | 8:117512383 | TTACACCCCAGAGAC[-/A]AACCGAGCCCTGTGC | 234779 |
rs212846045 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117521913 | TTCCTGCTCCCATCC[A/G]CCTCCCTGCCTTCCA | 234779 |
rs212859404 | snp | A/C | | | intron-variant | Plcg2 | Mm_Celera | 8:117595996 | CTTTATTTAAAAAAA[A/C]CAAACAAACAAACCA | 234779 |
rs212867799 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117552117 | GAAAATGACTCCGCA[A/G]GATTGGATTGTAAGC | 234779 |
rs212888142 | in-del | -/TGTG | | | intron-variant | Plcg2 | GRCm38.p3 | 8:117518526 | GTGTAGGTGTATATA[-/TGTG]TGTATGTAGGTGTGT | 234779 |
rs212906990 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117600229 | CAGCTCTCCATGTTG[A/G]CAGATGTCTAAGAAA | 234779 |
rs212949730 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117562750 | CCCTCAGCAGCGCAC[A/G]GATAGTTTATTTCTT | 234779 |
rs212958358 | in-del | -/A | | | intron-variant | Plcg2 | Mm_Celera | 8:117573079 | TGCCTGCAGGCACAT[-/A]ATGTCACCATATGTG | 234779 |
rs212968261 | in-del | -/GTGTG | | | intron-variant | Plcg2 | Mm_Celera | 8:117571853 | ATGTAGTGTATATGT[-/GTGTG]GTGTGGTGTGTATGC | 234779 |
rs212971959 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117633755 | CAAGCTCTTATGGAC[C/T]GAGCATTTCCCCAGC | 234779 |
rs212986111 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117525603 | TAATATGCGATGTGC[A/G]CATTTGTATGAATGG | 234779 |
rs212986872 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117519302 | GAGTCCTGCAAACAC[A/G]ATCATAGCTAATTTT | 234779 |
rs213023480 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117557090 | TATACACATGACACA[A/G]CATACACATCTCACA | 234779 |
rs213025266 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117550629 | ATTGGTGAGCTTTCG[A/G]GAGAGATTGTTGAGT | 234779 |
rs213035661 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117616218 | TCTTCTTCAGGAATT[C/T]AGCCCCTGGGAGGAT | 234779 |
rs213041926 | in-del | -/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117543658 | GAACCTTTCCTTTCC[-/T]ATAAAGAACACAGTG | 234779 |
rs213047935 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117592224 | AGGTGGGCAGAGAAG[A/G]GACTCCCCTGAGTTT | 234779 |
rs213051697 | snp | G/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117600748 | GCAGGCTTTGAACTT[G/T]TGTTCCTCCGGCCTT | 234779 |
rs213075028 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117558243 | GTTGACGGTAACCCA[A/G]AATGATTGAATGATT | 234779 |
rs213088288 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117556199 | GAGATCATACTTCAT[A/G]TCTGCTAATGCATGC | 234779 |
rs213110029 | snp | A/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117542674 | GTATTATCCATTCAT[A/T]CGTCGTCTCCAGCAT | 234779 |
rs213141488 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117586232 | TTTCCAGCTGGACAG[A/G]AGGCAGGGATGGGAT | 234779 |
rs213148625 | snp | A/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117501570 | TCTTGTGAGGTCACA[A/T]CCTGGCTTGTGTTGA | 234779 |
rs213155011 | in-del | -/CAGCCTGA | | | intron-variant | Plcg2 | Mm_Celera | 8:117538513 | TTTCGAACTTCAGAT[-/CAGCCTGA]CTCCACCTCCTGAGT | 234779 |
rs213155160 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117564708 | TTGGGTGTCTGGTTG[A/G]AGTGCATGGGTTTAG | 234779 |
rs213164921 | in-del | -/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117502567 | CACCCTCTTAGTTGA[-/T]TTTAAAAAAACCATA | 234779 |
rs213166687 | snp | A/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117551376 | CCATTGAGGGGGGGT[A/T]CCAGGTTTTACACAT | 234779 |
rs213176639 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117514199 | GAGCTTAGCCAGGCC[C/T]GAGGACACTGGGTTC | 234779 |
rs213191548 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117593252 | TAAGGCATGAAATGA[A/G]GCACAGTGAGGCTCA | 234779 |
rs213195709 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117521511 | GGTGCTGGGACATGG[A/G]TGCTCTTAAGAAGTT | 234779 |
rs213209852 | snp | A/C | | | intron-variant | Plcg2 | GRCm38.p3 | 8:117629204 | GGAAACAAAAAAAAA[A/C]AAACAAACAAACAAA | 234779 |
rs213220376 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117506694 | CCCAGCCTCTGGAGG[C/T]TGAGGCAGGATTAGA | 234779 |
rs213223830 | snp | A/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117621969 | AGCTTCAACACCACA[A/T]GGTGGGGACCATATT | 234779 |
rs213245499 | in-del | -/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117502673 | ATGTACATTGGTAGG[-/T]TTTGCTTTTGCCTAT | 234779 |
rs213270808 | snp | A/C | | | intron-variant | Plcg2 | GRCm38.p3 | 8:117507227 | TCACTCCCCCCCCCC[A/C]ACCGCCCCCCCCCCC | 234779 |
rs213271657 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117501041 | ACCCACTCTTCAAAG[A/G]GTCGGCCAGTTTTGT | 234779 |
rs213288059 | snp | A/C | | | intron-variant | Plcg2 | Mm_Celera | 8:117514791 | AAGGAAAGTGGTTCG[A/C]GACCTGACTGGCTGC | 234779 |
rs213296774 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117573880 | GGTAGAGGTGAACCC[C/T]CTCTCTAACCACCCT | 234779 |
rs213313694 | in-del | -/AAAC | | | intron-variant | Plcg2 | Mm_Celera | 8:117569413 | TATTACAGCTTAAAA[-/AAAC]AAAAAGTGTGTTTCT | 234779 |
rs213321239 | snp | A/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117580678 | CAAATGAGTAGGGTG[A/T]TGAAGGGAGTGAGCA | 234779 |
rs213329475 | in-del | -/GA | | | intron-variant | Plcg2 | Mm_Celera | 8:117589793 | TCAATGAGTTGTCAG[-/GA]GAGGGCAGAGCGAGC | 234779 |
rs213333137 | snp | C/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117621103 | GGATGCCATCTCCAG[C/G]ATATCACAAGAAAGC | 234779 |
rs213337593 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117563257 | ATGTTTCACTATGTA[A/G]CCCAGGGTTGAGAAA | 234779 |
rs213345801 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117537225 | GAGTGCAGGCCCTCA[C/T]GCTTGCATGGCCAGT | 234779 |
rs213358842 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117513834 | GCTTTATCATTCCCA[A/G]GTGAAACAAACCAAA | 234779 |
rs213364609 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117543199 | GACTTTGGGGCTGGG[A/G]ATATGGCTCAGGGGT | 234779 |
rs213375266 | snp | C/T | | | synonymous-codon | Plcg2 | Mm_Celera | 8:117586487 | GGGTCCCAAGGGTGA[C/T]GTCGACGTCAACGTG | 234779 |
rs213375967 | snp | A/C | | | intron-variant | Plcg2 | Mm_Celera | 8:117608031 | GCCAACGAAAGGCTG[A/C]AGAGTCTGGAGCAGT | 234779 |
rs213377298 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117580186 | GTCAGTGTTCTTAAC[C/T]GCTGAGCCATCTCTC | 234779 |
rs213403627 | snp | A/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117568760 | GGGACCAGGGCTTTG[A/T]ATGTGCTAGGCCATA | 234779 |
rs213415494 | in-del | -/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117563017 | ATTGTAGGTATGGGA[-/T]TTTTTTTTTTAAAAG | 234779 |
