Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5335 |
| ensemblid | ENSG00000124181.15 |
| hgncid | 9065 |
| symbol | PLCG1 |
| name | phospholipase C gamma 1 |
| refseq_nuc | NM_002660.3 |
| refseq_prot | NP_002651.2 |
| ensembl_nuc | ENST00000685551.1 |
| ensembl_prot | ENSP00000508698.1 |
| mane_status | MANE Select |
| chr | chr20 |
| start | 41137543 |
| end | 41177626 |
| strand | + |
| ver | v1.2 |
| region | chr20:41137543-41177626 |
| region5000 | chr20:41132543-41182626 |
| regionname0 | PLCG1_chr20_41137543_41177626 |
| regionname5000 | PLCG1_chr20_41132543_41182626 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 1291 | 288 | 76 | 41 | 140 | 10 | 20 | 100 | PLCG1_chr20_41132543_41182626 | PLCG1 | MAGAA others(1286): Show |
chr20 | 41132543 | 41182626 |
| a0002 | 1/0 | 1291 | 72 | 2 | 23 | 32 | 3 | 11 | 28 | PLCG1_chr20_41132543_41182626 | PLCG1 | MAGAA others(1286): Show |
chr20 | 41132543 | 41182626 |
| a0003 | 0/0 | 1291 | 28 | 12 | 10 | 1 | 3 | 2 | 1 | PLCG1_chr20_41132543_41182626 | PLCG1 | MAGAA others(1286): Show |
chr20 | 41132543 | 41182626 |
| a0004 | 0/0 | 1291 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | MAGAA others(1286): Show |
chr20 | 41132543 | 41182626 |
| a0005 | 0/0 | 1291 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLCG1_chr20_41132543_41182626 | PLCG1 | MAGAA others(1286): Show |
chr20 | 41132543 | 41182626 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 3873 | 280 | 75 | 40 | 136 | 8 | 20 | PLCG1_chr20_41132543_41182626 | PLCG1 | ATGGC others(3868): Show |
chr20 | 41132543 | 41182626 | ||
| a0001c0005 | 0/0 | 3873 | 2 | 0 | 0 | 0 | 2 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | ATGGC others(3868): Show |
chr20 | 41132543 | 41182626 | ||
| a0001c0007 | 0/0 | 3873 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | ATGGC others(3868): Show |
chr20 | 41132543 | 41182626 | ||
| a0001c0008 | 0/0 | 3873 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | ATGGC others(3868): Show |
chr20 | 41132543 | 41182626 | ||
| a0001c0009 | 0/0 | 3873 | 1 | 0 | 1 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | ATGGC others(3868): Show |
chr20 | 41132543 | 41182626 | ||
| a0001c0010 | 0/0 | 3873 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | ATGGC others(3868): Show |
chr20 | 41132543 | 41182626 | ||
| a0001c0011 | 0/0 | 3873 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | ATGGC others(3868): Show |
chr20 | 41132543 | 41182626 | ||
| a0001c0015 | 0/0 | 3873 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | ATGGC others(3868): Show |
chr20 | 41132543 | 41182626 | ||
| a0002c0002 | 1/0 | 3873 | 68 | 2 | 22 | 32 | 3 | 8 | PLCG1_chr20_41132543_41182626 | PLCG1 | ATGGC others(3868): Show |
chr20 | 41132543 | 41182626 | ||
| a0002c0004 | 0/0 | 3873 | 2 | 0 | 1 | 0 | 0 | 1 | PLCG1_chr20_41132543_41182626 | PLCG1 | ATGGC others(3868): Show |
chr20 | 41132543 | 41182626 | ||
| a0002c0012 | 0/0 | 3873 | 1 | 0 | 0 | 0 | 0 | 1 | PLCG1_chr20_41132543_41182626 | PLCG1 | ATGGC others(3868): Show |
chr20 | 41132543 | 41182626 | ||
| a0002c0013 | 0/0 | 3873 | 1 | 0 | 0 | 0 | 0 | 1 | PLCG1_chr20_41132543_41182626 | PLCG1 | ATGGC others(3868): Show |
chr20 | 41132543 | 41182626 | ||
| a0003c0003 | 0/0 | 3873 | 28 | 12 | 10 | 1 | 3 | 2 | PLCG1_chr20_41132543_41182626 | PLCG1 | ATGGC others(3868): Show |
chr20 | 41132543 | 41182626 | ||
| a0004c0014 | 0/0 | 3873 | 1 | 0 | 0 | 0 | 0 | 1 | PLCG1_chr20_41132543_41182626 | PLCG1 | ATGGC others(3868): Show |
chr20 | 41132543 | 41182626 | ||
| a0005c0006 | 0/0 | 3873 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | ATGGC others(3868): Show |
chr20 | 41132543 | 41182626 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 7092 | 209 | 36 | 31 | 123 | 5 | 14 | PLCG1_chr20_41132543_41182626 | PLCG1 | GTCTG others(7087): Show |
chr20 | 41132543 | 41182626 |
| a0001c0001t0003 | 0/0 | 7092 | 20 | 16 | 4 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | GTCTG others(7087): Show |
chr20 | 41132543 | 41182626 |
| a0001c0001t0004 | 0/1 | 7096 | 20 | 4 | 4 | 4 | 3 | 4 | PLCG1_chr20_41132543_41182626 | PLCG1 | GTCTG others(7091): Show |
chr20 | 41132543 | 41182626 |
| a0001c0001t0005 | 0/0 | 7096 | 7 | 0 | 0 | 7 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | GTCTG others(7091): Show |
chr20 | 41132543 | 41182626 |
| a0001c0001t0006 | 0/0 | 7092 | 7 | 7 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | GTCTG others(7087): Show |
chr20 | 41132543 | 41182626 |
| a0001c0001t0007 | 0/0 | 7094 | 5 | 5 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | GTCTG others(7089): Show |
chr20 | 41132543 | 41182626 |
| a0001c0001t0008 | 0/0 | 7096 | 2 | 0 | 1 | 0 | 0 | 1 | PLCG1_chr20_41132543_41182626 | PLCG1 | GTCTG others(7091): Show |
chr20 | 41132543 | 41182626 |
| a0001c0001t0011 | 0/0 | 7092 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | CTCTG others(7087): Show |
chr20 | 41132543 | 41182626 |
| a0001c0001t0012 | 0/0 | 7092 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | GTCTG others(7087): Show |
chr20 | 41132543 | 41182626 |
| a0001c0001t0014 | 0/0 | 7066 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | GTCTG others(7061): Show |
chr20 | 41132543 | 41182626 |
| a0001c0001t0015 | 0/0 | 7092 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | GTCTG others(7087): Show |
chr20 | 41132543 | 41182626 |
| a0001c0001t0016 | 0/0 | 7092 | 1 | 0 | 0 | 0 | 0 | 1 | PLCG1_chr20_41132543_41182626 | PLCG1 | GTCTG others(7087): Show |
chr20 | 41132543 | 41182626 |
| a0001c0001t0018 | 0/0 | 7096 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | GTCTG others(7091): Show |
chr20 | 41132543 | 41182626 |
| a0001c0001t0019 | 0/0 | 7096 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | GTCTG others(7091): Show |
chr20 | 41132543 | 41182626 |
| a0001c0001t0020 | 0/0 | 7092 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | GTCTG others(7087): Show |
chr20 | 41132543 | 41182626 |
| a0001c0001t0021 | 0/0 | 7096 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | GTCTG others(7091): Show |
chr20 | 41132543 | 41182626 |
| a0001c0001t0022 | 0/0 | 7092 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | GTCTG others(7087): Show |
chr20 | 41132543 | 41182626 |
| a0001c0005t0001 | 0/0 | 7092 | 2 | 0 | 0 | 0 | 2 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | GTCTG others(7087): Show |
chr20 | 41132543 | 41182626 |
| a0001c0007t0001 | 0/0 | 7092 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | GTCTG others(7087): Show |
chr20 | 41132543 | 41182626 |
| a0001c0008t0001 | 0/0 | 7092 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | GTCTG others(7087): Show |
chr20 | 41132543 | 41182626 |
| a0001c0009t0001 | 0/0 | 7092 | 1 | 0 | 1 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | GTCTG others(7087): Show |
chr20 | 41132543 | 41182626 |
| a0001c0010t0001 | 0/0 | 7092 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | GTCTG others(7087): Show |
chr20 | 41132543 | 41182626 |
| a0001c0011t0001 | 0/0 | 7092 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | GTCTG others(7087): Show |
chr20 | 41132543 | 41182626 |
| a0001c0015t0001 | 0/0 | 7092 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | GTCTG others(7087): Show |
chr20 | 41132543 | 41182626 |
| a0002c0002t0001 | 1/0 | 7092 | 62 | 1 | 19 | 32 | 3 | 6 | PLCG1_chr20_41132543_41182626 | PLCG1 | GTCTG others(7087): Show |
chr20 | 41132543 | 41182626 |
| a0002c0002t0008 | 0/0 | 7096 | 3 | 0 | 2 | 0 | 0 | 1 | PLCG1_chr20_41132543_41182626 | PLCG1 | GTCTG others(7091): Show |
chr20 | 41132543 | 41182626 |
| a0002c0002t0010 | 0/0 | 7092 | 2 | 0 | 1 | 0 | 0 | 1 | PLCG1_chr20_41132543_41182626 | PLCG1 | GTCTG others(7087): Show |
chr20 | 41132543 | 41182626 |
| a0002c0002t0013 | 0/0 | 7100 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | GTCTG others(7095): Show |
chr20 | 41132543 | 41182626 |
| a0002c0004t0001 | 0/0 | 7092 | 2 | 0 | 1 | 0 | 0 | 1 | PLCG1_chr20_41132543_41182626 | PLCG1 | GTCTG others(7087): Show |
chr20 | 41132543 | 41182626 |
| a0002c0012t0001 | 0/0 | 7092 | 1 | 0 | 0 | 0 | 0 | 1 | PLCG1_chr20_41132543_41182626 | PLCG1 | GTCTG others(7087): Show |
chr20 | 41132543 | 41182626 |
| a0002c0013t0017 | 0/0 | 7092 | 1 | 0 | 0 | 0 | 0 | 1 | PLCG1_chr20_41132543_41182626 | PLCG1 | GTCTG others(7087): Show |
chr20 | 41132543 | 41182626 |
| a0003c0003t0002 | 0/0 | 7100 | 25 | 9 | 10 | 1 | 3 | 2 | PLCG1_chr20_41132543_41182626 | PLCG1 | GTCTG others(7095): Show |
chr20 | 41132543 | 41182626 |
| a0003c0003t0009 | 0/0 | 7096 | 3 | 3 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | GTCTG others(7091): Show |
chr20 | 41132543 | 41182626 |
| a0004c0014t0002 | 0/0 | 7100 | 1 | 0 | 0 | 0 | 0 | 1 | PLCG1_chr20_41132543_41182626 | PLCG1 | GTCTG others(7095): Show |
chr20 | 41132543 | 41182626 |
| a0005c0006t0001 | 0/0 | 7092 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | GTCTG others(7087): Show |
chr20 | 41132543 | 41182626 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 16 | 0 | 5 | 11 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0004 | 0/0 | 7 | 0 | 4 | 3 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0006 | 0/0 | 6 | 0 | 0 | 4 | 0 | 2 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0015 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0017 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0040 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0046 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0003g0011 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0003g0012 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0004g0056 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0004g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0004g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0004g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0004g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0004g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0004g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0004g0230 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0004g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0004g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0004g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0004g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0004g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0005g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0005g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0005g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0005g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0005g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0006g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0006g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0006g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0006g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0006g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0006g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0007g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0007g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0007g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0007g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0007g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0008g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0008g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0011g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0012g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0014g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0015g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0016g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0018g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0019g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0020g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0021g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0001t0022g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0005t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0005t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0007t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0008t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0009t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0010t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0011t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0001c0015t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0002c0002t0001g0001 | 0/0 | 23 | 0 | 9 | 11 | 0 | 3 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0002c0002t0001g0003 | 1/0 | 8 | 0 | 2 | 3 | 0 | 2 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0002c0002t0001g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0002c0002t0001g0058 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0002c0002t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0002c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0002c0002t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0002c0002t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0002c0002t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0002c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0002c0002t0008g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0002c0002t0008g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0002c0002t0008g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0002c0002t0010g0049 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0002c0002t0013g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0002c0004t0001g0047 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0002c0012t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0002c0013t0017g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0003c0003t0002g0009 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0003c0003t0002g0024 