Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 389072 |
|---|---|
| ensemblid | ENSG00000178385.15 |
| hgncid | 34006 |
| symbol | PLEKHM3 |
| name | pleckstrin homology domain containing M3 |
| refseq_nuc | NM_001080475.3 |
| refseq_prot | NP_001073944.1 |
| ensembl_nuc | ENST00000427836.8 |
| ensembl_prot | ENSP00000417003.2 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 207821288 |
| end | 208025527 |
| strand | - |
| ver | v1.2 |
| region | chr2:207821288-208025527 |
| region5000 | chr2:207816288-208030527 |
| regionname0 | PLEKHM3_chr2_207821288_208025527 |
| regionname5000 | PLEKHM3_chr2_207816288_208030527 |
| 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 | 1/1 | 761 | 189 | 70 | 36 | 47 | 14 | 20 | 28 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0002 | 0/0 | 761 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0003 | 0/0 | 761 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0004 | 0/0 | 761 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0005 | 0/0 | 761 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0006 | 0/0 | 761 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0007 | 0/0 | 761 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0008 | 0/0 | 761 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 2286 | 66 | 25 | 9 | 15 | 7 | 10 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| c0002 | 0/0 | 2286 | 44 | 25 | 11 | 7 | 1 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| c0003 | 0/0 | 2286 | 38 | 11 | 13 | 6 | 6 | 2 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| c0004 | 1/1 | 2286 | 38 | 7 | 3 | 18 | 0 | 8 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| c0005 | 0/0 | 2286 | 3 | 2 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| c0006 | 0/0 | 2286 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| c0007 | 0/0 | 2286 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| c0008 | 0/0 | 2286 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| c0009 | 0/0 | 2286 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| c0010 | 0/0 | 2286 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| c0011 | 0/0 | 2286 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| c0012 | 0/0 | 2286 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| c0013 | 0/0 | 2286 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| c0014 | 0/0 | 2286 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| c0015 | 0/0 | 2286 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 7489 | 46 | 10 | 19 | 5 | 4 | 7 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| t0002 | 0/1 | 7489 | 35 | 3 | 8 | 16 | 3 | 4 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| t0003 | 0/0 | 7470 | 32 | 7 | 4 | 13 | 5 | 3 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| t0004 | 0/0 | 7470 | 6 | 5 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| t0005 | 0/0 | 7489 | 6 | 6 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| t0006 | 0/0 | 7489 | 6 | 6 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| t0007 | 0/0 | 7489 | 5 | 0 | 0 | 5 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| t0008 | 0/0 | 7489 | 4 | 0 | 3 | 0 | 1 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| t0009 | 0/0 | 7489 | 3 | 3 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| t0010 | 0/0 | 7489 | 3 | 0 | 0 | 3 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| t0011 | 0/0 | 7469 | 3 | 0 | 0 | 3 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| t0012 | 0/0 | 7470 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| t0013 | 0/0 | 7472 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| t0014 | 0/0 | 7489 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| t0015 | 0/0 | 7470 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| t0016 | 0/0 | 7470 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| t0017 | 0/0 | 7470 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| t0018 | 0/0 | 7489 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| t0019 | 0/0 | 7470 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| t0020 | 0/0 | 7470 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| t0021 | 0/0 | 7470 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| t0022 | 0/0 | 7489 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| t0023 | 0/0 | 7470 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| t0024 | 0/0 | 7470 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| t0025 | 0/0 | 7469 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| t0026 | 0/0 | 7469 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| t0027 | 0/0 | 7489 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| t0028 | 0/0 | 7489 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| t0029 | 0/0 | 7489 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| t0030 | 0/0 | 7489 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| t0031 | 0/0 | 7489 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| t0032 | 0/0 | 7470 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| t0033 | 0/0 | 7470 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| t0034 | 0/0 | 7489 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| t0035 | 0/0 | 7470 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| t0036 | 0/0 | 7470 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| t0037 | 0/0 | 7470 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| t0038 | 0/0 | 7470 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| t0039 | 0/0 | 7472 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| t0040 | 0/0 | 7472 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| t0041 | 0/0 | 7470 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| t0042 | 0/0 | 7470 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| t0043 | 0/0 | 7489 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| t0044 | 0/0 | 7489 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| t0045 | 0/0 | 7489 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| t0046 | 0/0 | 7489 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| t0047 | 0/0 | 7489 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| t0048 | 0/0 | 7489 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| t0049 | 0/0 | 7489 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| t0050 | 0/0 | 7468 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| t0051 | 0/0 | 7470 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| t0052 | 0/0 | 7470 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| t0053 | 0/0 | 7468 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| t0054 | 0/0 | 7470 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| t0055 | 0/0 | 7470 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| t0056 | 0/0 | 7469 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| t0057 | 0/0 | 7469 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| t0058 | 0/0 | 7470 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| t0059 | 0/0 | 7472 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| 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 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0112 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0189 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| 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 | 0/0 | 2286 | 66 | 25 | 9 | 15 | 7 | 10 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0002 | 0/0 | 2286 | 44 | 25 | 11 | 7 | 1 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0003 | 0/0 | 2286 | 38 | 11 | 13 | 6 | 6 | 2 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0004 | 1/1 | 2286 | 38 | 7 | 3 | 18 | 0 | 8 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0008 | 0/0 | 2286 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0009 | 0/0 | 2286 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0015 | 0/0 | 2286 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0002c0005 | 0/0 | 2286 | 3 | 2 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0002c0006 | 0/0 | 2286 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0003c0014 | 0/0 | 2286 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0004c0012 | 0/0 | 2286 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0005c0011 | 0/0 | 2286 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0006c0010 | 0/0 | 2286 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0007c0007 | 0/0 | 2286 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0008c0013 | 0/0 | 2286 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 9774 | 16 | 3 | 7 | 1 | 2 | 3 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0001t0002 | 0/0 | 9774 | 8 | 2 | 0 | 5 | 0 | 1 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0001t0003 | 0/0 | 9755 | 14 | 2 | 1 | 5 | 5 | 1 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0001t0004 | 0/0 | 9755 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0001t0005 | 0/0 | 9774 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0001t0009 | 0/0 | 9774 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0001t0011 | 0/0 | 9754 | 3 | 0 | 0 | 3 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0001t0013 | 0/0 | 9757 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0001t0015 | 0/0 | 9755 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0001t0016 | 0/0 | 9755 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0001t0017 | 0/0 | 9755 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0001t0018 | 0/0 | 9774 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0001t0019 | 0/0 | 9755 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0001t0020 | 0/0 | 9755 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0001t0021 | 0/0 | 9755 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0001t0024 | 0/0 | 9755 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0001t0027 | 0/0 | 9774 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0001t0032 | 0/0 | 9755 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0001t0033 | 0/0 | 9755 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0001t0034 | 0/0 | 9774 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0001t0044 | 0/0 | 9774 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0001t0046 | 0/0 | 9774 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0001t0047 | 0/0 | 9774 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0001t0049 | 0/0 | 9774 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0001t0051 | 0/0 | 9755 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0001t0055 | 0/0 | 9755 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0002t0001 | 0/0 | 9774 | 14 | 4 | 6 | 3 | 1 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0002t0002 | 0/0 | 9774 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0002t0003 | 0/0 | 9755 | 6 | 2 | 3 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0002t0004 | 0/0 | 9755 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0002t0005 | 0/0 | 9774 | 4 | 4 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0002t0006 | 0/0 | 9774 | 6 | 6 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0002t0013 | 0/0 | 9757 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0002t0026 | 0/0 | 9754 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0002t0037 | 0/0 | 9755 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0002t0038 | 0/0 | 9755 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0002t0041 | 0/0 | 9755 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0002t0045 | 0/0 | 9774 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0002t0050 | 0/0 | 9753 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0002t0052 | 0/0 | 9755 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0002t0054 | 0/0 | 9755 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0002t0058 | 0/0 | 9755 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0002t0059 | 0/0 | 9757 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0003t0001 | 0/0 | 9774 | 8 | 0 | 5 | 1 | 1 | 1 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0003t0002 | 0/0 | 9774 | 11 | 1 | 5 | 2 | 3 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0003t0003 | 0/0 | 9755 | 3 | 1 | 0 | 1 | 0 | 1 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0003t0004 | 0/0 | 9755 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0003t0007 | 0/0 | 9774 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0003t0008 | 0/0 | 9774 | 4 | 0 | 3 | 0 | 1 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0003t0009 | 0/0 | 9774 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0003t0012 | 0/0 | 9755 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0003t0014 | 0/0 | 9774 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0003t0023 | 0/0 | 9755 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0003t0028 | 0/0 | 9774 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0003t0029 | 0/0 | 9774 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0003t0056 | 0/0 | 9754 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0003t0057 | 0/0 | 9754 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0004t0001 | 1/0 | 9774 | 7 | 2 | 1 | 0 | 0 | 3 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0004t0002 | 0/1 | 9774 | 12 | 0 | 2 | 6 | 0 | 3 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0004t0003 | 0/0 | 9755 | 6 | 1 | 0 | 4 | 0 | 1 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0004t0007 | 0/0 | 9774 | 4 | 0 | 0 | 4 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0004t0010 | 0/0 | 9774 | 3 | 0 | 0 | 3 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0004t0014 | 0/0 | 9774 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0004t0030 | 0/0 | 9774 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0004t0039 | 0/0 | 9757 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0004t0040 | 0/0 | 9757 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0004t0042 | 0/0 | 9755 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0004t0048 | 0/0 | 9774 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0008t0053 | 0/0 | 9753 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0009t0031 | 0/0 | 9774 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0001c0015t0003 | 0/0 | 9755 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0002c0005t0001 | 0/0 | 9774 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0002c0005t0004 | 0/0 | 9755 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0002c0005t0036 | 0/0 | 9755 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0002c0006t0025 | 0/0 | 9754 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0002c0006t0035 | 0/0 | 9755 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0003c0014t0043 | 0/0 | 9774 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0004c0012t0003 | 0/0 | 9755 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0005c0011t0022 | 0/0 | 9774 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0006c0010t0003 | 0/0 | 9755 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0007c0007t0002 | 0/0 | 9774 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| a0008c0013t0002 | 0/0 | 9774 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | copy fasta | chr2 | 207816288 | 208030527 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0003g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0004g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0005g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0005g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0009g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0009g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0011g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0011g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0011g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0013g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0015g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0016g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0017g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0018g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0019g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0020g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0021g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0024g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0027g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0032g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0033g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0034g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0044g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0046g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0047g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0049g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0051g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0001t0055g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0002t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0002t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0002t0003g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0002t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0002t0003g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0002t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0002t0003g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0002t0003g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0002t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0002t0005g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0002t0005g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0002t0005g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0002t0005g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0002t0006g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0002t0006g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0002t0006g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0002t0006g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0002t0006g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0002t0006g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0002t0013g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0002t0026g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0002t0037g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0002t0038g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0002t0041g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0002t0045g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0002t0050g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0002t0052g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0002t0054g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0002t0058g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0002t0059g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0003t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0003t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0003t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0003t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0003t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0003t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0003t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0003t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0003t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0003t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0003t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0003t0002g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0003t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0003t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0003t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0003t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0003t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0003t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0003t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0003t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0003t0003g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0003t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0003t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0003t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0003t0007g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0003t0008g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0003t0008g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0003t0008g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0003t0008g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0003t0009g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0003t0012g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0003t0012g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0003t0014g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0003t0023g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0003t0028g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0003t0029g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0003t0056g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0003t0057g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0004t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0004t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0004t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0004t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0004t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0004t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0004t0001g0189 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0004t0002g0112 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0004t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0004t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0004t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0004t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0004t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0004t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0004t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0004t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0004t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0004t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0004t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0004t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0004t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0004t0003g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0004t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0004t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0004t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0004t0007g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0004t0007g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0004t0007g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0004t0007g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0004t0010g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0004t0010g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0004t0010g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0004t0014g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0004t0030g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0004t0039g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0004t0040g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0004t0042g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0004t0048g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0008t0053g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0009t0031g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0001c0015t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0002c0005t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0002c0005t0004g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0002c0005t0036g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0002c0006t0025g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0002c0006t0035g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0003c0014t0043g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0004c0012t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0005c0011t0022g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0006c0010t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0007c0007t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| a0008c0013t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0001 | g0028 | EUR | GBR | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0012 | EUR | GBR | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0144 | EUR | FIN | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG00280 | hp2 | a0001 | c0003 | t0008 | g0027 | EUR | FIN | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0071 | EUR | FIN | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG00323 | hp2 | a0001 | c0003 | t0002 | g0024 | EUR | FIN | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0062 | EAS | CHS | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG00408 | hp2 | a0001 | c0004 | t0003 | g0096 | EAS | CHS | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG00423 | hp1 | a0001 | c0004 | t0002 | g0148 | EAS | CHS | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG00423 | hp2 | a0001 | c0001 | t0032 | g0049 | EAS | CHS | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG00438 | hp1 | a0001 | c0003 | t0002 | g0040 | EAS | CHS | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0141 | EAS | CHS | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | CHS | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG00558 | hp2 | a0001 | c0004 | t0002 | g0143 | EAS | CHS | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0154 | EAS | CHS | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG00621 | hp2 | a0001 | c0002 | t0002 | g0170 | EAS | CHS | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG00639 | hp1 | a0001 | c0002 | t0041 | g0164 | AMR | PUR | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG00639 | hp2 | a0001 | c0003 | t0008 | g0026 | AMR | PUR | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG00642 | hp2 | a0001 | c0004 | t0002 | g0136 | AMR | PUR | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG01069 | hp2 | a0001 | c0003 | t0002 | g0021 | AMR | PUR | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG01071 | hp1 | a0007 | c0007 | t0002 | g0057 | AMR | PUR | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG01071 | hp2 | a0001 | c0003 | t0001 | g0022 | AMR | PUR | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG01074 | hp1 | a0001 | c0003 | t0002 | g0018 | AMR | PUR | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0139 | AMR | PUR | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0064 | AMR | PUR | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG01109 | hp1 | a0001 | c0004 | t0001 | g0107 | AMR | PUR | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG01109 | hp2 | a0002 | c0005 | t0004 | g0094 | AMR | PUR | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG01168 | hp1 | a0001 | c0001 | t0047 | g0059 | AMR | PUR | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG01168 | hp2 | a0001 | c0002 | t0038 | g0182 | AMR | PUR | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG01192 | hp1 | a0001 | c0003 | t0001 | g0044 | AMR | PUR | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0102 | AMR | PUR | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG01243 | hp1 | a0001 | c0003 | t0001 | g0091 | AMR | PUR | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG01256 | hp1 | a0001 | c0003 | t0001 | g0043 | AMR | CLM | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG01256 | hp2 | a0001 | c0002 | t0003 | g0133 | AMR | CLM | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG01261 | hp2 | a0001 | c0002 | t0003 | g0171 | AMR | CLM | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG01346 | hp1 | a0001 | c0003 | t0008 | g0050 | AMR | CLM | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0106 | AMR | CLM | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG01358 | hp2 | a0001 | c0003 | t0002 | g0023 | AMR | CLM | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0105 | AMR | CLM | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0052 | EUR | IBS | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | IBS | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG01516 | hp1 | a0001 | c0003 | t0002 | g0037 | EUR | IBS | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0053 | EUR | IBS | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0051 | EUR | IBS | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG01517 | hp2 | a0001 | c0003 | t0002 | g0038 | EUR | IBS | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG01884 | hp1 | a0001 | c0002 | t0003 | g0184 | AFR | ACB | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG01884 | hp2 | a0001 | c0002 | t0006 | g0198 | AFR | ACB | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG01891 | hp1 | a0001 | c0003 | t0012 | g0090 | AFR | ACB | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0169 | AMR | PEL | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG01928 | hp2 | a0001 | c0003 | t0002 | g0072 | AMR | PEL | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG01952 | hp1 | a0001 | c0003 | t0002 | g0081 | AMR | PEL | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG01952 | hp2 | a0001 | c0003 | t0008 | g0076 | AMR | PEL | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG02056 | hp1 | a0006 | c0010 | t0003 | g0101 | EAS | KHV | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG02056 | hp2 | a0001 | c0004 | t0010 | g0157 | EAS | KHV | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0031 | EAS | KHV | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG02071 | hp2 | a0001 | c0004 | t0002 | g0155 | EAS | KHV | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0058 | EAS | KHV | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG02080 | hp2 | a0001 | c0004 | t0003 | g0147 | EAS | KHV | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG02135 | hp1 | a0001 | c0004 | t0003 | g0104 | EAS | KHV | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0030 | EAS | KHV | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG02145 | hp1 | a0001 | c0002 | t0006 | g0199 | AFR | ACB | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG02145 | hp2 | a0001 | c0001 | t0009 | g0007 | AFR | ACB | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG02257 | hp1 | a0003 | c0014 | t0043 | g0084 | AFR | ACB | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG02257 | hp2 | a0001 | c0001 | t0020 | g0115 | AFR | ACB | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG02258 | hp1 | a0001 | c0003 | t0014 | g0099 | AFR | ACB | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0088 | AFR | ACB | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0168 | AMR | PEL | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG02293 | hp2 | a0001 | c0003 | t0001 | g0025 | AMR | PEL | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG02300 | hp1 | a0001 | c0004 | t0002 | g0138 | AMR | PEL | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG02300 | hp2 | a0001 | c0002 | t0003 | g0103 | AMR | PEL | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0177 | AFR | GWD | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG02572 | hp2 | a0001 | c0004 | t0014 | g0130 | AFR | GWD | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG02615 | hp2 | a0001 | c0002 | t0058 | g0197 | AFR | GWD | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG02622 | hp1 | a0001 | c0002 | t0050 | g0188 | AFR | GWD | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG02622 | hp2 | a0001 | c0004 | t0001 | g0185 | AFR | GWD | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG02630 | hp1 | a0001 | c0004 | t0001 | g0127 | AFR | GWD | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG02630 | hp2 | a0001 | c0003 | t0004 | g0172 | AFR | GWD | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG02647 | hp1 | a0001 | c0001 | t0044 | g0116 | AFR | GWD | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG02647 | hp2 | a0001 | c0002 | t0006 | g0196 | AFR | GWD | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG02683 | hp1 | a0001 | c0004 | t0002 | g0114 | SAS | PJL | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG02683 | hp2 | a0001 | c0001 | t0046 | g0089 | SAS | PJL | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG02698 | hp1 | a0001 | c0001 | t0034 | g0047 | SAS | PJL | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG02698 | hp2 | a0001 | c0003 | t0001 | g0092 | SAS | PJL | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG02809 | hp1 | a0001 | c0004 | t0042 | g0035 | AFR | GWD | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG02809 | hp2 | a0001 | c0002 | t0003 | g0129 | AFR | GWD | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG02818 | hp1 | a0001 | c0002 | t0004 | g0122 | AFR | GWD | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG02818 | hp2 | a0001 | c0001 | t0021 | g0121 | AFR | GWD | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0126 | AFR | GWD | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG02886 | hp2 | a0001 | c0002 | t0006 | g0194 | AFR | GWD | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG02895 | hp1 | a0001 | c0002 | t0059 | g0200 | AFR | GWD | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG02895 | hp2 | a0001 | c0002 | t0006 | g0195 | AFR | GWD | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG02896 | hp1 | a0001 | c0015 | t0003 | g0093 | AFR | GWD | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG02896 | hp2 | a0002 | c0005 | t0001 | g0132 | AFR | GWD | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG02922 | hp1 | a0001 | c0002 | t0045 | g0190 | AFR | ESN | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG02922 | hp2 | a0001 | c0001 | t0009 | g0006 | AFR | ESN | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0135 | AFR | ESN | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0120 | AFR | ESN | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG02976 | hp2 | a0001 | c0002 | t0005 | g0162 | AFR | ESN | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG03041 | hp1 | a0001 | c0001 | t0018 | g0002 | AFR | GWD | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG03041 | hp2 | a0001 | c0002 | t0052 | g0160 | AFR | GWD | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG03098 | hp1 | a0001 | c0002 | t0037 | g0110 | AFR | MSL | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG03098 | hp2 | a0005 | c0011 | t0022 | g0111 | AFR | MSL | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG03130 | hp1 | a0001 | c0003 | t0023 | g0087 | AFR | ESN | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG03130 | hp2 | a0001 | c0001 | t0015 | g0004 | AFR | ESN | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG03139 | hp1 | a0001 | c0003 | t0012 | g0176 | AFR | ESN | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG03139 | hp2 | a0001 | c0004 | t0039 | g0036 | AFR | ESN | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG03195 | hp1 | a0001 | c0002 | t0005 | g0161 | AFR | ESN | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | ESN | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG03209 | hp1 | a0001 | c0001 | t0013 | g0175 | AFR | MSL | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG03209 | hp2 | a0001 | c0002 | t0005 | g0183 | AFR | MSL | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG03239 | hp1 | a0001 | c0004 | t0048 | g0166 | SAS | PJL | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG03453 | hp1 | a0001 | c0002 | t0026 | g0085 | AFR | MSL | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0124 | AFR | MSL | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG03486 | hp1 | a0001 | c0004 | t0040 | g0186 | AFR | MSL | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG03486 | hp2 | a0001 | c0001 | t0024 | g0117 | AFR | MSL | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG03492 | hp1 | a0001 | c0004 | t0001 | g0179 | SAS | PJL | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0020 | SAS | PJL | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0086 | AFR | ESN | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG03516 | hp2 | a0001 | c0004 | t0003 | g0128 | AFR | ESN | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG03579 | hp1 | a0001 | c0001 | t0051 | g0123 | AFR | MSL | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG03579 | hp2 | a0001 | c0003 | t0057 | g0191 | AFR | MSL | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG03669 | hp2 | a0001 | c0004 | t0002 | g0163 | SAS | PJL | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG03688 | hp1 | a0001 | c0001 | t0027 | g0041 | SAS | STU | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG03688 | hp2 | a0001 | c0004 | t0003 | g0108 | SAS | STU | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG03710 | hp1 | a0001 | c0004 | t0002 | g0113 | SAS | PJL | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG04115 | hp1 | a0001 | c0001 | t0049 | g0075 | SAS | STU | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG04115 | hp2 | a0001 | c0004 | t0001 | g0153 | SAS | STU | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG04184 | hp1 | a0001 | c0004 | t0001 | g0152 | SAS | BEB | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG04184 | hp2 | a0001 | c0001 | t0055 | g0029 | SAS | BEB | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG04204 | hp1 | a0001 | c0003 | t0003 | g0073 | SAS | STU | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0039 | SAS | STU | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| NA18522 | hp1 | a0002 | c0006 | t0025 | g0187 | AFR | YRI | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0134 | AFR | YRI | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| NA18747 | hp1 | a0001 | c0003 | t0003 | g0067 | EAS | CHB | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| NA18747 | hp2 | a0001 | c0004 | t0010 | g0150 | EAS | CHB | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| NA18906 | hp1 | a0001 | c0003 | t0004 | g0100 | AFR | YRI | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| NA18906 | hp2 | a0001 | c0002 | t0005 | g0159 | AFR | YRI | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| NA18941 | hp1 | a0001 | c0004 | t0007 | g0146 | EAS | JPT | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| NA18951 | hp1 | a0001 | c0003 | t0029 | g0054 | EAS | JPT | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| NA18951 | hp2 | a0001 | c0002 | t0002 | g0140 | EAS | JPT | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| NA18954 | hp1 | a0001 | c0004 | t0002 | g0131 | EAS | JPT | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| NA18956 | hp1 | a0004 | c0012 | t0003 | g0095 | EAS | JPT | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| NA18956 | hp2 | a0001 | c0004 | t0030 | g0167 | EAS | JPT | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| NA18959 | hp2 | a0001 | c0004 | t0010 | g0145 | EAS | JPT | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| NA18962 | hp1 | a0001 | c0004 | t0003 | g0165 | EAS | JPT | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| NA18962 | hp2 | a0001 | c0003 | t0007 | g0065 | EAS | JPT | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| NA18968 | hp1 | a0001 | c0001 | t0011 | g0077 | EAS | JPT | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| NA18968 | hp2 | a0001 | c0004 | t0007 | g0178 | EAS | JPT | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| NA18969 | hp2 | a0001 | c0009 | t0031 | g0156 | EAS | JPT | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| NA18972 | hp1 | a0001 | c0004 | t0002 | g0151 | EAS | JPT | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| NA18972 | hp2 | a0001 | c0001 | t0011 | g0078 | EAS | JPT | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| NA18985 | hp1 | a0001 | c0004 | t0002 | g0158 | EAS | JPT | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| NA18985 | hp2 | a0001 | c0003 | t0001 | g0009 | EAS | JPT | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| NA19005 | hp1 | a0001 | c0004 | t0007 | g0181 | EAS | JPT | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| NA19005 | hp2 | a0001 | c0001 | t0011 | g0079 | EAS | JPT | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| NA19007 | hp1 | a0008 | c0013 | t0002 | g0109 | EAS | JPT | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0142 | EAS | JPT | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| NA19030 | hp1 | a0001 | c0008 | t0053 | g0173 | AFR | LWK | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| NA19030 | hp2 | a0001 | c0001 | t0016 | g0005 | AFR | LWK | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| NA19043 | hp1 | a0001 | c0003 | t0003 | g0174 | AFR | LWK | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | LWK | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| NA19067 | hp1 | a0001 | c0003 | t0002 | g0082 | EAS | JPT | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| NA19067 | hp2 | a0001 | c0002 | t0054 | g0149 | EAS | JPT | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| NA19082 | hp1 | a0001 | c0004 | t0007 | g0180 | EAS | JPT | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| NA19087 | hp1 | a0001 | c0002 | t0003 | g0137 | EAS | JPT | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| NA19240 | hp1 | a0001 | c0003 | t0009 | g0001 | AFR | YRI | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0119 | AFR | YRI | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| NA20129 | hp1 | a0001 | c0001 | t0019 | g0008 | AFR | ASW | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | ASW | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0034 | EUR | TSI | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| NA20805 | hp2 | a0001 | c0003 | t0028 | g0010 | EUR | TSI | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG02109 | hp1 | a0002 | c0006 | t0035 | g0097 | AFR | ACB | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG02109 | hp2 | a0001 | c0001 | t0017 | g0003 | AFR | ACB | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG02486 | hp1 | a0001 | c0003 | t0056 | g0192 | AFR | ACB | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG02486 | hp2 | a0001 | c0002 | t0006 | g0193 | AFR | ACB | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG02559 | hp1 | a0001 | c0002 | t0013 | g0125 | AFR | ACB | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| HG02559 | hp2 | a0001 | c0001 | t0033 | g0016 | AFR | ACB | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| NA20300 | hp1 | a0002 | c0005 | t0036 | g0098 | AFR | USA | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| NA20300 | hp2 | a0001 | c0003 | t0002 | g0066 | AFR | USA | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0004 | t0002 | g0112 | REF | REF | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| homoSapiens_grch38 | hp1 | a0001 | c0004 | t0001 | g0189 | REF | REF | PLEKHM3_chr2_207816288_208030527 | PLEKHM3 | chr2 | 207816288 | 208030527 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:207946464
|
T | A | 1 | a0004 | 1 | NA18956.hp1 | missense_variant | MODERATE | c.1595A>T | p.Asn532Ile | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/8 | 2052/9774 | 1595/2286 | 532/761 | chr2 | 207946464 | ||
| chr2:207976821
|
C | G | 1 | a0005 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.1376G>C | p.Arg459Thr | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/8 | 1833/9774 | 1376/2286 | 459/761 | chr2 | 207976821 | ||
| chr2:207977227
|
A | T | 1 | a0002 | 5 | HG01109.hp2 HG02109.hp1 HG02896.hp2 others(2): Show |
missense_variant | MODERATE | c.970T>A | p.Ser324Thr | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/8 | 1427/9774 | 970/2286 | 324/761 | chr2 | 207977227 | ||
| chr2:207977284
|
C | G | 1 | a0006 | 1 | HG02056.hp1 | missense_variant | MODERATE | c.913G>C | p.Glu305Gln | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/8 | 1370/9774 | 913/2286 | 305/761 | chr2 | 207977284 | ||
| chr2:207977461
|
C | T | 1 | a0007 | 1 | HG01071.hp1 | missense_variant | MODERATE | c.736G>A | p.Asp246Asn | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/8 | 1193/9774 | 736/2286 | 246/761 | chr2 | 207977461 | ||
| chr2:208001095
|
T | C | 1 | a0008 | 1 | NA19007.hp1 | missense_variant | MODERATE | c.545A>G | p.His182Arg | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/8 | 1002/9774 | 545/2286 | 182/761 | chr2 | 208001095 | ||
| chr2:208001476
|
G | A | 1 | a0003 | 1 | HG02257.hp1 | missense_variant | MODERATE | c.164C>T | p.Thr55Ile | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/8 | 621/9774 | 164/2286 | 55/761 | chr2 | 208001476 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:207946373
|
C | T | 10 | a0001c0001a0001c0002a0001c0008others(7): Show | 120 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(117): Show |
synonymous_variant | LOW | c.1686G>A | p.Lys562Lys | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/8 | 2143/9774 | 1686/2286 | 562/761 | chr2 | 207946373 | ||
| chr2:207977240
|
A | G | 8 | a0001c0001a0001c0003a0001c0008others(5): Show | 113 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(110): Show |
synonymous_variant | LOW | c.957T>C | p.Asn319Asn | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/8 | 1414/9774 | 957/2286 | 319/761 | chr2 | 207977240 | ||
| chr2:207977429
|
C | T | 2 | a0001c0008a0001c0009 | 2 | NA18969.hp2 NA19030.hp1 |
synonymous_variant | LOW | c.768G>A | p.Thr256Thr | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/8 | 1225/9774 | 768/2286 | 256/761 | chr2 | 207977429 | ||
| chr2:208001499
|
C | A | 1 | a0001c0015 | 1 | HG02896.hp1 | synonymous_variant | LOW | c.141G>T | p.Gly47Gly | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/8 | 598/9774 | 141/2286 | 47/761 | chr2 | 208001499 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:207821307
|
T | TGA | 5 | a0001c0001t0013a0001c0002t0013a0001c0002t0059others(2): Show | 5 | HG02559.hp1 HG02895.hp1 HG03139.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*7010_*7011dupTC | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 7011 | chr2 | 207821307 | |||||
| chr2:207821541
|
C | A | 1 | a0001c0001t0044 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6778G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 6778 | chr2 | 207821541 | |||||
| chr2:207821686
|
C | T | 34 | a0001c0001t0003a0001c0001t0004a0001c0001t0011others(31): Show | 63 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*6633G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 6633 | chr2 | 207821686 | |||||
| chr2:207821871
|
G | A | 7 | a0001c0001t0004a0001c0001t0016a0001c0001t0021others(4): Show | 9 | HG01109.hp2 HG02559.hp2 HG02630.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*6448C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 6448 | chr2 | 207821871 | |||||
| chr2:207822001
|
G | T | 1 | a0001c0001t0051 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6318C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 6318 | chr2 | 207822001 | |||||
| chr2:207822315
|
G | T | 2 | a0001c0003t0007a0001c0004t0007 | 5 | NA18941.hp1 NA18962.hp2 NA18968.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6004C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 6004 | chr2 | 207822315 | |||||
| chr2:207822784
|
G | C | 7 | a0001c0001t0004a0001c0001t0016a0001c0001t0021others(4): Show | 9 | HG01109.hp2 HG02559.hp2 HG02630.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*5535C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 5535 | chr2 | 207822784 | |||||
| chr2:207822868
|
CA | C | 1 | a0001c0001t0011 | 3 | NA18968.hp1 NA18972.hp2 NA19005.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5450delT | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 5450 | chr2 | 207822868 | |||||
| chr2:207822958
|
G | C | 1 | a0001c0001t0032 | 1 | HG00423.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5361C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 5361 | chr2 | 207822958 | |||||
| chr2:207823091
|
GCTTCATT others(12): Show |
G | 45 | a0001c0001t0003a0001c0001t0004a0001c0001t0011others(42): Show | 75 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*5209_*5227delTTCC others(15): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 5209 | chr2 | 207823091 | |||||
| chr2:207823161
|
C | T | 5 | a0001c0001t0013a0001c0002t0013a0001c0002t0059others(2): Show | 5 | HG02559.hp1 HG02895.hp1 HG03139.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5158G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 5158 | chr2 | 207823161 | |||||
| chr2:207823508
|
G | A | 3 | a0001c0001t0013a0001c0002t0013a0001c0002t0059 | 3 | HG02559.hp1 HG02895.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4811C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 4811 | chr2 | 207823508 | |||||
| chr2:207823578
|
A | G | 1 | a0001c0004t0030 | 1 | NA18956.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4741T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 4741 | chr2 | 207823578 | |||||
| chr2:207823595
|
T | C | 5 | a0001c0001t0013a0001c0002t0013a0001c0002t0059others(2): Show | 5 | HG02559.hp1 HG02895.hp1 HG03139.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4724A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 4724 | chr2 | 207823595 | |||||
| chr2:207823688
|
C | G | 2 | a0001c0002t0050a0001c0008t0053 | 2 | HG02622.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4631G>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 4631 | chr2 | 207823688 | |||||
| chr2:207823718
|
C | T | 5 | a0001c0001t0013a0001c0002t0013a0001c0002t0059others(2): Show | 5 | HG02559.hp1 HG02895.hp1 HG03139.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4601G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 4601 | chr2 | 207823718 | |||||
| chr2:207823774
|
C | T | 7 | a0001c0001t0004a0001c0001t0016a0001c0001t0021others(4): Show | 9 | HG01109.hp2 HG02559.hp2 HG02630.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4545G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 4545 | chr2 | 207823774 | |||||
| chr2:207823806
|
T | C | 5 | a0001c0001t0013a0001c0002t0013a0001c0002t0059others(2): Show | 5 | HG02559.hp1 HG02895.hp1 HG03139.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4513A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 4513 | chr2 | 207823806 | |||||
| chr2:207823866
|
G | A | 2 | a0001c0003t0012a0002c0005t0036 | 3 | HG01891.hp1 HG03139.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4453C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 4453 | chr2 | 207823866 | |||||
| chr2:207823872
|
A | C | 1 | a0001c0001t0020 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4447T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 4447 | chr2 | 207823872 | |||||
| chr2:207823894
|
A | G | 1 | a0001c0002t0037 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4425T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 4425 | chr2 | 207823894 | |||||
| chr2:207823924
|
T | C | 5 | a0001c0001t0013a0001c0002t0013a0001c0002t0059others(2): Show | 5 | HG02559.hp1 HG02895.hp1 HG03139.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4395A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 4395 | chr2 | 207823924 | |||||
| chr2:207824123
|
C | T | 1 | a0001c0001t0033 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4196G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 4196 | chr2 | 207824123 | |||||
| chr2:207824164
|
T | C | 5 | a0001c0001t0017a0001c0001t0024a0001c0001t0051others(2): Show | 5 | HG02109.hp1 HG02109.hp2 HG03130.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4155A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 4155 | chr2 | 207824164 | |||||
| chr2:207824174
|
G | A | 1 | a0001c0002t0045 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4145C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 4145 | chr2 | 207824174 | |||||
| chr2:207824430
|
G | A | 1 | a0001c0002t0050 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3889C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 3889 | chr2 | 207824430 | |||||
| chr2:207824453
|
T | C | 39 | a0001c0001t0003a0001c0001t0004a0001c0001t0011others(36): Show | 68 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*3866A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 3866 | chr2 | 207824453 | |||||
| chr2:207824457
|
C | A | 2 | a0001c0001t0017a0001c0003t0023 | 2 | HG02109.hp2 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3862G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 3862 | chr2 | 207824457 | |||||
| chr2:207824458
|
G | A | 1 | a0001c0001t0046 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3861C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 3861 | chr2 | 207824458 | |||||
| chr2:207824691
|
T | C | 2 | a0001c0003t0014a0001c0004t0014 | 2 | HG02258.hp1 HG02572.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3628A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 3628 | chr2 | 207824691 | |||||
| chr2:207824799
|
G | A | 2 | a0001c0001t0047a0001c0004t0040 | 2 | HG01168.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3520C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 3520 | chr2 | 207824799 | |||||
| chr2:207824831
|
A | G | 1 | a0001c0003t0029 | 1 | NA18951.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3488T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 3488 | chr2 | 207824831 | |||||
| chr2:207824849
|
T | A | 1 | a0001c0001t0020 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3470A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 3470 | chr2 | 207824849 | |||||
| chr2:207824943
|
G | A | 2 | a0001c0002t0050a0001c0008t0053 | 2 | HG02622.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3376C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 3376 | chr2 | 207824943 | |||||
| chr2:207825059
|
T | C | 38 | a0001c0001t0003a0001c0001t0004a0001c0001t0011others(35): Show | 67 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*3260A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 3260 | chr2 | 207825059 | |||||
| chr2:207825181
|
C | A | 18 | a0001c0001t0003a0001c0001t0011a0001c0001t0015others(15): Show | 45 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*3138G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 3138 | chr2 | 207825181 | |||||
| chr2:207825391
|
CAT | C | 2 | a0001c0002t0050a0001c0008t0053 | 2 | HG02622.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2926_*2927delAT | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 2926 | chr2 | 207825391 | |||||
| chr2:207825392
|
A | G | 1 | a0003c0014t0043 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2927T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 2927 | chr2 | 207825392 | |||||
| chr2:207825557
|
A | G | 45 | a0001c0001t0003a0001c0001t0004a0001c0001t0011others(42): Show | 75 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*2762T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 2762 | chr2 | 207825557 | |||||
| chr2:207825647
|
A | G | 1 | a0002c0005t0036 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2672T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 2672 | chr2 | 207825647 | |||||
| chr2:207825680
|
G | C | 1 | a0001c0001t0049 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2639C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 2639 | chr2 | 207825680 | |||||
| chr2:207825728
|
G | A | 5 | a0001c0001t0017a0001c0001t0024a0001c0001t0051others(2): Show | 5 | HG02109.hp1 HG02109.hp2 HG03130.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2591C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 2591 | chr2 | 207825728 | |||||
| chr2:207825736
|
G | T | 45 | a0001c0001t0003a0001c0001t0004a0001c0001t0011others(42): Show | 75 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*2583C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 2583 | chr2 | 207825736 | |||||
| chr2:207825741
|
G | A | 4 | a0001c0001t0017a0001c0001t0024a0001c0003t0023others(1): Show | 4 | HG02109.hp1 HG02109.hp2 HG03130.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2578C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 2578 | chr2 | 207825741 | |||||
| chr2:207825943
|
G | A | 7 | a0001c0001t0017a0001c0001t0024a0001c0001t0051others(4): Show | 7 | HG02109.hp1 HG02109.hp2 HG02622.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2376C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 2376 | chr2 | 207825943 | |||||
| chr2:207825972
|
G | A | 5 | a0001c0001t0017a0001c0001t0024a0001c0001t0051others(2): Show | 5 | HG02109.hp1 HG02109.hp2 HG03130.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2347C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 2347 | chr2 | 207825972 | |||||
| chr2:207825973
|
G | A | 7 | a0001c0001t0004a0001c0001t0016a0001c0001t0021others(4): Show | 9 | HG01109.hp2 HG02559.hp2 HG02630.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2346C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 2346 | chr2 | 207825973 | |||||
| chr2:207826099
|
G | A | 2 | a0001c0001t0016a0001c0009t0031 | 2 | NA18969.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2220C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 2220 | chr2 | 207826099 | |||||
| chr2:207826135
|
G | A | 1 | a0001c0001t0051 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2184C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 2184 | chr2 | 207826135 | |||||
| chr2:207826173
|
C | T | 2 | a0001c0001t0017a0001c0003t0023 | 2 | HG02109.hp2 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2146G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 2146 | chr2 | 207826173 | |||||
| chr2:207826452
|
C | T | 4 | a0001c0001t0017a0001c0001t0024a0001c0003t0023others(1): Show | 4 | HG02109.hp1 HG02109.hp2 HG03130.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1867G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 1867 | chr2 | 207826452 | |||||
| chr2:207826503
|
C | T | 2 | a0001c0001t0027a0001c0001t0034 | 2 | HG02698.hp1 HG03688.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1816G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 1816 | chr2 | 207826503 | |||||
| chr2:207826568
|
C | T | 20 | a0001c0001t0003a0001c0001t0004a0001c0001t0011others(17): Show | 49 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*1751G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 1751 | chr2 | 207826568 | |||||
| chr2:207826807
|
C | T | 15 | a0001c0001t0002a0001c0002t0002a0001c0002t0058others(12): Show | 49 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*1512G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 1512 | chr2 | 207826807 | |||||
| chr2:207827182
|
T | C | 4 | a0001c0001t0005a0001c0001t0018a0001c0002t0005others(1): Show | 8 | HG02258.hp2 HG02976.hp2 HG03041.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1137A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 1137 | chr2 | 207827182 | |||||
| chr2:207827254
|
C | T | 1 | a0001c0003t0028 | 1 | NA20805.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1065G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 1065 | chr2 | 207827254 | |||||
| chr2:207827285
|
A | G | 1 | a0001c0001t0027 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1034T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 1034 | chr2 | 207827285 | |||||
| chr2:207827451
|
GA | G | 4 | a0001c0002t0026a0001c0003t0056a0001c0003t0057others(1): Show | 4 | HG02486.hp1 HG03453.hp1 HG03579.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*867delT | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 867 | chr2 | 207827451 | |||||
| chr2:207827493
|
T | C | 3 | a0001c0001t0020a0001c0001t0021a0001c0003t0057 | 3 | HG02257.hp2 HG02818.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*826A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 826 | chr2 | 207827493 | |||||
| chr2:207827560
|
G | A | 1 | a0001c0003t0008 | 4 | HG00280.hp2 HG00639.hp2 HG01346.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*759C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 759 | chr2 | 207827560 | |||||
| chr2:207827581
|
C | T | 1 | a0001c0004t0010 | 3 | HG02056.hp2 NA18747.hp2 NA18959.hp2 |
3_prime_UTR_variant | MODIFIER | c.*738G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 738 | chr2 | 207827581 | |||||
| chr2:207827685
|
T | C | 1 | a0001c0008t0053 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*634A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 634 | chr2 | 207827685 | |||||
| chr2:207827985
|
A | G | 2 | a0001c0001t0024a0001c0003t0023 | 2 | HG03130.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*334T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 334 | chr2 | 207827985 | |||||
| chr2:207828157
|
C | G | 1 | a0005c0011t0022 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*162G>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 162 | chr2 | 207828157 | |||||
| chr2:207828157
|
C | T | 3 | a0001c0001t0020a0001c0001t0021a0001c0003t0012 | 4 | HG01891.hp1 HG02257.hp2 HG02818.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*162G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 162 | chr2 | 207828157 | |||||
| chr2:207828172
|
G | A | 1 | a0001c0002t0054 | 1 | NA19067.hp2 | 3_prime_UTR_variant | MODIFIER | c.*147C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 8/8 | 147 | chr2 | 207828172 | |||||
| chr2:208001942
|
G | A | 1 | a0001c0001t0055 | 1 | HG04184.hp2 | 5_prime_UTR_variant | MODIFIER | c.-303C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/8 | 303 | chr2 | 208001942 | |||||
| chr2:208025399
|
G | A | 2 | a0001c0003t0056a0001c0003t0057 | 2 | HG02486.hp1 HG03579.hp2 |
5_prime_UTR_variant | MODIFIER | c.-329C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/8 | 23760 | chr2 | 208025399 | |||||
| chr2:208025462
|
G | A | 3 | a0001c0002t0006a0001c0002t0058a0001c0002t0059 | 8 | HG01884.hp2 HG02145.hp1 HG02486.hp2 others(5): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-392C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/8 | chr2 | 208025462 | ||||||
| chr2:208025474
|
C | T | 1 | a0001c0001t0019 | 1 | NA20129.hp1 | 5_prime_UTR_variant | MODIFIER | c.-404G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/8 | 23835 | chr2 | 208025474 | |||||
| chr2:208025490
|
C | T | 6 | a0001c0001t0009a0001c0001t0015a0001c0001t0016others(3): Show | 7 | HG02109.hp2 HG02145.hp2 HG02922.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-420G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/8 | 23851 | chr2 | 208025490 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:207828537
|
C | G | 122 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(119): Show | 122 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.2109-41G>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207828537 | ||||||
| chr2:207828583
|
T | C | 122 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(119): Show | 122 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.2109-87A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207828583 | ||||||
| chr2:207828741
|
C | T | 1 | a0001c0004t0003g0104 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2109-245G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207828741 | ||||||
| chr2:207828906
|
A | G | 123 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(120): Show | 123 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.2109-410T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207828906 | ||||||
| chr2:207829207
|
A | G | 122 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(119): Show | 122 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.2109-711T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207829207 | ||||||
| chr2:207829641
|
C | T | 4 | a0001c0001t0015g0004a0001c0001t0046g0089a0001c0002t0001g0135others(1): Show | 4 | HG02683.hp2 HG02896.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2109-1145G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207829641 | ||||||
| chr2:207830299
|
A | G | 196 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(193): Show | 196 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.2109-1803T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207830299 | ||||||
| chr2:207830380
|
G | A | 2 | a0001c0002t0002g0140a0001c0004t0002g0155 | 2 | HG02071.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.2109-1884C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207830380 | ||||||
| chr2:207830457
|
T | C | 1 | a0001c0002t0002g0170 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2109-1961A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207830457 | ||||||
| chr2:207830571
|
C | T | 1 | a0002c0005t0036g0098 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2109-2075G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207830571 | ||||||
| chr2:207830607
|
C | CA | 5 | a0001c0001t0044g0116a0001c0002t0026g0085a0001c0003t0001g0091others(2): Show | 5 | HG01243.hp1 HG02647.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.2109-2112dupT | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207830607 | ||||||
| chr2:207830607
|
C | CAA | 117 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(114): Show | 117 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.2109-2113_2109-211 others(6): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207830607 | ||||||
| chr2:207830664
|
A | ATAAGTGT others(23): Show |
1 | a0001c0004t0001g0179 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.2109-2198_2109-216 others(34): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207830664 | ||||||
| chr2:207830664
|
ATAAGTGT others(23): Show |