rs213421934 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117531777 | GCTGGGATTAAAGGC[A/G]TGCGCCACCACGCCC | 234779 |
rs213441756 | in-del | -/TTA | | | upstream-variant-2KB | Plcg2 | Mm_Celera | 8:117496389 | TTATTTCTTTTTTTT[-/TTA]AAGATTTATTTATTA | 234779 |
rs213476344 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117537570 | GGTACTTGTTAAGCT[C/T]TTGAATATGAACTTA | 234779 |
rs213478354 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117531459 | CTGTCCACTACCAAA[C/T]GTCATGCATGATAGG | 234779 |
rs213481799 | in-del | -/TTTTAT | | | intron-variant | Plcg2 | Mm_Celera | 8:117560393 | GTCCACTTCTGTGTC[-/TTTTAT]TTTGTTTTGTTTTTT | 234779 |
rs213513228 | snp | A/C | | | intron-variant | Plcg2 | Mm_Celera | 8:117501430 | CCCCCCAACGATGAA[A/C]TAGCCTGGAAACTCC | 234779 |
rs213513856 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117519822 | GCTTGGCCGTGAGGC[C/T]GGCCTTTTGTCATCC | 234779 |
rs213521836 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117564185 | TTTTTGGTTGTCATT[C/T]ACAAAAGAGATCAGC | 234779 |
rs213536572 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117608696 | AGAAAGCCGCAGCCA[C/T]CCCCCTGCCTCTTCC | 234779 |
rs213538545 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117514331 | CTTGCACTTGGGAGA[C/T]GGAGGCAGGAGGATC | 234779 |
rs213551865 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117526889 | GGAGGCTTGGCCGGC[A/G]CTGTGGGTAGAGGAA | 234779 |
rs213569451 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117634733 | GCCACAGGTGACCTG[C/T]GAGGTAGGGTGGGAG | 234779 |
rs213586315 | snp | G/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117558234 | GGTTCTGGGGTTGAC[G/T]GTAACCCAGAATGAT | 234779 |
rs213594996 | snp | G/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117601592 | AGCCACCATGTGGAT[G/T]CTGGGAACTGAACCT | 234779 |
rs213603685 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117569741 | ACATTTAAAACCCAG[A/G]GGTCTAGGTGAGGCT | 234779 |
rs213621900 | snp | A/C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117616194 | GCTATTGGGAGAAGG[A/C/T]GCACCCCATCTTCTT | 234779 |
rs213626455 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117521447 | CCCAAGTTCCTTTGC[C/T]TGCCATTTGATCAGT | 234779 |
rs213633050 | in-del | -/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117619907 | GATCTGTGCTTTTTA[-/T]TTTTTTAAAAAAATA | 234779 |
rs213648526 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117564686 | CCTGCTTCTGCAGTG[C/T]CTTTGGTTGGGTGTC | 234779 |
rs213658317 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117609112 | GCAGACGCTGGCTCA[A/G]TGCTGTATCGGGTTC | 234779 |
rs213660251 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117601028 | AGATGGCGTAGTAAC[C/T]CCGGCCTCTGCCGTC | 234779 |
rs213708983 | in-del | -/TGTCTGGCATT | | | intron-variant | Plcg2 | Mm_Celera | 8:117560093 | ATAGAGGTGACTCTG[-/TGTCTGGCATT]TCCGTCTGTCTCTTG | 234779 |
rs213714419 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117580867 | AGGGGAATGGGTAGG[C/T]GGTGCATCTCGAGTT | 234779 |
rs213714943 | in-del | -/GATGCACGTG | | | intron-variant | Plcg2 | GRCm38.p3 | 8:117549633 | AGGGCCAGCCTTACA[-/GATGCACGTG]GCCACACCCAGCTTT | 234779 |
rs213724452 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117614356 | GTGTCTTCCTCAGTC[A/G]TTCCCACTTTAGGTT | 234779 |
rs213731471 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117519130 | CCTCACTGAGATTTG[A/G]TTCCCATGCCACGGA | 234779 |
rs213733354 | in-del | -/C | | | intron-variant | Plcg2 | Mm_Celera | 8:117558651 | CTCTTTCCTCTTCCT[-/C]TCTTCCTCTCTCTCC | 234779 |
rs213747403 | snp | A/C | | | intron-variant | Plcg2 | Mm_Celera | 8:117543385 | CGAGTCAGTAACTCG[A/C]TGCCTTAGTTTCCCC | 234779 |
rs213763111 | in-del | -/TTTA | | | intron-variant, upstream-variant-2KB | Plcg2 | Mm_Celera | 8:117506343 | CCAGCTCATTAGTCG[-/TTTA]TTTAGTCTTCTGGTA | 234779 |
rs213771741 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117563144 | ACAGACGGCTGTGAG[C/T]TGCCAGGTGGGTGTG | 234779 |
rs213776911 | in-del | -/TGC | | | intron-variant | Plcg2 | Mm_Celera | 8:117520414 | CCTCTGTCTCCTGAG[-/TGC]TGCTGGGATTAAAGG | 234779 |
rs213780231 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117555170 | TCTCCAGTGAGCATC[A/G]GTCCCTCTCCTGCTA | 234779 |
rs213802988 | snp | G/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117607981 | CTCCTAGATGCTGAC[G/T]CTCTTGTAAAAGCAT | 234779 |
rs213835182 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117562703 | AGGAACACCTGCGCT[A/G]TTTTCCATACTGGTC | 234779 |
rs213854795 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117606997 | GGCAGTTGAGGTGGG[A/G]GCACTAGTATGAGGT | 234779 |
rs213881370 | snp | G/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117500895 | GCTGGGGGAAACCTT[G/T]CCTGGGCATCTAACA | 234779 |
rs213884993 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117524492 | CTCACCCAGACATAG[C/T]CTGCTGAAGGCTGGG | 234779 |
rs213917017 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117567480 | CACGTGGTCCGGGGA[A/G]CCCCCATAGGAGGCT | 234779 |
rs213935579 | snp | A/C | | | intron-variant | Plcg2 | Mm_Celera | 8:117574663 | GACCAAACCGCATAC[A/C]ACAAGGCAGGGCAAA | 234779 |
rs213959395 | snp | C/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117599685 | CCATTTTACTGGTGA[C/G]GAAACTGAGGTTATT | 234779 |
rs213966581 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117621928 | ATGCTCACCATTGCC[A/G]TCAGTGAGTGACTCT | 234779 |
rs213975672 | snp | C/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117512961 | TGTGAATGTTTGTAA[C/G]AGGGCCGATGGAGGG | 234779 |
rs213977183 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117519757 | TTCTGATTCGCATTT[C/T]GCTGGTTGTTGGTTG | 234779 |
rs213978712 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117634509 | TCCCCTCCAATCCCC[C/T]AAAGTCTTGGAGCTT | 234779 |
rs213978866 | snp | A/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117628051 | AGAGGCCTTTTTTTT[A/T]TGATTAAAAATATTC | 234779 |
rs213982581 | snp | A/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117586156 | ACACTTCTTCTCTTT[A/T]GCTCAGTCCCCACCT | 234779 |
rs214007469 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117633746 | CGTACAGCCCAAGCT[C/T]TTATGGACCGAGCAT | 234779 |
rs214025497 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117513676 | CATCTGCAGACTGGC[C/T]TGCTGCAAGCCTCAC | 234779 |
rs214067268 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117526268 | GAGGGAGGGAGAAAG[A/G]GACCTGGCTGTCATC | 234779 |