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0003c0003t0002g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0003c0003t0002g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0003c0003t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0003c0003t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0003c0003t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0003c0003t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0003c0003t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0003c0003t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0003c0003t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0003c0003t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0003c0003t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0003c0003t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0003c0003t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0003c0003t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0003c0003t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0003c0003t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0003c0003t0009g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0003c0003t0009g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0004c0014t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| a0005c0006t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0005 | t0001 | g0151 | EUR | GBR | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0043 | EUR | GBR | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0185 | EUR | GBR | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0153 | EUR | GBR | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0043 | EUR | FIN | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG00280 | hp2 | a0001 | c0005 | t0001 | g0150 | EUR | FIN | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG00323 | hp1 | a0001 | c0001 | t0004 | g0237 | EUR | FIN | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG00323 | hp2 | a0003 | c0003 | t0002 | g0024 | EUR | FIN | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG00544 | hp1 | a0001 | c0015 | t0001 | g0005 | EAS | CHS | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG00621 | hp2 | a0001 | c0001 | t0018 | g0057 | EAS | CHS | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0175 | AMR | PUR | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG00733 | hp1 | a0003 | c0003 | t0002 | g0009 | AMR | PUR | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG00733 | hp2 | a0002 | c0002 | t0001 | g0182 | AMR | PUR | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0056 | AMR | PUR | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG00735 | hp2 | a0002 | c0002 | t0008 | g0102 | AMR | PUR | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0105 | AMR | PUR | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG00741 | hp1 | a0001 | c0009 | t0001 | g0106 | AMR | PUR | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG00741 | hp2 | a0002 | c0002 | t0010 | g0049 | AMR | PUR | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0184 | AMR | PUR | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01070 | hp2 | a0003 | c0003 | t0002 | g0074 | AMR | PUR | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01074 | hp2 | a0002 | c0002 | t0001 | g0205 | AMR | PUR | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01081 | hp1 | a0002 | c0004 | t0001 | g0047 | AMR | PUR | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0068 | AMR | PUR | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0012 | AMR | PUR | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01243 | hp2 | a0003 | c0003 | t0002 | g0215 | AMR | PUR | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | CLM | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01256 | hp2 | a0002 | c0002 | t0001 | g0192 | AMR | CLM | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0183 | AMR | CLM | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0012 | AMR | CLM | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01261 | hp2 | a0001 | c0001 | t0004 | g0120 | AMR | CLM | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01346 | hp1 | a0003 | c0003 | t0002 | g0024 | AMR | CLM | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01358 | hp2 | a0001 | c0001 | t0004 | g0056 | AMR | CLM | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01361 | hp2 | a0003 | c0003 | t0002 | g0213 | AMR | CLM | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0186 | AMR | CLM | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | CLM | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0101 | EUR | IBS | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0179 | EUR | IBS | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0177 | EUR | IBS | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01516 | hp2 | a0001 | c0001 | t0004 | g0236 | EUR | IBS | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01891 | hp1 | a0001 | c0001 | t0006 | g0170 | AFR | ACB | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0069 | AFR | ACB | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01943 | hp1 | a0003 | c0003 | t0002 | g0009 | AMR | PEL | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01943 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0244 | AMR | PEL | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01981 | hp1 | a0003 | c0003 | t0002 | g0211 | AMR | PEL | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02027 | hp2 | a0001 | c0011 | t0001 | g0029 | EAS | KHV | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02055 | hp1 | a0001 | c0001 | t0007 | g0108 | AFR | ACB | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0070 | AFR | ACB | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | KHV | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | KHV | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02083 | hp1 | a0001 | c0001 | t0004 | g0057 | EAS | KHV | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02148 | hp2 | a0003 | c0003 | t0002 | g0009 | AMR | PEL | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | CDX | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CDX | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02165 | hp2 | a0001 | c0001 | t0004 | g0235 | EAS | CDX | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0180 | AFR | ACB | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0118 | AFR | ACB | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02258 | hp2 | a0001 | c0001 | t0006 | g0171 | AFR | ACB | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02280 | hp1 | a0001 | c0001 | t0015 | g0203 | AFR | ACB | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ACB | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02293 | hp1 | a0003 | c0003 | t0002 | g0009 | AMR | PEL | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02300 | hp1 | a0003 | c0003 | t0002 | g0009 | AMR | PEL | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02451 | hp1 | a0001 | c0001 | t0011 | g0124 | AFR | ACB | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02572 | hp2 | a0001 | c0001 | t0021 | g0115 | AFR | GWD | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02615 | hp1 | a0003 | c0003 | t0009 | g0051 | AFR | GWD | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0063 | AFR | GWD | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | GWD | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02622 | hp2 | a0001 | c0001 | t0006 | g0045 | AFR | GWD | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02683 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0178 | SAS | PJL | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02735 | hp2 | a0003 | c0003 | t0002 | g0210 | SAS | PJL | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0234 | AFR | GWD | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0062 | AFR | GWD | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02895 | hp1 | a0003 | c0003 | t0002 | g0050 | AFR | GWD | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0067 | AFR | GWD | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02897 | hp1 | a0003 | c0003 | t0002 | g0050 | AFR | GWD | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0117 | AFR | ESN | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02922 | hp2 | a0001 | c0010 | t0001 | g0013 | AFR | ESN | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0061 | AFR | ESN | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02965 | hp2 | a0001 | c0001 | t0007 | g0111 | AFR | ESN | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0073 | AFR | ESN | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0003 | SAS | PJL | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG03017 | hp2 | a0001 | c0001 | t0004 | g0229 | SAS | PJL | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG03098 | hp1 | a0001 | c0001 | t0012 | g0123 | AFR | MSL | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | MSL | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG03139 | hp1 | a0003 | c0003 | t0002 | g0052 | AFR | ESN | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ESN | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0012 | AFR | ESN | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | ESN | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG03209 | hp1 | a0003 | c0003 | t0002 | g0206 | AFR | MSL | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | MSL | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0065 | AFR | MSL | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG03225 | hp2 | a0001 | c0001 | t0007 | g0225 | AFR | MSL | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG03239 | hp1 | a0001 | c0001 | t0004 | g0233 | SAS | PJL | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG03453 | hp1 | a0003 | c0003 | t0002 | g0052 | AFR | MSL | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG03486 | hp1 | a0003 | c0003 | t0009 | g0051 | AFR | MSL | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG03490 | hp1 | a0001 | c0001 | t0004 | g0227 | SAS | PJL | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG03491 | hp2 | a0002 | c0013 | t0017 | g0193 | SAS | PJL | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG03492 | hp2 | a0001 | c0001 | t0004 | g0228 | SAS | PJL | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG03516 | hp1 | a0001 | c0001 | t0006 | g0122 | AFR | ESN | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG03516 | hp2 | a0001 | c0001 | t0006 | g0045 | AFR | ESN | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0022 | AFR | GWD | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | MSL | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG03579 | hp2 | a0003 | c0003 | t0002 | g0217 | AFR | MSL | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG03654 | hp1 | a0004 | c0014 | t0002 | g0176 | SAS | PJL | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | STU | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | STU | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG03831 | hp1 | a0002 | c0004 | t0001 | g0047 | SAS | BEB | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG03831 | hp2 | a0002 | c0002 | t0010 | g0049 | SAS | BEB | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | BEB | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | BEB | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0003 | SAS | BEB | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG04184 | hp2 | a0003 | c0003 | t0002 | g0216 | SAS | BEB | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG04199 | hp1 | a0001 | c0001 | t0008 | g0053 | SAS | STU | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG04199 | hp2 | a0002 | c0002 | t0008 | g0200 | SAS | STU | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | STU | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG04204 | hp2 | a0002 | c0012 | t0001 | g0001 | SAS | STU | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | STU | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG04228 | hp2 | a0001 | c0001 | t0016 | g0082 | SAS | STU | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18522 | hp1 | a0001 | c0001 | t0007 | g0109 | AFR | YRI | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | YRI | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | CHB | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | CHB | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0188 | EAS | CHB | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0066 | AFR | YRI | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18906 | hp2 | a0003 | c0003 | t0009 | g0214 | AFR | YRI | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0072 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18950 | hp1 | a0001 | c0001 | t0022 | g0075 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0246 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18953 | hp1 | a0002 | c0002 | t0001 | g0247 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18957 | hp1 | a0002 | c0002 | t0001 | g0187 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18964 | hp2 | a0001 | c0007 | t0001 | g0089 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18967 | hp1 | a0002 | c0002 | t0001 | g0194 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18968 | hp2 | a0001 | c0008 | t0001 | g0224 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0071 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18977 | hp1 | a0001 | c0001 | t0005 | g0239 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18978 | hp1 | a0001 | c0001 | t0005 | g0242 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18978 | hp2 | a0005 | c0006 | t0001 | g0191 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18980 | hp2 | a0001 | c0001 | t0004 | g0231 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18984 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18985 