| geneid | 23228 |
|---|---|
| ensemblid | ENSG00000154822.18 |
| hgncid | 9064 |
| symbol | PLCL2 |
| name | phospholipase C like 2 |
| refseq_nuc | NM_001144382.2 |
| refseq_prot | NP_001137854.1 |
| ensembl_nuc | ENST00000615277.5 |
| ensembl_prot | ENSP00000478458.1 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 16884955 |
| end | 17090604 |
| strand | + |
| ver | v1.2 |
| region | chr3:16884955-17090604 |
| region5000 | chr3:16879955-17095604 |
| regionname0 | PLCL2_chr3_16884955_17090604 |
| regionname5000 | PLCL2_chr3_16879955_17095604 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0000 | 0/0 | 0 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| a0001 | 1/1 | 1127 | 242 | 81 | 49 | 67 | 10 | 33 | 49 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| a0002 | 0/0 | 1127 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| a0003 | 0/0 | 1127 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| a0004 | 0/0 | 1127 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 3384 | 89 | 32 | 13 | 29 | 3 | 12 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| c0002 | 1/0 | 3384 | 86 | 35 | 13 | 24 | 4 | 9 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| c0003 | 0/0 | 3384 | 33 | 10 | 13 | 5 | 2 | 3 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| c0004 | 0/0 | 3384 | 15 | 0 | 6 | 5 | 0 | 4 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| c0005 | 0/1 | 3384 | 4 | 0 | 0 | 0 | 1 | 2 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| c0006 | 0/0 | 3384 | 4 | 0 | 0 | 3 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| c0007 | 0/0 | 3384 | 3 | 2 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| c0008 | 0/0 | 3384 | 2 | 0 | 1 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| c0009 | 0/0 | 3384 | 2 | 2 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| c0010 | 0/0 | 3384 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| c0011 | 0/0 | 3384 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| c0012 | 0/0 | 3384 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| c0013 | 0/0 | 3384 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| c0014 | 0/0 | 3384 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| c0015 | 0/0 | 3384 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| c0016 | 0/0 | 3384 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| c0017 | 0/0 | 3384 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| c0018 | 0/0 | 3384 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| c0019 | 0/0 | 3384 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| c0020 | 0/0 | 3384 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| c0021 | 0/0 | 3384 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 778 | 206 | 65 | 42 | 62 | 6 | 29 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| t0002 | 0/0 | 778 | 29 | 15 | 4 | 6 | 2 | 2 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| t0003 | 0/0 | 778 | 8 | 0 | 3 | 0 | 2 | 3 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| t0004 | 0/0 | 778 | 5 | 5 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| t0005 | 0/0 | 778 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| t0006 | 0/0 | 778 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0179 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0241 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0000c0007 | 0/0 | 3384 | 3 | 2 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| a0000c0019 | 0/0 | 3384 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| a0001c0001 | 0/0 | 3384 | 89 | 32 | 13 | 29 | 3 | 12 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| a0001c0002 | 1/0 | 3384 | 86 | 35 | 13 | 24 | 4 | 9 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| a0001c0003 | 0/0 | 3384 | 33 | 10 | 13 | 5 | 2 | 3 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| a0001c0004 | 0/0 | 3384 | 15 | 0 | 6 | 5 | 0 | 4 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| a0001c0005 | 0/1 | 3384 | 4 | 0 | 0 | 0 | 1 | 2 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| a0001c0006 | 0/0 | 3384 | 4 | 0 | 0 | 3 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| a0001c0008 | 0/0 | 3384 | 2 | 0 | 1 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| a0001c0011 | 0/0 | 3384 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| a0001c0012 | 0/0 | 3384 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| a0001c0013 | 0/0 | 3384 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| a0001c0014 | 0/0 | 3384 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| a0001c0016 | 0/0 | 3384 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| a0001c0017 | 0/0 | 3384 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| a0001c0018 | 0/0 | 3384 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| a0001c0020 | 0/0 | 3384 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| a0001c0021 | 0/0 | 3384 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| a0002c0009 | 0/0 | 3384 | 2 | 2 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| a0003c0010 | 0/0 | 3384 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| a0004c0015 | 0/0 | 3384 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0000c0007t0002 | 0/0 | 4161 | 3 | 2 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| a0000c0019t0002 | 0/0 | 4161 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| a0001c0001t0001 | 0/0 | 4161 | 67 | 19 | 10 | 27 | 1 | 10 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| a0001c0001t0002 | 0/0 | 4161 | 21 | 12 | 3 | 2 | 2 | 2 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| a0001c0001t0006 | 0/0 | 4161 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| a0001c0002t0001 | 1/0 | 4161 | 84 | 35 | 11 | 24 | 4 | 9 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| a0001c0002t0003 | 0/0 | 4161 | 2 | 0 | 2 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| a0001c0003t0001 | 0/0 | 4161 | 23 | 5 | 12 | 5 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| a0001c0003t0003 | 0/0 | 4161 | 5 | 0 | 1 | 0 | 2 | 2 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| a0001c0003t0004 | 0/0 | 4161 | 5 | 5 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| a0001c0004t0001 | 0/0 | 4161 | 11 | 0 | 6 | 1 | 0 | 4 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| a0001c0004t0002 | 0/0 | 4161 | 4 | 0 | 0 | 4 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| a0001c0005t0001 | 0/1 | 4161 | 4 | 0 | 0 | 0 | 1 | 2 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| a0001c0006t0001 | 0/0 | 4161 | 4 | 0 | 0 | 3 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| a0001c0008t0001 | 0/0 | 4161 | 2 | 0 | 1 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| a0001c0011t0001 | 0/0 | 4161 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| a0001c0012t0001 | 0/0 | 4161 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| a0001c0013t0001 | 0/0 | 4161 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| a0001c0014t0001 | 0/0 | 4161 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| a0001c0016t0001 | 0/0 | 4161 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| a0001c0017t0001 | 0/0 | 4161 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| a0001c0018t0005 | 0/0 | 4161 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| a0001c0020t0003 | 0/0 | 4161 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| a0001c0021t0001 | 0/0 | 4161 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| a0002c0009t0001 | 0/0 | 4161 | 2 | 2 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| a0003c0010t0001 | 0/0 | 4161 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| a0004c0015t0001 | 0/0 | 4161 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | copy fasta | chr3 | 16879955 | 17095604 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0000c0007t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0000c0007t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0000c0007t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0000c0019t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0001t0006g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0001g0241 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0003g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0002t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0003t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0003t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0003t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0003t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0003t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0003t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0003t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0003t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0003t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0003t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0003t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0003t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0003t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0003t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0003t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0003t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0003t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0003t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0003t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0003t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0003t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0003t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0003t0003g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0003t0003g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0003t0003g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0003t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0003t0003g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0003t0004g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0003t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0003t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0003t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0004t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0004t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0004t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0004t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0004t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0004t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0004t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0004t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0004t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0004t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0004t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0004t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0004t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0004t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0005t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0005t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0005t0001g0179 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0005t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0006t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0006t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0006t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0006t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0008t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0008t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0011t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0012t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0013t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0014t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0016t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0017t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0018t0005g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0020t0003g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0001c0021t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0002c0009t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0002c0009t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0003c0010t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| a0004c0015t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0100 | EUR | GBR | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0138 | EUR | GBR | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0054 | EUR | FIN | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG00280 | hp2 | a0001 | c0003 | t0003 | g0232 | EUR | FIN | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0145 | EUR | FIN | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0098 | EUR | FIN | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0113 | EAS | CHS | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG00741 | hp1 | a0001 | c0002 | t0003 | g0064 | AMR | PUR | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG00741 | hp2 | a0001 | c0003 | t0003 | g0231 | AMR | PUR | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0071 | AMR | PUR | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG01069 | hp2 | a0001 | c0004 | t0001 | g0162 | AMR | PUR | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0024 | AMR | PUR | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0073 | AMR | PUR | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG01081 | hp1 | a0001 | c0016 | t0001 | g0093 | AMR | PUR | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG01099 | hp1 | a0001 | c0003 | t0001 | g0189 | AMR | PUR | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0143 | AMR | PUR | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0028 | AMR | PUR | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG01106 | hp2 | a0001 | c0003 | t0001 | g0235 | AMR | PUR | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0151 | AMR | PUR | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0097 | AMR | PUR | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG01175 | hp1 | a0001 | c0008 | t0001 | g0242 | AMR | PUR | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG01243 | hp1 | a0000 | c0007 | t0002 | g0146 | AMR | PUR | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG01243 | hp2 | a0001 | c0003 | t0001 | g0192 | AMR | PUR | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0025 | AMR | CLM | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0070 | AMR | CLM | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0026 | AMR | CLM | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0099 | AMR | CLM | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG01433 | hp2 | a0001 | c0003 | t0001 | g0187 | AMR | CLM | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0108 | EUR | IBS | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG01515 | hp2 | a0001 | c0005 | t0001 | g0063 | EUR | IBS | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0046 | EUR | IBS | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG01516 | hp2 | a0001 | c0003 | t0003 | g0216 | EUR | IBS | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG01891 | hp1 | a0000 | c0019 | t0002 | g0148 | AFR | ACB | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0233 | AFR | ACB | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG01928 | hp2 | a0001 | c0003 | t0001 | g0191 | AMR | PEL | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG01934 | hp1 | a0001 | c0003 | t0001 | g0094 | AMR | PEL | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG01934 | hp2 | a0001 | c0004 | t0001 | g0164 | AMR | PEL | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG01943 | hp1 | a0001 | c0003 | t0001 | g0190 | AMR | PEL | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG01952 | hp1 | a0001 | c0003 | t0001 | g0044 | AMR | PEL | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG01952 | hp2 | a0001 | c0004 | t0001 | g0163 | AMR | PEL | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG01975 | hp1 | a0001 | c0003 | t0001 | g0194 | AMR | PEL | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG01975 | hp2 | a0001 | c0004 | t0001 | g0165 | AMR | PEL | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG01978 | hp1 | a0001 | c0003 | t0001 | g0248 | AMR | PEL | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG01978 | hp2 | a0001 | c0018 | t0005 | g0029 | AMR | PEL | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0212 | AMR | PEL | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG01993 | hp2 | a0001 | c0021 | t0001 | g0177 | AMR | PEL | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0027 | AMR | PEL | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02004 | hp2 | a0001 | c0003 | t0001 | g0180 | AMR | PEL | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0061 | EAS | KHV | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02055 | hp1 | a0001 | c0012 | t0001 | g0005 | AFR | ACB | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02074 | hp1 | a0001 | c0004 | t0002 | g0173 | EAS | KHV | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0114 | EAS | KHV | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | KHV | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0031 | EAS | KHV | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0095 | EAS | KHV | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02155 | hp1 | a0001 | c0004 | t0002 | g0172 | EAS | CDX | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02155 | hp2 | a0001 | c0006 | t0001 | g0160 | EAS | CDX | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | CDX | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0111 | EAS | CDX | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0007 | AFR | ACB | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0032 | AFR | ACB | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0238 | AFR | ACB | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02273 | hp1 | a0001 | c0003 | t0001 | g0188 | AMR | PEL | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02273 | hp2 | a0001 | c0004 | t0001 | g0167 | AMR | PEL | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02280 | hp1 | a0001 | c0003 | t0001 | g0003 | AFR | ACB | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02280 | hp2 | a0001 | c0002 | t0001 | g0210 | AFR | ACB | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02300 | hp1 | a0001 | c0004 | t0001 | g0166 | AMR | PEL | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02300 | hp2 | a0001 | c0002 | t0003 | g0065 | AMR | PEL | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0080 | AFR | ACB | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02602 | hp2 | a0001 | c0020 | t0003 | g0178 | SAS | PJL | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | GWD | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0199 | AFR | GWD | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02683 | hp1 | a0001 | c0003 | t0003 | g0209 | SAS | PJL | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02683 | hp2 | a0001 | c0006 | t0001 | g0161 | SAS | PJL | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0074 | AFR | GWD | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0137 | AFR | GWD | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0205 | AFR | GWD | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0133 | AFR | GWD | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0096 | SAS | PJL | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0069 | SAS | PJL | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0159 | AFR | GWD | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0047 | AFR | GWD | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0092 | AFR | GWD | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0136 | AFR | GWD | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0091 | AFR | GWD | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0125 | AFR | GWD | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | GWD | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0126 | AFR | GWD | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0240 | AFR | ESN | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | ESN | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | ESN | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02965 | hp2 | a0001 | c0013 | t0001 | g0198 | AFR | ESN | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0156 | AFR | ESN | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0122 | AFR | ESN | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02976 | hp1 | a0000 | c0007 | t0002 | g0213 | AFR | ESN | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | ESN | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0244 | SAS | PJL | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0223 | SAS | PJL | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0132 | AFR | GWD | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0010 | AFR | MSL | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0079 | AFR | MSL | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG03130 | hp1 | a0001 | c0003 | t0001 | g0106 | AFR | ESN | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | ESN | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG03139 | hp1 | a0001 | c0003 | t0004 | g0128 | AFR | ESN | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0206 | AFR | ESN | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0066 | AFR | ESN | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0129 | AFR | ESN | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | MSL | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0076 | AFR | MSL | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG03225 | hp1 | a0002 | c0009 | t0001 | g0154 | AFR | MSL | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG03225 | hp2 | a0001 | c0003 | t0001 | g0030 | AFR | MSL | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0134 | AFR | MSL | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0121 | AFR | MSL | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0068 | AFR | MSL | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | MSL | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0140 | SAS | PJL | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG03490 | hp2 | a0001 | c0003 | t0003 | g0215 | SAS | PJL | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG03491 | hp1 | a0001 | c0004 | t0001 | g0002 | SAS | PJL | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG03491 | hp2 | a0001 | c0005 | t0001 | g0019 | SAS | PJL | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0141 | SAS | PJL | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG03492 | hp2 | a0001 | c0004 | t0001 | g0002 | SAS | PJL | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG03516 | hp1 | a0001 | c0003 | t0001 | g0211 | AFR | ESN | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0130 | AFR | ESN | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0149 | AFR | GWD | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | GWD | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0048 | SAS | PJL | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG03704 | hp1 | a0001 | c0005 | t0001 | g0185 | SAS | PJL | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG03710 | hp2 | a0001 | c0003 | t0001 | g0184 | SAS | PJL | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | BEB | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0085 | SAS | BEB | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0245 | SAS | BEB | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0058 | SAS | BEB | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | BEB | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG03927 | hp2 | a0001 | c0004 | t0001 | g0176 | SAS | BEB | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0060 | SAS | STU | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | STU | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG04199 | hp1 | a0001 | c0008 | t0001 | g0123 | SAS | STU | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0158 | SAS | STU | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG04228 | hp1 | a0003 | c0010 | t0001 | g0049 | SAS | STU | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | STU | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | YRI | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA18522 | hp2 | a0001 | c0003 | t0004 | g0152 | AFR | YRI | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0045 | EAS | CHB | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CHB | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA18906 | hp1 | a0001 | c0003 | t0004 | g0001 | AFR | YRI | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA18906 | hp2 | a0002 | c0009 | t0001 | g0155 | AFR | YRI | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA18949 | hp1 | a0001 | c0002 | t0001 | g0062 | EAS | JPT | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA18950 | hp2 | a0001 | c0004 | t0001 | g0168 | EAS | JPT | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA18956 | hp2 | a0001 | c0003 | t0001 | g0116 | EAS | JPT | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA18966 | hp1 | a0001 | c0004 | t0002 | g0175 | EAS | JPT | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA18966 | hp2 | a0004 | c0015 | t0001 | g0072 | EAS | JPT | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA18973 | hp2 | a0001 | c0003 | t0001 | g0186 | EAS | JPT | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0107 | EAS | JPT | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA18991 | hp2 | a0001 | c0003 | t0001 | g0181 | EAS | JPT | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA18993 | hp1 | a0001 | c0017 | t0001 | g0050 | EAS | JPT | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0052 | EAS | JPT | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | LWK | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0075 | AFR | LWK | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA19043 | hp1 | a0001 | c0001 | t0006 | g0222 | AFR | LWK | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA19043 | hp2 | a0001 | c0014 | t0001 | g0104 | AFR | LWK | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA19056 | hp2 | a0001 | c0006 | t0001 | g0174 | EAS | JPT | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA19065 | hp1 | a0001 | c0003 | t0001 | g0018 | EAS | JPT | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA19079 | hp2 | a0001 | c0003 | t0001 | g0193 | EAS | JPT | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA19088 | hp1 | a0001 | c0004 | t0002 | g0171 | EAS | JPT | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA19240 | hp1 | a0000 | c0007 | t0002 | g0147 | AFR | YRI | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | YRI | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA20129 | hp1 | a0001 | c0003 | t0001 | g0196 | AFR | ASW | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0077 | AFR | ASW | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA20905 | hp1 | a0001 | c0004 | t0001 | g0169 | SAS | GIH | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0057 | SAS | GIH | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0142 | AMR | CLM | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | CLM | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02109 | hp1 | a0001 | c0011 | t0001 | g0004 | AFR | ACB | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0131 | AFR | ACB | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02486 | hp1 | a0001 | c0003 | t0004 | g0153 | AFR | ACB | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0120 | AFR | ACB | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0124 | AFR | ACB | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0207 | AFR | ACB | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | MSL | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0208 | AFR | MSL | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG06807 | hp1 | a0001 | c0003 | t0004 | g0001 | AFR | USA | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0204 | AFR | USA | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA18955 | hp1 | a0001 | c0006 | t0001 | g0170 | EAS | JPT | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0214 | AFR | USA | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0011 | AFR | USA | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0078 | AFR | LWK | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0144 | AFR | LWK | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0005 | t0001 | g0179 | REF | REF | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0241 | REF | REF | PLCL2_chr3_16879955_17095604 | PLCL2 | chr3 | 16879955 | 17095604 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:16885062
|
G | A | 1 | a0003 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.23G>A | p.Gly8Asp | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/6 | 108/4161 | 23/3384 | 8/1127 | chr3 | 16885062 | ||
| chr3:16885313
|
C | T | 1 | a0000 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.274C>T | p.Leu92Phe | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/6 | 359/4161 | 274/3384 | 92/1127 | chr3 | 16885313 | ||
| chr3:16885324
|
G | T | 1 | a0000 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.285G>T | p.Glu95Asp | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/6 | 370/4161 | 285/3384 | 95/1127 | chr3 | 16885324 | ||
| chr3:17011833
|
T | G | 1 | a0004 | 1 | NA18966.hp2 | missense_variant | MODERATE | c.2487T>G | p.Phe829Leu | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 2/6 | 2572/4161 | 2487/3384 | 829/1127 | chr3 | 17011833 | ||
| chr3:17014786
|
C | T | 1 | a0002 | 2 | HG03225.hp1 NA18906.hp2 |
missense_variant | MODERATE | c.2893C>T | p.Pro965Ser | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/6 | 2978/4161 | 2893/3384 | 965/1127 | chr3 | 17014786 | ||
| chr3:17089910
|
T | G | 1 | a0000 | 4 | HG01243.hp1 HG01891.hp1 HG02976.hp1 others(1): Show |
stop_lost | HIGH | c.3382T>G | p.Ter1128Glyext*? | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 6/6 | 3467/4161 | 3382/3384 | 1128/1127 | chr3 | 17089910 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:16885267
|
C | T | 4 | a0001c0004a0001c0006a0001c0020others(1): Show | 21 | HG01069.hp2 HG01934.hp2 HG01952.hp2 others(18): Show |
synonymous_variant | LOW | c.228C>T | p.Pro76Pro | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/6 | 313/4161 | 228/3384 | 76/1127 | chr3 | 16885267 | ||
| chr3:17009836
|
T | C | 9 | a0000c0007a0000c0019a0001c0001others(6): Show | 105 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(102): Show |
synonymous_variant | LOW | c.490T>C | p.Leu164Leu | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 2/6 | 575/4161 | 490/3384 | 164/1127 | chr3 | 17009836 | ||
| chr3:17009958
|
C | A | 2 | a0001c0004a0001c0008 | 17 | HG01069.hp2 HG01175.hp1 HG01934.hp2 others(14): Show |
synonymous_variant | LOW | c.612C>A | p.Arg204Arg | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 2/6 | 697/4161 | 612/3384 | 204/1127 | chr3 | 17009958 | ||
| chr3:17011101
|
C | T | 1 | a0001c0021 | 1 | HG01993.hp2 | synonymous_variant | LOW | c.1755C>T | p.Asp585Asp | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 2/6 | 1840/4161 | 1755/3384 | 585/1127 | chr3 | 17011101 | ||
| chr3:17011200
|
G | C | 2 | a0001c0011a0001c0012 | 2 | HG02055.hp1 HG02109.hp1 |
synonymous_variant | LOW | c.1854G>C | p.Leu618Leu | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 2/6 | 1939/4161 | 1854/3384 | 618/1127 | chr3 | 17011200 | ||
| chr3:17011254
|
G | C | 1 | a0001c0011 | 1 | HG02109.hp1 | synonymous_variant | LOW | c.1908G>C | p.Ser636Ser | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 2/6 | 1993/4161 | 1908/3384 | 636/1127 | chr3 | 17011254 | ||
| chr3:17011509
|
C | T | 1 | a0001c0005 | 4 | HG01515.hp2 HG03491.hp2 HG03704.hp1 others(1): Show |
synonymous_variant | LOW | c.2163C>T | p.Asn721Asn | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 2/6 | 2248/4161 | 2163/3384 | 721/1127 | chr3 | 17011509 | ||
| chr3:17012007
|
A | G | 15 | a0000c0007a0000c0019a0001c0001others(12): Show | 158 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(155): Show |
synonymous_variant | LOW | c.2661A>G | p.Gly887Gly | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 2/6 | 2746/4161 | 2661/3384 | 887/1127 | chr3 | 17012007 | ||
| chr3:17012077
|
C | T | 1 | a0001c0017 | 1 | NA18993.hp1 | synonymous_variant | LOW | c.2731C>T | p.Leu911Leu | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 2/6 | 2816/4161 | 2731/3384 | 911/1127 | chr3 | 17012077 | ||
| chr3:17012121
|
C | T | 1 | a0001c0016 | 1 | HG01081.hp1 | synonymous_variant | LOW | c.2775C>T | p.Pro925Pro | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 2/6 | 2860/4161 | 2775/3384 | 925/1127 | chr3 | 17012121 | ||
| chr3:17014809
|
C | T | 1 | a0001c0014 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.2916C>T | p.Asn972Asn | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/6 | 3001/4161 | 2916/3384 | 972/1127 | chr3 | 17014809 | ||
| chr3:17089882
|
C | T | 2 | a0001c0013a0001c0018 | 2 | HG01978.hp2 HG02965.hp2 |
synonymous_variant | LOW | c.3354C>T | p.Pro1118Pro | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 6/6 | 3439/4161 | 3354/3384 | 1118/1127 | chr3 | 17089882 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:17089929
|
C | T | 3 | a0001c0002t0003a0001c0003t0003a0001c0020t0003 | 8 | HG00280.hp2 HG00741.hp1 HG00741.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*17C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 6/6 | 17 | chr3 | 17089929 | |||||
| chr3:17090009
|
C | T | 3 | a0001c0002t0003a0001c0003t0003a0001c0020t0003 | 8 | HG00280.hp2 HG00741.hp1 HG00741.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*97C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 6/6 | 97 | chr3 | 17090009 | |||||
| chr3:17090091
|
A | G | 1 | a0001c0001t0006 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*179A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 6/6 | 179 | chr3 | 17090091 | |||||
| chr3:17090248
|
T | C | 1 | a0001c0018t0005 | 1 | HG01978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*336T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 6/6 | 336 | chr3 | 17090248 | |||||
| chr3:17090414
|
G | A | 1 | a0001c0003t0004 | 5 | HG02486.hp1 HG03139.hp1 HG06807.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*502G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 6/6 | 502 | chr3 | 17090414 | |||||
| chr3:17090513
|
A | G | 4 | a0000c0007t0002a0000c0019t0002a0001c0001t0002others(1): Show | 29 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*601A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 6/6 | 601 | chr3 | 17090513 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:16885451
|
G | A | 3 | a0001c0003t0001g0003a0001c0011t0001g0004a0001c0012t0001g0005 | 3 | HG02055.hp1 HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.327+85G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16885451 | ||||||
| chr3:16885663
|
C | A | 158 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0019t0002g0148others(155): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.327+297C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16885663 | ||||||
| chr3:16885997
|
C | T | 1 | a0001c0003t0001g0248 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.327+631C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16885997 | ||||||
| chr3:16886263
|
C | T | 1 | a0001c0001t0002g0159 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.327+897C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16886263 | ||||||
| chr3:16886438
|
T | A | 2 | a0001c0006t0001g0160a0001c0006t0001g0161 | 2 | HG02155.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.327+1072T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16886438 | ||||||
| chr3:16886528
|
T | C | 20 | a0001c0004t0001g0002a0001c0004t0001g0162a0001c0004t0001g0163others(17): Show | 21 | HG01069.hp2 HG01934.hp2 HG01952.hp2 others(18): Show |
intron_variant | MODIFIER | c.327+1162T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16886528 | ||||||
| chr3:16886567
|
T | A | 46 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0195others(43): Show | 47 | HG01069.hp2 HG01099.hp1 HG01243.hp2 others(44): Show |
intron_variant | MODIFIER | c.327+1201T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16886567 | ||||||
| chr3:16886593
|
G | A | 39 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0195others(36): Show | 40 | HG01069.hp2 HG01099.hp1 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.327+1227G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16886593 | ||||||
| chr3:16886628
|
G | A | 5 | a0001c0001t0002g0204a0001c0002t0001g0205a0001c0002t0001g0206others(2): Show | 5 | HG02559.hp2 HG02723.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.327+1262G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16886628 | ||||||
| chr3:16886638
|
G | C | 46 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0195others(43): Show | 47 | HG01069.hp2 HG01099.hp1 HG01243.hp2 others(44): Show |
intron_variant | MODIFIER | c.327+1272G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16886638 | ||||||
| chr3:16886692
|
G | A | 3 | a0001c0003t0001g0003a0001c0011t0001g0004a0001c0012t0001g0005 | 3 | HG02055.hp1 HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.327+1326G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16886692 | ||||||
| chr3:16887115
|
T | A | 1 | a0001c0002t0001g0006 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.327+1749T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16887115 | ||||||
| chr3:16887122
|
C | T | 20 | a0001c0004t0001g0002a0001c0004t0001g0162a0001c0004t0001g0163others(17): Show | 21 | HG01069.hp2 HG01934.hp2 HG01952.hp2 others(18): Show |
intron_variant | MODIFIER | c.327+1756C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16887122 | ||||||
| chr3:16887169
|
G | A | 1 | a0001c0005t0001g0179 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.327+1803G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16887169 | ||||||
| chr3:16887381
|
T | C | 1 | a0001c0003t0003g0209 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.327+2015T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16887381 | ||||||
| chr3:16887415
|
C | T | 19 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0195others(16): Show | 19 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.327+2049C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16887415 | ||||||
| chr3:16887589
|
T | C | 26 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0195others(23): Show | 26 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(23): Show |
intron_variant | MODIFIER | c.327+2223T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16887589 | ||||||
| chr3:16887610
|
T | C | 46 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0195others(43): Show | 47 | HG01069.hp2 HG01099.hp1 HG01243.hp2 others(44): Show |
intron_variant | MODIFIER | c.327+2244T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16887610 | ||||||
| chr3:16887834
|
A | G | 20 | a0001c0004t0001g0002a0001c0004t0001g0162a0001c0004t0001g0163others(17): Show | 21 | HG01069.hp2 HG01934.hp2 HG01952.hp2 others(18): Show |
intron_variant | MODIFIER | c.327+2468A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16887834 | ||||||
| chr3:16887855
|
A | G | 1 | a0001c0002t0001g0158 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.327+2489A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16887855 | ||||||
| chr3:16887989
|
A | G | 150 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0019t0002g0148others(147): Show | 151 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.327+2623A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16887989 | ||||||
| chr3:16888094
|
C | T | 44 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0195others(41): Show | 45 | HG01069.hp2 HG01099.hp1 HG01243.hp2 others(42): Show |
intron_variant | MODIFIER | c.327+2728C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16888094 | ||||||
| chr3:16888177
|
G | A | 5 | a0001c0001t0001g0197a0001c0003t0001g0003a0001c0011t0001g0004others(2): Show | 5 | HG02055.hp1 HG02109.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.327+2811G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16888177 | ||||||
| chr3:16888477
|
C | G | 1 | a0001c0001t0001g0157 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.327+3111C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16888477 | ||||||
| chr3:16888548
|
G | A | 117 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(114): Show | 117 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.327+3182G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16888548 | ||||||
| chr3:16888551
|
A | G | 2 | a0001c0002t0001g0125a0001c0002t0001g0126 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.327+3185A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16888551 | ||||||
| chr3:16888726
|
A | T | 1 | a0001c0020t0003g0178 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.327+3360A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16888726 | ||||||
| chr3:16888778
|
G | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG02027.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.327+3412G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16888778 | ||||||
| chr3:16889151
|
A | G | 1 | a0001c0021t0001g0177 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.327+3785A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16889151 | ||||||
| chr3:16889366
|
G | T | 1 | a0001c0002t0001g0124 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.327+4000G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16889366 | ||||||
| chr3:16889410
|
A | G | 1 | a0001c0001t0002g0156 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.327+4044A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16889410 | ||||||
| chr3:16889477
|
C | T | 10 | a0001c0001t0001g0197a0001c0001t0001g0243a0001c0001t0001g0244others(7): Show | 10 | HG01123.hp2 HG02055.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.327+4111C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16889477 | ||||||
| chr3:16889522
|
G | C | 5 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(2): Show | 5 | NA18747.hp2 NA18942.hp1 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.327+4156G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16889522 | ||||||
| chr3:16889600
|
G | A | 1 | a0001c0003t0001g0180 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.327+4234G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16889600 | ||||||
| chr3:16889872
|
A | AT | 13 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(10): Show | 13 | HG00408.hp1 HG00408.hp2 HG02129.hp1 others(10): Show |
intron_variant | MODIFIER | c.327+4515dupT | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16889872 | |||||
| chr3:16890020
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.327+4654A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16890020 | ||||||
| chr3:16890040
|
C | A | 5 | a0001c0001t0001g0197a0001c0003t0001g0003a0001c0011t0001g0004others(2): Show | 5 | HG02055.hp1 HG02109.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.327+4674C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16890040 | ||||||
| chr3:16890061
|
C | T | 20 | a0001c0004t0001g0002a0001c0004t0001g0162a0001c0004t0001g0163others(17): Show | 21 | HG01069.hp2 HG01934.hp2 HG01952.hp2 others(18): Show |
intron_variant | MODIFIER | c.327+4695C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16890061 | ||||||
| chr3:16890119
|
C | T | 1 | a0001c0001t0001g0109 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.327+4753C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16890119 | ||||||
| chr3:16890125
|
A | G | 1 | a0001c0001t0001g0108 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.327+4759A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16890125 | ||||||
| chr3:16890350
|
A | G | 1 | a0001c0002t0001g0107 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.327+4984A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16890350 | ||||||
| chr3:16890867
|
A | G | 20 | a0001c0004t0001g0002a0001c0004t0001g0162a0001c0004t0001g0163others(17): Show | 21 | HG01069.hp2 HG01934.hp2 HG01952.hp2 others(18): Show |
intron_variant | MODIFIER | c.327+5501A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16890867 | ||||||
| chr3:16890931
|
G | T | 1 | a0001c0002t0001g0006 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.327+5565G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16890931 | ||||||
| chr3:16891174
|
G | C | 2 | a0001c0002t0001g0007a0001c0002t0001g0210 | 2 | HG02257.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.327+5808G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16891174 | ||||||
| chr3:16891190
|
A | G | 1 | a0001c0003t0001g0106 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.327+5824A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16891190 | ||||||
| chr3:16891211
|
C | T | 21 | a0001c0004t0001g0002a0001c0004t0001g0162a0001c0004t0001g0163others(18): Show | 22 | HG01069.hp2 HG01175.hp1 HG01934.hp2 others(19): Show |
intron_variant | MODIFIER | c.327+5845C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16891211 | ||||||
| chr3:16891436
|
T | C | 1 | a0001c0003t0001g0181 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.327+6070T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16891436 | ||||||
| chr3:16891490
|
G | A | 43 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0195others(40): Show | 44 | HG01069.hp2 HG01099.hp1 HG01175.hp1 others(41): Show |
intron_variant | MODIFIER | c.327+6124G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16891490 | ||||||
| chr3:16891518
|
GTTTTGGT others(3): Show |
G | 5 | a0001c0001t0001g0197a0001c0003t0001g0003a0001c0011t0001g0004others(2): Show | 5 | HG02055.hp1 HG02109.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.327+6156_327+6165d others(12): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16891518 | |||||
| chr3:16891567
|
G | C | 1 | a0001c0002t0001g0020 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.327+6201G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16891567 | ||||||
| chr3:16891975
|
C | T | 4 | a0001c0002t0001g0205a0001c0002t0001g0206a0001c0002t0001g0207others(1): Show | 4 | HG02559.hp2 HG02723.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+6609C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16891975 | ||||||
| chr3:16892106
|
A | C | 1 | a0001c0003t0001g0196 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.327+6740A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16892106 | ||||||
| chr3:16892132
|
A | T | 1 | a0001c0002t0001g0105 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.327+6766A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16892132 | ||||||
| chr3:16892298
|
G | A | 1 | a0001c0006t0001g0160 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.327+6932G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16892298 | ||||||
| chr3:16892315
|
T | C | 1 | a0001c0002t0001g0111 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.327+6949T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16892315 | ||||||
| chr3:16892431
|
G | A | 1 | a0001c0003t0001g0211 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.327+7065G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16892431 | ||||||
| chr3:16892439
|
CT | C | 140 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(137): Show | 141 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.327+7074delT | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16892439 | ||||||
| chr3:16892625
|
T | A | 1 | a0001c0003t0003g0215 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.327+7259T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16892625 | ||||||
| chr3:16892822
|
T | G | 4 | a0001c0002t0001g0021a0001c0002t0001g0022a0001c0002t0001g0023others(1): Show | 4 | NA18950.hp1 NA18955.hp2 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+7456T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16892822 | ||||||
| chr3:16892865
|
A | T | 5 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(2): Show | 5 | HG02965.hp1 HG02976.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.327+7499A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16892865 | ||||||
| chr3:16893067
|
T | C | 1 | a0001c0014t0001g0104 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.327+7701T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16893067 | ||||||
| chr3:16893196
|
T | C | 1 | a0001c0001t0001g0243 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.327+7830T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16893196 | ||||||
| chr3:16893197
|
C | A | 1 | a0001c0001t0001g0243 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.327+7831C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16893197 | ||||||
| chr3:16893251
|
T | C | 5 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0001g0245others(2): Show | 5 | HG01123.hp2 HG03017.hp1 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.327+7885T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16893251 | ||||||
| chr3:16893314
|
TAAC | T | 4 | a0001c0003t0001g0003a0001c0011t0001g0004a0001c0012t0001g0005others(1): Show | 4 | HG02055.hp1 HG02109.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+7952_327+7954d others(5): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16893314 | |||||
| chr3:16893668
|
G | T | 1 | a0001c0002t0001g0096 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.327+8302G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16893668 | ||||||
| chr3:16893701
|
A | G | 2 | a0001c0004t0001g0176a0001c0008t0001g0123 | 2 | HG03927.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.327+8335A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16893701 | ||||||
| chr3:16893820
|
A | C | 5 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(2): Show | 5 | HG02965.hp1 HG02976.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.327+8454A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16893820 | ||||||
| chr3:16893940
|
T | C | 143 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(140): Show | 144 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.327+8574T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16893940 | ||||||
| chr3:16893949
|
T | C | 20 | a0001c0001t0001g0195a0001c0003t0001g0018a0001c0003t0001g0180others(17): Show | 20 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.327+8583T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16893949 | ||||||
| chr3:16894572
|
G | A | 2 | a0001c0002t0001g0113a0001c0002t0001g0114 | 2 | HG00408.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.327+9206G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16894572 | ||||||
| chr3:16894573
|
G | A | 1 | a0001c0003t0003g0216 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.327+9207G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16894573 | ||||||
| chr3:16894665
|
C | T | 2 | a0002c0009t0001g0154a0002c0009t0001g0155 | 2 | HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.327+9299C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16894665 | ||||||
| chr3:16894711
|
A | G | 2 | a0002c0009t0001g0154a0002c0009t0001g0155 | 2 | HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.327+9345A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16894711 | ||||||
| chr3:16894732
|
GGCCATTT others(4588): Show |
G | 1 | a0001c0002t0001g0208 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.327+9367_327+13961 others(3): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16894732 | ||||||
| chr3:16894740
|
G | A | 1 | a0001c0006t0001g0160 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.327+9374G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16894740 | ||||||
| chr3:16894744
|
ATTCTC | A | 2 | a0001c0004t0001g0002a0001c0004t0001g0169 | 3 | HG03491.hp1 HG03492.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.327+9381_327+9385d others(7): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16894744 | |||||
| chr3:16894811
|
W | A | 244 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(241): Show | 246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.327+9445T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16894811 | ||||||
| chr3:16894811
|
W | T | 2 | a0001c0001t0001g0197a0001c0002t0001g0240 | 2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.327+9445A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16894811 | ||||||
| chr3:16895061
|
C | CGTATCTA others(27): Show |
1 | a0001c0014t0001g0104 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.327+9706_327+9739d others(36): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16895061 | |||||
| chr3:16895068
|
A | G | 1 | a0001c0001t0001g0239 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.327+9702A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16895068 | ||||||
| chr3:16895072
|
A | AGATATAG others(27): Show |
3 | a0001c0001t0001g0243a0001c0003t0001g0094a0001c0004t0002g0175 | 3 | HG01934.hp1 HG03704.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.327+9761_327+9794d others(36): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16895072 | |||||
| chr3:16895072
|
A | C | 2 | a0002c0009t0001g0154a0002c0009t0001g0155 | 2 | HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.327+9706A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16895072 | ||||||
| chr3:16895072
|
AGATATAG others(27): Show |
A | 20 | a0001c0001t0001g0195a0001c0003t0001g0018a0001c0003t0001g0180others(17): Show | 20 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.327+9761_327+9794d others(36): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16895072 | |||||
| chr3:16895106
|
C | A | 6 | a0001c0001t0001g0197a0001c0003t0001g0003a0001c0011t0001g0004others(3): Show | 6 | HG02055.hp1 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.327+9740C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16895106 | ||||||
| chr3:16895106
|
C | T | 1 | a0001c0002t0001g0095 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.327+9740C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16895106 | ||||||
| chr3:16895334
|
A | C | 20 | a0001c0001t0001g0195a0001c0003t0001g0018a0001c0003t0001g0180others(17): Show | 20 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.327+9968A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16895334 | ||||||
| chr3:16895382
|
C | T | 2 | a0002c0009t0001g0154a0002c0009t0001g0155 | 2 | HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.327+10016C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16895382 | ||||||
| chr3:16895733
|
C | T | 1 | a0001c0003t0004g0153 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.327+10367C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16895733 | ||||||
| chr3:16895741
|
A | G | 1 | a0001c0016t0001g0093 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.327+10375A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16895741 | ||||||
| chr3:16895777
|
G | C | 1 | a0001c0002t0001g0024 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.327+10411G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16895777 | ||||||
| chr3:16895781
|
C | T | 5 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(2): Show | 5 | HG02965.hp1 HG02976.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.327+10415C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16895781 | ||||||
| chr3:16895972
|
T | A | 2 | a0002c0009t0001g0154a0002c0009t0001g0155 | 2 | HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.327+10606T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16895972 | ||||||
| chr3:16896067
|
G | A | 4 | a0001c0003t0001g0003a0001c0011t0001g0004a0001c0012t0001g0005others(1): Show | 4 | HG02055.hp1 HG02109.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+10701G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16896067 | ||||||
| chr3:16896156
|
T | C | 1 | a0001c0002t0001g0115 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.327+10790T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16896156 | ||||||
| chr3:16896197
|
C | T | 2 | a0001c0002t0001g0091a0001c0002t0001g0092 | 2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.327+10831C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16896197 | ||||||
| chr3:16896415
|
A | C | 20 | a0001c0001t0001g0195a0001c0003t0001g0018a0001c0003t0001g0180others(17): Show | 20 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.327+11049A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16896415 | ||||||
| chr3:16896475
|
T | C | 1 | a0001c0004t0001g0162 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.327+11109T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16896475 | ||||||
| chr3:16896596
|
A | T | 1 | a0001c0001t0001g0090 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.327+11230A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16896596 | ||||||
| chr3:16896669
|
G | A | 4 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0219others(1): Show | 4 | HG02895.hp2 HG03041.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+11303G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16896669 | ||||||
| chr3:16896695
|
C | T | 2 | a0002c0009t0001g0154a0002c0009t0001g0155 | 2 | HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.327+11329C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16896695 | ||||||
| chr3:16896913
|
C | T | 4 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103others(1): Show | 4 | HG02818.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+11547C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16896913 | ||||||
| chr3:16897072
|
G | A | 1 | a0001c0001t0002g0127 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.327+11706G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16897072 | ||||||
| chr3:16897125
|
G | T | 32 | a0001c0001t0001g0195a0001c0001t0001g0197a0001c0001t0001g0200others(29): Show | 32 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(29): Show |
intron_variant | MODIFIER | c.327+11759G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16897125 | ||||||
| chr3:16897290
|
A | G | 4 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0182others(1): Show | 4 | NA18991.hp1 NA18993.hp2 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+11924A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16897290 | ||||||
| chr3:16897293
|
A | G | 1 | a0001c0001t0002g0151 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.327+11927A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16897293 | ||||||
| chr3:16897301
|
T | TA | 6 | a0001c0001t0001g0203a0001c0002t0001g0212a0001c0003t0001g0003others(3): Show | 6 | HG01981.hp1 HG02055.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.327+11947dupA | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16897301 | |||||
| chr3:16897395
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.327+12029G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16897395 | ||||||
| chr3:16897723
|
T | C | 1 | a0001c0001t0006g0222 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.327+12357T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16897723 | ||||||
| chr3:16897844
|
A | G | 2 | a0002c0009t0001g0154a0002c0009t0001g0155 | 2 | HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.327+12478A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16897844 | ||||||
| chr3:16897937
|
C | A | 4 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0027others(1): Show | 4 | HG01106.hp1 HG01255.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+12571C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16897937 | ||||||
| chr3:16897947
|
C | A | 143 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(140): Show | 144 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.327+12581C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16897947 | ||||||
| chr3:16897989
|
A | AT | 54 | a0001c0001t0001g0195a0001c0001t0001g0197a0001c0001t0001g0200others(51): Show | 55 | HG00099.hp1 HG00323.hp2 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.327+12633dupT | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16897989 | |||||
| chr3:16897989
|
AT | A | 10 | a0001c0002t0001g0007a0001c0002t0001g0008a0001c0002t0001g0009others(7): Show | 10 | HG02257.hp1 HG02280.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.327+12633delT | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16897989 | |||||
| chr3:16898008
|
C | T | 1 | a0001c0002t0001g0011 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.327+12642C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16898008 | ||||||
| chr3:16898130
|
C | T | 1 | a0001c0012t0001g0005 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.327+12764C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16898130 | ||||||
| chr3:16898243
|
C | G | 7 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(4): Show | 7 | HG02559.hp2 HG02723.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.327+12877C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16898243 | ||||||
| chr3:16898255
|
T | C | 210 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(207): Show | 212 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.327+12889T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16898255 | ||||||
| chr3:16898414
|
G | GA | 5 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0001g0245others(2): Show | 5 | HG01123.hp2 HG03017.hp1 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.327+13055dupA | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16898414 | |||||
| chr3:16898563
|
A | G | 1 | a0001c0001t0001g0195 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.327+13197A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16898563 | ||||||
| chr3:16898659
|
G | T | 20 | a0001c0002t0001g0098a0001c0002t0001g0099a0001c0002t0001g0100others(17): Show | 21 | HG00099.hp1 HG00323.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.327+13293G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16898659 | ||||||
| chr3:16898755
|
G | A | 9 | a0001c0001t0001g0195a0001c0003t0001g0018a0001c0003t0001g0181others(6): Show | 9 | HG01943.hp2 HG03491.hp2 HG03704.hp1 others(6): Show |
intron_variant | MODIFIER | c.327+13389G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16898755 | ||||||
| chr3:16898843
|
A | G | 1 | a0001c0001t0001g0203 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.327+13477A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16898843 | ||||||
| chr3:16898873
|
T | C | 21 | a0001c0001t0001g0195a0001c0001t0001g0197a0001c0001t0001g0200others(18): Show | 21 | HG01943.hp2 HG02055.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.327+13507T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16898873 | ||||||
| chr3:16899015
|
C | T | 1 | a0001c0002t0001g0087 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.327+13649C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16899015 | ||||||
| chr3:16899452
|
A | G | 1 | a0001c0002t0001g0214 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.327+14086A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16899452 | ||||||
| chr3:16899472
|
T | C | 1 | a0001c0001t0001g0088 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.327+14106T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16899472 | ||||||
| chr3:16899580
|
T | G | 5 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(2): Show | 5 | HG02965.hp1 HG02976.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.327+14214T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16899580 | ||||||
| chr3:16899588
|
C | T | 3 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010 | 3 | HG02896.hp2 HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.327+14222C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16899588 | ||||||
| chr3:16899781
|
A | C | 1 | a0001c0003t0004g0153 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.327+14415A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16899781 | ||||||
| chr3:16899989
|
G | C | 212 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(209): Show | 214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.327+14623G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16899989 | ||||||
| chr3:16900217
|