rs214097710 | snp | A/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117515975 | TCTGTGTCTGGGGAT[A/T]TTTTTAATGTACATA | 234779 |
rs214106148 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117569293 | CGTTGAAGTGACCTC[A/G]ATAGTAGCCTAGGCT | 234779 |
rs214140250 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117549727 | GAGCCATCTCCCTGG[C/T]CCTGGAATCTAAAAC | 234779 |
rs214145913 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117560200 | TCTCCCTCTCATCTG[C/T]CATCTCCTGGCTGCC | 234779 |
rs214145978 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117553183 | AGTTCCTAGCCCTCA[A/G]TCTCCCCAAGAGAAT | 234779 |
rs214160414 | snp | C/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117603600 | GCTCTCTGAGAGGCC[C/G]TTGGTCCCTCTTAAA | 234779 |
rs214162497 | in-del | -/TG | | | intron-variant | Plcg2 | GRCm38.p3 | 8:117518426 | GTATATGTGTGTGTA[-/TG]TGTGTGTGTGGATGT | 234779 |
rs214167868 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117591698 | AGACCGGTTTGGGTC[C/T]GCAGTGTCTGTGCTT | 234779 |
rs214205288 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117559658 | GCAAACACTACCCTG[C/T]ATGGAGAACTTGGCA | 234779 |
rs214217935 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117602778 | GGGCAGTTCTGGGTC[A/G]TGGAGCTTCCCTGGG | 234779 |
rs214232607 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117520831 | CAGTGAAGCATGAGT[C/T]CTGGGCTGGGGAGAT | 234779 |
rs214242011 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117524977 | GGCGTCGGTAAGGCG[A/G]TAGCAGCCTAGCCTT | 234779 |
rs214254915 | in-del | -/TGCTCTAGGTGTGAAGGATAG | | | intron-variant | Plcg2 | Mm_Celera | 8:117548221 | AGGGAGAGAGAGCCA[-/TGCTCTAGGTGTGAAGGATAG]GAGGACATCACCAGG | 234779 |
rs214275269 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117553507 | GTGCAGAGAAGTCAC[A/G]TGCAGTTTAGTTGTT | 234779 |
rs214283220 | snp | G/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117568068 | TCAGAGGACGTTGGG[G/T]TGATTCCTCCAGCTG | 234779 |
rs214293865 | snp | A/C | | | intron-variant | Plcg2 | Mm_Celera | 8:117597428 | TAGGACCCAGGACCC[A/C]ATATTCCAACCATGT | 234779 |
rs214297403 | snp | A/G | | | intron-variant, upstream-variant-2KB | Plcg2 | Mm_Celera | 8:117506165 | TGGCTTGCTCGGCTA[A/G]TTTTCCTAGGATGAC | 234779 |
rs214308136 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117530852 | TCCTTGCTTCAAAAG[A/G]CATCAGACAGATTAC | 234779 |
rs214316421 | in-del | -/GT | | | intron-variant | Plcg2 | Mm_Celera | 8:117507664 | CTGCAAGAGCAGTCA[-/GT]GTGCTCTTAACCACA | 234779 |
rs214328412 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117625218 | GGAGGCAGGGGCTAG[C/T]ACATGTCTGTGAATT | 234779 |
rs214329070 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117573169 | TAGCTGTGAGCTGCC[A/G]TGTGGGCTCTGAGAA | 234779 |
rs214344903 | snp | G/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117516731 | TTTGGGTTTTTATGT[G/T]ATCCCATGTTTTCCT | 234779 |
rs214346872 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117510194 | ACACAGGTGTAATAG[C/T]GGCACAAAAGTTGTA | 234779 |
rs214367707 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117584028 | CTTGGGACTAGAACC[C/T]AAGAGTTCTAGATGC | 234779 |
rs214371464 | snp | C/G/T | | | intron-variant | Plcg2 | GRCm38.p3 | 8:117565804 | CACGCGGCTCTTCTC[C/G/T]GACGATGACAAAGGC | 234779 |
rs214407235 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117510604 | GATGGAAGACACCAA[A/G]GAAACAAGGCCTTCT | 234779 |
rs214409774 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117527743 | CACTCAGGGGAGACC[C/T]TGAAAAGCAGGCACC | 234779 |
rs214413225 | in-del | -/TCCA | | | intron-variant | Plcg2 | Mm_Celera | 8:117631981 | AAGGAAAGAATCCGG[-/TCCA]TCCAGAGCATCACAG | 234779 |
rs214441673 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117571176 | GGCAAGGTGGACAGA[A/G]TGTTTGCCAGGCTGT | 234779 |
rs214442832 | in-del | -/TTTTTTTTA | | | intron-variant | Plcg2 | Mm_Celera | 8:117578773 | CTTCAGTTTTTTTTT[-/TTTTTTTTA]AAACCTGAGGCTTTG | 234779 |
rs214465809 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117592166 | CCTGCCCCAGATGTT[C/T]CCCTGCGACACTGCT | 234779 |
rs214494753 | in-del | -/C | | | intron-variant | Plcg2 | Mm_Celera | 8:117599480 | GGTGCATTTCCAGTG[-/C]CCCCCCCCAATCCCC | 234779 |
rs214497402 | in-del | -/GA | | | intron-variant | Plcg2 | Mm_Celera | 8:117570910 | TGTGTGTGTGTGTGT[-/GA]GTGCTTCTGAATTTG | 234779 |
rs214523319 | snp | C/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117506654 | AGACCCTGCAAAGCC[C/G]GGTGTGGTAACTCAA | 234779 |
rs214546147 | snp | A/C | | | intron-variant | Plcg2 | Mm_Celera | 8:117514765 | TAGAGCTAATCGGTG[A/C]GTAGGAAGAAAAGGA | 234779 |
rs214546211 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117538635 | CATCTGAGGTACATT[C/T]CCAGGCCTAATGCCA | 234779 |
rs214546330 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117600109 | TCTTCATGTCTCTGT[A/G]CTCAGCTTTCCCATC | 234779 |
rs214555473 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117581535 | AGACCTCAGGATGGC[A/G]TGCGTGTGGCCCAGA | 234779 |
rs214558061 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117522471 | GAGGTCAGAAGATCC[C/T]TGGAACTGGAGTTAC | 234779 |
rs214567210 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117588943 | GGCCCTGGGGTCAGT[C/T]TCCAGTACTGAGGAA | 234779 |
rs214595343 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117542607 | GGTCCTGGCGATTGG[A/G]ACTTACACGTATTTT | 234779 |
rs214608212 | snp | G/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117508279 | AATAATTTTTTTTTG[G/T]TTTTGTTTTTCGAGA | 234779 |
rs214613745 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117629738 | CTTCAGAATCTAGAA[C/T]ACAATACCATTAGAG | 234779 |
rs214621516 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117503812 | TAGGCTCTAGCAGGT[C/T]AGATACGGTGCTGGA | 234779 |
rs214629889 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117576290 | CAGTCCTGTGTTGCT[A/G]AAGTAGGGCCTCACC | 234779 |
rs214672770 | snp | C/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117550414 | AGCTGCACCTATCCA[C/G]TGTGGTGTGTGCGAC | 234779 |
rs214683437 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117539135 | TACATAAGGTGCCTA[C/T]TGTCCAAGTACAGCG | 234779 |
rs214690213 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117582101 | GGAAGCAGGGGACCA[A/G]CAGCAAGGTCCACTT | 234779 |
rs214700924 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117540273 | CCTGGGCCTGAGGGA[C/T]GGGAACCCTGAATAA | 234779 |
rs214705373 | in-del | -/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117531843 | CAATTCAGGACCACT[-/G]GGGTTTTCCAGAGAC | 234779 |