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18988 | hp1 | a0001 | c0001 | t0005 | g0020 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18998 | hp1 | a0001 | c0001 | t0005 | g0240 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19001 | hp1 | a0003 | c0003 | t0002 | g0212 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19002 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0190 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19030 | hp1 | a0001 | c0001 | t0006 | g0114 | AFR | LWK | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19030 | hp2 | a0001 | c0001 | t0007 | g0110 | AFR | LWK | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | LWK | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | LWK | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19054 | hp1 | a0002 | c0002 | t0001 | g0181 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19057 | hp1 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19058 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19065 | hp2 | a0001 | c0001 | t0005 | g0020 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0202 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19068 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19074 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19077 | hp2 | a0001 | c0001 | t0004 | g0232 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19078 | hp2 | a0002 | c0002 | t0001 | g0163 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19082 | hp1 | a0001 | c0001 | t0005 | g0241 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19082 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19084 | hp2 | a0001 | c0001 | t0005 | g0020 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19240 | hp1 | a0001 | c0001 | t0014 | g0059 | AFR | YRI | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA19240 | hp2 | a0003 | c0003 | t0002 | g0208 | AFR | YRI | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA20129 | hp1 | a0002 | c0002 | t0013 | g0201 | AFR | ASW | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0119 | AFR | ASW | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA20752 | hp1 | a0003 | c0003 | t0002 | g0209 | EUR | TSI | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA20752 | hp2 | a0001 | c0001 | t0004 | g0104 | EUR | TSI | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0031 | EUR | TSI | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA20805 | hp2 | a0003 | c0003 | t0002 | g0218 | EUR | TSI | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | GIH | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | GIH | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01123 | hp1 | a0001 | c0001 | t0008 | g0048 | AMR | CLM | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG01123 | hp2 | a0002 | c0002 | t0008 | g0245 | AMR | CLM | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0064 | AFR | ACB | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | ACB | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | MSL | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG03471 | hp2 | a0001 | c0001 | t0020 | g0160 | AFR | MSL | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG06807 | hp1 | a0001 | c0001 | t0019 | g0116 | AFR | USA | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | USA | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18955 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA20300 | hp1 | a0003 | c0003 | t0002 | g0219 | AFR | USA | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | USA | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA21309 | hp1 | a0001 | c0001 | t0006 | g0172 | AFR | LWK | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| NA21309 | hp2 | a0003 | c0003 | t0002 | g0207 | AFR | LWK | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0004 | g0230 | REF | REF | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0003 | REF | REF | PLCG1_chr20_41132543_41182626 | PLCG1 | chr20 | 41132543 | 41182626 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:41160107 | T | G | 1 | a0005 | 1 | NA18978.hp2 | missense_variant&splice_region_variant | MODERATE | c.466T>G | p.Trp156Gly | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 4/32 | 565/7092 | 466/3876 | 156/1291 | chr20 | 41160107 | |||
| chr20:41160109 | G | T | 1 | a0005 | 1 | NA18978.hp2 | missense_variant | MODERATE | c.468G>T | p.Trp156Cys | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 4/32 | 567/7092 | 468/3876 | 156/1291 | chr20 | 41160109 | |||
| chr20:41160111 | T | G | 1 | a0005 | 1 | NA18978.hp2 | missense_variant | MODERATE | c.470T>G | p.Leu157Arg | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 4/32 | 569/7092 | 470/3876 | 157/1291 | chr20 | 41160111 | |||
| chr20:41163423 | A | G | 2 | a0003 a0004 |
29 | HG00323.hp2 HG00733.hp1 HG01070.hp2 others(26): Show |
missense_variant | MODERATE | c.835A>G | p.Ser279Gly | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 9/32 | 934/7092 | 835/3876 | 279/1291 | chr20 | 41163423 | |||
| chr20:41168825 | T | C | 2 | a0001 a0003 |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(312): Show |
missense_variant | MODERATE | c.2438T>C | p.Ile813Thr | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 21/32 | 2537/7092 | 2438/3876 | 813/1291 | chr20 | 41168825 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:41137674 | C | G | 1 | a0001c0015 | 1 | HG00544.hp1 | synonymous_variant | LOW | c.33C>G | p.Gly11Gly | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/32 | 132/7092 | 33/3876 | 11/1291 | chr20 | 41137674 | |||
| chr20:41160112 | C | G | 1 | a0005c0006 | 1 | NA18978.hp2 | synonymous_variant | LOW | c.471C>G | p.Leu157Leu | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 4/32 | 570/7092 | 471/3876 | 157/1291 | chr20 | 41160112 | |||
| chr20:41165731 | G | A | 1 | a0001c0007 | 1 | NA18964.hp2 | synonymous_variant | LOW | c.1704G>A | p.Leu568Leu | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 16/32 | 1803/7092 | 1704/3876 | 568/1291 | chr20 | 41165731 | |||
| chr20:41166245 | G | A | 1 | a0002c0004 | 2 | HG01081.hp1 HG03831.hp1 |
synonymous_variant | LOW | c.1851G>A | p.Gly617Gly | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 17/32 | 1950/7092 | 1851/3876 | 617/1291 | chr20 | 41166245 | |||
| chr20:41169112 | G | A | 1 | a0001c0008 | 1 | NA18968.hp2 | synonymous_variant | LOW | c.2517G>A | p.Leu839Leu | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 22/32 | 2616/7092 | 2517/3876 | 839/1291 | chr20 | 41169112 | |||
| chr20:41170170 | G | A | 1 | a0001c0009 | 1 | HG00741.hp1 | synonymous_variant | LOW | c.2709G>A | p.Ser903Ser | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 24/32 | 2808/7092 | 2709/3876 | 903/1291 | chr20 | 41170170 | |||
| chr20:41170236 | G | A | 1 | a0001c0010 | 1 | HG02922.hp2 | synonymous_variant | LOW | c.2775G>A | p.Lys925Lys | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 24/32 | 2874/7092 | 2775/3876 | 925/1291 | chr20 | 41170236 | |||
| chr20:41172488 | C | T | 1 | a0002c0013 | 1 | HG03491.hp2 | synonymous_variant | LOW | c.2973C>T | p.Tyr991Tyr | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 26/32 | 3072/7092 | 2973/3876 | 991/1291 | chr20 | 41172488 | |||
| chr20:41174174 | G | T | 1 | a0001c0005 | 2 | HG00099.hp1 HG00280.hp2 |
synonymous_variant | LOW | c.3696G>T | p.Arg1232Arg | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 31/32 | 3795/7092 | 3696/3876 | 1232/1291 | chr20 | 41174174 | |||
| chr20:41174258 | C | T | 1 | a0001c0011 | 1 | HG02027.hp2 | synonymous_variant | LOW | c.3780C>T | p.Asp1260Asp | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 31/32 | 3879/7092 | 3780/3876 | 1260/1291 | chr20 | 41174258 | |||
| chr20:41174494 | A | G | 1 | a0002c0012 | 1 | HG04204.hp2 | synonymous_variant | LOW | c.3861A>G | p.Gly1287Gly | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 32/32 | 3960/7092 | 3861/3876 | 1287/1291 | chr20 | 41174494 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:41137543 | G | C | 1 | a0001c0001t0011 | 1 | HG02451.hp1 | 5_prime_UTR_variant | MODIFIER | c.-99G>C | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/32 | 99 | chr20 | 41137543 | ||||||
| chr20:41137558 | C | T | 1 | a0001c0001t0022 | 1 | NA18950.hp1 | 5_prime_UTR_variant | MODIFIER | c.-84C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/32 | 84 | chr20 | 41137558 | ||||||
| chr20:41174582 | A | AAG | 1 | a0001c0001t0007 | 5 | HG02055.hp1 HG02965.hp2 HG03225.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*74_*75dupAG | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 32/32 | 76 | INFO_REALIGN_3_PRIME | chr20 | 41174582 | |||||
| chr20:41174589 | C | A | 1 | a0001c0001t0012 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*80C>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 32/32 | 80 | chr20 | 41174589 | ||||||
| chr20:41175296 | G | T | 1 | a0001c0001t0021 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*787G>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 32/32 | 787 | chr20 | 41175296 | ||||||
| chr20:41175815 | A | G | 1 | a0001c0001t0020 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1306A>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 32/32 | 1306 | chr20 | 41175815 | ||||||
| chr20:41175899 | C | G | 1 | a0001c0001t0019 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1390C>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 32/32 | 1390 | chr20 | 41175899 | ||||||
| chr20:41176263 | T | TCAAA | 5 | a0001c0001t0008 a0002c0002t0008 a0002c0002t0013 others(2): Show |
32 | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*1757_*1760dupAACA | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 32/32 | 1761 | INFO_REALIGN_3_PRIME | chr20 | 41176263 | |||||
| chr20:41176272 | G | A | 2 | a0001c0001t0003 a0001c0001t0014 |
21 | HG01109.hp2 HG01167.hp1 HG01243.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1763G>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 32/32 | 1763 | chr20 | 41176272 | ||||||
| chr20:41176615 | C | G | 1 | a0001c0001t0018 | 1 | HG00621.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2106C>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 32/32 | 2106 | chr20 | 41176615 | ||||||
| chr20:41176697 | T | TTTGA | 6 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0018 others(3): Show |
30 | HG00323.hp1 HG00621.hp2 HG00735.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*2192_*2195dupATTG | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 32/32 | 2196 | INFO_REALIGN_3_PRIME | chr20 | 41176697 | |||||
| chr20:41176792 | T | C | 1 | a0001c0001t0015 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2283T>C | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 32/32 | 2283 | chr20 | 41176792 | ||||||
| chr20:41176809 | G | GTGTT | 3 | a0003c0003t0002 a0003c0003t0009 a0004c0014t0002 |
29 | HG00323.hp2 HG00733.hp1 HG01070.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*2305_*2308dupTGTT | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 32/32 | 2309 | INFO_REALIGN_3_PRIME | chr20 | 41176809 | |||||
| chr20:41176925 | A | T | 1 | a0002c0013t0017 | 1 | HG03491.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2416A>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 32/32 | 2416 | chr20 | 41176925 | ||||||
| chr20:41177111 | G | A | 1 | a0001c0001t0016 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2602G>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 32/32 | 2602 | chr20 | 41177111 | ||||||
| chr20:41177205 | C | T | 1 | a0001c0001t0006 | 7 | HG01891.hp1 HG02258.hp2 HG02622.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2696C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 32/32 | 2696 | chr20 | 41177205 | ||||||
| chr20:41177223 | AGTGACAG others(19): Show |
A | 1 | a0001c0001t0014 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2715_*2740delGTGA others(22): Show |
PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 32/32 | 2715 | chr20 | 41177223 | ||||||
| chr20:41177472 | C | T | 1 | a0002c0002t0010 | 2 | HG00741.hp2 HG03831.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2963C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 32/32 | 2963 | chr20 | 41177472 | ||||||
| chr20:41177623 | C | T | 1 | a0001c0001t0005 | 7 | NA18977.hp1 NA18978.hp1 NA18988.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3114C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 32/32 | 3114 | chr20 | 41177623 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:41137952 | C | G | 2 | a0001c0001t0001g0248 a0001c0001t0001g0249 |
2 | HG02056.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.217+94C>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41137952 | |||||||
| chr20:41137996 | C | T | 6 | a0002c0002t0001g0010 a0002c0002t0001g0058 a0002c0002t0001g0244 others(3): Show |
11 | HG01123.hp2 HG01978.hp2 NA18942.hp2 others(8): Show |
intron_variant | MODIFIER | c.217+138C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41137996 | |||||||
| chr20:41138006 | G | T | 1 | a0001c0001t0001g0243 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.217+148G>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41138006 | |||||||
| chr20:41138478 | A | AT | 21 | a0001c0001t0001g0226 a0001c0001t0001g0238 a0001c0001t0004g0056 others(18): Show |
24 | HG00323.hp1 HG00621.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.217+637dupT | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr20 | 41138478 | ||||||
| chr20:41138478 | AT | A | 21 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(18): Show |
29 | HG01109.hp2 HG01167.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.217+637delT | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr20 | 41138478 | ||||||