A | 2 | a0001c0001t0055g0029a0001c0004t0003g0096 | 2 | HG00408.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.2109-2198_2109-216 others(34): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207830664 | ||||||
| chr2:207830680
|
GAAGGAC | G | 119 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(116): Show | 119 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.2109-2190_2109-218 others(10): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207830680 | ||||||
| chr2:207830687
|
A | T | 119 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(116): Show | 119 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.2109-2191T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207830687 | ||||||
| chr2:207830688
|
C | G | 119 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(116): Show | 119 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.2109-2192G>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207830688 | ||||||
| chr2:207830690
|
T | C | 119 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(116): Show | 119 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.2109-2194A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207830690 | ||||||
| chr2:207830694
|
C | A | 119 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(116): Show | 119 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.2109-2198G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207830694 | ||||||
| chr2:207830695
|
T | G | 119 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(116): Show | 119 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.2109-2199A>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207830695 | ||||||
| chr2:207830703
|
C | G | 8 | a0001c0001t0019g0008a0001c0002t0050g0188a0001c0002t0059g0200others(5): Show | 8 | HG02622.hp1 HG02622.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.2109-2207G>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207830703 | ||||||
| chr2:207830708
|
A | G | 119 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(116): Show | 119 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.2109-2212T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207830708 | ||||||
| chr2:207830710
|
G | C | 119 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(116): Show | 119 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.2109-2214C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207830710 | ||||||
| chr2:207830711
|
T | A | 119 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(116): Show | 119 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.2109-2215A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207830711 | ||||||
| chr2:207830712
|
G | C | 119 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(116): Show | 119 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.2109-2216C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207830712 | ||||||
| chr2:207830714
|
C | T | 119 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(116): Show | 119 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.2109-2218G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207830714 | ||||||
| chr2:207830718
|
A | C | 119 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(116): Show | 119 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.2109-2222T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207830718 | ||||||
| chr2:207830719
|
G | GAAGTGTC others(17): Show |
2 | a0001c0001t0013g0175a0001c0004t0001g0127 | 2 | HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2109-2224_2109-222 others(28): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207830719 | ||||||
| chr2:207830719
|
G | T | 119 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(116): Show | 119 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.2109-2223C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207830719 | ||||||
| chr2:207830925
|
G | A | 2 | a0001c0001t0009g0006a0001c0001t0051g0123 | 2 | HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2109-2429C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207830925 | ||||||
| chr2:207830957
|
G | A | 2 | a0001c0002t0037g0110a0001c0002t0038g0182 | 2 | HG01168.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2109-2461C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207830957 | ||||||
| chr2:207830969
|
G | A | 1 | a0001c0001t0055g0029 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2109-2473C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207830969 | ||||||
| chr2:207830972
|
T | C | 1 | a0001c0001t0003g0034 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2109-2476A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207830972 | ||||||
| chr2:207831133
|
G | A | 1 | a0001c0001t0051g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2109-2637C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207831133 | ||||||
| chr2:207831224
|
C | G | 1 | a0001c0001t0051g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2109-2728G>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207831224 | ||||||
| chr2:207831252
|
A | T | 1 | a0001c0003t0001g0009 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2109-2756T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207831252 | ||||||
| chr2:207831408
|
T | G | 123 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(120): Show | 123 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.2109-2912A>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207831408 | ||||||
| chr2:207831601
|
T | C | 123 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(120): Show | 123 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.2109-3105A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207831601 | ||||||
| chr2:207831666
|
C | T | 1 | a0001c0002t0059g0200 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2109-3170G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207831666 | ||||||
| chr2:207831833
|
C | T | 2 | a0001c0003t0012g0090a0001c0003t0012g0176 | 2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2109-3337G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207831833 | ||||||
| chr2:207831842
|
C | T | 1 | a0001c0001t0051g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2109-3346G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207831842 | ||||||
| chr2:207831872
|
C | T | 2 | a0001c0001t0013g0175a0001c0004t0001g0127 | 2 | HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2109-3376G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207831872 | ||||||
| chr2:207832099
|
G | T | 2 | a0001c0002t0001g0105a0001c0002t0001g0106 | 2 | HG01346.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.2109-3603C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207832099 | ||||||
| chr2:207832251
|
T | C | 1 | a0001c0003t0001g0091 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2109-3755A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207832251 | ||||||
| chr2:207832359
|
G | A | 2 | a0001c0001t0001g0118a0001c0002t0006g0196 | 2 | HG02647.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2109-3863C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207832359 | ||||||
| chr2:207832501
|
A | G | 2 | a0001c0001t0017g0003a0001c0001t0033g0016 | 2 | HG02109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.2109-4005T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207832501 | ||||||
| chr2:207832531
|
C | T | 1 | a0001c0002t0001g0102 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2109-4035G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207832531 | ||||||
| chr2:207832620
|
C | T | 2 | a0001c0001t0001g0042a0001c0001t0001g0060 | 2 | HG01243.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.2109-4124G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207832620 | ||||||
| chr2:207832718
|
G | T | 1 | a0001c0002t0004g0122 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2109-4222C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207832718 | ||||||
| chr2:207832778
|
C | T | 1 | a0001c0003t0004g0100 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2109-4282G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207832778 | ||||||
| chr2:207832840
|
G | A | 3 | a0001c0002t0026g0085a0001c0003t0001g0091a0001c0008t0053g0173 | 3 | HG01243.hp1 HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2109-4344C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207832840 | ||||||
| chr2:207832871
|
G | C | 2 | a0001c0001t0024g0117a0001c0003t0023g0087 | 2 | HG03130.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2109-4375C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207832871 | ||||||
| chr2:207832938
|
C | T | 122 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(119): Show | 122 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.2109-4442G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207832938 | ||||||
| chr2:207832939
|
C | G | 123 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(120): Show | 123 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.2109-4443G>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207832939 | ||||||
| chr2:207832973
|
G | A | 1 | a0001c0002t0001g0126 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2109-4477C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207832973 | ||||||
| chr2:207832994
|
C | A | 2 | a0001c0001t0024g0117a0001c0003t0023g0087 | 2 | HG03130.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2109-4498G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207832994 | ||||||
| chr2:207833004
|
T | C | 123 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(120): Show | 123 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.2109-4508A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207833004 | ||||||
| chr2:207833111
|
C | CA | 10 | a0001c0001t0003g0058a0001c0001t0003g0062a0001c0001t0016g0005others(7): Show | 10 | HG00408.hp1 HG00639.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.2109-4616dupT | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207833111 | ||||||
| chr2:207833111
|
CA | C | 76 | a0001c0001t0001g0045a0001c0001t0001g0068a0001c0001t0001g0071others(73): Show | 76 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.2109-4616delT | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207833111 | ||||||
| chr2:207833111
|
CAA | C | 6 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0002t0003g0129others(3): Show | 6 | HG02809.hp2 HG03195.hp2 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.2109-4617_2109-461 others(6): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207833111 | ||||||
| chr2:207833268
|
G | T | 123 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(120): Show | 123 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.2109-4772C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207833268 | ||||||
| chr2:207833341
|
T | C | 1 | a0001c0002t0001g0139 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2109-4845A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207833341 | ||||||
| chr2:207833583
|
A | C | 1 | a0001c0001t0051g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2109-5087T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207833583 | ||||||
| chr2:207833660
|
A | G | 123 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(120): Show | 123 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.2109-5164T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207833660 | ||||||
| chr2:207833676
|
C | T | 10 | a0001c0001t0004g0120a0001c0001t0019g0008a0001c0002t0004g0122others(7): Show | 10 | HG02622.hp1 HG02622.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.2109-5180G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207833676 | ||||||
| chr2:207834063
|
C | T | 3 | a0001c0002t0026g0085a0001c0003t0001g0091a0001c0008t0053g0173 | 3 | HG01243.hp1 HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2109-5567G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207834063 | ||||||
| chr2:207834130
|
C | CT | 121 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(118): Show | 121 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.2109-5635dupA | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207834130 | ||||||
| chr2:207834146
|
G | A | 1 | a0001c0002t0003g0184 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2109-5650C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207834146 | ||||||
| chr2:207834206
|
C | T | 123 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(120): Show | 123 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.2109-5710G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207834206 | ||||||
| chr2:207834324
|
T | C | 1 | a0001c0001t0002g0069 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2109-5828A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207834324 | ||||||
| chr2:207834342
|
T | C | 123 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(120): Show | 123 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.2109-5846A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207834342 | ||||||
| chr2:207834409
|
A | C | 196 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(193): Show | 196 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.2109-5913T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207834409 | ||||||
| chr2:207834434
|
CT | C | 123 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(120): Show | 123 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.2109-5939delA | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207834434 | ||||||
| chr2:207834555
|
A | G | 1 | a0001c0002t0037g0110 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2109-6059T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207834555 | ||||||
| chr2:207834572
|
T | C | 2 | a0001c0004t0039g0036a0001c0004t0042g0035 | 2 | HG02809.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2109-6076A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207834572 | ||||||
| chr2:207834613
|
T | C | 196 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(193): Show | 196 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.2109-6117A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207834613 | ||||||
| chr2:207834679
|
C | G | 1 | a0001c0001t0002g0032 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2109-6183G>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207834679 | ||||||
| chr2:207834764
|
G | A | 2 | a0001c0004t0030g0167a0008c0013t0002g0109 | 2 | NA18956.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.2109-6268C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207834764 | ||||||
| chr2:207834943
|
G | GT | 8 | a0001c0001t0003g0011a0001c0001t0003g0119a0001c0001t0004g0086others(5): Show | 8 | HG01109.hp2 HG01168.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.2109-6448dupA | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207834943 | ||||||
| chr2:207834948
|
T | G | 1 | a0001c0004t0001g0179 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.2109-6452A>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207834948 | ||||||
| chr2:207834962
|
C | T | 1 | a0001c0004t0001g0127 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2109-6466G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207834962 | ||||||
| chr2:207835026
|
T | C | 121 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(118): Show | 121 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.2109-6530A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207835026 | ||||||
| chr2:207835034
|
G | A | 120 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(117): Show | 120 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.2109-6538C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207835034 | ||||||
| chr2:207835041
|
A | G | 108 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(105): Show | 108 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.2109-6545T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207835041 | ||||||
| chr2:207835193
|
T | C | 2 | a0001c0002t0002g0140a0001c0004t0002g0155 | 2 | HG02071.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.2109-6697A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207835193 | ||||||
| chr2:207835347
|
C | T | 1 | a0001c0002t0006g0193 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2109-6851G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207835347 | ||||||
| chr2:207835875
|
G | T | 123 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(120): Show | 123 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.2109-7379C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207835875 | ||||||
| chr2:207836008
|
A | C | 2 | a0001c0003t0012g0090a0001c0003t0012g0176 | 2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2109-7512T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207836008 | ||||||
| chr2:207836057
|
G | C | 1 | a0001c0001t0051g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2109-7561C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207836057 | ||||||
| chr2:207836187
|
T | C | 123 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(120): Show | 123 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.2109-7691A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207836187 | ||||||
| chr2:207836190
|
T | C | 1 | a0001c0001t0051g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2109-7694A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207836190 | ||||||
| chr2:207836219
|
A | G | 123 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(120): Show | 123 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.2109-7723T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207836219 | ||||||
| chr2:207836288
|
C | T | 8 | a0001c0001t0004g0120a0001c0001t0019g0008a0001c0002t0004g0122others(5): Show | 8 | HG02622.hp1 HG02809.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.2109-7792G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207836288 | ||||||
| chr2:207836299
|
G | A | 123 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(120): Show | 123 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.2109-7803C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207836299 | ||||||
| chr2:207836314
|
A | ACTCT | 5 | a0001c0001t0001g0074a0001c0001t0003g0062a0001c0002t0001g0134others(2): Show | 5 | HG00408.hp1 HG01496.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.2109-7819_2109-781 others(8): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207836314 | ||||||
| chr2:207836315
|
G | C | 119 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(116): Show | 119 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.2109-7819C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207836315 | ||||||
| chr2:207836317
|
C | CTG | 5 | a0001c0001t0013g0175a0001c0002t0026g0085a0001c0004t0001g0127others(2): Show | 5 | HG02622.hp2 HG02630.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.2109-7822_2109-782 others(6): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207836317 | ||||||
| chr2:207836318
|
T | TGTC | 114 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(111): Show | 114 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.2109-7823_2109-782 others(7): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207836318 | ||||||
| chr2:207836319
|
A | C | 5 | a0001c0001t0013g0175a0001c0002t0026g0085a0001c0004t0001g0127others(2): Show | 5 | HG02622.hp2 HG02630.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.2109-7823T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207836319 | ||||||
| chr2:207836319
|
A | T | 114 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(111): Show | 114 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.2109-7823T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207836319 | ||||||
| chr2:207836320
|
A | T | 5 | a0001c0001t0013g0175a0001c0002t0026g0085a0001c0004t0001g0127others(2): Show | 5 | HG02622.hp2 HG02630.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.2109-7824T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207836320 | ||||||
| chr2:207836327
|
A | C | 2 | a0001c0002t0037g0110a0001c0002t0038g0182 | 2 | HG01168.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2109-7831T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207836327 | ||||||
| chr2:207836346
|
A | C | 8 | a0001c0001t0001g0118a0001c0001t0004g0086a0001c0001t0009g0007others(5): Show | 8 | HG01109.hp2 HG02145.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.2109-7850T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207836346 | ||||||
| chr2:207836642
|
A | C | 1 | a0001c0003t0008g0076 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2109-8146T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207836642 | ||||||
| chr2:207837011
|
C | T | 2 | a0001c0001t0003g0051a0001c0001t0003g0052 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.2109-8515G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207837011 | ||||||
| chr2:207837015
|
C | T | 1 | a0001c0003t0008g0026 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2109-8519G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207837015 | ||||||
| chr2:207837192
|
C | T | 2 | a0001c0001t0020g0115a0001c0001t0021g0121 | 2 | HG02257.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.2109-8696G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207837192 | ||||||
| chr2:207837548
|
T | C | 120 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(117): Show | 120 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.2109-9052A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207837548 | ||||||
| chr2:207837548
|
T | G | 2 | a0001c0003t0001g0043a0001c0003t0028g0010 | 2 | HG01256.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2109-9052A>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207837548 | ||||||
| chr2:207837576
|
G | C | 1 | a0001c0001t0001g0019 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2109-9080C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207837576 | ||||||
| chr2:207837632
|
C | CTTT | 13 | a0001c0001t0001g0118a0001c0001t0003g0052a0001c0001t0004g0086others(10): Show | 13 | HG01109.hp2 HG01256.hp2 HG01515.hp1 others(10): Show |
intron_variant | MODIFIER | c.2109-9139_2109-913 others(7): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207837632 | ||||||
| chr2:207837632
|
C | CTTTT | 96 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0042others(93): Show | 96 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.2109-9140_2109-913 others(8): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207837632 | ||||||
| chr2:207837632
|
C | CTTTTT | 11 | a0001c0001t0001g0013a0001c0001t0020g0115a0001c0001t0044g0116others(8): Show | 11 | HG01109.hp1 HG01891.hp2 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.2109-9141_2109-913 others(9): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207837632 | ||||||
| chr2:207837632
|
CT | C | 5 | a0001c0002t0005g0162a0001c0002t0037g0110a0001c0002t0038g0182others(2): Show | 5 | HG01168.hp2 HG01256.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2109-9137delA | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207837632 | ||||||
| chr2:207837675
|
T | A | 2 | a0001c0004t0002g0113a0001c0004t0002g0114 | 2 | HG02683.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.2109-9179A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207837675 | ||||||
| chr2:207837687
|
C | T | 2 | a0001c0003t0012g0090a0001c0003t0012g0176 | 2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2109-9191G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207837687 | ||||||
| chr2:207837688
|
G | A | 2 | a0001c0004t0030g0167a0008c0013t0002g0109 | 2 | NA18956.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.2109-9192C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207837688 | ||||||
| chr2:207837741
|
G | A | 2 | a0001c0003t0004g0172a0002c0005t0004g0094 | 2 | HG01109.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2109-9245C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207837741 | ||||||
| chr2:207837744
|
G | A | 1 | a0001c0001t0004g0120 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2109-9248C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207837744 | ||||||
| chr2:207837758
|
T | C | 120 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(117): Show | 120 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.2109-9262A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207837758 | ||||||
| chr2:207837761
|
AT | A | 74 | a0001c0001t0001g0045a0001c0001t0001g0068a0001c0001t0001g0071others(71): Show | 74 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.2109-9266delA | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207837761 | ||||||
| chr2:207837761
|
ATT | A | 7 | a0001c0002t0003g0137a0001c0002t0037g0110a0001c0003t0007g0065others(4): Show | 7 | HG02056.hp2 HG03098.hp1 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.2109-9267_2109-926 others(6): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207837761 | ||||||
| chr2:207837761
|
ATTT | A | 5 | a0001c0001t0003g0031a0001c0002t0001g0135a0001c0002t0006g0199others(2): Show | 5 | HG01168.hp2 HG01243.hp1 HG02071.hp1 others(2): Show |
intron_variant | MODIFIER | c.2109-9268_2109-926 others(7): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207837761 | ||||||
| chr2:207837761
|
ATTTT | A | 74 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0061others(71): Show | 74 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.2109-9269_2109-926 others(8): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207837761 | ||||||
| chr2:207837761
|
ATTTTT | A | 29 | a0001c0001t0001g0013a0001c0001t0001g0033a0001c0001t0001g0042others(26): Show | 29 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(26): Show |
intron_variant | MODIFIER | c.2109-9270_2109-926 others(9): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207837761 | ||||||
| chr2:207837761
|
ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0051g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2109-9277_2109-926 others(16): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207837761 | ||||||
| chr2:207837925
|
C | G | 1 | a0001c0004t0002g0158 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2109-9429G>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207837925 | ||||||
| chr2:207837926
|
A | C | 1 | a0001c0004t0002g0158 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2109-9430T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207837926 | ||||||
| chr2:207837928
|
G | C | 1 | a0001c0004t0002g0158 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2109-9432C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207837928 | ||||||
| chr2:207837929
|
C | A | 1 | a0001c0004t0002g0158 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2109-9433G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207837929 | ||||||
| chr2:207837951
|
T | G | 2 | a0001c0002t0037g0110a0001c0002t0038g0182 | 2 | HG01168.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2109-9455A>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207837951 | ||||||
| chr2:207838270
|
A | T | 1 | a0001c0004t0003g0096 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2109-9774T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207838270 | ||||||
| chr2:207838795
|
G | A | 113 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0033others(110): Show | 113 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.2109-10299C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207838795 | ||||||
| chr2:207838978
|
C | T | 113 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0033others(110): Show | 113 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.2109-10482G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207838978 | ||||||
| chr2:207839248
|
G | A | 1 | a0001c0002t0054g0149 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.2109-10752C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207839248 | ||||||
| chr2:207839423
|
T | C | 4 | a0001c0001t0013g0175a0001c0001t0020g0115a0001c0001t0021g0121others(1): Show | 4 | HG02257.hp2 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2109-10927A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207839423 | ||||||
| chr2:207839579
|
G | T | 93 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0033others(90): Show | 93 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.2109-11083C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207839579 | ||||||
| chr2:207839623
|
T | C | 114 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(111): Show | 114 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.2109-11127A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207839623 | ||||||
| chr2:207839663
|
T | C | 3 | a0001c0003t0004g0172a0001c0015t0003g0093a0002c0005t0004g0094 | 3 | HG01109.hp2 HG02630.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.2109-11167A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207839663 | ||||||
| chr2:207839668
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2109-11172G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207839668 | ||||||
| chr2:207839768
|
C | T | 23 | a0001c0001t0003g0011a0001c0001t0003g0119a0001c0001t0004g0120others(20): Show | 23 | HG01168.hp2 HG01891.hp1 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.2109-11272G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207839768 | ||||||
| chr2:207839805
|
C | T | 4 | a0001c0001t0017g0003a0001c0002t0037g0110a0001c0003t0001g0043others(1): Show | 4 | HG01256.hp1 HG02109.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2109-11309G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207839805 | ||||||
| chr2:207840204
|
T | A | 1 | a0001c0002t0045g0190 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2109-11708A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207840204 | ||||||
| chr2:207840236
|
G | T | 47 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(44): Show | 47 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.2109-11740C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207840236 | ||||||
| chr2:207840252
|
A | G | 1 | a0001c0002t0026g0085 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2109-11756T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207840252 | ||||||
| chr2:207840319
|
C | T | 1 | a0001c0002t0038g0182 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2109-11823G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207840319 | ||||||
| chr2:207840334
|
G | GTGTGTGC others(17): Show |
1 | a0001c0003t0007g0065 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2109-11862_2109-11 others(30): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207840334 | ||||||
| chr2:207840367
|
C | A | 112 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(109): Show | 112 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.2109-11871G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207840367 | ||||||
| chr2:207840474
|
G | T | 1 | a0001c0002t0037g0110 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2109-11978C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207840474 | ||||||
| chr2:207840503
|
G | A | 8 | a0001c0001t0004g0120a0001c0001t0016g0005a0001c0001t0019g0008others(5): Show | 8 | HG02622.hp1 HG02622.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.2109-12007C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207840503 | ||||||
| chr2:207840651
|
C | A | 1 | a0001c0001t0051g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2109-12155G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207840651 | ||||||
| chr2:207840798
|
TG | T | 15 | a0001c0001t0003g0119a0001c0001t0004g0086a0001c0001t0009g0007others(12): Show | 15 | HG01109.hp2 HG01168.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.2109-12303delC | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207840798 | ||||||
| chr2:207840799
|
G | GT | 31 | a0001c0001t0001g0063a0001c0001t0001g0080a0001c0001t0001g0118others(28): Show | 31 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(28): Show |
intron_variant | MODIFIER | c.2109-12304dupA | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207840799 | ||||||
| chr2:207840799
|
G | GTT | 6 | a0001c0001t0033g0016a0001c0002t0001g0169a0001c0003t0001g0091others(3): Show | 6 | HG01243.hp1 HG01928.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.2109-12305_2109-12 others(8): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207840799 | ||||||
| chr2:207840799
|
G | T | 46 | a0001c0001t0001g0033a0001c0001t0002g0032a0001c0001t0002g0055others(43): Show | 46 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.2109-12303C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207840799 | ||||||
| chr2:207840799
|
GT | G | 15 | a0001c0001t0001g0017a0001c0001t0002g0069a0001c0001t0021g0121others(12): Show | 15 | HG00642.hp2 HG02258.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.2109-12304delA | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207840799 | ||||||
| chr2:207840805
|
T | A | 46 | a0001c0001t0001g0033a0001c0001t0002g0032a0001c0001t0002g0055others(43): Show | 46 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.2109-12309A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207840805 | ||||||
| chr2:207840806
|
T | A | 14 | a0001c0001t0003g0119a0001c0001t0004g0086a0001c0001t0009g0007others(11): Show | 14 | HG01109.hp2 HG01168.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.2109-12310A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207840806 | ||||||
| chr2:207840809
|
T | A | 2 | a0001c0004t0003g0128a0004c0012t0003g0095 | 2 | HG03516.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.2109-12313A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207840809 | ||||||
| chr2:207840812
|
T | A | 10 | a0001c0001t0003g0119a0001c0001t0004g0086a0001c0001t0009g0007others(7): Show | 10 | HG01109.hp2 HG02145.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.2109-12316A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207840812 | ||||||
| chr2:207840813
|
T | A | 11 | a0001c0001t0004g0120a0001c0001t0013g0175a0001c0001t0016g0005others(8): Show | 11 | HG02622.hp1 HG02622.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.2109-12317A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207840813 | ||||||
| chr2:207840869
|
C | T | 10 | a0001c0001t0003g0119a0001c0001t0004g0086a0001c0001t0009g0007others(7): Show | 10 | HG01109.hp2 HG02145.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.2109-12373G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207840869 | ||||||
| chr2:207841057
|
G | A | 1 | a0001c0002t0045g0190 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2109-12561C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207841057 | ||||||
| chr2:207841098
|
C | T | 6 | a0001c0001t0013g0175a0001c0002t0038g0182a0001c0003t0012g0090others(3): Show | 6 | HG01168.hp2 HG01891.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.2109-12602G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207841098 | ||||||
| chr2:207841290
|
C | A | 1 | a0001c0002t0045g0190 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2109-12794G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207841290 | ||||||
| chr2:207841371
|
G | A | 61 | a0001c0001t0001g0033a0001c0001t0002g0032a0001c0001t0002g0055others(58): Show | 61 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.2109-12875C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207841371 | ||||||
| chr2:207841379
|
C | G | 1 | a0001c0001t0001g0045 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2109-12883G>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207841379 | ||||||
| chr2:207841397
|
C | T | 1 | a0005c0011t0022g0111 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2109-12901G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207841397 | ||||||
| chr2:207841425
|
G | C | 10 | a0001c0001t0003g0119a0001c0001t0004g0086a0001c0001t0009g0007others(7): Show | 10 | HG01109.hp2 HG02145.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.2109-12929C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207841425 | ||||||
| chr2:207841448
|
CAA | C | 5 | a0001c0002t0002g0170a0001c0003t0002g0040a0001c0003t0029g0054others(2): Show | 5 | HG00438.hp1 HG00621.hp2 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.2109-12954_2109-12 others(8): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207841448 | ||||||
| chr2:207841448
|
CAAA | C | 17 | a0001c0001t0001g0118a0001c0001t0002g0014a0001c0002t0001g0126others(14): Show | 17 | HG00408.hp2 HG00642.hp2 HG01516.hp1 others(14): Show |
intron_variant | MODIFIER | c.2109-12955_2109-12 others(9): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207841448 | ||||||
| chr2:207841448
|
CAAAA | C | 6 | a0001c0001t0002g0015a0001c0003t0001g0028a0001c0003t0002g0024others(3): Show | 6 | HG00099.hp1 HG00323.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.2109-12956_2109-12 others(10): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207841448 | ||||||
| chr2:207841460
|
AAAAAAAA others(15): Show |
A | 2 | a0001c0002t0037g0110a0001c0002t0038g0182 | 2 | HG01168.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2109-12986_2109-12 others(28): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207841460 | ||||||
| chr2:207841462
|
AAAAAAAA others(15): Show |
A | 2 | a0001c0001t0013g0175a0001c0004t0001g0127 | 2 | HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2109-12988_2109-12 others(28): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207841462 | ||||||
| chr2:207841467
|
AAAAAAAA others(18): Show |
A | 3 | a0001c0001t0016g0005a0001c0004t0001g0185a0001c0004t0040g0186 | 3 | HG02622.hp2 HG03486.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2109-12996_2109-12 others(31): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207841467 | ||||||
| chr2:207841468
|
AAAAAAAA others(17): Show |
A | 45 | a0001c0001t0001g0033a0001c0001t0002g0032a0001c0001t0002g0055others(42): Show | 45 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.2109-12996_2109-12 others(30): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207841468 | ||||||
| chr2:207841470
|
AAAAAAAA others(15): Show |
A | 9 | a0001c0001t0004g0086a0001c0001t0009g0007a0001c0001t0024g0117others(6): Show | 9 | HG01109.hp2 HG02145.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.2109-12996_2109-12 others(28): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207841470 | ||||||
| chr2:207841476
|
A | AATATATA others(3): Show |
1 | a0001c0002t0045g0190 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2109-12981_2109-12 others(16): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207841476 | ||||||
| chr2:207841476
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0046 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2109-12981_2109-12 others(17): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207841476 | ||||||
| chr2:207841478
|
A | AATATATA others(1): Show |
6 | a0001c0001t0001g0013a0001c0001t0001g0070a0001c0001t0003g0034others(3): Show | 6 | HG00280.hp1 HG00642.hp1 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.2109-12983_2109-12 others(14): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207841478 | ||||||
| chr2:207841478
|
A | AATATATA others(3): Show |
1 | a0001c0001t0034g0047 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2109-12983_2109-12 others(16): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207841478 | ||||||
| chr2:207841478
|
A | AATATATA others(7): Show |
1 | a0001c0001t0002g0039 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2109-12983_2109-12 others(20): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207841478 | ||||||
| chr2:207841478
|
A | AATATATA others(11): Show |
1 | a0001c0001t0033g0016 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2109-12983_2109-12 others(24): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207841478 | ||||||
| chr2:207841478
|
A | T | 6 | a0001c0001t0001g0046a0001c0002t0002g0140a0001c0002t0045g0190others(3): Show | 6 | HG00408.hp2 HG01069.hp1 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.2109-12982T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207841478 | ||||||
| chr2:207841478
|
AAAATATA others(9): Show |
A | 1 | a0001c0001t0051g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2109-12998_2109-12 others(22): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207841478 | ||||||
| chr2:207841479
|
AAAT | A | 28 | a0001c0001t0003g0030a0001c0001t0003g0031a0001c0001t0005g0088others(25): Show | 28 | HG00423.hp1 HG00558.hp2 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.2109-12986_2109-12 others(9): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207841479 | ||||||
| chr2:207841480
|
A | AAAAATAT others(6): Show |
1 | a0001c0002t0006g0195 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2109-12985_2109-12 others(19): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207841480 | ||||||
| chr2:207841480
|
A | AAAAATAT others(8): Show |
1 | a0001c0002t0001g0134 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2109-12985_2109-12 others(21): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207841480 | ||||||
| chr2:207841480
|
A | AAAAATAT others(10): Show |
1 | a0001c0003t0001g0091 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2109-12985_2109-12 others(23): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207841480 | ||||||
| chr2:207841480
|
A | AAAAATAT others(14): Show |
1 | a0001c0002t0006g0194 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2109-12985_2109-12 others(27): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207841480 | ||||||
| chr2:207841480
|
A | AAAATATA others(3): Show |
1 | a0002c0005t0001g0132 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2109-12985_2109-12 others(16): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207841480 | ||||||
| chr2:207841480
|
A | AAAATATA others(5): Show |
1 | a0001c0001t0021g0121 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2109-12985_2109-12 others(18): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207841480 | ||||||
| chr2:207841480
|
A | AAAATATA others(7): Show |
2 | a0001c0001t0027g0041a0001c0001t0049g0075 | 2 | HG03688.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.2109-12985_2109-12 others(20): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207841480 | ||||||
| chr2:207841480
|
A | AAAATATA others(9): Show |
2 | a0001c0002t0006g0193a0001c0003t0001g0009 | 2 | HG02486.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.2109-12985_2109-12 others(22): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207841480 | ||||||
| chr2:207841480
|
A | AAAATATA others(13): Show |
1 | a0001c0001t0017g0003 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2109-12985_2109-12 others(26): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207841480 | ||||||
| chr2:207841480
|
A | AAATATAT others(4): Show |
5 | a0001c0001t0001g0017a0001c0001t0003g0058a0001c0002t0006g0198others(2): Show | 5 | HG01346.hp1 HG01884.hp2 HG02080.hp1 others(2): Show |
intron_variant | MODIFIER | c.2109-12985_2109-12 others(17): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207841480 | ||||||
| chr2:207841480
|
A | AAATATAT others(6): Show |
1 | a0001c0001t0001g0045 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2109-12985_2109-12 others(19): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207841480 | ||||||
| chr2:207841480
|
A | AAATATAT others(8): Show |
2 | a0001c0001t0001g0042a0001c0003t0009g0001 | 2 | HG01243.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2109-12985_2109-12 others(21): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207841480 | ||||||
| chr2:207841480
|
A | AATATATA others(1): Show |
5 | a0001c0002t0001g0141a0001c0002t0001g0142a0001c0002t0001g0169others(2): Show | 5 | HG00438.hp2 HG00639.hp1 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.2109-12992_2109-12 others(14): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207841480 | ||||||
| chr2:207841480
|
A | AATATATA others(3): Show |
4 | a0001c0001t0020g0115a0001c0002t0001g0168a0001c0003t0008g0027others(1): Show | 4 | HG00280.hp2 HG01952.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.2109-12994_2109-12 others(16): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207841480 | ||||||
| chr2:207841480
|
A | AATATATA others(5): Show |
2 | a0001c0001t0001g0060a0001c0003t0008g0026 | 2 | HG00639.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.2109-12996_2109-12 others(18): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207841480 | ||||||
| chr2:207841480
|
A | AATATATA others(9): Show |
1 | a0001c0002t0058g0197 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2109-13000_2109-12 others(22): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207841480 | ||||||
| chr2:207841480
|
A | AATATATA others(11): Show |
4 | a0001c0001t0001g0080a0001c0001t0044g0116a0001c0002t0059g0200others(1): Show | 4 | HG01891.hp1 HG02647.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2109-13002_2109-12 others(24): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207841480 | ||||||
| chr2:207841480
|
A | ATATATAT others(6): Show |
2 | a0001c0002t0006g0199a0001c0003t0014g0099 | 2 | HG02145.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.2109-12985_2109-12 others(19): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207841480 | ||||||
| chr2:207841480
|
A | ATATATAT others(10): Show |
1 | a0002c0005t0036g0098 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2109-12985_2109-12 others(23): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207841480 | ||||||
| chr2:207841480
|
A | ATATATAT others(12): Show |
1 | a0001c0008t0053g0173 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2109-12985_2109-12 others(25): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207841480 | ||||||
| chr2:207841480
|
A | T | 25 | a0001c0001t0001g0013a0001c0001t0001g0046a0001c0001t0001g0070others(22): Show | 25 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(22): Show |
intron_variant | MODIFIER | c.2109-12984T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207841480 | ||||||
| chr2:207841481
|
AT | A | 2 | a0001c0004t0001g0152a0001c0004t0007g0180 | 2 | HG04184.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.2109-12986delA | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207841481 | ||||||
| chr2:207841481
|
ATAT | A | 2 | a0001c0001t0001g0068a0001c0004t0003g0165 | 2 | HG01081.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.2109-12988_2109-12 others(9): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207841481 | ||||||
| chr2:207841484
|
T | A | 2 | a0001c0004t0001g0152a0001c0004t0030g0167 | 2 | HG04184.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.2109-12988A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207841484 | ||||||
| chr2:207841488
|
T | A | 1 | a0001c0001t0002g0069 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2109-12992A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207841488 | ||||||
| chr2:207841498
|
T | C | 61 | a0001c0001t0001g0033a0001c0001t0002g0032a0001c0001t0002g0055others(58): Show | 61 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.2109-13002A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207841498 | ||||||
| chr2:207841713
|
C | A | 2 | a0001c0004t0039g0036a0001c0004t0042g0035 | 2 | HG02809.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2109-13217G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207841713 | ||||||
| chr2:207841713
|
C | T | 59 | a0001c0001t0001g0033a0001c0001t0002g0032a0001c0001t0002g0055others(56): Show | 59 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.2109-13217G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207841713 | ||||||
| chr2:207841753
|
A | G | 2 | a0001c0003t0004g0172a0002c0005t0004g0094 | 2 | HG01109.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2109-13257T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207841753 | ||||||
| chr2:207841881
|
T | C | 14 | a0001c0001t0003g0119a0001c0001t0004g0086a0001c0001t0009g0007others(11): Show | 14 | HG01109.hp2 HG01168.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.2109-13385A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207841881 | ||||||
| chr2:207842078
|
T | C | 63 | a0001c0001t0001g0033a0001c0001t0002g0032a0001c0001t0002g0055others(60): Show | 63 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.2109-13582A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207842078 | ||||||
| chr2:207842138
|
C | T | 1 | a0001c0002t0037g0110 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2109-13642G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207842138 | ||||||
| chr2:207842159
|
G | A | 2 | a0001c0004t0039g0036a0001c0004t0042g0035 | 2 | HG02809.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2109-13663C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207842159 | ||||||
| chr2:207842176
|
C | T | 47 | a0001c0001t0001g0033a0001c0001t0002g0032a0001c0001t0002g0055others(44): Show | 47 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.2109-13680G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207842176 | ||||||
| chr2:207842225
|
C | T | 47 | a0001c0001t0001g0033a0001c0001t0002g0032a0001c0001t0002g0055others(44): Show | 47 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.2109-13729G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207842225 | ||||||
| chr2:207842305
|
A | G | 1 | a0001c0003t0023g0087 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2109-13809T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207842305 | ||||||
| chr2:207842314
|
A | G | 1 | a0005c0011t0022g0111 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2109-13818T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207842314 | ||||||
| chr2:207842343
|
G | A | 14 | a0001c0001t0003g0119a0001c0001t0004g0086a0001c0001t0009g0007others(11): Show | 14 | HG01109.hp2 HG01168.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.2109-13847C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207842343 | ||||||
| chr2:207842476
|
T | C | 1 | a0001c0002t0038g0182 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2109-13980A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207842476 | ||||||
| chr2:207842548
|
G | A | 1 | a0001c0003t0028g0010 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2109-14052C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207842548 | ||||||
| chr2:207842582
|
TGAAGGAG others(4): Show |
T | 14 | a0001c0001t0003g0119a0001c0001t0004g0086a0001c0001t0009g0007others(11): Show | 14 | HG01109.hp2 HG01168.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.2109-14097_2109-14 others(17): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207842582 | ||||||
| chr2:207842602
|
G | C | 60 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(57): Show | 60 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.2109-14106C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207842602 | ||||||
| chr2:207842618
|
A | G | 2 | a0001c0002t0006g0198a0002c0005t0001g0132 | 2 | HG01884.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.2109-14122T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207842618 | ||||||
| chr2:207842709
|
G | A | 1 | a0001c0002t0045g0190 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2109-14213C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207842709 | ||||||
| chr2:207842920
|
G | A | 61 | a0001c0001t0001g0033a0001c0001t0002g0032a0001c0001t0002g0055others(58): Show | 61 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.2109-14424C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207842920 | ||||||
| chr2:207843084
|
A | G | 123 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(120): Show | 123 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.2109-14588T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207843084 | ||||||
| chr2:207843207
|
C | T | 1 | a0001c0009t0031g0156 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2109-14711G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207843207 | ||||||
| chr2:207843236
|
A | G | 48 | a0001c0001t0001g0033a0001c0001t0002g0032a0001c0001t0002g0055others(45): Show | 48 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.2109-14740T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207843236 | ||||||
| chr2:207843252
|
G | A | 1 | a0001c0001t0003g0012 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2109-14756C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207843252 | ||||||
| chr2:207843537
|
C | T | 2 | a0001c0002t0038g0182a0001c0004t0001g0127 | 2 | HG01168.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.2109-15041G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207843537 | ||||||
| chr2:207843623
|
C | A | 1 | a0001c0001t0003g0119 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2109-15127G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207843623 | ||||||
| chr2:207843623
|
C | T | 2 | a0001c0002t0038g0182a0001c0004t0001g0127 | 2 | HG01168.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.2109-15127G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207843623 | ||||||
| chr2:207843774
|
C | A | 51 | a0001c0001t0001g0033a0001c0001t0002g0032a0001c0001t0002g0055others(48): Show | 51 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.2109-15278G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207843774 | ||||||
| chr2:207843780
|
C | T | 39 | a0001c0001t0001g0033a0001c0001t0002g0032a0001c0001t0002g0055others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.2109-15284G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207843780 | ||||||
| chr2:207843781
|
G | A | 3 | a0001c0001t0013g0175a0001c0002t0038g0182a0001c0004t0001g0127 | 3 | HG01168.hp2 HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2109-15285C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207843781 | ||||||
| chr2:207843836
|
T | C | 39 | a0001c0001t0001g0033a0001c0001t0002g0032a0001c0001t0002g0055others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.2109-15340A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207843836 | ||||||
| chr2:207843973
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2109-15477G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207843973 | ||||||
| chr2:207844122
|
C | T | 8 | a0001c0001t0004g0120a0001c0001t0016g0005a0001c0001t0019g0008others(5): Show | 8 | HG02622.hp1 HG02622.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.2109-15626G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207844122 | ||||||
| chr2:207844297
|
A | C | 15 | a0001c0001t0003g0119a0001c0001t0004g0086a0001c0001t0009g0007others(12): Show | 15 | HG01109.hp2 HG01168.hp2 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.2109-15801T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207844297 | ||||||
| chr2:207844300
|
T | A | 9 | a0001c0001t0001g0017a0001c0001t0020g0115a0001c0001t0021g0121others(6): Show | 9 | HG02145.hp1 HG02257.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.2109-15804A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207844300 | ||||||
| chr2:207844303
|
CT | C | 53 | a0001c0001t0001g0033a0001c0001t0002g0032a0001c0001t0002g0055others(50): Show | 53 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.2109-15808delA | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207844303 | ||||||
| chr2:207844303
|
CTT | C | 58 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(55): Show | 58 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.2109-15809_2109-15 others(8): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207844303 | ||||||
| chr2:207844333
|
C | T | 1 | a0001c0001t0002g0032 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2109-15837G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207844333 | ||||||
| chr2:207844341
|
T | C | 124 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(121): Show | 124 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.2109-15845A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207844341 | ||||||
| chr2:207844385
|
C | G | 1 | a0001c0002t0038g0182 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2109-15889G>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207844385 | ||||||
| chr2:207844403
|
C | T | 47 | a0001c0001t0001g0033a0001c0001t0002g0032a0001c0001t0002g0055others(44): Show | 47 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.2109-15907G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207844403 | ||||||
| chr2:207844414
|
T | C | 124 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(121): Show | 124 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.2109-15918A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207844414 | ||||||
| chr2:207844447
|
C | T | 1 | a0001c0001t0001g0080 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2109-15951G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207844447 | ||||||
| chr2:207844449
|
CCCA | C | 60 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(57): Show | 60 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.2109-15956_2109-15 others(9): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207844449 | ||||||
| chr2:207844469
|
A | AT | 64 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(61): Show | 64 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.2109-15974dupA | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207844469 | ||||||
| chr2:207844476
|
T | G | 62 | a0001c0001t0001g0033a0001c0001t0002g0032a0001c0001t0002g0055others(59): Show | 62 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.2109-15980A>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207844476 | ||||||
| chr2:207844557
|
A | C | 62 | a0001c0001t0001g0033a0001c0001t0002g0032a0001c0001t0002g0055others(59): Show | 62 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.2109-16061T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207844557 | ||||||
| chr2:207844595
|
T | C | 2 | a0001c0002t0037g0110a0001c0002t0038g0182 | 2 | HG01168.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2109-16099A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207844595 | ||||||
| chr2:207844965
|
G | T | 122 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(119): Show | 122 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.2108+16140C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207844965 | ||||||
| chr2:207845007
|
C | A | 1 | a0001c0002t0038g0182 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2108+16098G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207845007 | ||||||
| chr2:207845193
|
T | C | 10 | a0001c0001t0003g0119a0001c0001t0004g0086a0001c0001t0009g0007others(7): Show | 10 | HG01109.hp2 HG02145.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.2108+15912A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207845193 | ||||||
| chr2:207845325
|
A | G | 1 | a0001c0002t0045g0190 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2108+15780T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207845325 | ||||||
| chr2:207845469
|
C | G | 2 | a0001c0001t0013g0175a0001c0004t0001g0127 | 2 | HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2108+15636G>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207845469 | ||||||
| chr2:207845751
|
T | C | 1 | a0001c0001t0004g0086 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2108+15354A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207845751 | ||||||
| chr2:207845753
|
T | C | 1 | a0001c0003t0008g0076 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2108+15352A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207845753 | ||||||
| chr2:207845803
|
A | T | 1 | a0001c0002t0045g0190 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2108+15302T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207845803 | ||||||
| chr2:207845935
|
G | A | 1 | a0001c0002t0045g0190 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2108+15170C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207845935 | ||||||
| chr2:207845960
|
A | T | 1 | a0001c0001t0049g0075 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2108+15145T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207845960 | ||||||
| chr2:207846082
|
G | C | 1 | a0002c0005t0036g0098 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2108+15023C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207846082 | ||||||
| chr2:207846182
|
G | A | 1 | a0001c0003t0009g0001 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2108+14923C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207846182 | ||||||
| chr2:207846273
|
C | G | 1 | a0001c0004t0002g0143 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2108+14832G>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207846273 | ||||||
| chr2:207846637
|
C | A | 1 | a0001c0004t0042g0035 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2108+14468G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207846637 | ||||||
| chr2:207846645
|
C | A | 1 | a0001c0001t0051g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2108+14460G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207846645 | ||||||
| chr2:207846673
|
A | G | 3 | a0001c0003t0012g0090a0001c0003t0012g0176a0002c0005t0036g0098 | 3 | HG01891.hp1 HG03139.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2108+14432T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207846673 | ||||||
| chr2:207846678
|
G | A | 1 | a0001c0003t0001g0091 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2108+14427C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207846678 | ||||||
| chr2:207846735
|
A | T | 1 | a0001c0001t0051g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2108+14370T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207846735 | ||||||
| chr2:207846775
|
T | C | 1 | a0001c0002t0005g0183 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2108+14330A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207846775 | ||||||
| chr2:207846800
|
G | A | 4 | a0001c0003t0008g0026a0001c0003t0008g0027a0001c0003t0008g0050others(1): Show | 4 | HG00280.hp2 HG00639.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.2108+14305C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207846800 | ||||||
| chr2:207846849
|
A | C | 1 | a0001c0002t0045g0190 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2108+14256T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207846849 | ||||||
| chr2:207847031
|
T | C | 1 | a0008c0013t0002g0109 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2108+14074A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207847031 | ||||||
| chr2:207847062
|
T | C | 5 | a0001c0001t0013g0175a0001c0002t0037g0110a0001c0002t0038g0182others(2): Show | 5 | HG01168.hp2 HG02630.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2108+14043A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207847062 | ||||||
| chr2:207847524
|
C | T | 2 | a0001c0003t0004g0172a0002c0005t0004g0094 | 2 | HG01109.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2108+13581G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207847524 | ||||||
| chr2:207847565
|
G | A | 1 | a0001c0003t0001g0043 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2108+13540C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207847565 | ||||||
| chr2:207847637
|
T | C | 107 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(104): Show | 107 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.2108+13468A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207847637 | ||||||
| chr2:207847686
|
C | T | 121 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(118): Show | 121 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.2108+13419G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207847686 | ||||||
| chr2:207847935
|
T | C | 1 | a0001c0001t0034g0047 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2108+13170A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207847935 | ||||||
| chr2:207848131
|
A | G | 122 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(119): Show | 122 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.2108+12974T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207848131 | ||||||
| chr2:207848303
|
G | A | 123 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(120): Show | 123 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.2108+12802C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207848303 | ||||||
| chr2:207848547
|
C | T | 106 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(103): Show | 106 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.2108+12558G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207848547 | ||||||
| chr2:207848614
|
T | C | 10 | a0001c0001t0003g0119a0001c0001t0004g0086a0001c0001t0009g0007others(7): Show | 10 | HG01109.hp2 HG02145.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.2108+12491A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207848614 | ||||||
| chr2:207848760
|
C | A | 10 | a0001c0001t0003g0119a0001c0001t0004g0086a0001c0001t0009g0007others(7): Show | 10 | HG01109.hp2 HG02145.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.2108+12345G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207848760 | ||||||
| chr2:207848950
|
G | A | 1 | a0001c0002t0041g0164 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2108+12155C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207848950 | ||||||
| chr2:207849059
|
C | T | 1 | a0001c0002t0045g0190 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2108+12046G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207849059 | ||||||
| chr2:207849092
|
T | C | 1 | a0001c0002t0038g0182 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2108+12013A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207849092 | ||||||