rs214736917 | in-del | -/A | | | intron-variant | Plcg2 | Mm_Celera | 8:117515510 | AAAAAACAAACAAAC[-/A]AAAAAAACAAAAAAA | 234779 |
rs214754353 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117533535 | GTGGCCCACCACACC[A/G]GTTTTATGATGGCAG | 234779 |
rs214765635 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117576856 | AGGACCATACGGGGA[C/T]GAGGCTGTTAGAATA | 234779 |
rs214772157 | in-del | -/CT | | | intron-variant | Plcg2 | Mm_Celera | 8:117543602 | CAAAGCTATAGAAAG[-/CT]CTCTGCACAGCGGTA | 234779 |
rs214774268 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117546224 | GGAGGGACAGAGTAT[C/T]ACGTAGCCCAGGCTG | 234779 |
rs214797753 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117595873 | GGAGCAAACACTTTC[A/G]GCTTCACAGGCTGAA | 234779 |
rs214802704 | in-del | -/A | | | intron-variant | Plcg2 | Mm_Celera | 8:117514300 | GAGCTCTAAGCTGGG[-/A]CAAGGATCTTTAATC | 234779 |
rs214813084 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117565389 | GTGCTGATCAACTCA[A/G]TCCCTTCTGTACAGT | 234779 |
rs214822826 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117533068 | CAAGTGTCAAGGTCC[C/T]GTGACCAGAGAGTGG | 234779 |
rs214826091 | snp | A/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117623926 | CTAGTCCATAGGAGT[A/T]AAGGCTCTAGGTAGG | 234779 |
rs214846037 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117596825 | CCTTGGGGTGGTCAA[C/T]AGGCATGAAATGAGC | 234779 |
rs214848170 | snp | G/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117521998 | AGAGTAGGTCATGTA[G/T]GTAGTTTAAACACTG | 234779 |
rs214856376 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117570644 | ACCCAAGTGGGTACC[A/G]TGCTTGGCACAGACA | 234779 |
rs214867229 | snp | G/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117616743 | CACAGGTTCTAATAG[G/T]GCTACTCCCTGGGCC | 234779 |
rs214871216 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117521964 | GCTGCTTCTGGGCCA[A/G]CGAGGCTCAGATGAC | 234779 |
rs214920467 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117570160 | ACAGAGCCCAAGAGA[C/T]CACCTGGGGTCAGGC | 234779 |
rs214930471 | snp | G/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117565694 | GCACAAGGGCCTCGC[G/T]CCCTCCACAGGACCC | 234779 |
rs214941213 | snp | A/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117587295 | AAACCAAAAAAAAAG[A/T]GAGGTTAGCCCTTCA | 234779 |
rs214944744 | snp | A/G | | | synonymous-codon | Plcg2 | Mm_Celera | 8:117610863 | CCCCAAGGGACAGAG[A/G]GTTGACTCTTCGAAC | 234779 |
rs214980461 | in-del | -/TAGTA | | | intron-variant | Plcg2 | Mm_Celera | 8:117538388 | AGTTCCATAGCAGTG[-/TAGTA]TATCGCCTCCATATC | 234779 |
rs214983324 | in-del | -/CAGGTGT | | | intron-variant | Plcg2 | Mm_Celera | 8:117564139 | TGTCTGTATAAAAGA[-/CAGGTGT]CAGCTGCCCCTTGGG | 234779 |
rs214986323 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117545827 | CAACCACTTCGCCAA[C/T]GGTGCCACCTCCCAG | 234779 |
rs214989749 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117565271 | GTCAGTTCAGCACAA[C/T]TCACTAAGAGAGTGT | 234779 |
rs214995702 | snp | C/G/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117552372 | GGCTGAGGCAGGAGG[C/G/T]TTATGAGCTCGAGGC | 234779 |
rs215005204 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117610094 | TTAAAGATTTATTCA[C/T]TATTATACATAAGTA | 234779 |
rs215010894 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117588133 | AACCATATCTAGTTC[C/T]AGCCTCAGGGGATCT | 234779 |
rs215115128 | in-del | -/TTATTTTATT | | | intron-variant | Plcg2 | Mm_Celera | 8:117534543 | TATTTTATTTTCATC[-/TTATTTTATT]TTATTTTATTTTATT | 234779 |
rs215125263 | snp | A/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117545798 | ATTGTACTCAGGTCC[A/T]CCTGATTGCACAGCA | 234779 |
rs215130519 | snp | G/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117522357 | TCTAGCCCTGAGACA[G/T]TTAACCTTTTTTTTT | 234779 |
rs215130654 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117515350 | TGTAGGGCCGGGCGT[A/G]GTGGCGCACGCCTTT | 234779 |
rs215141261 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117502963 | TGGAGCTGGAGTTTG[A/G]TGGTCTTAAGCTGCC | 234779 |
rs215147046 | snp | A/C | | | intron-variant | Plcg2 | Mm_Celera | 8:117617524 | GCTATGTGCTTCTTC[A/C]GATTAGCCCAGCAAT | 234779 |
rs215152694 | snp | C/G/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117588098 | GAGTTTGGTGCCCAG[C/G/T]ATCCACATGGGAGGC | 234779 |
rs215157045 | snp | A/C | | | intron-variant | Plcg2 | Mm_Celera | 8:117503453 | CAGCAGAGAGCTCCT[A/C]GGAGGAGCCAGGGAG | 234779 |
rs215182573 | in-del | -/TGG | | | intron-variant | Plcg2 | Mm_Celera | 8:117509184 | TGATGATGATGATGA[-/TGG]TGGTGGTGGTGGTGG | 234779 |
rs215186840 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117587086 | CAAGCCAAGTGCCTC[A/G]CTCACCTCATGGTGA | 234779 |
rs215192344 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117515713 | TATGGTGATTCAGTA[A/G]TGACCATCTGCATAG | 234779 |
rs215215968 | snp | C/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117593436 | CTCACGTCAGGTGTT[C/G]TGCCGATGGCAGTAG | 234779 |
rs215232550 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117502246 | TGATACTCAGAGCTC[C/T]GATCACCTGGCTGAT | 234779 |
rs215236087 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117551999 | AGAAGCAGGAGGAGG[A/G]AGGATGGAATAGGGG | 234779 |
rs215241977 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117527318 | TCCCGCCTATAAAAC[A/G]GGGCACAATGTGAAC | 234779 |
rs215259315 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117594916 | CCTGAACAGATCGTG[A/G]TCAGATGATCCGTTT | 234779 |
rs215314136 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117532951 | CTATCCCACTGTTGG[A/G]GCTCTTATGTATTTG | 234779 |
rs215322549 | snp | G/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117543464 | ACTGAAACCCTACTG[G/T]GTGGTCCTGTGTGTG | 234779 |
rs215330535 | snp | G/T | | | downstream-variant-500B | Plcg2 | Mm_Celera | 8:117635411 | AGTTGTCTAGACAAA[G/T]CTACATGGAATCTGC | 234779 |
rs215331634 | in-del | -/C | | | intron-variant | Plcg2 | Mm_Celera | 8:117551265 | TTGTCATGGAAACAG[-/C]TAATGAAGTAATCTG | 234779 |
rs215336827 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117520820 | TGAGCAGGGAACAGT[A/G]AAGCATGAGTTCTGG | 234779 |
rs215349821 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117594703 | AAAGGCCTGCGCCCC[C/T]ACACCTTTTTGATAC | 234779 |
rs215349918 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117586583 | GAGTCTGGGTCCCTC[C/T]TCCCCTCACAGAGCC | 234779 |
rs215350955 | in-del | -/CCGT | | | intron-variant | Plcg2 | Mm_Celera | 8:117576353 | CTTTCTGACACACCC[-/CCGT]CCCCGTCCCCCCACC | 234779 |