| chr20:41138558 | C | G | 1 | a0001c0001t0007g0225 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.217+700C>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41138558 | |||||||
| chr20:41138780 | G | C | 2 | a0003c0003t0002g0024 a0003c0003t0002g0074 |
3 | HG00323.hp2 HG01070.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.217+922G>C | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41138780 | |||||||
| chr20:41138957 | G | T | 4 | a0001c0001t0001g0023 a0001c0001t0001g0054 a0001c0001t0001g0055 others(1): Show |
7 | HG02015.hp1 HG02155.hp1 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.217+1099G>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41138957 | |||||||
| chr20:41139104 | T | C | 38 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(35): Show |
74 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.217+1246T>C | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41139104 | |||||||
| chr20:41139314 | G | C | 1 | a0002c0002t0001g0244 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.217+1456G>C | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41139314 | |||||||
| chr20:41139544 | T | G | 1 | a0001c0001t0001g0226 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.217+1686T>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41139544 | |||||||
| chr20:41139590 | G | C | 1 | a0001c0001t0014g0059 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.217+1732G>C | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41139590 | |||||||
| chr20:41139691 | G | A | 1 | a0001c0001t0022g0075 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.217+1833G>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41139691 | |||||||
| chr20:41139795 | G | T | 2 | a0001c0001t0001g0222 a0001c0001t0001g0223 |
2 | HG02135.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.217+1937G>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41139795 | |||||||
| chr20:41139852 | A | G | 3 | a0001c0001t0001g0053 a0001c0001t0001g0221 a0001c0001t0008g0053 |
3 | HG02523.hp2 HG04199.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.217+1994A>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41139852 | |||||||
| chr20:41139882 | A | C | 5 | a0001c0001t0005g0020 a0001c0001t0005g0239 a0001c0001t0005g0240 others(2): Show |
7 | NA18977.hp1 NA18978.hp1 NA18988.hp1 others(4): Show |
intron_variant | MODIFIER | c.217+2024A>C | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41139882 | |||||||
| chr20:41140183 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.217+2325C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41140183 | |||||||
| chr20:41140212 | G | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0100 a0001c0001t0001g0101 |
4 | HG00642.hp2 HG01168.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.217+2354G>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41140212 | |||||||
| chr20:41140213 | A | G | 1 | a0001c0001t0003g0073 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.217+2355A>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41140213 | |||||||
| chr20:41140681 | G | A | 1 | a0002c0002t0008g0102 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.217+2823G>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41140681 | |||||||
| chr20:41140826 | C | T | 1 | a0001c0001t0001g0221 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.217+2968C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41140826 | |||||||
| chr20:41141335 | T | C | 166 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(163): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.217+3477T>C | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41141335 | |||||||
| chr20:41141396 | G | T | 7 | a0001c0001t0004g0057 a0001c0001t0005g0020 a0001c0001t0005g0239 others(4): Show |
9 | HG00621.hp2 HG02083.hp1 NA18977.hp1 others(6): Show |
intron_variant | MODIFIER | c.217+3538G>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41141396 | |||||||
| chr20:41141476 | C | T | 20 | a0003c0003t0002g0009 a0003c0003t0002g0024 a0003c0003t0002g0050 others(17): Show |
28 | HG00323.hp2 HG00733.hp1 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.217+3618C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41141476 | |||||||
| chr20:41141673 | A | G | 3 | a0001c0001t0001g0044 a0001c0001t0001g0161 a0001c0001t0001g0162 |
4 | HG02976.hp1 HG03579.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.217+3815A>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41141673 | |||||||
| chr20:41141968 | G | A | 1 | a0001c0001t0001g0076 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.217+4110G>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41141968 | |||||||
| chr20:41142009 | C | T | 1 | a0001c0001t0020g0160 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.217+4151C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41142009 | |||||||
| chr20:41142038 | T | G | 1 | a0001c0001t0001g0103 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.217+4180T>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41142038 | |||||||
| chr20:41142128 | C | T | 1 | a0002c0002t0001g0205 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.217+4270C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41142128 | |||||||
| chr20:41142137 | A | C | 1 | a0003c0003t0002g0219 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.217+4279A>C | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41142137 | |||||||
| chr20:41142279 | AGGGAACA others(5): Show |
A | 1 | a0001c0001t0001g0204 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.217+4424_217+4435d others(14): Show |
PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr20 | 41142279 | ||||||
| chr20:41142392 | C | T | 1 | a0001c0001t0015g0203 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.217+4534C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41142392 | |||||||
| chr20:41142490 | G | T | 1 | a0002c0002t0001g0202 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.217+4632G>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41142490 | |||||||
| chr20:41142664 | G | A | 2 | a0003c0003t0002g0050 a0003c0003t0002g0206 |
3 | HG02895.hp1 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.217+4806G>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41142664 | |||||||
| chr20:41142803 | G | A | 9 | a0001c0001t0001g0107 a0001c0001t0004g0104 a0001c0001t0004g0105 others(6): Show |
9 | HG00738.hp1 HG00741.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.217+4945G>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41142803 | |||||||
| chr20:41142922 | G | C | 1 | a0002c0002t0001g0163 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.217+5064G>C | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41142922 | |||||||
| chr20:41142992 | G | A | 1 | a0001c0001t0001g0112 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.217+5134G>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41142992 | |||||||
| chr20:41143307 | T | C | 200 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(197): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.217+5449T>C | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41143307 | |||||||
| chr20:41143477 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.217+5619A>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41143477 | |||||||
| chr20:41143543 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.217+5685G>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41143543 | |||||||
| chr20:41143704 | T | G | 1 | a0001c0001t0001g0161 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.217+5846T>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41143704 | |||||||
| chr20:41143832 | A | G | 5 | a0001c0001t0007g0108 a0001c0001t0007g0109 a0001c0001t0007g0110 others(2): Show |
5 | HG02055.hp1 HG02965.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.217+5974A>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41143832 | |||||||
| chr20:41143973 | G | A | 2 | a0001c0001t0001g0077 a0001c0001t0001g0078 |
2 | NA18947.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.217+6115G>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41143973 | |||||||
| chr20:41144048 | A | G | 3 | a0002c0002t0008g0102 a0002c0002t0008g0200 a0002c0002t0013g0201 |
3 | HG00735.hp2 HG04199.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.217+6190A>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41144048 | |||||||
| chr20:41144180 | C | A | 1 | a0001c0001t0006g0114 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.217+6322C>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41144180 | |||||||
| chr20:41144193 | G | A | 4 | a0001c0001t0001g0044 a0001c0001t0001g0159 a0001c0001t0001g0161 others(1): Show |
5 | HG01884.hp2 HG02976.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.217+6335G>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41144193 | |||||||
| chr20:41144301 | T | A | 9 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(6): Show |
9 | HG02135.hp2 HG03688.hp2 NA18946.hp1 others(6): Show |
intron_variant | MODIFIER | c.217+6443T>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41144301 | |||||||
| chr20:41144395 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.217+6537C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41144395 | |||||||
| chr20:41144533 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.217+6675G>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41144533 | |||||||
| chr20:41144599 | G | A | 24 | a0001c0001t0004g0056 a0001c0001t0004g0057 a0001c0001t0004g0117 others(21): Show |
27 | HG00323.hp1 HG00621.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.217+6741G>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41144599 | |||||||
| chr20:41144667 | A | G | 2 | a0001c0001t0001g0197 a0001c0001t0001g0198 |
2 | HG02572.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.217+6809A>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41144667 | |||||||
| chr20:41144715 | T | C | 1 | a0001c0001t0001g0046 | 2 | HG00738.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.217+6857T>C | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41144715 | |||||||
| chr20:41144784 | C | T | 1 | a0001c0001t0004g0120 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.217+6926C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41144784 | |||||||
| chr20:41144808 | G | T | 3 | a0001c0001t0001g0015 a0001c0001t0001g0046 a0001c0001t0001g0196 |
7 | HG00642.hp1 HG00738.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.217+6950G>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41144808 | |||||||
| chr20:41145092 | G | A | 1 | a0001c0001t0015g0203 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.217+7234G>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41145092 | |||||||
| chr20:41145482 | C | T | 2 | a0001c0001t0003g0069 a0001c0001t0003g0070 |
2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.217+7624C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41145482 | |||||||
| chr20:41145485 | C | T | 2 | a0001c0001t0003g0069 a0001c0001t0003g0070 |
2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.217+7627C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41145485 | |||||||
| chr20:41145523 | T | C | 201 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(198): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.217+7665T>C | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41145523 | |||||||
| chr20:41145534 | C | T | 1 | a0001c0001t0003g0068 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.217+7676C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41145534 | |||||||
| chr20:41145586 | A | T | 1 | a0001c0001t0001g0226 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.217+7728A>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41145586 | |||||||
| chr20:41145752 | G | T | 1 | a0001c0001t0015g0203 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.217+7894G>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41145752 | |||||||
| chr20:41146297 | C | G | 5 | a0001c0001t0001g0022 a0001c0001t0003g0012 a0001c0001t0003g0022 others(2): Show |
8 | HG01243.hp1 HG01261.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.217+8439C>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41146297 | |||||||
| chr20:41146426 | C | T | 2 | a0001c0001t0001g0107 a0001c0009t0001g0106 |
2 | HG00741.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.217+8568C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41146426 | |||||||
| chr20:41146684 | G | C | 2 | a0003c0003t0002g0050 a0003c0003t0002g0206 |
3 | HG02895.hp1 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.217+8826G>C | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41146684 | |||||||
| chr20:41146769 | C | T | 3 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0014g0059 |
3 | HG02135.hp2 NA19079.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.217+8911C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41146769 | |||||||
| chr20:41146854 | G | A | 24 | a0001c0001t0004g0056 a0001c0001t0004g0057 a0001c0001t0004g0117 others(21): Show |
27 | HG00323.hp1 HG00621.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.217+8996G>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41146854 | |||||||
| chr20:41146968 | T | G | 1 | a0003c0003t0002g0207 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.217+9110T>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41146968 | |||||||
| chr20:41147016 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.217+9158G>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41147016 | |||||||
| chr20:41147266 | C | G | 1 | a0001c0001t0020g0160 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.217+9408C>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41147266 | |||||||
| chr20:41147355 | A | C | 1 | a0001c0001t0006g0045 | 2 | HG02622.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.217+9497A>C | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41147355 | |||||||
