| geneid | 57088 |
|---|---|
| ensemblid | ENSG00000114698.15 |
| hgncid | 16497 |
| symbol | PLSCR4 |
| name | phospholipid scramblase 4 |
| refseq_nuc | NM_020353.3 |
| refseq_prot | NP_065086.2 |
| ensembl_nuc | ENST00000354952.7 |
| ensembl_prot | ENSP00000347038.2 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 146192335 |
| end | 146251105 |
| strand | - |
| ver | v1.2 |
| region | chr3:146192335-146251105 |
| region5000 | chr3:146187335-146256105 |
| regionname0 | PLSCR4_chr3_146192335_146251105 |
| regionname5000 | PLSCR4_chr3_146187335_146256105 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 329 | 263 | 56 | 40 | 132 | 6 | 28 | 99 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0002 | 0/1 | 329 | 85 | 7 | 28 | 34 | 4 | 11 | 25 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0003 | 0/0 | 329 | 24 | 22 | 2 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0004 | 0/0 | 329 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0005 | 0/0 | 314 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0006 | 0/0 | 329 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| 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 | 1/0 | 990 | 262 | 56 | 39 | 132 | 6 | 28 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| c0002 | 0/1 | 990 | 84 | 7 | 28 | 33 | 4 | 11 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| c0003 | 0/0 | 990 | 24 | 22 | 2 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| c0004 | 0/0 | 990 | 4 | 4 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| c0005 | 0/0 | 990 | 3 | 3 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| c0006 | 0/0 | 990 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| c0007 | 0/0 | 990 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| c0008 | 0/0 | 990 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| 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 | 0/0 | 2243 | 115 | 13 | 26 | 58 | 4 | 14 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| t0002 | 1/1 | 2244 | 57 | 1 | 13 | 31 | 0 | 10 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| t0003 | 0/0 | 2243 | 38 | 9 | 11 | 9 | 4 | 5 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| t0004 | 0/0 | 2243 | 35 | 1 | 5 | 28 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| t0005 | 0/0 | 2242 | 28 | 0 | 0 | 24 | 2 | 2 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| t0006 | 0/0 | 2243 | 17 | 10 | 2 | 1 | 0 | 4 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| t0007 | 0/0 | 2243 | 16 | 5 | 1 | 9 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| t0008 | 0/0 | 2243 | 9 | 0 | 7 | 0 | 0 | 2 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| t0009 | 0/0 | 2242 | 8 | 7 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| t0010 | 0/0 | 2243 | 8 | 8 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| t0011 | 0/0 | 2242 | 7 | 6 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| t0012 | 0/0 | 2242 | 6 | 6 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| t0013 | 0/0 | 2243 | 6 | 6 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| t0014 | 0/0 | 2243 | 4 | 4 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| t0015 | 0/0 | 2243 | 4 | 3 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| t0016 | 0/0 | 2243 | 2 | 2 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| t0017 | 0/0 | 2243 | 2 | 0 | 0 | 2 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| t0018 | 0/0 | 2243 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| t0019 | 0/0 | 2243 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| t0020 | 0/0 | 2243 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| t0021 | 0/0 | 2242 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| t0022 | 0/0 | 2242 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| t0023 | 0/0 | 2244 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| t0024 | 0/0 | 2243 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| t0025 | 0/0 | 2244 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| t0026 | 0/0 | 2243 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| t0027 | 0/0 | 2242 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| t0028 | 0/0 | 2243 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| t0029 | 0/0 | 2243 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| t0030 | 0/0 | 2244 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| t0031 | 0/0 | 2243 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| t0032 | 0/0 | 2243 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| t0033 | 0/0 | 2244 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| t0034 | 0/0 | 2242 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| t0035 | 0/0 | 2243 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| 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 | 6 | 0 | 0 | 6 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0003 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0004 | 0/0 | 4 | 0 | 0 | 1 | 0 | 3 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0005 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0008 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0018 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0026 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0038 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0039 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0042 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0087 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0268 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 990 | 262 | 56 | 39 | 132 | 6 | 28 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0001c0007 | 0/0 | 990 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0002c0002 | 0/1 | 990 | 84 | 7 | 28 | 33 | 4 | 11 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0002c0008 | 0/0 | 990 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0003c0003 | 0/0 | 990 | 24 | 22 | 2 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0004c0004 | 0/0 | 990 | 4 | 4 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0005c0005 | 0/0 | 990 | 3 | 3 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0006c0006 | 0/0 | 990 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3232 | 92 | 9 | 16 | 53 | 3 | 11 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0001c0001t0002 | 1/0 | 3233 | 35 | 1 | 6 | 22 | 0 | 5 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0001c0001t0003 | 0/0 | 3232 | 34 | 8 | 10 | 9 | 3 | 4 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0001c0001t0004 | 0/0 | 3232 | 20 | 1 | 4 | 14 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0001c0001t0005 | 0/0 | 3231 | 21 | 0 | 0 | 20 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0001c0001t0006 | 0/0 | 3232 | 11 | 5 | 2 | 1 | 0 | 3 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0001c0001t0007 | 0/0 | 3232 | 13 | 5 | 0 | 8 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0001c0001t0008 | 0/0 | 3232 | 2 | 0 | 0 | 0 | 0 | 2 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0001c0001t0009 | 0/0 | 3231 | 6 | 5 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0001c0001t0010 | 0/0 | 3232 | 2 | 2 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0001c0001t0012 | 0/0 | 3231 | 5 | 5 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0001c0001t0013 | 0/0 | 3232 | 5 | 5 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0001c0001t0014 | 0/0 | 3232 | 3 | 3 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0001c0001t0015 | 0/0 | 3232 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0001c0001t0016 | 0/0 | 3232 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0001c0001t0017 | 0/0 | 3232 | 2 | 0 | 0 | 2 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0001c0001t0020 | 0/0 | 3232 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0001c0001t0022 | 0/0 | 3231 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0001c0001t0023 | 0/0 | 3233 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0001c0001t0024 | 0/0 | 3232 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0001c0001t0025 | 0/0 | 3233 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0001c0001t0027 | 0/0 | 3231 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0001c0001t0030 | 0/0 | 3233 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0001c0001t0034 | 0/0 | 3231 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0001c0001t0035 | 0/0 | 3232 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0001c0007t0003 | 0/0 | 3232 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0002c0002t0001 | 0/0 | 3232 | 19 | 0 | 10 | 5 | 1 | 3 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0002c0002t0002 | 0/1 | 3233 | 20 | 0 | 7 | 8 | 0 | 4 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0002c0002t0003 | 0/0 | 3232 | 3 | 1 | 0 | 0 | 1 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0002c0002t0004 | 0/0 | 3232 | 15 | 0 | 1 | 14 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0002c0002t0005 | 0/0 | 3231 | 7 | 0 | 0 | 4 | 2 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0002c0002t0006 | 0/0 | 3232 | 2 | 1 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0002c0002t0007 | 0/0 | 3232 | 3 | 0 | 1 | 1 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0002c0002t0008 | 0/0 | 3232 | 7 | 0 | 7 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0002c0002t0009 | 0/0 | 3231 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0002c0002t0013 | 0/0 | 3232 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0002c0002t0015 | 0/0 | 3232 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0002c0002t0016 | 0/0 | 3232 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0002c0002t0026 | 0/0 | 3232 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0002c0002t0029 | 0/0 | 3232 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0002c0002t0031 | 0/0 | 3232 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0002c0002t0032 | 0/0 | 3232 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0002c0008t0002 | 0/0 | 3233 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0003c0003t0001 | 0/0 | 3232 | 2 | 2 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0003c0003t0006 | 0/0 | 3232 | 2 | 2 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0003c0003t0010 | 0/0 | 3232 | 6 | 6 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0003c0003t0011 | 0/0 | 3231 | 7 | 6 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0003c0003t0012 | 0/0 | 3231 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0003c0003t0014 | 0/0 | 3232 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0003c0003t0015 | 0/0 | 3232 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0003c0003t0018 | 0/0 | 3232 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0003c0003t0019 | 0/0 | 3232 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0003c0003t0028 | 0/0 | 3232 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0003c0003t0033 | 0/0 | 3233 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0004c0004t0001 | 0/0 | 3232 | 2 | 2 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0004c0004t0006 | 0/0 | 3232 | 2 | 2 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0005c0005t0009 | 0/0 | 3231 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0005c0005t0015 | 0/0 | 3232 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0005c0005t0021 | 0/0 | 3231 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| a0006c0006t0002 | 0/0 | 3233 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | copy fasta | chr3 | 146187335 | 146256105 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0002g0001 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0002g0003 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0002g0087 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0003g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0003g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0003g0018 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0003g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0004g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0004g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0004g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0004g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0004g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0004g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0004g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0004g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0004g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0004g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0004g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0004g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0005g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0005g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0005g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0005g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0005g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0005g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0005g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0005g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0005g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0005g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0005g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0005g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0005g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0005g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0005g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0005g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0005g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0005g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0006g0004 | 0/0 | 4 | 0 | 0 | 1 | 0 | 3 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0006g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0006g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0006g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0006g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0006g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0006g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0007g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0007g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0007g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0007g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0007g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0007g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0007g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0007g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0007g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0007g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0007g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0007g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0008g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0009g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0009g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0009g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0009g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0009g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0010g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0010g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0012g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0012g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0012g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0012g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0012g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0013g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0013g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0013g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0013g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0013g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0014g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0014g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0015g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0016g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0017g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0017g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0020g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0022g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0023g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0024g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0025g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0027g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0030g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0034g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0001t0035g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0001c0007t0003g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0001g0038 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0002g0008 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0002g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0002g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0002g0268 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0002g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0003g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0003g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0003g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0004g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0004g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0004g0039 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0004g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0004g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0004g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0005g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0005g0042 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0005g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0005g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0005g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0006g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0006g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0007g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0007g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0007g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0008g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0008g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0008g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0008g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0008g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0009g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0013g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0015g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0016g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0026g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0029g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0031g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0002t0032g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0002c0008t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0003c0003t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0003c0003t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0003c0003t0006g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0003c0003t0010g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0003c0003t0010g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0003c0003t0010g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0003c0003t0010g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0003c0003t0010g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0003c0003t0010g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0003c0003t0011g0005 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0003c0003t0011g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0003c0003t0011g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0003c0003t0011g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0003c0003t0011g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0003c0003t0012g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0003c0003t0014g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0003c0003t0015g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0003c0003t0018g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0003c0003t0019g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0003c0003t0028g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0003c0003t0033g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0004c0004t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0004c0004t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0004c0004t0006g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0004c0004t0006g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0005c0005t0009g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0005c0005t0015g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0005c0005t0021g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| a0006c0006t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0238 | EUR | GBR | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0018 | EUR | GBR | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG00408 | hp1 | a0002 | c0008 | t0002 | g0266 | EAS | CHS | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0099 | EAS | CHS | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG00423 | hp1 | a0002 | c0002 | t0007 | g0292 | EAS | CHS | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | CHS | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | CHS | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | CHS | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | CHS | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG00558 | hp2 | a0002 | c0002 | t0004 | g0039 | EAS | CHS | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG00597 | hp1 | a0001 | c0001 | t0005 | g0201 | EAS | CHS | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG00597 | hp2 | a0002 | c0002 | t0004 | g0254 | EAS | CHS | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG00609 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | CHS | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | CHS | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG00621 | hp1 | a0002 | c0002 | t0004 | g0002 | EAS | CHS | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | CHS | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0168 | AMR | PUR | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0257 | AMR | PUR | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | CHS | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG00735 | hp1 | a0002 | c0002 | t0008 | g0043 | AMR | PUR | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG00735 | hp2 | a0001 | c0007 | t0003 | g0190 | AMR | PUR | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0056 | AMR | PUR | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0018 | AMR | PUR | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0038 | AMR | PUR | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0197 | AMR | PUR | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01069 | hp2 | a0002 | c0002 | t0008 | g0040 | AMR | PUR | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01070 | hp1 | a0002 | c0002 | t0002 | g0287 | AMR | PUR | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01070 | hp2 | a0001 | c0001 | t0006 | g0029 | AMR | PUR | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01071 | hp1 | a0001 | c0001 | t0006 | g0029 | AMR | PUR | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01071 | hp2 | a0002 | c0002 | t0008 | g0040 | AMR | PUR | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0034 | AMR | PUR | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0133 | AMR | PUR | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01081 | hp1 | a0002 | c0002 | t0015 | g0264 | AMR | PUR | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01099 | hp1 | a0002 | c0002 | t0008 | g0277 | AMR | PUR | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01099 | hp2 | a0001 | c0001 | t0004 | g0017 | AMR | PUR | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0170 | AMR | PUR | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01106 | hp2 | a0002 | c0002 | t0008 | g0043 | AMR | PUR | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0246 | AMR | PUR | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01167 | hp2 | a0002 | c0002 | t0002 | g0037 | AMR | PUR | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0092 | AMR | PUR | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01169 | hp2 | a0002 | c0002 | t0002 | g0037 | AMR | PUR | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0083 | AMR | PUR | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01192 | hp2 | a0002 | c0002 | t0029 | g0279 | AMR | PUR | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01243 | hp1 | a0002 | c0002 | t0007 | g0306 | AMR | PUR | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01243 | hp2 | a0001 | c0001 | t0009 | g0122 | AMR | PUR | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01255 | hp1 | a0003 | c0003 | t0028 | g0156 | AMR | CLM | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01255 | hp2 | a0002 | c0002 | t0008 | g0286 | AMR | CLM | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | CLM | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0108 | AMR | CLM | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01261 | hp2 | a0002 | c0002 | t0008 | g0282 | AMR | CLM | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | CLM | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01358 | hp2 | a0002 | c0002 | t0002 | g0008 | AMR | CLM | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0265 | AMR | CLM | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01433 | hp1 | a0003 | c0003 | t0011 | g0005 | AMR | CLM | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01496 | hp2 | a0002 | c0002 | t0002 | g0262 | AMR | CLM | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0026 | EUR | IBS | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0038 | EUR | IBS | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0187 | EUR | IBS | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01516 | hp2 | a0002 | c0002 | t0005 | g0042 | EUR | IBS | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01517 | hp1 | a0002 | c0002 | t0005 | g0042 | EUR | IBS | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0026 | EUR | IBS | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01891 | hp1 | a0003 | c0003 | t0010 | g0157 | AFR | ACB | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01891 | hp2 | a0003 | c0003 | t0018 | g0047 | AFR | ACB | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01943 | hp1 | a0001 | c0001 | t0004 | g0213 | AMR | PEL | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PEL | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01978 | hp2 | a0002 | c0002 | t0002 | g0289 | AMR | PEL | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0245 | AMR | PEL | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01981 | hp2 | a0001 | c0001 | t0004 | g0208 | AMR | PEL | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0034 | AMR | PEL | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0247 | AMR | PEL | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PEL | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02015 | hp1 | a0001 | c0001 | t0004 | g0194 | EAS | KHV | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | KHV | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02027 | hp2 | a0001 | c0001 | t0004 | g0076 | EAS | KHV | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02055 | hp2 | a0005 | c0005 | t0021 | g0314 | AFR | ACB | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | KHV | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02080 | hp2 | a0002 | c0002 | t0002 | g0008 | EAS | KHV | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02129 | hp1 | a0001 | c0001 | t0004 | g0183 | EAS | KHV | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0291 | EAS | KHV | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0112 | AFR | ACB | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02145 | hp2 | a0001 | c0001 | t0007 | g0024 | AFR | ACB | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02155 | hp1 | a0001 | c0001 | t0004 | g0068 | EAS | CDX | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | CDX | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | CDX | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | CDX | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02257 | hp1 | a0003 | c0003 | t0011 | g0049 | AFR | ACB | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02257 | hp2 | a0001 | c0001 | t0009 | g0163 | AFR | ACB | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02258 | hp1 | a0003 | c0003 | t0011 | g0046 | AFR | ACB | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02258 | hp2 | a0003 | c0003 | t0001 | g0301 | AFR | ACB | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02273 | hp1 | a0001 | c0001 | t0004 | g0131 | AMR | PEL | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0193 | AMR | PEL | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02280 | hp1 | a0003 | c0003 | t0010 | g0159 | AFR | ACB | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02280 | hp2 | a0001 | c0001 | t0006 | g0123 | AFR | ACB | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02293 | hp1 | a0002 | c0002 | t0004 | g0039 | AMR | PEL | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02293 | hp2 | a0002 | c0002 | t0001 | g0244 | AMR | PEL | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0189 | AMR | PEL | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02300 | hp2 | a0002 | c0002 | t0002 | g0269 | AMR | PEL | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0078 | AFR | ACB | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02451 | hp2 | a0003 | c0003 | t0011 | g0005 | AFR | ACB | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02523 | hp1 | a0002 | c0002 | t0005 | g0041 | EAS | KHV | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | KHV | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02572 | hp1 | a0002 | c0002 | t0006 | g0090 | AFR | GWD | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0128 | AFR | GWD | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02602 | hp2 | a0001 | c0001 | t0004 | g0084 | SAS | PJL | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02615 | hp1 | a0003 | c0003 | t0010 | g0310 | AFR | GWD | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02615 | hp2 | a0001 | c0001 | t0013 | g0079 | AFR | GWD | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02622 | hp1 | a0003 | c0003 | t0011 | g0048 | AFR | GWD | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02622 | hp2 | a0001 | c0001 | t0013 | g0119 | AFR | GWD | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02630 | hp2 | a0001 | c0001 | t0010 | g0151 | AFR | GWD | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02647 | hp1 | a0003 | c0003 | t0010 | g0161 | AFR | GWD | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02647 | hp2 | a0001 | c0001 | t0012 | g0150 | AFR | GWD | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02683 | hp2 | a0001 | c0001 | t0023 | g0144 | SAS | PJL | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02698 | hp1 | a0002 | c0002 | t0005 | g0293 | SAS | PJL | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02698 | hp2 | a0002 | c0002 | t0002 | g0298 | SAS | PJL | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02717 | hp1 | a0003 | c0003 | t0010 | g0160 | AFR | GWD | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02717 | hp2 | a0001 | c0001 | t0006 | g0192 | AFR | GWD | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02818 | hp1 | a0001 | c0001 | t0013 | g0059 | AFR | GWD | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02818 | hp2 | a0004 | c0004 | t0001 | g0153 | AFR | GWD | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0272 | AFR | GWD | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02895 | hp1 | a0001 | c0001 | t0012 | g0148 | AFR | GWD | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02895 | hp2 | a0001 | c0001 | t0014 | g0025 | AFR | GWD | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0014 | AFR | GWD | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02896 | hp2 | a0001 | c0001 | t0012 | g0299 | AFR | GWD | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02897 | hp1 | a0001 | c0001 | t0014 | g0025 | AFR | GWD | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0014 | AFR | GWD | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02922 | hp1 | a0003 | c0003 | t0014 | g0052 | AFR | ESN | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02922 | hp2 | a0001 | c0001 | t0012 | g0147 | AFR | ESN | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02965 | hp1 | a0002 | c0002 | t0013 | g0305 | AFR | ESN | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02965 | hp2 | a0001 | c0001 | t0035 | g0319 | AFR | ESN | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02970 | hp1 | a0004 | c0004 | t0006 | g0154 | AFR | ESN | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02970 | hp2 | a0001 | c0001 | t0024 | g0217 | AFR | ESN | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02976 | hp1 | a0003 | c0003 | t0019 | g0045 | AFR | ESN | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02976 | hp2 | a0001 | c0001 | t0009 | g0164 | AFR | ESN | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG03017 | hp1 | a0002 | c0002 | t0002 | g0008 | SAS | PJL | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG03017 | hp2 | a0001 | c0001 | t0006 | g0004 | SAS | PJL | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG03041 | hp1 | a0002 | c0002 | t0026 | g0304 | AFR | GWD | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG03041 | hp2 | a0003 | c0003 | t0011 | g0044 | AFR | GWD | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG03098 | hp1 | a0001 | c0001 | t0013 | g0058 | AFR | MSL | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG03098 | hp2 | a0001 | c0001 | t0007 | g0091 | AFR | MSL | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0118 | AFR | ESN | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | ESN | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG03139 | hp1 | a0001 | c0001 | t0009 | g0022 | AFR | ESN | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | ESN | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG03195 | hp2 | a0003 | c0003 | t0001 | g0300 | AFR | ESN | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | MSL | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG03225 | hp1 | a0001 | c0001 | t0009 | g0053 | AFR | MSL | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG03225 | hp2 | a0001 | c0001 | t0012 | g0273 | AFR | MSL | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0207 | SAS | PJL | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0057 | SAS | PJL | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG03453 | hp1 | a0005 | c0005 | t0009 | g0317 | AFR | MSL | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG03453 | hp2 | a0001 | c0001 | t0016 | g0255 | AFR | MSL | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG03486 | hp1 | a0002 | c0002 | t0009 | g0089 | AFR | MSL | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG03486 | hp2 | a0001 | c0001 | t0022 | g0162 | AFR | MSL | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG03490 | hp1 | a0002 | c0002 | t0001 | g0259 | SAS | PJL | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG03490 | hp2 | a0001 | c0001 | t0006 | g0004 | SAS | PJL | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG03491 | hp1 | a0001 | c0001 | t0008 | g0016 | SAS | PJL | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG03491 | hp2 | a0002 | c0002 | t0002 | g0260 | SAS | PJL | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG03492 | hp1 | a0001 | c0001 | t0008 | g0016 | SAS | PJL | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG03492 | hp2 | a0001 | c0001 | t0006 | g0004 | SAS | PJL | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG03516 | hp1 | a0003 | c0003 | t0012 | g0311 | AFR | ESN | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG03516 | hp2 | a0001 | c0001 | t0014 | g0270 | AFR | ESN | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0070 | AFR | GWD | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG03540 | hp2 | a0001 | c0001 | t0007 | g0271 | AFR | GWD | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG03579 | hp1 | a0003 | c0003 | t0010 | g0158 | AFR | MSL | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG03579 | hp2 | a0003 | c0003 | t0006 | g0012 | AFR | MSL | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0288 | SAS | PJL | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0225 | SAS | PJL | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0138 | SAS | PJL | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG03669 | hp2 | a0001 | c0001 | t0005 | g0095 | SAS | PJL | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0146 | SAS | STU | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG03688 | hp2 | a0002 | c0002 | t0003 | g0296 | SAS | STU | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG03704 | hp2 | a0002 | c0002 | t0006 | g0295 | SAS | PJL | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0209 | SAS | PJL | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0256 | SAS | PJL | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG03831 | hp1 | a0002 | c0002 | t0007 | g0297 | SAS | BEB | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | BEB | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | BEB | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0200 | SAS | BEB | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | BEB | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | BEB | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0082 | SAS | BEB | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | BEB | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | STU | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | STU | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG04184 | hp1 | a0006 | c0006 | t0002 | g0127 | SAS | BEB | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG04184 | hp2 | a0002 | c0002 | t0002 | g0136 | SAS | BEB | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0134 | SAS | STU | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | STU | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18522 | hp1 | a0001 | c0001 | t0010 | g0149 | AFR | YRI | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18522 | hp2 | a0001 | c0001 | t0034 | g0320 | AFR | YRI | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18747 | hp1 | a0001 | c0001 | t0005 | g0110 | EAS | CHB | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | CHB | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18906 | hp1 | a0004 | c0004 | t0006 | g0155 | AFR | YRI | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18906 | hp2 | a0001 | c0001 | t0015 | g0216 | AFR | YRI | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18939 | hp2 | a0001 | c0001 | t0005 | g0085 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18941 | hp2 | a0001 | c0001 | t0005 | g0094 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18942 | hp2 | a0001 | c0001 | t0007 | g0109 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18943 | hp2 | a0002 | c0002 | t0002 | g0276 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18944 | hp1 | a0002 | c0002 | t0004 | g0002 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18944 | hp2 | a0001 | c0001 | t0007 | g0240 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18946 | hp1 | a0001 | c0001 | t0025 | g0071 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18946 | hp2 | a0001 | c0001 | t0004 | g0120 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18950 | hp1 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18950 | hp2 | a0001 | c0001 | t0004 | g0235 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18952 | hp2 | a0002 | c0002 | t0004 | g0258 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18953 | hp1 | a0001 | c0001 | t0007 | g0075 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18953 | hp2 | a0002 | c0002 | t0004 | g0002 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18954 | hp1 | a0002 | c0002 | t0001 | g0281 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18954 | hp2 | a0001 | c0001 | t0007 | g0111 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18959 | hp2 | a0001 | c0001 | t0027 | g0195 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18961 | hp2 | a0001 | c0001 | t0004 | g0073 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18963 | hp1 | a0001 | c0001 | t0004 | g0226 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18964 | hp2 | a0002 | c0002 | t0005 | g0041 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18967 | hp1 | a0001 | c0001 | t0005 | g0015 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18967 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18968 | hp2 | a0001 | c0001 | t0004 | g0171 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18969 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18970 | hp1 | a0002 | c0002 | t0004 | g0002 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18979 | hp2 | a0001 | c0001 | t0005 | g0115 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18980 | hp1 | a0001 | c0001 | t0005 | g0015 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18980 | hp2 | a0001 | c0001 | t0005 | g0178 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18982 | hp2 | a0002 | c0002 | t0004 | g0253 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18986 | hp1 | a0001 | c0001 | t0004 | g0017 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18988 | hp1 | a0001 | c0001 | t0004 | g0142 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18988 | hp2 | a0001 | c0001 | t0005 | g0117 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18991 | hp1 | a0001 | c0001 | t0005 | g0021 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18993 | hp1 | a0001 | c0001 | t0004 | g0097 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18993 | hp2 | a0002 | c0002 | t0005 | g0251 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18994 | hp2 | a0002 | c0002 | t0004 | g0035 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18995 | hp1 | a0001 | c0001 | t0005 | g0218 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18995 | hp2 | a0002 | c0002 | t0031 | g0275 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA18999 | hp2 | a0001 | c0001 | t0005 | g0182 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19000 | hp1 | a0002 | c0002 | t0002 | g0267 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19000 | hp2 | a0002 | c0002 | t0004 | g0263 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19002 | hp1 | a0001 | c0001 | t0017 | g0212 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19002 | hp2 | a0002 | c0002 | t0002 | g0294 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19003 | hp2 | a0001 | c0001 | t0017 | g0211 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19004 | hp1 | a0001 | c0001 | t0005 | g0019 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19004 | hp2 | a0002 | c0002 | t0002 | g0249 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0241 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19009 | hp1 | a0001 | c0001 | t0005 | g0021 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19010 | hp2 | a0001 | c0001 | t0007 | g0139 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19011 | hp1 | a0001 | c0001 | t0005 | g0172 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19012 | hp1 | a0001 | c0001 | t0005 | g0121 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19030 | hp1 | a0005 | c0005 | t0015 | g0318 | AFR | LWK | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19030 | hp2 | a0001 | c0001 | t0013 | g0285 | AFR | LWK | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0069 | AFR | LWK | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19043 | hp2 | a0001 | c0001 | t0006 | g0261 | AFR | LWK | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19062 | hp1 | a0001 | c0001 | t0005 | g0313 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0239 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19063 | hp2 | a0002 | c0002 | t0004 | g0002 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19065 | hp2 | a0002 | c0002 | t0004 | g0290 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19066 | hp1 | a0001 | c0001 | t0005 | g0100 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19070 | hp1 | a0001 | c0001 | t0007 | g0203 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19070 | hp2 | a0001 | c0001 | t0007 | g0102 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19072 | hp1 | a0001 | c0001 | t0005 | g0019 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19078 | hp1 | a0002 | c0002 | t0004 | g0035 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19078 | hp2 | a0001 | c0001 | t0004 | g0232 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19079 | hp2 | a0002 | c0002 | t0005 | g0250 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19081 | hp1 | a0001 | c0001 | t0005 | g0126 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19081 | hp2 | a0002 | c0002 | t0004 | g0002 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19085 | hp1 | a0001 | c0001 | t0007 | g0106 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19086 | hp1 | a0001 | c0001 | t0004 | g0179 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19087 | hp1 | a0002 | c0002 | t0001 | g0252 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19087 | hp2 | a0001 | c0001 | t0030 | g0231 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19088 | hp2 | a0001 | c0001 | t0006 | g0004 | EAS | JPT | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19240 | hp1 | a0003 | c0003 | t0006 | g0012 | AFR | YRI | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA19240 | hp2 | a0002 | c0002 | t0003 | g0307 | AFR | YRI | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA20129 | hp1 | a0003 | c0003 | t0011 | g0005 | AFR | ASW | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA20129 | hp2 | a0001 | c0001 | t0020 | g0050 | AFR | ASW | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0051 | EUR | TSI | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA20805 | hp2 | a0002 | c0002 | t0003 | g0278 | EUR | TSI | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0173 | AMR | CLM | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0280 | AMR | CLM | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02109 | hp1 | a0001 | c0001 | t0006 | g0124 | AFR | ACB | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02109 | hp2 | a0003 | c0003 | t0033 | g0309 | AFR | ACB | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02559 | hp1 | a0001 | c0001 | t0006 | g0284 | AFR | ACB | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG02559 | hp2 | a0001 | c0001 | t0009 | g0022 | AFR | ACB | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG03471 | hp1 | a0001 | c0001 | t0007 | g0024 | AFR | MSL | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG03471 | hp2 | a0002 | c0002 | t0032 | g0302 | AFR | MSL | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0088 | AFR | USA | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| HG06807 | hp2 | a0001 | c0001 | t0007 | g0063 | AFR | USA | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | USA | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA20300 | hp2 | a0004 | c0004 | t0001 | g0152 | AFR | USA | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA21309 | hp1 | a0002 | c0002 | t0016 | g0303 | AFR | LWK | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| NA21309 | hp2 | a0003 | c0003 | t0015 | g0308 | AFR | LWK | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0002 | g0268 | REF | REF | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0087 | REF | REF | PLSCR4_chr3_146187335_146256105 | PLSCR4 | chr3 | 146187335 | 146256105 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:146199886
|
C | T | 1 | a0004 | 4 | HG02818.hp2 HG02970.hp1 NA18906.hp1 others(1): Show |
missense_variant | MODERATE | c.551G>A | p.Arg184Gln | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 6/9 | 718/3233 | 551/990 | 184/329 | chr3 | 146199886 | ||
| chr3:146199965
|
C | T | 1 | a0006 | 1 | HG04184.hp1 | missense_variant | MODERATE | c.472G>A | p.Glu158Lys | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 6/9 | 639/3233 | 472/990 | 158/329 | chr3 | 146199965 | ||
| chr3:146199974
|
T | C | 1 | a0002 | 85 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(82): Show |
missense_variant | MODERATE | c.463A>G | p.Ile155Val | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 6/9 | 630/3233 | 463/990 | 155/329 | chr3 | 146199974 | ||
| chr3:146220832
|
T | C | 3 | a0002a0003a0005 | 112 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(109): Show |
missense_variant | MODERATE | c.101A>G | p.Asn34Ser | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/9 | 268/3233 | 101/990 | 34/329 | chr3 | 146220832 | ||
| chr3:146222069
|
C | G | 1 | a0005 | 3 | HG02055.hp2 HG03453.hp1 NA19030.hp1 |
start_lost | HIGH | c.3G>C | p.Met1? | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 2/9 | 170/3233 | 3/990 | 1/329 | chr3 | 146222069 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:146194423
|
T | C | 1 | a0001c0007 | 1 | HG00735.hp2 | synonymous_variant | LOW | c.978A>G | p.Gln326Gln | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 9/9 | 1145/3233 | 978/990 | 326/329 | chr3 | 146194423 | ||
| chr3:146196749
|
C | T | 1 | a0002c0008 | 1 | HG00408.hp1 | synonymous_variant | LOW | c.669G>A | p.Ala223Ala | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 7/9 | 836/3233 | 669/990 | 223/329 | chr3 | 146196749 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:146192598
|
A | G | 4 | a0001c0001t0016a0001c0001t0024a0002c0002t0016others(1): Show | 4 | HG01255.hp1 HG02970.hp2 HG03453.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1813T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 9/9 | 1813 | chr3 | 146192598 | |||||
| chr3:146192643
|
T | C | 18 | a0001c0001t0006a0001c0001t0007a0001c0001t0008others(15): Show | 52 | HG00423.hp1 HG00735.hp1 HG01069.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*1768A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 9/9 | 1768 | chr3 | 146192643 | |||||
| chr3:146192756
|
T | C | 4 | a0001c0001t0007a0001c0001t0035a0002c0002t0007others(1): Show | 18 | HG00423.hp1 HG01192.hp2 HG01243.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1655A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 9/9 | 1655 | chr3 | 146192756 | |||||
| chr3:146192780
|
G | A | 1 | a0001c0001t0022 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1631C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 9/9 | 1631 | chr3 | 146192780 | |||||
| chr3:146192813
|
CT | C | 5 | a0001c0001t0009a0001c0001t0034a0002c0002t0009others(2): Show | 16 | HG01243.hp2 HG01433.hp1 HG02257.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1597delA | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 9/9 | 1597 | chr3 | 146192813 | |||||
| chr3:146192820
|
T | A | 5 | a0001c0001t0005a0001c0001t0013a0002c0002t0005others(2): Show | 35 | HG00597.hp1 HG01516.hp2 HG01517.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*1591A>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 9/9 | 1591 | chr3 | 146192820 | |||||
| chr3:146192820
|
TA | T | 5 | a0001c0001t0012a0001c0001t0022a0001c0001t0027others(2): Show | 9 | HG02055.hp2 HG02647.hp2 HG02895.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1590delT | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 9/9 | 1590 | chr3 | 146192820 | |||||
| chr3:146192821
|
A | T | 2 | a0001c0001t0004a0002c0002t0004 | 35 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*1590T>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 9/9 | 1590 | chr3 | 146192821 | |||||
| chr3:146192926
|
C | T | 2 | a0001c0001t0010a0003c0003t0010 | 8 | HG01891.hp1 HG02280.hp1 HG02615.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1485G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 9/9 | 1485 | chr3 | 146192926 | |||||
| chr3:146193051
|
TA | T | 50 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(47): Show | 291 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(288): Show |
3_prime_UTR_variant | MODIFIER | c.*1359delT | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 9/9 | 1359 | chr3 | 146193051 | |||||
| chr3:146193289
|
G | A | 1 | a0002c0002t0026 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1122C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 9/9 | 1122 | chr3 | 146193289 | |||||
| chr3:146193377
|
C | T | 7 | a0001c0001t0006a0001c0001t0008a0002c0002t0006others(4): Show | 27 | HG00735.hp1 HG01069.hp2 HG01070.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1034G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 9/9 | 1034 | chr3 | 146193377 | |||||
| chr3:146193577
|
C | T | 1 | a0005c0005t0021 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*834G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 9/9 | 834 | chr3 | 146193577 | |||||
| chr3:146193677
|
G | A | 1 | a0001c0001t0017 | 2 | NA19002.hp1 NA19003.hp2 |
3_prime_UTR_variant | MODIFIER | c.*734C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 9/9 | 734 | chr3 | 146193677 | |||||
| chr3:146193681
|
G | A | 8 | a0001c0001t0001a0001c0001t0017a0001c0001t0020others(5): Show | 120 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*730C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 9/9 | 730 | chr3 | 146193681 | |||||
| chr3:146193688
|
T | C | 1 | a0003c0003t0028 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*723A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 9/9 | 723 | chr3 | 146193688 | |||||
| chr3:146193920
|
TTC | T | 2 | a0001c0001t0005a0002c0002t0005 | 28 | HG00597.hp1 HG01516.hp2 HG01517.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*489_*490delGA | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 9/9 | 489 | chr3 | 146193920 | |||||
| chr3:146193946
|
A | G | 24 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(21): Show | 215 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*465T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 9/9 | 465 | chr3 | 146193946 | |||||
| chr3:146193994
|
T | C | 1 | a0002c0002t0031 | 1 | NA18995.hp2 | 3_prime_UTR_variant | MODIFIER | c.*417A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 9/9 | 417 | chr3 | 146193994 | |||||
| chr3:146194000
|
C | T | 1 | a0001c0001t0023 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*411G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 9/9 | 411 | chr3 | 146194000 | |||||
| chr3:146194268
|
C | T | 9 | a0001c0001t0009a0001c0001t0012a0001c0001t0022others(6): Show | 24 | HG01243.hp2 HG01433.hp1 HG02055.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*143G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 9/9 | 143 | chr3 | 146194268 | |||||
| chr3:146194390
|
T | G | 17 | a0001c0001t0006a0001c0001t0007a0001c0001t0014others(14): Show | 46 | HG00423.hp1 HG01070.hp2 HG01071.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*21A>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 9/9 | 21 | chr3 | 146194390 | |||||
| chr3:146250993
|
G | T | 1 | a0001c0001t0020 | 1 | NA20129.hp2 | 5_prime_UTR_variant | MODIFIER | c.-55C>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/9 | 28922 | chr3 | 146250993 | |||||
| chr3:146251048
|
G | A | 2 | a0001c0001t0034a0001c0001t0035 | 2 | HG02965.hp2 NA18522.hp2 |
5_prime_UTR_variant | MODIFIER | c.-110C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/9 | 28977 | chr3 | 146251048 | |||||
| chr3:146251051
|
A | G | 3 | a0003c0003t0011a0003c0003t0018a0003c0003t0019 | 9 | HG01433.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-113T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/9 | 28980 | chr3 | 146251051 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:146194512
|
C | T | 30 | a0001c0001t0003g0006a0001c0001t0003g0018a0001c0001t0003g0051others(27): Show | 33 | HG00099.hp2 HG00408.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.946-57G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 8/8 | chr3 | 146194512 | ||||||
| chr3:146194626
|
G | T | 1 | a0002c0002t0029g0279 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.946-171C>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 8/8 | chr3 | 146194626 | ||||||
| chr3:146194761
|
C | T | 205 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(202): Show | 232 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(229): Show |
intron_variant | MODIFIER | c.946-306G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 8/8 | chr3 | 146194761 | ||||||
| chr3:146194793
|
G | A | 2 | a0001c0001t0008g0016a0002c0002t0008g0282 | 3 | HG01261.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.945+331C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 8/8 | chr3 | 146194793 | ||||||
| chr3:146195311
|
T | C | 6 | a0001c0001t0003g0014a0001c0001t0003g0070a0001c0001t0003g0112others(3): Show | 7 | HG02145.hp1 HG02886.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.787-29A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 7/8 | chr3 | 146195311 | ||||||
| chr3:146195316
|
G | C | 1 | a0001c0001t0003g0064 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.787-34C>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 7/8 | chr3 | 146195316 | ||||||
| chr3:146195398
|
T | C | 6 | a0001c0001t0003g0014a0001c0001t0003g0070a0001c0001t0003g0112others(3): Show | 7 | HG02145.hp1 HG02886.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.787-116A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 7/8 | chr3 | 146195398 | ||||||
| chr3:146195455
|
T | A | 2 | a0001c0001t0004g0068a0001c0001t0004g0076 | 2 | HG02027.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.787-173A>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 7/8 | chr3 | 146195455 | ||||||
| chr3:146195657
|
T | G | 31 | a0001c0001t0003g0014a0001c0001t0003g0070a0001c0001t0003g0112others(28): Show | 35 | HG01243.hp2 HG01433.hp1 HG02055.hp2 others(32): Show |
intron_variant | MODIFIER | c.787-375A>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 7/8 | chr3 | 146195657 | ||||||
| chr3:146195704
|
C | A | 2 | a0001c0001t0001g0199a0001c0001t0001g0242 | 2 | HG01081.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.787-422G>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 7/8 | chr3 | 146195704 | ||||||
| chr3:146195887
|
C | T | 2 | a0002c0002t0008g0043a0002c0002t0008g0277 | 3 | HG00735.hp1 HG01099.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.787-605G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 7/8 | chr3 | 146195887 | ||||||
| chr3:146196114
|
CT | C | 6 | a0003c0003t0010g0157a0003c0003t0010g0158a0003c0003t0010g0159others(3): Show | 6 | HG01891.hp1 HG02280.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.786+517delA | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 7/8 | chr3 | 146196114 | ||||||
| chr3:146196217
|
T | C | 1 | a0001c0001t0001g0166 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.786+415A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 7/8 | chr3 | 146196217 | ||||||
| chr3:146196309
|
G | A | 5 | a0001c0001t0009g0122a0003c0003t0011g0005a0003c0003t0011g0046others(2): Show | 7 | HG01243.hp2 HG01433.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.786+323C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 7/8 | chr3 | 146196309 | ||||||
| chr3:146196349
|
G | T | 1 | a0002c0002t0029g0279 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.786+283C>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 7/8 | chr3 | 146196349 | ||||||
| chr3:146196432
|
T | TA | 25 | a0001c0001t0007g0063a0001c0001t0009g0022a0001c0001t0009g0053others(22): Show | 28 | HG01243.hp2 HG01433.hp1 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.786+199dupT | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 7/8 | chr3 | 146196432 | ||||||
| chr3:146196579
|
C | T | 5 | a0001c0001t0003g0051a0001c0001t0003g0056a0001c0001t0003g0187others(2): Show | 5 | HG00735.hp2 HG00738.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.786+53G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 7/8 | chr3 | 146196579 | ||||||
| chr3:146196855
|
C | T | 2 | a0001c0001t0014g0270a0003c0003t0019g0045 | 2 | HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.625-62G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 6/8 | chr3 | 146196855 | ||||||
| chr3:146197201
|
T | A | 2 | a0001c0001t0012g0148a0001c0001t0012g0150 | 2 | HG02647.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.625-408A>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 6/8 | chr3 | 146197201 | ||||||
| chr3:146197226
|
C | T | 129 | a0001c0001t0001g0010a0001c0001t0001g0026a0001c0001t0001g0030others(126): Show | 151 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(148): Show |
intron_variant | MODIFIER | c.625-433G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 6/8 | chr3 | 146197226 | ||||||
| chr3:146197278
|
G | C | 1 | a0001c0001t0003g0170 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.625-485C>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 6/8 | chr3 | 146197278 | ||||||
| chr3:146197398
|
C | G | 1 | a0001c0001t0001g0198 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.625-605G>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 6/8 | chr3 | 146197398 | ||||||
| chr3:146197655
|
T | C | 4 | a0004c0004t0001g0152a0004c0004t0001g0153a0004c0004t0006g0154others(1): Show | 4 | HG02818.hp2 HG02970.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.625-862A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 6/8 | chr3 | 146197655 | ||||||
| chr3:146197839
|
T | C | 24 | a0001c0001t0007g0024a0001c0001t0007g0063a0001c0001t0009g0053others(21): Show | 27 | HG01255.hp1 HG01891.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.625-1046A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 6/8 | chr3 | 146197839 | ||||||
| chr3:146197902
|
A | G | 2 | a0001c0001t0001g0011a0001c0001t0003g0051 | 3 | HG02886.hp1 HG03209.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.625-1109T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 6/8 | chr3 | 146197902 | ||||||
| chr3:146197984
|
T | C | 1 | a0001c0001t0002g0141 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.625-1191A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 6/8 | chr3 | 146197984 | ||||||
| chr3:146198035
|
C | T | 148 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(145): Show | 174 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.625-1242G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 6/8 | chr3 | 146198035 | ||||||
| chr3:146198119
|
G | A | 9 | a0001c0001t0001g0010a0003c0003t0001g0300a0003c0003t0001g0301others(6): Show | 11 | HG02109.hp2 HG02258.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.625-1326C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 6/8 | chr3 | 146198119 | ||||||