rs215351019 | snp | G/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117576174 | ACTGAGCTAAATCCT[G/T]AACCCCATGCTCTAT | 234779 |
rs215358749 | in-del | -/A | | | intron-variant | Plcg2 | Mm_Celera | 8:117619225 | TGATACAACAACAAC[-/A]AAAAAGCCAAATCAA | 234779 |
rs215368017 | snp | C/T | | | utr-variant-3-prime | Plcg2 | Mm_Celera | 8:117634869 | CACGGTGTTCACGAG[C/T]GCATCTGGGTACGGG | 234779 |
rs215411534 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117544336 | TTATATTAATTATTT[C/T]CTTTTAAGTATTTAT | 234779 |
rs215453727 | in-del | -/T | | | upstream-variant-2KB | Plcg2 | Mm_Celera | 8:117497813 | AAGCGGAAAAATACA[-/T]TTTTTTTTTCCCCAG | 234779 |
rs215453900 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117544240 | TCAGAAATCCGCCTG[C/T]CTCTGCCTCCCAAGT | 234779 |
rs215472542 | snp | A/C | | | intron-variant | Plcg2 | Mm_Celera | 8:117596755 | TTCTGGGGCGATCTT[A/C]CTGAGGAGTGAGCCA | 234779 |
rs215478267 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117587019 | TGTTGCTTCTGCGTC[A/G]TTAGTTCACTGTGAG | 234779 |
rs215482086 | in-del | -/TCTAGTTG | | | intron-variant | Plcg2 | Mm_Celera | 8:117620966 | TTTGAGCCAACCATT[-/TCTAGTTG]GCAGATGTTTTAACT | 234779 |
rs215506759 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117501617 | TAGATGACTGTTCCT[C/T]TACCAGCTTTTCACT | 234779 |
rs215507461 | in-del | -/C | | | intron-variant | Plcg2 | Mm_Celera | 8:117614836 | CAGGCTTCAGAGACA[-/C]CCCCCCCCCCATCCC | 234779 |
rs215507946 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117623106 | GCGTTTCTTCCCTAC[C/T]TTAGACCACTTATGT | 234779 |
rs215508616 | snp | C/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117616237 | CCCTGGGAGGATACC[C/G]AGCTCCAGGAGATGG | 234779 |
rs215514322 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117559447 | CTTGCAGGGGATTCG[A/G]GTTTGATTCTCAGCA | 234779 |
rs215527990 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117509955 | ACAAGGCTATTGATT[A/G]CTTCTCACAAACTTA | 234779 |
rs215529452 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117539095 | AAGTCTTTAAAGAAC[A/G]AGAGGTTCTGAGGAG | 234779 |
rs215552946 | snp | A/C | | | intron-variant | Plcg2 | Mm_Celera | 8:117502140 | GCTCTCCCACCTAGG[A/C]GCCTTTCTGCCTTCC | 234779 |
rs215565050 | in-del | -/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117503703 | AAGCCACCATTAGTA[-/G]GGGGGCTGCCAGGCC | 234779 |
rs215567661 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117602695 | GAGTCAGGTCTTAGG[C/T]AGTTAGGAGGCTTAG | 234779 |
rs215578546 | snp | A/C | | | intron-variant | Plcg2 | Mm_Celera | 8:117538560 | CGCAGCACCATGCCC[A/C]GGTTCGACAGTCCTG | 234779 |
rs215612416 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117527366 | CTGTGGGGACGGAGT[A/G]AGTTAAGATCTGAGG | 234779 |
rs215625011 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117512087 | CAGTGATGATCCCTA[A/G]AGACCCAAGGAACTC | 234779 |
rs215654626 | snp | C/T | | | intron-variant | Plcg2 | GRCm38.p3 | 8:117570662 | CTTGGCACAGACATG[C/T]CCTCTGACCCTGCTG | 234779 |
rs215681445 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117584563 | ACGCCAAAGTTCTCA[C/T]AGTCCTGCTCTGTGA | 234779 |
rs215681777 | snp | C/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117540858 | GGGTTAGTTACAGGG[C/G]TGACAAGCATAAACA | 234779 |
rs215687455 | snp | A/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117517366 | GATGTTTGCTATCCA[A/T]GCGCTGGGGAGGGGA | 234779 |
rs215687565 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117632765 | CAACCTTCCTGATGC[C/T]ATGACCCTCGTGGTG | 234779 |
rs215703166 | snp | G/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117616827 | CCCCGGATTTCACAT[G/T]TAACCCAACACGCAG | 234779 |
rs215722946 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117632094 | GTACAGTCTCAGAGC[A/G]GATGAAATAATCTCC | 234779 |
rs215732309 | snp | A/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117553125 | CTGGGCTTGAAGTCT[A/T]CTGCTATCCCAGCAT | 234779 |
rs215755664 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117579147 | AAATGGTGGGTAGGT[C/T]CAGGAGGTGCTTATG | 234779 |
rs215765809 | in-del | -/TGACGC | | | intron-variant | Plcg2 | Mm_Celera | 8:117582881 | AGGACACAGCCTCAA[-/TGACGC]TACTCCAGGAACCAC | 234779 |
rs215775208 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117601489 | ACGTGTGCCTATTTG[C/T]CTGAATATGCACACA | 234779 |
rs215783781 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117527131 | GTGTGAGTCCACACG[C/T]GTGTAGGCATGTGCA | 234779 |
rs215802021 | in-del | -/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117632927 | TTGTTTGACATCCCC[-/T]CCCAAAAAAAAGGGG | 234779 |
rs215813710 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117541231 | TTGCAGGTAATCACG[A/G]ATGTCGTACAATAGC | 234779 |
rs215824409 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117514748 | TAGCACCCTTGAGAT[C/T]CTAGAGCTAATCGGT | 234779 |
rs215825236 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117558836 | ATCTCCCTAGACCAT[C/T]CAGGCTGGCCTCTAA | 234779 |
rs215827606 | in-del | -/TTT | | | intron-variant | Plcg2 | Mm_Celera | 8:117606586 | TATGTCTGGCACATC[-/TTT]TTTTTTTTTTTTTTT | 234779 |
rs215844336 | snp | A/G | | | upstream-variant-2KB | Plcg2 | Mm_Celera | 8:117497573 | CCACAACAGCCTGTG[A/G]CTCCAGCTTCAGAGA | 234779 |
rs215852460 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117613892 | ATCCAGTATGAAGGT[C/T]CCATGAACCTGTACT | 234779 |
rs215884323 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117536644 | CCACACCTCACGCTT[C/T]TCCATCTTACTGCTG | 234779 |
rs215885160 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117579544 | CCCACTCCAACAGGG[C/T]TATGCCTCCTAATAG | 234779 |
rs215899006 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117551875 | TTGTCATGCAACAAT[A/G]GGAGGAGAGGTCCTT | 234779 |
rs215944115 | snp | G/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117535888 | GAGGATACTTGGGGG[G/T]GGGGTGGGGGGGCGC | 234779 |
rs215971311 | snp | A/C | | | intron-variant | Plcg2 | Mm_Celera | 8:117631641 | GACAGGAAGAGTCAC[A/C]TGTCTGTCACTTTAG | 234779 |
rs215974097 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117583972 | TAAACTGAGGTCCTC[A/G]GAGAGAGCAGTATGA | 234779 |
rs215990078 | snp | A/G | | | upstream-variant-2KB | Plcg2 | GRCm38.p3 | 8:117496457 | CAGAAGAGGGCGTCA[A/G]ATCTCATTATGAATG | 234779 |
rs215993397 | snp | G/T | | | intron-variant | Plcg2 | GRCm38.p3 | 8:117539631 | CTCCCAGAGACCACC[G/T]CCCCCACCCCCTGCC | 234779 |
rs216003744 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117552578 | GGGGAAACAGAGGCA[A/G]GCAGAGTGAAATTGC | 234779 |