| chr20:41147406 | C | T | 201 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(198): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.217+9548C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41147406 | |||||||
| chr20:41147722 | G | A | 3 | a0001c0001t0001g0048 a0001c0001t0001g0174 a0001c0001t0008g0048 |
3 | HG01123.hp1 HG01255.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.217+9864G>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41147722 | |||||||
| chr20:41147805 | G | A | 20 | a0003c0003t0002g0009 a0003c0003t0002g0024 a0003c0003t0002g0050 others(17): Show |
28 | HG00323.hp2 HG00733.hp1 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.217+9947G>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41147805 | |||||||
| chr20:41147840 | T | C | 1 | a0002c0002t0008g0200 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.217+9982T>C | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41147840 | |||||||
| chr20:41147992 | C | T | 1 | a0001c0001t0001g0158 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.217+10134C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41147992 | |||||||
| chr20:41148247 | G | A | 2 | a0001c0001t0006g0170 a0001c0001t0006g0171 |
2 | HG01891.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.217+10389G>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41148247 | |||||||
| chr20:41148405 | G | A | 1 | a0001c0001t0004g0104 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.217+10547G>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41148405 | |||||||
| chr20:41148685 | C | G | 1 | a0002c0004t0001g0047 | 2 | HG01081.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.217+10827C>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41148685 | |||||||
| chr20:41148737 | T | C | 5 | a0001c0001t0007g0108 a0001c0001t0007g0109 a0001c0001t0007g0110 others(2): Show |
5 | HG02055.hp1 HG02965.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.218-10869T>C | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41148737 | |||||||
| chr20:41148764 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.218-10842C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41148764 | |||||||
| chr20:41149269 | T | C | 1 | a0001c0001t0001g0077 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.218-10337T>C | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41149269 | |||||||
| chr20:41149305 | C | G | 4 | a0001c0001t0004g0117 a0001c0001t0004g0118 a0001c0001t0004g0119 others(1): Show |
4 | HG02258.hp1 HG02922.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.218-10301C>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41149305 | |||||||
| chr20:41149314 | A | G | 25 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0016 others(22): Show |
36 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(33): Show |
intron_variant | MODIFIER | c.218-10292A>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41149314 | |||||||
| chr20:41149380 | G | T | 2 | a0001c0001t0001g0043 a0001c0001t0001g0156 |
3 | HG00099.hp2 HG00280.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.218-10226G>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41149380 | |||||||
| chr20:41149542 | T | C | 2 | a0001c0001t0004g0104 a0001c0001t0004g0105 |
2 | HG00738.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.218-10064T>C | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41149542 | |||||||
| chr20:41149653 | A | G | 1 | a0001c0001t0001g0155 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.218-9953A>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41149653 | |||||||
| chr20:41149742 | C | T | 1 | a0001c0001t0001g0042 | 2 | NA18964.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.218-9864C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41149742 | |||||||
| chr20:41149866 | T | C | 2 | a0002c0002t0001g0244 a0002c0002t0008g0245 |
2 | HG01123.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.218-9740T>C | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41149866 | |||||||
| chr20:41149869 | C | T | 1 | a0002c0002t0001g0194 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.218-9737C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41149869 | |||||||
| chr20:41149968 | C | T | 17 | a0001c0001t0001g0022 a0001c0001t0001g0154 a0001c0001t0003g0011 others(14): Show |
23 | HG01109.hp2 HG01167.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.218-9638C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41149968 | |||||||
| chr20:41150491 | A | G | 9 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(6): Show |
9 | HG02135.hp2 HG03688.hp2 NA18946.hp1 others(6): Show |
intron_variant | MODIFIER | c.218-9115A>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41150491 | |||||||
| chr20:41150681 | A | G | 1 | a0002c0013t0017g0193 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.218-8925A>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41150681 | |||||||
| chr20:41150890 | C | A | 2 | a0001c0001t0001g0112 a0001c0001t0001g0121 |
2 | NA19012.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.218-8716C>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41150890 | |||||||
| chr20:41150909 | A | T | 20 | a0003c0003t0002g0009 a0003c0003t0002g0024 a0003c0003t0002g0050 others(17): Show |
28 | HG00323.hp2 HG00733.hp1 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.218-8697A>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41150909 | |||||||
| chr20:41151091 | C | G | 2 | a0001c0001t0004g0104 a0001c0001t0004g0105 |
2 | HG00738.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.218-8515C>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41151091 | |||||||
| chr20:41151138 | C | G | 1 | a0001c0001t0001g0077 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.218-8468C>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41151138 | |||||||
| chr20:41151614 | T | C | 1 | a0001c0001t0001g0248 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.218-7992T>C | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41151614 | |||||||
| chr20:41151622 | C | T | 4 | a0001c0001t0006g0045 a0001c0001t0006g0170 a0001c0001t0006g0171 others(1): Show |
5 | HG01891.hp1 HG02258.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.218-7984C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41151622 | |||||||
| chr20:41151658 | A | G | 1 | a0002c0002t0001g0192 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.218-7948A>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41151658 | |||||||
| chr20:41151701 | C | G | 1 | a0001c0001t0004g0237 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.218-7905C>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41151701 | |||||||
| chr20:41151715 | A | T | 5 | a0001c0001t0007g0108 a0001c0001t0007g0109 a0001c0001t0007g0110 others(2): Show |
5 | HG02055.hp1 HG02965.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.218-7891A>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41151715 | |||||||
| chr20:41151970 | G | T | 1 | a0001c0001t0001g0158 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.218-7636G>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41151970 | |||||||
| chr20:41151976 | G | A | 1 | a0002c0002t0013g0201 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.218-7630G>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41151976 | |||||||
| chr20:41152073 | T | A | 2 | a0001c0001t0001g0107 a0001c0009t0001g0106 |
2 | HG00741.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.218-7533T>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41152073 | |||||||
| chr20:41152075 | A | T | 2 | a0001c0001t0001g0107 a0001c0009t0001g0106 |
2 | HG00741.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.218-7531A>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41152075 | |||||||
| chr20:41152076 | G | A | 2 | a0001c0001t0001g0107 a0001c0009t0001g0106 |
2 | HG00741.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.218-7530G>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41152076 | |||||||
| chr20:41152077 | C | A | 2 | a0001c0001t0001g0107 a0001c0009t0001g0106 |
2 | HG00741.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.218-7529C>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41152077 | |||||||
| chr20:41152079 | C | G | 2 | a0001c0001t0001g0107 a0001c0009t0001g0106 |
2 | HG00741.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.218-7527C>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41152079 | |||||||
| chr20:41152080 | C | G | 2 | a0001c0001t0001g0107 a0001c0009t0001g0106 |
2 | HG00741.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.218-7526C>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41152080 | |||||||
| chr20:41152097 | G | A | 1 | a0002c0002t0001g0175 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.218-7509G>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41152097 | |||||||
| chr20:41152242 | C | T | 39 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(36): Show |
75 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.218-7364C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41152242 | |||||||
| chr20:41152292 | G | A | 118 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(115): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.218-7314G>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41152292 | |||||||
| chr20:41152318 | C | T | 2 | a0001c0001t0001g0041 a0001c0001t0001g0153 |
3 | HG00140.hp2 HG01192.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.218-7288C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41152318 | |||||||
| chr20:41152458 | G | A | 1 | a0001c0001t0001g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.218-7148G>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41152458 | |||||||
| chr20:41153052 | A | C | 2 | a0001c0001t0001g0107 a0001c0009t0001g0106 |
2 | HG00741.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.218-6554A>C | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41153052 | |||||||
| chr20:41153062 | G | T | 1 | a0001c0001t0004g0105 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.218-6544G>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41153062 | |||||||
| chr20:41153166 | A | G | 1 | a0001c0001t0005g0242 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.218-6440A>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41153166 | |||||||
| chr20:41153455 | T | A | 13 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(10): Show |
14 | HG01891.hp1 HG02135.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.218-6151T>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41153455 | |||||||
| chr20:41153463 | T | C | 4 | a0001c0001t0001g0044 a0001c0001t0001g0159 a0001c0001t0001g0161 others(1): Show |
5 | HG01884.hp2 HG02976.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.218-6143T>C | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41153463 | |||||||
| chr20:41153623 | A | G | 1 | a0001c0001t0022g0075 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.218-5983A>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41153623 | |||||||
| chr20:41154259 | A | G | 69 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(66): Show |
105 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.218-5347A>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41154259 | |||||||
| chr20:41154394 | C | A | 68 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(65): Show |
104 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(101): Show |
intron_variant | MODIFIER | c.218-5212C>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41154394 | |||||||
| chr20:41154748 | A | G | 1 | a0001c0001t0004g0237 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.218-4858A>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41154748 | |||||||
| chr20:41154782 | A | G | 3 | a0002c0002t0001g0072 a0002c0002t0001g0190 a0005c0006t0001g0191 |
3 | NA18948.hp2 NA18978.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.218-4824A>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41154782 | |||||||
| chr20:41154834 | C | T | 1 | a0001c0001t0004g0236 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.218-4772C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41154834 | |||||||
| chr20:41154963 | A | G | 2 | a0001c0001t0004g0104 a0001c0001t0004g0105 |
2 | HG00738.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.218-4643A>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41154963 | |||||||
| chr20:41154966 | G | C | 14 | a0001c0001t0001g0025 a0001c0001t0001g0164 a0001c0001t0001g0165 others(11): Show |
16 | HG01891.hp1 HG02135.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.218-4640G>C | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41154966 | |||||||
| chr20:41155661 | C | T | 1 | a0003c0003t0002g0207 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.218-3945C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41155661 | |||||||
| chr20:41155761 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.218-3845C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41155761 | |||||||
| chr20:41155785 | A | G | 4 | a0001c0001t0001g0040 a0001c0001t0001g0152 a0001c0005t0001g0150 others(1): Show |
5 | HG00099.hp1 HG00280.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.218-3821A>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41155785 | |||||||
| chr20:41156579 | C | T | 3 | a0001c0001t0004g0117 a0001c0001t0004g0118 a0001c0001t0004g0119 |
3 | HG02258.hp1 HG02922.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.218-3027C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41156579 | |||||||
| chr20:41156589 | G | A | 26 | a0001c0001t0007g0108 a0001c0001t0007g0109 a0001c0001t0007g0110 others(23): Show |