C | G | 1 | a0001c0001t0001g0086 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.327+14851C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16900217 | ||||||
| chr3:16900246
|
G | A | 1 | a0001c0002t0001g0098 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.327+14880G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16900246 | ||||||
| chr3:16900841
|
T | C | 211 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(208): Show | 213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.327+15475T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16900841 | ||||||
| chr3:16900919
|
G | A | 212 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(209): Show | 214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.327+15553G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16900919 | ||||||
| chr3:16901018
|
A | C | 21 | a0001c0002t0001g0098a0001c0002t0001g0099a0001c0002t0001g0100others(18): Show | 22 | HG00099.hp1 HG00323.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.327+15652A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16901018 | ||||||
| chr3:16901162
|
T | C | 32 | a0001c0001t0001g0195a0001c0001t0001g0197a0001c0001t0001g0200others(29): Show | 32 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(29): Show |
intron_variant | MODIFIER | c.327+15796T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16901162 | ||||||
| chr3:16901208
|
C | G | 1 | a0001c0002t0001g0085 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.327+15842C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16901208 | ||||||
| chr3:16901259
|
G | A | 1 | a0001c0002t0001g0096 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.327+15893G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16901259 | ||||||
| chr3:16901289
|
G | C | 145 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(142): Show | 146 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.327+15923G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16901289 | ||||||
| chr3:16901404
|
A | G | 3 | a0001c0003t0001g0003a0001c0011t0001g0004a0001c0012t0001g0005 | 3 | HG02055.hp1 HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.327+16038A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16901404 | ||||||
| chr3:16901569
|
A | G | 20 | a0001c0001t0001g0195a0001c0003t0001g0018a0001c0003t0001g0180others(17): Show | 20 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.327+16203A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16901569 | ||||||
| chr3:16901873
|
C | G | 3 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202 | 3 | HG02976.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.327+16507C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16901873 | ||||||
| chr3:16901944
|
C | T | 4 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083others(1): Show | 4 | HG01256.hp1 HG01928.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+16578C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16901944 | ||||||
| chr3:16901957
|
A | G | 2 | a0002c0009t0001g0154a0002c0009t0001g0155 | 2 | HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.327+16591A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16901957 | ||||||
| chr3:16902148
|
C | T | 28 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(25): Show | 28 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.327+16782C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16902148 | ||||||
| chr3:16902223
|
G | A | 4 | a0001c0003t0001g0030a0001c0003t0001g0094a0001c0003t0001g0106others(1): Show | 4 | HG01934.hp1 HG01978.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+16857G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16902223 | ||||||
| chr3:16902301
|
T | C | 20 | a0001c0001t0001g0195a0001c0003t0001g0018a0001c0003t0001g0180others(17): Show | 20 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.327+16935T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16902301 | ||||||
| chr3:16902382
|
C | T | 32 | a0001c0001t0001g0195a0001c0001t0001g0197a0001c0001t0001g0200others(29): Show | 32 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(29): Show |
intron_variant | MODIFIER | c.327+17016C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16902382 | ||||||
| chr3:16902562
|
C | T | 1 | a0001c0002t0001g0238 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.327+17196C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16902562 | ||||||
| chr3:16902620
|
G | T | 1 | a0001c0001t0001g0247 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.327+17254G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16902620 | ||||||
| chr3:16902681
|
G | A | 2 | a0002c0009t0001g0154a0002c0009t0001g0155 | 2 | HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.327+17315G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16902681 | ||||||
| chr3:16902820
|
C | G | 143 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(140): Show | 144 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.327+17454C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16902820 | ||||||
| chr3:16902826
|
C | CA | 44 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0219others(41): Show | 45 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.327+17479dupA | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16902826 | |||||
| chr3:16902826
|
CA | C | 37 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083others(34): Show | 37 | HG01074.hp1 HG01074.hp2 HG01256.hp1 others(34): Show |
intron_variant | MODIFIER | c.327+17479delA | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16902826 | |||||
| chr3:16902843
|
A | ATGC | 18 | a0001c0001t0001g0195a0001c0003t0001g0003a0001c0003t0001g0018others(15): Show | 18 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.327+17477_327+1747 others(7): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16902843 | ||||||
| chr3:16902845
|
A | G | 18 | a0001c0001t0001g0195a0001c0003t0001g0003a0001c0003t0001g0018others(15): Show | 18 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.327+17479A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16902845 | ||||||
| chr3:16902849
|
A | ATGTGTGT | 7 | a0001c0003t0001g0187a0001c0003t0001g0188a0001c0003t0001g0189others(4): Show | 7 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.327+17483_327+1748 others(11): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16902849 | ||||||
| chr3:16902849
|
A | ATGTGTGT others(2): Show |
8 | a0001c0001t0001g0195a0001c0003t0001g0018a0001c0003t0001g0180others(5): Show | 8 | HG01943.hp2 HG01975.hp1 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.327+17483_327+1748 others(13): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16902849 | ||||||
| chr3:16902853
|
C | CAT | 3 | a0001c0001t0001g0203a0001c0005t0001g0179a0001c0014t0001g0104 | 3 | HG02965.hp1 NA19043.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.327+17487_327+1748 others(6): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16902853 | ||||||
| chr3:16902853
|
C | CATGT | 3 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202 | 3 | HG02976.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.327+17487_327+1748 others(8): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16902853 | ||||||
| chr3:16902853
|
C | CATGTGTG others(7): Show |
2 | a0001c0003t0001g0196a0002c0009t0001g0154 | 2 | HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.327+17487_327+1748 others(18): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16902853 | ||||||
| chr3:16902853
|
C | CATGTGTG others(9): Show |
2 | a0001c0005t0001g0019a0002c0009t0001g0155 | 2 | HG03491.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.327+17487_327+1748 others(20): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16902853 | ||||||
| chr3:16902853
|
C | CATGTGTG others(13): Show |
1 | a0001c0005t0001g0185 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.327+17487_327+1748 others(24): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16902853 | ||||||
| chr3:16902853
|
C | CGT | 5 | a0001c0002t0001g0206a0001c0002t0001g0207a0001c0002t0001g0208others(2): Show | 5 | HG02559.hp2 HG02683.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.327+17515_327+1751 others(6): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16902853 | |||||
| chr3:16902853
|
C | CGTGT | 19 | a0001c0001t0006g0222a0001c0004t0001g0002a0001c0004t0001g0162others(16): Show | 20 | HG01069.hp2 HG01934.hp2 HG01975.hp2 others(17): Show |
intron_variant | MODIFIER | c.327+17513_327+1751 others(8): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16902853 | |||||
| chr3:16902853
|
C | CGTGTGT | 6 | a0001c0002t0001g0098a0001c0002t0001g0099a0001c0002t0001g0100others(3): Show | 6 | HG00099.hp1 HG00323.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.327+17511_327+1751 others(10): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16902853 | |||||
| chr3:16902853
|
C | T | 18 | a0001c0001t0001g0195a0001c0003t0001g0003a0001c0003t0001g0018others(15): Show | 18 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.327+17487C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16902853 | ||||||
| chr3:16902853
|
CGTGT | C | 4 | a0001c0001t0002g0129a0001c0001t0002g0130a0001c0001t0002g0151others(1): Show | 4 | HG01109.hp1 HG02970.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+17513_327+1751 others(8): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16902853 | |||||
| chr3:16902854
|
G | A | 1 | a0001c0003t0001g0184 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.327+17488G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16902854 | ||||||
| chr3:16902873
|
TGTGTGTG others(3): Show |
T | 1 | a0001c0002t0001g0112 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.327+17508_327+1751 others(14): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16902873 | ||||||
| chr3:16902879
|
TGTGB | T | 117 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(114): Show | 117 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.327+17514_327+1751 others(8): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16902879 | ||||||
| chr3:16902881
|
T | C | 30 | a0001c0001t0001g0195a0001c0001t0001g0200a0001c0001t0001g0201others(27): Show | 30 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(27): Show |
intron_variant | MODIFIER | c.327+17515T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16902881 | ||||||
| chr3:16902881
|
T | TGTGTGTG others(7): Show |
1 | a0001c0003t0001g0184 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.327+17516_327+1751 others(18): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16902881 | |||||
| chr3:16902881
|
TGB | T | 21 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(18): Show | 22 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.327+17516_327+1751 others(6): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16902881 | ||||||
| chr3:16902883
|
B | C | 38 | a0001c0001t0001g0195a0001c0001t0001g0197a0001c0001t0001g0200others(35): Show | 38 | HG01099.hp1 HG01109.hp1 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.327+17517G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16902883 | ||||||
| chr3:16902883
|
B | T | 70 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103others(67): Show | 71 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.327+17517C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16902883 | ||||||
| chr3:16902885
|
C | T | 1 | a0001c0004t0002g0175 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.327+17519C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16902885 | ||||||
| chr3:16903105
|
GACGATTT others(15): Show |
G | 1 | a0001c0005t0001g0185 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.327+17741_327+1776 others(26): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16903105 | |||||
| chr3:16903108
|
G | A | 2 | a0001c0003t0004g0152a0001c0003t0004g0153 | 2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.327+17742G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16903108 | ||||||
| chr3:16903262
|
T | G | 1 | a0001c0014t0001g0104 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.327+17896T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16903262 | ||||||
| chr3:16903281
|
A | T | 2 | a0002c0009t0001g0154a0002c0009t0001g0155 | 2 | HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.327+17915A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16903281 | ||||||
| chr3:16903604
|
G | A | 1 | a0001c0004t0002g0171 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.327+18238G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16903604 | ||||||
| chr3:16903630
|
C | T | 1 | a0001c0002t0001g0199 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.327+18264C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16903630 | ||||||
| chr3:16903736
|
C | T | 3 | a0001c0002t0001g0007a0001c0002t0001g0199a0001c0002t0001g0210 | 3 | HG02257.hp1 HG02280.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.327+18370C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16903736 | ||||||
| chr3:16903958
|
T | G | 1 | a0001c0002t0001g0032 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.327+18592T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16903958 | ||||||
| chr3:16904067
|
T | C | 1 | a0001c0002t0001g0223 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.327+18701T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16904067 | ||||||
| chr3:16904083
|
GAGCACCT | G | 5 | a0001c0001t0001g0197a0001c0003t0001g0003a0001c0011t0001g0004others(2): Show | 5 | HG02055.hp1 HG02109.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.327+18720_327+1872 others(11): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16904083 | |||||
| chr3:16904306
|
C | CAAAAAAA others(4): Show |
1 | a0001c0001t0001g0203 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.327+18941_327+1895 others(15): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16904306 | |||||
| chr3:16904306
|
C | CAAAAAAA others(10): Show |
1 | a0001c0001t0001g0197 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.327+18951_327+1895 others(21): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16904306 | |||||
| chr3:16904306
|
C | CAAAAAAA others(11): Show |
3 | a0001c0003t0001g0003a0001c0011t0001g0004a0001c0013t0001g0198 | 3 | HG02109.hp1 HG02280.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.327+18951_327+1895 others(22): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16904306 | |||||
| chr3:16904306
|
C | CAAAAAAA others(12): Show |
4 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(1): Show | 4 | HG02055.hp1 HG02976.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+18951_327+1895 others(23): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16904306 | |||||
| chr3:16904306
|
C | CAAAAAAA others(13): Show |
11 | a0001c0001t0001g0195a0001c0003t0001g0184a0001c0003t0001g0187others(8): Show | 11 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.327+18951_327+1895 others(24): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16904306 | |||||
| chr3:16904306
|
C | CAAAAAAA others(14): Show |
7 | a0001c0003t0001g0180a0001c0003t0001g0186a0001c0003t0001g0193others(4): Show | 7 | HG01978.hp1 HG02004.hp2 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.327+18951_327+1895 others(25): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16904306 | |||||
| chr3:16904306
|
C | CAAAAAAA others(15): Show |
3 | a0001c0003t0001g0018a0001c0003t0001g0181a0001c0005t0001g0179 | 3 | NA18991.hp2 NA19065.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.327+18951_327+1895 others(26): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16904306 | |||||
| chr3:16904397
|
G | A | 1 | a0001c0002t0001g0033 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.327+19031G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16904397 | ||||||
| chr3:16904581
|
C | A | 4 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133others(1): Show | 4 | HG02109.hp2 HG02723.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+19215C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16904581 | ||||||
| chr3:16904737
|
A | G | 1 | a0001c0001t0001g0236 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.327+19371A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16904737 | ||||||
| chr3:16904781
|
GT | G | 30 | a0001c0001t0001g0195a0001c0001t0001g0197a0001c0001t0001g0200others(27): Show | 30 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(27): Show |
intron_variant | MODIFIER | c.327+19416delT | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16904781 | ||||||
| chr3:16904787
|
G | A | 12 | a0001c0001t0002g0129a0001c0001t0002g0130a0001c0001t0002g0131others(9): Show | 12 | HG01109.hp1 HG02109.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.327+19421G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16904787 | ||||||
| chr3:16905187
|
C | T | 3 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202 | 3 | HG02976.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.327+19821C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16905187 | ||||||
| chr3:16905341
|
C | A | 30 | a0001c0001t0001g0195a0001c0001t0001g0197a0001c0001t0001g0200others(27): Show | 30 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(27): Show |
intron_variant | MODIFIER | c.327+19975C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16905341 | ||||||
| chr3:16905428
|
C | T | 4 | a0001c0003t0001g0003a0001c0011t0001g0004a0001c0012t0001g0005others(1): Show | 4 | HG02055.hp1 HG02109.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+20062C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16905428 | ||||||
| chr3:16905556
|
TA | T | 3 | a0001c0002t0001g0007a0001c0002t0001g0199a0001c0002t0001g0210 | 3 | HG02257.hp1 HG02280.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.327+20191delA | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16905556 | ||||||
| chr3:16905959
|
A | G | 124 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(121): Show | 125 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.327+20593A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16905959 | ||||||
| chr3:16906236
|
C | T | 8 | a0001c0001t0001g0197a0001c0002t0001g0007a0001c0002t0001g0199others(5): Show | 8 | HG02055.hp1 HG02109.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.327+20870C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16906236 | ||||||
| chr3:16906271
|
G | A | 2 | a0001c0001t0001g0224a0001c0001t0001g0239 | 2 | HG02622.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.327+20905G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16906271 | ||||||
| chr3:16906331
|
C | T | 1 | a0001c0001t0002g0127 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.327+20965C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16906331 | ||||||
| chr3:16906352
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.327+20986C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16906352 | ||||||
| chr3:16906414
|
A | G | 1 | a0001c0002t0001g0068 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.327+21048A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16906414 | ||||||
| chr3:16906433
|
C | T | 1 | a0001c0004t0001g0167 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.327+21067C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16906433 | ||||||
| chr3:16906959
|
G | C | 168 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(165): Show | 170 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.327+21593G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16906959 | ||||||
| chr3:16907106
|
C | A | 1 | a0001c0001t0001g0203 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.327+21740C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16907106 | ||||||
| chr3:16907186
|
CT | C | 34 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(31): Show | 35 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.327+21821delT | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16907186 | ||||||
| chr3:16907274
|
A | G | 2 | a0001c0002t0001g0066a0001c0002t0001g0214 | 2 | HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.327+21908A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16907274 | ||||||
| chr3:16907377
|
T | A | 9 | a0001c0001t0001g0197a0001c0001t0006g0222a0001c0002t0001g0007others(6): Show | 9 | HG02055.hp1 HG02109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.327+22011T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16907377 | ||||||
| chr3:16907716
|
C | A | 1 | a0001c0002t0001g0240 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.327+22350C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16907716 | ||||||
| chr3:16907821
|
G | T | 1 | a0001c0001t0001g0203 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.327+22455G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16907821 | ||||||
| chr3:16907862
|
C | T | 1 | a0001c0014t0001g0104 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.327+22496C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16907862 | ||||||
| chr3:16908022
|
G | A | 116 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(113): Show | 117 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.327+22656G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16908022 | ||||||
| chr3:16908236
|
C | G | 1 | a0001c0001t0001g0086 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.327+22870C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16908236 | ||||||
| chr3:16908248
|
A | G | 8 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(5): Show | 8 | HG02559.hp2 HG02723.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.327+22882A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16908248 | ||||||
| chr3:16908437
|
C | T | 1 | a0001c0001t0001g0234 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.327+23071C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16908437 | ||||||
| chr3:16908809
|
T | C | 1 | a0001c0002t0001g0158 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.327+23443T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16908809 | ||||||
| chr3:16908847
|
A | G | 3 | a0001c0002t0001g0068a0001c0002t0001g0091a0001c0002t0001g0092 | 3 | HG02818.hp2 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.327+23481A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16908847 | ||||||
| chr3:16908867
|
A | G | 24 | a0001c0002t0001g0098a0001c0002t0001g0099a0001c0002t0001g0100others(21): Show | 25 | HG00099.hp1 HG00323.hp2 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.327+23501A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16908867 | ||||||
| chr3:16909194
|
T | G | 1 | a0001c0002t0001g0045 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.327+23828T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16909194 | ||||||
| chr3:16910063
|
G | A | 1 | a0001c0005t0001g0185 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.327+24697G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16910063 | ||||||
| chr3:16910083
|
A | G | 2 | a0002c0009t0001g0154a0002c0009t0001g0155 | 2 | HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.327+24717A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16910083 | ||||||
| chr3:16910120
|
A | G | 2 | a0001c0002t0003g0064a0001c0002t0003g0065 | 2 | HG00741.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.327+24754A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16910120 | ||||||
| chr3:16910152
|
T | C | 4 | a0001c0003t0001g0003a0001c0011t0001g0004a0001c0012t0001g0005others(1): Show | 4 | HG02055.hp1 HG02109.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+24786T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16910152 | ||||||
| chr3:16910158
|
T | A | 148 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(145): Show | 150 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.327+24792T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16910158 | ||||||
| chr3:16910276
|
T | C | 175 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(172): Show | 177 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.327+24910T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16910276 | ||||||
| chr3:16910394
|
G | A | 1 | a0001c0002t0001g0020 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.327+25028G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16910394 | ||||||
| chr3:16910447
|
C | T | 1 | a0001c0006t0001g0160 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.327+25081C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16910447 | ||||||
| chr3:16910463
|
C | A | 1 | a0001c0001t0001g0090 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.327+25097C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16910463 | ||||||
| chr3:16910521
|
G | C | 1 | a0001c0002t0001g0223 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.327+25155G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16910521 | ||||||
| chr3:16910755
|
A | T | 4 | a0001c0003t0001g0003a0001c0011t0001g0004a0001c0012t0001g0005others(1): Show | 4 | HG02055.hp1 HG02109.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+25389A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16910755 | ||||||
| chr3:16910796
|
T | G | 2 | a0001c0002t0001g0024a0001c0002t0001g0073 | 2 | HG01074.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.327+25430T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16910796 | ||||||
| chr3:16910797
|
T | C | 2 | a0001c0002t0001g0024a0001c0002t0001g0073 | 2 | HG01074.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.327+25431T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16910797 | ||||||
| chr3:16910868
|
A | G | 1 | a0001c0001t0006g0222 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.327+25502A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16910868 | ||||||
| chr3:16910912
|
C | T | 1 | a0002c0009t0001g0155 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.327+25546C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16910912 | ||||||
| chr3:16910972
|
G | A | 19 | a0001c0003t0001g0018a0001c0003t0001g0180a0001c0003t0001g0181others(16): Show | 19 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.327+25606G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16910972 | ||||||
| chr3:16911018
|
G | A | 1 | a0001c0003t0004g0128 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.327+25652G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16911018 | ||||||
| chr3:16911147
|
G | A | 4 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103others(1): Show | 4 | HG02818.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+25781G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16911147 | ||||||
| chr3:16911183
|
G | A | 1 | a0001c0003t0003g0216 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.327+25817G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16911183 | ||||||
| chr3:16911196
|
T | C | 2 | a0001c0002t0001g0091a0001c0002t0001g0092 | 2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.327+25830T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16911196 | ||||||
| chr3:16911252
|
C | CA | 9 | a0001c0001t0001g0086a0001c0001t0001g0150a0001c0001t0001g0203others(6): Show | 10 | HG02055.hp2 HG02132.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.327+25907dupA | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16911252 | |||||
| chr3:16911252
|
CA | C | 8 | a0001c0001t0001g0067a0001c0001t0001g0157a0001c0002t0001g0033others(5): Show | 8 | HG01516.hp2 HG02135.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.327+25907delA | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16911252 | |||||
| chr3:16911845
|
A | G | 139 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(136): Show | 140 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.327+26479A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16911845 | ||||||
| chr3:16911963
|
A | G | 4 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103others(1): Show | 4 | HG02818.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+26597A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16911963 | ||||||
| chr3:16912150
|
C | T | 3 | a0001c0002t0001g0098a0001c0002t0001g0099a0001c0002t0001g0100 | 3 | HG00099.hp1 HG00323.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.327+26784C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16912150 | ||||||
| chr3:16912778
|
A | G | 1 | a0001c0003t0001g0192 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.327+27412A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16912778 | ||||||
| chr3:16912808
|
C | T | 1 | a0001c0004t0001g0162 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.327+27442C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16912808 | ||||||
| chr3:16913153
|
C | A | 21 | a0001c0002t0001g0098a0001c0002t0001g0099a0001c0002t0001g0100others(18): Show | 22 | HG00099.hp1 HG00323.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.327+27787C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16913153 | ||||||
| chr3:16913182
|
T | A | 1 | a0001c0001t0001g0195 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.327+27816T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16913182 | ||||||
| chr3:16913449
|
T | C | 1 | a0001c0016t0001g0093 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.327+28083T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16913449 | ||||||
| chr3:16913728
|
C | T | 19 | a0001c0003t0001g0018a0001c0003t0001g0180a0001c0003t0001g0181others(16): Show | 19 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.327+28362C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16913728 | ||||||
| chr3:16913767
|
G | A | 100 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(97): Show | 100 | HG00280.hp2 HG00408.hp1 HG00741.hp1 others(97): Show |
intron_variant | MODIFIER | c.327+28401G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16913767 | ||||||
| chr3:16913822
|
G | T | 25 | a0001c0002t0001g0098a0001c0002t0001g0099a0001c0002t0001g0100others(22): Show | 26 | HG00099.hp1 HG00323.hp2 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.327+28456G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16913822 | ||||||
| chr3:16913899
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.327+28533G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16913899 | ||||||
| chr3:16914616
|
G | A | 1 | a0001c0008t0001g0242 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.327+29250G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16914616 | ||||||
| chr3:16914786
|
G | T | 30 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(27): Show | 30 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.327+29420G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16914786 | ||||||
| chr3:16915163
|
A | T | 1 | a0001c0002t0001g0124 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.327+29797A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16915163 | ||||||
| chr3:16915245
|
C | A | 1 | a0001c0002t0001g0046 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.327+29879C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16915245 | ||||||
| chr3:16915468
|
T | TTTC | 3 | a0001c0002t0001g0007a0001c0002t0001g0199a0001c0002t0001g0210 | 3 | HG02257.hp1 HG02280.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.327+30102_327+3010 others(7): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16915468 | ||||||
| chr3:16915840
|
G | T | 98 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(95): Show | 98 | HG00280.hp2 HG00408.hp1 HG00741.hp2 others(95): Show |
intron_variant | MODIFIER | c.327+30474G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16915840 | ||||||
| chr3:16915878
|
G | T | 4 | a0001c0003t0001g0003a0001c0011t0001g0004a0001c0012t0001g0005others(1): Show | 4 | HG02055.hp1 HG02109.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+30512G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16915878 | ||||||
| chr3:16916219
|
C | T | 98 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(95): Show | 98 | HG00280.hp2 HG00408.hp1 HG00741.hp2 others(95): Show |
intron_variant | MODIFIER | c.327+30853C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16916219 | ||||||
| chr3:16916264
|
G | A | 4 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(1): Show | 4 | HG02896.hp2 HG03098.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+30898G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16916264 | ||||||
| chr3:16916662
|
G | C | 206 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(203): Show | 208 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.327+31296G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16916662 | ||||||
| chr3:16916829
|
G | T | 1 | a0001c0016t0001g0093 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.327+31463G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16916829 | ||||||
| chr3:16916863
|
C | T | 1 | a0001c0002t0001g0205 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.327+31497C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16916863 | ||||||
| chr3:16916875
|
C | T | 96 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(93): Show | 96 | HG00280.hp2 HG00408.hp1 HG00741.hp2 others(93): Show |
intron_variant | MODIFIER | c.327+31509C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16916875 | ||||||
| chr3:16916902
|
C | T | 1 | a0001c0014t0001g0104 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.327+31536C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16916902 | ||||||
| chr3:16916927
|
T | C | 3 | a0001c0002t0001g0007a0001c0002t0001g0199a0001c0002t0001g0210 | 3 | HG02257.hp1 HG02280.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.327+31561T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16916927 | ||||||
| chr3:16916970
|
C | T | 1 | a0001c0001t0002g0145 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.327+31604C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16916970 | ||||||
| chr3:16916971
|
G | A | 98 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(95): Show | 98 | HG00280.hp2 HG00408.hp1 HG00741.hp2 others(95): Show |
intron_variant | MODIFIER | c.327+31605G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16916971 | ||||||
| chr3:16916975
|
G | A | 3 | a0001c0002t0001g0007a0001c0002t0001g0199a0001c0002t0001g0210 | 3 | HG02257.hp1 HG02280.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.327+31609G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16916975 | ||||||
| chr3:16917006
|
A | G | 21 | a0001c0002t0001g0098a0001c0002t0001g0099a0001c0002t0001g0100others(18): Show | 22 | HG00099.hp1 HG00323.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.327+31640A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16917006 | ||||||
| chr3:16917340
|
A | G | 4 | a0001c0003t0001g0003a0001c0011t0001g0004a0001c0012t0001g0005others(1): Show | 4 | HG02055.hp1 HG02109.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+31974A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16917340 | ||||||
| chr3:16917361
|
C | A | 1 | a0001c0002t0001g0011 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.327+31995C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16917361 | ||||||
| chr3:16917420
|
G | C | 3 | a0001c0002t0001g0007a0001c0002t0001g0199a0001c0002t0001g0210 | 3 | HG02257.hp1 HG02280.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.327+32054G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16917420 | ||||||
| chr3:16917583
|
C | A | 135 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(132): Show | 136 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.327+32217C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16917583 | ||||||
| chr3:16917586
|
T | C | 3 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202 | 3 | HG02976.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.327+32220T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16917586 | ||||||
| chr3:16917827
|
G | A | 124 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(121): Show | 125 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.327+32461G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16917827 | ||||||
| chr3:16917956
|
A | G | 1 | a0001c0001t0001g0197 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.327+32590A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16917956 | ||||||
| chr3:16918012
|
G | GA | 19 | a0001c0003t0001g0018a0001c0003t0001g0180a0001c0003t0001g0181others(16): Show | 19 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.327+32652dupA | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16918012 | |||||
| chr3:16918040
|
C | T | 98 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(95): Show | 98 | HG00280.hp2 HG00408.hp1 HG00741.hp2 others(95): Show |
intron_variant | MODIFIER | c.327+32674C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16918040 | ||||||
| chr3:16918160
|
G | A | 98 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(95): Show | 98 | HG00280.hp2 HG00408.hp1 HG00741.hp2 others(95): Show |
intron_variant | MODIFIER | c.327+32794G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16918160 | ||||||
| chr3:16918287
|
A | G | 3 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017 | 3 | NA18942.hp1 NA18949.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.327+32921A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16918287 | ||||||
| chr3:16918397
|
C | T | 1 | a0001c0006t0001g0161 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.327+33031C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16918397 | ||||||
| chr3:16918450
|
T | C | 2 | a0001c0002t0001g0025a0001c0002t0001g0026 | 2 | HG01255.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.327+33084T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16918450 | ||||||
| chr3:16918472
|
G | A | 24 | a0001c0002t0001g0098a0001c0002t0001g0099a0001c0002t0001g0100others(21): Show | 25 | HG00099.hp1 HG00323.hp2 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.327+33106G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16918472 | ||||||
| chr3:16918689
|
G | A | 71 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(68): Show | 71 | HG00280.hp2 HG00408.hp1 HG00741.hp1 others(68): Show |
intron_variant | MODIFIER | c.327+33323G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16918689 | ||||||
| chr3:16918816
|
G | A | 1 | a0001c0002t0001g0045 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.327+33450G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16918816 | ||||||
| chr3:16918818
|
A | G | 2 | a0001c0001t0001g0197a0001c0001t0006g0222 | 2 | HG02258.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.327+33452A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16918818 | ||||||
| chr3:16919773
|
A | G | 105 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(102): Show | 105 | HG00280.hp2 HG00408.hp1 HG00741.hp1 others(102): Show |
intron_variant | MODIFIER | c.327+34407A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16919773 | ||||||
| chr3:16919960
|
C | T | 16 | a0001c0003t0001g0018a0001c0003t0001g0180a0001c0003t0001g0181others(13): Show | 16 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.327+34594C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16919960 | ||||||
| chr3:16920017
|
A | C | 3 | a0001c0002t0001g0233a0001c0002t0001g0238a0001c0002t0001g0240 | 3 | HG01891.hp2 HG02258.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.327+34651A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16920017 | ||||||
| chr3:16920106
|
A | C | 1 | a0001c0001t0001g0239 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.327+34740A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16920106 | ||||||
| chr3:16920438
|
A | G | 10 | a0001c0002t0001g0031a0001c0002t0001g0111a0001c0002t0001g0113others(7): Show | 10 | HG00408.hp2 HG00741.hp1 HG02129.hp1 others(7): Show |
intron_variant | MODIFIER | c.327+35072A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16920438 | ||||||
| chr3:16920867
|
T | A | 19 | a0001c0003t0001g0018a0001c0003t0001g0180a0001c0003t0001g0181others(16): Show | 19 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.327+35501T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16920867 | ||||||
| chr3:16921182
|
A | T | 1 | a0001c0002t0001g0097 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.327+35816A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16921182 | ||||||
| chr3:16921274
|
C | G | 1 | a0001c0014t0001g0104 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.327+35908C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16921274 | ||||||
| chr3:16921356
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.327+35990C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16921356 | ||||||
| chr3:16921537
|
G | A | 1 | a0001c0002t0001g0074 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.327+36171G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16921537 | ||||||
| chr3:16922551
|
C | T | 1 | a0001c0001t0001g0234 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.327+37185C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16922551 | ||||||
| chr3:16922620
|
A | G | 2 | a0002c0009t0001g0154a0002c0009t0001g0155 | 2 | HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.327+37254A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16922620 | ||||||
| chr3:16922718
|
A | G | 1 | a0001c0013t0001g0198 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.327+37352A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16922718 | ||||||
| chr3:16922766
|
TAG | T | 67 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(64): Show | 67 | HG00280.hp2 HG00408.hp1 HG00741.hp2 others(64): Show |
intron_variant | MODIFIER | c.327+37404_327+3740 others(6): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16922766 | |||||
| chr3:16923366
|
A | G | 2 | a0001c0001t0002g0130a0001c0001t0002g0156 | 2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.327+38000A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16923366 | ||||||
| chr3:16923529
|
T | C | 78 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(75): Show | 78 | HG00280.hp2 HG00408.hp1 HG00741.hp1 others(75): Show |
intron_variant | MODIFIER | c.327+38163T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16923529 | ||||||
| chr3:16923558
|
A | G | 2 | a0001c0001t0001g0197a0001c0001t0006g0222 | 2 | HG02258.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.327+38192A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16923558 | ||||||
| chr3:16923626
|
T | C | 1 | a0001c0001t0001g0035 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.327+38260T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16923626 | ||||||
| chr3:16923631
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.327+38265C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16923631 | ||||||
| chr3:16923719
|
C | T | 2 | a0002c0009t0001g0154a0002c0009t0001g0155 | 2 | HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.327+38353C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16923719 | ||||||
| chr3:16923724
|
T | C | 105 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(102): Show | 105 | HG00280.hp2 HG00408.hp1 HG00741.hp1 others(102): Show |
intron_variant | MODIFIER | c.327+38358T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16923724 | ||||||
| chr3:16923953
|
T | TC | 78 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(75): Show | 78 | HG00280.hp2 HG00408.hp1 HG00741.hp1 others(75): Show |
intron_variant | MODIFIER | c.327+38587_327+3858 others(5): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16923953 | ||||||
| chr3:16924382
|
C | T | 2 | a0002c0009t0001g0154a0002c0009t0001g0155 | 2 | HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.327+39016C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16924382 | ||||||
| chr3:16924433
|
C | T | 3 | a0001c0003t0001g0003a0001c0011t0001g0004a0001c0012t0001g0005 | 3 | HG02055.hp1 HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.327+39067C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16924433 | ||||||
| chr3:16924681
|
G | A | 4 | a0001c0003t0001g0003a0001c0011t0001g0004a0001c0012t0001g0005others(1): Show | 4 | HG02055.hp1 HG02109.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+39315G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16924681 | ||||||
| chr3:16924857
|
G | C | 9 | a0001c0002t0001g0074a0001c0002t0001g0075a0001c0002t0001g0076others(6): Show | 9 | HG02559.hp1 HG02717.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.327+39491G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16924857 | ||||||
| chr3:16924895
|
G | A | 135 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(132): Show | 136 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.327+39529G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16924895 | ||||||
| chr3:16924927
|
G | GT | 3 | a0001c0001t0001g0197a0001c0001t0001g0247a0001c0013t0001g0198 | 3 | HG02258.hp2 HG02965.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.327+39564dupT | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16924927 | |||||
| chr3:16924931
|
G | T | 100 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(97): Show | 100 | HG00280.hp2 HG00408.hp1 HG00741.hp1 others(97): Show |
intron_variant | MODIFIER | c.327+39565G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16924931 | ||||||
| chr3:16925016
|
C | T | 4 | a0001c0003t0001g0003a0001c0011t0001g0004a0001c0012t0001g0005others(1): Show | 4 | HG02055.hp1 HG02109.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+39650C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16925016 | ||||||
| chr3:16925063
|
A | G | 19 | a0001c0003t0001g0018a0001c0003t0001g0180a0001c0003t0001g0181others(16): Show | 19 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.327+39697A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16925063 | ||||||
| chr3:16925086
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.327+39720G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16925086 | ||||||
| chr3:16925189
|
C | T | 24 | a0001c0002t0001g0098a0001c0002t0001g0099a0001c0002t0001g0100others(21): Show | 25 | HG00099.hp1 HG00323.hp2 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.327+39823C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16925189 | ||||||
| chr3:16925226
|
GT | G | 124 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(121): Show | 125 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.327+39874delT | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16925226 | |||||
| chr3:16925313
|
A | ATATT | 8 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(5): Show | 8 | HG02559.hp2 HG02723.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.327+39951_327+3995 others(8): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16925313 | |||||
| chr3:16925412
|
C | T | 1 | a0001c0002t0001g0079 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.327+40046C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16925412 | ||||||
| chr3:16925506
|
C | T | 135 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(132): Show | 136 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.327+40140C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16925506 | ||||||
| chr3:16925729
|
A | T | 98 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(95): Show | 98 | HG00280.hp2 HG00408.hp1 HG00741.hp2 others(95): Show |
intron_variant | MODIFIER | c.327+40363A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16925729 | ||||||
| chr3:16925731
|
A | G | 1 | a0001c0014t0001g0104 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.327+40365A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16925731 | ||||||
| chr3:16926108
|
AT | A | 19 | a0001c0003t0001g0018a0001c0003t0001g0180a0001c0003t0001g0181others(16): Show | 19 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.327+40750delT | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16926108 | |||||
| chr3:16926781
|
G | A | 3 | a0001c0002t0001g0075a0001c0003t0001g0181a0001c0003t0001g0186 | 3 | NA18973.hp2 NA18991.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.327+41415G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16926781 | ||||||
| chr3:16926918
|
C | T | 9 | a0001c0002t0001g0074a0001c0002t0001g0075a0001c0002t0001g0076others(6): Show | 9 | HG02559.hp1 HG02717.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.327+41552C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16926918 | ||||||
| chr3:16926933
|
T | A | 1 | a0001c0003t0003g0209 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.327+41567T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16926933 | ||||||
| chr3:16926934
|
T | A | 1 | a0001c0003t0003g0209 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.327+41568T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16926934 | ||||||
| chr3:16926935
|
T | A | 1 | a0001c0003t0003g0209 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.327+41569T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16926935 | ||||||
| chr3:16926936
|
T | A | 1 | a0001c0003t0003g0209 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.327+41570T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16926936 | ||||||
| chr3:16926945
|
C | G | 3 | a0001c0002t0001g0007a0001c0002t0001g0199a0001c0002t0001g0210 | 3 | HG02257.hp1 HG02280.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.327+41579C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16926945 | ||||||
| chr3:16927192
|
C | G | 4 | a0001c0003t0004g0001a0001c0003t0004g0128a0001c0003t0004g0152others(1): Show | 5 | HG02486.hp1 HG03139.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.327+41826C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16927192 | ||||||
| chr3:16927230
|
G | A | 4 | a0001c0003t0001g0003a0001c0011t0001g0004a0001c0012t0001g0005others(1): Show | 4 | HG02055.hp1 HG02109.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+41864G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16927230 | ||||||
| chr3:16927474
|
C | T | 8 | a0001c0001t0001g0197a0001c0002t0001g0007a0001c0002t0001g0199others(5): Show | 8 | HG02055.hp1 HG02109.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.327+42108C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16927474 | ||||||
| chr3:16927538
|
A | G | 1 | a0001c0013t0001g0198 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.327+42172A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16927538 | ||||||
| chr3:16927611
|
T | C | 1 | a0001c0008t0001g0123 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.327+42245T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16927611 | ||||||
| chr3:16927711
|
T | TACCTGCC others(16): Show |
2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG00323.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.327+42349_327+4237 others(27): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16927711 | |||||
| chr3:16927823
|
C | T | 1 | a0001c0001t0006g0222 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.327+42457C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16927823 | ||||||
| chr3:16928107
|
G | C | 4 | a0001c0003t0001g0003a0001c0011t0001g0004a0001c0012t0001g0005others(1): Show | 4 | HG02055.hp1 HG02109.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+42741G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16928107 | ||||||
| chr3:16928158
|
T | C | 1 | a0001c0001t0002g0135 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.327+42792T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16928158 | ||||||
| chr3:16928548
|
A | G | 2 | a0002c0009t0001g0154a0002c0009t0001g0155 | 2 | HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.327+43182A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16928548 | ||||||
| chr3:16928783
|
C | T | 4 | a0001c0002t0001g0205a0001c0002t0001g0206a0001c0002t0001g0207others(1): Show | 4 | HG02559.hp2 HG02723.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+43417C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16928783 | ||||||
| chr3:16928919
|
G | A | 9 | a0001c0001t0006g0222a0001c0002t0001g0008a0001c0002t0001g0009others(6): Show | 9 | HG02559.hp2 HG02723.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.327+43553G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16928919 | ||||||
| chr3:16928957
|
C | CA | 247 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(244): Show | 249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.327+43591_327+4359 others(5): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16928957 | ||||||
| chr3:16928976
|
G | GA | 247 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(244): Show | 249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.327+43612dupA | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16928976 | |||||
| chr3:16929062
|
CT | C | 247 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(244): Show | 249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.327+43699delT | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16929062 | |||||
| chr3:16929066
|
G | A | 247 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(244): Show | 249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.327+43700G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16929066 | ||||||
| chr3:16929069
|
C | A | 247 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(244): Show | 249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.327+43703C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16929069 | ||||||
| chr3:16929071
|
T | A | 247 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(244): Show | 249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.327+43705T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16929071 | ||||||
| chr3:16929074
|
A | G | 247 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(244): Show | 249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.327+43708A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16929074 | ||||||
| chr3:16929081
|
C | G | 247 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(244): Show | 249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.327+43715C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16929081 | ||||||
| chr3:16929082
|
C | A | 247 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(244): Show | 249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.327+43716C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16929082 | ||||||
| chr3:16929083
|
GC | G | 247 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(244): Show | 249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.327+43718delC | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16929083 | ||||||
| chr3:16929087
|
C | G | 247 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(244): Show | 249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.327+43721C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16929087 | ||||||
| chr3:16929088
|
A | C | 247 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(244): Show | 249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.327+43722A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16929088 | ||||||
| chr3:16929090
|
A | T | 247 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(244): Show | 249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.327+43724A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16929090 | ||||||
| chr3:16929097
|
A | T | 247 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(244): Show | 249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.327+43731A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16929097 | ||||||
| chr3:16929098
|
G | T | 247 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(244): Show | 249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.327+43732G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16929098 | ||||||
| chr3:16929099
|
T | TA | 247 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(244): Show | 249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.327+43735dupA | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16929099 | |||||
| chr3:16929103
|
T | G | 247 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(244): Show | 249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.327+43737T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16929103 | ||||||
| chr3:16929108
|
GC | G | 247 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(244): Show | 249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.327+43743delC | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16929108 | ||||||
| chr3:16929112
|
TG | T | 244 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(241): Show | 246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.327+43747delG | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16929112 | ||||||
| chr3:16929113
|
G | A | 3 | a0001c0002t0001g0120a0001c0002t0001g0121a0001c0002t0001g0122 | 3 | HG02486.hp2 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.327+43747G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16929113 | ||||||
| chr3:16929115
|
G | A | 244 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(241): Show | 246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.327+43749G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16929115 | ||||||
| chr3:16929115
|
GGAT | G | 3 | a0001c0002t0001g0120a0001c0002t0001g0121a0001c0002t0001g0122 | 3 | HG02486.hp2 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.327+43750_327+4375 others(7): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16929115 | ||||||
| chr3:16929119
|
A | G | 244 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(241): Show | 246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.327+43753A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16929119 | ||||||
| chr3:16929121
|
C | G | 3 | a0001c0002t0001g0120a0001c0002t0001g0121a0001c0002t0001g0122 | 3 | HG02486.hp2 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.327+43755C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16929121 | ||||||
| chr3:16929121
|
CTG | C | 244 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(241): Show | 246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.327+43756_327+4375 others(6): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16929121 | ||||||
| chr3:16929122
|
T | C | 3 | a0001c0002t0001g0120a0001c0002t0001g0121a0001c0002t0001g0122 | 3 | HG02486.hp2 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.327+43756T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16929122 | ||||||
| chr3:16929123
|
G | C | 3 | a0001c0002t0001g0120a0001c0002t0001g0121a0001c0002t0001g0122 | 3 | HG02486.hp2 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.327+43757G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16929123 | ||||||
| chr3:16929124
|
C | A | 247 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(244): Show | 249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.327+43758C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16929124 | ||||||
| chr3:16929126
|
C | A | 2 | a0002c0009t0001g0154a0002c0009t0001g0155 | 2 | HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.327+43760C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16929126 | ||||||
| chr3:16929126
|
C | G | 245 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(242): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.327+43760C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16929126 | ||||||
| chr3:16929130
|
A | G | 247 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(244): Show | 249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.327+43764A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16929130 | ||||||
| chr3:16929135
|
T | A | 247 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(244): Show | 249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.327+43769T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16929135 | ||||||
| chr3:16929140
|
A | G | 247 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(244): Show | 249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.327+43774A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16929140 | ||||||
| chr3:16929145
|
A | G | 247 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(244): Show | 249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.327+43779A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16929145 | ||||||
| chr3:16929152
|
AC | A | 247 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(244): Show | 249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.327+43787delC | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16929152 | ||||||
| chr3:16929177
|
C | G | 247 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(244): Show | 249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.327+43811C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16929177 | ||||||
| chr3:16929184
|
T | G | 247 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(244): Show | 249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.327+43818T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16929184 | ||||||
| chr3:16929186
|
G | T | 247 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(244): Show | 249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.327+43820G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16929186 | ||||||
| chr3:16929195
|
A | G | 4 | a0001c0005t0001g0019a0001c0005t0001g0063a0001c0005t0001g0179others(1): Show | 4 | HG01515.hp2 HG03491.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+43829A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16929195 | ||||||
| chr3:16929213
|
C | G | 247 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(244): Show | 249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.327+43847C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16929213 | ||||||
| chr3:16929214
|
T | C | 247 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(244): Show | 249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.327+43848T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16929214 | ||||||
| chr3:16929215
|
A | T | 247 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(244): Show | 249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.327+43849A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16929215 | ||||||
| chr3:16929289
|
T | C | 105 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(102): Show | 105 | HG00408.hp1 HG00741.hp2 HG01081.hp2 others(102): Show |
intron_variant | MODIFIER | c.327+43923T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16929289 | ||||||
| chr3:16929314
|
A | G | 4 | a0001c0005t0001g0019a0001c0005t0001g0063a0001c0005t0001g0179others(1): Show | 4 | HG01515.hp2 HG03491.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+43948A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16929314 | ||||||
| chr3:16929336
|
T | A | 1 | a0001c0003t0001g0187 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.327+43970T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16929336 | ||||||
| chr3:16929363
|
C | T | 8 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(5): Show | 8 | HG02559.hp2 HG02723.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.327+43997C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16929363 | ||||||
| chr3:16929409
|
G | A | 1 | a0001c0014t0001g0104 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.327+44043G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16929409 | ||||||
| chr3:16929446
|
A | G | 61 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(58): Show | 61 | HG00280.hp2 HG00408.hp1 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.327+44080A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16929446 | ||||||
| chr3:16929709
|
G | C | 1 | a0000c0007t0002g0146 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.327+44343G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16929709 | ||||||
| chr3:16929756
|
T | G | 110 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(107): Show | 110 | HG00280.hp2 HG00408.hp1 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.327+44390T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16929756 | ||||||
| chr3:16929867
|
T | C | 9 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(6): Show | 9 | HG02559.hp2 HG02723.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.327+44501T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16929867 | ||||||
| chr3:16930341
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.327+44975G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16930341 | ||||||
| chr3:16930384
|
