Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 153478 |
|---|---|
| ensemblid | ENSG00000153404.15 |
| hgncid | 29399 |
| symbol | PLEKHG4B |
| name | pleckstrin homology and RhoGEF domain containing G4B |
| refseq_nuc | NM_052909.5 |
| refseq_prot | NP_443141.4 |
| ensembl_nuc | ENST00000637938.2 |
| ensembl_prot | ENSP00000490806.1 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 92168 |
| end | 189966 |
| strand | + |
| ver | v1.2 |
| region | chr5:92168-189966 |
| region5000 | chr5:87168-194966 |
| regionname0 | PLEKHG4B_chr5_92168_189966 |
| regionname5000 | PLEKHG4B_chr5_87168_194966 |
| 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 | 0/0 | 1627 | 78 | 27 | 22 | 21 | 3 | 5 | 14 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0002 | 0/0 | 1627 | 23 | 0 | 11 | 7 | 2 | 3 | 6 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0003 | 0/0 | 1627 | 21 | 2 | 7 | 8 | 2 | 2 | 6 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0004 | 0/1 | 1627 | 11 | 0 | 3 | 1 | 1 | 5 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0005 | 0/0 | 1627 | 7 | 1 | 5 | 1 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0006 | 0/0 | 1627 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0007 | 1/0 | 1627 | 6 | 0 | 0 | 4 | 0 | 1 | 2 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0008 | 0/0 | 1627 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0009 | 0/0 | 1627 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0010 | 0/0 | 1627 | 4 | 3 | 0 | 1 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0011 | 0/0 | 1627 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0012 | 0/0 | 1627 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0013 | 0/0 | 1627 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0014 | 0/0 | 1627 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0015 | 0/0 | 1627 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0016 | 0/0 | 1627 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0017 | 0/0 | 1627 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0018 | 0/0 | 1627 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0019 | 0/0 | 1627 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0020 | 0/0 | 1627 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0021 | 0/0 | 1627 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0022 | 0/0 | 1627 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0023 | 0/0 | 1627 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0024 | 0/0 | 1627 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0025 | 0/0 | 1627 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0026 | 0/0 | 1627 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0027 | 0/0 | 1627 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0028 | 0/0 | 1627 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0029 | 0/0 | 1627 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0030 | 0/0 | 1627 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0031 | 0/0 | 1627 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0032 | 0/0 | 1627 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0033 | 0/0 | 1627 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0034 | 0/0 | 1627 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0035 | 0/0 | 1627 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0036 | 0/0 | 1627 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0037 | 0/0 | 1627 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0038 | 0/0 | 1627 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0039 | 0/0 | 1627 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0040 | 0/0 | 1627 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0041 | 0/0 | 1627 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| 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 | 4884 | 36 | 4 | 14 | 13 | 2 | 3 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0002 | 0/0 | 4884 | 19 | 2 | 6 | 8 | 1 | 2 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0003 | 0/0 | 4884 | 12 | 0 | 8 | 1 | 1 | 2 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0004 | 0/0 | 4884 | 12 | 2 | 2 | 6 | 1 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0005 | 0/0 | 4884 | 9 | 0 | 2 | 5 | 1 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0006 | 0/1 | 4884 | 8 | 0 | 2 | 0 | 1 | 4 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0007 | 0/0 | 4884 | 7 | 7 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0008 | 0/0 | 4884 | 7 | 1 | 5 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0009 | 0/0 | 4884 | 5 | 0 | 4 | 0 | 1 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0010 | 1/0 | 4884 | 5 | 0 | 0 | 3 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0011 | 0/0 | 4884 | 3 | 3 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0012 | 0/0 | 4884 | 3 | 3 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0013 | 0/0 | 4884 | 3 | 0 | 0 | 3 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0014 | 0/0 | 4884 | 3 | 2 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0015 | 0/0 | 4884 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0016 | 0/0 | 4884 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0017 | 0/0 | 4884 | 2 | 0 | 1 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0018 | 0/0 | 4884 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0019 | 0/0 | 4884 | 2 | 0 | 1 | 0 | 1 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0020 | 0/0 | 4884 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0021 | 0/0 | 4884 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0022 | 0/0 | 4884 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0023 | 0/0 | 4884 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0024 | 0/0 | 4884 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0025 | 0/0 | 4884 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0026 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0027 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0028 | 0/0 | 4884 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0029 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0030 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0031 | 0/0 | 4884 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0032 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0033 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0034 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0035 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0036 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0037 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0038 | 0/0 | 4884 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0039 | 0/0 | 4884 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0040 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0041 | 0/0 | 4884 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0042 | 0/0 | 4884 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0043 | 0/0 | 4884 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0044 | 0/0 | 4884 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0045 | 0/0 | 4884 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0046 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0047 | 0/0 | 4884 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0048 | 0/0 | 4884 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0049 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0050 | 0/0 | 4884 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0051 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0052 | 0/0 | 4884 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0053 | 0/0 | 4884 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0054 | 0/0 | 4884 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0055 | 0/0 | 4884 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0056 | 0/0 | 4884 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0057 | 0/0 | 4884 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0058 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0059 | 0/0 | 4884 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0060 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0061 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0062 | 0/0 | 4884 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0063 | 0/0 | 4884 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0064 | 0/0 | 4884 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0065 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0066 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0067 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0068 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0069 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0070 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0071 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0072 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0073 | 0/0 | 4884 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0074 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0075 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0076 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0077 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0078 | 0/0 | 4884 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0079 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0080 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| c0081 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 7712 | 11 | 1 | 1 | 9 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0002 | 0/0 | 7691 | 7 | 0 | 5 | 1 | 1 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0003 | 0/0 | 7695 | 7 | 1 | 0 | 3 | 0 | 3 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0004 | 0/0 | 7704 | 5 | 0 | 5 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0005 | 0/0 | 7712 | 4 | 2 | 0 | 1 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0006 | 0/0 | 7716 | 4 | 2 | 0 | 1 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0007 | 0/0 | 7716 | 4 | 0 | 0 | 2 | 1 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0008 | 0/0 | 7711 | 4 | 4 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0009 | 0/0 | 7699 | 4 | 0 | 2 | 2 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0010 | 0/0 | 7699 | 3 | 0 | 1 | 0 | 1 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0011 | 0/0 | 7695 | 3 | 0 | 1 | 2 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0012 | 0/0 | 7704 | 3 | 0 | 3 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0013 | 0/0 | 7708 | 3 | 0 | 1 | 1 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0014 | 0/0 | 7712 | 3 | 0 | 0 | 3 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0015 | 0/0 | 7712 | 3 | 0 | 2 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0016 | 0/0 | 7716 | 3 | 0 | 0 | 3 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0017 | 0/0 | 7703 | 3 | 0 | 2 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0018 | 0/0 | 7711 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0019 | 0/0 | 7719 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0020 | 0/0 | 7707 | 2 | 1 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0021 | 0/0 | 7694 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0022 | 0/0 | 7708 | 2 | 0 | 2 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0023 | 0/0 | 7704 | 2 | 1 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0024 | 0/0 | 7704 | 2 | 1 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0025 | 0/0 | 7708 | 2 | 1 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0026 | 1/0 | 7708 | 2 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0027 | 0/0 | 7712 | 2 | 0 | 2 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0028 | 0/0 | 7712 | 2 | 0 | 1 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0029 | 0/0 | 7716 | 2 | 1 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0030 | 0/0 | 7720 | 2 | 1 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0031 | 0/0 | 7720 | 2 | 0 | 2 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0032 | 0/0 | 7711 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0033 | 0/0 | 7718 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0034 | 0/0 | 7687 | 2 | 1 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0035 | 0/0 | 7671 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0036 | 0/0 | 7720 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0037 | 0/0 | 7707 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0038 | 0/0 | 7671 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0039 | 0/0 | 7671 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0040 | 0/0 | 7667 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0041 | 0/0 | 7707 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0042 | 0/0 | 7704 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0043 | 0/0 | 7704 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0044 | 0/0 | 7699 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0045 | 0/0 | 7707 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0046 | 0/0 | 7707 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0047 | 0/0 | 7716 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0048 | 0/0 | 7716 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0049 | 0/0 | 7707 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0050 | 0/0 | 7715 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0051 | 0/0 | 7711 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0052 | 0/0 | 7719 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0053 | 0/0 | 7711 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0054 | 0/0 | 7707 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0055 | 0/0 | 7715 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0056 | 0/0 | 7719 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0057 | 0/0 | 7707 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0058 | 0/0 | 7719 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0059 | 0/0 | 7710 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0060 | 0/0 | 7699 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0061 | 0/0 | 7679 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0062 | 0/0 | 7695 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0063 | 0/0 | 7699 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0064 | 0/0 | 7694 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0065 | 0/0 | 7691 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0066 | 0/0 | 7699 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0067 | 0/0 | 7699 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0068 | 0/0 | 7711 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0069 | 0/0 | 7711 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0070 | 0/0 | 7695 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0071 | 0/0 | 7699 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0072 | 0/0 | 7703 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0073 | 0/0 | 7712 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0074 | 0/0 | 7720 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0075 | 0/0 | 7691 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0076 | 0/0 | 7671 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0077 | 0/0 | 7667 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0078 | 0/0 | 7667 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0079 | 0/0 | 7700 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0080 | 0/0 | 7708 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0081 | 0/0 | 7704 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0082 | 0/0 | 7704 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0083 | 0/0 | 7704 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0084 | 0/0 | 7704 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0085 | 0/0 | 7708 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0086 | 0/0 | 7708 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0087 | 0/0 | 7708 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0088 | 0/0 | 7712 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0089 | 0/0 | 7712 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0090 | 0/0 | 7712 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0091 | 0/0 | 7712 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0092 | 0/0 | 7712 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0093 | 0/0 | 7712 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0094 | 0/0 | 7712 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0095 | 0/0 | 7712 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0096 | 0/0 | 7712 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0097 | 0/0 | 7716 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0098 | 0/0 | 7716 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0099 | 0/0 | 7716 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0100 | 0/0 | 7716 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0101 | 0/0 | 7716 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0102 | 0/0 | 7716 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0103 | 0/0 | 7716 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0104 | 0/0 | 7720 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0105 | 0/0 | 7720 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0106 | 0/0 | 7720 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0107 | 0/0 | 7720 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0108 | 0/0 | 7724 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0109 | 0/0 | 7707 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0110 | 0/0 | 7707 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0111 | 0/0 | 7716 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0112 | 0/0 | 7715 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0113 | 0/0 | 7715 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0114 | 0/0 | 7722 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0115 | 0/0 | 7722 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0116 | 0/0 | 7699 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0117 | 0/0 | 7707 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0118 | 0/0 | 7691 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0119 | 0/0 | 7695 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0120 | 0/0 | 7699 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0121 | 0/0 | 7699 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0122 | 0/0 | 7716 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0123 | 0/0 | 7683 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0124 | 0/0 | 7687 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0125 | 0/0 | 7691 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0126 | 0/0 | 7691 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0127 | 0/0 | 7695 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0128 | 0/0 | 7695 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0129 | 0/0 | 7695 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0130 | 0/0 | 7695 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0131 | 0/0 | 7699 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0132 | 0/0 | 7697 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0133 | 0/0 | 7703 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0134 | 0/1 | 7705 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0135 | 0/0 | 7703 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| t0136 | 0/0 | 7693 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| 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 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0011 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0168 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| 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 | 4884 | 36 | 4 | 14 | 13 | 2 | 3 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0002 | 0/0 | 4884 | 19 | 2 | 6 | 8 | 1 | 2 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0007 | 0/0 | 4884 | 7 | 7 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0011 | 0/0 | 4884 | 3 | 3 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0015 | 0/0 | 4884 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0016 | 0/0 | 4884 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0032 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0035 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0036 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0037 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0048 | 0/0 | 4884 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0049 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0051 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0052 | 0/0 | 4884 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0061 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0002c0003 | 0/0 | 4884 | 12 | 0 | 8 | 1 | 1 | 2 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0002c0005 | 0/0 | 4884 | 9 | 0 | 2 | 5 | 1 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0002c0039 | 0/0 | 4884 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0002c0057 | 0/0 | 4884 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0003c0004 | 0/0 | 4884 | 12 | 2 | 2 | 6 | 1 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0003c0009 | 0/0 | 4884 | 5 | 0 | 4 | 0 | 1 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0003c0017 | 0/0 | 4884 | 2 | 0 | 1 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0003c0044 | 0/0 | 4884 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0003c0056 | 0/0 | 4884 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0004c0006 | 0/1 | 4884 | 8 | 0 | 2 | 0 | 1 | 4 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0004c0041 | 0/0 | 4884 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0004c0043 | 0/0 | 4884 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0004c0054 | 0/0 | 4884 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0005c0008 | 0/0 | 4884 | 7 | 1 | 5 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0006c0021 | 0/0 | 4884 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0006c0068 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0006c0070 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0006c0071 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0006c0072 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0006c0073 | 0/0 | 4884 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0007c0010 | 1/0 | 4884 | 5 | 0 | 0 | 3 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0007c0038 | 0/0 | 4884 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0008c0024 | 0/0 | 4884 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0008c0025 | 0/0 | 4884 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0008c0079 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0009c0012 | 0/0 | 4884 | 3 | 3 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0009c0034 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0010c0014 | 0/0 | 4884 | 3 | 2 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0010c0069 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0011c0023 | 0/0 | 4884 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0011c0078 | 0/0 | 4884 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0012c0013 | 0/0 | 4884 | 3 | 0 | 0 | 3 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0013c0020 | 0/0 | 4884 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0013c0067 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0014c0027 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0014c0065 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0014c0066 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0015c0076 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0015c0077 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0016c0018 | 0/0 | 4884 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0017c0029 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0017c0030 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0018c0022 | 0/0 | 4884 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0019c0019 | 0/0 | 4884 | 2 | 0 | 1 | 0 | 1 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0020c0081 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0021c0026 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0022c0046 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0023c0055 | 0/0 | 4884 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0024c0042 | 0/0 | 4884 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0025c0045 | 0/0 | 4884 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0026c0050 | 0/0 | 4884 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0027c0053 | 0/0 | 4884 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0028c0040 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0029c0033 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0030c0047 | 0/0 | 4884 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0031c0031 | 0/0 | 4884 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0032c0058 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0033c0028 | 0/0 | 4884 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0034c0059 | 0/0 | 4884 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0035c0060 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0036c0075 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0037c0074 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0038c0080 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0039c0062 | 0/0 | 4884 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0040c0063 | 0/0 | 4884 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0041c0064 | 0/0 | 4884 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 12595 | 4 | 0 | 0 | 4 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0001t0004 | 0/0 | 12587 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0001t0005 | 0/0 | 12595 | 2 | 1 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0001t0006 | 0/0 | 12599 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0001t0007 | 0/0 | 12599 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0001t0012 | 0/0 | 12587 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0001t0014 | 0/0 | 12595 | 3 | 0 | 0 | 3 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0001t0015 | 0/0 | 12595 | 3 | 0 | 2 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0001t0024 | 0/0 | 12587 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0001t0027 | 0/0 | 12595 | 2 | 0 | 2 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0001t0028 | 0/0 | 12595 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0001t0030 | 0/0 | 12603 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0001t0031 | 0/0 | 12603 | 2 | 0 | 2 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0001t0032 | 0/0 | 12594 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0001t0073 | 0/0 | 12595 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0001t0079 | 0/0 | 12583 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0001t0091 | 0/0 | 12595 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0001t0092 | 0/0 | 12595 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0001t0093 | 0/0 | 12595 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0001t0097 | 0/0 | 12599 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0001t0098 | 0/0 | 12599 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0001t0099 | 0/0 | 12599 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0001t0102 | 0/0 | 12599 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0001t0104 | 0/0 | 12603 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0001t0113 | 0/0 | 12598 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0002t0001 | 0/0 | 12595 | 3 | 0 | 1 | 2 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0002t0006 | 0/0 | 12599 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0002t0007 | 0/0 | 12599 | 2 | 0 | 0 | 1 | 1 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0002t0012 | 0/0 | 12587 | 2 | 0 | 2 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0002t0013 | 0/0 | 12591 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0002t0022 | 0/0 | 12591 | 2 | 0 | 2 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0002t0024 | 0/0 | 12587 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0002t0025 | 0/0 | 12591 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0002t0081 | 0/0 | 12587 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0002t0082 | 0/0 | 12587 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0002t0086 | 0/0 | 12591 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0002t0087 | 0/0 | 12591 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0002t0094 | 0/0 | 12595 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0002t0101 | 0/0 | 12599 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0007t0008 | 0/0 | 12594 | 4 | 4 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0007t0100 | 0/0 | 12599 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0007t0109 | 0/0 | 12590 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0007t0110 | 0/0 | 12590 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0011t0029 | 0/0 | 12599 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0011t0048 | 0/0 | 12599 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0011t0106 | 0/0 | 12603 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0015t0035 | 0/0 | 12554 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0015t0076 | 0/0 | 12554 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0016t0005 | 0/0 | 12595 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0016t0025 | 0/0 | 12591 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0032t0103 | 0/0 | 12599 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0035t0030 | 0/0 | 12603 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0036t0077 | 0/0 | 12550 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0037t0006 | 0/0 | 12599 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0048t0013 | 0/0 | 12591 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0049t0096 | 0/0 | 12595 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0051t0078 | 0/0 | 12550 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0052t0118 | 0/0 | 12574 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0001c0061t0001 | 0/0 | 12595 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0002c0003t0002 | 0/0 | 12574 | 3 | 0 | 3 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0002c0003t0011 | 0/0 | 12578 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0002c0003t0066 | 0/0 | 12582 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0002c0003t0071 | 0/0 | 12582 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0002c0003t0124 | 0/0 | 12570 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0002c0003t0128 | 0/0 | 12578 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0002c0003t0130 | 0/0 | 12578 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0002c0003t0132 | 0/0 | 12580 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0002c0003t0135 | 0/0 | 12586 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0002c0003t0136 | 0/0 | 12576 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0002c0005t0002 | 0/0 | 12574 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0002c0005t0003 | 0/0 | 12578 | 3 | 0 | 0 | 2 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0002c0005t0070 | 0/0 | 12578 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0002c0005t0072 | 0/0 | 12586 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0002c0005t0075 | 0/0 | 12574 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0002c0005t0127 | 0/0 | 12578 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0002c0005t0129 | 0/0 | 12578 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0002c0039t0009 | 0/0 | 12582 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0002c0057t0003 | 0/0 | 12578 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0003c0004t0001 | 0/0 | 12595 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0003c0004t0004 | 0/0 | 12587 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0003c0004t0007 | 0/0 | 12599 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0003c0004t0016 | 0/0 | 12599 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0003c0004t0028 | 0/0 | 12595 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0003c0004t0084 | 0/0 | 12587 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0003c0004t0089 | 0/0 | 12595 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0003c0004t0105 | 0/0 | 12603 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0003c0004t0108 | 0/0 | 12607 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0003c0004t0116 | 0/0 | 12582 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0003c0004t0117 | 0/0 | 12590 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0003c0009t0017 | 0/0 | 12586 | 2 | 0 | 2 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0003c0009t0119 | 0/0 | 12578 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0003c0009t0120 | 0/0 | 12582 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0003c0009t0121 | 0/0 | 12582 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0003c0017t0016 | 0/0 | 12599 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0003c0017t0074 | 0/0 | 12603 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0003c0044t0001 | 0/0 | 12595 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0003c0056t0017 | 0/0 | 12586 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0004c0006t0002 | 0/0 | 12574 | 3 | 0 | 2 | 0 | 1 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0004c0006t0003 | 0/0 | 12578 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0004c0006t0065 | 0/0 | 12574 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0004c0006t0123 | 0/0 | 12566 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0004c0006t0125 | 0/0 | 12574 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0004c0006t0134 | 0/1 | 12588 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0004c0041t0003 | 0/0 | 12578 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0004c0043t0126 | 0/0 | 12574 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0004c0054t0034 | 0/0 | 12570 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0005c0008t0004 | 0/0 | 12587 | 3 | 0 | 3 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0005c0008t0023 | 0/0 | 12587 | 2 | 1 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0005c0008t0083 | 0/0 | 12587 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0005c0008t0111 | 0/0 | 12599 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0006c0021t0018 | 0/0 | 12594 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0006c0021t0056 | 0/0 | 12602 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0006c0068t0058 | 0/0 | 12602 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0006c0070t0054 | 0/0 | 12590 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0006c0071t0018 | 0/0 | 12594 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0006c0072t0036 | 0/0 | 12603 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0006c0073t0020 | 0/0 | 12590 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0007c0010t0005 | 0/0 | 12595 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0007c0010t0026 | 1/0 | 12591 | 2 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0007c0010t0080 | 0/0 | 12591 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0007c0010t0095 | 0/0 | 12595 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0007c0038t0013 | 0/0 | 12591 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0008c0024t0021 | 0/0 | 12577 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0008c0025t0045 | 0/0 | 12590 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0008c0025t0069 | 0/0 | 12594 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0008c0079t0068 | 0/0 | 12594 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0009c0012t0033 | 0/0 | 12601 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0009c0012t0114 | 0/0 | 12605 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0009c0012t0115 | 0/0 | 12605 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0009c0034t0033 | 0/0 | 12601 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0010c0014t0019 | 0/0 | 12602 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0010c0014t0055 | 0/0 | 12598 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0010c0014t0057 | 0/0 | 12590 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0010c0069t0019 | 0/0 | 12602 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0011c0023t0041 | 0/0 | 12590 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0011c0023t0044 | 0/0 | 12582 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0011c0078t0059 | 0/0 | 12593 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0012c0013t0009 | 0/0 | 12582 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0012c0013t0133 | 0/0 | 12586 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0013c0020t0050 | 0/0 | 12598 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0013c0020t0052 | 0/0 | 12602 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0013c0067t0046 | 0/0 | 12590 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0014c0027t0049 | 0/0 | 12590 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0014c0065t0038 | 0/0 | 12554 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0014c0066t0051 | 0/0 | 12594 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0015c0076t0067 | 0/0 | 12582 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0015c0077t0053 | 0/0 | 12594 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0016c0018t0003 | 0/0 | 12578 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0016c0018t0034 | 0/0 | 12570 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0017c0029t0112 | 0/0 | 12598 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0017c0030t0039 | 0/0 | 12554 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0018c0022t0011 | 0/0 | 12578 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0019c0019t0010 | 0/0 | 12582 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0019c0019t0062 | 0/0 | 12578 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0020c0081t0064 | 0/0 | 12577 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0021c0026t0060 | 0/0 | 12582 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0022c0046t0047 | 0/0 | 12599 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0023c0055t0029 | 0/0 | 12599 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0024c0042t0006 | 0/0 | 12599 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0025c0045t0122 | 0/0 | 12599 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0026c0050t0009 | 0/0 | 12582 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0027c0053t0107 | 0/0 | 12603 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0028c0040t0090 | 0/0 | 12595 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0029c0033t0042 | 0/0 | 12587 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0030c0047t0131 | 0/0 | 12582 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0031c0031t0085 | 0/0 | 12591 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0032c0058t0040 | 0/0 | 12550 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0033c0028t0088 | 0/0 | 12595 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0034c0059t0001 | 0/0 | 12595 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0035c0060t0020 | 0/0 | 12590 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0036c0075t0061 | 0/0 | 12562 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0037c0074t0037 | 0/0 | 12590 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0038c0080t0043 | 0/0 | 12587 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0039c0062t0010 | 0/0 | 12582 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0040c0063t0063 | 0/0 | 12582 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| a0041c0064t0010 | 0/0 | 12582 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | copy fasta | chr5 | 87168 | 194966 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0001t0004g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0001t0005g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0001t0005g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0001t0006g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0001t0007g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0001t0012g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0001t0014g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0001t0014g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0001t0014g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0001t0015g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0001t0015g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0001t0015g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0001t0024g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0001t0027g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0001t0027g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0001t0028g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0001t0030g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0001t0031g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0001t0031g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0001t0032g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0001t0032g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0001t0073g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0001t0079g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0001t0091g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0001t0092g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0001t0093g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0001t0097g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0001t0098g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0001t0099g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0001t0102g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0001t0104g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0001t0113g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0002t0006g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0002t0007g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0002t0007g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0002t0012g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0002t0012g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0002t0013g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0002t0022g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0002t0022g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0002t0024g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0002t0025g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0002t0081g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0002t0082g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0002t0086g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0002t0087g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0002t0094g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0002t0101g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0007t0008g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0007t0008g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0007t0008g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0007t0008g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0007t0100g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0007t0109g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0007t0110g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0011t0029g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0011t0048g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0011t0106g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0015t0035g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0015t0076g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0016t0005g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0016t0025g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0032t0103g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0035t0030g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0036t0077g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0037t0006g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0048t0013g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0049t0096g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0051t0078g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0052t0118g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0001c0061t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0002c0003t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0002c0003t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0002c0003t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0002c0003t0011g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0002c0003t0066g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0002c0003t0071g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0002c0003t0124g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0002c0003t0128g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0002c0003t0130g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0002c0003t0132g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0002c0003t0135g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0002c0003t0136g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0002c0005t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0002c0005t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0002c0005t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0002c0005t0003g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0002c0005t0070g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0002c0005t0072g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0002c0005t0075g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0002c0005t0127g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0002c0005t0129g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0002c0039t0009g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0002c0057t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0003c0004t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0003c0004t0004g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0003c0004t0007g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0003c0004t0016g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0003c0004t0016g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0003c0004t0028g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0003c0004t0084g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0003c0004t0089g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0003c0004t0105g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0003c0004t0108g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0003c0004t0116g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0003c0004t0117g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0003c0009t0017g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0003c0009t0017g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0003c0009t0119g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0003c0009t0120g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0003c0009t0121g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0003c0017t0016g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0003c0017t0074g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0003c0044t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0003c0056t0017g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0004c0006t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0004c0006t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0004c0006t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0004c0006t0003g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0004c0006t0065g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0004c0006t0123g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0004c0006t0125g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0004c0006t0134g0011 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0004c0041t0003g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0004c0043t0126g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0004c0054t0034g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0005c0008t0004g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0005c0008t0004g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0005c0008t0004g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0005c0008t0023g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0005c0008t0023g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0005c0008t0083g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0005c0008t0111g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0006c0021t0018g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0006c0021t0056g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0006c0068t0058g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0006c0070t0054g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0006c0071t0018g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0006c0072t0036g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0006c0073t0020g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0007c0010t0005g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0007c0010t0026g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0007c0010t0026g0168 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0007c0010t0080g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0007c0010t0095g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0007c0038t0013g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0008c0024t0021g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0008c0024t0021g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0008c0025t0045g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0008c0025t0069g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0008c0079t0068g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0009c0012t0033g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0009c0012t0114g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0009c0012t0115g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0009c0034t0033g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0010c0014t0019g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0010c0014t0055g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0010c0014t0057g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0010c0069t0019g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0011c0023t0041g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0011c0023t0044g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0011c0078t0059g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0012c0013t0009g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0012c0013t0009g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0012c0013t0133g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0013c0020t0050g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0013c0020t0052g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0013c0067t0046g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0014c0027t0049g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0014c0065t0038g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0014c0066t0051g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0015c0076t0067g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0015c0077t0053g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0016c0018t0003g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0016c0018t0034g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0017c0029t0112g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0017c0030t0039g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0018c0022t0011g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0018c0022t0011g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0019c0019t0010g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0019c0019t0062g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0020c0081t0064g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0021c0026t0060g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0022c0046t0047g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0023c0055t0029g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0024c0042t0006g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0025c0045t0122g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0026c0050t0009g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0027c0053t0107g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0028c0040t0090g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0029c0033t0042g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0030c0047t0131g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0031c0031t0085g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0032c0058t0040g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0033c0028t0088g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0034c0059t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0035c0060t0020g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0036c0075t0061g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0037c0074t0037g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0038c0080t0043g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0039c0062t0010g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0040c0063t0063g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| a0041c0064t0010g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0007 | g0060 | EUR | GBR | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG00099 | hp2 | a0002 | c0003 | t0066 | g0209 | EUR | GBR | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG00140 | hp1 | a0003 | c0004 | t0089 | g0014 | EUR | GBR | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG00140 | hp2 | a0002 | c0005 | t0129 | g0043 | EUR | GBR | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG00280 | hp1 | a0001 | c0001 | t0099 | g0089 | EUR | FIN | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG00280 | hp2 | a0040 | c0063 | t0063 | g0189 | EUR | FIN | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG00323 | hp1 | a0001 | c0001 | t0104 | g0023 | EUR | FIN | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG00323 | hp2 | a0019 | c0019 | t0010 | g0164 | EUR | FIN | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG00438 | hp1 | a0001 | c0001 | t0030 | g0027 | EAS | CHS | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG00438 | hp2 | a0001 | c0001 | t0014 | g0115 | EAS | CHS | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG00597 | hp1 | a0031 | c0031 | t0085 | g0108 | EAS | CHS | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG00597 | hp2 | a0018 | c0022 | t0011 | g0196 | EAS | CHS | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG00639 | hp1 | a0002 | c0003 | t0130 | g0130 | AMR | PUR | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG00639 | hp2 | a0002 | c0003 | t0128 | g0029 | AMR | PUR | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG00642 | hp1 | a0001 | c0002 | t0094 | g0021 | AMR | PUR | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG00642 | hp2 | a0005 | c0008 | t0004 | g0001 | AMR | PUR | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG00673 | hp1 | a0002 | c0005 | t0003 | g0031 | EAS | CHS | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG00673 | hp2 | a0033 | c0028 | t0088 | g0008 | EAS | CHS | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG00733 | hp1 | a0002 | c0005 | t0127 | g0124 | AMR | PUR | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG00733 | hp2 | a0001 | c0002 | t0012 | g0072 | AMR | PUR | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG00735 | hp1 | a0001 | c0001 | t0113 | g0044 | AMR | PUR | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG00735 | hp2 | a0002 | c0003 | t0002 | g0132 | AMR | PUR | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG00738 | hp1 | a0004 | c0006 | t0002 | g0065 | AMR | PUR | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG00738 | hp2 | a0001 | c0001 | t0073 | g0107 | AMR | PUR | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG00741 | hp1 | a0001 | c0052 | t0118 | g0121 | AMR | PUR | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG00741 | hp2 | a0001 | c0002 | t0022 | g0015 | AMR | PUR | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG01069 | hp1 | a0002 | c0003 | t0002 | g0098 | AMR | PUR | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG01069 | hp2 | a0003 | c0017 | t0074 | g0050 | AMR | PUR | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG01070 | hp1 | a0005 | c0008 | t0004 | g0038 | AMR | PUR | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG01070 | hp2 | a0001 | c0001 | t0027 | g0052 | AMR | PUR | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG01071 | hp1 | a0002 | c0003 | t0002 | g0101 | AMR | PUR | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG01071 | hp2 | a0001 | c0001 | t0027 | g0053 | AMR | PUR | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG01074 | hp1 | a0002 | c0003 | t0011 | g0210 | AMR | PUR | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG01074 | hp2 | a0001 | c0001 | t0012 | g0069 | AMR | PUR | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG01081 | hp1 | a0004 | c0006 | t0002 | g0119 | AMR | PUR | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG01081 | hp2 | a0041 | c0064 | t0010 | g0190 | AMR | PUR | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG01099 | hp1 | a0011 | c0078 | t0059 | g0185 | AMR | PUR | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG01099 | hp2 | a0001 | c0001 | t0015 | g0022 | AMR | PUR | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG01106 | hp1 | a0001 | c0002 | t0012 | g0066 | AMR | PUR | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG01106 | hp2 | a0002 | c0003 | t0124 | g0017 | AMR | PUR | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG01175 | hp1 | a0026 | c0050 | t0009 | g0141 | AMR | PUR | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG01175 | hp2 | a0003 | c0009 | t0120 | g0013 | AMR | PUR | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG01192 | hp1 | a0002 | c0005 | t0070 | g0100 | AMR | PUR | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG01192 | hp2 | a0001 | c0001 | t0092 | g0054 | AMR | PUR | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG01243 | hp1 | a0003 | c0009 | t0017 | g0088 | AMR | PUR | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG01243 | hp2 | a0001 | c0001 | t0028 | g0046 | AMR | PUR | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG01255 | hp1 | a0001 | c0048 | t0013 | g0055 | AMR | CLM | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG01255 | hp2 | a0005 | c0008 | t0004 | g0061 | AMR | CLM | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG01256 | hp1 | a0003 | c0009 | t0017 | g0093 | AMR | CLM | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG01256 | hp2 | a0003 | c0004 | t0084 | g0041 | AMR | CLM | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG01261 | hp1 | a0004 | c0043 | t0126 | g0099 | AMR | CLM | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG01261 | hp2 | a0006 | c0073 | t0020 | g0193 | AMR | CLM | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG01515 | hp1 | a0003 | c0009 | t0119 | g0049 | EUR | IBS | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG01515 | hp2 | a0004 | c0006 | t0002 | g0051 | EUR | IBS | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG01928 | hp1 | a0003 | c0009 | t0121 | g0092 | AMR | PEL | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG01928 | hp2 | a0002 | c0039 | t0009 | g0030 | AMR | PEL | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG01952 | hp1 | a0001 | c0001 | t0004 | g0020 | AMR | PEL | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG01952 | hp2 | a0001 | c0001 | t0031 | g0111 | AMR | PEL | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG01975 | hp1 | a0005 | c0008 | t0083 | g0042 | AMR | PEL | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0074 | AMR | PEL | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG01978 | hp1 | a0001 | c0001 | t0024 | g0135 | AMR | PEL | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG01978 | hp2 | a0001 | c0002 | t0022 | g0138 | AMR | PEL | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG02004 | hp1 | a0001 | c0001 | t0031 | g0112 | AMR | PEL | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG02004 | hp2 | a0019 | c0019 | t0062 | g0191 | AMR | PEL | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | KHV | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG02080 | hp2 | a0001 | c0001 | t0014 | g0033 | EAS | KHV | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG02083 | hp1 | a0003 | c0004 | t0001 | g0087 | EAS | KHV | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG02083 | hp2 | a0007 | c0038 | t0013 | g0102 | EAS | KHV | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG02132 | hp1 | a0001 | c0002 | t0081 | g0034 | EAS | KHV | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG02132 | hp2 | a0001 | c0001 | t0102 | g0057 | EAS | KHV | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG02145 | hp1 | a0016 | c0018 | t0003 | g0005 | AFR | ACB | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG02145 | hp2 | a0008 | c0024 | t0021 | g0176 | AFR | ACB | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG02165 | hp1 | a0007 | c0010 | t0080 | g0117 | EAS | CDX | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG02165 | hp2 | a0001 | c0001 | t0006 | g0075 | EAS | CDX | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG02257 | hp1 | a0015 | c0076 | t0067 | g0192 | AFR | ACB | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG02257 | hp2 | a0001 | c0007 | t0100 | g0025 | AFR | ACB | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0123 | AFR | ACB | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG02258 | hp2 | a0010 | c0069 | t0019 | g0204 | AFR | ACB | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG02273 | hp1 | a0023 | c0055 | t0029 | g0079 | AMR | PEL | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG02273 | hp2 | a0001 | c0001 | t0091 | g0120 | AMR | PEL | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG02280 | hp1 | a0011 | c0023 | t0044 | g0187 | AFR | ACB | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG02280 | hp2 | a0001 | c0011 | t0048 | g0179 | AFR | ACB | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG02300 | hp1 | a0001 | c0001 | t0015 | g0037 | AMR | PEL | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG02300 | hp2 | a0005 | c0008 | t0023 | g0039 | AMR | PEL | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG02451 | hp1 | a0013 | c0020 | t0050 | g0182 | AFR | ACB | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG02451 | hp2 | a0010 | c0014 | t0055 | g0201 | AFR | ACB | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG02602 | hp1 | a0001 | c0001 | t0097 | g0086 | SAS | PJL | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG02602 | hp2 | a0004 | c0006 | t0003 | g0047 | SAS | PJL | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG02622 | hp1 | a0011 | c0023 | t0041 | g0184 | AFR | GWD | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG02622 | hp2 | a0017 | c0030 | t0039 | g0140 | AFR | GWD | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG02647 | hp1 | a0006 | c0068 | t0058 | g0194 | AFR | GWD | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG02647 | hp2 | a0001 | c0037 | t0006 | g0045 | AFR | GWD | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG02683 | hp1 | a0003 | c0056 | t0017 | g0080 | SAS | PJL | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG02683 | hp2 | a0001 | c0001 | t0007 | g0056 | SAS | PJL | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG02717 | hp1 | a0001 | c0049 | t0096 | g0063 | AFR | GWD | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG02717 | hp2 | a0015 | c0077 | t0053 | g0181 | AFR | GWD | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG02723 | hp1 | a0001 | c0007 | t0110 | g0151 | AFR | GWD | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG02723 | hp2 | a0001 | c0002 | t0006 | g0134 | AFR | GWD | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG02735 | hp1 | a0001 | c0002 | t0013 | g0109 | SAS | PJL | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG02735 | hp2 | a0024 | c0042 | t0006 | g0012 | SAS | PJL | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG02809 | hp1 | a0014 | c0066 | t0051 | g0170 | AFR | GWD | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG02809 | hp2 | a0032 | c0058 | t0040 | g0158 | AFR | GWD | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG02818 | hp1 | a0022 | c0046 | t0047 | g0180 | AFR | GWD | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG02818 | hp2 | a0021 | c0026 | t0060 | g0169 | AFR | GWD | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG02886 | hp1 | a0001 | c0015 | t0076 | g0154 | AFR | GWD | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG02886 | hp2 | a0009 | c0012 | t0114 | g0156 | AFR | GWD | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG02896 | hp1 | a0001 | c0007 | t0008 | g0145 | AFR | GWD | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG02896 | hp2 | a0006 | c0070 | t0054 | g0207 | AFR | GWD | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG02897 | hp1 | a0001 | c0007 | t0008 | g0143 | AFR | GWD | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG02897 | hp2 | a0006 | c0072 | t0036 | g0206 | AFR | GWD | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG02922 | hp1 | a0001 | c0016 | t0005 | g0160 | AFR | ESN | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG02922 | hp2 | a0006 | c0071 | t0018 | g0202 | AFR | ESN | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG03017 | hp1 | a0004 | c0041 | t0003 | g0077 | SAS | PJL | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG03017 | hp2 | a0001 | c0001 | t0005 | g0090 | SAS | PJL | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG03041 | hp1 | a0013 | c0067 | t0046 | g0186 | AFR | GWD | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG03041 | hp2 | a0006 | c0021 | t0056 | g0199 | AFR | GWD | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG03098 | hp1 | a0001 | c0032 | t0103 | g0007 | AFR | MSL | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG03098 | hp2 | a0035 | c0060 | t0020 | g0188 | AFR | MSL | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG03139 | hp1 | a0001 | c0051 | t0078 | g0148 | AFR | ESN | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG03139 | hp2 | a0009 | c0012 | t0115 | g0157 | AFR | ESN | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG03195 | hp1 | a0001 | c0015 | t0035 | g0122 | AFR | ESN | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG03195 | hp2 | a0006 | c0021 | t0018 | g0198 | AFR | ESN | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG03209 | hp1 | a0001 | c0061 | t0001 | g0006 | AFR | MSL | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG03209 | hp2 | a0009 | c0012 | t0033 | g0161 | AFR | MSL | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG03225 | hp1 | a0036 | c0075 | t0061 | g0178 | AFR | MSL | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG03225 | hp2 | a0001 | c0001 | t0079 | g0059 | AFR | MSL | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG03453 | hp1 | a0001 | c0016 | t0025 | g0152 | AFR | MSL | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG03453 | hp2 | a0001 | c0001 | t0032 | g0094 | AFR | MSL | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG03486 | hp1 | a0020 | c0081 | t0064 | g0200 | AFR | MSL | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG03486 | hp2 | a0009 | c0034 | t0033 | g0162 | AFR | MSL | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG03491 | hp1 | a0002 | c0003 | t0136 | g0071 | SAS | PJL | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG03491 | hp2 | a0001 | c0002 | t0101 | g0068 | SAS | PJL | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG03516 | hp1 | a0001 | c0011 | t0029 | g0136 | AFR | ESN | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG03516 | hp2 | a0028 | c0040 | t0090 | g0127 | AFR | ESN | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG03540 | hp1 | a0001 | c0007 | t0109 | g0147 | AFR | GWD | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG03540 | hp2 | a0003 | c0004 | t0116 | g0103 | AFR | GWD | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG03579 | hp1 | a0016 | c0018 | t0034 | g0004 | AFR | MSL | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG03579 | hp2 | a0010 | c0014 | t0019 | g0205 | AFR | MSL | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG03669 | hp1 | a0002 | c0003 | t0135 | g0128 | SAS | PJL | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG03669 | hp2 | a0025 | c0045 | t0122 | g0002 | SAS | PJL | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG03710 | hp1 | a0007 | c0010 | t0026 | g0035 | SAS | PJL | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG03710 | hp2 | a0003 | c0004 | t0028 | g0058 | SAS | PJL | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG03831 | hp1 | a0002 | c0005 | t0003 | g0167 | SAS | BEB | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG03831 | hp2 | a0027 | c0053 | t0107 | g0009 | SAS | BEB | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG04115 | hp1 | a0004 | c0006 | t0123 | g0003 | SAS | STU | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG04115 | hp2 | a0004 | c0006 | t0065 | g0208 | SAS | STU | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG04204 | hp1 | a0039 | c0062 | t0010 | g0165 | SAS | STU | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG04204 | hp2 | a0004 | c0006 | t0125 | g0048 | SAS | STU | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| NA18522 | hp1 | a0037 | c0074 | t0037 | g0203 | AFR | YRI | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| NA18522 | hp2 | a0001 | c0011 | t0106 | g0085 | AFR | YRI | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| NA18747 | hp1 | a0003 | c0004 | t0105 | g0081 | EAS | CHB | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| NA18747 | hp2 | a0030 | c0047 | t0131 | g0067 | EAS | CHB | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| NA18906 | hp1 | a0014 | c0027 | t0049 | g0171 | AFR | YRI | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| NA18906 | hp2 | a0013 | c0020 | t0052 | g0183 | AFR | YRI | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| NA18947 | hp2 | a0003 | c0004 | t0108 | g0010 | EAS | JPT | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| NA18954 | hp1 | a0002 | c0005 | t0075 | g0076 | EAS | JPT | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| NA18954 | hp2 | a0002 | c0005 | t0002 | g0064 | EAS | JPT | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| NA18957 | hp1 | a0001 | c0001 | t0015 | g0131 | EAS | JPT | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| NA18957 | hp2 | a0001 | c0002 | t0086 | g0104 | EAS | JPT | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| NA18970 | hp1 | a0007 | c0010 | t0005 | g0113 | EAS | JPT | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| NA18970 | hp2 | a0004 | c0054 | t0034 | g0139 | EAS | JPT | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| NA18971 | hp1 | a0005 | c0008 | t0111 | g0091 | EAS | JPT | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| NA18971 | hp2 | a0002 | c0003 | t0071 | g0095 | EAS | JPT | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| NA18973 | hp1 | a0012 | c0013 | t0009 | g0016 | EAS | JPT | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| NA18977 | hp1 | a0034 | c0059 | t0001 | g0114 | EAS | JPT | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| NA18977 | hp2 | a0003 | c0044 | t0001 | g0116 | EAS | JPT | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| NA18979 | hp1 | a0012 | c0013 | t0009 | g0019 | EAS | JPT | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| NA18979 | hp2 | a0003 | c0004 | t0016 | g0133 | EAS | JPT | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| NA18983 | hp1 | a0003 | c0004 | t0007 | g0097 | EAS | JPT | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| NA18983 | hp2 | a0001 | c0002 | t0082 | g0126 | EAS | JPT | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| NA18984 | hp1 | a0018 | c0022 | t0011 | g0195 | EAS | JPT | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| NA18984 | hp2 | a0001 | c0002 | t0025 | g0073 | EAS | JPT | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| NA18995 | hp1 | a0001 | c0001 | t0093 | g0105 | EAS | JPT | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| NA18995 | hp2 | a0007 | c0010 | t0095 | g0106 | EAS | JPT | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| NA19007 | hp1 | a0001 | c0002 | t0087 | g0040 | EAS | JPT | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| NA19012 | hp1 | a0010 | c0014 | t0057 | g0197 | EAS | JPT | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| NA19012 | hp2 | a0001 | c0002 | t0007 | g0083 | EAS | JPT | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| NA19030 | hp1 | a0014 | c0065 | t0038 | g0166 | AFR | LWK | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| NA19030 | hp2 | a0029 | c0033 | t0042 | g0163 | AFR | LWK | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| NA19043 | hp1 | a0017 | c0029 | t0112 | g0155 | AFR | LWK | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| NA19043 | hp2 | a0008 | c0025 | t0069 | g0174 | AFR | LWK | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| NA19056 | hp1 | a0002 | c0005 | t0072 | g0153 | EAS | JPT | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| NA19066 | hp1 | a0002 | c0005 | t0003 | g0096 | EAS | JPT | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| NA19066 | hp2 | a0003 | c0017 | t0016 | g0110 | EAS | JPT | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| NA19068 | hp1 | a0012 | c0013 | t0133 | g0118 | EAS | JPT | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| NA19068 | hp2 | a0001 | c0001 | t0098 | g0129 | EAS | JPT | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| NA19084 | hp2 | a0001 | c0001 | t0014 | g0125 | EAS | JPT | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| NA19088 | hp1 | a0003 | c0004 | t0016 | g0078 | EAS | JPT | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| NA19088 | hp2 | a0002 | c0057 | t0003 | g0026 | EAS | JPT | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| NA20129 | hp1 | a0003 | c0004 | t0117 | g0070 | AFR | ASW | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| NA20129 | hp2 | a0001 | c0007 | t0008 | g0150 | AFR | ASW | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG01123 | hp1 | a0002 | c0003 | t0132 | g0028 | AMR | CLM | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG01123 | hp2 | a0003 | c0004 | t0004 | g0036 | AMR | CLM | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG02109 | hp1 | a0001 | c0001 | t0032 | g0144 | AFR | ACB | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG02109 | hp2 | a0008 | c0024 | t0021 | g0175 | AFR | ACB | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG02486 | hp1 | a0008 | c0025 | t0045 | g0172 | AFR | ACB | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG02486 | hp2 | a0038 | c0080 | t0043 | g0177 | AFR | ACB | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG03471 | hp1 | a0001 | c0035 | t0030 | g0137 | AFR | MSL | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG03471 | hp2 | a0008 | c0079 | t0068 | g0173 | AFR | MSL | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG06807 | hp1 | a0001 | c0036 | t0077 | g0149 | AFR | USA | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| HG06807 | hp2 | a0001 | c0002 | t0024 | g0024 | AFR | USA | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| NA20300 | hp1 | a0005 | c0008 | t0023 | g0062 | AFR | USA | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| NA20300 | hp2 | a0001 | c0007 | t0008 | g0146 | AFR | USA | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| homoSapiens_chm13v2 | hp1 | a0004 | c0006 | t0134 | g0011 | REF | REF | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| homoSapiens_grch38 | hp1 | a0007 | c0010 | t0026 | g0168 | REF | REF | PLEKHG4B_chr5_87168_194966 | PLEKHG4B | chr5 | 87168 | 194966 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:113285
|
C | T | 1 | a0020 | 1 | HG03486.hp1 | missense_variant | MODERATE | c.80C>T | p.Thr27Met | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/20 | 144/12591 | 80/4884 | 27/1627 | chr5 | 113285 | ||
| chr5:113350
|
G | A | 1 | a0021 | 1 | HG02818.hp2 | missense_variant | MODERATE | c.145G>A | p.Val49Met | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/20 | 209/12591 | 145/4884 | 49/1627 | chr5 | 113350 | ||
| chr5:139610
|
C | T | 2 | a0011a0015 | 5 | HG01099.hp1 HG02257.hp1 HG02280.hp1 others(2): Show |
missense_variant | MODERATE | c.371C>T | p.Thr124Met | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/20 | 435/12591 | 371/4884 | 124/1627 | chr5 | 139610 | ||
| chr5:139868
|
G | C | 16 | a0006a0008a0010others(13): Show | 38 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(35): Show |
missense_variant | MODERATE | c.629G>C | p.Ser210Thr | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/20 | 693/12591 | 629/4884 | 210/1627 | chr5 | 139868 | ||
| chr5:140009
|
A | G | 18 | a0006a0008a0010others(15): Show | 40 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(37): Show |
missense_variant | MODERATE | c.770A>G | p.His257Arg | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/20 | 834/12591 | 770/4884 | 257/1627 | chr5 | 140009 | ||
| chr5:140149
|
A | G | 1 | a0016 | 2 | HG02145.hp1 HG03579.hp1 |
missense_variant | MODERATE | c.910A>G | p.Asn304Asp | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/20 | 974/12591 | 910/4884 | 304/1627 | chr5 | 140149 | ||
| chr5:140149
|
A | T | 1 | a0034 | 1 | NA18977.hp1 | missense_variant | MODERATE | c.910A>T | p.Asn304Tyr | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/20 | 974/12591 | 910/4884 | 304/1627 | chr5 | 140149 | ||
| chr5:140417
|
T | C | 18 | a0006a0008a0010others(15): Show | 40 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(37): Show |
missense_variant | MODERATE | c.1178T>C | p.Val393Ala | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/20 | 1242/12591 | 1178/4884 | 393/1627 | chr5 | 140417 | ||
| chr5:140521
|
G | A | 4 | a0019a0039a0040others(1): Show | 5 | HG00280.hp2 HG00323.hp2 HG01081.hp2 others(2): Show |
missense_variant | MODERATE | c.1282G>A | p.Ala428Thr | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/20 | 1346/12591 | 1282/4884 | 428/1627 | chr5 | 140521 | ||
| chr5:140698
|
G | T | 5 | a0006a0010a0018others(2): Show | 15 | HG00597.hp2 HG01261.hp2 HG02258.hp2 others(12): Show |
missense_variant | MODERATE | c.1459G>T | p.Gly487Cys | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/20 | 1523/12591 | 1459/4884 | 487/1627 | chr5 | 140698 | ||
| chr5:143082
|
G | A | 14 | a0006a0008a0010others(11): Show | 31 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(28): Show |
missense_variant | MODERATE | c.1513G>A | p.Gly505Ser | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 4/20 | 1577/12591 | 1513/4884 | 505/1627 | chr5 | 143082 | ||
| chr5:143142
|
C | T | 1 | a0041 | 1 | HG01081.hp2 | missense_variant | MODERATE | c.1573C>T | p.His525Tyr | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 4/20 | 1637/12591 | 1573/4884 | 525/1627 | chr5 | 143142 | ||
| chr5:143244
|
G | A | 1 | a0008 | 5 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(2): Show |
missense_variant | MODERATE | c.1675G>A | p.Val559Ile | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 4/20 | 1739/12591 | 1675/4884 | 559/1627 | chr5 | 143244 | ||
| chr5:143419
|
G | A | 17 | a0006a0008a0010others(14): Show | 39 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(36): Show |
missense_variant | MODERATE | c.1727G>A | p.Arg576His | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 5/20 | 1791/12591 | 1727/4884 | 576/1627 | chr5 | 143419 | ||
| chr5:155361
|
C | T | 1 | a0037 | 1 | NA18522.hp1 | missense_variant | MODERATE | c.2126C>T | p.Ala709Val | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 9/20 | 2190/12591 | 2126/4884 | 709/1627 | chr5 | 155361 | ||
| chr5:156093
|
A | G | 1 | a0035 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.2231A>G | p.Gln744Arg | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 10/20 | 2295/12591 | 2231/4884 | 744/1627 | chr5 | 156093 | ||
| chr5:156787
|
C | T | 1 | a0040 | 1 | HG00280.hp2 | missense_variant | MODERATE | c.2363C>T | p.Ala788Val | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/20 | 2427/12591 | 2363/4884 | 788/1627 | chr5 | 156787 | ||
| chr5:161808
|
T | A | 1 | a0033 | 1 | HG00673.hp2 | missense_variant | MODERATE | c.2513T>A | p.Leu838Gln | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 12/20 | 2577/12591 | 2513/4884 | 838/1627 | chr5 | 161808 | ||
| chr5:161808
|
T | C | 2 | a0017a0032 | 3 | HG02622.hp2 HG02809.hp2 NA19043.hp1 |
missense_variant | MODERATE | c.2513T>C | p.Leu838Pro | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 12/20 | 2577/12591 | 2513/4884 | 838/1627 | chr5 | 161808 | ||
| chr5:161930
|
G | A | 1 | a0031 | 1 | HG00597.hp1 | missense_variant | MODERATE | c.2635G>A | p.Glu879Lys | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 12/20 | 2699/12591 | 2635/4884 | 879/1627 | chr5 | 161930 | ||
| chr5:163103
|
G | A | 1 | a0030 | 1 | NA18747.hp2 | missense_variant | MODERATE | c.3031G>A | p.Gly1011Ser | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/20 | 3095/12591 | 3031/4884 | 1011/1627 | chr5 | 163103 | ||
| chr5:163119
|
C | T | 2 | a0005a0031 | 8 | HG00597.hp1 HG00642.hp2 HG01070.hp1 others(5): Show |
missense_variant | MODERATE | c.3047C>T | p.Ala1016Val | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/20 | 3111/12591 | 3047/4884 | 1016/1627 | chr5 | 163119 | ||
| chr5:163145
|
A | C | 38 | a0001a0002a0003others(35): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
missense_variant | MODERATE | c.3073A>C | p.Thr1025Pro | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/20 | 3137/12591 | 3073/4884 | 1025/1627 | chr5 | 163145 | ||
| chr5:163151
|
C | G | 21 | a0003a0004a0006others(18): Show | 72 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(69): Show |
missense_variant | MODERATE | c.3079C>G | p.Arg1027Gly | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/20 | 3143/12591 | 3079/4884 | 1027/1627 | chr5 | 163151 | ||
| chr5:163337
|
C | T | 1 | a0029 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.3265C>T | p.Pro1089Ser | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/20 | 3329/12591 | 3265/4884 | 1089/1627 | chr5 | 163337 | ||
| chr5:163503
|
C | T | 1 | a0022 | 1 | HG02818.hp1 | missense_variant | MODERATE | c.3431C>T | p.Ser1144Leu | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/20 | 3495/12591 | 3431/4884 | 1144/1627 | chr5 | 163503 | ||
| chr5:163509
|
T | C | 5 | a0009a0011a0015others(2): Show | 11 | HG01099.hp1 HG02257.hp1 HG02280.hp1 others(8): Show |
missense_variant | MODERATE | c.3437T>C | p.Leu1146Pro | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/20 | 3501/12591 | 3437/4884 | 1146/1627 | chr5 | 163509 | ||
| chr5:169465
|
G | A | 1 | a0038 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.3602G>A | p.Arg1201Gln | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 14/20 | 3666/12591 | 3602/4884 | 1201/1627 | chr5 | 169465 | ||
| chr5:169474
|
A | G | 1 | a0025 | 1 | HG03669.hp2 | missense_variant | MODERATE | c.3611A>G | p.His1204Arg | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 14/20 | 3675/12591 | 3611/4884 | 1204/1627 | chr5 | 169474 | ||
| chr5:171305
|
A | G | 1 | a0027 | 1 | HG03831.hp2 | missense_variant | MODERATE | c.3911A>G | p.Gln1304Arg | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 16/20 | 3975/12591 | 3911/4884 | 1304/1627 | chr5 | 171305 | ||
| chr5:173988
|
G | A | 1 | a0023 | 1 | HG02273.hp1 | missense_variant | MODERATE | c.4292G>A | p.Arg1431Gln | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/20 | 4356/12591 | 4292/4884 | 1431/1627 | chr5 | 173988 | ||
| chr5:173991
|
G | A | 7 | a0002a0004a0012others(4): Show | 42 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(39): Show |
missense_variant | MODERATE | c.4295G>A | p.Arg1432Gln | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/20 | 4359/12591 | 4295/4884 | 1432/1627 | chr5 | 173991 | ||
| chr5:181615
|
C | G | 7 | a0002a0004a0012others(4): Show | 43 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(40): Show |
missense_variant | MODERATE | c.4504C>G | p.Arg1502Gly | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 19/20 | 4568/12591 | 4504/4884 | 1502/1627 | chr5 | 181615 | ||
| chr5:182139
|
G | T | 1 | a0026 | 1 | HG01175.hp1 | missense_variant | MODERATE | c.4700G>T | p.Gly1567Val | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 4764/12591 | 4700/4884 | 1567/1627 | chr5 | 182139 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:113307
|
G | A | 2 | a0014c0027a0021c0026 | 2 | HG02818.hp2 NA18906.hp1 |
synonymous_variant | LOW | c.102G>A | p.Pro34Pro | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/20 | 166/12591 | 102/4884 | 34/1627 | chr5 | 113307 | ||
| chr5:113376
|
C | T | 4 | a0008c0024a0008c0025a0008c0079others(1): Show | 6 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(3): Show |
synonymous_variant | LOW | c.171C>T | p.Asp57Asp | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/20 | 235/12591 | 171/4884 | 57/1627 | chr5 | 113376 | ||
| chr5:139587
|
C | T | 30 | a0006c0021a0006c0068a0006c0070others(27): Show | 39 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(36): Show |
synonymous_variant | LOW | c.348C>T | p.Pro116Pro | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/20 | 412/12591 | 348/4884 | 116/1627 | chr5 | 139587 | ||
| chr5:139728
|
C | T | 1 | a0001c0061 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.489C>T | p.Phe163Phe | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/20 | 553/12591 | 489/4884 | 163/1627 | chr5 | 139728 | ||
| chr5:139740
|
G | A | 30 | a0006c0021a0006c0068a0006c0070others(27): Show | 39 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(36): Show |
synonymous_variant | LOW | c.501G>A | p.Val167Val | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/20 | 565/12591 | 501/4884 | 167/1627 | chr5 | 139740 | ||
| chr5:140238
|
G | A | 1 | a0036c0075 | 1 | HG03225.hp1 | synonymous_variant | LOW | c.999G>A | p.Pro333Pro | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/20 | 1063/12591 | 999/4884 | 333/1627 | chr5 | 140238 | ||
| chr5:140673
|
A | G | 29 | a0006c0021a0006c0068a0006c0070others(26): Show | 38 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(35): Show |
synonymous_variant | LOW | c.1434A>G | p.Pro478Pro | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/20 | 1498/12591 | 1434/4884 | 478/1627 | chr5 | 140673 | ||
| chr5:143120
|
C | T | 1 | a0032c0058 | 1 | HG02809.hp2 | synonymous_variant | LOW | c.1551C>T | p.Ser517Ser | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 4/20 | 1615/12591 | 1551/4884 | 517/1627 | chr5 | 143120 | ||
| chr5:156172
|
G | A | 29 | a0006c0021a0006c0068a0006c0070others(26): Show | 38 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(35): Show |
synonymous_variant | LOW | c.2310G>A | p.Ala770Ala | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 10/20 | 2374/12591 | 2310/4884 | 770/1627 | chr5 | 156172 | ||
| chr5:156803
|
C | T | 1 | a0002c0057 | 1 | NA19088.hp2 | synonymous_variant | LOW | c.2379C>T | p.Tyr793Tyr | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/20 | 2443/12591 | 2379/4884 | 793/1627 | chr5 | 156803 | ||
| chr5:161869
|
C | T | 1 | a0003c0056 | 1 | HG02683.hp1 | synonymous_variant | LOW | c.2574C>T | p.Ser858Ser | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 12/20 | 2638/12591 | 2574/4884 | 858/1627 | chr5 | 161869 | ||
| chr5:162814
|
G | C | 10 | a0001c0032a0001c0035a0001c0036others(7): Show | 11 | HG02257.hp1 HG02647.hp1 HG03041.hp1 others(8): Show |
synonymous_variant | LOW | c.2742G>C | p.Ser914Ser | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/20 | 2806/12591 | 2742/4884 | 914/1627 | chr5 | 162814 | ||
| chr5:162994
|
C | T | 1 | a0037c0074 | 1 | NA18522.hp1 | synonymous_variant | LOW | c.2922C>T | p.Pro974Pro | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/20 | 2986/12591 | 2922/4884 | 974/1627 | chr5 | 162994 | ||
| chr5:163060
|
G | A | 3 | a0001c0011a0001c0032a0001c0037 | 5 | HG02280.hp2 HG02647.hp2 HG03098.hp1 others(2): Show |
synonymous_variant | LOW | c.2988G>A | p.Thr996Thr | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/20 | 3052/12591 | 2988/4884 | 996/1627 | chr5 | 163060 | ||
| chr5:163090
|
G | C | 56 | a0001c0002a0001c0007a0001c0015others(53): Show | 126 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(123): Show |
synonymous_variant | LOW | c.3018G>C | p.Ala1006Ala | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/20 | 3082/12591 | 3018/4884 | 1006/1627 | chr5 | 163090 | ||
| chr5:163381
|
T | C | 1 | a0004c0041 | 1 | HG03017.hp1 | synonymous_variant | LOW | c.3309T>C | p.His1103His | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/20 | 3373/12591 | 3309/4884 | 1103/1627 | chr5 | 163381 | ||
| chr5:163471
|
G | A | 1 | a0001c0048 | 1 | HG01255.hp1 | synonymous_variant | LOW | c.3399G>A | p.Pro1133Pro | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/20 | 3463/12591 | 3399/4884 | 1133/1627 | chr5 | 163471 | ||
| chr5:163507
|
G | A | 16 | a0001c0007a0001c0035a0001c0049others(13): Show | 27 | HG00597.hp2 HG01928.hp2 HG02257.hp2 others(24): Show |
synonymous_variant | LOW | c.3435G>A | p.Gly1145Gly | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/20 | 3499/12591 | 3435/4884 | 1145/1627 | chr5 | 163507 | ||
| chr5:169397
|
G | A | 4 | a0001c0016a0001c0035a0001c0049others(1): Show | 5 | HG02717.hp1 HG02922.hp1 HG03453.hp1 others(2): Show |
synonymous_variant | LOW | c.3534G>A | p.Arg1178Arg | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 14/20 | 3598/12591 | 3534/4884 | 1178/1627 | chr5 | 169397 | ||
| chr5:171378
|
C | T | 2 | a0003c0044a0034c0059 | 2 | NA18977.hp1 NA18977.hp2 |
synonymous_variant | LOW | c.3984C>T | p.Val1328Val | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 16/20 | 4048/12591 | 3984/4884 | 1328/1627 | chr5 | 171378 | ||
| chr5:181545
|
T | G | 32 | a0001c0015a0001c0036a0001c0051others(29): Show | 69 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(66): Show |
synonymous_variant | LOW | c.4434T>G | p.Gly1478Gly | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 19/20 | 4498/12591 | 4434/4884 | 1478/1627 | chr5 | 181545 | ||
| chr5:181629
|
T | C | 3 | a0009c0012a0009c0034a0011c0078 | 5 | HG01099.hp1 HG02886.hp2 HG03139.hp2 others(2): Show |
synonymous_variant | LOW | c.4518T>C | p.Cys1506Cys | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 19/20 | 4582/12591 | 4518/4884 | 1506/1627 | chr5 | 181629 | ||
| chr5:181647
|
A | G | 32 | a0001c0015a0001c0036a0001c0037others(29): Show | 69 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(66): Show |
synonymous_variant | LOW | c.4536A>G | p.Arg1512Arg | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 19/20 | 4600/12591 | 4536/4884 | 1512/1627 | chr5 | 181647 | ||
| chr5:182152
|
C | T | 1 | a0006c0071 | 1 | HG02922.hp2 | synonymous_variant | LOW | c.4713C>T | p.Ser1571Ser | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 4777/12591 | 4713/4884 | 1571/1627 | chr5 | 182152 | ||
| chr5:182176
|
A | G | 7 | a0001c0052a0003c0009a0003c0056others(4): Show | 12 | HG00280.hp2 HG00323.hp2 HG00741.hp1 others(9): Show |
synonymous_variant | LOW | c.4737A>G | p.Leu1579Leu | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 4801/12591 | 4737/4884 | 1579/1627 | chr5 | 182176 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:92191
|
G | A | 1 | a0001c0015t0035 | 1 | HG03195.hp1 | 5_prime_UTR_variant | MODIFIER | c.-41G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/20 | 41 | chr5 | 92191 | |||||
| chr5:92226
|
T | G | 46 | a0001c0011t0048a0002c0003t0011a0002c0003t0066others(43): Show | 48 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(45): Show |
5_prime_UTR_variant | MODIFIER | c.-6T>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/20 | 6 | chr5 | 92226 | |||||
| chr5:182382
|
G | A | 2 | a0006c0072t0036a0037c0074t0037 | 2 | HG02897.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*59G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 59 | chr5 | 182382 | |||||
| chr5:182472
|
C | A | 3 | a0002c0003t0071a0002c0005t0070a0002c0005t0072 | 3 | HG01192.hp1 NA18971.hp2 NA19056.hp1 |
3_prime_UTR_variant | MODIFIER | c.*149C>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 149 | chr5 | 182472 | |||||
| chr5:182715
|
C | A | 2 | a0001c0001t0073a0003c0017t0074 | 2 | HG00738.hp2 HG01069.hp2 |
3_prime_UTR_variant | MODIFIER | c.*392C>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 392 | chr5 | 182715 | |||||
| chr5:182812
|
A | C | 2 | a0008c0025t0069a0008c0079t0068 | 2 | HG03471.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*489A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 489 | chr5 | 182812 | |||||
| chr5:182906
|
G | A | 1 | a0002c0005t0075 | 1 | NA18954.hp1 | 3_prime_UTR_variant | MODIFIER | c.*583G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 583 | chr5 | 182906 | |||||
| chr5:182932
|
C | T | 1 | a0015c0076t0067 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*609C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 609 | chr5 | 182932 | |||||
| chr5:183008
|
G | C | 7 | a0001c0015t0035a0001c0015t0076a0001c0036t0077others(4): Show | 7 | HG02622.hp2 HG02809.hp2 HG02886.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*685G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 685 | chr5 | 183008 | |||||
| chr5:183019
|
A | G | 35 | a0002c0003t0002a0002c0003t0011a0002c0003t0066others(32): Show | 43 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*696A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 696 | chr5 | 183019 | |||||
| chr5:183089
|
C | G | 1 | a0020c0081t0064 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*766C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 766 | chr5 | 183089 | |||||
| chr5:183178
|
C | T | 1 | a0002c0003t0136 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*855C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 855 | chr5 | 183178 | |||||
| chr5:183213
|
TCAAAC | T | 2 | a0008c0024t0021a0020c0081t0064 | 3 | HG02109.hp2 HG02145.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*893_*897delAACCA | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 893 | INFO_REALIGN_3_PRIME | chr5 | 183213 | ||||
| chr5:183286
|
A | G | 57 | a0001c0015t0035a0001c0015t0076a0001c0036t0077others(54): Show | 67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*963A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 963 | chr5 | 183286 | |||||
| chr5:183401
|
A | G | 57 | a0001c0015t0035a0001c0015t0076a0001c0036t0077others(54): Show | 67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*1078A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 1078 | chr5 | 183401 | |||||
| chr5:183514
|
C | T | 3 | a0002c0003t0135a0017c0030t0039a0032c0058t0040 | 3 | HG02622.hp2 HG02809.hp2 HG03669.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1191C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 1191 | chr5 | 183514 | |||||
| chr5:183566
|
C | T | 2 | a0006c0073t0020a0035c0060t0020 | 2 | HG01261.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1243C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 1243 | chr5 | 183566 | |||||
| chr5:183654
|
A | G | 2 | a0003c0004t0116a0003c0004t0117 | 2 | HG03540.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1331A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 1331 | chr5 | 183654 | |||||
| chr5:183668
|
C | T | 7 | a0001c0015t0035a0001c0015t0076a0001c0036t0077others(4): Show | 7 | HG02622.hp2 HG02809.hp2 HG02886.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1345C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 1345 | chr5 | 183668 | |||||
| chr5:183709
|
C | A | 8 | a0001c0015t0035a0001c0015t0076a0001c0036t0077others(5): Show | 8 | HG02622.hp2 HG02809.hp2 HG02886.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1386C>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 1386 | chr5 | 183709 | |||||
| chr5:183720
|
G | C | 7 | a0001c0015t0035a0001c0015t0076a0001c0036t0077others(4): Show | 7 | HG02622.hp2 HG02809.hp2 HG02886.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1397G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 1397 | chr5 | 183720 | |||||
| chr5:183970
|
C | CAGAT | 2 | a0004c0006t0134a0011c0023t0041 | 2 | HG02622.hp1 homoSapiens_chm13v2.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1664_*1667dupAGAT | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 1668 | INFO_REALIGN_3_PRIME | chr5 | 183970 | ||||
| chr5:183970
|
C | T | 1 | a0021c0026t0060 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1647C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 1647 | chr5 | 183970 | |||||
| chr5:183970
|
CAGATAGA others(17): Show |
C | 1 | a0036c0075t0061 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1668_*1691delCGAT others(20): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 1668 | INFO_REALIGN_3_PRIME | chr5 | 183970 | ||||
| chr5:183970
|
CAGATAGA others(25): Show |
C | 7 | a0001c0015t0035a0001c0015t0076a0001c0036t0077others(4): Show | 7 | HG02622.hp2 HG02809.hp2 HG02886.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1668_*1699delCGAT others(28): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 1668 | INFO_REALIGN_3_PRIME | chr5 | 183970 | ||||
| chr5:183971
|
AGATAGAT others(13): Show |
A | 1 | a0004c0006t0123 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1668_*1687delCGAT others(16): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 1668 | INFO_REALIGN_3_PRIME | chr5 | 183971 | ||||
| chr5:183975
|
AGATAGAT others(9): Show |
A | 3 | a0002c0003t0124a0004c0054t0034a0016c0018t0034 | 3 | HG01106.hp2 HG03579.hp1 NA18970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1668_*1683delCGAT others(12): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 1668 | INFO_REALIGN_3_PRIME | chr5 | 183975 | ||||
| chr5:183979
|
AGATAGAT others(5): Show |
A | 8 | a0001c0052t0118a0002c0003t0002a0002c0005t0002others(5): Show | 12 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1668_*1679delCGAT others(8): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 1668 | INFO_REALIGN_3_PRIME | chr5 | 183979 | ||||
| chr5:183983
|
AGATAGAT others(1): Show |
A | 15 | a0002c0003t0011a0002c0003t0128a0002c0003t0130others(12): Show | 18 | HG00140.hp2 HG00597.hp2 HG00639.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1668_*1675delCGAT others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 1668 | INFO_REALIGN_3_PRIME | chr5 | 183983 | ||||
| chr5:183987
|
A | AGATCGAT others(1): Show |
4 | a0006c0073t0020a0010c0014t0057a0011c0078t0059others(1): Show | 4 | HG01099.hp1 HG01261.hp2 HG03098.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1671_*1672insCGAT others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 1672 | INFO_REALIGN_3_PRIME | chr5 | 183987 | ||||
| chr5:183987
|
AGATC | A | 15 | a0001c0001t0079a0002c0003t0066a0002c0003t0071others(12): Show | 16 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1668_*1671delCGAT | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 1668 | INFO_REALIGN_3_PRIME | chr5 | 183987 | ||||
| chr5:183991
|
C | A | 10 | a0001c0002t0022a0002c0003t0135a0002c0005t0072others(7): Show | 13 | HG00741.hp2 HG01243.hp1 HG01256.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1668C>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 1668 | chr5 | 183991 | |||||
| chr5:183991
|
C | CGATA | 25 | a0001c0001t0001a0001c0001t0005a0001c0001t0014others(22): Show | 36 | HG00140.hp1 HG00438.hp2 HG00642.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*1703_*1706dupTAGA | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 1707 | INFO_REALIGN_3_PRIME | chr5 | 183991 | ||||
| chr5:183991
|
C | CGATAGAT others(1): Show |
23 | a0001c0001t0006a0001c0001t0007a0001c0001t0097others(20): Show | 25 | HG00099.hp1 HG00280.hp1 HG02132.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1699_*1706dupTAGA others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 1707 | INFO_REALIGN_3_PRIME | chr5 | 183991 | ||||
| chr5:183991
|
C | CGATAGAT others(5): Show |
11 | a0001c0001t0030a0001c0001t0031a0001c0001t0104others(8): Show | 12 | HG00323.hp1 HG00438.hp1 HG01069.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1695_*1706dupTAGA others(8): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 1707 | INFO_REALIGN_3_PRIME | chr5 | 183991 | ||||
| chr5:183991
|
C | CGATAGAT others(9): Show |
2 | a0003c0004t0108a0013c0020t0052 | 2 | NA18906.hp2 NA18947.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1691_*1706dupTAGA others(12): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 1707 | INFO_REALIGN_3_PRIME | chr5 | 183991 | ||||
| chr5:183991
|
C | CGATCGAT others(1): Show |
7 | a0001c0007t0109a0001c0007t0110a0003c0004t0117others(4): Show | 7 | HG02717.hp2 HG02723.hp1 HG02896.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1671_*1672insCGAT others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 1672 | INFO_REALIGN_3_PRIME | chr5 | 183991 | ||||
| chr5:183991
|
C | CGATCGAT others(5): Show |
5 | a0001c0001t0032a0001c0007t0008a0006c0021t0018others(2): Show | 9 | HG02109.hp1 HG02451.hp2 HG02896.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1671_*1672insCGAT others(8): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 1672 | INFO_REALIGN_3_PRIME | chr5 | 183991 | ||||
| chr5:183991
|
C | CGATCGAT others(13): Show |
3 | a0006c0021t0056a0010c0014t0019a0010c0069t0019 | 3 | HG02258.hp2 HG03041.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1671_*1672insCGAT others(16): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 1672 | INFO_REALIGN_3_PRIME | chr5 | 183991 | ||||
| chr5:183991
|
C | CGATCGAT others(5): Show |
2 | a0008c0025t0069a0008c0079t0068 | 2 | HG03471.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1671_*1672insCGAT others(8): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 1672 | INFO_REALIGN_3_PRIME | chr5 | 183991 | ||||
| chr5:183991
|
C | CGATCGAT others(9): Show |
5 | a0001c0001t0113a0006c0068t0058a0009c0012t0033others(2): Show | 5 | HG00735.hp1 HG02647.hp1 HG03209.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1671_*1672insCGAT others(12): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 1672 | INFO_REALIGN_3_PRIME | chr5 | 183991 | ||||
| chr5:183991
|
C | CGATCGAT others(13): Show |
2 | a0009c0012t0114a0009c0012t0115 | 2 | HG02886.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1671_*1672insCGAT others(16): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 1672 | INFO_REALIGN_3_PRIME | chr5 | 183991 | ||||
| chr5:183991
|
CGATA | C | 14 | a0001c0001t0004a0001c0001t0012a0001c0001t0024others(11): Show | 18 | HG00642.hp2 HG00733.hp2 HG01070.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1703_*1706delTAGA | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 1703 | INFO_REALIGN_3_PRIME | chr5 | 183991 | ||||
| chr5:183995
|
A | C | 2 | a0006c0073t0020a0035c0060t0020 | 2 | HG01261.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1672A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 1672 | chr5 | 183995 | |||||
| chr5:183999
|
A | C | 2 | a0006c0073t0020a0035c0060t0020 | 2 | HG01261.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1676A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 1676 | chr5 | 183999 | |||||
| chr5:184003
|
A | C | 3 | a0001c0002t0022a0006c0073t0020a0035c0060t0020 | 4 | HG00741.hp2 HG01261.hp2 HG01978.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1680A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 1680 | chr5 | 184003 | |||||
| chr5:184023
|