| chr3:146198126
|
C | T | 2 | a0002c0002t0008g0043a0002c0002t0008g0277 | 3 | HG00735.hp1 HG01099.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.625-1333G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 6/8 | chr3 | 146198126 | ||||||
| chr3:146198192
|
T | G | 19 | a0001c0001t0007g0024a0001c0001t0007g0063a0001c0001t0009g0053others(16): Show | 21 | HG01255.hp1 HG01891.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.625-1399A>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 6/8 | chr3 | 146198192 | ||||||
| chr3:146198256
|
G | A | 1 | a0001c0001t0003g0057 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.625-1463C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 6/8 | chr3 | 146198256 | ||||||
| chr3:146198270
|
T | C | 19 | a0001c0001t0007g0024a0001c0001t0007g0063a0001c0001t0009g0053others(16): Show | 21 | HG01255.hp1 HG01891.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.625-1477A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 6/8 | chr3 | 146198270 | ||||||
| chr3:146198293
|
C | T | 19 | a0001c0001t0007g0024a0001c0001t0007g0063a0001c0001t0009g0053others(16): Show | 21 | HG01255.hp1 HG01891.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.625-1500G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 6/8 | chr3 | 146198293 | ||||||
| chr3:146198361
|
A | G | 19 | a0001c0001t0007g0024a0001c0001t0007g0063a0001c0001t0009g0053others(16): Show | 21 | HG01255.hp1 HG01891.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.624+1452T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 6/8 | chr3 | 146198361 | ||||||
| chr3:146198378
|
A | T | 1 | a0002c0002t0002g0276 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.624+1435T>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 6/8 | chr3 | 146198378 | ||||||
| chr3:146198531
|
G | C | 149 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(146): Show | 177 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.624+1282C>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 6/8 | chr3 | 146198531 | ||||||
| chr3:146198629
|
A | C | 19 | a0001c0001t0007g0024a0001c0001t0007g0063a0001c0001t0009g0053others(16): Show | 21 | HG01255.hp1 HG01891.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.624+1184T>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 6/8 | chr3 | 146198629 | ||||||
| chr3:146198701
|
C | T | 1 | a0001c0001t0003g0256 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.624+1112G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 6/8 | chr3 | 146198701 | ||||||
| chr3:146198737
|
C | T | 1 | a0001c0001t0002g0141 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.624+1076G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 6/8 | chr3 | 146198737 | ||||||
| chr3:146198752
|
G | A | 1 | a0001c0001t0001g0010 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.624+1061C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 6/8 | chr3 | 146198752 | ||||||
| chr3:146198858
|
C | G | 19 | a0001c0001t0007g0024a0001c0001t0007g0063a0001c0001t0009g0053others(16): Show | 21 | HG01255.hp1 HG01891.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.624+955G>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 6/8 | chr3 | 146198858 | ||||||
| chr3:146198962
|
A | G | 19 | a0001c0001t0007g0024a0001c0001t0007g0063a0001c0001t0009g0053others(16): Show | 21 | HG01255.hp1 HG01891.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.624+851T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 6/8 | chr3 | 146198962 | ||||||
| chr3:146199210
|
A | G | 89 | a0001c0001t0003g0014a0001c0001t0003g0070a0001c0001t0003g0112others(86): Show | 111 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.624+603T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 6/8 | chr3 | 146199210 | ||||||
| chr3:146199731
|
T | C | 1 | a0001c0001t0001g0191 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.624+82A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 6/8 | chr3 | 146199731 | ||||||
| chr3:146199803
|
A | G | 7 | a0003c0003t0011g0005a0003c0003t0011g0044a0003c0003t0011g0046others(4): Show | 9 | HG01433.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.624+10T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 6/8 | chr3 | 146199803 | ||||||
| chr3:146200140
|
T | G | 9 | a0001c0001t0007g0024a0001c0001t0007g0063a0001c0001t0009g0053others(6): Show | 11 | HG02145.hp2 HG02257.hp2 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.398-101A>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 5/8 | chr3 | 146200140 | ||||||
| chr3:146200388
|
T | C | 19 | a0001c0001t0007g0024a0001c0001t0007g0063a0001c0001t0009g0053others(16): Show | 21 | HG01255.hp1 HG01891.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.398-349A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 5/8 | chr3 | 146200388 | ||||||
| chr3:146200524
|
T | C | 3 | a0001c0001t0006g0123a0001c0001t0006g0124a0001c0001t0009g0122 | 3 | HG01243.hp2 HG02109.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.398-485A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 5/8 | chr3 | 146200524 | ||||||
| chr3:146200712
|
C | G | 1 | a0001c0001t0001g0062 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.397+323G>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 5/8 | chr3 | 146200712 | ||||||
| chr3:146200756
|
T | C | 12 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0248others(9): Show | 17 | HG01358.hp1 HG02683.hp2 HG03669.hp1 others(14): Show |
intron_variant | MODIFIER | c.397+279A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 5/8 | chr3 | 146200756 | ||||||
| chr3:146200813
|
A | T | 1 | a0003c0003t0010g0160 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.397+222T>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 5/8 | chr3 | 146200813 | ||||||
| chr3:146200919
|
T | C | 2 | a0001c0001t0002g0072a0001c0001t0025g0071 | 2 | NA18946.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.397+116A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 5/8 | chr3 | 146200919 | ||||||
| chr3:146200976
|
G | C | 19 | a0001c0001t0007g0024a0001c0001t0007g0063a0001c0001t0009g0053others(16): Show | 21 | HG01255.hp1 HG01891.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.397+59C>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 5/8 | chr3 | 146200976 | ||||||
| chr3:146201160
|
T | C | 4 | a0001c0001t0001g0191a0001c0001t0001g0196a0001c0001t0003g0173others(1): Show | 4 | HG01069.hp1 HG01123.hp1 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.355-83A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 4/8 | chr3 | 146201160 | ||||||
| chr3:146201188
|
T | C | 1 | a0002c0002t0013g0305 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.355-111A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 4/8 | chr3 | 146201188 | ||||||
| chr3:146201470
|
C | T | 9 | a0001c0001t0007g0024a0001c0001t0007g0063a0001c0001t0009g0053others(6): Show | 11 | HG02145.hp2 HG02257.hp2 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.355-393G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 4/8 | chr3 | 146201470 | ||||||
| chr3:146201479
|
C | T | 19 | a0001c0001t0007g0024a0001c0001t0007g0063a0001c0001t0009g0053others(16): Show | 21 | HG01255.hp1 HG01891.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.355-402G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 4/8 | chr3 | 146201479 | ||||||
| chr3:146201611
|
T | G | 19 | a0001c0001t0007g0024a0001c0001t0007g0063a0001c0001t0009g0053others(16): Show | 21 | HG01255.hp1 HG01891.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.355-534A>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 4/8 | chr3 | 146201611 | ||||||
| chr3:146201620
|
T | C | 1 | a0001c0001t0001g0210 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.355-543A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 4/8 | chr3 | 146201620 | ||||||
| chr3:146201673
|
G | T | 7 | a0003c0003t0011g0005a0003c0003t0011g0044a0003c0003t0011g0046others(4): Show | 9 | HG01433.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.355-596C>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 4/8 | chr3 | 146201673 | ||||||
| chr3:146201776
|
A | C | 1 | a0001c0001t0015g0216 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.355-699T>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 4/8 | chr3 | 146201776 | ||||||
| chr3:146202056
|
C | T | 19 | a0001c0001t0007g0024a0001c0001t0007g0063a0001c0001t0009g0053others(16): Show | 21 | HG01255.hp1 HG01891.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.355-979G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 4/8 | chr3 | 146202056 | ||||||
| chr3:146202248
|
A | G | 19 | a0001c0001t0007g0024a0001c0001t0007g0063a0001c0001t0009g0053others(16): Show | 21 | HG01255.hp1 HG01891.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.355-1171T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 4/8 | chr3 | 146202248 | ||||||
| chr3:146202309
|
G | T | 214 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(211): Show | 259 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(256): Show |
intron_variant | MODIFIER | c.355-1232C>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 4/8 | chr3 | 146202309 | ||||||
| chr3:146202336
|
TG | T | 2 | a0001c0001t0001g0011a0001c0001t0003g0051 | 3 | HG02886.hp1 HG03209.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.355-1260delC | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 4/8 | chr3 | 146202336 | ||||||
| chr3:146202413
|
A | G | 1 | a0001c0001t0006g0192 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.355-1336T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 4/8 | chr3 | 146202413 | ||||||
| chr3:146202519
|
T | C | 1 | a0003c0003t0011g0048 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.355-1442A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 4/8 | chr3 | 146202519 | ||||||
| chr3:146202621
|
T | C | 18 | a0001c0001t0007g0024a0001c0001t0007g0063a0001c0001t0009g0053others(15): Show | 20 | HG01255.hp1 HG01891.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.355-1544A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 4/8 | chr3 | 146202621 | ||||||
| chr3:146202626
|
A | G | 4 | a0004c0004t0001g0152a0004c0004t0001g0153a0004c0004t0006g0154others(1): Show | 4 | HG02818.hp2 HG02970.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.355-1549T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 4/8 | chr3 | 146202626 | ||||||
| chr3:146202679
|
G | A | 1 | a0001c0001t0001g0010 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.355-1602C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 4/8 | chr3 | 146202679 | ||||||
| chr3:146202701
|
A | G | 1 | a0001c0001t0005g0182 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.355-1624T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 4/8 | chr3 | 146202701 | ||||||
| chr3:146202826
|
T | C | 18 | a0001c0001t0007g0024a0001c0001t0007g0063a0001c0001t0009g0053others(15): Show | 20 | HG01255.hp1 HG01891.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.355-1749A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 4/8 | chr3 | 146202826 | ||||||
| chr3:146202893
|
T | C | 213 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(210): Show | 258 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(255): Show |
intron_variant | MODIFIER | c.355-1816A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 4/8 | chr3 | 146202893 | ||||||
| chr3:146203053
|
T | C | 1 | a0001c0001t0002g0185 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.355-1976A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 4/8 | chr3 | 146203053 | ||||||
| chr3:146203076
|
C | T | 2 | a0001c0001t0009g0163a0001c0001t0022g0162 | 2 | HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.355-1999G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 4/8 | chr3 | 146203076 | ||||||
| chr3:146203197
|
C | G | 1 | a0001c0001t0003g0239 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.355-2120G>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 4/8 | chr3 | 146203197 | ||||||
| chr3:146203198
|
G | A | 90 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0028others(87): Show | 104 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.355-2121C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 4/8 | chr3 | 146203198 | ||||||
| chr3:146203339
|
ATG | A | 9 | a0001c0001t0007g0024a0001c0001t0007g0063a0001c0001t0009g0053others(6): Show | 11 | HG02145.hp2 HG02257.hp2 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.355-2264_355-2263d others(4): Show |
PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 4/8 | chr3 | 146203339 | ||||||
| chr3:146203358
|
T | C | 90 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0028others(87): Show | 104 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.355-2281A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 4/8 | chr3 | 146203358 | ||||||
| chr3:146203972
|
C | T | 1 | a0004c0004t0001g0153 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.354+2554G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 4/8 | chr3 | 146203972 | ||||||
| chr3:146204102
|
T | C | 224 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(221): Show | 269 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(266): Show |
intron_variant | MODIFIER | c.354+2424A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 4/8 | chr3 | 146204102 | ||||||
| chr3:146204160
|
T | G | 25 | a0001c0001t0001g0028a0001c0001t0001g0032a0001c0001t0001g0202others(22): Show | 31 | HG00099.hp1 HG00423.hp2 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.354+2366A>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 4/8 | chr3 | 146204160 | ||||||
| chr3:146204167
|
T | C | 223 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(220): Show | 268 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(265): Show |
intron_variant | MODIFIER | c.354+2359A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 4/8 | chr3 | 146204167 | ||||||
| chr3:146204183
|
A | C | 3 | a0001c0001t0001g0204a0001c0001t0017g0211a0001c0001t0017g0212 | 3 | HG00621.hp2 NA19002.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.354+2343T>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 4/8 | chr3 | 146204183 | ||||||
| chr3:146204183
|
A | G | 14 | a0001c0001t0001g0011a0001c0001t0001g0143a0001c0001t0001g0145others(11): Show | 20 | HG01358.hp1 HG02683.hp2 HG02886.hp1 others(17): Show |
intron_variant | MODIFIER | c.354+2343T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 4/8 | chr3 | 146204183 | ||||||
| chr3:146204220
|
T | C | 14 | a0001c0001t0001g0011a0001c0001t0001g0143a0001c0001t0001g0145others(11): Show | 20 | HG01358.hp1 HG02683.hp2 HG02886.hp1 others(17): Show |
intron_variant | MODIFIER | c.354+2306A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 4/8 | chr3 | 146204220 | ||||||
| chr3:146204277
|
A | G | 4 | a0004c0004t0001g0152a0004c0004t0001g0153a0004c0004t0006g0154others(1): Show | 4 | HG02818.hp2 HG02970.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.354+2249T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 4/8 | chr3 | 146204277 | ||||||
| chr3:146204443
|
G | A | 101 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0028others(98): Show | 115 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.354+2083C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 4/8 | chr3 | 146204443 | ||||||
| chr3:146204714
|
A | G | 3 | a0001c0001t0001g0210a0001c0001t0001g0215a0001c0001t0002g0209 | 3 | HG02683.hp1 HG03710.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.354+1812T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 4/8 | chr3 | 146204714 | ||||||
| chr3:146204973
|
A | G | 1 | a0001c0001t0007g0203 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.354+1553T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 4/8 | chr3 | 146204973 | ||||||
| chr3:146205018
|
G | C | 1 | a0002c0002t0001g0134 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.354+1508C>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 4/8 | chr3 | 146205018 | ||||||
| chr3:146205087
|
G | C | 127 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0027others(124): Show | 149 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.354+1439C>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 4/8 | chr3 | 146205087 | ||||||
| chr3:146205272
|
A | G | 1 | a0001c0001t0001g0010 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.354+1254T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 4/8 | chr3 | 146205272 | ||||||
| chr3:146205357
|
A | G | 108 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0028others(105): Show | 124 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.354+1169T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 4/8 | chr3 | 146205357 | ||||||
| chr3:146205479
|
C | A | 2 | a0001c0001t0001g0011a0001c0001t0003g0051 | 3 | HG02886.hp1 HG03209.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.354+1047G>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 4/8 | chr3 | 146205479 | ||||||
| chr3:146205480
|
A | C | 2 | a0001c0001t0001g0011a0001c0001t0003g0051 | 3 | HG02886.hp1 HG03209.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.354+1046T>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 4/8 | chr3 | 146205480 | ||||||
| chr3:146205536
|
A | C | 1 | a0001c0001t0017g0211 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.354+990T>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 4/8 | chr3 | 146205536 | ||||||
| chr3:146205624
|
G | A | 1 | a0002c0002t0001g0252 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.354+902C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 4/8 | chr3 | 146205624 | ||||||
| chr3:146205728
|
G | T | 2 | a0001c0001t0009g0163a0001c0001t0022g0162 | 2 | HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.354+798C>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 4/8 | chr3 | 146205728 | ||||||
| chr3:146205820
|
G | T | 1 | a0002c0002t0031g0275 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.354+706C>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 4/8 | chr3 | 146205820 | ||||||
| chr3:146205964
|
C | T | 17 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0248others(14): Show | 22 | HG01358.hp1 HG02630.hp2 HG02647.hp2 others(19): Show |
intron_variant | MODIFIER | c.354+562G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 4/8 | chr3 | 146205964 | ||||||
| chr3:146205969
|
A | G | 101 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0028others(98): Show | 115 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.354+557T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 4/8 | chr3 | 146205969 | ||||||
| chr3:146205976
|
T | A | 34 | a0001c0001t0001g0062a0001c0001t0001g0065a0001c0001t0001g0066others(31): Show | 40 | HG00408.hp2 HG00639.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.354+550A>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 4/8 | chr3 | 146205976 | ||||||
| chr3:146206113
|
G | A | 1 | a0001c0001t0009g0164 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.354+413C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 4/8 | chr3 | 146206113 | ||||||
| chr3:146206243
|
T | G | 2 | a0001c0001t0009g0163a0001c0001t0022g0162 | 2 | HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.354+283A>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 4/8 | chr3 | 146206243 | ||||||
| chr3:146206377
|
A | G | 1 | a0001c0001t0006g0192 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.354+149T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 4/8 | chr3 | 146206377 | ||||||
| chr3:146206482
|
T | C | 1 | a0005c0005t0015g0318 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.354+44A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 4/8 | chr3 | 146206482 | ||||||
| chr3:146206489
|
A | G | 6 | a0001c0001t0007g0024a0001c0001t0009g0053a0001c0001t0009g0164others(3): Show | 8 | HG02145.hp2 HG02895.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.354+37T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 4/8 | chr3 | 146206489 | ||||||
| chr3:146206796
|
T | A | 8 | a0002c0002t0001g0034a0002c0002t0001g0244a0002c0002t0001g0245others(5): Show | 10 | HG01074.hp1 HG01109.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.119-35A>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146206796 | ||||||
| chr3:146206797
|
T | C | 8 | a0002c0002t0001g0034a0002c0002t0001g0244a0002c0002t0001g0245others(5): Show | 10 | HG01074.hp1 HG01109.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.119-36A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146206797 | ||||||
| chr3:146206804
|
A | AT | 128 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0027others(125): Show | 150 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.119-44_119-43insA | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146206804 | ||||||
| chr3:146206845
|
C | T | 215 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(212): Show | 258 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(255): Show |
intron_variant | MODIFIER | c.119-84G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146206845 | ||||||
| chr3:146206871
|
G | A | 1 | a0002c0002t0016g0303 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.119-110C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146206871 | ||||||
| chr3:146207083
|
T | C | 1 | a0001c0001t0001g0221 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.119-322A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146207083 | ||||||
| chr3:146207193
|
G | T | 2 | a0002c0002t0007g0306a0002c0002t0026g0304 | 2 | HG01243.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.119-432C>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146207193 | ||||||
| chr3:146207295
|
G | C | 1 | a0002c0002t0006g0090 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.119-534C>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146207295 | ||||||
| chr3:146207323
|
C | T | 1 | a0001c0001t0001g0010 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.119-562G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146207323 | ||||||
| chr3:146207407
|
C | T | 17 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0248others(14): Show | 22 | HG01358.hp1 HG02630.hp2 HG02647.hp2 others(19): Show |
intron_variant | MODIFIER | c.119-646G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146207407 | ||||||
| chr3:146207440
|
TG | T | 17 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0248others(14): Show | 22 | HG01358.hp1 HG02630.hp2 HG02647.hp2 others(19): Show |
intron_variant | MODIFIER | c.119-680delC | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146207440 | ||||||
| chr3:146207516
|
T | C | 6 | a0003c0003t0010g0157a0003c0003t0010g0158a0003c0003t0010g0159others(3): Show | 6 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.119-755A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146207516 | ||||||
| chr3:146207554
|
C | G | 4 | a0002c0002t0002g0037a0002c0002t0002g0268a0002c0002t0002g0287others(1): Show | 5 | HG01070.hp1 HG01081.hp1 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.119-793G>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146207554 | ||||||
| chr3:146207679
|
G | A | 5 | a0001c0001t0001g0116a0001c0001t0005g0021a0001c0001t0005g0115others(2): Show | 6 | NA18979.hp2 NA18988.hp2 NA18990.hp1 others(3): Show |
intron_variant | MODIFIER | c.119-918C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146207679 | ||||||
| chr3:146207723
|
A | G | 1 | a0003c0003t0011g0044 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.119-962T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146207723 | ||||||
| chr3:146207785
|
T | C | 33 | a0001c0001t0001g0026a0001c0001t0001g0055a0001c0001t0001g0074others(30): Show | 37 | HG00544.hp1 HG00639.hp2 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.119-1024A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146207785 | ||||||
| chr3:146208319
|
T | C | 12 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0248others(9): Show | 17 | HG01358.hp1 HG02683.hp2 HG03669.hp1 others(14): Show |
intron_variant | MODIFIER | c.119-1558A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146208319 | ||||||
| chr3:146208433
|
A | C | 17 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0248others(14): Show | 22 | HG01358.hp1 HG02630.hp2 HG02647.hp2 others(19): Show |
intron_variant | MODIFIER | c.119-1672T>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146208433 | ||||||
| chr3:146208546
|
C | T | 5 | a0001c0001t0010g0149a0001c0001t0010g0151a0001c0001t0012g0147others(2): Show | 5 | HG02630.hp2 HG02647.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.119-1785G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146208546 | ||||||
| chr3:146208651
|
T | C | 215 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(212): Show | 258 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(255): Show |
intron_variant | MODIFIER | c.119-1890A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146208651 | ||||||
| chr3:146208912
|
G | A | 7 | a0003c0003t0011g0005a0003c0003t0011g0044a0003c0003t0011g0046others(4): Show | 9 | HG01433.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.119-2151C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146208912 | ||||||
| chr3:146208927
|
A | G | 1 | a0001c0001t0002g0140 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.119-2166T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146208927 | ||||||
| chr3:146208951
|
G | A | 2 | a0002c0002t0004g0035a0002c0002t0004g0263 | 3 | NA18994.hp2 NA19000.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.119-2190C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146208951 | ||||||
| chr3:146208952
|
C | T | 2 | a0002c0002t0004g0035a0002c0002t0004g0263 | 3 | NA18994.hp2 NA19000.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.119-2191G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146208952 | ||||||
| chr3:146208992
|
C | T | 109 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0027others(106): Show | 126 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.119-2231G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146208992 | ||||||
| chr3:146209262
|
G | A | 1 | a0001c0001t0001g0010 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.119-2501C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146209262 | ||||||
| chr3:146209336
|
G | A | 2 | a0001c0001t0001g0011a0001c0001t0003g0051 | 3 | HG02886.hp1 HG03209.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.119-2575C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146209336 | ||||||
| chr3:146209336
|
G | C | 1 | a0002c0002t0002g0267 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.119-2575C>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146209336 | ||||||
| chr3:146209363
|
C | G | 1 | a0001c0001t0002g0185 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.119-2602G>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146209363 | ||||||
| chr3:146209375
|
C | T | 1 | a0001c0001t0001g0054 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.119-2614G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146209375 | ||||||
| chr3:146209527
|
C | T | 1 | a0001c0001t0007g0139 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.119-2766G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146209527 | ||||||
| chr3:146209634
|
T | A | 2 | a0001c0001t0001g0011a0001c0001t0003g0051 | 3 | HG02886.hp1 HG03209.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.119-2873A>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146209634 | ||||||
| chr3:146209814
|
C | T | 17 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0248others(14): Show | 22 | HG01358.hp1 HG02630.hp2 HG02647.hp2 others(19): Show |
intron_variant | MODIFIER | c.119-3053G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146209814 | ||||||
| chr3:146209939
|
A | G | 1 | a0001c0001t0001g0010 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.119-3178T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146209939 | ||||||
| chr3:146209949
|
A | G | 2 | a0001c0001t0003g0006a0001c0001t0003g0180 | 4 | NA18939.hp1 NA18970.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.119-3188T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146209949 | ||||||
| chr3:146209971
|
G | A | 7 | a0003c0003t0011g0005a0003c0003t0011g0044a0003c0003t0011g0046others(4): Show | 9 | HG01433.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.119-3210C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146209971 | ||||||
| chr3:146209980
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.119-3219A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146209980 | ||||||
| chr3:146210189
|
T | C | 5 | a0001c0001t0012g0299a0004c0004t0001g0152a0004c0004t0001g0153others(2): Show | 5 | HG02818.hp2 HG02896.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.119-3428A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146210189 | ||||||
| chr3:146210192
|
C | T | 12 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0248others(9): Show | 17 | HG01358.hp1 HG02683.hp2 HG03669.hp1 others(14): Show |
intron_variant | MODIFIER | c.119-3431G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146210192 | ||||||
| chr3:146210265
|
T | C | 6 | a0003c0003t0006g0012a0003c0003t0010g0310a0003c0003t0012g0311others(3): Show | 7 | HG02109.hp2 HG02615.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.119-3504A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146210265 | ||||||
| chr3:146210381
|
G | T | 1 | a0001c0001t0001g0065 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.119-3620C>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146210381 | ||||||
| chr3:146210524
|
A | G | 1 | a0003c0003t0012g0311 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.119-3763T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146210524 | ||||||
| chr3:146210601
|
C | T | 2 | a0001c0001t0001g0081a0001c0001t0002g0082 | 2 | HG03942.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.119-3840G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146210601 | ||||||
| chr3:146210627
|
AAATGTAC | A | 76 | a0002c0002t0001g0034a0002c0002t0001g0036a0002c0002t0001g0038others(73): Show | 96 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.119-3873_119-3867d others(9): Show |
PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146210627 | ||||||
| chr3:146210699
|
T | A | 110 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0027others(107): Show | 127 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.119-3938A>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146210699 | ||||||
| chr3:146210847
|
G | GT | 7 | a0001c0001t0001g0054a0001c0001t0007g0024a0001c0001t0009g0053others(4): Show | 9 | HG02145.hp2 HG02895.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.119-4087dupA | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146210847 | ||||||
| chr3:146210847
|
GT | G | 115 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0027others(112): Show | 132 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.119-4087delA | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146210847 | ||||||
| chr3:146210847
|
GTT | G | 12 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0248others(9): Show | 17 | HG01358.hp1 HG02683.hp2 HG03669.hp1 others(14): Show |
intron_variant | MODIFIER | c.119-4088_119-4087d others(4): Show |
PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146210847 | ||||||
| chr3:146210869
|