rs216008654 | in-del | -/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117539631 | CTCCCAGAGACCACC[-/G]CCCCCACCCCCTGCC | 234779 |
rs216020447 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117583141 | CCCACAGTCTTATTC[C/T]ATTTGCATAATGACT | 234779 |
rs216028392 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117588933 | ACATGCATATGGCCC[C/T]GGGGTCAGTTTCCAG | 234779 |
rs216035514 | in-del | -/TTATGT/TTATTT | | | intron-variant | Plcg2 | Mm_Celera | 8:117601467 | ACAAACTAAAAAAAA[-/TTATGT/TTATTT]ATATACACGTGTGCC | 234779 |
rs216036647 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117596175 | TCTTCATTTCGGTCC[C/T]CTAAGGACGGGTAAC | 234779 |
rs216077916 | in-del | -/TTTA | | | intron-variant | Plcg2 | Mm_Celera | 8:117528327 | TTTTTTTGTTTTTTG[-/TTTA]TTTGTTTGTTTGTTT | 234779 |
rs216089676 | in-del | -/CTTCACCTATAA | | | intron-variant | Plcg2 | Mm_Celera | 8:117504024 | TCTCAGCACTAGAAC[-/CTTCACCTATAA]CTTCACCTATAACAG | 234779 |
rs216092092 | in-del | -/TG | | | intron-variant | Plcg2 | Mm_Celera | 8:117629262 | TGTAATGAAAATCTC[-/TG]TGAGTTCAAGGCCAG | 234779 |
rs216113374 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117630759 | TGACTTCAGAAGTGA[A/G]CCTTTGCATTCTGCA | 234779 |
rs216114015 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117540237 | CAGAGAGGCAGGAGG[A/G]ACTCTGTAGAAAGGC | 234779 |
rs216126115 | in-del | -/GGAAC | | | intron-variant | Plcg2 | Mm_Celera | 8:117612469 | CACTTGAAGGCCAGA[-/GGAAC]AGGGTGTCTATGTCA | 234779 |
rs216130913 | snp | C/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117508012 | CTGGTCAAGCTGAGC[C/G]ATTCTGCATAGTCCT | 234779 |
rs216132964 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117623085 | ATACTAAGAGTCCCA[A/G]TTCGGGCGTTTCTTC | 234779 |
rs216154686 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117566407 | TAGGGTGGAGAAGTG[C/T]CATGGCTTAGCTGAC | 234779 |
rs216180569 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117508955 | GCAGGATGTGCCAGC[C/T]GGCCAGTGAGGATGG | 234779 |
rs216181684 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117582035 | AGCAAAAGTGACATC[C/T]GGTTGGGCAATAGAT | 234779 |
rs216188645 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117611829 | ATTTAACAACTACAC[C/T]CACCTCAGCTCTAGG | 234779 |
rs216194366 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117516927 | CCATCATCCACTCTC[A/G]CCAGGATGCAGGCTT | 234779 |
rs216222880 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117630305 | TATTCAGTAGGTCGA[A/G]GCAGGATTGCCCAAG | 234779 |
rs216240457 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117561400 | AGCCAACCACTGGGC[A/G]AGGCACCCATTTTAC | 234779 |
rs216246049 | snp | G/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117557239 | AGGTCCCAGATTCCA[G/T]CCCCCAGCAGAAACA | 234779 |
rs216256702 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117507272 | CTTTCTGTTTCTACA[A/G]ATGCCATTTATAGAA | 234779 |
rs216282241 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117553919 | ATTCATTTTCTTTCT[C/T]CTTCTCCTCTTCTCC | 234779 |
rs216292248 | snp | A/G | | | intron-variant, upstream-variant-2KB | Plcg2 | Mm_Celera | 8:117504884 | GCTTAGTAGCCAAAC[A/G]CCTAACGATTTATTT | 234779 |
rs216302532 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117560360 | TGGTCACACTGTCTC[C/T]ATGGTGGTGGAGTTG | 234779 |
rs216311252 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117612411 | TACATAGATTGCACA[C/T]GTGTGTGGAGGTTGG | 234779 |
rs216315194 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117598354 | CCCATGGCAGGCAAA[C/T]ACTTCTTTCCCTGAG | 234779 |
rs216317553 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117523197 | GTTCTGGAGATCAAC[C/T]CAGGATGTCAGGTTT | 234779 |
rs216424589 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117551470 | TTGCTGTTTGTGTGC[C/T]GTTTGTGTCGTGTTG | 234779 |
rs216429674 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117546295 | ACTTCTGATTTTCCC[A/G]CCTAGACCTCCCAAT | 234779 |
rs216435402 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117514279 | GGCCTGCCTGGGCTA[C/T]GGAGCGAGCTCTAAG | 234779 |
rs216441676 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117523151 | GTCAGAGGATAACCT[A/G]AAGGGATCAATTCTT | 234779 |
rs216468445 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117598328 | TGCTGGGAATCGAAC[C/T]GGGGGCCTTGCCCAT | 234779 |
rs216473525 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117588992 | AAAGTTACTAGTGAG[A/G]TTGCATGATCTGATC | 234779 |
rs216481258 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117581484 | CAGATTGCTTAGGTA[A/G]CTATCGTGCACATCT | 234779 |
rs216488444 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117553547 | AATGCGGGGCTGAAA[A/G]AGGATGGGGTGGGGT | 234779 |
rs216493279 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117629716 | TTTAAGGCAGAGTGC[C/T]GAAGTACTTCAGAAT | 234779 |
rs216519356 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117626914 | TTCACAGGAAAACCA[A/G]TCAGCACTTGCGGCT | 234779 |
rs216557792 | snp | G/T | | | upstream-variant-2KB | Plcg2 | Mm_Celera | 8:117497517 | GAGAGCACATATTGC[G/T]CCTACAGAGACTGGA | 234779 |
rs216600064 | in-del | -/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117558971 | TTTTGTTTTGTTTTG[-/T]TTTTTAAAAATAGAT | 234779 |
rs216600738 | snp | C/T | | | synonymous-codon | Plcg2 | Mm_Celera | 8:117590191 | GAAGTACTACCTGAC[C/T]GACAACCTCACGTTC | 234779 |
rs216611391 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117532491 | CTGGGGATTAAAGGA[A/G]TGCGCCACCACCGCC | 234779 |
rs216624907 | snp | G/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117541216 | TCGGGGCCCAATCCT[G/T]TGCAGGTAATCACGG | 234779 |
rs216625231 | snp | C/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117530229 | AAACTGATGTGGGGA[C/G]TGGCAGATAAAACCA | 234779 |
rs216630766 | snp | A/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117503851 | ACCGAGCCTGTCAGA[A/T]CGGCTTTGCTTATTC | 234779 |
rs216651345 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117572793 | GGAGGGGTGCAGCTT[A/G]CTGGCTTGCTCAGCA | 234779 |
rs216652576 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117575316 | GAAGATGCCGTTAAA[C/T]GTTCCCCTGTGATAC | 234779 |
rs216659168 | in-del | -/C | | | intron-variant | Plcg2 | Mm_Celera | 8:117519072 | ACTCCCTCCAGACCT[-/C]CCCCCCCAACTTCCT | 234779 |
rs216663392 | in-del | -/GGGAGG | | | intron-variant | Plcg2 | Mm_Celera | 8:117627146 | AGGGAGGCTGGGAGT[-/GGGAGG]AGGTTTTGAATGGAT | 234779 |
rs216668529 | in-del | -/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117628043 | TAAATATTAGAGGCC[-/T]TTTTTTTTTGATTAA | 234779 |