34 | HG00323.hp2 HG00733.hp1 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.218-3017G>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41156589 | |||||||
| chr20:41156802 | G | A | 1 | a0001c0001t0015g0203 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.218-2804G>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41156802 | |||||||
| chr20:41156949 | A | G | 1 | a0001c0001t0006g0045 | 2 | HG02622.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.218-2657A>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41156949 | |||||||
| chr20:41156994 | T | G | 16 | a0001c0001t0001g0022 a0001c0001t0003g0011 a0001c0001t0003g0012 others(13): Show |
22 | HG01109.hp2 HG01167.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.218-2612T>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41156994 | |||||||
| chr20:41157040 | T | C | 2 | a0001c0001t0004g0057 a0001c0001t0018g0057 |
2 | HG00621.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.218-2566T>C | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41157040 | |||||||
| chr20:41157134 | A | G | 5 | a0001c0001t0007g0108 a0001c0001t0007g0109 a0001c0001t0007g0110 others(2): Show |
5 | HG02055.hp1 HG02965.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.218-2472A>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41157134 | |||||||
| chr20:41157204 | C | CTG | 9 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0004g0227 others(6): Show |
9 | HG00741.hp1 HG02572.hp1 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.218-2366_218-2365d others(4): Show |
PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr20 | 41157204 | ||||||
| chr20:41157204 | C | CTGTG | 46 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0018 others(43): Show |
61 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.218-2368_218-2365d others(6): Show |
PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr20 | 41157204 | ||||||
| chr20:41157204 | C | CTGTGTG | 27 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0034 others(24): Show |
38 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.218-2370_218-2365d others(8): Show |
PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr20 | 41157204 | ||||||
| chr20:41157204 | C | CTGTGTGT others(1): Show |
44 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0014 others(41): Show |
69 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.218-2372_218-2365d others(10): Show |
PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr20 | 41157204 | ||||||
| chr20:41157204 | C | CTGTGTGT others(3): Show |
20 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0038 others(17): Show |
41 | HG00438.hp2 HG00673.hp2 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.218-2374_218-2365d others(12): Show |
PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr20 | 41157204 | ||||||
| chr20:41157204 | C | CTGTGTGT others(5): Show |
16 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0028 others(13): Show |
29 | HG01167.hp1 HG01928.hp2 HG01934.hp2 others(26): Show |
intron_variant | MODIFIER | c.218-2376_218-2365d others(14): Show |
PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr20 | 41157204 | ||||||
| chr20:41157204 | C | CTGTGTGT others(7): Show |
6 | a0001c0001t0001g0044 a0001c0001t0001g0095 a0001c0001t0003g0067 others(3): Show |
7 | HG01109.hp2 HG02896.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.218-2378_218-2365d others(16): Show |
PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr20 | 41157204 | ||||||
| chr20:41157204 | C | CTGTGTGT others(9): Show |
11 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(8): Show |
14 | HG01243.hp1 HG01261.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.218-2380_218-2365d others(18): Show |
PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr20 | 41157204 | ||||||
| chr20:41157204 | C | CTGTGTGT others(11): Show |
4 | a0001c0001t0001g0022 a0001c0001t0001g0099 a0001c0001t0003g0022 others(1): Show |
4 | HG02071.hp2 HG02976.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.218-2382_218-2365d others(20): Show |
PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr20 | 41157204 | ||||||
| chr20:41157204 | C | CTGTGTGT others(13): Show |
1 | a0001c0001t0001g0161 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.218-2384_218-2365d others(22): Show |
PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr20 | 41157204 | ||||||
| chr20:41157204 | C | CTGTGTGT others(15): Show |
1 | a0001c0001t0003g0065 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.218-2386_218-2365d others(24): Show |
PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr20 | 41157204 | ||||||
| chr20:41157204 | CTG | C | 54 | a0001c0001t0001g0015 a0001c0001t0001g0025 a0001c0001t0001g0031 others(51): Show |
89 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.218-2366_218-2365d others(4): Show |
PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr20 | 41157204 | ||||||
| chr20:41157204 | CTGTG | C | 3 | a0001c0001t0006g0114 a0002c0002t0001g0175 a0002c0002t0001g0246 |
3 | HG00639.hp1 NA18952.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.218-2368_218-2365d others(6): Show |
PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr20 | 41157204 | ||||||
| chr20:41157204 | CTGTGTGT others(1): Show |
C | 2 | a0003c0003t0002g0024 a0003c0003t0002g0074 |
3 | HG00323.hp2 HG01070.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.218-2372_218-2365d others(10): Show |
PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr20 | 41157204 | ||||||
| chr20:41157204 | CTGTGTGT others(5): Show |
C | 1 | a0002c0002t0001g0178 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.218-2376_218-2365d others(14): Show |
PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr20 | 41157204 | ||||||
| chr20:41157204 | CTGTGTGT others(9): Show |
C | 1 | a0002c0002t0001g0177 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.218-2380_218-2365d others(18): Show |
PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr20 | 41157204 | ||||||
| chr20:41157276 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.218-2330G>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41157276 | |||||||
| chr20:41157604 | G | A | 1 | a0002c0002t0008g0200 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.218-2002G>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41157604 | |||||||
| chr20:41157621 | C | T | 1 | a0001c0001t0006g0171 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.218-1985C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41157621 | |||||||
| chr20:41157692 | C | T | 2 | a0001c0001t0003g0069 a0001c0001t0003g0070 |
2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.218-1914C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41157692 | |||||||
| chr20:41157723 | A | T | 1 | a0001c0001t0001g0189 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.218-1883A>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41157723 | |||||||
| chr20:41157814 | G | A | 16 | a0001c0001t0001g0022 a0001c0001t0001g0125 a0001c0001t0001g0126 others(13): Show |
22 | HG01109.hp2 HG01167.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.218-1792G>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41157814 | |||||||
| chr20:41158220 | C | T | 8 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(5): Show |
8 | HG03688.hp2 NA18946.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.218-1386C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41158220 | |||||||
| chr20:41158255 | G | A | 1 | a0001c0001t0001g0084 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.218-1351G>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41158255 | |||||||
| chr20:41158277 | G | T | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | NA18982.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.218-1329G>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41158277 | |||||||
| chr20:41158316 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.218-1290C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41158316 | |||||||
| chr20:41158443 | G | A | 1 | a0001c0001t0006g0114 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.218-1163G>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41158443 | |||||||
| chr20:41158720 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.218-886C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41158720 | |||||||
| chr20:41158736 | C | G | 1 | a0001c0001t0001g0155 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.218-870C>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41158736 | |||||||
| chr20:41158863 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.218-743A>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41158863 | |||||||
| chr20:41158890 | T | C | 3 | a0001c0001t0004g0056 a0001c0001t0004g0234 a0001c0001t0004g0236 |
4 | HG00735.hp1 HG01358.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.218-716T>C | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41158890 | |||||||
| chr20:41159297 | T | C | 179 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(176): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.218-309T>C | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41159297 | |||||||
| chr20:41159327 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.218-279A>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41159327 | |||||||
| chr20:41159371 | A | T | 39 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(36): Show |
75 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.218-235A>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41159371 | |||||||
| chr20:41159452 | C | T | 5 | a0001c0001t0007g0108 a0001c0001t0007g0109 a0001c0001t0007g0110 others(2): Show |
5 | HG02055.hp1 HG02965.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.218-154C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 1/31 | chr20 | 41159452 | |||||||
| chr20:41159771 | G | C | 1 | a0001c0001t0001g0095 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.370+13G>C | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 2/31 | chr20 | 41159771 | |||||||
| chr20:41160046 | C | T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0155 others(1): Show |
9 | NA18612.hp2 NA18939.hp1 NA18944.hp2 others(6): Show |
intron_variant | MODIFIER | c.465-60C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 3/31 | chr20 | 41160046 | |||||||
| chr20:41160176 | A | G | 5 | a0001c0001t0007g0108 a0001c0001t0007g0109 a0001c0001t0007g0110 others(2): Show |
5 | HG02055.hp1 HG02965.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.512+23A>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 4/31 | chr20 | 41160176 | |||||||
| chr20:41160194 | T | A | 1 | a0001c0001t0001g0121 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.512+41T>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 4/31 | chr20 | 41160194 | |||||||
| chr20:41160215 | A | G | 200 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(197): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.512+62A>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 4/31 | chr20 | 41160215 | |||||||
| chr20:41160221 | C | CT | 2 | a0001c0001t0005g0020 a0001c0001t0005g0241 |
4 | NA18988.hp1 NA19065.hp2 NA19082.hp1 others(1): Show |
intron_variant | MODIFIER | c.512+69dupT | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr20 | 41160221 | ||||||
| chr20:41160234 | C | A | 3 | a0001c0001t0007g0109 a0001c0001t0007g0111 a0001c0001t0007g0225 |
3 | HG02965.hp2 HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.512+81C>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 4/31 | chr20 | 41160234 | |||||||
| chr20:41160298 | C | T | 1 | a0001c0001t0011g0124 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.512+145C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 4/31 | chr20 | 41160298 | |||||||
| chr20:41160617 | T | C | 2 | a0001c0001t0006g0170 a0001c0001t0006g0171 |
2 | HG01891.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.512+464T>C | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 4/31 | chr20 | 41160617 | |||||||
| chr20:41160732 | A | C | 1 | a0001c0001t0001g0130 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.512+579A>C | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 4/31 | chr20 | 41160732 | |||||||
| chr20:41160821 | A | T | 26 | a0001c0001t0004g0056 a0001c0001t0004g0057 a0001c0001t0004g0104 others(23): Show |
29 | HG00323.hp1 HG00621.hp2 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.512+668A>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 4/31 | chr20 | 41160821 | |||||||
| chr20:41161075 | A | G | 8 | a0001c0001t0001g0014 a0001c0001t0001g0042 a0001c0001t0001g0060 others(5): Show |
12 | HG01081.hp2 HG01256.hp1 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.512+922A>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 4/31 | chr20 | 41161075 | |||||||
| chr20:41161089 | G | C | 4 | a0001c0001t0001g0044 a0001c0001t0001g0159 a0001c0001t0001g0161 others(1): Show |
5 | HG01884.hp2 HG02976.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.512+936G>C | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 4/31 | chr20 | 41161089 | |||||||
| chr20:41161191 | G | A | 1 | a0002c0002t0001g0205 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.512+1038G>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 4/31 | chr20 | 41161191 | |||||||
| chr20:41161260 | C | G | 5 | a0001c0001t0007g0108 a0001c0001t0007g0109 a0001c0001t0007g0110 others(2): Show |
5 | HG02055.hp1 HG02965.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.512+1107C>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 4/31 | chr20 | 41161260 | |||||||
| chr20:41161294 | G | A | 5 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(2): Show |
5 | HG02074.hp2 NA18943.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.512+1141G>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 4/31 | chr20 | 41161294 | |||||||