A | AGAT | 5 | a0009c0012t0033a0009c0012t0114a0009c0012t0115others(2): Show | 5 | HG01099.hp1 HG02886.hp2 HG03139.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1701_*1703dupGAT | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 1704 | INFO_REALIGN_3_PRIME | chr5 | 184023 | ||||
| chr5:184153
|
G | T | 1 | a0014c0065t0038 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1830G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 1830 | chr5 | 184153 | |||||
| chr5:184221
|
G | A | 89 | a0001c0001t0032a0001c0001t0113a0001c0007t0008others(86): Show | 103 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*1898G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 1898 | chr5 | 184221 | |||||
| chr5:184278
|
C | T | 56 | a0001c0015t0035a0001c0015t0076a0001c0036t0077others(53): Show | 66 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*1955C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 1955 | chr5 | 184278 | |||||
| chr5:184329
|
C | T | 1 | a0020c0081t0064 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2006C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 2006 | chr5 | 184329 | |||||
| chr5:184545
|
G | C | 1 | a0036c0075t0061 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2222G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 2222 | chr5 | 184545 | |||||
| chr5:184587
|
A | G | 48 | a0001c0052t0118a0002c0003t0002a0002c0003t0011others(45): Show | 58 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*2264A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 2264 | chr5 | 184587 | |||||
| chr5:184635
|
A | G | 51 | a0001c0052t0118a0002c0003t0002a0002c0003t0011others(48): Show | 61 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*2312A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 2312 | chr5 | 184635 | |||||
| chr5:184645
|
A | G | 51 | a0001c0052t0118a0002c0003t0002a0002c0003t0011others(48): Show | 61 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*2322A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 2322 | chr5 | 184645 | |||||
| chr5:184744
|
G | A | 3 | a0011c0023t0041a0011c0023t0044a0015c0076t0067 | 3 | HG02257.hp1 HG02280.hp1 HG02622.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2421G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 2421 | chr5 | 184744 | |||||
| chr5:184801
|
CACTTG | C | 94 | a0001c0001t0032a0001c0001t0113a0001c0007t0008others(91): Show | 108 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*2485_*2489delCTTG others(1): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 2485 | INFO_REALIGN_3_PRIME | chr5 | 184801 | ||||
| chr5:184822
|
C | T | 8 | a0001c0015t0035a0001c0015t0076a0001c0036t0077others(5): Show | 8 | HG02622.hp2 HG02809.hp2 HG02886.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2499C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 2499 | chr5 | 184822 | |||||
| chr5:184879
|
A | C | 1 | a0022c0046t0047 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2556A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 2556 | chr5 | 184879 | |||||
| chr5:184936
|
C | T | 8 | a0001c0015t0035a0001c0015t0076a0001c0036t0077others(5): Show | 8 | HG02622.hp2 HG02809.hp2 HG02886.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2613C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 2613 | chr5 | 184936 | |||||
| chr5:184941
|
A | G | 8 | a0001c0015t0035a0001c0015t0076a0001c0036t0077others(5): Show | 8 | HG02622.hp2 HG02809.hp2 HG02886.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2618A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 2618 | chr5 | 184941 | |||||
| chr5:184977
|
C | T | 49 | a0001c0052t0118a0002c0003t0002a0002c0003t0011others(46): Show | 59 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*2654C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 2654 | chr5 | 184977 | |||||
| chr5:184979
|
C | T | 39 | a0001c0001t0032a0001c0001t0113a0001c0007t0008others(36): Show | 43 | HG00735.hp1 HG01099.hp1 HG01261.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*2656C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 2656 | chr5 | 184979 | |||||
| chr5:185045
|
G | T | 94 | a0001c0001t0032a0001c0001t0113a0001c0007t0008others(91): Show | 108 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*2722G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 2722 | chr5 | 185045 | |||||
| chr5:185050
|
A | G | 1 | a0001c0032t0103 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2727A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 2727 | chr5 | 185050 | |||||
| chr5:185062
|
C | T | 11 | a0001c0052t0118a0003c0009t0017a0003c0009t0119others(8): Show | 12 | HG00280.hp2 HG00323.hp2 HG00741.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2739C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 2739 | chr5 | 185062 | |||||
| chr5:185194
|
G | A | 2 | a0017c0030t0039a0032c0058t0040 | 2 | HG02622.hp2 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2871G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 2871 | chr5 | 185194 | |||||
| chr5:185254
|
G | A | 48 | a0001c0052t0118a0002c0003t0002a0002c0003t0011others(45): Show | 58 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*2931G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 2931 | chr5 | 185254 | |||||
| chr5:185303
|
C | T | 3 | a0001c0001t0012a0001c0002t0012a0003c0004t0084 | 4 | HG00733.hp2 HG01074.hp2 HG01106.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2980C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 2980 | chr5 | 185303 | |||||
| chr5:185358
|
C | T | 3 | a0011c0023t0041a0011c0023t0044a0015c0076t0067 | 3 | HG02257.hp1 HG02280.hp1 HG02622.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3035C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 3035 | chr5 | 185358 | |||||
| chr5:185366
|
C | T | 2 | a0010c0014t0019a0010c0069t0019 | 2 | HG02258.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3043C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 3043 | chr5 | 185366 | |||||
| chr5:185383
|
C | T | 37 | a0002c0003t0002a0002c0003t0011a0002c0003t0066others(34): Show | 46 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*3060C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 3060 | chr5 | 185383 | |||||
| chr5:185404
|
A | T | 48 | a0001c0052t0118a0002c0003t0002a0002c0003t0011others(45): Show | 58 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*3081A>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 3081 | chr5 | 185404 | |||||
| chr5:185929
|
C | G | 1 | a0001c0001t0079 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3606C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 3606 | chr5 | 185929 | |||||
| chr5:185980
|
T | C | 55 | a0001c0015t0035a0001c0015t0076a0001c0036t0077others(52): Show | 65 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*3657T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 3657 | chr5 | 185980 | |||||
| chr5:186004
|
G | A | 1 | a0022c0046t0047 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3681G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 3681 | chr5 | 186004 | |||||
| chr5:186130
|
G | A | 6 | a0003c0004t0116a0003c0004t0117a0008c0025t0045others(3): Show | 6 | HG02451.hp1 HG02486.hp1 HG03041.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3807G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 3807 | chr5 | 186130 | |||||
| chr5:186209
|
G | A | 2 | a0001c0015t0035a0001c0015t0076 | 2 | HG02886.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3886G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 3886 | chr5 | 186209 | |||||
| chr5:186231
|
C | A | 1 | a0003c0004t0084 | 1 | HG01256.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3908C>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 3908 | chr5 | 186231 | |||||
| chr5:186340
|
G | C | 1 | a0029c0033t0042 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4017G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 4017 | chr5 | 186340 | |||||
| chr5:186385
|
C | T | 5 | a0001c0001t0004a0001c0002t0087a0003c0004t0004others(2): Show | 7 | HG00642.hp2 HG01070.hp1 HG01123.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4062C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 4062 | chr5 | 186385 | |||||
| chr5:186488
|
G | A | 7 | a0001c0015t0035a0001c0015t0076a0001c0036t0077others(4): Show | 7 | HG01261.hp2 HG02886.hp1 HG02897.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4165G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 4165 | chr5 | 186488 | |||||
| chr5:186515
|
C | G | 46 | a0001c0001t0031a0001c0001t0102a0001c0015t0035others(43): Show | 56 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*4192C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 4192 | chr5 | 186515 | |||||
| chr5:187103
|
T | C | 37 | a0002c0003t0002a0002c0003t0011a0002c0003t0066others(34): Show | 46 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*4780T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 4780 | chr5 | 187103 | |||||
| chr5:187127
|
A | G | 2 | a0006c0073t0020a0035c0060t0020 | 2 | HG01261.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4804A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 4804 | chr5 | 187127 | |||||
| chr5:187187
|
G | A | 139 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(136): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*4864G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 4864 | chr5 | 187187 | |||||
| chr5:187484
|
C | T | 1 | a0006c0068t0058 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5161C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 5161 | chr5 | 187484 | |||||
| chr5:187485
|
G | A | 1 | a0033c0028t0088 | 1 | HG00673.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5162G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 5162 | chr5 | 187485 | |||||
| chr5:187497
|
C | T | 4 | a0002c0003t0130a0002c0003t0132a0002c0003t0136others(1): Show | 4 | HG00639.hp1 HG01123.hp1 HG03491.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5174C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 5174 | chr5 | 187497 | |||||
| chr5:187602
|
C | T | 50 | a0001c0002t0094a0001c0002t0101a0001c0052t0118others(47): Show | 59 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*5279C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 5279 | chr5 | 187602 | |||||
| chr5:187732
|
C | T | 1 | a0014c0065t0038 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5409C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 5409 | chr5 | 187732 | |||||
| chr5:187773
|
C | A | 86 | a0001c0001t0032a0001c0001t0079a0001c0001t0113others(83): Show | 100 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*5450C>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 5450 | chr5 | 187773 | |||||
| chr5:187780
|
G | A | 2 | a0014c0027t0049a0014c0066t0051 | 2 | HG02809.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5457G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 5457 | chr5 | 187780 | |||||
| chr5:187820
|
C | G | 1 | a0002c0003t0135 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5497C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 5497 | chr5 | 187820 | |||||
| chr5:187838
|
C | T | 1 | a0001c0001t0015 | 3 | HG01099.hp2 HG02300.hp1 NA18957.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5515C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 5515 | chr5 | 187838 | |||||
| chr5:187901
|
G | A | 3 | a0014c0027t0049a0014c0066t0051a0021c0026t0060 | 3 | HG02809.hp1 HG02818.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5578G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 5578 | chr5 | 187901 | |||||
| chr5:187909
|
G | A | 1 | a0004c0043t0126 | 1 | HG01261.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5586G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 5586 | chr5 | 187909 | |||||
| chr5:188020
|
G | A | 1 | a0002c0005t0075 | 1 | NA18954.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5697G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 5697 | chr5 | 188020 | |||||
| chr5:188025
|
C | T | 1 | a0001c0001t0093 | 1 | NA18995.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5702C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 5702 | chr5 | 188025 | |||||
| chr5:188101
|
C | T | 3 | a0001c0001t0079a0001c0036t0077a0001c0051t0078 | 3 | HG03139.hp1 HG03225.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5778C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 5778 | chr5 | 188101 | |||||
| chr5:188137
|
G | A | 2 | a0019c0019t0062a0040c0063t0063 | 2 | HG00280.hp2 HG02004.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5814G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 5814 | chr5 | 188137 | |||||
| chr5:188198
|
C | G | 1 | a0005c0008t0111 | 1 | NA18971.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5875C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 5875 | chr5 | 188198 | |||||
| chr5:188206
|
G | C | 116 | a0001c0001t0004a0001c0001t0012a0001c0001t0027others(113): Show | 137 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*5883G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 5883 | chr5 | 188206 | |||||
| chr5:188215
|
A | G | 115 | a0001c0001t0004a0001c0001t0027a0001c0001t0028others(112): Show | 135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*5892A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 5892 | chr5 | 188215 | |||||
| chr5:188265
|
T | C | 23 | a0001c0001t0032a0001c0001t0091a0001c0007t0008others(20): Show | 27 | HG02109.hp1 HG02258.hp2 HG02273.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*5942T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 5942 | chr5 | 188265 | |||||
| chr5:188322
|
G | C | 23 | a0001c0001t0032a0001c0001t0092a0001c0007t0008others(20): Show | 27 | HG01192.hp2 HG02109.hp1 HG02258.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*5999G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 5999 | chr5 | 188322 | |||||
| chr5:188504
|
G | C | 7 | a0001c0052t0118a0003c0009t0120a0019c0019t0010others(4): Show | 7 | HG00280.hp2 HG00323.hp2 HG00741.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*6181G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 6181 | chr5 | 188504 | |||||
| chr5:188531
|
T | C | 1 | a0036c0075t0061 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6208T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 6208 | chr5 | 188531 | |||||
| chr5:188543
|
C | T | 2 | a0006c0073t0020a0035c0060t0020 | 2 | HG01261.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6220C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 6220 | chr5 | 188543 | |||||
| chr5:188545
|
C | T | 3 | a0001c0015t0035a0001c0015t0076a0036c0075t0061 | 3 | HG02886.hp1 HG03195.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6222C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 6222 | chr5 | 188545 | |||||
| chr5:188576
|
CAT | C | 3 | a0002c0003t0132a0002c0003t0136a0004c0006t0134 | 3 | HG01123.hp1 HG03491.hp1 homoSapiens_chm13v2.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6254_*6255delAT | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 6254 | chr5 | 188576 | |||||
| chr5:188604
|
T | C | 50 | a0001c0001t0014a0001c0001t0027a0001c0001t0091others(47): Show | 61 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*6281T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 6281 | chr5 | 188604 | |||||
| chr5:188610
|
G | A | 2 | a0001c0001t0113a0010c0014t0057 | 2 | HG00735.hp1 NA19012.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6287G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 6287 | chr5 | 188610 | |||||
| chr5:188632
|
C | T | 43 | a0001c0001t0014a0001c0001t0027a0001c0001t0091others(40): Show | 54 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*6309C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 6309 | chr5 | 188632 | |||||
| chr5:188735
|
T | G | 2 | a0006c0073t0020a0035c0060t0020 | 2 | HG01261.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6412T>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 6412 | chr5 | 188735 | |||||
| chr5:188781
|
G | C | 118 | a0001c0001t0004a0001c0001t0005a0001c0001t0006others(115): Show | 138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*6458G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 6458 | chr5 | 188781 | |||||
| chr5:188803
|
A | G | 35 | a0001c0001t0028a0001c0001t0031a0001c0001t0032others(32): Show | 41 | HG00323.hp1 HG00735.hp1 HG01243.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*6480A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 6480 | chr5 | 188803 | |||||
| chr5:188834
|
C | T | 1 | a0005c0008t0111 | 1 | NA18971.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6511C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 6511 | chr5 | 188834 | |||||
| chr5:189017
|
C | T | 1 | a0001c0007t0110 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6694C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 6694 | chr5 | 189017 | |||||
| chr5:189018
|
G | A | 2 | a0001c0015t0035a0001c0015t0076 | 2 | HG02886.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6695G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 6695 | chr5 | 189018 | |||||
| chr5:189073
|
A | C | 1 | a0013c0067t0046 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6750A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 6750 | chr5 | 189073 | |||||
| chr5:189077
|
C | T | 1 | a0017c0029t0112 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6754C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 6754 | chr5 | 189077 | |||||
| chr5:189104
|
T | C | 1 | a0022c0046t0047 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6781T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 6781 | chr5 | 189104 | |||||
| chr5:189110
|
C | T | 6 | a0001c0001t0079a0001c0051t0078a0010c0014t0057others(3): Show | 6 | HG02809.hp1 HG02818.hp2 HG03139.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*6787C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 6787 | chr5 | 189110 | |||||
| chr5:189243
|
C | T | 7 | a0006c0073t0020a0009c0012t0033a0009c0012t0114others(4): Show | 7 | HG01099.hp1 HG01261.hp2 HG02886.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*6920C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 6920 | chr5 | 189243 | |||||
| chr5:189303
|
C | T | 2 | a0005c0008t0111a0031c0031t0085 | 2 | HG00597.hp1 NA18971.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6980C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 6980 | chr5 | 189303 | |||||
| chr5:189304
|
G | A | 1 | a0014c0065t0038 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6981G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 6981 | chr5 | 189304 | |||||
| chr5:189389
|
C | T | 5 | a0009c0012t0033a0009c0012t0114a0009c0012t0115others(2): Show | 5 | HG01099.hp1 HG02886.hp2 HG03139.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*7066C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 7066 | chr5 | 189389 | |||||
| chr5:189620
|
G | A | 6 | a0001c0001t0079a0001c0051t0078a0011c0023t0041others(3): Show | 6 | HG02622.hp1 HG02809.hp1 HG02818.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*7297G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 7297 | chr5 | 189620 | |||||
| chr5:189684
|
T | C | 89 | a0001c0001t0027a0001c0001t0032a0001c0001t0079others(86): Show | 104 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*7361T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 7361 | chr5 | 189684 | |||||
| chr5:189699
|
CAGTA | C | 36 | a0001c0001t0032a0001c0001t0079a0001c0001t0113others(33): Show | 41 | HG00735.hp1 HG01099.hp1 HG01261.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*7379_*7382delTAAG | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 7379 | INFO_REALIGN_3_PRIME | chr5 | 189699 | ||||
| chr5:189706
|
C | A | 90 | a0001c0001t0027a0001c0001t0032a0001c0001t0079others(87): Show | 105 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*7383C>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 7383 | chr5 | 189706 | |||||
| chr5:189783
|
C | T | 1 | a0004c0006t0065 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7460C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 7460 | chr5 | 189783 | |||||
| chr5:189935
|
A | G | 1 | a0003c0004t0105 | 1 | NA18747.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7612A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 20/20 | 7612 | chr5 | 189935 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:92311
|
G | T | 18 | a0002c0003t0011g0210a0002c0003t0066g0209a0004c0006t0065g0208others(15): Show | 18 | HG00099.hp2 HG00597.hp2 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.45+35G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 92311 | ||||||
| chr5:92328
|
A | G | 42 | a0001c0011t0048g0179a0002c0003t0011g0210a0002c0003t0066g0209others(39): Show | 42 | HG00099.hp2 HG00280.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.45+52A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 92328 | ||||||
| chr5:92333
|
G | A | 18 | a0002c0003t0011g0210a0002c0003t0066g0209a0004c0006t0065g0208others(15): Show | 18 | HG00099.hp2 HG00597.hp2 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.45+57G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 92333 | ||||||
| chr5:92336
|
C | CGGGTGGG others(18): Show |
5 | a0006c0070t0054g0207a0006c0073t0020g0193a0008c0024t0021g0176others(2): Show | 5 | HG01261.hp2 HG02145.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+72_45+73insCGGG others(21): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92336 | |||||
| chr5:92349
|
G | C | 37 | a0001c0011t0048g0179a0002c0003t0011g0210a0002c0003t0066g0209others(34): Show | 37 | HG00099.hp2 HG00280.hp2 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.45+73G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 92349 | ||||||
| chr5:92360
|
C | CGGGGGTG others(359): Show |
1 | a0005c0008t0004g0001 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.45+88_45+89insGTGG others(362): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92360 | |||||
| chr5:92368
|
G | GGGCGCGG others(478): Show |
1 | a0011c0023t0044g0187 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.45+94_45+95insCGCG others(481): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92368 | |||||
| chr5:92369
|
G | GGCGCCAG others(360): Show |
1 | a0025c0045t0122g0002 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.45+94_45+95insCGCC others(363): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCCGG others(360): Show |
1 | a0004c0006t0123g0003 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.45+94_45+95insCGCC others(363): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCCGG others(115): Show |
1 | a0016c0018t0034g0004 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.45+94_45+95insCGCC others(118): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCCGG others(140): Show |
1 | a0016c0018t0003g0005 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.45+94_45+95insCGCC others(143): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCCGG others(238): Show |
1 | a0001c0061t0001g0006 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.45+94_45+95insCGCC others(241): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCCGG others(433): Show |
1 | a0001c0032t0103g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.45+94_45+95insCGCC others(436): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCCGG others(362): Show |
1 | a0033c0028t0088g0008 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.45+94_45+95insCGCC others(365): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCCGG others(361): Show |
2 | a0003c0004t0108g0010a0027c0053t0107g0009 | 2 | HG03831.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.45+94_45+95insCGCC others(364): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCCGG others(559): Show |
1 | a0024c0042t0006g0012 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.45+94_45+95insCGCC others(562): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCCGG others(632): Show |
1 | a0004c0006t0134g0011 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.45+94_45+95insCGCC others(635): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCCGG others(610): Show |
1 | a0003c0009t0120g0013 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.45+94_45+95insCGCC others(613): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCCGG others(334): Show |
6 | a0001c0002t0001g0018a0001c0002t0022g0015a0002c0003t0124g0017others(3): Show | 6 | HG00140.hp1 HG00741.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.45+94_45+95insCGCC others(337): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCCGG others(361): Show |
1 | a0001c0001t0004g0020 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.45+94_45+95insCGCC others(364): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCCGG others(360): Show |
1 | a0001c0002t0094g0021 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.45+94_45+95insCGCC others(363): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCCGG others(360): Show |
1 | a0001c0001t0015g0022 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.45+94_45+95insCGCC others(363): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCCGG others(237): Show |
1 | a0001c0007t0100g0025 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.45+94_45+95insCGCC others(240): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCCGG others(360): Show |
1 | a0001c0001t0104g0023 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.45+94_45+95insCGCC others(363): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCCGG others(286): Show |
1 | a0001c0001t0015g0131 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.45+94_45+95insCGCC others(289): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCCGG others(557): Show |
1 | a0001c0002t0024g0024 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.45+94_45+95insCGCC others(560): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCCGG others(359): Show |
101 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0005g0090others(98): Show | 101 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.45+94_45+95insCGCC others(362): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCCGG others(481): Show |
2 | a0001c0001t0030g0027a0002c0057t0003g0026 | 2 | HG00438.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.45+94_45+95insCGCC others(484): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCCGG others(361): Show |
1 | a0001c0001t0098g0129 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.45+94_45+95insCGCC others(364): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCCGG others(359): Show |
1 | a0002c0003t0130g0130 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.45+94_45+95insCGCC others(362): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCCGG others(361): Show |
1 | a0002c0003t0002g0132 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.45+94_45+95insCGCC others(364): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCCGG others(361): Show |
1 | a0003c0004t0016g0133 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.45+94_45+95insCGCC others(364): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCCGG others(262): Show |
1 | a0001c0002t0006g0134 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.45+94_45+95insCGCC others(265): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCCGG others(360): Show |
1 | a0001c0001t0024g0135 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.45+94_45+95insCGCC others(363): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCCGG others(361): Show |
1 | a0001c0011t0029g0136 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.45+94_45+95insCGCC others(364): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCCGG others(362): Show |
1 | a0001c0035t0030g0137 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.45+94_45+95insCGCC others(365): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCCGG others(361): Show |
1 | a0001c0002t0022g0138 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.45+94_45+95insCGCC others(364): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCCGG others(359): Show |
1 | a0004c0054t0034g0139 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.45+94_45+95insCGCC others(362): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCCGG others(314): Show |
1 | a0017c0030t0039g0140 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.45+94_45+95insCGCC others(317): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCCGG others(361): Show |
1 | a0026c0050t0009g0141 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.45+94_45+95insCGCC others(364): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCCGG others(360): Show |
1 | a0001c0001t0001g0142 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.45+94_45+95insCGCC others(363): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCCGG others(165): Show |
1 | a0001c0007t0008g0143 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.45+94_45+95insCGCC others(168): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCCGG others(89): Show |
1 | a0001c0001t0032g0144 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.45+94_45+95insCGCC others(92): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCCGG others(114): Show |
5 | a0001c0007t0008g0145a0001c0007t0008g0146a0001c0007t0109g0147others(2): Show | 5 | HG02896.hp1 HG03139.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+94_45+95insCGCC others(117): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCCGG others(285): Show |
1 | a0001c0007t0008g0150 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.45+94_45+95insCGCC others(288): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCCGG others(334): Show |
7 | a0001c0007t0110g0151a0001c0015t0076g0154a0001c0016t0025g0152others(4): Show | 7 | HG02723.hp1 HG02886.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.45+94_45+95insCGCC others(337): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCCGG others(264): Show |
1 | a0032c0058t0040g0158 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.45+94_45+95insCGCC others(267): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCCGG others(309): Show |
2 | a0001c0001t0001g0159a0001c0016t0005g0160 | 2 | HG02922.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.45+94_45+95insCGCC others(312): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCCGG others(334): Show |
2 | a0009c0012t0033g0161a0009c0034t0033g0162 | 2 | HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.45+94_45+95insCGCC others(337): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCCGG others(501): Show |
1 | a0021c0026t0060g0169 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.45+94_45+95insCGCC others(504): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCCGG others(476): Show |
2 | a0014c0027t0049g0171a0014c0066t0051g0170 | 2 | HG02809.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.45+94_45+95insCGCC others(479): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCCGG others(315): Show |
1 | a0029c0033t0042g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.45+94_45+95insCGCC others(318): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCCGG others(294): Show |
2 | a0019c0019t0010g0164a0039c0062t0010g0165 | 2 | HG00323.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.45+94_45+95insCGCC others(297): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCGGG others(502): Show |
1 | a0008c0025t0045g0172 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.45+94_45+95insCGCG others(505): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCGGG others(501): Show |
2 | a0008c0024t0021g0176a0008c0025t0069g0174 | 2 | HG02145.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.45+94_45+95insCGCG others(504): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCGGG others(213): Show |
1 | a0014c0065t0038g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.45+94_45+95insCGCG others(216): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCGGG others(526): Show |
2 | a0008c0024t0021g0175a0008c0079t0068g0173 | 2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.45+94_45+95insCGCG others(529): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCGGG others(528): Show |
1 | a0038c0080t0043g0177 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.45+94_45+95insCGCG others(531): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCGGG others(245): Show |
1 | a0036c0075t0061g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.45+94_45+95insCGCG others(248): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCGGG others(39): Show |
13 | a0002c0003t0011g0210a0004c0006t0065g0208a0006c0021t0018g0198others(10): Show | 13 | HG00597.hp2 HG01074.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.45+94_45+95insCGCG others(42): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCGGG others(88): Show |
1 | a0002c0003t0066g0209 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.45+94_45+95insCGCG others(91): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCGGG others(451): Show |
1 | a0001c0011t0048g0179 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.45+94_45+95insCGCG others(454): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCGGG others(1086): Show |
1 | a0022c0046t0047g0180 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.45+94_45+95insCGCG others(1089): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCGGG others(476): Show |
5 | a0011c0023t0041g0184a0011c0078t0059g0185a0013c0020t0050g0182others(2): Show | 5 | HG01099.hp1 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+94_45+95insCGCG others(479): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCGGG others(633): Show |
1 | a0013c0067t0046g0186 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.45+94_45+95insCGCG others(636): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCGGG others(526): Show |
1 | a0006c0068t0058g0194 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.45+94_45+95insCGCG others(529): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCGGG others(525): Show |
1 | a0006c0071t0018g0202 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.45+94_45+95insCGCG others(528): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCGGG others(477): Show |
1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.45+94_45+95insCGCG others(480): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCGGG others(426): Show |
2 | a0040c0063t0063g0189a0041c0064t0010g0190 | 2 | HG00280.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.45+94_45+95insCGCG others(429): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCGGG others(501): Show |
1 | a0006c0073t0020g0193 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.45+94_45+95insCGCG others(504): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCGGG others(426): Show |
1 | a0006c0070t0054g0207 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.45+94_45+95insCGCG others(429): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCGGG others(427): Show |
1 | a0019c0019t0062g0191 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.45+94_45+95insCGCG others(430): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGCGCGGG others(476): Show |
1 | a0015c0076t0067g0192 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.45+94_45+95insCGCG others(479): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92369
|
G | GGGCGCCG others(434): Show |
1 | a0002c0005t0003g0167 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.45+95_45+96insCGCC others(437): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92369 | |||||
| chr5:92378
|
C | G | 5 | a0002c0003t0066g0209a0006c0068t0058g0194a0006c0070t0054g0207others(2): Show | 5 | HG00099.hp2 HG01261.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+102C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 92378 | ||||||
| chr5:92381
|
A | G | 8 | a0001c0007t0008g0143a0001c0007t0008g0150a0002c0003t0066g0209others(5): Show | 8 | HG00099.hp2 HG01261.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.45+105A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 92381 | ||||||
| chr5:92388
|
G | GT | 5 | a0002c0003t0066g0209a0006c0068t0058g0194a0006c0070t0054g0207others(2): Show | 5 | HG00099.hp2 HG01261.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+112_45+113insT | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 92388 | ||||||
| chr5:92389
|
C | A | 1 | a0022c0046t0047g0180 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.45+113C>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 92389 | ||||||
| chr5:92389
|
C | CGGGTGGG others(43): Show |
1 | a0002c0003t0011g0210 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.45+151_45+152insGG others(48): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92389 | |||||
| chr5:92389
|
C | CGGGTGGG others(455): Show |
3 | a0010c0014t0057g0197a0018c0022t0011g0195a0018c0022t0011g0196 | 3 | HG00597.hp2 NA18984.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.45+151_45+152insGG others(460): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92389 | |||||
| chr5:92389
|
C | CGGGTGGG others(480): Show |
8 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0072t0036g0206others(5): Show | 8 | HG02258.hp2 HG02451.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.45+151_45+152insGG others(485): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92389 | |||||
| chr5:92389
|
C | G | 5 | a0002c0003t0066g0209a0006c0068t0058g0194a0006c0070t0054g0207others(2): Show | 5 | HG00099.hp2 HG01261.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+113C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 92389 | ||||||
| chr5:92413
|
T | TGGGGTGG others(44): Show |
1 | a0004c0006t0065g0208 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.45+151_45+152insGG others(49): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92413 | |||||
| chr5:92414
|
G | C | 1 | a0001c0007t0008g0150 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.45+138G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 92414 | ||||||
| chr5:92418
|
T | TG | 5 | a0001c0002t0094g0021a0002c0003t0135g0128a0002c0005t0003g0167others(2): Show | 5 | HG00642.hp1 HG00642.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.45+147dupG | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92418 | |||||
| chr5:92426
|
C | CCGGAGTA others(56): Show |
1 | a0001c0007t0100g0025 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.45+150_45+151insCG others(61): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 92426 | ||||||
| chr5:92426
|
C | CCGGAGTA others(32): Show |
1 | a0001c0007t0008g0143 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.45+150_45+151insCG others(37): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 92426 | ||||||
| chr5:92426
|
C | CCGGGGTA others(82): Show |
1 | a0016c0018t0003g0005 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.45+150_45+151insCG others(87): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 92426 | ||||||
| chr5:92426
|
C | CCGGGGTA others(81): Show |
9 | a0001c0001t0032g0144a0001c0007t0008g0145a0001c0007t0008g0146others(6): Show | 9 | HG02109.hp1 HG02809.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.45+150_45+151insCG others(86): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 92426 | ||||||
| chr5:92426
|
C | CCGGGGTA others(82): Show |
1 | a0017c0030t0039g0140 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.45+150_45+151insCG others(87): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 92426 | ||||||
| chr5:92428
|
A | T | 13 | a0001c0001t0032g0144a0001c0007t0008g0143a0001c0007t0008g0145others(10): Show | 13 | HG02109.hp1 HG02145.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.45+152A>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 92428 | ||||||
| chr5:92430
|
C | G | 13 | a0001c0001t0032g0144a0001c0007t0008g0143a0001c0007t0008g0145others(10): Show | 13 | HG02109.hp1 HG02145.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.45+154C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 92430 | ||||||
| chr5:92433
|
A | G | 13 | a0001c0001t0032g0144a0001c0007t0008g0143a0001c0007t0008g0145others(10): Show | 13 | HG02109.hp1 HG02145.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.45+157A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 92433 | ||||||
| chr5:92437
|
G | C | 13 | a0001c0001t0032g0144a0001c0007t0008g0143a0001c0007t0008g0145others(10): Show | 13 | HG02109.hp1 HG02145.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.45+161G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 92437 | ||||||
| chr5:92440
|
A | G | 3 | a0017c0030t0039g0140a0029c0033t0042g0163a0032c0058t0040g0158 | 3 | HG02622.hp2 HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.45+164A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 92440 | ||||||
| chr5:92448
|
C | CGGGTGGG others(18): Show |
1 | a0016c0018t0003g0005 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.45+184_45+185insGG others(23): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92448 | |||||
| chr5:92461
|
C | G | 2 | a0001c0007t0008g0150a0001c0007t0100g0025 | 2 | HG02257.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.45+185C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 92461 | ||||||
| chr5:92464
|
G | A | 1 | a0016c0018t0003g0005 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.45+188G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 92464 | ||||||
| chr5:92485
|
G | C | 1 | a0036c0075t0061g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.45+209G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 92485 | ||||||
| chr5:92500
|
G | A | 5 | a0001c0001t0032g0144a0001c0007t0008g0143a0001c0007t0008g0145others(2): Show | 5 | HG02109.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+224G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 92500 | ||||||
| chr5:92514
|
A | G | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.45+238A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 92514 | ||||||
| chr5:92527
|
G | GGC | 39 | a0001c0002t0024g0024a0001c0007t0110g0151a0001c0011t0048g0179others(36): Show | 39 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.45+255_45+256dupCG | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 92527 | |||||
| chr5:92610
|
T | G | 3 | a0014c0027t0049g0171a0014c0066t0051g0170a0021c0026t0060g0169 | 3 | HG02809.hp1 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.45+334T>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 92610 | ||||||
| chr5:92634
|
C | T | 1 | a0036c0075t0061g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.45+358C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 92634 | ||||||
| chr5:92662
|
G | A | 6 | a0014c0065t0038g0166a0016c0018t0003g0005a0016c0018t0034g0004others(3): Show | 6 | HG02145.hp1 HG02622.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.45+386G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 92662 | ||||||
| chr5:92709
|
C | T | 1 | a0014c0065t0038g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.45+433C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 92709 | ||||||
| chr5:92812
|
T | G | 1 | a0018c0022t0011g0195 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.45+536T>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 92812 | ||||||
| chr5:92821
|
G | T | 1 | a0022c0046t0047g0180 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.45+545G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 92821 | ||||||
| chr5:92965
|
C | T | 1 | a0014c0065t0038g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.45+689C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 92965 | ||||||
| chr5:93203
|
A | G | 13 | a0001c0001t0032g0144a0001c0007t0008g0143a0001c0007t0008g0145others(10): Show | 13 | HG02109.hp1 HG02886.hp2 HG02896.hp1 others(10): Show |
intron_variant | MODIFIER | c.45+927A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 93203 | ||||||
| chr5:93217
|
G | A | 41 | a0001c0011t0048g0179a0006c0021t0018g0198a0006c0021t0056g0199others(38): Show | 41 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.45+941G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 93217 | ||||||
| chr5:93235
|
T | A | 6 | a0008c0024t0021g0175a0008c0024t0021g0176a0008c0025t0045g0172others(3): Show | 6 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.45+959T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 93235 | ||||||
| chr5:93272
|
A | C | 38 | a0001c0011t0048g0179a0006c0021t0018g0198a0006c0021t0056g0199others(35): Show | 38 | HG00597.hp2 HG01099.hp1 HG01261.hp2 others(35): Show |
intron_variant | MODIFIER | c.45+996A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 93272 | ||||||
| chr5:93465
|
C | T | 36 | a0001c0011t0048g0179a0006c0068t0058g0194a0006c0070t0054g0207others(33): Show | 36 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.45+1189C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 93465 | ||||||
| chr5:93604
|
G | A | 1 | a0010c0014t0055g0201 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.45+1328G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 93604 | ||||||
| chr5:93614
|
G | A | 3 | a0014c0027t0049g0171a0014c0066t0051g0170a0021c0026t0060g0169 | 3 | HG02809.hp1 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.45+1338G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 93614 | ||||||
| chr5:93617
|
A | G | 1 | a0008c0025t0045g0172 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.45+1341A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 93617 | ||||||
| chr5:93635
|
C | T | 1 | a0021c0026t0060g0169 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.45+1359C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 93635 | ||||||
| chr5:93681
|
C | T | 1 | a0036c0075t0061g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.45+1405C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 93681 | ||||||
| chr5:94000
|
T | C | 1 | a0016c0018t0034g0004 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.45+1724T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 94000 | ||||||
| chr5:94116
|
C | T | 1 | a0001c0002t0082g0126 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.45+1840C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 94116 | ||||||
| chr5:94149
|
A | G | 1 | a0014c0065t0038g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.45+1873A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 94149 | ||||||
| chr5:94202
|
C | T | 1 | a0001c0001t0014g0125 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.45+1926C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 94202 | ||||||
| chr5:94220
|
C | G | 1 | a0039c0062t0010g0165 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.45+1944C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 94220 | ||||||
| chr5:94282
|
G | A | 2 | a0002c0003t0128g0029a0002c0003t0132g0028 | 2 | HG00639.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.45+2006G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 94282 | ||||||
| chr5:94376
|
C | T | 41 | a0001c0011t0048g0179a0006c0021t0018g0198a0006c0021t0056g0199others(38): Show | 41 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.45+2100C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 94376 | ||||||
| chr5:94390
|
CAG | C | 9 | a0001c0011t0048g0179a0011c0023t0041g0184a0011c0023t0044g0187others(6): Show | 9 | HG01099.hp1 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.45+2117_45+2118del others(2): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 94390 | |||||
| chr5:94456
|
G | GGTAGGCT others(106): Show |
1 | a0001c0036t0077g0149 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.45+2244_45+2245ins others(113): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 94456 | |||||
| chr5:94475
|
G | A | 1 | a0017c0029t0112g0155 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.45+2199G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 94475 | ||||||
| chr5:94480
|
G | A | 1 | a0001c0032t0103g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.45+2204G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 94480 | ||||||
| chr5:94503
|
G | GGCAGGTT others(215): Show |
5 | a0019c0019t0010g0164a0019c0019t0062g0191a0039c0062t0010g0165others(2): Show | 5 | HG00280.hp2 HG00323.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.45+2292_45+2293ins others(222): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 94503 | |||||
| chr5:94503
|
G | GGCAGGTT others(104): Show |
36 | a0001c0011t0048g0179a0006c0021t0018g0198a0006c0021t0056g0199others(33): Show | 36 | HG00597.hp2 HG01099.hp1 HG01261.hp2 others(33): Show |
intron_variant | MODIFIER | c.45+2244_45+2245ins others(111): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 94503 | |||||
| chr5:95091
|
G | C | 1 | a0022c0046t0047g0180 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.45+2815G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 95091 | ||||||
| chr5:95264
|
G | A | 1 | a0018c0022t0011g0196 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.45+2988G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 95264 | ||||||
| chr5:95608
|
A | G | 9 | a0001c0011t0048g0179a0011c0023t0041g0184a0011c0023t0044g0187others(6): Show | 9 | HG01099.hp1 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.45+3332A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 95608 | ||||||
| chr5:95949
|
G | A | 15 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(12): Show | 15 | HG00597.hp2 HG01261.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.45+3673G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 95949 | ||||||
| chr5:96116
|
A | T | 1 | a0002c0003t0002g0132 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.45+3840A>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 96116 | ||||||
| chr5:96339
|
G | A | 1 | a0036c0075t0061g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.45+4063G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 96339 | ||||||
| chr5:96458
|
G | A | 209 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0142others(206): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.45+4182G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 96458 | ||||||
| chr5:96562
|
C | G | 1 | a0012c0013t0009g0019 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.45+4286C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 96562 | ||||||
| chr5:96621
|
T | C | 42 | a0001c0011t0048g0179a0001c0036t0077g0149a0006c0021t0018g0198others(39): Show | 42 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.45+4345T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 96621 | ||||||
| chr5:96675
|
G | A | 1 | a0015c0076t0067g0192 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.45+4399G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 96675 | ||||||
| chr5:96819
|
G | A | 1 | a0014c0065t0038g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.45+4543G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 96819 | ||||||
| chr5:97060
|
C | G | 1 | a0002c0005t0127g0124 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.45+4784C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 97060 | ||||||
| chr5:97086
|
A | G | 6 | a0008c0024t0021g0175a0008c0024t0021g0176a0008c0025t0045g0172others(3): Show | 6 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.45+4810A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 97086 | ||||||
| chr5:97189
|
A | G | 1 | a0014c0065t0038g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.45+4913A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 97189 | ||||||
| chr5:97212
|
C | CAAACCCC others(46): Show |
1 | a0002c0003t0002g0132 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.45+4951_45+5003dup others(53): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 97212 | |||||
| chr5:97312
|
A | AAAGTCCA others(99): Show |
41 | a0001c0011t0048g0179a0006c0021t0018g0198a0006c0021t0056g0199others(38): Show | 41 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.45+5041_45+5042ins others(106): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 97312 | |||||
| chr5:97312
|
A | AAAGTCCA others(99): Show |
1 | a0014c0065t0038g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.45+5041_45+5042ins others(106): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 97312 | |||||
| chr5:97350
|