| chr2:207849099
|
C | T | 1 | a0001c0002t0038g0182 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2108+12006G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207849099 | ||||||
| chr2:207849131
|
C | T | 1 | a0001c0002t0006g0193 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2108+11974G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207849131 | ||||||
| chr2:207849248
|
C | A | 1 | a0001c0004t0001g0127 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2108+11857G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207849248 | ||||||
| chr2:207849248
|
C | T | 3 | a0001c0001t0017g0003a0001c0001t0033g0016a0001c0008t0053g0173 | 3 | HG02109.hp2 HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2108+11857G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207849248 | ||||||
| chr2:207849282
|
C | T | 1 | a0002c0006t0035g0097 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2108+11823G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207849282 | ||||||
| chr2:207849758
|
G | C | 3 | a0001c0001t0017g0003a0001c0001t0033g0016a0001c0008t0053g0173 | 3 | HG02109.hp2 HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2108+11347C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207849758 | ||||||
| chr2:207849857
|
T | C | 11 | a0001c0001t0003g0119a0001c0001t0004g0086a0001c0001t0009g0007others(8): Show | 11 | HG01109.hp2 HG01243.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.2108+11248A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207849857 | ||||||
| chr2:207850058
|
A | G | 1 | a0001c0002t0037g0110 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2108+11047T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207850058 | ||||||
| chr2:207850450
|
C | T | 3 | a0001c0001t0004g0086a0001c0003t0004g0172a0002c0005t0004g0094 | 3 | HG01109.hp2 HG02630.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2108+10655G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207850450 | ||||||
| chr2:207850486
|
G | A | 1 | a0001c0002t0045g0190 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2108+10619C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207850486 | ||||||
| chr2:207850590
|
G | A | 103 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(100): Show | 103 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.2108+10515C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207850590 | ||||||
| chr2:207850865
|
C | A | 1 | a0001c0001t0003g0119 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2108+10240G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207850865 | ||||||
| chr2:207850926
|
G | A | 1 | a0001c0002t0045g0190 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2108+10179C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207850926 | ||||||
| chr2:207851057
|
G | T | 1 | a0001c0001t0051g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2108+10048C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207851057 | ||||||
| chr2:207851148
|
C | T | 3 | a0001c0001t0015g0004a0001c0002t0001g0135a0001c0015t0003g0093 | 3 | HG02896.hp1 HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2108+9957G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207851148 | ||||||
| chr2:207851153
|
C | CA | 113 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0033others(110): Show | 113 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.2108+9951dupT | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207851153 | ||||||
| chr2:207851153
|
C | CAA | 7 | a0001c0001t0001g0017a0001c0001t0003g0058a0001c0001t0004g0086others(4): Show | 7 | HG02080.hp1 HG02615.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.2108+9950_2108+995 others(6): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207851153 | ||||||
| chr2:207851230
|
G | A | 116 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(113): Show | 116 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.2108+9875C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207851230 | ||||||
| chr2:207851282
|
C | T | 9 | a0001c0001t0003g0119a0001c0001t0004g0086a0001c0001t0009g0007others(6): Show | 9 | HG01109.hp2 HG01243.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2108+9823G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207851282 | ||||||
| chr2:207851295
|
T | C | 7 | a0001c0001t0003g0058a0001c0001t0003g0062a0001c0002t0001g0141others(4): Show | 7 | HG00408.hp1 HG00438.hp2 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.2108+9810A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207851295 | ||||||
| chr2:207851405
|
G | A | 3 | a0001c0002t0037g0110a0001c0004t0039g0036a0001c0004t0042g0035 | 3 | HG02809.hp1 HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2108+9700C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207851405 | ||||||
| chr2:207851487
|
G | A | 2 | a0001c0001t0013g0175a0001c0004t0001g0127 | 2 | HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2108+9618C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207851487 | ||||||
| chr2:207851599
|
G | A | 3 | a0001c0001t0013g0175a0001c0002t0038g0182a0001c0004t0001g0127 | 3 | HG01168.hp2 HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2108+9506C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207851599 | ||||||
| chr2:207851740
|
C | CA | 11 | a0001c0001t0001g0019a0001c0001t0001g0061a0001c0001t0001g0063others(8): Show | 11 | HG00621.hp2 HG01168.hp1 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.2108+9364dupT | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207851740 | ||||||
| chr2:207851740
|
C | CAA | 8 | a0001c0001t0001g0118a0001c0001t0005g0088a0001c0002t0001g0126others(5): Show | 8 | HG02258.hp2 HG02809.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.2108+9363_2108+936 others(6): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207851740 | ||||||
| chr2:207851740
|
C | CAAAAAAA others(3): Show |
1 | a0001c0004t0001g0127 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2108+9355_2108+936 others(14): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207851740 | ||||||
| chr2:207851740
|
C | CAAAAAAA others(4): Show |
1 | a0001c0001t0013g0175 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2108+9354_2108+936 others(15): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207851740 | ||||||
| chr2:207851740
|
C | CAAAAAAA others(9): Show |
1 | a0001c0002t0045g0190 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2108+9349_2108+936 others(20): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207851740 | ||||||
| chr2:207851740
|
C | CAAAAAAA others(13): Show |
1 | a0001c0002t0038g0182 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2108+9345_2108+936 others(24): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207851740 | ||||||
| chr2:207851740
|
CA | C | 57 | a0001c0001t0001g0033a0001c0001t0002g0032a0001c0001t0002g0055others(54): Show | 57 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.2108+9364delT | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207851740 | ||||||
| chr2:207851740
|
CAA | C | 5 | a0001c0001t0019g0008a0001c0002t0037g0110a0001c0004t0039g0036others(2): Show | 5 | HG02809.hp1 HG02896.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.2108+9363_2108+936 others(6): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207851740 | ||||||
| chr2:207851740
|
CAAA | C | 9 | a0001c0001t0003g0119a0001c0001t0004g0086a0001c0001t0009g0007others(6): Show | 9 | HG01109.hp2 HG01243.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2108+9362_2108+936 others(7): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207851740 | ||||||
| chr2:207851822
|
G | C | 1 | a0001c0001t0001g0068 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2108+9283C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207851822 | ||||||
| chr2:207851842
|
C | A | 1 | a0001c0002t0003g0103 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2108+9263G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207851842 | ||||||
| chr2:207851922
|
G | A | 3 | a0001c0001t0013g0175a0001c0002t0038g0182a0001c0004t0001g0127 | 3 | HG01168.hp2 HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2108+9183C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207851922 | ||||||
| chr2:207851935
|
C | T | 124 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(121): Show | 124 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.2108+9170G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207851935 | ||||||
| chr2:207852021
|
T | C | 113 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(110): Show | 113 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.2108+9084A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207852021 | ||||||
| chr2:207852040
|
C | T | 1 | a0001c0003t0001g0028 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2108+9065G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207852040 | ||||||
| chr2:207852180
|
G | A | 10 | a0001c0001t0003g0119a0001c0001t0004g0086a0001c0001t0009g0007others(7): Show | 10 | HG01109.hp2 HG01243.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.2108+8925C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207852180 | ||||||
| chr2:207852261
|
C | G | 1 | a0001c0002t0045g0190 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2108+8844G>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207852261 | ||||||
| chr2:207852270
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2108+8835G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207852270 | ||||||
| chr2:207852470
|
G | T | 125 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(122): Show | 125 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.2108+8635C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207852470 | ||||||
| chr2:207852562
|
T | C | 1 | a0001c0002t0026g0085 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2108+8543A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207852562 | ||||||
| chr2:207852716
|
A | G | 125 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(122): Show | 125 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.2108+8389T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207852716 | ||||||
| chr2:207852716
|
A | T | 1 | a0001c0003t0001g0025 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2108+8389T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207852716 | ||||||
| chr2:207852850
|
G | GA | 13 | a0001c0001t0003g0119a0001c0001t0004g0086a0001c0001t0009g0007others(10): Show | 13 | HG01109.hp2 HG01243.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.2108+8254dupT | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207852850 | ||||||
| chr2:207853059
|
T | C | 37 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0042others(34): Show | 37 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.2108+8046A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207853059 | ||||||
| chr2:207853117
|
A | G | 3 | a0001c0001t0004g0086a0001c0003t0004g0172a0002c0005t0004g0094 | 3 | HG01109.hp2 HG02630.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2108+7988T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207853117 | ||||||
| chr2:207853331
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2108+7774G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207853331 | ||||||
| chr2:207853417
|
C | CA | 17 | a0001c0001t0003g0119a0001c0001t0004g0086a0001c0001t0009g0007others(14): Show | 17 | HG00280.hp1 HG01109.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.2108+7687dupT | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207853417 | ||||||
| chr2:207853602
|
C | T | 1 | a0001c0002t0026g0085 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2108+7503G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207853602 | ||||||
| chr2:207853725
|
C | T | 61 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(58): Show | 61 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.2108+7380G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207853725 | ||||||
| chr2:207853874
|
G | A | 1 | a0001c0003t0008g0026 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2108+7231C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207853874 | ||||||
| chr2:207853904
|
G | T | 1 | a0001c0004t0001g0127 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2108+7201C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207853904 | ||||||
| chr2:207854081
|
AT | A | 47 | a0001c0001t0001g0033a0001c0001t0002g0032a0001c0001t0002g0055others(44): Show | 47 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.2108+7023delA | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207854081 | ||||||
| chr2:207854334
|
A | G | 57 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(54): Show | 57 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.2108+6771T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207854334 | ||||||
| chr2:207854454
|
T | C | 1 | a0001c0002t0001g0126 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2108+6651A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207854454 | ||||||
| chr2:207854809
|
A | C | 2 | a0001c0001t0013g0175a0001c0002t0026g0085 | 2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2108+6296T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207854809 | ||||||
| chr2:207855084
|
T | C | 1 | a0001c0001t0051g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2108+6021A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207855084 | ||||||
| chr2:207855165
|
C | T | 1 | a0001c0004t0001g0127 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2108+5940G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207855165 | ||||||
| chr2:207855200
|
G | T | 1 | a0001c0003t0002g0024 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2108+5905C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207855200 | ||||||
| chr2:207855325
|
A | G | 1 | a0001c0001t0016g0005 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2108+5780T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207855325 | ||||||
| chr2:207855353
|
C | T | 1 | a0001c0002t0038g0182 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2108+5752G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207855353 | ||||||
| chr2:207855365
|
G | A | 54 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(51): Show | 54 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.2108+5740C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207855365 | ||||||
| chr2:207855443
|
C | T | 1 | a0002c0006t0025g0187 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2108+5662G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207855443 | ||||||
| chr2:207855680
|
T | C | 1 | a0001c0002t0002g0140 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2108+5425A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207855680 | ||||||
| chr2:207855719
|
T | A | 1 | a0001c0004t0039g0036 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2108+5386A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207855719 | ||||||
| chr2:207855873
|
C | T | 1 | a0001c0004t0042g0035 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2108+5232G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207855873 | ||||||
| chr2:207855957
|
G | T | 1 | a0001c0001t0051g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2108+5148C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207855957 | ||||||
| chr2:207856192
|
G | T | 2 | a0001c0002t0001g0105a0001c0002t0001g0106 | 2 | HG01346.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.2108+4913C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207856192 | ||||||
| chr2:207856334
|
T | G | 122 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(119): Show | 122 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.2108+4771A>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207856334 | ||||||
| chr2:207856343
|
G | C | 2 | a0001c0003t0012g0090a0001c0003t0012g0176 | 2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2108+4762C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207856343 | ||||||
| chr2:207856374
|
T | C | 9 | a0001c0001t0003g0119a0001c0001t0004g0086a0001c0001t0009g0007others(6): Show | 9 | HG01109.hp2 HG01243.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2108+4731A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207856374 | ||||||
| chr2:207856566
|
C | T | 1 | a0001c0002t0003g0103 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2108+4539G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207856566 | ||||||
| chr2:207856778
|
G | A | 3 | a0001c0003t0002g0072a0001c0003t0002g0081a0001c0004t0002g0138 | 3 | HG01928.hp2 HG01952.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.2108+4327C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207856778 | ||||||
| chr2:207857627
|
A | C | 1 | a0001c0001t0001g0068 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2108+3478T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207857627 | ||||||
| chr2:207857667
|
C | T | 106 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(103): Show | 106 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.2108+3438G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207857667 | ||||||
| chr2:207857761
|
G | T | 2 | a0001c0001t0017g0003a0001c0001t0033g0016 | 2 | HG02109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.2108+3344C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207857761 | ||||||
| chr2:207857844
|
T | C | 1 | a0001c0001t0033g0016 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2108+3261A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207857844 | ||||||
| chr2:207858119
|
T | G | 1 | a0001c0001t0002g0039 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2108+2986A>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207858119 | ||||||
| chr2:207858136
|
A | ATG | 6 | a0001c0001t0017g0003a0001c0002t0005g0159a0001c0003t0003g0174others(3): Show | 6 | HG02109.hp2 HG03669.hp2 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.2108+2967_2108+296 others(6): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207858136 | ||||||
| chr2:207858136
|
A | ATGTG | 2 | a0001c0001t0001g0068a0001c0004t0002g0143 | 2 | HG00558.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.2108+2965_2108+296 others(8): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207858136 | ||||||
| chr2:207858136
|
A | ATGTGTG | 3 | a0001c0001t0033g0016a0001c0003t0056g0192a0001c0003t0057g0191 | 3 | HG02486.hp1 HG02559.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2108+2963_2108+296 others(10): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207858136 | ||||||
| chr2:207858136
|
A | ATGTGTGT others(1): Show |
2 | a0001c0002t0026g0085a0001c0008t0053g0173 | 2 | HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2108+2961_2108+296 others(12): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207858136 | ||||||
| chr2:207858136
|
A | ATGTGTGT others(3): Show |
1 | a0001c0001t0013g0175 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2108+2959_2108+296 others(14): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207858136 | ||||||
| chr2:207858136
|
ATGTGTGT others(3): Show |
A | 1 | a0001c0003t0008g0027 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2108+2959_2108+296 others(14): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207858136 | ||||||
| chr2:207858136
|
ATGTGTGT others(7): Show |
A | 1 | a0001c0004t0030g0167 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2108+2955_2108+296 others(18): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207858136 | ||||||
| chr2:207858170
|
G | A | 7 | a0001c0001t0001g0046a0001c0001t0004g0120a0001c0001t0019g0008others(4): Show | 7 | HG00639.hp1 HG01069.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2108+2935C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207858170 | ||||||
| chr2:207858170
|
G | GTA | 3 | a0001c0001t0016g0005a0001c0004t0001g0185a0001c0004t0040g0186 | 3 | HG02622.hp2 HG03486.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2108+2934_2108+293 others(6): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207858170 | ||||||
| chr2:207858172
|
G | A | 56 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0042others(53): Show | 56 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.2108+2933C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207858172 | ||||||
| chr2:207858174
|
G | A | 58 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(55): Show | 58 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.2108+2931C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207858174 | ||||||
| chr2:207858174
|
G | GTGTA | 3 | a0001c0003t0007g0065a0001c0004t0003g0128a0002c0006t0025g0187 | 3 | HG03516.hp2 NA18522.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.2108+2930_2108+293 others(8): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207858174 | ||||||
| chr2:207858174
|
G | GTGTATAT others(3): Show |
2 | a0001c0002t0037g0110a0001c0004t0039g0036 | 2 | HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2108+2930_2108+293 others(14): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207858174 | ||||||
| chr2:207858174
|
G | GTGTGTA | 5 | a0001c0001t0001g0033a0001c0001t0002g0055a0001c0001t0002g0056others(2): Show | 5 | HG01358.hp1 HG01891.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2108+2930_2108+293 others(10): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207858174 | ||||||
| chr2:207858174
|
G | GTGTGTAT others(3): Show |
3 | a0001c0003t0004g0172a0001c0004t0001g0127a0002c0005t0004g0094 | 3 | HG01109.hp2 HG02630.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2108+2930_2108+293 others(14): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207858174 | ||||||
| chr2:207858174
|
G | GTGTGTAT others(5): Show |
1 | a0001c0001t0024g0117 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2108+2930_2108+293 others(16): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207858174 | ||||||
| chr2:207858174
|
G | GTGTGTGT others(1): Show |
27 | a0001c0001t0002g0032a0001c0001t0003g0012a0001c0001t0003g0020others(24): Show | 27 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(24): Show |
intron_variant | MODIFIER | c.2108+2930_2108+293 others(12): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207858174 | ||||||
| chr2:207858174
|
G | GTGTGTGT others(5): Show |
2 | a0001c0002t0006g0196a0001c0002t0013g0125 | 2 | HG02559.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.2108+2930_2108+293 others(16): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207858174 | ||||||
| chr2:207858174
|
G | GTGTGTGT others(7): Show |
1 | a0001c0004t0042g0035 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2108+2930_2108+293 others(18): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207858174 | ||||||
| chr2:207858174
|
G | GTGTGTGT others(3): Show |
2 | a0001c0001t0003g0011a0001c0001t0055g0029 | 2 | HG04184.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2108+2930_2108+293 others(14): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207858174 | ||||||
| chr2:207858174
|
G | GTGTGTGT others(5): Show |
2 | a0001c0001t0003g0064a0001c0002t0003g0137 | 2 | HG01081.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.2108+2930_2108+293 others(16): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207858174 | ||||||
| chr2:207858174
|
G | GTGTGTGT others(7): Show |
1 | a0001c0003t0001g0091 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2108+2930_2108+293 others(18): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207858174 | ||||||
| chr2:207858174
|
G | GTGTGTGT others(9): Show |
1 | a0001c0001t0009g0007 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2108+2930_2108+293 others(20): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207858174 | ||||||
| chr2:207858174
|
G | GTGTGTGT others(11): Show |
1 | a0001c0001t0003g0119 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2108+2930_2108+293 others(22): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207858174 | ||||||
| chr2:207858174
|
G | GTGTGTGT others(13): Show |
1 | a0001c0001t0004g0086 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2108+2930_2108+293 others(24): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207858174 | ||||||
| chr2:207858174
|
G | GTGTGTGT others(4): Show |
1 | a0001c0002t0003g0133 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2108+2930_2108+293 others(15): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207858174 | ||||||
| chr2:207858176
|
A | AT | 2 | a0001c0001t0001g0061a0001c0001t0003g0062 | 2 | HG00408.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.2108+2928dupA | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207858176 | ||||||
| chr2:207858176
|
A | ATT | 9 | a0001c0001t0002g0039a0001c0001t0003g0034a0001c0001t0020g0115others(6): Show | 9 | HG02257.hp2 HG02486.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.2108+2928_2108+292 others(6): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207858176 | ||||||
| chr2:207858176
|
A | G | 6 | a0001c0001t0013g0175a0001c0001t0017g0003a0001c0001t0033g0016others(3): Show | 6 | HG01168.hp2 HG02109.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.2108+2929T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207858176 | ||||||
| chr2:207858178
|
A | ATT | 31 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0042others(28): Show | 31 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.2108+2926_2108+292 others(6): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207858178 | ||||||
| chr2:207858178
|
A | G | 1 | a0002c0005t0036g0098 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2108+2927T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207858178 | ||||||
| chr2:207858178
|
A | T | 14 | a0001c0001t0001g0046a0001c0001t0001g0061a0001c0001t0002g0039others(11): Show | 14 | HG00408.hp1 HG00639.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.2108+2927T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207858178 | ||||||
| chr2:207858180
|
A | ATTTT | 7 | a0001c0001t0044g0116a0001c0002t0026g0085a0001c0002t0058g0197others(4): Show | 7 | HG01891.hp1 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2108+2921_2108+292 others(8): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207858180 | ||||||
| chr2:207858180
|
A | T | 50 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(47): Show | 50 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(47): Show |
intron_variant | MODIFIER | c.2108+2925T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207858180 | ||||||
| chr2:207858182
|
T | A | 53 | a0001c0001t0001g0033a0001c0001t0002g0032a0001c0001t0002g0055others(50): Show | 53 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.2108+2923A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207858182 | ||||||
| chr2:207858183
|
T | A | 1 | a0001c0001t0003g0053 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2108+2922A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207858183 | ||||||
| chr2:207858184
|
T | A | 3 | a0001c0002t0045g0190a0001c0004t0039g0036a0001c0004t0042g0035 | 3 | HG02809.hp1 HG02922.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2108+2921A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207858184 | ||||||
| chr2:207858269
|
G | A | 2 | a0001c0003t0012g0090a0001c0003t0012g0176 | 2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2108+2836C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207858269 | ||||||
| chr2:207858390
|
G | A | 3 | a0001c0001t0015g0004a0001c0002t0001g0135a0001c0015t0003g0093 | 3 | HG02896.hp1 HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2108+2715C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207858390 | ||||||
| chr2:207858485
|
A | AT | 10 | a0001c0001t0013g0175a0001c0002t0002g0140a0001c0002t0004g0122others(7): Show | 10 | HG00408.hp2 HG01168.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.2108+2619dupA | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207858485 | ||||||
| chr2:207858485
|
AT | A | 11 | a0001c0001t0001g0118a0001c0001t0003g0119a0001c0001t0004g0086others(8): Show | 11 | HG01109.hp2 HG01243.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.2108+2619delA | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207858485 | ||||||
| chr2:207858512
|
C | T | 107 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(104): Show | 107 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.2108+2593G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207858512 | ||||||
| chr2:207858566
|
T | C | 15 | a0001c0001t0003g0119a0001c0001t0004g0086a0001c0001t0009g0007others(12): Show | 15 | HG01109.hp2 HG01168.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.2108+2539A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207858566 | ||||||
| chr2:207858638
|
G | T | 1 | a0001c0001t0001g0074 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2108+2467C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207858638 | ||||||
| chr2:207858669
|
C | T | 3 | a0001c0001t0016g0005a0001c0004t0001g0185a0001c0004t0040g0186 | 3 | HG02622.hp2 HG03486.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2108+2436G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207858669 | ||||||
| chr2:207858774
|
C | T | 9 | a0001c0001t0003g0119a0001c0001t0004g0086a0001c0001t0009g0007others(6): Show | 9 | HG01109.hp2 HG01243.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2108+2331G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207858774 | ||||||
| chr2:207858843
|
C | A | 50 | a0001c0001t0001g0033a0001c0001t0002g0032a0001c0001t0002g0055others(47): Show | 50 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.2108+2262G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207858843 | ||||||
| chr2:207858865
|
G | C | 3 | a0001c0001t0017g0003a0001c0001t0033g0016a0001c0008t0053g0173 | 3 | HG02109.hp2 HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2108+2240C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207858865 | ||||||
| chr2:207859055
|
C | G | 119 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(116): Show | 119 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.2108+2050G>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207859055 | ||||||
| chr2:207859128
|
T | C | 2 | a0001c0003t0014g0099a0001c0004t0014g0130 | 2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.2108+1977A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207859128 | ||||||
| chr2:207859136
|
C | CT | 94 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0033others(91): Show | 94 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.2108+1968dupA | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207859136 | ||||||
| chr2:207859136
|
CT | C | 7 | a0001c0002t0013g0125a0001c0003t0002g0040a0001c0004t0001g0152others(4): Show | 7 | HG00438.hp1 HG02257.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.2108+1968delA | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207859136 | ||||||
| chr2:207859136
|
CTTTTTTT | C | 9 | a0001c0001t0001g0017a0001c0001t0020g0115a0001c0001t0021g0121others(6): Show | 9 | HG02145.hp1 HG02257.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.2108+1962_2108+196 others(11): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207859136 | ||||||
| chr2:207859198
|
C | T | 2 | a0001c0003t0012g0090a0001c0003t0012g0176 | 2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2108+1907G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207859198 | ||||||
| chr2:207859211
|
T | G | 1 | a0001c0001t0003g0030 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2108+1894A>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207859211 | ||||||
| chr2:207859604
|
G | GT | 7 | a0001c0001t0001g0118a0001c0001t0002g0015a0001c0002t0003g0133others(4): Show | 7 | HG01256.hp2 HG02145.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.2108+1500dupA | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207859604 | ||||||
| chr2:207859659
|
G | A | 1 | a0001c0003t0001g0091 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2108+1446C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207859659 | ||||||
| chr2:207859722
|
T | C | 5 | a0001c0001t0004g0086a0001c0001t0024g0117a0001c0002t0013g0125others(2): Show | 5 | HG01109.hp2 HG02559.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2108+1383A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207859722 | ||||||
| chr2:207859766
|
T | C | 1 | a0004c0012t0003g0095 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.2108+1339A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207859766 | ||||||
| chr2:207860151
|
C | CTG | 17 | a0001c0001t0003g0012a0001c0001t0003g0030a0001c0001t0003g0051others(14): Show | 17 | HG00099.hp2 HG01243.hp1 HG01515.hp1 others(14): Show |
intron_variant | MODIFIER | c.2108+952_2108+953d others(4): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207860151 | ||||||
| chr2:207860151
|
C | CTGTG | 16 | a0001c0001t0003g0020a0001c0001t0003g0031a0001c0001t0003g0083others(13): Show | 16 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(13): Show |
intron_variant | MODIFIER | c.2108+950_2108+953d others(6): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207860151 | ||||||
| chr2:207860151
|
C | CTGTGTG | 20 | a0001c0001t0001g0068a0001c0001t0009g0006a0001c0001t0015g0004others(17): Show | 20 | HG00438.hp1 HG00558.hp2 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.2108+948_2108+953d others(8): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207860151 | ||||||
| chr2:207860151
|
C | CTGTGTGT others(1): Show |
19 | a0001c0001t0003g0011a0001c0001t0003g0119a0001c0001t0005g0088others(16): Show | 19 | HG01192.hp2 HG01884.hp1 HG02080.hp2 others(16): Show |
intron_variant | MODIFIER | c.2108+946_2108+953d others(10): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207860151 | ||||||
| chr2:207860151
|
C | CTGTGTGT others(3): Show |
18 | a0001c0001t0001g0118a0001c0001t0003g0064a0001c0001t0004g0120others(15): Show | 18 | HG00642.hp2 HG01081.hp1 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.2108+944_2108+953d others(12): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207860151 | ||||||
| chr2:207860151
|
C | CTGTGTGT others(5): Show |
8 | a0001c0001t0003g0053a0001c0001t0046g0089a0001c0002t0001g0105others(5): Show | 8 | HG00323.hp2 HG01496.hp1 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.2108+942_2108+953d others(14): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207860151 | ||||||
| chr2:207860151
|
C | CTGTGTGT others(7): Show |
11 | a0001c0001t0002g0055a0001c0001t0002g0056a0001c0001t0011g0078others(8): Show | 11 | HG02293.hp2 HG02630.hp1 HG03669.hp2 others(8): Show |
intron_variant | MODIFIER | c.2108+940_2108+953d others(16): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207860151 | ||||||
| chr2:207860151
|
C | CTGTGTGT others(9): Show |
3 | a0001c0001t0011g0077a0001c0004t0002g0148a0008c0013t0002g0109 | 3 | HG00423.hp1 NA18968.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.2108+938_2108+953d others(18): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207860151 | ||||||
| chr2:207860151
|
C | CTGTGTGT others(11): Show |
3 | a0001c0001t0001g0033a0001c0003t0002g0072a0001c0004t0003g0165 | 3 | HG01358.hp1 HG01928.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.2108+936_2108+953d others(20): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207860151 | ||||||
| chr2:207860151
|
C | G | 4 | a0001c0002t0037g0110a0001c0003t0001g0022a0001c0003t0002g0018others(1): Show | 4 | HG01069.hp2 HG01071.hp2 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.2108+954G>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207860151 | ||||||
| chr2:207860151
|
CTG | C | 6 | a0001c0002t0038g0182a0001c0003t0002g0023a0001c0003t0023g0087others(3): Show | 6 | HG01168.hp2 HG01358.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.2108+952_2108+953d others(4): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207860151 | ||||||
| chr2:207860151
|
CTGTG | C | 10 | a0001c0001t0002g0032a0001c0001t0017g0003a0001c0002t0001g0154others(7): Show | 10 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(7): Show |
intron_variant | MODIFIER | c.2108+950_2108+953d others(6): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207860151 | ||||||
| chr2:207860151
|
CTGTGTG | C | 10 | a0001c0001t0001g0013a0001c0001t0001g0061a0001c0001t0002g0014others(7): Show | 10 | HG01891.hp2 HG01928.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.2108+948_2108+953d others(8): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207860151 | ||||||
| chr2:207860151
|
CTGTGTGT others(1): Show |
C | 35 | a0001c0001t0001g0019a0001c0001t0001g0042a0001c0001t0001g0045others(32): Show | 35 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.2108+946_2108+953d others(10): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207860151 | ||||||
| chr2:207860151
|
CTGTGTGT others(3): Show |
C | 7 | a0001c0001t0001g0017a0001c0001t0020g0115a0001c0001t0021g0121others(4): Show | 7 | HG02257.hp1 HG02257.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.2108+944_2108+953d others(12): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207860151 | ||||||
| chr2:207860151
|
CTGTGTGT others(5): Show |
C | 5 | a0001c0001t0005g0124a0001c0001t0018g0002a0001c0001t0027g0041others(2): Show | 5 | HG01109.hp2 HG02630.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2108+942_2108+953d others(14): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207860151 | ||||||
| chr2:207860151
|
CTGTGTGT others(7): Show |
C | 1 | a0001c0001t0004g0086 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2108+940_2108+953d others(16): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207860151 | ||||||
| chr2:207860151
|
CTGTGTGT others(9): Show |
C | 1 | a0001c0003t0008g0026 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2108+938_2108+953d others(18): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207860151 | ||||||
| chr2:207860151
|
CTGTGTGT others(13): Show |
C | 1 | a0001c0002t0059g0200 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2108+934_2108+953d others(22): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207860151 | ||||||
| chr2:207860207
|
A | G | 5 | a0001c0001t0004g0120a0001c0001t0019g0008a0001c0002t0004g0122others(2): Show | 5 | HG02622.hp1 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.2108+898T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207860207 | ||||||
| chr2:207860338
|
C | T | 2 | a0001c0001t0001g0042a0001c0001t0001g0060 | 2 | HG01243.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.2108+767G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207860338 | ||||||
| chr2:207860548
|
G | C | 2 | a0001c0003t0012g0090a0001c0003t0012g0176 | 2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2108+557C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207860548 | ||||||
| chr2:207860602
|
C | T | 1 | a0001c0003t0007g0065 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2108+503G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207860602 | ||||||
| chr2:207860643
|
C | T | 1 | a0001c0001t0032g0049 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2108+462G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207860643 | ||||||
| chr2:207860664
|
G | A | 2 | a0001c0003t0056g0192a0001c0003t0057g0191 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2108+441C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207860664 | ||||||
| chr2:207860871
|
A | C | 2 | a0001c0001t0024g0117a0001c0002t0013g0125 | 2 | HG02559.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2108+234T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 7/7 | chr2 | 207860871 | ||||||
| chr2:207861517
|
C | T | 119 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(116): Show | 119 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.1951-255G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207861517 | ||||||
| chr2:207861527
|
AC | A | 37 | a0001c0001t0001g0033a0001c0001t0002g0032a0001c0001t0002g0055others(34): Show | 37 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.1951-266delG | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207861527 | ||||||
| chr2:207861640
|
A | C | 1 | a0001c0001t0001g0068 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1951-378T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207861640 | ||||||
| chr2:207861722
|
A | T | 1 | a0001c0001t0051g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1951-460T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207861722 | ||||||
| chr2:207861725
|
G | C | 4 | a0001c0002t0006g0193a0001c0002t0006g0194a0001c0002t0006g0195others(1): Show | 4 | HG02145.hp1 HG02486.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1951-463C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207861725 | ||||||
| chr2:207861942
|
G | A | 9 | a0001c0001t0001g0118a0001c0001t0005g0088a0001c0002t0001g0126others(6): Show | 9 | HG02258.hp2 HG02809.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1951-680C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207861942 | ||||||
| chr2:207862139
|
T | C | 1 | a0001c0004t0002g0155 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1951-877A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207862139 | ||||||
| chr2:207862355
|
G | T | 1 | a0001c0001t0047g0059 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1951-1093C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207862355 | ||||||
| chr2:207862412
|
AGATT | A | 32 | a0001c0001t0002g0032a0001c0001t0002g0055a0001c0001t0002g0056others(29): Show | 32 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.1951-1154_1951-115 others(8): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207862412 | ||||||
| chr2:207862418
|
C | G | 32 | a0001c0001t0002g0032a0001c0001t0002g0055a0001c0001t0002g0056others(29): Show | 32 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.1951-1156G>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207862418 | ||||||
| chr2:207862694
|
A | T | 3 | a0001c0001t0013g0175a0001c0002t0038g0182a0001c0004t0001g0127 | 3 | HG01168.hp2 HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1951-1432T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207862694 | ||||||
| chr2:207862846
|
T | C | 1 | a0001c0001t0024g0117 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1951-1584A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207862846 | ||||||
| chr2:207863011
|
C | T | 1 | a0001c0004t0001g0127 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1951-1749G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207863011 | ||||||
| chr2:207863138
|
G | A | 1 | a0001c0002t0013g0125 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1951-1876C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207863138 | ||||||
| chr2:207863265
|
C | T | 57 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0042others(54): Show | 57 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.1951-2003G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207863265 | ||||||
| chr2:207863361
|
G | C | 1 | a0001c0001t0013g0175 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1951-2099C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207863361 | ||||||
| chr2:207863912
|
A | AAT | 43 | a0001c0001t0001g0033a0001c0001t0002g0032a0001c0001t0002g0055others(40): Show | 43 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.1951-2651_1951-265 others(6): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207863912 | ||||||
| chr2:207863914
|
A | T | 101 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0033others(98): Show | 101 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.1951-2652T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207863914 | ||||||
| chr2:207863993
|
T | C | 62 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0042others(59): Show | 62 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.1951-2731A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207863993 | ||||||
| chr2:207864021
|
G | C | 1 | a0001c0001t0004g0086 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1951-2759C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207864021 | ||||||
| chr2:207864174
|
A | G | 1 | a0001c0001t0017g0003 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1951-2912T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207864174 | ||||||
| chr2:207864213
|
C | G | 1 | a0004c0012t0003g0095 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1951-2951G>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207864213 | ||||||
| chr2:207864385
|
A | G | 1 | a0001c0002t0038g0182 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1951-3123T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207864385 | ||||||
| chr2:207864471
|
A | G | 1 | a0001c0001t0009g0007 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1951-3209T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207864471 | ||||||
| chr2:207864816
|
C | T | 41 | a0001c0001t0001g0017a0001c0001t0002g0032a0001c0001t0002g0039others(38): Show | 41 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.1951-3554G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207864816 | ||||||
| chr2:207865046
|
G | T | 1 | a0001c0004t0048g0166 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1951-3784C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865046 | ||||||
| chr2:207865064
|
T | C | 1 | a0001c0001t0049g0075 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1951-3802A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865064 | ||||||
| chr2:207865340
|
A | G | 5 | a0001c0001t0004g0086a0001c0001t0044g0116a0001c0003t0004g0172others(2): Show | 5 | HG01109.hp2 HG02257.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1951-4078T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865340 | ||||||
| chr2:207865378
|
C | T | 1 | a0001c0002t0038g0182 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1951-4116G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865378 | ||||||
| chr2:207865380
|
A | G | 32 | a0001c0001t0004g0086a0001c0001t0004g0120a0001c0001t0013g0175others(29): Show | 32 | HG01109.hp2 HG02145.hp1 HG02257.hp1 others(29): Show |
intron_variant | MODIFIER | c.1951-4118T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865380 | ||||||
| chr2:207865402
|
A | C | 1 | a0001c0002t0026g0085 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1951-4140T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865402 | ||||||
| chr2:207865409
|
T | C | 2 | a0001c0004t0001g0185a0001c0004t0040g0186 | 2 | HG02622.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1951-4147A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865409 | ||||||
| chr2:207865517
|
C | T | 9 | a0001c0001t0020g0115a0001c0001t0021g0121a0001c0001t0051g0123others(6): Show | 9 | HG02145.hp1 HG02257.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1951-4255G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865517 | ||||||
| chr2:207865663
|
G | C | 123 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(120): Show | 123 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.1951-4401C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865663 | ||||||
| chr2:207865781
|
C | CAA | 5 | a0001c0001t0055g0029a0001c0003t0001g0091a0001c0003t0012g0090others(2): Show | 5 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1951-4521_1951-452 others(6): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865781 | ||||||
| chr2:207865781
|
C | CAAA | 9 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0051g0123others(6): Show | 9 | HG00280.hp2 HG00323.hp2 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.1951-4522_1951-452 others(7): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865781 | ||||||
| chr2:207865781
|
C | CAAAA | 10 | a0001c0003t0001g0044a0001c0003t0002g0023a0001c0003t0002g0038others(7): Show | 10 | HG00423.hp1 HG00639.hp2 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.1951-4523_1951-452 others(8): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865781 | ||||||
| chr2:207865781
|
C | CAAAAAA | 5 | a0001c0001t0003g0011a0001c0003t0002g0037a0001c0003t0002g0040others(2): Show | 5 | HG00438.hp1 HG01516.hp1 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.1951-4525_1951-452 others(10): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865781 | ||||||
| chr2:207865795
|
AAAAAAAA others(5): Show |
A | 1 | a0001c0004t0001g0185 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1951-4545_1951-453 others(16): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865795 | ||||||
| chr2:207865796
|
AAAAAAAG others(4): Show |
A | 1 | a0001c0002t0050g0188 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1951-4545_1951-453 others(15): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865796 | ||||||
| chr2:207865796
|
AAAAAAAG others(6): Show |
A | 1 | a0001c0001t0019g0008 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1951-4547_1951-453 others(17): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865796 | ||||||
| chr2:207865796
|
AAAAAAAG others(10): Show |
A | 2 | a0001c0004t0001g0127a0001c0004t0014g0130 | 2 | HG02572.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1951-4551_1951-453 others(21): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865796 | ||||||
| chr2:207865797
|
A | T | 2 | a0001c0001t0001g0017a0001c0004t0040g0186 | 2 | HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1951-4535T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865797 | ||||||
| chr2:207865797
|
AAAAAAGA others(5): Show |
A | 4 | a0001c0001t0004g0120a0001c0002t0003g0129a0001c0002t0004g0122others(1): Show | 4 | HG02809.hp2 HG02818.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1951-4547_1951-453 others(16): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865797 | ||||||
| chr2:207865797
|
AAAAAAGA others(7): Show |
A | 1 | a0001c0001t0013g0175 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1951-4549_1951-453 others(18): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865797 | ||||||
| chr2:207865797
|
AAAAAAGA others(9): Show |
A | 1 | a0002c0005t0036g0098 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1951-4551_1951-453 others(20): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865797 | ||||||
| chr2:207865798
|
AAAAAGAT others(8): Show |
A | 1 | a0001c0002t0026g0085 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1951-4551_1951-453 others(19): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865798 | ||||||
| chr2:207865798
|
AAAAAGAT others(10): Show |
A | 1 | a0001c0003t0014g0099 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1951-4553_1951-453 others(21): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865798 | ||||||
| chr2:207865799
|
A | AATATATA others(3): Show |
1 | a0001c0001t0003g0119 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1951-4538_1951-453 others(14): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865799 | ||||||
| chr2:207865799
|
A | ATATATAT others(6): Show |
1 | a0002c0005t0004g0094 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1951-4538_1951-453 others(17): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865799 | ||||||
| chr2:207865799
|
A | ATATATAT others(8): Show |
1 | a0001c0002t0006g0196 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1951-4538_1951-453 others(19): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865799 | ||||||
| chr2:207865799
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0009g0007 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1951-4538_1951-453 others(25): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865799 | ||||||
| chr2:207865799
|
A | T | 4 | a0001c0001t0001g0017a0001c0001t0016g0005a0001c0003t0004g0172others(1): Show | 4 | HG02615.hp1 HG02630.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1951-4537T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865799 | ||||||
| chr2:207865801
|
A | AAAAAAAA others(29): Show |
1 | a0001c0001t0003g0053 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1951-4540_1951-453 others(40): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865801 | ||||||
| chr2:207865801
|
A | AAAAAAAA others(33): Show |
1 | a0004c0012t0003g0095 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1951-4540_1951-453 others(44): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865801 | ||||||
| chr2:207865801
|
A | AAAAAAAA others(14): Show |
1 | a0001c0001t0011g0078 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1951-4540_1951-453 others(25): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865801 | ||||||
| chr2:207865801
|
A | AAAAAAAA others(20): Show |
1 | a0001c0002t0001g0139 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1951-4540_1951-453 others(31): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865801 | ||||||
| chr2:207865801
|
A | AAAAAAAA others(22): Show |
1 | a0001c0003t0028g0010 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1951-4540_1951-453 others(33): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865801 | ||||||
| chr2:207865801
|
A | AAAAAAAA others(34): Show |
1 | a0001c0001t0002g0039 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1951-4540_1951-453 others(45): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865801 | ||||||
| chr2:207865801
|
A | AAAAAAAA others(9): Show |
1 | a0001c0001t0002g0032 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1951-4540_1951-453 others(20): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865801 | ||||||
| chr2:207865801
|
A | AAAAAAAA others(11): Show |
1 | a0001c0001t0003g0012 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1951-4540_1951-453 others(22): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865801 | ||||||
| chr2:207865801
|
A | AAAAAAAA others(15): Show |
1 | a0001c0004t0010g0157 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1951-4540_1951-453 others(26): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865801 | ||||||
| chr2:207865801
|
A | AAAAAAAA others(25): Show |
1 | a0001c0001t0003g0083 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1951-4540_1951-453 others(36): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865801 | ||||||
| chr2:207865801
|
A | AAAAAAAA others(35): Show |
1 | a0001c0002t0001g0105 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1951-4540_1951-453 others(46): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865801 | ||||||
| chr2:207865801
|
A | AAAAAAAA others(24): Show |
1 | a0001c0001t0009g0006 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1951-4540_1951-453 others(35): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865801 | ||||||
| chr2:207865801
|
A | AAAAAAAA others(30): Show |
1 | a0001c0002t0001g0106 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1951-4540_1951-453 others(41): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865801 | ||||||
| chr2:207865801
|
A | AAAAAAAA others(36): Show |
1 | a0001c0004t0003g0147 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1951-4540_1951-453 others(47): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865801 | ||||||
| chr2:207865801
|
A | AAAAAAAA others(7): Show |
1 | a0001c0001t0003g0020 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1951-4540_1951-453 others(18): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865801 | ||||||
| chr2:207865801
|
A | AAAAAAAA others(13): Show |
1 | a0001c0001t0011g0077 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1951-4540_1951-453 others(24): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865801 | ||||||
| chr2:207865801
|
A | AAAAAAAA others(15): Show |
2 | a0001c0001t0011g0079a0001c0001t0021g0121 | 2 | HG02818.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1951-4540_1951-453 others(26): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865801 | ||||||
| chr2:207865801
|
A | AAAAAAAA others(21): Show |
2 | a0001c0001t0024g0117a0001c0002t0013g0125 | 2 | HG02559.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1951-4540_1951-453 others(32): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865801 | ||||||
| chr2:207865801
|
A | AAAAAAAA others(27): Show |
1 | a0001c0002t0001g0102 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1951-4540_1951-453 others(38): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865801 | ||||||
| chr2:207865801
|
A | AAAAAAAA others(35): Show |
1 | a0001c0001t0020g0115 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1951-4540_1951-453 others(46): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865801 | ||||||
| chr2:207865801
|
A | AAAAAAAA others(26): Show |
1 | a0001c0001t0002g0055 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1951-4540_1951-453 others(37): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865801 | ||||||
| chr2:207865801
|
A | AAAAAAAA others(30): Show |
1 | a0001c0002t0003g0137 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1951-4540_1951-453 others(41): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865801 | ||||||
| chr2:207865801
|
A | AAAAAAAA others(31): Show |
1 | a0001c0002t0003g0133 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1951-4540_1951-453 others(42): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865801 | ||||||
| chr2:207865801
|
A | AAAAAAAA others(26): Show |
1 | a0001c0001t0046g0089 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1951-4540_1951-453 others(37): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865801 | ||||||
| chr2:207865801
|
A | AAAAAAAA others(34): Show |
1 | a0001c0001t0003g0064 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1951-4540_1951-453 others(45): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865801 | ||||||
| chr2:207865801
|
A | AAAAAAAA others(5): Show |
1 | a0001c0004t0002g0163 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1951-4540_1951-453 others(16): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865801 | ||||||
| chr2:207865801
|
A | AAAAAAAA others(11): Show |
1 | a0001c0002t0006g0193 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1951-4540_1951-453 others(22): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865801 | ||||||
| chr2:207865801
|
A | AAAAAAAA others(19): Show |
1 | a0001c0003t0023g0087 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1951-4540_1951-453 others(30): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865801 | ||||||
| chr2:207865801
|
A | AAAAAAAA others(21): Show |
1 | a0001c0002t0054g0149 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1951-4540_1951-453 others(32): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865801 | ||||||
| chr2:207865801
|
A | AAAAAAAA others(27): Show |
1 | a0001c0001t0002g0056 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1951-4540_1951-453 others(38): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865801 | ||||||
| chr2:207865801
|
A | AAAAAAAA others(8): Show |
1 | a0001c0004t0002g0136 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1951-4540_1951-453 others(19): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865801 | ||||||
| chr2:207865801
|
A | AAAAAAAA others(14): Show |
1 | a0001c0002t0006g0194 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1951-4540_1951-453 others(25): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865801 | ||||||
| chr2:207865801
|
A | AAAAAAAA others(20): Show |
1 | a0001c0002t0006g0195 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1951-4540_1951-453 others(31): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865801 | ||||||
| chr2:207865801
|
A | AAAAAAAA others(7): Show |
1 | a0001c0004t0003g0096 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1951-4540_1951-453 others(18): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865801 | ||||||
| chr2:207865801
|
A | AAAAAAAA others(13): Show |
1 | a0001c0003t0009g0001 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1951-4540_1951-453 others(24): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865801 | ||||||
| chr2:207865801
|
A | AAAAAAAA others(17): Show |
1 | a0001c0002t0006g0199 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1951-4540_1951-453 others(28): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865801 | ||||||
| chr2:207865801
|
A | AAAAAATA others(7): Show |
1 | a0001c0004t0002g0155 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1951-4540_1951-453 others(18): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865801 | ||||||
| chr2:207865801
|
A | AAAAATAT others(16): Show |
1 | a0001c0002t0001g0134 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1951-4540_1951-453 others(27): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865801 | ||||||
| chr2:207865801
|
A | AAAATATA others(3): Show |
2 | a0001c0002t0002g0140a0001c0003t0029g0054 | 2 | NA18951.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.1951-4540_1951-453 others(14): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865801 | ||||||
| chr2:207865801
|
A | T | 9 | a0001c0001t0001g0017a0001c0001t0001g0118a0001c0001t0003g0119others(6): Show | 9 | HG01109.hp2 HG02145.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1951-4539T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865801 | ||||||
| chr2:207865801
|
AAG | A | 6 | a0001c0001t0001g0019a0001c0001t0001g0061a0001c0001t0001g0063others(3): Show | 6 | HG01515.hp2 HG01884.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1951-4541_1951-454 others(6): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865801 | ||||||
| chr2:207865801
|
AAGAT | A | 28 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0060others(25): Show | 28 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.1951-4543_1951-454 others(8): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865801 | ||||||
| chr2:207865801
|
AAGATATA others(3): Show |
A | 1 | a0001c0001t0005g0088 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1951-4549_1951-454 others(14): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865801 | ||||||
| chr2:207865802
|
AG | A | 3 | a0001c0001t0015g0004a0001c0001t0033g0016a0001c0004t0003g0128 | 3 | HG02559.hp2 HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1951-4541delC | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865802 | ||||||
| chr2:207865802
|
AGAT | A | 9 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0003g0058others(6): Show | 9 | HG00423.hp2 HG01069.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.1951-4543_1951-454 others(7): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865802 | ||||||
| chr2:207865802
|
AGATAT | A | 3 | a0001c0001t0001g0013a0001c0001t0001g0071a0001c0002t0041g0164 | 3 | HG00323.hp1 HG00639.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.1951-4545_1951-454 others(9): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865802 | ||||||
| chr2:207865803
|
G | A | 26 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0069others(23): Show | 26 | HG00280.hp2 HG00323.hp2 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.1951-4541C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865803 | ||||||
| chr2:207865803
|
G | GAT | 9 | a0001c0001t0001g0068a0001c0003t0001g0092a0001c0003t0003g0067others(6): Show | 9 | HG01081.hp2 HG02698.hp2 NA18747.hp1 others(6): Show |
intron_variant | MODIFIER | c.1951-4543_1951-454 others(6): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865803 | ||||||
| chr2:207865803
|
G | GATAT | 4 | a0001c0003t0001g0028a0001c0004t0001g0179a0001c0004t0030g0167others(1): Show | 4 | HG00099.hp1 HG03492.hp1 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.1951-4545_1951-454 others(8): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865803 | ||||||
| chr2:207865803
|
G | GATATAT | 4 | a0001c0002t0002g0170a0001c0003t0001g0043a0001c0004t0002g0131others(1): Show | 4 | HG00621.hp2 HG01256.hp1 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.1951-4547_1951-454 others(10): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865803 | ||||||
| chr2:207865803
|
G | T | 83 | a0001c0001t0001g0017a0001c0001t0001g0118a0001c0001t0002g0032others(80): Show | 83 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.1951-4541C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865803 | ||||||
| chr2:207865805
|
T | A | 20 | a0001c0001t0001g0019a0001c0001t0001g0061a0001c0001t0001g0063others(17): Show | 20 | HG01168.hp1 HG01243.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.1951-4543A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865805 | ||||||
| chr2:207865807
|
T | A | 53 | a0001c0001t0001g0019a0001c0001t0001g0033a0001c0001t0001g0042others(50): Show | 53 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.1951-4545A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865807 | ||||||
| chr2:207865809
|
T | A | 52 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0033others(49): Show | 52 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.1951-4547A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865809 | ||||||
| chr2:207865811
|
T | A | 42 | a0001c0001t0001g0013a0001c0001t0001g0033a0001c0001t0001g0045others(39): Show | 42 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(39): Show |
intron_variant | MODIFIER | c.1951-4549A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865811 | ||||||
| chr2:207865813
|
T | A | 30 | a0001c0001t0001g0013a0001c0001t0001g0046a0001c0001t0001g0070others(27): Show | 30 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(27): Show |
intron_variant | MODIFIER | c.1951-4551A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865813 | ||||||
| chr2:207865815
|
T | A | 9 | a0001c0001t0001g0074a0001c0001t0001g0080a0001c0001t0005g0088others(6): Show | 9 | HG00423.hp2 HG01496.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.1951-4553A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865815 | ||||||