| chr20:41161393 | G | C | 1 | a0001c0001t0001g0238 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.513-1059G>C | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 4/31 | chr20 | 41161393 | |||||||
| chr20:41161645 | C | T | 5 | a0001c0001t0007g0108 a0001c0001t0007g0109 a0001c0001t0007g0110 others(2): Show |
5 | HG02055.hp1 HG02965.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.513-807C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 4/31 | chr20 | 41161645 | |||||||
| chr20:41161795 | C | T | 10 | a0001c0001t0001g0031 a0001c0001t0001g0048 a0001c0001t0001g0053 others(7): Show |
11 | HG00642.hp2 HG01123.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.513-657C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 4/31 | chr20 | 41161795 | |||||||
| chr20:41161821 | G | A | 1 | a0002c0013t0017g0193 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.513-631G>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 4/31 | chr20 | 41161821 | |||||||
| chr20:41161860 | C | T | 1 | a0001c0001t0006g0114 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.513-592C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 4/31 | chr20 | 41161860 | |||||||
| chr20:41161877 | C | T | 2 | a0001c0005t0001g0150 a0001c0005t0001g0151 |
2 | HG00099.hp1 HG00280.hp2 |
intron_variant | MODIFIER | c.513-575C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 4/31 | chr20 | 41161877 | |||||||
| chr20:41161989 | C | A | 1 | a0001c0001t0001g0156 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.513-463C>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 4/31 | chr20 | 41161989 | |||||||
| chr20:41161995 | A | T | 8 | a0003c0003t0002g0024 a0003c0003t0002g0074 a0003c0003t0002g0209 others(5): Show |
9 | HG00323.hp2 HG01070.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.513-457A>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 4/31 | chr20 | 41161995 | |||||||
| chr20:41162036 | C | T | 1 | a0002c0002t0001g0188 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.513-416C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 4/31 | chr20 | 41162036 | |||||||
| chr20:41162229 | G | GT | 3 | a0001c0001t0003g0069 a0001c0001t0003g0070 a0003c0003t0002g0212 |
3 | HG01891.hp2 HG02055.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.513-218dupT | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr20 | 41162229 | ||||||
| chr20:41162234 | TG | T | 15 | a0003c0003t0002g0009 a0003c0003t0002g0050 a0003c0003t0002g0052 others(12): Show |
21 | HG00733.hp1 HG01070.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.513-217delG | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 4/31 | chr20 | 41162234 | |||||||
| chr20:41162235 | G | GT | 102 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(99): Show |
138 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.513-197dupT | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr20 | 41162235 | ||||||
| chr20:41162235 | G | GTT | 50 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(47): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.513-198_513-197dup others(2): Show |
PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr20 | 41162235 | ||||||
| chr20:41162235 | G | GTTT | 10 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(7): Show |
11 | HG01433.hp1 HG02074.hp2 HG02165.hp1 others(8): Show |
intron_variant | MODIFIER | c.513-199_513-197dup others(3): Show |
PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr20 | 41162235 | ||||||
| chr20:41162235 | G | GTTTTT | 7 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(4): Show |
7 | HG02135.hp2 HG03688.hp2 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.513-201_513-197dup others(5): Show |
PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr20 | 41162235 | ||||||
| chr20:41162235 | G | T | 6 | a0001c0001t0003g0069 a0001c0001t0003g0070 a0003c0003t0002g0024 others(3): Show |
7 | HG00323.hp2 HG01346.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.513-217G>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 4/31 | chr20 | 41162235 | |||||||
| chr20:41162241 | T | G | 2 | a0001c0001t0011g0124 a0001c0001t0020g0160 |
2 | HG02451.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.513-211T>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 4/31 | chr20 | 41162241 | |||||||
| chr20:41162256 | G | T | 1 | a0002c0002t0001g0187 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.513-196G>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 4/31 | chr20 | 41162256 | |||||||
| chr20:41162387 | C | T | 4 | a0001c0001t0001g0044 a0001c0001t0001g0159 a0001c0001t0001g0161 others(1): Show |
5 | HG01884.hp2 HG02976.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.513-65C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 4/31 | chr20 | 41162387 | |||||||
| chr20:41162429 | T | C | 1 | a0001c0001t0001g0137 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.513-23T>C | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 4/31 | chr20 | 41162429 | |||||||
| chr20:41162432 | G | C | 1 | a0001c0001t0015g0203 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.513-20G>C | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 4/31 | chr20 | 41162432 | |||||||
| chr20:41162609 | G | A | 3 | a0001c0001t0004g0227 a0001c0001t0004g0228 a0001c0001t0004g0229 |
3 | HG03017.hp2 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.598-33G>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 5/31 | chr20 | 41162609 | |||||||
| chr20:41163101 | C | T | 28 | a0001c0001t0003g0012 a0001c0001t0003g0066 a0001c0001t0004g0056 others(25): Show |
34 | HG00323.hp1 HG00621.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.717-102C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 7/31 | chr20 | 41163101 | |||||||
| chr20:41163187 | C | T | 1 | a0003c0003t0002g0210 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.717-16C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 7/31 | chr20 | 41163187 | |||||||
| chr20:41163282 | C | T | 1 | a0001c0001t0001g0046 | 2 | HG00738.hp2 HG02559.hp2 |
splice_region_variant&intron_variant | LOW | c.789+7C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 8/31 | chr20 | 41163282 | |||||||
| chr20:41163354 | C | T | 1 | a0002c0002t0001g0178 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.790-24C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 8/31 | chr20 | 41163354 | |||||||
| chr20:41163362 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.790-16C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 8/31 | chr20 | 41163362 | |||||||
| chr20:41163596 | G | A | 1 | a0001c0001t0001g0041 | 2 | HG01192.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.891+117G>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 9/31 | chr20 | 41163596 | |||||||
| chr20:41163656 | T | C | 4 | a0001c0001t0006g0045 a0001c0001t0006g0170 a0001c0001t0006g0171 others(1): Show |
5 | HG01891.hp1 HG02258.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.892-59T>C | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 9/31 | chr20 | 41163656 | |||||||
| chr20:41163898 | C | T | 39 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(36): Show |
75 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.1011-23C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 10/31 | chr20 | 41163898 | |||||||
| chr20:41164052 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1097-29C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 11/31 | chr20 | 41164052 | |||||||
| chr20:41164401 | G | A | 3 | a0001c0001t0001g0017 a0001c0001t0001g0103 a0001c0001t0001g0133 |
5 | HG01361.hp1 HG02451.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1217+200G>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 12/31 | chr20 | 41164401 | |||||||
| chr20:41164440 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1217+239G>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 12/31 | chr20 | 41164440 | |||||||
| chr20:41165107 | G | C | 5 | a0001c0001t0007g0108 a0001c0001t0007g0109 a0001c0001t0007g0110 others(2): Show |
5 | HG02055.hp1 HG02965.hp2 HG03225.hp2 others(2): Show |
splice_region_variant&intron_variant | LOW | c.1386+6G>C | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 13/31 | chr20 | 41165107 | |||||||
| chr20:41165194 | G | T | 1 | a0001c0001t0007g0110 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1387-51G>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 13/31 | chr20 | 41165194 | |||||||
| chr20:41165207 | C | A | 2 | a0001c0001t0001g0044 a0001c0001t0001g0161 |
3 | HG02976.hp1 HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1387-38C>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 13/31 | chr20 | 41165207 | |||||||
| chr20:41165849 | G | A | 199 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(196): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.1799+23G>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 16/31 | chr20 | 41165849 | |||||||
| chr20:41165864 | G | A | 14 | a0001c0001t0001g0022 a0001c0001t0003g0011 a0001c0001t0003g0022 others(11): Show |
17 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.1799+38G>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 16/31 | chr20 | 41165864 | |||||||
| chr20:41165944 | C | T | 1 | a0002c0004t0001g0047 | 2 | HG01081.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1799+118C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 16/31 | chr20 | 41165944 | |||||||
| chr20:41165990 | A | AC | 48 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(45): Show |
90 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.1799+174dupC | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr20 | 41165990 | ||||||
| chr20:41165992 | C | T | 12 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(9): Show |
13 | HG01891.hp1 HG02135.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1799+166C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 16/31 | chr20 | 41165992 | |||||||
| chr20:41165993 | C | G | 1 | a0001c0001t0001g0220 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1799+167C>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 16/31 | chr20 | 41165993 | |||||||
| chr20:41166038 | TTTGGTTC others(33): Show |
T | 1 | a0001c0001t0001g0145 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1800-151_1800-112d others(42): Show |
PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr20 | 41166038 | ||||||
| chr20:41166102 | C | G | 1 | a0001c0001t0001g0146 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1800-92C>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 16/31 | chr20 | 41166102 | |||||||
| chr20:41166135 | T | G | 3 | a0002c0002t0001g0175 a0002c0002t0001g0179 a0002c0002t0001g0205 |
3 | HG00639.hp1 HG01074.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.1800-59T>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 16/31 | chr20 | 41166135 | |||||||
| chr20:41166945 | A | G | 1 | a0001c0001t0001g0204 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2301+86A>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 19/31 | chr20 | 41166945 | |||||||
| chr20:41167032 | G | A | 14 | a0001c0001t0001g0022 a0001c0001t0003g0011 a0001c0001t0003g0022 others(11): Show |
17 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.2301+173G>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 19/31 | chr20 | 41167032 | |||||||
| chr20:41167073 | A | G | 1 | a0001c0001t0012g0123 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2301+214A>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 19/31 | chr20 | 41167073 | |||||||
| chr20:41167086 | T | C | 1 | a0002c0002t0001g0205 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2301+227T>C | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 19/31 | chr20 | 41167086 | |||||||
| chr20:41167089 | T | C | 2 | a0001c0001t0011g0124 a0001c0001t0012g0123 |
2 | HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2301+230T>C | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 19/31 | chr20 | 41167089 | |||||||
| chr20:41167427 | T | G | 10 | a0001c0001t0001g0031 a0001c0001t0001g0048 a0001c0001t0001g0053 others(7): Show |
11 | HG00642.hp2 HG01123.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.2302-425T>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 19/31 | chr20 | 41167427 | |||||||
| chr20:41167460 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2302-392G>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 19/31 | chr20 | 41167460 | |||||||
| chr20:41167640 | G | C | 1 | a0001c0001t0004g0231 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2302-212G>C | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 19/31 | chr20 | 41167640 | |||||||
| chr20:41167651 | T | G | 4 | a0001c0001t0006g0045 a0001c0001t0006g0170 a0001c0001t0006g0171 others(1): Show |
5 | HG01891.hp1 HG02258.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.2302-201T>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 19/31 | chr20 | 41167651 | |||||||
| chr20:41167759 | C | A | 1 | a0003c0003t0002g0208 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2302-93C>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 19/31 | chr20 | 41167759 | |||||||
| chr20:41168059 | G | A | 2 | a0001c0001t0001g0107 a0001c0009t0001g0106 |
2 | HG00741.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2379+130G>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 20/31 | chr20 | 41168059 | |||||||
| chr20:41168091 | G | A | 2 | a0001c0001t0011g0124 a0001c0001t0012g0123 |
2 | HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2379+162G>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 20/31 | chr20 | 41168091 | |||||||
| chr20:41168163 | T | C | 2 | a0001c0001t0004g0104 a0001c0001t0004g0105 |
2 | HG00738.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.2379+234T>C | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 20/31 | chr20 | 41168163 | |||||||