C | A | 2 | a0001c0002t0001g0032a0001c0002t0001g0085 | 2 | HG02257.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.327+45018C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16930384 | ||||||
| chr3:16930600
|
G | A | 4 | a0001c0005t0001g0019a0001c0005t0001g0063a0001c0005t0001g0179others(1): Show | 4 | HG01515.hp2 HG03491.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+45234G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16930600 | ||||||
| chr3:16930719
|
G | A | 101 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(98): Show | 101 | HG00280.hp2 HG00408.hp1 HG00741.hp2 others(98): Show |
intron_variant | MODIFIER | c.327+45353G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16930719 | ||||||
| chr3:16931134
|
C | G | 8 | a0001c0003t0001g0030a0001c0003t0001g0094a0001c0003t0001g0106others(5): Show | 9 | HG01934.hp1 HG01978.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.327+45768C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16931134 | ||||||
| chr3:16931157
|
A | AT | 50 | a0001c0001t0001g0088a0001c0001t0001g0109a0001c0001t0001g0237others(47): Show | 51 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.327+45802dupT | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16931157 | |||||
| chr3:16931157
|
A | T | 1 | a0001c0005t0001g0185 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.327+45791A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16931157 | ||||||
| chr3:16931313
|
A | G | 1 | a0001c0001t0001g0197 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.327+45947A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16931313 | ||||||
| chr3:16931599
|
T | C | 4 | a0001c0005t0001g0019a0001c0005t0001g0063a0001c0005t0001g0179others(1): Show | 4 | HG01515.hp2 HG03491.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+46233T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16931599 | ||||||
| chr3:16931613
|
C | A | 4 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0219others(1): Show | 4 | HG02895.hp2 HG03041.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+46247C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16931613 | ||||||
| chr3:16931672
|
C | T | 3 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202 | 3 | HG02976.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.327+46306C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16931672 | ||||||
| chr3:16931681
|
C | T | 2 | a0001c0001t0001g0101a0001c0001t0001g0102 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.327+46315C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16931681 | ||||||
| chr3:16931687
|
G | T | 1 | a0001c0008t0001g0242 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.327+46321G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16931687 | ||||||
| chr3:16931788
|
G | C | 4 | a0001c0002t0001g0205a0001c0002t0001g0206a0001c0002t0001g0207others(1): Show | 4 | HG02559.hp2 HG02723.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+46422G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16931788 | ||||||
| chr3:16931859
|
A | G | 1 | a0001c0001t0001g0246 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.327+46493A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16931859 | ||||||
| chr3:16931951
|
A | C | 1 | a0001c0002t0001g0062 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.327+46585A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16931951 | ||||||
| chr3:16932038
|
C | T | 1 | a0001c0012t0001g0005 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.327+46672C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16932038 | ||||||
| chr3:16932051
|
C | T | 5 | a0001c0002t0001g0024a0001c0002t0001g0069a0001c0002t0001g0070others(2): Show | 5 | HG01069.hp1 HG01074.hp1 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.327+46685C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16932051 | ||||||
| chr3:16932213
|
C | T | 4 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(1): Show | 4 | HG02965.hp1 HG02976.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+46847C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16932213 | ||||||
| chr3:16932270
|
G | A | 28 | a0001c0002t0001g0098a0001c0002t0001g0099a0001c0002t0001g0100others(25): Show | 29 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.327+46904G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16932270 | ||||||
| chr3:16932453
|
T | C | 2 | a0002c0009t0001g0154a0002c0009t0001g0155 | 2 | HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.327+47087T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16932453 | ||||||
| chr3:16932515
|
A | G | 8 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(5): Show | 8 | HG02559.hp2 HG02723.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.327+47149A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16932515 | ||||||
| chr3:16932631
|
T | G | 104 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(101): Show | 104 | HG00408.hp1 HG01081.hp2 HG01099.hp1 others(101): Show |
intron_variant | MODIFIER | c.327+47265T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16932631 | ||||||
| chr3:16933041
|
C | G | 3 | a0001c0002t0001g0007a0001c0002t0001g0199a0001c0002t0001g0210 | 3 | HG02257.hp1 HG02280.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.327+47675C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16933041 | ||||||
| chr3:16933118
|
C | A | 133 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(130): Show | 134 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.327+47752C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16933118 | ||||||
| chr3:16933136
|
T | C | 69 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(66): Show | 69 | HG00408.hp1 HG01081.hp2 HG01123.hp2 others(66): Show |
intron_variant | MODIFIER | c.327+47770T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16933136 | ||||||
| chr3:16933277
|
A | G | 2 | a0001c0001t0001g0197a0001c0001t0006g0222 | 2 | HG02258.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.327+47911A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16933277 | ||||||
| chr3:16933379
|
C | T | 17 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(14): Show | 17 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.327+48013C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16933379 | ||||||
| chr3:16933599
|
C | T | 1 | a0001c0001t0002g0143 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.327+48233C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16933599 | ||||||
| chr3:16933623
|
T | C | 4 | a0001c0005t0001g0019a0001c0005t0001g0063a0001c0005t0001g0179others(1): Show | 4 | HG01515.hp2 HG03491.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+48257T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16933623 | ||||||
| chr3:16933971
|
G | A | 8 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(5): Show | 8 | HG02559.hp2 HG02723.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.327+48605G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16933971 | ||||||
| chr3:16933998
|
C | T | 1 | a0001c0001t0001g0013 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.327+48632C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16933998 | ||||||
| chr3:16934890
|
ATAT | A | 4 | a0001c0005t0001g0019a0001c0005t0001g0063a0001c0005t0001g0179others(1): Show | 4 | HG01515.hp2 HG03491.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+49529_327+4953 others(7): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16934890 | |||||
| chr3:16935081
|
G | A | 3 | a0001c0002t0001g0120a0001c0002t0001g0121a0001c0002t0001g0122 | 3 | HG02486.hp2 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.327+49715G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16935081 | ||||||
| chr3:16935194
|
T | A | 1 | a0001c0002t0001g0097 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.327+49828T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16935194 | ||||||
| chr3:16935330
|
T | A | 1 | a0001c0002t0001g0212 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.327+49964T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16935330 | ||||||
| chr3:16935371
|
A | G | 73 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(70): Show | 73 | HG00408.hp1 HG01081.hp2 HG01123.hp2 others(70): Show |
intron_variant | MODIFIER | c.327+50005A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16935371 | ||||||
| chr3:16935396
|
A | G | 14 | a0001c0001t0001g0067a0001c0001t0001g0139a0001c0001t0002g0127others(11): Show | 14 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.327+50030A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16935396 | ||||||
| chr3:16935621
|
G | C | 4 | a0001c0003t0004g0001a0001c0003t0004g0128a0001c0003t0004g0152others(1): Show | 5 | HG02486.hp1 HG03139.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.327+50255G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16935621 | ||||||
| chr3:16935789
|
T | C | 11 | a0001c0002t0001g0007a0001c0002t0001g0008a0001c0002t0001g0009others(8): Show | 11 | HG02257.hp1 HG02280.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.327+50423T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16935789 | ||||||
| chr3:16935967
|
T | C | 17 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(14): Show | 17 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.327+50601T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16935967 | ||||||
| chr3:16936083
|
A | G | 1 | a0001c0001t0001g0247 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.327+50717A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16936083 | ||||||
| chr3:16936390
|
G | T | 1 | a0001c0016t0001g0093 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.327+51024G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16936390 | ||||||
| chr3:16936638
|
G | T | 2 | a0001c0003t0004g0152a0001c0003t0004g0153 | 2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.327+51272G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16936638 | ||||||
| chr3:16936668
|
T | C | 17 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(14): Show | 17 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.327+51302T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16936668 | ||||||
| chr3:16936852
|
A | G | 1 | a0001c0001t0001g0119 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.327+51486A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16936852 | ||||||
| chr3:16936961
|
T | C | 1 | a0001c0001t0002g0136 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.327+51595T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16936961 | ||||||
| chr3:16937150
|
T | C | 137 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(134): Show | 138 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.327+51784T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16937150 | ||||||
| chr3:16937207
|
T | C | 15 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(12): Show | 15 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.327+51841T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16937207 | ||||||
| chr3:16937572
|
A | T | 1 | a0001c0014t0001g0104 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.327+52206A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16937572 | ||||||
| chr3:16937613
|
A | G | 7 | a0001c0004t0001g0162a0001c0004t0001g0163a0001c0004t0001g0164others(4): Show | 7 | HG01069.hp2 HG01934.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.327+52247A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16937613 | ||||||
| chr3:16937672
|
A | T | 1 | a0001c0002t0001g0024 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.327+52306A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16937672 | ||||||
| chr3:16937778
|
G | C | 1 | a0001c0012t0001g0005 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.327+52412G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16937778 | ||||||
| chr3:16938002
|
T | C | 4 | a0001c0005t0001g0019a0001c0005t0001g0063a0001c0005t0001g0179others(1): Show | 4 | HG01515.hp2 HG03491.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+52636T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16938002 | ||||||
| chr3:16938085
|
G | A | 1 | a0001c0002t0001g0212 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.327+52719G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16938085 | ||||||
| chr3:16938263
|
A | G | 69 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(66): Show | 69 | HG00408.hp1 HG01081.hp2 HG01123.hp2 others(66): Show |
intron_variant | MODIFIER | c.327+52897A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16938263 | ||||||
| chr3:16938276
|
G | A | 1 | a0001c0003t0003g0216 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.327+52910G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16938276 | ||||||
| chr3:16938395
|
A | T | 4 | a0001c0005t0001g0019a0001c0005t0001g0063a0001c0005t0001g0179others(1): Show | 4 | HG01515.hp2 HG03491.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+53029A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16938395 | ||||||
| chr3:16938495
|
A | G | 17 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(14): Show | 17 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.327+53129A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16938495 | ||||||
| chr3:16938590
|
A | G | 2 | a0002c0009t0001g0154a0002c0009t0001g0155 | 2 | HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.327+53224A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16938590 | ||||||
| chr3:16938683
|
T | G | 17 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(14): Show | 17 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.327+53317T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16938683 | ||||||
| chr3:16938853
|
C | T | 1 | a0001c0001t0001g0234 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.327+53487C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16938853 | ||||||
| chr3:16938880
|
G | T | 1 | a0001c0003t0001g0191 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.327+53514G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16938880 | ||||||
| chr3:16938935
|
C | T | 4 | a0001c0005t0001g0019a0001c0005t0001g0063a0001c0005t0001g0179others(1): Show | 4 | HG01515.hp2 HG03491.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+53569C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16938935 | ||||||
| chr3:16939094
|
C | A | 73 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(70): Show | 73 | HG00408.hp1 HG01081.hp2 HG01123.hp2 others(70): Show |
intron_variant | MODIFIER | c.327+53728C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16939094 | ||||||
| chr3:16939150
|
G | T | 4 | a0001c0003t0001g0003a0001c0011t0001g0004a0001c0012t0001g0005others(1): Show | 4 | HG02055.hp1 HG02109.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+53784G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16939150 | ||||||
| chr3:16939406
|
T | C | 8 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(5): Show | 8 | HG02559.hp2 HG02723.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.327+54040T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16939406 | ||||||
| chr3:16939530
|
G | A | 75 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(72): Show | 75 | HG00408.hp1 HG01081.hp2 HG01123.hp2 others(72): Show |
intron_variant | MODIFIER | c.327+54164G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16939530 | ||||||
| chr3:16939897
|
T | C | 1 | a0001c0003t0001g0193 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.327+54531T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16939897 | ||||||
| chr3:16939908
|
G | A | 1 | a0001c0017t0001g0050 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.327+54542G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16939908 | ||||||
| chr3:16939919
|
C | A | 1 | a0001c0001t0001g0086 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.327+54553C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16939919 | ||||||
| chr3:16940052
|
A | T | 4 | a0001c0003t0001g0030a0001c0003t0001g0094a0001c0003t0001g0106others(1): Show | 4 | HG01934.hp1 HG01978.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+54686A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16940052 | ||||||
| chr3:16940191
|
G | T | 91 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(88): Show | 91 | HG00408.hp1 HG01081.hp2 HG01099.hp1 others(88): Show |
intron_variant | MODIFIER | c.327+54825G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16940191 | ||||||
| chr3:16940638
|
G | A | 4 | a0001c0002t0001g0033a0001c0002t0001g0051a0001c0002t0001g0052others(1): Show | 4 | NA18944.hp1 NA18986.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+55272G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16940638 | ||||||
| chr3:16940642
|
G | GA | 2 | a0001c0003t0004g0001a0001c0003t0004g0128 | 3 | HG03139.hp1 HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.327+55281dupA | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16940642 | |||||
| chr3:16940659
|
T | C | 4 | a0001c0005t0001g0019a0001c0005t0001g0063a0001c0005t0001g0179others(1): Show | 4 | HG01515.hp2 HG03491.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+55293T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16940659 | ||||||
| chr3:16940869
|
G | C | 10 | a0001c0001t0002g0129a0001c0001t0002g0130a0001c0001t0002g0131others(7): Show | 10 | HG01109.hp1 HG02109.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.327+55503G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16940869 | ||||||
| chr3:16940926
|
G | A | 1 | a0001c0003t0001g0106 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.327+55560G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16940926 | ||||||
| chr3:16940992
|
C | T | 1 | a0000c0019t0002g0148 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.327+55626C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16940992 | ||||||
| chr3:16941281
|
A | T | 4 | a0001c0005t0001g0019a0001c0005t0001g0063a0001c0005t0001g0179others(1): Show | 4 | HG01515.hp2 HG03491.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+55915A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16941281 | ||||||
| chr3:16941538
|
A | G | 2 | a0001c0001t0001g0221a0001c0001t0001g0225 | 2 | HG01081.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.327+56172A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16941538 | ||||||
| chr3:16941567
|
A | G | 3 | a0001c0003t0001g0180a0001c0003t0001g0194a0001c0021t0001g0177 | 3 | HG01975.hp1 HG01993.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.327+56201A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16941567 | ||||||
| chr3:16941595
|
T | C | 1 | a0001c0001t0002g0204 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.327+56229T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16941595 | ||||||
| chr3:16941723
|
G | C | 2 | a0001c0001t0001g0197a0001c0001t0006g0222 | 2 | HG02258.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.327+56357G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16941723 | ||||||
| chr3:16941868
|
TA | T | 17 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(14): Show | 17 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.327+56513delA | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16941868 | |||||
| chr3:16941944
|
A | G | 38 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(35): Show | 39 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.327+56578A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16941944 | ||||||
| chr3:16941960
|
G | A | 95 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(92): Show | 97 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.327+56594G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16941960 | ||||||
| chr3:16942090
|
A | T | 1 | a0001c0002t0001g0045 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.327+56724A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16942090 | ||||||
| chr3:16942184
|
A | G | 27 | a0001c0002t0001g0098a0001c0002t0001g0099a0001c0002t0001g0100others(24): Show | 28 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.327+56818A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16942184 | ||||||
| chr3:16942342
|
A | T | 156 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(153): Show | 158 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.327+56976A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16942342 | ||||||
| chr3:16942594
|
C | T | 2 | a0001c0011t0001g0004a0001c0012t0001g0005 | 2 | HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.327+57228C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16942594 | ||||||
| chr3:16942922
|
T | A | 57 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(54): Show | 58 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.327+57556T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16942922 | ||||||
| chr3:16943294
|
T | A | 10 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(7): Show | 10 | HG02559.hp2 HG02723.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.327+57928T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16943294 | ||||||
| chr3:16943301
|
G | A | 167 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(164): Show | 169 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.327+57935G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16943301 | ||||||
| chr3:16943583
|
T | A | 1 | a0001c0002t0001g0021 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.327+58217T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16943583 | ||||||
| chr3:16943647
|
G | A | 11 | a0001c0001t0006g0222a0001c0002t0001g0008a0001c0002t0001g0009others(8): Show | 11 | HG02559.hp2 HG02723.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.327+58281G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16943647 | ||||||
| chr3:16943662
|
T | G | 1 | a0001c0005t0001g0019 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.327+58296T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16943662 | ||||||
| chr3:16943718
|
G | A | 1 | a0001c0002t0001g0045 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.327+58352G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16943718 | ||||||
| chr3:16943780
|
C | T | 104 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(101): Show | 105 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.327+58414C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16943780 | ||||||
| chr3:16943946
|
A | G | 4 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(1): Show | 4 | HG02896.hp2 HG03098.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+58580A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16943946 | ||||||
| chr3:16944110
|
T | C | 4 | a0001c0004t0001g0162a0001c0004t0001g0163a0001c0004t0001g0164others(1): Show | 4 | HG01069.hp2 HG01934.hp2 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+58744T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16944110 | ||||||
| chr3:16944347
|
A | G | 1 | a0001c0003t0001g0211 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.327+58981A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16944347 | ||||||
| chr3:16944375
|
T | C | 4 | a0001c0005t0001g0019a0001c0005t0001g0063a0001c0005t0001g0179others(1): Show | 4 | HG01515.hp2 HG03491.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+59009T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16944375 | ||||||
| chr3:16944475
|
TA | T | 28 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(25): Show | 28 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.327+59110delA | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16944475 | ||||||
| chr3:16944644
|
G | A | 1 | a0001c0001t0001g0243 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.327+59278G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16944644 | ||||||
| chr3:16944759
|
G | GT | 10 | a0001c0001t0001g0118a0001c0001t0002g0129a0001c0001t0002g0151others(7): Show | 10 | HG00099.hp1 HG00323.hp2 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.327+59407dupT | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16944759 | |||||
| chr3:16944798
|
C | T | 28 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(25): Show | 28 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.327+59432C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16944798 | ||||||
| chr3:16944820
|
C | T | 1 | a0001c0002t0001g0024 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.327+59454C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16944820 | ||||||
| chr3:16944834
|
A | G | 1 | a0001c0003t0001g0211 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.327+59468A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16944834 | ||||||
| chr3:16944884
|
C | T | 1 | a0001c0001t0002g0136 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.327+59518C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16944884 | ||||||
| chr3:16944921
|
G | A | 1 | a0001c0002t0001g0047 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.327+59555G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16944921 | ||||||
| chr3:16945082
|
C | T | 1 | a0001c0003t0003g0231 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.327+59716C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16945082 | ||||||
| chr3:16945106
|
C | A | 1 | a0001c0003t0001g0187 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.327+59740C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16945106 | ||||||
| chr3:16945239
|
TAC | T | 88 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0016others(85): Show | 89 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.327+59895_327+5989 others(6): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16945239 | |||||
| chr3:16945239
|
TACAC | T | 108 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(105): Show | 109 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.327+59893_327+5989 others(8): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16945239 | |||||
| chr3:16945257
|
CACACAT | C | 3 | a0001c0005t0001g0063a0001c0005t0001g0179a0001c0005t0001g0185 | 3 | HG01515.hp2 HG03704.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.327+59897_327+5990 others(10): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16945257 | |||||
| chr3:16945264
|
A | G | 1 | a0001c0001t0001g0088 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.327+59898A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16945264 | ||||||
| chr3:16945312
|
C | T | 6 | a0001c0002t0001g0125a0001c0002t0001g0126a0001c0002t0001g0205others(3): Show | 6 | HG02559.hp2 HG02723.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.327+59946C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16945312 | ||||||
| chr3:16945313
|
G | A | 156 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(153): Show | 158 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.327+59947G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16945313 | ||||||
| chr3:16945341
|
C | T | 4 | a0001c0005t0001g0019a0001c0005t0001g0063a0001c0005t0001g0179others(1): Show | 4 | HG01515.hp2 HG03491.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+59975C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16945341 | ||||||
| chr3:16945386
|
T | C | 1 | a0001c0002t0001g0054 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.327+60020T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16945386 | ||||||
| chr3:16945497
|
A | T | 30 | a0001c0002t0001g0098a0001c0002t0001g0099a0001c0002t0001g0100others(27): Show | 31 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.327+60131A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16945497 | ||||||
| chr3:16945581
|
A | G | 17 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(14): Show | 17 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.327+60215A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16945581 | ||||||
| chr3:16945813
|
C | T | 1 | a0001c0014t0001g0104 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.327+60447C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16945813 | ||||||
| chr3:16945856
|
A | G | 1 | a0001c0001t0001g0043 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.327+60490A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16945856 | ||||||
| chr3:16945963
|
T | C | 3 | a0001c0002t0001g0098a0001c0002t0001g0099a0001c0002t0001g0100 | 3 | HG00099.hp1 HG00323.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.327+60597T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16945963 | ||||||
| chr3:16946282
|
T | C | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.327+60916T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16946282 | ||||||
| chr3:16946333
|
G | A | 1 | a0001c0003t0001g0211 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.327+60967G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16946333 | ||||||
| chr3:16946410
|
T | C | 4 | a0001c0005t0001g0019a0001c0005t0001g0063a0001c0005t0001g0179others(1): Show | 4 | HG01515.hp2 HG03491.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+61044T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16946410 | ||||||
| chr3:16946448
|
C | T | 4 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(1): Show | 4 | HG02965.hp1 HG02976.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+61082C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16946448 | ||||||
| chr3:16946719
|
A | T | 1 | a0001c0002t0001g0011 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.327+61353A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16946719 | ||||||
| chr3:16946725
|
G | C | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.327+61359G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16946725 | ||||||
| chr3:16946790
|
A | G | 2 | a0001c0001t0001g0221a0001c0001t0001g0225 | 2 | HG01081.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.327+61424A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16946790 | ||||||
| chr3:16946953
|
C | CT | 14 | a0001c0002t0001g0007a0001c0002t0001g0008a0001c0002t0001g0009others(11): Show | 14 | HG02027.hp2 HG02257.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.327+61607dupT | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16946953 | |||||
| chr3:16946953
|
C | CTTTTT | 75 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(72): Show | 76 | HG00323.hp2 HG00408.hp1 HG01099.hp1 others(73): Show |
intron_variant | MODIFIER | c.327+61603_327+6160 others(9): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16946953 | |||||
| chr3:16946953
|
C | CTTTTTT | 42 | a0001c0001t0001g0042a0001c0001t0001g0053a0001c0001t0001g0118others(39): Show | 43 | HG00099.hp1 HG00741.hp2 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.327+61602_327+6160 others(10): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16946953 | |||||
| chr3:16946953
|
C | CTTTTTTT | 7 | a0001c0001t0001g0197a0001c0001t0006g0222a0001c0003t0001g0116others(4): Show | 7 | HG00280.hp2 HG01106.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.327+61601_327+6160 others(11): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16946953 | |||||
| chr3:16946953
|
C | CTTTTTTT others(1): Show |
26 | a0000c0007t0002g0146a0000c0007t0002g0213a0000c0019t0002g0148others(23): Show | 26 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.327+61600_327+6160 others(12): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16946953 | |||||
| chr3:16946953
|
C | CTTTTTTT others(2): Show |
6 | a0000c0007t0002g0147a0001c0001t0002g0135a0001c0001t0002g0140others(3): Show | 6 | HG01123.hp1 HG02129.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.327+61599_327+6160 others(13): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16946953 | |||||
| chr3:16947015
|
G | T | 17 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(14): Show | 17 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.327+61649G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16947015 | ||||||
| chr3:16947040
|
C | T | 3 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010 | 3 | HG02896.hp2 HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.327+61674C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16947040 | ||||||
| chr3:16947127
|
A | AT | 68 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(65): Show | 68 | HG00408.hp1 HG01081.hp2 HG01123.hp2 others(65): Show |
intron_variant | MODIFIER | c.327+61774dupT | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16947127 | |||||
| chr3:16947132
|
T | A | 45 | a0001c0002t0001g0011a0001c0002t0001g0098a0001c0002t0001g0099others(42): Show | 46 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.327+61766T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16947132 | ||||||
| chr3:16947187
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.327+61821C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16947187 | ||||||
| chr3:16947261
|
C | T | 4 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(1): Show | 4 | HG02896.hp2 HG03098.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+61895C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16947261 | ||||||
| chr3:16947760
|
C | A | 1 | a0001c0002t0001g0021 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.328-61914C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16947760 | ||||||
| chr3:16947815
|
C | T | 17 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(14): Show | 17 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.328-61859C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16947815 | ||||||
| chr3:16947816
|
G | A | 1 | a0001c0001t0001g0036 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.328-61858G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16947816 | ||||||
| chr3:16947826
|
A | C | 4 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133others(1): Show | 4 | HG02109.hp2 HG02723.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-61848A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16947826 | ||||||
| chr3:16947962
|
G | C | 17 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(14): Show | 17 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.328-61712G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16947962 | ||||||
| chr3:16948432
|
A | G | 1 | a0001c0003t0003g0216 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.328-61242A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16948432 | ||||||
| chr3:16948454
|
A | T | 4 | a0001c0005t0001g0019a0001c0005t0001g0063a0001c0005t0001g0179others(1): Show | 4 | HG01515.hp2 HG03491.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-61220A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16948454 | ||||||
| chr3:16948488
|
G | T | 1 | a0001c0001t0001g0229 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.328-61186G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16948488 | ||||||
| chr3:16948511
|
T | A | 80 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(77): Show | 81 | HG00408.hp1 HG01081.hp2 HG01123.hp2 others(78): Show |
intron_variant | MODIFIER | c.328-61163T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16948511 | ||||||
| chr3:16948531
|
A | G | 1 | a0003c0010t0001g0049 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.328-61143A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16948531 | ||||||
| chr3:16948627
|
A | G | 7 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(4): Show | 7 | HG02055.hp1 HG02109.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.328-61047A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16948627 | ||||||
| chr3:16948798
|
A | C | 1 | a0001c0002t0001g0223 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.328-60876A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16948798 | ||||||
| chr3:16948995
|
G | A | 1 | a0001c0003t0001g0211 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.328-60679G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16948995 | ||||||
| chr3:16949015
|
A | G | 1 | a0001c0014t0001g0104 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.328-60659A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16949015 | ||||||
| chr3:16949204
|
AAGAT | A | 79 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(76): Show | 80 | HG00408.hp1 HG01081.hp2 HG01123.hp2 others(77): Show |
intron_variant | MODIFIER | c.328-60466_328-6046 others(8): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16949204 | |||||
| chr3:16949258
|
T | A | 71 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(68): Show | 72 | HG00408.hp1 HG01081.hp2 HG01123.hp2 others(69): Show |
intron_variant | MODIFIER | c.328-60416T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16949258 | ||||||
| chr3:16949281
|
C | T | 4 | a0001c0005t0001g0019a0001c0005t0001g0063a0001c0005t0001g0179others(1): Show | 4 | HG01515.hp2 HG03491.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-60393C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16949281 | ||||||
| chr3:16949701
|
G | A | 3 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0247 | 3 | HG03017.hp1 HG03710.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.328-59973G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16949701 | ||||||
| chr3:16949739
|
C | T | 3 | a0001c0011t0001g0004a0001c0012t0001g0005a0001c0013t0001g0198 | 3 | HG02055.hp1 HG02109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.328-59935C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16949739 | ||||||
| chr3:16950066
|
G | A | 6 | a0001c0002t0001g0046a0001c0002t0001g0048a0001c0002t0001g0080others(3): Show | 6 | HG01081.hp1 HG01516.hp1 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.328-59608G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16950066 | ||||||
| chr3:16950316
|
A | T | 1 | a0001c0001t0006g0222 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.328-59358A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16950316 | ||||||
| chr3:16950413
|
C | G | 3 | a0001c0011t0001g0004a0001c0012t0001g0005a0001c0013t0001g0198 | 3 | HG02055.hp1 HG02109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.328-59261C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16950413 | ||||||
| chr3:16950665
|
A | C | 2 | a0001c0002t0001g0111a0001c0006t0001g0160 | 2 | HG02155.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.328-59009A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16950665 | ||||||
| chr3:16950710
|
A | G | 1 | a0001c0001t0001g0237 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.328-58964A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16950710 | ||||||
| chr3:16950792
|
A | G | 1 | a0001c0003t0003g0209 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.328-58882A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16950792 | ||||||
| chr3:16951014
|
T | G | 3 | a0001c0011t0001g0004a0001c0012t0001g0005a0001c0013t0001g0198 | 3 | HG02055.hp1 HG02109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.328-58660T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16951014 | ||||||
| chr3:16951070
|
G | T | 11 | a0001c0001t0006g0222a0001c0002t0001g0008a0001c0002t0001g0009others(8): Show | 11 | HG02559.hp2 HG02723.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.328-58604G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16951070 | ||||||
| chr3:16951213
|
C | T | 3 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017 | 3 | NA18942.hp1 NA18949.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.328-58461C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16951213 | ||||||
| chr3:16951675
|
C | T | 5 | a0001c0001t0001g0139a0001c0001t0002g0140a0001c0001t0002g0141others(2): Show | 5 | HG01123.hp1 HG02683.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.328-57999C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16951675 | ||||||
| chr3:16951750
|
T | C | 2 | a0001c0004t0001g0176a0001c0008t0001g0123 | 2 | HG03927.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.328-57924T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16951750 | ||||||
| chr3:16951833
|
G | T | 1 | a0001c0001t0002g0143 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.328-57841G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16951833 | ||||||
| chr3:16951859
|
T | TGGGAATG others(312): Show |
1 | a0001c0001t0001g0221 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.328-57803_328-5780 others(323): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16951859 | |||||
| chr3:16951859
|
T | TGGGAATG others(321): Show |
1 | a0001c0001t0001g0225 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.328-57803_328-5780 others(332): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16951859 | |||||
| chr3:16952360
|
C | CA | 68 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0017others(65): Show | 68 | HG00408.hp1 HG00408.hp2 HG00741.hp1 others(65): Show |
intron_variant | MODIFIER | c.328-57283dupA | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16952360 | |||||
| chr3:16952360
|
C | CAA | 28 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0016others(25): Show | 28 | HG00280.hp2 HG01106.hp2 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.328-57284_328-5728 others(6): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16952360 | |||||
| chr3:16952360
|
C | CAAA | 7 | a0001c0001t0001g0103a0001c0002t0001g0075a0001c0002t0001g0076others(4): Show | 7 | HG01516.hp2 HG02155.hp2 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.328-57285_328-5728 others(7): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16952360 | |||||
| chr3:16952360
|
C | CAAAA | 18 | a0001c0001t0001g0053a0001c0001t0001g0217a0001c0001t0001g0218others(15): Show | 19 | HG01175.hp2 HG01934.hp2 HG01975.hp2 others(16): Show |
intron_variant | MODIFIER | c.328-57286_328-5728 others(8): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16952360 | |||||
| chr3:16952360
|
C | CAAAAAA | 10 | a0001c0001t0001g0225a0001c0002t0001g0099a0001c0002t0001g0100others(7): Show | 10 | HG00099.hp1 HG00741.hp2 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.328-57288_328-5728 others(10): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16952360 | |||||
| chr3:16952360
|
CA | C | 17 | a0001c0001t0002g0127a0001c0001t0002g0135a0001c0001t0002g0136others(14): Show | 17 | HG00099.hp2 HG01099.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.328-57283delA | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16952360 | |||||
| chr3:16952360
|
CAA | C | 8 | a0001c0001t0002g0145a0001c0003t0001g0003a0001c0003t0001g0094others(5): Show | 8 | HG00323.hp1 HG01934.hp1 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.328-57284_328-5728 others(6): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16952360 | |||||
| chr3:16952360
|
CAAA | C | 16 | a0001c0003t0001g0181a0001c0003t0001g0184a0001c0003t0001g0186others(13): Show | 17 | HG01243.hp2 HG01433.hp2 HG01515.hp2 others(14): Show |
intron_variant | MODIFIER | c.328-57285_328-5728 others(7): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16952360 | |||||
| chr3:16952360
|
CAAAA | C | 15 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(12): Show | 15 | HG01099.hp1 HG01943.hp1 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.328-57286_328-5728 others(8): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16952360 | |||||
| chr3:16952395
|
C | A | 1 | a0001c0001t0001g0197 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.328-57279C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16952395 | ||||||
| chr3:16952558
|
A | G | 1 | a0001c0001t0006g0222 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.328-57116A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16952558 | ||||||
| chr3:16952604
|
T | C | 2 | a0001c0005t0001g0063a0001c0005t0001g0179 | 2 | HG01515.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.328-57070T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16952604 | ||||||
| chr3:16952643
|
A | G | 7 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(4): Show | 7 | HG02055.hp1 HG02109.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.328-57031A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16952643 | ||||||
| chr3:16953000
|
C | G | 170 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(167): Show | 172 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.328-56674C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16953000 | ||||||
| chr3:16953011
|
A | T | 1 | a0001c0003t0001g0196 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.328-56663A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16953011 | ||||||
| chr3:16953163
|
A | C | 1 | a0001c0001t0001g0203 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.328-56511A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16953163 | ||||||
| chr3:16953377
|
T | C | 1 | a0001c0002t0001g0212 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.328-56297T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16953377 | ||||||
| chr3:16953521
|
A | T | 1 | a0001c0001t0001g0202 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.328-56153A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16953521 | ||||||
| chr3:16953587
|
T | C | 1 | a0001c0001t0006g0222 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.328-56087T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16953587 | ||||||
| chr3:16953654
|
A | G | 1 | a0001c0002t0001g0066 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.328-56020A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16953654 | ||||||
| chr3:16953673
|
G | A | 27 | a0001c0002t0001g0098a0001c0002t0001g0099a0001c0002t0001g0100others(24): Show | 28 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.328-56001G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16953673 | ||||||
| chr3:16953750
|
T | C | 1 | a0001c0002t0001g0047 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.328-55924T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16953750 | ||||||
| chr3:16953781
|
A | T | 10 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(7): Show | 10 | HG02559.hp2 HG02723.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.328-55893A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16953781 | ||||||
| chr3:16953834
|
C | A | 88 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(85): Show | 89 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.328-55840C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16953834 | ||||||
| chr3:16953919
|
T | A | 3 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202 | 3 | HG02976.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.328-55755T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16953919 | ||||||
| chr3:16953946
|
C | G | 2 | a0001c0002t0001g0032a0001c0002t0001g0085 | 2 | HG02257.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.328-55728C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16953946 | ||||||
| chr3:16953959
|
G | C | 4 | a0001c0005t0001g0019a0001c0005t0001g0063a0001c0005t0001g0179others(1): Show | 4 | HG01515.hp2 HG03491.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-55715G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16953959 | ||||||
| chr3:16953983
|
T | C | 1 | a0001c0002t0001g0051 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.328-55691T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16953983 | ||||||
| chr3:16954147
|
G | A | 4 | a0001c0005t0001g0019a0001c0005t0001g0063a0001c0005t0001g0179others(1): Show | 4 | HG01515.hp2 HG03491.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-55527G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16954147 | ||||||
| chr3:16954266
|
C | A | 95 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(92): Show | 96 | HG00408.hp1 HG01081.hp2 HG01099.hp1 others(93): Show |
intron_variant | MODIFIER | c.328-55408C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16954266 | ||||||
| chr3:16954295
|
C | G | 1 | a0004c0015t0001g0072 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.328-55379C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16954295 | ||||||
| chr3:16954327
|
T | G | 3 | a0001c0011t0001g0004a0001c0012t0001g0005a0001c0013t0001g0198 | 3 | HG02055.hp1 HG02109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.328-55347T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16954327 | ||||||
| chr3:16954353
|
C | A | 2 | a0001c0002t0001g0091a0001c0002t0001g0092 | 2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.328-55321C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16954353 | ||||||
| chr3:16954474
|
C | A | 1 | a0001c0001t0001g0227 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.328-55200C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16954474 | ||||||
| chr3:16954489
|
G | A | 1 | a0000c0019t0002g0148 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.328-55185G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16954489 | ||||||
| chr3:16954543
|
G | A | 154 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(151): Show | 156 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.328-55131G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16954543 | ||||||
| chr3:16954650
|
A | C | 1 | a0001c0014t0001g0104 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.328-55024A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16954650 | ||||||
| chr3:16954709
|
G | A | 10 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(7): Show | 10 | HG02559.hp2 HG02723.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.328-54965G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16954709 | ||||||
| chr3:16954724
|
T | C | 1 | a0001c0001t0001g0088 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.328-54950T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16954724 | ||||||
| chr3:16954907
|
T | C | 2 | a0001c0001t0001g0037a0001c0001t0001g0108 | 2 | HG01255.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.328-54767T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16954907 | ||||||
| chr3:16955020
|
C | G | 1 | a0001c0001t0001g0221 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.328-54654C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16955020 | ||||||
| chr3:16955100
|
A | C | 1 | a0001c0004t0001g0164 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.328-54574A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16955100 | ||||||
| chr3:16955105
|
A | C | 1 | a0001c0004t0001g0164 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.328-54569A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16955105 | ||||||
| chr3:16955109
|
C | T | 1 | a0001c0004t0001g0164 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.328-54565C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16955109 | ||||||
| chr3:16955131
|
G | A | 139 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(136): Show | 141 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.328-54543G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16955131 | ||||||
| chr3:16955239
|
A | C | 4 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(1): Show | 4 | HG02896.hp2 HG03098.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-54435A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16955239 | ||||||
| chr3:16955267
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.328-54407C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16955267 | ||||||
| chr3:16955268
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.328-54406A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16955268 | ||||||
| chr3:16955309
|
C | G | 2 | a0002c0009t0001g0154a0002c0009t0001g0155 | 2 | HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.328-54365C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16955309 | ||||||
| chr3:16955356
|
C | G | 1 | a0001c0002t0001g0068 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.328-54318C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16955356 | ||||||
| chr3:16955381
|
A | G | 17 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(14): Show | 17 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.328-54293A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16955381 | ||||||
| chr3:16955435
|
A | G | 2 | a0001c0001t0002g0143a0001c0004t0001g0166 | 2 | HG01099.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.328-54239A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16955435 | ||||||
| chr3:16955617
|
G | A | 3 | a0001c0011t0001g0004a0001c0012t0001g0005a0001c0013t0001g0198 | 3 | HG02055.hp1 HG02109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.328-54057G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16955617 | ||||||
| chr3:16955832
|
C | G | 1 | a0001c0003t0001g0235 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.328-53842C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16955832 | ||||||
| chr3:16955841
|
G | C | 3 | a0001c0003t0004g0001a0001c0003t0004g0152a0001c0003t0004g0153 | 4 | HG02486.hp1 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-53833G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16955841 | ||||||
| chr3:16955881
|
G | A | 17 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(14): Show | 17 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.328-53793G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16955881 | ||||||
| chr3:16955948
|
G | T | 2 | a0001c0001t0001g0037a0001c0001t0001g0108 | 2 | HG01255.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.328-53726G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16955948 | ||||||
| chr3:16955966
|
A | G | 1 | a0001c0001t0001g0067 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.328-53708A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16955966 | ||||||
| chr3:16955981
|
C | T | 4 | a0001c0005t0001g0019a0001c0005t0001g0063a0001c0005t0001g0179others(1): Show | 4 | HG01515.hp2 HG03491.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-53693C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16955981 | ||||||
| chr3:16956018
|
A | T | 1 | a0001c0002t0001g0069 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.328-53656A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16956018 | ||||||
| chr3:16956037
|
T | A | 140 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(137): Show | 142 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.328-53637T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16956037 | ||||||
| chr3:16956046
|
C | T | 4 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(1): Show | 4 | HG02896.hp2 HG03098.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-53628C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16956046 | ||||||
| chr3:16956198
|
G | A | 1 | a0001c0001t0002g0145 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.328-53476G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16956198 | ||||||
| chr3:16956198
|
G | C | 64 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(61): Show | 64 | HG00408.hp1 HG01081.hp2 HG01123.hp2 others(61): Show |
intron_variant | MODIFIER | c.328-53476G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16956198 | ||||||
| chr3:16956205
|
C | A | 1 | a0001c0002t0001g0212 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.328-53469C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16956205 | ||||||
| chr3:16956277
|
T | C | 27 | a0001c0002t0001g0098a0001c0002t0001g0099a0001c0002t0001g0100others(24): Show | 28 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.328-53397T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16956277 | ||||||
| chr3:16956278
|
T | G | 37 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(34): Show | 37 | HG00408.hp1 HG01175.hp2 HG01255.hp1 others(34): Show |
intron_variant | MODIFIER | c.328-53396T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16956278 | ||||||
| chr3:16956282
|
A | G | 27 | a0001c0002t0001g0098a0001c0002t0001g0099a0001c0002t0001g0100others(24): Show | 28 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.328-53392A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16956282 | ||||||
| chr3:16956343
|
A | G | 244 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(241): Show | 246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.328-53331A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16956343 | ||||||
| chr3:16956368
|
G | A | 7 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103others(4): Show | 7 | HG01074.hp1 HG01515.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.328-53306G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16956368 | ||||||
| chr3:16956380
|
C | A | 1 | a0001c0001t0006g0222 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.328-53294C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16956380 | ||||||
| chr3:16956425
|
G | C | 1 | a0001c0001t0001g0203 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.328-53249G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16956425 | ||||||
| chr3:16956480
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.328-53194C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16956480 | ||||||
| chr3:16956512
|
A | T | 1 | a0001c0003t0001g0211 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.328-53162A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16956512 | ||||||
| chr3:16956582
|
T | C | 4 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(1): Show | 4 | HG02965.hp1 HG02976.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-53092T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16956582 | ||||||
| chr3:16956696
|
G | A | 210 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(207): Show | 212 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.328-52978G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16956696 | ||||||
| chr3:16956863
|
A | G | 1 | a0001c0001t0001g0237 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.328-52811A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16956863 | ||||||
| chr3:16956894
|
A | T | 1 | a0001c0002t0001g0033 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.328-52780A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16956894 | ||||||
| chr3:16957015
|
T | G | 30 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(27): Show | 30 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.328-52659T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16957015 | ||||||
| chr3:16957188
|
A | G | 10 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(7): Show | 10 | HG02559.hp2 HG02723.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.328-52486A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16957188 | ||||||
| chr3:16957283
|
T | C | 3 | a0001c0011t0001g0004a0001c0012t0001g0005a0001c0013t0001g0198 | 3 | HG02055.hp1 HG02109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.328-52391T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16957283 | ||||||
| chr3:16957331
|
G | C | 8 | a0001c0003t0001g0116a0001c0003t0001g0235a0001c0003t0003g0209others(5): Show | 8 | HG00280.hp2 HG00741.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.328-52343G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16957331 | ||||||
| chr3:16957446
|
C | A | 1 | a0001c0003t0003g0215 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.328-52228C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16957446 | ||||||
| chr3:16957449
|
G | C | 30 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(27): Show | 30 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(27): Show |
intron_variant | MODIFIER | c.328-52225G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16957449 | ||||||
| chr3:16957521
|
C | G | 2 | a0001c0001t0002g0130a0001c0001t0002g0156 | 2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.328-52153C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16957521 | ||||||
| chr3:16957670
|
G | C | 13 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(10): Show | 13 | HG02055.hp1 HG02109.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.328-52004G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16957670 | ||||||
| chr3:16957815
|
G | T | 13 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(10): Show | 13 | HG02055.hp1 HG02109.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.328-51859G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16957815 | ||||||
| chr3:16957885
|
G | A | 7 | a0001c0004t0001g0162a0001c0004t0001g0163a0001c0004t0001g0164others(4): Show | 7 | HG01069.hp2 HG01934.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.328-51789G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16957885 | ||||||
| chr3:16957886
|
T | C | 7 | a0001c0004t0001g0162a0001c0004t0001g0163a0001c0004t0001g0164others(4): Show | 7 | HG01069.hp2 HG01934.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.328-51788T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16957886 | ||||||
| chr3:16957914
|
G | A | 2 | a0001c0001t0001g0037a0001c0001t0001g0108 | 2 | HG01255.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.328-51760G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16957914 | ||||||
| chr3:16958171
|
A | T | 154 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(151): Show | 156 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.328-51503A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16958171 | ||||||
| chr3:16958172
|
G | C | 1 | a0001c0001t0006g0222 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.328-51502G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16958172 | ||||||
| chr3:16958220
|
T | C | 1 | a0001c0001t0002g0132 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.328-51454T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16958220 | ||||||
| chr3:16958224
|
G | A | 1 | a0001c0003t0001g0003 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.328-51450G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16958224 | ||||||
| chr3:16958233
|
C | T | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.328-51441C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16958233 | ||||||
| chr3:16958460
|
T | TA | 11 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(8): Show | 11 | HG02559.hp2 HG02723.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.328-51207dupA | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16958460 | |||||
| chr3:16958642
|
A | G | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.328-51032A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16958642 | ||||||
| chr3:16958674
|
A | G | 4 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(1): Show | 4 | HG02896.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-51000A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16958674 | ||||||
| chr3:16958736
|
G | A | 156 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(153): Show | 158 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.328-50938G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16958736 | ||||||
| chr3:16958823
|
G | A | 3 | a0001c0002t0001g0120a0001c0002t0001g0121a0001c0002t0001g0122 | 3 | HG02486.hp2 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.328-50851G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16958823 | ||||||
| chr3:16958953
|
C | T | 5 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(2): Show | 5 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.328-50721C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16958953 | ||||||
| chr3:16959289
|
G | A | 1 | a0001c0001t0001g0227 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.328-50385G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16959289 | ||||||
| chr3:16959418
|
G | C | 173 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(170): Show | 175 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.328-50256G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16959418 | ||||||
| chr3:16959472
|
C | T | 1 | a0001c0005t0001g0185 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.328-50202C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16959472 | ||||||
| chr3:16959629
|
C | T | 1 | a0001c0001t0001g0237 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.328-50045C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16959629 | ||||||
| chr3:16959639
|
G | T | 1 | a0001c0003t0001g0211 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.328-50035G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16959639 | ||||||
| chr3:16959673
|
T | G | 61 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(58): Show | 61 | HG00408.hp1 HG01081.hp2 HG01123.hp2 others(58): Show |
intron_variant | MODIFIER | c.328-50001T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16959673 | ||||||
| chr3:16959744
|