T | G | 4 | a0004c0004t0001g0152a0004c0004t0001g0153a0004c0004t0006g0154others(1): Show | 4 | HG02818.hp2 HG02970.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.119-4108A>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146210869 | ||||||
| chr3:146211060
|
G | A | 101 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0028others(98): Show | 115 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.119-4299C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146211060 | ||||||
| chr3:146211063
|
C | CAT | 116 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(113): Show | 134 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.119-4304_119-4303d others(4): Show |
PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146211063 | ||||||
| chr3:146211086
|
G | C | 8 | a0002c0002t0003g0307a0002c0002t0006g0090a0002c0002t0007g0306others(5): Show | 8 | HG01243.hp1 HG02572.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.119-4325C>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146211086 | ||||||
| chr3:146211129
|
C | T | 101 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0028others(98): Show | 115 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.119-4368G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146211129 | ||||||
| chr3:146211163
|
T | C | 82 | a0002c0002t0001g0034a0002c0002t0001g0036a0002c0002t0001g0038others(79): Show | 102 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.119-4402A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146211163 | ||||||
| chr3:146211203
|
C | T | 1 | a0001c0001t0013g0059 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.119-4442G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146211203 | ||||||
| chr3:146211380
|
C | T | 110 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0027others(107): Show | 127 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.119-4619G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146211380 | ||||||
| chr3:146211393
|
T | G | 2 | a0001c0001t0001g0011a0001c0001t0003g0051 | 3 | HG02886.hp1 HG03209.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.119-4632A>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146211393 | ||||||
| chr3:146211471
|
G | C | 1 | a0001c0001t0001g0174 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.119-4710C>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146211471 | ||||||
| chr3:146211528
|
A | T | 2 | a0001c0001t0009g0163a0001c0001t0022g0162 | 2 | HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.119-4767T>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146211528 | ||||||
| chr3:146211591
|
G | A | 5 | a0001c0001t0012g0299a0004c0004t0001g0152a0004c0004t0001g0153others(2): Show | 5 | HG02818.hp2 HG02896.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.119-4830C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146211591 | ||||||
| chr3:146211619
|
C | A | 2 | a0001c0001t0009g0163a0001c0001t0022g0162 | 2 | HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.119-4858G>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146211619 | ||||||
| chr3:146211749
|
T | A | 12 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0248others(9): Show | 17 | HG01358.hp1 HG02683.hp2 HG03669.hp1 others(14): Show |
intron_variant | MODIFIER | c.119-4988A>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146211749 | ||||||
| chr3:146211842
|
T | G | 3 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0020g0050 | 3 | HG02055.hp1 HG02630.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.119-5081A>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146211842 | ||||||
| chr3:146211883
|
T | C | 4 | a0004c0004t0001g0152a0004c0004t0001g0153a0004c0004t0006g0154others(1): Show | 4 | HG02818.hp2 HG02970.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.119-5122A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146211883 | ||||||
| chr3:146211956
|
T | A | 1 | a0001c0001t0001g0061 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.119-5195A>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146211956 | ||||||
| chr3:146212057
|
A | G | 17 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0248others(14): Show | 22 | HG01358.hp1 HG02630.hp2 HG02647.hp2 others(19): Show |
intron_variant | MODIFIER | c.119-5296T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146212057 | ||||||
| chr3:146212230
|
T | C | 3 | a0001c0001t0006g0123a0001c0001t0006g0124a0001c0001t0009g0122 | 3 | HG01243.hp2 HG02109.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.119-5469A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146212230 | ||||||
| chr3:146212280
|
T | C | 110 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0027others(107): Show | 127 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.119-5519A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146212280 | ||||||
| chr3:146212348
|
T | C | 2 | a0001c0001t0001g0011a0001c0001t0003g0051 | 3 | HG02886.hp1 HG03209.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.119-5587A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146212348 | ||||||
| chr3:146212399
|
T | TTGTGCTG | 6 | a0003c0003t0010g0157a0003c0003t0010g0158a0003c0003t0010g0159others(3): Show | 6 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.119-5645_119-5639d others(9): Show |
PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146212399 | ||||||
| chr3:146212432
|
G | T | 5 | a0003c0003t0010g0157a0003c0003t0010g0158a0003c0003t0010g0160others(2): Show | 5 | HG01255.hp1 HG01891.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.119-5671C>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146212432 | ||||||
| chr3:146212437
|
G | GT | 289 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(286): Show | 344 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(341): Show |
intron_variant | MODIFIER | c.119-5677dupA | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146212437 | ||||||
| chr3:146212456
|
G | GT | 16 | a0001c0001t0001g0011a0001c0001t0001g0098a0001c0001t0002g0072others(13): Show | 19 | HG01109.hp2 HG01255.hp1 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.119-5696dupA | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146212456 | ||||||
| chr3:146212456
|
G | GTT | 99 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0028others(96): Show | 113 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.119-5697_119-5696d others(4): Show |
PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146212456 | ||||||
| chr3:146212459
|
T | TC | 8 | a0002c0002t0003g0307a0002c0002t0006g0090a0002c0002t0007g0306others(5): Show | 8 | HG01243.hp1 HG02572.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.119-5699_119-5698i others(3): Show |
PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146212459 | ||||||
| chr3:146212469
|
T | A | 8 | a0002c0002t0003g0307a0002c0002t0006g0090a0002c0002t0007g0306others(5): Show | 8 | HG01243.hp1 HG02572.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.119-5708A>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146212469 | ||||||
| chr3:146212920
|
A | G | 1 | a0001c0001t0001g0191 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.119-6159T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146212920 | ||||||
| chr3:146212964
|
G | A | 1 | a0001c0001t0001g0010 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.119-6203C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146212964 | ||||||
| chr3:146213147
|
C | T | 223 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(220): Show | 268 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(265): Show |
intron_variant | MODIFIER | c.119-6386G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146213147 | ||||||
| chr3:146213334
|
C | CTTTTT | 21 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0184others(18): Show | 26 | HG01106.hp1 HG01358.hp1 HG02630.hp2 others(23): Show |
intron_variant | MODIFIER | c.119-6578_119-6574d others(7): Show |
PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146213334 | ||||||
| chr3:146213334
|
C | CTTTTTT | 93 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0027others(90): Show | 108 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.119-6579_119-6574d others(8): Show |
PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146213334 | ||||||
| chr3:146213334
|
C | CTTTTTTT | 11 | a0001c0001t0001g0199a0001c0001t0001g0202a0001c0001t0001g0230others(8): Show | 13 | HG00423.hp2 HG01433.hp1 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.119-6580_119-6574d others(9): Show |
PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146213334 | ||||||
| chr3:146213334
|
CT | C | 6 | a0001c0001t0001g0010a0001c0001t0003g0088a0001c0001t0003g0112others(3): Show | 7 | HG01255.hp1 HG02145.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.119-6574delA | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146213334 | ||||||
| chr3:146213357
|
T | C | 2 | a0001c0001t0001g0186a0001c0001t0001g0219 | 2 | HG01109.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.119-6596A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146213357 | ||||||
| chr3:146213370
|
C | T | 1 | a0002c0002t0005g0293 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.119-6609G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146213370 | ||||||
| chr3:146213387
|
A | G | 1 | a0001c0001t0009g0163 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.119-6626T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146213387 | ||||||
| chr3:146213451
|
T | C | 215 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(212): Show | 258 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(255): Show |
intron_variant | MODIFIER | c.119-6690A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146213451 | ||||||
| chr3:146213618
|
C | T | 1 | a0001c0001t0013g0058 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.119-6857G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146213618 | ||||||
| chr3:146213793
|
C | A | 17 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0248others(14): Show | 22 | HG01358.hp1 HG02630.hp2 HG02647.hp2 others(19): Show |
intron_variant | MODIFIER | c.118+7022G>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146213793 | ||||||
| chr3:146213908
|
GTTTTAT | G | 4 | a0004c0004t0001g0152a0004c0004t0001g0153a0004c0004t0006g0154others(1): Show | 4 | HG02818.hp2 HG02970.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.118+6901_118+6906d others(8): Show |
PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146213908 | ||||||
| chr3:146213975
|
A | G | 60 | a0002c0002t0001g0034a0002c0002t0001g0036a0002c0002t0001g0038others(57): Show | 79 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.118+6840T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146213975 | ||||||
| chr3:146214111
|
ATCTTCCT others(305): Show |
A | 223 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(220): Show | 268 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(265): Show |
intron_variant | MODIFIER | c.118+6392_118+6703d others(2): Show |
PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146214111 | ||||||
| chr3:146214117
|
C | CT | 6 | a0001c0001t0001g0081a0001c0001t0001g0114a0001c0001t0001g0166others(3): Show | 6 | HG01168.hp2 HG02071.hp2 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.118+6697dupA | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146214117 | ||||||
| chr3:146214134
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.118+6681A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146214134 | ||||||
| chr3:146214438
|
T | C | 4 | a0003c0003t0010g0310a0003c0003t0012g0311a0003c0003t0015g0308others(1): Show | 4 | HG02109.hp2 HG02615.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.118+6377A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146214438 | ||||||
| chr3:146214612
|
G | A | 5 | a0001c0001t0010g0149a0001c0001t0010g0151a0001c0001t0012g0147others(2): Show | 5 | HG02630.hp2 HG02647.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.118+6203C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146214612 | ||||||
| chr3:146214787
|
G | A | 2 | a0001c0001t0003g0006a0001c0001t0003g0180 | 4 | NA18939.hp1 NA18970.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.118+6028C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146214787 | ||||||
| chr3:146214902
|
T | A | 2 | a0001c0001t0003g0018a0001c0001t0003g0088 | 3 | HG00099.hp2 HG00741.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.118+5913A>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146214902 | ||||||
| chr3:146214977
|
C | T | 215 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(212): Show | 258 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(255): Show |
intron_variant | MODIFIER | c.118+5838G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146214977 | ||||||
| chr3:146215272
|
G | A | 12 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0248others(9): Show | 17 | HG01358.hp1 HG02683.hp2 HG03669.hp1 others(14): Show |
intron_variant | MODIFIER | c.118+5543C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146215272 | ||||||
| chr3:146215303
|
C | T | 223 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(220): Show | 268 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(265): Show |
intron_variant | MODIFIER | c.118+5512G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146215303 | ||||||
| chr3:146215379
|
C | G | 4 | a0002c0002t0001g0034a0002c0002t0001g0244a0002c0002t0001g0245others(1): Show | 5 | HG01074.hp1 HG01109.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.118+5436G>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146215379 | ||||||
| chr3:146215570
|
G | A | 1 | a0002c0002t0002g0268 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.118+5245C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146215570 | ||||||
| chr3:146215599
|
A | G | 1 | a0001c0001t0001g0077 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.118+5216T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146215599 | ||||||
| chr3:146215636
|
TG | T | 8 | a0001c0001t0009g0163a0001c0001t0022g0162a0003c0003t0010g0157others(5): Show | 8 | HG01255.hp1 HG01891.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.118+5178delC | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146215636 | ||||||
| chr3:146215698
|
T | C | 103 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0027others(100): Show | 118 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.118+5117A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146215698 | ||||||
| chr3:146215748
|
C | G | 2 | a0001c0001t0009g0163a0001c0001t0022g0162 | 2 | HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.118+5067G>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146215748 | ||||||
| chr3:146215817
|
C | T | 1 | a0002c0002t0004g0290 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.118+4998G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146215817 | ||||||
| chr3:146215861
|
A | G | 215 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(212): Show | 258 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(255): Show |
intron_variant | MODIFIER | c.118+4954T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146215861 | ||||||
| chr3:146215916
|
G | A | 4 | a0004c0004t0001g0152a0004c0004t0001g0153a0004c0004t0006g0154others(1): Show | 4 | HG02818.hp2 HG02970.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.118+4899C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146215916 | ||||||
| chr3:146215948
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.118+4867G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146215948 | ||||||
| chr3:146215990
|
G | A | 17 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0248others(14): Show | 22 | HG01358.hp1 HG02630.hp2 HG02647.hp2 others(19): Show |
intron_variant | MODIFIER | c.118+4825C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146215990 | ||||||
| chr3:146215997
|
G | A | 103 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0027others(100): Show | 118 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.118+4818C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146215997 | ||||||
| chr3:146216002
|
G | A | 5 | a0001c0001t0010g0149a0001c0001t0010g0151a0001c0001t0012g0147others(2): Show | 5 | HG02630.hp2 HG02647.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.118+4813C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146216002 | ||||||
| chr3:146216087
|
G | A | 1 | a0002c0002t0002g0294 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.118+4728C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146216087 | ||||||
| chr3:146216155
|
C | T | 6 | a0003c0003t0006g0012a0003c0003t0010g0310a0003c0003t0012g0311others(3): Show | 7 | HG02109.hp2 HG02615.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.118+4660G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146216155 | ||||||
| chr3:146216163
|
G | A | 4 | a0001c0001t0001g0233a0001c0001t0003g0051a0001c0001t0004g0232others(1): Show | 4 | NA18950.hp2 NA18951.hp1 NA19078.hp2 others(1): Show |
intron_variant | MODIFIER | c.118+4652C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146216163 | ||||||
| chr3:146216232
|
A | AAAAC | 6 | a0003c0003t0006g0012a0003c0003t0010g0310a0003c0003t0012g0311others(3): Show | 7 | HG02109.hp2 HG02615.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.118+4579_118+4582d others(6): Show |
PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146216232 | ||||||
| chr3:146216405
|
G | A | 1 | a0002c0002t0002g0269 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.118+4410C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146216405 | ||||||
| chr3:146216431
|
T | TA | 33 | a0001c0001t0001g0062a0001c0001t0001g0065a0001c0001t0001g0066others(30): Show | 39 | HG00408.hp2 HG00639.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.118+4383dupT | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146216431 | ||||||
| chr3:146216432
|
A | T | 58 | a0002c0002t0001g0034a0002c0002t0001g0036a0002c0002t0001g0038others(55): Show | 77 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.118+4383T>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146216432 | ||||||
| chr3:146216507
|
G | A | 103 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0027others(100): Show | 118 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.118+4308C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146216507 | ||||||
| chr3:146216530
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.118+4285A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146216530 | ||||||
| chr3:146216558
|
C | T | 1 | a0001c0001t0001g0010 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.118+4257G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146216558 | ||||||
| chr3:146216701
|
T | C | 1 | a0001c0001t0001g0010 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.118+4114A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146216701 | ||||||
| chr3:146216738
|
AC | A | 103 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0027others(100): Show | 118 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.118+4076delG | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146216738 | ||||||
| chr3:146216792
|
C | T | 5 | a0001c0001t0010g0149a0001c0001t0010g0151a0001c0001t0012g0147others(2): Show | 5 | HG02630.hp2 HG02647.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.118+4023G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146216792 | ||||||
| chr3:146216807
|
T | C | 1 | a0002c0002t0007g0306 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.118+4008A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146216807 | ||||||
| chr3:146216849
|
C | T | 1 | a0001c0001t0001g0010 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.118+3966G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146216849 | ||||||
| chr3:146216978
|
C | A | 2 | a0003c0003t0001g0300a0003c0003t0001g0301 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.118+3837G>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146216978 | ||||||
| chr3:146217006
|
T | C | 214 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0027others(211): Show | 256 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(253): Show |
intron_variant | MODIFIER | c.118+3809A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146217006 | ||||||
| chr3:146217351
|
C | T | 1 | a0001c0001t0001g0080 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.118+3464G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146217351 | ||||||
| chr3:146217376
|
G | A | 17 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0248others(14): Show | 22 | HG01358.hp1 HG02630.hp2 HG02647.hp2 others(19): Show |
intron_variant | MODIFIER | c.118+3439C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146217376 | ||||||
| chr3:146217717
|
G | A | 3 | a0001c0001t0001g0210a0001c0001t0001g0215a0001c0001t0002g0209 | 3 | HG02683.hp1 HG03710.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.118+3098C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146217717 | ||||||
| chr3:146217737
|
T | C | 8 | a0001c0001t0007g0024a0001c0001t0009g0053a0001c0001t0009g0163others(5): Show | 10 | HG02145.hp2 HG02257.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.118+3078A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146217737 | ||||||
| chr3:146217898
|
A | G | 6 | a0003c0003t0006g0012a0003c0003t0010g0310a0003c0003t0012g0311others(3): Show | 7 | HG02109.hp2 HG02615.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.118+2917T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146217898 | ||||||
| chr3:146218013
|
A | G | 17 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0248others(14): Show | 22 | HG01358.hp1 HG02630.hp2 HG02647.hp2 others(19): Show |
intron_variant | MODIFIER | c.118+2802T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146218013 | ||||||
| chr3:146218027
|
C | T | 8 | a0001c0001t0007g0024a0001c0001t0009g0053a0001c0001t0009g0163others(5): Show | 10 | HG02145.hp2 HG02257.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.118+2788G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146218027 | ||||||
| chr3:146218033
|
T | A | 1 | a0001c0001t0001g0010 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.118+2782A>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146218033 | ||||||
| chr3:146218109
|
A | G | 218 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(215): Show | 264 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(261): Show |
intron_variant | MODIFIER | c.118+2706T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146218109 | ||||||
| chr3:146218134
|
GA | G | 6 | a0003c0003t0010g0157a0003c0003t0010g0158a0003c0003t0010g0159others(3): Show | 6 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.118+2680delT | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146218134 | ||||||
| chr3:146218279
|
T | A | 106 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0027others(103): Show | 124 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.118+2536A>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146218279 | ||||||
| chr3:146218325
|
T | G | 106 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0027others(103): Show | 124 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.118+2490A>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146218325 | ||||||
| chr3:146218362
|
T | G | 106 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0027others(103): Show | 124 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.118+2453A>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146218362 | ||||||
| chr3:146218535
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.118+2280A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146218535 | ||||||
| chr3:146218541
|
A | G | 226 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(223): Show | 274 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(271): Show |
intron_variant | MODIFIER | c.118+2274T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146218541 | ||||||
| chr3:146218760
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.118+2055G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146218760 | ||||||
| chr3:146218765
|
C | A | 1 | a0001c0001t0001g0010 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.118+2050G>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146218765 | ||||||
| chr3:146218778
|
A | G | 1 | a0001c0001t0001g0010 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.118+2037T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146218778 | ||||||
| chr3:146218821
|
T | A | 103 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0027others(100): Show | 118 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.118+1994A>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146218821 | ||||||
| chr3:146218875
|
A | G | 1 | a0001c0001t0005g0110 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.118+1940T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146218875 | ||||||
| chr3:146218939
|
A | G | 94 | a0001c0001t0012g0299a0002c0002t0001g0034a0002c0002t0001g0036others(91): Show | 116 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.118+1876T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146218939 | ||||||
| chr3:146218991
|
T | C | 6 | a0003c0003t0006g0012a0003c0003t0010g0310a0003c0003t0012g0311others(3): Show | 7 | HG02109.hp2 HG02615.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.118+1824A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146218991 | ||||||
| chr3:146219047
|
A | C | 223 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(220): Show | 268 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(265): Show |
intron_variant | MODIFIER | c.118+1768T>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146219047 | ||||||
| chr3:146219159
|
A | G | 5 | a0001c0001t0010g0149a0001c0001t0010g0151a0001c0001t0012g0147others(2): Show | 5 | HG02630.hp2 HG02647.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.118+1656T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146219159 | ||||||
| chr3:146219335
|
G | A | 1 | a0001c0001t0001g0199 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.118+1480C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146219335 | ||||||
| chr3:146219376
|
C | G | 103 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0027others(100): Show | 118 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.118+1439G>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146219376 | ||||||
| chr3:146219378
|
T | C | 89 | a0002c0002t0001g0034a0002c0002t0001g0036a0002c0002t0001g0038others(86): Show | 111 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.118+1437A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146219378 | ||||||
| chr3:146219421
|
A | G | 7 | a0003c0003t0011g0005a0003c0003t0011g0044a0003c0003t0011g0046others(4): Show | 9 | HG01433.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.118+1394T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146219421 | ||||||
| chr3:146219477
|
C | A | 4 | a0004c0004t0001g0152a0004c0004t0001g0153a0004c0004t0006g0154others(1): Show | 4 | HG02818.hp2 HG02970.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.118+1338G>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146219477 | ||||||
| chr3:146219599
|
G | C | 1 | a0001c0001t0003g0180 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.118+1216C>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146219599 | ||||||
| chr3:146219621
|
C | A | 1 | a0001c0001t0001g0010 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.118+1194G>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146219621 | ||||||
| chr3:146219749
|
T | A | 103 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0027others(100): Show | 118 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.118+1066A>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146219749 | ||||||
| chr3:146219797
|
G | A | 1 | a0001c0001t0001g0010 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.118+1018C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146219797 | ||||||
| chr3:146219869
|
G | A | 2 | a0001c0001t0017g0211a0001c0001t0017g0212 | 2 | NA19002.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.118+946C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146219869 | ||||||
| chr3:146220016
|
A | T | 5 | a0001c0001t0010g0149a0001c0001t0010g0151a0001c0001t0012g0147others(2): Show | 5 | HG02630.hp2 HG02647.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.118+799T>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146220016 | ||||||
| chr3:146220062
|
A | T | 1 | a0004c0004t0001g0152 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.118+753T>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146220062 | ||||||
| chr3:146220209
|
A | G | 4 | a0004c0004t0001g0152a0004c0004t0001g0153a0004c0004t0006g0154others(1): Show | 4 | HG02818.hp2 HG02970.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.118+606T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146220209 | ||||||
| chr3:146220653
|
T | A | 1 | a0001c0001t0002g0033 | 2 | HG02165.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.118+162A>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146220653 | ||||||
| chr3:146220694
|
T | C | 95 | a0001c0001t0001g0010a0002c0002t0001g0034a0002c0002t0001g0036others(92): Show | 118 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(115): Show |
intron_variant | MODIFIER | c.118+121A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146220694 | ||||||
| chr3:146220741
|
C | A | 223 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(220): Show | 268 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(265): Show |
intron_variant | MODIFIER | c.118+74G>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 3/8 | chr3 | 146220741 | ||||||
| chr3:146220995
|
C | T | 90 | a0001c0001t0001g0010a0002c0002t0001g0034a0002c0002t0001g0036others(87): Show | 113 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.8-70G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 2/8 | chr3 | 146220995 | ||||||
| chr3:146221024
|
T | C | 6 | a0003c0003t0010g0157a0003c0003t0010g0158a0003c0003t0010g0159others(3): Show | 6 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.8-99A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 2/8 | chr3 | 146221024 | ||||||
| chr3:146221159
|
T | A | 90 | a0002c0002t0001g0034a0002c0002t0001g0036a0002c0002t0001g0038others(87): Show | 112 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.8-234A>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 2/8 | chr3 | 146221159 | ||||||
| chr3:146221202
|
G | A | 90 | a0002c0002t0001g0034a0002c0002t0001g0036a0002c0002t0001g0038others(87): Show | 112 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.8-277C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 2/8 | chr3 | 146221202 | ||||||
| chr3:146221253
|
T | A | 91 | a0001c0001t0001g0010a0002c0002t0001g0034a0002c0002t0001g0036others(88): Show | 114 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.8-328A>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 2/8 | chr3 | 146221253 | ||||||
| chr3:146221261
|
T | A | 91 | a0001c0001t0001g0010a0002c0002t0001g0034a0002c0002t0001g0036others(88): Show | 114 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.8-336A>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 2/8 | chr3 | 146221261 | ||||||
| chr3:146221286
|
A | C | 1 | a0001c0001t0001g0010 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.8-361T>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 2/8 | chr3 | 146221286 | ||||||
| chr3:146221376
|