| chr20:41168383 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2380-384G>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 20/31 | chr20 | 41168383 | |||||||
| chr20:41168428 | A | G | 2 | a0001c0001t0006g0114 a0001c0001t0006g0122 |
2 | HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2380-339A>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 20/31 | chr20 | 41168428 | |||||||
| chr20:41168443 | C | T | 1 | a0002c0002t0001g0186 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2380-324C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 20/31 | chr20 | 41168443 | |||||||
| chr20:41168530 | G | T | 1 | a0003c0003t0002g0212 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2380-237G>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 20/31 | chr20 | 41168530 | |||||||
| chr20:41168552 | C | T | 1 | a0003c0003t0002g0074 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.2380-215C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 20/31 | chr20 | 41168552 | |||||||
| chr20:41168558 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2380-209C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 20/31 | chr20 | 41168558 | |||||||
| chr20:41168698 | C | T | 2 | a0001c0001t0001g0107 a0001c0009t0001g0106 |
2 | HG00741.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2380-69C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 20/31 | chr20 | 41168698 | |||||||
| chr20:41168874 | A | G | 1 | a0001c0001t0001g0196 | 1 | HG02486.hp1 | splice_region_variant&intron_variant | LOW | c.2483+4A>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 21/31 | chr20 | 41168874 | |||||||
| chr20:41168900 | C | T | 1 | a0001c0001t0020g0160 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2483+30C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 21/31 | chr20 | 41168900 | |||||||
| chr20:41169005 | C | A | 1 | a0001c0001t0003g0070 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2484-74C>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 21/31 | chr20 | 41169005 | |||||||
| chr20:41169006 | C | T | 28 | a0001c0001t0003g0012 a0001c0001t0003g0066 a0001c0001t0004g0056 others(25): Show |
34 | HG00323.hp1 HG00621.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.2484-73C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 21/31 | chr20 | 41169006 | |||||||
| chr20:41169054 | G | A | 1 | a0001c0001t0003g0070 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2484-25G>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 21/31 | chr20 | 41169054 | |||||||
| chr20:41169180 | GACCAGAA others(2): Show |
G | 2 | a0001c0001t0001g0032 a0001c0001t0001g0238 |
3 | HG00423.hp2 HG02074.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.2580+9_2580+17delA others(8): Show |
PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 22/31 | INFO_REALIGN_3_PRIME | chr20 | 41169180 | ||||||
| chr20:41169238 | C | T | 1 | a0001c0001t0012g0123 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2580+63C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 22/31 | chr20 | 41169238 | |||||||
| chr20:41169310 | G | A | 1 | a0003c0003t0009g0214 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2580+135G>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 22/31 | chr20 | 41169310 | |||||||
| chr20:41169312 | C | G | 1 | a0001c0001t0001g0128 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2580+137C>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 22/31 | chr20 | 41169312 | |||||||
| chr20:41169434 | T | C | 1 | a0001c0001t0001g0220 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2581-23T>C | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 22/31 | chr20 | 41169434 | |||||||
| chr20:41169454 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG03688.hp2 | splice_region_variant&intron_variant | LOW | c.2581-3C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 22/31 | chr20 | 41169454 | |||||||
| chr20:41169643 | C | T | 5 | a0001c0001t0007g0108 a0001c0001t0007g0109 a0001c0001t0007g0110 others(2): Show |
5 | HG02055.hp1 HG02965.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.2650+117C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 23/31 | chr20 | 41169643 | |||||||
| chr20:41169778 | G | C | 202 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(199): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.2650+252G>C | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 23/31 | chr20 | 41169778 | |||||||
| chr20:41169810 | T | TTGTA | 17 | a0001c0001t0001g0022 a0001c0001t0001g0154 a0001c0001t0003g0011 others(14): Show |
20 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.2650+285_2650+288d others(6): Show |
PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 23/31 | INFO_REALIGN_3_PRIME | chr20 | 41169810 | ||||||
| chr20:41169837 | T | G | 1 | a0001c0001t0001g0136 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2651-275T>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 23/31 | chr20 | 41169837 | |||||||
| chr20:41169844 | G | T | 1 | a0001c0001t0001g0243 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2651-268G>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 23/31 | chr20 | 41169844 | |||||||
| chr20:41169941 | T | C | 7 | a0001c0001t0001g0107 a0001c0001t0007g0108 a0001c0001t0007g0109 others(4): Show |
7 | HG00741.hp1 HG02055.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.2651-171T>C | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 23/31 | chr20 | 41169941 | |||||||
| chr20:41170045 | C | T | 2 | a0001c0001t0001g0091 a0001c0001t0001g0092 |
2 | NA18952.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.2651-67C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 23/31 | chr20 | 41170045 | |||||||
| chr20:41170046 | G | A | 2 | a0001c0001t0001g0041 a0001c0001t0001g0153 |
3 | HG00140.hp2 HG01192.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.2651-66G>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 23/31 | chr20 | 41170046 | |||||||
| chr20:41170433 | A | T | 39 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(36): Show |
75 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.2808+164A>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 24/31 | chr20 | 41170433 | |||||||
| chr20:41170843 | G | C | 1 | a0001c0001t0001g0199 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2808+574G>C | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 24/31 | chr20 | 41170843 | |||||||
| chr20:41171166 | G | A | 3 | a0001c0001t0001g0019 a0001c0001t0001g0134 a0001c0001t0001g0138 |
5 | HG01993.hp2 HG02273.hp1 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.2808+897G>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 24/31 | chr20 | 41171166 | |||||||
| chr20:41171308 | C | T | 1 | a0002c0002t0001g0185 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2809-885C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 24/31 | chr20 | 41171308 | |||||||
| chr20:41171583 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2809-610T>C | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 24/31 | chr20 | 41171583 | |||||||
| chr20:41171586 | C | CA | 10 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0133 others(7): Show |
10 | HG00642.hp2 HG01515.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.2809-584dupA | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 24/31 | INFO_REALIGN_3_PRIME | chr20 | 41171586 | ||||||
| chr20:41171586 | C | CAA | 63 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(60): Show |
96 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(93): Show |
intron_variant | MODIFIER | c.2809-585_2809-584d others(4): Show |
PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 24/31 | INFO_REALIGN_3_PRIME | chr20 | 41171586 | ||||||
| chr20:41171586 | C | CAAA | 8 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0054 others(5): Show |
11 | HG01069.hp2 HG01071.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.2809-586_2809-584d others(5): Show |
PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 24/31 | INFO_REALIGN_3_PRIME | chr20 | 41171586 | ||||||
| chr20:41171586 | CA | C | 84 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(81): Show |
136 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.2809-584delA | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 24/31 | INFO_REALIGN_3_PRIME | chr20 | 41171586 | ||||||
| chr20:41171586 | CAA | C | 21 | a0001c0001t0001g0081 a0001c0001t0001g0098 a0001c0001t0001g0166 others(18): Show |
23 | HG00323.hp1 HG00621.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.2809-585_2809-584d others(4): Show |
PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 24/31 | INFO_REALIGN_3_PRIME | chr20 | 41171586 | ||||||
| chr20:41171633 | G | A | 2 | a0001c0001t0004g0227 a0001c0001t0004g0228 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2809-560G>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 24/31 | chr20 | 41171633 | |||||||
| chr20:41171915 | C | T | 1 | a0002c0002t0001g0183 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.2809-278C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 24/31 | chr20 | 41171915 | |||||||
| chr20:41171952 | C | A | 1 | a0001c0001t0001g0038 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.2809-241C>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 24/31 | chr20 | 41171952 | |||||||
| chr20:41171952 | C | T | 4 | a0001c0001t0006g0045 a0001c0001t0006g0170 a0001c0001t0006g0171 others(1): Show |
5 | HG01891.hp1 HG02258.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.2809-241C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 24/31 | chr20 | 41171952 | |||||||
| chr20:41171974 | T | C | 1 | a0001c0001t0001g0086 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2809-219T>C | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 24/31 | chr20 | 41171974 | |||||||
| chr20:41172067 | G | GTA | 2 | a0001c0001t0001g0036 a0001c0001t0001g0141 |
3 | NA18985.hp2 NA19058.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.2809-125_2809-124d others(4): Show |
PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 24/31 | INFO_REALIGN_3_PRIME | chr20 | 41172067 | ||||||
| chr20:41172070 | C | G | 2 | a0001c0001t0001g0036 a0001c0001t0001g0141 |
3 | NA18985.hp2 NA19058.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.2809-123C>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 24/31 | chr20 | 41172070 | |||||||
| chr20:41172070 | C | T | 42 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0018 others(39): Show |
68 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.2809-123C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 24/31 | chr20 | 41172070 | |||||||
| chr20:41172372 | C | T | 5 | a0001c0001t0007g0108 a0001c0001t0007g0109 a0001c0001t0007g0110 others(2): Show |
5 | HG02055.hp1 HG02965.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.2906-49C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 25/31 | chr20 | 41172372 | |||||||
| chr20:41173047 | G | A | 1 | a0001c0001t0020g0160 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3279+170G>A | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 27/31 | chr20 | 41173047 | |||||||
| chr20:41173075 | G | C | 3 | a0001c0001t0003g0062 a0001c0001t0003g0063 a0001c0001t0003g0073 |
3 | HG02615.hp2 HG02809.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.3279+198G>C | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 27/31 | chr20 | 41173075 | |||||||
| chr20:41173247 | C | T | 1 | a0002c0002t0001g0183 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.3280-173C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 27/31 | chr20 | 41173247 | |||||||
| chr20:41173259 | G | C | 9 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(6): Show |
9 | HG02135.hp2 HG03688.hp2 NA18946.hp1 others(6): Show |
intron_variant | MODIFIER | c.3280-161G>C | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 27/31 | chr20 | 41173259 | |||||||
| chr20:41173274 | TGTC | T | 3 | a0001c0001t0001g0044 a0001c0001t0001g0161 a0001c0001t0001g0162 |
4 | HG02976.hp1 HG03579.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.3280-143_3280-141d others(5): Show |
PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 27/31 | INFO_REALIGN_3_PRIME | chr20 | 41173274 | ||||||
| chr20:41173277 | C | G | 1 | a0002c0002t0001g0003 | 2 | HG03017.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.3280-143C>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 27/31 | chr20 | 41173277 | |||||||
| chr20:41173358 | C | T | 1 | a0001c0001t0020g0160 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3280-62C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 27/31 | chr20 | 41173358 | |||||||
| chr20:41173397 | G | C | 1 | a0001c0001t0005g0020 | 3 | NA18988.hp1 NA19065.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.3280-23G>C | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 27/31 | chr20 | 41173397 | |||||||
| chr20:41173617 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3395-35C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 28/31 | chr20 | 41173617 | |||||||
| chr20:41173630 | C | G | 1 | a0002c0002t0001g0182 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.3395-22C>G | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 28/31 | chr20 | 41173630 | |||||||
| chr20:41174027 | G | C | 1 | a0001c0001t0001g0153 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.3645+16G>C | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 30/31 | chr20 | 41174027 | |||||||
| chr20:41174438 | C | T | 2 | a0001c0001t0001g0030 a0001c0001t0001g0094 |
3 | NA18942.hp1 NA19084.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.3834-29C>T | PLCG1 | ENSG00000124181.15 | transcript | ENST00000685551.1 | protein_coding | 31/31 | chr20 | 41174438 |