T | C | 168 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(165): Show | 170 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.328-49930T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16959744 | ||||||
| chr3:16959871
|
C | T | 1 | a0001c0001t0002g0136 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.328-49803C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16959871 | ||||||
| chr3:16959906
|
C | T | 4 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(1): Show | 4 | HG02965.hp1 HG02976.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-49768C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16959906 | ||||||
| chr3:16960020
|
G | A | 4 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(1): Show | 4 | HG02965.hp1 HG02976.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-49654G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16960020 | ||||||
| chr3:16960072
|
T | C | 154 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(151): Show | 156 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.328-49602T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16960072 | ||||||
| chr3:16960175
|
C | A | 11 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(8): Show | 11 | HG02559.hp2 HG02723.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.328-49499C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16960175 | ||||||
| chr3:16960235
|
C | T | 34 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(31): Show | 34 | HG00408.hp1 HG01175.hp2 HG01255.hp1 others(31): Show |
intron_variant | MODIFIER | c.328-49439C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16960235 | ||||||
| chr3:16960579
|
GT | G | 157 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(154): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.328-49093delT | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16960579 | |||||
| chr3:16960613
|
C | T | 61 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(58): Show | 61 | HG00408.hp1 HG01081.hp2 HG01123.hp2 others(58): Show |
intron_variant | MODIFIER | c.328-49061C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16960613 | ||||||
| chr3:16960644
|
C | A | 1 | a0001c0003t0001g0188 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.328-49030C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16960644 | ||||||
| chr3:16960959
|
G | C | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.328-48715G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16960959 | ||||||
| chr3:16961079
|
G | A | 1 | a0001c0002t0001g0092 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.328-48595G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16961079 | ||||||
| chr3:16961127
|
G | A | 108 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(105): Show | 110 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.328-48547G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16961127 | ||||||
| chr3:16961167
|
C | T | 4 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(1): Show | 4 | HG02965.hp1 HG02976.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-48507C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16961167 | ||||||
| chr3:16961440
|
G | A | 4 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133others(1): Show | 4 | HG02109.hp2 HG02723.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-48234G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16961440 | ||||||
| chr3:16961632
|
C | T | 1 | a0001c0014t0001g0104 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.328-48042C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16961632 | ||||||
| chr3:16961636
|
C | G | 11 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(8): Show | 11 | HG02559.hp2 HG02723.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.328-48038C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16961636 | ||||||
| chr3:16961797
|
C | A | 4 | a0001c0005t0001g0019a0001c0005t0001g0063a0001c0005t0001g0179others(1): Show | 4 | HG01515.hp2 HG03491.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-47877C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16961797 | ||||||
| chr3:16962037
|
A | G | 57 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(54): Show | 58 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.328-47637A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16962037 | ||||||
| chr3:16962168
|
A | G | 1 | a0001c0002t0001g0073 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.328-47506A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16962168 | ||||||
| chr3:16962285
|
A | G | 1 | a0001c0001t0001g0084 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.328-47389A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16962285 | ||||||
| chr3:16962423
|
C | CT | 88 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(85): Show | 89 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.328-47239dupT | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16962423 | |||||
| chr3:16962436
|
C | T | 89 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(86): Show | 90 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.328-47238C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16962436 | ||||||
| chr3:16962535
|
T | A | 17 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(14): Show | 17 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.328-47139T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16962535 | ||||||
| chr3:16962755
|
C | G | 1 | a0001c0001t0001g0203 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.328-46919C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16962755 | ||||||
| chr3:16962792
|
G | A | 106 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(103): Show | 108 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.328-46882G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16962792 | ||||||
| chr3:16962991
|
TA | T | 3 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202 | 3 | HG02976.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.328-46682delA | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16962991 | ||||||
| chr3:16963019
|
G | T | 5 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(2): Show | 5 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.328-46655G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16963019 | ||||||
| chr3:16963197
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.328-46477G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16963197 | ||||||
| chr3:16963197
|
G | T | 1 | a0001c0002t0001g0100 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.328-46477G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16963197 | ||||||
| chr3:16963267
|
G | T | 2 | a0001c0002t0001g0076a0001c0002t0001g0077 | 2 | HG03209.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.328-46407G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16963267 | ||||||
| chr3:16963481
|
A | C | 2 | a0001c0011t0001g0004a0001c0012t0001g0005 | 2 | HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.328-46193A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16963481 | ||||||
| chr3:16963575
|
C | A | 1 | a0001c0001t0001g0236 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.328-46099C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16963575 | ||||||
| chr3:16963624
|
A | G | 3 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010 | 3 | HG02896.hp2 HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.328-46050A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16963624 | ||||||
| chr3:16963651
|
A | C | 1 | a0001c0003t0001g0211 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.328-46023A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16963651 | ||||||
| chr3:16963959
|
G | A | 2 | a0001c0002t0001g0021a0001c0002t0001g0112 | 2 | NA18950.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.328-45715G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16963959 | ||||||
| chr3:16964083
|
T | TA | 4 | a0001c0005t0001g0019a0001c0005t0001g0063a0001c0005t0001g0179others(1): Show | 4 | HG01515.hp2 HG03491.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-45590dupA | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16964083 | |||||
| chr3:16964122
|
A | G | 1 | a0001c0003t0001g0193 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.328-45552A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16964122 | ||||||
| chr3:16964146
|
A | G | 1 | a0001c0001t0001g0226 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.328-45528A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16964146 | ||||||
| chr3:16964341
|
T | G | 171 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(168): Show | 173 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.328-45333T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16964341 | ||||||
| chr3:16964552
|
G | T | 1 | a0001c0002t0001g0210 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.328-45122G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16964552 | ||||||
| chr3:16964728
|
G | T | 1 | a0001c0002t0001g0205 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.328-44946G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16964728 | ||||||
| chr3:16964729
|
G | A | 2 | a0001c0011t0001g0004a0001c0012t0001g0005 | 2 | HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.328-44945G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16964729 | ||||||
| chr3:16964782
|
A | G | 3 | a0001c0011t0001g0004a0001c0012t0001g0005a0001c0013t0001g0198 | 3 | HG02055.hp1 HG02109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.328-44892A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16964782 | ||||||
| chr3:16964909
|
G | T | 154 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(151): Show | 156 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.328-44765G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16964909 | ||||||
| chr3:16964975
|
G | T | 1 | a0001c0001t0001g0103 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.328-44699G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16964975 | ||||||
| chr3:16965037
|
G | T | 61 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(58): Show | 61 | HG00408.hp1 HG01081.hp2 HG01123.hp2 others(58): Show |
intron_variant | MODIFIER | c.328-44637G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16965037 | ||||||
| chr3:16965077
|
A | G | 166 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(163): Show | 168 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.328-44597A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16965077 | ||||||
| chr3:16965094
|
C | A | 97 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(94): Show | 98 | HG00408.hp1 HG01081.hp2 HG01099.hp1 others(95): Show |
intron_variant | MODIFIER | c.328-44580C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16965094 | ||||||
| chr3:16965099
|
C | A | 97 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(94): Show | 98 | HG00408.hp1 HG01081.hp2 HG01099.hp1 others(95): Show |
intron_variant | MODIFIER | c.328-44575C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16965099 | ||||||
| chr3:16965103
|
T | C | 97 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(94): Show | 98 | HG00408.hp1 HG01081.hp2 HG01099.hp1 others(95): Show |
intron_variant | MODIFIER | c.328-44571T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16965103 | ||||||
| chr3:16965122
|
C | T | 97 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(94): Show | 98 | HG00408.hp1 HG01081.hp2 HG01099.hp1 others(95): Show |
intron_variant | MODIFIER | c.328-44552C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16965122 | ||||||
| chr3:16965145
|
T | C | 1 | a0001c0014t0001g0104 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.328-44529T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16965145 | ||||||
| chr3:16965166
|
G | A | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.328-44508G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16965166 | ||||||
| chr3:16965171
|
T | C | 1 | a0001c0001t0001g0014 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.328-44503T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16965171 | ||||||
| chr3:16965194
|
G | A | 6 | a0001c0002t0001g0125a0001c0002t0001g0126a0001c0002t0001g0205others(3): Show | 6 | HG02559.hp2 HG02723.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.328-44480G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16965194 | ||||||
| chr3:16965203
|
A | G | 2 | a0001c0001t0001g0197a0001c0001t0006g0222 | 2 | HG02258.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.328-44471A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16965203 | ||||||
| chr3:16965232
|
C | A | 97 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(94): Show | 98 | HG00408.hp1 HG01081.hp2 HG01099.hp1 others(95): Show |
intron_variant | MODIFIER | c.328-44442C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16965232 | ||||||
| chr3:16965260
|
C | T | 97 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(94): Show | 98 | HG00408.hp1 HG01081.hp2 HG01099.hp1 others(95): Show |
intron_variant | MODIFIER | c.328-44414C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16965260 | ||||||
| chr3:16965261
|
G | C | 3 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202 | 3 | HG02976.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.328-44413G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16965261 | ||||||
| chr3:16965272
|
A | G | 1 | a0001c0001t0001g0197 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.328-44402A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16965272 | ||||||
| chr3:16965289
|
G | A | 1 | a0001c0002t0001g0095 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.328-44385G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16965289 | ||||||
| chr3:16965489
|
C | G | 27 | a0001c0002t0001g0098a0001c0002t0001g0099a0001c0002t0001g0100others(24): Show | 28 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.328-44185C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16965489 | ||||||
| chr3:16965490
|
T | A | 27 | a0001c0002t0001g0098a0001c0002t0001g0099a0001c0002t0001g0100others(24): Show | 28 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.328-44184T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16965490 | ||||||
| chr3:16965579
|
G | A | 1 | a0001c0014t0001g0104 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.328-44095G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16965579 | ||||||
| chr3:16965628
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.328-44046C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16965628 | ||||||
| chr3:16965787
|
T | C | 3 | a0001c0011t0001g0004a0001c0012t0001g0005a0001c0013t0001g0198 | 3 | HG02055.hp1 HG02109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.328-43887T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16965787 | ||||||
| chr3:16965796
|
G | T | 1 | a0001c0008t0001g0242 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.328-43878G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16965796 | ||||||
| chr3:16965919
|
G | A | 1 | a0001c0002t0001g0149 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.328-43755G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16965919 | ||||||
| chr3:16965921
|
G | A | 4 | a0001c0005t0001g0019a0001c0005t0001g0063a0001c0005t0001g0179others(1): Show | 4 | HG01515.hp2 HG03491.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-43753G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16965921 | ||||||
| chr3:16965984
|
A | C | 1 | a0001c0002t0001g0122 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.328-43690A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16965984 | ||||||
| chr3:16966151
|
A | G | 1 | a0001c0003t0001g0211 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.328-43523A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16966151 | ||||||
| chr3:16966156
|
G | T | 15 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(12): Show | 15 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.328-43518G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16966156 | ||||||
| chr3:16966181
|
A | G | 1 | a0001c0001t0001g0108 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.328-43493A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16966181 | ||||||
| chr3:16966200
|
T | C | 57 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(54): Show | 58 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.328-43474T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16966200 | ||||||
| chr3:16966201
|
G | T | 57 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(54): Show | 58 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.328-43473G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16966201 | ||||||
| chr3:16966204
|
C | T | 57 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(54): Show | 58 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.328-43470C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16966204 | ||||||
| chr3:16966228
|
A | G | 58 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(55): Show | 59 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.328-43446A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16966228 | ||||||
| chr3:16966332
|
G | A | 3 | a0001c0002t0001g0056a0001c0002t0001g0105a0001c0017t0001g0050 | 3 | NA18942.hp2 NA18993.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.328-43342G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16966332 | ||||||
| chr3:16966357
|
A | G | 58 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(55): Show | 59 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.328-43317A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16966357 | ||||||
| chr3:16966526
|
G | A | 61 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(58): Show | 61 | HG00408.hp1 HG01081.hp2 HG01123.hp2 others(58): Show |
intron_variant | MODIFIER | c.328-43148G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16966526 | ||||||
| chr3:16966628
|
G | A | 1 | a0001c0001t0001g0239 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.328-43046G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16966628 | ||||||
| chr3:16966666
|
A | T | 17 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(14): Show | 17 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.328-43008A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16966666 | ||||||
| chr3:16966738
|
A | G | 63 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(60): Show | 63 | HG00408.hp1 HG01081.hp2 HG01123.hp2 others(60): Show |
intron_variant | MODIFIER | c.328-42936A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16966738 | ||||||
| chr3:16966800
|
A | C | 3 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0002g0142 | 3 | HG01123.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.328-42874A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16966800 | ||||||
| chr3:16966955
|
G | C | 2 | a0001c0011t0001g0004a0001c0012t0001g0005 | 2 | HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.328-42719G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16966955 | ||||||
| chr3:16967138
|
G | A | 1 | a0001c0002t0001g0207 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.328-42536G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16967138 | ||||||
| chr3:16967202
|
A | G | 3 | a0001c0002t0001g0007a0001c0002t0001g0199a0001c0002t0001g0210 | 3 | HG02257.hp1 HG02280.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.328-42472A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16967202 | ||||||
| chr3:16967476
|
G | A | 3 | a0001c0011t0001g0004a0001c0012t0001g0005a0001c0013t0001g0198 | 3 | HG02055.hp1 HG02109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.328-42198G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16967476 | ||||||
| chr3:16967856
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.328-41818G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16967856 | ||||||
| chr3:16967867
|
G | A | 17 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(14): Show | 17 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.328-41807G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16967867 | ||||||
| chr3:16967917
|
T | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0039a0001c0001t0001g0109 | 3 | HG02074.hp2 NA18944.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.328-41757T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16967917 | ||||||
| chr3:16967931
|
A | G | 4 | a0001c0005t0001g0019a0001c0005t0001g0063a0001c0005t0001g0179others(1): Show | 4 | HG01515.hp2 HG03491.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-41743A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16967931 | ||||||
| chr3:16967970
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.328-41704C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16967970 | ||||||
| chr3:16968162
|
G | A | 8 | a0001c0002t0001g0031a0001c0002t0001g0111a0001c0002t0001g0113others(5): Show | 8 | HG00408.hp2 HG00741.hp1 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.328-41512G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16968162 | ||||||
| chr3:16968310
|
A | G | 5 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(2): Show | 5 | HG02896.hp2 HG03098.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.328-41364A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16968310 | ||||||
| chr3:16968370
|
A | G | 5 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(2): Show | 5 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.328-41304A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16968370 | ||||||
| chr3:16968510
|
A | T | 4 | a0001c0005t0001g0019a0001c0005t0001g0063a0001c0005t0001g0179others(1): Show | 4 | HG01515.hp2 HG03491.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-41164A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16968510 | ||||||
| chr3:16968601
|
T | G | 157 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(154): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.328-41073T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16968601 | ||||||
| chr3:16968612
|
G | A | 4 | a0001c0002t0001g0214a0001c0002t0001g0233a0001c0002t0001g0238others(1): Show | 4 | HG01891.hp2 HG02258.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-41062G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16968612 | ||||||
| chr3:16968716
|
C | G | 4 | a0001c0005t0001g0019a0001c0005t0001g0063a0001c0005t0001g0179others(1): Show | 4 | HG01515.hp2 HG03491.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-40958C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16968716 | ||||||
| chr3:16968821
|
T | A | 5 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(2): Show | 5 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.328-40853T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16968821 | ||||||
| chr3:16968899
|
G | C | 4 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0219others(1): Show | 4 | HG02895.hp2 HG03041.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-40775G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16968899 | ||||||
| chr3:16968909
|
T | C | 35 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(32): Show | 35 | HG00408.hp1 HG01175.hp2 HG01255.hp1 others(32): Show |
intron_variant | MODIFIER | c.328-40765T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16968909 | ||||||
| chr3:16969095
|
C | G | 4 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0219others(1): Show | 4 | HG02895.hp2 HG03041.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-40579C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16969095 | ||||||
| chr3:16969372
|
T | A | 1 | a0001c0003t0001g0211 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.328-40302T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16969372 | ||||||
| chr3:16969405
|
G | A | 3 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202 | 3 | HG02976.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.328-40269G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16969405 | ||||||
| chr3:16969446
|
A | G | 4 | a0001c0003t0004g0001a0001c0003t0004g0128a0001c0003t0004g0152others(1): Show | 5 | HG02486.hp1 HG03139.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.328-40228A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16969446 | ||||||
| chr3:16969726
|
G | A | 170 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(167): Show | 172 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.328-39948G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16969726 | ||||||
| chr3:16969761
|
G | C | 1 | a0001c0001t0002g0143 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.328-39913G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16969761 | ||||||
| chr3:16969982
|
C | G | 139 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(136): Show | 141 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.328-39692C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16969982 | ||||||
| chr3:16970038
|
T | TTA | 27 | a0001c0002t0001g0021a0001c0002t0001g0022a0001c0002t0001g0023others(24): Show | 28 | HG00280.hp2 HG00741.hp2 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.328-39616_328-3961 others(6): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16970038 | |||||
| chr3:16970038
|
T | TTATA | 4 | a0001c0002t0001g0098a0001c0002t0001g0099a0001c0002t0001g0100others(1): Show | 4 | HG00099.hp1 HG00323.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-39618_328-3961 others(8): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16970038 | |||||
| chr3:16970038
|
T | TTATATAT others(1): Show |
3 | a0001c0011t0001g0004a0001c0012t0001g0005a0001c0013t0001g0198 | 3 | HG02055.hp1 HG02109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.328-39622_328-3961 others(12): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16970038 | |||||
| chr3:16970054
|
A | ATTTT | 3 | a0001c0001t0001g0086a0001c0001t0001g0090a0001c0001t0001g0109 | 3 | HG02132.hp1 HG02602.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.328-39619_328-3961 others(8): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16970054 | |||||
| chr3:16970054
|
A | T | 2 | a0001c0003t0004g0001a0001c0003t0004g0128 | 3 | HG03139.hp1 HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.328-39620A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16970054 | ||||||
| chr3:16970056
|
A | ATTTT | 32 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(29): Show | 32 | HG01175.hp2 HG01255.hp1 HG01256.hp1 others(29): Show |
intron_variant | MODIFIER | c.328-39617_328-3961 others(8): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16970056 | |||||
| chr3:16970056
|
A | T | 18 | a0001c0001t0001g0043a0001c0001t0001g0086a0001c0001t0001g0090others(15): Show | 19 | HG01515.hp2 HG01934.hp1 HG01978.hp2 others(16): Show |
intron_variant | MODIFIER | c.328-39618A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16970056 | ||||||
| chr3:16970058
|
A | ATATT | 14 | a0001c0001t0001g0195a0001c0001t0001g0200a0001c0001t0001g0201others(11): Show | 14 | HG01943.hp2 HG02622.hp1 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.328-39615_328-3961 others(8): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16970058 | |||||
| chr3:16970058
|
A | ATT | 42 | a0000c0007t0002g0146a0001c0001t0001g0101a0001c0001t0001g0102others(39): Show | 42 | HG01081.hp2 HG01099.hp1 HG01123.hp2 others(39): Show |
intron_variant | MODIFIER | c.328-39613_328-3961 others(6): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16970058 | |||||
| chr3:16970058
|
A | T | 81 | a0000c0007t0002g0147a0000c0007t0002g0213a0000c0019t0002g0148others(78): Show | 82 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.328-39616A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16970058 | ||||||
| chr3:16970136
|
G | A | 4 | a0001c0004t0002g0171a0001c0004t0002g0172a0001c0004t0002g0173others(1): Show | 4 | HG02074.hp1 HG02155.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-39538G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16970136 | ||||||
| chr3:16970189
|
C | T | 80 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(77): Show | 81 | HG00408.hp1 HG01081.hp2 HG01123.hp2 others(78): Show |
intron_variant | MODIFIER | c.328-39485C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16970189 | ||||||
| chr3:16970210
|
C | A | 5 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(2): Show | 5 | HG02896.hp2 HG03098.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.328-39464C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16970210 | ||||||
| chr3:16970217
|
C | A | 4 | a0001c0005t0001g0019a0001c0005t0001g0063a0001c0005t0001g0179others(1): Show | 4 | HG01515.hp2 HG03491.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-39457C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16970217 | ||||||
| chr3:16970217
|
C | G | 1 | a0001c0020t0003g0178 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.328-39457C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16970217 | ||||||
| chr3:16970331
|
A | G | 1 | a0001c0001t0001g0234 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.328-39343A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16970331 | ||||||
| chr3:16970348
|
G | A | 1 | a0001c0004t0001g0002 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.328-39326G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16970348 | ||||||
| chr3:16970460
|
A | G | 1 | a0001c0002t0001g0087 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.328-39214A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16970460 | ||||||
| chr3:16970470
|
A | G | 4 | a0001c0005t0001g0019a0001c0005t0001g0063a0001c0005t0001g0179others(1): Show | 4 | HG01515.hp2 HG03491.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-39204A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16970470 | ||||||
| chr3:16970515
|
T | G | 7 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(4): Show | 7 | HG02055.hp1 HG02109.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.328-39159T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16970515 | ||||||
| chr3:16970806
|
T | C | 3 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017 | 3 | NA18942.hp1 NA18949.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.328-38868T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16970806 | ||||||
| chr3:16970838
|
CT | C | 11 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(8): Show | 11 | HG02559.hp2 HG02723.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.328-38832delT | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16970838 | |||||
| chr3:16970840
|
T | G | 3 | a0001c0002t0001g0120a0001c0002t0001g0121a0001c0002t0001g0122 | 3 | HG02486.hp2 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.328-38834T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16970840 | ||||||
| chr3:16970882
|
G | A | 1 | a0001c0002t0001g0021 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.328-38792G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16970882 | ||||||
| chr3:16970903
|
G | A | 1 | a0001c0002t0001g0149 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.328-38771G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16970903 | ||||||
| chr3:16970905
|
G | A | 11 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(8): Show | 11 | HG02559.hp2 HG02723.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.328-38769G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16970905 | ||||||
| chr3:16970937
|
A | G | 1 | a0001c0001t0001g0203 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.328-38737A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16970937 | ||||||
| chr3:16970987
|
G | A | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.328-38687G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16970987 | ||||||
| chr3:16970993
|
T | G | 1 | a0003c0010t0001g0049 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.328-38681T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16970993 | ||||||
| chr3:16971100
|
C | A | 1 | a0001c0002t0001g0047 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.328-38574C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16971100 | ||||||
| chr3:16971147
|
T | C | 6 | a0001c0002t0001g0031a0001c0002t0001g0111a0001c0002t0001g0113others(3): Show | 6 | HG00408.hp2 HG02129.hp1 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.328-38527T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16971147 | ||||||
| chr3:16971298
|
C | A | 7 | a0001c0001t0001g0229a0001c0003t0001g0003a0001c0003t0001g0030others(4): Show | 7 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.328-38376C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16971298 | ||||||
| chr3:16971412
|
A | G | 1 | a0001c0003t0001g0211 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.328-38262A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16971412 | ||||||
| chr3:16971456
|
G | A | 126 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(123): Show | 127 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.328-38218G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16971456 | ||||||
| chr3:16971572
|
C | T | 1 | a0001c0013t0001g0198 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.328-38102C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16971572 | ||||||
| chr3:16971631
|
A | T | 4 | a0001c0005t0001g0019a0001c0005t0001g0063a0001c0005t0001g0179others(1): Show | 4 | HG01515.hp2 HG03491.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-38043A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16971631 | ||||||
| chr3:16971661
|
T | C | 1 | a0001c0005t0001g0179 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.328-38013T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16971661 | ||||||
| chr3:16971710
|
C | A | 34 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(31): Show | 34 | HG00408.hp1 HG01175.hp2 HG01255.hp1 others(31): Show |
intron_variant | MODIFIER | c.328-37964C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16971710 | ||||||
| chr3:16971804
|
T | A | 1 | a0001c0003t0001g0211 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.328-37870T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16971804 | ||||||
| chr3:16971887
|
G | A | 13 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(10): Show | 14 | HG01515.hp2 HG01934.hp1 HG01978.hp2 others(11): Show |
intron_variant | MODIFIER | c.328-37787G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16971887 | ||||||
| chr3:16971915
|
C | G | 4 | a0001c0005t0001g0019a0001c0005t0001g0063a0001c0005t0001g0179others(1): Show | 4 | HG01515.hp2 HG03491.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-37759C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16971915 | ||||||
| chr3:16971980
|
C | T | 1 | a0001c0003t0001g0211 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.328-37694C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16971980 | ||||||
| chr3:16972056
|
T | A | 247 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(244): Show | 249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.328-37618T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16972056 | ||||||
| chr3:16972128
|
G | A | 1 | a0001c0003t0003g0215 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.328-37546G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16972128 | ||||||
| chr3:16972214
|
C | T | 97 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(94): Show | 98 | HG00408.hp1 HG01081.hp2 HG01099.hp1 others(95): Show |
intron_variant | MODIFIER | c.328-37460C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16972214 | ||||||
| chr3:16972441
|
G | A | 9 | a0001c0002t0001g0074a0001c0002t0001g0075a0001c0002t0001g0076others(6): Show | 9 | HG02559.hp1 HG02717.hp1 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.328-37233G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16972441 | ||||||
| chr3:16972460
|
A | C | 1 | a0001c0014t0001g0104 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.328-37214A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16972460 | ||||||
| chr3:16972918
|
G | A | 11 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(8): Show | 11 | HG02559.hp2 HG02723.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.328-36756G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16972918 | ||||||
| chr3:16973040
|
T | A | 3 | a0001c0002t0001g0007a0001c0002t0001g0199a0001c0002t0001g0210 | 3 | HG02257.hp1 HG02280.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.328-36634T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16973040 | ||||||
| chr3:16973207
|
C | G | 1 | a0001c0002t0001g0075 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.328-36467C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16973207 | ||||||
| chr3:16973216
|
A | T | 1 | a0001c0004t0002g0172 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.328-36458A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16973216 | ||||||
| chr3:16973293
|
A | G | 1 | a0001c0003t0003g0216 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.328-36381A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16973293 | ||||||
| chr3:16973297
|
C | A | 1 | a0001c0001t0001g0236 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.328-36377C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16973297 | ||||||
| chr3:16973314
|
A | G | 64 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(61): Show | 64 | HG00408.hp1 HG01081.hp2 HG01123.hp2 others(61): Show |
intron_variant | MODIFIER | c.328-36360A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16973314 | ||||||
| chr3:16973351
|
T | G | 2 | a0001c0011t0001g0004a0001c0012t0001g0005 | 2 | HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.328-36323T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16973351 | ||||||
| chr3:16973355
|
C | CT | 69 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(66): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.328-36303dupT | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16973355 | |||||
| chr3:16973355
|
CT | C | 17 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(14): Show | 17 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.328-36303delT | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16973355 | |||||
| chr3:16973414
|
T | C | 27 | a0001c0002t0001g0098a0001c0002t0001g0099a0001c0002t0001g0100others(24): Show | 28 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.328-36260T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16973414 | ||||||
| chr3:16973425
|
A | G | 3 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202 | 3 | HG02976.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.328-36249A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16973425 | ||||||
| chr3:16973435
|
A | C | 7 | a0001c0004t0001g0162a0001c0004t0001g0163a0001c0004t0001g0164others(4): Show | 7 | HG01069.hp2 HG01934.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.328-36239A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16973435 | ||||||
| chr3:16973757
|
G | T | 13 | a0001c0002t0001g0024a0001c0002t0001g0046a0001c0002t0001g0047others(10): Show | 13 | HG01069.hp1 HG01074.hp1 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.328-35917G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16973757 | ||||||
| chr3:16973824
|
A | T | 1 | a0001c0002t0001g0111 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.328-35850A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16973824 | ||||||
| chr3:16973881
|
C | T | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.328-35793C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16973881 | ||||||
| chr3:16973883
|
A | G | 1 | a0001c0002t0001g0046 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.328-35791A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16973883 | ||||||
| chr3:16973889
|
G | A | 1 | a0001c0001t0001g0239 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.328-35785G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16973889 | ||||||
| chr3:16973929
|
A | G | 1 | a0001c0001t0001g0013 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.328-35745A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16973929 | ||||||
| chr3:16973979
|
G | A | 2 | a0001c0005t0001g0063a0001c0005t0001g0179 | 2 | HG01515.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.328-35695G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16973979 | ||||||
| chr3:16974000
|
G | A | 3 | a0001c0001t0001g0197a0001c0001t0002g0127a0001c0001t0006g0222 | 3 | HG02258.hp2 NA18986.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.328-35674G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16974000 | ||||||
| chr3:16974045
|
T | A | 1 | a0001c0004t0002g0172 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.328-35629T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16974045 | ||||||
| chr3:16974200
|
G | A | 11 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(8): Show | 11 | HG02559.hp2 HG02723.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.328-35474G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16974200 | ||||||
| chr3:16974303
|
G | A | 4 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133others(1): Show | 4 | HG02109.hp2 HG02723.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-35371G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16974303 | ||||||
| chr3:16974443
|
T | C | 63 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(60): Show | 63 | HG00408.hp1 HG01081.hp2 HG01123.hp2 others(60): Show |
intron_variant | MODIFIER | c.328-35231T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16974443 | ||||||
| chr3:16974467
|
T | C | 2 | a0001c0001t0001g0101a0001c0001t0001g0102 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.328-35207T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16974467 | ||||||
| chr3:16974635
|
T | C | 61 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(58): Show | 61 | HG00408.hp1 HG01081.hp2 HG01123.hp2 others(58): Show |
intron_variant | MODIFIER | c.328-35039T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16974635 | ||||||
| chr3:16974754
|
A | G | 2 | a0001c0001t0001g0118a0001c0001t0001g0228 | 2 | NA18956.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.328-34920A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16974754 | ||||||
| chr3:16974897
|
GT | G | 3 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202 | 3 | HG02976.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.328-34776delT | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16974897 | ||||||
| chr3:16974905
|
G | T | 1 | a0001c0002t0001g0075 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.328-34769G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16974905 | ||||||
| chr3:16974945
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.328-34729C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16974945 | ||||||
| chr3:16975002
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.328-34672C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16975002 | ||||||
| chr3:16975168
|
G | A | 3 | a0001c0011t0001g0004a0001c0012t0001g0005a0001c0013t0001g0198 | 3 | HG02055.hp1 HG02109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.328-34506G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16975168 | ||||||
| chr3:16975227
|
C | T | 168 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(165): Show | 170 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.328-34447C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16975227 | ||||||
| chr3:16975244
|
C | A | 4 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103others(1): Show | 4 | HG02818.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-34430C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16975244 | ||||||
| chr3:16975302
|
A | C | 140 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(137): Show | 142 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.328-34372A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16975302 | ||||||
| chr3:16975368
|
C | T | 4 | a0001c0005t0001g0019a0001c0005t0001g0063a0001c0005t0001g0179others(1): Show | 4 | HG01515.hp2 HG03491.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-34306C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16975368 | ||||||
| chr3:16975509
|
G | A | 27 | a0001c0002t0001g0098a0001c0002t0001g0099a0001c0002t0001g0100others(24): Show | 28 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.328-34165G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16975509 | ||||||
| chr3:16975595
|
T | C | 1 | a0001c0020t0003g0178 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.328-34079T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16975595 | ||||||
| chr3:16975635
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.328-34039C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16975635 | ||||||
| chr3:16975925
|
G | C | 1 | a0001c0013t0001g0198 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.328-33749G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16975925 | ||||||
| chr3:16976046
|
G | T | 1 | a0001c0014t0001g0104 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.328-33628G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16976046 | ||||||
| chr3:16976126
|
C | T | 29 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(26): Show | 29 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.328-33548C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16976126 | ||||||
| chr3:16976199
|
C | T | 27 | a0001c0002t0001g0098a0001c0002t0001g0099a0001c0002t0001g0100others(24): Show | 28 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.328-33475C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16976199 | ||||||
| chr3:16976320
|
A | G | 1 | a0001c0002t0001g0006 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.328-33354A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16976320 | ||||||
| chr3:16976658
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.328-33016C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16976658 | ||||||
| chr3:16976745
|
G | A | 1 | a0001c0014t0001g0104 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.328-32929G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16976745 | ||||||
| chr3:16976764
|
G | T | 77 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(74): Show | 78 | HG00408.hp1 HG01081.hp2 HG01123.hp2 others(75): Show |
intron_variant | MODIFIER | c.328-32910G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16976764 | ||||||
| chr3:16976912
|
C | T | 1 | a0001c0005t0001g0179 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.328-32762C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16976912 | ||||||
| chr3:16977041
|
T | C | 1 | a0000c0019t0002g0148 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.328-32633T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16977041 | ||||||
| chr3:16977114
|
G | GCA | 23 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133others(20): Show | 23 | HG00741.hp1 HG01099.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.328-32543_328-3254 others(6): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16977114 | |||||
| chr3:16977187
|
C | T | 1 | a0001c0003t0001g0211 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.328-32487C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16977187 | ||||||
| chr3:16977389
|
C | T | 1 | a0001c0002t0001g0066 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.328-32285C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16977389 | ||||||
| chr3:16978076
|
A | G | 3 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202 | 3 | HG02976.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.328-31598A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16978076 | ||||||
| chr3:16978198
|
T | C | 17 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(14): Show | 17 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.328-31476T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16978198 | ||||||
| chr3:16978359
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.328-31315C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16978359 | ||||||
| chr3:16978365
|
C | T | 156 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(153): Show | 158 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.328-31309C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16978365 | ||||||
| chr3:16978418
|
T | C | 27 | a0001c0002t0001g0098a0001c0002t0001g0099a0001c0002t0001g0100others(24): Show | 28 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.328-31256T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16978418 | ||||||
| chr3:16978531
|
A | T | 63 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(60): Show | 63 | HG00408.hp1 HG01081.hp2 HG01123.hp2 others(60): Show |
intron_variant | MODIFIER | c.328-31143A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16978531 | ||||||
| chr3:16978738
|
G | A | 1 | a0001c0002t0001g0066 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.328-30936G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16978738 | ||||||
| chr3:16978882
|
A | G | 1 | a0001c0001t0001g0225 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.328-30792A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16978882 | ||||||
| chr3:16978932
|
C | T | 76 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(73): Show | 77 | HG00408.hp1 HG01081.hp2 HG01123.hp2 others(74): Show |
intron_variant | MODIFIER | c.328-30742C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16978932 | ||||||
| chr3:16979078
|
G | A | 1 | a0001c0003t0001g0018 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.328-30596G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16979078 | ||||||
| chr3:16979081
|
A | G | 77 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(74): Show | 78 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.328-30593A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16979081 | ||||||
| chr3:16979234
|
A | G | 4 | a0001c0005t0001g0019a0001c0005t0001g0063a0001c0005t0001g0179others(1): Show | 4 | HG01515.hp2 HG03491.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-30440A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16979234 | ||||||
| chr3:16979357
|
T | TTAA | 17 | a0001c0001t0001g0108a0001c0001t0001g0200a0001c0001t0001g0201others(14): Show | 17 | HG01074.hp2 HG01515.hp1 HG01975.hp1 others(14): Show |
intron_variant | MODIFIER | c.328-30316_328-3031 others(7): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16979357 | |||||
| chr3:16979360
|
A | AATTG | 228 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(225): Show | 230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.328-30312_328-3031 others(8): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16979360 | |||||
| chr3:16979360
|
A | G | 19 | a0001c0001t0001g0108a0001c0001t0001g0200a0001c0001t0001g0201others(16): Show | 19 | HG00280.hp2 HG01074.hp2 HG01515.hp1 others(16): Show |
intron_variant | MODIFIER | c.328-30314A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16979360 | ||||||
| chr3:16979482
|
T | C | 159 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(156): Show | 161 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.328-30192T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16979482 | ||||||
| chr3:16979483
|
G | A | 19 | a0001c0002t0001g0098a0001c0002t0001g0099a0001c0002t0001g0100others(16): Show | 20 | HG00099.hp1 HG00323.hp2 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.328-30191G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16979483 | ||||||
| chr3:16979509
|
A | G | 159 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(156): Show | 161 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.328-30165A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16979509 | ||||||
| chr3:16979510
|
T | G | 159 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(156): Show | 161 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.328-30164T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16979510 | ||||||
| chr3:16979516
|
G | A | 11 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(8): Show | 11 | HG02559.hp2 HG02723.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.328-30158G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16979516 | ||||||
| chr3:16979545
|
C | G | 159 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(156): Show | 161 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.328-30129C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16979545 | ||||||
| chr3:16979570
|
C | T | 57 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(54): Show | 58 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.328-30104C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16979570 | ||||||
| chr3:16979662
|
A | G | 27 | a0001c0002t0001g0098a0001c0002t0001g0099a0001c0002t0001g0100others(24): Show | 28 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.328-30012A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16979662 | ||||||
| chr3:16979664
|
C | T | 78 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(75): Show | 79 | HG00408.hp1 HG01081.hp2 HG01123.hp2 others(76): Show |
intron_variant | MODIFIER | c.328-30010C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16979664 | ||||||
| chr3:16979686
|
G | C | 4 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(1): Show | 4 | HG02965.hp1 HG02976.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-29988G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16979686 | ||||||
| chr3:16979688
|
A | G | 28 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(25): Show | 28 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.328-29986A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16979688 | ||||||
| chr3:16979689
|
G | T | 1 | a0001c0003t0003g0209 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.328-29985G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16979689 | ||||||
| chr3:16979697
|
C | G | 1 | a0001c0001t0001g0230 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.328-29977C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16979697 | ||||||
| chr3:16979706
|
G | T | 1 | a0001c0001t0001g0103 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.328-29968G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16979706 | ||||||
| chr3:16979714
|
T | G | 1 | a0001c0001t0001g0197 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.328-29960T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16979714 | ||||||
| chr3:16979753
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.328-29921G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16979753 | ||||||
| chr3:16979776
|
T | C | 1 | a0001c0001t0001g0053 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.328-29898T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16979776 | ||||||
| chr3:16979777
|
T | C | 1 | a0001c0001t0001g0053 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.328-29897T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16979777 | ||||||
| chr3:16979787
|
T | C | 1 | a0001c0001t0001g0053 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.328-29887T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16979787 | ||||||
| chr3:16979793
|
C | G | 2 | a0001c0001t0001g0053a0001c0003t0004g0153 | 2 | HG01175.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.328-29881C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16979793 | ||||||
| chr3:16979840
|
A | G | 2 | a0001c0001t0001g0226a0001c0001t0001g0230 | 2 | HG03831.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.328-29834A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16979840 | ||||||
| chr3:16979976
|
C | G | 1 | a0001c0002t0001g0031 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.328-29698C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16979976 | ||||||
| chr3:16979993
|
T | C | 159 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(156): Show | 161 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.328-29681T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16979993 | ||||||
| chr3:16980071
|
C | T | 1 | a0001c0002t0001g0062 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.328-29603C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16980071 | ||||||
| chr3:16980101
|
A | C | 170 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(167): Show | 172 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.328-29573A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16980101 | ||||||
| chr3:16980106
|
A | ACCTCCCT others(682): Show |
25 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(22): Show | 25 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.328-29558_328-2955 others(693): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980106 | |||||
| chr3:16980106
|
A | ACCTCCCT others(683): Show |
1 | a0001c0001t0001g0150 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.328-29558_328-2955 others(694): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980106 | |||||
| chr3:16980106
|
A | ACCTCCCT others(682): Show |
1 | a0001c0001t0002g0159 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.328-29558_328-2955 others(693): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980106 | |||||
| chr3:16980106
|
A | ACCTCCCT others(683): Show |
1 | a0001c0001t0002g0151 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.328-29558_328-2955 others(694): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980106 | |||||
| chr3:16980106
|
A | ACCTCCCT others(776): Show |
1 | a0001c0001t0001g0226 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.328-29549_328-2954 others(787): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980106 | |||||
| chr3:16980121
|
G | A | 1 | a0001c0002t0001g0107 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.328-29553G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16980121 | ||||||
| chr3:16980126
|
A | G | 217 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(214): Show | 219 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.328-29548A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16980126 | ||||||
| chr3:16980136
|
GT | G | 28 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(25): Show | 28 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.328-29537delT | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16980136 | ||||||
| chr3:16980137
|
T | C | 1 | a0001c0001t0001g0226 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.328-29537T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16980137 | ||||||
| chr3:16980138
|
G | C | 28 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(25): Show | 28 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.328-29536G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16980138 | ||||||
| chr3:16980138
|
G | GGGGGGCT others(730): Show |
1 | a0001c0014t0001g0104 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.328-29531_328-2953 others(741): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980138 | |||||
| chr3:16980138
|
G | GGGGGGCT others(723): Show |
1 | a0001c0001t0001g0225 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.328-29531_328-2953 others(734): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980138 | |||||
| chr3:16980138
|
G | GGGGGGGC others(674): Show |
1 | a0001c0002t0001g0046 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.328-29521_328-2952 others(685): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980138 | |||||
| chr3:16980138
|
G | GGGGGGGC others(546): Show |
1 | a0001c0002t0001g0057 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.328-29521_328-2952 others(557): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980138 | |||||
| chr3:16980138
|
G | GGGGGGGC others(774): Show |
4 | a0001c0002t0001g0074a0001c0002t0001g0078a0001c0002t0001g0079others(1): Show | 4 | HG02559.hp1 HG02717.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-29521_328-2952 others(785): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980138 | |||||
| chr3:16980138
|
G | GGGGGGGC others(773): Show |
17 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(14): Show | 17 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.328-29521_328-2952 others(784): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980138 | |||||
| chr3:16980138
|
G | GGGGGGGC others(773): Show |
1 | a0001c0011t0001g0004 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.328-29521_328-2952 others(784): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980138 | |||||
| chr3:16980138
|
G | GGGGGGGC others(773): Show |
1 | a0001c0001t0001g0203 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.328-29521_328-2952 others(784): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980138 | |||||
| chr3:16980138
|
G | GGGGGGGC others(773): Show |
3 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202 | 3 | HG02976.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.328-29521_328-2952 others(784): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980138 | |||||
| chr3:16980138
|
G | GGGGGGGC others(775): Show |
1 | a0001c0012t0001g0005 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.328-29521_328-2952 others(786): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980138 | |||||
| chr3:16980138
|
G | GGGGGGGC others(773): Show |
3 | a0001c0005t0001g0019a0001c0005t0001g0179a0001c0005t0001g0185 | 3 | HG03491.hp2 HG03704.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.328-29521_328-2952 others(784): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980138 | |||||
| chr3:16980138
|
G | GGGGGGGC others(773): Show |
12 | a0001c0001t0001g0197a0001c0002t0001g0007a0001c0002t0001g0008others(9): Show | 13 | HG02257.hp1 HG02258.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.328-29521_328-2952 others(784): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980138 | |||||
| chr3:16980138
|
G | GGGGGGGC others(774): Show |
1 | a0001c0003t0004g0153 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.328-29521_328-2952 others(785): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980138 | |||||
| chr3:16980138
|
G | GGGGGGGC others(773): Show |
1 | a0001c0001t0001g0221 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.328-29521_328-2952 others(784): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980138 | |||||
| chr3:16980138
|
G | GGGGGGGC others(773): Show |
48 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(45): Show | 48 | HG01123.hp2 HG01255.hp1 HG01256.hp1 others(45): Show |
intron_variant | MODIFIER | c.328-29521_328-2952 others(784): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980138 | |||||
| chr3:16980138
|
G | GGGGGGGC others(774): Show |
1 | a0001c0001t0001g0088 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.328-29521_328-2952 others(785): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980138 | |||||
| chr3:16980138
|
G | GGGGGGGC others(774): Show |
1 | a0001c0001t0001g0053 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.328-29521_328-2952 others(785): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980138 | |||||
| chr3:16980138
|
G | GGGGGGGC others(774): Show |
1 | a0001c0001t0001g0243 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.328-29521_328-2952 others(785): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980138 | |||||
| chr3:16980138
|
G | GGGGGGGC others(775): Show |
1 | a0001c0001t0001g0035 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.328-29521_328-2952 others(786): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980138 | |||||
| chr3:16980138
|
G | GGGGGGGC others(900): Show |
1 | a0001c0001t0001g0247 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.328-29521_328-2952 others(911): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980138 | |||||
| chr3:16980138
|
G | GGGGGGGC others(774): Show |
1 | a0001c0001t0001g0230 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.328-29521_328-2952 others(785): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980138 | |||||
| chr3:16980138
|
G | GGGGGGGC others(773): Show |
5 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(2): Show | 5 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.328-29521_328-2952 others(784): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980138 | |||||
| chr3:16980138
|
G | GGGGGGGC others(773): Show |
2 | a0001c0001t0001g0118a0001c0001t0001g0228 | 2 | NA18956.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.328-29521_328-2952 others(784): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980138 | |||||