C | G | 42 | a0001c0011t0048g0179a0006c0021t0018g0198a0006c0021t0056g0199others(39): Show | 42 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.45+5074C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 97350 | ||||||
| chr5:97365
|
G | A | 42 | a0001c0011t0048g0179a0006c0021t0018g0198a0006c0021t0056g0199others(39): Show | 42 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.45+5089G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 97365 | ||||||
| chr5:97365
|
G | GAAGTCAA others(46): Show |
18 | a0001c0001t0032g0144a0001c0007t0008g0143a0001c0007t0008g0145others(15): Show | 18 | HG02109.hp1 HG02145.hp1 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.45+5126_45+5127ins others(53): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 97365 | |||||
| chr5:97370
|
C | A | 1 | a0002c0005t0003g0167 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.45+5094C>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 97370 | ||||||
| chr5:97447
|
T | C | 41 | a0001c0011t0048g0179a0006c0021t0018g0198a0006c0021t0056g0199others(38): Show | 41 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.45+5171T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 97447 | ||||||
| chr5:97535
|
C | T | 1 | a0001c0001t0005g0123 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.45+5259C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 97535 | ||||||
| chr5:97585
|
C | T | 3 | a0014c0027t0049g0171a0014c0066t0051g0170a0021c0026t0060g0169 | 3 | HG02809.hp1 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.45+5309C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 97585 | ||||||
| chr5:97656
|
C | T | 6 | a0008c0024t0021g0175a0008c0024t0021g0176a0008c0025t0045g0172others(3): Show | 6 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.45+5380C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 97656 | ||||||
| chr5:97676
|
G | GC | 42 | a0001c0011t0048g0179a0006c0021t0018g0198a0006c0021t0056g0199others(39): Show | 42 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.45+5400_45+5401ins others(1): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 97676 | ||||||
| chr5:97818
|
C | G | 15 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(12): Show | 15 | HG00597.hp2 HG01261.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.45+5542C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 97818 | ||||||
| chr5:97848
|
T | C | 2 | a0015c0076t0067g0192a0015c0077t0053g0181 | 2 | HG02257.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.45+5572T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 97848 | ||||||
| chr5:97919
|
A | G | 2 | a0019c0019t0010g0164a0039c0062t0010g0165 | 2 | HG00323.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.45+5643A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 97919 | ||||||
| chr5:97920
|
T | G | 2 | a0002c0005t0003g0031a0002c0039t0009g0030 | 2 | HG00673.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.45+5644T>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 97920 | ||||||
| chr5:97995
|
A | G | 2 | a0001c0015t0035g0122a0001c0015t0076g0154 | 2 | HG02886.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.45+5719A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 97995 | ||||||
| chr5:98004
|
T | G | 1 | a0036c0075t0061g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.45+5728T>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 98004 | ||||||
| chr5:98011
|
A | G | 2 | a0019c0019t0010g0164a0039c0062t0010g0165 | 2 | HG00323.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.45+5735A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 98011 | ||||||
| chr5:98121
|
C | T | 4 | a0014c0027t0049g0171a0014c0066t0051g0170a0021c0026t0060g0169others(1): Show | 4 | HG02809.hp1 HG02818.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+5845C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 98121 | ||||||
| chr5:98199
|
G | C | 1 | a0001c0002t0001g0032 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.45+5923G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 98199 | ||||||
| chr5:98207
|
A | T | 1 | a0002c0005t0127g0124 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.45+5931A>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 98207 | ||||||
| chr5:98247
|
G | T | 6 | a0001c0011t0048g0179a0011c0023t0041g0184a0011c0023t0044g0187others(3): Show | 6 | HG01099.hp1 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.45+5971G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 98247 | ||||||
| chr5:98300
|
G | A | 1 | a0002c0003t0066g0209 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.45+6024G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 98300 | ||||||
| chr5:98425
|
C | CT | 97 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0142others(94): Show | 97 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.45+6177dupT | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 98425 | |||||
| chr5:98425
|
C | CTT | 47 | a0001c0001t0014g0115a0001c0001t0030g0027a0001c0001t0031g0111others(44): Show | 47 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.45+6176_45+6177dup others(2): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 98425 | |||||
| chr5:98425
|
CT | C | 13 | a0001c0007t0008g0143a0001c0007t0008g0145a0001c0007t0008g0146others(10): Show | 13 | HG02258.hp2 HG02622.hp2 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.45+6177delT | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 98425 | |||||
| chr5:98425
|
CTT | C | 15 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(12): Show | 15 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(12): Show |
intron_variant | MODIFIER | c.45+6176_45+6177del others(2): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 98425 | |||||
| chr5:98603
|
T | TG | 3 | a0001c0035t0030g0137a0002c0005t0003g0096a0039c0062t0010g0165 | 3 | HG03471.hp1 HG04204.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.45+6327_45+6328ins others(1): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 98603 | ||||||
| chr5:98603
|
T | TGTG | 2 | a0001c0001t0001g0159a0001c0037t0006g0045 | 2 | HG02647.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.45+6327_45+6328ins others(3): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 98603 | ||||||
| chr5:98603
|
T | TTG | 33 | a0001c0001t0007g0056a0001c0001t0014g0033a0001c0001t0027g0052others(30): Show | 33 | HG00741.hp2 HG01069.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.45+6369_45+6370dup others(2): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 98603 | |||||
| chr5:98603
|
T | TTGTG | 13 | a0001c0001t0001g0142a0001c0001t0032g0144a0004c0006t0003g0047others(10): Show | 13 | HG02109.hp1 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.45+6367_45+6370dup others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 98603 | |||||
| chr5:98603
|
T | TTGTGTG | 6 | a0001c0001t0028g0046a0010c0014t0057g0197a0018c0022t0011g0195others(3): Show | 6 | HG00597.hp2 HG01243.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.45+6365_45+6370dup others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 98603 | |||||
| chr5:98603
|
T | TTGTGTGT others(3): Show |
4 | a0009c0012t0033g0161a0009c0012t0114g0156a0009c0012t0115g0157others(1): Show | 4 | HG02809.hp2 HG02886.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+6361_45+6370dup others(10): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 98603 | |||||
| chr5:98603
|
T | TTGTGTGT others(5): Show |
1 | a0009c0034t0033g0162 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.45+6359_45+6370dup others(12): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 98603 | |||||
| chr5:98603
|
TTG | T | 22 | a0001c0001t0005g0090a0001c0001t0015g0022a0001c0001t0032g0094others(19): Show | 22 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(19): Show |
intron_variant | MODIFIER | c.45+6369_45+6370del others(2): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 98603 | |||||
| chr5:98603
|
TTGTG | T | 7 | a0001c0052t0118g0121a0002c0003t0071g0095a0002c0003t0124g0017others(4): Show | 7 | HG00323.hp2 HG00741.hp1 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.45+6367_45+6370del others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 98603 | |||||
| chr5:98603
|
TTGTGTG | T | 6 | a0001c0061t0001g0006a0013c0020t0050g0182a0013c0067t0046g0186others(3): Show | 6 | HG02451.hp1 HG02809.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.45+6365_45+6370del others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 98603 | |||||
| chr5:98603
|
TTGTGTGT others(3): Show |
T | 3 | a0019c0019t0062g0191a0040c0063t0063g0189a0041c0064t0010g0190 | 3 | HG00280.hp2 HG01081.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.45+6361_45+6370del others(10): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 98603 | |||||
| chr5:98603
|
TTGTGTGT others(15): Show |
T | 1 | a0002c0003t0130g0130 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.45+6349_45+6370del others(22): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 98603 | |||||
| chr5:98638
|
T | A | 1 | a0003c0004t0007g0097 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.45+6362T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 98638 | ||||||
| chr5:98708
|
C | G | 3 | a0019c0019t0062g0191a0040c0063t0063g0189a0041c0064t0010g0190 | 3 | HG00280.hp2 HG01081.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.45+6432C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 98708 | ||||||
| chr5:98752
|
C | T | 1 | a0001c0001t0032g0144 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.45+6476C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 98752 | ||||||
| chr5:98764
|
C | T | 12 | a0001c0011t0048g0179a0011c0023t0041g0184a0011c0023t0044g0187others(9): Show | 12 | HG00280.hp2 HG01081.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.45+6488C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 98764 | ||||||
| chr5:98772
|
C | T | 1 | a0014c0065t0038g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.45+6496C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 98772 | ||||||
| chr5:98837
|
C | CT | 20 | a0001c0001t0032g0094a0001c0001t0091g0120a0001c0002t0001g0032others(17): Show | 20 | HG00735.hp2 HG01099.hp1 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.45+6580dupT | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 98837 | |||||
| chr5:98837
|
C | CTTTTTTT others(1): Show |
15 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(12): Show | 15 | HG00597.hp2 HG01261.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.45+6573_45+6580dup others(8): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 98837 | |||||
| chr5:98837
|
C | CTTTTTTT others(3): Show |
1 | a0020c0081t0064g0200 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.45+6571_45+6580dup others(10): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 98837 | |||||
| chr5:98837
|
CT | C | 5 | a0002c0003t0002g0098a0002c0003t0011g0210a0003c0009t0119g0049others(2): Show | 5 | HG01069.hp1 HG01074.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+6580delT | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 98837 | |||||
| chr5:98941
|
G | A | 1 | a0001c0002t0022g0138 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.45+6665G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 98941 | ||||||
| chr5:99155
|
C | CA | 40 | a0001c0001t0014g0033a0001c0011t0048g0179a0006c0021t0018g0198others(37): Show | 40 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.45+6891dupA | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 99155 | |||||
| chr5:99170
|
G | A | 1 | a0013c0067t0046g0186 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.45+6894G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 99170 | ||||||
| chr5:99170
|
G | GTA | 7 | a0001c0001t0004g0020a0001c0002t0007g0060a0001c0007t0008g0143others(4): Show | 7 | HG00099.hp1 HG01255.hp2 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.45+6936_45+6937dup others(2): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 99170 | |||||
| chr5:99170
|
G | GTATA | 3 | a0012c0013t0009g0016a0013c0020t0052g0183a0015c0077t0053g0181 | 3 | HG02717.hp2 NA18906.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.45+6934_45+6937dup others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 99170 | |||||
| chr5:99170
|
G | GTATATA | 6 | a0001c0001t0015g0131a0009c0012t0114g0156a0011c0023t0044g0187others(3): Show | 6 | HG01099.hp1 HG02145.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.45+6932_45+6937dup others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 99170 | |||||
| chr5:99170
|
G | GTATATAT others(5): Show |
1 | a0012c0013t0009g0019 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.45+6926_45+6937dup others(12): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 99170 | |||||
| chr5:99170
|
G | GTATATAT others(7): Show |
2 | a0001c0001t0091g0120a0014c0065t0038g0166 | 2 | HG02273.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.45+6924_45+6937dup others(14): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 99170 | |||||
| chr5:99170
|
G | GTGTATAT others(3): Show |
1 | a0001c0036t0077g0149 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.45+6895_45+6896ins others(10): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 99170 | |||||
| chr5:99170
|
GTA | G | 6 | a0001c0001t0099g0089a0001c0007t0008g0146a0001c0049t0096g0063others(3): Show | 6 | HG00280.hp1 HG00738.hp1 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.45+6936_45+6937del others(2): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 99170 | |||||
| chr5:99170
|
GTATA | G | 13 | a0001c0001t0005g0090a0001c0001t0032g0094a0001c0002t0012g0066others(10): Show | 13 | HG00733.hp1 HG00741.hp1 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.45+6934_45+6937del others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 99170 | |||||
| chr5:99170
|
GTATATA | G | 27 | a0001c0001t0001g0159a0001c0001t0012g0069a0001c0001t0024g0135others(24): Show | 27 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.45+6932_45+6937del others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 99170 | |||||
| chr5:99170
|
GTATATAT others(1): Show |
G | 25 | a0001c0001t0001g0142a0001c0001t0005g0123a0001c0001t0015g0022others(22): Show | 25 | HG00140.hp1 HG00639.hp2 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.45+6930_45+6937del others(8): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 99170 | |||||
| chr5:99170
|
GTATATAT others(3): Show |
G | 67 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0006g0075others(64): Show | 67 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.45+6928_45+6937del others(10): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 99170 | |||||
| chr5:99170
|
GTATATAT others(5): Show |
G | 3 | a0007c0010t0080g0117a0010c0069t0019g0204a0040c0063t0063g0189 | 3 | HG00280.hp2 HG02165.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.45+6926_45+6937del others(12): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 99170 | |||||
| chr5:99170
|
GTATATAT others(7): Show |
G | 4 | a0001c0011t0048g0179a0010c0014t0019g0205a0010c0014t0055g0201others(1): Show | 4 | HG02280.hp2 HG02451.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+6924_45+6937del others(14): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 99170 | |||||
| chr5:99170
|
GTATATAT others(9): Show |
G | 10 | a0002c0005t0003g0031a0006c0071t0018g0202a0006c0072t0036g0206others(7): Show | 10 | HG00673.hp1 HG01081.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.45+6922_45+6937del others(16): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 99170 | |||||
| chr5:99170
|
GTATATAT others(11): Show |
G | 15 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(12): Show | 15 | HG00323.hp2 HG00597.hp2 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.45+6920_45+6937del others(18): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 99170 | |||||
| chr5:99170
|
GTATATAT others(13): Show |
G | 1 | a0039c0062t0010g0165 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.45+6918_45+6937del others(20): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 99170 | |||||
| chr5:99170
|
GTATATAT others(17): Show |
G | 1 | a0001c0002t0001g0018 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.45+6914_45+6937del others(24): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 99170 | |||||
| chr5:99202
|
ATATATAT others(4): Show |
A | 1 | a0001c0002t0025g0073 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.45+6928_45+6938del others(11): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 99202 | |||||
| chr5:99214
|
T | A | 1 | a0003c0004t0004g0036 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.45+6938T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 99214 | ||||||
| chr5:99227
|
G | A | 1 | a0022c0046t0047g0180 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.45+6951G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 99227 | ||||||
| chr5:99461
|
G | A | 1 | a0014c0065t0038g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.45+7185G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 99461 | ||||||
| chr5:99479
|
G | A | 1 | a0036c0075t0061g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.45+7203G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 99479 | ||||||
| chr5:99583
|
TG | T | 9 | a0001c0011t0048g0179a0011c0023t0041g0184a0011c0023t0044g0187others(6): Show | 9 | HG01099.hp1 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.45+7308delG | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 99583 | ||||||
| chr5:99669
|
G | A | 26 | a0001c0001t0007g0056a0001c0001t0027g0052a0001c0001t0027g0053others(23): Show | 26 | HG00597.hp1 HG00673.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.45+7393G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 99669 | ||||||
| chr5:99879
|
C | T | 1 | a0041c0064t0010g0190 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.45+7603C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 99879 | ||||||
| chr5:100060
|
C | G | 2 | a0019c0019t0010g0164a0039c0062t0010g0165 | 2 | HG00323.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.45+7784C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 100060 | ||||||
| chr5:100232
|
C | T | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.45+7956C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 100232 | ||||||
| chr5:100320
|
C | A | 1 | a0001c0001t0006g0075 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.45+8044C>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 100320 | ||||||
| chr5:100345
|
T | TCTGTAGG others(735): Show |
1 | a0006c0068t0058g0194 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.45+8077_45+8078ins others(742): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 100345 | |||||
| chr5:100345
|
T | TCTGTAGG others(258): Show |
1 | a0006c0070t0054g0207 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.45+8077_45+8078ins others(265): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 100345 | |||||
| chr5:100354
|
G | A | 13 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0071t0018g0202others(10): Show | 13 | HG00597.hp2 HG01261.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.45+8078G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 100354 | ||||||
| chr5:100355
|
A | G | 1 | a0001c0002t0012g0072 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.45+8079A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 100355 | ||||||
| chr5:100356
|
A | AAGACTGT others(46): Show |
1 | a0028c0040t0090g0127 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.45+8096_45+8148dup others(53): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 100356 | |||||
| chr5:100356
|
A | AAGACTGT others(152): Show |
1 | a0041c0064t0010g0190 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.45+8121_45+8122ins others(159): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 100356 | |||||
| chr5:100356
|
A | AAGACTGT others(735): Show |
2 | a0014c0027t0049g0171a0014c0066t0051g0170 | 2 | HG02809.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.45+8121_45+8122ins others(742): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 100356 | |||||
| chr5:100356
|
A | AAGACTGT others(9106): Show |
1 | a0040c0063t0063g0189 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.45+8121_45+8122ins others(9113): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 100356 | |||||
| chr5:100356
|
A | G | 2 | a0006c0068t0058g0194a0006c0070t0054g0207 | 2 | HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.45+8080A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 100356 | ||||||
| chr5:100372
|
T | A | 1 | a0026c0050t0009g0141 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.45+8096T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 100372 | ||||||
| chr5:100372
|
T | TAATCCAT others(364): Show |
1 | a0008c0025t0045g0172 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.45+8121_45+8122ins others(371): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 100372 | |||||
| chr5:100372
|
T | TAATCCAT others(205): Show |
2 | a0006c0021t0018g0198a0006c0021t0056g0199 | 2 | HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.45+8121_45+8122ins others(212): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 100372 | |||||
| chr5:100378
|
A | ATATAAAG others(258): Show |
1 | a0019c0019t0062g0191 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.45+8121_45+8122ins others(265): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 100378 | |||||
| chr5:100387
|
C | CCTGGAAA others(258): Show |
6 | a0006c0071t0018g0202a0006c0072t0036g0206a0010c0014t0057g0197others(3): Show | 6 | HG00597.hp2 HG02897.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.45+8121_45+8122ins others(265): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 100387 | |||||
| chr5:100387
|
C | T | 1 | a0006c0070t0054g0207 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.45+8111C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 100387 | ||||||
| chr5:100398
|
C | T | 25 | a0001c0011t0048g0179a0006c0073t0020g0193a0008c0024t0021g0175others(22): Show | 25 | HG00323.hp2 HG01099.hp1 HG01261.hp2 others(22): Show |
intron_variant | MODIFIER | c.45+8122C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 100398 | ||||||
| chr5:100404
|
G | A | 5 | a0008c0024t0021g0175a0008c0024t0021g0176a0008c0025t0069g0174others(2): Show | 5 | HG02109.hp2 HG02145.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.45+8128G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 100404 | ||||||
| chr5:100420
|
G | C | 1 | a0036c0075t0061g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.45+8144G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 100420 | ||||||
| chr5:100425
|
A | T | 40 | a0001c0011t0048g0179a0006c0021t0018g0198a0006c0021t0056g0199others(37): Show | 40 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.45+8149A>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 100425 | ||||||
| chr5:100440
|
C | T | 2 | a0006c0021t0018g0198a0006c0021t0056g0199 | 2 | HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.45+8164C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 100440 | ||||||
| chr5:100445
|
AAAAAGCC others(998): Show |
A | 1 | a0002c0005t0127g0124 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.45+8222_45+9226del | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 100445 | |||||
| chr5:100451
|
C | CCTGTAGG others(46): Show |
1 | a0011c0078t0059g0185 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.45+8216_45+8217ins others(53): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 100451 | |||||
| chr5:100451
|
C | CCTGTAGG others(205): Show |
1 | a0036c0075t0061g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.45+8201_45+8202ins others(212): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 100451 | |||||
| chr5:100451
|
C | CCTGTAGG others(46): Show |
12 | a0006c0073t0020g0193a0008c0024t0021g0175a0008c0024t0021g0176others(9): Show | 12 | HG01261.hp2 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.45+8201_45+8202ins others(53): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 100451 | |||||
| chr5:100451
|
C | CCTGTAGG others(417): Show |
1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.45+8201_45+8202ins others(424): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 100451 | |||||
| chr5:100451
|
C | T | 11 | a0006c0070t0054g0207a0006c0071t0018g0202a0006c0072t0036g0206others(8): Show | 11 | HG00280.hp2 HG00597.hp2 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.45+8175C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 100451 | ||||||
| chr5:100478
|
A | AAATCCAT others(46): Show |
1 | a0029c0033t0042g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.45+8254_45+8255ins others(53): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 100478 | |||||
| chr5:100478
|
A | T | 26 | a0001c0001t0032g0144a0006c0021t0018g0198a0006c0021t0056g0199others(23): Show | 26 | HG00280.hp2 HG00323.hp2 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.45+8202A>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 100478 | ||||||
| chr5:100484
|
A | ATATAAAG others(152): Show |
2 | a0019c0019t0010g0164a0039c0062t0010g0165 | 2 | HG00323.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.45+8216_45+8217ins others(159): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 100484 | |||||
| chr5:100484
|
A | G | 1 | a0041c0064t0010g0190 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.45+8208A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 100484 | ||||||
| chr5:100498
|
A | G | 3 | a0014c0027t0049g0171a0014c0066t0051g0170a0019c0019t0062g0191 | 3 | HG02004.hp2 HG02809.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.45+8222A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 100498 | ||||||
| chr5:100504
|
C | T | 10 | a0001c0011t0048g0179a0008c0025t0045g0172a0011c0023t0041g0184others(7): Show | 10 | HG01099.hp1 HG02257.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.45+8228C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 100504 | ||||||
| chr5:100531
|
A | AAATCCAT others(46): Show |
4 | a0001c0001t0005g0090a0001c0001t0005g0123a0001c0001t0099g0089others(1): Show | 4 | HG00280.hp1 HG00741.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+8487_45+8539dup others(53): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 100531 | |||||
| chr5:100531
|
A | AAATCCAT others(99): Show |
2 | a0017c0030t0039g0140a0032c0058t0040g0158 | 2 | HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.45+8434_45+8539dup others(106): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 100531 | |||||
| chr5:100531
|
A | AAATCCAT others(152): Show |
2 | a0016c0018t0003g0005a0016c0018t0034g0004 | 2 | HG02145.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.45+8381_45+8539dup others(159): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 100531 | |||||
| chr5:100531
|
A | T | 37 | a0001c0001t0032g0144a0001c0002t0094g0021a0001c0007t0008g0143others(34): Show | 37 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.45+8255A>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 100531 | ||||||
| chr5:100546
|
C | T | 5 | a0006c0068t0058g0194a0014c0027t0049g0171a0014c0066t0051g0170others(2): Show | 5 | HG00280.hp2 HG02647.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+8270C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 100546 | ||||||
| chr5:100557
|
C | T | 22 | a0001c0011t0048g0179a0006c0070t0054g0207a0006c0071t0018g0202others(19): Show | 22 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.45+8281C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 100557 | ||||||
| chr5:100584
|
T | A | 1 | a0014c0065t0038g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.45+8308T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 100584 | ||||||
| chr5:100589
|
C | CAT | 2 | a0019c0019t0010g0164a0039c0062t0010g0165 | 2 | HG00323.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.45+8317_45+8318dup others(2): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 100589 | |||||
| chr5:100599
|
C | T | 11 | a0006c0073t0020g0193a0008c0024t0021g0175a0008c0024t0021g0176others(8): Show | 11 | HG01261.hp2 HG02109.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.45+8323C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 100599 | ||||||
| chr5:100604
|
A | G | 3 | a0019c0019t0010g0164a0039c0062t0010g0165a0041c0064t0010g0190 | 3 | HG00323.hp2 HG01081.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.45+8328A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 100604 | ||||||
| chr5:100610
|
C | T | 13 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0070t0054g0207others(10): Show | 13 | HG00280.hp2 HG00597.hp2 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.45+8334C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 100610 | ||||||
| chr5:100637
|
T | A | 11 | a0001c0011t0048g0179a0011c0023t0041g0184a0011c0023t0044g0187others(8): Show | 11 | HG01099.hp1 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.45+8361T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 100637 | ||||||
| chr5:100652
|
C | T | 3 | a0006c0068t0058g0194a0014c0027t0049g0171a0014c0066t0051g0170 | 3 | HG02647.hp1 HG02809.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.45+8376C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 100652 | ||||||
| chr5:100657
|
A | G | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.45+8381A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 100657 | ||||||
| chr5:100663
|
C | T | 27 | a0001c0011t0048g0179a0006c0021t0018g0198a0006c0021t0056g0199others(24): Show | 27 | HG00323.hp2 HG01081.hp2 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.45+8387C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 100663 | ||||||
| chr5:100690
|
T | A | 11 | a0006c0073t0020g0193a0008c0024t0021g0175a0008c0024t0021g0176others(8): Show | 11 | HG01261.hp2 HG02109.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.45+8414T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 100690 | ||||||
| chr5:100690
|
T | TAATCCAT others(2218): Show |
1 | a0001c0036t0077g0149 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.45+8539_45+8540ins others(2225): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 100690 | |||||
| chr5:100703
|
G | A | 1 | a0036c0075t0061g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.45+8427G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 100703 | ||||||
| chr5:100716
|
C | CCTGTAGG others(841): Show |
1 | a0001c0007t0008g0145 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.45+8539_45+8540ins others(848): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 100716 | |||||
| chr5:100716
|
C | T | 14 | a0001c0011t0048g0179a0011c0023t0041g0184a0011c0023t0044g0187others(11): Show | 14 | HG00323.hp2 HG01081.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.45+8440C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 100716 | ||||||
| chr5:100743
|
T | A | 1 | a0014c0065t0038g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.45+8467T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 100743 | ||||||
| chr5:100747
|
C | T | 1 | a0031c0031t0085g0108 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.45+8471C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 100747 | ||||||
| chr5:100758
|
C | T | 2 | a0019c0019t0062g0191a0040c0063t0063g0189 | 2 | HG00280.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.45+8482C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 100758 | ||||||
| chr5:100763
|
A | G | 4 | a0001c0001t0079g0059a0001c0002t0094g0021a0007c0010t0026g0035others(1): Show | 4 | HG00597.hp1 HG00642.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+8487A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 100763 | ||||||
| chr5:100769
|
C | T | 15 | a0001c0001t0079g0059a0001c0002t0094g0021a0006c0073t0020g0193others(12): Show | 15 | HG00597.hp1 HG00642.hp1 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.45+8493C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 100769 | ||||||
| chr5:100796
|
T | A | 5 | a0001c0001t0079g0059a0001c0002t0094g0021a0007c0010t0026g0035others(2): Show | 5 | HG00597.hp1 HG00642.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.45+8520T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 100796 | ||||||
| chr5:100796
|
T | TAATCCAT others(2324): Show |
1 | a0001c0051t0078g0148 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.45+8539_45+8540ins others(2331): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 100796 | |||||
| chr5:100811
|
C | T | 9 | a0001c0011t0048g0179a0011c0023t0041g0184a0011c0023t0044g0187others(6): Show | 9 | HG01099.hp1 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.45+8535C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 100811 | ||||||
| chr5:100816
|
G | A | 47 | a0001c0001t0032g0144a0001c0001t0079g0059a0001c0002t0094g0021others(44): Show | 47 | HG00597.hp1 HG00597.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.45+8540G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 100816 | ||||||
| chr5:100816
|
G | GAAAAGCC others(470): Show |
2 | a0008c0025t0069g0174a0008c0079t0068g0173 | 2 | HG03471.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.45+8545_45+8546ins others(477): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 100816 | |||||
| chr5:100816
|
G | GAAAAGCC others(629): Show |
1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.45+8545_45+8546ins others(636): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 100816 | |||||
| chr5:100816
|
G | GAAAAGTC others(46): Show |
1 | a0001c0002t0013g0109 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.45+8573_45+8625dup others(53): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 100816 | |||||
| chr5:100822
|
T | C | 18 | a0001c0001t0032g0144a0001c0007t0008g0143a0001c0007t0008g0145others(15): Show | 18 | HG00323.hp2 HG01081.hp2 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.45+8546T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 100822 | ||||||
| chr5:100822
|
T | TCTGTAGG others(205): Show |
2 | a0006c0072t0036g0206a0037c0074t0037g0203 | 2 | HG02897.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.45+8572_45+8573ins others(212): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 100822 | |||||
| chr5:100822
|
T | TCTGTAGG others(364): Show |
1 | a0006c0070t0054g0207 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.45+8572_45+8573ins others(371): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 100822 | |||||
| chr5:100822
|
T | TCTGTAGG others(417): Show |
1 | a0018c0022t0011g0196 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.45+8572_45+8573ins others(424): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 100822 | |||||
| chr5:100825
|
G | A | 1 | a0008c0025t0045g0172 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.45+8549G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 100825 | ||||||
| chr5:100825
|
G | GTAGGGGA others(46): Show |
1 | a0002c0003t0002g0132 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.45+8601_45+8602ins others(53): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 100825 | |||||
| chr5:100849
|
A | AAATCCAT others(364): Show |
1 | a0001c0049t0096g0063 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.45+8598_45+8599ins others(371): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 100849 | |||||
| chr5:100849
|
A | T | 48 | a0001c0001t0032g0144a0001c0001t0079g0059a0001c0002t0094g0021others(45): Show | 48 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.45+8573A>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 100849 | ||||||
| chr5:100864
|
C | CCTGGAAA others(258): Show |
2 | a0010c0014t0057g0197a0018c0022t0011g0195 | 2 | NA18984.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.45+8598_45+8599ins others(265): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 100864 | |||||
| chr5:100864
|
C | T | 3 | a0008c0025t0069g0174a0008c0079t0068g0173a0041c0064t0010g0190 | 3 | HG01081.hp2 HG03471.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.45+8588C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 100864 | ||||||
| chr5:100869
|
A | G | 1 | a0008c0025t0045g0172 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.45+8593A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 100869 | ||||||
| chr5:100875
|
T | C | 40 | a0001c0001t0032g0144a0001c0007t0008g0143a0001c0007t0008g0145others(37): Show | 40 | HG00597.hp2 HG01081.hp2 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.45+8599T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 100875 | ||||||
| chr5:100875
|
T | TCTGTAGG others(311): Show |
2 | a0006c0021t0018g0198a0006c0021t0056g0199 | 2 | HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.45+8651_45+8652ins others(318): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 100875 | |||||
| chr5:100902
|
T | A | 9 | a0001c0001t0079g0059a0001c0002t0094g0021a0001c0049t0096g0063others(6): Show | 9 | HG00323.hp2 HG00597.hp1 HG00642.hp1 others(6): Show |
intron_variant | MODIFIER | c.45+8626T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 100902 | ||||||
| chr5:100902
|
T | TAATCCAT others(1213): Show |
2 | a0012c0013t0009g0016a0012c0013t0009g0019 | 2 | NA18973.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.45+8651_45+8652ins others(1220): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 100902 | |||||
| chr5:100902
|
T | TAATCCAT others(948): Show |
5 | a0001c0002t0006g0134a0001c0011t0029g0136a0001c0011t0106g0085others(2): Show | 5 | HG02647.hp2 HG02723.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+8678_45+8679ins others(955): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 100902 | |||||
| chr5:100902
|
T | TAATCCAT others(1107): Show |
1 | a0001c0007t0100g0025 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.45+8678_45+8679ins others(1114): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 100902 | |||||
| chr5:100902
|
T | TAATCCAT others(1160): Show |
2 | a0001c0001t0097g0086a0001c0001t0104g0023 | 2 | HG00323.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.45+8678_45+8679ins others(1167): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 100902 | |||||
| chr5:100902
|
TAATCCAT others(998): Show |
T | 5 | a0009c0012t0033g0161a0009c0012t0114g0156a0009c0012t0115g0157others(2): Show | 5 | HG02886.hp2 HG03139.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.45+8655_45+9659del | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 100902 | |||||
| chr5:100915
|
G | GCTCTGGA others(682): Show |
2 | a0014c0027t0049g0171a0014c0066t0051g0170 | 2 | HG02809.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.45+8640_45+8641ins others(689): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 100915 | |||||
| chr5:100917
|
C | CCTGGAAA others(152): Show |
1 | a0011c0023t0044g0187 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.45+8651_45+8652ins others(159): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 100917 | |||||
| chr5:100917
|
C | CCTGGGAA others(576): Show |
1 | a0008c0025t0045g0172 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.45+8645_45+8646ins others(583): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 100917 | |||||
| chr5:100917
|
C | CCTGGGAA others(205): Show |
1 | a0006c0071t0018g0202 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.45+8645_45+8646ins others(212): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 100917 | |||||
| chr5:100917
|
C | T | 4 | a0006c0068t0058g0194a0035c0060t0020g0188a0036c0075t0061g0178others(1): Show | 4 | HG00280.hp2 HG02647.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+8641C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 100917 | ||||||
| chr5:100928
|
T | C | 41 | a0001c0001t0032g0144a0001c0007t0008g0143a0001c0007t0008g0145others(38): Show | 41 | HG00323.hp2 HG01099.hp1 HG01261.hp1 others(38): Show |
intron_variant | MODIFIER | c.45+8652T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 100928 | ||||||
| chr5:100955
|
A | T | 48 | a0001c0001t0032g0144a0001c0002t0024g0024a0001c0007t0008g0143others(45): Show | 48 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.45+8679A>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 100955 | ||||||
| chr5:100970
|
C | CCTGGAAA others(8943): Show |
1 | a0019c0019t0062g0191 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.45+8731_45+8732ins others(8950): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 100970 | |||||
| chr5:100970
|
C | T | 9 | a0001c0011t0048g0179a0008c0025t0045g0172a0011c0023t0041g0184others(6): Show | 9 | HG01099.hp1 HG02257.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.45+8694C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 100970 | ||||||
| chr5:100971
|
C | G | 1 | a0040c0063t0063g0189 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.45+8695C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 100971 | ||||||
| chr5:100975
|
A | AAAAAGCC others(46): Show |
1 | a0021c0026t0060g0169 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.45+8704_45+8705ins others(53): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 100975 | |||||
| chr5:100975
|
A | G | 2 | a0019c0019t0010g0164a0039c0062t0010g0165 | 2 | HG00323.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.45+8699A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 100975 | ||||||
| chr5:100981
|
T | C | 28 | a0004c0006t0125g0048a0004c0043t0126g0099a0006c0021t0018g0198others(25): Show | 28 | HG00323.hp2 HG01081.hp2 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.45+8705T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 100981 | ||||||
| chr5:100981
|
T | TCTGTAGG others(205): Show |
3 | a0013c0020t0050g0182a0013c0020t0052g0183a0013c0067t0046g0186 | 3 | HG02451.hp1 HG03041.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.45+8731_45+8732ins others(212): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 100981 | |||||
| chr5:100984
|
G | A | 1 | a0001c0007t0008g0145 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.45+8708G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 100984 | ||||||
| chr5:100998
|
G | A | 1 | a0001c0007t0008g0145 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.45+8722G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 100998 | ||||||
| chr5:100998
|
G | GTTGTGAG others(841): Show |
1 | a0001c0007t0008g0143 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.45+8731_45+8732ins others(848): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 100998 | |||||
| chr5:101008
|
A | AAATCCAT others(99): Show |
1 | a0003c0044t0001g0116 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.45+8761_45+8866dup others(106): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101008 | |||||
| chr5:101008
|
A | AAATCCAT others(46): Show |
3 | a0002c0003t0002g0098a0002c0003t0002g0101a0002c0005t0070g0100 | 3 | HG01069.hp1 HG01071.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.45+8753_45+8754ins others(53): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101008 | |||||
| chr5:101008
|
A | AAATCCAT others(470): Show |
1 | a0032c0058t0040g0158 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.45+8751_45+8752ins others(477): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101008 | |||||
| chr5:101008
|
A | T | 61 | a0001c0001t0032g0144a0001c0001t0079g0059a0001c0001t0097g0086others(58): Show | 61 | HG00323.hp1 HG00323.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.45+8732A>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101008 | ||||||
| chr5:101008
|
AAATCCAT others(46): Show |
A | 1 | a0001c0048t0013g0055 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.45+8814_45+8866del others(53): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101008 | |||||
| chr5:101023
|
C | T | 4 | a0011c0023t0044g0187a0014c0027t0049g0171a0014c0066t0051g0170others(1): Show | 4 | HG00280.hp2 HG02280.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+8747C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101023 | ||||||
| chr5:101028
|
A | G | 8 | a0001c0011t0048g0179a0011c0023t0041g0184a0011c0078t0059g0185others(5): Show | 8 | HG00323.hp2 HG01099.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.45+8752A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101028 | ||||||
| chr5:101029
|
A | G | 4 | a0001c0001t0032g0144a0001c0007t0008g0146a0001c0007t0008g0150others(1): Show | 4 | HG02109.hp1 HG03540.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+8753A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101029 | ||||||
| chr5:101034
|
T | C | 36 | a0001c0001t0032g0144a0001c0007t0008g0143a0001c0007t0008g0145others(33): Show | 36 | HG00597.hp2 HG01099.hp1 HG01261.hp1 others(33): Show |
intron_variant | MODIFIER | c.45+8758T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101034 | ||||||
| chr5:101034
|
T | TCTATAGG others(837): Show |
1 | a0004c0006t0123g0003 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.45+8760_45+8761ins others(844): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101034 | |||||
| chr5:101034
|
T | TCTGTAGG others(256): Show |
1 | a0025c0045t0122g0002 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.45+8837_45+8838ins others(263): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101034 | |||||
| chr5:101061
|
T | A | 24 | a0001c0001t0079g0059a0001c0001t0097g0086a0001c0001t0104g0023others(21): Show | 24 | HG00323.hp1 HG00597.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.45+8785T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101061 | ||||||
| chr5:101061
|
T | TAATCCAT others(46): Show |
94 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0142others(91): Show | 94 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.45+8837_45+8838ins others(53): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101061 | |||||
| chr5:101061
|
T | TAATCCAT others(415): Show |
1 | a0001c0015t0035g0122 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.45+8837_45+8838ins others(422): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101061 | |||||
| chr5:101061
|
T | TAATCCAT others(468): Show |
1 | a0001c0015t0076g0154 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.45+8837_45+8838ins others(475): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101061 | |||||
| chr5:101061
|
T | TAATCCAT others(470): Show |
1 | a0022c0046t0047g0180 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.45+8799_45+8800ins others(477): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101061 | |||||
| chr5:101074
|
G | A | 1 | a0040c0063t0063g0189 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.45+8798G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101074 | ||||||
| chr5:101076
|
C | CCTGGAAA others(364): Show |
2 | a0019c0019t0010g0164a0039c0062t0010g0165 | 2 | HG00323.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.45+8810_45+8811ins others(371): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101076 | |||||
| chr5:101076
|
C | T | 8 | a0001c0011t0048g0179a0008c0025t0069g0174a0008c0079t0068g0173others(5): Show | 8 | HG01099.hp1 HG02257.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.45+8800C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101076 | ||||||
| chr5:101081
|
A | AAAAAGCC others(46): Show |
5 | a0006c0073t0020g0193a0010c0014t0019g0205a0010c0014t0055g0201others(2): Show | 5 | HG01261.hp2 HG02258.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.45+8810_45+8811ins others(53): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101081 | |||||
| chr5:101081
|
A | G | 4 | a0001c0007t0008g0143a0001c0007t0008g0145a0004c0006t0125g0048others(1): Show | 4 | HG01261.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+8805A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101081 | ||||||
| chr5:101082
|
A | AAAAGTCT others(258): Show |
5 | a0001c0011t0048g0179a0011c0023t0041g0184a0011c0078t0059g0185others(2): Show | 5 | HG01099.hp1 HG02257.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.45+8837_45+8838ins others(265): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101082 | |||||
| chr5:101087
|
T | C | 23 | a0001c0001t0032g0144a0001c0007t0008g0146a0001c0007t0008g0150others(20): Show | 23 | HG00280.hp2 HG01261.hp2 HG02004.hp2 others(20): Show |
intron_variant | MODIFIER | c.45+8811T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101087 | ||||||
| chr5:101087
|
T | TCTGTAGG others(258): Show |
1 | a0004c0041t0003g0077 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.45+8837_45+8838ins others(265): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101087 | |||||
| chr5:101087
|
T | TCTGTAGG others(99): Show |
1 | a0036c0075t0061g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.45+8857_45+8858ins others(106): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101087 | |||||
| chr5:101090
|
G | GTAGGGGA others(46): Show |
1 | a0026c0050t0009g0141 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.45+8837_45+8838ins others(53): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101090 | |||||
| chr5:101090
|
GTAGGGGA others(998): Show |
G | 1 | a0014c0065t0038g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.45+8864_45+9868del | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101090 | |||||
| chr5:101114
|
T | A | 21 | a0001c0001t0028g0046a0001c0001t0032g0144a0001c0001t0098g0129others(18): Show | 21 | HG01074.hp1 HG01243.hp2 HG01256.hp1 others(18): Show |
intron_variant | MODIFIER | c.45+8838T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101114 | ||||||
| chr5:101114
|
T | TAATCCAT others(152): Show |
1 | a0001c0002t0012g0072 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.45+8866_45+8867ins others(159): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101114 | |||||
| chr5:101127
|
G | A | 3 | a0001c0007t0008g0146a0001c0007t0008g0150a0001c0007t0109g0147 | 3 | HG03540.hp1 NA20129.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.45+8851G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101127 | ||||||
| chr5:101129
|
C | T | 2 | a0006c0021t0018g0198a0006c0021t0056g0199 | 2 | HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.45+8853C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101129 | ||||||
| chr5:101134
|
A | G | 4 | a0012c0013t0009g0016a0012c0013t0009g0019a0021c0026t0060g0169others(1): Show | 4 | HG02818.hp2 HG03225.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+8858A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101134 | ||||||
| chr5:101140
|
T | C | 33 | a0001c0007t0008g0143a0001c0007t0008g0145a0001c0007t0008g0146others(30): Show | 33 | HG00280.hp2 HG00323.hp2 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.45+8864T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101140 | ||||||
| chr5:101140
|
TCTATAGG others(362): Show |
T | 2 | a0003c0009t0017g0093a0004c0006t0002g0051 | 2 | HG01256.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.45+8867_45+9235del | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101140 | |||||
| chr5:101143
|
A | ATAGGGGA others(1742): Show |
2 | a0008c0024t0021g0175a0008c0024t0021g0176 | 2 | HG02109.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.45+8878_45+8879ins others(1749): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101143 | |||||
| chr5:101143
|
A | G | 55 | a0001c0001t0028g0046a0001c0001t0032g0144a0001c0001t0098g0129others(52): Show | 55 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.45+8867A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101143 | ||||||
| chr5:101155
|
T | C | 59 | a0001c0001t0028g0046a0001c0001t0032g0144a0001c0001t0098g0129others(56): Show | 59 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.45+8879T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101155 | ||||||
| chr5:101167
|
T | A | 5 | a0001c0007t0008g0146a0001c0007t0008g0150a0001c0007t0109g0147others(2): Show | 5 | HG03471.hp2 HG03540.hp1 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.45+8891T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101167 | ||||||
| chr5:101167
|
T | TAATCCAT others(258): Show |
1 | a0001c0001t0098g0129 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.45+8905_45+8906ins others(265): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101167 | |||||
| chr5:101167
|
T | TAATCCAT others(46): Show |
2 | a0011c0023t0041g0184a0011c0078t0059g0185 | 2 | HG01099.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.45+8916_45+8917ins others(53): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101167 | |||||