rs216678869 | snp | A/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117622606 | CGTAAGGTTAAAAAA[A/T]TTTCCCTGTCAAAAG | 234779 |
rs216692335 | snp | C/T | | | intron-variant, upstream-variant-2KB | Plcg2 | Mm_Celera | 8:117504819 | TGGGGATCACCTGGT[C/T]CCAAAGGTAGCGAGC | 234779 |
rs216721393 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117598854 | TCCCACCCTGCCGCT[A/G]CCTCGTAACTTTGTG | 234779 |
rs216731728 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117503380 | TTGAGTTTGCGTTCT[A/G]AAATGCTGCCAGCCA | 234779 |
rs216750556 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117552964 | CTTGGTCACTGAATG[A/G]CGATGAGCAGAGAGG | 234779 |
rs216768169 | in-del | -/TGT | | | intron-variant | Plcg2 | Mm_Celera | 8:117623028 | CTGCAGCTCCTTCTC[-/TGT]TGTTGTTATCATTTG | 234779 |
rs216771292 | in-del | -/TATCTATCTATC | | | intron-variant | Plcg2 | Mm_Celera | 8:117590694 | AGATATTTATCTATT[-/TATCTATCTATC]TATCTATCTATCTAT | 234779 |
rs216788402 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117623994 | GGTGTAATTTTCAGC[A/G]ATAGAGCCGTCACAT | 234779 |
rs216801207 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117508795 | TGGCTGGGAGTGAGG[A/G]TGAGGAGTCTCATCA | 234779 |
rs216845721 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117576461 | CTGAAACCCAGAAGG[C/T]ATTGGCCAGCATCGG | 234779 |
rs216857899 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117503030 | AAGAGCAACAAGTGC[C/T]CTTAACTGCTGAGCC | 234779 |
rs216858859 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117547865 | CCTGTAGGTACCGGA[C/T]CCTACTGGCCTCTCA | 234779 |
rs216860238 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117509781 | GCCTGGATGTGTGGG[A/G]AGACTGGATGGAGGA | 234779 |
rs216860587 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117623317 | TTGGCCCTTAGCCTA[C/T]GGCAGCTCTCCTCCT | 234779 |
rs216861966 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117503416 | CTGAGAACCTCAGGG[A/G]CTCGGGGCAAGAAGC | 234779 |
rs216877112 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117618203 | ACTCATTCAAGGTCA[C/T]AGGCTGGCACTTGCC | 234779 |
rs216890281 | snp | A/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117591247 | AAAATTATGAGTATG[A/T]GCGGTTTTGCCTGCA | 234779 |
rs216891248 | snp | A/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117534261 | TTCAGGTCCTTCCCT[A/T]TACTTGAGTTCCTGG | 234779 |
rs216910216 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117571295 | ATGTGTGCATGTGAG[C/T]ATGTATGTTTGTGTT | 234779 |
rs216927666 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117617567 | GCGATGCTGCCTCTT[C/T]ACATCAAGAAAAGTG | 234779 |
rs216930393 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117554173 | GATGACAACTATCTC[C/T]TAGGGTTTGAGGACT | 234779 |
rs216932694 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117522562 | GCAAGTGATCTTAAC[C/T]ACGGAGCCATCCCTC | 234779 |
rs216948721 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117577611 | GTGGCTGCGTTCACA[C/T]GGTGGTGACTGCTGA | 234779 |
rs216966364 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117576937 | CACAACTGACTTCAT[A/G]TGGTCCTGTTTCCAA | 234779 |
rs216995221 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117528406 | GGTGTTTGGTTCAGA[A/G]CATCACAAAATGAGA | 234779 |
rs217013784 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117625138 | CCATTGTGGTAATCC[A/G]GGGAGTGAAAATTGC | 234779 |
rs217029892 | in-del | -/AGATAGATAGATAGATAGAT | | | intron-variant | Plcg2 | Mm_Celera | 8:117519997 | GAGACCTTGCCTCTA[-/AGATAGATAGATAGATAGAT]AGATAGATAGATAGA | 234779 |
rs217030298 | snp | G/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117571626 | ACCACAGTACCCAGA[G/T]AGAAGACCTCCAATG | 234779 |
rs217047837 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117618044 | AAACCGGCTGGGCCC[A/G]ACTCAGGAGGGAGAC | 234779 |
rs217050083 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117527809 | ACTCTTGTAGACACC[C/T]GGAAATCTCTTGCCC | 234779 |
rs217051282 | in-del | -/C | | | upstream-variant-2KB | Plcg2 | Mm_Celera | 8:117496914 | GGGACACAATGTAAA[-/C]AGGGAACAGTGGCAA | 234779 |
rs217072544 | in-del | -/GGGG | | | intron-variant | Plcg2 | Mm_Celera | 8:117582718 | GAGCTTTTAATGGCA[-/GGGG]TATTGTTCTGTATCT | 234779 |
rs217072825 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117586134 | TATTAACCTATAAGC[A/G]ACAGTAACACTTCTT | 234779 |
rs217079969 | in-del | -/GT | | | intron-variant | Plcg2 | Mm_Celera | 8:117582484 | GCTCTAGCCTAGCTA[-/GT]CAGCTTGTCTCATAC | 234779 |
rs217084228 | in-del | -/C | | | intron-variant | Plcg2 | Mm_Celera | 8:117573282 | ACAACAACAAAAAAT[-/C]TCACCGGCATAAGCT | 234779 |
rs217085276 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117500468 | AGACTGTTCAAGAGA[C/T]GGATAGTCCCTGTTT | 234779 |
rs217088266 | snp | A/C | | | intron-variant, upstream-variant-2KB | Plcg2 | Mm_Celera | 8:117505387 | GCCTGGAACTTGGAA[A/C]GTAGCTGAGGATGAC | 234779 |
rs217093171 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117620415 | CCAACCCATCAGCTG[C/T]TGAGATGGAGCCCTG | 234779 |
rs217100716 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117541995 | TAACAGCTATCAATA[A/G]TAAAGGTATCCAGCG | 234779 |
rs217102679 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117550404 | GGTGTTGTACAGCTG[C/T]ACCTATCCAGTGTGG | 234779 |
rs217125763 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117528467 | CTACCATTTGCAAGC[C/T]GTGTGACTTGGTCTG | 234779 |
rs217129359 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117592132 | GTAACCAAAATCTTT[C/T]TGAGCCTCACCCGTG | 234779 |
rs217129449 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117585738 | TTGGGGTCTCTCACA[C/T]TATGTGAGATGTGGA | 234779 |
rs217146754 | in-del | -/AATGC | | | intron-variant | Plcg2 | Mm_Celera | 8:117542641 | GGGGGTGGGGAGCAG[-/AATGC]AATGCAACCGCTAGT | 234779 |
rs217146879 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117621081 | GGCCTCTCTACCCTT[A/G]GAATGGGGATGCCAT | 234779 |
rs217159303 | snp | C/T | | | upstream-variant-2KB | Plcg2 | GRCm38.p3 | 8:117497752 | ATTCAGAGATGTAAT[C/T]TTGTCATTCTGCCTT | 234779 |
rs217160996 | snp | A/C | | | intron-variant | Plcg2 | Mm_Celera | 8:117571725 | AGTCAGAGACATGTG[A/C]CAGAGACACCAGAGG | 234779 |
rs217181333 | snp | A/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117499071 | GCCGACACGCCCTGG[A/T]AACAGGTGGCTTTCT | 234779 |
rs217198554 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117525628 | GAATGGCTGTGTGTG[C/T]CTGTGTCACAGCAGG | 234779 |
rs217200618 | in-del | -/ATGTGT | | | intron-variant | Plcg2 | GRCm38.p3 | 8:117549324 | TGTATGTGTGTGTGC[-/ATGTGT]ATGTGTGCTGTGTGT | 234779 |