G | C | 60 | a0002c0002t0001g0034a0002c0002t0001g0036a0002c0002t0001g0038others(57): Show | 79 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.8-451C>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 2/8 | chr3 | 146221376 | ||||||
| chr3:146221580
|
C | CA | 119 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0027others(116): Show | 139 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.7+484dupT | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 2/8 | chr3 | 146221580 | ||||||
| chr3:146221630
|
A | C | 6 | a0001c0001t0001g0283a0001c0001t0003g0272a0001c0001t0006g0261others(3): Show | 6 | HG02886.hp2 HG03209.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.7+435T>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 2/8 | chr3 | 146221630 | ||||||
| chr3:146221782
|
CTTT | C | 12 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0248others(9): Show | 17 | HG01358.hp1 HG02683.hp2 HG03669.hp1 others(14): Show |
intron_variant | MODIFIER | c.7+280_7+282delAAA | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 2/8 | chr3 | 146221782 | ||||||
| chr3:146221802
|
T | G | 2 | a0001c0001t0009g0163a0001c0001t0022g0162 | 2 | HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.7+263A>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 2/8 | chr3 | 146221802 | ||||||
| chr3:146221904
|
C | T | 210 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(207): Show | 253 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(250): Show |
intron_variant | MODIFIER | c.7+161G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 2/8 | chr3 | 146221904 | ||||||
| chr3:146221945
|
A | G | 5 | a0001c0001t0012g0299a0004c0004t0001g0152a0004c0004t0001g0153others(2): Show | 5 | HG02818.hp2 HG02896.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.7+120T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 2/8 | chr3 | 146221945 | ||||||
| chr3:146221968
|
C | CA | 58 | a0002c0002t0001g0034a0002c0002t0001g0036a0002c0002t0001g0038others(55): Show | 77 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.7+96dupT | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 2/8 | chr3 | 146221968 | ||||||
| chr3:146221989
|
T | G | 96 | a0001c0001t0001g0010a0001c0001t0012g0299a0002c0002t0001g0034others(93): Show | 119 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.7+76A>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 2/8 | chr3 | 146221989 | ||||||
| chr3:146222060
|
C | G | 2 | a0001c0001t0001g0222a0001c0001t0005g0201 | 2 | HG00597.hp1 HG02040.hp2 |
splice_region_variant&intron_variant | LOW | c.7+5G>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 2/8 | chr3 | 146222060 | ||||||
| chr3:146222105
|
A | C | 1 | a0001c0001t0001g0010 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-21-13T>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146222105 | ||||||
| chr3:146222129
|
T | C | 4 | a0001c0001t0001g0145a0001c0001t0001g0248a0001c0001t0002g0146others(1): Show | 4 | HG01358.hp1 HG02683.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.-21-37A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146222129 | ||||||
| chr3:146222264
|
A | C | 60 | a0002c0002t0001g0034a0002c0002t0001g0036a0002c0002t0001g0038others(57): Show | 79 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.-21-172T>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146222264 | ||||||
| chr3:146222276
|
G | A | 83 | a0002c0002t0001g0034a0002c0002t0001g0036a0002c0002t0001g0038others(80): Show | 103 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.-21-184C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146222276 | ||||||
| chr3:146222352
|
A | T | 7 | a0001c0001t0001g0093a0001c0001t0007g0024a0001c0001t0009g0053others(4): Show | 9 | HG02027.hp1 HG02145.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-21-260T>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146222352 | ||||||
| chr3:146222378
|
T | G | 12 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0248others(9): Show | 17 | HG01358.hp1 HG02683.hp2 HG03669.hp1 others(14): Show |
intron_variant | MODIFIER | c.-21-286A>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146222378 | ||||||
| chr3:146222462
|
A | C | 1 | a0002c0002t0002g0262 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-21-370T>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146222462 | ||||||
| chr3:146222474
|
G | A | 1 | a0001c0001t0004g0084 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-21-382C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146222474 | ||||||
| chr3:146222496
|
C | G | 215 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(212): Show | 258 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(255): Show |
intron_variant | MODIFIER | c.-21-404G>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146222496 | ||||||
| chr3:146222589
|
A | T | 223 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(220): Show | 268 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(265): Show |
intron_variant | MODIFIER | c.-21-497T>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146222589 | ||||||
| chr3:146222681
|
G | A | 1 | a0001c0001t0001g0010 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-21-589C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146222681 | ||||||
| chr3:146222786
|
T | C | 96 | a0001c0001t0001g0010a0001c0001t0012g0299a0002c0002t0001g0034others(93): Show | 119 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.-21-694A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146222786 | ||||||
| chr3:146222938
|
A | T | 1 | a0002c0002t0002g0249 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-21-846T>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146222938 | ||||||
| chr3:146223077
|
G | A | 1 | a0001c0001t0003g0200 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-21-985C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146223077 | ||||||
| chr3:146223099
|
C | CATGTT | 223 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(220): Show | 268 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(265): Show |
intron_variant | MODIFIER | c.-21-1012_-21-1008d others(7): Show |
PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146223099 | ||||||
| chr3:146223175
|
A | G | 100 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0028others(97): Show | 114 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.-21-1083T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146223175 | ||||||
| chr3:146223182
|
A | C | 1 | a0002c0002t0006g0295 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-21-1090T>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146223182 | ||||||
| chr3:146223198
|
C | T | 6 | a0001c0001t0001g0027a0001c0001t0001g0188a0001c0001t0003g0187others(3): Show | 8 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.-21-1106G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146223198 | ||||||
| chr3:146223233
|
T | A | 96 | a0001c0001t0001g0010a0001c0001t0012g0299a0002c0002t0001g0034others(93): Show | 119 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.-21-1141A>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146223233 | ||||||
| chr3:146223377
|
T | C | 1 | a0001c0001t0009g0163 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-21-1285A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146223377 | ||||||
| chr3:146223402
|
C | T | 213 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(210): Show | 255 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(252): Show |
intron_variant | MODIFIER | c.-21-1310G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146223402 | ||||||
| chr3:146223416
|
TAAC | T | 90 | a0002c0002t0001g0034a0002c0002t0001g0036a0002c0002t0001g0038others(87): Show | 112 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.-21-1327_-21-1325d others(5): Show |
PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146223416 | ||||||
| chr3:146223429
|
A | C | 1 | a0001c0001t0003g0064 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-21-1337T>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146223429 | ||||||
| chr3:146223474
|
T | TA | 8 | a0001c0001t0007g0024a0001c0001t0009g0053a0001c0001t0009g0163others(5): Show | 10 | HG02145.hp2 HG02257.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.-21-1383dupT | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146223474 | ||||||
| chr3:146223477
|
G | T | 8 | a0001c0001t0007g0024a0001c0001t0009g0053a0001c0001t0009g0163others(5): Show | 10 | HG02145.hp2 HG02257.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.-21-1385C>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146223477 | ||||||
| chr3:146223502
|
C | A | 2 | a0001c0001t0001g0060a0001c0001t0004g0120 | 2 | NA18946.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.-21-1410G>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146223502 | ||||||
| chr3:146223558
|
G | A | 1 | a0001c0001t0006g0123 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-21-1466C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146223558 | ||||||
| chr3:146223610
|
T | G | 1 | a0001c0001t0001g0220 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-21-1518A>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146223610 | ||||||
| chr3:146223774
|
C | T | 1 | a0001c0001t0001g0080 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-21-1682G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146223774 | ||||||
| chr3:146223790
|
A | G | 1 | a0001c0001t0002g0138 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-21-1698T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146223790 | ||||||
| chr3:146223821
|
C | T | 223 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(220): Show | 268 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(265): Show |
intron_variant | MODIFIER | c.-21-1729G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146223821 | ||||||
| chr3:146223834
|
T | C | 1 | a0001c0001t0001g0010 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-21-1742A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146223834 | ||||||
| chr3:146223847
|
AAT | A | 96 | a0001c0001t0001g0010a0001c0001t0012g0299a0002c0002t0001g0034others(93): Show | 119 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.-21-1757_-21-1756d others(4): Show |
PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146223847 | ||||||
| chr3:146223870
|
ATATAT | A | 96 | a0001c0001t0001g0010a0001c0001t0012g0299a0002c0002t0001g0034others(93): Show | 119 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.-21-1783_-21-1779d others(7): Show |
PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146223870 | ||||||
| chr3:146223925
|
A | G | 96 | a0001c0001t0001g0010a0001c0001t0012g0299a0002c0002t0001g0034others(93): Show | 119 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.-21-1833T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146223925 | ||||||
| chr3:146223953
|
A | C | 96 | a0001c0001t0001g0010a0001c0001t0012g0299a0002c0002t0001g0034others(93): Show | 119 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.-21-1861T>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146223953 | ||||||
| chr3:146223958
|
ATATT | A | 95 | a0001c0001t0012g0299a0002c0002t0001g0034a0002c0002t0001g0036others(92): Show | 117 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.-21-1870_-21-1867d others(6): Show |
PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146223958 | ||||||
| chr3:146223974
|
T | C | 1 | a0001c0001t0006g0284 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-21-1882A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146223974 | ||||||
| chr3:146224038
|
G | C | 1 | a0002c0002t0005g0251 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-21-1946C>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146224038 | ||||||
| chr3:146224099
|
T | C | 3 | a0001c0001t0006g0123a0001c0001t0006g0124a0001c0001t0009g0122 | 3 | HG01243.hp2 HG02109.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.-21-2007A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146224099 | ||||||
| chr3:146224104
|
A | C | 96 | a0001c0001t0001g0010a0001c0001t0012g0299a0002c0002t0001g0034others(93): Show | 119 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.-21-2012T>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146224104 | ||||||
| chr3:146224107
|
T | C | 1 | a0002c0002t0008g0282 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-21-2015A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146224107 | ||||||
| chr3:146224144
|
C | T | 96 | a0001c0001t0001g0010a0001c0001t0012g0299a0002c0002t0001g0034others(93): Show | 119 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.-21-2052G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146224144 | ||||||
| chr3:146224171
|
T | C | 4 | a0001c0001t0001g0125a0001c0001t0003g0112a0001c0001t0003g0118others(1): Show | 4 | HG02145.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-21-2079A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146224171 | ||||||
| chr3:146224228
|
A | G | 96 | a0001c0001t0001g0010a0001c0001t0012g0299a0002c0002t0001g0034others(93): Show | 119 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.-21-2136T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146224228 | ||||||
| chr3:146224237
|
T | G | 2 | a0001c0001t0009g0163a0001c0001t0022g0162 | 2 | HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-21-2145A>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146224237 | ||||||
| chr3:146224241
|
T | C | 1 | a0001c0001t0001g0010 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-21-2149A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146224241 | ||||||
| chr3:146224336
|
T | C | 96 | a0001c0001t0001g0010a0001c0001t0012g0299a0002c0002t0001g0034others(93): Show | 119 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.-21-2244A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146224336 | ||||||
| chr3:146224337
|
A | T | 5 | a0001c0001t0010g0149a0001c0001t0010g0151a0001c0001t0012g0147others(2): Show | 5 | HG02630.hp2 HG02647.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-21-2245T>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146224337 | ||||||
| chr3:146224338
|
G | A | 8 | a0001c0001t0007g0024a0001c0001t0009g0053a0001c0001t0009g0163others(5): Show | 10 | HG02145.hp2 HG02257.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.-21-2246C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146224338 | ||||||
| chr3:146224346
|
G | A | 1 | a0001c0001t0005g0172 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-21-2254C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146224346 | ||||||
| chr3:146224413
|
G | A | 95 | a0001c0001t0012g0299a0002c0002t0001g0034a0002c0002t0001g0036others(92): Show | 117 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.-21-2321C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146224413 | ||||||
| chr3:146224418
|
C | T | 2 | a0001c0001t0001g0167a0001c0001t0003g0168 | 2 | HG00642.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.-21-2326G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146224418 | ||||||
| chr3:146224438
|
CTCGCGGT others(124): Show |
C | 5 | a0001c0001t0010g0149a0001c0001t0010g0151a0001c0001t0012g0147others(2): Show | 5 | HG02630.hp2 HG02647.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-21-2477_-21-2347d others(2): Show |
PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146224438 | ||||||
| chr3:146224444
|
G | A | 96 | a0001c0001t0001g0010a0001c0001t0012g0299a0002c0002t0001g0034others(93): Show | 119 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.-21-2352C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146224444 | ||||||
| chr3:146224469
|
C | T | 96 | a0001c0001t0001g0010a0001c0001t0012g0299a0002c0002t0001g0034others(93): Show | 119 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.-21-2377G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146224469 | ||||||
| chr3:146224534
|
G | T | 1 | a0001c0001t0001g0010 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-21-2442C>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146224534 | ||||||
| chr3:146224542
|
G | A | 5 | a0001c0001t0012g0299a0004c0004t0001g0152a0004c0004t0001g0153others(2): Show | 5 | HG02818.hp2 HG02896.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-21-2450C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146224542 | ||||||
| chr3:146224543
|
C | T | 1 | a0001c0001t0003g0057 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-21-2451G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146224543 | ||||||
| chr3:146224572
|
G | A | 102 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0027others(99): Show | 117 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.-21-2480C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146224572 | ||||||
| chr3:146224615
|
G | A | 119 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0027others(116): Show | 139 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.-21-2523C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146224615 | ||||||
| chr3:146224646
|
A | G | 1 | a0001c0001t0001g0010 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-21-2554T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146224646 | ||||||
| chr3:146224653
|
A | C | 1 | a0001c0001t0001g0010 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-21-2561T>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146224653 | ||||||
| chr3:146224682
|
C | T | 1 | a0001c0001t0012g0299 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-21-2590G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146224682 | ||||||
| chr3:146224687
|
G | A | 6 | a0001c0001t0007g0024a0001c0001t0009g0053a0001c0001t0009g0164others(3): Show | 8 | HG02145.hp2 HG02895.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.-21-2595C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146224687 | ||||||
| chr3:146224726
|
C | T | 1 | a0003c0003t0010g0160 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-21-2634G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146224726 | ||||||
| chr3:146224766
|
G | A | 5 | a0001c0001t0012g0299a0004c0004t0001g0152a0004c0004t0001g0153others(2): Show | 5 | HG02818.hp2 HG02896.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-21-2674C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146224766 | ||||||
| chr3:146224821
|
TACAAAGG others(43): Show |
T | 60 | a0002c0002t0001g0034a0002c0002t0001g0036a0002c0002t0001g0038others(57): Show | 79 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.-21-2779_-21-2730d others(52): Show |
PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146224821 | ||||||
| chr3:146224870
|
A | C | 3 | a0005c0005t0009g0317a0005c0005t0015g0318a0005c0005t0021g0314 | 3 | HG02055.hp2 HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-21-2778T>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146224870 | ||||||
| chr3:146224921
|
C | T | 1 | a0001c0001t0005g0085 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-21-2829G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146224921 | ||||||
| chr3:146224969
|
G | A | 91 | a0001c0001t0004g0213a0002c0002t0001g0034a0002c0002t0001g0036others(88): Show | 113 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.-21-2877C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146224969 | ||||||
| chr3:146225006
|
T | G | 2 | a0001c0001t0013g0058a0001c0001t0013g0059 | 2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-21-2914A>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146225006 | ||||||
| chr3:146225053
|
T | G | 1 | a0001c0001t0001g0010 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-21-2961A>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146225053 | ||||||
| chr3:146225082
|
A | T | 8 | a0001c0001t0007g0024a0001c0001t0009g0053a0001c0001t0009g0163others(5): Show | 10 | HG02145.hp2 HG02257.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.-21-2990T>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146225082 | ||||||
| chr3:146225121
|
A | G | 1 | a0001c0001t0001g0010 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-21-3029T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146225121 | ||||||
| chr3:146225127
|
T | C | 1 | a0001c0001t0001g0010 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-21-3035A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146225127 | ||||||
| chr3:146225143
|
C | T | 1 | a0001c0001t0001g0010 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-21-3051G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146225143 | ||||||
| chr3:146225248
|
C | G | 96 | a0001c0001t0001g0010a0001c0001t0012g0299a0002c0002t0001g0034others(93): Show | 119 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.-21-3156G>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146225248 | ||||||
| chr3:146225291
|
T | C | 5 | a0001c0001t0012g0299a0004c0004t0001g0152a0004c0004t0001g0153others(2): Show | 5 | HG02818.hp2 HG02896.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-21-3199A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146225291 | ||||||
| chr3:146225325
|
G | A | 1 | a0001c0001t0001g0010 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-21-3233C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146225325 | ||||||
| chr3:146225326
|
A | T | 1 | a0001c0001t0001g0010 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-21-3234T>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146225326 | ||||||
| chr3:146225335
|
T | C | 1 | a0001c0001t0001g0010 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-21-3243A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146225335 | ||||||
| chr3:146225344
|
A | G | 12 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0248others(9): Show | 17 | HG01358.hp1 HG02683.hp2 HG03669.hp1 others(14): Show |
intron_variant | MODIFIER | c.-21-3252T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146225344 | ||||||
| chr3:146225407
|
CTGCCAGT others(4): Show |
C | 90 | a0002c0002t0001g0034a0002c0002t0001g0036a0002c0002t0001g0038others(87): Show | 112 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.-21-3326_-21-3316d others(13): Show |
PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146225407 | ||||||
| chr3:146225418
|
G | C | 5 | a0001c0001t0012g0299a0004c0004t0001g0152a0004c0004t0001g0153others(2): Show | 5 | HG02818.hp2 HG02896.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-21-3326C>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146225418 | ||||||
| chr3:146225430
|
T | C | 96 | a0001c0001t0001g0010a0001c0001t0012g0299a0002c0002t0001g0034others(93): Show | 119 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.-21-3338A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146225430 | ||||||
| chr3:146225467
|
T | C | 1 | a0001c0001t0001g0010 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-21-3375A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146225467 | ||||||
| chr3:146225480
|
G | A | 1 | a0001c0001t0001g0060 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-21-3388C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146225480 | ||||||
| chr3:146225486
|
G | A | 1 | a0001c0001t0001g0010 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-21-3394C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146225486 | ||||||
| chr3:146225495
|
G | A | 83 | a0002c0002t0001g0034a0002c0002t0001g0036a0002c0002t0001g0038others(80): Show | 103 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.-21-3403C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146225495 | ||||||
| chr3:146225555
|
A | T | 100 | a0001c0001t0010g0149a0001c0001t0010g0151a0001c0001t0012g0147others(97): Show | 122 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.-21-3463T>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146225555 | ||||||
| chr3:146225563
|
C | G | 100 | a0001c0001t0010g0149a0001c0001t0010g0151a0001c0001t0012g0147others(97): Show | 122 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.-21-3471G>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146225563 | ||||||
| chr3:146225571
|
C | T | 1 | a0001c0001t0003g0092 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-21-3479G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146225571 | ||||||
| chr3:146225572
|
G | A | 2 | a0001c0001t0001g0011a0001c0001t0003g0051 | 3 | HG02886.hp1 HG03209.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-21-3480C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146225572 | ||||||
| chr3:146225573
|
C | A | 1 | a0001c0001t0001g0165 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-21-3481G>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146225573 | ||||||
| chr3:146225597
|
T | C | 101 | a0001c0001t0001g0010a0001c0001t0010g0149a0001c0001t0010g0151others(98): Show | 124 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.-21-3505A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146225597 | ||||||
| chr3:146225642
|
G | A | 1 | a0001c0001t0001g0105 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-21-3550C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146225642 | ||||||
| chr3:146225669
|
G | T | 11 | a0001c0001t0001g0010a0001c0001t0010g0149a0001c0001t0010g0151others(8): Show | 12 | HG02630.hp2 HG02647.hp2 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.-21-3577C>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146225669 | ||||||
| chr3:146225672
|
C | A | 89 | a0002c0002t0001g0034a0002c0002t0001g0036a0002c0002t0001g0038others(86): Show | 111 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.-21-3580G>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146225672 | ||||||
| chr3:146225672
|
C | T | 1 | a0001c0001t0001g0010 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-21-3580G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146225672 | ||||||
| chr3:146225673
|
A | G | 100 | a0001c0001t0001g0010a0001c0001t0010g0149a0001c0001t0010g0151others(97): Show | 123 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.-21-3581T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146225673 | ||||||
| chr3:146225696
|
G | A | 121 | a0001c0001t0001g0028a0001c0001t0001g0032a0001c0001t0001g0135others(118): Show | 148 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.-21-3604C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146225696 | ||||||
| chr3:146225704
|
C | T | 60 | a0002c0002t0001g0034a0002c0002t0001g0036a0002c0002t0001g0038others(57): Show | 79 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.-21-3612G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146225704 | ||||||
| chr3:146225708
|
G | T | 60 | a0002c0002t0001g0034a0002c0002t0001g0036a0002c0002t0001g0038others(57): Show | 79 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.-21-3616C>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146225708 | ||||||
| chr3:146225729
|
T | C | 219 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(216): Show | 265 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(262): Show |
intron_variant | MODIFIER | c.-21-3637A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146225729 | ||||||
| chr3:146225732
|
G | T | 11 | a0002c0002t0003g0307a0002c0002t0006g0090a0002c0002t0007g0306others(8): Show | 11 | HG01243.hp1 HG02055.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-21-3640C>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146225732 | ||||||
| chr3:146225788
|
G | A | 1 | a0002c0002t0001g0245 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-21-3696C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146225788 | ||||||
| chr3:146225798
|
G | A | 77 | a0002c0002t0001g0034a0002c0002t0001g0036a0002c0002t0001g0038others(74): Show | 97 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.-21-3706C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146225798 | ||||||
| chr3:146225910
|
C | T | 1 | a0001c0001t0001g0186 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-21-3818G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146225910 | ||||||
| chr3:146225914
|
G | A | 96 | a0001c0001t0001g0010a0001c0001t0012g0299a0002c0002t0001g0034others(93): Show | 119 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.-21-3822C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146225914 | ||||||
| chr3:146225918
|
T | C | 1 | a0001c0001t0005g0110 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-21-3826A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146225918 | ||||||
| chr3:146225965
|
G | A | 1 | a0001c0001t0001g0010 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-21-3873C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146225965 | ||||||
| chr3:146225973
|
A | G | 226 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(223): Show | 274 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(271): Show |
intron_variant | MODIFIER | c.-21-3881T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146225973 | ||||||
| chr3:146226005
|
A | C | 95 | a0001c0001t0012g0299a0002c0002t0001g0034a0002c0002t0001g0036others(92): Show | 117 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.-21-3913T>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146226005 | ||||||
| chr3:146226048
|
AAT | A | 12 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0248others(9): Show | 17 | HG01358.hp1 HG02683.hp2 HG03669.hp1 others(14): Show |
intron_variant | MODIFIER | c.-21-3958_-21-3957d others(4): Show |
PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146226048 | ||||||
| chr3:146226090
|
AAC | A | 12 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0248others(9): Show | 17 | HG01358.hp1 HG02683.hp2 HG03669.hp1 others(14): Show |
intron_variant | MODIFIER | c.-21-4000_-21-3999d others(4): Show |
PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146226090 | ||||||
| chr3:146226135
|
G | T | 8 | a0002c0002t0003g0307a0002c0002t0006g0090a0002c0002t0007g0306others(5): Show | 8 | HG01243.hp1 HG02572.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-21-4043C>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146226135 | ||||||
| chr3:146226279
|
T | G | 96 | a0001c0001t0001g0010a0001c0001t0012g0299a0002c0002t0001g0034others(93): Show | 119 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.-21-4187A>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146226279 | ||||||
| chr3:146226305
|
C | T | 1 | a0001c0001t0001g0010 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-21-4213G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146226305 | ||||||
| chr3:146226359
|
T | A | 218 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(215): Show | 264 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(261): Show |
intron_variant | MODIFIER | c.-21-4267A>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146226359 | ||||||
| chr3:146226441
|
A | G | 95 | a0001c0001t0012g0299a0002c0002t0001g0034a0002c0002t0001g0036others(92): Show | 117 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.-21-4349T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146226441 | ||||||
| chr3:146226464
|
T | C | 25 | a0001c0001t0001g0026a0001c0001t0001g0055a0001c0001t0001g0074others(22): Show | 29 | HG00544.hp1 HG00639.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.-21-4372A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146226464 | ||||||
| chr3:146226476
|
T | C | 122 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0027others(119): Show | 145 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.-21-4384A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146226476 | ||||||
| chr3:146226481
|
G | A | 1 | a0001c0001t0005g0172 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-21-4389C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146226481 | ||||||
| chr3:146226549
|