| chr2:207865817
|
T | A | 3 | a0001c0001t0032g0049a0001c0002t0003g0103a0001c0003t0007g0065 | 3 | HG00423.hp2 HG02300.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.1951-4555A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865817 | ||||||
| chr2:207865819
|
T | A | 1 | a0001c0003t0007g0065 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1951-4557A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865819 | ||||||
| chr2:207865821
|
T | A | 1 | a0001c0003t0007g0065 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1951-4559A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865821 | ||||||
| chr2:207865859
|
G | C | 1 | a0001c0004t0010g0145 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1951-4597C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207865859 | ||||||
| chr2:207866002
|
G | A | 42 | a0001c0001t0001g0017a0001c0001t0002g0032a0001c0001t0002g0039others(39): Show | 42 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1951-4740C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207866002 | ||||||
| chr2:207866219
|
G | C | 1 | a0001c0001t0001g0080 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1951-4957C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207866219 | ||||||
| chr2:207866258
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1951-4996G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207866258 | ||||||
| chr2:207866259
|
G | A | 1 | a0001c0003t0001g0091 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1951-4997C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207866259 | ||||||
| chr2:207866364
|
C | T | 1 | a0001c0004t0001g0127 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1951-5102G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207866364 | ||||||
| chr2:207866623
|
C | T | 1 | a0005c0011t0022g0111 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1951-5361G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207866623 | ||||||
| chr2:207866650
|
G | C | 1 | a0001c0001t0001g0033 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1951-5388C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207866650 | ||||||
| chr2:207866919
|
G | A | 2 | a0001c0002t0006g0198a0002c0005t0001g0132 | 2 | HG01884.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1951-5657C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207866919 | ||||||
| chr2:207867164
|
G | C | 2 | a0001c0003t0056g0192a0001c0003t0057g0191 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1951-5902C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207867164 | ||||||
| chr2:207867830
|
T | A | 41 | a0001c0001t0002g0032a0001c0001t0002g0039a0001c0001t0002g0055others(38): Show | 41 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.1951-6568A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207867830 | ||||||
| chr2:207867852
|
T | C | 2 | a0001c0003t0008g0050a0001c0003t0008g0076 | 2 | HG01346.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.1951-6590A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207867852 | ||||||
| chr2:207867925
|
G | A | 9 | a0001c0001t0004g0120a0001c0001t0016g0005a0001c0001t0019g0008others(6): Show | 9 | HG02622.hp1 HG02622.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1951-6663C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207867925 | ||||||
| chr2:207867978
|
T | C | 45 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0042others(42): Show | 45 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.1951-6716A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207867978 | ||||||
| chr2:207868056
|
T | C | 1 | a0001c0002t0002g0170 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1951-6794A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207868056 | ||||||
| chr2:207868062
|
A | T | 2 | a0001c0001t0024g0117a0001c0002t0013g0125 | 2 | HG02559.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1951-6800T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207868062 | ||||||
| chr2:207868135
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1951-6873G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207868135 | ||||||
| chr2:207868274
|
A | AT | 55 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0045others(52): Show | 55 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.1951-7013dupA | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207868274 | ||||||
| chr2:207868274
|
A | ATT | 11 | a0001c0001t0001g0042a0001c0001t0001g0060a0001c0001t0020g0115others(8): Show | 11 | HG01243.hp2 HG01884.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1951-7014_1951-701 others(6): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207868274 | ||||||
| chr2:207868276
|
T | TA | 63 | a0001c0001t0001g0017a0001c0001t0001g0033a0001c0001t0002g0032others(60): Show | 63 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.1951-7015_1951-701 others(5): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207868276 | ||||||
| chr2:207868277
|
T | A | 7 | a0001c0001t0004g0086a0001c0001t0044g0116a0001c0003t0002g0081others(4): Show | 7 | HG01109.hp2 HG01952.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1951-7015A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207868277 | ||||||
| chr2:207868278
|
T | A | 1 | a0001c0002t0026g0085 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1951-7016A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207868278 | ||||||
| chr2:207868279
|
T | A | 7 | a0001c0001t0003g0119a0001c0002t0006g0196a0001c0002t0037g0110others(4): Show | 7 | HG02622.hp2 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1951-7017A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207868279 | ||||||
| chr2:207868387
|
G | A | 1 | a0001c0001t0013g0175 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1951-7125C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207868387 | ||||||
| chr2:207868560
|
A | C | 3 | a0001c0001t0024g0117a0001c0002t0013g0125a0001c0003t0001g0091 | 3 | HG01243.hp1 HG02559.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1951-7298T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207868560 | ||||||
| chr2:207868575
|
C | T | 2 | a0001c0001t0009g0007a0001c0002t0006g0196 | 2 | HG02145.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1951-7313G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207868575 | ||||||
| chr2:207869119
|
A | T | 2 | a0001c0001t0001g0017a0001c0002t0026g0085 | 2 | HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1951-7857T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207869119 | ||||||
| chr2:207869668
|
C | T | 5 | a0001c0001t0004g0086a0001c0001t0044g0116a0001c0003t0004g0172others(2): Show | 5 | HG01109.hp2 HG02257.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1951-8406G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207869668 | ||||||
| chr2:207869960
|
T | C | 6 | a0001c0002t0026g0085a0001c0002t0038g0182a0001c0003t0014g0099others(3): Show | 6 | HG01168.hp2 HG02258.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1951-8698A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207869960 | ||||||
| chr2:207870023
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1951-8761G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207870023 | ||||||
| chr2:207870236
|
T | C | 9 | a0001c0001t0004g0120a0001c0001t0016g0005a0001c0001t0019g0008others(6): Show | 9 | HG02622.hp1 HG02622.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1951-8974A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207870236 | ||||||
| chr2:207870330
|
T | C | 1 | a0002c0005t0036g0098 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1951-9068A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207870330 | ||||||
| chr2:207870382
|
C | T | 43 | a0001c0001t0002g0032a0001c0001t0002g0039a0001c0001t0002g0055others(40): Show | 43 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.1951-9120G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207870382 | ||||||
| chr2:207870513
|
C | T | 43 | a0001c0001t0002g0032a0001c0001t0002g0039a0001c0001t0002g0055others(40): Show | 43 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.1951-9251G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207870513 | ||||||
| chr2:207870515
|
A | T | 1 | a0001c0004t0001g0153 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1951-9253T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207870515 | ||||||
| chr2:207870818
|
G | A | 75 | a0001c0001t0001g0017a0001c0001t0002g0032a0001c0001t0002g0039others(72): Show | 75 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.1951-9556C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207870818 | ||||||
| chr2:207870965
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1951-9703C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207870965 | ||||||
| chr2:207871184
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1951-9922G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207871184 | ||||||
| chr2:207871469
|
T | A | 9 | a0001c0001t0020g0115a0001c0001t0021g0121a0001c0001t0051g0123others(6): Show | 9 | HG02145.hp1 HG02257.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1951-10207A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207871469 | ||||||
| chr2:207871597
|
G | A | 3 | a0001c0002t0058g0197a0001c0002t0059g0200a0005c0011t0022g0111 | 3 | HG02615.hp2 HG02895.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1951-10335C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207871597 | ||||||
| chr2:207871644
|
T | C | 8 | a0001c0001t0020g0115a0001c0001t0021g0121a0001c0002t0001g0134others(5): Show | 8 | HG02145.hp1 HG02257.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1951-10382A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207871644 | ||||||
| chr2:207871679
|
T | G | 11 | a0001c0001t0001g0017a0001c0001t0020g0115a0001c0001t0021g0121others(8): Show | 11 | HG02145.hp1 HG02257.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1951-10417A>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207871679 | ||||||
| chr2:207871689
|
G | C | 1 | a0001c0003t0001g0092 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1951-10427C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207871689 | ||||||
| chr2:207871728
|
A | C | 2 | a0001c0001t0024g0117a0001c0002t0013g0125 | 2 | HG02559.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1951-10466T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207871728 | ||||||
| chr2:207871757
|
T | C | 1 | a0001c0001t0001g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1951-10495A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207871757 | ||||||
| chr2:207871992
|
G | C | 50 | a0001c0001t0002g0032a0001c0001t0002g0039a0001c0001t0002g0055others(47): Show | 50 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.1951-10730C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207871992 | ||||||
| chr2:207872551
|
G | T | 75 | a0001c0001t0001g0017a0001c0001t0002g0032a0001c0001t0002g0039others(72): Show | 75 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.1951-11289C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207872551 | ||||||
| chr2:207872569
|
G | T | 2 | a0001c0004t0002g0113a0001c0004t0002g0114 | 2 | HG02683.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1951-11307C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207872569 | ||||||
| chr2:207872616
|
T | A | 1 | a0001c0002t0038g0182 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1951-11354A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207872616 | ||||||
| chr2:207872666
|
C | T | 2 | a0001c0004t0039g0036a0001c0004t0042g0035 | 2 | HG02809.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1951-11404G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207872666 | ||||||
| chr2:207872696
|
C | T | 2 | a0001c0004t0039g0036a0001c0004t0042g0035 | 2 | HG02809.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1951-11434G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207872696 | ||||||
| chr2:207872795
|
C | A | 2 | a0001c0001t0024g0117a0001c0002t0013g0125 | 2 | HG02559.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1951-11533G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207872795 | ||||||
| chr2:207872825
|
TCAAACAA others(1): Show |
T | 4 | a0001c0003t0001g0043a0001c0004t0001g0152a0001c0004t0001g0153others(1): Show | 4 | HG01256.hp1 HG04115.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.1951-11571_1951-11 others(14): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207872825 | ||||||
| chr2:207873030
|
T | C | 1 | a0001c0003t0012g0176 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1951-11768A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207873030 | ||||||
| chr2:207873254
|
C | T | 1 | a0001c0001t0001g0033 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1951-11992G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207873254 | ||||||
| chr2:207873362
|
A | G | 3 | a0001c0002t0037g0110a0001c0004t0039g0036a0001c0004t0042g0035 | 3 | HG02809.hp1 HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1951-12100T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207873362 | ||||||
| chr2:207873469
|
C | A | 1 | a0008c0013t0002g0109 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1951-12207G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207873469 | ||||||
| chr2:207873615
|
C | T | 2 | a0001c0003t0012g0090a0001c0003t0012g0176 | 2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1951-12353G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207873615 | ||||||
| chr2:207874255
|
C | G | 1 | a0001c0001t0001g0080 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1951-12993G>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207874255 | ||||||
| chr2:207874259
|
A | T | 2 | a0001c0002t0026g0085a0001c0004t0001g0127 | 2 | HG02630.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1951-12997T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207874259 | ||||||
| chr2:207874600
|
TC | T | 5 | a0001c0001t0004g0086a0001c0001t0044g0116a0001c0003t0004g0172others(2): Show | 5 | HG01109.hp2 HG02257.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1951-13339delG | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207874600 | ||||||
| chr2:207874832
|
C | T | 1 | a0001c0004t0002g0112 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1951-13570G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207874832 | ||||||
| chr2:207874902
|
A | G | 1 | a0001c0002t0038g0182 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1951-13640T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207874902 | ||||||
| chr2:207875222
|
A | C | 1 | a0001c0001t0003g0119 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1951-13960T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207875222 | ||||||
| chr2:207875456
|
A | G | 1 | a0001c0002t0026g0085 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1951-14194T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207875456 | ||||||
| chr2:207875472
|
C | G | 1 | a0001c0001t0009g0006 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1951-14210G>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207875472 | ||||||
| chr2:207875514
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1951-14252C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207875514 | ||||||
| chr2:207875583
|
G | C | 1 | a0001c0003t0001g0025 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1951-14321C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207875583 | ||||||
| chr2:207875650
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1951-14388C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207875650 | ||||||
| chr2:207875716
|
T | C | 3 | a0001c0001t0024g0117a0001c0001t0033g0016a0001c0002t0013g0125 | 3 | HG02559.hp1 HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1951-14454A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207875716 | ||||||
| chr2:207875814
|
A | C | 1 | a0001c0002t0038g0182 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1951-14552T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207875814 | ||||||
| chr2:207875817
|
A | AAAC | 3 | a0001c0001t0003g0030a0001c0002t0026g0085a0001c0003t0003g0067 | 3 | HG02135.hp2 HG03453.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.1951-14558_1951-14 others(9): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207875817 | ||||||
| chr2:207876148
|
G | A | 1 | a0001c0001t0003g0011 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1951-14886C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207876148 | ||||||
| chr2:207876304
|
G | A | 2 | a0001c0004t0001g0127a0002c0005t0036g0098 | 2 | HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1951-15042C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207876304 | ||||||
| chr2:207876478
|
A | T | 1 | a0001c0003t0001g0025 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1951-15216T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207876478 | ||||||
| chr2:207876798
|
G | A | 5 | a0001c0001t0004g0086a0001c0001t0044g0116a0001c0003t0004g0172others(2): Show | 5 | HG01109.hp2 HG02257.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1951-15536C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207876798 | ||||||
| chr2:207877277
|
T | C | 1 | a0001c0003t0003g0067 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1951-16015A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207877277 | ||||||
| chr2:207877500
|
T | G | 1 | a0001c0001t0001g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1951-16238A>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207877500 | ||||||
| chr2:207877535
|
C | T | 40 | a0001c0001t0002g0032a0001c0001t0002g0039a0001c0001t0002g0055others(37): Show | 40 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.1951-16273G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207877535 | ||||||
| chr2:207877619
|
A | T | 41 | a0001c0001t0002g0032a0001c0001t0002g0039a0001c0001t0002g0055others(38): Show | 41 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.1951-16357T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207877619 | ||||||
| chr2:207877879
|
C | T | 2 | a0001c0001t0001g0017a0001c0001t0013g0175 | 2 | HG02615.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1951-16617G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207877879 | ||||||
| chr2:207877952
|
T | C | 1 | a0001c0003t0001g0028 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1951-16690A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207877952 | ||||||
| chr2:207878012
|
C | T | 1 | a0001c0001t0003g0083 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1951-16750G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207878012 | ||||||
| chr2:207878013
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1951-16751C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207878013 | ||||||
| chr2:207878142
|
T | C | 9 | a0001c0001t0020g0115a0001c0001t0021g0121a0001c0001t0051g0123others(6): Show | 9 | HG02145.hp1 HG02257.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1951-16880A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207878142 | ||||||
| chr2:207878152
|
G | A | 1 | a0001c0001t0002g0048 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1951-16890C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207878152 | ||||||
| chr2:207878251
|
C | T | 199 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1951-16989G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207878251 | ||||||
| chr2:207878303
|
A | AT | 50 | a0001c0001t0002g0032a0001c0001t0002g0039a0001c0001t0002g0055others(47): Show | 50 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.1951-17042dupA | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207878303 | ||||||
| chr2:207878306
|
A | T | 1 | a0002c0006t0025g0187 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1951-17044T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207878306 | ||||||
| chr2:207878560
|
A | G | 1 | a0001c0001t0002g0048 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1951-17298T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207878560 | ||||||
| chr2:207878581
|
C | A | 46 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0042others(43): Show | 46 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(43): Show |
intron_variant | MODIFIER | c.1951-17319G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207878581 | ||||||
| chr2:207878621
|
A | G | 1 | a0001c0004t0001g0179 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1951-17359T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207878621 | ||||||
| chr2:207878722
|
T | C | 1 | a0001c0001t0001g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1951-17460A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207878722 | ||||||
| chr2:207878940
|
C | G | 41 | a0001c0001t0002g0032a0001c0001t0002g0039a0001c0001t0002g0055others(38): Show | 41 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.1951-17678G>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207878940 | ||||||
| chr2:207879261
|
A | G | 11 | a0001c0001t0001g0017a0001c0001t0013g0175a0001c0001t0020g0115others(8): Show | 11 | HG02145.hp1 HG02257.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1951-17999T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207879261 | ||||||
| chr2:207879280
|
A | G | 1 | a0001c0001t0001g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1951-18018T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207879280 | ||||||
| chr2:207879662
|
T | G | 11 | a0001c0001t0001g0017a0001c0001t0013g0175a0001c0001t0020g0115others(8): Show | 11 | HG02145.hp1 HG02257.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1951-18400A>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207879662 | ||||||
| chr2:207879772
|
C | T | 6 | a0001c0001t0004g0086a0001c0001t0044g0116a0001c0003t0001g0091others(3): Show | 6 | HG01109.hp2 HG01243.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1951-18510G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207879772 | ||||||
| chr2:207879787
|
A | T | 11 | a0001c0001t0001g0017a0001c0001t0013g0175a0001c0001t0020g0115others(8): Show | 11 | HG02145.hp1 HG02257.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1951-18525T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207879787 | ||||||
| chr2:207879830
|
T | G | 5 | a0001c0003t0001g0025a0001c0003t0002g0024a0001c0003t0002g0037others(2): Show | 5 | HG00323.hp2 HG01516.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1951-18568A>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207879830 | ||||||
| chr2:207879840
|
G | C | 2 | a0001c0003t0014g0099a0001c0004t0014g0130 | 2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1951-18578C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207879840 | ||||||
| chr2:207880089
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1951-18827G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207880089 | ||||||
| chr2:207880128
|
C | T | 2 | a0001c0003t0012g0090a0001c0003t0012g0176 | 2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1951-18866G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207880128 | ||||||
| chr2:207880256
|
A | C | 32 | a0001c0001t0002g0032a0001c0001t0002g0039a0001c0001t0002g0055others(29): Show | 32 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.1951-18994T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207880256 | ||||||
| chr2:207880297
|
C | A | 1 | a0001c0001t0001g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1951-19035G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207880297 | ||||||
| chr2:207880361
|
C | A | 1 | a0002c0005t0036g0098 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1951-19099G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207880361 | ||||||
| chr2:207880410
|
G | GA | 109 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(106): Show | 109 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.1951-19149dupT | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207880410 | ||||||
| chr2:207880410
|
G | GAA | 13 | a0001c0001t0017g0003a0001c0001t0033g0016a0001c0001t0049g0075others(10): Show | 13 | HG00438.hp2 HG01168.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.1951-19150_1951-19 others(8): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207880410 | ||||||
| chr2:207880424
|
C | T | 1 | a0001c0004t0001g0127 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1951-19162G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207880424 | ||||||
| chr2:207880485
|
C | T | 1 | a0001c0002t0038g0182 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1951-19223G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207880485 | ||||||
| chr2:207880486
|
G | T | 6 | a0001c0001t0004g0120a0001c0001t0019g0008a0001c0002t0003g0129others(3): Show | 6 | HG02622.hp1 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1951-19224C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207880486 | ||||||
| chr2:207880563
|
A | G | 1 | a0001c0001t0001g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1951-19301T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207880563 | ||||||
| chr2:207880627
|
T | C | 2 | a0001c0003t0056g0192a0001c0003t0057g0191 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1951-19365A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207880627 | ||||||
| chr2:207880762
|
C | CAAAAAAA others(3): Show |
4 | a0001c0002t0026g0085a0001c0002t0038g0182a0001c0004t0039g0036others(1): Show | 4 | HG01168.hp2 HG02809.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1951-19510_1951-19 others(16): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207880762 | ||||||
| chr2:207880762
|
C | CAAAAAAA others(4): Show |
7 | a0001c0001t0001g0017a0001c0001t0003g0011a0001c0001t0004g0086others(4): Show | 7 | HG01109.hp2 HG01243.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1951-19511_1951-19 others(17): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207880762 | ||||||
| chr2:207880762
|
C | CAAAAAAA others(5): Show |
19 | a0001c0001t0002g0032a0001c0001t0002g0039a0001c0001t0002g0055others(16): Show | 19 | HG00558.hp1 HG01358.hp2 HG01516.hp2 others(16): Show |
intron_variant | MODIFIER | c.1951-19512_1951-19 others(18): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207880762 | ||||||
| chr2:207880762
|
C | CAAAAAAA others(6): Show |
36 | a0001c0001t0003g0051a0001c0001t0003g0083a0001c0001t0009g0006others(33): Show | 36 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(33): Show |
intron_variant | MODIFIER | c.1951-19513_1951-19 others(19): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207880762 | ||||||
| chr2:207880762
|
C | CAAAAAAA others(7): Show |
43 | a0001c0001t0001g0033a0001c0001t0001g0068a0001c0001t0002g0014others(40): Show | 43 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(40): Show |
intron_variant | MODIFIER | c.1951-19514_1951-19 others(20): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207880762 | ||||||
| chr2:207880762
|
C | CAAAAAAA others(8): Show |
19 | a0001c0001t0001g0118a0001c0001t0003g0020a0001c0001t0003g0030others(16): Show | 19 | HG00423.hp1 HG00438.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.1951-19515_1951-19 others(21): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207880762 | ||||||
| chr2:207880762
|
C | CAAAAAAA others(9): Show |
3 | a0001c0001t0001g0019a0001c0002t0001g0102a0001c0004t0002g0163 | 3 | HG01192.hp2 HG01515.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1951-19516_1951-19 others(22): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207880762 | ||||||
| chr2:207880762
|
C | CAAAAAAA others(10): Show |
1 | a0001c0001t0034g0047 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1951-19517_1951-19 others(23): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207880762 | ||||||
| chr2:207880762
|
C | CAAAAAAA others(11): Show |
5 | a0001c0001t0001g0061a0001c0001t0003g0031a0001c0001t0015g0004others(2): Show | 5 | HG01168.hp1 HG02071.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1951-19518_1951-19 others(24): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207880762 | ||||||
| chr2:207880762
|
C | CAAAAAAA others(12): Show |
12 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0063others(9): Show | 12 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.1951-19519_1951-19 others(25): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207880762 | ||||||
| chr2:207880762
|
C | CAAAAAAA others(13): Show |
6 | a0001c0001t0001g0074a0001c0002t0001g0141a0001c0002t0001g0154others(3): Show | 6 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(3): Show |
intron_variant | MODIFIER | c.1951-19520_1951-19 others(26): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207880762 | ||||||
| chr2:207880762
|
C | CAAAAAAA others(14): Show |
4 | a0001c0001t0001g0080a0001c0001t0049g0075a0001c0002t0001g0169others(1): Show | 4 | HG01928.hp1 HG02896.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.1951-19521_1951-19 others(27): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207880762 | ||||||
| chr2:207880762
|
C | CAAAAAAA others(15): Show |
2 | a0001c0001t0018g0002a0001c0002t0006g0198 | 2 | HG01884.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1951-19522_1951-19 others(28): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207880762 | ||||||
| chr2:207880762
|
C | CAAAAAAA others(16): Show |
2 | a0001c0001t0003g0062a0001c0001t0005g0124 | 2 | HG00408.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1951-19523_1951-19 others(29): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207880762 | ||||||
| chr2:207880762
|
C | CAAAAAAA others(17): Show |
4 | a0001c0001t0001g0071a0001c0001t0003g0058a0001c0002t0001g0142others(1): Show | 4 | HG00323.hp1 HG02080.hp1 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.1951-19524_1951-19 others(30): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207880762 | ||||||
| chr2:207880762
|
CAAAAAAA others(3): Show |
C | 8 | a0001c0001t0020g0115a0001c0001t0051g0123a0001c0002t0001g0134others(5): Show | 8 | HG02145.hp1 HG02257.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1951-19510_1951-19 others(16): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207880762 | ||||||
| chr2:207880762
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0002t0037g0110 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1951-19512_1951-19 others(18): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207880762 | ||||||
| chr2:207880767
|
A | AAAAAAAA others(6): Show |
1 | a0001c0003t0029g0054 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1951-19506_1951-19 others(19): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207880767 | ||||||
| chr2:207880783
|
A | AAAAAAAA others(6): Show |
1 | a0001c0003t0057g0191 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1951-19522_1951-19 others(19): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207880783 | ||||||
| chr2:207880783
|
A | AAAAAAAA others(5): Show |
1 | a0001c0003t0056g0192 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1951-19522_1951-19 others(18): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207880783 | ||||||
| chr2:207880788
|
A | AAAAAAAA others(7): Show |
1 | a0001c0008t0053g0173 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1951-19527_1951-19 others(20): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207880788 | ||||||
| chr2:207880789
|
C | A | 2 | a0001c0004t0002g0158a0001c0004t0007g0178 | 2 | NA18968.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.1951-19527G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207880789 | ||||||
| chr2:207880790
|
C | A | 2 | a0001c0004t0002g0158a0001c0004t0007g0178 | 2 | NA18968.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.1951-19528G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207880790 | ||||||
| chr2:207880794
|
A | AAAAAAAA others(4): Show |
1 | a0001c0004t0007g0178 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1951-19533_1951-19 others(17): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207880794 | ||||||
| chr2:207880798
|
C | A | 1 | a0001c0004t0007g0178 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1951-19536G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207880798 | ||||||
| chr2:207880802
|
C | A | 1 | a0001c0004t0002g0158 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1951-19540G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207880802 | ||||||
| chr2:207880810
|
A | C | 11 | a0001c0001t0013g0175a0001c0001t0020g0115a0001c0001t0021g0121others(8): Show | 11 | HG02145.hp1 HG02257.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1951-19548T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207880810 | ||||||
| chr2:207880814
|
A | C | 1 | a0001c0004t0002g0158 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1951-19552T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207880814 | ||||||
| chr2:207880816
|
C | A | 1 | a0001c0004t0002g0158 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1951-19554G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207880816 | ||||||
| chr2:207880867
|
C | CT | 118 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(115): Show | 118 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.1951-19606dupA | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207880867 | ||||||
| chr2:207881069
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1951-19807G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207881069 | ||||||
| chr2:207881071
|
T | A | 1 | a0001c0001t0001g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1951-19809A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207881071 | ||||||
| chr2:207881072
|
A | T | 1 | a0001c0001t0001g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1951-19810T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207881072 | ||||||
| chr2:207881073
|
A | C | 1 | a0001c0001t0001g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1951-19811T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207881073 | ||||||
| chr2:207881074
|
A | T | 1 | a0001c0001t0001g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1951-19812T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207881074 | ||||||
| chr2:207881336
|
T | C | 1 | a0001c0001t0021g0121 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1951-20074A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207881336 | ||||||
| chr2:207881402
|
C | T | 72 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(69): Show | 72 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.1951-20140G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207881402 | ||||||
| chr2:207881420
|
T | C | 3 | a0001c0002t0037g0110a0001c0004t0039g0036a0001c0004t0042g0035 | 3 | HG02809.hp1 HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1951-20158A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207881420 | ||||||
| chr2:207881774
|
C | T | 1 | a0002c0005t0036g0098 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1951-20512G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207881774 | ||||||
| chr2:207881918
|
C | T | 46 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0042others(43): Show | 46 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(43): Show |
intron_variant | MODIFIER | c.1951-20656G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207881918 | ||||||
| chr2:207881968
|
C | T | 2 | a0001c0004t0039g0036a0001c0004t0042g0035 | 2 | HG02809.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1951-20706G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207881968 | ||||||
| chr2:207882321
|
G | C | 4 | a0001c0001t0017g0003a0001c0001t0033g0016a0001c0002t0045g0190others(1): Show | 4 | HG02109.hp2 HG02559.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1951-21059C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207882321 | ||||||
| chr2:207882322
|
C | T | 2 | a0001c0003t0056g0192a0001c0003t0057g0191 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1951-21060G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207882322 | ||||||
| chr2:207882468
|
C | T | 11 | a0001c0001t0004g0120a0001c0001t0016g0005a0001c0001t0019g0008others(8): Show | 11 | HG02622.hp1 HG02622.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.1951-21206G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207882468 | ||||||
| chr2:207882537
|
G | A | 1 | a0006c0010t0003g0101 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1951-21275C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207882537 | ||||||
| chr2:207882568
|
C | T | 2 | a0001c0002t0002g0140a0001c0004t0002g0155 | 2 | HG02071.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.1951-21306G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207882568 | ||||||
| chr2:207882612
|
C | CA | 93 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0033others(90): Show | 93 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.1951-21351dupT | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207882612 | ||||||
| chr2:207882654
|
G | A | 15 | a0001c0001t0004g0086a0001c0001t0004g0120a0001c0001t0016g0005others(12): Show | 15 | HG01109.hp2 HG01243.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.1951-21392C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207882654 | ||||||
| chr2:207882724
|
A | C | 1 | a0001c0001t0001g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1951-21462T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207882724 | ||||||
| chr2:207882835
|
T | A | 9 | a0001c0001t0004g0120a0001c0001t0016g0005a0001c0001t0019g0008others(6): Show | 9 | HG02622.hp1 HG02622.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1951-21573A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207882835 | ||||||
| chr2:207882836
|
T | A | 15 | a0001c0001t0004g0120a0001c0001t0016g0005a0001c0001t0019g0008others(12): Show | 15 | HG02258.hp1 HG02572.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.1951-21574A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207882836 | ||||||
| chr2:207882837
|
A | T | 1 | a0001c0001t0024g0117 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1951-21575T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207882837 | ||||||
| chr2:207882967
|
C | T | 1 | a0001c0002t0006g0193 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1951-21705G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207882967 | ||||||
| chr2:207883039
|
C | A | 1 | a0001c0004t0002g0113 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1951-21777G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207883039 | ||||||
| chr2:207883040
|
G | A | 1 | a0001c0001t0049g0075 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1951-21778C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207883040 | ||||||
| chr2:207883055
|
A | C | 1 | a0001c0002t0003g0137 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1951-21793T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207883055 | ||||||
| chr2:207883089
|
G | A | 1 | a0001c0015t0003g0093 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1951-21827C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207883089 | ||||||
| chr2:207883111
|
T | C | 1 | a0001c0001t0001g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1951-21849A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207883111 | ||||||
| chr2:207883499
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1951-22237G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207883499 | ||||||
| chr2:207883621
|
A | G | 1 | a0001c0001t0049g0075 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1951-22359T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207883621 | ||||||
| chr2:207883836
|
G | A | 6 | a0001c0001t0033g0016a0001c0002t0037g0110a0001c0002t0045g0190others(3): Show | 6 | HG02559.hp2 HG02809.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1951-22574C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207883836 | ||||||
| chr2:207883965
|
G | T | 1 | a0001c0004t0007g0178 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1951-22703C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207883965 | ||||||
| chr2:207884036
|
C | T | 73 | a0001c0001t0001g0013a0001c0001t0001g0033a0001c0001t0001g0042others(70): Show | 73 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.1951-22774G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207884036 | ||||||
| chr2:207884064
|
C | T | 11 | a0001c0001t0004g0120a0001c0001t0005g0088a0001c0001t0005g0124others(8): Show | 11 | HG01168.hp2 HG02258.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1951-22802G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207884064 | ||||||
| chr2:207884097
|
G | A | 1 | a0001c0004t0003g0108 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1951-22835C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207884097 | ||||||
| chr2:207884147
|
C | CA | 6 | a0001c0002t0001g0102a0001c0002t0003g0171a0001c0003t0001g0009others(3): Show | 6 | HG01192.hp2 HG01261.hp2 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.1951-22886dupT | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207884147 | ||||||
| chr2:207884175
|
T | C | 3 | a0001c0002t0001g0126a0001c0004t0039g0036a0001c0004t0042g0035 | 3 | HG02809.hp1 HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1951-22913A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207884175 | ||||||
| chr2:207884207
|
T | G | 49 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0074others(46): Show | 49 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.1951-22945A>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207884207 | ||||||
| chr2:207884283
|
T | C | 39 | a0001c0001t0001g0033a0001c0001t0001g0080a0001c0001t0002g0032others(36): Show | 39 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.1951-23021A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207884283 | ||||||
| chr2:207884439
|
T | C | 8 | a0001c0001t0002g0032a0001c0001t0002g0048a0001c0001t0011g0077others(5): Show | 8 | HG00558.hp1 HG02071.hp2 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.1951-23177A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207884439 | ||||||
| chr2:207884511
|
A | G | 5 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0002t0001g0177others(2): Show | 5 | HG02572.hp1 HG02630.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1951-23249T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207884511 | ||||||
| chr2:207884579
|
A | T | 9 | a0001c0001t0004g0086a0001c0001t0013g0175a0001c0001t0024g0117others(6): Show | 9 | HG01109.hp2 HG01243.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1951-23317T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207884579 | ||||||
| chr2:207884705
|
C | A | 1 | a0001c0002t0001g0102 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1951-23443G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207884705 | ||||||
| chr2:207884812
|
C | T | 8 | a0001c0001t0004g0086a0001c0001t0024g0117a0001c0001t0033g0016others(5): Show | 8 | HG01109.hp2 HG01243.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1951-23550G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207884812 | ||||||
| chr2:207884845
|
C | G | 81 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0042others(78): Show | 81 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.1951-23583G>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207884845 | ||||||
| chr2:207885404
|
T | C | 1 | a0001c0004t0010g0157 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1950+23110A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207885404 | ||||||
| chr2:207885532
|
A | G | 19 | a0001c0001t0005g0088a0001c0001t0021g0121a0001c0001t0051g0123others(16): Show | 19 | HG01168.hp2 HG02258.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.1950+22982T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207885532 | ||||||
| chr2:207885748
|
C | T | 1 | a0001c0002t0041g0164 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1950+22766G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207885748 | ||||||
| chr2:207885910
|
T | C | 1 | a0001c0004t0002g0148 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1950+22604A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207885910 | ||||||
| chr2:207885989
|
A | G | 22 | a0001c0001t0005g0088a0001c0001t0021g0121a0001c0001t0024g0117others(19): Show | 22 | HG01168.hp2 HG01243.hp1 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.1950+22525T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207885989 | ||||||
| chr2:207886025
|
T | C | 133 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.1950+22489A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207886025 | ||||||
| chr2:207886117
|
CA | C | 6 | a0001c0001t0004g0086a0001c0001t0033g0016a0001c0002t0001g0135others(3): Show | 6 | HG01109.hp2 HG01243.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1950+22396delT | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207886117 | ||||||
| chr2:207886215
|
T | A | 1 | a0001c0002t0013g0125 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1950+22299A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207886215 | ||||||
| chr2:207886221
|
C | T | 1 | a0001c0003t0002g0072 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1950+22293G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207886221 | ||||||
| chr2:207886248
|
C | T | 6 | a0001c0002t0001g0134a0001c0002t0006g0193a0001c0002t0006g0194others(3): Show | 6 | HG02145.hp1 HG02486.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1950+22266G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207886248 | ||||||
| chr2:207886472
|
T | C | 6 | a0001c0001t0004g0120a0001c0001t0019g0008a0001c0002t0003g0129others(3): Show | 6 | HG02622.hp1 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1950+22042A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207886472 | ||||||
| chr2:207886675
|
G | A | 1 | a0005c0011t0022g0111 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1950+21839C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207886675 | ||||||
| chr2:207886745
|
T | C | 2 | a0001c0003t0003g0073a0001c0004t0003g0108 | 2 | HG03688.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1950+21769A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207886745 | ||||||
| chr2:207887245
|
T | C | 6 | a0001c0001t0004g0120a0001c0001t0019g0008a0001c0002t0003g0129others(3): Show | 6 | HG02622.hp1 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1950+21269A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207887245 | ||||||
| chr2:207887427
|
A | G | 7 | a0001c0001t0004g0086a0001c0001t0013g0175a0001c0001t0033g0016others(4): Show | 7 | HG01109.hp2 HG01243.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1950+21087T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207887427 | ||||||
| chr2:207887599
|
G | C | 1 | a0001c0002t0038g0182 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1950+20915C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207887599 | ||||||
| chr2:207887699
|
A | G | 139 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(136): Show | 139 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.1950+20815T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207887699 | ||||||
| chr2:207887730
|
T | C | 1 | a0001c0003t0004g0100 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1950+20784A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207887730 | ||||||
| chr2:207887792
|
G | A | 1 | a0001c0001t0001g0045 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1950+20722C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207887792 | ||||||
| chr2:207887807
|
T | A | 1 | a0001c0004t0002g0143 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1950+20707A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207887807 | ||||||
| chr2:207887939
|
C | A | 2 | a0001c0002t0006g0198a0002c0005t0001g0132 | 2 | HG01884.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1950+20575G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207887939 | ||||||
| chr2:207887980
|
GATCTGCA others(10): Show |
G | 1 | a0001c0004t0007g0178 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1950+20517_1950+20 others(23): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207887980 | ||||||
| chr2:207888153
|
T | C | 1 | a0001c0004t0003g0104 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1950+20361A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207888153 | ||||||
| chr2:207888312
|
C | T | 6 | a0001c0001t0004g0086a0001c0001t0033g0016a0001c0002t0001g0135others(3): Show | 6 | HG01109.hp2 HG01243.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1950+20202G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207888312 | ||||||
| chr2:207888354
|
T | TAC | 80 | a0001c0001t0001g0017a0001c0001t0001g0068a0001c0001t0003g0030others(77): Show | 80 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.1950+20158_1950+20 others(8): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207888354 | ||||||
| chr2:207888354
|
T | TACAC | 6 | a0001c0002t0013g0125a0001c0003t0001g0092a0001c0003t0003g0073others(3): Show | 6 | HG01891.hp1 HG02109.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1950+20156_1950+20 others(10): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207888354 | ||||||
| chr2:207888354
|
T | TACACAC | 10 | a0001c0001t0013g0175a0001c0002t0001g0134a0001c0002t0006g0193others(7): Show | 10 | HG02145.hp1 HG02486.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1950+20154_1950+20 others(12): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207888354 | ||||||
| chr2:207888354
|
TAC | T | 53 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0042others(50): Show | 53 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.1950+20158_1950+20 others(8): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207888354 | ||||||
| chr2:207888384
|
T | C | 1 | a0002c0006t0025g0187 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1950+20130A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207888384 | ||||||
| chr2:207888505
|
T | C | 6 | a0001c0001t0004g0086a0001c0001t0033g0016a0001c0002t0001g0135others(3): Show | 6 | HG01109.hp2 HG01243.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1950+20009A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207888505 | ||||||
| chr2:207888542
|
G | A | 3 | a0001c0001t0001g0118a0001c0001t0044g0116a0001c0002t0059g0200 | 3 | HG02647.hp1 HG02895.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1950+19972C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207888542 | ||||||
| chr2:207888543
|
C | T | 47 | a0001c0001t0001g0033a0001c0001t0001g0080a0001c0001t0002g0032others(44): Show | 47 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.1950+19971G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207888543 | ||||||
| chr2:207888545
|
C | T | 2 | a0001c0002t0001g0102a0001c0002t0001g0139 | 2 | HG01074.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.1950+19969G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207888545 | ||||||
| chr2:207888643
|
C | T | 1 | a0001c0003t0001g0091 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1950+19871G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207888643 | ||||||
| chr2:207888687
|
C | G | 9 | a0001c0001t0013g0175a0001c0002t0001g0134a0001c0002t0006g0193others(6): Show | 9 | HG02145.hp1 HG02486.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1950+19827G>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207888687 | ||||||
| chr2:207888848
|
G | A | 1 | a0001c0002t0038g0182 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1950+19666C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207888848 | ||||||
| chr2:207888864
|
G | A | 1 | a0001c0004t0048g0166 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1950+19650C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207888864 | ||||||
| chr2:207889434
|
A | AAC | 23 | a0001c0001t0003g0051a0001c0001t0003g0052a0001c0001t0011g0077others(20): Show | 23 | HG00408.hp2 HG00438.hp1 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.1950+19078_1950+19 others(8): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207889434 | ||||||
| chr2:207889434
|
A | AACAC | 31 | a0001c0001t0001g0033a0001c0001t0003g0053a0001c0002t0002g0140others(28): Show | 31 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.1950+19076_1950+19 others(10): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207889434 | ||||||
| chr2:207889434
|
A | AACACAC | 29 | a0001c0001t0001g0080a0001c0001t0002g0032a0001c0001t0003g0012others(26): Show | 29 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(26): Show |
intron_variant | MODIFIER | c.1950+19074_1950+19 others(12): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207889434 | ||||||
| chr2:207889434
|
A | AACACACA others(1): Show |
12 | a0001c0001t0001g0068a0001c0001t0002g0055a0001c0001t0003g0011others(9): Show | 12 | HG00558.hp2 HG01081.hp1 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.1950+19072_1950+19 others(14): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207889434 | ||||||
| chr2:207889434
|
A | AACACACA others(3): Show |
5 | a0001c0001t0002g0056a0001c0001t0009g0006a0001c0002t0038g0182others(2): Show | 5 | HG01168.hp2 HG02922.hp2 NA18941.hp1 others(2): Show |
intron_variant | MODIFIER | c.1950+19070_1950+19 others(16): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207889434 | ||||||
| chr2:207889434
|
A | AACACACA others(5): Show |
5 | a0001c0001t0002g0039a0001c0002t0001g0102a0001c0002t0054g0149others(2): Show | 5 | HG01192.hp2 HG04204.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.1950+19068_1950+19 others(18): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207889434 | ||||||
| chr2:207889434
|
A | AACACACA others(7): Show |
3 | a0001c0001t0003g0031a0001c0001t0003g0083a0001c0004t0003g0104 | 3 | HG02071.hp1 HG02135.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.1950+19066_1950+19 others(20): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207889434 | ||||||
| chr2:207889434
|
A | AACACACA others(11): Show |
1 | a0001c0001t0003g0030 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1950+19062_1950+19 others(24): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207889434 | ||||||
| chr2:207889434
|
AAC | A | 11 | a0001c0002t0001g0134a0001c0002t0006g0193a0001c0002t0006g0194others(8): Show | 11 | HG00280.hp2 HG00323.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1950+19078_1950+19 others(8): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207889434 | ||||||
| chr2:207889434
|
AACAC | A | 7 | a0001c0002t0045g0190a0001c0003t0009g0001a0001c0004t0001g0127others(4): Show | 7 | HG02572.hp2 HG02630.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1950+19076_1950+19 others(10): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207889434 | ||||||
| chr2:207889434
|
AACACAC | A | 3 | a0001c0001t0013g0175a0001c0002t0003g0184a0001c0002t0006g0196 | 3 | HG01884.hp1 HG02647.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1950+19074_1950+19 others(12): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207889434 | ||||||
| chr2:207889434
|
AACACACA others(3): Show |
A | 1 | a0001c0002t0001g0135 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1950+19070_1950+19 others(16): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207889434 | ||||||
| chr2:207889434
|
AACACACA others(5): Show |
A | 5 | a0001c0001t0004g0086a0001c0001t0033g0016a0001c0003t0001g0091others(2): Show | 5 | HG01109.hp2 HG01243.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1950+19068_1950+19 others(18): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207889434 | ||||||
| chr2:207889434
|
AACACACA others(9): Show |
A | 1 | a0001c0001t0002g0014 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1950+19064_1950+19 others(22): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207889434 | ||||||
| chr2:207889434
|
AACACACA others(11): Show |
A | 7 | a0001c0001t0001g0013a0001c0001t0001g0070a0001c0001t0001g0071others(4): Show | 7 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(4): Show |
intron_variant | MODIFIER | c.1950+19062_1950+19 others(24): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207889434 | ||||||
| chr2:207889434
|
AACACACA others(13): Show |
A | 37 | a0001c0001t0001g0019a0001c0001t0001g0042a0001c0001t0001g0045others(34): Show | 37 | HG00408.hp1 HG00438.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.1950+19060_1950+19 others(26): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207889434 | ||||||
| chr2:207889434
|
AACACACA others(15): Show |
A | 1 | a0001c0001t0027g0041 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1950+19058_1950+19 others(28): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207889434 | ||||||
| chr2:207889834
|
C | T | 1 | a0001c0003t0009g0001 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1950+18680G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207889834 | ||||||
| chr2:207889865
|
T | G | 9 | a0001c0001t0013g0175a0001c0002t0001g0134a0001c0002t0006g0193others(6): Show | 9 | HG02145.hp1 HG02486.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1950+18649A>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207889865 | ||||||
| chr2:207889872
|
C | T | 1 | a0001c0001t0009g0007 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1950+18642G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207889872 | ||||||
| chr2:207889881
|
G | A | 1 | a0001c0001t0024g0117 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1950+18633C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207889881 | ||||||
| chr2:207889960
|
C | T | 2 | a0001c0004t0039g0036a0001c0004t0042g0035 | 2 | HG02809.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1950+18554G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207889960 | ||||||
| chr2:207889998
|
T | A | 1 | a0001c0003t0008g0076 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1950+18516A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207889998 | ||||||
| chr2:207890402
|
T | G | 6 | a0001c0001t0004g0120a0001c0001t0019g0008a0001c0002t0003g0129others(3): Show | 6 | HG02622.hp1 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1950+18112A>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207890402 | ||||||
| chr2:207890497
|
G | A | 3 | a0001c0001t0019g0008a0001c0002t0003g0129a0001c0002t0050g0188 | 3 | HG02622.hp1 HG02809.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1950+18017C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207890497 | ||||||
| chr2:207890497
|
G | T | 6 | a0001c0001t0004g0086a0001c0001t0033g0016a0001c0002t0001g0135others(3): Show | 6 | HG01109.hp2 HG01243.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1950+18017C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207890497 | ||||||
| chr2:207890632
|
T | A | 128 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.1950+17882A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207890632 | ||||||
| chr2:207890976
|
T | C | 1 | a0001c0001t0001g0080 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1950+17538A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207890976 | ||||||
| chr2:207891047
|
T | C | 187 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(184): Show | 187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.1950+17467A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207891047 | ||||||
| chr2:207891111
|
G | A | 2 | a0001c0001t0002g0055a0001c0001t0002g0056 | 2 | NA18954.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.1950+17403C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207891111 | ||||||
| chr2:207891180
|
G | C | 4 | a0001c0001t0001g0019a0001c0001t0001g0061a0001c0001t0001g0063others(1): Show | 4 | HG01168.hp1 HG01515.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1950+17334C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207891180 | ||||||
| chr2:207891207
|
C | T | 1 | a0001c0001t0051g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1950+17307G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207891207 | ||||||
| chr2:207891366
|
C | T | 1 | a0001c0001t0013g0175 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1950+17148G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207891366 | ||||||
| chr2:207891461
|
C | T | 9 | a0001c0001t0013g0175a0001c0002t0001g0134a0001c0002t0006g0193others(6): Show | 9 | HG02145.hp1 HG02486.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1950+17053G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207891461 | ||||||
| chr2:207891623
|
G | A | 1 | a0001c0004t0001g0107 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1950+16891C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207891623 | ||||||
| chr2:207891628
|
C | T | 38 | a0001c0001t0001g0033a0001c0001t0001g0080a0001c0001t0002g0032others(35): Show | 38 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.1950+16886G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207891628 | ||||||
| chr2:207891722
|
T | C | 1 | a0001c0002t0026g0085 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1950+16792A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207891722 | ||||||
| chr2:207891753
|
A | C | 2 | a0001c0001t0027g0041a0001c0001t0034g0047 | 2 | HG02698.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1950+16761T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207891753 | ||||||
| chr2:207891761
|
T | A | 1 | a0001c0002t0013g0125 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1950+16753A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207891761 | ||||||
| chr2:207891908
|
G | A | 46 | a0001c0001t0001g0017a0001c0001t0001g0033a0001c0001t0001g0080others(43): Show | 46 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1950+16606C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207891908 | ||||||
| chr2:207891921
|
G | A | 2 | a0001c0001t0003g0011a0001c0001t0009g0007 | 2 | HG02145.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1950+16593C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207891921 | ||||||
| chr2:207892020
|
C | T | 47 | a0001c0001t0001g0017a0001c0001t0001g0033a0001c0001t0001g0080others(44): Show | 47 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.1950+16494G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207892020 | ||||||
| chr2:207892022
|
C | A | 6 | a0001c0001t0004g0086a0001c0001t0033g0016a0001c0002t0001g0135others(3): Show | 6 | HG01109.hp2 HG01243.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1950+16492G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207892022 | ||||||
| chr2:207892371
|
T | C | 1 | a0001c0002t0003g0184 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1950+16143A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207892371 | ||||||
| chr2:207892640
|
G | A | 2 | a0001c0001t0017g0003a0001c0003t0023g0087 | 2 | HG02109.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1950+15874C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207892640 | ||||||
| chr2:207892686
|
C | T | 1 | a0001c0001t0003g0011 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1950+15828G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207892686 | ||||||
| chr2:207892701
|
G | C | 61 | a0001c0001t0001g0033a0001c0001t0001g0080a0001c0001t0002g0032others(58): Show | 61 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.1950+15813C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207892701 | ||||||
| chr2:207892701
|
G | T | 1 | a0002c0005t0036g0098 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1950+15813C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207892701 | ||||||
| chr2:207893051
|
T | C | 1 | a0001c0001t0016g0005 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1950+15463A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207893051 | ||||||
| chr2:207893100
|
G | A | 1 | a0001c0002t0013g0125 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1950+15414C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207893100 | ||||||
| chr2:207893110
|
C | T | 1 | a0001c0001t0015g0004 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1950+15404G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207893110 | ||||||
| chr2:207893125
|
CA | C | 45 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0042others(42): Show | 45 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(42): Show |
intron_variant | MODIFIER | c.1950+15388delT | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207893125 | ||||||
| chr2:207893134
|
C | G | 126 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(123): Show | 126 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.1950+15380G>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207893134 | ||||||
| chr2:207893338
|
G | A | 1 | a0001c0001t0013g0175 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1950+15176C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207893338 | ||||||
| chr2:207893345
|
C | G | 44 | a0001c0001t0001g0033a0001c0001t0001g0080a0001c0001t0002g0032others(41): Show | 44 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(41): Show |
intron_variant | MODIFIER | c.1950+15169G>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207893345 | ||||||
| chr2:207893390
|
C | G | 45 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0042others(42): Show | 45 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(42): Show |
intron_variant | MODIFIER | c.1950+15124G>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207893390 | ||||||
| chr2:207893455
|