rs217201464 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117627206 | CTTTAAGAGGAAGCC[C/T]CTGAATGTGTGCAAG | 234779 |
rs217209067 | in-del | -/ACAC | | | intron-variant | Plcg2 | Mm_Celera | 8:117567769 | ATATGTACAACACTT[-/ACAC]ACACACACACACACA | 234779 |
rs217216222 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117577071 | TAGGCTGGCTATACT[A/G]TATAGTTACTTTTCT | 234779 |
rs217237488 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117615036 | CTGCAGCAGGATTGC[C/T]TGCTGCAAAAGAAAT | 234779 |
rs217238275 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117624082 | ATTTTTGGCCAACTT[C/T]TCAATTAGATGTGAC | 234779 |
rs217238967 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117621919 | AAAACTTCAATGCTC[A/G]CCATTGCCATCAGTG | 234779 |
rs217241694 | snp | G/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117542588 | AAGAAGATTGCATTT[G/T]GTTGGTCCTGGCGAT | 234779 |
rs217243017 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117519949 | TTAGAAAGATCCTAT[C/T]TCAAATACTGTAAGC | 234779 |
rs217252515 | snp | G/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117546122 | GGATTACATGCTGGG[G/T]TTTTTTTTTGTGGCC | 234779 |
rs217275673 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117568831 | GCAAGTGTATGAGCC[C/T]ATGGGGCCCATTTTT | 234779 |
rs217292728 | snp | A/C | | | intron-variant | Plcg2 | Mm_Celera | 8:117526186 | TGTGTTCTTGGCAGA[A/C]ATGGGGGCTTGCATG | 234779 |
rs217331636 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117615721 | CTTGGCCTGTGTCAT[C/T]AGGACGAGGCCCTAA | 234779 |
rs217344973 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117563812 | CAACACTGCTTGTGT[A/G]ATATTTGGGATAATT | 234779 |
rs217346817 | in-del | -/A | | | intron-variant | Plcg2 | Mm_Celera | 8:117546176 | CCTAAACTTGCAAAC[-/A]ATTGAGCTGAAAAAA | 234779 |
rs217359241 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117572778 | TGAGGCAGAAGCCAC[A/G]GAGGGGTGCAGCTTA | 234779 |
rs217378376 | in-del | -/AT | | | intron-variant | Plcg2 | Mm_Celera | 8:117545735 | CTCCCCTGTGCTGCG[-/AT]TACAAGCATATGCCA | 234779 |
rs217402325 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117563327 | TGGTGAAGCAGCCCT[C/T]TTCCTCCTCCTCTGC | 234779 |
rs217402635 | snp | A/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117569223 | ACTTTCTGTTGTTGT[A/T]AAGACAGCATGCCTC | 234779 |
rs217403783 | snp | C/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117503765 | TATGCAGAAGAACCA[C/G]CTGTTCTCATTTTTT | 234779 |
rs217405382 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117572409 | TTAGTCTTGAACTCA[C/T]GATCTTCTTCTTCTG | 234779 |
rs217409910 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117568058 | ATCACTGACTTCAGA[A/G]GACGTTGGGTTGATT | 234779 |
rs217421963 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117533606 | CTCCAGCTGCTCCTC[A/G]CTCTCTGATTATTGG | 234779 |
rs217438390 | snp | A/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117528943 | AGGAAGAGAGGGTGG[A/T]GTGGGTACAGAATGG | 234779 |
rs217449768 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117567405 | GCAGGGGGCAAGGAT[A/G]GATGGATGGAGGAGA | 234779 |
rs217473928 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117572281 | CATTCTCTCCTTCCA[C/T]TGTGAGGACCCTAGG | 234779 |
rs217491890 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117618665 | GTTAGAGCACAGAAT[C/T]TGCATTTGCATCTTA | 234779 |
rs217494974 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117619569 | GAAGCTGGGGCTGGT[A/G]AGATGGCTCAGCAGG | 234779 |
rs217498172 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117529363 | GAACTGTTTCTTTGA[A/G]CTGGTGGCAGGCTCT | 234779 |
rs217500107 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117524005 | TGCGCCTTACCCTTC[C/T]TTCGTTGGTGACAAG | 234779 |
rs217532294 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117560271 | GGTTTTACACACTGA[A/G]GTCTTAGGGTGTTGT | 234779 |
rs217534033 | snp | C/T | | | upstream-variant-2KB | Plcg2 | Mm_Celera | 8:117497723 | ACTGTATAGCCCTAG[C/T]TGGCCTTGAACTAAT | 234779 |
rs217544592 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117510786 | CATAACTCCTCACAA[A/G]GGAGAAATGATTTTT | 234779 |
rs217565370 | in-del | -/TCT | | | intron-variant | Plcg2 | Mm_Celera | 8:117541725 | GACCCTGTAGGCACA[-/TCT]GAGAGAAAGTTGCCT | 234779 |
rs217569887 | snp | A/C | | | intron-variant | Plcg2 | Mm_Celera | 8:117614131 | CCCTCCCAGCGCAGA[A/C]CCGGGAGACTTCCAA | 234779 |
rs217571098 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117603714 | GTATTTTTAAAAGGC[A/G]TATGCTCCCCTTGAA | 234779 |
rs217574789 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117524477 | TGTTGGCTGAAAGCC[C/T]TCACCCAGACATAGT | 234779 |
rs217588847 | in-del | -/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117558298 | CTGTCGTGCTGCTGA[-/G]GTGACATTTGACATG | 234779 |
rs217590414 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117591660 | CTCTTTCAGTGCCCT[A/G]AGGTCTGGGGCTTTG | 234779 |
rs217624641 | in-del | -/AGTGA | | | intron-variant | Plcg2 | Mm_Celera | 8:117538389 | GTTCCATAGCAGTGT[-/AGTGA]ATCGCCTCCATATCT | 234779 |
rs217650253 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117604471 | ATCCCTTTAGGGTCC[A/G]CAGCGTTTATTCCCT | 234779 |
rs217675918 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117534668 | TCTGCTTATAGAATG[C/T]TGGGATTAAAGGCAC | 234779 |
rs217708627 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117524963 | TGAGGAGTTCTGGTG[A/G]CGTCGGTAAGGCGGT | 234779 |
rs217711823 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117517304 | TAGGCATGAAGATCC[A/G]AGTGCAGCCCTCAGC | 234779 |
rs217712560 | in-del | -/TGTT | | | intron-variant | Plcg2 | Mm_Celera | 8:117602014 | ACTCCCAAGTCACAC[-/TGTT]TGTTTGTTTGTTTGT | 234779 |
rs217738677 | snp | C/T | | | intron-variant | Plcg2 | Mm_Celera | 8:117516861 | TGTGGTGGGCTTGGA[C/T]GATGTGGTCAGTTTT | 234779 |
rs217739190 | snp | A/G | | | intron-variant, upstream-variant-2KB | Plcg2 | Mm_Celera | 8:117505041 | TAGTCACCTTATACT[A/G]GGCTGTTGGCTCAGT | 234779 |
rs217743528 | snp | A/C | | | intron-variant | Plcg2 | Mm_Celera | 8:117529695 | AGGCAAGGTGCTCAC[A/C]TTGGAAGTGTCAGGA | 234779 |
rs217743560 | snp | A/C | | | intron-variant | Plcg2 | Mm_Celera | 8:117619941 | CTATTGTAAAAATTC[A/C]AATAAACATTACACA | 234779 |
rs217747254 | snp | A/G | | | intron-variant | Plcg2 | Mm_Celera | 8:117548964 | ACATGTACAAATATG[A/G]CTCTTTCTCTTTGGC | 234779 |
rs217755831 | in-del | -/TATATATATG | | | intron-variant | Plcg2 | Mm_Celera | 8:117624201 | CAGATTGACTTCATA[-/TATATATATG]TATATATATATTTCA | 234779 |