C | A | 92 | a0001c0001t0001g0010a0001c0001t0012g0299a0002c0002t0001g0034others(89): Show | 115 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.-21-4457G>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146226549 | ||||||
| chr3:146226604
|
T | C | 96 | a0001c0001t0001g0010a0001c0001t0012g0299a0002c0002t0001g0034others(93): Show | 119 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.-21-4512A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146226604 | ||||||
| chr3:146226703
|
G | A | 6 | a0003c0003t0010g0157a0003c0003t0010g0158a0003c0003t0010g0159others(3): Show | 6 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-21-4611C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146226703 | ||||||
| chr3:146226749
|
G | C | 1 | a0001c0001t0006g0124 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-21-4657C>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146226749 | ||||||
| chr3:146226905
|
A | G | 90 | a0002c0002t0001g0034a0002c0002t0001g0036a0002c0002t0001g0038others(87): Show | 112 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.-21-4813T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146226905 | ||||||
| chr3:146226970
|
ATATTC | A | 95 | a0001c0001t0012g0299a0002c0002t0001g0034a0002c0002t0001g0036others(92): Show | 117 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.-21-4883_-21-4879d others(7): Show |
PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146226970 | ||||||
| chr3:146227034
|
G | A | 1 | a0001c0001t0001g0010 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-21-4942C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146227034 | ||||||
| chr3:146227142
|
G | A | 2 | a0003c0003t0006g0012a0003c0003t0014g0052 | 3 | HG02922.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-21-5050C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146227142 | ||||||
| chr3:146227275
|
G | T | 1 | a0001c0001t0001g0010 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-21-5183C>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146227275 | ||||||
| chr3:146227304
|
C | T | 1 | a0001c0001t0001g0010 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-21-5212G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146227304 | ||||||
| chr3:146227325
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-21-5233C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146227325 | ||||||
| chr3:146227464
|
G | A | 5 | a0001c0001t0010g0149a0001c0001t0010g0151a0001c0001t0012g0147others(2): Show | 5 | HG02630.hp2 HG02647.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-21-5372C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146227464 | ||||||
| chr3:146227513
|
C | A | 1 | a0001c0001t0001g0010 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-21-5421G>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146227513 | ||||||
| chr3:146227514
|
C | A | 1 | a0001c0001t0001g0010 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-21-5422G>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146227514 | ||||||
| chr3:146227560
|
T | C | 3 | a0005c0005t0009g0317a0005c0005t0015g0318a0005c0005t0021g0314 | 3 | HG02055.hp2 HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-21-5468A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146227560 | ||||||
| chr3:146227570
|
A | G | 5 | a0001c0001t0001g0010a0003c0003t0010g0310a0003c0003t0012g0311others(2): Show | 6 | HG02109.hp2 HG02615.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.-21-5478T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146227570 | ||||||
| chr3:146227608
|
C | G | 226 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(223): Show | 274 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(271): Show |
intron_variant | MODIFIER | c.-21-5516G>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146227608 | ||||||
| chr3:146227618
|
T | TC | 38 | a0001c0001t0001g0010a0001c0001t0012g0299a0002c0002t0003g0307others(35): Show | 42 | HG01243.hp1 HG01255.hp1 HG01433.hp1 others(39): Show |
intron_variant | MODIFIER | c.-21-5527dupG | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146227618 | ||||||
| chr3:146227622
|
A | G | 1 | a0001c0001t0001g0010 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-21-5530T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146227622 | ||||||
| chr3:146227716
|
T | C | 37 | a0001c0001t0012g0299a0002c0002t0003g0307a0002c0002t0006g0090others(34): Show | 40 | HG01243.hp1 HG01255.hp1 HG01433.hp1 others(37): Show |
intron_variant | MODIFIER | c.-21-5624A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146227716 | ||||||
| chr3:146227773
|
G | T | 1 | a0003c0003t0019g0045 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-21-5681C>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146227773 | ||||||
| chr3:146227820
|
G | A | 39 | a0001c0001t0001g0010a0001c0001t0001g0283a0001c0001t0012g0299others(36): Show | 43 | HG01243.hp1 HG01255.hp1 HG01433.hp1 others(40): Show |
intron_variant | MODIFIER | c.-21-5728C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146227820 | ||||||
| chr3:146227859
|
C | T | 15 | a0002c0002t0003g0307a0002c0002t0006g0090a0002c0002t0007g0306others(12): Show | 16 | HG01243.hp1 HG02055.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.-21-5767G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146227859 | ||||||
| chr3:146228039
|
A | G | 38 | a0001c0001t0001g0010a0001c0001t0012g0299a0002c0002t0003g0307others(35): Show | 42 | HG01243.hp1 HG01255.hp1 HG01433.hp1 others(39): Show |
intron_variant | MODIFIER | c.-21-5947T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146228039 | ||||||
| chr3:146228362
|
T | G | 37 | a0001c0001t0012g0299a0002c0002t0003g0307a0002c0002t0006g0090others(34): Show | 40 | HG01243.hp1 HG01255.hp1 HG01433.hp1 others(37): Show |
intron_variant | MODIFIER | c.-21-6270A>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146228362 | ||||||
| chr3:146228494
|
T | C | 5 | a0001c0001t0001g0010a0003c0003t0010g0310a0003c0003t0012g0311others(2): Show | 6 | HG02109.hp2 HG02615.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.-21-6402A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146228494 | ||||||
| chr3:146228600
|
T | C | 1 | a0003c0003t0001g0301 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-21-6508A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146228600 | ||||||
| chr3:146228644
|
AG | A | 5 | a0001c0001t0010g0149a0001c0001t0010g0151a0001c0001t0012g0147others(2): Show | 5 | HG02630.hp2 HG02647.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-21-6553delC | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146228644 | ||||||
| chr3:146228724
|
A | T | 1 | a0001c0001t0002g0185 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-21-6632T>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146228724 | ||||||
| chr3:146228726
|
TGA | T | 196 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0027others(193): Show | 236 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.-21-6636_-21-6635d others(4): Show |
PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146228726 | ||||||
| chr3:146228735
|
A | G | 4 | a0003c0003t0010g0310a0003c0003t0012g0311a0003c0003t0015g0308others(1): Show | 4 | HG02109.hp2 HG02615.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-21-6643T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146228735 | ||||||
| chr3:146228765
|
G | A | 4 | a0004c0004t0001g0152a0004c0004t0001g0153a0004c0004t0006g0154others(1): Show | 4 | HG02818.hp2 HG02970.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-21-6673C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146228765 | ||||||
| chr3:146228769
|
G | A | 1 | a0001c0001t0001g0010 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-21-6677C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146228769 | ||||||
| chr3:146228813
|
A | G | 1 | a0005c0005t0009g0317 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-21-6721T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146228813 | ||||||
| chr3:146228874
|
A | G | 1 | a0003c0003t0011g0044 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-21-6782T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146228874 | ||||||
| chr3:146228922
|
A | G | 5 | a0001c0001t0010g0149a0001c0001t0010g0151a0001c0001t0012g0147others(2): Show | 5 | HG02630.hp2 HG02647.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-21-6830T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146228922 | ||||||
| chr3:146228950
|
A | G | 1 | a0001c0001t0004g0097 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-21-6858T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146228950 | ||||||
| chr3:146229029
|
T | C | 218 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(215): Show | 264 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(261): Show |
intron_variant | MODIFIER | c.-21-6937A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146229029 | ||||||
| chr3:146229064
|
A | G | 1 | a0001c0001t0001g0010 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-21-6972T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146229064 | ||||||
| chr3:146229243
|
G | A | 6 | a0003c0003t0010g0157a0003c0003t0010g0158a0003c0003t0010g0159others(3): Show | 6 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-21-7151C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146229243 | ||||||
| chr3:146229263
|
A | C | 2 | a0003c0003t0001g0300a0003c0003t0001g0301 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-21-7171T>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146229263 | ||||||
| chr3:146229370
|
T | C | 174 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0027others(171): Show | 212 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(209): Show |
intron_variant | MODIFIER | c.-21-7278A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146229370 | ||||||
| chr3:146229462
|
T | C | 211 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0027others(208): Show | 256 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(253): Show |
intron_variant | MODIFIER | c.-21-7370A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146229462 | ||||||
| chr3:146229463
|
G | A | 1 | a0001c0001t0001g0214 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-21-7371C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146229463 | ||||||
| chr3:146229536
|
T | C | 212 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(209): Show | 258 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(255): Show |
intron_variant | MODIFIER | c.-21-7444A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146229536 | ||||||
| chr3:146229581
|
A | ATTTTAT | 177 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0027others(174): Show | 215 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(212): Show |
intron_variant | MODIFIER | c.-21-7495_-21-7490d others(8): Show |
PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146229581 | ||||||
| chr3:146229588
|
TTTTCATT others(6): Show |
T | 13 | a0002c0002t0003g0307a0002c0002t0006g0090a0002c0002t0007g0306others(10): Show | 13 | HG01243.hp1 HG02055.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.-21-7509_-21-7497d others(15): Show |
PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146229588 | ||||||
| chr3:146229588
|
TTTTCATT others(18): Show |
T | 12 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0248others(9): Show | 17 | HG01358.hp1 HG02683.hp2 HG03669.hp1 others(14): Show |
intron_variant | MODIFIER | c.-21-7521_-21-7497d others(27): Show |
PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146229588 | ||||||
| chr3:146229592
|
C | A | 6 | a0001c0001t0001g0135a0001c0001t0001g0215a0001c0001t0001g0316others(3): Show | 8 | HG00438.hp1 HG00609.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-21-7500G>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146229592 | ||||||
| chr3:146229592
|
CATTT | C | 65 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0001g0055others(62): Show | 74 | HG00099.hp2 HG00408.hp2 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.-21-7504_-21-7501d others(6): Show |
PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146229592 | ||||||
| chr3:146229592
|
CATTTATT others(1): Show |
C | 11 | a0001c0001t0001g0010a0001c0001t0001g0060a0001c0001t0001g0086others(8): Show | 12 | HG01255.hp1 HG01891.hp1 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.-21-7508_-21-7501d others(10): Show |
PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146229592 | ||||||
| chr3:146229593
|
A | T | 6 | a0001c0001t0001g0135a0001c0001t0001g0215a0001c0001t0001g0316others(3): Show | 8 | HG00438.hp1 HG00609.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-21-7501T>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146229593 | ||||||
| chr3:146229596
|
T | TTC | 6 | a0001c0001t0001g0135a0001c0001t0001g0215a0001c0001t0001g0316others(3): Show | 8 | HG00438.hp1 HG00609.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-21-7505_-21-7504i others(4): Show |
PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146229596 | ||||||
| chr3:146229600
|
T | C | 2 | a0001c0001t0015g0216a0001c0001t0024g0217 | 2 | HG02970.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-21-7508A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146229600 | ||||||
| chr3:146229604
|
T | C | 1 | a0001c0001t0005g0218 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-21-7512A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146229604 | ||||||
| chr3:146229605
|
A | ATTTAT | 4 | a0004c0004t0001g0152a0004c0004t0001g0153a0004c0004t0006g0154others(1): Show | 4 | HG02818.hp2 HG02970.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-21-7518_-21-7514d others(7): Show |
PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146229605 | ||||||
| chr3:146229608
|
TA | T | 13 | a0002c0002t0003g0307a0002c0002t0006g0090a0002c0002t0007g0306others(10): Show | 13 | HG01243.hp1 HG02055.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.-21-7517delT | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146229608 | ||||||
| chr3:146229612
|
T | C | 13 | a0002c0002t0003g0307a0002c0002t0006g0090a0002c0002t0007g0306others(10): Show | 13 | HG01243.hp1 HG02055.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.-21-7520A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146229612 | ||||||
| chr3:146229620
|
TA | T | 12 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0248others(9): Show | 17 | HG01358.hp1 HG02683.hp2 HG03669.hp1 others(14): Show |
intron_variant | MODIFIER | c.-21-7529delT | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146229620 | ||||||
| chr3:146229624
|
T | C | 12 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0248others(9): Show | 17 | HG01358.hp1 HG02683.hp2 HG03669.hp1 others(14): Show |
intron_variant | MODIFIER | c.-21-7532A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146229624 | ||||||
| chr3:146229633
|
A | G | 6 | a0003c0003t0010g0157a0003c0003t0010g0158a0003c0003t0010g0159others(3): Show | 6 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-21-7541T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146229633 | ||||||
| chr3:146229641
|
A | ATTTATTT others(5): Show |
1 | a0001c0001t0001g0176 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-21-7550_-21-7549i others(14): Show |
PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146229641 | ||||||
| chr3:146229641
|
A | ATTTATTT others(1): Show |
8 | a0001c0001t0001g0177a0001c0001t0001g0228a0002c0002t0001g0245others(5): Show | 8 | HG01981.hp1 HG01993.hp1 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.-21-7550_-21-7549i others(10): Show |
PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146229641 | ||||||
| chr3:146229641
|
A | ATTTT | 60 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0181others(57): Show | 75 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.-21-7550_-21-7549i others(6): Show |
PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146229641 | ||||||
| chr3:146229641
|
A | T | 222 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(219): Show | 262 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(259): Show |
intron_variant | MODIFIER | c.-21-7549T>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146229641 | ||||||
| chr3:146229717
|
C | T | 174 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0027others(171): Show | 212 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(209): Show |
intron_variant | MODIFIER | c.-21-7625G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146229717 | ||||||
| chr3:146229760
|
A | G | 226 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(223): Show | 274 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(271): Show |
intron_variant | MODIFIER | c.-21-7668T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146229760 | ||||||
| chr3:146229828
|
G | C | 212 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(209): Show | 258 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(255): Show |
intron_variant | MODIFIER | c.-21-7736C>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146229828 | ||||||
| chr3:146229973
|
T | C | 1 | a0001c0001t0013g0285 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-21-7881A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146229973 | ||||||
| chr3:146229983
|
G | A | 1 | a0001c0001t0001g0011 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-21-7891C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146229983 | ||||||
| chr3:146230028
|
T | C | 2 | a0003c0003t0006g0012a0003c0003t0014g0052 | 3 | HG02922.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-21-7936A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146230028 | ||||||
| chr3:146230029
|
A | C | 6 | a0003c0003t0010g0157a0003c0003t0010g0158a0003c0003t0010g0159others(3): Show | 6 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-21-7937T>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146230029 | ||||||
| chr3:146230069
|
G | A | 6 | a0003c0003t0010g0157a0003c0003t0010g0158a0003c0003t0010g0159others(3): Show | 6 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-21-7977C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146230069 | ||||||
| chr3:146230135
|
T | C | 7 | a0001c0001t0007g0024a0001c0001t0009g0163a0001c0001t0009g0164others(4): Show | 9 | HG02145.hp2 HG02257.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-21-8043A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146230135 | ||||||
| chr3:146230135
|
T | G | 1 | a0002c0002t0004g0290 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-21-8043A>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146230135 | ||||||
| chr3:146230136
|
T | G | 1 | a0001c0001t0001g0010 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-21-8044A>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146230136 | ||||||
| chr3:146230195
|
AAAT | A | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-21-8106_-21-8104d others(5): Show |
PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146230195 | ||||||
| chr3:146230237
|
T | C | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-21-8145A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146230237 | ||||||
| chr3:146230256
|
C | A | 197 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0027others(194): Show | 237 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(234): Show |
intron_variant | MODIFIER | c.-21-8164G>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146230256 | ||||||
| chr3:146230315
|
T | C | 1 | a0001c0001t0007g0111 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-21-8223A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146230315 | ||||||
| chr3:146230462
|
A | G | 167 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0027others(164): Show | 204 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(201): Show |
intron_variant | MODIFIER | c.-21-8370T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146230462 | ||||||
| chr3:146230580
|
T | C | 3 | a0005c0005t0009g0317a0005c0005t0015g0318a0005c0005t0021g0314 | 3 | HG02055.hp2 HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-21-8488A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146230580 | ||||||
| chr3:146230610
|
T | C | 1 | a0001c0001t0007g0091 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-21-8518A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146230610 | ||||||
| chr3:146230635
|
A | T | 2 | a0003c0003t0001g0300a0003c0003t0001g0301 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-21-8543T>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146230635 | ||||||
| chr3:146230681
|
AGAGAGGG others(4): Show |
A | 1 | a0002c0002t0008g0286 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-21-8600_-21-8590d others(13): Show |
PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146230681 | ||||||
| chr3:146230697
|
G | A | 1 | a0001c0001t0002g0133 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-21-8605C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146230697 | ||||||
| chr3:146230731
|
G | A | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-21-8639C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146230731 | ||||||
| chr3:146230783
|
C | T | 2 | a0001c0001t0001g0176a0001c0001t0004g0097 | 2 | NA18978.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.-21-8691G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146230783 | ||||||
| chr3:146230935
|
T | C | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-21-8843A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146230935 | ||||||
| chr3:146230971
|
A | G | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-21-8879T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146230971 | ||||||
| chr3:146230984
|
A | ACTGACAG others(313): Show |
5 | a0003c0003t0010g0158a0003c0003t0010g0159a0003c0003t0010g0160others(2): Show | 5 | HG01255.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-21-8893_-21-8892i others(322): Show |
PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146230984 | ||||||
| chr3:146230984
|
A | ACTGACAG others(314): Show |
2 | a0001c0001t0009g0053a0003c0003t0010g0157 | 2 | HG01891.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-21-8893_-21-8892i others(323): Show |
PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146230984 | ||||||
| chr3:146231022
|
C | G | 1 | a0001c0001t0001g0011 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-21-8930G>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146231022 | ||||||
| chr3:146231052
|
T | C | 1 | a0001c0001t0001g0219 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-21-8960A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146231052 | ||||||
| chr3:146231076
|
G | A | 216 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(213): Show | 263 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(260): Show |
intron_variant | MODIFIER | c.-21-8984C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146231076 | ||||||
| chr3:146231181
|
C | G | 1 | a0001c0001t0001g0175 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-21-9089G>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146231181 | ||||||
| chr3:146231288
|
C | T | 223 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(220): Show | 270 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(267): Show |
intron_variant | MODIFIER | c.-21-9196G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146231288 | ||||||
| chr3:146231323
|
G | A | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-21-9231C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146231323 | ||||||
| chr3:146231323
|
G | C | 3 | a0005c0005t0009g0317a0005c0005t0015g0318a0005c0005t0021g0314 | 3 | HG02055.hp2 HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-21-9231C>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146231323 | ||||||
| chr3:146231549
|
C | T | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-21-9457G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146231549 | ||||||
| chr3:146231589
|
A | C | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-21-9497T>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146231589 | ||||||
| chr3:146231630
|
C | T | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-21-9538G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146231630 | ||||||
| chr3:146231647
|
T | C | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-21-9555A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146231647 | ||||||
| chr3:146231692
|
AT | A | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-21-9601delA | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146231692 | ||||||
| chr3:146231745
|
T | G | 4 | a0004c0004t0001g0152a0004c0004t0001g0153a0004c0004t0006g0154others(1): Show | 4 | HG02818.hp2 HG02970.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-21-9653A>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146231745 | ||||||
| chr3:146231757
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-21-9665C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146231757 | ||||||
| chr3:146231771
|
G | A | 2 | a0001c0001t0001g0114a0001c0001t0001g0220 | 2 | HG02071.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.-21-9679C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146231771 | ||||||
| chr3:146231826
|
G | T | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-21-9734C>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146231826 | ||||||
| chr3:146231896
|
T | C | 5 | a0001c0001t0010g0149a0001c0001t0010g0151a0001c0001t0012g0147others(2): Show | 5 | HG02630.hp2 HG02647.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-21-9804A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146231896 | ||||||
| chr3:146231926
|
T | C | 1 | a0001c0001t0005g0100 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-21-9834A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146231926 | ||||||
| chr3:146231949
|
G | GT | 215 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0026others(212): Show | 261 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(258): Show |
intron_variant | MODIFIER | c.-21-9858dupA | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146231949 | ||||||
| chr3:146232047
|
G | A | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-21-9955C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146232047 | ||||||
| chr3:146232223
|
A | G | 4 | a0003c0003t0010g0310a0003c0003t0012g0311a0003c0003t0015g0308others(1): Show | 4 | HG02109.hp2 HG02615.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-21-10131T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146232223 | ||||||
| chr3:146232241
|
T | G | 1 | a0003c0003t0010g0160 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-21-10149A>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146232241 | ||||||
| chr3:146232307
|
T | A | 20 | a0001c0001t0001g0010a0001c0001t0009g0053a0001c0001t0012g0299others(17): Show | 21 | HG01243.hp1 HG01255.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.-21-10215A>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146232307 | ||||||
| chr3:146232319
|
T | G | 13 | a0001c0001t0001g0010a0001c0001t0012g0299a0002c0002t0003g0307others(10): Show | 14 | HG01243.hp1 HG02055.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-21-10227A>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146232319 | ||||||
| chr3:146232396
|
T | C | 1 | a0005c0005t0015g0318 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-21-10304A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146232396 | ||||||
| chr3:146232407
|
T | C | 7 | a0003c0003t0011g0005a0003c0003t0011g0044a0003c0003t0011g0046others(4): Show | 9 | HG01433.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-21-10315A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146232407 | ||||||
| chr3:146232537
|
C | T | 24 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0248others(21): Show | 31 | HG01358.hp1 HG01433.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.-21-10445G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146232537 | ||||||
| chr3:146232560
|
G | A | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-21-10468C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146232560 | ||||||
| chr3:146232602
|
A | G | 1 | a0001c0001t0001g0169 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-21-10510T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146232602 | ||||||
| chr3:146232654
|
T | A | 1 | a0001c0001t0012g0299 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-21-10562A>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146232654 | ||||||
| chr3:146232691
|
G | C | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-21-10599C>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146232691 | ||||||
| chr3:146232705
|
T | C | 12 | a0001c0001t0012g0299a0002c0002t0003g0307a0002c0002t0007g0306others(9): Show | 12 | HG01243.hp1 HG02055.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.-21-10613A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146232705 | ||||||
| chr3:146232707
|
T | C | 223 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(220): Show | 270 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(267): Show |
intron_variant | MODIFIER | c.-21-10615A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146232707 | ||||||
| chr3:146232959
|
AC | A | 179 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0026others(176): Show | 218 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(215): Show |
intron_variant | MODIFIER | c.-21-10868delG | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146232959 | ||||||
| chr3:146233083
|
C | A | 223 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(220): Show | 270 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(267): Show |
intron_variant | MODIFIER | c.-21-10991G>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146233083 | ||||||
| chr3:146233120
|
G | T | 12 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0248others(9): Show | 17 | HG01358.hp1 HG02683.hp2 HG03669.hp1 others(14): Show |
intron_variant | MODIFIER | c.-21-11028C>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146233120 | ||||||
| chr3:146233124
|
T | C | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-21-11032A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146233124 | ||||||
| chr3:146233308
|
T | A | 5 | a0001c0001t0010g0149a0001c0001t0010g0151a0001c0001t0012g0147others(2): Show | 5 | HG02630.hp2 HG02647.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-21-11216A>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146233308 | ||||||
| chr3:146233410
|
T | C | 7 | a0001c0001t0007g0024a0001c0001t0009g0163a0001c0001t0009g0164others(4): Show | 9 | HG02145.hp2 HG02257.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-21-11318A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146233410 | ||||||
| chr3:146233431
|
G | A | 2 | a0003c0003t0001g0300a0003c0003t0001g0301 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-21-11339C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146233431 | ||||||
| chr3:146233459
|
A | G | 7 | a0003c0003t0011g0005a0003c0003t0011g0044a0003c0003t0011g0046others(4): Show | 9 | HG01433.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-21-11367T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146233459 | ||||||
| chr3:146233543
|
C | T | 199 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0026others(196): Show | 242 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(239): Show |
intron_variant | MODIFIER | c.-21-11451G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146233543 | ||||||
| chr3:146233609
|
T | G | 1 | a0002c0002t0001g0252 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-21-11517A>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146233609 | ||||||