G | A | 1 | a0001c0001t0009g0007 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1950+15059C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207893455 | ||||||
| chr2:207893607
|
C | T | 1 | a0001c0001t0016g0005 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1950+14907G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207893607 | ||||||
| chr2:207893683
|
G | C | 46 | a0001c0001t0001g0033a0001c0001t0001g0080a0001c0001t0002g0032others(43): Show | 46 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1950+14831C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207893683 | ||||||
| chr2:207894091
|
G | A | 1 | a0002c0006t0025g0187 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1950+14423C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207894091 | ||||||
| chr2:207894266
|
C | G | 1 | a0002c0005t0036g0098 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1950+14248G>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207894266 | ||||||
| chr2:207894384
|
C | T | 1 | a0001c0002t0003g0184 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1950+14130G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207894384 | ||||||
| chr2:207894441
|
A | G | 1 | a0001c0002t0013g0125 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1950+14073T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207894441 | ||||||
| chr2:207894641
|
G | C | 57 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(54): Show | 57 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.1950+13873C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207894641 | ||||||
| chr2:207894774
|
C | T | 6 | a0001c0001t0004g0120a0001c0001t0019g0008a0001c0002t0003g0129others(3): Show | 6 | HG02622.hp1 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1950+13740G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207894774 | ||||||
| chr2:207894837
|
G | A | 5 | a0001c0001t0021g0121a0001c0002t0038g0182a0001c0003t0009g0001others(2): Show | 5 | HG01168.hp2 HG02818.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1950+13677C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207894837 | ||||||
| chr2:207894974
|
C | T | 1 | a0001c0003t0002g0066 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1950+13540G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207894974 | ||||||
| chr2:207895157
|
G | T | 3 | a0001c0001t0016g0005a0001c0002t0026g0085a0001c0002t0038g0182 | 3 | HG01168.hp2 HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1950+13357C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207895157 | ||||||
| chr2:207895225
|
T | G | 3 | a0001c0001t0016g0005a0001c0002t0026g0085a0001c0002t0038g0182 | 3 | HG01168.hp2 HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1950+13289A>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207895225 | ||||||
| chr2:207895266
|
C | T | 6 | a0001c0001t0004g0086a0001c0001t0033g0016a0001c0002t0001g0135others(3): Show | 6 | HG01109.hp2 HG01243.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1950+13248G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207895266 | ||||||
| chr2:207895518
|
T | C | 1 | a0001c0004t0007g0178 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1950+12996A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207895518 | ||||||
| chr2:207895646
|
T | C | 3 | a0001c0001t0003g0011a0001c0001t0009g0007a0001c0001t0017g0003 | 3 | HG02109.hp2 HG02145.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1950+12868A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207895646 | ||||||
| chr2:207895825
|
AT | A | 9 | a0001c0001t0013g0175a0001c0002t0001g0134a0001c0002t0006g0193others(6): Show | 9 | HG02145.hp1 HG02486.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1950+12688delA | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207895825 | ||||||
| chr2:207895916
|
T | C | 118 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0033others(115): Show | 118 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.1950+12598A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207895916 | ||||||
| chr2:207896036
|
T | C | 1 | a0001c0001t0004g0086 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1950+12478A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207896036 | ||||||
| chr2:207896207
|
C | T | 121 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0033others(118): Show | 121 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.1950+12307G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207896207 | ||||||
| chr2:207896373
|
GC | G | 96 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0033others(93): Show | 96 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.1950+12140delG | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207896373 | ||||||
| chr2:207896375
|
C | T | 96 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0033others(93): Show | 96 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.1950+12139G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207896375 | ||||||
| chr2:207896378
|
A | G | 96 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0033others(93): Show | 96 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.1950+12136T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207896378 | ||||||
| chr2:207896432
|
A | T | 1 | a0001c0001t0003g0051 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1950+12082T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207896432 | ||||||
| chr2:207896511
|
G | T | 51 | a0001c0001t0001g0033a0001c0001t0001g0080a0001c0001t0002g0032others(48): Show | 51 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.1950+12003C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207896511 | ||||||
| chr2:207896624
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1950+11890G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207896624 | ||||||
| chr2:207896828
|
G | A | 1 | a0002c0006t0035g0097 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1950+11686C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207896828 | ||||||
| chr2:207896938
|
C | T | 5 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0002t0001g0177others(2): Show | 5 | HG02572.hp1 HG02630.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1950+11576G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207896938 | ||||||
| chr2:207897155
|
T | C | 4 | a0001c0003t0009g0001a0001c0003t0014g0099a0001c0004t0014g0130others(1): Show | 4 | HG02258.hp1 HG02572.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1950+11359A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207897155 | ||||||
| chr2:207897401
|
A | G | 6 | a0001c0001t0004g0086a0001c0001t0033g0016a0001c0002t0001g0135others(3): Show | 6 | HG01109.hp2 HG01243.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1950+11113T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207897401 | ||||||
| chr2:207897932
|
T | G | 6 | a0001c0001t0005g0088a0001c0002t0005g0159a0001c0002t0005g0161others(3): Show | 6 | HG02258.hp2 HG02976.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1950+10582A>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207897932 | ||||||
| chr2:207898095
|
T | C | 9 | a0001c0001t0013g0175a0001c0002t0001g0134a0001c0002t0006g0193others(6): Show | 9 | HG02145.hp1 HG02486.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1950+10419A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207898095 | ||||||
| chr2:207898140
|
G | A | 1 | a0001c0002t0041g0164 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1950+10374C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207898140 | ||||||
| chr2:207898154
|
C | T | 1 | a0001c0001t0003g0083 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1950+10360G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207898154 | ||||||
| chr2:207898752
|
G | A | 1 | a0001c0002t0026g0085 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1950+9762C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207898752 | ||||||
| chr2:207898756
|
C | T | 1 | a0001c0001t0016g0005 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1950+9758G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207898756 | ||||||
| chr2:207898757
|
G | T | 2 | a0001c0001t0009g0007a0001c0001t0017g0003 | 2 | HG02109.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1950+9757C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207898757 | ||||||
| chr2:207898765
|
G | A | 2 | a0001c0003t0003g0073a0001c0004t0003g0108 | 2 | HG03688.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1950+9749C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207898765 | ||||||
| chr2:207898786
|
C | T | 3 | a0001c0001t0011g0077a0001c0001t0011g0078a0001c0001t0011g0079 | 3 | NA18968.hp1 NA18972.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1950+9728G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207898786 | ||||||
| chr2:207898947
|
G | A | 1 | a0001c0002t0003g0184 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1950+9567C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207898947 | ||||||
| chr2:207899010
|
T | C | 9 | a0001c0001t0003g0011a0001c0001t0004g0086a0001c0001t0009g0007others(6): Show | 9 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1950+9504A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207899010 | ||||||
| chr2:207899127
|
C | T | 9 | a0001c0002t0001g0134a0001c0002t0006g0193a0001c0002t0006g0194others(6): Show | 9 | HG02145.hp1 HG02486.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1950+9387G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207899127 | ||||||
| chr2:207899166
|
C | T | 1 | a0001c0002t0003g0184 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1950+9348G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207899166 | ||||||
| chr2:207899282
|
T | C | 9 | a0001c0001t0013g0175a0001c0002t0001g0134a0001c0002t0006g0193others(6): Show | 9 | HG02145.hp1 HG02486.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1950+9232A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207899282 | ||||||
| chr2:207899302
|
G | A | 1 | a0001c0004t0002g0131 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1950+9212C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207899302 | ||||||
| chr2:207899310
|
C | T | 1 | a0001c0001t0033g0016 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1950+9204G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207899310 | ||||||
| chr2:207899384
|
G | A | 1 | a0001c0002t0001g0168 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1950+9130C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207899384 | ||||||
| chr2:207899400
|
C | A | 1 | a0001c0003t0002g0023 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1950+9114G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207899400 | ||||||
| chr2:207899557
|
T | C | 2 | a0001c0003t0009g0001a0001c0015t0003g0093 | 2 | HG02896.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1950+8957A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207899557 | ||||||
| chr2:207900338
|
T | C | 1 | a0001c0002t0003g0184 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1950+8176A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207900338 | ||||||
| chr2:207900391
|
T | C | 6 | a0001c0001t0004g0120a0001c0001t0019g0008a0001c0002t0003g0129others(3): Show | 6 | HG02622.hp1 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1950+8123A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207900391 | ||||||
| chr2:207900449
|
G | C | 1 | a0001c0002t0001g0177 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1950+8065C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207900449 | ||||||
| chr2:207900462
|
G | T | 1 | a0001c0004t0048g0166 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1950+8052C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207900462 | ||||||
| chr2:207900779
|
C | A | 1 | a0001c0001t0013g0175 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1950+7735G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207900779 | ||||||
| chr2:207900846
|
C | T | 10 | a0001c0001t0003g0011a0001c0001t0004g0086a0001c0001t0009g0007others(7): Show | 10 | HG01109.hp2 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1950+7668G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207900846 | ||||||
| chr2:207900974
|
T | C | 44 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0042others(41): Show | 44 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(41): Show |
intron_variant | MODIFIER | c.1950+7540A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207900974 | ||||||
| chr2:207901292
|
G | T | 1 | a0001c0001t0001g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1950+7222C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207901292 | ||||||
| chr2:207901324
|
T | C | 6 | a0001c0001t0004g0120a0001c0001t0019g0008a0001c0002t0003g0129others(3): Show | 6 | HG02622.hp1 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1950+7190A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207901324 | ||||||
| chr2:207901664
|
A | G | 1 | a0001c0002t0037g0110 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1950+6850T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207901664 | ||||||
| chr2:207901812
|
G | A | 2 | a0001c0001t0001g0017a0001c0002t0003g0184 | 2 | HG01884.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1950+6702C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207901812 | ||||||
| chr2:207901826
|
T | C | 1 | a0001c0001t0009g0007 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1950+6688A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207901826 | ||||||
| chr2:207902241
|
C | T | 37 | a0001c0001t0001g0033a0001c0001t0001g0080a0001c0001t0002g0032others(34): Show | 37 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.1950+6273G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207902241 | ||||||
| chr2:207902261
|
T | C | 45 | a0001c0001t0001g0033a0001c0001t0001g0080a0001c0001t0002g0032others(42): Show | 45 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.1950+6253A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207902261 | ||||||
| chr2:207902275
|
T | C | 2 | a0001c0004t0039g0036a0001c0004t0042g0035 | 2 | HG02809.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1950+6239A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207902275 | ||||||
| chr2:207902682
|
C | T | 1 | a0001c0002t0001g0154 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1950+5832G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207902682 | ||||||
| chr2:207902811
|
C | CCCAT | 9 | a0001c0001t0003g0011a0001c0001t0004g0086a0001c0001t0009g0007others(6): Show | 9 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1950+5699_1950+570 others(8): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207902811 | ||||||
| chr2:207902827
|
C | T | 2 | a0001c0003t0009g0001a0001c0015t0003g0093 | 2 | HG02896.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1950+5687G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207902827 | ||||||
| chr2:207902831
|
TCCAC | T | 15 | a0001c0001t0001g0017a0001c0001t0013g0175a0001c0001t0024g0117others(12): Show | 15 | HG01884.hp1 HG02145.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.1950+5679_1950+568 others(8): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207902831 | ||||||
| chr2:207902851
|
C | T | 15 | a0001c0001t0001g0017a0001c0001t0013g0175a0001c0001t0024g0117others(12): Show | 15 | HG01884.hp1 HG02145.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.1950+5663G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207902851 | ||||||
| chr2:207902855
|
C | CCCACCCA others(5): Show |
1 | a0001c0001t0051g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1950+5658_1950+565 others(16): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207902855 | ||||||
| chr2:207902855
|
C | CCCATCCA others(5): Show |
103 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0033others(100): Show | 103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.1950+5647_1950+565 others(16): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207902855 | ||||||
| chr2:207902855
|
C | CCCATCCA others(9): Show |
6 | a0001c0001t0004g0120a0001c0001t0019g0008a0001c0002t0003g0129others(3): Show | 6 | HG02622.hp1 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1950+5658_1950+565 others(20): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207902855 | ||||||
| chr2:207902855
|
C | T | 15 | a0001c0001t0001g0017a0001c0001t0013g0175a0001c0001t0024g0117others(12): Show | 15 | HG01884.hp1 HG02145.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.1950+5659G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207902855 | ||||||
| chr2:207902921
|
G | A | 2 | a0001c0002t0001g0105a0001c0002t0001g0106 | 2 | HG01346.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.1950+5593C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207902921 | ||||||
| chr2:207903015
|
CTT | C | 3 | a0001c0001t0004g0086a0001c0001t0033g0016a0003c0014t0043g0084 | 3 | HG02257.hp1 HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1950+5497_1950+549 others(6): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207903015 | ||||||
| chr2:207903210
|
A | G | 1 | a0001c0004t0002g0151 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1950+5304T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207903210 | ||||||
| chr2:207903299
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1950+5215C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207903299 | ||||||
| chr2:207903643
|
G | T | 44 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0042others(41): Show | 44 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(41): Show |
intron_variant | MODIFIER | c.1950+4871C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207903643 | ||||||
| chr2:207903771
|
C | T | 1 | a0002c0005t0036g0098 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1950+4743G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207903771 | ||||||
| chr2:207903816
|
G | A | 4 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0060others(1): Show | 4 | HG00323.hp1 HG01069.hp1 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.1950+4698C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207903816 | ||||||
| chr2:207903860
|
C | T | 7 | a0001c0001t0001g0017a0001c0001t0004g0120a0001c0001t0019g0008others(4): Show | 7 | HG02615.hp1 HG02622.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1950+4654G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207903860 | ||||||
| chr2:207904087
|
G | A | 2 | a0001c0001t0021g0121a0001c0002t0038g0182 | 2 | HG01168.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1950+4427C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207904087 | ||||||
| chr2:207904173
|
T | C | 1 | a0001c0002t0013g0125 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1950+4341A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207904173 | ||||||
| chr2:207904233
|
A | G | 1 | a0001c0001t0016g0005 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1950+4281T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207904233 | ||||||
| chr2:207904391
|
C | T | 1 | a0001c0002t0003g0184 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1950+4123G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207904391 | ||||||
| chr2:207904619
|
G | A | 14 | a0001c0001t0001g0017a0001c0001t0004g0086a0001c0001t0009g0007others(11): Show | 14 | HG01109.hp2 HG01884.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1950+3895C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207904619 | ||||||
| chr2:207904836
|
T | C | 2 | a0001c0001t0001g0017a0001c0002t0003g0184 | 2 | HG01884.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1950+3678A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207904836 | ||||||
| chr2:207904891
|
A | G | 1 | a0001c0004t0002g0131 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1950+3623T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207904891 | ||||||
| chr2:207905070
|
A | G | 6 | a0001c0001t0004g0120a0001c0001t0019g0008a0001c0002t0003g0129others(3): Show | 6 | HG02622.hp1 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1950+3444T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207905070 | ||||||
| chr2:207905524
|
C | T | 1 | a0001c0002t0003g0184 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1950+2990G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207905524 | ||||||
| chr2:207905660
|
G | A | 1 | a0001c0001t0003g0064 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1950+2854C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207905660 | ||||||
| chr2:207905877
|
G | C | 1 | a0001c0004t0002g0163 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1950+2637C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207905877 | ||||||
| chr2:207905897
|
G | C | 3 | a0001c0004t0001g0152a0001c0004t0001g0153a0001c0004t0002g0112 | 3 | HG04115.hp2 HG04184.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1950+2617C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207905897 | ||||||
| chr2:207906084
|
G | A | 1 | a0001c0004t0002g0112 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1950+2430C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207906084 | ||||||
| chr2:207906134
|
C | T | 124 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(121): Show | 124 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.1950+2380G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207906134 | ||||||
| chr2:207906266
|
T | C | 9 | a0001c0001t0013g0175a0001c0002t0001g0134a0001c0002t0006g0193others(6): Show | 9 | HG02145.hp1 HG02486.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1950+2248A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207906266 | ||||||
| chr2:207906286
|
T | A | 1 | a0001c0002t0037g0110 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1950+2228A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207906286 | ||||||
| chr2:207906287
|
T | A | 1 | a0001c0002t0037g0110 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1950+2227A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207906287 | ||||||
| chr2:207906448
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1950+2066C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207906448 | ||||||
| chr2:207906475
|
C | T | 4 | a0001c0001t0001g0118a0001c0001t0020g0115a0001c0001t0044g0116others(1): Show | 4 | HG02257.hp2 HG02647.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1950+2039G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207906475 | ||||||
| chr2:207906515
|
G | A | 1 | a0001c0004t0010g0150 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1950+1999C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207906515 | ||||||
| chr2:207906541
|
C | T | 9 | a0001c0001t0013g0175a0001c0002t0001g0134a0001c0002t0006g0193others(6): Show | 9 | HG02145.hp1 HG02486.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1950+1973G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207906541 | ||||||
| chr2:207906564
|
G | A | 5 | a0001c0001t0016g0005a0001c0001t0024g0117a0001c0008t0053g0173others(2): Show | 5 | HG03098.hp2 HG03486.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.1950+1950C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207906564 | ||||||
| chr2:207906617
|
C | T | 1 | a0001c0004t0001g0185 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1950+1897G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207906617 | ||||||
| chr2:207906627
|
A | G | 1 | a0001c0001t0001g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1950+1887T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207906627 | ||||||
| chr2:207906661
|
T | C | 1 | a0001c0002t0026g0085 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1950+1853A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207906661 | ||||||
| chr2:207906784
|
C | CAAAT | 10 | a0001c0001t0001g0017a0001c0001t0004g0086a0001c0001t0009g0007others(7): Show | 10 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1950+1726_1950+172 others(8): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207906784 | ||||||
| chr2:207906987
|
C | T | 1 | a0001c0002t0037g0110 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1950+1527G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207906987 | ||||||
| chr2:207907045
|
T | C | 1 | a0001c0001t0013g0175 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1950+1469A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207907045 | ||||||
| chr2:207907240
|
G | A | 1 | a0001c0002t0003g0184 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1950+1274C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207907240 | ||||||
| chr2:207907394
|
C | T | 2 | a0001c0001t0001g0017a0001c0002t0037g0110 | 2 | HG02615.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1950+1120G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207907394 | ||||||
| chr2:207907448
|
G | A | 1 | a0001c0001t0013g0175 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1950+1066C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207907448 | ||||||
| chr2:207907480
|
C | T | 1 | a0001c0003t0012g0176 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1950+1034G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207907480 | ||||||
| chr2:207907528
|
A | C | 1 | a0001c0004t0003g0147 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1950+986T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207907528 | ||||||
| chr2:207907965
|
T | C | 1 | a0001c0002t0003g0184 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1950+549A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207907965 | ||||||
| chr2:207908015
|
A | G | 8 | a0001c0001t0005g0088a0001c0001t0051g0123a0001c0002t0005g0159others(5): Show | 8 | HG02258.hp2 HG02976.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.1950+499T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207908015 | ||||||
| chr2:207908124
|
C | T | 6 | a0001c0001t0004g0120a0001c0001t0019g0008a0001c0002t0003g0129others(3): Show | 6 | HG02622.hp1 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1950+390G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207908124 | ||||||
| chr2:207908189
|
T | C | 1 | a0001c0002t0026g0085 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1950+325A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207908189 | ||||||
| chr2:207908275
|
G | A | 5 | a0001c0001t0016g0005a0001c0001t0024g0117a0001c0008t0053g0173others(2): Show | 5 | HG03098.hp2 HG03486.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.1950+239C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207908275 | ||||||
| chr2:207908312
|
G | C | 1 | a0001c0001t0001g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1950+202C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 6/7 | chr2 | 207908312 | ||||||
| chr2:207908654
|
T | C | 1 | a0001c0002t0037g0110 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1887-77A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207908654 | ||||||
| chr2:207908730
|
C | T | 10 | a0001c0001t0004g0086a0001c0001t0009g0007a0001c0001t0017g0003others(7): Show | 10 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1887-153G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207908730 | ||||||
| chr2:207908757
|
C | T | 1 | a0001c0002t0003g0184 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1887-180G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207908757 | ||||||
| chr2:207908803
|
G | A | 1 | a0001c0002t0058g0197 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1887-226C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207908803 | ||||||
| chr2:207908828
|
C | A | 44 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0042others(41): Show | 44 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(41): Show |
intron_variant | MODIFIER | c.1887-251G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207908828 | ||||||
| chr2:207909108
|
A | G | 2 | a0001c0001t0009g0007a0001c0001t0017g0003 | 2 | HG02109.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1887-531T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207909108 | ||||||
| chr2:207909136
|
C | T | 124 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(121): Show | 124 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.1887-559G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207909136 | ||||||
| chr2:207909159
|
C | T | 1 | a0001c0001t0002g0039 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1887-582G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207909159 | ||||||
| chr2:207909161
|
G | A | 5 | a0001c0001t0016g0005a0001c0001t0024g0117a0001c0008t0053g0173others(2): Show | 5 | HG03098.hp2 HG03486.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.1887-584C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207909161 | ||||||
| chr2:207909183
|
A | G | 2 | a0001c0001t0001g0074a0007c0007t0002g0057 | 2 | HG01071.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.1887-606T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207909183 | ||||||
| chr2:207909302
|
A | G | 10 | a0001c0001t0013g0175a0001c0002t0001g0134a0001c0002t0006g0193others(7): Show | 10 | HG02145.hp1 HG02486.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1887-725T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207909302 | ||||||
| chr2:207909593
|
G | A | 1 | a0001c0002t0013g0125 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1887-1016C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207909593 | ||||||
| chr2:207909621
|
C | A | 124 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(121): Show | 124 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.1887-1044G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207909621 | ||||||
| chr2:207909709
|
A | G | 1 | a0001c0001t0016g0005 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1887-1132T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207909709 | ||||||
| chr2:207910050
|
G | A | 1 | a0001c0004t0003g0147 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1887-1473C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207910050 | ||||||
| chr2:207910214
|
C | G | 1 | a0001c0002t0003g0103 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1887-1637G>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207910214 | ||||||
| chr2:207910217
|
C | A | 88 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0033others(85): Show | 88 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.1887-1640G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207910217 | ||||||
| chr2:207910237
|
G | A | 1 | a0001c0001t0005g0088 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1887-1660C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207910237 | ||||||
| chr2:207910422
|
C | T | 1 | a0001c0002t0003g0184 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1887-1845G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207910422 | ||||||
| chr2:207910666
|
T | A | 1 | a0002c0006t0025g0187 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1887-2089A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207910666 | ||||||
| chr2:207910709
|
C | T | 3 | a0001c0003t0014g0099a0001c0004t0003g0128a0001c0004t0014g0130 | 3 | HG02258.hp1 HG02572.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1887-2132G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207910709 | ||||||
| chr2:207911029
|
C | T | 2 | a0001c0001t0002g0055a0001c0001t0002g0056 | 2 | NA18954.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.1887-2452G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207911029 | ||||||
| chr2:207911067
|
C | G | 1 | a0001c0003t0008g0027 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1887-2490G>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207911067 | ||||||
| chr2:207911113
|
T | A | 1 | a0001c0001t0001g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1887-2536A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207911113 | ||||||
| chr2:207911132
|
A | G | 126 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(123): Show | 126 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.1887-2555T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207911132 | ||||||
| chr2:207911186
|
G | A | 1 | a0001c0002t0038g0182 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1887-2609C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207911186 | ||||||
| chr2:207911210
|
G | A | 9 | a0001c0001t0003g0011a0001c0001t0004g0120a0001c0001t0019g0008others(6): Show | 9 | HG01168.hp2 HG02622.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1887-2633C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207911210 | ||||||
| chr2:207911457
|
T | C | 1 | a0005c0011t0022g0111 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1887-2880A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207911457 | ||||||
| chr2:207911507
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1887-2930G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207911507 | ||||||
| chr2:207911755
|
G | C | 5 | a0001c0001t0016g0005a0001c0001t0024g0117a0001c0008t0053g0173others(2): Show | 5 | HG03098.hp2 HG03486.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.1887-3178C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207911755 | ||||||
| chr2:207911947
|
G | A | 1 | a0001c0003t0003g0174 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1887-3370C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207911947 | ||||||
| chr2:207912054
|
T | G | 1 | a0001c0003t0001g0025 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1887-3477A>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207912054 | ||||||
| chr2:207912085
|
C | T | 89 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0033others(86): Show | 89 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.1887-3508G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207912085 | ||||||
| chr2:207912251
|
T | C | 1 | a0001c0001t0016g0005 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1887-3674A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207912251 | ||||||
| chr2:207912613
|
G | A | 7 | a0001c0001t0004g0086a0001c0001t0009g0007a0001c0001t0017g0003others(4): Show | 7 | HG01109.hp2 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1887-4036C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207912613 | ||||||
| chr2:207912638
|
A | G | 44 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0042others(41): Show | 44 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(41): Show |
intron_variant | MODIFIER | c.1887-4061T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207912638 | ||||||
| chr2:207912643
|
A | G | 89 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0033others(86): Show | 89 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.1887-4066T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207912643 | ||||||
| chr2:207912837
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1887-4260G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207912837 | ||||||
| chr2:207912976
|
T | A | 1 | a0001c0002t0002g0170 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1887-4399A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207912976 | ||||||
| chr2:207913080
|
G | T | 1 | a0001c0001t0003g0011 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1887-4503C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207913080 | ||||||
| chr2:207913135
|
G | A | 1 | a0001c0004t0001g0179 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1887-4558C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207913135 | ||||||
| chr2:207913137
|
A | G | 1 | a0001c0001t0001g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1887-4560T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207913137 | ||||||
| chr2:207913186
|
C | T | 2 | a0001c0001t0001g0074a0007c0007t0002g0057 | 2 | HG01071.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.1887-4609G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207913186 | ||||||
| chr2:207913435
|
G | T | 5 | a0001c0001t0016g0005a0001c0001t0024g0117a0001c0008t0053g0173others(2): Show | 5 | HG03098.hp2 HG03486.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.1887-4858C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207913435 | ||||||
| chr2:207913457
|
A | G | 1 | a0001c0002t0006g0199 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1887-4880T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207913457 | ||||||
| chr2:207913613
|
G | A | 3 | a0001c0001t0024g0117a0001c0008t0053g0173a0005c0011t0022g0111 | 3 | HG03098.hp2 HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1887-5036C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207913613 | ||||||
| chr2:207913682
|
A | G | 1 | a0001c0002t0003g0184 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1887-5105T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207913682 | ||||||
| chr2:207913723
|
AT | A | 44 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0042others(41): Show | 44 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(41): Show |
intron_variant | MODIFIER | c.1887-5147delA | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207913723 | ||||||
| chr2:207913743
|
A | G | 5 | a0001c0001t0016g0005a0001c0001t0024g0117a0001c0008t0053g0173others(2): Show | 5 | HG03098.hp2 HG03486.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.1887-5166T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207913743 | ||||||
| chr2:207913856
|
A | C | 1 | a0001c0002t0037g0110 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1887-5279T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207913856 | ||||||
| chr2:207913874
|
C | T | 4 | a0001c0001t0024g0117a0001c0008t0053g0173a0002c0005t0036g0098others(1): Show | 4 | HG03098.hp2 HG03486.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1887-5297G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207913874 | ||||||
| chr2:207913932
|
AAC | A | 114 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.1887-5357_1887-535 others(6): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207913932 | ||||||
| chr2:207913934
|
C | A | 4 | a0001c0003t0012g0090a0001c0003t0012g0176a0001c0003t0056g0192others(1): Show | 4 | HG01891.hp1 HG02486.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1887-5357G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207913934 | ||||||
| chr2:207913963
|
G | A | 5 | a0001c0001t0016g0005a0001c0001t0024g0117a0001c0008t0053g0173others(2): Show | 5 | HG03098.hp2 HG03486.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.1887-5386C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207913963 | ||||||
| chr2:207914079
|
G | A | 35 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0042others(32): Show | 35 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(32): Show |
intron_variant | MODIFIER | c.1887-5502C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207914079 | ||||||
| chr2:207914131
|
T | C | 9 | a0001c0001t0013g0175a0001c0002t0001g0134a0001c0002t0006g0193others(6): Show | 9 | HG02145.hp1 HG02486.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1887-5554A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207914131 | ||||||
| chr2:207914224
|
C | T | 8 | a0001c0002t0001g0134a0001c0002t0006g0193a0001c0002t0006g0194others(5): Show | 8 | HG02145.hp1 HG02486.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1887-5647G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207914224 | ||||||
| chr2:207914266
|
C | T | 1 | a0001c0001t0004g0086 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1887-5689G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207914266 | ||||||
| chr2:207914411
|
T | C | 3 | a0001c0001t0003g0051a0001c0001t0003g0052a0001c0001t0003g0053 | 3 | HG01515.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1887-5834A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207914411 | ||||||
| chr2:207914493
|
C | T | 2 | a0001c0001t0009g0007a0001c0001t0017g0003 | 2 | HG02109.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1887-5916G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207914493 | ||||||
| chr2:207914498
|
C | CA | 16 | a0001c0001t0004g0086a0001c0001t0005g0088a0001c0001t0009g0007others(13): Show | 16 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1887-5922dupT | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207914498 | ||||||
| chr2:207914509
|
A | C | 2 | a0001c0002t0003g0184a0001c0002t0013g0125 | 2 | HG01884.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1887-5932T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207914509 | ||||||
| chr2:207914681
|
CA | C | 53 | a0001c0001t0001g0017a0001c0001t0003g0011a0001c0001t0004g0086others(50): Show | 53 | HG01109.hp2 HG01168.hp2 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.1887-6105delT | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207914681 | ||||||
| chr2:207914681
|
CAA | C | 44 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0042others(41): Show | 44 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(41): Show |
intron_variant | MODIFIER | c.1887-6106_1887-610 others(6): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207914681 | ||||||
| chr2:207914687
|
A | G | 6 | a0001c0001t0004g0120a0001c0001t0019g0008a0001c0002t0003g0129others(3): Show | 6 | HG02622.hp1 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1887-6110T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207914687 | ||||||
| chr2:207914698
|
A | G | 2 | a0001c0003t0009g0001a0001c0015t0003g0093 | 2 | HG02896.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1887-6121T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207914698 | ||||||
| chr2:207914882
|
T | G | 1 | a0001c0001t0016g0005 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1887-6305A>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207914882 | ||||||
| chr2:207914947
|
C | T | 1 | a0001c0004t0002g0131 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1887-6370G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207914947 | ||||||
| chr2:207915050
|
G | C | 2 | a0001c0003t0008g0050a0001c0003t0008g0076 | 2 | HG01346.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.1887-6473C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207915050 | ||||||
| chr2:207915073
|
C | T | 3 | a0001c0001t0021g0121a0001c0002t0026g0085a0001c0002t0038g0182 | 3 | HG01168.hp2 HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1887-6496G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207915073 | ||||||
| chr2:207915210
|
T | C | 1 | a0001c0002t0003g0103 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1887-6633A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207915210 | ||||||
| chr2:207915696
|
C | A | 5 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0002t0001g0177others(2): Show | 5 | HG02572.hp1 HG02630.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1887-7119G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207915696 | ||||||
| chr2:207915726
|
T | G | 5 | a0001c0001t0016g0005a0001c0001t0024g0117a0001c0008t0053g0173others(2): Show | 5 | HG03098.hp2 HG03486.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.1887-7149A>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207915726 | ||||||
| chr2:207916160
|
G | C | 1 | a0001c0002t0003g0184 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1887-7583C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207916160 | ||||||
| chr2:207916300
|
A | G | 6 | a0001c0001t0004g0120a0001c0001t0019g0008a0001c0002t0003g0129others(3): Show | 6 | HG02622.hp1 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1887-7723T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207916300 | ||||||
| chr2:207916391
|
C | T | 1 | a0004c0012t0003g0095 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1887-7814G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207916391 | ||||||
| chr2:207916704
|
C | A | 1 | a0001c0001t0003g0011 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1887-8127G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207916704 | ||||||
| chr2:207916773
|
T | C | 2 | a0001c0003t0002g0072a0001c0004t0002g0138 | 2 | HG01928.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.1887-8196A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207916773 | ||||||
| chr2:207916946
|
A | T | 9 | a0001c0001t0013g0175a0001c0002t0001g0134a0001c0002t0006g0193others(6): Show | 9 | HG02145.hp1 HG02486.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1887-8369T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207916946 | ||||||
| chr2:207917206
|
T | C | 1 | a0001c0004t0001g0185 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1887-8629A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207917206 | ||||||
| chr2:207917324
|
G | C | 2 | a0001c0002t0003g0184a0001c0002t0013g0125 | 2 | HG01884.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1887-8747C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207917324 | ||||||
| chr2:207917530
|
G | A | 2 | a0001c0003t0056g0192a0001c0003t0057g0191 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1887-8953C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207917530 | ||||||
| chr2:207917662
|
T | C | 1 | a0001c0004t0002g0151 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1887-9085A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207917662 | ||||||
| chr2:207917855
|
G | T | 6 | a0001c0001t0004g0086a0001c0001t0033g0016a0001c0002t0001g0135others(3): Show | 6 | HG01109.hp2 HG01243.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1887-9278C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207917855 | ||||||
| chr2:207917894
|
G | T | 125 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(122): Show | 125 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.1887-9317C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207917894 | ||||||
| chr2:207917905
|
T | G | 1 | a0001c0001t0003g0031 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1887-9328A>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207917905 | ||||||
| chr2:207918116
|
T | G | 9 | a0001c0001t0013g0175a0001c0002t0001g0134a0001c0002t0006g0193others(6): Show | 9 | HG02145.hp1 HG02486.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1887-9539A>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207918116 | ||||||
| chr2:207918195
|
A | G | 1 | a0001c0001t0013g0175 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1887-9618T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207918195 | ||||||
| chr2:207918244
|
C | T | 35 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0042others(32): Show | 35 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(32): Show |
intron_variant | MODIFIER | c.1887-9667G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207918244 | ||||||
| chr2:207918304
|
C | T | 1 | a0001c0001t0032g0049 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1887-9727G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207918304 | ||||||
| chr2:207918323
|
C | T | 10 | a0001c0001t0004g0086a0001c0001t0009g0007a0001c0001t0017g0003others(7): Show | 10 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1887-9746G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207918323 | ||||||
| chr2:207918350
|
G | A | 9 | a0001c0001t0003g0011a0001c0001t0004g0120a0001c0001t0019g0008others(6): Show | 9 | HG01168.hp2 HG02622.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1887-9773C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207918350 | ||||||
| chr2:207918436
|
G | C | 1 | a0001c0001t0009g0006 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1887-9859C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207918436 | ||||||
| chr2:207918521
|
C | CAACA | 8 | a0001c0002t0001g0134a0001c0002t0006g0193a0001c0002t0006g0194others(5): Show | 8 | HG02145.hp1 HG02486.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1887-9948_1887-994 others(8): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207918521 | ||||||
| chr2:207918521
|
CAACAAAC others(16): Show |
C | 8 | a0001c0001t0005g0088a0001c0001t0016g0005a0001c0001t0051g0123others(5): Show | 8 | HG02258.hp2 HG02976.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.1887-9967_1887-994 others(27): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207918521 | ||||||
| chr2:207918543
|
A | C | 1 | a0001c0004t0002g0143 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1887-9966T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207918543 | ||||||
| chr2:207918544
|
A | C | 1 | a0001c0001t0013g0175 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1887-9967T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207918544 | ||||||
| chr2:207918547
|
C | A | 1 | a0001c0001t0013g0175 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1887-9970G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207918547 | ||||||
| chr2:207918641
|
A | C | 2 | a0001c0002t0003g0184a0001c0002t0038g0182 | 2 | HG01168.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.1887-10064T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207918641 | ||||||
| chr2:207918715
|
G | A | 1 | a0001c0001t0027g0041 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1887-10138C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207918715 | ||||||
| chr2:207918779
|
C | T | 6 | a0001c0001t0004g0120a0001c0001t0019g0008a0001c0002t0003g0129others(3): Show | 6 | HG02622.hp1 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1887-10202G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207918779 | ||||||
| chr2:207918895
|
A | T | 8 | a0001c0002t0001g0134a0001c0002t0006g0193a0001c0002t0006g0194others(5): Show | 8 | HG02145.hp1 HG02486.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1887-10318T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207918895 | ||||||
| chr2:207918946
|
A | C | 7 | a0001c0001t0004g0120a0001c0001t0013g0175a0001c0001t0019g0008others(4): Show | 7 | HG02622.hp1 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1887-10369T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207918946 | ||||||
| chr2:207918948
|
A | C | 1 | a0001c0002t0026g0085 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1887-10371T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207918948 | ||||||
| chr2:207919270
|
C | G | 1 | a0001c0002t0013g0125 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1887-10693G>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207919270 | ||||||
| chr2:207919712
|
A | C | 5 | a0001c0003t0001g0091a0001c0003t0012g0090a0001c0003t0012g0176others(2): Show | 5 | HG01243.hp1 HG01891.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1887-11135T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207919712 | ||||||
| chr2:207919953
|
G | GAC | 18 | a0001c0001t0001g0068a0001c0001t0005g0088a0001c0001t0016g0005others(15): Show | 18 | HG01081.hp2 HG01884.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.1886+10971_1886+10 others(8): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207919953 | ||||||
| chr2:207919977
|
C | T | 1 | a0001c0001t0003g0011 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1886+10949G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207919977 | ||||||
| chr2:207920124
|
T | A | 1 | a0001c0002t0001g0126 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1886+10802A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207920124 | ||||||
| chr2:207920146
|
T | C | 1 | a0001c0002t0001g0177 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1886+10780A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207920146 | ||||||
| chr2:207920176
|
C | G | 15 | a0001c0001t0005g0088a0001c0001t0016g0005a0001c0001t0024g0117others(12): Show | 15 | HG02258.hp1 HG02258.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.1886+10750G>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207920176 | ||||||
| chr2:207920540
|
A | C | 1 | a0008c0013t0002g0109 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1886+10386T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207920540 | ||||||
| chr2:207920579
|
GA | G | 123 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(120): Show | 123 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.1886+10346delT | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207920579 | ||||||
| chr2:207920653
|
A | AT | 32 | a0001c0001t0001g0033a0001c0001t0002g0039a0001c0001t0002g0055others(29): Show | 32 | HG00099.hp2 HG00423.hp2 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.1886+10272dupA | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207920653 | ||||||
| chr2:207920653
|
AT | A | 9 | a0001c0001t0004g0120a0001c0001t0019g0008a0001c0001t0021g0121others(6): Show | 9 | HG01168.hp2 HG02622.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1886+10272delA | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207920653 | ||||||
| chr2:207920896
|
G | C | 10 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0004g0086others(7): Show | 10 | HG01109.hp2 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1886+10030C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207920896 | ||||||
| chr2:207921020
|
C | G | 2 | a0001c0001t0013g0175a0001c0002t0026g0085 | 2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1886+9906G>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207921020 | ||||||
| chr2:207921127
|
C | T | 1 | a0001c0002t0013g0125 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1886+9799G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207921127 | ||||||
| chr2:207921172
|
T | C | 59 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(56): Show | 59 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.1886+9754A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207921172 | ||||||
| chr2:207921179
|
G | A | 7 | a0001c0001t0005g0088a0001c0001t0016g0005a0001c0002t0005g0159others(4): Show | 7 | HG02258.hp2 HG02976.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1886+9747C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207921179 | ||||||
| chr2:207921230
|
G | A | 10 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0004g0086others(7): Show | 10 | HG01109.hp2 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1886+9696C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207921230 | ||||||
| chr2:207921342
|
T | C | 128 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(125): Show | 128 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.1886+9584A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207921342 | ||||||
| chr2:207921656
|
C | G | 1 | a0001c0002t0026g0085 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1886+9270G>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207921656 | ||||||
| chr2:207921841
|
A | T | 1 | a0001c0002t0001g0177 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1886+9085T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207921841 | ||||||
| chr2:207921883
|
C | T | 1 | a0001c0001t0013g0175 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1886+9043G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207921883 | ||||||
| chr2:207922076
|
T | G | 2 | a0001c0001t0003g0011a0001c0001t0021g0121 | 2 | HG02818.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1886+8850A>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207922076 | ||||||
| chr2:207922583
|
C | T | 1 | a0001c0002t0026g0085 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1886+8343G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207922583 | ||||||
| chr2:207922811
|
CA | C | 15 | a0001c0001t0005g0088a0001c0001t0016g0005a0001c0001t0024g0117others(12): Show | 15 | HG01069.hp2 HG02258.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1886+8114delT | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207922811 | ||||||
| chr2:207922826
|
A | G | 1 | a0001c0001t0013g0175 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1886+8100T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207922826 | ||||||
| chr2:207922963
|
T | A | 2 | a0001c0003t0004g0100a0001c0003t0014g0099 | 2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1886+7963A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207922963 | ||||||
| chr2:207923516
|
A | C | 1 | a0001c0003t0023g0087 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1886+7410T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923516 | ||||||
| chr2:207923561
|
G | A | 1 | a0001c0001t0003g0011 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1886+7365C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923561 | ||||||
| chr2:207923568
|
T | C | 1 | a0001c0001t0003g0011 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1886+7358A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923568 | ||||||
| chr2:207923594
|
C | T | 2 | a0001c0001t0002g0055a0001c0001t0002g0056 | 2 | NA18954.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.1886+7332G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923594 | ||||||
| chr2:207923619
|
C | T | 1 | a0001c0002t0013g0125 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1886+7307G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923619 | ||||||
| chr2:207923827
|
A | G | 1 | a0001c0001t0003g0034 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1886+7099T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923827 | ||||||
| chr2:207923855
|
G | A | 3 | a0001c0003t0001g0091a0001c0003t0012g0090a0001c0003t0012g0176 | 3 | HG01243.hp1 HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1886+7071C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923855 | ||||||
| chr2:207923855
|
G | GCA | 25 | a0001c0002t0001g0177a0001c0002t0052g0160a0001c0003t0001g0025others(22): Show | 25 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(22): Show |
intron_variant | MODIFIER | c.1886+7069_1886+707 others(6): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923855 | ||||||
| chr2:207923855
|
G | GCACA | 20 | a0001c0001t0003g0064a0001c0003t0001g0009a0001c0003t0001g0092others(17): Show | 20 | HG00408.hp2 HG00438.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1886+7067_1886+707 others(8): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923855 | ||||||
| chr2:207923855
|
G | GCACACA | 18 | a0001c0001t0001g0033a0001c0001t0001g0080a0001c0001t0002g0032others(15): Show | 18 | HG00558.hp1 HG01109.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.1886+7065_1886+707 others(10): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923855 | ||||||
| chr2:207923855
|
G | GCACACAC others(3): Show |
1 | a0005c0011t0022g0111 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1886+7061_1886+707 others(14): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923855 | ||||||
| chr2:207923855
|
G | GCACACAC others(9): Show |
1 | a0001c0002t0001g0134 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1886+7055_1886+707 others(20): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923855 | ||||||
| chr2:207923855
|
G | GCACACAC others(11): Show |
1 | a0001c0008t0053g0173 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1886+7053_1886+707 others(22): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923855 | ||||||
| chr2:207923855
|
G | GCACACAC others(13): Show |
1 | a0001c0001t0024g0117 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1886+7051_1886+707 others(24): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923855 | ||||||
| chr2:207923855
|
G | GCACACAC others(17): Show |
1 | a0001c0001t0003g0011 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1886+7047_1886+707 others(28): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923855 | ||||||
| chr2:207923855
|
GCACA | G | 2 | a0001c0002t0003g0184a0001c0002t0037g0110 | 2 | HG01884.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1886+7067_1886+707 others(8): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923855 | ||||||
| chr2:207923857
|
A | G | 2 | a0001c0001t0003g0012a0001c0001t0003g0020 | 2 | HG00099.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1886+7069T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923857 | ||||||
| chr2:207923876
|
CACACAT | C | 5 | a0001c0003t0002g0066a0001c0003t0008g0026a0001c0003t0008g0027others(2): Show | 5 | HG00280.hp2 HG00639.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.1886+7044_1886+704 others(10): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923876 | ||||||
| chr2:207923878
|
C | T | 7 | a0001c0002t0003g0184a0001c0002t0006g0193a0001c0002t0006g0194others(4): Show | 7 | HG01884.hp1 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1886+7048G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923878 | ||||||
| chr2:207923880
|
C | CACACACA others(13): Show |
2 | a0001c0003t0004g0100a0001c0003t0014g0099 | 2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1886+7045_1886+704 others(24): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923880 | ||||||
| chr2:207923880
|
C | CACACACA others(9): Show |
1 | a0001c0004t0014g0130 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1886+7045_1886+704 others(20): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923880 | ||||||
| chr2:207923880
|
C | CACACACA others(15): Show |
1 | a0002c0005t0001g0132 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1886+7045_1886+704 others(26): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923880 | ||||||
| chr2:207923880
|
C | CACACACA others(17): Show |
1 | a0001c0001t0002g0069 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1886+7045_1886+704 others(28): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923880 | ||||||
| chr2:207923880
|
C | CACACACA others(5): Show |
3 | a0001c0001t0003g0058a0001c0001t0003g0062a0001c0002t0002g0170 | 3 | HG00408.hp1 HG00621.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.1886+7045_1886+704 others(16): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923880 | ||||||
| chr2:207923880
|
C | CACACACA others(7): Show |
3 | a0001c0001t0003g0030a0001c0002t0001g0168a0001c0002t0001g0169 | 3 | HG01928.hp1 HG02135.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.1886+7045_1886+704 others(18): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923880 | ||||||
| chr2:207923880
|
C | CACACACA others(9): Show |
4 | a0001c0001t0002g0048a0001c0001t0003g0031a0001c0001t0034g0047others(1): Show | 4 | HG02056.hp1 HG02071.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.1886+7045_1886+704 others(20): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923880 | ||||||
| chr2:207923880
|
C | CACACACA others(11): Show |
2 | a0001c0001t0001g0070a0001c0002t0001g0141 | 2 | HG00438.hp2 HG00642.hp1 |
intron_variant | MODIFIER | c.1886+7045_1886+704 others(22): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923880 | ||||||
| chr2:207923880
|
C | CACACACA others(15): Show |
1 | a0001c0001t0003g0034 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1886+7045_1886+704 others(26): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923880 | ||||||
| chr2:207923880
|
C | CACACACA others(19): Show |
1 | a0001c0001t0001g0061 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1886+7045_1886+704 others(30): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923880 | ||||||
| chr2:207923880
|
C | CACACACA others(21): Show |
1 | a0001c0001t0020g0115 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1886+7045_1886+704 others(32): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923880 | ||||||
| chr2:207923880
|
C | CACACACA others(23): Show |
1 | a0001c0001t0001g0074 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1886+7045_1886+704 others(34): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923880 | ||||||
| chr2:207923880
|
C | CACACACA others(3): Show |
1 | a0001c0001t0001g0046 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1886+7045_1886+704 others(14): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923880 | ||||||
| chr2:207923880
|
C | CACACACA others(7): Show |
2 | a0001c0001t0015g0004a0001c0001t0027g0041 | 2 | HG03130.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1886+7045_1886+704 others(18): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923880 | ||||||
| chr2:207923880
|
C | CACACACA others(9): Show |
4 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0060others(1): Show | 4 | HG00323.hp1 HG01243.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.1886+7045_1886+704 others(20): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923880 | ||||||
| chr2:207923880
|
C | CACACACA others(11): Show |
2 | a0001c0001t0049g0075a0001c0002t0041g0164 | 2 | HG00639.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1886+7045_1886+704 others(22): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923880 | ||||||
| chr2:207923880
|
C | CACACACA others(13): Show |
2 | a0001c0001t0001g0013a0001c0001t0001g0019 | 2 | HG01515.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.1886+7045_1886+704 others(24): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923880 | ||||||
| chr2:207923880
|
C | CACACACA others(15): Show |
4 | a0001c0001t0001g0063a0001c0001t0047g0059a0001c0002t0001g0144others(1): Show | 4 | HG00280.hp1 HG01168.hp1 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.1886+7045_1886+704 others(26): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923880 | ||||||
| chr2:207923880
|
C | CACACACA others(17): Show |
1 | a0001c0002t0059g0200 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1886+7045_1886+704 others(28): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923880 | ||||||
| chr2:207923880
|
C | CACACACA others(19): Show |
1 | a0001c0001t0001g0068 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1886+7045_1886+704 others(30): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923880 | ||||||
| chr2:207923880
|