| chr5:101182
|
T | C | 31 | a0001c0001t0028g0046a0001c0001t0032g0144a0001c0001t0098g0129others(28): Show | 31 | HG00323.hp2 HG00597.hp2 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.45+8906T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101182 | ||||||
| chr5:101188
|
A | G | 1 | a0011c0023t0044g0187 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.45+8912A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101188 | ||||||
| chr5:101193
|
T | C | 27 | a0001c0007t0008g0143a0001c0007t0008g0145a0001c0011t0048g0179others(24): Show | 27 | HG00597.hp2 HG00741.hp1 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.45+8917T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101193 | ||||||
| chr5:101193
|
T | TCTATAGG others(362): Show |
1 | a0001c0036t0077g0149 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.45+8919_45+8920ins others(369): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101193 | |||||
| chr5:101196
|
G | A | 6 | a0001c0001t0028g0046a0002c0003t0011g0210a0002c0005t0002g0064others(3): Show | 6 | HG01074.hp1 HG01243.hp2 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.45+8920G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101196 | ||||||
| chr5:101208
|
C | T | 5 | a0001c0001t0028g0046a0002c0003t0011g0210a0002c0005t0002g0064others(2): Show | 5 | HG01074.hp1 HG01243.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+8932C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101208 | ||||||
| chr5:101220
|
T | A | 6 | a0001c0011t0048g0179a0004c0006t0125g0048a0004c0041t0003g0077others(3): Show | 6 | HG01261.hp1 HG02280.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.45+8944T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101220 | ||||||
| chr5:101235
|
C | T | 8 | a0001c0001t0028g0046a0002c0003t0011g0210a0002c0005t0002g0064others(5): Show | 8 | HG00597.hp2 HG01074.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.45+8959C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101235 | ||||||
| chr5:101240
|
A | G | 2 | a0001c0007t0008g0143a0001c0007t0008g0145 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.45+8964A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101240 | ||||||
| chr5:101246
|
T | C | 30 | a0001c0001t0032g0144a0001c0011t0048g0179a0001c0051t0078g0148others(27): Show | 30 | HG00323.hp2 HG00597.hp2 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.45+8970T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101246 | ||||||
| chr5:101246
|
TCTGTAGG others(97): Show |
T | 3 | a0002c0003t0011g0210a0002c0005t0002g0064a0003c0004t0016g0078 | 3 | HG01074.hp1 NA18954.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.45+8983_45+9086del | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101246 | |||||
| chr5:101254
|
G | GGA | 37 | a0001c0001t0028g0046a0001c0001t0032g0144a0001c0007t0008g0143others(34): Show | 37 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.45+8981_45+8982dup others(2): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101254 | |||||
| chr5:101254
|
G | GGAGAGAC others(101): Show |
2 | a0013c0020t0050g0182a0013c0020t0052g0183 | 2 | HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.45+8982_45+8983ins others(108): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101254 | |||||
| chr5:101254
|
G | GGAGAGAC others(48): Show |
1 | a0008c0025t0069g0174 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.45+8982_45+8983ins others(55): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101254 | |||||
| chr5:101254
|
G | GGAGAGAC others(525): Show |
1 | a0008c0079t0068g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.45+8982_45+8983ins others(532): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101254 | |||||
| chr5:101254
|
G | GGAGAGAC others(101): Show |
1 | a0006c0068t0058g0194 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.45+8982_45+8983ins others(108): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101254 | |||||
| chr5:101254
|
G | GGAGAGAC others(101): Show |
1 | a0006c0072t0036g0206 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.45+8982_45+8983ins others(108): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101254 | |||||
| chr5:101254
|
G | GGAGAGAC others(48): Show |
1 | a0006c0071t0018g0202 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.45+8982_45+8983ins others(55): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101254 | |||||
| chr5:101254
|
G | GGAGAGAC others(1267): Show |
1 | a0006c0021t0018g0198 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.45+8982_45+8983ins others(1274): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101254 | |||||
| chr5:101254
|
G | GGAGAGAC others(1214): Show |
1 | a0037c0074t0037g0203 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.45+8982_45+8983ins others(1221): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101254 | |||||
| chr5:101254
|
G | GGAGAGAC others(48): Show |
2 | a0006c0073t0020g0193a0010c0014t0055g0201 | 2 | HG01261.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.45+8982_45+8983ins others(55): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101254 | |||||
| chr5:101254
|
G | GGAGAGAC others(207): Show |
1 | a0013c0067t0046g0186 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.45+8982_45+8983ins others(214): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101254 | |||||
| chr5:101254
|
G | GGAGAGAC others(101): Show |
3 | a0001c0011t0048g0179a0015c0076t0067g0192a0015c0077t0053g0181 | 3 | HG02257.hp1 HG02280.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.45+8982_45+8983ins others(108): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101254 | |||||
| chr5:101271
|
A | T | 37 | a0001c0001t0028g0046a0001c0001t0032g0144a0001c0007t0008g0146others(34): Show | 37 | HG00323.hp2 HG00597.hp2 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.45+8995A>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101271 | ||||||
| chr5:101286
|
C | CCTGGAAA others(99): Show |
2 | a0011c0023t0041g0184a0011c0078t0059g0185 | 2 | HG01099.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.45+9014_45+9015ins others(106): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101286 | |||||
| chr5:101286
|
C | T | 17 | a0001c0011t0048g0179a0008c0025t0045g0172a0008c0025t0069g0174others(14): Show | 17 | HG00280.hp2 HG00323.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.45+9010C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101286 | ||||||
| chr5:101287
|
C | G | 1 | a0041c0064t0010g0190 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.45+9011C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101287 | ||||||
| chr5:101288
|
T | G | 2 | a0004c0006t0125g0048a0004c0043t0126g0099 | 2 | HG01261.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.45+9012T>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101288 | ||||||
| chr5:101291
|
G | A | 48 | a0001c0001t0028g0046a0001c0001t0032g0144a0001c0007t0008g0143others(45): Show | 48 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.45+9015G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101291 | ||||||
| chr5:101292
|
A | G | 1 | a0036c0075t0061g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.45+9016A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101292 | ||||||
| chr5:101297
|
C | CCTGTAGG others(99): Show |
1 | a0011c0023t0044g0187 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.45+9100_45+9101ins others(106): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101297 | |||||
| chr5:101297
|
C | CCTGTAGG others(152): Show |
1 | a0001c0001t0079g0059 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.45+9115_45+9116ins others(159): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101297 | |||||
| chr5:101297
|
C | T | 12 | a0001c0001t0028g0046a0001c0001t0032g0144a0001c0007t0008g0143others(9): Show | 12 | HG00323.hp2 HG01243.hp2 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.45+9021C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101297 | ||||||
| chr5:101324
|
T | A | 6 | a0001c0001t0028g0046a0001c0051t0078g0148a0003c0004t0001g0087others(3): Show | 6 | HG01243.hp2 HG02083.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.45+9048T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101324 | ||||||
| chr5:101325
|
A | G | 2 | a0014c0027t0049g0171a0014c0066t0051g0170 | 2 | HG02809.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.45+9049A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101325 | ||||||
| chr5:101339
|
C | CCTGGAAA others(99): Show |
1 | a0008c0025t0069g0174 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.45+9153_45+9154ins others(106): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101339 | |||||
| chr5:101339
|
C | T | 2 | a0018c0022t0011g0195a0040c0063t0063g0189 | 2 | HG00280.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.45+9063C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101339 | ||||||
| chr5:101344
|
A | AAAAAGTC others(44): Show |
1 | a0001c0036t0077g0149 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.45+9073_45+9074ins others(51): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101344 | |||||
| chr5:101344
|
A | G | 5 | a0001c0001t0028g0046a0003c0004t0001g0087a0004c0006t0125g0048others(2): Show | 5 | HG01243.hp2 HG01261.hp1 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+9068A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101344 | ||||||
| chr5:101350
|
C | T | 16 | a0001c0007t0008g0143a0001c0007t0008g0145a0001c0007t0008g0146others(13): Show | 16 | HG00280.hp2 HG01081.hp2 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.45+9074C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101350 | ||||||
| chr5:101377
|
T | A | 5 | a0001c0001t0014g0033a0001c0007t0008g0143a0001c0007t0008g0145others(2): Show | 5 | HG01261.hp1 HG02080.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+9101T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101377 | ||||||
| chr5:101377
|
T | TAATCCAT others(521): Show |
1 | a0038c0080t0043g0177 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.45+9113_45+9114ins others(528): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101377 | |||||
| chr5:101392
|
C | CCTGGAAA others(46): Show |
3 | a0013c0020t0050g0182a0013c0020t0052g0183a0013c0067t0046g0186 | 3 | HG02451.hp1 HG03041.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.45+9126_45+9127ins others(53): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101392 | |||||
| chr5:101392
|
C | T | 5 | a0006c0021t0056g0199a0006c0071t0018g0202a0011c0023t0044g0187others(2): Show | 5 | HG02280.hp1 HG02486.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.45+9116C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101392 | ||||||
| chr5:101403
|
C | CCTGTAGG others(1318): Show |
1 | a0006c0068t0058g0194 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.45+9153_45+9154ins others(1325): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101403 | |||||
| chr5:101403
|
C | CCTGTAGG others(3067): Show |
2 | a0014c0027t0049g0171a0014c0066t0051g0170 | 2 | HG02809.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.45+9153_45+9154ins others(3074): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101403 | |||||
| chr5:101403
|
C | T | 9 | a0001c0007t0008g0143a0001c0007t0008g0145a0001c0036t0077g0149others(6): Show | 9 | HG00280.hp2 HG01074.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.45+9127C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101403 | ||||||
| chr5:101411
|
GGA | G | 3 | a0002c0003t0011g0210a0002c0005t0002g0064a0003c0004t0016g0078 | 3 | HG01074.hp1 NA18954.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.45+9140_45+9141del others(2): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101411 | |||||
| chr5:101430
|
A | AAATCCAT others(46): Show |
1 | a0008c0025t0045g0172 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.45+9168_45+9169ins others(53): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101430 | |||||
| chr5:101430
|
A | T | 38 | a0001c0001t0028g0046a0001c0001t0032g0144a0001c0007t0008g0146others(35): Show | 38 | HG00323.hp2 HG00597.hp2 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.45+9154A>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101430 | ||||||
| chr5:101445
|
C | CCTGGAAA others(46): Show |
1 | a0011c0023t0044g0187 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.45+9170_45+9171ins others(53): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101445 | |||||
| chr5:101445
|
C | CCTGGAAA others(46): Show |
2 | a0006c0073t0020g0193a0010c0014t0055g0201 | 2 | HG01261.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.45+9170_45+9171ins others(53): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101445 | |||||
| chr5:101445
|
C | T | 8 | a0001c0011t0048g0179a0006c0068t0058g0194a0008c0025t0069g0174others(5): Show | 8 | HG01099.hp1 HG02257.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.45+9169C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101445 | ||||||
| chr5:101447
|
G | T | 58 | a0001c0001t0028g0046a0001c0001t0032g0144a0001c0007t0008g0143others(55): Show | 58 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.45+9171G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101447 | ||||||
| chr5:101450
|
G | A | 46 | a0001c0001t0028g0046a0001c0001t0032g0144a0001c0007t0008g0143others(43): Show | 46 | HG00280.hp2 HG00323.hp2 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.45+9174G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101450 | ||||||
| chr5:101450
|
G | GAAAAGCC others(99): Show |
1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.45+9206_45+9207ins others(106): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101450 | |||||
| chr5:101456
|
C | CCTGTAGG others(1477): Show |
1 | a0006c0071t0018g0202 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.45+9206_45+9207ins others(1484): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101456 | |||||
| chr5:101456
|
C | CCTGTAGG others(576): Show |
1 | a0019c0019t0062g0191 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.45+9206_45+9207ins others(583): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101456 | |||||
| chr5:101456
|
C | T | 10 | a0001c0007t0008g0143a0001c0007t0008g0145a0001c0036t0077g0149others(7): Show | 10 | HG01261.hp1 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.45+9180C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101456 | ||||||
| chr5:101466
|
A | AGACTGTT others(462): Show |
1 | a0001c0051t0078g0148 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.45+9192_45+9193ins others(469): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101466 | |||||
| chr5:101483
|
A | T | 39 | a0001c0001t0028g0046a0001c0001t0032g0144a0001c0007t0008g0143others(36): Show | 39 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.45+9207A>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101483 | ||||||
| chr5:101498
|
C | CCTGGAAA others(46): Show |
1 | a0010c0014t0019g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.45+9226_45+9227ins others(53): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101498 | |||||
| chr5:101498
|
C | T | 2 | a0014c0027t0049g0171a0014c0066t0051g0170 | 2 | HG02809.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.45+9222C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101498 | ||||||
| chr5:101498
|
CCTGGGAA others(46): Show |
C | 1 | a0001c0002t0081g0034 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.45+9227_45+9279del others(53): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101498 | |||||
| chr5:101500
|
T | G | 1 | a0003c0004t0001g0087 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.45+9224T>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101500 | ||||||
| chr5:101503
|
G | A | 50 | a0001c0001t0028g0046a0001c0001t0032g0144a0001c0007t0008g0143others(47): Show | 50 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.45+9227G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101503 | ||||||
| chr5:101503
|
G | GAAAAGTC others(46): Show |
2 | a0016c0018t0003g0005a0016c0018t0034g0004 | 2 | HG02145.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.45+9232_45+9233ins others(53): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101503 | |||||
| chr5:101503
|
GAAAAGCC others(152): Show |
G | 1 | a0003c0004t0001g0087 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.45+9260_45+9418del | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101503 | |||||
| chr5:101509
|
C | CCTGTAGG others(523): Show |
1 | a0006c0070t0054g0207 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.45+9274_45+9275ins others(530): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101509 | |||||
| chr5:101509
|
C | CCTGTAGG others(470): Show |
1 | a0006c0072t0036g0206 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.45+9274_45+9275ins others(477): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101509 | |||||
| chr5:101509
|
C | T | 16 | a0001c0007t0008g0143a0001c0007t0008g0145a0001c0011t0048g0179others(13): Show | 16 | HG00323.hp2 HG01261.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.45+9233C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101509 | ||||||
| chr5:101536
|
T | A | 10 | a0001c0007t0008g0143a0001c0007t0008g0145a0001c0011t0048g0179others(7): Show | 10 | HG01261.hp1 HG02257.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.45+9260T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101536 | ||||||
| chr5:101536
|
T | TAATCCAT others(46): Show |
3 | a0013c0020t0050g0182a0013c0020t0052g0183a0013c0067t0046g0186 | 3 | HG02451.hp1 HG03041.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.45+9274_45+9275ins others(53): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101536 | |||||
| chr5:101536
|
T | TAATCCAT others(1477): Show |
2 | a0010c0014t0057g0197a0018c0022t0011g0195 | 2 | NA18984.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.45+9274_45+9275ins others(1484): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101536 | |||||
| chr5:101536
|
T | TAATCCAT others(1371): Show |
1 | a0018c0022t0011g0196 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.45+9274_45+9275ins others(1378): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101536 | |||||
| chr5:101551
|
T | C | 32 | a0001c0001t0028g0046a0001c0001t0032g0144a0001c0007t0008g0143others(29): Show | 32 | HG00597.hp2 HG01074.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.45+9275T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101551 | ||||||
| chr5:101551
|
T | TCTGGAAA others(46): Show |
1 | a0010c0069t0019g0204 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.45+9285_45+9286ins others(53): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101551 | |||||
| chr5:101551
|
T | TCTGGAAA others(258): Show |
1 | a0037c0074t0037g0203 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.45+9327_45+9328ins others(265): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101551 | |||||
| chr5:101556
|
A | AAAAAGCC others(628): Show |
1 | a0001c0007t0109g0147 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.45+9285_45+9286ins others(635): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101556 | |||||
| chr5:101556
|
A | AAAAAGTC others(46): Show |
2 | a0001c0016t0005g0160a0001c0016t0025g0152 | 2 | HG02922.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.45+9313_45+9365dup others(53): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101556 | |||||
| chr5:101556
|
A | G | 1 | a0006c0070t0054g0207 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.45+9280A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101556 | ||||||
| chr5:101557
|
A | AAAAGCCT others(575): Show |
2 | a0001c0007t0008g0146a0001c0007t0008g0150 | 2 | NA20129.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.45+9285_45+9286ins others(582): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101557 | |||||
| chr5:101557
|
A | AAAAGCCT others(522): Show |
1 | a0001c0001t0032g0144 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.45+9285_45+9286ins others(529): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101557 | |||||
| chr5:101557
|
A | G | 1 | a0038c0080t0043g0177 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.45+9281A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101557 | ||||||
| chr5:101562
|
T | C | 30 | a0001c0011t0048g0179a0002c0003t0011g0210a0002c0005t0002g0064others(27): Show | 30 | HG01074.hp1 HG01081.hp2 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.45+9286T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101562 | ||||||
| chr5:101562
|
T | TCTGTAGG others(46): Show |
1 | a0019c0019t0010g0164 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.45+9312_45+9313ins others(53): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101562 | |||||
| chr5:101562
|
T | TCTGTAGG others(4127): Show |
1 | a0039c0062t0010g0165 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.45+9312_45+9313ins others(4134): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101562 | |||||
| chr5:101562
|
T | TCTGTAGG others(468): Show |
1 | a0004c0006t0125g0048 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.45+9312_45+9313ins others(475): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101562 | |||||
| chr5:101562
|
T | TCTGTAGG others(468): Show |
1 | a0004c0043t0126g0099 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.45+9312_45+9313ins others(475): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101562 | |||||
| chr5:101564
|
T | TGTAGGGG others(576): Show |
1 | a0015c0076t0067g0192 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.45+9312_45+9313ins others(583): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101564 | |||||
| chr5:101564
|
T | TGTAGGGG others(629): Show |
1 | a0015c0077t0053g0181 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.45+9312_45+9313ins others(636): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101564 | |||||
| chr5:101565
|
G | A | 2 | a0001c0002t0081g0034a0004c0006t0002g0051 | 2 | HG01515.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.45+9289G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101565 | ||||||
| chr5:101577
|
C | T | 1 | a0004c0006t0002g0051 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.45+9301C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101577 | ||||||
| chr5:101589
|
A | AAATCCAT others(152): Show |
1 | a0012c0013t0133g0118 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.45+9332_45+9333ins others(159): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101589 | |||||
| chr5:101589
|
A | AAATCCAT others(311): Show |
1 | a0001c0049t0096g0063 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.45+9380_45+9381ins others(318): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101589 | |||||
| chr5:101589
|
A | AAATCCAT others(5876): Show |
1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.45+9327_45+9328ins others(5883): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101589 | |||||
| chr5:101589
|
A | T | 32 | a0001c0002t0081g0034a0001c0007t0008g0143a0001c0007t0008g0145others(29): Show | 32 | HG00280.hp2 HG00323.hp2 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.45+9313A>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101589 | ||||||
| chr5:101604
|
C | CCTGGAAA others(152): Show |
1 | a0019c0019t0010g0164 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.45+9332_45+9333ins others(159): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101604 | |||||
| chr5:101604
|
C | T | 6 | a0004c0006t0002g0051a0006c0021t0018g0198a0008c0079t0068g0173others(3): Show | 6 | HG01515.hp2 HG02486.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.45+9328C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101604 | ||||||
| chr5:101606
|
T | G | 3 | a0002c0003t0011g0210a0002c0005t0002g0064a0003c0004t0016g0078 | 3 | HG01074.hp1 NA18954.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.45+9330T>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101606 | ||||||
| chr5:101609
|
G | A | 51 | a0001c0001t0032g0144a0001c0002t0081g0034a0001c0007t0008g0143others(48): Show | 51 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.45+9333G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101609 | ||||||
| chr5:101610
|
A | AAAAGCCT others(470): Show |
1 | a0006c0021t0056g0199 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.45+9338_45+9339ins others(477): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101610 | |||||
| chr5:101610
|
A | C | 1 | a0021c0026t0060g0169 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.45+9334A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101610 | ||||||
| chr5:101615
|
T | C | 27 | a0001c0036t0077g0149a0001c0051t0078g0148a0002c0003t0011g0210others(24): Show | 27 | HG00597.hp2 HG01074.hp1 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.45+9339T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101615 | ||||||
| chr5:101615
|
T | TCTATAGG others(309): Show |
2 | a0001c0007t0008g0143a0001c0007t0008g0145 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.45+9341_45+9342ins others(316): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101615 | |||||
| chr5:101615
|
T | TCTGTAGG others(152): Show |
1 | a0020c0081t0064g0200 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.45+9380_45+9381ins others(159): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101615 | |||||
| chr5:101618
|
G | A | 1 | a0001c0002t0081g0034 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.45+9342G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101618 | ||||||
| chr5:101642
|
T | A | 17 | a0001c0007t0008g0143a0001c0007t0008g0145a0002c0003t0011g0210others(14): Show | 17 | HG01074.hp1 HG01099.hp1 HG02004.hp2 others(14): Show |
intron_variant | MODIFIER | c.45+9366T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101642 | ||||||
| chr5:101657
|
T | C | 21 | a0001c0011t0048g0179a0001c0036t0077g0149a0001c0051t0078g0148others(18): Show | 21 | HG00280.hp2 HG01074.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.45+9381T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101657 | ||||||
| chr5:101662
|
A | G | 3 | a0002c0003t0011g0210a0002c0005t0002g0064a0003c0004t0016g0078 | 3 | HG01074.hp1 NA18954.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.45+9386A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101662 | ||||||
| chr5:101668
|
C | CCTGTAGG others(46): Show |
1 | a0001c0011t0048g0179 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.45+9418_45+9419ins others(53): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101668 | |||||
| chr5:101668
|
C | T | 15 | a0001c0001t0032g0144a0001c0007t0008g0143a0001c0007t0008g0145others(12): Show | 15 | HG00323.hp2 HG00597.hp2 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.45+9392C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101668 | ||||||
| chr5:101671
|
G | GTAGGGGA others(152): Show |
6 | a0001c0001t0004g0020a0003c0004t0004g0036a0005c0008t0004g0001others(3): Show | 6 | HG00642.hp2 HG01070.hp1 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.45+9419_45+9577dup others(159): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101671 | |||||
| chr5:101695
|
A | AAATCCAT others(2007): Show |
1 | a0036c0075t0061g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.45+9471_45+9472ins others(2014): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101695 | |||||
| chr5:101695
|
A | AAATCCAT others(46): Show |
1 | a0001c0036t0077g0149 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.45+9433_45+9434ins others(53): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101695 | |||||
| chr5:101695
|
A | T | 26 | a0001c0007t0008g0143a0001c0007t0008g0145a0002c0003t0011g0210others(23): Show | 26 | HG00280.hp2 HG00323.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.45+9419A>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101695 | ||||||
| chr5:101701
|
A | T | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.45+9425A>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101701 | ||||||
| chr5:101710
|
C | CCTGGAAA others(46): Show |
1 | a0011c0023t0044g0187 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.45+9444_45+9445ins others(53): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101710 | |||||
| chr5:101710
|
C | T | 7 | a0001c0011t0048g0179a0001c0051t0078g0148a0002c0003t0011g0210others(4): Show | 7 | HG01074.hp1 HG02280.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.45+9434C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101710 | ||||||
| chr5:101715
|
A | G | 2 | a0001c0002t0001g0018a0004c0006t0002g0051 | 2 | HG01515.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.45+9439A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101715 | ||||||
| chr5:101721
|
C | T | 20 | a0001c0001t0032g0144a0001c0002t0001g0018a0001c0007t0008g0146others(17): Show | 20 | HG01074.hp1 HG01099.hp1 HG02004.hp2 others(17): Show |
intron_variant | MODIFIER | c.45+9445C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101721 | ||||||
| chr5:101748
|
T | A | 10 | a0001c0011t0048g0179a0002c0003t0011g0210a0002c0005t0002g0064others(7): Show | 10 | HG01074.hp1 HG01099.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.45+9472T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101748 | ||||||
| chr5:101748
|
T | TAATCCAT others(735): Show |
1 | a0008c0025t0069g0174 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.45+9524_45+9525ins others(742): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101748 | |||||
| chr5:101763
|
C | CCTGGAAA others(46): Show |
1 | a0010c0014t0019g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.45+9497_45+9498ins others(53): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101763 | |||||
| chr5:101763
|
C | T | 6 | a0006c0068t0058g0194a0006c0071t0018g0202a0010c0014t0057g0197others(3): Show | 6 | HG00597.hp2 HG02647.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.45+9487C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101763 | ||||||
| chr5:101768
|
A | G | 2 | a0002c0003t0011g0210a0002c0005t0002g0064 | 2 | HG01074.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.45+9492A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101768 | ||||||
| chr5:101774
|
C | CCTGTAGG others(152): Show |
3 | a0001c0007t0008g0143a0001c0007t0008g0145a0001c0036t0077g0149 | 3 | HG02896.hp1 HG02897.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.45+9524_45+9525ins others(159): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101774 | |||||
| chr5:101774
|
C | CCTGTAGG others(1000): Show |
1 | a0006c0070t0054g0207 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.45+9524_45+9525ins others(1007): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101774 | |||||
| chr5:101774
|
C | T | 14 | a0002c0003t0011g0210a0002c0005t0002g0064a0006c0068t0058g0194others(11): Show | 14 | HG00597.hp2 HG01074.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.45+9498C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101774 | ||||||
| chr5:101776
|
T | C | 5 | a0011c0023t0041g0184a0011c0078t0059g0185a0013c0020t0050g0182others(2): Show | 5 | HG01099.hp1 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+9500T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101776 | ||||||
| chr5:101777
|
GTAGGGGA others(152): Show |
G | 1 | a0002c0005t0129g0043 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.45+9705_45+9863del | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101777 | |||||
| chr5:101801
|
T | A | 12 | a0001c0011t0048g0179a0006c0021t0018g0198a0006c0021t0056g0199others(9): Show | 12 | HG00597.hp2 HG02280.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.45+9525T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101801 | ||||||
| chr5:101801
|
T | TAATCCAT others(2908): Show |
1 | a0010c0069t0019g0204 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.45+9539_45+9540ins others(2915): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101801 | |||||
| chr5:101814
|
G | A | 1 | a0021c0026t0060g0169 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.45+9538G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101814 | ||||||
| chr5:101816
|
C | CCTGGAAA others(205): Show |
1 | a0001c0051t0078g0148 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.45+9545_45+9546ins others(212): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101816 | |||||
| chr5:101816
|
C | T | 8 | a0001c0007t0008g0143a0001c0007t0008g0145a0001c0036t0077g0149others(5): Show | 8 | HG02258.hp2 HG02896.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.45+9540C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101816 | ||||||
| chr5:101822
|
G | A | 51 | a0001c0001t0032g0144a0001c0007t0008g0143a0001c0007t0008g0145others(48): Show | 51 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.45+9546G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101822 | ||||||
| chr5:101827
|
T | C | 34 | a0001c0007t0008g0143a0001c0007t0008g0145a0001c0036t0077g0149others(31): Show | 34 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.45+9551T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101827 | ||||||
| chr5:101827
|
T | TCTGTAGG others(258): Show |
1 | a0006c0021t0018g0198 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.45+9553_45+9554ins others(265): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101827 | |||||
| chr5:101830
|
A | ATAGGGGA others(1634): Show |
1 | a0001c0001t0032g0144 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.45+9567_45+9568ins others(1641): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101830 | |||||
| chr5:101830
|
A | ATAGGGGA others(1793): Show |
3 | a0001c0007t0008g0146a0001c0007t0008g0150a0001c0007t0109g0147 | 3 | HG03540.hp1 NA20129.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.45+9567_45+9568ins others(1800): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101830 | |||||
| chr5:101830
|
A | ATAGGGGA others(46): Show |
1 | a0016c0018t0034g0004 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.45+9603_45+9604ins others(53): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101830 | |||||
| chr5:101830
|
A | G | 47 | a0001c0007t0008g0143a0001c0007t0008g0145a0001c0036t0077g0149others(44): Show | 47 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.45+9554A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101830 | ||||||
| chr5:101854
|
T | A | 18 | a0001c0001t0032g0144a0001c0007t0008g0143a0001c0007t0008g0145others(15): Show | 18 | HG01074.hp1 HG01515.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.45+9578T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101854 | ||||||
| chr5:101854
|
T | TAATCCAT others(99): Show |
1 | a0021c0026t0060g0169 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.45+9603_45+9604ins others(106): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101854 | |||||
| chr5:101869
|
C | CCTGGAAA others(947): Show |
1 | a0006c0021t0056g0199 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.45+9645_45+9646ins others(954): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101869 | |||||
| chr5:101869
|
C | T | 15 | a0002c0003t0011g0210a0006c0021t0018g0198a0006c0068t0058g0194others(12): Show | 15 | HG00280.hp2 HG00597.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.45+9593C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101869 | ||||||
| chr5:101871
|
T | G | 1 | a0004c0006t0002g0051 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.45+9595T>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101871 | ||||||
| chr5:101874
|
A | AAAAAGCC others(46): Show |
1 | a0010c0014t0055g0201 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.45+9603_45+9604ins others(53): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101874 | |||||
| chr5:101874
|
A | G | 3 | a0004c0006t0002g0051a0019c0019t0010g0164a0020c0081t0064g0200 | 3 | HG00323.hp2 HG01515.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.45+9598A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101874 | ||||||
| chr5:101875
|
A | G | 2 | a0001c0001t0006g0075a0007c0038t0013g0102 | 2 | HG02083.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.45+9599A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101875 | ||||||
| chr5:101880
|
T | C | 33 | a0001c0001t0032g0144a0001c0007t0008g0143a0001c0007t0008g0145others(30): Show | 33 | HG00323.hp2 HG01099.hp1 HG01261.hp2 others(30): Show |
intron_variant | MODIFIER | c.45+9604T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101880 | ||||||
| chr5:101880
|
T | TCTGTAGG others(2855): Show |
1 | a0010c0014t0019g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.45+9630_45+9631ins others(2862): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101880 | |||||
| chr5:101880
|
T | TCTGTAGG others(205): Show |
3 | a0017c0030t0039g0140a0029c0033t0042g0163a0032c0058t0040g0158 | 3 | HG02622.hp2 HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.45+9630_45+9631ins others(212): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101880 | |||||
| chr5:101883
|
G | GTAGGGGA others(46): Show |
2 | a0001c0002t0024g0024a0001c0007t0110g0151 | 2 | HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.45+9631_45+9683dup others(53): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101883 | |||||
| chr5:101907
|
A | AAATCCAT others(152): Show |
1 | a0001c0001t0079g0059 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.45+9656_45+9657ins others(159): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101907 | |||||
| chr5:101907
|
A | T | 24 | a0001c0001t0032g0144a0001c0007t0008g0143a0001c0007t0008g0145others(21): Show | 24 | HG00280.hp2 HG01081.hp2 HG02004.hp2 others(21): Show |
intron_variant | MODIFIER | c.45+9631A>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101907 | ||||||
| chr5:101922
|
C | CCTGGAAA others(4233): Show |
1 | a0019c0019t0010g0164 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.45+9656_45+9657ins others(4240): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101922 | |||||
| chr5:101922
|
C | CCTGGAAA others(2113): Show |
1 | a0040c0063t0063g0189 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.45+9656_45+9657ins others(2120): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101922 | |||||
| chr5:101922
|
C | CCTGGAAA others(1212): Show |
1 | a0019c0019t0062g0191 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.45+9656_45+9657ins others(1219): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101922 | |||||
| chr5:101922
|
C | T | 14 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(11): Show | 14 | HG00597.hp2 HG01081.hp2 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.45+9646C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101922 | ||||||
| chr5:101927
|
A | G | 2 | a0002c0003t0011g0210a0004c0006t0002g0051 | 2 | HG01074.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.45+9651A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101927 | ||||||
| chr5:101933
|
T | C | 29 | a0001c0001t0032g0144a0001c0007t0008g0143a0001c0007t0008g0145others(26): Show | 29 | HG00280.hp2 HG01081.hp2 HG01099.hp1 others(26): Show |
intron_variant | MODIFIER | c.45+9657T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101933 | ||||||
| chr5:101933
|
T | CCTGTAGG others(2325): Show |
1 | a0010c0014t0055g0201 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.45+9656_45+9657ins others(2332): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101933 | ||||||
| chr5:101933
|
T | TCTGTAGG others(1265): Show |
1 | a0038c0080t0043g0177 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.45+9659_45+9660ins others(1272): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101933 | |||||
| chr5:101936
|
A | G | 51 | a0001c0001t0032g0144a0001c0007t0008g0143a0001c0007t0008g0145others(48): Show | 51 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.45+9660A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101936 | ||||||
| chr5:101960
|
T | A | 6 | a0008c0024t0021g0175a0008c0024t0021g0176a0008c0025t0045g0172others(3): Show | 6 | HG02109.hp2 HG02145.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.45+9684T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101960 | ||||||
| chr5:101960
|
T | TAATCCAT others(99): Show |
1 | a0001c0001t0001g0142 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.45+9705_45+9810dup others(106): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101960 | |||||
| chr5:101975
|
C | CCTGGAAA others(258): Show |
2 | a0011c0023t0041g0184a0011c0078t0059g0185 | 2 | HG01099.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.45+9704_45+9705ins others(265): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101975 | |||||
| chr5:101975
|
C | CCTGGAAA others(4233): Show |
1 | a0021c0026t0060g0169 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.45+9704_45+9705ins others(4240): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 101975 | |||||
| chr5:101975
|
C | T | 9 | a0008c0024t0021g0175a0008c0024t0021g0176a0008c0025t0045g0172others(6): Show | 9 | HG02109.hp2 HG02145.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.45+9699C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101975 | ||||||
| chr5:101980
|
A | G | 1 | a0020c0081t0064g0200 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.45+9704A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101980 | ||||||
| chr5:101981
|
G | A | 39 | a0004c0006t0002g0051a0006c0021t0018g0198a0006c0021t0056g0199others(36): Show | 39 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.45+9705G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101981 | ||||||
| chr5:101986
|
T | C | 22 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(19): Show | 22 | HG00597.hp2 HG01261.hp2 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.45+9710T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101986 | ||||||
| chr5:101989
|
A | G | 39 | a0004c0006t0002g0051a0006c0021t0018g0198a0006c0021t0056g0199others(36): Show | 39 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.45+9713A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 101989 | ||||||
| chr5:102013
|
T | A | 22 | a0004c0006t0002g0051a0006c0021t0018g0198a0006c0021t0056g0199others(19): Show | 22 | HG00597.hp2 HG01261.hp2 HG01515.hp2 others(19): Show |
intron_variant | MODIFIER | c.45+9737T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 102013 | ||||||
| chr5:102013
|
T | TAATCCAT others(2484): Show |
1 | a0020c0081t0064g0200 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.45+9789_45+9790ins others(2491): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 102013 | |||||
| chr5:102028
|
C | CCTGGAAA others(576): Show |
1 | a0011c0023t0044g0187 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.45+9762_45+9763ins others(583): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 102028 | |||||
| chr5:102028
|
C | CCTGGAAA others(205): Show |
3 | a0013c0020t0050g0182a0013c0020t0052g0183a0013c0067t0046g0186 | 3 | HG02451.hp1 HG03041.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.45+9762_45+9763ins others(212): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 102028 | |||||
| chr5:102028
|
C | CCTGGAAA others(364): Show |
1 | a0008c0079t0068g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.45+9762_45+9763ins others(371): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 102028 | |||||
| chr5:102028
|
C | CCTGGAAA others(10540): Show |
1 | a0041c0064t0010g0190 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.45+9762_45+9763ins others(10547): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 102028 | |||||
| chr5:102028
|
C | T | 9 | a0001c0011t0048g0179a0008c0025t0069g0174a0011c0023t0041g0184others(6): Show | 9 | HG01099.hp1 HG02257.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.45+9752C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 102028 | ||||||
| chr5:102039
|
T | C | 5 | a0019c0019t0010g0164a0019c0019t0062g0191a0039c0062t0010g0165others(2): Show | 5 | HG00280.hp2 HG00323.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.45+9763T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 102039 | ||||||
| chr5:102039
|
T | CCTGTAGG others(894): Show |
1 | a0006c0072t0036g0206 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.45+9762_45+9763ins others(901): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 102039 | ||||||
| chr5:102066
|
A | AAATCCAT others(470): Show |
3 | a0008c0024t0021g0175a0008c0024t0021g0176a0008c0025t0045g0172 | 3 | HG02109.hp2 HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.45+9815_45+9816ins others(477): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 102066 | |||||
| chr5:102066
|
A | AAATCCAT others(46): Show |
1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.45+9804_45+9805ins others(53): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 102066 | |||||
| chr5:102066
|
A | T | 21 | a0001c0011t0048g0179a0008c0025t0069g0174a0008c0079t0068g0173others(18): Show | 21 | HG00280.hp2 HG00323.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.45+9790A>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 102066 | ||||||
| chr5:102081
|
C | CCTGGAAA others(3173): Show |
1 | a0022c0046t0047g0180 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.45+9815_45+9816ins others(3180): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 102081 | |||||
| chr5:102081
|
C | T | 1 | a0036c0075t0061g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.45+9805C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 102081 | ||||||
| chr5:102092
|
T | C | 15 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(12): Show | 15 | HG00597.hp2 HG01261.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.45+9816T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 102092 | ||||||
| chr5:102095
|
A | ATAGGGGA others(46): Show |
1 | a0001c0002t0101g0068 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.45+9834_45+9886dup others(53): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 102095 | |||||
| chr5:102095
|
A | ATAGGGGA others(46): Show |
1 | a0001c0052t0118g0121 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.45+9868_45+9869ins others(53): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 102095 | |||||
| chr5:102095
|
A | G | 41 | a0001c0011t0048g0179a0006c0021t0018g0198a0006c0021t0056g0199others(38): Show | 41 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.45+9819A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 102095 | ||||||
| chr5:102163
|
C | CTGTGAGG others(205): Show |
1 | a0001c0015t0035g0122 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.45+9895_45+9896ins others(212): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 102163 | |||||
| chr5:102163
|
C | T | 42 | a0001c0011t0048g0179a0006c0021t0018g0198a0006c0021t0056g0199others(39): Show | 42 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.45+9887C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 102163 | ||||||
| chr5:102186
|
C | T | 1 | a0022c0046t0047g0180 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.45+9910C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 102186 | ||||||
| chr5:102368
|
C | T | 1 | a0036c0075t0061g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.45+10092C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 102368 | ||||||
| chr5:102444
|
T | C | 1 | a0002c0005t0002g0064 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.45+10168T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 102444 | ||||||
| chr5:102497
|
C | G | 3 | a0019c0019t0062g0191a0040c0063t0063g0189a0041c0064t0010g0190 | 3 | HG00280.hp2 HG01081.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.45+10221C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 102497 | ||||||
| chr5:102529
|
TG | T | 5 | a0009c0012t0033g0161a0009c0012t0114g0156a0009c0012t0115g0157others(2): Show | 5 | HG02886.hp2 HG03139.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.45+10256delG | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 102529 | |||||
| chr5:102574
|
C | T | 28 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0159others(25): Show | 28 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(25): Show |
intron_variant | MODIFIER | c.45+10298C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 102574 | ||||||
| chr5:102651
|
G | C | 3 | a0019c0019t0062g0191a0040c0063t0063g0189a0041c0064t0010g0190 | 3 | HG00280.hp2 HG01081.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.45+10375G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 102651 | ||||||
| chr5:102654
|
G | A | 42 | a0001c0011t0048g0179a0006c0021t0018g0198a0006c0021t0056g0199others(39): Show | 42 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.45+10378G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 102654 | ||||||
| chr5:102660
|
C | T | 4 | a0008c0024t0021g0175a0008c0024t0021g0176a0008c0025t0045g0172others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+10384C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 102660 | ||||||
| chr5:102666
|
T | C | 42 | a0001c0011t0048g0179a0006c0021t0018g0198a0006c0021t0056g0199others(39): Show | 42 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.45+10390T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 102666 | ||||||
| chr5:102727
|
A | G | 1 | a0014c0065t0038g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.45+10451A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 102727 | ||||||
| chr5:102837
|
C | T | 1 | a0022c0046t0047g0180 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.46-10414C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 102837 | ||||||
| chr5:102852
|
G | A | 1 | a0001c0002t0001g0032 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.46-10399G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 102852 | ||||||
| chr5:102886
|
T | C | 1 | a0001c0001t0028g0046 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.46-10365T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 102886 | ||||||
| chr5:102926
|
T | C | 1 | a0006c0070t0054g0207 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.46-10325T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 102926 | ||||||
| chr5:102933
|
C | A | 42 | a0001c0011t0048g0179a0006c0021t0018g0198a0006c0021t0056g0199others(39): Show | 42 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.46-10318C>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 102933 | ||||||
| chr5:102955
|
T | C | 1 | a0036c0075t0061g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.46-10296T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 102955 | ||||||
| chr5:102957
|
T | G | 42 | a0001c0011t0048g0179a0006c0021t0018g0198a0006c0021t0056g0199others(39): Show | 42 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.46-10294T>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 102957 | ||||||
| chr5:102994
|
G | A | 3 | a0019c0019t0062g0191a0040c0063t0063g0189a0041c0064t0010g0190 | 3 | HG00280.hp2 HG01081.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.46-10257G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 102994 | ||||||
| chr5:103007
|
G | A | 3 | a0019c0019t0062g0191a0040c0063t0063g0189a0041c0064t0010g0190 | 3 | HG00280.hp2 HG01081.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.46-10244G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 103007 | ||||||
| chr5:103106
|
C | T | 1 | a0001c0001t0001g0142 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.46-10145C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 103106 | ||||||
| chr5:103244
|
C | G | 3 | a0019c0019t0062g0191a0040c0063t0063g0189a0041c0064t0010g0190 | 3 | HG00280.hp2 HG01081.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.46-10007C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 103244 | ||||||
| chr5:103533
|
T | C | 1 | a0003c0009t0017g0093 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.46-9718T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 103533 | ||||||
| chr5:103645
|
C | G | 42 | a0001c0011t0048g0179a0006c0021t0018g0198a0006c0021t0056g0199others(39): Show | 42 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.46-9606C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 103645 | ||||||
| chr5:103756
|
A | C | 1 | a0014c0065t0038g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.46-9495A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 103756 | ||||||