| chr3:146233667
|
T | C | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-21-11575A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146233667 | ||||||
| chr3:146233716
|
T | C | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-21-11624A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146233716 | ||||||
| chr3:146233757
|
C | CA | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-21-11666dupT | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146233757 | ||||||
| chr3:146233969
|
A | ATATATT | 223 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(220): Show | 270 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(267): Show |
intron_variant | MODIFIER | c.-21-11878_-21-1187 others(10): Show |
PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146233969 | ||||||
| chr3:146233977
|
C | T | 223 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(220): Show | 270 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(267): Show |
intron_variant | MODIFIER | c.-21-11885G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146233977 | ||||||
| chr3:146233987
|
T | C | 1 | a0001c0001t0012g0299 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-21-11895A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146233987 | ||||||
| chr3:146234054
|
T | C | 13 | a0001c0001t0001g0010a0001c0001t0012g0299a0002c0002t0003g0307others(10): Show | 14 | HG01243.hp1 HG02055.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-21-11962A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146234054 | ||||||
| chr3:146234075
|
C | T | 5 | a0001c0001t0010g0149a0001c0001t0010g0151a0001c0001t0012g0147others(2): Show | 5 | HG02630.hp2 HG02647.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-21-11983G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146234075 | ||||||
| chr3:146234245
|
T | C | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-21-12153A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146234245 | ||||||
| chr3:146234255
|
T | C | 1 | a0001c0001t0013g0119 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-21-12163A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146234255 | ||||||
| chr3:146234328
|
A | G | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-21-12236T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146234328 | ||||||
| chr3:146234361
|
C | G | 12 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0248others(9): Show | 17 | HG01358.hp1 HG02683.hp2 HG03669.hp1 others(14): Show |
intron_variant | MODIFIER | c.-21-12269G>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146234361 | ||||||
| chr3:146234375
|
T | A | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-21-12283A>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146234375 | ||||||
| chr3:146234405
|
C | T | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-21-12313G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146234405 | ||||||
| chr3:146234489
|
A | G | 5 | a0001c0001t0010g0149a0001c0001t0010g0151a0001c0001t0012g0147others(2): Show | 5 | HG02630.hp2 HG02647.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-21-12397T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146234489 | ||||||
| chr3:146234516
|
A | G | 230 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(227): Show | 279 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(276): Show |
intron_variant | MODIFIER | c.-21-12424T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146234516 | ||||||
| chr3:146234534
|
A | G | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-21-12442T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146234534 | ||||||
| chr3:146234723
|
T | A | 1 | a0002c0002t0002g0287 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-21-12631A>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146234723 | ||||||
| chr3:146234733
|
A | G | 1 | a0001c0001t0009g0053 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-21-12641T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146234733 | ||||||
| chr3:146234805
|
T | C | 215 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0026others(212): Show | 261 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(258): Show |
intron_variant | MODIFIER | c.-21-12713A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146234805 | ||||||
| chr3:146234845
|
C | G | 1 | a0001c0001t0023g0144 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-21-12753G>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146234845 | ||||||
| chr3:146234859
|
G | T | 1 | a0002c0002t0001g0257 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-21-12767C>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146234859 | ||||||
| chr3:146234886
|
A | C | 1 | a0001c0001t0001g0174 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-21-12794T>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146234886 | ||||||
| chr3:146234896
|
C | A | 1 | a0001c0001t0009g0053 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-21-12804G>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146234896 | ||||||
| chr3:146234931
|
T | C | 68 | a0001c0001t0001g0274a0001c0001t0001g0283a0001c0001t0003g0272others(65): Show | 87 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.-21-12839A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146234931 | ||||||
| chr3:146234975
|
A | C | 6 | a0003c0003t0006g0012a0003c0003t0010g0310a0003c0003t0012g0311others(3): Show | 7 | HG02109.hp2 HG02615.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-21-12883T>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146234975 | ||||||
| chr3:146235096
|
A | AT | 12 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0248others(9): Show | 17 | HG01358.hp1 HG02683.hp2 HG03669.hp1 others(14): Show |
intron_variant | MODIFIER | c.-21-13005dupA | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146235096 | ||||||
| chr3:146235104
|
G | A | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-21-13012C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146235104 | ||||||
| chr3:146235222
|
T | C | 1 | a0002c0002t0001g0288 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-21-13130A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146235222 | ||||||
| chr3:146235242
|
C | T | 212 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(209): Show | 256 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(253): Show |
intron_variant | MODIFIER | c.-21-13150G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146235242 | ||||||
| chr3:146235466
|
C | T | 8 | a0001c0001t0001g0010a0001c0001t0009g0053a0003c0003t0010g0157others(5): Show | 9 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-21-13374G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146235466 | ||||||
| chr3:146235502
|
A | T | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-21-13410T>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146235502 | ||||||
| chr3:146235529
|
C | A | 212 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(209): Show | 256 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(253): Show |
intron_variant | MODIFIER | c.-21-13437G>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146235529 | ||||||
| chr3:146235577
|
G | T | 212 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(209): Show | 256 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(253): Show |
intron_variant | MODIFIER | c.-21-13485C>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146235577 | ||||||
| chr3:146235688
|
A | G | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-21-13596T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146235688 | ||||||
| chr3:146235803
|
C | A | 1 | a0001c0001t0012g0299 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-21-13711G>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146235803 | ||||||
| chr3:146235835
|
C | T | 7 | a0003c0003t0011g0005a0003c0003t0011g0044a0003c0003t0011g0046others(4): Show | 9 | HG01433.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-21-13743G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146235835 | ||||||
| chr3:146235905
|
G | A | 165 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0026others(162): Show | 200 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(197): Show |
intron_variant | MODIFIER | c.-21-13813C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146235905 | ||||||
| chr3:146235950
|
C | T | 212 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(209): Show | 256 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(253): Show |
intron_variant | MODIFIER | c.-21-13858G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146235950 | ||||||
| chr3:146236034
|
T | C | 1 | a0001c0001t0001g0316 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-21-13942A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146236034 | ||||||
| chr3:146236064
|
T | G | 21 | a0001c0001t0001g0062a0001c0001t0001g0065a0001c0001t0001g0066others(18): Show | 25 | HG00408.hp2 HG00639.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.-21-13972A>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146236064 | ||||||
| chr3:146236102
|
A | C | 218 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(215): Show | 262 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(259): Show |
intron_variant | MODIFIER | c.-21-14010T>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146236102 | ||||||
| chr3:146236129
|
A | G | 7 | a0001c0001t0007g0024a0001c0001t0009g0163a0001c0001t0009g0164others(4): Show | 9 | HG02145.hp2 HG02257.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-21-14037T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146236129 | ||||||
| chr3:146236158
|
G | A | 1 | a0001c0001t0001g0010 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-21-14066C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146236158 | ||||||
| chr3:146236205
|
T | A | 5 | a0001c0001t0007g0024a0001c0001t0009g0164a0001c0001t0014g0025others(2): Show | 7 | HG02145.hp2 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-21-14113A>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146236205 | ||||||
| chr3:146236264
|
A | C | 211 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0026others(208): Show | 254 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(251): Show |
intron_variant | MODIFIER | c.-21-14172T>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146236264 | ||||||
| chr3:146236265
|
G | A | 1 | a0001c0001t0001g0011 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-21-14173C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146236265 | ||||||
| chr3:146236298
|
G | C | 175 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0026others(172): Show | 211 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(208): Show |
intron_variant | MODIFIER | c.-21-14206C>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146236298 | ||||||
| chr3:146236368
|
C | T | 212 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(209): Show | 256 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(253): Show |
intron_variant | MODIFIER | c.-21-14276G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146236368 | ||||||
| chr3:146236465
|
A | C | 212 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(209): Show | 256 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(253): Show |
intron_variant | MODIFIER | c.-21-14373T>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146236465 | ||||||
| chr3:146236596
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-22+14364G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146236596 | ||||||
| chr3:146236674
|
T | G | 6 | a0003c0003t0006g0012a0003c0003t0014g0052a0004c0004t0001g0152others(3): Show | 7 | HG02818.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+14286A>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146236674 | ||||||
| chr3:146236699
|
C | T | 175 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0026others(172): Show | 211 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(208): Show |
intron_variant | MODIFIER | c.-22+14261G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146236699 | ||||||
| chr3:146236708
|
G | A | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+14252C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146236708 | ||||||
| chr3:146236716
|
G | A | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+14244C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146236716 | ||||||
| chr3:146236725
|
TG | T | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+14234delC | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146236725 | ||||||
| chr3:146236764
|
G | A | 2 | a0001c0001t0009g0163a0001c0001t0022g0162 | 2 | HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-22+14196C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146236764 | ||||||
| chr3:146236774
|
A | ACTGG | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+14185_-22+1418 others(8): Show |
PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146236774 | ||||||
| chr3:146236874
|
C | A | 212 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(209): Show | 256 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(253): Show |
intron_variant | MODIFIER | c.-22+14086G>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146236874 | ||||||
| chr3:146236968
|
A | G | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+13992T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146236968 | ||||||
| chr3:146237055
|
AAAAG | A | 5 | a0003c0003t0010g0157a0003c0003t0010g0158a0003c0003t0010g0159others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22+13901_-22+1390 others(8): Show |
PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146237055 | ||||||
| chr3:146237058
|
A | C | 5 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(2): Show | 5 | HG00673.hp1 HG02165.hp1 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.-22+13902T>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146237058 | ||||||
| chr3:146237078
|
C | T | 5 | a0001c0001t0010g0149a0001c0001t0010g0151a0001c0001t0012g0147others(2): Show | 5 | HG02630.hp2 HG02647.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22+13882G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146237078 | ||||||
| chr3:146237083
|
C | T | 212 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(209): Show | 256 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(253): Show |
intron_variant | MODIFIER | c.-22+13877G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146237083 | ||||||
| chr3:146237114
|
C | T | 4 | a0001c0001t0001g0125a0001c0001t0003g0112a0001c0001t0003g0118others(1): Show | 4 | HG02145.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-22+13846G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146237114 | ||||||
| chr3:146237287
|
C | T | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+13673G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146237287 | ||||||
| chr3:146237457
|
C | T | 2 | a0001c0001t0009g0163a0001c0001t0022g0162 | 2 | HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-22+13503G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146237457 | ||||||
| chr3:146237556
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-22+13404T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146237556 | ||||||
| chr3:146237592
|
A | G | 207 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0026others(204): Show | 250 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(247): Show |
intron_variant | MODIFIER | c.-22+13368T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146237592 | ||||||
| chr3:146237610
|
A | AAC | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+13349_-22+1335 others(6): Show |
PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146237610 | ||||||
| chr3:146237793
|
A | T | 1 | a0001c0001t0003g0173 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-22+13167T>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146237793 | ||||||
| chr3:146237917
|
A | C | 5 | a0001c0001t0001g0010a0003c0003t0010g0310a0003c0003t0012g0311others(2): Show | 6 | HG02109.hp2 HG02615.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.-22+13043T>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146237917 | ||||||
| chr3:146237949
|
C | T | 175 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0026others(172): Show | 211 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(208): Show |
intron_variant | MODIFIER | c.-22+13011G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146237949 | ||||||
| chr3:146238019
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-22+12941G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146238019 | ||||||
| chr3:146238135
|
C | A | 2 | a0001c0001t0001g0011a0001c0001t0003g0051 | 3 | HG02886.hp1 HG03209.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-22+12825G>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146238135 | ||||||
| chr3:146238168
|
A | G | 1 | a0002c0002t0001g0244 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-22+12792T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146238168 | ||||||
| chr3:146238204
|
C | CA | 26 | a0001c0001t0001g0098a0001c0001t0001g0224a0001c0001t0003g0099others(23): Show | 26 | HG00408.hp2 HG01243.hp1 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.-22+12755dupT | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146238204 | ||||||
| chr3:146238277
|
C | T | 5 | a0001c0001t0010g0149a0001c0001t0010g0151a0001c0001t0012g0147others(2): Show | 5 | HG02630.hp2 HG02647.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22+12683G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146238277 | ||||||
| chr3:146238282
|
C | T | 7 | a0003c0003t0011g0005a0003c0003t0011g0044a0003c0003t0011g0046others(4): Show | 9 | HG01433.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-22+12678G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146238282 | ||||||
| chr3:146238470
|
T | C | 24 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0248others(21): Show | 31 | HG01358.hp1 HG01433.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.-22+12490A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146238470 | ||||||
| chr3:146238489
|
A | G | 1 | a0001c0001t0005g0172 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-22+12471T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146238489 | ||||||
| chr3:146238585
|
C | T | 1 | a0001c0001t0005g0100 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-22+12375G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146238585 | ||||||
| chr3:146238587
|
C | G | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+12373G>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146238587 | ||||||
| chr3:146238651
|
C | G | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+12309G>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146238651 | ||||||
| chr3:146238651
|
C | T | 2 | a0001c0001t0009g0163a0001c0001t0022g0162 | 2 | HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-22+12309G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146238651 | ||||||
| chr3:146238791
|
G | C | 25 | a0001c0001t0001g0054a0001c0001t0001g0060a0001c0001t0001g0101others(22): Show | 29 | HG01257.hp2 NA18747.hp1 NA18941.hp1 others(26): Show |
intron_variant | MODIFIER | c.-22+12169C>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146238791 | ||||||
| chr3:146238997
|
A | G | 6 | a0003c0003t0010g0157a0003c0003t0010g0158a0003c0003t0010g0159others(3): Show | 6 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-22+11963T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146238997 | ||||||
| chr3:146239006
|
C | T | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+11954G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146239006 | ||||||
| chr3:146239478
|
C | A | 212 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(209): Show | 256 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(253): Show |
intron_variant | MODIFIER | c.-22+11482G>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146239478 | ||||||
| chr3:146239519
|
C | CA | 8 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0116others(5): Show | 9 | HG02071.hp2 HG02145.hp1 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.-22+11440dupT | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146239519 | ||||||
| chr3:146239519
|
CA | C | 24 | a0001c0001t0001g0060a0001c0001t0001g0221a0001c0001t0001g0230others(21): Show | 26 | HG01255.hp1 HG01891.hp1 HG01978.hp1 others(23): Show |
intron_variant | MODIFIER | c.-22+11440delT | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146239519 | ||||||
| chr3:146239519
|
CAA | C | 164 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0026others(161): Show | 199 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(196): Show |
intron_variant | MODIFIER | c.-22+11439_-22+1144 others(6): Show |
PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146239519 | ||||||
| chr3:146239519
|
CAAA | C | 37 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0248others(34): Show | 45 | HG01243.hp1 HG01358.hp1 HG01433.hp1 others(42): Show |
intron_variant | MODIFIER | c.-22+11438_-22+1144 others(7): Show |
PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146239519 | ||||||
| chr3:146239521
|
A | C | 1 | a0001c0001t0004g0131 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-22+11439T>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146239521 | ||||||
| chr3:146239531
|
A | C | 5 | a0001c0001t0007g0024a0001c0001t0009g0164a0001c0001t0014g0025others(2): Show | 7 | HG02145.hp2 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+11429T>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146239531 | ||||||
| chr3:146239660
|
A | G | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+11300T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146239660 | ||||||
| chr3:146239682
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-22+11278C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146239682 | ||||||
| chr3:146239701
|
C | T | 2 | a0001c0001t0013g0058a0001c0001t0013g0059 | 2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-22+11259G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146239701 | ||||||
| chr3:146239880
|
T | G | 1 | a0001c0001t0001g0010 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-22+11080A>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146239880 | ||||||
| chr3:146239891
|
G | GA | 8 | a0001c0001t0003g0118a0003c0003t0011g0005a0003c0003t0011g0044others(5): Show | 10 | HG01433.hp1 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-22+11068dupT | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146239891 | ||||||
| chr3:146239921
|
A | G | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+11039T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146239921 | ||||||
| chr3:146240000
|
T | C | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+10960A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146240000 | ||||||
| chr3:146240030
|
T | G | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+10930A>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146240030 | ||||||
| chr3:146240291
|
TA | T | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+10668delT | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146240291 | ||||||
| chr3:146240302
|
C | T | 12 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0248others(9): Show | 17 | HG01358.hp1 HG02683.hp2 HG03669.hp1 others(14): Show |
intron_variant | MODIFIER | c.-22+10658G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146240302 | ||||||
| chr3:146240332
|
G | A | 5 | a0001c0001t0007g0024a0001c0001t0009g0164a0001c0001t0014g0025others(2): Show | 7 | HG02145.hp2 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+10628C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146240332 | ||||||
| chr3:146240334
|
T | C | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+10626A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146240334 | ||||||
| chr3:146240386
|
G | A | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+10574C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146240386 | ||||||
| chr3:146240414
|
C | T | 13 | a0001c0001t0001g0010a0001c0001t0012g0299a0002c0002t0003g0307others(10): Show | 14 | HG01243.hp1 HG02055.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-22+10546G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146240414 | ||||||
| chr3:146240415
|
G | A | 2 | a0001c0001t0001g0223a0001c0001t0001g0224 | 2 | NA18942.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.-22+10545C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146240415 | ||||||
| chr3:146240434
|
C | T | 1 | a0001c0001t0003g0170 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-22+10526G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146240434 | ||||||
| chr3:146240437
|
C | T | 1 | a0001c0001t0002g0137 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-22+10523G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146240437 | ||||||
| chr3:146240470
|
TG | T | 24 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0248others(21): Show | 31 | HG01358.hp1 HG01433.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.-22+10489delC | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146240470 | ||||||
| chr3:146240558
|
C | A | 1 | a0002c0002t0007g0292 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-22+10402G>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146240558 | ||||||
| chr3:146240631
|
G | T | 1 | a0001c0001t0001g0010 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-22+10329C>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146240631 | ||||||
| chr3:146240681
|
G | A | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+10279C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146240681 | ||||||
| chr3:146240690
|
G | A | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+10270C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146240690 | ||||||
| chr3:146240705
|
C | A | 1 | a0001c0001t0003g0225 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-22+10255G>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146240705 | ||||||
| chr3:146240705
|
C | T | 1 | a0001c0001t0004g0171 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-22+10255G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146240705 | ||||||
| chr3:146240713
|
T | TC | 175 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0026others(172): Show | 211 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(208): Show |
intron_variant | MODIFIER | c.-22+10246dupG | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146240713 | ||||||
| chr3:146240721
|
C | T | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+10239G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146240721 | ||||||
| chr3:146240806
|
T | C | 2 | a0001c0001t0009g0022a0001c0001t0013g0119 | 3 | HG02559.hp2 HG02622.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-22+10154A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146240806 | ||||||
| chr3:146240828
|
T | C | 13 | a0001c0001t0001g0010a0001c0001t0012g0299a0002c0002t0003g0307others(10): Show | 14 | HG01243.hp1 HG02055.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-22+10132A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146240828 | ||||||
| chr3:146240904
|
T | C | 1 | a0001c0001t0001g0169 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-22+10056A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146240904 | ||||||
| chr3:146240950
|
C | T | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+10010G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146240950 | ||||||
| chr3:146241034
|
T | C | 226 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(223): Show | 272 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(269): Show |
intron_variant | MODIFIER | c.-22+9926A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146241034 | ||||||
| chr3:146241043
|
T | C | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+9917A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146241043 | ||||||
| chr3:146241120
|
G | A | 1 | a0001c0001t0004g0226 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-22+9840C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146241120 | ||||||
| chr3:146241437
|
T | A | 1 | a0001c0001t0002g0227 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-22+9523A>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146241437 | ||||||
| chr3:146241492
|
T | A | 1 | a0002c0002t0005g0293 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-22+9468A>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146241492 | ||||||
| chr3:146241571
|
C | T | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+9389G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146241571 | ||||||
| chr3:146241584
|
T | C | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+9376A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146241584 | ||||||
| chr3:146241608
|
CA | C | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+9351delT | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146241608 | ||||||
| chr3:146241682
|
G | C | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+9278C>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146241682 | ||||||
| chr3:146241701
|
G | A | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+9259C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146241701 | ||||||
| chr3:146241758
|
C | G | 1 | a0001c0001t0016g0255 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-22+9202G>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146241758 | ||||||
| chr3:146241803
|
A | C | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+9157T>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146241803 | ||||||
| chr3:146241853
|
G | A | 1 | a0001c0001t0004g0120 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-22+9107C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146241853 | ||||||
| chr3:146241896
|
C | A | 1 | a0001c0001t0001g0011 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-22+9064G>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146241896 | ||||||
| chr3:146242026
|
T | C | 230 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(227): Show | 279 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(276): Show |
intron_variant | MODIFIER | c.-22+8934A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146242026 | ||||||
| chr3:146242051
|
G | A | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+8909C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146242051 | ||||||
| chr3:146242218
|
A | G | 1 | a0002c0002t0016g0303 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-22+8742T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146242218 | ||||||
| chr3:146242243
|
G | C | 1 | a0001c0001t0005g0121 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-22+8717C>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146242243 | ||||||
| chr3:146242369
|
C | T | 1 | a0002c0002t0004g0254 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-22+8591G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146242369 | ||||||
| chr3:146242413
|
C | T | 1 | a0001c0001t0003g0057 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-22+8547G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146242413 | ||||||
| chr3:146242444
|
G | A | 2 | a0001c0001t0009g0163a0001c0001t0022g0162 | 2 | HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-22+8516C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146242444 | ||||||