C | CACACACA others(21): Show |
1 | a0001c0002t0001g0139 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1886+7045_1886+704 others(32): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923880 | ||||||
| chr2:207923880
|
C | CACACACA others(27): Show |
1 | a0001c0001t0001g0118 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1886+7045_1886+704 others(38): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923880 | ||||||
| chr2:207923880
|
C | CACACAT | 2 | a0001c0002t0038g0182a0001c0004t0002g0131 | 2 | HG01168.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.1886+7045_1886+704 others(10): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923880 | ||||||
| chr2:207923880
|
C | CACACATA others(1): Show |
3 | a0001c0004t0030g0167a0001c0004t0039g0036a0001c0004t0042g0035 | 3 | HG02809.hp1 HG03139.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.1886+7045_1886+704 others(12): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923880 | ||||||
| chr2:207923880
|
C | CACACATA others(3): Show |
1 | a0001c0002t0001g0154 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1886+7045_1886+704 others(14): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923880 | ||||||
| chr2:207923880
|
C | CACACATA others(5): Show |
1 | a0001c0001t0018g0002 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1886+7045_1886+704 others(16): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923880 | ||||||
| chr2:207923880
|
C | CACACATA others(7): Show |
2 | a0001c0001t0001g0017a0001c0001t0005g0124 | 2 | HG02615.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1886+7045_1886+704 others(18): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923880 | ||||||
| chr2:207923880
|
C | CACACATA others(11): Show |
1 | a0001c0001t0044g0116 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1886+7045_1886+704 others(22): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923880 | ||||||
| chr2:207923880
|
C | CACAT | 3 | a0001c0001t0005g0088a0001c0001t0016g0005a0001c0002t0005g0161 | 3 | HG02258.hp2 HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1886+7045_1886+704 others(8): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923880 | ||||||
| chr2:207923880
|
C | CACATATA others(7): Show |
1 | a0007c0007t0002g0057 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1886+7045_1886+704 others(18): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923880 | ||||||
| chr2:207923880
|
C | CAT | 2 | a0001c0001t0003g0119a0001c0002t0005g0159 | 2 | NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1886+7044_1886+704 others(6): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923880 | ||||||
| chr2:207923880
|
C | T | 8 | a0001c0002t0003g0184a0001c0002t0006g0193a0001c0002t0006g0194others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1886+7046G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923880 | ||||||
| chr2:207923880
|
CATAT | C | 3 | a0001c0003t0001g0091a0001c0003t0012g0090a0001c0003t0012g0176 | 3 | HG01243.hp1 HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1886+7042_1886+704 others(8): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923880 | ||||||
| chr2:207923882
|
T | C | 76 | a0001c0001t0003g0012a0001c0001t0003g0020a0001c0001t0003g0064others(73): Show | 76 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.1886+7044A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923882 | ||||||
| chr2:207923884
|
T | C | 34 | a0001c0001t0003g0012a0001c0001t0003g0020a0001c0001t0003g0083others(31): Show | 34 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(31): Show |
intron_variant | MODIFIER | c.1886+7042A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923884 | ||||||
| chr2:207923886
|
T | C | 19 | a0001c0001t0003g0012a0001c0001t0003g0020a0001c0001t0003g0083others(16): Show | 19 | HG00099.hp2 HG00423.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.1886+7040A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923886 | ||||||
| chr2:207923888
|
T | C | 1 | a0008c0013t0002g0109 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1886+7038A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923888 | ||||||
| chr2:207923897
|
A | T | 1 | a0001c0002t0003g0184 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1886+7029T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923897 | ||||||
| chr2:207923899
|
A | T | 14 | a0001c0001t0001g0080a0001c0001t0002g0039a0001c0001t0002g0055others(11): Show | 14 | HG01109.hp1 HG01192.hp2 HG01515.hp1 others(11): Show |
intron_variant | MODIFIER | c.1886+7027T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923899 | ||||||
| chr2:207923901
|
A | T | 23 | a0001c0001t0001g0033a0001c0001t0001g0080a0001c0001t0002g0039others(20): Show | 23 | HG01081.hp1 HG01109.hp1 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.1886+7025T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923901 | ||||||
| chr2:207923901
|
ATATATTT others(1): Show |
A | 7 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0004g0086others(4): Show | 7 | HG01109.hp2 HG02559.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1886+7017_1886+702 others(12): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923901 | ||||||
| chr2:207923902
|
TA | T | 3 | a0001c0002t0037g0110a0001c0008t0053g0173a0005c0011t0022g0111 | 3 | HG03098.hp1 HG03098.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1886+7023delT | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923902 | ||||||
| chr2:207923903
|
A | ATTTTT | 4 | a0001c0001t0011g0077a0001c0001t0021g0121a0001c0002t0002g0140others(1): Show | 4 | HG02818.hp2 NA18951.hp2 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.1886+7022_1886+702 others(9): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923903 | ||||||
| chr2:207923903
|
A | ATTTTTTT | 5 | a0001c0001t0003g0012a0001c0001t0003g0020a0001c0002t0003g0137others(2): Show | 5 | HG00099.hp2 HG01261.hp2 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.1886+7022_1886+702 others(11): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923903 | ||||||
| chr2:207923903
|
A | T | 39 | a0001c0001t0001g0033a0001c0001t0001g0080a0001c0001t0002g0032others(36): Show | 39 | HG00558.hp1 HG00642.hp2 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.1886+7023T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923903 | ||||||
| chr2:207923904
|
TA | T | 2 | a0001c0001t0024g0117a0001c0002t0001g0134 | 2 | HG03486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1886+7021delT | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923904 | ||||||
| chr2:207923905
|
A | ATTT | 11 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0002g0048others(8): Show | 11 | HG00323.hp1 HG00621.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.1886+7018_1886+702 others(7): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923905 | ||||||
| chr2:207923905
|
A | T | 84 | a0001c0001t0001g0013a0001c0001t0001g0033a0001c0001t0001g0042others(81): Show | 84 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.1886+7021T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923905 | ||||||
| chr2:207923906
|
T | TA | 5 | a0001c0002t0001g0126a0001c0002t0006g0198a0001c0003t0003g0174others(2): Show | 5 | HG01884.hp2 HG02886.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1886+7019_1886+702 others(5): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923906 | ||||||
| chr2:207923906
|
T | TATA | 3 | a0001c0001t0009g0007a0001c0002t0005g0183a0001c0004t0001g0127 | 3 | HG02145.hp2 HG02630.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1886+7019_1886+702 others(7): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923906 | ||||||
| chr2:207923906
|
T | TATATATA others(12): Show |
1 | a0001c0001t0013g0175 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1886+7019_1886+702 others(23): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923906 | ||||||
| chr2:207923907
|
T | A | 30 | a0001c0001t0001g0068a0001c0001t0001g0118a0001c0001t0003g0119others(27): Show | 30 | HG01081.hp2 HG01346.hp1 HG01952.hp2 others(27): Show |
intron_variant | MODIFIER | c.1886+7019A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923907 | ||||||
| chr2:207923908
|
T | A | 5 | a0001c0002t0005g0162a0001c0002t0005g0183a0001c0002t0006g0198others(2): Show | 5 | HG01884.hp2 HG02630.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1886+7018A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923908 | ||||||
| chr2:207923909
|
T | A | 6 | a0001c0001t0001g0118a0001c0001t0003g0119a0001c0001t0016g0005others(3): Show | 6 | HG01952.hp2 HG02647.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1886+7017A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923909 | ||||||
| chr2:207923911
|
T | A | 2 | a0001c0001t0001g0118a0001c0001t0016g0005 | 2 | HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1886+7015A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923911 | ||||||
| chr2:207923936
|
T | C | 1 | a0001c0004t0002g0158 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1886+6990A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207923936 | ||||||
| chr2:207924025
|
C | A | 3 | a0001c0001t0002g0032a0001c0002t0002g0140a0001c0002t0003g0137 | 3 | HG00558.hp1 NA18951.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1886+6901G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207924025 | ||||||
| chr2:207924028
|
T | C | 125 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(122): Show | 125 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.1886+6898A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207924028 | ||||||
| chr2:207924149
|
C | G | 1 | a0001c0003t0002g0072 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1886+6777G>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207924149 | ||||||
| chr2:207924196
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1886+6730G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207924196 | ||||||
| chr2:207924264
|
C | T | 5 | a0001c0001t0004g0120a0001c0001t0019g0008a0001c0002t0003g0129others(2): Show | 5 | HG02622.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1886+6662G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207924264 | ||||||
| chr2:207924265
|
G | C | 1 | a0002c0006t0025g0187 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1886+6661C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207924265 | ||||||
| chr2:207924270
|
T | C | 14 | a0001c0001t0005g0088a0001c0001t0016g0005a0001c0001t0024g0117others(11): Show | 14 | HG02258.hp1 HG02258.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.1886+6656A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207924270 | ||||||
| chr2:207924323
|
G | A | 5 | a0001c0001t0003g0119a0001c0001t0009g0007a0001c0001t0017g0003others(2): Show | 5 | HG02109.hp2 HG02145.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1886+6603C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207924323 | ||||||
| chr2:207924511
|
C | T | 1 | a0001c0002t0003g0184 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1886+6415G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207924511 | ||||||
| chr2:207924583
|
G | C | 8 | a0001c0002t0006g0193a0001c0002t0006g0194a0001c0002t0006g0195others(5): Show | 8 | HG02145.hp1 HG02486.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1886+6343C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207924583 | ||||||
| chr2:207924824
|
C | T | 1 | a0001c0003t0023g0087 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1886+6102G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207924824 | ||||||
| chr2:207924992
|
C | T | 1 | a0001c0001t0013g0175 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1886+5934G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207924992 | ||||||
| chr2:207925116
|
T | G | 7 | a0001c0001t0005g0088a0001c0001t0016g0005a0001c0002t0005g0159others(4): Show | 7 | HG02258.hp2 HG02976.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1886+5810A>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207925116 | ||||||
| chr2:207925117
|
A | C | 3 | a0001c0003t0004g0100a0001c0003t0014g0099a0001c0004t0014g0130 | 3 | HG02258.hp1 HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1886+5809T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207925117 | ||||||
| chr2:207925118
|
G | A | 1 | a0001c0001t0003g0020 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1886+5808C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207925118 | ||||||
| chr2:207925139
|
TG | T | 2 | a0001c0001t0001g0042a0001c0001t0001g0060 | 2 | HG01243.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1886+5786delC | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207925139 | ||||||
| chr2:207925146
|
TG | T | 43 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(40): Show | 43 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.1886+5779delC | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207925146 | ||||||
| chr2:207925147
|
G | T | 14 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0060others(11): Show | 14 | HG00323.hp1 HG01069.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1886+5779C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207925147 | ||||||
| chr2:207925371
|
A | AGGCTCAT others(34): Show |
1 | a0001c0001t0013g0175 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1886+5514_1886+555 others(45): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207925371 | ||||||
| chr2:207925437
|
T | C | 1 | a0002c0006t0025g0187 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1886+5489A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207925437 | ||||||
| chr2:207925542
|
G | A | 3 | a0001c0004t0007g0178a0001c0004t0007g0180a0001c0004t0007g0181 | 3 | NA18968.hp2 NA19005.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1886+5384C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207925542 | ||||||
| chr2:207925547
|
G | A | 1 | a0005c0011t0022g0111 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1886+5379C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207925547 | ||||||
| chr2:207925769
|
C | T | 8 | a0001c0002t0006g0193a0001c0002t0006g0194a0001c0002t0006g0195others(5): Show | 8 | HG02145.hp1 HG02486.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1886+5157G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207925769 | ||||||
| chr2:207925876
|
G | A | 124 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(121): Show | 124 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.1886+5050C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207925876 | ||||||
| chr2:207925935
|
T | C | 1 | a0001c0001t0034g0047 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1886+4991A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207925935 | ||||||
| chr2:207926028
|
G | A | 1 | a0001c0001t0001g0045 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1886+4898C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207926028 | ||||||
| chr2:207926054
|
T | C | 7 | a0001c0001t0024g0117a0001c0002t0001g0134a0001c0003t0004g0100others(4): Show | 7 | HG02258.hp1 HG02572.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1886+4872A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207926054 | ||||||
| chr2:207926120
|
T | C | 1 | a0001c0001t0016g0005 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1886+4806A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207926120 | ||||||
| chr2:207926233
|
A | G | 14 | a0001c0001t0005g0088a0001c0001t0016g0005a0001c0001t0024g0117others(11): Show | 14 | HG02258.hp1 HG02258.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.1886+4693T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207926233 | ||||||
| chr2:207926264
|
T | C | 2 | a0001c0001t0001g0068a0001c0002t0001g0177 | 2 | HG01081.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1886+4662A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207926264 | ||||||
| chr2:207926901
|
C | G | 5 | a0001c0001t0001g0013a0001c0001t0001g0070a0001c0001t0003g0034others(2): Show | 5 | HG00280.hp1 HG00642.hp1 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1886+4025G>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207926901 | ||||||
| chr2:207927077
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1886+3849C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207927077 | ||||||
| chr2:207927101
|
T | C | 7 | a0001c0002t0006g0193a0001c0002t0006g0194a0001c0002t0006g0195others(4): Show | 7 | HG02145.hp1 HG02486.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1886+3825A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207927101 | ||||||
| chr2:207927439
|
C | G | 2 | a0001c0003t0003g0073a0001c0004t0003g0108 | 2 | HG03688.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1886+3487G>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207927439 | ||||||
| chr2:207927494
|
C | T | 1 | a0001c0002t0006g0198 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1886+3432G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207927494 | ||||||
| chr2:207927515
|
C | CA | 19 | a0001c0001t0005g0088a0001c0001t0016g0005a0001c0001t0024g0117others(16): Show | 19 | HG00423.hp2 HG01256.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.1886+3410dupT | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207927515 | ||||||
| chr2:207927515
|
CA | C | 58 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0042others(55): Show | 58 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.1886+3410delT | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207927515 | ||||||
| chr2:207927590
|
G | A | 1 | a0008c0013t0002g0109 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1886+3336C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207927590 | ||||||
| chr2:207927640
|
G | A | 3 | a0001c0002t0045g0190a0001c0003t0003g0174a0001c0003t0004g0172 | 3 | HG02630.hp2 HG02922.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1886+3286C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207927640 | ||||||
| chr2:207927743
|
T | C | 1 | a0001c0001t0011g0078 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1886+3183A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207927743 | ||||||
| chr2:207927785
|
G | A | 5 | a0001c0001t0003g0119a0001c0001t0009g0007a0001c0001t0017g0003others(2): Show | 5 | HG02109.hp2 HG02145.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1886+3141C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207927785 | ||||||
| chr2:207927845
|
T | C | 1 | a0001c0001t0001g0070 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1886+3081A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207927845 | ||||||
| chr2:207927895
|
T | G | 14 | a0001c0001t0005g0088a0001c0001t0016g0005a0001c0001t0024g0117others(11): Show | 14 | HG02258.hp1 HG02258.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.1886+3031A>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207927895 | ||||||
| chr2:207928006
|
T | A | 1 | a0001c0001t0003g0011 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1886+2920A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207928006 | ||||||
| chr2:207928007
|
A | T | 1 | a0001c0002t0026g0085 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1886+2919T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207928007 | ||||||
| chr2:207928012
|
A | C | 58 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(55): Show | 58 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.1886+2914T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207928012 | ||||||
| chr2:207928020
|
T | G | 125 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(122): Show | 125 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.1886+2906A>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207928020 | ||||||
| chr2:207928022
|
A | C | 125 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(122): Show | 125 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.1886+2904T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207928022 | ||||||
| chr2:207928083
|
C | T | 2 | a0001c0003t0002g0037a0001c0003t0002g0038 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1886+2843G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207928083 | ||||||
| chr2:207928142
|
T | G | 2 | a0001c0001t0001g0068a0001c0002t0003g0184 | 2 | HG01081.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.1886+2784A>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207928142 | ||||||
| chr2:207928178
|
A | G | 32 | a0001c0001t0001g0033a0001c0001t0001g0080a0001c0001t0002g0032others(29): Show | 32 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.1886+2748T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207928178 | ||||||
| chr2:207928216
|
T | C | 1 | a0001c0001t0017g0003 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1886+2710A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207928216 | ||||||
| chr2:207928497
|
A | C | 5 | a0001c0001t0003g0011a0001c0001t0013g0175a0001c0002t0045g0190others(2): Show | 5 | HG02630.hp2 HG02922.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1886+2429T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207928497 | ||||||
| chr2:207928609
|
G | T | 122 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(119): Show | 122 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.1886+2317C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207928609 | ||||||
| chr2:207928809
|
G | A | 1 | a0001c0002t0045g0190 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1886+2117C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207928809 | ||||||
| chr2:207929020
|
G | A | 3 | a0001c0001t0003g0011a0001c0001t0013g0175a0001c0002t0045g0190 | 3 | HG02922.hp1 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1886+1906C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207929020 | ||||||
| chr2:207929229
|
C | T | 5 | a0001c0003t0001g0091a0001c0003t0012g0090a0001c0003t0012g0176others(2): Show | 5 | HG01243.hp1 HG01891.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1886+1697G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207929229 | ||||||
| chr2:207929342
|
T | C | 1 | a0001c0001t0003g0020 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1886+1584A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207929342 | ||||||
| chr2:207929496
|
T | C | 3 | a0001c0001t0002g0032a0001c0002t0002g0140a0001c0002t0003g0137 | 3 | HG00558.hp1 NA18951.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1886+1430A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207929496 | ||||||
| chr2:207929513
|
A | G | 1 | a0001c0002t0037g0110 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1886+1413T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207929513 | ||||||
| chr2:207929777
|
C | T | 2 | a0001c0001t0009g0007a0001c0001t0017g0003 | 2 | HG02109.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1886+1149G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207929777 | ||||||
| chr2:207929898
|
T | A | 2 | a0001c0001t0001g0068a0001c0002t0003g0184 | 2 | HG01081.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.1886+1028A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207929898 | ||||||
| chr2:207930322
|
C | G | 1 | a0001c0002t0006g0195 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1886+604G>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207930322 | ||||||
| chr2:207930350
|
G | C | 1 | a0001c0003t0012g0176 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1886+576C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207930350 | ||||||
| chr2:207930361
|
C | T | 7 | a0001c0001t0004g0120a0001c0001t0019g0008a0001c0001t0021g0121others(4): Show | 7 | HG01168.hp2 HG02622.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1886+565G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207930361 | ||||||
| chr2:207930572
|
G | A | 2 | a0001c0003t0008g0026a0001c0003t0008g0027 | 2 | HG00280.hp2 HG00639.hp2 |
intron_variant | MODIFIER | c.1886+354C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207930572 | ||||||
| chr2:207930573
|
G | A | 1 | a0005c0011t0022g0111 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1886+353C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207930573 | ||||||
| chr2:207930607
|
A | G | 44 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(41): Show | 44 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(41): Show |
intron_variant | MODIFIER | c.1886+319T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207930607 | ||||||
| chr2:207930630
|
C | T | 1 | a0001c0004t0039g0036 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1886+296G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207930630 | ||||||
| chr2:207930640
|
T | C | 1 | a0001c0004t0002g0112 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1886+286A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207930640 | ||||||
| chr2:207930736
|
C | A | 1 | a0001c0003t0009g0001 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1886+190G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207930736 | ||||||
| chr2:207930743
|
G | T | 1 | a0001c0002t0001g0169 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1886+183C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207930743 | ||||||
| chr2:207930744
|
G | T | 1 | a0001c0002t0001g0169 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1886+182C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 5/7 | chr2 | 207930744 | ||||||
| chr2:207931354
|
C | T | 121 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(118): Show | 121 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1693-235G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207931354 | ||||||
| chr2:207931394
|
C | T | 1 | a0001c0002t0038g0182 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1693-275G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207931394 | ||||||
| chr2:207931738
|
T | G | 1 | a0001c0002t0037g0110 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1693-619A>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207931738 | ||||||
| chr2:207931811
|
A | G | 2 | a0001c0003t0003g0067a0001c0004t0010g0145 | 2 | NA18747.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.1693-692T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207931811 | ||||||
| chr2:207931847
|
C | T | 8 | a0001c0003t0004g0100a0001c0003t0009g0001a0001c0003t0014g0099others(5): Show | 8 | HG02258.hp1 HG02572.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1693-728G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207931847 | ||||||
| chr2:207932181
|
T | C | 121 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(118): Show | 121 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1693-1062A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207932181 | ||||||
| chr2:207932271
|
CAAT | C | 2 | a0001c0001t0002g0055a0001c0001t0002g0056 | 2 | NA18954.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.1693-1155_1693-115 others(7): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207932271 | ||||||
| chr2:207932512
|
GA | G | 11 | a0001c0001t0005g0088a0001c0001t0016g0005a0001c0001t0024g0117others(8): Show | 11 | HG02258.hp2 HG02976.hp2 HG03041.hp2 others(8): Show |
intron_variant | MODIFIER | c.1693-1394delT | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207932512 | ||||||
| chr2:207932913
|
C | T | 11 | a0001c0001t0005g0088a0001c0001t0016g0005a0001c0001t0024g0117others(8): Show | 11 | HG02258.hp2 HG02976.hp2 HG03041.hp2 others(8): Show |
intron_variant | MODIFIER | c.1693-1794G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207932913 | ||||||
| chr2:207932917
|
C | T | 1 | a0001c0002t0002g0140 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1693-1798G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207932917 | ||||||
| chr2:207933084
|
T | C | 1 | a0001c0002t0045g0190 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1693-1965A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207933084 | ||||||
| chr2:207933123
|
T | C | 2 | a0001c0001t0001g0068a0001c0002t0003g0184 | 2 | HG01081.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.1693-2004A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207933123 | ||||||
| chr2:207933226
|
G | A | 11 | a0001c0001t0005g0088a0001c0001t0016g0005a0001c0001t0024g0117others(8): Show | 11 | HG02258.hp2 HG02976.hp2 HG03041.hp2 others(8): Show |
intron_variant | MODIFIER | c.1693-2107C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207933226 | ||||||
| chr2:207933229
|
T | C | 1 | a0005c0011t0022g0111 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1693-2110A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207933229 | ||||||
| chr2:207933230
|
C | A | 14 | a0001c0001t0003g0011a0001c0001t0005g0088a0001c0001t0013g0175others(11): Show | 14 | HG02258.hp2 HG02922.hp1 HG02976.hp2 others(11): Show |
intron_variant | MODIFIER | c.1693-2111G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207933230 | ||||||
| chr2:207933284
|
T | C | 11 | a0001c0001t0005g0088a0001c0001t0016g0005a0001c0001t0024g0117others(8): Show | 11 | HG02258.hp2 HG02976.hp2 HG03041.hp2 others(8): Show |
intron_variant | MODIFIER | c.1693-2165A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207933284 | ||||||
| chr2:207933394
|
T | C | 32 | a0001c0001t0001g0033a0001c0001t0001g0080a0001c0001t0002g0032others(29): Show | 32 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.1693-2275A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207933394 | ||||||
| chr2:207933471
|
G | A | 23 | a0001c0001t0001g0068a0001c0001t0003g0011a0001c0001t0005g0088others(20): Show | 23 | HG01081.hp2 HG01884.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.1693-2352C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207933471 | ||||||
| chr2:207933591
|
G | A | 11 | a0001c0001t0005g0088a0001c0001t0016g0005a0001c0001t0024g0117others(8): Show | 11 | HG02258.hp2 HG02976.hp2 HG03041.hp2 others(8): Show |
intron_variant | MODIFIER | c.1693-2472C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207933591 | ||||||
| chr2:207934108
|
G | T | 32 | a0001c0001t0001g0033a0001c0001t0001g0080a0001c0001t0002g0032others(29): Show | 32 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.1693-2989C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207934108 | ||||||
| chr2:207934287
|
G | A | 1 | a0001c0002t0026g0085 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1693-3168C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207934287 | ||||||
| chr2:207934722
|
C | T | 14 | a0001c0001t0003g0011a0001c0001t0005g0088a0001c0001t0013g0175others(11): Show | 14 | HG02258.hp2 HG02922.hp1 HG02976.hp2 others(11): Show |
intron_variant | MODIFIER | c.1693-3603G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207934722 | ||||||
| chr2:207934869
|
C | T | 4 | a0001c0001t0024g0117a0001c0002t0001g0134a0001c0008t0053g0173others(1): Show | 4 | HG03098.hp2 HG03486.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1693-3750G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207934869 | ||||||
| chr2:207935161
|
C | CA | 4 | a0001c0003t0001g0022a0001c0003t0002g0018a0001c0003t0002g0021others(1): Show | 4 | HG01069.hp2 HG01071.hp2 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.1693-4043dupT | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207935161 | ||||||
| chr2:207935328
|
G | A | 1 | a0001c0002t0037g0110 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1693-4209C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207935328 | ||||||
| chr2:207935391
|
C | T | 1 | a0001c0001t0003g0011 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1693-4272G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207935391 | ||||||
| chr2:207935418
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1693-4299G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207935418 | ||||||
| chr2:207935419
|
G | A | 3 | a0001c0001t0003g0011a0001c0001t0013g0175a0001c0002t0045g0190 | 3 | HG02922.hp1 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1693-4300C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207935419 | ||||||
| chr2:207935755
|
A | G | 3 | a0001c0004t0001g0185a0001c0004t0040g0186a0002c0006t0035g0097 | 3 | HG02109.hp1 HG02622.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1693-4636T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207935755 | ||||||
| chr2:207935858
|
T | C | 22 | a0001c0001t0003g0011a0001c0001t0005g0088a0001c0001t0013g0175others(19): Show | 22 | HG01884.hp1 HG02145.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.1693-4739A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207935858 | ||||||
| chr2:207936263
|
C | A | 11 | a0001c0001t0005g0088a0001c0001t0016g0005a0001c0001t0024g0117others(8): Show | 11 | HG02258.hp2 HG02976.hp2 HG03041.hp2 others(8): Show |
intron_variant | MODIFIER | c.1693-5144G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207936263 | ||||||
| chr2:207936545
|
T | C | 14 | a0001c0001t0003g0011a0001c0001t0005g0088a0001c0001t0013g0175others(11): Show | 14 | HG02258.hp2 HG02922.hp1 HG02976.hp2 others(11): Show |
intron_variant | MODIFIER | c.1693-5426A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207936545 | ||||||
| chr2:207936846
|
A | AGT | 25 | a0001c0001t0001g0045a0001c0001t0015g0004a0001c0001t0018g0002others(22): Show | 25 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.1693-5729_1693-572 others(6): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207936846 | ||||||
| chr2:207936846
|
A | AGTGT | 5 | a0001c0002t0001g0177a0001c0002t0006g0198a0001c0002t0037g0110others(2): Show | 5 | HG01884.hp2 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1693-5731_1693-572 others(8): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207936846 | ||||||
| chr2:207936846
|
A | AGTGTGTG others(3): Show |
1 | a0001c0002t0045g0190 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1693-5737_1693-572 others(14): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207936846 | ||||||
| chr2:207936846
|
AGT | A | 25 | a0001c0001t0001g0017a0001c0001t0001g0061a0001c0001t0001g0063others(22): Show | 25 | HG00408.hp1 HG01109.hp2 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1693-5729_1693-572 others(6): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207936846 | ||||||
| chr2:207936846
|
AGTGT | A | 38 | a0001c0001t0001g0033a0001c0001t0001g0080a0001c0001t0002g0032others(35): Show | 38 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.1693-5731_1693-572 others(8): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207936846 | ||||||
| chr2:207936846
|
AGTGTGT | A | 2 | a0001c0002t0054g0149a0004c0012t0003g0095 | 2 | NA18956.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1693-5733_1693-572 others(10): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207936846 | ||||||
| chr2:207936846
|
AGTGTGTG others(3): Show |
A | 1 | a0001c0001t0013g0175 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1693-5737_1693-572 others(14): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207936846 | ||||||
| chr2:207936846
|
AGTGTGTG others(5): Show |
A | 1 | a0001c0002t0003g0184 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1693-5739_1693-572 others(16): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207936846 | ||||||
| chr2:207937074
|
G | T | 1 | a0001c0004t0002g0158 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1693-5955C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207937074 | ||||||
| chr2:207937131
|
C | T | 8 | a0001c0001t0004g0120a0001c0001t0019g0008a0001c0001t0021g0121others(5): Show | 8 | HG01168.hp2 HG02622.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1693-6012G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207937131 | ||||||
| chr2:207937444
|
C | T | 37 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0042others(34): Show | 37 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(34): Show |
intron_variant | MODIFIER | c.1693-6325G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207937444 | ||||||
| chr2:207937569
|
C | T | 1 | a0001c0004t0010g0150 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1693-6450G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207937569 | ||||||
| chr2:207937570
|
T | TA | 6 | a0001c0001t0003g0058a0001c0002t0003g0184a0001c0003t0001g0025others(3): Show | 6 | HG00323.hp2 HG01192.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.1693-6452dupT | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207937570 | ||||||
| chr2:207937744
|
G | A | 1 | a0001c0002t0037g0110 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1693-6625C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207937744 | ||||||
| chr2:207938115
|
A | AT | 7 | a0001c0002t0006g0193a0001c0002t0006g0194a0001c0002t0006g0195others(4): Show | 7 | HG02145.hp1 HG02486.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1693-6997dupA | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207938115 | ||||||
| chr2:207938191
|
C | T | 1 | a0001c0015t0003g0093 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1693-7072G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207938191 | ||||||
| chr2:207938259
|
T | C | 1 | a0001c0002t0037g0110 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1693-7140A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207938259 | ||||||
| chr2:207938479
|
C | T | 1 | a0001c0002t0045g0190 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1693-7360G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207938479 | ||||||
| chr2:207938559
|
G | C | 14 | a0001c0001t0005g0088a0001c0001t0016g0005a0001c0001t0024g0117others(11): Show | 14 | HG02258.hp1 HG02258.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.1693-7440C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207938559 | ||||||
| chr2:207938824
|
G | A | 3 | a0001c0001t0003g0011a0001c0001t0013g0175a0001c0002t0045g0190 | 3 | HG02922.hp1 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1692+7543C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207938824 | ||||||
| chr2:207938836
|
A | C | 124 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(121): Show | 124 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.1692+7531T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207938836 | ||||||
| chr2:207938892
|
T | C | 1 | a0008c0013t0002g0109 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1692+7475A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207938892 | ||||||
| chr2:207939023
|
T | C | 8 | a0001c0001t0004g0120a0001c0001t0019g0008a0001c0001t0021g0121others(5): Show | 8 | HG01168.hp2 HG02622.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1692+7344A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207939023 | ||||||
| chr2:207939053
|
C | T | 1 | a0001c0002t0003g0184 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1692+7314G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207939053 | ||||||
| chr2:207939402
|
C | T | 3 | a0001c0001t0003g0011a0001c0001t0013g0175a0001c0002t0045g0190 | 3 | HG02922.hp1 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1692+6965G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207939402 | ||||||
| chr2:207939584
|
C | T | 1 | a0001c0001t0013g0175 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1692+6783G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207939584 | ||||||
| chr2:207939908
|
T | G | 1 | a0001c0004t0002g0148 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1692+6459A>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207939908 | ||||||
| chr2:207940211
|
A | G | 1 | a0001c0004t0010g0150 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1692+6156T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207940211 | ||||||
| chr2:207940305
|
C | T | 1 | a0001c0002t0037g0110 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1692+6062G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207940305 | ||||||
| chr2:207940436
|
A | G | 7 | a0001c0001t0005g0088a0001c0001t0016g0005a0001c0002t0005g0159others(4): Show | 7 | HG02258.hp2 HG02976.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1692+5931T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207940436 | ||||||
| chr2:207940774
|
C | T | 2 | a0001c0004t0039g0036a0001c0004t0042g0035 | 2 | HG02809.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1692+5593G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207940774 | ||||||
| chr2:207940868
|
A | G | 59 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(56): Show | 59 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.1692+5499T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207940868 | ||||||
| chr2:207941402
|
G | C | 1 | a0001c0001t0013g0175 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1692+4965C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207941402 | ||||||
| chr2:207941798
|
G | A | 1 | a0001c0002t0003g0184 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1692+4569C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207941798 | ||||||
| chr2:207942175
|
A | C | 1 | a0006c0010t0003g0101 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1692+4192T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207942175 | ||||||
| chr2:207942216
|
G | T | 59 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(56): Show | 59 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.1692+4151C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207942216 | ||||||
| chr2:207942257
|
C | T | 7 | a0001c0002t0006g0193a0001c0002t0006g0194a0001c0002t0006g0195others(4): Show | 7 | HG02145.hp1 HG02486.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1692+4110G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207942257 | ||||||
| chr2:207942362
|
A | C | 2 | a0001c0001t0002g0055a0001c0001t0002g0056 | 2 | NA18954.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.1692+4005T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207942362 | ||||||
| chr2:207942380
|
T | G | 1 | a0001c0002t0001g0177 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1692+3987A>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207942380 | ||||||
| chr2:207942526
|
GATTCTGT others(12): Show |
G | 14 | a0001c0001t0005g0088a0001c0001t0016g0005a0001c0001t0024g0117others(11): Show | 14 | HG02258.hp1 HG02258.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.1692+3822_1692+384 others(23): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207942526 | ||||||
| chr2:207942667
|
G | A | 3 | a0001c0001t0001g0118a0001c0001t0044g0116a0001c0002t0059g0200 | 3 | HG02647.hp1 HG02895.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1692+3700C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207942667 | ||||||
| chr2:207942808
|
G | A | 1 | a0001c0002t0026g0085 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1692+3559C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207942808 | ||||||
| chr2:207943086
|
T | C | 1 | a0001c0001t0002g0069 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1692+3281A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207943086 | ||||||
| chr2:207943117
|
G | C | 1 | a0001c0002t0003g0184 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1692+3250C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207943117 | ||||||
| chr2:207943120
|
T | C | 32 | a0001c0001t0001g0033a0001c0001t0001g0080a0001c0001t0002g0032others(29): Show | 32 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.1692+3247A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207943120 | ||||||
| chr2:207943183
|
T | C | 1 | a0001c0001t0032g0049 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1692+3184A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207943183 | ||||||
| chr2:207943363
|
C | G | 32 | a0001c0001t0001g0033a0001c0001t0001g0080a0001c0001t0002g0032others(29): Show | 32 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.1692+3004G>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207943363 | ||||||
| chr2:207943724
|
C | T | 61 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(58): Show | 61 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.1692+2643G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207943724 | ||||||
| chr2:207943792
|
C | G | 2 | a0001c0004t0039g0036a0001c0004t0042g0035 | 2 | HG02809.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1692+2575G>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207943792 | ||||||
| chr2:207943846
|
C | T | 13 | a0001c0001t0005g0088a0001c0001t0024g0117a0001c0002t0001g0134others(10): Show | 13 | HG02258.hp1 HG02258.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.1692+2521G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207943846 | ||||||
| chr2:207943851
|
G | C | 2 | a0001c0001t0001g0068a0001c0002t0003g0184 | 2 | HG01081.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.1692+2516C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207943851 | ||||||
| chr2:207943867
|
C | CAA | 10 | a0001c0001t0005g0088a0001c0001t0024g0117a0001c0002t0001g0134others(7): Show | 10 | HG02258.hp1 HG02258.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1692+2498_1692+249 others(6): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207943867 | ||||||
| chr2:207943867
|
CA | C | 61 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(58): Show | 61 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.1692+2499delT | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207943867 | ||||||
| chr2:207943867
|
CAA | C | 39 | a0001c0001t0001g0033a0001c0001t0001g0068a0001c0001t0002g0032others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.1692+2498_1692+249 others(6): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207943867 | ||||||
| chr2:207943870
|
A | G | 2 | a0001c0001t0001g0068a0001c0002t0003g0184 | 2 | HG01081.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.1692+2497T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207943870 | ||||||
| chr2:207944182
|
T | C | 2 | a0001c0001t0001g0068a0001c0002t0003g0184 | 2 | HG01081.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.1692+2185A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207944182 | ||||||
| chr2:207944383
|
G | A | 3 | a0001c0001t0003g0011a0001c0001t0013g0175a0001c0002t0045g0190 | 3 | HG02922.hp1 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1692+1984C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207944383 | ||||||
| chr2:207944599
|
T | C | 1 | a0002c0005t0004g0094 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1692+1768A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207944599 | ||||||
| chr2:207944775
|
C | T | 32 | a0001c0001t0001g0033a0001c0001t0001g0080a0001c0001t0002g0032others(29): Show | 32 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.1692+1592G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207944775 | ||||||
| chr2:207944845
|
C | G | 59 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(56): Show | 59 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.1692+1522G>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207944845 | ||||||
| chr2:207944983
|
T | C | 7 | a0001c0001t0004g0120a0001c0001t0019g0008a0001c0001t0021g0121others(4): Show | 7 | HG01168.hp2 HG02622.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1692+1384A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207944983 | ||||||
| chr2:207945198
|
C | T | 1 | a0001c0001t0013g0175 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1692+1169G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207945198 | ||||||
| chr2:207945317
|
C | T | 1 | a0001c0002t0003g0184 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1692+1050G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207945317 | ||||||
| chr2:207945336
|
T | C | 1 | a0001c0003t0002g0024 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1692+1031A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207945336 | ||||||
| chr2:207945465
|
G | C | 1 | a0001c0001t0001g0046 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1692+902C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207945465 | ||||||
| chr2:207945607
|
A | G | 8 | a0001c0001t0004g0120a0001c0001t0019g0008a0001c0001t0021g0121others(5): Show | 8 | HG01168.hp2 HG02622.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1692+760T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207945607 | ||||||
| chr2:207945694
|
G | A | 32 | a0001c0001t0001g0033a0001c0001t0001g0080a0001c0001t0002g0032others(29): Show | 32 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.1692+673C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207945694 | ||||||
| chr2:207945756
|
C | T | 6 | a0001c0001t0005g0088a0001c0002t0005g0159a0001c0002t0005g0161others(3): Show | 6 | HG02258.hp2 HG02976.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1692+611G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207945756 | ||||||
| chr2:207945762
|
G | A | 1 | a0001c0003t0001g0044 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1692+605C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207945762 | ||||||
| chr2:207945950
|
C | A | 1 | a0001c0001t0055g0029 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1692+417G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207945950 | ||||||
| chr2:207946154
|
T | C | 2 | a0001c0001t0009g0007a0001c0001t0017g0003 | 2 | HG02109.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1692+213A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207946154 | ||||||
| chr2:207946258
|
A | G | 3 | a0001c0001t0003g0119a0001c0001t0051g0123a0001c0002t0001g0126 | 3 | HG02886.hp1 HG03579.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1692+109T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 4/7 | chr2 | 207946258 | ||||||
| chr2:207946560
|
C | T | 32 | a0001c0001t0001g0033a0001c0001t0001g0080a0001c0001t0002g0032others(29): Show | 32 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.1547-48G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207946560 | ||||||
| chr2:207946670
|
C | T | 1 | a0001c0001t0013g0175 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1547-158G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207946670 | ||||||
| chr2:207946914
|
T | A | 1 | a0001c0004t0003g0128 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1547-402A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207946914 | ||||||
| chr2:207946942
|
T | G | 12 | a0001c0001t0002g0048a0001c0001t0002g0069a0001c0001t0003g0030others(9): Show | 12 | HG00408.hp1 HG00438.hp2 HG00621.hp1 others(9): Show |
intron_variant | MODIFIER | c.1547-430A>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207946942 | ||||||
| chr2:207947158
|
T | C | 33 | a0001c0001t0001g0033a0001c0001t0001g0080a0001c0001t0002g0032others(30): Show | 33 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.1547-646A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207947158 | ||||||
| chr2:207947164
|
C | T | 1 | a0001c0004t0002g0155 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1547-652G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207947164 | ||||||
| chr2:207947201
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1547-689A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207947201 | ||||||
| chr2:207947279
|
C | T | 3 | a0001c0001t0003g0119a0001c0001t0051g0123a0001c0002t0001g0126 | 3 | HG02886.hp1 HG03579.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1547-767G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207947279 | ||||||
| chr2:207947435
|
G | A | 1 | a0001c0002t0003g0129 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1547-923C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207947435 | ||||||
| chr2:207947496
|
C | T | 10 | a0001c0001t0005g0088a0001c0001t0024g0117a0001c0002t0001g0134others(7): Show | 10 | HG02258.hp2 HG02976.hp2 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.1547-984G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207947496 | ||||||
| chr2:207947503
|
C | G | 13 | a0001c0001t0005g0088a0001c0001t0024g0117a0001c0002t0001g0134others(10): Show | 13 | HG02258.hp1 HG02258.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.1547-991G>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207947503 | ||||||
| chr2:207947652
|
TC | T | 32 | a0001c0001t0001g0033a0001c0001t0001g0080a0001c0001t0002g0032others(29): Show | 32 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.1547-1141delG | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207947652 | ||||||
| chr2:207947654
|
T | G | 32 | a0001c0001t0001g0033a0001c0001t0001g0080a0001c0001t0002g0032others(29): Show | 32 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.1547-1142A>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207947654 | ||||||
| chr2:207947731
|
C | T | 2 | a0001c0003t0001g0091a0001c0003t0012g0090 | 2 | HG01243.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.1547-1219G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207947731 | ||||||
| chr2:207947859
|
A | G | 6 | a0001c0001t0005g0088a0001c0002t0005g0159a0001c0002t0005g0161others(3): Show | 6 | HG02258.hp2 HG02976.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1547-1347T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207947859 | ||||||
| chr2:207947953
|
G | A | 1 | a0002c0005t0001g0132 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1547-1441C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207947953 | ||||||
| chr2:207948019
|
T | C | 1 | a0003c0014t0043g0084 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1547-1507A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207948019 | ||||||
| chr2:207948019
|
T | G | 3 | a0001c0001t0011g0077a0001c0001t0011g0078a0001c0001t0011g0079 | 3 | NA18968.hp1 NA18972.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1547-1507A>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207948019 | ||||||
| chr2:207948052
|
A | G | 8 | a0001c0001t0004g0120a0001c0001t0019g0008a0001c0001t0021g0121others(5): Show | 8 | HG01168.hp2 HG02622.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1547-1540T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207948052 | ||||||
| chr2:207948094
|
A | T | 1 | a0001c0001t0003g0064 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1547-1582T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207948094 | ||||||
| chr2:207948291
|
AT | A | 6 | a0001c0002t0006g0193a0001c0002t0006g0194a0001c0002t0006g0195others(3): Show | 6 | HG02145.hp1 HG02486.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1547-1780delA | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207948291 | ||||||
| chr2:207948349
|
C | CT | 22 | a0001c0001t0001g0118a0001c0001t0003g0083a0001c0001t0024g0117others(19): Show | 22 | HG00280.hp2 HG01192.hp1 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1547-1838dupA | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207948349 | ||||||
| chr2:207948349
|
C | CTT | 47 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0042others(44): Show | 47 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.1547-1839_1547-183 others(6): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207948349 | ||||||
| chr2:207948349
|
C | CTTT | 13 | a0001c0001t0001g0068a0001c0001t0003g0011a0001c0001t0003g0030others(10): Show | 13 | HG00639.hp1 HG01081.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1547-1840_1547-183 others(7): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207948349 | ||||||
| chr2:207948349
|
C | CTTTT | 5 | a0001c0001t0001g0019a0001c0001t0001g0061a0001c0001t0001g0063others(2): Show | 5 | HG01168.hp1 HG01515.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1547-1841_1547-183 others(8): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207948349 | ||||||
| chr2:207948349
|
CT | C | 10 | a0001c0001t0003g0052a0001c0001t0004g0120a0001c0001t0019g0008others(7): Show | 10 | HG01168.hp2 HG01515.hp1 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.1547-1838delA | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207948349 | ||||||
| chr2:207948546
|
G | GT | 27 | a0001c0002t0006g0199a0001c0003t0001g0022a0001c0003t0001g0025others(24): Show | 27 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.1547-2035dupA | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207948546 | ||||||
| chr2:207948546
|
G | T | 1 | a0001c0003t0002g0082 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1547-2034C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207948546 | ||||||
| chr2:207948546
|
GT | G | 52 | a0001c0001t0001g0033a0001c0001t0001g0080a0001c0001t0002g0032others(49): Show | 52 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.1547-2035delA | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207948546 | ||||||
| chr2:207948546
|
GTT | G | 69 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(66): Show | 69 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.1547-2036_1547-203 others(6): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207948546 | ||||||
| chr2:207948559
|
T | C | 3 | a0001c0001t0011g0077a0001c0001t0011g0078a0001c0001t0011g0079 | 3 | NA18968.hp1 NA18972.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1547-2047A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207948559 | ||||||
| chr2:207948598
|
C | T | 6 | a0001c0002t0006g0193a0001c0002t0006g0194a0001c0002t0006g0195others(3): Show | 6 | HG02145.hp1 HG02486.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1547-2086G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207948598 | ||||||
| chr2:207948607
|
G | A | 13 | a0001c0001t0005g0088a0001c0001t0024g0117a0001c0002t0001g0134others(10): Show | 13 | HG02258.hp1 HG02258.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.1547-2095C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207948607 | ||||||
| chr2:207948610
|
T | C | 76 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(73): Show | 76 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.1547-2098A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207948610 | ||||||
| chr2:207948733
|
C | T | 32 | a0001c0001t0001g0033a0001c0001t0001g0080a0001c0001t0002g0032others(29): Show | 32 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.1547-2221G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207948733 | ||||||
| chr2:207948765
|
G | A | 3 | a0001c0001t0003g0011a0001c0001t0013g0175a0001c0002t0045g0190 | 3 | HG02922.hp1 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1547-2253C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207948765 | ||||||
| chr2:207948913
|
G | A | 32 | a0001c0001t0001g0033a0001c0001t0001g0080a0001c0001t0002g0032others(29): Show | 32 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.1547-2401C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207948913 | ||||||
| chr2:207948981
|
TC | T | 60 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(57): Show | 60 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(57): Show |
intron_variant | MODIFIER | c.1547-2470delG | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207948981 | ||||||
| chr2:207949321
|
G | A | 60 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(57): Show | 60 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(57): Show |
intron_variant | MODIFIER | c.1547-2809C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207949321 | ||||||
| chr2:207949774
|
A | T | 5 | a0001c0002t0045g0190a0001c0003t0003g0174a0001c0003t0004g0100others(2): Show | 5 | HG02258.hp1 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1547-3262T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207949774 | ||||||
| chr2:207949785
|
T | A | 6 | a0001c0002t0006g0193a0001c0002t0006g0194a0001c0002t0006g0195others(3): Show | 6 | HG02145.hp1 HG02486.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1547-3273A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207949785 | ||||||
| chr2:207950098
|
C | T | 1 | a0001c0001t0013g0175 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1547-3586G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207950098 | ||||||
| chr2:207950561
|
G | A | 7 | a0001c0002t0006g0193a0001c0002t0006g0194a0001c0002t0006g0195others(4): Show | 7 | HG02145.hp1 HG02486.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1547-4049C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207950561 | ||||||
| chr2:207951206
|
T | C | 1 | a0001c0002t0026g0085 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1547-4694A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207951206 | ||||||
| chr2:207951380
|
G | A | 3 | a0001c0001t0011g0077a0001c0001t0011g0078a0001c0001t0011g0079 | 3 | NA18968.hp1 NA18972.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1547-4868C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207951380 | ||||||
| chr2:207951703
|
G | T | 1 | a0001c0001t0046g0089 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1547-5191C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207951703 | ||||||
| chr2:207951861
|
G | A | 6 | a0001c0001t0005g0088a0001c0002t0005g0159a0001c0002t0005g0161others(3): Show | 6 | HG02258.hp2 HG02976.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1547-5349C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207951861 | ||||||
| chr2:207951878
|
C | T | 6 | a0001c0001t0005g0088a0001c0002t0005g0159a0001c0002t0005g0161others(3): Show | 6 | HG02258.hp2 HG02976.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1547-5366G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207951878 | ||||||
| chr2:207952163
|
A | G | 1 | a0001c0001t0013g0175 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1547-5651T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207952163 | ||||||
| chr2:207952204
|
GA | G | 4 | a0001c0001t0024g0117a0001c0002t0001g0134a0001c0008t0053g0173others(1): Show | 4 | HG03098.hp2 HG03486.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1547-5693delT | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207952204 | ||||||
| chr2:207952361
|
T | C | 1 | a0001c0002t0003g0184 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1547-5849A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207952361 | ||||||
| chr2:207952459
|
C | T | 1 | a0001c0002t0045g0190 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1547-5947G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207952459 | ||||||
| chr2:207952478
|
T | C | 32 | a0001c0001t0001g0033a0001c0001t0001g0080a0001c0001t0002g0032others(29): Show | 32 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.1547-5966A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207952478 | ||||||
| chr2:207952548
|
C | T | 5 | a0001c0001t0003g0119a0001c0001t0009g0007a0001c0001t0017g0003others(2): Show | 5 | HG02109.hp2 HG02145.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1547-6036G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207952548 | ||||||
| chr2:207952959
|
A | G | 1 | a0001c0002t0037g0110 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1547-6447T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207952959 | ||||||
| chr2:207952961
|
C | T | 2 | a0001c0002t0001g0105a0001c0002t0001g0106 | 2 | HG01346.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.1547-6449G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207952961 | ||||||
| chr2:207953110
|
T | C | 59 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(56): Show | 59 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.1547-6598A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207953110 | ||||||
| chr2:207953160
|
C | A | 1 | a0001c0003t0028g0010 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1547-6648G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207953160 | ||||||
| chr2:207953163
|
A | AT | 92 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(89): Show | 92 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.1547-6652dupA | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207953163 | ||||||
| chr2:207953169
|
T | C | 6 | a0001c0001t0005g0088a0001c0002t0005g0159a0001c0002t0005g0161others(3): Show | 6 | HG02258.hp2 HG02976.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1547-6657A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207953169 | ||||||
| chr2:207953221
|
A | C | 1 | a0001c0001t0003g0020 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1547-6709T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207953221 | ||||||
| chr2:207953390
|
AT | A | 92 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(89): Show | 92 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.1547-6879delA | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207953390 | ||||||
| chr2:207953454
|
T | C | 6 | a0001c0002t0006g0193a0001c0002t0006g0194a0001c0002t0006g0195others(3): Show | 6 | HG02145.hp1 HG02486.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1547-6942A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207953454 | ||||||
| chr2:207953535
|
C | T | 1 | a0001c0001t0003g0119 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1547-7023G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207953535 | ||||||
| chr2:207953560
|
G | A | 6 | a0001c0001t0005g0088a0001c0002t0005g0159a0001c0002t0005g0161others(3): Show | 6 | HG02258.hp2 HG02976.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1547-7048C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207953560 | ||||||
| chr2:207953746
|
C | A | 1 | a0001c0001t0001g0060 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1547-7234G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207953746 | ||||||
| chr2:207953824
|
C | CA | 37 | a0001c0001t0001g0080a0001c0001t0002g0032a0001c0001t0002g0039others(34): Show | 37 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.1547-7313dupT | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207953824 | ||||||
| chr2:207953824
|