| chr3:16980138
|
G | GGGGGGGC others(774): Show |
1 | a0001c0001t0001g0237 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.328-29521_328-2952 others(785): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980138 | |||||
| chr3:16980138
|
G | GGGGGGGC others(773): Show |
1 | a0001c0002t0001g0080 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.328-29521_328-2952 others(784): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980138 | |||||
| chr3:16980138
|
G | GGGGGGGC others(773): Show |
51 | a0001c0002t0001g0006a0001c0002t0001g0020a0001c0002t0001g0021others(48): Show | 51 | HG00280.hp1 HG00741.hp1 HG01074.hp2 others(48): Show |
intron_variant | MODIFIER | c.328-29521_328-2952 others(784): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980138 | |||||
| chr3:16980138
|
G | GGGGGGGC others(774): Show |
3 | a0001c0002t0001g0047a0001c0002t0001g0061a0001c0002t0001g0113 | 3 | HG00408.hp2 HG02027.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.328-29521_328-2952 others(785): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980138 | |||||
| chr3:16980138
|
G | GGGGGGGC others(775): Show |
1 | a0001c0002t0001g0212 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.328-29521_328-2952 others(786): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980138 | |||||
| chr3:16980138
|
G | GGGGGGGC others(773): Show |
3 | a0001c0002t0001g0024a0001c0002t0001g0070a0001c0002t0001g0071 | 3 | HG01069.hp1 HG01074.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.328-29521_328-2952 others(784): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980138 | |||||
| chr3:16980138
|
G | GGGGGGGC others(774): Show |
1 | a0001c0002t0001g0096 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.328-29521_328-2952 others(785): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980138 | |||||
| chr3:16980138
|
G | GGGGGGGC others(773): Show |
1 | a0001c0001t0001g0090 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.328-29521_328-2952 others(784): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980138 | |||||
| chr3:16980138
|
G | GGGGGGGC others(773): Show |
1 | a0001c0002t0001g0068 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.328-29521_328-2952 others(784): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980138 | |||||
| chr3:16980138
|
G | GGGGGGGC others(774): Show |
2 | a0001c0002t0001g0059a0001c0002t0001g0095 | 2 | HG02135.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.328-29521_328-2952 others(785): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980138 | |||||
| chr3:16980138
|
G | GGGGGGGC others(775): Show |
1 | a0001c0002t0001g0048 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.328-29521_328-2952 others(786): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980138 | |||||
| chr3:16980138
|
G | GGGGGGGC others(776): Show |
1 | a0001c0002t0001g0076 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.328-29521_328-2952 others(787): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980138 | |||||
| chr3:16980138
|
G | GGGGGGGC others(778): Show |
1 | a0001c0001t0001g0034 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.328-29521_328-2952 others(789): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980138 | |||||
| chr3:16980138
|
G | GGGGGGGC others(774): Show |
1 | a0001c0001t0001g0117 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.328-29521_328-2952 others(785): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980138 | |||||
| chr3:16980138
|
G | GGGGGGGC others(775): Show |
1 | a0001c0002t0001g0060 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.328-29521_328-2952 others(786): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980138 | |||||
| chr3:16980138
|
G | GGGGGGGC others(773): Show |
5 | a0001c0002t0001g0125a0001c0002t0001g0126a0001c0002t0001g0205others(2): Show | 5 | HG02559.hp2 HG02723.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.328-29521_328-2952 others(784): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980138 | |||||
| chr3:16980138
|
G | GGGGGGGC others(773): Show |
1 | a0001c0002t0001g0206 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.328-29521_328-2952 others(784): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980138 | |||||
| chr3:16980138
|
G | GGGGGGGC others(778): Show |
1 | a0001c0002t0001g0062 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.328-29521_328-2952 others(789): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980138 | |||||
| chr3:16980138
|
G | GGGGGGGC others(774): Show |
1 | a0001c0001t0006g0222 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.328-29521_328-2952 others(785): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980138 | |||||
| chr3:16980138
|
G | GGGGGGGC others(780): Show |
6 | a0001c0003t0001g0235a0001c0003t0003g0209a0001c0003t0003g0215others(3): Show | 6 | HG00280.hp2 HG00741.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.328-29521_328-2952 others(791): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980138 | |||||
| chr3:16980138
|
G | GGGGGGGC others(780): Show |
16 | a0001c0002t0001g0098a0001c0002t0001g0099a0001c0002t0001g0100others(13): Show | 17 | HG00099.hp1 HG00323.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.328-29521_328-2952 others(791): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980138 | |||||
| chr3:16980138
|
G | GGGGGGGC others(780): Show |
2 | a0001c0003t0001g0116a0001c0020t0003g0178 | 2 | HG02602.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.328-29521_328-2952 others(791): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980138 | |||||
| chr3:16980138
|
G | GGGGGGGC others(781): Show |
1 | a0001c0004t0002g0173 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.328-29521_328-2952 others(792): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980138 | |||||
| chr3:16980138
|
G | GGGGGGGC others(774): Show |
1 | a0001c0003t0001g0211 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.328-29521_328-2952 others(785): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980138 | |||||
| chr3:16980138
|
G | GGGGGGGC others(781): Show |
1 | a0001c0004t0001g0176 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.328-29521_328-2952 others(792): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980138 | |||||
| chr3:16980138
|
G | GGGGGGGC others(782): Show |
1 | a0001c0004t0001g0164 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.328-29521_328-2952 others(793): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980138 | |||||
| chr3:16980138
|
G | GGGGGGGG others(783): Show |
1 | a0001c0002t0001g0069 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.328-29530_328-2952 others(794): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980138 | |||||
| chr3:16980139
|
G | GGGGGGCT others(772): Show |
1 | a0001c0005t0001g0063 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.328-29521_328-2952 others(783): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980139 | |||||
| chr3:16980142
|
G | GGGCTGAC others(773): Show |
1 | a0001c0013t0001g0198 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.328-29521_328-2952 others(784): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980142 | |||||
| chr3:16980215
|
G | C | 4 | a0001c0002t0001g0031a0001c0002t0001g0111a0001c0002t0001g0113others(1): Show | 4 | HG00408.hp2 HG02129.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-29459G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16980215 | ||||||
| chr3:16980253
|
C | T | 5 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(2): Show | 5 | HG02896.hp2 HG03098.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.328-29421C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16980253 | ||||||
| chr3:16980293
|
T | C | 81 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(78): Show | 82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.328-29381T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16980293 | ||||||
| chr3:16980316
|
G | T | 1 | a0001c0003t0001g0211 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.328-29358G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16980316 | ||||||
| chr3:16980339
|
C | T | 1 | a0001c0002t0001g0048 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.328-29335C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16980339 | ||||||
| chr3:16980351
|
T | G | 3 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202 | 3 | HG02976.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.328-29323T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16980351 | ||||||
| chr3:16980380
|
AGGGCGGC others(33): Show |
A | 2 | a0001c0001t0001g0041a0001c0001t0002g0145 | 2 | HG00323.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.328-29287_328-2924 others(44): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980380 | |||||
| chr3:16980396
|
G | C | 1 | a0001c0002t0001g0054 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.328-29278G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16980396 | ||||||
| chr3:16980420
|
G | A | 28 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(25): Show | 28 | HG00099.hp2 HG01099.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.328-29254G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16980420 | ||||||
| chr3:16980503
|
G | A | 5 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0001g0245others(2): Show | 5 | HG01123.hp2 HG03017.hp1 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.328-29171G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16980503 | ||||||
| chr3:16980529
|
C | CA | 13 | a0001c0002t0001g0024a0001c0002t0001g0046a0001c0002t0001g0047others(10): Show | 13 | HG01069.hp1 HG01074.hp1 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.328-29144dupA | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980529 | |||||
| chr3:16980579
|
G | T | 1 | a0001c0014t0001g0104 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.328-29095G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16980579 | ||||||
| chr3:16980594
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.328-29080C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16980594 | ||||||
| chr3:16980610
|
G | C | 1 | a0001c0002t0001g0007 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.328-29064G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16980610 | ||||||
| chr3:16980696
|
C | A | 3 | a0001c0002t0001g0007a0001c0002t0001g0199a0001c0002t0001g0210 | 3 | HG02257.hp1 HG02280.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.328-28978C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16980696 | ||||||
| chr3:16980697
|
G | A | 5 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(2): Show | 5 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.328-28977G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16980697 | ||||||
| chr3:16980728
|
C | CG | 8 | a0001c0001t0001g0082a0001c0001t0002g0131a0001c0002t0001g0010others(5): Show | 8 | HG01099.hp1 HG01256.hp1 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.328-28942dupG | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16980728 | |||||
| chr3:16980750
|
C | T | 8 | a0001c0003t0001g0116a0001c0003t0001g0235a0001c0003t0003g0209others(5): Show | 8 | HG00280.hp2 HG00741.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.328-28924C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16980750 | ||||||
| chr3:16980813
|
A | G | 170 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(167): Show | 172 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.328-28861A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16980813 | ||||||
| chr3:16980825
|
C | T | 78 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(75): Show | 79 | HG00408.hp1 HG01081.hp2 HG01123.hp2 others(76): Show |
intron_variant | MODIFIER | c.328-28849C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16980825 | ||||||
| chr3:16980870
|
C | G | 4 | a0001c0002t0001g0214a0001c0002t0001g0233a0001c0002t0001g0238others(1): Show | 4 | HG01891.hp2 HG02258.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-28804C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16980870 | ||||||
| chr3:16980899
|
C | T | 81 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(78): Show | 82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.328-28775C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16980899 | ||||||
| chr3:16980919
|
C | T | 2 | a0001c0002t0001g0054a0001c0002t0001g0073 | 2 | HG00280.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.328-28755C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16980919 | ||||||
| chr3:16980943
|
G | A | 2 | a0001c0001t0001g0221a0001c0001t0001g0225 | 2 | HG01081.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.328-28731G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16980943 | ||||||
| chr3:16980976
|
A | C | 1 | a0001c0001t0001g0038 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.328-28698A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16980976 | ||||||
| chr3:16980981
|
C | T | 1 | a0001c0004t0002g0173 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.328-28693C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16980981 | ||||||
| chr3:16980994
|
A | G | 4 | a0001c0004t0002g0171a0001c0004t0002g0172a0001c0004t0002g0173others(1): Show | 4 | HG02074.hp1 HG02155.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-28680A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16980994 | ||||||
| chr3:16981001
|
T | C | 81 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(78): Show | 82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.328-28673T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16981001 | ||||||
| chr3:16981016
|
A | G | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.328-28658A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16981016 | ||||||
| chr3:16981073
|
C | T | 6 | a0001c0001t0001g0014a0001c0001t0001g0034a0001c0001t0001g0036others(3): Show | 6 | HG02135.hp1 HG02165.hp1 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.328-28601C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16981073 | ||||||
| chr3:16981150
|
G | GGGGAGA | 169 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(166): Show | 171 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.328-28509_328-2850 others(10): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16981150 | |||||
| chr3:16981280
|
C | T | 1 | a0001c0003t0001g0211 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.328-28394C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16981280 | ||||||
| chr3:16981299
|
A | C | 81 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(78): Show | 82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.328-28375A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16981299 | ||||||
| chr3:16981353
|
A | G | 27 | a0001c0002t0001g0098a0001c0002t0001g0099a0001c0002t0001g0100others(24): Show | 28 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.328-28321A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16981353 | ||||||
| chr3:16981438
|
C | A | 1 | a0001c0001t0002g0159 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.328-28236C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16981438 | ||||||
| chr3:16981830
|
C | T | 8 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103others(5): Show | 8 | HG02818.hp1 HG02895.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.328-27844C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16981830 | ||||||
| chr3:16982285
|
G | A | 1 | a0002c0009t0001g0154 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.328-27389G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16982285 | ||||||
| chr3:16982299
|
G | A | 4 | a0001c0005t0001g0019a0001c0005t0001g0063a0001c0005t0001g0179others(1): Show | 4 | HG01515.hp2 HG03491.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-27375G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16982299 | ||||||
| chr3:16982399
|
G | C | 5 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(2): Show | 5 | HG02896.hp2 HG03098.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.328-27275G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16982399 | ||||||
| chr3:16982470
|
G | A | 17 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(14): Show | 17 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.328-27204G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16982470 | ||||||
| chr3:16982756
|
A | G | 159 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(156): Show | 161 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.328-26918A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16982756 | ||||||
| chr3:16982959
|
A | G | 7 | a0001c0004t0001g0162a0001c0004t0001g0163a0001c0004t0001g0164others(4): Show | 7 | HG01069.hp2 HG01934.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.328-26715A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16982959 | ||||||
| chr3:16983073
|
A | G | 21 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(18): Show | 21 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.328-26601A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16983073 | ||||||
| chr3:16983081
|
T | C | 3 | a0001c0011t0001g0004a0001c0012t0001g0005a0001c0013t0001g0198 | 3 | HG02055.hp1 HG02109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.328-26593T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16983081 | ||||||
| chr3:16983102
|
G | A | 2 | a0001c0001t0001g0042a0001c0001t0001g0067 | 2 | HG01346.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.328-26572G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16983102 | ||||||
| chr3:16983174
|
T | G | 17 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(14): Show | 17 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.328-26500T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16983174 | ||||||
| chr3:16983225
|
TC | T | 51 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(48): Show | 52 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.328-26446delC | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16983225 | |||||
| chr3:16983227
|
C | A | 31 | a0001c0002t0001g0098a0001c0002t0001g0099a0001c0002t0001g0100others(28): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.328-26447C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16983227 | ||||||
| chr3:16983485
|
A | G | 62 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(59): Show | 62 | HG01081.hp2 HG01123.hp2 HG01175.hp2 others(59): Show |
intron_variant | MODIFIER | c.328-26189A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16983485 | ||||||
| chr3:16983687
|
G | T | 2 | a0001c0001t0001g0101a0001c0001t0001g0102 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.328-25987G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16983687 | ||||||
| chr3:16983991
|
G | T | 3 | a0001c0002t0001g0074a0001c0002t0001g0078a0001c0002t0001g0079 | 3 | HG02717.hp1 HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.328-25683G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16983991 | ||||||
| chr3:16984091
|
T | C | 52 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(49): Show | 53 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.328-25583T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16984091 | ||||||
| chr3:16984114
|
A | G | 107 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(104): Show | 108 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.328-25560A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16984114 | ||||||
| chr3:16984197
|
A | T | 17 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(14): Show | 17 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.328-25477A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16984197 | ||||||
| chr3:16984476
|
A | G | 1 | a0001c0003t0001g0211 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.328-25198A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16984476 | ||||||
| chr3:16984482
|
C | A | 2 | a0001c0001t0001g0197a0001c0001t0006g0222 | 2 | HG02258.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.328-25192C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16984482 | ||||||
| chr3:16984631
|
G | A | 170 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(167): Show | 172 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.328-25043G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16984631 | ||||||
| chr3:16984863
|
C | T | 1 | a0001c0002t0001g0112 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.328-24811C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16984863 | ||||||
| chr3:16984921
|
G | T | 65 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(62): Show | 65 | HG00408.hp1 HG01081.hp2 HG01123.hp2 others(62): Show |
intron_variant | MODIFIER | c.328-24753G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16984921 | ||||||
| chr3:16984931
|
T | TA | 13 | a0001c0002t0001g0024a0001c0002t0001g0046a0001c0002t0001g0047others(10): Show | 13 | HG01069.hp1 HG01074.hp1 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.328-24733dupA | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16984931 | |||||
| chr3:16985044
|
C | T | 4 | a0001c0002t0001g0214a0001c0002t0001g0233a0001c0002t0001g0238others(1): Show | 4 | HG01891.hp2 HG02258.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-24630C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16985044 | ||||||
| chr3:16985221
|
C | T | 3 | a0001c0011t0001g0004a0001c0012t0001g0005a0001c0013t0001g0198 | 3 | HG02055.hp1 HG02109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.328-24453C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16985221 | ||||||
| chr3:16985272
|
T | A | 52 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(49): Show | 53 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.328-24402T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16985272 | ||||||
| chr3:16985320
|
T | C | 1 | a0001c0003t0001g0211 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.328-24354T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16985320 | ||||||
| chr3:16985402
|
A | C | 7 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(4): Show | 7 | HG02055.hp1 HG02109.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.328-24272A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16985402 | ||||||
| chr3:16985410
|
G | C | 1 | a0001c0004t0001g0166 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.328-24264G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16985410 | ||||||
| chr3:16985671
|
C | A | 7 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(4): Show | 7 | HG02055.hp1 HG02109.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.328-24003C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16985671 | ||||||
| chr3:16985713
|
A | G | 8 | a0001c0003t0001g0116a0001c0003t0001g0235a0001c0003t0003g0209others(5): Show | 8 | HG00280.hp2 HG00741.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.328-23961A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16985713 | ||||||
| chr3:16985900
|
C | A | 11 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(8): Show | 11 | HG02559.hp2 HG02723.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.328-23774C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16985900 | ||||||
| chr3:16986091
|
G | T | 1 | a0001c0004t0001g0002 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.328-23583G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16986091 | ||||||
| chr3:16986092
|
G | T | 1 | a0001c0004t0001g0002 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.328-23582G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16986092 | ||||||
| chr3:16986346
|
C | T | 1 | a0001c0001t0001g0119 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.328-23328C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16986346 | ||||||
| chr3:16986587
|
G | A | 2 | a0001c0001t0001g0197a0001c0001t0006g0222 | 2 | HG02258.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.328-23087G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16986587 | ||||||
| chr3:16986602
|
C | G | 1 | a0001c0002t0001g0060 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.328-23072C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16986602 | ||||||
| chr3:16986631
|
G | T | 4 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(1): Show | 4 | HG02965.hp1 HG02976.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-23043G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16986631 | ||||||
| chr3:16986673
|
G | C | 1 | a0001c0001t0001g0202 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.328-23001G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16986673 | ||||||
| chr3:16986735
|
T | C | 17 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(14): Show | 17 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.328-22939T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16986735 | ||||||
| chr3:16986886
|
T | C | 159 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(156): Show | 161 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.328-22788T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16986886 | ||||||
| chr3:16987054
|
G | T | 1 | a0001c0001t0002g0134 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.328-22620G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16987054 | ||||||
| chr3:16987124
|
C | T | 1 | a0001c0001t0001g0197 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.328-22550C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16987124 | ||||||
| chr3:16987478
|
A | G | 1 | a0001c0002t0001g0051 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.328-22196A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16987478 | ||||||
| chr3:16987524
|
A | C | 1 | a0001c0001t0001g0157 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.328-22150A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16987524 | ||||||
| chr3:16987530
|
G | A | 17 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(14): Show | 17 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.328-22144G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16987530 | ||||||
| chr3:16987572
|
C | G | 4 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(1): Show | 4 | HG02965.hp1 HG02976.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-22102C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16987572 | ||||||
| chr3:16987781
|
T | C | 5 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0001g0245others(2): Show | 5 | HG01123.hp2 HG03017.hp1 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.328-21893T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16987781 | ||||||
| chr3:16987963
|
G | A | 170 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(167): Show | 172 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.328-21711G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16987963 | ||||||
| chr3:16987995
|
C | T | 1 | a0001c0013t0001g0198 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.328-21679C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16987995 | ||||||
| chr3:16987996
|
G | A | 17 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(14): Show | 17 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.328-21678G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16987996 | ||||||
| chr3:16988022
|
T | C | 1 | a0001c0001t0001g0037 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.328-21652T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16988022 | ||||||
| chr3:16988032
|
A | C | 1 | a0001c0003t0003g0215 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.328-21642A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16988032 | ||||||
| chr3:16988039
|
T | C | 1 | a0001c0003t0001g0235 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.328-21635T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16988039 | ||||||
| chr3:16988061
|
C | T | 17 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(14): Show | 17 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.328-21613C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16988061 | ||||||
| chr3:16988104
|
A | G | 18 | a0001c0001t0001g0224a0001c0003t0001g0018a0001c0003t0001g0044others(15): Show | 18 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.328-21570A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16988104 | ||||||
| chr3:16988380
|
A | T | 15 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(12): Show | 15 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.328-21294A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16988380 | ||||||
| chr3:16988495
|
A | G | 1 | a0001c0013t0001g0198 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.328-21179A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16988495 | ||||||
| chr3:16988661
|
T | G | 1 | a0001c0002t0001g0057 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.328-21013T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16988661 | ||||||
| chr3:16988724
|
C | T | 2 | a0001c0001t0001g0197a0001c0001t0006g0222 | 2 | HG02258.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.328-20950C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16988724 | ||||||
| chr3:16988747
|
T | A | 2 | a0001c0002t0001g0008a0001c0002t0001g0010 | 2 | HG02896.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.328-20927T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16988747 | ||||||
| chr3:16989017
|
TTCTC | T | 55 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(52): Show | 56 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.328-20648_328-2064 others(8): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16989017 | |||||
| chr3:16989168
|
C | T | 3 | a0001c0011t0001g0004a0001c0012t0001g0005a0001c0013t0001g0198 | 3 | HG02055.hp1 HG02109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.328-20506C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16989168 | ||||||
| chr3:16989211
|
G | C | 1 | a0001c0001t0001g0150 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.328-20463G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16989211 | ||||||
| chr3:16989461
|
A | G | 1 | a0001c0001t0002g0144 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.328-20213A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16989461 | ||||||
| chr3:16989905
|
T | C | 81 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(78): Show | 82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.328-19769T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16989905 | ||||||
| chr3:16989906
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.328-19768G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16989906 | ||||||
| chr3:16990115
|
G | A | 28 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(25): Show | 28 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.328-19559G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16990115 | ||||||
| chr3:16990121
|
G | A | 7 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(4): Show | 7 | HG02055.hp1 HG02109.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.328-19553G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16990121 | ||||||
| chr3:16990128
|
G | GTGA | 102 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(99): Show | 103 | HG00408.hp1 HG01081.hp2 HG01099.hp1 others(100): Show |
intron_variant | MODIFIER | c.328-19538_328-1953 others(7): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16990128 | |||||
| chr3:16990139
|
A | G | 1 | a0001c0005t0001g0019 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.328-19535A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16990139 | ||||||
| chr3:16990140
|
G | A | 1 | a0001c0005t0001g0019 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.328-19534G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16990140 | ||||||
| chr3:16990141
|
C | T | 1 | a0001c0005t0001g0019 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.328-19533C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16990141 | ||||||
| chr3:16990411
|
C | T | 1 | a0001c0016t0001g0093 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.328-19263C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16990411 | ||||||
| chr3:16990534
|
G | C | 2 | a0001c0001t0001g0221a0001c0001t0001g0225 | 2 | HG01081.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.328-19140G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16990534 | ||||||
| chr3:16990609
|
C | T | 3 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202 | 3 | HG02976.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.328-19065C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16990609 | ||||||
| chr3:16990789
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.328-18885C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16990789 | ||||||
| chr3:16990831
|
A | T | 1 | a0001c0002t0001g0210 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.328-18843A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16990831 | ||||||
| chr3:16991141
|
G | C | 1 | a0001c0003t0001g0190 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.328-18533G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16991141 | ||||||
| chr3:16991226
|
C | T | 1 | a0001c0001t0001g0246 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.328-18448C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16991226 | ||||||
| chr3:16991768
|
C | G | 3 | a0001c0011t0001g0004a0001c0012t0001g0005a0001c0013t0001g0198 | 3 | HG02055.hp1 HG02109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.328-17906C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16991768 | ||||||
| chr3:16991898
|
A | G | 24 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(21): Show | 24 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(21): Show |
intron_variant | MODIFIER | c.328-17776A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16991898 | ||||||
| chr3:16992181
|
G | A | 17 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(14): Show | 17 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.328-17493G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16992181 | ||||||
| chr3:16992432
|
C | A | 4 | a0001c0005t0001g0019a0001c0005t0001g0063a0001c0005t0001g0179others(1): Show | 4 | HG01515.hp2 HG03491.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-17242C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16992432 | ||||||
| chr3:16992477
|
A | G | 1 | a0001c0001t0001g0034 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.328-17197A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16992477 | ||||||
| chr3:16992599
|
G | C | 24 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(21): Show | 24 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(21): Show |
intron_variant | MODIFIER | c.328-17075G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16992599 | ||||||
| chr3:16992834
|
A | C | 17 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(14): Show | 17 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.328-16840A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16992834 | ||||||
| chr3:16993011
|
C | A | 17 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(14): Show | 17 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.328-16663C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16993011 | ||||||
| chr3:16993028
|
G | A | 1 | a0001c0001t0006g0222 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.328-16646G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16993028 | ||||||
| chr3:16993260
|
T | G | 2 | a0001c0011t0001g0004a0001c0012t0001g0005 | 2 | HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.328-16414T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16993260 | ||||||
| chr3:16993280
|
T | C | 1 | a0001c0001t0001g0197 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.328-16394T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16993280 | ||||||
| chr3:16993356
|
T | C | 4 | a0001c0005t0001g0019a0001c0005t0001g0063a0001c0005t0001g0179others(1): Show | 4 | HG01515.hp2 HG03491.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-16318T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16993356 | ||||||
| chr3:16993474
|
G | A | 3 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202 | 3 | HG02976.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.328-16200G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16993474 | ||||||
| chr3:16993586
|
T | A | 159 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(156): Show | 161 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.328-16088T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16993586 | ||||||
| chr3:16993816
|
C | T | 11 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(8): Show | 11 | HG02559.hp2 HG02723.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.328-15858C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16993816 | ||||||
| chr3:16993907
|
G | C | 170 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(167): Show | 172 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.328-15767G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16993907 | ||||||
| chr3:16994231
|
A | G | 3 | a0001c0011t0001g0004a0001c0012t0001g0005a0001c0013t0001g0198 | 3 | HG02055.hp1 HG02109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.328-15443A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16994231 | ||||||
| chr3:16994260
|
C | T | 1 | a0003c0010t0001g0049 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.328-15414C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16994260 | ||||||
| chr3:16994262
|
T | C | 1 | a0001c0001t0001g0089 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.328-15412T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16994262 | ||||||
| chr3:16994332
|
G | A | 15 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(12): Show | 15 | HG01515.hp2 HG02559.hp2 HG02723.hp1 others(12): Show |
intron_variant | MODIFIER | c.328-15342G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16994332 | ||||||
| chr3:16994443
|
A | G | 1 | a0001c0014t0001g0104 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.328-15231A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16994443 | ||||||
| chr3:16994513
|
ACCTCTAA others(1): Show |
A | 3 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202 | 3 | HG02976.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.328-15160_328-1515 others(12): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16994513 | ||||||
| chr3:16994726
|
C | T | 4 | a0001c0001t0001g0221a0001c0001t0001g0225a0001c0011t0001g0004others(1): Show | 4 | HG01081.hp2 HG02055.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-14948C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16994726 | ||||||
| chr3:16994767
|
C | T | 1 | a0001c0003t0001g0211 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.328-14907C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16994767 | ||||||
| chr3:16994835
|
G | A | 19 | a0001c0002t0001g0098a0001c0002t0001g0099a0001c0002t0001g0100others(16): Show | 20 | HG00099.hp1 HG00323.hp2 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.328-14839G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16994835 | ||||||
| chr3:16994838
|
A | G | 1 | a0001c0001t0001g0203 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.328-14836A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16994838 | ||||||
| chr3:16994839
|
T | C | 1 | a0001c0001t0001g0195 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.328-14835T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16994839 | ||||||
| chr3:16994895
|
G | C | 13 | a0001c0002t0001g0024a0001c0002t0001g0046a0001c0002t0001g0047others(10): Show | 13 | HG01069.hp1 HG01074.hp1 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.328-14779G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16994895 | ||||||
| chr3:16994950
|
T | C | 17 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(14): Show | 17 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.328-14724T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16994950 | ||||||
| chr3:16994959
|
C | G | 1 | a0001c0002t0001g0068 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.328-14715C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16994959 | ||||||
| chr3:16995025
|
A | T | 5 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(2): Show | 5 | HG02896.hp2 HG03098.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.328-14649A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16995025 | ||||||
| chr3:16995055
|
T | C | 1 | a0001c0014t0001g0104 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.328-14619T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16995055 | ||||||
| chr3:16995106
|
A | C | 17 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(14): Show | 17 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.328-14568A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16995106 | ||||||
| chr3:16995147
|
A | T | 63 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(60): Show | 63 | HG00408.hp1 HG01081.hp2 HG01123.hp2 others(60): Show |
intron_variant | MODIFIER | c.328-14527A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16995147 | ||||||
| chr3:16995222
|
G | T | 6 | a0001c0002t0001g0125a0001c0002t0001g0126a0001c0002t0001g0205others(3): Show | 6 | HG02559.hp2 HG02723.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.328-14452G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16995222 | ||||||
| chr3:16995253
|
C | G | 6 | a0001c0002t0001g0125a0001c0002t0001g0126a0001c0002t0001g0205others(3): Show | 6 | HG02559.hp2 HG02723.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.328-14421C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16995253 | ||||||
| chr3:16995383
|
A | T | 170 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(167): Show | 172 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.328-14291A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16995383 | ||||||
| chr3:16995415
|
C | G | 2 | a0002c0009t0001g0154a0002c0009t0001g0155 | 2 | HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.328-14259C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16995415 | ||||||
| chr3:16995415
|
C | T | 31 | a0001c0002t0001g0098a0001c0002t0001g0099a0001c0002t0001g0100others(28): Show | 32 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.328-14259C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16995415 | ||||||
| chr3:16995431
|
G | A | 1 | a0001c0001t0001g0237 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.328-14243G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16995431 | ||||||
| chr3:16995555
|
A | G | 1 | a0001c0002t0001g0212 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.328-14119A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16995555 | ||||||
| chr3:16995791
|
A | G | 1 | a0001c0002t0001g0214 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.328-13883A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16995791 | ||||||
| chr3:16996344
|
C | T | 2 | a0001c0002t0001g0054a0001c0002t0001g0073 | 2 | HG00280.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.328-13330C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16996344 | ||||||
| chr3:16996377
|
C | T | 201 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(198): Show | 203 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.328-13297C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16996377 | ||||||
| chr3:16996525
|
A | T | 17 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(14): Show | 17 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.328-13149A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16996525 | ||||||
| chr3:16996562
|
G | A | 1 | a0001c0002t0001g0011 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.328-13112G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16996562 | ||||||
| chr3:16996706
|
A | G | 1 | a0001c0014t0001g0104 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.328-12968A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16996706 | ||||||
| chr3:16996744
|
G | A | 2 | a0001c0001t0001g0139a0001c0006t0001g0161 | 2 | HG02683.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.328-12930G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16996744 | ||||||
| chr3:16996803
|
G | A | 9 | a0001c0002t0001g0006a0001c0002t0001g0055a0001c0002t0001g0056others(6): Show | 9 | HG02027.hp2 NA18942.hp2 NA18945.hp2 others(6): Show |
intron_variant | MODIFIER | c.328-12871G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16996803 | ||||||
| chr3:16997003
|
T | C | 1 | a0001c0003t0001g0196 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.328-12671T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16997003 | ||||||
| chr3:16997422
|
T | C | 2 | a0001c0002t0001g0054a0001c0002t0001g0073 | 2 | HG00280.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.328-12252T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16997422 | ||||||
| chr3:16997427
|
GT | G | 65 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(62): Show | 65 | HG00408.hp1 HG01081.hp2 HG01123.hp2 others(62): Show |
intron_variant | MODIFIER | c.328-12243delT | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16997427 | |||||
| chr3:16997429
|
T | A | 2 | a0002c0009t0001g0154a0002c0009t0001g0155 | 2 | HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.328-12245T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16997429 | ||||||
| chr3:16997492
|
A | G | 48 | a0001c0002t0001g0098a0001c0002t0001g0099a0001c0002t0001g0100others(45): Show | 49 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.328-12182A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16997492 | ||||||
| chr3:16997507
|
C | T | 1 | a0001c0001t0002g0130 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.328-12167C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16997507 | ||||||
| chr3:16997512
|
C | T | 1 | a0001c0002t0001g0080 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.328-12162C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16997512 | ||||||
| chr3:16997528
|
TTTTC | T | 17 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(14): Show | 17 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.328-12142_328-1213 others(8): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16997528 | |||||
| chr3:16997532
|
C | CT | 26 | a0001c0001t0001g0243a0001c0002t0001g0098a0001c0002t0001g0099others(23): Show | 27 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.328-12126dupT | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16997532 | |||||
| chr3:16997731
|
G | A | 17 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(14): Show | 17 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.328-11943G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16997731 | ||||||
| chr3:16997775
|
T | A | 1 | a0001c0001t0001g0040 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.328-11899T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16997775 | ||||||
| chr3:16997784
|
T | C | 159 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(156): Show | 161 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.328-11890T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16997784 | ||||||
| chr3:16997807
|
G | A | 3 | a0001c0002t0001g0033a0001c0002t0001g0052a0001c0002t0001g0107 | 3 | NA18986.hp2 NA19009.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.328-11867G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16997807 | ||||||
| chr3:16997829
|
T | C | 77 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(74): Show | 78 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.328-11845T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16997829 | ||||||
| chr3:16997845
|
T | G | 17 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(14): Show | 17 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.328-11829T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16997845 | ||||||
| chr3:16998199
|
A | AT | 159 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(156): Show | 161 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.328-11466dupT | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16998199 | |||||
| chr3:16998714
|
A | G | 1 | a0001c0002t0001g0047 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.328-10960A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16998714 | ||||||
| chr3:16998803
|
G | A | 11 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(8): Show | 11 | HG02559.hp2 HG02723.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.328-10871G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16998803 | ||||||
| chr3:16998849
|
C | T | 4 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(1): Show | 4 | HG02965.hp1 HG02976.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-10825C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16998849 | ||||||
| chr3:16998868
|
A | G | 77 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(74): Show | 78 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.328-10806A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16998868 | ||||||
| chr3:16999009
|
AGGTCATT others(1): Show |
A | 3 | a0001c0011t0001g0004a0001c0012t0001g0005a0001c0013t0001g0198 | 3 | HG02055.hp1 HG02109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.328-10663_328-1065 others(12): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16999009 | |||||
| chr3:16999020
|
T | A | 3 | a0001c0011t0001g0004a0001c0012t0001g0005a0001c0013t0001g0198 | 3 | HG02055.hp1 HG02109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.328-10654T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16999020 | ||||||
| chr3:16999021
|
C | T | 3 | a0001c0011t0001g0004a0001c0012t0001g0005a0001c0013t0001g0198 | 3 | HG02055.hp1 HG02109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.328-10653C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16999021 | ||||||
| chr3:16999164
|
G | GT | 5 | a0001c0001t0001g0053a0001c0001t0002g0131a0001c0002t0001g0061others(2): Show | 5 | HG01175.hp2 HG01978.hp1 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.328-10502dupT | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 16999164 | |||||
| chr3:16999175
|
CT | C | 4 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0027others(1): Show | 4 | HG01106.hp1 HG01255.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-10498delT | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16999175 | ||||||
| chr3:16999207
|
T | A | 8 | a0001c0003t0001g0116a0001c0003t0001g0235a0001c0003t0003g0209others(5): Show | 8 | HG00280.hp2 HG00741.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.328-10467T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16999207 | ||||||
| chr3:16999229
|
C | T | 3 | a0001c0011t0001g0004a0001c0012t0001g0005a0001c0013t0001g0198 | 3 | HG02055.hp1 HG02109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.328-10445C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16999229 | ||||||
| chr3:16999267
|
G | A | 5 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(2): Show | 5 | HG02896.hp2 HG03098.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.328-10407G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16999267 | ||||||
| chr3:16999378
|
C | T | 17 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(14): Show | 17 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.328-10296C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16999378 | ||||||
| chr3:16999485
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.328-10189C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16999485 | ||||||
| chr3:16999652
|
C | G | 4 | a0001c0005t0001g0019a0001c0005t0001g0063a0001c0005t0001g0179others(1): Show | 4 | HG01515.hp2 HG03491.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-10022C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16999652 | ||||||
| chr3:16999695
|
A | C | 3 | a0001c0002t0001g0068a0001c0002t0001g0091a0001c0002t0001g0092 | 3 | HG02818.hp2 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.328-9979A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16999695 | ||||||
| chr3:16999700
|
A | G | 1 | a0001c0001t0006g0222 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.328-9974A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16999700 | ||||||
| chr3:16999802
|
TG | T | 11 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(8): Show | 11 | HG02559.hp2 HG02723.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.328-9871delG | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16999802 | ||||||
| chr3:16999823
|
A | G | 4 | a0001c0005t0001g0019a0001c0005t0001g0063a0001c0005t0001g0179others(1): Show | 4 | HG01515.hp2 HG03491.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-9851A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 16999823 | ||||||
| chr3:17000128
|
G | C | 1 | a0001c0003t0001g0211 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.328-9546G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17000128 | ||||||
| chr3:17000150
|
C | T | 1 | a0001c0002t0001g0006 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.328-9524C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17000150 | ||||||
| chr3:17000334
|
A | G | 1 | a0001c0002t0001g0112 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.328-9340A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17000334 | ||||||
| chr3:17000427
|
CATTT | C | 82 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(79): Show | 83 | HG00408.hp1 HG01081.hp2 HG01123.hp2 others(80): Show |
intron_variant | MODIFIER | c.328-9244_328-9241d others(6): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 17000427 | |||||
| chr3:17000443
|
G | T | 4 | a0001c0005t0001g0019a0001c0005t0001g0063a0001c0005t0001g0179others(1): Show | 4 | HG01515.hp2 HG03491.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-9231G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17000443 | ||||||
| chr3:17000476
|
A | C | 17 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(14): Show | 17 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.328-9198A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17000476 | ||||||
| chr3:17000548
|
A | G | 6 | a0001c0002t0001g0125a0001c0002t0001g0126a0001c0002t0001g0205others(3): Show | 6 | HG02559.hp2 HG02723.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.328-9126A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17000548 | ||||||
| chr3:17000565
|
C | A | 17 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(14): Show | 17 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.328-9109C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17000565 | ||||||
| chr3:17000709
|
A | C | 2 | a0001c0001t0001g0197a0001c0001t0006g0222 | 2 | HG02258.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.328-8965A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17000709 | ||||||
| chr3:17000722
|
G | A | 63 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(60): Show | 63 | HG00408.hp1 HG01081.hp2 HG01123.hp2 others(60): Show |
intron_variant | MODIFIER | c.328-8952G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17000722 | ||||||
| chr3:17000811
|
C | T | 77 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(74): Show | 78 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.328-8863C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17000811 | ||||||
| chr3:17000912
|
G | T | 2 | a0001c0001t0001g0197a0001c0001t0006g0222 | 2 | HG02258.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.328-8762G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17000912 | ||||||
| chr3:17001080
|
T | C | 1 | a0001c0001t0006g0222 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.328-8594T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17001080 | ||||||
| chr3:17001189
|
G | C | 7 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(4): Show | 7 | HG02055.hp1 HG02109.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.328-8485G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17001189 | ||||||
| chr3:17001488
|
T | C | 1 | a0001c0002t0001g0066 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.328-8186T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17001488 | ||||||
| chr3:17001554
|
T | G | 1 | a0001c0001t0001g0081 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.328-8120T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17001554 | ||||||
| chr3:17001669
|
A | G | 1 | a0001c0014t0001g0104 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.328-8005A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17001669 | ||||||
| chr3:17001789
|
T | C | 1 | a0001c0004t0001g0002 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.328-7885T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17001789 | ||||||
| chr3:17001869
|
A | AT | 12 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(9): Show | 12 | HG02280.hp2 HG02559.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.328-7794dupT | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 17001869 | |||||
| chr3:17001869
|
AT | A | 5 | a0001c0002t0001g0048a0001c0005t0001g0019a0001c0005t0001g0063others(2): Show | 5 | HG01515.hp2 HG03491.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.328-7794delT | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 17001869 | |||||
| chr3:17001909
|
A | G | 1 | a0004c0015t0001g0072 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.328-7765A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17001909 | ||||||
| chr3:17001921
|
T | C | 159 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(156): Show | 161 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.328-7753T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17001921 | ||||||
| chr3:17001928
|
T | G | 57 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(54): Show | 58 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.328-7746T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17001928 | ||||||
| chr3:17002085
|
A | G | 27 | a0001c0002t0001g0098a0001c0002t0001g0099a0001c0002t0001g0100others(24): Show | 28 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.328-7589A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17002085 | ||||||
| chr3:17002482
|
G | T | 1 | a0001c0003t0001g0106 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.328-7192G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17002482 | ||||||
| chr3:17002614
|
G | A | 1 | a0001c0001t0001g0224 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.328-7060G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17002614 | ||||||
| chr3:17002629
|
T | C | 4 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(1): Show | 4 | HG02965.hp1 HG02976.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-7045T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17002629 | ||||||
| chr3:17002729
|
C | T | 1 | a0001c0003t0001g0187 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.328-6945C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17002729 | ||||||
| chr3:17002832
|
G | T | 1 | a0001c0005t0001g0019 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.328-6842G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17002832 | ||||||
| chr3:17002860
|
T | C | 1 | a0001c0001t0001g0195 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.328-6814T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17002860 | ||||||
| chr3:17002920
|
T | G | 76 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(73): Show | 77 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.328-6754T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17002920 | ||||||
| chr3:17003140
|
T | C | 2 | a0001c0005t0001g0063a0001c0005t0001g0179 | 2 | HG01515.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.328-6534T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17003140 | ||||||
| chr3:17003338
|
T | G | 2 | a0001c0001t0001g0221a0001c0001t0001g0225 | 2 | HG01081.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.328-6336T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17003338 | ||||||
| chr3:17003871
|
T | C | 159 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(156): Show | 161 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.328-5803T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17003871 | ||||||
| chr3:17003881
|
A | G | 17 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(14): Show | 17 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.328-5793A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17003881 | ||||||
| chr3:17003901
|
A | C | 1 | a0001c0002t0001g0111 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.328-5773A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17003901 | ||||||
| chr3:17004046
|
C | G | 3 | a0001c0011t0001g0004a0001c0012t0001g0005a0001c0013t0001g0198 | 3 | HG02055.hp1 HG02109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.328-5628C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17004046 | ||||||
| chr3:17004094
|
A | G | 103 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(100): Show | 104 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.328-5580A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17004094 | ||||||
| chr3:17004166
|
A | T | 11 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(8): Show | 11 | HG02559.hp2 HG02723.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.328-5508A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17004166 | ||||||
| chr3:17004176
|
G | T | 3 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202 | 3 | HG02976.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.328-5498G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17004176 | ||||||
| chr3:17004188
|
T | C | 1 | a0001c0002t0001g0047 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.328-5486T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17004188 | ||||||
| chr3:17004236
|
G | A | 48 | a0001c0002t0001g0098a0001c0002t0001g0099a0001c0002t0001g0100others(45): Show | 49 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.328-5438G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17004236 | ||||||
| chr3:17004432
|
C | T | 6 | a0001c0001t0001g0014a0001c0001t0001g0034a0001c0001t0001g0036others(3): Show | 6 | HG02135.hp1 HG02165.hp1 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.328-5242C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17004432 | ||||||
| chr3:17004644
|
T | C | 1 | a0001c0001t0001g0042 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.328-5030T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17004644 | ||||||
| chr3:17004660
|
G | A | 170 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(167): Show | 172 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.328-5014G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17004660 | ||||||
| chr3:17004662
|
G | A | 4 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(1): Show | 4 | HG02965.hp1 HG02976.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-5012G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17004662 | ||||||
| chr3:17004777
|
G | GT | 11 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(8): Show | 11 | HG02559.hp2 HG02723.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.328-4890dupT | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 17004777 | |||||
| chr3:17004796
|
T | C | 28 | a0001c0002t0001g0098a0001c0002t0001g0099a0001c0002t0001g0100others(25): Show | 29 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.328-4878T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17004796 | ||||||
| chr3:17004797
|
A | T | 1 | a0001c0002t0001g0061 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.328-4877A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17004797 | ||||||
| chr3:17005005
|
AC | A | 110 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(107): Show | 111 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.328-4666delC | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 17005005 | |||||
| chr3:17005128
|
G | A | 1 | a0001c0013t0001g0198 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.328-4546G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17005128 | ||||||
| chr3:17005225
|
G | A | 1 | a0001c0003t0001g0184 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.328-4449G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17005225 | ||||||
| chr3:17005342
|