| chr5:103789
|
G | A | 36 | a0001c0011t0048g0179a0006c0021t0018g0198a0006c0021t0056g0199others(33): Show | 36 | HG00597.hp2 HG01099.hp1 HG01261.hp2 others(33): Show |
intron_variant | MODIFIER | c.46-9462G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 103789 | ||||||
| chr5:103875
|
C | T | 42 | a0001c0011t0048g0179a0006c0021t0018g0198a0006c0021t0056g0199others(39): Show | 42 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.46-9376C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 103875 | ||||||
| chr5:103884
|
C | G | 2 | a0016c0018t0003g0005a0016c0018t0034g0004 | 2 | HG02145.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.46-9367C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 103884 | ||||||
| chr5:103941
|
G | A | 42 | a0001c0011t0048g0179a0006c0021t0018g0198a0006c0021t0056g0199others(39): Show | 42 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.46-9310G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 103941 | ||||||
| chr5:104035
|
C | CCCAGTCC others(125): Show |
1 | a0016c0018t0003g0005 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.46-9153_46-9022dup others(132): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 104035 | |||||
| chr5:104035
|
CCCAGTCC others(59): Show |
C | 6 | a0014c0065t0038g0166a0019c0019t0010g0164a0019c0019t0062g0191others(3): Show | 6 | HG00280.hp2 HG00323.hp2 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.46-9087_46-9022del others(66): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 104035 | |||||
| chr5:104098
|
A | T | 36 | a0001c0011t0048g0179a0006c0021t0018g0198a0006c0021t0056g0199others(33): Show | 36 | HG00597.hp2 HG01099.hp1 HG01261.hp2 others(33): Show |
intron_variant | MODIFIER | c.46-9153A>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 104098 | ||||||
| chr5:104101
|
G | GC | 35 | a0001c0011t0048g0179a0006c0021t0018g0198a0006c0021t0056g0199others(32): Show | 35 | HG00597.hp2 HG01099.hp1 HG01261.hp2 others(32): Show |
intron_variant | MODIFIER | c.46-9148dupC | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 104101 | |||||
| chr5:104102
|
CCAGTCCC others(25): Show |
C | 1 | a0010c0069t0019g0204 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.46-9147_46-9116del others(32): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 104102 | |||||
| chr5:104131
|
TCAGCCAG others(26): Show |
T | 2 | a0003c0004t0028g0058a0003c0004t0105g0081 | 2 | HG03710.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.46-9087_46-9055del others(33): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 104131 | |||||
| chr5:104164
|
A | T | 1 | a0010c0069t0019g0204 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.46-9087A>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 104164 | ||||||
| chr5:104182
|
G | A | 1 | a0001c0001t0079g0059 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.46-9069G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 104182 | ||||||
| chr5:104183
|
A | G | 1 | a0022c0046t0047g0180 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.46-9068A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 104183 | ||||||
| chr5:104227
|
A | G | 3 | a0019c0019t0062g0191a0040c0063t0063g0189a0041c0064t0010g0190 | 3 | HG00280.hp2 HG01081.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.46-9024A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 104227 | ||||||
| chr5:104245
|
C | G | 9 | a0001c0011t0048g0179a0011c0023t0041g0184a0011c0023t0044g0187others(6): Show | 9 | HG01099.hp1 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.46-9006C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 104245 | ||||||
| chr5:104555
|
C | A | 6 | a0008c0024t0021g0175a0008c0024t0021g0176a0008c0025t0045g0172others(3): Show | 6 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.46-8696C>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 104555 | ||||||
| chr5:104561
|
C | T | 2 | a0001c0015t0035g0122a0001c0015t0076g0154 | 2 | HG02886.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.46-8690C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 104561 | ||||||
| chr5:104562
|
G | A | 41 | a0001c0011t0048g0179a0006c0021t0018g0198a0006c0021t0056g0199others(38): Show | 41 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.46-8689G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 104562 | ||||||
| chr5:104635
|
G | C | 1 | a0014c0065t0038g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.46-8616G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 104635 | ||||||
| chr5:104871
|
C | T | 3 | a0010c0014t0057g0197a0018c0022t0011g0195a0018c0022t0011g0196 | 3 | HG00597.hp2 NA18984.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.46-8380C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 104871 | ||||||
| chr5:104936
|
G | C | 3 | a0013c0020t0050g0182a0013c0020t0052g0183a0013c0067t0046g0186 | 3 | HG02451.hp1 HG03041.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.46-8315G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 104936 | ||||||
| chr5:105008
|
G | A | 1 | a0001c0001t0028g0046 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.46-8243G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 105008 | ||||||
| chr5:105042
|
A | G | 1 | a0019c0019t0010g0164 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.46-8209A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 105042 | ||||||
| chr5:105077
|
CTGGTGTT others(53): Show |
C | 2 | a0004c0006t0125g0048a0004c0043t0126g0099 | 2 | HG01261.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.46-8139_46-8080del others(60): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 105077 | |||||
| chr5:105137
|
T | TTGGTGTT others(415): Show |
1 | a0032c0058t0040g0158 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.46-8080_46-8079ins others(422): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 105137 | |||||
| chr5:105137
|
T | TTGGTGTT others(355): Show |
1 | a0020c0081t0064g0200 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.46-8080_46-8079ins others(362): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 105137 | |||||
| chr5:105137
|
T | TTGGTGTT others(355): Show |
1 | a0022c0046t0047g0180 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.46-8080_46-8079ins others(362): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 105137 | |||||
| chr5:105137
|
T | TTGGTGTT others(355): Show |
39 | a0001c0011t0048g0179a0006c0021t0018g0198a0006c0021t0056g0199others(36): Show | 39 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.46-8080_46-8079ins others(362): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 105137 | |||||
| chr5:105137
|
T | TTGGTGTT others(54): Show |
13 | a0001c0001t0032g0144a0001c0007t0008g0143a0001c0007t0008g0145others(10): Show | 13 | HG02109.hp1 HG02145.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.46-8074_46-8073ins others(61): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 105137 | |||||
| chr5:105147
|
C | T | 10 | a0001c0001t0097g0086a0001c0001t0104g0023a0001c0002t0006g0134others(7): Show | 10 | HG00323.hp1 HG02257.hp2 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.46-8104C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 105147 | ||||||
| chr5:105301
|
G | A | 9 | a0001c0011t0048g0179a0011c0023t0041g0184a0011c0023t0044g0187others(6): Show | 9 | HG01099.hp1 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.46-7950G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 105301 | ||||||
| chr5:105431
|
T | A | 3 | a0013c0020t0050g0182a0013c0020t0052g0183a0013c0067t0046g0186 | 3 | HG02451.hp1 HG03041.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.46-7820T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 105431 | ||||||
| chr5:105486
|
G | A | 2 | a0003c0009t0119g0049a0003c0017t0074g0050 | 2 | HG01069.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.46-7765G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 105486 | ||||||
| chr5:105623
|
C | A | 4 | a0006c0072t0036g0206a0010c0014t0019g0205a0010c0014t0055g0201others(1): Show | 4 | HG02258.hp2 HG02451.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.46-7628C>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 105623 | ||||||
| chr5:105652
|
G | C | 3 | a0019c0019t0062g0191a0040c0063t0063g0189a0041c0064t0010g0190 | 3 | HG00280.hp2 HG01081.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.46-7599G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 105652 | ||||||
| chr5:105750
|
T | A | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.46-7501T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 105750 | ||||||
| chr5:105802
|
G | A | 1 | a0001c0001t0015g0131 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.46-7449G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 105802 | ||||||
| chr5:105881
|
G | T | 6 | a0008c0024t0021g0175a0008c0024t0021g0176a0008c0025t0045g0172others(3): Show | 6 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.46-7370G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 105881 | ||||||
| chr5:105882
|
G | A | 2 | a0019c0019t0010g0164a0039c0062t0010g0165 | 2 | HG00323.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.46-7369G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 105882 | ||||||
| chr5:105886
|
A | G | 1 | a0031c0031t0085g0108 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.46-7365A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 105886 | ||||||
| chr5:105893
|
G | A | 1 | a0014c0065t0038g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.46-7358G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 105893 | ||||||
| chr5:106222
|
G | A | 1 | a0015c0076t0067g0192 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.46-7029G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 106222 | ||||||
| chr5:106437
|
T | C | 42 | a0001c0011t0048g0179a0006c0021t0018g0198a0006c0021t0056g0199others(39): Show | 42 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.46-6814T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 106437 | ||||||
| chr5:106555
|
A | C | 1 | a0036c0075t0061g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.46-6696A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 106555 | ||||||
| chr5:106560
|
G | T | 1 | a0036c0075t0061g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.46-6691G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 106560 | ||||||
| chr5:106583
|
A | G | 2 | a0019c0019t0010g0164a0039c0062t0010g0165 | 2 | HG00323.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.46-6668A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 106583 | ||||||
| chr5:106663
|
C | T | 2 | a0001c0036t0077g0149a0001c0051t0078g0148 | 2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.46-6588C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 106663 | ||||||
| chr5:106681
|
G | T | 3 | a0017c0030t0039g0140a0029c0033t0042g0163a0032c0058t0040g0158 | 3 | HG02622.hp2 HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.46-6570G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 106681 | ||||||
| chr5:106690
|
G | A | 2 | a0014c0065t0038g0166a0022c0046t0047g0180 | 2 | HG02818.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.46-6561G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 106690 | ||||||
| chr5:106704
|
C | T | 15 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(12): Show | 15 | HG00597.hp2 HG01261.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.46-6547C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 106704 | ||||||
| chr5:106870
|
TGAG | T | 15 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(12): Show | 15 | HG00597.hp2 HG01261.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.46-6379_46-6377del others(3): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 106870 | |||||
| chr5:106918
|
G | A | 5 | a0019c0019t0010g0164a0019c0019t0062g0191a0039c0062t0010g0165others(2): Show | 5 | HG00280.hp2 HG00323.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.46-6333G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 106918 | ||||||
| chr5:106997
|
G | A | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.46-6254G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 106997 | ||||||
| chr5:107075
|
T | C | 40 | a0001c0011t0048g0179a0006c0021t0018g0198a0006c0021t0056g0199others(37): Show | 40 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.46-6176T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 107075 | ||||||
| chr5:107132
|
C | T | 3 | a0017c0030t0039g0140a0029c0033t0042g0163a0032c0058t0040g0158 | 3 | HG02622.hp2 HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.46-6119C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 107132 | ||||||
| chr5:107133
|
A | G | 2 | a0014c0065t0038g0166a0022c0046t0047g0180 | 2 | HG02818.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.46-6118A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 107133 | ||||||
| chr5:107161
|
G | T | 3 | a0019c0019t0062g0191a0040c0063t0063g0189a0041c0064t0010g0190 | 3 | HG00280.hp2 HG01081.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.46-6090G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 107161 | ||||||
| chr5:107189
|
C | G | 1 | a0001c0001t0005g0123 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.46-6062C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 107189 | ||||||
| chr5:107204
|
G | A | 2 | a0019c0019t0010g0164a0039c0062t0010g0165 | 2 | HG00323.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.46-6047G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 107204 | ||||||
| chr5:107342
|
C | G | 24 | a0001c0001t0007g0056a0001c0001t0027g0052a0001c0001t0027g0053others(21): Show | 24 | HG00597.hp1 HG00673.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.46-5909C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 107342 | ||||||
| chr5:107357
|
A | G | 2 | a0001c0001t0014g0115a0001c0001t0014g0125 | 2 | HG00438.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.46-5894A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 107357 | ||||||
| chr5:107395
|
A | G | 1 | a0002c0005t0075g0076 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.46-5856A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 107395 | ||||||
| chr5:107396
|
C | T | 15 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(12): Show | 15 | HG00597.hp2 HG01261.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.46-5855C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 107396 | ||||||
| chr5:107547
|
G | T | 1 | a0001c0001t0005g0123 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.46-5704G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 107547 | ||||||
| chr5:107558
|
G | A | 2 | a0035c0060t0020g0188a0036c0075t0061g0178 | 2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.46-5693G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 107558 | ||||||
| chr5:107649
|
C | T | 2 | a0008c0025t0069g0174a0008c0079t0068g0173 | 2 | HG03471.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.46-5602C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 107649 | ||||||
| chr5:107774
|
G | T | 1 | a0001c0001t0001g0159 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.46-5477G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 107774 | ||||||
| chr5:107775
|
C | T | 1 | a0001c0001t0001g0159 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.46-5476C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 107775 | ||||||
| chr5:107795
|
G | T | 2 | a0014c0065t0038g0166a0022c0046t0047g0180 | 2 | HG02818.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.46-5456G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 107795 | ||||||
| chr5:107979
|
C | T | 2 | a0035c0060t0020g0188a0036c0075t0061g0178 | 2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.46-5272C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 107979 | ||||||
| chr5:108087
|
C | T | 1 | a0006c0072t0036g0206 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.46-5164C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 108087 | ||||||
| chr5:108240
|
C | A | 1 | a0016c0018t0003g0005 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.46-5011C>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 108240 | ||||||
| chr5:108270
|
C | T | 3 | a0017c0030t0039g0140a0029c0033t0042g0163a0032c0058t0040g0158 | 3 | HG02622.hp2 HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.46-4981C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 108270 | ||||||
| chr5:108322
|
C | T | 3 | a0017c0030t0039g0140a0029c0033t0042g0163a0032c0058t0040g0158 | 3 | HG02622.hp2 HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.46-4929C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 108322 | ||||||
| chr5:108365
|
C | T | 1 | a0014c0065t0038g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.46-4886C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 108365 | ||||||
| chr5:108366
|
G | A | 1 | a0004c0006t0134g0011 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.46-4885G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 108366 | ||||||
| chr5:108497
|
CGGTGCAG others(21): Show |
C | 2 | a0004c0006t0125g0048a0004c0043t0126g0099 | 2 | HG01261.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.46-4710_46-4683del others(28): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 108497 | |||||
| chr5:108510
|
TGGTGTAG others(216): Show |
T | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.46-4682_46-4460del | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 108510 | |||||
| chr5:108567
|
GGGTGTAG others(21): Show |
G | 11 | a0001c0001t0001g0159a0001c0001t0004g0020a0001c0001t0006g0075others(8): Show | 11 | HG00438.hp1 HG00733.hp1 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.46-4625_46-4598del others(28): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 108567 | |||||
| chr5:108582
|
G | GGGTGCAG others(47): Show |
9 | a0001c0011t0048g0179a0011c0023t0041g0184a0011c0023t0044g0187others(6): Show | 9 | HG01099.hp1 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.46-4668_46-4615dup others(54): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 108582 | |||||
| chr5:108583
|
G | GGTGCAGA others(21): Show |
1 | a0014c0065t0038g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.46-4641_46-4640ins others(28): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 108583 | |||||
| chr5:108611
|
G | GGTGCAGA others(50): Show |
1 | a0014c0065t0038g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.46-4626_46-4625ins others(57): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 108611 | |||||
| chr5:108657
|
T | C | 1 | a0001c0002t0001g0074 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.46-4594T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 108657 | ||||||
| chr5:108661
|
CAGACTGG others(17): Show |
C | 1 | a0037c0074t0037g0203 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.46-4583_46-4560del others(24): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 108661 | |||||
| chr5:108685
|
T | TAGAC | 37 | a0001c0001t0032g0144a0001c0007t0008g0143a0001c0007t0008g0145others(34): Show | 37 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.46-4565_46-4562dup others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 108685 | |||||
| chr5:108692
|
A | G | 1 | a0036c0075t0061g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.46-4559A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 108692 | ||||||
| chr5:108692
|
A | GGTGCAGA others(162): Show |
1 | a0006c0073t0020g0193 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.46-4560_46-4559ins others(169): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 108692 | ||||||
| chr5:108723
|
G | A | 2 | a0001c0002t0024g0024a0001c0007t0110g0151 | 2 | HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.46-4528G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 108723 | ||||||
| chr5:108733
|
G | GGGTGTAG others(47): Show |
8 | a0011c0023t0041g0184a0011c0023t0044g0187a0011c0078t0059g0185others(5): Show | 8 | HG01099.hp1 HG02257.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.46-4477_46-4476ins others(54): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 108733 | |||||
| chr5:108733
|
G | GGGTGTAG others(129): Show |
1 | a0001c0011t0048g0179 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.46-4477_46-4476ins others(136): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 108733 | |||||
| chr5:108733
|
G | GGTGTAGA others(77): Show |
5 | a0019c0019t0010g0164a0019c0019t0062g0191a0039c0062t0010g0165others(2): Show | 5 | HG00280.hp2 HG00323.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.46-4517_46-4516ins others(84): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 108733 | |||||
| chr5:108733
|
GGGTGTAG others(21): Show |
G | 3 | a0017c0030t0039g0140a0029c0033t0042g0163a0032c0058t0040g0158 | 3 | HG02622.hp2 HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.46-4476_46-4449del others(28): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 108733 | |||||
| chr5:108776
|
G | A | 1 | a0005c0008t0023g0039 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.46-4475G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 108776 | ||||||
| chr5:108804
|
G | A | 1 | a0001c0001t0001g0142 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.46-4447G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 108804 | ||||||
| chr5:108971
|
G | T | 35 | a0001c0001t0032g0144a0001c0007t0008g0143a0001c0007t0008g0145others(32): Show | 35 | HG00323.hp2 HG00597.hp2 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.46-4280G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 108971 | ||||||
| chr5:108998
|
G | A | 2 | a0001c0001t0006g0075a0007c0038t0013g0102 | 2 | HG02083.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.46-4253G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 108998 | ||||||
| chr5:109014
|
G | T | 3 | a0019c0019t0010g0164a0039c0062t0010g0165a0040c0063t0063g0189 | 3 | HG00280.hp2 HG00323.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.46-4237G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 109014 | ||||||
| chr5:109091
|
T | TG | 3 | a0019c0019t0062g0191a0040c0063t0063g0189a0041c0064t0010g0190 | 3 | HG00280.hp2 HG01081.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.46-4160_46-4159ins others(1): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 109091 | ||||||
| chr5:109164
|
A | G | 54 | a0001c0001t0032g0144a0001c0007t0008g0143a0001c0007t0008g0145others(51): Show | 54 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.46-4087A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 109164 | ||||||
| chr5:109261
|
G | A | 1 | a0004c0006t0125g0048 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.46-3990G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 109261 | ||||||
| chr5:109390
|
C | CT | 6 | a0001c0011t0048g0179a0011c0023t0041g0184a0011c0023t0044g0187others(3): Show | 6 | HG01099.hp1 HG02280.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.46-3860dupT | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 109390 | |||||
| chr5:109397
|
C | CA | 29 | a0001c0001t0001g0082a0001c0001t0001g0142a0001c0001t0015g0037others(26): Show | 29 | HG00642.hp2 HG00673.hp2 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.46-3830dupA | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 109397 | |||||
| chr5:109397
|
C | CAA | 5 | a0008c0024t0021g0176a0008c0025t0045g0172a0035c0060t0020g0188others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.46-3831_46-3830dup others(2): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 109397 | |||||
| chr5:109397
|
C | CAAA | 18 | a0001c0001t0032g0144a0001c0007t0008g0143a0001c0007t0008g0145others(15): Show | 18 | HG00597.hp2 HG01261.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.46-3832_46-3830dup others(3): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 109397 | |||||
| chr5:109397
|
C | CAAAA | 6 | a0001c0036t0077g0149a0006c0021t0018g0198a0006c0070t0054g0207others(3): Show | 6 | HG02258.hp2 HG02809.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.46-3833_46-3830dup others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 109397 | |||||
| chr5:109397
|
C | CAAAAAAA others(5): Show |
2 | a0016c0018t0034g0004a0022c0046t0047g0180 | 2 | HG02818.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.46-3841_46-3830dup others(12): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 109397 | |||||
| chr5:109397
|
C | CAAAAAAA others(8): Show |
1 | a0016c0018t0003g0005 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.46-3844_46-3830dup others(15): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 109397 | |||||
| chr5:109397
|
CA | C | 5 | a0001c0001t0079g0059a0015c0076t0067g0192a0015c0077t0053g0181others(2): Show | 5 | HG00323.hp2 HG02257.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.46-3830delA | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 109397 | |||||
| chr5:109420
|
A | T | 5 | a0019c0019t0010g0164a0019c0019t0062g0191a0039c0062t0010g0165others(2): Show | 5 | HG00280.hp2 HG00323.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.46-3831A>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 109420 | ||||||
| chr5:109423
|
C | A | 5 | a0019c0019t0010g0164a0019c0019t0062g0191a0039c0062t0010g0165others(2): Show | 5 | HG00280.hp2 HG00323.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.46-3828C>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 109423 | ||||||
| chr5:109424
|
C | T | 18 | a0001c0001t0032g0144a0001c0007t0008g0143a0001c0007t0008g0145others(15): Show | 18 | HG00280.hp2 HG00323.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.46-3827C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 109424 | ||||||
| chr5:109470
|
A | ACC | 5 | a0013c0020t0050g0182a0013c0020t0052g0183a0013c0067t0046g0186others(2): Show | 5 | HG02257.hp1 HG02451.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.46-3779_46-3778dup others(2): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 109470 | |||||
| chr5:109474
|
A | C | 43 | a0001c0001t0032g0144a0001c0007t0008g0143a0001c0007t0008g0145others(40): Show | 43 | HG00597.hp2 HG01099.hp1 HG01261.hp2 others(40): Show |
intron_variant | MODIFIER | c.46-3777A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 109474 | ||||||
| chr5:109474
|
A | G | 5 | a0019c0019t0010g0164a0019c0019t0062g0191a0039c0062t0010g0165others(2): Show | 5 | HG00280.hp2 HG00323.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.46-3777A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 109474 | ||||||
| chr5:109477
|
C | G | 5 | a0008c0024t0021g0175a0008c0024t0021g0176a0008c0025t0045g0172others(2): Show | 5 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.46-3774C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 109477 | ||||||
| chr5:109510
|
G | A | 1 | a0002c0003t0130g0130 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.46-3741G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 109510 | ||||||
| chr5:109542
|
G | A | 2 | a0014c0027t0049g0171a0021c0026t0060g0169 | 2 | HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.46-3709G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 109542 | ||||||
| chr5:109699
|
A | G | 1 | a0022c0046t0047g0180 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.46-3552A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 109699 | ||||||
| chr5:109797
|
A | G | 6 | a0001c0011t0048g0179a0010c0014t0019g0205a0010c0069t0019g0204others(3): Show | 6 | HG01099.hp1 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.46-3454A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 109797 | ||||||
| chr5:109821
|
G | A | 1 | a0030c0047t0131g0067 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.46-3430G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 109821 | ||||||
| chr5:109839
|
C | T | 1 | a0001c0002t0025g0073 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.46-3412C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 109839 | ||||||
| chr5:109944
|
C | A | 1 | a0014c0065t0038g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.46-3307C>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 109944 | ||||||
| chr5:109974
|
G | A | 4 | a0001c0002t0006g0134a0001c0011t0029g0136a0001c0011t0106g0085others(1): Show | 4 | HG02647.hp2 HG02723.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-3277G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 109974 | ||||||
| chr5:110028
|
ACACC | A | 6 | a0008c0024t0021g0175a0008c0024t0021g0176a0008c0025t0045g0172others(3): Show | 6 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.46-3219_46-3216del others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 110028 | |||||
| chr5:110077
|
C | T | 2 | a0016c0018t0003g0005a0016c0018t0034g0004 | 2 | HG02145.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.46-3174C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 110077 | ||||||
| chr5:110153
|
C | T | 2 | a0014c0027t0049g0171a0021c0026t0060g0169 | 2 | HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.46-3098C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 110153 | ||||||
| chr5:110155
|
G | A | 40 | a0001c0011t0048g0179a0006c0021t0018g0198a0006c0021t0056g0199others(37): Show | 40 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.46-3096G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 110155 | ||||||
| chr5:110165
|
C | T | 1 | a0001c0032t0103g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.46-3086C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 110165 | ||||||
| chr5:110166
|
GTGCACAC others(50): Show |
G | 3 | a0001c0002t0025g0073a0002c0005t0003g0096a0002c0005t0075g0076 | 3 | NA18954.hp1 NA18984.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.46-3060_46-3004del others(57): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 110166 | |||||
| chr5:110173
|
C | T | 2 | a0035c0060t0020g0188a0036c0075t0061g0178 | 2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.46-3078C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 110173 | ||||||
| chr5:110176
|
C | T | 2 | a0014c0027t0049g0171a0021c0026t0060g0169 | 2 | HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.46-3075C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 110176 | ||||||
| chr5:110190
|
C | T | 5 | a0013c0020t0050g0182a0013c0020t0052g0183a0013c0067t0046g0186others(2): Show | 5 | HG02257.hp1 HG02451.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.46-3061C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 110190 | ||||||
| chr5:110233
|
C | T | 40 | a0001c0011t0048g0179a0006c0021t0018g0198a0006c0021t0056g0199others(37): Show | 40 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.46-3018C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 110233 | ||||||
| chr5:110317
|
C | T | 1 | a0005c0008t0111g0091 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.46-2934C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 110317 | ||||||
| chr5:110340
|
G | A | 1 | a0001c0035t0030g0137 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.46-2911G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 110340 | ||||||
| chr5:110369
|
A | ATGCACAC others(83): Show |
1 | a0001c0001t0032g0094 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.46-2854_46-2765dup others(90): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 110369 | |||||
| chr5:110378
|
T | TCCACACA others(53): Show |
30 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(27): Show | 30 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.46-2823_46-2822ins others(60): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 110378 | |||||
| chr5:110378
|
T | TCCACACA others(53): Show |
9 | a0001c0011t0048g0179a0011c0023t0041g0184a0011c0023t0044g0187others(6): Show | 9 | HG01099.hp1 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.46-2818_46-2817ins others(60): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 110378 | |||||
| chr5:110404
|
C | CACACCCA others(23): Show |
1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.46-2823_46-2822ins others(30): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 110404 | |||||
| chr5:110427
|
A | C | 1 | a0002c0003t0128g0029 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.46-2824A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 110427 | ||||||
| chr5:110516
|
A | G | 41 | a0001c0011t0048g0179a0006c0021t0018g0198a0006c0021t0056g0199others(38): Show | 41 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.46-2735A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 110516 | ||||||
| chr5:110545
|
CGTGCACA others(53): Show |
C | 1 | a0017c0030t0039g0140 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.46-2694_46-2635del others(60): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 110545 | |||||
| chr5:110563
|
A | C | 1 | a0001c0002t0082g0126 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.46-2688A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 110563 | ||||||
| chr5:110590
|
A | G | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.46-2661A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 110590 | ||||||
| chr5:110635
|
G | A | 4 | a0002c0005t0003g0031a0002c0039t0009g0030a0004c0006t0125g0048others(1): Show | 4 | HG00673.hp1 HG01261.hp1 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.46-2616G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 110635 | ||||||
| chr5:110692
|
C | G | 1 | a0014c0065t0038g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.46-2559C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 110692 | ||||||
| chr5:110965
|
T | C | 40 | a0001c0011t0048g0179a0006c0021t0018g0198a0006c0021t0056g0199others(37): Show | 40 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.46-2286T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 110965 | ||||||
| chr5:111015
|
G | A | 1 | a0032c0058t0040g0158 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.46-2236G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 111015 | ||||||
| chr5:111048
|
G | A | 49 | a0001c0001t0032g0144a0001c0007t0008g0143a0001c0007t0008g0145others(46): Show | 49 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.46-2203G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 111048 | ||||||
| chr5:111277
|
G | A | 1 | a0005c0008t0111g0091 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.46-1974G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 111277 | ||||||
| chr5:111405
|
G | A | 1 | a0009c0012t0114g0156 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.46-1846G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 111405 | ||||||
| chr5:111594
|
C | T | 1 | a0022c0046t0047g0180 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.46-1657C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 111594 | ||||||
| chr5:111671
|
G | A | 1 | a0014c0065t0038g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.46-1580G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 111671 | ||||||
| chr5:111746
|
C | G | 1 | a0003c0009t0017g0088 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.46-1505C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 111746 | ||||||
| chr5:111781
|
T | C | 4 | a0001c0011t0048g0179a0011c0023t0041g0184a0011c0023t0044g0187others(1): Show | 4 | HG01099.hp1 HG02280.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.46-1470T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 111781 | ||||||
| chr5:111804
|
G | A | 5 | a0013c0020t0050g0182a0013c0020t0052g0183a0013c0067t0046g0186others(2): Show | 5 | HG02257.hp1 HG02451.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.46-1447G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 111804 | ||||||
| chr5:111854
|
G | A | 6 | a0008c0024t0021g0175a0008c0024t0021g0176a0008c0025t0045g0172others(3): Show | 6 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.46-1397G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 111854 | ||||||
| chr5:111874
|
C | T | 1 | a0001c0002t0006g0134 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.46-1377C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 111874 | ||||||
| chr5:111885
|
AGGCCCAC others(36): Show |
A | 6 | a0001c0002t0082g0126a0002c0003t0002g0098a0002c0003t0002g0101others(3): Show | 6 | HG01069.hp1 HG01071.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.46-1300_46-1258del others(43): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 111885 | |||||
| chr5:111901
|
A | C | 2 | a0004c0006t0125g0048a0004c0043t0126g0099 | 2 | HG01261.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.46-1350A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 111901 | ||||||
| chr5:111949
|
CTGTG | C | 38 | a0001c0011t0048g0179a0006c0068t0058g0194a0006c0070t0054g0207others(35): Show | 38 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.46-1299_46-1296del others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 111949 | |||||
| chr5:112240
|
A | G | 41 | a0001c0011t0048g0179a0006c0021t0018g0198a0006c0021t0056g0199others(38): Show | 41 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.46-1011A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 112240 | ||||||
| chr5:112407
|
G | A | 2 | a0004c0006t0002g0051a0004c0041t0003g0077 | 2 | HG01515.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.46-844G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 112407 | ||||||
| chr5:112418
|
A | G | 3 | a0010c0014t0057g0197a0018c0022t0011g0195a0018c0022t0011g0196 | 3 | HG00597.hp2 NA18984.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.46-833A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 112418 | ||||||
| chr5:112593
|
G | A | 5 | a0002c0003t0002g0098a0002c0003t0002g0101a0002c0003t0071g0095others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.46-658G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 112593 | ||||||
| chr5:112597
|
G | A | 41 | a0001c0011t0048g0179a0006c0021t0018g0198a0006c0021t0056g0199others(38): Show | 41 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.46-654G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 112597 | ||||||
| chr5:112712
|
G | A | 1 | a0014c0065t0038g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.46-539G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 112712 | ||||||
| chr5:112745
|
C | T | 1 | a0026c0050t0009g0141 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.46-506C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 112745 | ||||||
| chr5:112763
|
A | C | 15 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(12): Show | 15 | HG00597.hp2 HG01261.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.46-488A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 112763 | ||||||
| chr5:112782
|
T | C | 41 | a0001c0011t0048g0179a0006c0021t0018g0198a0006c0021t0056g0199others(38): Show | 41 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.46-469T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 112782 | ||||||
| chr5:112836
|
G | A | 1 | a0002c0003t0071g0095 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.46-415G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 112836 | ||||||
| chr5:112896
|
G | T | 9 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0014g0033others(6): Show | 9 | HG00438.hp2 HG02080.hp2 NA18947.hp2 others(6): Show |
intron_variant | MODIFIER | c.46-355G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 112896 | ||||||
| chr5:112960
|
G | A | 1 | a0001c0011t0048g0179 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.46-291G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 1/19 | chr5 | 112960 | ||||||
| chr5:113462
|
T | C | 41 | a0001c0011t0048g0179a0006c0021t0018g0198a0006c0021t0056g0199others(38): Show | 41 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.243+14T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 113462 | ||||||
| chr5:113499
|
G | C | 5 | a0019c0019t0010g0164a0019c0019t0062g0191a0039c0062t0010g0165others(2): Show | 5 | HG00280.hp2 HG00323.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.243+51G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 113499 | ||||||
| chr5:113571
|
T | G | 2 | a0001c0001t0113g0044a0003c0004t0089g0014 | 2 | HG00140.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.243+123T>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 113571 | ||||||
| chr5:113713
|
A | G | 8 | a0001c0001t0032g0144a0001c0007t0008g0143a0001c0007t0008g0145others(5): Show | 8 | HG02109.hp1 HG02896.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.243+265A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 113713 | ||||||
| chr5:113720
|
A | G | 1 | a0014c0065t0038g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.243+272A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 113720 | ||||||
| chr5:113832
|
T | C | 1 | a0014c0065t0038g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.243+384T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 113832 | ||||||
| chr5:113956
|
C | A | 15 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(12): Show | 15 | HG00597.hp2 HG01261.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.243+508C>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 113956 | ||||||
| chr5:114019
|
C | T | 5 | a0019c0019t0010g0164a0019c0019t0062g0191a0039c0062t0010g0165others(2): Show | 5 | HG00280.hp2 HG00323.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.243+571C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 114019 | ||||||
| chr5:114258
|
C | T | 1 | a0001c0011t0048g0179 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.243+810C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 114258 | ||||||
| chr5:114260
|
C | T | 1 | a0001c0011t0048g0179 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.243+812C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 114260 | ||||||
| chr5:114263
|
C | A | 1 | a0001c0011t0048g0179 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.243+815C>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 114263 | ||||||
| chr5:114265
|
T | A | 1 | a0001c0011t0048g0179 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.243+817T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 114265 | ||||||
| chr5:114313
|
C | T | 1 | a0001c0036t0077g0149 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.243+865C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 114313 | ||||||
| chr5:114459
|
T | C | 15 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(12): Show | 15 | HG00597.hp2 HG01261.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.243+1011T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 114459 | ||||||
| chr5:114462
|
T | G | 6 | a0003c0004t0016g0078a0003c0004t0016g0133a0003c0004t0028g0058others(3): Show | 6 | HG02273.hp1 HG03710.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.243+1014T>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 114462 | ||||||
| chr5:114494
|
G | C | 2 | a0004c0006t0125g0048a0004c0043t0126g0099 | 2 | HG01261.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.243+1046G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 114494 | ||||||
| chr5:114542
|
C | T | 1 | a0002c0005t0003g0167 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.243+1094C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 114542 | ||||||
| chr5:114562
|
A | G | 1 | a0011c0023t0044g0187 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.243+1114A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 114562 | ||||||
| chr5:115128
|
C | G | 4 | a0001c0011t0048g0179a0011c0023t0041g0184a0011c0023t0044g0187others(1): Show | 4 | HG01099.hp1 HG02280.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.243+1680C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 115128 | ||||||
| chr5:115341
|
G | A | 1 | a0004c0006t0123g0003 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.243+1893G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 115341 | ||||||
| chr5:115418
|
G | T | 1 | a0001c0001t0001g0142 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.243+1970G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 115418 | ||||||
| chr5:115527
|
G | T | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.243+2079G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 115527 | ||||||
| chr5:115580
|
G | A | 41 | a0001c0011t0048g0179a0006c0021t0018g0198a0006c0021t0056g0199others(38): Show | 41 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.243+2132G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 115580 | ||||||
| chr5:115777
|
T | A | 1 | a0022c0046t0047g0180 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.243+2329T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 115777 | ||||||
| chr5:115837
|
A | C | 1 | a0002c0003t0124g0017 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.243+2389A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 115837 | ||||||
| chr5:115839
|
G | A | 1 | a0017c0030t0039g0140 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.243+2391G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 115839 | ||||||
| chr5:115881
|
A | G | 1 | a0014c0065t0038g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.243+2433A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 115881 | ||||||
| chr5:115913
|
C | T | 2 | a0001c0001t0073g0107a0001c0002t0001g0074 | 2 | HG00738.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.243+2465C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 115913 | ||||||
| chr5:115964
|
G | A | 6 | a0008c0024t0021g0175a0008c0024t0021g0176a0008c0025t0045g0172others(3): Show | 6 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.243+2516G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 115964 | ||||||
| chr5:116057
|
C | T | 2 | a0001c0001t0027g0052a0001c0001t0027g0053 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.243+2609C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 116057 | ||||||
| chr5:116186
|
T | C | 40 | a0001c0011t0048g0179a0006c0021t0018g0198a0006c0021t0056g0199others(37): Show | 40 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.243+2738T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 116186 | ||||||
| chr5:116516
|
C | T | 5 | a0019c0019t0010g0164a0019c0019t0062g0191a0039c0062t0010g0165others(2): Show | 5 | HG00280.hp2 HG00323.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.243+3068C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 116516 | ||||||
| chr5:116613
|
A | G | 2 | a0003c0009t0119g0049a0003c0017t0074g0050 | 2 | HG01069.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.243+3165A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 116613 | ||||||
| chr5:117080
|
A | G | 41 | a0001c0011t0048g0179a0006c0021t0018g0198a0006c0021t0056g0199others(38): Show | 41 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.243+3632A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 117080 | ||||||
| chr5:117132
|
A | T | 5 | a0019c0019t0010g0164a0019c0019t0062g0191a0039c0062t0010g0165others(2): Show | 5 | HG00280.hp2 HG00323.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.243+3684A>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 117132 | ||||||
| chr5:117136
|
A | G | 1 | a0008c0025t0045g0172 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.243+3688A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 117136 | ||||||
| chr5:117242
|
A | G | 1 | a0037c0074t0037g0203 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.243+3794A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 117242 | ||||||
| chr5:117295
|
C | T | 3 | a0008c0024t0021g0175a0008c0024t0021g0176a0008c0025t0045g0172 | 3 | HG02109.hp2 HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.243+3847C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 117295 | ||||||
| chr5:117304
|
T | C | 1 | a0027c0053t0107g0009 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.243+3856T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 117304 | ||||||
| chr5:117545
|
T | C | 1 | a0001c0036t0077g0149 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.243+4097T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 117545 | ||||||
| chr5:117547
|
T | C | 1 | a0014c0065t0038g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.243+4099T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 117547 | ||||||
| chr5:117714
|
G | A | 2 | a0002c0003t0066g0209a0004c0006t0065g0208 | 2 | HG00099.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.243+4266G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 117714 | ||||||
| chr5:117778
|
A | C | 2 | a0017c0030t0039g0140a0029c0033t0042g0163 | 2 | HG02622.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.243+4330A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 117778 | ||||||
| chr5:117935
|
T | C | 1 | a0006c0070t0054g0207 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+4487T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 117935 | ||||||
| chr5:118048
|
T | C | 40 | a0001c0011t0048g0179a0006c0021t0018g0198a0006c0021t0056g0199others(37): Show | 40 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.243+4600T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 118048 | ||||||
| chr5:118054
|
A | G | 1 | a0014c0065t0038g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.243+4606A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 118054 | ||||||
| chr5:118291
|
C | T | 130 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0142others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.243+4843C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 118291 | ||||||
| chr5:118310
|
C | T | 1 | a0002c0003t0135g0128 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.243+4862C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 118310 | ||||||
| chr5:118725
|
A | G | 1 | a0001c0061t0001g0006 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.243+5277A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 118725 | ||||||
| chr5:118772
|
A | C | 1 | a0002c0005t0002g0064 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.243+5324A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 118772 | ||||||
| chr5:118798
|
T | TTA | 6 | a0002c0005t0127g0124a0019c0019t0010g0164a0019c0019t0062g0191others(3): Show | 6 | HG00280.hp2 HG00323.hp2 HG00733.hp1 others(3): Show |
intron_variant | MODIFIER | c.243+5362_243+5363d others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 118798 | |||||
| chr5:118832
|
C | T | 4 | a0016c0018t0034g0004a0029c0033t0042g0163a0032c0058t0040g0158others(1): Show | 4 | HG02809.hp2 HG03225.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.243+5384C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 118832 | ||||||
| chr5:118842
|
T | C | 1 | a0022c0046t0047g0180 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.243+5394T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 118842 | ||||||
| chr5:118851
|
C | T | 1 | a0001c0002t0012g0072 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.243+5403C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 118851 | ||||||
| chr5:118855
|
CT | C | 208 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0142others(205): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.243+5420delT | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 118855 | |||||
| chr5:118911
|
T | C | 42 | a0001c0011t0048g0179a0001c0016t0025g0152a0001c0051t0078g0148others(39): Show | 42 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.243+5463T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 118911 | ||||||
| chr5:118995
|
C | T | 1 | a0004c0006t0003g0047 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.243+5547C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 118995 | ||||||
| chr5:119034
|
A | T | 4 | a0001c0001t0079g0059a0001c0011t0106g0085a0016c0018t0003g0005others(1): Show | 4 | HG02145.hp1 HG03225.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.243+5586A>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 119034 | ||||||
| chr5:119250
|
C | A | 1 | a0036c0075t0061g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.243+5802C>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 119250 | ||||||
| chr5:119370
|
T | C | 1 | a0014c0065t0038g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.243+5922T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 119370 | ||||||
| chr5:119473
|