| chr3:146242523
|
C | A | 216 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(213): Show | 263 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(260): Show |
intron_variant | MODIFIER | c.-22+8437G>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146242523 | ||||||
| chr3:146242680
|
A | T | 6 | a0003c0003t0010g0157a0003c0003t0010g0158a0003c0003t0010g0159others(3): Show | 6 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-22+8280T>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146242680 | ||||||
| chr3:146242687
|
G | A | 6 | a0003c0003t0010g0157a0003c0003t0010g0158a0003c0003t0010g0159others(3): Show | 6 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-22+8273C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146242687 | ||||||
| chr3:146242701
|
G | T | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+8259C>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146242701 | ||||||
| chr3:146242721
|
C | T | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+8239G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146242721 | ||||||
| chr3:146242724
|
G | A | 4 | a0001c0001t0001g0145a0001c0001t0001g0248a0001c0001t0002g0146others(1): Show | 4 | HG01358.hp1 HG02683.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.-22+8236C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146242724 | ||||||
| chr3:146242764
|
T | A | 2 | a0001c0001t0009g0163a0001c0001t0022g0162 | 2 | HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-22+8196A>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146242764 | ||||||
| chr3:146242816
|
G | C | 12 | a0001c0001t0012g0299a0002c0002t0003g0307a0002c0002t0007g0306others(9): Show | 12 | HG01243.hp1 HG02055.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.-22+8144C>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146242816 | ||||||
| chr3:146242959
|
C | A | 1 | a0002c0002t0002g0294 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-22+8001G>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146242959 | ||||||
| chr3:146242976
|
C | T | 8 | a0001c0001t0001g0010a0001c0001t0009g0053a0003c0003t0010g0157others(5): Show | 9 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-22+7984G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146242976 | ||||||
| chr3:146242981
|
A | G | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+7979T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146242981 | ||||||
| chr3:146243022
|
A | G | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+7938T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146243022 | ||||||
| chr3:146243052
|
G | A | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+7908C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146243052 | ||||||
| chr3:146243168
|
G | A | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+7792C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146243168 | ||||||
| chr3:146243236
|
A | ATC | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+7722_-22+7723d others(4): Show |
PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146243236 | ||||||
| chr3:146243238
|
CT | C | 7 | a0003c0003t0011g0005a0003c0003t0011g0044a0003c0003t0011g0046others(4): Show | 9 | HG01433.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-22+7721delA | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146243238 | ||||||
| chr3:146243306
|
A | G | 2 | a0003c0003t0001g0300a0003c0003t0001g0301 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-22+7654T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146243306 | ||||||
| chr3:146243387
|
G | T | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+7573C>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146243387 | ||||||
| chr3:146243428
|
A | C | 1 | a0001c0001t0003g0056 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-22+7532T>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146243428 | ||||||
| chr3:146243452
|
A | C | 212 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(209): Show | 256 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(253): Show |
intron_variant | MODIFIER | c.-22+7508T>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146243452 | ||||||
| chr3:146243495
|
G | A | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+7465C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146243495 | ||||||
| chr3:146243509
|
A | T | 219 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(216): Show | 263 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(260): Show |
intron_variant | MODIFIER | c.-22+7451T>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146243509 | ||||||
| chr3:146243625
|
G | A | 171 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0026others(168): Show | 207 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(204): Show |
intron_variant | MODIFIER | c.-22+7335C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146243625 | ||||||
| chr3:146243708
|
C | T | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+7252G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146243708 | ||||||
| chr3:146243759
|
C | A | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+7201G>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146243759 | ||||||
| chr3:146243760
|
G | A | 3 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230 | 3 | HG01257.hp1 HG01978.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.-22+7200C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146243760 | ||||||
| chr3:146243816
|
G | C | 12 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0248others(9): Show | 17 | HG01358.hp1 HG02683.hp2 HG03669.hp1 others(14): Show |
intron_variant | MODIFIER | c.-22+7144C>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146243816 | ||||||
| chr3:146243887
|
T | C | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+7073A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146243887 | ||||||
| chr3:146243960
|
C | T | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+7000G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146243960 | ||||||
| chr3:146243969
|
C | T | 1 | a0001c0001t0001g0010 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-22+6991G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146243969 | ||||||
| chr3:146243986
|
T | G | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+6974A>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146243986 | ||||||
| chr3:146244008
|
C | T | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+6952G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146244008 | ||||||
| chr3:146244010
|
C | T | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+6950G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146244010 | ||||||
| chr3:146244068
|
G | A | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+6892C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146244068 | ||||||
| chr3:146244152
|
T | C | 13 | a0001c0001t0001g0010a0001c0001t0012g0299a0002c0002t0003g0307others(10): Show | 14 | HG01243.hp1 HG02055.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-22+6808A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146244152 | ||||||
| chr3:146244168
|
T | C | 4 | a0004c0004t0001g0152a0004c0004t0001g0153a0004c0004t0006g0154others(1): Show | 4 | HG02818.hp2 HG02970.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-22+6792A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146244168 | ||||||
| chr3:146244192
|
C | T | 2 | a0001c0001t0012g0147a0001c0001t0012g0148 | 2 | HG02895.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-22+6768G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146244192 | ||||||
| chr3:146244204
|
C | T | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+6756G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146244204 | ||||||
| chr3:146244208
|
C | T | 212 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(209): Show | 256 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(253): Show |
intron_variant | MODIFIER | c.-22+6752G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146244208 | ||||||
| chr3:146244240
|
T | C | 6 | a0003c0003t0010g0157a0003c0003t0010g0158a0003c0003t0010g0159others(3): Show | 6 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-22+6720A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146244240 | ||||||
| chr3:146244263
|
C | T | 2 | a0003c0003t0001g0300a0003c0003t0001g0301 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-22+6697G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146244263 | ||||||
| chr3:146244398
|
T | A | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+6562A>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146244398 | ||||||
| chr3:146244456
|
C | T | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+6504G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146244456 | ||||||
| chr3:146244472
|
C | T | 1 | a0001c0001t0003g0170 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-22+6488G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146244472 | ||||||
| chr3:146244490
|
A | C | 219 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(216): Show | 263 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(260): Show |
intron_variant | MODIFIER | c.-22+6470T>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146244490 | ||||||
| chr3:146244583
|
G | A | 212 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(209): Show | 256 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(253): Show |
intron_variant | MODIFIER | c.-22+6377C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146244583 | ||||||
| chr3:146244593
|
C | A | 1 | a0001c0001t0030g0231 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-22+6367G>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146244593 | ||||||
| chr3:146244856
|
A | C | 1 | a0001c0001t0009g0053 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-22+6104T>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146244856 | ||||||
| chr3:146244899
|
C | T | 1 | a0001c0001t0001g0010 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-22+6061G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146244899 | ||||||
| chr3:146244905
|
T | C | 94 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0027others(91): Show | 109 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.-22+6055A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146244905 | ||||||
| chr3:146244947
|
A | G | 212 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(209): Show | 256 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(253): Show |
intron_variant | MODIFIER | c.-22+6013T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146244947 | ||||||
| chr3:146245038
|
C | T | 212 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(209): Show | 256 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(253): Show |
intron_variant | MODIFIER | c.-22+5922G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146245038 | ||||||
| chr3:146245114
|
G | A | 4 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0004g0232others(1): Show | 4 | NA18950.hp2 NA18951.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22+5846C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146245114 | ||||||
| chr3:146245211
|
A | G | 1 | a0001c0001t0001g0010 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-22+5749T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146245211 | ||||||
| chr3:146245219
|
A | C | 1 | a0002c0002t0004g0253 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-22+5741T>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146245219 | ||||||
| chr3:146245281
|
C | A | 3 | a0001c0001t0006g0123a0001c0001t0006g0124a0001c0001t0009g0122 | 3 | HG01243.hp2 HG02109.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.-22+5679G>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146245281 | ||||||
| chr3:146245303
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-22+5657G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146245303 | ||||||
| chr3:146245324
|
C | G | 6 | a0001c0001t0001g0026a0001c0001t0001g0165a0001c0001t0001g0166others(3): Show | 7 | HG00642.hp1 HG01256.hp1 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+5636G>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146245324 | ||||||
| chr3:146245358
|
T | C | 2 | a0003c0003t0001g0300a0003c0003t0001g0301 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-22+5602A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146245358 | ||||||
| chr3:146245395
|
A | T | 7 | a0003c0003t0011g0005a0003c0003t0011g0044a0003c0003t0011g0046others(4): Show | 9 | HG01433.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-22+5565T>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146245395 | ||||||
| chr3:146245489
|
G | A | 4 | a0002c0002t0002g0298a0002c0002t0003g0296a0002c0002t0006g0295others(1): Show | 4 | HG02698.hp2 HG03688.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22+5471C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146245489 | ||||||
| chr3:146245573
|
A | C | 212 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(209): Show | 256 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(253): Show |
intron_variant | MODIFIER | c.-22+5387T>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146245573 | ||||||
| chr3:146245739
|
CAATA | C | 212 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(209): Show | 256 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(253): Show |
intron_variant | MODIFIER | c.-22+5217_-22+5220d others(6): Show |
PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146245739 | ||||||
| chr3:146245854
|
G | T | 212 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(209): Show | 256 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(253): Show |
intron_variant | MODIFIER | c.-22+5106C>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146245854 | ||||||
| chr3:146245868
|
C | T | 13 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0248others(10): Show | 18 | HG01358.hp1 HG02683.hp2 HG03669.hp1 others(15): Show |
intron_variant | MODIFIER | c.-22+5092G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146245868 | ||||||
| chr3:146246029
|
G | A | 8 | a0002c0002t0003g0307a0002c0002t0007g0306a0002c0002t0013g0305others(5): Show | 8 | HG01243.hp1 HG02055.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-22+4931C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146246029 | ||||||
| chr3:146246094
|
G | A | 213 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(210): Show | 257 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(254): Show |
intron_variant | MODIFIER | c.-22+4866C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146246094 | ||||||
| chr3:146246158
|
T | C | 5 | a0001c0001t0010g0149a0001c0001t0010g0151a0001c0001t0012g0147others(2): Show | 5 | HG02630.hp2 HG02647.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22+4802A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146246158 | ||||||
| chr3:146246381
|
T | C | 209 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(206): Show | 253 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(250): Show |
intron_variant | MODIFIER | c.-22+4579A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146246381 | ||||||
| chr3:146246381
|
T | G | 4 | a0002c0002t0001g0252a0002c0002t0002g0249a0002c0002t0005g0250others(1): Show | 4 | NA18993.hp2 NA19004.hp2 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22+4579A>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146246381 | ||||||
| chr3:146246481
|
T | A | 1 | a0001c0001t0001g0236 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-22+4479A>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146246481 | ||||||
| chr3:146246566
|
TA | T | 12 | a0001c0001t0012g0299a0002c0002t0003g0307a0002c0002t0007g0306others(9): Show | 12 | HG01243.hp1 HG02055.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.-22+4393delT | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146246566 | ||||||
| chr3:146246601
|
G | A | 5 | a0001c0001t0010g0149a0001c0001t0010g0151a0001c0001t0012g0147others(2): Show | 5 | HG02630.hp2 HG02647.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22+4359C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146246601 | ||||||
| chr3:146246620
|
A | T | 1 | a0001c0001t0012g0299 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-22+4340T>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146246620 | ||||||
| chr3:146247002
|
C | T | 220 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(217): Show | 264 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(261): Show |
intron_variant | MODIFIER | c.-22+3958G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146247002 | ||||||
| chr3:146247031
|
T | C | 3 | a0001c0001t0006g0123a0001c0001t0006g0124a0001c0001t0009g0122 | 3 | HG01243.hp2 HG02109.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.-22+3929A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146247031 | ||||||
| chr3:146247054
|
T | A | 213 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(210): Show | 257 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(254): Show |
intron_variant | MODIFIER | c.-22+3906A>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146247054 | ||||||
| chr3:146247116
|
T | C | 4 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0003g0239others(1): Show | 7 | HG00099.hp1 HG03017.hp2 HG03490.hp2 others(4): Show |
intron_variant | MODIFIER | c.-22+3844A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146247116 | ||||||
| chr3:146247209
|
A | T | 1 | a0001c0001t0001g0054 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-22+3751T>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146247209 | ||||||
| chr3:146247218
|
C | T | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+3742G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146247218 | ||||||
| chr3:146247259
|
G | A | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+3701C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146247259 | ||||||
| chr3:146247394
|
T | A | 1 | a0001c0001t0003g0241 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-22+3566A>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146247394 | ||||||
| chr3:146247395
|
A | G | 7 | a0001c0001t0009g0053a0003c0003t0010g0157a0003c0003t0010g0158others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+3565T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146247395 | ||||||
| chr3:146247396
|
TA | T | 164 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0026others(161): Show | 199 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(196): Show |
intron_variant | MODIFIER | c.-22+3563delT | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146247396 | ||||||
| chr3:146247626
|
T | C | 1 | a0001c0001t0001g0010 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-22+3334A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146247626 | ||||||
| chr3:146247630
|
G | A | 8 | a0001c0001t0001g0010a0001c0001t0009g0053a0003c0003t0010g0157others(5): Show | 9 | HG01255.hp1 HG01891.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-22+3330C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146247630 | ||||||
| chr3:146247656
|
T | G | 4 | a0004c0004t0001g0152a0004c0004t0001g0153a0004c0004t0006g0154others(1): Show | 4 | HG02818.hp2 HG02970.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-22+3304A>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146247656 | ||||||
| chr3:146247676
|
G | A | 1 | a0001c0001t0007g0240 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-22+3284C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146247676 | ||||||
| chr3:146247688
|
T | C | 1 | a0002c0002t0032g0302 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-22+3272A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146247688 | ||||||
| chr3:146247801
|
T | G | 5 | a0002c0002t0003g0307a0002c0002t0007g0306a0002c0002t0013g0305others(2): Show | 5 | HG01243.hp1 HG02965.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22+3159A>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146247801 | ||||||
| chr3:146247832
|
G | A | 216 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0026others(213): Show | 262 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(259): Show |
intron_variant | MODIFIER | c.-22+3128C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146247832 | ||||||
| chr3:146247902
|
G | A | 216 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0026others(213): Show | 262 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(259): Show |
intron_variant | MODIFIER | c.-22+3058C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146247902 | ||||||
| chr3:146247911
|
C | T | 4 | a0004c0004t0001g0152a0004c0004t0001g0153a0004c0004t0006g0154others(1): Show | 4 | HG02818.hp2 HG02970.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-22+3049G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146247911 | ||||||
| chr3:146247912
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-22+3048C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146247912 | ||||||
| chr3:146248157
|
C | T | 2 | a0003c0003t0006g0012a0003c0003t0014g0052 | 3 | HG02922.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-22+2803G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146248157 | ||||||
| chr3:146248252
|
A | G | 7 | a0003c0003t0011g0005a0003c0003t0011g0044a0003c0003t0011g0046others(4): Show | 9 | HG01433.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-22+2708T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146248252 | ||||||
| chr3:146248343
|
C | T | 217 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(214): Show | 264 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(261): Show |
intron_variant | MODIFIER | c.-22+2617G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146248343 | ||||||
| chr3:146248385
|
A | G | 13 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0248others(10): Show | 18 | HG01358.hp1 HG02683.hp2 HG03669.hp1 others(15): Show |
intron_variant | MODIFIER | c.-22+2575T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146248385 | ||||||
| chr3:146248398
|
G | A | 8 | a0002c0002t0003g0307a0002c0002t0007g0306a0002c0002t0013g0305others(5): Show | 8 | HG01243.hp1 HG02055.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-22+2562C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146248398 | ||||||
| chr3:146248489
|
G | GAC | 16 | a0001c0001t0003g0241a0001c0001t0005g0126a0001c0001t0009g0163others(13): Show | 18 | HG01433.hp1 HG01891.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.-22+2469_-22+2470d others(4): Show |
PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146248489 | ||||||
| chr3:146248489
|
G | GACAC | 7 | a0001c0001t0002g0023a0001c0001t0007g0024a0001c0001t0009g0164others(4): Show | 10 | HG02015.hp2 HG02145.hp2 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.-22+2467_-22+2470d others(6): Show |
PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146248489 | ||||||
| chr3:146248491
|
C | G | 1 | a0005c0005t0009g0317 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-22+2469G>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146248491 | ||||||
| chr3:146248494
|
A | G | 1 | a0001c0001t0001g0010 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-22+2466T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146248494 | ||||||
| chr3:146248544
|
T | TTTAAC | 217 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(214): Show | 264 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(261): Show |
intron_variant | MODIFIER | c.-22+2415_-22+2416i others(7): Show |
PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146248544 | ||||||
| chr3:146248586
|
A | C | 1 | a0001c0001t0002g0013 | 2 | NA19003.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.-22+2374T>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146248586 | ||||||
| chr3:146248727
|
T | G | 170 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0026others(167): Show | 205 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(202): Show |
intron_variant | MODIFIER | c.-22+2233A>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146248727 | ||||||
| chr3:146248794
|
C | T | 204 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0026others(201): Show | 250 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(247): Show |
intron_variant | MODIFIER | c.-22+2166G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146248794 | ||||||
| chr3:146248870
|
C | T | 217 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(214): Show | 264 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(261): Show |
intron_variant | MODIFIER | c.-22+2090G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146248870 | ||||||
| chr3:146248965
|
T | C | 181 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0026others(178): Show | 219 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(216): Show |
intron_variant | MODIFIER | c.-22+1995A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146248965 | ||||||
| chr3:146249026
|
C | T | 7 | a0003c0003t0011g0005a0003c0003t0011g0044a0003c0003t0011g0046others(4): Show | 9 | HG01433.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-22+1934G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146249026 | ||||||
| chr3:146249123
|
G | C | 217 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(214): Show | 264 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(261): Show |
intron_variant | MODIFIER | c.-22+1837C>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146249123 | ||||||
| chr3:146249301
|
A | G | 5 | a0002c0002t0001g0034a0002c0002t0001g0244a0002c0002t0001g0245others(2): Show | 6 | HG01074.hp1 HG01109.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.-22+1659T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146249301 | ||||||
| chr3:146249386
|
T | C | 217 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(214): Show | 264 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(261): Show |
intron_variant | MODIFIER | c.-22+1574A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146249386 | ||||||
| chr3:146249686
|
G | A | 1 | a0001c0001t0001g0010 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-22+1274C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146249686 | ||||||
| chr3:146249710
|
G | A | 1 | a0004c0004t0006g0155 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-22+1250C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146249710 | ||||||
| chr3:146249759
|
T | G | 1 | a0001c0001t0001g0010 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-22+1201A>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146249759 | ||||||
| chr3:146249839
|
T | C | 4 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0004g0128others(1): Show | 4 | HG02055.hp1 HG02572.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-22+1121A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146249839 | ||||||
| chr3:146249933
|
T | C | 216 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0026others(213): Show | 262 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(259): Show |
intron_variant | MODIFIER | c.-22+1027A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146249933 | ||||||
| chr3:146249943
|
C | T | 217 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(214): Show | 264 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(261): Show |
intron_variant | MODIFIER | c.-22+1017G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146249943 | ||||||
| chr3:146250012
|
T | G | 2 | a0001c0001t0001g0242a0001c0001t0001g0243 | 2 | HG01081.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.-22+948A>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146250012 | ||||||
| chr3:146250026
|
T | C | 6 | a0003c0003t0006g0012a0003c0003t0010g0310a0003c0003t0012g0311others(3): Show | 7 | HG02109.hp2 HG02615.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+934A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146250026 | ||||||
| chr3:146250117
|
A | G | 99 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0027others(96): Show | 117 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.-22+843T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146250117 | ||||||
| chr3:146250231
|
T | C | 1 | a0002c0002t0008g0043 | 2 | HG00735.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.-22+729A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146250231 | ||||||
| chr3:146250279
|
G | A | 2 | a0001c0001t0001g0312a0001c0001t0005g0313 | 2 | NA18999.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.-22+681C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146250279 | ||||||
| chr3:146250311
|
T | G | 184 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0027others(181): Show | 221 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(218): Show |
intron_variant | MODIFIER | c.-22+649A>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146250311 | ||||||
| chr3:146250473
|
T | C | 1 | a0005c0005t0021g0314 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-22+487A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146250473 | ||||||
| chr3:146250476
|
G | A | 1 | a0001c0001t0001g0010 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-22+484C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146250476 | ||||||
| chr3:146250482
|
A | T | 1 | a0001c0001t0001g0010 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-22+478T>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146250482 | ||||||
| chr3:146250520
|
T | C | 1 | a0001c0001t0001g0010 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-22+440A>G | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146250520 | ||||||
| chr3:146250594
|
C | G | 1 | a0001c0001t0001g0135 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-22+366G>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146250594 | ||||||
| chr3:146250701
|
G | A | 1 | a0001c0001t0001g0315 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-22+259C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146250701 | ||||||
| chr3:146250765
|
G | A | 226 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(223): Show | 272 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(269): Show |
intron_variant | MODIFIER | c.-22+195C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146250765 | ||||||
| chr3:146250786
|
G | A | 1 | a0001c0001t0001g0316 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-22+174C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146250786 | ||||||
| chr3:146250832
|
G | A | 2 | a0005c0005t0009g0317a0005c0005t0015g0318 | 2 | HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-22+128C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146250832 | ||||||
| chr3:146250885
|
A | G | 1 | a0001c0001t0009g0053 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-22+75T>C | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146250885 | ||||||
| chr3:146250893
|
G | A | 1 | a0001c0001t0001g0010 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-22+67C>T | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146250893 | ||||||
| chr3:146250905
|
C | T | 11 | a0001c0001t0001g0011a0001c0001t0003g0051a0003c0003t0006g0012others(8): Show | 15 | HG01433.hp1 HG01891.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-22+55G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146250905 | ||||||
| chr3:146250951
|
C | T | 1 | a0001c0001t0001g0010 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-22+9G>A | PLSCR4 | ENSG00000114698.15 | transcript | ENST00000354952.7 | protein_coding | 1/8 | chr3 | 146250951 |