C | G | 1 | a0001c0002t0001g0068 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.328-4332C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17005342 | ||||||
| chr3:17005370
|
T | TC | 106 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(103): Show | 107 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.328-4301dupC | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 17005370 | |||||
| chr3:17005374
|
G | A | 166 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(163): Show | 168 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.328-4300G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17005374 | ||||||
| chr3:17005540
|
A | T | 113 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(110): Show | 114 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.328-4134A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17005540 | ||||||
| chr3:17005563
|
G | C | 4 | a0001c0003t0004g0001a0001c0003t0004g0128a0001c0003t0004g0152others(1): Show | 5 | HG02486.hp1 HG03139.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.328-4111G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17005563 | ||||||
| chr3:17005631
|
T | C | 155 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(152): Show | 157 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.328-4043T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17005631 | ||||||
| chr3:17005724
|
A | G | 1 | a0001c0002t0001g0007 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.328-3950A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17005724 | ||||||
| chr3:17005794
|
C | A | 25 | a0001c0003t0001g0116a0001c0003t0001g0211a0001c0003t0001g0235others(22): Show | 26 | HG00280.hp2 HG00741.hp2 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.328-3880C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17005794 | ||||||
| chr3:17005796
|
G | A | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.328-3878G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17005796 | ||||||
| chr3:17005861
|
G | A | 1 | a0001c0004t0002g0172 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.328-3813G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17005861 | ||||||
| chr3:17006185
|
G | T | 1 | a0001c0013t0001g0198 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.328-3489G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17006185 | ||||||
| chr3:17006228
|
C | A | 6 | a0001c0002t0001g0125a0001c0002t0001g0126a0001c0002t0001g0205others(3): Show | 6 | HG02559.hp2 HG02723.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.328-3446C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17006228 | ||||||
| chr3:17006472
|
A | G | 3 | a0001c0002t0001g0007a0001c0002t0001g0199a0001c0002t0001g0210 | 3 | HG02257.hp1 HG02280.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.328-3202A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17006472 | ||||||
| chr3:17006539
|
C | T | 3 | a0001c0002t0001g0007a0001c0002t0001g0199a0001c0002t0001g0210 | 3 | HG02257.hp1 HG02280.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.328-3135C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17006539 | ||||||
| chr3:17006593
|
G | A | 1 | a0001c0011t0001g0004 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.328-3081G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17006593 | ||||||
| chr3:17006773
|
T | C | 24 | a0001c0003t0001g0116a0001c0003t0001g0235a0001c0003t0003g0209others(21): Show | 25 | HG00280.hp2 HG00741.hp2 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.328-2901T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17006773 | ||||||
| chr3:17006880
|
C | G | 1 | a0001c0002t0001g0060 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.328-2794C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17006880 | ||||||
| chr3:17006944
|
CAG | C | 3 | a0001c0005t0001g0019a0001c0005t0001g0063a0001c0005t0001g0179 | 3 | HG01515.hp2 HG03491.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.328-2728_328-2727d others(4): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 17006944 | |||||
| chr3:17006968
|
A | G | 3 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202 | 3 | HG02976.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.328-2706A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17006968 | ||||||
| chr3:17006995
|
G | A | 156 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(153): Show | 158 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.328-2679G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17006995 | ||||||
| chr3:17007180
|
G | A | 2 | a0001c0001t0001g0139a0001c0006t0001g0161 | 2 | HG02683.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.328-2494G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17007180 | ||||||
| chr3:17007222
|
C | T | 3 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202 | 3 | HG02976.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.328-2452C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17007222 | ||||||
| chr3:17007223
|
G | A | 24 | a0001c0003t0001g0116a0001c0003t0001g0235a0001c0003t0003g0209others(21): Show | 25 | HG00280.hp2 HG00741.hp2 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.328-2451G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17007223 | ||||||
| chr3:17007309
|
C | T | 1 | a0001c0005t0001g0185 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.328-2365C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17007309 | ||||||
| chr3:17007310
|
G | A | 4 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(1): Show | 4 | HG02965.hp1 HG02976.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-2364G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17007310 | ||||||
| chr3:17007461
|
A | G | 1 | a0001c0002t0001g0011 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.328-2213A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17007461 | ||||||
| chr3:17007929
|
G | T | 1 | a0001c0001t0001g0067 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.328-1745G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17007929 | ||||||
| chr3:17007981
|
A | G | 1 | a0001c0001t0001g0053 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.328-1693A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17007981 | ||||||
| chr3:17008473
|
T | C | 45 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0116others(42): Show | 46 | HG00280.hp2 HG00741.hp2 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.328-1201T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17008473 | ||||||
| chr3:17008554
|
C | T | 3 | a0001c0011t0001g0004a0001c0012t0001g0005a0001c0013t0001g0198 | 3 | HG02055.hp1 HG02109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.328-1120C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17008554 | ||||||
| chr3:17008988
|
A | AT | 19 | a0001c0001t0001g0042a0001c0001t0001g0117a0001c0001t0001g0119others(16): Show | 19 | HG00408.hp1 HG01099.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.328-672dupT | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 17008988 | |||||
| chr3:17009078
|
G | A | 1 | a0001c0005t0001g0019 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.328-596G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17009078 | ||||||
| chr3:17009153
|
T | G | 1 | a0001c0002t0001g0111 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.328-521T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17009153 | ||||||
| chr3:17009159
|
A | G | 6 | a0001c0002t0001g0125a0001c0002t0001g0126a0001c0002t0001g0205others(3): Show | 6 | HG02559.hp2 HG02723.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.328-515A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17009159 | ||||||
| chr3:17009395
|
T | C | 1 | a0001c0003t0001g0211 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.328-279T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17009395 | ||||||
| chr3:17009478
|
CTGT | C | 17 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(14): Show | 17 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.328-193_328-191del others(3): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 17009478 | |||||
| chr3:17009501
|
G | C | 170 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(167): Show | 172 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.328-173G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17009501 | ||||||
| chr3:17009589
|
T | A | 51 | a0001c0003t0001g0003a0001c0003t0001g0018a0001c0003t0001g0030others(48): Show | 53 | HG00280.hp2 HG00741.hp2 HG01069.hp2 others(50): Show |
intron_variant | MODIFIER | c.328-85T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17009589 | ||||||
| chr3:17009664
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.328-10T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 1/5 | chr3 | 17009664 | ||||||
| chr3:17012306
|
G | C | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.2814+146G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 2/5 | chr3 | 17012306 | ||||||
| chr3:17012382
|
G | T | 1 | a0001c0002t0001g0205 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2814+222G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 2/5 | chr3 | 17012382 | ||||||
| chr3:17012398
|
C | T | 1 | a0001c0001t0006g0222 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2814+238C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 2/5 | chr3 | 17012398 | ||||||
| chr3:17012493
|
C | T | 28 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(25): Show | 28 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.2814+333C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 2/5 | chr3 | 17012493 | ||||||
| chr3:17012552
|
A | G | 1 | a0001c0001t0001g0012 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2814+392A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 2/5 | chr3 | 17012552 | ||||||
| chr3:17012622
|
A | G | 17 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(14): Show | 17 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.2814+462A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 2/5 | chr3 | 17012622 | ||||||
| chr3:17012992
|
T | C | 2 | a0001c0002t0003g0064a0001c0002t0003g0065 | 2 | HG00741.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.2814+832T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 2/5 | chr3 | 17012992 | ||||||
| chr3:17013146
|
G | A | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.2814+986G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 2/5 | chr3 | 17013146 | ||||||
| chr3:17013151
|
G | A | 1 | a0001c0002t0001g0055 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.2814+991G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 2/5 | chr3 | 17013151 | ||||||
| chr3:17013176
|
G | GC | 4 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(1): Show | 4 | HG02965.hp1 HG02976.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.2814+1017dupC | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 17013176 | |||||
| chr3:17013297
|
C | T | 3 | a0001c0011t0001g0004a0001c0012t0001g0005a0001c0013t0001g0198 | 3 | HG02055.hp1 HG02109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2814+1137C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 2/5 | chr3 | 17013297 | ||||||
| chr3:17013448
|
C | G | 1 | a0001c0002t0001g0210 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2815-1260C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 2/5 | chr3 | 17013448 | ||||||
| chr3:17013653
|
A | G | 2 | a0001c0011t0001g0004a0001c0012t0001g0005 | 2 | HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.2815-1055A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 2/5 | chr3 | 17013653 | ||||||
| chr3:17013816
|
G | C | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.2815-892G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 2/5 | chr3 | 17013816 | ||||||
| chr3:17014189
|
A | C | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.2815-519A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 2/5 | chr3 | 17014189 | ||||||
| chr3:17014334
|
A | AT | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.2815-365dupT | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 17014334 | |||||
| chr3:17014383
|
G | T | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.2815-325G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 2/5 | chr3 | 17014383 | ||||||
| chr3:17014469
|
A | G | 1 | a0001c0002t0001g0066 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2815-239A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 2/5 | chr3 | 17014469 | ||||||
| chr3:17014539
|
G | A | 168 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(165): Show | 170 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.2815-169G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 2/5 | chr3 | 17014539 | ||||||
| chr3:17014594
|
T | C | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.2815-114T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 2/5 | chr3 | 17014594 | ||||||
| chr3:17014664
|
A | G | 6 | a0001c0002t0001g0125a0001c0002t0001g0126a0001c0002t0001g0205others(3): Show | 6 | HG02559.hp2 HG02723.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2815-44A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 2/5 | chr3 | 17014664 | ||||||
| chr3:17015602
|
C | A | 4 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(1): Show | 4 | HG02965.hp1 HG02976.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.3018+691C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17015602 | ||||||
| chr3:17015624
|
GT | G | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3018+715delT | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 17015624 | |||||
| chr3:17015666
|
T | TC | 13 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(10): Show | 14 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.3018+756dupC | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 17015666 | |||||
| chr3:17015744
|
G | A | 1 | a0001c0002t0001g0032 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3018+833G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17015744 | ||||||
| chr3:17015798
|
C | T | 1 | a0001c0001t0002g0142 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.3018+887C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17015798 | ||||||
| chr3:17015811
|
C | A | 4 | a0001c0005t0001g0019a0001c0005t0001g0063a0001c0005t0001g0179others(1): Show | 4 | HG01515.hp2 HG03491.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.3018+900C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17015811 | ||||||
| chr3:17015837
|
C | T | 1 | a0001c0014t0001g0104 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3018+926C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17015837 | ||||||
| chr3:17016097
|
T | G | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3018+1186T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17016097 | ||||||
| chr3:17016196
|
A | G | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3018+1285A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17016196 | ||||||
| chr3:17016756
|
C | CA | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3018+1851dupA | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 17016756 | |||||
| chr3:17016831
|
C | G | 1 | a0001c0001t0002g0156 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3018+1920C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17016831 | ||||||
| chr3:17016908
|
G | A | 3 | a0001c0002t0001g0007a0001c0002t0001g0199a0001c0002t0001g0210 | 3 | HG02257.hp1 HG02280.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.3018+1997G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17016908 | ||||||
| chr3:17017191
|
C | T | 2 | a0001c0004t0001g0176a0001c0008t0001g0123 | 2 | HG03927.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.3018+2280C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17017191 | ||||||
| chr3:17017329
|
C | T | 1 | a0001c0002t0001g0096 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3018+2418C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17017329 | ||||||
| chr3:17017419
|
T | G | 2 | a0001c0001t0001g0226a0001c0001t0001g0230 | 2 | HG03831.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.3018+2508T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17017419 | ||||||
| chr3:17017521
|
T | TAA | 17 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(14): Show | 17 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.3018+2612_3018+261 others(6): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 17017521 | |||||
| chr3:17017640
|
T | C | 2 | a0001c0002t0001g0006a0001c0002t0001g0062 | 2 | NA18945.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.3018+2729T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17017640 | ||||||
| chr3:17017788
|
A | G | 1 | a0001c0001t0002g0136 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3018+2877A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17017788 | ||||||
| chr3:17017831
|
TAATAA | T | 4 | a0001c0005t0001g0019a0001c0005t0001g0063a0001c0005t0001g0179others(1): Show | 4 | HG01515.hp2 HG03491.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.3018+2925_3018+292 others(9): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 17017831 | |||||
| chr3:17017879
|
G | A | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3018+2968G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17017879 | ||||||
| chr3:17017889
|
C | T | 1 | a0001c0006t0001g0161 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3018+2978C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17017889 | ||||||
| chr3:17018021
|
A | G | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3018+3110A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17018021 | ||||||
| chr3:17018109
|
C | G | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3018+3198C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17018109 | ||||||
| chr3:17018356
|
G | A | 24 | a0001c0003t0001g0116a0001c0003t0001g0235a0001c0003t0003g0209others(21): Show | 25 | HG00280.hp2 HG00741.hp2 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.3018+3445G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17018356 | ||||||
| chr3:17018488
|
T | C | 1 | a0001c0001t0001g0225 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3018+3577T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17018488 | ||||||
| chr3:17018631
|
G | T | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3018+3720G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17018631 | ||||||
| chr3:17018652
|
C | T | 17 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(14): Show | 17 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.3018+3741C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17018652 | ||||||
| chr3:17018710
|
C | T | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3018+3799C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17018710 | ||||||
| chr3:17018711
|
G | A | 28 | a0001c0003t0001g0116a0001c0003t0001g0235a0001c0003t0003g0209others(25): Show | 29 | HG00280.hp2 HG00741.hp2 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.3018+3800G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17018711 | ||||||
| chr3:17018833
|
C | T | 7 | a0001c0005t0001g0019a0001c0005t0001g0063a0001c0005t0001g0179others(4): Show | 7 | HG01515.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.3018+3922C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17018833 | ||||||
| chr3:17018930
|
G | T | 5 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0001g0245others(2): Show | 5 | HG01123.hp2 HG03017.hp1 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.3018+4019G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17018930 | ||||||
| chr3:17019027
|
T | C | 2 | a0001c0011t0001g0004a0001c0012t0001g0005 | 2 | HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.3018+4116T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17019027 | ||||||
| chr3:17019458
|
T | A | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3018+4547T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17019458 | ||||||
| chr3:17019527
|
A | T | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3018+4616A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17019527 | ||||||
| chr3:17019536
|
G | A | 13 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(10): Show | 14 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.3018+4625G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17019536 | ||||||
| chr3:17019559
|
G | GTAA | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3018+4660_3018+466 others(7): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 17019559 | |||||
| chr3:17019611
|
C | T | 17 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(14): Show | 17 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.3018+4700C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17019611 | ||||||
| chr3:17019641
|
A | T | 2 | a0001c0001t0001g0197a0001c0001t0006g0222 | 2 | HG02258.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.3018+4730A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17019641 | ||||||
| chr3:17019688
|
T | A | 6 | a0001c0001t0002g0129a0001c0001t0002g0130a0001c0001t0002g0151others(3): Show | 6 | HG01109.hp1 HG02809.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.3018+4777T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17019688 | ||||||
| chr3:17019724
|
G | A | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3018+4813G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17019724 | ||||||
| chr3:17019750
|
A | G | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3018+4839A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17019750 | ||||||
| chr3:17019797
|
T | TTAAA | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3018+4888_3018+488 others(8): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 17019797 | |||||
| chr3:17019905
|
T | C | 1 | a0001c0004t0001g0165 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.3018+4994T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17019905 | ||||||
| chr3:17020223
|
A | G | 1 | a0001c0002t0001g0212 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.3018+5312A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17020223 | ||||||
| chr3:17020404
|
G | A | 4 | a0001c0005t0001g0019a0001c0005t0001g0063a0001c0005t0001g0179others(1): Show | 4 | HG01515.hp2 HG03491.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.3018+5493G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17020404 | ||||||
| chr3:17020552
|
A | AT | 24 | a0001c0003t0001g0116a0001c0003t0001g0235a0001c0003t0003g0209others(21): Show | 25 | HG00280.hp2 HG00741.hp2 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.3018+5650dupT | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 17020552 | |||||
| chr3:17020572
|
A | C | 11 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(8): Show | 11 | HG02559.hp2 HG02723.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.3018+5661A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17020572 | ||||||
| chr3:17020622
|
G | A | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3018+5711G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17020622 | ||||||
| chr3:17020700
|
GCT | G | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3018+5796_3018+579 others(6): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 17020700 | |||||
| chr3:17020830
|
A | G | 1 | a0001c0001t0001g0197 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3018+5919A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17020830 | ||||||
| chr3:17020912
|
T | G | 1 | a0001c0002t0001g0068 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3018+6001T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17020912 | ||||||
| chr3:17020961
|
G | C | 2 | a0001c0002t0001g0006a0001c0002t0001g0062 | 2 | NA18945.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.3018+6050G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17020961 | ||||||
| chr3:17021032
|
A | G | 1 | a0001c0002t0001g0095 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.3018+6121A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17021032 | ||||||
| chr3:17021035
|
A | G | 1 | a0001c0001t0001g0203 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3018+6124A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17021035 | ||||||
| chr3:17021157
|
T | C | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3018+6246T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17021157 | ||||||
| chr3:17021243
|
G | A | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3018+6332G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17021243 | ||||||
| chr3:17021253
|
C | T | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3018+6342C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17021253 | ||||||
| chr3:17021353
|
C | T | 1 | a0001c0005t0001g0185 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3018+6442C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17021353 | ||||||
| chr3:17021398
|
A | G | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3018+6487A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17021398 | ||||||
| chr3:17021434
|
A | G | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3018+6523A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17021434 | ||||||
| chr3:17021461
|
T | C | 2 | a0001c0001t0001g0197a0001c0001t0006g0222 | 2 | HG02258.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.3018+6550T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17021461 | ||||||
| chr3:17021595
|
T | TAC | 53 | a0001c0001t0001g0110a0001c0001t0001g0118a0001c0001t0001g0228others(50): Show | 53 | HG00280.hp1 HG00280.hp2 HG01074.hp2 others(50): Show |
intron_variant | MODIFIER | c.3018+6719_3018+672 others(6): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 17021595 | |||||
| chr3:17021595
|
T | TACAC | 21 | a0001c0001t0001g0103a0001c0001t0006g0222a0001c0002t0001g0024others(18): Show | 21 | HG00099.hp1 HG00323.hp2 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.3018+6717_3018+672 others(8): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 17021595 | |||||
| chr3:17021595
|
TAC | T | 72 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(69): Show | 73 | HG00408.hp1 HG00741.hp2 HG01069.hp2 others(70): Show |
intron_variant | MODIFIER | c.3018+6719_3018+672 others(6): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 17021595 | |||||
| chr3:17021595
|
TACAC | T | 22 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(19): Show | 22 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.3018+6717_3018+672 others(8): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 17021595 | |||||
| chr3:17021595
|
TACACAC | T | 10 | a0001c0001t0001g0042a0001c0001t0001g0067a0001c0001t0002g0137others(7): Show | 10 | HG01346.hp1 HG01934.hp1 HG01978.hp2 others(7): Show |
intron_variant | MODIFIER | c.3018+6715_3018+672 others(10): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 17021595 | |||||
| chr3:17021595
|
TACACACA others(1): Show |
T | 34 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(31): Show | 35 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.3018+6713_3018+672 others(12): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 17021595 | |||||
| chr3:17021595
|
TACACACA others(3): Show |
T | 1 | a0001c0014t0001g0104 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3018+6711_3018+672 others(14): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 17021595 | |||||
| chr3:17021628
|
A | C | 1 | a0001c0001t0001g0201 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3018+6717A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17021628 | ||||||
| chr3:17021630
|
A | C | 7 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(4): Show | 7 | HG02055.hp1 HG02109.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.3018+6719A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17021630 | ||||||
| chr3:17021690
|
T | C | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3018+6779T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17021690 | ||||||
| chr3:17021703
|
C | T | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3018+6792C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17021703 | ||||||
| chr3:17021704
|
T | G | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3018+6793T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17021704 | ||||||
| chr3:17021813
|
C | A | 1 | a0001c0008t0001g0242 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3018+6902C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17021813 | ||||||
| chr3:17021876
|
C | A | 3 | a0001c0011t0001g0004a0001c0012t0001g0005a0001c0013t0001g0198 | 3 | HG02055.hp1 HG02109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.3018+6965C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17021876 | ||||||
| chr3:17021984
|
G | A | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3018+7073G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17021984 | ||||||
| chr3:17021993
|
A | T | 1 | a0001c0002t0001g0062 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.3018+7082A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17021993 | ||||||
| chr3:17022074
|
T | G | 1 | a0001c0001t0006g0222 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3018+7163T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17022074 | ||||||
| chr3:17022126
|
T | C | 1 | a0001c0002t0001g0080 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3018+7215T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17022126 | ||||||
| chr3:17022240
|
G | T | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3018+7329G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17022240 | ||||||
| chr3:17022252
|
A | G | 62 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(59): Show | 62 | HG00408.hp1 HG01123.hp2 HG01175.hp2 others(59): Show |
intron_variant | MODIFIER | c.3018+7341A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17022252 | ||||||
| chr3:17022464
|
GTTC | G | 6 | a0001c0002t0001g0125a0001c0002t0001g0126a0001c0002t0001g0205others(3): Show | 6 | HG02559.hp2 HG02723.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.3018+7558_3018+756 others(7): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 17022464 | |||||
| chr3:17022501
|
A | C | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3018+7590A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17022501 | ||||||
| chr3:17022611
|
G | A | 1 | a0001c0001t0001g0247 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3018+7700G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17022611 | ||||||
| chr3:17022633
|
T | C | 158 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(155): Show | 160 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.3018+7722T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17022633 | ||||||
| chr3:17022756
|
A | C | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3018+7845A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17022756 | ||||||
| chr3:17022898
|
G | T | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3018+7987G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17022898 | ||||||
| chr3:17022956
|
C | T | 1 | a0001c0001t0002g0204 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3018+8045C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17022956 | ||||||
| chr3:17022984
|
C | T | 1 | a0001c0003t0001g0211 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3018+8073C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17022984 | ||||||
| chr3:17023021
|
G | A | 3 | a0001c0002t0001g0007a0001c0002t0001g0199a0001c0002t0001g0210 | 3 | HG02257.hp1 HG02280.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.3018+8110G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17023021 | ||||||
| chr3:17023181
|
A | G | 1 | a0001c0001t0001g0229 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.3018+8270A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17023181 | ||||||
| chr3:17023304
|
G | C | 1 | a0001c0001t0001g0043 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.3018+8393G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17023304 | ||||||
| chr3:17023335
|
C | A | 1 | a0001c0002t0001g0085 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3018+8424C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17023335 | ||||||
| chr3:17023339
|
T | A | 1 | a0001c0001t0001g0201 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3018+8428T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17023339 | ||||||
| chr3:17023401
|
C | A | 158 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(155): Show | 160 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.3018+8490C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17023401 | ||||||
| chr3:17023624
|
T | A | 204 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(201): Show | 206 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.3018+8713T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17023624 | ||||||
| chr3:17023643
|
C | T | 17 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(14): Show | 17 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.3018+8732C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17023643 | ||||||
| chr3:17023702
|
T | C | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3018+8791T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17023702 | ||||||
| chr3:17023748
|
A | G | 29 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(26): Show | 29 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.3018+8837A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17023748 | ||||||
| chr3:17023798
|
A | T | 4 | a0001c0003t0004g0001a0001c0003t0004g0128a0001c0003t0004g0152others(1): Show | 5 | HG02486.hp1 HG03139.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.3018+8887A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17023798 | ||||||
| chr3:17023801
|
A | G | 64 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(61): Show | 64 | HG00408.hp1 HG01081.hp2 HG01123.hp2 others(61): Show |
intron_variant | MODIFIER | c.3018+8890A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17023801 | ||||||
| chr3:17024091
|
A | C | 1 | a0001c0002t0001g0240 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3018+9180A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17024091 | ||||||
| chr3:17024193
|
A | G | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3018+9282A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17024193 | ||||||
| chr3:17024220
|
C | T | 1 | a0000c0007t0002g0213 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3018+9309C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17024220 | ||||||
| chr3:17024221
|
G | A | 1 | a0001c0002t0001g0027 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.3018+9310G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17024221 | ||||||
| chr3:17024316
|
G | C | 3 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202 | 3 | HG02976.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3018+9405G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17024316 | ||||||
| chr3:17024421
|
G | A | 2 | a0001c0001t0001g0203a0001c0002t0001g0078 | 2 | HG02965.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3018+9510G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17024421 | ||||||
| chr3:17024761
|
CCTT | C | 4 | a0001c0005t0001g0019a0001c0005t0001g0063a0001c0005t0001g0179others(1): Show | 4 | HG01515.hp2 HG03491.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.3018+9853_3018+985 others(7): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 17024761 | |||||
| chr3:17024777
|
TG | T | 3 | a0001c0011t0001g0004a0001c0012t0001g0005a0001c0013t0001g0198 | 3 | HG02055.hp1 HG02109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.3018+9869delG | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 17024777 | |||||
| chr3:17024787
|
C | G | 6 | a0001c0002t0001g0125a0001c0002t0001g0126a0001c0002t0001g0205others(3): Show | 6 | HG02559.hp2 HG02723.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.3018+9876C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17024787 | ||||||
| chr3:17024807
|
C | T | 11 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(8): Show | 11 | HG02559.hp2 HG02723.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.3018+9896C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17024807 | ||||||
| chr3:17024898
|
A | C | 1 | a0001c0001t0001g0224 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3018+9987A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17024898 | ||||||
| chr3:17024922
|
C | G | 11 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(8): Show | 11 | HG02559.hp2 HG02723.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.3018+10011C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17024922 | ||||||
| chr3:17024929
|
T | A | 91 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(88): Show | 92 | HG00280.hp2 HG00408.hp1 HG00741.hp2 others(89): Show |
intron_variant | MODIFIER | c.3018+10018T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17024929 | ||||||
| chr3:17024976
|
C | T | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3018+10065C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17024976 | ||||||
| chr3:17025058
|
G | A | 5 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(2): Show | 5 | HG02896.hp2 HG03098.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.3018+10147G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17025058 | ||||||
| chr3:17025110
|
G | A | 1 | a0001c0003t0003g0232 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.3018+10199G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17025110 | ||||||
| chr3:17025352
|
G | A | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3018+10441G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17025352 | ||||||
| chr3:17025354
|
C | T | 20 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(17): Show | 20 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.3018+10443C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17025354 | ||||||
| chr3:17025398
|
C | A | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3018+10487C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17025398 | ||||||
| chr3:17025399
|
A | C | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3018+10488A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17025399 | ||||||
| chr3:17025400
|
A | G | 1 | a0001c0001t0001g0203 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3018+10489A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17025400 | ||||||
| chr3:17025444
|
T | C | 1 | a0001c0003t0003g0209 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3018+10533T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17025444 | ||||||
| chr3:17025543
|
A | G | 1 | a0001c0001t0002g0204 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3018+10632A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17025543 | ||||||
| chr3:17025593
|
T | C | 34 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(31): Show | 34 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.3018+10682T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17025593 | ||||||
| chr3:17025648
|
T | A | 1 | a0001c0005t0001g0185 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3018+10737T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17025648 | ||||||
| chr3:17025700
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.3018+10789G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17025700 | ||||||
| chr3:17025881
|
A | G | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3018+10970A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17025881 | ||||||
| chr3:17025898
|
AAGACTC | A | 4 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(1): Show | 4 | HG02965.hp1 HG02976.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.3018+10989_3018+10 others(12): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 17025898 | |||||
| chr3:17025907
|
C | T | 1 | a0001c0002t0001g0121 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3018+10996C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17025907 | ||||||
| chr3:17025989
|
G | T | 6 | a0001c0001t0002g0129a0001c0001t0002g0130a0001c0001t0002g0151others(3): Show | 6 | HG01109.hp1 HG02809.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.3018+11078G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17025989 | ||||||
| chr3:17026085
|
C | A | 2 | a0001c0002t0001g0008a0001c0002t0001g0010 | 2 | HG02896.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.3018+11174C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17026085 | ||||||
| chr3:17026214
|
A | C | 1 | a0001c0002t0001g0006 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.3018+11303A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17026214 | ||||||
| chr3:17026479
|
T | C | 24 | a0001c0003t0001g0116a0001c0003t0001g0235a0001c0003t0003g0209others(21): Show | 25 | HG00280.hp2 HG00741.hp2 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.3018+11568T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17026479 | ||||||
| chr3:17026721
|
G | A | 64 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(61): Show | 64 | HG00408.hp1 HG01081.hp2 HG01123.hp2 others(61): Show |
intron_variant | MODIFIER | c.3018+11810G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17026721 | ||||||
| chr3:17027071
|
T | G | 168 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(165): Show | 170 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.3018+12160T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17027071 | ||||||
| chr3:17027084
|
G | A | 168 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(165): Show | 170 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.3018+12173G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17027084 | ||||||
| chr3:17027085
|
T | G | 4 | a0001c0005t0001g0019a0001c0005t0001g0063a0001c0005t0001g0179others(1): Show | 4 | HG01515.hp2 HG03491.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.3018+12174T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17027085 | ||||||
| chr3:17027194
|
A | G | 1 | a0001c0002t0001g0074 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3018+12283A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17027194 | ||||||
| chr3:17027407
|
A | G | 7 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(4): Show | 7 | HG02055.hp1 HG02109.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.3018+12496A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17027407 | ||||||
| chr3:17027518
|
A | T | 1 | a0001c0014t0001g0104 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3018+12607A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17027518 | ||||||
| chr3:17027747
|
G | A | 5 | a0001c0002t0001g0031a0001c0002t0001g0111a0001c0002t0001g0113others(2): Show | 5 | HG00408.hp2 HG02129.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.3018+12836G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17027747 | ||||||
| chr3:17027865
|
A | G | 1 | a0001c0001t0002g0135 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.3018+12954A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17027865 | ||||||
| chr3:17028166
|
TAG | T | 3 | a0001c0002t0001g0007a0001c0002t0001g0199a0001c0002t0001g0210 | 3 | HG02257.hp1 HG02280.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.3018+13258_3018+13 others(8): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 17028166 | |||||
| chr3:17028190
|
C | A | 11 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(8): Show | 11 | HG02559.hp2 HG02723.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.3018+13279C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17028190 | ||||||
| chr3:17028482
|
CT | C | 64 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(61): Show | 64 | HG00408.hp1 HG01081.hp2 HG01123.hp2 others(61): Show |
intron_variant | MODIFIER | c.3018+13582delT | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 17028482 | |||||
| chr3:17028825
|
C | G | 64 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(61): Show | 64 | HG00408.hp1 HG01081.hp2 HG01123.hp2 others(61): Show |
intron_variant | MODIFIER | c.3018+13914C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17028825 | ||||||
| chr3:17028839
|
C | T | 1 | a0001c0002t0001g0080 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3018+13928C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17028839 | ||||||
| chr3:17028851
|
C | T | 2 | a0001c0001t0001g0157a0001c0002t0001g0054 | 2 | HG00280.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.3018+13940C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17028851 | ||||||
| chr3:17028902
|
T | C | 6 | a0001c0002t0001g0125a0001c0002t0001g0126a0001c0002t0001g0205others(3): Show | 6 | HG02559.hp2 HG02723.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.3019-13972T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17028902 | ||||||
| chr3:17028970
|
C | T | 1 | a0001c0001t0006g0222 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3019-13904C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17028970 | ||||||
| chr3:17028971
|
A | T | 1 | a0001c0001t0001g0227 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3019-13903A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17028971 | ||||||
| chr3:17029027
|
G | A | 23 | a0001c0003t0001g0235a0001c0003t0003g0209a0001c0003t0003g0215others(20): Show | 24 | HG00280.hp2 HG00741.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.3019-13847G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17029027 | ||||||
| chr3:17029090
|
T | C | 168 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(165): Show | 170 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.3019-13784T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17029090 | ||||||
| chr3:17029266
|
C | T | 1 | a0001c0014t0001g0104 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3019-13608C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17029266 | ||||||
| chr3:17029363
|
GA | G | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3019-13500delA | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 17029363 | |||||
| chr3:17029363
|
GAAAA | G | 17 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(14): Show | 17 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.3019-13503_3019-13 others(10): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 17029363 | |||||
| chr3:17029367
|
A | G | 30 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(27): Show | 30 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.3019-13507A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17029367 | ||||||
| chr3:17029373
|
A | C | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3019-13501A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17029373 | ||||||
| chr3:17029380
|
G | A | 171 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(168): Show | 173 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.3019-13494G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17029380 | ||||||
| chr3:17029391
|
C | CT | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3019-13481dupT | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 17029391 | |||||
| chr3:17029449
|
T | C | 1 | a0001c0017t0001g0050 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.3019-13425T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17029449 | ||||||
| chr3:17029622
|
A | T | 1 | a0001c0001t0001g0197 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3019-13252A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17029622 | ||||||
| chr3:17029846
|
C | T | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3019-13028C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17029846 | ||||||
| chr3:17029930
|
A | G | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3019-12944A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17029930 | ||||||
| chr3:17030485
|
A | G | 74 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(71): Show | 75 | HG00408.hp1 HG01081.hp2 HG01123.hp2 others(72): Show |
intron_variant | MODIFIER | c.3019-12389A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17030485 | ||||||
| chr3:17030534
|
A | G | 2 | a0001c0006t0001g0170a0001c0006t0001g0174 | 2 | NA18955.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.3019-12340A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17030534 | ||||||
| chr3:17030689
|
C | T | 1 | a0001c0001t0002g0135 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.3019-12185C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17030689 | ||||||
| chr3:17030720
|
C | T | 3 | a0001c0002t0001g0075a0001c0002t0001g0076a0001c0002t0001g0077 | 3 | HG03209.hp2 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.3019-12154C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17030720 | ||||||
| chr3:17030984
|
A | T | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3019-11890A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17030984 | ||||||
| chr3:17030985
|
AT | A | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3019-11886delT | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 17030985 | |||||
| chr3:17030987
|
T | G | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3019-11887T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17030987 | ||||||
| chr3:17030987
|
T | TTAG | 65 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(62): Show | 65 | HG00408.hp1 HG01081.hp2 HG01123.hp2 others(62): Show |
intron_variant | MODIFIER | c.3019-11884_3019-11 others(9): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 17030987 | |||||
| chr3:17031159
|
A | G | 74 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(71): Show | 75 | HG00408.hp1 HG01081.hp2 HG01123.hp2 others(72): Show |
intron_variant | MODIFIER | c.3019-11715A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17031159 | ||||||
| chr3:17031306
|
A | G | 17 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(14): Show | 17 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.3019-11568A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17031306 | ||||||
| chr3:17031438
|
A | G | 7 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(4): Show | 7 | HG02055.hp1 HG02109.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.3019-11436A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17031438 | ||||||
| chr3:17031476
|
G | C | 1 | a0001c0014t0001g0104 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3019-11398G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17031476 | ||||||
| chr3:17031505
|
A | G | 169 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(166): Show | 171 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.3019-11369A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17031505 | ||||||
| chr3:17031540
|
T | C | 74 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(71): Show | 75 | HG00408.hp1 HG01081.hp2 HG01123.hp2 others(72): Show |
intron_variant | MODIFIER | c.3019-11334T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17031540 | ||||||
| chr3:17031641
|
C | T | 1 | a0001c0003t0004g0128 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3019-11233C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17031641 | ||||||
| chr3:17031643
|
A | G | 4 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0182others(1): Show | 4 | NA18991.hp1 NA18993.hp2 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.3019-11231A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17031643 | ||||||
| chr3:17031675
|
A | G | 1 | a0001c0002t0001g0097 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3019-11199A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17031675 | ||||||
| chr3:17031873
|
G | C | 1 | a0001c0001t0001g0234 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3019-11001G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17031873 | ||||||
| chr3:17031929
|
C | CT | 17 | a0001c0001t0006g0222a0001c0002t0001g0125a0001c0002t0001g0126others(14): Show | 18 | HG01934.hp1 HG01978.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.3019-10925dupT | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 17031929 | |||||
| chr3:17031929
|
CT | C | 37 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(34): Show | 38 | HG00280.hp2 HG00323.hp2 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.3019-10925delT | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 17031929 | |||||
| chr3:17031994
|
G | T | 6 | a0001c0002t0001g0125a0001c0002t0001g0126a0001c0002t0001g0205others(3): Show | 6 | HG02559.hp2 HG02723.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.3019-10880G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17031994 | ||||||
| chr3:17032039
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.3019-10835C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17032039 | ||||||
| chr3:17032121
|
T | C | 3 | a0001c0011t0001g0004a0001c0012t0001g0005a0001c0013t0001g0198 | 3 | HG02055.hp1 HG02109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.3019-10753T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17032121 | ||||||
| chr3:17032240
|
A | G | 3 | a0001c0003t0001g0044a0001c0003t0001g0187a0001c0003t0001g0188 | 3 | HG01433.hp2 HG01952.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.3019-10634A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17032240 | ||||||
| chr3:17032473
|
C | T | 26 | a0001c0001t0001g0197a0001c0001t0006g0222a0001c0003t0001g0211others(23): Show | 27 | HG00280.hp2 HG00741.hp2 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.3019-10401C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17032473 | ||||||
| chr3:17032474
|
G | A | 1 | a0001c0003t0001g0184 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3019-10400G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17032474 | ||||||
| chr3:17032500
|
T | C | 1 | a0001c0001t0001g0083 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.3019-10374T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17032500 | ||||||
| chr3:17032650
|
G | GTA | 65 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(62): Show | 65 | HG00408.hp1 HG01081.hp2 HG01123.hp2 others(62): Show |
intron_variant | MODIFIER | c.3019-10223_3019-10 others(8): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 17032650 | |||||
| chr3:17032674
|
G | A | 2 | a0001c0004t0001g0176a0001c0008t0001g0123 | 2 | HG03927.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.3019-10200G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17032674 | ||||||
| chr3:17032771
|
T | A | 74 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(71): Show | 75 | HG00408.hp1 HG01081.hp2 HG01123.hp2 others(72): Show |
intron_variant | MODIFIER | c.3019-10103T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17032771 | ||||||
| chr3:17032789
|
G | C | 19 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(16): Show | 19 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.3019-10085G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17032789 | ||||||
| chr3:17032874
|
A | C | 1 | a0001c0001t0001g0083 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.3019-10000A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17032874 | ||||||
| chr3:17032908
|
C | T | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3019-9966C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17032908 | ||||||
| chr3:17033379
|
A | G | 104 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(101): Show | 105 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.3019-9495A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17033379 | ||||||
| chr3:17033567
|
G | A | 74 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(71): Show | 75 | HG00408.hp1 HG01081.hp2 HG01123.hp2 others(72): Show |
intron_variant | MODIFIER | c.3019-9307G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17033567 | ||||||
| chr3:17033666
|
A | G | 1 | a0001c0003t0001g0211 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3019-9208A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17033666 | ||||||
| chr3:17034276
|
C | A | 96 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(93): Show | 96 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.3019-8598C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17034276 | ||||||
| chr3:17034397
|
A | G | 6 | a0001c0002t0001g0125a0001c0002t0001g0126a0001c0002t0001g0205others(3): Show | 6 | HG02559.hp2 HG02723.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.3019-8477A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17034397 | ||||||
| chr3:17034421
|
A | T | 162 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(159): Show | 164 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.3019-8453A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17034421 | ||||||
| chr3:17034519
|
T | G | 1 | a0000c0007t0002g0147 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3019-8355T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17034519 | ||||||
| chr3:17034619
|
C | G | 3 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202 | 3 | HG02976.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3019-8255C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17034619 | ||||||
| chr3:17034781
|
C | G | 3 | a0001c0001t0001g0035a0001c0001t0001g0039a0001c0001t0001g0109 | 3 | HG02074.hp2 NA18944.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.3019-8093C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17034781 | ||||||
| chr3:17034810
|
A | T | 1 | a0001c0002t0003g0064 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.3019-8064A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17034810 | ||||||
| chr3:17034882
|
C | T | 1 | a0001c0002t0001g0223 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3019-7992C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17034882 | ||||||
| chr3:17034889
|
T | C | 2 | a0001c0011t0001g0004a0001c0012t0001g0005 | 2 | HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.3019-7985T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17034889 | ||||||
| chr3:17034911
|
C | CCTT | 168 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(165): Show | 170 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.3019-7962_3019-796 others(7): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 17034911 | |||||
| chr3:17034926
|
T | C | 74 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(71): Show | 74 | HG00408.hp1 HG01081.hp2 HG01123.hp2 others(71): Show |
intron_variant | MODIFIER | c.3019-7948T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17034926 | ||||||
| chr3:17034927
|
G | A | 1 | a0001c0001t0001g0036 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.3019-7947G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17034927 | ||||||
| chr3:17034932
|
C | T | 1 | a0001c0013t0001g0198 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3019-7942C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17034932 | ||||||
| chr3:17035051
|
A | G | 1 | a0001c0003t0001g0211 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3019-7823A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17035051 | ||||||
| chr3:17035068
|
C | G | 104 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(101): Show | 104 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.3019-7806C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17035068 | ||||||
| chr3:17035234
|
C | G | 2 | a0001c0002t0003g0064a0001c0002t0003g0065 | 2 | HG00741.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.3019-7640C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17035234 | ||||||
| chr3:17035281
|
A | ATAACTGT others(42): Show |
3 | a0001c0011t0001g0004a0001c0012t0001g0005a0001c0013t0001g0198 | 3 | HG02055.hp1 HG02109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.3019-7566_3019-751 others(53): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 17035281 | |||||
| chr3:17035371
|
A | C | 2 | a0001c0001t0001g0197a0001c0001t0006g0222 | 2 | HG02258.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.3019-7503A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17035371 | ||||||
| chr3:17035392
|
G | A | 1 | a0001c0002t0001g0066 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3019-7482G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17035392 | ||||||
| chr3:17035423
|
T | TC | 165 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(162): Show | 167 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.3019-7450dupC | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 17035423 | |||||
| chr3:17035474
|
G | A | 5 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(2): Show | 5 | HG02896.hp2 HG03098.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.3019-7400G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17035474 | ||||||
| chr3:17035479
|
C | A | 29 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(26): Show | 29 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.3019-7395C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17035479 | ||||||
| chr3:17035614
|
A | G | 2 | a0001c0003t0004g0152a0001c0003t0004g0153 | 2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.3019-7260A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17035614 | ||||||
| chr3:17035744
|
C | T | 4 | a0001c0003t0001g0211a0001c0011t0001g0004a0001c0012t0001g0005others(1): Show | 4 | HG02055.hp1 HG02109.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.3019-7130C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17035744 | ||||||
| chr3:17035776
|
C | T | 165 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(162): Show | 167 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.3019-7098C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17035776 | ||||||
| chr3:17036007
|
A | G | 2 | a0001c0004t0001g0165a0001c0004t0001g0166 | 2 | HG01975.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.3019-6867A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17036007 | ||||||
| chr3:17036132
|
G | C | 1 | a0001c0002t0001g0007 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3019-6742G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17036132 | ||||||
| chr3:17036227
|
G | A | 3 | a0001c0011t0001g0004a0001c0012t0001g0005a0001c0013t0001g0198 | 3 | HG02055.hp1 HG02109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.3019-6647G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17036227 | ||||||
| chr3:17036239
|
C | T | 23 | a0001c0003t0001g0235a0001c0003t0003g0209a0001c0003t0003g0215others(20): Show | 24 | HG00280.hp2 HG00741.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.3019-6635C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17036239 | ||||||
| chr3:17036453
|
G | C | 1 | a0001c0001t0001g0221 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3019-6421G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17036453 | ||||||
| chr3:17036464
|
C | T | 1 | a0001c0003t0003g0215 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.3019-6410C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17036464 | ||||||
| chr3:17036610
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3019-6264G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17036610 | ||||||
| chr3:17036667
|
A | G | 4 | a0001c0002t0001g0214a0001c0002t0001g0233a0001c0002t0001g0238others(1): Show | 4 | HG01891.hp2 HG02258.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.3019-6207A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17036667 | ||||||
| chr3:17036717
|
G | A | 2 | a0001c0001t0001g0221a0001c0001t0001g0225 | 2 | HG01081.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.3019-6157G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17036717 | ||||||
| chr3:17036724
|
T | C | 7 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(4): Show | 7 | HG02055.hp1 HG02109.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.3019-6150T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17036724 | ||||||
| chr3:17036832
|
G | A | 23 | a0001c0003t0001g0235a0001c0003t0003g0209a0001c0003t0003g0215others(20): Show | 24 | HG00280.hp2 HG00741.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.3019-6042G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17036832 | ||||||
| chr3:17036938
|
C | T | 64 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(61): Show | 64 | HG00408.hp1 HG01081.hp2 HG01123.hp2 others(61): Show |
intron_variant | MODIFIER | c.3019-5936C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17036938 | ||||||
| chr3:17036945
|