G | A | 1 | a0019c0019t0010g0164 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.243+6025G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 119473 | ||||||
| chr5:119811
|
C | A | 5 | a0019c0019t0010g0164a0019c0019t0062g0191a0039c0062t0010g0165others(2): Show | 5 | HG00280.hp2 HG00323.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.243+6363C>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 119811 | ||||||
| chr5:119851
|
C | G | 40 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(37): Show | 40 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.243+6403C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 119851 | ||||||
| chr5:119963
|
G | C | 15 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(12): Show | 15 | HG00597.hp2 HG01261.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.243+6515G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 119963 | ||||||
| chr5:119982
|
T | G | 8 | a0011c0023t0041g0184a0011c0023t0044g0187a0011c0078t0059g0185others(5): Show | 8 | HG01099.hp1 HG02257.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.243+6534T>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 119982 | ||||||
| chr5:120015
|
T | A | 40 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(37): Show | 40 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.243+6567T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 120015 | ||||||
| chr5:120109
|
C | T | 2 | a0001c0001t0001g0082a0034c0059t0001g0114 | 2 | NA18973.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.243+6661C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 120109 | ||||||
| chr5:120110
|
A | G | 1 | a0001c0061t0001g0006 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.243+6662A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 120110 | ||||||
| chr5:120165
|
A | T | 1 | a0003c0004t0001g0087 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.243+6717A>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 120165 | ||||||
| chr5:120196
|
T | C | 1 | a0027c0053t0107g0009 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.243+6748T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 120196 | ||||||
| chr5:120205
|
A | G | 2 | a0017c0030t0039g0140a0032c0058t0040g0158 | 2 | HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.243+6757A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 120205 | ||||||
| chr5:120233
|
C | T | 1 | a0041c0064t0010g0190 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.243+6785C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 120233 | ||||||
| chr5:120400
|
G | A | 1 | a0002c0005t0003g0031 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.243+6952G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 120400 | ||||||
| chr5:120609
|
C | T | 1 | a0036c0075t0061g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.243+7161C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 120609 | ||||||
| chr5:120866
|
T | C | 3 | a0002c0003t0071g0095a0002c0005t0070g0100a0002c0005t0072g0153 | 3 | HG01192.hp1 NA18971.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.243+7418T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 120866 | ||||||
| chr5:121014
|
A | G | 1 | a0001c0001t0005g0090 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.243+7566A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 121014 | ||||||
| chr5:121116
|
G | A | 10 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0007t0008g0143others(7): Show | 10 | HG02109.hp1 HG02723.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.243+7668G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 121116 | ||||||
| chr5:121139
|
C | T | 15 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(12): Show | 15 | HG00597.hp2 HG01261.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.243+7691C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 121139 | ||||||
| chr5:121140
|
G | A | 2 | a0035c0060t0020g0188a0036c0075t0061g0178 | 2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.243+7692G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 121140 | ||||||
| chr5:121201
|
C | T | 5 | a0001c0002t0006g0134a0001c0011t0029g0136a0001c0011t0106g0085others(2): Show | 5 | HG02647.hp2 HG02723.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.243+7753C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 121201 | ||||||
| chr5:121241
|
C | T | 5 | a0008c0024t0021g0175a0008c0024t0021g0176a0008c0025t0045g0172others(2): Show | 5 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.243+7793C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 121241 | ||||||
| chr5:121257
|
G | A | 38 | a0006c0021t0056g0199a0006c0068t0058g0194a0006c0070t0054g0207others(35): Show | 38 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.243+7809G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 121257 | ||||||
| chr5:121458
|
T | A | 2 | a0015c0076t0067g0192a0015c0077t0053g0181 | 2 | HG02257.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.243+8010T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 121458 | ||||||
| chr5:121538
|
A | C | 1 | a0022c0046t0047g0180 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.243+8090A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 121538 | ||||||
| chr5:121570
|
G | A | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.243+8122G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 121570 | ||||||
| chr5:121618
|
G | A | 1 | a0011c0023t0044g0187 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.243+8170G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 121618 | ||||||
| chr5:121630
|
G | A | 1 | a0002c0003t0124g0017 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.243+8182G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 121630 | ||||||
| chr5:121651
|
G | A | 1 | a0006c0070t0054g0207 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+8203G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 121651 | ||||||
| chr5:121830
|
G | A | 1 | a0014c0065t0038g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.243+8382G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 121830 | ||||||
| chr5:121892
|
G | A | 1 | a0001c0001t0028g0046 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.243+8444G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 121892 | ||||||
| chr5:122008
|
GACA | G | 2 | a0019c0019t0010g0164a0039c0062t0010g0165 | 2 | HG00323.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.243+8565_243+8567d others(5): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 122008 | |||||
| chr5:122154
|
A | G | 10 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0007t0008g0143others(7): Show | 10 | HG02109.hp1 HG02723.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.243+8706A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 122154 | ||||||
| chr5:122294
|
A | G | 3 | a0014c0027t0049g0171a0021c0026t0060g0169a0038c0080t0043g0177 | 3 | HG02486.hp2 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.243+8846A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 122294 | ||||||
| chr5:122376
|
G | T | 2 | a0035c0060t0020g0188a0036c0075t0061g0178 | 2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.243+8928G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 122376 | ||||||
| chr5:122380
|
G | A | 10 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0007t0008g0143others(7): Show | 10 | HG02109.hp1 HG02723.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.243+8932G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 122380 | ||||||
| chr5:122401
|
T | TTTTA | 4 | a0001c0001t0031g0111a0001c0001t0031g0112a0001c0037t0006g0045others(1): Show | 4 | HG01928.hp1 HG01952.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.243+8985_243+8988d others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 122401 | |||||
| chr5:122401
|
TTTTA | T | 54 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0007t0008g0143others(51): Show | 54 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.243+8985_243+8988d others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 122401 | |||||
| chr5:122410
|
T | A | 40 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(37): Show | 40 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.243+8962T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 122410 | ||||||
| chr5:122459
|
T | G | 40 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(37): Show | 40 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.243+9011T>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 122459 | ||||||
| chr5:122473
|
A | G | 39 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(36): Show | 39 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.243+9025A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 122473 | ||||||
| chr5:122513
|
A | T | 1 | a0022c0046t0047g0180 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.243+9065A>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 122513 | ||||||
| chr5:122555
|
G | A | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.243+9107G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 122555 | ||||||
| chr5:122602
|
G | A | 9 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0070t0054g0207others(6): Show | 9 | HG00597.hp2 HG01261.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.243+9154G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 122602 | ||||||
| chr5:122710
|
G | A | 1 | a0036c0075t0061g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.243+9262G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 122710 | ||||||
| chr5:122767
|
A | T | 15 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(12): Show | 15 | HG00597.hp2 HG01261.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.243+9319A>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 122767 | ||||||
| chr5:123447
|
G | A | 1 | a0027c0053t0107g0009 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.243+9999G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 123447 | ||||||
| chr5:123533
|
C | T | 1 | a0007c0010t0026g0035 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.243+10085C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 123533 | ||||||
| chr5:123630
|
A | T | 3 | a0008c0024t0021g0175a0008c0024t0021g0176a0008c0025t0045g0172 | 3 | HG02109.hp2 HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.243+10182A>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 123630 | ||||||
| chr5:123763
|
G | A | 39 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(36): Show | 39 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.243+10315G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 123763 | ||||||
| chr5:123805
|
A | G | 1 | a0014c0065t0038g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.243+10357A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 123805 | ||||||
| chr5:123959
|
G | A | 1 | a0001c0001t0014g0125 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.243+10511G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 123959 | ||||||
| chr5:123979
|
G | A | 5 | a0008c0024t0021g0175a0008c0024t0021g0176a0008c0025t0045g0172others(2): Show | 5 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.243+10531G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 123979 | ||||||
| chr5:124111
|
C | A | 15 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(12): Show | 15 | HG00597.hp2 HG01261.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.243+10663C>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 124111 | ||||||
| chr5:124290
|
G | A | 5 | a0001c0016t0005g0160a0001c0016t0025g0152a0001c0035t0030g0137others(2): Show | 5 | HG02717.hp1 HG02922.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.243+10842G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 124290 | ||||||
| chr5:124307
|
G | A | 1 | a0022c0046t0047g0180 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.243+10859G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 124307 | ||||||
| chr5:124644
|
C | T | 2 | a0017c0030t0039g0140a0032c0058t0040g0158 | 2 | HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.243+11196C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 124644 | ||||||
| chr5:124765
|
C | T | 3 | a0002c0003t0002g0098a0002c0003t0002g0101a0002c0003t0011g0210 | 3 | HG01069.hp1 HG01071.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.243+11317C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 124765 | ||||||
| chr5:124835
|
C | A | 1 | a0004c0041t0003g0077 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.243+11387C>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 124835 | ||||||
| chr5:124935
|
A | AC | 41 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(38): Show | 41 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.243+11488dupC | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 124935 | |||||
| chr5:124949
|
A | G | 1 | a0022c0046t0047g0180 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.243+11501A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 124949 | ||||||
| chr5:125001
|
C | T | 8 | a0011c0023t0041g0184a0011c0023t0044g0187a0011c0078t0059g0185others(5): Show | 8 | HG01099.hp1 HG02257.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.243+11553C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 125001 | ||||||
| chr5:125119
|
T | C | 40 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(37): Show | 40 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.243+11671T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 125119 | ||||||
| chr5:125243
|
G | A | 2 | a0019c0019t0062g0191a0040c0063t0063g0189 | 2 | HG00280.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.243+11795G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 125243 | ||||||
| chr5:125306
|
G | A | 1 | a0002c0003t0136g0071 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.243+11858G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 125306 | ||||||
| chr5:125316
|
T | G | 40 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(37): Show | 40 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.243+11868T>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 125316 | ||||||
| chr5:125360
|
A | G | 1 | a0001c0007t0100g0025 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.243+11912A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 125360 | ||||||
| chr5:125553
|
A | G | 1 | a0036c0075t0061g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.243+12105A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 125553 | ||||||
| chr5:125664
|
A | G | 40 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(37): Show | 40 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.243+12216A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 125664 | ||||||
| chr5:125832
|
T | C | 2 | a0003c0009t0120g0013a0024c0042t0006g0012 | 2 | HG01175.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.243+12384T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 125832 | ||||||
| chr5:126008
|
A | G | 40 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(37): Show | 40 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.243+12560A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 126008 | ||||||
| chr5:126448
|
G | GT | 4 | a0002c0003t0135g0128a0004c0006t0065g0208a0004c0006t0123g0003others(1): Show | 4 | HG03669.hp1 HG03669.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.243+13006dupT | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 126448 | |||||
| chr5:126508
|
A | G | 5 | a0019c0019t0010g0164a0019c0019t0062g0191a0039c0062t0010g0165others(2): Show | 5 | HG00280.hp2 HG00323.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.244-12975A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 126508 | ||||||
| chr5:126753
|
G | A | 39 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(36): Show | 39 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.244-12730G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 126753 | ||||||
| chr5:126967
|
G | A | 1 | a0001c0001t0028g0046 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.244-12516G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 126967 | ||||||
| chr5:127011
|
G | C | 10 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0007t0008g0143others(7): Show | 10 | HG02109.hp1 HG02723.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.244-12472G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 127011 | ||||||
| chr5:127134
|
G | A | 1 | a0001c0001t0001g0159 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.244-12349G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 127134 | ||||||
| chr5:127174
|
T | C | 2 | a0016c0018t0003g0005a0016c0018t0034g0004 | 2 | HG02145.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.244-12309T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 127174 | ||||||
| chr5:127212
|
G | C | 1 | a0001c0001t0092g0054 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.244-12271G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 127212 | ||||||
| chr5:127273
|
TC | T | 2 | a0001c0001t0001g0082a0012c0013t0009g0016 | 2 | NA18973.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.244-12209delC | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 127273 | ||||||
| chr5:127340
|
T | A | 6 | a0002c0003t0135g0128a0002c0005t0003g0096a0004c0006t0065g0208others(3): Show | 6 | HG02273.hp1 HG02809.hp1 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.244-12143T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 127340 | ||||||
| chr5:127340
|
T | TATTATTA | 2 | a0001c0002t0007g0060a0002c0003t0066g0209 | 2 | HG00099.hp1 HG00099.hp2 |
intron_variant | MODIFIER | c.244-12143_244-1214 others(11): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 127340 | ||||||
| chr5:127340
|
T | TTATTATT others(4): Show |
1 | a0001c0002t0082g0126 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.244-12142_244-1214 others(15): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 127340 | |||||
| chr5:127340
|
T | TTTA | 20 | a0002c0003t0002g0132a0003c0004t0108g0010a0004c0054t0034g0139others(17): Show | 20 | HG00735.hp2 HG01175.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.244-12105_244-1210 others(7): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 127340 | |||||
| chr5:127340
|
T | TTTATTA | 78 | a0001c0001t0001g0142a0001c0001t0001g0159a0001c0001t0007g0056others(75): Show | 78 | HG00140.hp1 HG00323.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.244-12108_244-1210 others(10): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 127340 | |||||
| chr5:127340
|
T | TTTATTAT others(2): Show |
45 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0014g0033others(42): Show | 45 | HG00323.hp2 HG00438.hp2 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.244-12111_244-1210 others(13): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 127340 | |||||
| chr5:127340
|
T | TTTATTAT others(5): Show |
19 | a0001c0001t0005g0123a0001c0001t0006g0075a0001c0001t0030g0027others(16): Show | 19 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(16): Show |
intron_variant | MODIFIER | c.244-12114_244-1210 others(16): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 127340 | |||||
| chr5:127340
|
T | TTTATTAT others(8): Show |
2 | a0001c0001t0005g0090a0041c0064t0010g0190 | 2 | HG01081.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.244-12117_244-1210 others(19): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 127340 | |||||
| chr5:127340
|
T | TTTATTAT others(11): Show |
2 | a0017c0030t0039g0140a0036c0075t0061g0178 | 2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.244-12120_244-1210 others(22): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 127340 | |||||
| chr5:127340
|
T | TTTTTTAT others(5): Show |
4 | a0008c0024t0021g0175a0008c0024t0021g0176a0008c0025t0045g0172others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.244-12141_244-1214 others(16): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 127340 | |||||
| chr5:127340
|
TTTATTAT others(8): Show |
T | 1 | a0001c0002t0001g0018 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.244-12117_244-1210 others(19): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 127340 | |||||
| chr5:127412
|
G | A | 2 | a0001c0001t0113g0044a0003c0004t0089g0014 | 2 | HG00140.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.244-12071G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 127412 | ||||||
| chr5:127414
|
G | T | 3 | a0019c0019t0062g0191a0040c0063t0063g0189a0041c0064t0010g0190 | 3 | HG00280.hp2 HG01081.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.244-12069G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 127414 | ||||||
| chr5:127419
|
C | T | 40 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(37): Show | 40 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.244-12064C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 127419 | ||||||
| chr5:127621
|
G | A | 39 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(36): Show | 39 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.244-11862G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 127621 | ||||||
| chr5:127635
|
G | A | 4 | a0014c0027t0049g0171a0014c0066t0051g0170a0021c0026t0060g0169others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.244-11848G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 127635 | ||||||
| chr5:127790
|
G | A | 40 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(37): Show | 40 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.244-11693G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 127790 | ||||||
| chr5:127850
|
G | A | 1 | a0038c0080t0043g0177 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.244-11633G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 127850 | ||||||
| chr5:128348
|
A | C | 1 | a0014c0065t0038g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.244-11135A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 128348 | ||||||
| chr5:128348
|
A | G | 40 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(37): Show | 40 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.244-11135A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 128348 | ||||||
| chr5:128449
|
A | G | 1 | a0003c0056t0017g0080 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.244-11034A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 128449 | ||||||
| chr5:128601
|
T | C | 41 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(38): Show | 41 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.244-10882T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 128601 | ||||||
| chr5:128671
|
T | G | 1 | a0001c0007t0008g0150 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.244-10812T>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 128671 | ||||||
| chr5:128757
|
A | G | 5 | a0009c0012t0114g0156a0014c0027t0049g0171a0014c0066t0051g0170others(2): Show | 5 | HG02486.hp2 HG02809.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.244-10726A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 128757 | ||||||
| chr5:128917
|
G | A | 41 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(38): Show | 41 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.244-10566G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 128917 | ||||||
| chr5:128942
|
A | G | 2 | a0001c0036t0077g0149a0001c0051t0078g0148 | 2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.244-10541A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 128942 | ||||||
| chr5:128944
|
C | T | 15 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(12): Show | 15 | HG00597.hp2 HG01261.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.244-10539C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 128944 | ||||||
| chr5:129279
|
A | G | 1 | a0014c0065t0038g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.244-10204A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 129279 | ||||||
| chr5:129345
|
G | A | 5 | a0001c0001t0006g0075a0001c0001t0030g0027a0001c0001t0093g0105others(2): Show | 5 | HG00438.hp1 HG02083.hp2 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.244-10138G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 129345 | ||||||
| chr5:129368
|
C | T | 1 | a0014c0065t0038g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.244-10115C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 129368 | ||||||
| chr5:129451
|
C | T | 1 | a0037c0074t0037g0203 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.244-10032C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 129451 | ||||||
| chr5:129591
|
A | G | 51 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0007t0008g0143others(48): Show | 51 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.244-9892A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 129591 | ||||||
| chr5:129626
|
T | C | 1 | a0032c0058t0040g0158 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.244-9857T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 129626 | ||||||
| chr5:130007
|
A | G | 1 | a0016c0018t0034g0004 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.244-9476A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 130007 | ||||||
| chr5:130061
|
A | AAGAGAGA others(1): Show |
5 | a0008c0025t0069g0174a0008c0079t0068g0173a0015c0076t0067g0192others(2): Show | 5 | HG02257.hp1 HG02486.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.244-9421_244-9414d others(10): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 130061 | |||||
| chr5:130061
|
A | AAGAGAGA others(3): Show |
25 | a0006c0068t0058g0194a0006c0071t0018g0202a0006c0072t0036g0206others(22): Show | 25 | HG00597.hp2 HG01099.hp1 HG01261.hp2 others(22): Show |
intron_variant | MODIFIER | c.244-9414_244-9413i others(12): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 130061 | |||||
| chr5:130061
|
A | AAGAGAGA others(5): Show |
2 | a0006c0021t0018g0198a0006c0021t0056g0199 | 2 | HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.244-9414_244-9413i others(14): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 130061 | |||||
| chr5:130061
|
A | AAGAGAGA others(11): Show |
1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.244-9414_244-9413i others(20): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 130061 | |||||
| chr5:130066
|
AGAGT | A | 5 | a0019c0019t0010g0164a0019c0019t0062g0191a0039c0062t0010g0165others(2): Show | 5 | HG00280.hp2 HG00323.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.244-9413_244-9410d others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 130066 | |||||
| chr5:130070
|
T | A | 35 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(32): Show | 35 | HG00597.hp2 HG01099.hp1 HG01261.hp2 others(32): Show |
intron_variant | MODIFIER | c.244-9413T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 130070 | ||||||
| chr5:130373
|
T | G | 41 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(38): Show | 41 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.244-9110T>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 130373 | ||||||
| chr5:130390
|
A | G | 41 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(38): Show | 41 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.244-9093A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 130390 | ||||||
| chr5:130654
|
T | TA | 3 | a0008c0024t0021g0175a0008c0024t0021g0176a0008c0025t0045g0172 | 3 | HG02109.hp2 HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.244-8826dupA | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 130654 | |||||
| chr5:130741
|
GCACCGCT others(9): Show |
G | 1 | a0002c0003t0002g0101 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.244-8739_244-8724d others(18): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 130741 | |||||
| chr5:130746
|
G | A | 4 | a0014c0027t0049g0171a0014c0066t0051g0170a0021c0026t0060g0169others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.244-8737G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 130746 | ||||||
| chr5:130944
|
A | G | 1 | a0003c0009t0121g0092 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.244-8539A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 130944 | ||||||
| chr5:131015
|
G | A | 5 | a0008c0024t0021g0175a0008c0024t0021g0176a0008c0025t0045g0172others(2): Show | 5 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.244-8468G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 131015 | ||||||
| chr5:131085
|
G | A | 1 | a0006c0068t0058g0194 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.244-8398G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 131085 | ||||||
| chr5:131091
|
G | T | 1 | a0018c0022t0011g0196 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.244-8392G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 131091 | ||||||
| chr5:131118
|
C | CTTTTTTT others(1): Show |
37 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(34): Show | 37 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.244-8362_244-8355d others(10): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 131118 | |||||
| chr5:131144
|
G | A | 10 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0007t0008g0143others(7): Show | 10 | HG02109.hp1 HG02723.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.244-8339G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 131144 | ||||||
| chr5:131259
|
T | C | 188 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0142others(185): Show | 188 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.244-8224T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 131259 | ||||||
| chr5:131295
|
A | G | 40 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(37): Show | 40 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.244-8188A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 131295 | ||||||
| chr5:131301
|
C | T | 40 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(37): Show | 40 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.244-8182C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 131301 | ||||||
| chr5:131314
|
A | C | 1 | a0001c0001t0028g0046 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.244-8169A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 131314 | ||||||
| chr5:131393
|
A | G | 40 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(37): Show | 40 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.244-8090A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 131393 | ||||||
| chr5:131488
|
C | T | 40 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(37): Show | 40 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.244-7995C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 131488 | ||||||
| chr5:131532
|
G | A | 2 | a0001c0001t0014g0115a0001c0001t0014g0125 | 2 | HG00438.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.244-7951G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 131532 | ||||||
| chr5:131563
|
G | T | 1 | a0014c0065t0038g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.244-7920G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 131563 | ||||||
| chr5:131576
|
G | A | 4 | a0014c0027t0049g0171a0014c0066t0051g0170a0021c0026t0060g0169others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.244-7907G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 131576 | ||||||
| chr5:131851
|
T | C | 3 | a0011c0023t0041g0184a0011c0023t0044g0187a0011c0078t0059g0185 | 3 | HG01099.hp1 HG02280.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.244-7632T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 131851 | ||||||
| chr5:131860
|
A | G | 4 | a0001c0001t0031g0111a0001c0001t0031g0112a0001c0001t0102g0057others(1): Show | 4 | HG01928.hp1 HG01952.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.244-7623A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 131860 | ||||||
| chr5:131938
|
T | C | 40 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(37): Show | 40 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.244-7545T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 131938 | ||||||
| chr5:132008
|
A | G | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.244-7475A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 132008 | ||||||
| chr5:132055
|
G | A | 40 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(37): Show | 40 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.244-7428G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 132055 | ||||||
| chr5:132066
|
G | A | 1 | a0001c0051t0078g0148 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.244-7417G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 132066 | ||||||
| chr5:132071
|
G | A | 2 | a0015c0076t0067g0192a0015c0077t0053g0181 | 2 | HG02257.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.244-7412G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 132071 | ||||||
| chr5:132115
|
G | A | 41 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(38): Show | 41 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.244-7368G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 132115 | ||||||
| chr5:132116
|
C | T | 1 | a0014c0065t0038g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.244-7367C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 132116 | ||||||
| chr5:132543
|
G | T | 40 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(37): Show | 40 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.244-6940G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 132543 | ||||||
| chr5:132722
|
C | T | 4 | a0014c0027t0049g0171a0014c0066t0051g0170a0021c0026t0060g0169others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.244-6761C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 132722 | ||||||
| chr5:132753
|
C | T | 40 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(37): Show | 40 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.244-6730C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 132753 | ||||||
| chr5:132818
|
G | A | 9 | a0011c0023t0041g0184a0011c0023t0044g0187a0011c0078t0059g0185others(6): Show | 9 | HG01099.hp1 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.244-6665G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 132818 | ||||||
| chr5:132902
|
A | G | 3 | a0019c0019t0062g0191a0040c0063t0063g0189a0041c0064t0010g0190 | 3 | HG00280.hp2 HG01081.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.244-6581A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 132902 | ||||||
| chr5:133065
|
T | C | 1 | a0001c0015t0035g0122 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.244-6418T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 133065 | ||||||
| chr5:133072
|
G | A | 5 | a0008c0024t0021g0175a0008c0024t0021g0176a0008c0025t0045g0172others(2): Show | 5 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.244-6411G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 133072 | ||||||
| chr5:133167
|
G | A | 5 | a0008c0024t0021g0175a0008c0024t0021g0176a0008c0025t0045g0172others(2): Show | 5 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.244-6316G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 133167 | ||||||
| chr5:133180
|
A | G | 41 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(38): Show | 41 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.244-6303A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 133180 | ||||||
| chr5:133259
|
G | GA | 4 | a0014c0027t0049g0171a0014c0066t0051g0170a0021c0026t0060g0169others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.244-6222dupA | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 133259 | |||||
| chr5:133340
|
C | T | 4 | a0014c0027t0049g0171a0014c0066t0051g0170a0021c0026t0060g0169others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.244-6143C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 133340 | ||||||
| chr5:133393
|
C | T | 1 | a0001c0002t0001g0018 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.244-6090C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 133393 | ||||||
| chr5:133450
|
G | A | 40 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(37): Show | 40 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.244-6033G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 133450 | ||||||
| chr5:133549
|
T | G | 15 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(12): Show | 15 | HG00597.hp2 HG01261.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.244-5934T>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 133549 | ||||||
| chr5:133894
|
G | A | 1 | a0006c0071t0018g0202 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.244-5589G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 133894 | ||||||
| chr5:133913
|
G | GAC | 3 | a0006c0021t0018g0198a0006c0021t0056g0199a0020c0081t0064g0200 | 3 | HG03041.hp2 HG03195.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.244-5563_244-5562d others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 133913 | |||||
| chr5:133913
|
G | GACACAC | 9 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0007t0008g0143others(6): Show | 9 | HG02109.hp1 HG02723.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.244-5567_244-5562d others(8): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 133913 | |||||
| chr5:133913
|
G | GACACACA others(1): Show |
12 | a0006c0068t0058g0194a0006c0070t0054g0207a0006c0071t0018g0202others(9): Show | 12 | HG00597.hp2 HG02145.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.244-5569_244-5562d others(10): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 133913 | |||||
| chr5:133913
|
G | GACACACA others(3): Show |
5 | a0006c0073t0020g0193a0016c0018t0034g0004a0017c0029t0112g0155others(2): Show | 5 | HG01261.hp2 HG02622.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.244-5562_244-5561i others(12): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 133913 | |||||
| chr5:133922
|
G | A | 55 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0007t0008g0143others(52): Show | 55 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.244-5561G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 133922 | ||||||
| chr5:133924
|
A | G | 1 | a0002c0039t0009g0030 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.244-5559A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 133924 | ||||||
| chr5:133941
|
C | CACACACA others(13): Show |
3 | a0011c0023t0041g0184a0011c0023t0044g0187a0011c0078t0059g0185 | 3 | HG01099.hp1 HG02280.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.244-5541_244-5540i others(22): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 133941 | |||||
| chr5:133941
|
C | CACACACA others(9): Show |
3 | a0015c0076t0067g0192a0015c0077t0053g0181a0022c0046t0047g0180 | 3 | HG02257.hp1 HG02717.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.244-5541_244-5540i others(18): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 133941 | |||||
| chr5:133941
|
C | CACACACA others(11): Show |
3 | a0014c0027t0049g0171a0014c0066t0051g0170a0038c0080t0043g0177 | 3 | HG02486.hp2 HG02809.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.244-5541_244-5540i others(20): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 133941 | |||||
| chr5:133941
|
C | CACACACA others(5): Show |
4 | a0019c0019t0010g0164a0019c0019t0062g0191a0039c0062t0010g0165others(1): Show | 4 | HG00280.hp2 HG00323.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.244-5541_244-5540i others(14): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 133941 | |||||
| chr5:133941
|
C | CACACACA others(3): Show |
2 | a0036c0075t0061g0178a0041c0064t0010g0190 | 2 | HG01081.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.244-5541_244-5540i others(12): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 133941 | |||||
| chr5:133941
|
C | CACAT | 8 | a0008c0024t0021g0175a0008c0024t0021g0176a0008c0025t0045g0172others(5): Show | 8 | HG02109.hp2 HG02145.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.244-5541_244-5540i others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 133941 | |||||
| chr5:133941
|
C | T | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.244-5542C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 133941 | ||||||
| chr5:133943
|
T | C | 10 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0007t0008g0143others(7): Show | 10 | HG02109.hp1 HG02723.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.244-5540T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 133943 | ||||||
| chr5:133953
|
G | GTGGAATA others(27): Show |
1 | a0003c0017t0074g0050 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.244-5502_244-5469d others(36): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 133953 | |||||
| chr5:133969
|
T | C | 1 | a0014c0065t0038g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.244-5514T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 133969 | ||||||
| chr5:134030
|
A | G | 1 | a0016c0018t0034g0004 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.244-5453A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 134030 | ||||||
| chr5:134058
|
AATATATA others(13): Show |
A | 1 | a0001c0011t0029g0136 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.244-5412_244-5393d others(22): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 134058 | |||||
| chr5:134058
|
AATATATA others(17): Show |
A | 3 | a0001c0001t0097g0086a0001c0001t0104g0023a0001c0002t0006g0134 | 3 | HG00323.hp1 HG02602.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.244-5412_244-5389d others(26): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 134058 | |||||
| chr5:134058
|
AATATATA others(19): Show |
A | 4 | a0001c0001t0001g0082a0001c0037t0006g0045a0012c0013t0009g0016others(1): Show | 4 | HG02647.hp2 NA18973.hp1 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.244-5412_244-5387d others(28): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 134058 | |||||
| chr5:134058
|
AATATATA others(21): Show |
A | 1 | a0001c0011t0106g0085 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.244-5412_244-5385d others(30): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 134058 | |||||
| chr5:134058
|
AATATATA others(23): Show |
A | 1 | a0001c0032t0103g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.244-5412_244-5383d others(32): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 134058 | |||||
| chr5:134058
|
AATATATA others(27): Show |
A | 1 | a0019c0019t0062g0191 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.244-5412_244-5379d others(36): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 134058 | |||||
| chr5:134069
|
A | G | 1 | a0002c0005t0072g0153 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.244-5414A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 134069 | ||||||
| chr5:134076
|
A | AAT | 11 | a0001c0001t0015g0131a0001c0002t0012g0072a0001c0002t0081g0034others(8): Show | 11 | HG00642.hp1 HG00733.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.244-5362_244-5361d others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 134076 | |||||
| chr5:134076
|
A | AATAT | 10 | a0001c0001t0014g0125a0001c0001t0093g0105a0002c0003t0124g0017others(7): Show | 10 | HG00597.hp1 HG00639.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.244-5364_244-5361d others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 134076 | |||||
| chr5:134076
|
A | AATATAT | 2 | a0009c0012t0115g0157a0034c0059t0001g0114 | 2 | HG03139.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.244-5366_244-5361d others(8): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 134076 | |||||
| chr5:134076
|
AAT | A | 48 | a0001c0001t0004g0020a0001c0001t0024g0135a0001c0001t0027g0052others(45): Show | 48 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.244-5362_244-5361d others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 134076 | |||||
| chr5:134076
|
AATAT | A | 40 | a0001c0001t0001g0159a0001c0001t0014g0033a0001c0001t0014g0115others(37): Show | 40 | HG00438.hp2 HG00597.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.244-5364_244-5361d others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 134076 | |||||
| chr5:134076
|
AATATAT | A | 16 | a0001c0001t0073g0107a0001c0002t0024g0024a0001c0036t0077g0149others(13): Show | 16 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.244-5366_244-5361d others(8): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 134076 | |||||
| chr5:134076
|
AATATATA others(1): Show |
A | 10 | a0001c0001t0012g0069a0001c0002t0007g0060a0001c0051t0078g0148others(7): Show | 10 | HG00099.hp1 HG00099.hp2 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.244-5368_244-5361d others(10): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 134076 | |||||
| chr5:134076
|
AATATATA others(3): Show |
A | 7 | a0001c0001t0032g0144a0001c0016t0025g0152a0006c0068t0058g0194others(4): Show | 7 | HG02109.hp1 HG02647.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.244-5370_244-5361d others(12): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 134076 | |||||
| chr5:134076
|
AATATATA others(5): Show |
A | 3 | a0001c0001t0032g0094a0013c0020t0050g0182a0013c0020t0052g0183 | 3 | HG02451.hp1 HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.244-5372_244-5361d others(14): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 134076 | |||||
| chr5:134076
|
AATATATA others(7): Show |
A | 2 | a0015c0076t0067g0192a0020c0081t0064g0200 | 2 | HG02257.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.244-5374_244-5361d others(16): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 134076 | |||||
| chr5:134076
|
AATATATA others(9): Show |
A | 7 | a0001c0007t0008g0143a0001c0007t0008g0146a0001c0007t0109g0147others(4): Show | 7 | HG02451.hp2 HG02723.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.244-5376_244-5361d others(18): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 134076 | |||||
| chr5:134076
|
AATATATA others(11): Show |
A | 4 | a0001c0007t0008g0145a0011c0023t0041g0184a0011c0023t0044g0187others(1): Show | 4 | HG01099.hp1 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.244-5378_244-5361d others(20): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 134076 | |||||
| chr5:134076
|
AATATATA others(13): Show |
A | 3 | a0001c0007t0008g0150a0008c0025t0069g0174a0008c0079t0068g0173 | 3 | HG03471.hp2 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.244-5380_244-5361d others(22): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 134076 | |||||
| chr5:134076
|
AATATATA others(17): Show |
A | 2 | a0005c0008t0004g0061a0007c0038t0013g0102 | 2 | HG01255.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.244-5384_244-5361d others(26): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 134076 | |||||
| chr5:134076
|
AATATATA others(23): Show |
A | 1 | a0014c0065t0038g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.244-5390_244-5361d others(32): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 134076 | |||||
| chr5:134080
|
T | TATATATA others(21): Show |
1 | a0001c0001t0005g0123 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.244-5381_244-5380i others(30): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 134080 | |||||
| chr5:134080
|
T | TATATATA others(7): Show |
1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.244-5395_244-5394i others(16): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 134080 | |||||
| chr5:134081
|
A | G | 1 | a0003c0017t0016g0110 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.244-5402A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 134081 | ||||||
| chr5:134088
|
T | TG | 3 | a0008c0024t0021g0175a0008c0024t0021g0176a0008c0025t0045g0172 | 3 | HG02109.hp2 HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.244-5395_244-5394i others(3): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 134088 | ||||||
| chr5:134090
|
T | TAGA | 3 | a0008c0024t0021g0175a0008c0024t0021g0176a0008c0025t0045g0172 | 3 | HG02109.hp2 HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.244-5392_244-5391i others(5): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 134090 | |||||
| chr5:134100
|
T | C | 1 | a0004c0006t0002g0119 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.244-5383T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 134100 | ||||||
| chr5:134151
|
A | G | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.244-5332A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 134151 | ||||||
| chr5:134162
|
A | G | 1 | a0001c0001t0079g0059 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.244-5321A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 134162 | ||||||
| chr5:134174
|
G | GCAACCTG others(9): Show |
1 | a0002c0003t0002g0101 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.244-5308_244-5293d others(18): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 134174 | |||||
| chr5:134229
|
A | C | 4 | a0014c0027t0049g0171a0014c0066t0051g0170a0021c0026t0060g0169others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.244-5254A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 134229 | ||||||
| chr5:134252
|
TC | T | 2 | a0003c0044t0001g0116a0012c0013t0133g0118 | 2 | NA18977.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.244-5230delC | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 134252 | ||||||
| chr5:134333
|
G | A | 9 | a0011c0023t0041g0184a0011c0023t0044g0187a0011c0078t0059g0185others(6): Show | 9 | HG01099.hp1 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.244-5150G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 134333 | ||||||
| chr5:134443
|
A | G | 4 | a0014c0027t0049g0171a0014c0066t0051g0170a0021c0026t0060g0169others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.244-5040A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 134443 | ||||||
| chr5:134517
|
G | T | 1 | a0029c0033t0042g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.244-4966G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 134517 | ||||||
| chr5:134578
|
C | T | 1 | a0038c0080t0043g0177 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.244-4905C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 134578 | ||||||
| chr5:134581
|
T | C | 40 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(37): Show | 40 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.244-4902T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 134581 | ||||||
| chr5:134623
|
A | G | 40 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(37): Show | 40 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.244-4860A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 134623 | ||||||
| chr5:134631
|
T | C | 5 | a0008c0024t0021g0175a0008c0024t0021g0176a0008c0025t0045g0172others(2): Show | 5 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.244-4852T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 134631 | ||||||
| chr5:134640
|
C | A | 1 | a0036c0075t0061g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.244-4843C>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 134640 | ||||||
| chr5:134756
|
ACT | A | 2 | a0003c0004t0116g0103a0003c0004t0117g0070 | 2 | HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.244-4724_244-4723d others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 134756 | |||||
| chr5:134777
|
A | AAAG | 35 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(32): Show | 35 | HG00597.hp2 HG01099.hp1 HG01261.hp2 others(32): Show |
intron_variant | MODIFIER | c.244-4704_244-4703i others(5): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 134777 | |||||
| chr5:134777
|
A | G | 1 | a0001c0007t0100g0025 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.244-4706A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 134777 | ||||||
| chr5:134912
|
G | A | 40 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(37): Show | 40 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.244-4571G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 134912 | ||||||
| chr5:134917
|
C | T | 2 | a0002c0005t0003g0031a0002c0039t0009g0030 | 2 | HG00673.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.244-4566C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 134917 | ||||||
| chr5:134927
|
T | C | 40 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(37): Show | 40 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.244-4556T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 134927 | ||||||
| chr5:134986
|