CA | C | 12 | a0001c0001t0005g0088a0001c0001t0009g0007a0001c0001t0017g0003others(9): Show | 12 | HG02109.hp2 HG02145.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1547-7313delT | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207953824 | ||||||
| chr2:207953984
|
T | C | 33 | a0001c0001t0001g0033a0001c0001t0001g0080a0001c0001t0002g0032others(30): Show | 33 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.1547-7472A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207953984 | ||||||
| chr2:207954141
|
C | T | 4 | a0001c0002t0026g0085a0001c0003t0004g0100a0001c0003t0014g0099others(1): Show | 4 | HG02258.hp1 HG02572.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1547-7629G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207954141 | ||||||
| chr2:207954374
|
A | C | 6 | a0001c0001t0005g0088a0001c0002t0005g0159a0001c0002t0005g0161others(3): Show | 6 | HG02258.hp2 HG02976.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1547-7862T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207954374 | ||||||
| chr2:207954409
|
G | A | 1 | a0001c0001t0003g0011 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1547-7897C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207954409 | ||||||
| chr2:207954980
|
A | T | 1 | a0001c0003t0001g0092 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1547-8468T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207954980 | ||||||
| chr2:207955528
|
G | A | 104 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(101): Show | 104 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.1547-9016C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207955528 | ||||||
| chr2:207955764
|
CA | C | 13 | a0001c0001t0003g0011a0001c0001t0004g0120a0001c0001t0013g0175others(10): Show | 13 | HG01168.hp2 HG01884.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1547-9253delT | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207955764 | ||||||
| chr2:207955797
|
A | T | 3 | a0001c0002t0001g0134a0001c0008t0053g0173a0005c0011t0022g0111 | 3 | HG03098.hp2 NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1547-9285T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207955797 | ||||||
| chr2:207955953
|
T | C | 1 | a0001c0001t0002g0069 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1547-9441A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207955953 | ||||||
| chr2:207956036
|
G | A | 3 | a0001c0002t0001g0134a0001c0008t0053g0173a0005c0011t0022g0111 | 3 | HG03098.hp2 NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1547-9524C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207956036 | ||||||
| chr2:207956088
|
G | A | 1 | a0001c0002t0026g0085 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1547-9576C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207956088 | ||||||
| chr2:207956235
|
G | A | 6 | a0001c0001t0005g0088a0001c0002t0005g0159a0001c0002t0005g0161others(3): Show | 6 | HG02258.hp2 HG02976.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1547-9723C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207956235 | ||||||
| chr2:207956316
|
A | C | 107 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(104): Show | 107 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.1547-9804T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207956316 | ||||||
| chr2:207956429
|
A | C | 126 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(123): Show | 126 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.1547-9917T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207956429 | ||||||
| chr2:207956454
|
C | T | 2 | a0001c0003t0056g0192a0001c0003t0057g0191 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1547-9942G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207956454 | ||||||
| chr2:207956468
|
A | G | 116 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(113): Show | 116 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.1547-9956T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207956468 | ||||||
| chr2:207956543
|
A | T | 6 | a0001c0001t0005g0088a0001c0002t0005g0159a0001c0002t0005g0161others(3): Show | 6 | HG02258.hp2 HG02976.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1547-10031T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207956543 | ||||||
| chr2:207956544
|
A | T | 6 | a0001c0001t0005g0088a0001c0002t0005g0159a0001c0002t0005g0161others(3): Show | 6 | HG02258.hp2 HG02976.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1547-10032T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207956544 | ||||||
| chr2:207956556
|
A | T | 125 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(122): Show | 125 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.1547-10044T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207956556 | ||||||
| chr2:207956718
|
A | AT | 44 | a0001c0001t0001g0033a0001c0001t0002g0032a0001c0001t0002g0039others(41): Show | 44 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(41): Show |
intron_variant | MODIFIER | c.1547-10207dupA | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207956718 | ||||||
| chr2:207956718
|
A | ATT | 7 | a0001c0001t0001g0080a0001c0001t0046g0089a0001c0002t0001g0105others(4): Show | 7 | HG01496.hp1 HG02630.hp1 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.1547-10208_1547-10 others(8): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207956718 | ||||||
| chr2:207956718
|
A | ATTTTT | 20 | a0001c0001t0001g0019a0001c0001t0001g0061a0001c0001t0001g0063others(17): Show | 20 | HG00639.hp1 HG01109.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.1547-10211_1547-10 others(11): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207956718 | ||||||
| chr2:207956718
|
A | ATTTTTT | 17 | a0001c0001t0001g0013a0001c0001t0001g0046a0001c0001t0001g0060others(14): Show | 17 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(14): Show |
intron_variant | MODIFIER | c.1547-10212_1547-10 others(12): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207956718 | ||||||
| chr2:207956718
|
A | ATTTTTTT | 15 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0070others(12): Show | 15 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(12): Show |
intron_variant | MODIFIER | c.1547-10213_1547-10 others(13): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207956718 | ||||||
| chr2:207956718
|
ATT | A | 6 | a0001c0001t0005g0088a0001c0002t0005g0159a0001c0002t0005g0162others(3): Show | 6 | HG02258.hp2 HG02976.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1547-10208_1547-10 others(8): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207956718 | ||||||
| chr2:207956718
|
ATTTTTTT others(3): Show |
A | 12 | a0001c0001t0003g0011a0001c0001t0004g0120a0001c0001t0013g0175others(9): Show | 12 | HG01168.hp2 HG01884.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1547-10216_1547-10 others(16): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207956718 | ||||||
| chr2:207956841
|
A | C | 1 | a0001c0001t0046g0089 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1547-10329T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207956841 | ||||||
| chr2:207956853
|
A | C | 1 | a0001c0001t0046g0089 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1547-10341T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207956853 | ||||||
| chr2:207956862
|
G | C | 6 | a0001c0001t0005g0088a0001c0002t0005g0159a0001c0002t0005g0161others(3): Show | 6 | HG02258.hp2 HG02976.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1547-10350C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207956862 | ||||||
| chr2:207956876
|
T | C | 1 | a0001c0001t0003g0011 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1547-10364A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207956876 | ||||||
| chr2:207957044
|
G | A | 6 | a0001c0001t0005g0088a0001c0002t0005g0159a0001c0002t0005g0161others(3): Show | 6 | HG02258.hp2 HG02976.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1547-10532C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207957044 | ||||||
| chr2:207957097
|
G | A | 2 | a0001c0003t0001g0091a0001c0003t0012g0090 | 2 | HG01243.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.1547-10585C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207957097 | ||||||
| chr2:207957396
|
G | T | 92 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(89): Show | 92 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.1547-10884C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207957396 | ||||||
| chr2:207957446
|
C | T | 1 | a0001c0002t0003g0184 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1547-10934G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207957446 | ||||||
| chr2:207957714
|
A | C | 1 | a0002c0006t0035g0097 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1547-11202T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207957714 | ||||||
| chr2:207957846
|
A | G | 6 | a0001c0001t0005g0088a0001c0002t0005g0159a0001c0002t0005g0161others(3): Show | 6 | HG02258.hp2 HG02976.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1547-11334T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207957846 | ||||||
| chr2:207957927
|
G | A | 7 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0004g0086others(4): Show | 7 | HG01109.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1547-11415C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207957927 | ||||||
| chr2:207957994
|
T | G | 1 | a0001c0002t0045g0190 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1547-11482A>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207957994 | ||||||
| chr2:207958007
|
G | A | 6 | a0001c0001t0005g0088a0001c0002t0005g0159a0001c0002t0005g0161others(3): Show | 6 | HG02258.hp2 HG02976.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1547-11495C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207958007 | ||||||
| chr2:207958200
|
T | G | 126 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(123): Show | 126 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.1547-11688A>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207958200 | ||||||
| chr2:207958322
|
A | G | 4 | a0001c0003t0003g0073a0001c0004t0002g0113a0001c0004t0002g0114others(1): Show | 4 | HG02683.hp1 HG03688.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1547-11810T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207958322 | ||||||
| chr2:207958336
|
ACT | A | 12 | a0001c0001t0003g0011a0001c0001t0004g0120a0001c0001t0013g0175others(9): Show | 12 | HG01168.hp2 HG01884.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1547-11826_1547-11 others(8): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207958336 | ||||||
| chr2:207958483
|
T | A | 2 | a0001c0001t0015g0004a0001c0001t0016g0005 | 2 | HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1547-11971A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207958483 | ||||||
| chr2:207958512
|
A | G | 1 | a0001c0001t0001g0013 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1547-12000T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207958512 | ||||||
| chr2:207958735
|
T | C | 6 | a0001c0001t0005g0088a0001c0002t0005g0159a0001c0002t0005g0161others(3): Show | 6 | HG02258.hp2 HG02976.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1547-12223A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207958735 | ||||||
| chr2:207958783
|
G | A | 2 | a0001c0003t0003g0067a0001c0004t0010g0145 | 2 | NA18747.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.1547-12271C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207958783 | ||||||
| chr2:207958878
|
T | C | 4 | a0001c0002t0001g0134a0001c0002t0006g0198a0001c0008t0053g0173others(1): Show | 4 | HG01884.hp2 HG03098.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1547-12366A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207958878 | ||||||
| chr2:207959243
|
G | A | 1 | a0001c0004t0001g0127 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1547-12731C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207959243 | ||||||
| chr2:207959327
|
T | C | 10 | a0001c0001t0003g0119a0001c0001t0009g0007a0001c0001t0017g0003others(7): Show | 10 | HG00280.hp2 HG00639.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.1547-12815A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207959327 | ||||||
| chr2:207959683
|
C | A | 1 | a0001c0001t0003g0011 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1547-13171G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207959683 | ||||||
| chr2:207959973
|
T | C | 6 | a0001c0001t0005g0088a0001c0002t0005g0159a0001c0002t0005g0161others(3): Show | 6 | HG02258.hp2 HG02976.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1547-13461A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207959973 | ||||||
| chr2:207960230
|
C | T | 6 | a0001c0002t0006g0193a0001c0002t0006g0194a0001c0002t0006g0195others(3): Show | 6 | HG02145.hp1 HG02486.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1547-13718G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207960230 | ||||||
| chr2:207960292
|
T | C | 1 | a0001c0004t0010g0145 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1547-13780A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207960292 | ||||||
| chr2:207960694
|
A | G | 2 | a0001c0003t0002g0082a0001c0004t0039g0036 | 2 | HG03139.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.1547-14182T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207960694 | ||||||
| chr2:207960861
|
C | T | 10 | a0001c0001t0004g0120a0001c0001t0019g0008a0001c0001t0021g0121others(7): Show | 10 | HG01168.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1547-14349G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207960861 | ||||||
| chr2:207960978
|
T | C | 1 | a0001c0001t0013g0175 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1547-14466A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207960978 | ||||||
| chr2:207961019
|
C | T | 5 | a0001c0001t0001g0118a0001c0001t0024g0117a0001c0001t0044g0116others(2): Show | 5 | HG02647.hp1 HG02895.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1547-14507G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207961019 | ||||||
| chr2:207961305
|
T | A | 1 | a0001c0001t0013g0175 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1547-14793A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207961305 | ||||||
| chr2:207961701
|
G | A | 7 | a0001c0001t0021g0121a0001c0002t0001g0126a0001c0002t0003g0129others(4): Show | 7 | HG02559.hp1 HG02630.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1546+14950C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207961701 | ||||||
| chr2:207961732
|
G | C | 74 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0045others(71): Show | 74 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.1546+14919C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207961732 | ||||||
| chr2:207962074
|
G | A | 1 | a0001c0004t0002g0158 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1546+14577C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207962074 | ||||||
| chr2:207962288
|
C | T | 1 | a0001c0001t0055g0029 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1546+14363G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207962288 | ||||||
| chr2:207962333
|
T | C | 58 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0045others(55): Show | 58 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.1546+14318A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207962333 | ||||||
| chr2:207962399
|
T | C | 87 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0045others(84): Show | 87 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.1546+14252A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207962399 | ||||||
| chr2:207962688
|
G | A | 1 | a0001c0001t0055g0029 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1546+13963C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207962688 | ||||||
| chr2:207962740
|
T | C | 1 | a0001c0015t0003g0093 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1546+13911A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207962740 | ||||||
| chr2:207962743
|
T | C | 2 | a0001c0001t0005g0088a0001c0003t0023g0087 | 2 | HG02258.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1546+13908A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207962743 | ||||||
| chr2:207962756
|
C | T | 1 | a0001c0015t0003g0093 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1546+13895G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207962756 | ||||||
| chr2:207962924
|
T | TA | 32 | a0001c0001t0001g0080a0001c0001t0001g0118a0001c0001t0003g0119others(29): Show | 32 | HG00639.hp2 HG01109.hp2 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.1546+13726dupT | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207962924 | ||||||
| chr2:207962924
|
T | TAA | 52 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0045others(49): Show | 52 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.1546+13725_1546+13 others(8): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207962924 | ||||||
| chr2:207962924
|
TA | T | 7 | a0001c0001t0002g0014a0001c0001t0003g0011a0001c0002t0001g0105others(4): Show | 7 | HG01496.hp1 HG02965.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1546+13726delT | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207962924 | ||||||
| chr2:207962976
|
T | C | 4 | a0001c0004t0002g0158a0001c0004t0007g0178a0001c0004t0007g0180others(1): Show | 4 | NA18968.hp2 NA18985.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.1546+13675A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207962976 | ||||||
| chr2:207963074
|
G | T | 9 | a0001c0001t0005g0124a0001c0003t0004g0100a0001c0003t0014g0099others(6): Show | 9 | HG01109.hp2 HG02109.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1546+13577C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207963074 | ||||||
| chr2:207963241
|
AAAGGCTC others(1): Show |
A | 2 | a0001c0003t0001g0091a0001c0003t0012g0090 | 2 | HG01243.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.1546+13402_1546+13 others(14): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207963241 | ||||||
| chr2:207963451
|
C | A | 5 | a0001c0002t0005g0159a0001c0002t0005g0161a0001c0002t0005g0162others(2): Show | 5 | HG02976.hp2 HG03041.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1546+13200G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207963451 | ||||||
| chr2:207964176
|
C | T | 9 | a0001c0001t0005g0124a0001c0003t0004g0100a0001c0003t0014g0099others(6): Show | 9 | HG01109.hp2 HG02109.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1546+12475G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207964176 | ||||||
| chr2:207964234
|
A | G | 3 | a0001c0001t0003g0051a0001c0001t0003g0052a0001c0001t0003g0053 | 3 | HG01515.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1546+12417T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207964234 | ||||||
| chr2:207964258
|
A | C | 3 | a0001c0003t0003g0174a0001c0003t0004g0172a0001c0008t0053g0173 | 3 | HG02630.hp2 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1546+12393T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207964258 | ||||||
| chr2:207964346
|
C | T | 4 | a0001c0001t0009g0006a0001c0001t0009g0007a0001c0001t0017g0003others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1546+12305G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207964346 | ||||||
| chr2:207964458
|
G | A | 1 | a0001c0004t0003g0165 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1546+12193C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207964458 | ||||||
| chr2:207964496
|
G | C | 3 | a0001c0003t0003g0174a0001c0003t0004g0172a0001c0008t0053g0173 | 3 | HG02630.hp2 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1546+12155C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207964496 | ||||||
| chr2:207964660
|
C | T | 19 | a0001c0001t0001g0118a0001c0001t0003g0119a0001c0001t0004g0120others(16): Show | 19 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.1546+11991G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207964660 | ||||||
| chr2:207964803
|
A | G | 87 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0045others(84): Show | 87 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.1546+11848T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207964803 | ||||||
| chr2:207964931
|
G | A | 3 | a0001c0003t0003g0174a0001c0003t0004g0172a0001c0008t0053g0173 | 3 | HG02630.hp2 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1546+11720C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207964931 | ||||||
| chr2:207965042
|
T | C | 3 | a0001c0001t0019g0008a0001c0004t0039g0036a0001c0004t0042g0035 | 3 | HG02809.hp1 HG03139.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1546+11609A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207965042 | ||||||
| chr2:207965381
|
A | C | 1 | a0002c0005t0036g0098 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1546+11270T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207965381 | ||||||
| chr2:207965391
|
TA | T | 20 | a0001c0001t0001g0118a0001c0001t0003g0119a0001c0001t0004g0120others(17): Show | 20 | HG01256.hp2 HG01884.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1546+11259delT | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207965391 | ||||||
| chr2:207965548
|
A | T | 1 | a0001c0001t0001g0013 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1546+11103T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207965548 | ||||||
| chr2:207965669
|
G | A | 1 | a0001c0003t0009g0001 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1546+10982C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207965669 | ||||||
| chr2:207965934
|
C | G | 3 | a0001c0003t0003g0174a0001c0003t0004g0172a0001c0008t0053g0173 | 3 | HG02630.hp2 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1546+10717G>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207965934 | ||||||
| chr2:207965976
|
A | G | 1 | a0001c0003t0002g0018 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1546+10675T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207965976 | ||||||
| chr2:207966085
|
CTTAT | C | 3 | a0001c0004t0007g0178a0001c0004t0007g0180a0001c0004t0007g0181 | 3 | NA18968.hp2 NA19005.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1546+10562_1546+10 others(10): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207966085 | ||||||
| chr2:207966645
|
C | T | 7 | a0001c0002t0006g0193a0001c0002t0006g0194a0001c0002t0006g0195others(4): Show | 7 | HG01884.hp2 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1546+10006G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207966645 | ||||||
| chr2:207966646
|
G | A | 1 | a0001c0015t0003g0093 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1546+10005C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207966646 | ||||||
| chr2:207966792
|
A | T | 1 | a0001c0002t0026g0085 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1546+9859T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207966792 | ||||||
| chr2:207966804
|
C | T | 9 | a0001c0001t0005g0124a0001c0003t0004g0100a0001c0003t0014g0099others(6): Show | 9 | HG01109.hp2 HG02109.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1546+9847G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207966804 | ||||||
| chr2:207966831
|
G | A | 58 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0045others(55): Show | 58 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.1546+9820C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207966831 | ||||||
| chr2:207966851
|
A | G | 90 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0045others(87): Show | 90 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1546+9800T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207966851 | ||||||
| chr2:207966969
|
G | C | 1 | a0001c0002t0003g0184 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1546+9682C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207966969 | ||||||
| chr2:207967375
|
G | A | 15 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0002g0014others(12): Show | 15 | HG00099.hp2 HG01069.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.1546+9276C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207967375 | ||||||
| chr2:207967657
|
A | G | 9 | a0001c0001t0005g0124a0001c0003t0004g0100a0001c0003t0014g0099others(6): Show | 9 | HG01109.hp2 HG02109.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1546+8994T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207967657 | ||||||
| chr2:207967722
|
T | C | 3 | a0001c0001t0019g0008a0001c0004t0039g0036a0001c0004t0042g0035 | 3 | HG02809.hp1 HG03139.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1546+8929A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207967722 | ||||||
| chr2:207967767
|
C | A | 1 | a0001c0002t0003g0103 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1546+8884G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207967767 | ||||||
| chr2:207967816
|
C | G | 1 | a0001c0003t0002g0023 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1546+8835G>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207967816 | ||||||
| chr2:207967824
|
C | G | 90 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0045others(87): Show | 90 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1546+8827G>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207967824 | ||||||
| chr2:207967860
|
C | T | 18 | a0001c0001t0001g0118a0001c0001t0003g0119a0001c0001t0004g0120others(15): Show | 18 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.1546+8791G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207967860 | ||||||
| chr2:207968481
|
C | T | 2 | a0001c0002t0001g0126a0001c0004t0001g0127 | 2 | HG02630.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1546+8170G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207968481 | ||||||
| chr2:207968519
|
C | T | 4 | a0001c0001t0003g0051a0001c0001t0003g0052a0001c0001t0003g0053others(1): Show | 4 | HG01515.hp1 HG01516.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.1546+8132G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207968519 | ||||||
| chr2:207968533
|
T | C | 120 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0033others(117): Show | 120 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.1546+8118A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207968533 | ||||||
| chr2:207968600
|
G | A | 17 | a0001c0001t0001g0118a0001c0001t0003g0119a0001c0001t0004g0120others(14): Show | 17 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.1546+8051C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207968600 | ||||||
| chr2:207968754
|
A | G | 1 | a0001c0003t0002g0024 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1546+7897T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207968754 | ||||||
| chr2:207968765
|
G | A | 7 | a0001c0002t0001g0126a0001c0002t0003g0129a0001c0002t0004g0122others(4): Show | 7 | HG02559.hp1 HG02572.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1546+7886C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207968765 | ||||||
| chr2:207969114
|
C | T | 1 | a0001c0002t0038g0182 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1546+7537G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207969114 | ||||||
| chr2:207969247
|
C | G | 4 | a0002c0005t0001g0132a0002c0005t0036g0098a0002c0006t0025g0187others(1): Show | 4 | HG02109.hp1 HG02896.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1546+7404G>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207969247 | ||||||
| chr2:207969431
|
C | T | 1 | a0001c0004t0010g0157 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1546+7220G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207969431 | ||||||
| chr2:207969503
|
T | C | 164 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(161): Show | 164 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.1546+7148A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207969503 | ||||||
| chr2:207969536
|
T | C | 20 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0002g0014others(17): Show | 20 | HG00099.hp2 HG00323.hp2 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.1546+7115A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207969536 | ||||||
| chr2:207969753
|
C | T | 59 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0045others(56): Show | 59 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.1546+6898G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207969753 | ||||||
| chr2:207969767
|
C | T | 5 | a0001c0001t0001g0071a0001c0001t0001g0074a0001c0003t0001g0028others(2): Show | 5 | HG00099.hp1 HG00323.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.1546+6884G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207969767 | ||||||
| chr2:207969871
|
T | C | 17 | a0001c0001t0001g0118a0001c0001t0003g0119a0001c0001t0004g0120others(14): Show | 17 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.1546+6780A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207969871 | ||||||
| chr2:207970141
|
T | C | 116 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(113): Show | 116 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.1546+6510A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207970141 | ||||||
| chr2:207970142
|
G | C | 1 | a0001c0001t0019g0008 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1546+6509C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207970142 | ||||||
| chr2:207970158
|
C | T | 1 | a0001c0002t0003g0137 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1546+6493G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207970158 | ||||||
| chr2:207970220
|
G | GAA | 45 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(42): Show | 45 | HG00099.hp2 HG00323.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.1546+6430_1546+643 others(6): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207970220 | ||||||
| chr2:207970227
|
A | C | 20 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0002g0014others(17): Show | 20 | HG00099.hp2 HG00323.hp2 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.1546+6424T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207970227 | ||||||
| chr2:207970240
|
G | A | 1 | a0001c0002t0001g0134 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1546+6411C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207970240 | ||||||
| chr2:207970284
|
A | ACTCT | 44 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(41): Show | 44 | HG00099.hp2 HG00323.hp2 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.1546+6363_1546+636 others(8): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207970284 | ||||||
| chr2:207970354
|
A | G | 17 | a0001c0001t0001g0118a0001c0001t0003g0119a0001c0001t0004g0120others(14): Show | 17 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.1546+6297T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207970354 | ||||||
| chr2:207970976
|
G | T | 59 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0045others(56): Show | 59 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.1546+5675C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207970976 | ||||||
| chr2:207971459
|
A | G | 8 | a0001c0001t0005g0124a0001c0003t0004g0100a0001c0003t0014g0099others(5): Show | 8 | HG01109.hp2 HG02109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1546+5192T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207971459 | ||||||
| chr2:207971532
|
T | C | 2 | a0001c0004t0001g0185a0001c0004t0040g0186 | 2 | HG02622.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1546+5119A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207971532 | ||||||
| chr2:207971546
|
A | G | 8 | a0001c0002t0001g0135a0001c0002t0006g0193a0001c0002t0006g0194others(5): Show | 8 | HG01884.hp2 HG02145.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1546+5105T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207971546 | ||||||
| chr2:207971553
|
C | CT | 8 | a0001c0001t0005g0124a0001c0003t0004g0100a0001c0003t0014g0099others(5): Show | 8 | HG01109.hp2 HG02109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1546+5097dupA | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207971553 | ||||||
| chr2:207971692
|
CATTAATA others(13): Show |
C | 1 | a0001c0004t0001g0107 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1546+4939_1546+495 others(24): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207971692 | ||||||
| chr2:207972025
|
T | C | 1 | a0001c0001t0001g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1546+4626A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207972025 | ||||||
| chr2:207972352
|
C | CG | 25 | a0001c0001t0001g0033a0001c0001t0001g0063a0001c0001t0001g0070others(22): Show | 25 | HG00423.hp1 HG00621.hp2 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.1546+4298dupC | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207972352 | ||||||
| chr2:207972535
|
C | T | 5 | a0001c0001t0001g0017a0001c0001t0004g0086a0001c0003t0001g0091others(2): Show | 5 | HG01243.hp1 HG01891.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1546+4116G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207972535 | ||||||
| chr2:207972586
|
C | CA | 8 | a0001c0002t0005g0159a0001c0002t0005g0161a0001c0002t0005g0162others(5): Show | 8 | HG02976.hp2 HG03041.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.1546+4064dupT | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207972586 | ||||||
| chr2:207972586
|
CA | C | 7 | a0001c0001t0001g0074a0001c0001t0003g0083a0001c0002t0001g0135others(4): Show | 7 | HG01069.hp2 HG01243.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.1546+4064delT | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207972586 | ||||||
| chr2:207972603
|
A | G | 1 | a0001c0001t0001g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1546+4048T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207972603 | ||||||
| chr2:207972618
|
G | A | 1 | a0001c0003t0001g0009 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1546+4033C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207972618 | ||||||
| chr2:207972668
|
C | T | 1 | a0001c0001t0020g0115 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1546+3983G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207972668 | ||||||
| chr2:207972732
|
G | A | 2 | a0001c0004t0039g0036a0001c0004t0042g0035 | 2 | HG02809.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1546+3919C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207972732 | ||||||
| chr2:207972975
|
C | T | 7 | a0001c0001t0001g0118a0001c0001t0003g0119a0001c0001t0013g0175others(4): Show | 7 | HG02257.hp2 HG02647.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1546+3676G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207972975 | ||||||
| chr2:207973098
|
G | A | 110 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.1546+3553C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207973098 | ||||||
| chr2:207973162
|
T | C | 1 | a0001c0004t0001g0179 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1546+3489A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207973162 | ||||||
| chr2:207973204
|
T | A | 8 | a0001c0001t0005g0124a0001c0003t0004g0100a0001c0003t0014g0099others(5): Show | 8 | HG01109.hp2 HG02109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1546+3447A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207973204 | ||||||
| chr2:207973661
|
C | T | 59 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0045others(56): Show | 59 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.1546+2990G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207973661 | ||||||
| chr2:207973674
|
G | C | 8 | a0001c0001t0005g0124a0001c0003t0004g0100a0001c0003t0014g0099others(5): Show | 8 | HG01109.hp2 HG02109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1546+2977C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207973674 | ||||||
| chr2:207973770
|
GAGTTCA | G | 17 | a0001c0001t0001g0118a0001c0001t0003g0119a0001c0001t0004g0120others(14): Show | 17 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.1546+2875_1546+288 others(10): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207973770 | ||||||
| chr2:207973793
|
A | C | 1 | a0008c0013t0002g0109 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1546+2858T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207973793 | ||||||
| chr2:207973874
|
C | G | 7 | a0001c0002t0001g0126a0001c0002t0003g0129a0001c0002t0004g0122others(4): Show | 7 | HG02559.hp1 HG02572.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1546+2777G>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207973874 | ||||||
| chr2:207973966
|
T | C | 2 | a0001c0001t0001g0068a0001c0001t0001g0070 | 2 | HG00642.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.1546+2685A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207973966 | ||||||
| chr2:207974014
|
G | C | 85 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(82): Show | 85 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.1546+2637C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207974014 | ||||||
| chr2:207974071
|
C | T | 8 | a0001c0001t0005g0124a0001c0003t0004g0100a0001c0003t0014g0099others(5): Show | 8 | HG01109.hp2 HG02109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1546+2580G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207974071 | ||||||
| chr2:207974409
|
C | T | 1 | a0001c0004t0002g0148 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1546+2242G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207974409 | ||||||
| chr2:207974433
|
C | T | 5 | a0002c0005t0001g0132a0002c0005t0004g0094a0002c0005t0036g0098others(2): Show | 5 | HG01109.hp2 HG02109.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1546+2218G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207974433 | ||||||
| chr2:207974596
|
G | A | 17 | a0001c0001t0001g0118a0001c0001t0003g0119a0001c0001t0004g0120others(14): Show | 17 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.1546+2055C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207974596 | ||||||
| chr2:207974690
|
A | C | 1 | a0001c0001t0001g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1546+1961T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207974690 | ||||||
| chr2:207974708
|
T | C | 27 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(24): Show | 27 | HG00099.hp2 HG00323.hp2 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.1546+1943A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207974708 | ||||||
| chr2:207974797
|
C | T | 19 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0002g0014others(16): Show | 19 | HG00099.hp2 HG00323.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.1546+1854G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207974797 | ||||||
| chr2:207974835
|
C | CT | 16 | a0001c0001t0001g0118a0001c0001t0003g0119a0001c0001t0004g0120others(13): Show | 16 | HG02109.hp2 HG02257.hp2 HG02647.hp1 others(13): Show |
intron_variant | MODIFIER | c.1546+1815dupA | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207974835 | ||||||
| chr2:207974872
|
A | C | 113 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(110): Show | 113 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.1546+1779T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207974872 | ||||||
| chr2:207975284
|
A | G | 1 | a0001c0001t0019g0008 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1546+1367T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207975284 | ||||||
| chr2:207975479
|
C | G | 2 | a0001c0001t0003g0051a0001c0001t0003g0052 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1546+1172G>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207975479 | ||||||
| chr2:207975582
|
C | CT | 43 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0002g0014others(40): Show | 43 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.1546+1068dupA | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207975582 | ||||||
| chr2:207975582
|
C | CTT | 16 | a0001c0001t0001g0118a0001c0001t0003g0119a0001c0001t0004g0120others(13): Show | 16 | HG02109.hp2 HG02257.hp2 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.1546+1067_1546+106 others(6): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207975582 | ||||||
| chr2:207975582
|
CT | C | 56 | a0001c0001t0001g0017a0001c0001t0001g0033a0001c0001t0001g0045others(53): Show | 56 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.1546+1068delA | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207975582 | ||||||
| chr2:207975632
|
C | T | 8 | a0001c0001t0001g0017a0001c0001t0004g0086a0001c0003t0001g0091others(5): Show | 8 | HG01243.hp1 HG01891.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1546+1019G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207975632 | ||||||
| chr2:207975836
|
A | C | 1 | a0008c0013t0002g0109 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1546+815T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207975836 | ||||||
| chr2:207975897
|
C | T | 17 | a0001c0001t0001g0118a0001c0001t0003g0119a0001c0001t0004g0120others(14): Show | 17 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.1546+754G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207975897 | ||||||
| chr2:207975899
|
A | AT | 64 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0045others(61): Show | 64 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.1546+751dupA | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207975899 | ||||||
| chr2:207975899
|
A | ATT | 35 | a0001c0001t0001g0080a0001c0001t0001g0118a0001c0001t0003g0119others(32): Show | 35 | HG01109.hp2 HG01346.hp1 HG01928.hp2 others(32): Show |
intron_variant | MODIFIER | c.1546+750_1546+751d others(4): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207975899 | ||||||
| chr2:207976181
|
C | T | 2 | a0001c0001t0001g0118a0001c0001t0024g0117 | 2 | HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1546+470G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207976181 | ||||||
| chr2:207976409
|
A | G | 113 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(110): Show | 113 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.1546+242T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207976409 | ||||||
| chr2:207976549
|
A | C | 1 | a0001c0002t0013g0125 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1546+102T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 3/7 | chr2 | 207976549 | ||||||
| chr2:207977641
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.611-55C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207977641 | ||||||
| chr2:207977655
|
A | G | 1 | a0001c0001t0001g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.611-69T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207977655 | ||||||
| chr2:207977670
|
A | G | 105 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(102): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.611-84T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207977670 | ||||||
| chr2:207977813
|
C | T | 1 | a0001c0015t0003g0093 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.611-227G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207977813 | ||||||
| chr2:207977894
|
C | G | 8 | a0001c0001t0005g0124a0001c0003t0004g0100a0001c0003t0014g0099others(5): Show | 8 | HG01109.hp2 HG02109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.611-308G>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207977894 | ||||||
| chr2:207977904
|
T | C | 105 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(102): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.611-318A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207977904 | ||||||
| chr2:207977962
|
C | T | 1 | a0001c0001t0019g0008 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.611-376G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207977962 | ||||||
| chr2:207977979
|
C | T | 2 | a0001c0003t0056g0192a0001c0003t0057g0191 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.611-393G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207977979 | ||||||
| chr2:207978157
|
ACGTGCAA others(11): Show |
A | 16 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0002g0014others(13): Show | 16 | HG00099.hp2 HG00323.hp2 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.611-589_611-572del others(18): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207978157 | ||||||
| chr2:207978426
|
G | A | 1 | a0001c0001t0019g0008 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.611-840C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207978426 | ||||||
| chr2:207978505
|
G | A | 1 | a0001c0002t0001g0154 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.611-919C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207978505 | ||||||
| chr2:207978559
|
C | T | 8 | a0001c0001t0005g0124a0001c0003t0004g0100a0001c0003t0014g0099others(5): Show | 8 | HG01109.hp2 HG02109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.611-973G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207978559 | ||||||
| chr2:207979105
|
C | T | 59 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0045others(56): Show | 59 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.611-1519G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207979105 | ||||||
| chr2:207979286
|
G | A | 4 | a0001c0001t0004g0086a0001c0003t0001g0091a0001c0003t0012g0090others(1): Show | 4 | HG01243.hp1 HG01891.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.611-1700C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207979286 | ||||||
| chr2:207979300
|
C | T | 1 | a0001c0004t0030g0167 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.611-1714G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207979300 | ||||||
| chr2:207979377
|
T | C | 1 | a0001c0002t0050g0188 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.611-1791A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207979377 | ||||||
| chr2:207979443
|
A | G | 1 | a0001c0002t0003g0184 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.611-1857T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207979443 | ||||||
| chr2:207979488
|
C | A | 1 | a0001c0001t0019g0008 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.611-1902G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207979488 | ||||||
| chr2:207979499
|
A | C | 8 | a0001c0001t0005g0124a0001c0003t0004g0100a0001c0003t0014g0099others(5): Show | 8 | HG01109.hp2 HG02109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.611-1913T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207979499 | ||||||
| chr2:207979530
|
G | A | 8 | a0001c0002t0001g0135a0001c0002t0006g0193a0001c0002t0006g0194others(5): Show | 8 | HG01884.hp2 HG02145.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.611-1944C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207979530 | ||||||
| chr2:207980365
|
C | T | 17 | a0001c0001t0001g0118a0001c0001t0003g0119a0001c0001t0004g0120others(14): Show | 17 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.611-2779G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207980365 | ||||||
| chr2:207980368
|
C | T | 1 | a0001c0001t0055g0029 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.611-2782G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207980368 | ||||||
| chr2:207980388
|
C | T | 1 | a0001c0002t0001g0134 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.611-2802G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207980388 | ||||||
| chr2:207980629
|
C | T | 1 | a0001c0001t0002g0039 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.611-3043G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207980629 | ||||||
| chr2:207980847
|
G | A | 1 | a0001c0002t0002g0170 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.611-3261C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207980847 | ||||||
| chr2:207980942
|
A | G | 19 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0002g0014others(16): Show | 19 | HG00099.hp2 HG00323.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.611-3356T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207980942 | ||||||
| chr2:207981288
|
T | C | 1 | a0001c0015t0003g0093 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.611-3702A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207981288 | ||||||
| chr2:207981634
|
A | C | 2 | a0001c0001t0015g0004a0001c0001t0016g0005 | 2 | HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.611-4048T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207981634 | ||||||
| chr2:207981700
|
A | G | 3 | a0001c0001t0001g0042a0001c0001t0001g0068a0001c0001t0001g0070 | 3 | HG00642.hp1 HG01081.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.611-4114T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207981700 | ||||||
| chr2:207981816
|
A | G | 1 | a0001c0002t0003g0184 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.611-4230T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207981816 | ||||||
| chr2:207981873
|
A | G | 8 | a0001c0001t0005g0124a0001c0003t0004g0100a0001c0003t0014g0099others(5): Show | 8 | HG01109.hp2 HG02109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.611-4287T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207981873 | ||||||
| chr2:207982211
|
TCCTC | T | 17 | a0001c0001t0001g0118a0001c0001t0003g0119a0001c0001t0004g0120others(14): Show | 17 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.611-4629_611-4626d others(6): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207982211 | ||||||
| chr2:207982224
|
C | A | 1 | a0001c0003t0001g0009 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.611-4638G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207982224 | ||||||
| chr2:207982234
|
T | TC | 10 | a0001c0001t0001g0063a0001c0001t0003g0030a0001c0001t0032g0049others(7): Show | 10 | HG00423.hp2 HG00621.hp2 HG00639.hp1 others(7): Show |
intron_variant | MODIFIER | c.611-4649dupG | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207982234 | ||||||
| chr2:207982239
|
C | G | 1 | a0001c0001t0002g0048 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.611-4653G>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207982239 | ||||||
| chr2:207982243
|
C | T | 17 | a0001c0001t0001g0118a0001c0001t0003g0119a0001c0001t0004g0120others(14): Show | 17 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.611-4657G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207982243 | ||||||
| chr2:207982246
|
T | TC | 12 | a0001c0001t0001g0063a0001c0001t0003g0031a0001c0001t0009g0007others(9): Show | 12 | HG00423.hp1 HG00621.hp1 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.611-4661dupG | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207982246 | ||||||
| chr2:207982511
|
C | CTCT | 17 | a0001c0001t0001g0118a0001c0001t0003g0119a0001c0001t0004g0120others(14): Show | 17 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.611-4926_611-4925i others(5): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207982511 | ||||||
| chr2:207982513
|
T | A | 17 | a0001c0001t0001g0118a0001c0001t0003g0119a0001c0001t0004g0120others(14): Show | 17 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.611-4927A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207982513 | ||||||
| chr2:207982578
|
C | CT | 10 | a0001c0002t0001g0126a0001c0002t0003g0129a0001c0002t0004g0122others(7): Show | 10 | HG02071.hp2 HG02559.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.611-4993dupA | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207982578 | ||||||
| chr2:207982578
|
CT | C | 73 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0045others(70): Show | 73 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.611-4993delA | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207982578 | ||||||
| chr2:207982578
|
CTT | C | 5 | a0001c0001t0018g0002a0001c0003t0001g0009a0001c0003t0001g0044others(2): Show | 5 | HG01192.hp1 HG01952.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.611-4994_611-4993d others(4): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207982578 | ||||||
| chr2:207982589
|
T | TTA | 8 | a0001c0001t0005g0124a0001c0003t0004g0100a0001c0003t0014g0099others(5): Show | 8 | HG01109.hp2 HG02109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.611-5004_611-5003i others(4): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207982589 | ||||||
| chr2:207982610
|
C | T | 1 | a0001c0002t0001g0141 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.611-5024G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207982610 | ||||||
| chr2:207982739
|
C | T | 2 | a0001c0003t0008g0026a0001c0003t0008g0027 | 2 | HG00280.hp2 HG00639.hp2 |
intron_variant | MODIFIER | c.611-5153G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207982739 | ||||||
| chr2:207982860
|
G | T | 1 | a0001c0004t0002g0136 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.611-5274C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207982860 | ||||||
| chr2:207982928
|
T | C | 2 | a0001c0001t0002g0055a0001c0001t0002g0056 | 2 | NA18954.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.611-5342A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207982928 | ||||||
| chr2:207983051
|
A | AT | 87 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0033others(84): Show | 87 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.611-5466dupA | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207983051 | ||||||
| chr2:207983051
|
AT | A | 9 | a0001c0001t0004g0120a0001c0001t0005g0124a0001c0003t0004g0100others(6): Show | 9 | HG01109.hp2 HG02109.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.611-5466delA | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207983051 | ||||||
| chr2:207983138
|
G | A | 60 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0045others(57): Show | 60 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.611-5552C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207983138 | ||||||
| chr2:207983208
|
C | T | 8 | a0001c0001t0005g0124a0001c0003t0004g0100a0001c0003t0014g0099others(5): Show | 8 | HG01109.hp2 HG02109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.611-5622G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207983208 | ||||||
| chr2:207983215
|
C | G | 1 | a0001c0002t0006g0195 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.611-5629G>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207983215 | ||||||
| chr2:207983590
|
GA | G | 116 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(113): Show | 116 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.611-6005delT | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207983590 | ||||||
| chr2:207983898
|
C | G | 20 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(17): Show | 20 | HG00099.hp2 HG00323.hp2 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.611-6312G>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207983898 | ||||||
| chr2:207983966
|
C | A | 1 | a0001c0001t0002g0048 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.611-6380G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207983966 | ||||||
| chr2:207983966
|
C | T | 1 | a0001c0003t0007g0065 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.611-6380G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207983966 | ||||||
| chr2:207984141
|
T | C | 111 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(108): Show | 111 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.611-6555A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207984141 | ||||||
| chr2:207984344
|
C | A | 6 | a0001c0002t0001g0134a0001c0002t0001g0177a0001c0002t0037g0110others(3): Show | 6 | HG02572.hp1 HG02622.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.611-6758G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207984344 | ||||||
| chr2:207984429
|
T | C | 165 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.611-6843A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207984429 | ||||||
| chr2:207984537
|
C | T | 5 | a0001c0001t0001g0017a0001c0001t0004g0086a0001c0003t0001g0091others(2): Show | 5 | HG01243.hp1 HG01891.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.611-6951G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207984537 | ||||||
| chr2:207984601
|
A | G | 111 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(108): Show | 111 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.611-7015T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207984601 | ||||||
| chr2:207984672
|
C | T | 1 | a0001c0003t0002g0040 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.611-7086G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207984672 | ||||||
| chr2:207984783
|
C | G | 109 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.611-7197G>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207984783 | ||||||
| chr2:207984790
|
T | C | 1 | a0001c0004t0010g0157 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.611-7204A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207984790 | ||||||
| chr2:207984818
|
G | A | 1 | a0001c0001t0051g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.611-7232C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207984818 | ||||||
| chr2:207985035
|
G | A | 1 | a0001c0015t0003g0093 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.611-7449C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207985035 | ||||||
| chr2:207985182
|
A | C | 111 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(108): Show | 111 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.611-7596T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207985182 | ||||||
| chr2:207985484
|
A | T | 10 | a0001c0001t0001g0118a0001c0001t0003g0119a0001c0001t0004g0120others(7): Show | 10 | HG02257.hp2 HG02647.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.611-7898T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207985484 | ||||||
| chr2:207985508
|
C | A | 8 | a0001c0002t0001g0154a0001c0004t0002g0155a0001c0004t0002g0158others(5): Show | 8 | HG00621.hp1 HG02056.hp2 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.611-7922G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207985508 | ||||||
| chr2:207985583
|
C | T | 199 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.611-7997G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207985583 | ||||||
| chr2:207985595
|
G | A | 4 | a0001c0003t0001g0009a0001c0003t0001g0044a0001c0003t0002g0082others(1): Show | 4 | HG01192.hp1 HG01952.hp2 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.611-8009C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207985595 | ||||||
| chr2:207985627
|
A | T | 84 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(81): Show | 84 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.611-8041T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207985627 | ||||||
| chr2:207985763
|
G | C | 7 | a0001c0002t0001g0126a0001c0002t0003g0129a0001c0002t0004g0122others(4): Show | 7 | HG02559.hp1 HG02572.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.611-8177C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207985763 | ||||||
| chr2:207985881
|
G | A | 1 | a0001c0001t0003g0020 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.611-8295C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207985881 | ||||||
| chr2:207985983
|
G | A | 28 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0068others(25): Show | 28 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(25): Show |
intron_variant | MODIFIER | c.611-8397C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207985983 | ||||||
| chr2:207985987
|
C | CA | 8 | a0001c0001t0019g0008a0001c0002t0006g0194a0001c0004t0002g0113others(5): Show | 8 | HG00423.hp1 HG02683.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.611-8402dupT | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207985987 | ||||||
| chr2:207985987
|
CA | C | 94 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(91): Show | 94 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.611-8402delT | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207985987 | ||||||
| chr2:207986024
|
A | C | 84 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(81): Show | 84 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.611-8438T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207986024 | ||||||
| chr2:207986257
|
C | A | 84 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(81): Show | 84 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.611-8671G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207986257 | ||||||
| chr2:207986333
|
G | C | 17 | a0001c0001t0001g0118a0001c0001t0003g0119a0001c0001t0004g0120others(14): Show | 17 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.611-8747C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207986333 | ||||||
| chr2:207986534
|
C | T | 1 | a0001c0002t0038g0182 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.611-8948G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207986534 | ||||||
| chr2:207986597
|
C | T | 1 | a0001c0001t0003g0053 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.611-9011G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207986597 | ||||||
| chr2:207986676
|
G | GT | 86 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(83): Show | 86 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.611-9091dupA | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207986676 | ||||||
| chr2:207986806
|
G | A | 1 | a0001c0004t0002g0136 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.611-9220C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207986806 | ||||||
| chr2:207986838
|
A | AT | 36 | a0001c0001t0001g0017a0001c0001t0001g0068a0001c0001t0001g0118others(33): Show | 36 | HG00423.hp2 HG00621.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.611-9253dupA | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207986838 | ||||||
| chr2:207987019
|
A | G | 2 | a0001c0001t0004g0120a0001c0001t0021g0121 | 2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.611-9433T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207987019 | ||||||
| chr2:207987123
|
C | T | 1 | a0001c0002t0003g0133 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.611-9537G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207987123 | ||||||
| chr2:207987258
|
A | C | 101 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(98): Show | 101 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.611-9672T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207987258 | ||||||
| chr2:207987299
|
C | A | 1 | a0001c0015t0003g0093 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.611-9713G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207987299 | ||||||
| chr2:207987351
|
C | T | 18 | a0001c0001t0005g0124a0001c0002t0001g0126a0001c0002t0003g0129others(15): Show | 18 | HG01109.hp2 HG02109.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.611-9765G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207987351 | ||||||
| chr2:207987398
|
T | C | 103 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(100): Show | 103 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.611-9812A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207987398 | ||||||
| chr2:207987536
|
G | C | 17 | a0001c0001t0001g0118a0001c0001t0003g0119a0001c0001t0004g0120others(14): Show | 17 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.611-9950C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207987536 | ||||||
| chr2:207987665
|
T | C | 10 | a0001c0002t0001g0126a0001c0002t0003g0129a0001c0002t0004g0122others(7): Show | 10 | HG02559.hp1 HG02572.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.611-10079A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207987665 | ||||||
| chr2:207987730
|
A | G | 2 | a0001c0001t0005g0088a0001c0003t0023g0087 | 2 | HG02258.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.611-10144T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207987730 | ||||||
| chr2:207988053
|
C | A | 17 | a0001c0001t0001g0118a0001c0001t0003g0119a0001c0001t0004g0120others(14): Show | 17 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.611-10467G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207988053 | ||||||
| chr2:207988073
|
T | A | 1 | a0001c0004t0010g0157 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.611-10487A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207988073 | ||||||
| chr2:207988575
|
T | C | 29 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0046others(26): Show | 29 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.611-10989A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207988575 | ||||||
| chr2:207988681
|
T | C | 1 | a0001c0004t0001g0127 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.611-11095A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207988681 | ||||||
| chr2:207989066
|
T | A | 1 | a0001c0004t0002g0114 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.611-11480A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207989066 | ||||||
| chr2:207989722
|
C | T | 18 | a0001c0001t0001g0118a0001c0001t0003g0119a0001c0001t0004g0120others(15): Show | 18 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.610+11308G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207989722 | ||||||
| chr2:207990380
|
C | T | 1 | a0001c0002t0003g0137 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.610+10650G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207990380 | ||||||
| chr2:207990411
|
A | G | 19 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0002g0014others(16): Show | 19 | HG00099.hp2 HG00323.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.610+10619T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207990411 | ||||||
| chr2:207990594
|