C | T | 1 | a0001c0002t0001g0062 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.3019-5929C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17036945 | ||||||
| chr3:17037040
|
T | G | 6 | a0001c0002t0001g0125a0001c0002t0001g0126a0001c0002t0001g0205others(3): Show | 6 | HG02559.hp2 HG02723.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.3019-5834T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17037040 | ||||||
| chr3:17037148
|
A | G | 163 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(160): Show | 165 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.3019-5726A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17037148 | ||||||
| chr3:17037196
|
G | A | 4 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(1): Show | 4 | HG02965.hp1 HG02976.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.3019-5678G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17037196 | ||||||
| chr3:17037348
|
T | A | 38 | a0001c0002t0001g0125a0001c0002t0001g0126a0001c0002t0001g0205others(35): Show | 40 | HG00280.hp2 HG00741.hp2 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.3019-5526T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17037348 | ||||||
| chr3:17037656
|
GA | G | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3019-5211delA | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 17037656 | |||||
| chr3:17037709
|
A | T | 162 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(159): Show | 164 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.3019-5165A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17037709 | ||||||
| chr3:17037770
|
G | C | 62 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(59): Show | 62 | HG00408.hp1 HG01123.hp2 HG01175.hp2 others(59): Show |
intron_variant | MODIFIER | c.3019-5104G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17037770 | ||||||
| chr3:17038277
|
T | G | 162 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(159): Show | 164 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.3019-4597T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17038277 | ||||||
| chr3:17038439
|
C | T | 1 | a0001c0004t0002g0175 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3019-4435C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17038439 | ||||||
| chr3:17038468
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3019-4406C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17038468 | ||||||
| chr3:17038751
|
A | G | 1 | a0000c0007t0002g0147 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3019-4123A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17038751 | ||||||
| chr3:17038884
|
G | A | 1 | a0001c0002t0001g0114 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.3019-3990G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17038884 | ||||||
| chr3:17039004
|
A | G | 6 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(3): Show | 6 | HG02074.hp2 NA18942.hp1 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.3019-3870A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17039004 | ||||||
| chr3:17039047
|
C | T | 1 | a0001c0003t0001g0184 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3019-3827C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17039047 | ||||||
| chr3:17039055
|
A | G | 6 | a0001c0002t0001g0125a0001c0002t0001g0126a0001c0002t0001g0205others(3): Show | 6 | HG02559.hp2 HG02723.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.3019-3819A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17039055 | ||||||
| chr3:17039384
|
A | T | 5 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(2): Show | 5 | HG02896.hp2 HG03098.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.3019-3490A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17039384 | ||||||
| chr3:17039482
|
A | G | 167 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(164): Show | 169 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.3019-3392A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17039482 | ||||||
| chr3:17039498
|
A | G | 1 | a0001c0001t0001g0221 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3019-3376A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17039498 | ||||||
| chr3:17039624
|
C | T | 159 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(156): Show | 161 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.3019-3250C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17039624 | ||||||
| chr3:17040078
|
A | C | 6 | a0001c0002t0001g0125a0001c0002t0001g0126a0001c0002t0001g0205others(3): Show | 6 | HG02559.hp2 HG02723.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.3019-2796A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17040078 | ||||||
| chr3:17040085
|
T | C | 16 | a0001c0002t0001g0024a0001c0002t0001g0046a0001c0002t0001g0047others(13): Show | 16 | HG00099.hp1 HG00323.hp2 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.3019-2789T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17040085 | ||||||
| chr3:17040127
|
T | C | 62 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(59): Show | 62 | HG00408.hp1 HG01123.hp2 HG01175.hp2 others(59): Show |
intron_variant | MODIFIER | c.3019-2747T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17040127 | ||||||
| chr3:17040156
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.3019-2718C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17040156 | ||||||
| chr3:17040201
|
G | C | 5 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(2): Show | 5 | HG02896.hp2 HG03098.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.3019-2673G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17040201 | ||||||
| chr3:17040441
|
T | C | 1 | a0001c0001t0001g0108 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.3019-2433T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17040441 | ||||||
| chr3:17040585
|
C | T | 1 | a0001c0002t0001g0032 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3019-2289C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17040585 | ||||||
| chr3:17040862
|
T | C | 1 | a0001c0002t0001g0079 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3019-2012T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17040862 | ||||||
| chr3:17040972
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3019-1902T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17040972 | ||||||
| chr3:17041072
|
C | T | 2 | a0001c0001t0001g0221a0001c0001t0001g0225 | 2 | HG01081.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.3019-1802C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17041072 | ||||||
| chr3:17041079
|
C | T | 1 | a0001c0002t0001g0069 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3019-1795C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17041079 | ||||||
| chr3:17041347
|
G | A | 21 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(18): Show | 21 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.3019-1527G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17041347 | ||||||
| chr3:17041372
|
G | A | 1 | a0001c0001t0001g0227 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3019-1502G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17041372 | ||||||
| chr3:17041398
|
G | A | 1 | a0001c0001t0002g0136 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3019-1476G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17041398 | ||||||
| chr3:17041498
|
G | A | 5 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(2): Show | 5 | HG02896.hp2 HG03098.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.3019-1376G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17041498 | ||||||
| chr3:17041556
|
A | G | 163 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(160): Show | 165 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.3019-1318A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17041556 | ||||||
| chr3:17041682
|
G | A | 3 | a0001c0002t0001g0056a0001c0002t0001g0105a0001c0017t0001g0050 | 3 | NA18942.hp2 NA18993.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.3019-1192G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17041682 | ||||||
| chr3:17042012
|
A | G | 1 | a0001c0001t0006g0222 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3019-862A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17042012 | ||||||
| chr3:17042143
|
G | A | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3019-731G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17042143 | ||||||
| chr3:17042217
|
G | A | 159 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(156): Show | 161 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.3019-657G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17042217 | ||||||
| chr3:17042332
|
C | A | 70 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(67): Show | 70 | HG00408.hp1 HG01081.hp2 HG01123.hp2 others(67): Show |
intron_variant | MODIFIER | c.3019-542C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17042332 | ||||||
| chr3:17042372
|
A | G | 4 | a0001c0001t0002g0129a0001c0001t0002g0130a0001c0001t0002g0151others(1): Show | 4 | HG01109.hp1 HG02970.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3019-502A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17042372 | ||||||
| chr3:17042380
|
T | C | 1 | a0001c0014t0001g0104 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3019-494T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17042380 | ||||||
| chr3:17042432
|
A | C | 4 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0219others(1): Show | 4 | HG02895.hp2 HG03041.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.3019-442A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17042432 | ||||||
| chr3:17042532
|
A | G | 5 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(2): Show | 5 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.3019-342A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17042532 | ||||||
| chr3:17042565
|
G | A | 29 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(26): Show | 29 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.3019-309G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17042565 | ||||||
| chr3:17042628
|
G | C | 1 | a0001c0001t0006g0222 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3019-246G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17042628 | ||||||
| chr3:17042644
|
C | G | 1 | a0001c0014t0001g0104 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3019-230C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17042644 | ||||||
| chr3:17042824
|
G | A | 3 | a0001c0001t0001g0118a0001c0001t0001g0228a0001c0003t0001g0116 | 3 | NA18956.hp1 NA18956.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.3019-50G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 3/5 | chr3 | 17042824 | ||||||
| chr3:17042994
|
T | A | 6 | a0001c0002t0001g0125a0001c0002t0001g0126a0001c0002t0001g0205others(3): Show | 6 | HG02559.hp2 HG02723.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.3094+45T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17042994 | ||||||
| chr3:17043408
|
G | A | 162 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(159): Show | 164 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.3094+459G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17043408 | ||||||
| chr3:17043410
|
G | A | 1 | a0001c0002t0001g0149 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3094+461G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17043410 | ||||||
| chr3:17043626
|
TA | T | 30 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(27): Show | 30 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.3094+689delA | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17043626 | |||||
| chr3:17043638
|
A | G | 5 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(2): Show | 5 | HG02896.hp2 HG03098.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.3094+689A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17043638 | ||||||
| chr3:17043815
|
G | A | 1 | a0001c0002t0001g0007 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3094+866G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17043815 | ||||||
| chr3:17043823
|
T | A | 17 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(14): Show | 17 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.3094+874T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17043823 | ||||||
| chr3:17044178
|
C | T | 23 | a0001c0003t0001g0235a0001c0003t0003g0209a0001c0003t0003g0215others(20): Show | 24 | HG00280.hp2 HG00741.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.3094+1229C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17044178 | ||||||
| chr3:17044204
|
T | A | 2 | a0001c0002t0001g0125a0001c0002t0001g0126 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3094+1255T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17044204 | ||||||
| chr3:17044209
|
A | G | 2 | a0001c0002t0001g0058a0001c0002t0001g0158 | 2 | HG03834.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.3094+1260A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17044209 | ||||||
| chr3:17044262
|
G | A | 162 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(159): Show | 164 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.3094+1313G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17044262 | ||||||
| chr3:17044626
|
T | G | 5 | a0001c0002t0001g0031a0001c0002t0001g0111a0001c0002t0001g0113others(2): Show | 5 | HG00408.hp2 HG02129.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.3094+1677T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17044626 | ||||||
| chr3:17045075
|
C | G | 5 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(2): Show | 5 | HG02896.hp2 HG03098.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.3094+2126C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17045075 | ||||||
| chr3:17045087
|
A | G | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3094+2138A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17045087 | ||||||
| chr3:17045186
|
T | C | 167 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(164): Show | 169 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.3094+2237T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17045186 | ||||||
| chr3:17045521
|
A | G | 4 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(1): Show | 4 | HG02965.hp1 HG02976.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.3094+2572A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17045521 | ||||||
| chr3:17045891
|
T | C | 23 | a0001c0003t0001g0235a0001c0003t0003g0209a0001c0003t0003g0215others(20): Show | 24 | HG00280.hp2 HG00741.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.3094+2942T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17045891 | ||||||
| chr3:17046055
|
G | A | 1 | a0001c0005t0001g0019 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.3094+3106G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17046055 | ||||||
| chr3:17046062
|
T | C | 1 | a0001c0003t0001g0211 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3094+3113T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17046062 | ||||||
| chr3:17046110
|
A | G | 3 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0220 | 3 | HG03041.hp2 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.3094+3161A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17046110 | ||||||
| chr3:17046289
|
C | T | 1 | a0001c0002t0001g0032 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3094+3340C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17046289 | ||||||
| chr3:17046342
|
C | T | 29 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(26): Show | 29 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.3094+3393C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17046342 | ||||||
| chr3:17046734
|
G | T | 1 | a0001c0003t0001g0211 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3094+3785G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17046734 | ||||||
| chr3:17046907
|
C | T | 9 | a0001c0002t0001g0022a0001c0002t0001g0023a0001c0002t0001g0055others(6): Show | 9 | HG02027.hp2 NA18942.hp2 NA18955.hp2 others(6): Show |
intron_variant | MODIFIER | c.3094+3958C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17046907 | ||||||
| chr3:17047129
|
G | A | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3094+4180G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17047129 | ||||||
| chr3:17047171
|
A | C | 1 | a0001c0002t0001g0205 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3094+4222A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17047171 | ||||||
| chr3:17047208
|
A | T | 1 | a0001c0002t0001g0060 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3094+4259A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17047208 | ||||||
| chr3:17047381
|
A | AGCGTCGT others(10): Show |
168 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(165): Show | 170 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.3094+4434_3094+443 others(21): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17047381 | |||||
| chr3:17047472
|
T | G | 1 | a0001c0001t0002g0135 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.3094+4523T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17047472 | ||||||
| chr3:17047502
|
C | G | 1 | a0001c0001t0002g0135 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.3094+4553C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17047502 | ||||||
| chr3:17047517
|
C | T | 23 | a0001c0003t0001g0235a0001c0003t0003g0209a0001c0003t0003g0215others(20): Show | 24 | HG00280.hp2 HG00741.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.3094+4568C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17047517 | ||||||
| chr3:17047596
|
C | G | 1 | a0001c0002t0001g0052 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.3094+4647C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17047596 | ||||||
| chr3:17047632
|
G | C | 5 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0001g0245others(2): Show | 5 | HG01123.hp2 HG03017.hp1 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.3094+4683G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17047632 | ||||||
| chr3:17047703
|
G | A | 21 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(18): Show | 21 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.3094+4754G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17047703 | ||||||
| chr3:17047868
|
A | G | 1 | a0001c0014t0001g0104 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3094+4919A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17047868 | ||||||
| chr3:17047982
|
A | T | 7 | a0001c0003t0001g0235a0001c0003t0003g0209a0001c0003t0003g0215others(4): Show | 7 | HG00280.hp2 HG00741.hp2 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.3094+5033A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17047982 | ||||||
| chr3:17048009
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.3094+5060G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17048009 | ||||||
| chr3:17048084
|
C | CT | 123 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(120): Show | 123 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.3094+5149dupT | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17048084 | |||||
| chr3:17048084
|
C | CTT | 37 | a0001c0001t0001g0043a0001c0002t0001g0125a0001c0002t0001g0206others(34): Show | 39 | HG00280.hp2 HG00741.hp2 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.3094+5148_3094+514 others(6): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17048084 | |||||
| chr3:17048084
|
C | T | 1 | a0001c0002t0001g0055 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.3094+5135C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17048084 | ||||||
| chr3:17048099
|
C | G | 1 | a0001c0001t0001g0043 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.3094+5150C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17048099 | ||||||
| chr3:17048171
|
T | C | 2 | a0001c0002t0001g0125a0001c0002t0001g0126 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3094+5222T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17048171 | ||||||
| chr3:17048244
|
C | G | 10 | a0001c0001t0002g0129a0001c0001t0002g0130a0001c0001t0002g0131others(7): Show | 10 | HG01109.hp1 HG02109.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.3094+5295C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17048244 | ||||||
| chr3:17048494
|
T | C | 1 | a0001c0001t0001g0150 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3094+5545T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17048494 | ||||||
| chr3:17048842
|
A | G | 168 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(165): Show | 170 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.3094+5893A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17048842 | ||||||
| chr3:17048863
|
A | G | 5 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(2): Show | 5 | HG02896.hp2 HG03098.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.3094+5914A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17048863 | ||||||
| chr3:17049014
|
G | A | 2 | a0001c0001t0001g0226a0001c0001t0001g0230 | 2 | HG03831.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.3094+6065G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17049014 | ||||||
| chr3:17049100
|
G | GT | 28 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(25): Show | 29 | HG00280.hp2 HG00741.hp2 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.3094+6160dupT | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17049100 | |||||
| chr3:17049271
|
T | C | 5 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(2): Show | 5 | HG02896.hp2 HG03098.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.3094+6322T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17049271 | ||||||
| chr3:17049300
|
A | G | 16 | a0001c0004t0001g0002a0001c0004t0001g0162a0001c0004t0001g0163others(13): Show | 17 | HG01069.hp2 HG01175.hp1 HG01934.hp2 others(14): Show |
intron_variant | MODIFIER | c.3094+6351A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17049300 | ||||||
| chr3:17049563
|
A | C | 5 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(2): Show | 5 | HG02896.hp2 HG03098.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.3094+6614A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17049563 | ||||||
| chr3:17049785
|
G | A | 1 | a0001c0008t0001g0123 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3094+6836G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17049785 | ||||||
| chr3:17049962
|
A | G | 64 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(61): Show | 64 | HG00408.hp1 HG01081.hp2 HG01123.hp2 others(61): Show |
intron_variant | MODIFIER | c.3094+7013A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17049962 | ||||||
| chr3:17049984
|
C | G | 8 | a0001c0003t0001g0044a0001c0003t0001g0187a0001c0003t0001g0188others(5): Show | 8 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.3094+7035C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17049984 | ||||||
| chr3:17050029
|
C | A | 26 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103others(23): Show | 26 | HG01081.hp2 HG01123.hp2 HG01943.hp2 others(23): Show |
intron_variant | MODIFIER | c.3094+7080C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17050029 | ||||||
| chr3:17050109
|
A | G | 162 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(159): Show | 164 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.3094+7160A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17050109 | ||||||
| chr3:17050128
|
T | C | 2 | a0001c0002t0001g0022a0001c0002t0001g0023 | 2 | NA18955.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.3094+7179T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17050128 | ||||||
| chr3:17050418
|
GTATATAA others(10): Show |
G | 2 | a0002c0009t0001g0154a0002c0009t0001g0155 | 2 | HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3094+7470_3094+748 others(21): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17050418 | ||||||
| chr3:17050436
|
C | G | 2 | a0002c0009t0001g0154a0002c0009t0001g0155 | 2 | HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3094+7487C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17050436 | ||||||
| chr3:17050491
|
A | T | 1 | a0001c0001t0006g0222 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3094+7542A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17050491 | ||||||
| chr3:17050796
|
T | C | 1 | a0001c0002t0001g0087 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.3094+7847T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17050796 | ||||||
| chr3:17050821
|
G | C | 1 | a0001c0002t0001g0051 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.3094+7872G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17050821 | ||||||
| chr3:17050922
|
A | G | 5 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(2): Show | 5 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.3094+7973A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17050922 | ||||||
| chr3:17050942
|
A | T | 1 | a0001c0001t0001g0012 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.3094+7993A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17050942 | ||||||
| chr3:17050945
|
A | G | 3 | a0001c0011t0001g0004a0001c0012t0001g0005a0001c0013t0001g0198 | 3 | HG02055.hp1 HG02109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.3094+7996A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17050945 | ||||||
| chr3:17050976
|
A | C | 6 | a0001c0002t0001g0125a0001c0002t0001g0126a0001c0002t0001g0205others(3): Show | 6 | HG02559.hp2 HG02723.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.3094+8027A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17050976 | ||||||
| chr3:17051171
|
G | C | 1 | a0001c0001t0001g0053 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3094+8222G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17051171 | ||||||
| chr3:17051192
|
C | T | 1 | a0001c0002t0001g0032 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3094+8243C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17051192 | ||||||
| chr3:17051341
|
A | G | 3 | a0001c0011t0001g0004a0001c0012t0001g0005a0001c0013t0001g0198 | 3 | HG02055.hp1 HG02109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.3094+8392A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17051341 | ||||||
| chr3:17051405
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.3094+8456C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17051405 | ||||||
| chr3:17051406
|
G | A | 47 | a0001c0001t0001g0197a0001c0001t0001g0200a0001c0001t0001g0201others(44): Show | 49 | HG00280.hp2 HG00741.hp2 HG01069.hp2 others(46): Show |
intron_variant | MODIFIER | c.3094+8457G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17051406 | ||||||
| chr3:17051537
|
TG | T | 62 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(59): Show | 62 | HG00408.hp1 HG01123.hp2 HG01175.hp2 others(59): Show |
intron_variant | MODIFIER | c.3094+8594delG | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17051537 | |||||
| chr3:17051543
|
G | A | 106 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(103): Show | 108 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.3094+8594G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17051543 | ||||||
| chr3:17051543
|
GA | G | 7 | a0001c0002t0001g0031a0001c0002t0001g0111a0001c0002t0001g0113others(4): Show | 7 | HG00408.hp2 HG00741.hp1 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.3094+8602delA | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17051543 | |||||
| chr3:17051977
|
G | A | 4 | a0001c0002t0001g0031a0001c0002t0001g0111a0001c0002t0001g0113others(1): Show | 4 | HG00408.hp2 HG02129.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.3094+9028G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17051977 | ||||||
| chr3:17051980
|
C | T | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3094+9031C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17051980 | ||||||
| chr3:17052046
|
A | G | 167 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(164): Show | 169 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.3094+9097A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17052046 | ||||||
| chr3:17052130
|
C | T | 38 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(35): Show | 38 | HG00408.hp1 HG01175.hp2 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.3094+9181C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17052130 | ||||||
| chr3:17052134
|
G | A | 168 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(165): Show | 170 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.3094+9185G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17052134 | ||||||
| chr3:17052216
|
GA | G | 4 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0219others(1): Show | 4 | HG02895.hp2 HG03041.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.3094+9270delA | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17052216 | |||||
| chr3:17052236
|
C | CA | 33 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(30): Show | 33 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.3094+9304dupA | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17052236 | |||||
| chr3:17052236
|
CA | C | 14 | a0001c0002t0001g0023a0001c0002t0001g0033a0001c0002t0001g0125others(11): Show | 14 | HG00280.hp2 HG01106.hp2 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.3094+9304delA | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17052236 | |||||
| chr3:17052236
|
CAA | C | 16 | a0001c0004t0001g0002a0001c0004t0001g0162a0001c0004t0001g0163others(13): Show | 17 | HG01069.hp2 HG01175.hp1 HG01934.hp2 others(14): Show |
intron_variant | MODIFIER | c.3094+9303_3094+930 others(6): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17052236 | |||||
| chr3:17052253
|
A | AAAAAT | 18 | a0001c0003t0001g0018a0001c0003t0001g0180a0001c0003t0001g0181others(15): Show | 18 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.3094+9304_3094+930 others(9): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17052253 | ||||||
| chr3:17052253
|
A | AAT | 14 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103others(11): Show | 14 | HG01123.hp2 HG02451.hp2 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.3094+9304_3094+930 others(6): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17052253 | ||||||
| chr3:17052253
|
A | T | 5 | a0001c0001t0001g0038a0001c0001t0001g0117a0001c0001t0001g0119others(2): Show | 5 | HG00408.hp1 HG01943.hp2 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.3094+9304A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17052253 | ||||||
| chr3:17052255
|
T | G | 42 | a0001c0001t0001g0038a0001c0001t0001g0101a0001c0001t0001g0102others(39): Show | 42 | HG00408.hp1 HG01081.hp2 HG01099.hp1 others(39): Show |
intron_variant | MODIFIER | c.3094+9306T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17052255 | ||||||
| chr3:17052255
|
T | TG | 50 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(47): Show | 50 | HG00099.hp1 HG00323.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.3094+9315dupG | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17052255 | |||||
| chr3:17052256
|
G | T | 1 | a0001c0011t0001g0004 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3094+9307G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17052256 | ||||||
| chr3:17052262
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.3094+9313G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17052262 | ||||||
| chr3:17052262
|
G | GA | 8 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0229others(5): Show | 8 | HG03831.hp1 HG03927.hp1 HG04115.hp2 others(5): Show |
intron_variant | MODIFIER | c.3094+9313_3094+931 others(5): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17052262 | ||||||
| chr3:17052262
|
G | T | 4 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(1): Show | 4 | HG02965.hp1 HG02976.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.3094+9313G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17052262 | ||||||
| chr3:17052387
|
A | C | 3 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202 | 3 | HG02976.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3094+9438A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17052387 | ||||||
| chr3:17052814
|
G | A | 64 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(61): Show | 64 | HG00408.hp1 HG01081.hp2 HG01123.hp2 others(61): Show |
intron_variant | MODIFIER | c.3094+9865G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17052814 | ||||||
| chr3:17052869
|
C | T | 168 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(165): Show | 170 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.3094+9920C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17052869 | ||||||
| chr3:17052881
|
C | A | 201 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(198): Show | 203 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.3094+9932C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17052881 | ||||||
| chr3:17053003
|
C | T | 5 | a0001c0004t0001g0162a0001c0004t0001g0163a0001c0004t0001g0164others(2): Show | 5 | HG01069.hp2 HG01934.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.3094+10054C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17053003 | ||||||
| chr3:17053069
|
T | C | 167 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(164): Show | 169 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.3094+10120T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17053069 | ||||||
| chr3:17053325
|
C | T | 2 | a0001c0002t0001g0113a0001c0002t0001g0114 | 2 | HG00408.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.3094+10376C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17053325 | ||||||
| chr3:17053326
|
G | A | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3094+10377G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17053326 | ||||||
| chr3:17053414
|
C | T | 21 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(18): Show | 21 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.3094+10465C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17053414 | ||||||
| chr3:17053582
|
C | T | 1 | a0001c0006t0001g0174 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.3094+10633C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17053582 | ||||||
| chr3:17053597
|
A | T | 3 | a0001c0011t0001g0004a0001c0012t0001g0005a0001c0013t0001g0198 | 3 | HG02055.hp1 HG02109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.3094+10648A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17053597 | ||||||
| chr3:17053668
|
G | A | 1 | a0001c0003t0001g0211 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3094+10719G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17053668 | ||||||
| chr3:17053683
|
G | A | 14 | a0001c0002t0001g0024a0001c0002t0001g0046a0001c0002t0001g0048others(11): Show | 14 | HG00099.hp1 HG00323.hp2 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.3094+10734G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17053683 | ||||||
| chr3:17053909
|
A | G | 168 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(165): Show | 170 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.3094+10960A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17053909 | ||||||
| chr3:17053982
|
C | A | 5 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(2): Show | 5 | HG02896.hp2 HG03098.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.3094+11033C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17053982 | ||||||
| chr3:17054349
|
C | T | 5 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(2): Show | 5 | HG02896.hp2 HG03098.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.3094+11400C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17054349 | ||||||
| chr3:17054350
|
A | C | 1 | a0001c0003t0001g0211 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3094+11401A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17054350 | ||||||
| chr3:17054963
|
A | G | 1 | a0001c0002t0001g0087 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.3094+12014A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17054963 | ||||||
| chr3:17055079
|
C | T | 1 | a0001c0001t0001g0229 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.3094+12130C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17055079 | ||||||
| chr3:17055762
|
G | A | 64 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(61): Show | 64 | HG00408.hp1 HG01081.hp2 HG01123.hp2 others(61): Show |
intron_variant | MODIFIER | c.3095-12194G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17055762 | ||||||
| chr3:17055828
|
A | T | 14 | a0001c0001t0001g0139a0001c0001t0002g0127a0001c0001t0002g0135others(11): Show | 14 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.3095-12128A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17055828 | ||||||
| chr3:17055967
|
T | A | 1 | a0001c0002t0001g0212 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.3095-11989T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17055967 | ||||||
| chr3:17056058
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3095-11898C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17056058 | ||||||
| chr3:17056161
|
C | T | 6 | a0001c0002t0001g0125a0001c0002t0001g0126a0001c0002t0001g0205others(3): Show | 6 | HG02559.hp2 HG02723.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.3095-11795C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17056161 | ||||||
| chr3:17056262
|
A | G | 30 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(27): Show | 30 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.3095-11694A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17056262 | ||||||
| chr3:17056296
|
A | G | 2 | a0001c0001t0001g0197a0001c0001t0006g0222 | 2 | HG02258.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.3095-11660A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17056296 | ||||||
| chr3:17056416
|
A | G | 1 | a0001c0003t0001g0211 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3095-11540A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17056416 | ||||||
| chr3:17056865
|
G | A | 1 | a0001c0002t0001g0210 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3095-11091G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17056865 | ||||||
| chr3:17056907
|
A | G | 2 | a0001c0002t0001g0070a0001c0002t0001g0071 | 2 | HG01069.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.3095-11049A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17056907 | ||||||
| chr3:17056939
|
A | G | 2 | a0001c0002t0001g0032a0001c0002t0001g0085 | 2 | HG02257.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.3095-11017A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17056939 | ||||||
| chr3:17057008
|
G | C | 169 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(166): Show | 171 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.3095-10948G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17057008 | ||||||
| chr3:17057269
|
C | G | 30 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(27): Show | 30 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.3095-10687C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17057269 | ||||||
| chr3:17057398
|
T | C | 2 | a0001c0002t0001g0052a0001c0002t0001g0107 | 2 | NA18986.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.3095-10558T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17057398 | ||||||
| chr3:17057428
|
C | T | 1 | a0001c0002t0001g0007 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3095-10528C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17057428 | ||||||
| chr3:17057567
|
T | C | 1 | a0001c0001t0006g0222 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3095-10389T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17057567 | ||||||
| chr3:17057614
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.3095-10342G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17057614 | ||||||
| chr3:17057817
|
T | C | 169 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(166): Show | 171 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.3095-10139T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17057817 | ||||||
| chr3:17057870
|
C | T | 1 | a0001c0001t0001g0246 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.3095-10086C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17057870 | ||||||
| chr3:17057894
|
G | T | 2 | a0002c0009t0001g0154a0002c0009t0001g0155 | 2 | HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3095-10062G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17057894 | ||||||
| chr3:17057982
|
A | G | 2 | a0002c0009t0001g0154a0002c0009t0001g0155 | 2 | HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3095-9974A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17057982 | ||||||
| chr3:17058576
|
C | T | 19 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(16): Show | 19 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.3095-9380C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17058576 | ||||||
| chr3:17058741
|
T | A | 1 | a0001c0001t0006g0222 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3095-9215T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17058741 | ||||||
| chr3:17058755
|
A | C | 1 | a0001c0001t0001g0109 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.3095-9201A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17058755 | ||||||
| chr3:17058996
|
G | A | 71 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(68): Show | 71 | HG00408.hp1 HG01081.hp2 HG01123.hp2 others(68): Show |
intron_variant | MODIFIER | c.3095-8960G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17058996 | ||||||
| chr3:17059107
|
G | A | 2 | a0001c0001t0001g0197a0001c0001t0006g0222 | 2 | HG02258.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.3095-8849G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17059107 | ||||||
| chr3:17059172
|
A | G | 1 | a0001c0003t0001g0211 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3095-8784A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17059172 | ||||||
| chr3:17059378
|
CA | C | 17 | a0001c0001t0001g0017a0001c0001t0001g0243a0001c0001t0001g0244others(14): Show | 17 | HG01123.hp2 HG01243.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.3095-8561delA | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17059378 | |||||
| chr3:17059378
|
CAA | C | 151 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(148): Show | 153 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.3095-8562_3095-856 others(6): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17059378 | |||||
| chr3:17059442
|
G | A | 100 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(97): Show | 102 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.3095-8514G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17059442 | ||||||
| chr3:17059450
|
G | GTGTATAT others(11): Show |
1 | a0001c0002t0001g0011 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3095-8495_3095-849 others(22): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17059450 | |||||
| chr3:17059450
|
G | GTGTGTAT others(13): Show |
166 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(163): Show | 168 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.3095-8503_3095-850 others(24): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17059450 | |||||
| chr3:17059450
|
G | GTGTGTAT others(15): Show |
1 | a0001c0001t0001g0053 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3095-8503_3095-850 others(26): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17059450 | |||||
| chr3:17059588
|
A | G | 8 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103others(5): Show | 8 | HG02818.hp1 HG02895.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.3095-8368A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17059588 | ||||||
| chr3:17059739
|
G | A | 4 | a0001c0003t0004g0001a0001c0003t0004g0128a0001c0003t0004g0152others(1): Show | 5 | HG02486.hp1 HG03139.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.3095-8217G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17059739 | ||||||
| chr3:17059799
|
T | G | 1 | a0001c0001t0001g0203 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3095-8157T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17059799 | ||||||
| chr3:17059831
|
A | G | 4 | a0001c0005t0001g0019a0001c0005t0001g0063a0001c0005t0001g0179others(1): Show | 4 | HG01515.hp2 HG03491.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.3095-8125A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17059831 | ||||||
| chr3:17059980
|
G | A | 6 | a0001c0002t0001g0125a0001c0002t0001g0126a0001c0002t0001g0205others(3): Show | 6 | HG02559.hp2 HG02723.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.3095-7976G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17059980 | ||||||
| chr3:17060243
|
C | T | 3 | a0001c0002t0001g0206a0001c0002t0001g0207a0001c0002t0001g0208 | 3 | HG02559.hp2 HG03139.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3095-7713C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17060243 | ||||||
| chr3:17060312
|
C | A | 18 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(15): Show | 18 | HG01433.hp2 HG01515.hp2 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.3095-7644C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17060312 | ||||||
| chr3:17060524
|
C | CA | 3 | a0001c0002t0001g0120a0001c0002t0001g0121a0001c0002t0001g0122 | 3 | HG02486.hp2 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3095-7431dupA | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17060524 | |||||
| chr3:17060676
|
G | A | 22 | a0001c0003t0001g0235a0001c0003t0003g0209a0001c0003t0003g0215others(19): Show | 23 | HG00280.hp2 HG00741.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.3095-7280G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17060676 | ||||||
| chr3:17060926
|
A | AAAAATTT others(19): Show |
1 | a0001c0001t0001g0017 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.3095-7019_3095-701 others(30): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17060926 | |||||
| chr3:17061277
|
C | A | 18 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(15): Show | 18 | HG01433.hp2 HG01515.hp2 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.3095-6679C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17061277 | ||||||
| chr3:17061543
|
TTCA | T | 6 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(3): Show | 6 | HG02896.hp2 HG03098.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.3095-6412_3095-641 others(7): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17061543 | ||||||
| chr3:17061608
|
T | C | 2 | a0001c0001t0001g0221a0001c0001t0001g0225 | 2 | HG01081.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.3095-6348T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17061608 | ||||||
| chr3:17061731
|
A | AT | 3 | a0001c0011t0001g0004a0001c0012t0001g0005a0001c0013t0001g0198 | 3 | HG02055.hp1 HG02109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.3095-6224dupT | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17061731 | |||||
| chr3:17061988
|
C | G | 1 | a0001c0002t0001g0007 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3095-5968C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17061988 | ||||||
| chr3:17062511
|
T | C | 1 | a0001c0001t0001g0017 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.3095-5445T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17062511 | ||||||
| chr3:17062512
|
C | T | 1 | a0001c0001t0001g0017 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.3095-5444C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17062512 | ||||||
| chr3:17062513
|
T | C | 1 | a0001c0001t0001g0017 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.3095-5443T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17062513 | ||||||
| chr3:17062538
|
G | A | 1 | a0001c0002t0001g0062 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.3095-5418G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17062538 | ||||||
| chr3:17062661
|
T | G | 1 | a0001c0001t0002g0204 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3095-5295T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17062661 | ||||||
| chr3:17062720
|
T | G | 7 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(4): Show | 7 | HG02896.hp2 HG03098.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.3095-5236T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17062720 | ||||||
| chr3:17062994
|
A | T | 1 | a0001c0001t0001g0017 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.3095-4962A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17062994 | ||||||
| chr3:17063025
|
C | A | 9 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(6): Show | 9 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.3095-4931C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17063025 | ||||||
| chr3:17063103
|
A | T | 1 | a0001c0017t0001g0050 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.3095-4853A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17063103 | ||||||
| chr3:17063217
|
T | TCTTCCTC others(1): Show |
5 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0001g0245others(2): Show | 5 | HG01123.hp2 HG03017.hp1 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.3095-4733_3095-473 others(12): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063217 | |||||
| chr3:17063224
|
T | C | 76 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(73): Show | 76 | HG00408.hp1 HG01081.hp2 HG01099.hp1 others(73): Show |
intron_variant | MODIFIER | c.3095-4732T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17063224 | ||||||
| chr3:17063232
|
C | CCCTGCCT others(553): Show |
1 | a0001c0002t0001g0066 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3095-4721_3095-472 others(564): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063232 | |||||
| chr3:17063244
|
G | C | 1 | a0001c0002t0001g0066 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3095-4712G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17063244 | ||||||
| chr3:17063248
|
T | C | 1 | a0001c0002t0001g0066 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3095-4708T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17063248 | ||||||
| chr3:17063252
|
C | CCCTCCCT others(133): Show |
1 | a0001c0003t0001g0193 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.3095-4701_3095-470 others(144): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063252 | |||||
| chr3:17063252
|
C | CCCTCCCT others(117): Show |
1 | a0001c0003t0001g0191 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.3095-4701_3095-470 others(128): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063252 | |||||
| chr3:17063252
|
C | CCCTCCCT others(133): Show |
12 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(9): Show | 12 | HG01433.hp2 HG01943.hp1 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.3095-4701_3095-470 others(144): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063252 | |||||
| chr3:17063252
|
C | CCCTCCCT others(129): Show |
4 | a0001c0005t0001g0019a0001c0005t0001g0063a0001c0005t0001g0179others(1): Show | 4 | HG01515.hp2 HG03491.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.3095-4701_3095-470 others(140): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063252 | |||||
| chr3:17063252
|
C | CCCTCCCT others(241): Show |
2 | a0001c0002t0001g0058a0001c0002t0001g0158 | 2 | HG03834.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.3095-4701_3095-470 others(252): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063252 | |||||
| chr3:17063252
|
C | CCCTCCCT others(229): Show |
1 | a0001c0002t0001g0085 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3095-4701_3095-470 others(240): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063252 | |||||
| chr3:17063252
|
C | CCCTCCCT others(177): Show |
9 | a0001c0002t0001g0022a0001c0002t0001g0023a0001c0002t0001g0055others(6): Show | 9 | HG02027.hp2 NA18942.hp2 NA18955.hp2 others(6): Show |
intron_variant | MODIFIER | c.3095-4701_3095-470 others(188): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063252 | |||||
| chr3:17063252
|
C | CCCTCCCT others(241): Show |
3 | a0001c0002t0001g0054a0001c0002t0001g0112a0001c0003t0001g0184 | 3 | HG00280.hp1 HG03710.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.3095-4701_3095-470 others(252): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063252 | |||||
| chr3:17063252
|
C | CCCTCCCT others(237): Show |
8 | a0001c0002t0001g0020a0001c0002t0001g0027a0001c0002t0001g0028others(5): Show | 8 | HG01074.hp2 HG01106.hp1 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.3095-4701_3095-470 others(248): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063252 | |||||
| chr3:17063252
|
C | CCCTCCCT others(229): Show |
2 | a0001c0002t0001g0045a0001c0002t0001g0060 | 2 | HG04115.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.3095-4701_3095-470 others(240): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063252 | |||||
| chr3:17063252
|
C | CCCTCCCT others(225): Show |
7 | a0001c0001t0001g0139a0001c0002t0001g0021a0001c0002t0001g0032others(4): Show | 7 | HG02135.hp2 HG02257.hp2 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.3095-4701_3095-470 others(236): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063252 | |||||
| chr3:17063252
|
C | CCCTCCCT others(221): Show |
3 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0069 | 3 | HG01255.hp2 HG01346.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.3095-4701_3095-470 others(232): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063252 | |||||
| chr3:17063252
|
C | CCCTCCCT others(213): Show |
1 | a0001c0002t0001g0006 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.3095-4701_3095-470 others(224): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063252 | |||||
| chr3:17063252
|
C | CCCTCCCT others(209): Show |
1 | a0001c0002t0001g0062 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.3095-4701_3095-470 others(220): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063252 | |||||
| chr3:17063252
|
C | CCCTCCCT others(141): Show |
6 | a0001c0002t0001g0125a0001c0002t0001g0126a0001c0002t0001g0205others(3): Show | 6 | HG02559.hp2 HG02723.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.3095-4701_3095-470 others(152): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063252 | |||||
| chr3:17063252
|
C | CCCTCCCT others(137): Show |
5 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(2): Show | 5 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.3095-4701_3095-470 others(148): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063252 | |||||
| chr3:17063252
|
C | CCCTCCCT others(281): Show |
2 | a0002c0009t0001g0154a0002c0009t0001g0155 | 2 | HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3095-4701_3095-470 others(292): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063252 | |||||
| chr3:17063252
|
C | CCCTCCCT others(257): Show |
1 | a0001c0002t0001g0068 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3095-4701_3095-470 others(268): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063252 | |||||
| chr3:17063252
|
C | CCCTCCCT others(241): Show |
2 | a0001c0002t0001g0091a0001c0002t0001g0092 | 2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.3095-4701_3095-470 others(252): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063252 | |||||
| chr3:17063252
|
C | CCCTCCCT others(281): Show |
1 | a0001c0002t0003g0064 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.3095-4701_3095-470 others(292): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063252 | |||||
| chr3:17063252
|
C | CCCTCCCT others(265): Show |
1 | a0001c0002t0003g0065 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.3095-4701_3095-470 others(276): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063252 | |||||
| chr3:17063252
|
C | CCCTCCCT others(273): Show |
1 | a0001c0004t0001g0002 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.3095-4701_3095-470 others(284): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063252 | |||||
| chr3:17063252
|
C | CCCTCCCT others(281): Show |
41 | a0001c0002t0001g0007a0001c0002t0001g0024a0001c0002t0001g0046others(38): Show | 41 | HG00099.hp1 HG00323.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.3095-4701_3095-470 others(292): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063252 | |||||
| chr3:17063252
|
C | CCCTCCCT others(281): Show |
3 | a0001c0002t0001g0031a0001c0002t0001g0111a0001c0002t0001g0115 | 3 | HG02132.hp2 HG02165.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.3095-4701_3095-470 others(292): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063252 | |||||
| chr3:17063252
|
C | CCCTCCCT others(341): Show |
1 | a0001c0002t0001g0223 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3095-4701_3095-470 others(352): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063252 | |||||
| chr3:17063252
|
C | CCCTCCCT others(273): Show |
1 | a0001c0002t0001g0212 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.3095-4701_3095-470 others(284): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063252 | |||||
| chr3:17063252
|
C | CCCTCCCT others(245): Show |
2 | a0001c0002t0001g0113a0001c0002t0001g0114 | 2 | HG00408.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.3095-4701_3095-470 others(256): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063252 | |||||
| chr3:17063252
|
C | CCCTCCCT others(133): Show |
4 | a0001c0003t0004g0001a0001c0003t0004g0128a0001c0003t0004g0152others(1): Show | 5 | HG02486.hp1 HG03139.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.3095-4701_3095-470 others(144): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063252 | |||||
| chr3:17063252
|
C | CCCTCCCT others(533): Show |
1 | a0001c0003t0001g0211 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3095-4701_3095-470 others(544): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063252 | |||||
| chr3:17063252
|
C | CCCTCCCT others(281): Show |
1 | a0001c0004t0001g0176 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3095-4701_3095-470 others(292): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063252 | |||||
| chr3:17063252
|
C | CCCTCCCT others(277): Show |
2 | a0001c0004t0002g0173a0001c0008t0001g0123 | 2 | HG02074.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.3095-4701_3095-470 others(288): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063252 | |||||
| chr3:17063252
|
C | CCCTCCCT others(297): Show |
1 | a0001c0016t0001g0093 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3095-4701_3095-470 others(308): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063252 | |||||
| chr3:17063252
|
C | CCCTTCCT others(457): Show |
1 | a0001c0002t0001g0149 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3095-4693_3095-469 others(468): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063252 | |||||
| chr3:17063252
|
C | CCCTTCCT others(333): Show |
4 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(1): Show | 4 | HG02896.hp2 HG03098.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.3095-4693_3095-469 others(344): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063252 | |||||
| chr3:17063252
|
C | G | 1 | a0001c0002t0001g0066 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3095-4704C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17063252 | ||||||
| chr3:17063256
|
T | C | 7 | a0001c0003t0001g0235a0001c0003t0003g0209a0001c0003t0003g0215others(4): Show | 7 | HG00280.hp2 HG00741.hp2 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.3095-4700T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17063256 | ||||||
| chr3:17063256
|
T | TCCTCCCT others(715): Show |
1 | a0001c0001t0001g0101 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.3095-4693_3095-469 others(726): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(1565): Show |
3 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202 | 3 | HG02976.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3095-4693_3095-469 others(1576): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(529): Show |
1 | a0001c0013t0001g0198 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3095-4693_3095-469 others(540): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(481): Show |
1 | a0001c0011t0001g0004 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3095-4693_3095-469 others(492): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(777): Show |
3 | a0000c0007t0002g0147a0000c0007t0002g0213a0000c0019t0002g0148 | 3 | HG01891.hp1 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3095-4693_3095-469 others(788): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(773): Show |
1 | a0000c0007t0002g0146 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3095-4693_3095-469 others(784): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(813): Show |
1 | a0001c0001t0002g0151 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3095-4693_3095-469 others(824): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(813): Show |
1 | a0001c0001t0002g0129 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3095-4693_3095-469 others(824): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(664): Show |
1 | a0001c0014t0001g0104 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3095-4693_3095-469 others(675): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(653): Show |
1 | a0001c0001t0002g0135 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.3095-4693_3095-469 others(664): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(777): Show |
3 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0002g0142 | 3 | HG01123.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.3095-4693_3095-469 others(788): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(778): Show |
1 | a0001c0001t0002g0159 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3095-4693_3095-469 others(789): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(777): Show |
8 | a0001c0001t0002g0136a0001c0001t0002g0137a0001c0001t0002g0138others(5): Show | 8 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.3095-4693_3095-469 others(788): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(773): Show |
1 | a0001c0001t0001g0150 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3095-4693_3095-469 others(784): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(769): Show |
1 | a0001c0001t0002g0127 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.3095-4693_3095-469 others(780): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(777): Show |
1 | a0001c0001t0002g0130 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3095-4693_3095-469 others(788): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(681): Show |
1 | a0001c0001t0001g0197 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3095-4693_3095-469 others(692): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(769): Show |
3 | a0001c0001t0002g0131a0001c0001t0002g0133a0001c0001t0002g0134 | 3 | HG02109.hp2 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.3095-4693_3095-469 others(780): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(765): Show |
1 | a0001c0001t0002g0132 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3095-4693_3095-469 others(776): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(741): Show |
1 | a0001c0001t0001g0110 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3095-4693_3095-469 others(752): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(717): Show |
1 | a0001c0001t0001g0102 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.3095-4693_3095-469 others(728): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(721): Show |
1 | a0001c0001t0001g0227 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3095-4693_3095-469 others(732): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(741): Show |
1 | a0001c0001t0001g0226 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3095-4693_3095-469 others(752): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(741): Show |
5 | a0001c0001t0001g0195a0001c0001t0001g0229a0001c0001t0001g0230others(2): Show | 5 | HG01943.hp2 HG03927.hp1 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.3095-4693_3095-469 others(752): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(737): Show |
1 | a0001c0001t0001g0239 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3095-4693_3095-469 others(748): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(737): Show |
1 | a0001c0001t0001g0224 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3095-4693_3095-469 others(748): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(737): Show |