G | A | 3 | a0001c0003t0001g0022a0001c0003t0002g0018a0001c0003t0002g0021 | 3 | HG01069.hp2 HG01071.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.610+10436C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207990594 | ||||||
| chr2:207990625
|
G | A | 1 | a0001c0015t0003g0093 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.610+10405C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207990625 | ||||||
| chr2:207990816
|
T | C | 1 | a0001c0001t0019g0008 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.610+10214A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207990816 | ||||||
| chr2:207991374
|
C | T | 1 | a0001c0003t0029g0054 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.610+9656G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207991374 | ||||||
| chr2:207991603
|
GA | G | 103 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(100): Show | 103 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.610+9426delT | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207991603 | ||||||
| chr2:207992729
|
GA | G | 5 | a0001c0001t0001g0071a0001c0001t0001g0074a0001c0003t0001g0028others(2): Show | 5 | HG00099.hp1 HG00323.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.610+8300delT | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207992729 | ||||||
| chr2:207992838
|
G | T | 2 | a0001c0002t0002g0140a0001c0004t0003g0104 | 2 | HG02135.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.610+8192C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207992838 | ||||||
| chr2:207992930
|
A | G | 1 | a0001c0015t0003g0093 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.610+8100T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207992930 | ||||||
| chr2:207993180
|
G | C | 20 | a0001c0001t0001g0118a0001c0001t0003g0119a0001c0001t0004g0120others(17): Show | 20 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.610+7850C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207993180 | ||||||
| chr2:207993442
|
G | C | 8 | a0001c0002t0006g0193a0001c0002t0006g0194a0001c0002t0006g0195others(5): Show | 8 | HG01884.hp2 HG02145.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.610+7588C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207993442 | ||||||
| chr2:207993501
|
C | CT | 7 | a0001c0002t0001g0126a0001c0002t0003g0129a0001c0002t0004g0122others(4): Show | 7 | HG02559.hp1 HG02572.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.610+7528dupA | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207993501 | ||||||
| chr2:207993501
|
CT | C | 99 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.610+7528delA | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207993501 | ||||||
| chr2:207993528
|
T | TG | 103 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(100): Show | 103 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.610+7501dupC | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207993528 | ||||||
| chr2:207993700
|
C | T | 1 | a0001c0001t0001g0033 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.610+7330G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207993700 | ||||||
| chr2:207993933
|
C | T | 1 | a0001c0002t0005g0159 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.610+7097G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207993933 | ||||||
| chr2:207994211
|
T | G | 1 | a0001c0003t0002g0066 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.610+6819A>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207994211 | ||||||
| chr2:207994430
|
A | G | 1 | a0001c0001t0001g0033 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.610+6600T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207994430 | ||||||
| chr2:207994517
|
G | T | 1 | a0001c0001t0046g0089 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.610+6513C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207994517 | ||||||
| chr2:207994539
|
C | A | 1 | a0001c0001t0019g0008 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.610+6491G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207994539 | ||||||
| chr2:207995000
|
C | T | 16 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0002g0014others(13): Show | 16 | HG00099.hp2 HG00323.hp2 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.610+6030G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207995000 | ||||||
| chr2:207995003
|
G | A | 20 | a0001c0001t0001g0118a0001c0001t0003g0119a0001c0001t0004g0120others(17): Show | 20 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.610+6027C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207995003 | ||||||
| chr2:207995133
|
G | A | 1 | a0001c0015t0003g0093 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.610+5897C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207995133 | ||||||
| chr2:207995169
|
T | C | 19 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0002g0014others(16): Show | 19 | HG00099.hp2 HG00323.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.610+5861A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207995169 | ||||||
| chr2:207995192
|
C | T | 59 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0045others(56): Show | 59 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.610+5838G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207995192 | ||||||
| chr2:207995204
|
C | T | 2 | a0001c0001t0005g0088a0001c0003t0023g0087 | 2 | HG02258.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.610+5826G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207995204 | ||||||
| chr2:207995239
|
A | G | 1 | a0001c0002t0001g0139 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.610+5791T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207995239 | ||||||
| chr2:207995496
|
T | C | 1 | a0001c0001t0003g0011 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.610+5534A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207995496 | ||||||
| chr2:207995597
|
T | C | 2 | a0001c0004t0039g0036a0001c0004t0042g0035 | 2 | HG02809.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.610+5433A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207995597 | ||||||
| chr2:207995688
|
G | C | 1 | a0001c0004t0002g0151 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.610+5342C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207995688 | ||||||
| chr2:207995821
|
T | A | 1 | a0001c0002t0001g0135 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.610+5209A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207995821 | ||||||
| chr2:207995922
|
A | C | 19 | a0001c0001t0001g0118a0001c0001t0003g0119a0001c0001t0004g0120others(16): Show | 19 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.610+5108T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207995922 | ||||||
| chr2:207995970
|
G | A | 1 | a0001c0001t0004g0086 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.610+5060C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207995970 | ||||||
| chr2:207996077
|
A | G | 5 | a0001c0001t0001g0071a0001c0001t0001g0074a0001c0003t0001g0028others(2): Show | 5 | HG00099.hp1 HG00323.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.610+4953T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207996077 | ||||||
| chr2:207996112
|
C | T | 1 | a0005c0011t0022g0111 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.610+4918G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207996112 | ||||||
| chr2:207996259
|
C | T | 1 | a0001c0015t0003g0093 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.610+4771G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207996259 | ||||||
| chr2:207996871
|
T | C | 1 | a0001c0001t0019g0008 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.610+4159A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207996871 | ||||||
| chr2:207997007
|
C | CA | 99 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0033others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.610+4022dupT | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207997007 | ||||||
| chr2:207997007
|
C | CAA | 5 | a0001c0001t0001g0017a0001c0001t0004g0086a0001c0003t0001g0091others(2): Show | 5 | HG01243.hp1 HG01891.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.610+4021_610+4022d others(4): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207997007 | ||||||
| chr2:207997366
|
C | T | 104 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(101): Show | 104 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.610+3664G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207997366 | ||||||
| chr2:207997513
|
C | A | 2 | a0001c0001t0003g0119a0001c0003t0012g0176 | 2 | HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.610+3517G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207997513 | ||||||
| chr2:207997726
|
T | C | 105 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(102): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.610+3304A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207997726 | ||||||
| chr2:207997759
|
C | T | 1 | a0001c0003t0009g0001 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.610+3271G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207997759 | ||||||
| chr2:207998099
|
TG | T | 18 | a0001c0001t0001g0118a0001c0001t0003g0119a0001c0001t0004g0120others(15): Show | 18 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.610+2930delC | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207998099 | ||||||
| chr2:207998103
|
C | A | 18 | a0001c0001t0001g0118a0001c0001t0003g0119a0001c0001t0004g0120others(15): Show | 18 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.610+2927G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207998103 | ||||||
| chr2:207998201
|
G | A | 1 | a0001c0015t0003g0093 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.610+2829C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207998201 | ||||||
| chr2:207998561
|
G | T | 104 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(101): Show | 104 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.610+2469C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207998561 | ||||||
| chr2:207998705
|
T | C | 18 | a0001c0001t0001g0118a0001c0001t0003g0119a0001c0001t0004g0120others(15): Show | 18 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.610+2325A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207998705 | ||||||
| chr2:207998919
|
T | C | 1 | a0001c0002t0003g0184 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.610+2111A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207998919 | ||||||
| chr2:207999109
|
A | G | 1 | a0001c0001t0017g0003 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.610+1921T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207999109 | ||||||
| chr2:207999230
|
C | G | 2 | a0001c0003t0004g0100a0001c0003t0014g0099 | 2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.610+1800G>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207999230 | ||||||
| chr2:207999344
|
G | A | 1 | a0001c0015t0003g0093 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.610+1686C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207999344 | ||||||
| chr2:207999500
|
A | G | 60 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0045others(57): Show | 60 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.610+1530T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207999500 | ||||||
| chr2:207999544
|
G | C | 1 | a0001c0015t0003g0093 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.610+1486C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207999544 | ||||||
| chr2:207999931
|
T | C | 2 | a0001c0003t0001g0091a0001c0003t0012g0090 | 2 | HG01243.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.610+1099A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 207999931 | ||||||
| chr2:208000137
|
T | C | 7 | a0001c0003t0004g0100a0001c0003t0014g0099a0002c0005t0001g0132others(4): Show | 7 | HG01109.hp2 HG02109.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.610+893A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 208000137 | ||||||
| chr2:208000269
|
G | A | 1 | a0001c0015t0003g0093 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.610+761C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 208000269 | ||||||
| chr2:208000307
|
G | A | 1 | a0001c0003t0002g0081 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.610+723C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 208000307 | ||||||
| chr2:208000393
|
C | T | 1 | a0001c0003t0002g0072 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.610+637G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 208000393 | ||||||
| chr2:208000406
|
C | A | 2 | a0001c0003t0001g0091a0001c0003t0012g0090 | 2 | HG01243.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.610+624G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 208000406 | ||||||
| chr2:208000411
|
C | T | 1 | a0001c0001t0019g0008 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.610+619G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 2/7 | chr2 | 208000411 | ||||||
| chr2:208001998
|
T | C | 1 | a0001c0001t0019g0008 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-318-41A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208001998 | ||||||
| chr2:208002000
|
G | C | 7 | a0001c0001t0001g0118a0001c0001t0003g0119a0001c0001t0013g0175others(4): Show | 7 | HG02257.hp2 HG02647.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-318-43C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208002000 | ||||||
| chr2:208002280
|
A | C | 25 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(22): Show | 25 | HG00099.hp2 HG00323.hp2 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.-318-323T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208002280 | ||||||
| chr2:208002672
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-318-715G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208002672 | ||||||
| chr2:208002745
|
A | G | 1 | a0001c0001t0019g0008 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-318-788T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208002745 | ||||||
| chr2:208002895
|
T | C | 1 | a0001c0001t0001g0070 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-318-938A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208002895 | ||||||
| chr2:208003064
|
T | A | 1 | a0001c0001t0004g0086 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-318-1107A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208003064 | ||||||
| chr2:208003094
|
C | T | 15 | a0001c0002t0001g0126a0001c0002t0003g0129a0001c0002t0004g0122others(12): Show | 15 | HG01109.hp2 HG02109.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.-318-1137G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208003094 | ||||||
| chr2:208003095
|
G | A | 104 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(101): Show | 104 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.-318-1138C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208003095 | ||||||
| chr2:208003304
|
A | G | 19 | a0001c0001t0001g0118a0001c0001t0003g0119a0001c0001t0004g0120others(16): Show | 19 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.-318-1347T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208003304 | ||||||
| chr2:208003440
|
C | T | 1 | a0001c0001t0003g0034 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-318-1483G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208003440 | ||||||
| chr2:208003453
|
A | T | 1 | a0001c0001t0001g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-318-1496T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208003453 | ||||||
| chr2:208003456
|
A | G | 1 | a0001c0002t0026g0085 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-318-1499T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208003456 | ||||||
| chr2:208003755
|
T | C | 19 | a0001c0001t0001g0118a0001c0001t0003g0119a0001c0001t0004g0120others(16): Show | 19 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.-318-1798A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208003755 | ||||||
| chr2:208003774
|
CTT | C | 3 | a0001c0004t0003g0096a0001c0004t0010g0157a0006c0010t0003g0101 | 3 | HG00408.hp2 HG02056.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.-318-1819_-318-181 others(6): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208003774 | ||||||
| chr2:208003812
|
C | T | 5 | a0001c0001t0004g0086a0001c0002t0026g0085a0001c0003t0001g0091others(2): Show | 5 | HG01243.hp1 HG01891.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.-318-1855G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208003812 | ||||||
| chr2:208004056
|
T | C | 78 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0045others(75): Show | 78 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.-318-2099A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208004056 | ||||||
| chr2:208004258
|
T | C | 84 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(81): Show | 84 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.-318-2301A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208004258 | ||||||
| chr2:208004417
|
CA | C | 84 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(81): Show | 84 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.-318-2461delT | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208004417 | ||||||
| chr2:208004428
|
A | G | 2 | a0001c0001t0004g0120a0001c0001t0021g0121 | 2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-318-2471T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208004428 | ||||||
| chr2:208004440
|
C | T | 1 | a0001c0002t0005g0161 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-318-2483G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208004440 | ||||||
| chr2:208004598
|
G | A | 19 | a0001c0001t0001g0118a0001c0001t0003g0119a0001c0001t0004g0120others(16): Show | 19 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.-318-2641C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208004598 | ||||||
| chr2:208004601
|
C | T | 1 | a0001c0003t0001g0043 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-318-2644G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208004601 | ||||||
| chr2:208004713
|
G | A | 88 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0033others(85): Show | 88 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.-318-2756C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208004713 | ||||||
| chr2:208004789
|
C | T | 104 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(101): Show | 104 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.-318-2832G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208004789 | ||||||
| chr2:208004833
|
T | G | 7 | a0001c0002t0001g0126a0001c0002t0003g0129a0001c0002t0004g0122others(4): Show | 7 | HG02559.hp1 HG02572.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-318-2876A>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208004833 | ||||||
| chr2:208004863
|
C | A | 19 | a0001c0001t0001g0118a0001c0001t0003g0119a0001c0001t0004g0120others(16): Show | 19 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.-318-2906G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208004863 | ||||||
| chr2:208004876
|
G | C | 2 | a0001c0003t0001g0091a0001c0003t0012g0090 | 2 | HG01243.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.-318-2919C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208004876 | ||||||
| chr2:208004975
|
G | A | 59 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0045others(56): Show | 59 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.-318-3018C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208004975 | ||||||
| chr2:208005037
|
C | T | 84 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(81): Show | 84 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.-318-3080G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208005037 | ||||||
| chr2:208005040
|
GTCTTGAA others(1): Show |
G | 84 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(81): Show | 84 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.-318-3091_-318-308 others(12): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208005040 | ||||||
| chr2:208005105
|
G | A | 1 | a0001c0001t0003g0011 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-318-3148C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208005105 | ||||||
| chr2:208005254
|
G | C | 89 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(86): Show | 89 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.-318-3297C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208005254 | ||||||
| chr2:208005293
|
A | G | 59 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0045others(56): Show | 59 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.-318-3336T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208005293 | ||||||
| chr2:208005320
|
A | G | 1 | a0001c0001t0046g0089 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-318-3363T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208005320 | ||||||
| chr2:208005386
|
T | C | 1 | a0001c0003t0056g0192 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-318-3429A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208005386 | ||||||
| chr2:208005827
|
A | G | 105 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(102): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.-318-3870T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208005827 | ||||||
| chr2:208006013
|
T | C | 2 | a0001c0003t0001g0028a0001c0003t0001g0043 | 2 | HG00099.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.-318-4056A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208006013 | ||||||
| chr2:208006353
|
A | C | 1 | a0001c0002t0037g0110 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-318-4396T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208006353 | ||||||
| chr2:208006389
|
G | C | 2 | a0001c0003t0001g0091a0001c0003t0012g0090 | 2 | HG01243.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.-318-4432C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208006389 | ||||||
| chr2:208006717
|
G | A | 1 | a0002c0006t0025g0187 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-318-4760C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208006717 | ||||||
| chr2:208006890
|
C | T | 1 | a0001c0002t0001g0177 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-318-4933G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208006890 | ||||||
| chr2:208006905
|
C | T | 2 | a0002c0005t0036g0098a0002c0006t0035g0097 | 2 | HG02109.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-318-4948G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208006905 | ||||||
| chr2:208006921
|
A | C | 1 | a0001c0001t0019g0008 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-318-4964T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208006921 | ||||||
| chr2:208007262
|
C | T | 18 | a0001c0001t0001g0118a0001c0001t0003g0119a0001c0001t0004g0120others(15): Show | 18 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.-318-5305G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208007262 | ||||||
| chr2:208007490
|
A | G | 1 | a0001c0003t0001g0028 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-318-5533T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208007490 | ||||||
| chr2:208007531
|
A | T | 1 | a0001c0002t0045g0190 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-318-5574T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208007531 | ||||||
| chr2:208008075
|
C | A | 19 | a0001c0001t0001g0118a0001c0001t0003g0119a0001c0001t0004g0120others(16): Show | 19 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.-318-6118G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208008075 | ||||||
| chr2:208008189
|
G | C | 2 | a0001c0003t0001g0091a0001c0003t0012g0090 | 2 | HG01243.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.-318-6232C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208008189 | ||||||
| chr2:208008301
|
C | T | 1 | a0001c0002t0003g0171 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-318-6344G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208008301 | ||||||
| chr2:208008501
|
C | CA | 20 | a0001c0002t0003g0137a0001c0002t0003g0184a0001c0002t0005g0161others(17): Show | 20 | HG01884.hp1 HG01884.hp2 HG02071.hp2 others(17): Show |
intron_variant | MODIFIER | c.-318-6545dupT | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208008501 | ||||||
| chr2:208008501
|
C | CAA | 15 | a0001c0002t0001g0126a0001c0002t0003g0129a0001c0002t0005g0159others(12): Show | 15 | HG01168.hp2 HG02145.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.-318-6546_-318-654 others(6): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208008501 | ||||||
| chr2:208008501
|
C | CAAA | 13 | a0001c0001t0001g0118a0001c0001t0003g0119a0001c0001t0009g0006others(10): Show | 13 | HG01109.hp2 HG02109.hp2 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.-318-6547_-318-654 others(7): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208008501 | ||||||
| chr2:208008501
|
C | CAAAA | 6 | a0001c0001t0004g0120a0001c0001t0005g0124a0001c0001t0009g0007others(3): Show | 6 | HG02145.hp2 HG02257.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-318-6548_-318-654 others(8): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208008501 | ||||||
| chr2:208008501
|
CA | C | 5 | a0001c0002t0001g0134a0001c0002t0003g0103a0001c0004t0002g0138others(2): Show | 5 | HG02300.hp1 HG02300.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.-318-6545delT | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208008501 | ||||||
| chr2:208008501
|
CAAAAAAA others(1): Show |
C | 82 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0033others(79): Show | 82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.-318-6552_-318-654 others(12): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208008501 | ||||||
| chr2:208008540
|
T | A | 1 | a0001c0002t0038g0182 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-318-6583A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208008540 | ||||||
| chr2:208008542
|
T | G | 1 | a0001c0002t0038g0182 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-318-6585A>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208008542 | ||||||
| chr2:208008603
|
A | C | 1 | a0001c0001t0020g0115 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-318-6646T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208008603 | ||||||
| chr2:208008642
|
C | T | 18 | a0001c0001t0001g0118a0001c0001t0003g0119a0001c0001t0004g0120others(15): Show | 18 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.-318-6685G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208008642 | ||||||
| chr2:208008990
|
T | C | 18 | a0001c0001t0001g0118a0001c0001t0003g0119a0001c0001t0004g0120others(15): Show | 18 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.-318-7033A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208008990 | ||||||
| chr2:208009047
|
T | C | 60 | a0001c0002t0001g0102a0001c0002t0001g0105a0001c0002t0001g0106others(57): Show | 60 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.-318-7090A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208009047 | ||||||
| chr2:208009189
|
T | C | 1 | a0001c0002t0004g0122 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-318-7232A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208009189 | ||||||
| chr2:208009318
|
T | C | 1 | a0003c0014t0043g0084 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-318-7361A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208009318 | ||||||
| chr2:208009478
|
A | C | 3 | a0001c0001t0002g0055a0001c0001t0002g0056a0001c0003t0029g0054 | 3 | NA18951.hp1 NA18954.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.-318-7521T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208009478 | ||||||
| chr2:208009484
|
G | A | 118 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(115): Show | 118 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.-318-7527C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208009484 | ||||||
| chr2:208009530
|
A | G | 1 | a0001c0002t0052g0160 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-318-7573T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208009530 | ||||||
| chr2:208009650
|
A | G | 1 | a0001c0001t0001g0045 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-318-7693T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208009650 | ||||||
| chr2:208009817
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-318-7860G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208009817 | ||||||
| chr2:208009859
|
A | G | 103 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(100): Show | 103 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.-318-7902T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208009859 | ||||||
| chr2:208009970
|
A | G | 84 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(81): Show | 84 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.-318-8013T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208009970 | ||||||
| chr2:208010026
|
C | T | 1 | a0001c0004t0001g0153 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-318-8069G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208010026 | ||||||
| chr2:208010454
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-318-8497C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208010454 | ||||||
| chr2:208010579
|
C | CT | 18 | a0001c0001t0001g0118a0001c0001t0003g0119a0001c0001t0004g0120others(15): Show | 18 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.-318-8623dupA | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208010579 | ||||||
| chr2:208010631
|
C | T | 3 | a0001c0001t0003g0051a0001c0001t0003g0052a0001c0001t0003g0053 | 3 | HG01515.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-318-8674G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208010631 | ||||||
| chr2:208010870
|
C | T | 1 | a0001c0015t0003g0093 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-318-8913G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208010870 | ||||||
| chr2:208011027
|
T | C | 1 | a0001c0001t0004g0086 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-318-9070A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208011027 | ||||||
| chr2:208011064
|
C | CA | 7 | a0001c0001t0001g0070a0001c0001t0002g0032a0001c0001t0002g0069others(4): Show | 7 | HG00558.hp1 HG00642.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.-318-9108dupT | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208011064 | ||||||
| chr2:208011064
|
CA | C | 8 | a0001c0001t0001g0017a0001c0001t0004g0086a0001c0001t0019g0008others(5): Show | 8 | HG01074.hp1 HG01243.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.-318-9108delT | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208011064 | ||||||
| chr2:208011064
|
CAA | C | 18 | a0001c0001t0001g0118a0001c0001t0003g0119a0001c0001t0004g0120others(15): Show | 18 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.-318-9109_-318-910 others(6): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208011064 | ||||||
| chr2:208011077
|
A | C | 18 | a0001c0001t0001g0118a0001c0001t0003g0119a0001c0001t0004g0120others(15): Show | 18 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.-318-9120T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208011077 | ||||||
| chr2:208011107
|
T | C | 1 | a0001c0003t0008g0050 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-318-9150A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208011107 | ||||||
| chr2:208011231
|
C | A | 2 | a0001c0001t0001g0017a0001c0001t0019g0008 | 2 | HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-318-9274G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208011231 | ||||||
| chr2:208011245
|
C | T | 1 | a0001c0015t0003g0093 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-318-9288G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208011245 | ||||||
| chr2:208011624
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-318-9667C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208011624 | ||||||
| chr2:208011732
|
C | T | 2 | a0001c0003t0004g0100a0001c0003t0014g0099 | 2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-318-9775G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208011732 | ||||||
| chr2:208011785
|
C | CT | 62 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0042others(59): Show | 62 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.-318-9829dupA | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208011785 | ||||||
| chr2:208011785
|
C | CTT | 16 | a0001c0001t0003g0011a0001c0002t0001g0126a0001c0002t0003g0129others(13): Show | 16 | HG01192.hp1 HG01516.hp1 HG01517.hp2 others(13): Show |
intron_variant | MODIFIER | c.-318-9830_-318-982 others(6): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208011785 | ||||||
| chr2:208011785
|
CTTTTT | C | 15 | a0001c0001t0001g0118a0001c0001t0003g0119a0001c0001t0004g0120others(12): Show | 15 | HG02109.hp2 HG02145.hp2 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.-318-9833_-318-982 others(9): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208011785 | ||||||
| chr2:208011831
|
C | T | 4 | a0002c0005t0001g0132a0002c0005t0004g0094a0002c0005t0036g0098others(1): Show | 4 | HG01109.hp2 HG02109.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-318-9874G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208011831 | ||||||
| chr2:208012018
|
G | A | 58 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0045others(55): Show | 58 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.-318-10061C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208012018 | ||||||
| chr2:208012048
|
T | C | 2 | a0001c0003t0056g0192a0001c0003t0057g0191 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-318-10091A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208012048 | ||||||
| chr2:208012216
|
G | T | 1 | a0001c0015t0003g0093 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-318-10259C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208012216 | ||||||
| chr2:208012338
|
G | A | 2 | a0001c0003t0001g0091a0001c0003t0012g0090 | 2 | HG01243.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.-318-10381C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208012338 | ||||||
| chr2:208012804
|
G | C | 2 | a0001c0003t0056g0192a0001c0003t0057g0191 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-318-10847C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208012804 | ||||||
| chr2:208012814
|
T | C | 1 | a0001c0015t0003g0093 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-318-10857A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208012814 | ||||||
| chr2:208012900
|
C | A | 1 | a0001c0015t0003g0093 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-318-10943G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208012900 | ||||||
| chr2:208012977
|
A | G | 1 | a0001c0015t0003g0093 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-318-11020T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208012977 | ||||||
| chr2:208013299
|
C | A | 1 | a0001c0002t0004g0122 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-318-11342G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208013299 | ||||||
| chr2:208013337
|
G | A | 2 | a0001c0002t0001g0126a0001c0004t0001g0127 | 2 | HG02630.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-318-11380C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208013337 | ||||||
| chr2:208013351
|
A | G | 1 | a0001c0015t0003g0093 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-318-11394T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208013351 | ||||||
| chr2:208013632
|
T | C | 192 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(189): Show | 192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.-318-11675A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208013632 | ||||||
| chr2:208013905
|
T | G | 84 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(81): Show | 84 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.-319+11484A>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208013905 | ||||||
| chr2:208013971
|
C | T | 1 | a0001c0002t0001g0135 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-319+11418G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208013971 | ||||||
| chr2:208014015
|
A | G | 1 | a0001c0015t0003g0093 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-319+11374T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208014015 | ||||||
| chr2:208014189
|
A | T | 1 | a0001c0004t0048g0166 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-319+11200T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208014189 | ||||||
| chr2:208014367
|
G | A | 19 | a0001c0001t0001g0118a0001c0001t0003g0119a0001c0001t0004g0120others(16): Show | 19 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.-319+11022C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208014367 | ||||||
| chr2:208014387
|
G | A | 1 | a0001c0002t0003g0184 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-319+11002C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208014387 | ||||||
| chr2:208014434
|
A | G | 18 | a0001c0001t0001g0118a0001c0001t0003g0119a0001c0001t0004g0120others(15): Show | 18 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.-319+10955T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208014434 | ||||||
| chr2:208014470
|
C | T | 2 | a0001c0004t0039g0036a0001c0004t0042g0035 | 2 | HG02809.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-319+10919G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208014470 | ||||||
| chr2:208014537
|
G | A | 18 | a0001c0002t0001g0154a0001c0002t0003g0133a0001c0002t0038g0182others(15): Show | 18 | HG00621.hp1 HG01109.hp1 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.-319+10852C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208014537 | ||||||
| chr2:208014569
|
G | T | 1 | a0002c0005t0004g0094 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-319+10820C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208014569 | ||||||
| chr2:208014824
|
C | T | 19 | a0001c0001t0001g0118a0001c0001t0003g0119a0001c0001t0004g0120others(16): Show | 19 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.-319+10565G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208014824 | ||||||
| chr2:208014879
|
T | C | 18 | a0001c0001t0001g0118a0001c0001t0003g0119a0001c0001t0004g0120others(15): Show | 18 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.-319+10510A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208014879 | ||||||
| chr2:208014984
|
T | G | 1 | a0001c0001t0019g0008 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-319+10405A>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208014984 | ||||||
| chr2:208015108
|
C | T | 3 | a0001c0001t0001g0071a0001c0003t0001g0028a0001c0003t0001g0043 | 3 | HG00099.hp1 HG00323.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.-319+10281G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208015108 | ||||||
| chr2:208015208
|
A | C | 1 | a0001c0001t0001g0042 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-319+10181T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208015208 | ||||||
| chr2:208015267
|
C | A | 1 | a0001c0002t0001g0134 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-319+10122G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208015267 | ||||||
| chr2:208015435
|
A | T | 1 | a0001c0015t0003g0093 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-319+9954T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208015435 | ||||||
| chr2:208015445
|
C | T | 2 | a0001c0002t0001g0134a0002c0006t0025g0187 | 2 | NA18522.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-319+9944G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208015445 | ||||||
| chr2:208015475
|
C | CA | 102 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(99): Show | 102 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.-319+9913dupT | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208015475 | ||||||
| chr2:208015523
|
T | C | 1 | a0003c0014t0043g0084 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-319+9866A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208015523 | ||||||
| chr2:208015527
|
C | A | 19 | a0001c0001t0001g0118a0001c0001t0003g0119a0001c0001t0004g0120others(16): Show | 19 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.-319+9862G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208015527 | ||||||
| chr2:208015527
|
C | T | 84 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(81): Show | 84 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.-319+9862G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208015527 | ||||||
| chr2:208015595
|
C | T | 1 | a0001c0001t0044g0116 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-319+9794G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208015595 | ||||||
| chr2:208015715
|
A | T | 1 | a0001c0003t0009g0001 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-319+9674T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208015715 | ||||||
| chr2:208015739
|
A | G | 103 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(100): Show | 103 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.-319+9650T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208015739 | ||||||
| chr2:208015991
|
C | A | 2 | a0001c0003t0056g0192a0001c0003t0057g0191 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-319+9398G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208015991 | ||||||
| chr2:208016076
|
C | T | 1 | a0001c0003t0002g0072 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-319+9313G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208016076 | ||||||
| chr2:208016310
|
T | C | 5 | a0001c0002t0005g0159a0001c0002t0005g0161a0001c0002t0005g0162others(2): Show | 5 | HG02976.hp2 HG03041.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-319+9079A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208016310 | ||||||
| chr2:208016404
|
G | T | 7 | a0001c0001t0009g0006a0001c0001t0009g0007a0001c0001t0015g0004others(4): Show | 7 | HG02109.hp2 HG02145.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.-319+8985C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208016404 | ||||||
| chr2:208016411
|
A | G | 1 | a0001c0015t0003g0093 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-319+8978T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208016411 | ||||||
| chr2:208016518
|
G | A | 1 | a0001c0001t0004g0086 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-319+8871C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208016518 | ||||||
| chr2:208016605
|
G | A | 84 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(81): Show | 84 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.-319+8784C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208016605 | ||||||
| chr2:208016649
|
C | CA | 8 | a0001c0002t0006g0199a0001c0002t0037g0110a0001c0002t0041g0164others(5): Show | 8 | HG00639.hp1 HG01243.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.-319+8739dupT | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208016649 | ||||||
| chr2:208016649
|
CA | C | 93 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(90): Show | 93 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.-319+8739delT | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208016649 | ||||||
| chr2:208016649
|
CAAA | C | 19 | a0001c0001t0001g0118a0001c0001t0003g0119a0001c0001t0004g0120others(16): Show | 19 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.-319+8737_-319+873 others(7): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208016649 | ||||||
| chr2:208016670
|
T | TAC | 3 | a0001c0003t0008g0026a0001c0003t0008g0027a0001c0004t0048g0166 | 3 | HG00280.hp2 HG00639.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.-319+8717_-319+871 others(6): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208016670 | ||||||
| chr2:208016670
|
T | TACACACA others(5): Show |
1 | a0001c0001t0027g0041 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-319+8707_-319+871 others(16): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208016670 | ||||||
| chr2:208016670
|
T | TACACACA others(7): Show |
12 | a0001c0001t0001g0017a0001c0001t0004g0120a0001c0001t0005g0124others(9): Show | 12 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.-319+8705_-319+871 others(18): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208016670 | ||||||
| chr2:208016670
|
T | TACACACA others(9): Show |
50 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0046others(47): Show | 50 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(47): Show |
intron_variant | MODIFIER | c.-319+8703_-319+871 others(20): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208016670 | ||||||
| chr2:208016670
|
T | TACACACA others(11): Show |
9 | a0001c0001t0001g0074a0001c0001t0003g0119a0001c0003t0001g0091others(6): Show | 9 | HG01243.hp1 HG01496.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.-319+8701_-319+871 others(22): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208016670 | ||||||
| chr2:208016670
|
T | TACACACA others(13): Show |
16 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0002g0014others(13): Show | 16 | HG00099.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.-319+8699_-319+871 others(24): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208016670 | ||||||
| chr2:208016670
|
T | TACACACA others(15): Show |
8 | a0001c0001t0001g0033a0001c0001t0001g0080a0001c0001t0003g0011others(5): Show | 8 | HG00323.hp2 HG01358.hp1 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.-319+8697_-319+871 others(26): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208016670 | ||||||
| chr2:208016670
|
T | TACACACA others(17): Show |
3 | a0001c0001t0019g0008a0001c0003t0001g0025a0001c0003t0057g0191 | 3 | HG02293.hp2 HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-319+8695_-319+871 others(28): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208016670 | ||||||
| chr2:208016670
|
T | TACACACA others(19): Show |
1 | a0001c0001t0004g0086 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-319+8693_-319+871 others(30): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208016670 | ||||||
| chr2:208016670
|
T | TACACACA others(21): Show |
1 | a0001c0003t0056g0192 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-319+8718_-319+871 others(32): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208016670 | ||||||
| chr2:208016697
|
C | A | 1 | a0001c0003t0002g0081 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-319+8692G>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208016697 | ||||||
| chr2:208016755
|
C | T | 1 | a0001c0001t0018g0002 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-319+8634G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208016755 | ||||||
| chr2:208016915
|
T | C | 1 | a0001c0004t0030g0167 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-319+8474A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208016915 | ||||||
| chr2:208016948
|
T | A | 1 | a0001c0001t0003g0011 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-319+8441A>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208016948 | ||||||
| chr2:208017094
|
G | T | 18 | a0001c0001t0001g0118a0001c0001t0003g0119a0001c0001t0004g0120others(15): Show | 18 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.-319+8295C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208017094 | ||||||
| chr2:208017278
|
G | C | 2 | a0001c0003t0001g0091a0001c0003t0012g0090 | 2 | HG01243.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.-319+8111C>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208017278 | ||||||
| chr2:208017494
|
G | A | 1 | a0001c0003t0002g0082 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-319+7895C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208017494 | ||||||
| chr2:208017652
|
G | T | 1 | a0003c0014t0043g0084 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-319+7737C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208017652 | ||||||
| chr2:208017860
|
C | T | 19 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0002g0014others(16): Show | 19 | HG00099.hp2 HG00323.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.-319+7529G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208017860 | ||||||
| chr2:208017962
|
G | A | 1 | a0001c0015t0003g0093 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-319+7427C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208017962 | ||||||
| chr2:208018064
|
C | T | 1 | a0006c0010t0003g0101 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-319+7325G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208018064 | ||||||
| chr2:208018146
|
G | A | 1 | a0001c0004t0002g0112 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-319+7243C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208018146 | ||||||
| chr2:208018154
|
C | T | 84 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(81): Show | 84 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.-319+7235G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208018154 | ||||||
| chr2:208018328
|
A | G | 58 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0045others(55): Show | 58 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.-319+7061T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208018328 | ||||||
| chr2:208018371
|
CA | C | 115 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.-319+7017delT | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208018371 | ||||||
| chr2:208018500
|
A | C | 18 | a0001c0001t0001g0118a0001c0001t0003g0119a0001c0001t0004g0120others(15): Show | 18 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.-319+6889T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208018500 | ||||||
| chr2:208018613
|
T | C | 1 | a0001c0015t0003g0093 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-319+6776A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208018613 | ||||||
| chr2:208018656
|
A | C | 17 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0002g0014others(14): Show | 17 | HG00099.hp2 HG00323.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.-319+6733T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208018656 | ||||||
| chr2:208018671
|
G | A | 103 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(100): Show | 103 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.-319+6718C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208018671 | ||||||
| chr2:208019137
|
CA | C | 84 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(81): Show | 84 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.-319+6251delT | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208019137 | ||||||
| chr2:208019175
|
G | A | 1 | a0001c0001t0003g0083 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-319+6214C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208019175 | ||||||
| chr2:208019218
|
A | G | 2 | a0001c0003t0056g0192a0001c0003t0057g0191 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-319+6171T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208019218 | ||||||
| chr2:208019233
|
G | T | 1 | a0001c0004t0002g0131 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-319+6156C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208019233 | ||||||
| chr2:208019666
|
A | G | 1 | a0001c0001t0004g0086 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-319+5723T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208019666 | ||||||
| chr2:208019696
|
C | T | 1 | a0001c0003t0002g0040 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-319+5693G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208019696 | ||||||
| chr2:208019739
|
C | G | 1 | a0001c0002t0013g0125 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-319+5650G>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208019739 | ||||||
| chr2:208019916
|
C | T | 2 | a0002c0005t0036g0098a0002c0006t0035g0097 | 2 | HG02109.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-319+5473G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208019916 | ||||||
| chr2:208019971
|
G | A | 1 | a0001c0015t0003g0093 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-319+5418C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208019971 | ||||||
| chr2:208020156
|
CACAGGTA others(16): Show |
C | 1 | a0001c0001t0001g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-319+5210_-319+523 others(27): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208020156 | ||||||
| chr2:208020711
|
A | T | 1 | a0001c0001t0002g0039 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-319+4678T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208020711 | ||||||
| chr2:208020838
|
G | A | 17 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0002g0014others(14): Show | 17 | HG00099.hp2 HG00323.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.-319+4551C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208020838 | ||||||
| chr2:208020930
|
A | G | 27 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(24): Show | 27 | HG00099.hp2 HG00323.hp2 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.-319+4459T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208020930 | ||||||
| chr2:208021144
|
C | T | 1 | a0001c0015t0003g0093 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-319+4245G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208021144 | ||||||
| chr2:208021214
|
T | C | 1 | a0001c0002t0045g0190 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-319+4175A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208021214 | ||||||
| chr2:208021305
|
T | C | 1 | a0001c0002t0003g0184 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-319+4084A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208021305 | ||||||
| chr2:208021461
|
ATAATT | A | 3 | a0001c0003t0003g0174a0001c0003t0004g0172a0001c0008t0053g0173 | 3 | HG02630.hp2 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-319+3923_-319+392 others(9): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208021461 | ||||||
| chr2:208021482
|
G | A | 26 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(23): Show | 26 | HG00099.hp2 HG00323.hp2 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.-319+3907C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208021482 | ||||||
| chr2:208021535
|
A | G | 1 | a0001c0015t0003g0093 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-319+3854T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208021535 | ||||||
| chr2:208021681
|
C | T | 1 | a0001c0002t0059g0200 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-319+3708G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208021681 | ||||||
| chr2:208021862
|
C | T | 1 | a0001c0003t0009g0001 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-319+3527G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208021862 | ||||||
| chr2:208021949
|
A | C | 14 | a0001c0001t0001g0118a0001c0001t0003g0119a0001c0001t0009g0006others(11): Show | 14 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.-319+3440T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208021949 | ||||||
| chr2:208021957
|
T | C | 14 | a0001c0001t0001g0118a0001c0001t0003g0119a0001c0001t0009g0006others(11): Show | 14 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.-319+3432A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208021957 | ||||||
| chr2:208022573
|
G | T | 3 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0033g0016 | 3 | HG02559.hp2 HG03195.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-319+2816C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208022573 | ||||||
| chr2:208022674
|
G | GTCCTTCC others(26): Show |
1 | a0001c0003t0001g0092 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-319+2682_-319+271 others(37): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208022674 | ||||||
| chr2:208022730
|
G | T | 98 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(95): Show | 98 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.-319+2659C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208022730 | ||||||
| chr2:208022868
|
A | G | 1 | a0001c0001t0005g0124 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-319+2521T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208022868 | ||||||
| chr2:208022900
|
G | A | 26 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(23): Show | 26 | HG00099.hp2 HG00323.hp2 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.-319+2489C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208022900 | ||||||
| chr2:208022954
|
T | C | 3 | a0001c0002t0001g0168a0001c0002t0001g0169a0001c0002t0002g0170 | 3 | HG00621.hp2 HG01928.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.-319+2435A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208022954 | ||||||
| chr2:208022969
|
A | G | 1 | a0001c0001t0051g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-319+2420T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208022969 | ||||||
| chr2:208023205
|
G | A | 58 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0045others(55): Show | 58 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.-319+2184C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208023205 | ||||||
| chr2:208023306
|
C | CCCCATCT others(331): Show |
1 | a0001c0004t0014g0130 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-319+2082_-319+208 others(342): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208023306 | ||||||
| chr2:208023306
|
C | CCCCATCT others(332): Show |
1 | a0001c0002t0003g0129 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-319+2082_-319+208 others(343): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208023306 | ||||||
| chr2:208023306
|
C | CCCCATCT others(333): Show |
1 | a0001c0004t0003g0128 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-319+2082_-319+208 others(344): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208023306 | ||||||
| chr2:208023306
|
C | CCCCATCT others(335): Show |
5 | a0001c0001t0005g0124a0001c0001t0051g0123a0001c0002t0001g0126others(2): Show | 5 | HG02559.hp1 HG02630.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-319+2082_-319+208 others(346): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208023306 | ||||||
| chr2:208023306
|
C | CCCCATCT others(336): Show |
1 | a0001c0002t0004g0122 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-319+2082_-319+208 others(347): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208023306 | ||||||
| chr2:208023306
|
C | CCCCATCT others(338): Show |
1 | a0001c0001t0021g0121 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-319+2082_-319+208 others(349): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208023306 | ||||||
| chr2:208023306
|
C | CCCCATCT others(339): Show |
1 | a0001c0001t0004g0120 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-319+2082_-319+208 others(350): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208023306 | ||||||
| chr2:208023330
|
T | C | 1 | a0001c0004t0002g0112 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-319+2059A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208023330 | ||||||
| chr2:208023537
|
GCCT | G | 14 | a0001c0001t0001g0118a0001c0001t0003g0119a0001c0001t0009g0006others(11): Show | 14 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.-319+1849_-319+185 others(7): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208023537 | ||||||
| chr2:208023637
|
A | T | 14 | a0001c0001t0001g0118a0001c0001t0003g0119a0001c0001t0009g0006others(11): Show | 14 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.-319+1752T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208023637 | ||||||
| chr2:208023743
|
C | T | 2 | a0001c0004t0002g0113a0001c0004t0002g0114 | 2 | HG02683.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.-319+1646G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208023743 | ||||||
| chr2:208023750
|
T | C | 1 | a0001c0001t0004g0086 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-319+1639A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208023750 | ||||||
| chr2:208023873
|
AT | A | 79 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(76): Show | 79 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.-319+1515delA | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208023873 | ||||||
| chr2:208023890
|
T | C | 1 | a0001c0002t0003g0171 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-319+1499A>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208023890 | ||||||
| chr2:208023914
|
G | T | 7 | a0001c0001t0009g0006a0001c0001t0009g0007a0001c0001t0015g0004others(4): Show | 7 | HG02109.hp2 HG02145.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.-319+1475C>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208023914 | ||||||
| chr2:208023945
|
C | T | 7 | a0001c0001t0009g0006a0001c0001t0009g0007a0001c0001t0015g0004others(4): Show | 7 | HG02109.hp2 HG02145.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.-319+1444G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208023945 | ||||||
| chr2:208024009
|
G | A | 5 | a0001c0003t0003g0174a0001c0003t0004g0172a0001c0004t0001g0185others(2): Show | 5 | HG02622.hp2 HG02630.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-319+1380C>T | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208024009 | ||||||
| chr2:208024142
|
C | CAAAAT | 22 | a0001c0001t0001g0033a0001c0001t0002g0032a0001c0001t0003g0030others(19): Show | 22 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(19): Show |
intron_variant | MODIFIER | c.-319+1242_-319+124 others(9): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208024142 | ||||||
| chr2:208024142
|
C | CAAAATAA others(3): Show |
82 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0118others(79): Show | 82 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.-319+1237_-319+124 others(14): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208024142 | ||||||
| chr2:208024142
|
C | CAAAATAA others(8): Show |
18 | a0001c0001t0001g0013a0001c0001t0003g0012a0001c0002t0001g0102others(15): Show | 18 | HG00099.hp2 HG01109.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.-319+1232_-319+124 others(19): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208024142 | ||||||
| chr2:208024142
|
C | CAAAATAA others(13): Show |
5 | a0001c0001t0003g0011a0001c0002t0059g0200a0001c0003t0028g0010others(2): Show | 5 | HG00408.hp2 HG02895.hp1 NA18956.hp1 others(2): Show |
intron_variant | MODIFIER | c.-319+1227_-319+124 others(24): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208024142 | ||||||
| chr2:208024142
|
C | CAAAATAA others(18): Show |
2 | a0001c0003t0056g0192a0001c0003t0057g0191 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-319+1222_-319+124 others(29): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208024142 | ||||||
| chr2:208024142
|
C | CAAAATAA others(23): Show |
1 | a0002c0005t0004g0094 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-319+1217_-319+124 others(34): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208024142 | ||||||
| chr2:208024142
|
C | CAAACTAA others(68): Show |
1 | a0001c0015t0003g0093 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-319+1246_-319+124 others(79): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208024142 | ||||||
| chr2:208024142
|
CAAAATAA others(3): Show |
C | 6 | a0001c0001t0004g0086a0001c0001t0005g0088a0001c0001t0046g0089others(3): Show | 6 | HG02257.hp1 HG02258.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.-319+1237_-319+124 others(14): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208024142 | ||||||
| chr2:208024142
|
CAAAATAA others(18): Show |
C | 2 | a0001c0003t0001g0091a0001c0003t0012g0090 | 2 | HG01243.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.-319+1222_-319+124 others(29): Show |
PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208024142 | ||||||
| chr2:208024151
|
A | C | 1 | a0001c0015t0003g0093 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-319+1238T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208024151 | ||||||
| chr2:208024160
|
A | G | 7 | a0001c0001t0009g0006a0001c0001t0009g0007a0001c0001t0015g0004others(4): Show | 7 | HG02109.hp2 HG02145.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.-319+1229T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208024160 | ||||||
| chr2:208024170
|
A | C | 1 | a0001c0015t0003g0093 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-319+1219T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208024170 | ||||||
| chr2:208024175
|
A | C | 1 | a0001c0015t0003g0093 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-319+1214T>G | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208024175 | ||||||
| chr2:208024235
|
A | G | 1 | a0001c0003t0001g0009 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-319+1154T>C | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208024235 | ||||||
| chr2:208024518
|
A | T | 7 | a0001c0002t0006g0193a0001c0002t0006g0194a0001c0002t0006g0195others(4): Show | 7 | HG01884.hp2 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.-319+871T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208024518 | ||||||
| chr2:208024963
|
C | T | 1 | a0001c0003t0001g0092 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-319+426G>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208024963 | ||||||
| chr2:208025325
|
A | T | 93 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0019others(90): Show | 93 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.-319+64T>A | PLEKHM3 | ENSG00000178385.15 | transcript | ENST00000427836.8 | protein_coding | 1/7 | chr2 | 208025325 |