1 | a0001c0004t0001g0169 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3095-4693_3095-469 others(748): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(737): Show |
1 | a0001c0006t0001g0170 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.3095-4693_3095-469 others(748): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(743): Show |
1 | a0001c0006t0001g0174 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.3095-4693_3095-469 others(754): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(753): Show |
1 | a0001c0001t0001g0086 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.3095-4693_3095-469 others(764): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(753): Show |
1 | a0001c0001t0001g0036 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.3095-4693_3095-469 others(764): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(745): Show |
1 | a0001c0001t0001g0236 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3095-4693_3095-469 others(756): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(745): Show |
1 | a0001c0001t0001g0053 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3095-4693_3095-469 others(756): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(749): Show |
1 | a0001c0001t0001g0037 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.3095-4693_3095-469 others(760): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(557): Show |
1 | a0001c0001t0001g0225 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3095-4693_3095-469 others(568): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(741): Show |
1 | a0001c0001t0001g0103 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3095-4693_3095-469 others(752): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(749): Show |
1 | a0001c0001t0001g0014 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3095-4693_3095-469 others(760): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(761): Show |
1 | a0001c0001t0001g0040 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.3095-4693_3095-469 others(772): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(733): Show |
1 | a0001c0001t0001g0043 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.3095-4693_3095-469 others(744): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(749): Show |
16 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0039others(13): Show | 16 | HG01099.hp1 HG01243.hp2 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.3095-4693_3095-469 others(760): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(745): Show |
2 | a0001c0001t0001g0228a0001c0003t0001g0116 | 2 | NA18956.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.3095-4693_3095-469 others(756): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(737): Show |
2 | a0001c0001t0001g0015a0001c0001t0001g0016 | 2 | NA18949.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.3095-4693_3095-469 others(748): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(745): Show |
1 | a0001c0001t0001g0109 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.3095-4693_3095-469 others(756): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(776): Show |
1 | a0001c0001t0001g0157 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.3095-4693_3095-469 others(787): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(745): Show |
2 | a0001c0001t0001g0042a0001c0001t0001g0118 | 2 | HG01346.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.3095-4693_3095-469 others(756): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(545): Show |
1 | a0001c0001t0001g0221 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3095-4693_3095-469 others(556): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(745): Show |
2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG02027.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.3095-4693_3095-469 others(756): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(733): Show |
1 | a0001c0001t0001g0119 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.3095-4693_3095-469 others(744): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(797): Show |
1 | a0001c0001t0001g0218 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3095-4693_3095-469 others(808): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(749): Show |
3 | a0001c0001t0001g0217a0001c0001t0001g0219a0001c0001t0001g0220 | 3 | HG02895.hp2 HG03041.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.3095-4693_3095-469 others(760): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(729): Show |
1 | a0001c0006t0001g0160 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.3095-4693_3095-469 others(740): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(917): Show |
1 | a0001c0001t0001g0117 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.3095-4693_3095-469 others(928): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(734): Show |
1 | a0001c0001t0001g0088 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3095-4693_3095-469 others(745): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(1229): Show |
1 | a0001c0001t0001g0203 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3095-4693_3095-469 others(1240): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(705): Show |
1 | a0001c0001t0006g0222 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3095-4693_3095-469 others(716): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(728): Show |
1 | a0001c0001t0001g0017 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.3095-4693_3095-469 others(739): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(745): Show |
1 | a0001c0001t0001g0034 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.3095-4693_3095-469 others(756): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(965): Show |
1 | a0001c0001t0001g0243 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3095-4693_3095-469 others(976): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(969): Show |
1 | a0001c0001t0001g0247 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3095-4693_3095-469 others(980): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(969): Show |
2 | a0001c0001t0001g0244a0001c0001t0001g0245 | 2 | HG03017.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.3095-4693_3095-469 others(980): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063256
|
T | TCCTCCCT others(965): Show |
1 | a0001c0001t0001g0246 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.3095-4693_3095-469 others(976): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063256 | |||||
| chr3:17063260
|
C | CCCTCCCT others(145): Show |
1 | a0001c0003t0003g0216 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.3095-4693_3095-469 others(156): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063260 | |||||
| chr3:17063260
|
C | CCCTCCCT others(141): Show |
5 | a0001c0003t0001g0235a0001c0003t0003g0209a0001c0003t0003g0215others(2): Show | 5 | HG00280.hp2 HG00741.hp2 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.3095-4693_3095-469 others(152): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063260 | |||||
| chr3:17063260
|
C | CCCTCCCT others(125): Show |
1 | a0001c0020t0003g0178 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3095-4693_3095-469 others(136): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063260 | |||||
| chr3:17063264
|
T | C | 102 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(99): Show | 102 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.3095-4692T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17063264 | ||||||
| chr3:17063264
|
T | TCCTCCCT others(517): Show |
1 | a0001c0012t0001g0005 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3095-4685_3095-468 others(528): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063264 | |||||
| chr3:17063282
|
A | C | 207 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(204): Show | 209 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.3095-4674A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17063282 | ||||||
| chr3:17063315
|
C | G | 5 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(2): Show | 5 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.3095-4641C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17063315 | ||||||
| chr3:17063315
|
CT | C | 18 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(15): Show | 18 | HG01433.hp2 HG01515.hp2 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.3095-4632delT | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17063315 | |||||
| chr3:17063370
|
T | C | 1 | a0001c0002t0001g0011 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3095-4586T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17063370 | ||||||
| chr3:17063400
|
T | G | 4 | a0001c0005t0001g0019a0001c0005t0001g0063a0001c0005t0001g0179others(1): Show | 4 | HG01515.hp2 HG03491.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.3095-4556T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17063400 | ||||||
| chr3:17063894
|
C | T | 2 | a0001c0001t0001g0118a0001c0001t0001g0228 | 2 | NA18956.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.3095-4062C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17063894 | ||||||
| chr3:17063914
|
G | T | 3 | a0001c0001t0001g0035a0001c0001t0001g0039a0001c0001t0001g0109 | 3 | HG02074.hp2 NA18944.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.3095-4042G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17063914 | ||||||
| chr3:17063920
|
C | T | 1 | a0001c0002t0001g0149 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3095-4036C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17063920 | ||||||
| chr3:17064024
|
G | A | 1 | a0001c0014t0001g0104 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3095-3932G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17064024 | ||||||
| chr3:17064143
|
A | G | 75 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(72): Show | 75 | HG00408.hp1 HG01081.hp2 HG01099.hp1 others(72): Show |
intron_variant | MODIFIER | c.3095-3813A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17064143 | ||||||
| chr3:17064176
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3095-3780C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17064176 | ||||||
| chr3:17064535
|
C | T | 143 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(140): Show | 144 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.3095-3421C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17064535 | ||||||
| chr3:17064621
|
A | C | 5 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(2): Show | 5 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.3095-3335A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17064621 | ||||||
| chr3:17064928
|
C | CA | 53 | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0017others(50): Show | 53 | HG01099.hp1 HG01106.hp2 HG01243.hp2 others(50): Show |
intron_variant | MODIFIER | c.3095-3009dupA | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17064928 | |||||
| chr3:17064928
|
C | CAA | 5 | a0001c0002t0001g0079a0001c0003t0001g0188a0001c0003t0001g0193others(2): Show | 5 | HG02055.hp1 HG02273.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.3095-3010_3095-300 others(6): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 17064928 | |||||
| chr3:17065080
|
A | G | 1 | a0001c0001t0001g0090 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3095-2876A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17065080 | ||||||
| chr3:17065119
|
T | G | 2 | a0001c0001t0001g0197a0001c0001t0006g0222 | 2 | HG02258.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.3095-2837T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17065119 | ||||||
| chr3:17065316
|
T | A | 1 | a0001c0006t0001g0174 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.3095-2640T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17065316 | ||||||
| chr3:17065372
|
T | A | 1 | a0001c0006t0001g0174 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.3095-2584T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17065372 | ||||||
| chr3:17065750
|
T | C | 2 | a0001c0001t0001g0197a0001c0001t0006g0222 | 2 | HG02258.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.3095-2206T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17065750 | ||||||
| chr3:17066100
|
G | A | 2 | a0001c0001t0001g0197a0001c0001t0006g0222 | 2 | HG02258.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.3095-1856G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17066100 | ||||||
| chr3:17066128
|
G | A | 1 | a0001c0001t0002g0137 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3095-1828G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17066128 | ||||||
| chr3:17066319
|
G | A | 6 | a0001c0002t0001g0125a0001c0002t0001g0126a0001c0002t0001g0205others(3): Show | 6 | HG02559.hp2 HG02723.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.3095-1637G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17066319 | ||||||
| chr3:17066394
|
G | A | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3095-1562G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17066394 | ||||||
| chr3:17066454
|
G | A | 1 | a0001c0002t0001g0046 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.3095-1502G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17066454 | ||||||
| chr3:17066594
|
T | G | 1 | a0001c0003t0001g0187 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3095-1362T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17066594 | ||||||
| chr3:17066690
|
G | A | 1 | a0001c0002t0001g0085 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3095-1266G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17066690 | ||||||
| chr3:17067087
|
G | A | 18 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(15): Show | 18 | HG01433.hp2 HG01515.hp2 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.3095-869G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17067087 | ||||||
| chr3:17067159
|
T | A | 1 | a0001c0002t0001g0023 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.3095-797T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17067159 | ||||||
| chr3:17067213
|
A | G | 1 | a0001c0001t0001g0197 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3095-743A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17067213 | ||||||
| chr3:17067374
|
G | A | 1 | a0001c0001t0001g0119 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.3095-582G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17067374 | ||||||
| chr3:17067594
|
C | T | 6 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(3): Show | 6 | HG02896.hp2 HG03098.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.3095-362C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17067594 | ||||||
| chr3:17067704
|
A | G | 4 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0219others(1): Show | 4 | HG02895.hp2 HG03041.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.3095-252A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17067704 | ||||||
| chr3:17067706
|
G | A | 1 | a0001c0003t0001g0191 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.3095-250G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17067706 | ||||||
| chr3:17067847
|
C | T | 66 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(63): Show | 66 | HG00408.hp1 HG01081.hp2 HG01099.hp1 others(63): Show |
intron_variant | MODIFIER | c.3095-109C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 4/5 | chr3 | 17067847 | ||||||
| chr3:17068223
|
G | A | 1 | a0001c0001t0002g0135 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.3204+158G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17068223 | ||||||
| chr3:17068895
|
G | A | 1 | a0001c0012t0001g0005 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3204+830G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17068895 | ||||||
| chr3:17069014
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.3204+949G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17069014 | ||||||
| chr3:17069033
|
C | T | 4 | a0001c0005t0001g0019a0001c0005t0001g0063a0001c0005t0001g0179others(1): Show | 4 | HG01515.hp2 HG03491.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.3204+968C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17069033 | ||||||
| chr3:17069248
|
G | T | 5 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0001g0245others(2): Show | 5 | HG01123.hp2 HG03017.hp1 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.3204+1183G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17069248 | ||||||
| chr3:17069311
|
A | C | 1 | a0001c0003t0001g0211 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3204+1246A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17069311 | ||||||
| chr3:17069382
|
G | A | 149 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(146): Show | 150 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.3204+1317G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17069382 | ||||||
| chr3:17069572
|
G | T | 9 | a0001c0003t0001g0044a0001c0003t0001g0180a0001c0003t0001g0187others(6): Show | 9 | HG01433.hp2 HG01928.hp2 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.3204+1507G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17069572 | ||||||
| chr3:17069840
|
T | C | 1 | a0001c0003t0001g0235 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.3204+1775T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17069840 | ||||||
| chr3:17070132
|
G | C | 1 | a0001c0003t0001g0184 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3204+2067G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17070132 | ||||||
| chr3:17070483
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3204+2418G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17070483 | ||||||
| chr3:17070671
|
C | T | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3204+2606C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17070671 | ||||||
| chr3:17071410
|
T | TATTA | 3 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202 | 3 | HG02976.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3204+3347_3204+335 others(8): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 17071410 | |||||
| chr3:17071660
|
A | G | 6 | a0001c0002t0001g0125a0001c0002t0001g0126a0001c0002t0001g0205others(3): Show | 6 | HG02559.hp2 HG02723.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.3204+3595A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17071660 | ||||||
| chr3:17071823
|
T | C | 11 | a0001c0002t0001g0007a0001c0002t0001g0199a0001c0002t0001g0210others(8): Show | 11 | HG00280.hp2 HG00741.hp2 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.3204+3758T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17071823 | ||||||
| chr3:17072158
|
A | T | 2 | a0001c0002t0001g0022a0001c0002t0001g0023 | 2 | NA18955.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.3204+4093A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17072158 | ||||||
| chr3:17072390
|
C | T | 3 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202 | 3 | HG02976.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3204+4325C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17072390 | ||||||
| chr3:17072500
|
C | G | 1 | a0001c0013t0001g0198 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3204+4435C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17072500 | ||||||
| chr3:17072514
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.3204+4449C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17072514 | ||||||
| chr3:17072528
|
G | T | 1 | a0001c0003t0001g0211 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3204+4463G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17072528 | ||||||
| chr3:17072544
|
T | C | 127 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(124): Show | 128 | HG00280.hp2 HG00408.hp1 HG00741.hp2 others(125): Show |
intron_variant | MODIFIER | c.3204+4479T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17072544 | ||||||
| chr3:17072548
|
A | C | 22 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(19): Show | 22 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.3204+4483A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17072548 | ||||||
| chr3:17072561
|
T | A | 64 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(61): Show | 64 | HG00408.hp1 HG01081.hp2 HG01123.hp2 others(61): Show |
intron_variant | MODIFIER | c.3204+4496T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17072561 | ||||||
| chr3:17072572
|
G | A | 3 | a0001c0002t0001g0007a0001c0002t0001g0199a0001c0002t0001g0210 | 3 | HG02257.hp1 HG02280.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.3204+4507G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17072572 | ||||||
| chr3:17072583
|
C | T | 2 | a0001c0001t0001g0244a0001c0001t0001g0245 | 2 | HG03017.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.3204+4518C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17072583 | ||||||
| chr3:17072670
|
G | GA | 21 | a0001c0001t0001g0053a0001c0001t0001g0139a0001c0001t0001g0200others(18): Show | 21 | HG01175.hp2 HG02257.hp1 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.3204+4622dupA | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 17072670 | |||||
| chr3:17072670
|
GA | G | 24 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(21): Show | 24 | HG00099.hp2 HG01099.hp2 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.3204+4622delA | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 17072670 | |||||
| chr3:17072961
|
A | G | 2 | a0001c0001t0001g0197a0001c0001t0006g0222 | 2 | HG02258.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.3204+4896A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17072961 | ||||||
| chr3:17072979
|
G | A | 1 | a0001c0001t0001g0237 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3204+4914G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17072979 | ||||||
| chr3:17073123
|
G | A | 1 | a0001c0002t0001g0212 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.3204+5058G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17073123 | ||||||
| chr3:17073211
|
G | A | 1 | a0001c0002t0001g0048 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3204+5146G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17073211 | ||||||
| chr3:17073217
|
G | T | 5 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(2): Show | 5 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.3204+5152G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17073217 | ||||||
| chr3:17073318
|
T | G | 1 | a0001c0005t0001g0019 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.3204+5253T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17073318 | ||||||
| chr3:17073416
|
G | T | 9 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(6): Show | 10 | HG01934.hp1 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3204+5351G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17073416 | ||||||
| chr3:17073428
|
C | A | 64 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(61): Show | 64 | HG00408.hp1 HG01099.hp1 HG01123.hp2 others(61): Show |
intron_variant | MODIFIER | c.3204+5363C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17073428 | ||||||
| chr3:17073589
|
G | A | 7 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(4): Show | 7 | HG02257.hp1 HG02280.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.3204+5524G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17073589 | ||||||
| chr3:17073630
|
C | G | 23 | a0001c0002t0001g0125a0001c0002t0001g0126a0001c0002t0001g0205others(20): Show | 24 | HG00280.hp2 HG00741.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.3204+5565C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17073630 | ||||||
| chr3:17073689
|
T | G | 1 | a0001c0006t0001g0160 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.3204+5624T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17073689 | ||||||
| chr3:17073697
|
C | A | 5 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(2): Show | 5 | HG02896.hp2 HG03098.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.3204+5632C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17073697 | ||||||
| chr3:17073746
|
T | C | 1 | a0001c0001t0001g0041 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.3204+5681T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17073746 | ||||||
| chr3:17073829
|
A | C | 1 | a0001c0002t0001g0047 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3204+5764A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17073829 | ||||||
| chr3:17073977
|
A | G | 2 | a0000c0007t0002g0147a0000c0007t0002g0213 | 2 | HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3204+5912A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17073977 | ||||||
| chr3:17074085
|
C | T | 5 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(2): Show | 5 | HG02896.hp2 HG03098.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.3204+6020C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17074085 | ||||||
| chr3:17074428
|
T | A | 3 | a0001c0002t0001g0075a0001c0002t0001g0076a0001c0002t0001g0077 | 3 | HG03209.hp2 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.3204+6363T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17074428 | ||||||
| chr3:17074567
|
T | C | 73 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(70): Show | 73 | HG00408.hp1 HG01081.hp2 HG01099.hp1 others(70): Show |
intron_variant | MODIFIER | c.3204+6502T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17074567 | ||||||
| chr3:17074641
|
T | C | 1 | a0001c0003t0001g0211 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3204+6576T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17074641 | ||||||
| chr3:17074892
|
A | G | 153 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(150): Show | 154 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.3204+6827A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17074892 | ||||||
| chr3:17075026
|
C | A | 3 | a0001c0011t0001g0004a0001c0012t0001g0005a0001c0013t0001g0198 | 3 | HG02055.hp1 HG02109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.3204+6961C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17075026 | ||||||
| chr3:17075096
|
C | A | 1 | a0001c0002t0001g0020 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.3204+7031C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17075096 | ||||||
| chr3:17075353
|
G | A | 1 | a0001c0011t0001g0004 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3204+7288G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17075353 | ||||||
| chr3:17075410
|
T | C | 13 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(10): Show | 13 | HG02257.hp1 HG02280.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.3204+7345T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17075410 | ||||||
| chr3:17075518
|
G | A | 6 | a0001c0002t0001g0125a0001c0002t0001g0126a0001c0002t0001g0205others(3): Show | 6 | HG02559.hp2 HG02723.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.3204+7453G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17075518 | ||||||
| chr3:17075530
|
C | CAAACCTT others(54): Show |
1 | a0001c0008t0001g0123 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3204+7469_3204+752 others(65): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 17075530 | |||||
| chr3:17075540
|
A | G | 5 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(2): Show | 5 | HG02896.hp2 HG03098.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.3204+7475A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17075540 | ||||||
| chr3:17075545
|
T | TA | 34 | a0001c0001t0001g0195a0001c0001t0001g0197a0001c0001t0001g0217others(31): Show | 35 | HG00280.hp2 HG00741.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.3204+7499dupA | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 17075545 | |||||
| chr3:17075545
|
T | TAA | 67 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(64): Show | 67 | HG00408.hp1 HG01081.hp2 HG01099.hp1 others(64): Show |
intron_variant | MODIFIER | c.3204+7498_3204+749 others(6): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 17075545 | |||||
| chr3:17075545
|
T | TAAAAAAA others(55): Show |
1 | a0001c0004t0001g0176 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3204+7529_3204+753 others(66): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 17075545 | |||||
| chr3:17075545
|
TAA | T | 17 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(14): Show | 17 | HG01433.hp2 HG01515.hp2 HG01928.hp2 others(14): Show |
intron_variant | MODIFIER | c.3204+7498_3204+749 others(6): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 17075545 | |||||
| chr3:17075569
|
G | A | 26 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(23): Show | 26 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.3204+7504G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17075569 | ||||||
| chr3:17075575
|
G | T | 1 | a0001c0002t0001g0092 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3204+7510G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17075575 | ||||||
| chr3:17075615
|
C | T | 9 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(6): Show | 9 | HG02074.hp2 NA18942.hp1 NA18944.hp2 others(6): Show |
intron_variant | MODIFIER | c.3204+7550C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17075615 | ||||||
| chr3:17075638
|
C | T | 1 | a0001c0001t0001g0237 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3204+7573C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17075638 | ||||||
| chr3:17075859
|
C | G | 1 | a0001c0002t0001g0122 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.3204+7794C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17075859 | ||||||
| chr3:17075889
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3204+7824T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17075889 | ||||||
| chr3:17076186
|
A | G | 1 | a0001c0001t0001g0150 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3204+8121A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17076186 | ||||||
| chr3:17076215
|
G | C | 8 | a0001c0003t0001g0116a0001c0003t0001g0235a0001c0003t0003g0209others(5): Show | 8 | HG00280.hp2 HG00741.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.3204+8150G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17076215 | ||||||
| chr3:17076255
|
A | T | 68 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(65): Show | 68 | HG00408.hp1 HG01081.hp2 HG01099.hp1 others(65): Show |
intron_variant | MODIFIER | c.3204+8190A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17076255 | ||||||
| chr3:17076515
|
A | T | 5 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(2): Show | 5 | HG02896.hp2 HG03098.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.3204+8450A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17076515 | ||||||
| chr3:17076642
|
A | G | 6 | a0001c0002t0001g0125a0001c0002t0001g0126a0001c0002t0001g0205others(3): Show | 6 | HG02559.hp2 HG02723.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.3204+8577A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17076642 | ||||||
| chr3:17076676
|
C | T | 8 | a0001c0003t0001g0116a0001c0003t0001g0235a0001c0003t0003g0209others(5): Show | 8 | HG00280.hp2 HG00741.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.3204+8611C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17076676 | ||||||
| chr3:17076695
|
G | A | 1 | a0001c0002t0001g0149 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3204+8630G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17076695 | ||||||
| chr3:17076764
|
A | G | 2 | a0001c0002t0001g0022a0001c0002t0001g0023 | 2 | NA18955.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.3204+8699A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17076764 | ||||||
| chr3:17076922
|
A | C | 66 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(63): Show | 66 | HG00408.hp1 HG01081.hp2 HG01099.hp1 others(63): Show |
intron_variant | MODIFIER | c.3204+8857A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17076922 | ||||||
| chr3:17076946
|
T | G | 1 | a0001c0002t0003g0065 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.3204+8881T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17076946 | ||||||
| chr3:17076997
|
A | G | 1 | a0001c0001t0001g0103 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3204+8932A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17076997 | ||||||
| chr3:17077055
|
C | T | 8 | a0001c0003t0001g0116a0001c0003t0001g0235a0001c0003t0003g0209others(5): Show | 8 | HG00280.hp2 HG00741.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.3204+8990C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17077055 | ||||||
| chr3:17077056
|
G | A | 2 | a0001c0006t0001g0170a0001c0006t0001g0174 | 2 | NA18955.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.3204+8991G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17077056 | ||||||
| chr3:17077133
|
T | C | 2 | a0001c0003t0004g0152a0001c0003t0004g0153 | 2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.3204+9068T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17077133 | ||||||
| chr3:17077167
|
G | A | 15 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(12): Show | 15 | HG01433.hp2 HG01928.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.3204+9102G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17077167 | ||||||
| chr3:17077418
|
T | C | 68 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(65): Show | 68 | HG00408.hp1 HG01081.hp2 HG01099.hp1 others(65): Show |
intron_variant | MODIFIER | c.3204+9353T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17077418 | ||||||
| chr3:17077746
|
C | G | 132 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(129): Show | 133 | HG00280.hp2 HG00408.hp1 HG00741.hp2 others(130): Show |
intron_variant | MODIFIER | c.3204+9681C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17077746 | ||||||
| chr3:17077852
|
G | A | 1 | a0001c0001t0001g0227 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3204+9787G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17077852 | ||||||
| chr3:17077895
|
C | T | 2 | a0001c0001t0001g0197a0001c0001t0006g0222 | 2 | HG02258.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.3204+9830C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17077895 | ||||||
| chr3:17078024
|
C | A | 1 | a0001c0001t0001g0103 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3204+9959C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17078024 | ||||||
| chr3:17078455
|
C | CT | 26 | a0001c0001t0006g0222a0001c0002t0001g0007a0001c0002t0001g0199others(23): Show | 26 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(23): Show |
intron_variant | MODIFIER | c.3204+10401dupT | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 17078455 | |||||
| chr3:17078455
|
CT | C | 67 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(64): Show | 67 | HG00408.hp1 HG01081.hp2 HG01123.hp2 others(64): Show |
intron_variant | MODIFIER | c.3204+10401delT | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 17078455 | |||||
| chr3:17078505
|
G | A | 1 | a0001c0002t0001g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3204+10440G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17078505 | ||||||
| chr3:17078514
|
G | A | 1 | a0001c0002t0001g0048 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3204+10449G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17078514 | ||||||
| chr3:17078635
|
C | A | 3 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202 | 3 | HG02976.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3204+10570C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17078635 | ||||||
| chr3:17078714
|
T | C | 23 | a0001c0002t0001g0125a0001c0002t0001g0126a0001c0002t0001g0205others(20): Show | 24 | HG00280.hp2 HG00741.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.3204+10649T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17078714 | ||||||
| chr3:17078891
|
A | G | 21 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(18): Show | 21 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.3204+10826A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17078891 | ||||||
| chr3:17079064
|
G | A | 21 | a0001c0003t0001g0018a0001c0003t0001g0044a0001c0003t0001g0180others(18): Show | 21 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.3205-10669G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17079064 | ||||||
| chr3:17079105
|
G | A | 1 | a0001c0012t0001g0005 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3205-10628G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17079105 | ||||||
| chr3:17079630
|
C | T | 2 | a0001c0001t0001g0243a0001c0001t0001g0246 | 2 | HG01123.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.3205-10103C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17079630 | ||||||
| chr3:17079637
|
T | G | 4 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(1): Show | 4 | HG01934.hp1 HG02280.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.3205-10096T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17079637 | ||||||
| chr3:17079654
|
G | A | 1 | a0001c0001t0001g0017 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.3205-10079G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17079654 | ||||||
| chr3:17079691
|
G | A | 1 | a0001c0002t0001g0066 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3205-10042G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17079691 | ||||||
| chr3:17079918
|
G | A | 1 | a0001c0002t0001g0223 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3205-9815G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17079918 | ||||||
| chr3:17080075
|
G | A | 2 | a0001c0001t0001g0230a0001c0018t0005g0029 | 2 | HG01978.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.3205-9658G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17080075 | ||||||
| chr3:17080134
|
G | A | 1 | a0001c0002t0001g0055 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.3205-9599G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17080134 | ||||||
| chr3:17080200
|
G | A | 42 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(39): Show | 42 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(39): Show |
intron_variant | MODIFIER | c.3205-9533G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17080200 | ||||||
| chr3:17080271
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.3205-9462C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17080271 | ||||||
| chr3:17080277
|
G | A | 2 | a0001c0002t0001g0007a0001c0002t0001g0199 | 2 | HG02257.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.3205-9456G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17080277 | ||||||
| chr3:17080307
|
T | A | 6 | a0001c0003t0004g0001a0001c0003t0004g0128a0001c0003t0004g0152others(3): Show | 7 | HG02055.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.3205-9426T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17080307 | ||||||
| chr3:17080344
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3205-9389G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17080344 | ||||||
| chr3:17080394
|
A | G | 9 | a0001c0002t0001g0149a0001c0002t0003g0064a0001c0002t0003g0065others(6): Show | 9 | HG00280.hp2 HG00741.hp1 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.3205-9339A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17080394 | ||||||
| chr3:17080414
|
G | A | 2 | a0001c0013t0001g0198a0001c0018t0005g0029 | 2 | HG01978.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.3205-9319G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17080414 | ||||||
| chr3:17080425
|
C | T | 4 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(1): Show | 4 | HG01934.hp1 HG02280.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.3205-9308C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17080425 | ||||||
| chr3:17080439
|
C | T | 29 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(26): Show | 29 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.3205-9294C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17080439 | ||||||
| chr3:17080455
|
C | T | 1 | a0004c0015t0001g0072 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.3205-9278C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17080455 | ||||||
| chr3:17080512
|
G | A | 1 | a0001c0003t0001g0211 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3205-9221G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17080512 | ||||||
| chr3:17080576
|
G | A | 2 | a0001c0011t0001g0004a0001c0012t0001g0005 | 2 | HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.3205-9157G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17080576 | ||||||
| chr3:17080747
|
G | A | 1 | a0001c0003t0001g0211 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3205-8986G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17080747 | ||||||
| chr3:17080841
|
G | T | 1 | a0001c0001t0001g0239 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3205-8892G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17080841 | ||||||
| chr3:17080903
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.3205-8830C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17080903 | ||||||
| chr3:17080919
|
G | C | 1 | a0001c0014t0001g0104 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3205-8814G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17080919 | ||||||
| chr3:17080926
|
G | A | 2 | a0001c0013t0001g0198a0001c0018t0005g0029 | 2 | HG01978.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.3205-8807G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17080926 | ||||||
| chr3:17081261
|
C | G | 9 | a0001c0001t0001g0197a0001c0001t0006g0222a0001c0002t0001g0125others(6): Show | 9 | HG02258.hp2 HG02280.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.3205-8472C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17081261 | ||||||
| chr3:17081401
|
C | T | 5 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(2): Show | 5 | HG02257.hp1 HG02622.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.3205-8332C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17081401 | ||||||
| chr3:17081402
|
G | A | 1 | a0001c0003t0004g0152 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3205-8331G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17081402 | ||||||
| chr3:17081444
|
C | G | 2 | a0001c0011t0001g0004a0001c0012t0001g0005 | 2 | HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.3205-8289C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17081444 | ||||||
| chr3:17081448
|
T | C | 1 | a0001c0003t0001g0211 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3205-8285T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17081448 | ||||||
| chr3:17081465
|
G | A | 1 | a0001c0002t0001g0011 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3205-8268G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17081465 | ||||||
| chr3:17081515
|
C | T | 8 | a0001c0001t0001g0197a0001c0002t0001g0125a0001c0002t0001g0126others(5): Show | 8 | HG02258.hp2 HG02280.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.3205-8218C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17081515 | ||||||
| chr3:17081555
|
C | G | 2 | a0001c0011t0001g0004a0001c0012t0001g0005 | 2 | HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.3205-8178C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17081555 | ||||||
| chr3:17081618
|
C | A | 2 | a0001c0011t0001g0004a0001c0012t0001g0005 | 2 | HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.3205-8115C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17081618 | ||||||
| chr3:17081677
|
G | A | 1 | a0001c0014t0001g0104 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3205-8056G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17081677 | ||||||
| chr3:17081678
|
G | A | 1 | a0001c0002t0001g0011 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3205-8055G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17081678 | ||||||
| chr3:17081681
|
C | G | 9 | a0001c0001t0001g0197a0001c0001t0006g0222a0001c0002t0001g0125others(6): Show | 9 | HG02258.hp2 HG02280.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.3205-8052C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17081681 | ||||||
| chr3:17081732
|
C | G | 2 | a0001c0011t0001g0004a0001c0012t0001g0005 | 2 | HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.3205-8001C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17081732 | ||||||
| chr3:17081830
|
C | G | 2 | a0001c0011t0001g0004a0001c0012t0001g0005 | 2 | HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.3205-7903C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17081830 | ||||||
| chr3:17082139
|
G | GT | 49 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(46): Show | 50 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.3205-7573dupT | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 17082139 | |||||
| chr3:17082139
|
G | GTT | 30 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0197others(27): Show | 30 | HG00280.hp2 HG00741.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.3205-7574_3205-757 others(6): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 17082139 | |||||
| chr3:17082139
|
G | GTTT | 50 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(47): Show | 50 | HG00408.hp1 HG01099.hp1 HG01175.hp2 others(47): Show |
intron_variant | MODIFIER | c.3205-7575_3205-757 others(7): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 17082139 | |||||
| chr3:17082139
|
G | GTTTT | 13 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0034others(10): Show | 13 | HG01256.hp1 HG02027.hp1 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.3205-7576_3205-757 others(8): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 17082139 | |||||
| chr3:17082187
|
C | A | 208 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(205): Show | 210 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.3205-7546C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17082187 | ||||||
| chr3:17082237
|
G | C | 5 | a0001c0001t0001g0203a0001c0003t0001g0003a0001c0003t0001g0030others(2): Show | 5 | HG01934.hp1 HG02280.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.3205-7496G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17082237 | ||||||
| chr3:17082309
|
A | AT | 6 | a0001c0002t0001g0125a0001c0002t0001g0126a0001c0002t0001g0205others(3): Show | 6 | HG02559.hp2 HG02723.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.3205-7412dupT | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 17082309 | |||||
| chr3:17082326
|
T | G | 4 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(1): Show | 4 | HG01243.hp1 HG01891.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.3205-7407T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17082326 | ||||||
| chr3:17082364
|
T | C | 1 | a0001c0001t0002g0159 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3205-7369T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17082364 | ||||||
| chr3:17082406
|
A | C | 2 | a0001c0013t0001g0198a0001c0018t0005g0029 | 2 | HG01978.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.3205-7327A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17082406 | ||||||
| chr3:17082489
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3205-7244T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17082489 | ||||||
| chr3:17082543
|
C | G | 2 | a0001c0011t0001g0004a0001c0012t0001g0005 | 2 | HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.3205-7190C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17082543 | ||||||
| chr3:17082596
|
C | T | 4 | a0001c0001t0001g0139a0001c0002t0001g0032a0001c0002t0001g0085others(1): Show | 4 | HG02257.hp2 HG02683.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.3205-7137C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17082596 | ||||||
| chr3:17082597
|
C | G | 3 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017 | 3 | NA18942.hp1 NA18949.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.3205-7136C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17082597 | ||||||
| chr3:17082754
|
T | C | 2 | a0001c0002t0003g0064a0001c0002t0003g0065 | 2 | HG00741.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.3205-6979T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17082754 | ||||||
| chr3:17082813
|
A | C | 2 | a0001c0002t0001g0022a0001c0002t0001g0023 | 2 | NA18955.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.3205-6920A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17082813 | ||||||
| chr3:17082891
|
C | T | 7 | a0001c0001t0001g0014a0001c0001t0001g0034a0001c0001t0001g0036others(4): Show | 7 | HG01256.hp1 HG02165.hp1 NA18747.hp2 others(4): Show |
intron_variant | MODIFIER | c.3205-6842C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17082891 | ||||||
| chr3:17082892
|
A | G | 152 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(149): Show | 153 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.3205-6841A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17082892 | ||||||
| chr3:17082970
|
A | T | 147 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(144): Show | 148 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.3205-6763A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17082970 | ||||||
| chr3:17083089
|
C | T | 2 | a0001c0011t0001g0004a0001c0012t0001g0005 | 2 | HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.3205-6644C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17083089 | ||||||
| chr3:17083147
|
G | GGAAAAAG others(3): Show |
1 | a0001c0002t0001g0240 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3205-6584_3205-657 others(14): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 17083147 | |||||
| chr3:17083245
|
A | G | 64 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(61): Show | 64 | HG00408.hp1 HG01081.hp2 HG01175.hp2 others(61): Show |
intron_variant | MODIFIER | c.3205-6488A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17083245 | ||||||
| chr3:17083276
|
G | A | 1 | a0001c0003t0001g0211 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3205-6457G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17083276 | ||||||
| chr3:17083297
|
G | A | 2 | a0001c0005t0001g0063a0001c0005t0001g0179 | 2 | HG01515.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.3205-6436G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17083297 | ||||||
| chr3:17083406
|
C | G | 1 | a0001c0001t0001g0036 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.3205-6327C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17083406 | ||||||
| chr3:17083578
|
C | T | 4 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0219others(1): Show | 4 | HG02895.hp2 HG03041.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.3205-6155C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17083578 | ||||||
| chr3:17083663
|
G | T | 6 | a0001c0002t0001g0125a0001c0002t0001g0126a0001c0002t0001g0205others(3): Show | 6 | HG02559.hp2 HG02723.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.3205-6070G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17083663 | ||||||
| chr3:17083673
|
G | A | 5 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(2): Show | 5 | HG02257.hp1 HG02622.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.3205-6060G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17083673 | ||||||
| chr3:17083712
|
C | T | 1 | a0001c0002t0001g0048 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3205-6021C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17083712 | ||||||
| chr3:17084033
|
A | C | 17 | a0001c0002t0001g0115a0001c0003t0001g0018a0001c0003t0001g0180others(14): Show | 17 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.3205-5700A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17084033 | ||||||
| chr3:17084386
|
A | G | 1 | a0001c0001t0002g0159 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3205-5347A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17084386 | ||||||
| chr3:17084728
|
C | A | 1 | a0001c0002t0001g0240 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3205-5005C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17084728 | ||||||
| chr3:17084738
|
A | G | 1 | a0001c0002t0001g0240 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3205-4995A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17084738 | ||||||
| chr3:17084754
|
C | G | 27 | a0001c0002t0001g0115a0001c0002t0003g0064a0001c0002t0003g0065others(24): Show | 27 | HG00280.hp2 HG00741.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.3205-4979C>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17084754 | ||||||
| chr3:17084757
|
G | A | 1 | a0001c0002t0001g0240 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3205-4976G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17084757 | ||||||
| chr3:17084760
|
A | C | 1 | a0001c0002t0001g0240 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3205-4973A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17084760 | ||||||
| chr3:17084763
|
G | C | 1 | a0001c0002t0001g0240 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3205-4970G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17084763 | ||||||
| chr3:17084765
|
GAGGACCT others(9): Show |
G | 1 | a0001c0002t0001g0240 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3205-4967_3205-495 others(20): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17084765 | ||||||
| chr3:17084788
|
G | C | 1 | a0001c0002t0001g0240 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3205-4945G>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17084788 | ||||||
| chr3:17084789
|
G | T | 1 | a0001c0002t0001g0240 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3205-4944G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17084789 | ||||||
| chr3:17084791
|
A | T | 1 | a0001c0002t0001g0240 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3205-4942A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17084791 | ||||||
| chr3:17084793
|
A | T | 1 | a0001c0002t0001g0240 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3205-4940A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17084793 | ||||||
| chr3:17084794
|
T | G | 1 | a0001c0002t0001g0240 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3205-4939T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17084794 | ||||||
| chr3:17084795
|
C | A | 1 | a0001c0002t0001g0240 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3205-4938C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17084795 | ||||||
| chr3:17084796
|
T | C | 1 | a0001c0002t0001g0240 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3205-4937T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17084796 | ||||||
| chr3:17084797
|
A | T | 1 | a0001c0002t0001g0240 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3205-4936A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17084797 | ||||||
| chr3:17084799
|
A | T | 1 | a0001c0002t0001g0240 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3205-4934A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17084799 | ||||||
| chr3:17084800
|
A | T | 1 | a0001c0002t0001g0240 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3205-4933A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17084800 | ||||||
| chr3:17084803
|
A | C | 1 | a0001c0002t0001g0240 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3205-4930A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17084803 | ||||||
| chr3:17084808
|
A | G | 1 | a0001c0002t0001g0240 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3205-4925A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17084808 | ||||||
| chr3:17084836
|
A | T | 1 | a0001c0002t0001g0240 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3205-4897A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17084836 | ||||||
| chr3:17084862
|
G | A | 2 | a0001c0001t0001g0037a0001c0001t0001g0108 | 2 | HG01255.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.3205-4871G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17084862 | ||||||
| chr3:17084963
|
T | C | 2 | a0001c0013t0001g0198a0001c0018t0005g0029 | 2 | HG01978.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.3205-4770T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17084963 | ||||||
| chr3:17085058
|
C | T | 2 | a0001c0002t0001g0007a0001c0002t0001g0199 | 2 | HG02257.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.3205-4675C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17085058 | ||||||
| chr3:17085059
|
G | A | 65 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(62): Show | 65 | HG00408.hp1 HG01081.hp2 HG01175.hp2 others(62): Show |
intron_variant | MODIFIER | c.3205-4674G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17085059 | ||||||
| chr3:17085062
|
C | T | 4 | a0001c0001t0001g0014a0001c0001t0001g0034a0001c0001t0001g0082others(1): Show | 4 | HG01256.hp1 NA18747.hp2 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.3205-4671C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17085062 | ||||||
| chr3:17085176
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3205-4557C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17085176 | ||||||
| chr3:17085204
|
G | A | 64 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(61): Show | 64 | HG00408.hp1 HG01081.hp2 HG01175.hp2 others(61): Show |
intron_variant | MODIFIER | c.3205-4529G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17085204 | ||||||
| chr3:17085213
|
C | T | 40 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(37): Show | 40 | HG00408.hp1 HG01175.hp2 HG01255.hp1 others(37): Show |
intron_variant | MODIFIER | c.3205-4520C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17085213 | ||||||
| chr3:17085333
|
C | T | 8 | a0001c0002t0003g0064a0001c0002t0003g0065a0001c0003t0003g0209others(5): Show | 8 | HG00280.hp2 HG00741.hp1 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.3205-4400C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17085333 | ||||||
| chr3:17085354
|
A | C | 147 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(144): Show | 148 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.3205-4379A>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17085354 | ||||||
| chr3:17085384
|
C | T | 1 | a0001c0001t0002g0136 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3205-4349C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17085384 | ||||||
| chr3:17085436
|
CT | C | 45 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(42): Show | 46 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(43): Show |
intron_variant | MODIFIER | c.3205-4286delT | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 17085436 | |||||
| chr3:17085481
|
G | A | 3 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202 | 3 | HG02976.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3205-4252G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17085481 | ||||||
| chr3:17085534
|
T | C | 2 | a0001c0013t0001g0198a0001c0018t0005g0029 | 2 | HG01978.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.3205-4199T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17085534 | ||||||
| chr3:17085552
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.3205-4181G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17085552 | ||||||
| chr3:17085692
|
G | A | 1 | a0001c0003t0001g0211 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3205-4041G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17085692 | ||||||
| chr3:17085700
|
C | T | 16 | a0001c0002t0001g0115a0001c0003t0001g0018a0001c0003t0001g0180others(13): Show | 16 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.3205-4033C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17085700 | ||||||
| chr3:17085738
|
CATGCCCG others(47): Show |
C | 1 | a0001c0001t0001g0067 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3205-3992_3205-393 others(58): Show |
PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 17085738 | |||||
| chr3:17086043
|
A | T | 1 | a0001c0001t0001g0203 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3205-3690A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17086043 | ||||||
| chr3:17086077
|
A | T | 152 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(149): Show | 153 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.3205-3656A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17086077 | ||||||
| chr3:17086218
|
A | T | 1 | a0001c0001t0001g0117 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.3205-3515A>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17086218 | ||||||
| chr3:17086242
|
A | G | 1 | a0001c0002t0003g0064 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.3205-3491A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17086242 | ||||||
| chr3:17086294
|
C | A | 151 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(148): Show | 152 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.3205-3439C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17086294 | ||||||
| chr3:17086904
|
T | C | 1 | a0001c0002t0001g0205 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3205-2829T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17086904 | ||||||
| chr3:17086965
|
T | A | 1 | a0001c0003t0001g0187 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3205-2768T>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17086965 | ||||||
| chr3:17087281
|
T | C | 1 | a0001c0014t0001g0104 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3205-2452T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17087281 | ||||||
| chr3:17087437
|
C | T | 14 | a0001c0002t0001g0115a0001c0003t0001g0018a0001c0003t0001g0180others(11): Show | 14 | HG01433.hp2 HG01928.hp2 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.3205-2296C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17087437 | ||||||
| chr3:17087645
|
G | T | 4 | a0001c0003t0001g0003a0001c0003t0001g0030a0001c0003t0001g0094others(1): Show | 4 | HG01934.hp1 HG02280.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.3205-2088G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17087645 | ||||||
| chr3:17087738
|
G | T | 14 | a0001c0002t0001g0115a0001c0003t0001g0018a0001c0003t0001g0180others(11): Show | 14 | HG01433.hp2 HG01928.hp2 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.3205-1995G>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17087738 | ||||||
| chr3:17088160
|
T | G | 17 | a0001c0002t0001g0115a0001c0003t0001g0018a0001c0003t0001g0180others(14): Show | 17 | HG01099.hp1 HG01243.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.3205-1573T>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17088160 | ||||||
| chr3:17088166
|
C | T | 5 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(2): Show | 5 | HG02896.hp2 HG03098.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.3205-1567C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17088166 | ||||||
| chr3:17088344
|
G | A | 39 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(36): Show | 39 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.3205-1389G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17088344 | ||||||
| chr3:17088666
|
C | T | 2 | a0001c0011t0001g0004a0001c0012t0001g0005 | 2 | HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.3205-1067C>T | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17088666 | ||||||
| chr3:17088762
|
A | G | 1 | a0001c0016t0001g0093 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3205-971A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17088762 | ||||||
| chr3:17088958
|
T | C | 3 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103 | 3 | HG02896.hp1 HG02897.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.3205-775T>C | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17088958 | ||||||
| chr3:17089026
|
G | A | 1 | a0001c0002t0001g0006 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.3205-707G>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17089026 | ||||||
| chr3:17089590
|
A | G | 10 | a0001c0002t0003g0064a0001c0002t0003g0065a0001c0003t0003g0209others(7): Show | 10 | HG00280.hp2 HG00741.hp1 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.3205-143A>G | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17089590 | ||||||
| chr3:17089718
|
C | A | 39 | a0000c0007t0002g0146a0000c0007t0002g0147a0000c0007t0002g0213others(36): Show | 39 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.3205-15C>A | PLCL2 | ENSG00000154822.18 | transcript | ENST00000615277.5 | protein_coding | 5/5 | chr3 | 17089718 |