G | A | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.244-4497G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 134986 | ||||||
| chr5:135003
|
C | G | 1 | a0014c0065t0038g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.244-4480C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 135003 | ||||||
| chr5:135105
|
G | A | 1 | a0003c0009t0121g0092 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.244-4378G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 135105 | ||||||
| chr5:135187
|
C | CA | 14 | a0001c0001t0028g0046a0001c0001t0091g0120a0001c0001t0093g0105others(11): Show | 14 | HG01243.hp2 HG01515.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.244-4274dupA | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 135187 | |||||
| chr5:135187
|
C | CAAAAAAA others(5): Show |
1 | a0022c0046t0047g0180 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.244-4285_244-4274d others(14): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 135187 | |||||
| chr5:135187
|
C | CAAAAAAA others(9): Show |
1 | a0014c0066t0051g0170 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.244-4289_244-4274d others(18): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 135187 | |||||
| chr5:135187
|
C | CAAAAAAA others(10): Show |
1 | a0014c0027t0049g0171 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.244-4290_244-4274d others(19): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 135187 | |||||
| chr5:135187
|
C | CAAAAAAA others(11): Show |
3 | a0015c0077t0053g0181a0021c0026t0060g0169a0038c0080t0043g0177 | 3 | HG02486.hp2 HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.244-4291_244-4274d others(20): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 135187 | |||||
| chr5:135187
|
C | CAAAAAAA others(20): Show |
2 | a0013c0020t0050g0182a0013c0067t0046g0186 | 2 | HG02451.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.244-4274_244-4273i others(29): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 135187 | |||||
| chr5:135187
|
C | CAAAAAAA others(22): Show |
1 | a0013c0020t0052g0183 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.244-4274_244-4273i others(31): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 135187 | |||||
| chr5:135187
|
CA | C | 9 | a0001c0002t0101g0068a0001c0016t0005g0160a0001c0051t0078g0148others(6): Show | 9 | HG00323.hp2 HG00639.hp1 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.244-4274delA | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 135187 | |||||
| chr5:135187
|
CAAAAAAA | C | 15 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(12): Show | 15 | HG00597.hp2 HG01261.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.244-4280_244-4274d others(9): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 135187 | |||||
| chr5:135187
|
CAAAAAAA others(6): Show |
C | 1 | a0005c0008t0111g0091 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.244-4286_244-4274d others(15): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 135187 | |||||
| chr5:135288
|
G | T | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.244-4195G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 135288 | ||||||
| chr5:135352
|
T | A | 4 | a0001c0001t0012g0069a0001c0002t0012g0066a0002c0005t0127g0124others(1): Show | 4 | HG00733.hp1 HG01074.hp2 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.244-4131T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 135352 | ||||||
| chr5:135461
|
C | T | 40 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(37): Show | 40 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.244-4022C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 135461 | ||||||
| chr5:135476
|
T | C | 1 | a0002c0005t0003g0167 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.244-4007T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 135476 | ||||||
| chr5:135478
|
A | G | 1 | a0002c0005t0003g0167 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.244-4005A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 135478 | ||||||
| chr5:135614
|
C | T | 1 | a0014c0065t0038g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.244-3869C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 135614 | ||||||
| chr5:135665
|
C | CAA | 5 | a0001c0001t0098g0129a0016c0018t0034g0004a0022c0046t0047g0180others(2): Show | 5 | HG00673.hp2 HG01175.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.244-3801_244-3800d others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 135665 | |||||
| chr5:135665
|
C | CAAAAAAA others(7): Show |
1 | a0017c0029t0112g0155 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.244-3813_244-3800d others(16): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 135665 | |||||
| chr5:135665
|
CA | C | 12 | a0001c0001t0005g0123a0001c0001t0015g0037a0001c0001t0031g0111others(9): Show | 12 | HG00639.hp2 HG01070.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.244-3800delA | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 135665 | |||||
| chr5:135675
|
AAAAAAAA others(24): Show |
A | 4 | a0001c0002t0006g0134a0001c0011t0029g0136a0001c0011t0106g0085others(1): Show | 4 | HG02647.hp2 HG02723.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.244-3806_244-3776d others(33): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 135675 | |||||
| chr5:135676
|
A | T | 2 | a0001c0001t0024g0135a0004c0041t0003g0077 | 2 | HG01978.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.244-3807A>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 135676 | ||||||
| chr5:135677
|
AAAAAAAT others(16): Show |
A | 3 | a0001c0048t0013g0055a0004c0006t0134g0011a0005c0008t0111g0091 | 3 | HG01255.hp1 NA18971.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.244-3804_244-3782d others(25): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 135677 | |||||
| chr5:135677
|
AAAAAAAT others(24): Show |
A | 5 | a0001c0016t0005g0160a0001c0016t0025g0152a0001c0035t0030g0137others(2): Show | 5 | HG02717.hp1 HG02922.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.244-3804_244-3774d others(33): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 135677 | |||||
| chr5:135678
|
A | AATATATA others(3): Show |
1 | a0001c0001t0012g0069 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.244-3804_244-3803i others(12): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 135678 | |||||
| chr5:135678
|
A | AT | 2 | a0001c0001t0102g0057a0001c0002t0024g0024 | 2 | HG02132.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.244-3805_244-3804i others(3): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 135678 | ||||||
| chr5:135678
|
A | T | 7 | a0001c0001t0024g0135a0001c0002t0012g0072a0001c0002t0086g0104others(4): Show | 7 | HG00733.hp2 HG01069.hp2 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.244-3805A>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 135678 | ||||||
| chr5:135678
|
AAAAAATA others(17): Show |
A | 1 | a0001c0001t0079g0059 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.244-3803_244-3780d others(26): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 135678 | |||||
| chr5:135679
|
AAAAATAT others(4): Show |
A | 2 | a0001c0001t0073g0107a0029c0033t0042g0163 | 2 | HG00738.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.244-3802_244-3792d others(13): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 135679 | |||||
| chr5:135679
|
AAAAATAT others(10): Show |
A | 2 | a0001c0002t0025g0073a0002c0003t0002g0101 | 2 | HG01071.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.244-3802_244-3786d others(19): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 135679 | |||||
| chr5:135679
|
AAAAATAT others(16): Show |
A | 7 | a0001c0001t0027g0052a0001c0001t0027g0053a0001c0001t0113g0044others(4): Show | 7 | HG00140.hp1 HG00597.hp1 HG00733.hp1 others(4): Show |
intron_variant | MODIFIER | c.244-3802_244-3780d others(25): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 135679 | |||||
| chr5:135680
|
A | AATATATA others(3): Show |
1 | a0001c0001t0099g0089 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.244-3802_244-3801i others(12): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 135680 | |||||
| chr5:135680
|
A | AT | 9 | a0001c0001t0004g0020a0001c0001t0015g0022a0001c0001t0028g0046others(6): Show | 9 | HG00642.hp2 HG01069.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.244-3803_244-3802i others(3): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 135680 | ||||||
| chr5:135680
|
A | ATAT | 5 | a0001c0002t0007g0060a0001c0051t0078g0148a0002c0003t0066g0209others(2): Show | 5 | HG00099.hp1 HG00099.hp2 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.244-3803_244-3802i others(5): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 135680 | ||||||
| chr5:135680
|
A | ATATATAT others(2): Show |
2 | a0001c0061t0001g0006a0003c0004t0105g0081 | 2 | HG03209.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.244-3803_244-3802i others(11): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 135680 | ||||||
| chr5:135680
|
A | ATATATAT others(4): Show |
1 | a0001c0002t0012g0066 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.244-3803_244-3802i others(13): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 135680 | ||||||
| chr5:135680
|
A | T | 22 | a0001c0001t0006g0075a0001c0001t0012g0069a0001c0001t0024g0135others(19): Show | 22 | HG00639.hp2 HG00733.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.244-3803A>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 135680 | ||||||
| chr5:135680
|
AAAATATA others(7): Show |
A | 1 | a0001c0001t0015g0131 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.244-3801_244-3788d others(16): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 135680 | |||||
| chr5:135680
|
AAAATATA others(13): Show |
A | 1 | a0001c0002t0013g0109 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.244-3801_244-3782d others(22): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 135680 | |||||
| chr5:135682
|
A | AAAAAAAA others(13): Show |
1 | a0032c0058t0040g0158 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.244-3800_244-3799i others(22): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 135682 | |||||
| chr5:135682
|
A | AAAAAAAA others(9): Show |
1 | a0008c0079t0068g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.244-3800_244-3799i others(18): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 135682 | |||||
| chr5:135682
|
A | AAAAAAAA others(6): Show |
1 | a0008c0025t0045g0172 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.244-3800_244-3799i others(15): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 135682 | |||||
| chr5:135682
|
A | AAAAAAAA others(8): Show |
1 | a0008c0025t0069g0174 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.244-3800_244-3799i others(17): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 135682 | |||||
| chr5:135682
|
A | AAAAAAAA others(4): Show |
1 | a0008c0024t0021g0176 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.244-3800_244-3799i others(13): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 135682 | |||||
| chr5:135682
|
A | AAAAAAAA others(24): Show |
1 | a0019c0019t0062g0191 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.244-3800_244-3799i others(33): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 135682 | |||||
| chr5:135682
|
A | AAAAAAAA others(9): Show |
1 | a0041c0064t0010g0190 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.244-3800_244-3799i others(18): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 135682 | |||||
| chr5:135682
|
A | AAAAAAAA others(5): Show |
1 | a0040c0063t0063g0189 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.244-3800_244-3799i others(14): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 135682 | |||||
| chr5:135682
|
A | AAAAAAAA others(7): Show |
1 | a0038c0080t0043g0177 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.244-3800_244-3799i others(16): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 135682 | |||||
| chr5:135682
|
A | AAAAAAAT others(42): Show |
1 | a0021c0026t0060g0169 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.244-3800_244-3799i others(51): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 135682 | |||||
| chr5:135682
|
A | AAAT | 7 | a0001c0002t0007g0083a0001c0007t0008g0143a0001c0007t0008g0145others(4): Show | 7 | HG02165.hp1 HG02723.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.244-3800_244-3799i others(5): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 135682 | |||||
| chr5:135682
|
A | AAATAT | 6 | a0001c0001t0005g0090a0001c0001t0007g0056a0001c0001t0014g0033others(3): Show | 6 | HG01243.hp1 HG02080.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.244-3800_244-3799i others(7): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 135682 | |||||
| chr5:135682
|
A | AAT | 6 | a0001c0001t0091g0120a0002c0005t0070g0100a0002c0057t0003g0026others(3): Show | 6 | HG01192.hp1 HG01256.hp1 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.244-3756_244-3755d others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 135682 | |||||
| chr5:135682
|
A | AT | 5 | a0001c0001t0001g0084a0001c0001t0001g0142a0001c0011t0048g0179others(2): Show | 5 | HG02280.hp2 HG03209.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.244-3801_244-3800i others(3): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 135682 | ||||||
| chr5:135682
|
A | ATAT | 4 | a0001c0002t0087g0040a0002c0005t0003g0167a0003c0004t0001g0087others(1): Show | 4 | HG02083.hp1 HG03831.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.244-3801_244-3800i others(5): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 135682 | ||||||
| chr5:135682
|
A | ATATATAT others(4): Show |
1 | a0023c0055t0029g0079 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.244-3801_244-3800i others(13): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 135682 | ||||||
| chr5:135682
|
A | ATATATAT others(6): Show |
1 | a0003c0004t0028g0058 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.244-3801_244-3800i others(15): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 135682 | ||||||
| chr5:135682
|
A | ATATATAT others(8): Show |
2 | a0014c0027t0049g0171a0014c0066t0051g0170 | 2 | HG02809.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.244-3801_244-3800i others(17): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 135682 | ||||||
| chr5:135682
|
A | T | 59 | a0001c0001t0001g0159a0001c0001t0004g0020a0001c0001t0006g0075others(56): Show | 59 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(56): Show |
intron_variant | MODIFIER | c.244-3801A>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 135682 | ||||||
| chr5:135682
|
AATATAT | A | 7 | a0006c0021t0056g0199a0006c0068t0058g0194a0011c0078t0059g0185others(4): Show | 7 | HG01099.hp1 HG02451.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.244-3760_244-3755d others(8): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 135682 | |||||
| chr5:135682
|
AATATATA others(5): Show |
A | 1 | a0017c0030t0039g0140 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.244-3766_244-3755d others(14): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 135682 | |||||
| chr5:135683
|
AT | A | 8 | a0001c0002t0022g0015a0001c0002t0081g0034a0001c0007t0008g0150others(5): Show | 8 | HG00741.hp2 HG01123.hp1 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.244-3799delT | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 135683 | ||||||
| chr5:135683
|
ATATAT | A | 3 | a0006c0021t0018g0198a0006c0071t0018g0202a0018c0022t0011g0195 | 3 | HG02922.hp2 HG03195.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.244-3799_244-3795d others(7): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 135683 | ||||||
| chr5:135683
|
ATATATAT | A | 2 | a0015c0076t0067g0192a0015c0077t0053g0181 | 2 | HG02257.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.244-3799_244-3793d others(9): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 135683 | ||||||
| chr5:135683
|
ATATATAT others(2): Show |
A | 2 | a0001c0015t0035g0122a0001c0015t0076g0154 | 2 | HG02886.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.244-3799_244-3791d others(11): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 135683 | ||||||
| chr5:135683
|
ATATATAT others(4): Show |
A | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.244-3799_244-3789d others(13): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 135683 | ||||||
| chr5:135683
|
ATATATAT others(22): Show |
A | 1 | a0014c0065t0038g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.244-3799_244-3771d others(31): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 135683 | ||||||
| chr5:135684
|
T | A | 10 | a0001c0052t0118g0121a0006c0072t0036g0206a0010c0014t0055g0201others(7): Show | 10 | HG00741.hp1 HG02145.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.244-3799T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 135684 | ||||||
| chr5:135686
|
T | A | 14 | a0002c0003t0132g0028a0002c0003t0136g0071a0004c0006t0003g0047others(11): Show | 14 | HG01123.hp1 HG02145.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.244-3797T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 135686 | ||||||
| chr5:135688
|
T | A | 15 | a0002c0003t0132g0028a0002c0003t0136g0071a0006c0070t0054g0207others(12): Show | 15 | HG00597.hp2 HG01123.hp1 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.244-3795T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 135688 | ||||||
| chr5:135688
|
T | C | 1 | a0021c0026t0060g0169 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.244-3795T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 135688 | ||||||
| chr5:135690
|
T | A | 23 | a0002c0003t0136g0071a0006c0021t0018g0198a0006c0021t0056g0199others(20): Show | 23 | HG00597.hp2 HG01099.hp1 HG01261.hp2 others(20): Show |
intron_variant | MODIFIER | c.244-3793T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 135690 | ||||||
| chr5:135692
|
T | A | 22 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(19): Show | 22 | HG00597.hp2 HG01099.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.244-3791T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 135692 | ||||||
| chr5:135694
|
T | A | 22 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(19): Show | 22 | HG00597.hp2 HG01099.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.244-3789T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 135694 | ||||||
| chr5:135696
|
T | A | 24 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(21): Show | 24 | HG00597.hp2 HG01099.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.244-3787T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 135696 | ||||||
| chr5:135698
|
T | A | 19 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(16): Show | 19 | HG00597.hp2 HG01099.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.244-3785T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 135698 | ||||||
| chr5:135700
|
T | A | 11 | a0006c0068t0058g0194a0006c0071t0018g0202a0011c0023t0041g0184others(8): Show | 11 | HG00597.hp2 HG01099.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.244-3783T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 135700 | ||||||
| chr5:135700
|
T | C | 1 | a0038c0080t0043g0177 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.244-3783T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 135700 | ||||||
| chr5:135702
|
T | A | 7 | a0011c0023t0041g0184a0015c0076t0067g0192a0015c0077t0053g0181others(4): Show | 7 | HG00597.hp2 HG02257.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.244-3781T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 135702 | ||||||
| chr5:135702
|
T | C | 2 | a0014c0027t0049g0171a0014c0066t0051g0170 | 2 | HG02809.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.244-3781T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 135702 | ||||||
| chr5:135704
|
T | A | 1 | a0011c0023t0041g0184 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.244-3779T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 135704 | ||||||
| chr5:135714
|
T | A | 1 | a0001c0011t0048g0179 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.244-3769T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 135714 | ||||||
| chr5:135725
|
A | G | 6 | a0008c0025t0045g0172a0019c0019t0010g0164a0019c0019t0062g0191others(3): Show | 6 | HG00280.hp2 HG00323.hp2 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.244-3758A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 135725 | ||||||
| chr5:135729
|
G | A | 5 | a0014c0027t0049g0171a0014c0065t0038g0166a0014c0066t0051g0170others(2): Show | 5 | HG02486.hp2 HG02809.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.244-3754G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 135729 | ||||||
| chr5:135798
|
T | C | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.244-3685T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 135798 | ||||||
| chr5:135973
|
C | G | 6 | a0003c0004t0016g0078a0003c0004t0016g0133a0003c0004t0028g0058others(3): Show | 6 | HG02273.hp1 HG03710.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.244-3510C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 135973 | ||||||
| chr5:135995
|
G | C | 1 | a0001c0002t0082g0126 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.244-3488G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 135995 | ||||||
| chr5:136142
|
T | G | 26 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(23): Show | 26 | HG00597.hp2 HG01261.hp2 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.244-3341T>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 136142 | ||||||
| chr5:136276
|
A | G | 1 | a0036c0075t0061g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.244-3207A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 136276 | ||||||
| chr5:136349
|
A | G | 37 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(34): Show | 37 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.244-3134A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 136349 | ||||||
| chr5:136386
|
T | C | 40 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(37): Show | 40 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.244-3097T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 136386 | ||||||
| chr5:136531
|
C | T | 41 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(38): Show | 41 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.244-2952C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 136531 | ||||||
| chr5:136635
|
T | A | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.244-2848T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 136635 | ||||||
| chr5:136681
|
G | A | 2 | a0003c0009t0119g0049a0003c0017t0074g0050 | 2 | HG01069.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.244-2802G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 136681 | ||||||
| chr5:136794
|
G | A | 3 | a0008c0024t0021g0175a0008c0024t0021g0176a0008c0025t0045g0172 | 3 | HG02109.hp2 HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.244-2689G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 136794 | ||||||
| chr5:136872
|
A | C | 1 | a0014c0065t0038g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.244-2611A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 136872 | ||||||
| chr5:136950
|
A | G | 1 | a0014c0065t0038g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.244-2533A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 136950 | ||||||
| chr5:137051
|
A | G | 1 | a0001c0001t0073g0107 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.244-2432A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 137051 | ||||||
| chr5:137059
|
G | A | 1 | a0001c0061t0001g0006 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.244-2424G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 137059 | ||||||
| chr5:137139
|
C | T | 5 | a0019c0019t0010g0164a0019c0019t0062g0191a0039c0062t0010g0165others(2): Show | 5 | HG00280.hp2 HG00323.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.244-2344C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 137139 | ||||||
| chr5:137401
|
G | A | 24 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(21): Show | 24 | HG00597.hp2 HG01261.hp2 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.244-2082G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 137401 | ||||||
| chr5:137674
|
G | A | 2 | a0001c0015t0035g0122a0001c0015t0076g0154 | 2 | HG02886.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.244-1809G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 137674 | ||||||
| chr5:137802
|
G | A | 1 | a0007c0010t0095g0106 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.244-1681G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 137802 | ||||||
| chr5:138045
|
G | T | 1 | a0032c0058t0040g0158 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.244-1438G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 138045 | ||||||
| chr5:138252
|
T | C | 2 | a0004c0006t0002g0051a0004c0041t0003g0077 | 2 | HG01515.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.244-1231T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 138252 | ||||||
| chr5:138345
|
T | C | 59 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0007t0008g0143others(56): Show | 59 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.244-1138T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 138345 | ||||||
| chr5:138726
|
A | G | 3 | a0001c0001t0001g0082a0012c0013t0009g0016a0012c0013t0009g0019 | 3 | NA18973.hp1 NA18973.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.244-757A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 138726 | ||||||
| chr5:138797
|
G | A | 3 | a0001c0002t0001g0074a0001c0002t0094g0021a0001c0002t0101g0068 | 3 | HG00642.hp1 HG01975.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.244-686G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 138797 | ||||||
| chr5:139134
|
C | A | 11 | a0011c0023t0041g0184a0011c0023t0044g0187a0011c0078t0059g0185others(8): Show | 11 | HG01099.hp1 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.244-349C>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 139134 | ||||||
| chr5:139164
|
T | C | 55 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0007t0008g0143others(52): Show | 55 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.244-319T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 139164 | ||||||
| chr5:139180
|
G | C | 1 | a0001c0001t0005g0123 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.244-303G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 139180 | ||||||
| chr5:139216
|
C | T | 1 | a0001c0002t0013g0109 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.244-267C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 139216 | ||||||
| chr5:139279
|
C | T | 1 | a0022c0046t0047g0180 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.244-204C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 139279 | ||||||
| chr5:139340
|
A | G | 55 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0007t0008g0143others(52): Show | 55 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.244-143A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 139340 | ||||||
| chr5:139347
|
C | T | 2 | a0035c0060t0020g0188a0036c0075t0061g0178 | 2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.244-136C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 139347 | ||||||
| chr5:139425
|
T | C | 50 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0007t0008g0143others(47): Show | 50 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.244-58T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 2/19 | chr5 | 139425 | ||||||
| chr5:140723
|
GC | G | 3 | a0013c0020t0050g0182a0013c0020t0052g0183a0013c0067t0046g0186 | 3 | HG02451.hp1 HG03041.hp1 NA18906.hp2 |
splice_region_variant&intron_variant | LOW | c.1477+8delC | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | chr5 | 140723 | ||||||
| chr5:140734
|
C | T | 1 | a0036c0075t0061g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1477+18C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | chr5 | 140734 | ||||||
| chr5:140879
|
C | CCAACCCA others(161): Show |
1 | a0006c0071t0018g0202 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1477+164_1477+165i others(170): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 140879 | |||||
| chr5:140879
|
C | CCAACCCA others(183): Show |
13 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0070t0054g0207others(10): Show | 13 | HG00597.hp2 HG01261.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1477+164_1477+165i others(192): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 140879 | |||||
| chr5:140921
|
C | CCCCACCC others(184): Show |
1 | a0011c0023t0044g0187 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1477+231_1477+232i others(193): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 140921 | |||||
| chr5:140921
|
C | T | 14 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0070t0054g0207others(11): Show | 14 | HG00597.hp2 HG01261.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1477+205C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | chr5 | 140921 | ||||||
| chr5:140925
|
AC | A | 5 | a0008c0024t0021g0175a0008c0024t0021g0176a0008c0025t0045g0172others(2): Show | 5 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1477+214delC | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 140925 | |||||
| chr5:140945
|
CA | C | 2 | a0001c0002t0006g0134a0001c0011t0106g0085 | 2 | HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1477+230delA | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | chr5 | 140945 | ||||||
| chr5:140947
|
C | CCCCTTCC others(183): Show |
1 | a0011c0023t0041g0184 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1477+231_1477+232i others(192): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | chr5 | 140947 | ||||||
| chr5:140948
|
A | C | 4 | a0001c0002t0006g0134a0001c0011t0106g0085a0011c0023t0041g0184others(1): Show | 4 | HG01099.hp1 HG02622.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1477+232A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | chr5 | 140948 | ||||||
| chr5:140949
|
A | C | 3 | a0001c0002t0006g0134a0001c0011t0106g0085a0011c0078t0059g0185 | 3 | HG01099.hp1 HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1477+233A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | chr5 | 140949 | ||||||
| chr5:140950
|
C | T | 2 | a0001c0002t0006g0134a0001c0011t0106g0085 | 2 | HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1477+234C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | chr5 | 140950 | ||||||
| chr5:140951
|
C | T | 1 | a0011c0078t0059g0185 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1477+235C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | chr5 | 140951 | ||||||
| chr5:140955
|
C | G | 1 | a0011c0078t0059g0185 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1477+239C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | chr5 | 140955 | ||||||
| chr5:140967
|
A | C | 1 | a0011c0078t0059g0185 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1477+251A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | chr5 | 140967 | ||||||
| chr5:140971
|
C | A | 2 | a0001c0002t0006g0134a0001c0011t0106g0085 | 2 | HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1477+255C>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | chr5 | 140971 | ||||||
| chr5:140972
|
T | C | 2 | a0001c0002t0006g0134a0001c0011t0106g0085 | 2 | HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1477+256T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | chr5 | 140972 | ||||||
| chr5:140976
|
G | C | 3 | a0001c0002t0006g0134a0001c0011t0106g0085a0011c0078t0059g0185 | 3 | HG01099.hp1 HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1477+260G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | chr5 | 140976 | ||||||
| chr5:140976
|
G | GCTGCACA others(13): Show |
15 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0070t0054g0207others(12): Show | 15 | HG00597.hp2 HG01261.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1477+269_1477+270i others(22): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 140976 | |||||
| chr5:140983
|
A | ACCAACCC others(14): Show |
1 | a0010c0014t0019g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1477+269_1477+270i others(23): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 140983 | |||||
| chr5:140989
|
G | A | 19 | a0001c0002t0006g0134a0001c0011t0106g0085a0006c0021t0018g0198others(16): Show | 19 | HG00597.hp2 HG01099.hp1 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.1477+273G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | chr5 | 140989 | ||||||
| chr5:140993
|
T | A | 2 | a0001c0002t0006g0134a0001c0011t0106g0085 | 2 | HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1477+277T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | chr5 | 140993 | ||||||
| chr5:140993
|
T | C | 16 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0070t0054g0207others(13): Show | 16 | HG00597.hp2 HG01261.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1477+277T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | chr5 | 140993 | ||||||
| chr5:140996
|
C | A | 1 | a0011c0078t0059g0185 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1477+280C>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | chr5 | 140996 | ||||||
| chr5:141009
|
C | CA | 2 | a0001c0002t0006g0134a0001c0011t0106g0085 | 2 | HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1477+293_1477+294i others(3): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | chr5 | 141009 | ||||||
| chr5:141012
|
C | A | 2 | a0001c0002t0006g0134a0001c0011t0106g0085 | 2 | HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1477+296C>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | chr5 | 141012 | ||||||
| chr5:141015
|
T | A | 16 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0070t0054g0207others(13): Show | 16 | HG00597.hp2 HG01261.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1477+299T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | chr5 | 141015 | ||||||
| chr5:141015
|
T | C | 1 | a0011c0078t0059g0185 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1477+299T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | chr5 | 141015 | ||||||
| chr5:141016
|
CT | C | 2 | a0001c0002t0006g0134a0001c0011t0106g0085 | 2 | HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1477+301delT | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | chr5 | 141016 | ||||||
| chr5:141018
|
A | ACCCTGCA others(225): Show |
2 | a0014c0065t0038g0166a0035c0060t0020g0188 | 2 | HG03098.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1477+315_1477+316i others(234): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141018 | |||||
| chr5:141018
|
A | C | 19 | a0001c0002t0006g0134a0001c0011t0106g0085a0006c0021t0018g0198others(16): Show | 19 | HG00597.hp2 HG01099.hp1 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.1477+302A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | chr5 | 141018 | ||||||
| chr5:141027
|
A | AC | 16 | a0006c0068t0058g0194a0008c0024t0021g0175a0008c0024t0021g0176others(13): Show | 16 | HG00280.hp2 HG00323.hp2 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.1477+315dupC | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141027 | |||||
| chr5:141037
|
C | T | 1 | a0011c0078t0059g0185 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1477+321C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | chr5 | 141037 | ||||||
| chr5:141041
|
C | G | 1 | a0011c0078t0059g0185 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1477+325C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | chr5 | 141041 | ||||||
| chr5:141050
|
CCCA | C | 16 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0070t0054g0207others(13): Show | 16 | HG00597.hp2 HG01261.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1477+336_1477+338d others(5): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141050 | |||||
| chr5:141053
|
A | ACCCCCTC others(200): Show |
1 | a0011c0078t0059g0185 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1477+338_1477+339i others(209): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141053 | |||||
| chr5:141053
|
A | ACCCCTTC others(221): Show |
15 | a0006c0068t0058g0194a0008c0024t0021g0175a0008c0024t0021g0176others(12): Show | 15 | HG00280.hp2 HG00323.hp2 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.1477+338_1477+339i others(230): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141053 | |||||
| chr5:141053
|
A | ACCCCTTC others(221): Show |
2 | a0015c0076t0067g0192a0015c0077t0053g0181 | 2 | HG02257.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1477+338_1477+339i others(230): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141053 | |||||
| chr5:141077
|
A | C | 2 | a0001c0002t0006g0134a0001c0011t0106g0085 | 2 | HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1477+361A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | chr5 | 141077 | ||||||
| chr5:141078
|
A | C | 2 | a0001c0002t0006g0134a0001c0011t0106g0085 | 2 | HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1477+362A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | chr5 | 141078 | ||||||
| chr5:141082
|
C | CCCCTGCA others(424): Show |
2 | a0001c0002t0006g0134a0001c0011t0106g0085 | 2 | HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1477+369_1477+370i others(433): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141082 | |||||
| chr5:141103
|
TC | T | 23 | a0001c0002t0006g0134a0001c0011t0106g0085a0006c0021t0056g0199others(20): Show | 23 | HG00280.hp2 HG01099.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1477+392delC | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141103 | |||||
| chr5:141104
|
C | CCCCCTGC others(761): Show |
1 | a0021c0026t0060g0169 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1477+398_1477+399i others(770): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141104 | |||||
| chr5:141104
|
C | CCCCCTGC others(1004): Show |
1 | a0002c0003t0135g0128 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1477+400_1477+401i others(1013): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141104 | |||||
| chr5:141104
|
C | CCCCCTGC others(725): Show |
1 | a0001c0052t0118g0121 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1477+402_1477+403i others(734): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141104 | |||||
| chr5:141104
|
C | CCCCCTGC others(721): Show |
1 | a0001c0001t0028g0046 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1477+402_1477+403i others(730): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141104 | |||||
| chr5:141104
|
C | CCCCCTGC others(761): Show |
3 | a0014c0027t0049g0171a0014c0066t0051g0170a0038c0080t0043g0177 | 3 | HG02486.hp2 HG02809.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1477+402_1477+403i others(770): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141104 | |||||
| chr5:141104
|
C | CCCCCTGC others(719): Show |
1 | a0004c0043t0126g0099 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1477+402_1477+403i others(728): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141104 | |||||
| chr5:141104
|
C | CCCCCTGC others(727): Show |
1 | a0001c0002t0001g0032 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1477+402_1477+403i others(736): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141104 | |||||
| chr5:141104
|
C | CCCCCTGC others(725): Show |
1 | a0033c0028t0088g0008 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1477+402_1477+403i others(734): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141104 | |||||
| chr5:141104
|
C | CCCCCTGC others(728): Show |
1 | a0026c0050t0009g0141 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1477+402_1477+403i others(737): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141104 | |||||
| chr5:141104
|
C | CCCCCTGC others(725): Show |
1 | a0001c0032t0103g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1477+402_1477+403i others(734): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141104 | |||||
| chr5:141104
|
C | CCCCCTGC others(727): Show |
1 | a0001c0002t0022g0015 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1477+402_1477+403i others(736): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141104 | |||||
| chr5:141104
|
C | CCCCCTGC others(703): Show |
1 | a0012c0013t0009g0019 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1477+402_1477+403i others(712): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141104 | |||||
| chr5:141104
|
C | CCCCCTGC others(725): Show |
1 | a0003c0009t0017g0088 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1477+402_1477+403i others(734): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141104 | |||||
| chr5:141104
|
C | CCCCCTGC others(726): Show |
1 | a0001c0002t0101g0068 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1477+402_1477+403i others(735): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141104 | |||||
| chr5:141104
|
C | CCCCCTGC others(724): Show |
1 | a0029c0033t0042g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1477+402_1477+403i others(733): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141104 | |||||
| chr5:141104
|
C | CCCCCTGC others(918): Show |
1 | a0007c0010t0005g0113 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1477+402_1477+403i others(927): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141104 | |||||
| chr5:141104
|
C | CCCCCTGC others(917): Show |
1 | a0003c0009t0119g0049 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1477+402_1477+403i others(926): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141104 | |||||
| chr5:141104
|
C | CCCCCTGC others(726): Show |
1 | a0002c0005t0129g0043 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1477+402_1477+403i others(735): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141104 | |||||
| chr5:141104
|
C | CCCCCTGC others(698): Show |
1 | a0004c0041t0003g0077 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1477+402_1477+403i others(707): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141104 | |||||
| chr5:141104
|
C | CCCCCTGC others(725): Show |
1 | a0003c0009t0121g0092 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1477+402_1477+403i others(734): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141104 | |||||
| chr5:141104
|
C | CCCCCTGC others(725): Show |
2 | a0001c0001t0092g0054a0004c0006t0065g0208 | 2 | HG01192.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1477+402_1477+403i others(734): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141104 | |||||
| chr5:141104
|
C | CCCCCTGC others(575): Show |
9 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0007t0008g0143others(6): Show | 9 | HG02109.hp1 HG02723.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.1477+402_1477+403i others(584): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141104 | |||||
| chr5:141104
|
C | CCCCCTGC others(726): Show |
1 | a0016c0018t0003g0005 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1477+402_1477+403i others(735): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141104 | |||||
| chr5:141104
|
C | CCCCCTGC others(725): Show |
1 | a0031c0031t0085g0108 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1477+402_1477+403i others(734): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141104 | |||||
| chr5:141104
|
C | CCCCCTGC others(617): Show |
1 | a0002c0005t0003g0096 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1477+402_1477+403i others(626): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141104 | |||||
| chr5:141104
|
C | CCCCCTGC others(725): Show |
1 | a0002c0005t0070g0100 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1477+402_1477+403i others(734): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141104 | |||||
| chr5:141104
|
C | CCCCCTGC others(660): Show |
1 | a0003c0004t0016g0078 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1477+402_1477+403i others(669): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141104 | |||||
| chr5:141104
|
C | CCCCCTGC others(724): Show |
100 | a0001c0001t0001g0142a0001c0001t0004g0020a0001c0001t0005g0090others(97): Show | 100 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(97): Show |
intron_variant | MODIFIER | c.1477+402_1477+403i others(733): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141104 | |||||
| chr5:141104
|
C | CCCCCTGC others(724): Show |
4 | a0001c0001t0012g0069a0001c0002t0012g0066a0002c0005t0127g0124others(1): Show | 4 | HG00733.hp1 HG01074.hp2 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.1477+402_1477+403i others(733): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141104 | |||||
| chr5:141104
|
C | CCCCCTGC others(727): Show |
1 | a0001c0011t0029g0136 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1477+402_1477+403i others(736): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141104 | |||||
| chr5:141104
|
C | CCCCCTGC others(727): Show |
1 | a0017c0030t0039g0140 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1477+402_1477+403i others(736): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141104 | |||||
| chr5:141104
|
C | CCCCCTGC others(702): Show |
2 | a0001c0001t0001g0082a0012c0013t0009g0016 | 2 | NA18973.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.1477+402_1477+403i others(711): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141104 | |||||
| chr5:141104
|
C | CCCCCTGC others(722): Show |
1 | a0004c0006t0125g0048 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1477+402_1477+403i others(731): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141104 | |||||
| chr5:141104
|
C | CCCCCTGC others(577): Show |
1 | a0001c0007t0008g0145 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1477+402_1477+403i others(586): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141104 | |||||
| chr5:141104
|
C | CCCCCTGC others(731): Show |
1 | a0001c0002t0024g0024 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1477+402_1477+403i others(740): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141104 | |||||
| chr5:141104
|
C | CCCCCTGC others(725): Show |
1 | a0002c0057t0003g0026 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1477+402_1477+403i others(734): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141104 | |||||
| chr5:141104
|
C | CCCCCTGC others(725): Show |
1 | a0034c0059t0001g0114 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1477+402_1477+403i others(734): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141104 | |||||
| chr5:141104
|
C | CCCCCTGC others(724): Show |
1 | a0003c0044t0001g0116 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1477+402_1477+403i others(733): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141104 | |||||
| chr5:141104
|
C | CCCCCTGC others(724): Show |
16 | a0001c0001t0001g0084a0001c0001t0001g0159a0001c0001t0006g0075others(13): Show | 16 | HG00438.hp1 HG00438.hp2 HG02080.hp2 others(13): Show |
intron_variant | MODIFIER | c.1477+402_1477+403i others(733): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141104 | |||||
| chr5:141104
|
C | CCCCCTGC others(724): Show |
1 | a0001c0001t0015g0131 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1477+402_1477+403i others(733): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141104 | |||||
| chr5:141104
|
C | CCCCCTGC others(724): Show |
1 | a0004c0006t0002g0119 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1477+396_1477+397i others(733): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141104 | |||||
| chr5:141104
|
C | CCCCTGCA others(727): Show |
1 | a0010c0014t0019g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1477+391_1477+392i others(736): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141104 | |||||
| chr5:141104
|
C | CCCCTGCA others(339): Show |
1 | a0008c0079t0068g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1477+391_1477+392i others(348): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141104 | |||||
| chr5:141104
|
C | CCCCTGCA others(702): Show |
1 | a0004c0006t0134g0011 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1477+391_1477+392i others(711): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141104 | |||||
| chr5:141104
|
C | CCCCTGCA others(726): Show |
6 | a0006c0021t0018g0198a0006c0068t0058g0194a0006c0070t0054g0207others(3): Show | 6 | HG01261.hp2 HG02647.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1477+391_1477+392i others(735): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141104 | |||||
| chr5:141104
|
C | CCCCTGCA others(726): Show |
2 | a0018c0022t0011g0195a0018c0022t0011g0196 | 2 | HG00597.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.1477+391_1477+392i others(735): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141104 | |||||
| chr5:141104
|
C | CCCCTGCA others(727): Show |
1 | a0010c0014t0057g0197 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1477+391_1477+392i others(736): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141104 | |||||
| chr5:141104
|
C | CCCCTGCA others(773): Show |
1 | a0019c0019t0010g0164 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1477+391_1477+392i others(782): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141104 | |||||
| chr5:141104
|
C | CCCCTGCA others(771): Show |
1 | a0041c0064t0010g0190 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1477+391_1477+392i others(780): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141104 | |||||
| chr5:141104
|
C | CCCCTGCA others(772): Show |
1 | a0039c0062t0010g0165 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1477+391_1477+392i others(781): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141104 | |||||
| chr5:141104
|
C | CCCCTGCA others(773): Show |
1 | a0019c0019t0062g0191 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1477+391_1477+392i others(782): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141104 | |||||
| chr5:141130
|
C | CACACACC others(318): Show |
1 | a0036c0075t0061g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1477+414_1477+415i others(327): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | chr5 | 141130 | ||||||
| chr5:141130
|
C | CGCACACC others(273): Show |
1 | a0015c0076t0067g0192 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1477+423_1477+424i others(282): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141130 | |||||
| chr5:141130
|
C | CGCACACC others(319): Show |
1 | a0008c0024t0021g0175 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1477+423_1477+424i others(328): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141130 | |||||
| chr5:141130
|
C | CGCACACC others(272): Show |
1 | a0011c0078t0059g0185 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1477+423_1477+424i others(281): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141130 | |||||
| chr5:141130
|
C | CGCACACC others(312): Show |
1 | a0014c0065t0038g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1477+423_1477+424i others(321): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141130 | |||||
| chr5:141130
|
C | CGCACACC others(316): Show |
1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1477+423_1477+424i others(325): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141130 | |||||
| chr5:141130
|
C | CGCACACC others(318): Show |
3 | a0008c0024t0021g0176a0008c0025t0045g0172a0008c0025t0069g0174 | 3 | HG02145.hp2 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1477+423_1477+424i others(327): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141130 | |||||
| chr5:141130
|
C | CGCACACC others(706): Show |
5 | a0006c0021t0056g0199a0006c0071t0018g0202a0006c0072t0036g0206others(2): Show | 5 | HG02258.hp2 HG02451.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1477+423_1477+424i others(715): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141130 | |||||
| chr5:141130
|
C | CGCACACC others(751): Show |
1 | a0040c0063t0063g0189 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1477+423_1477+424i others(760): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141130 | |||||
| chr5:141130
|
C | CGCACACC others(271): Show |
1 | a0015c0077t0053g0181 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1477+423_1477+424i others(280): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141130 | |||||
| chr5:141130
|
C | CGCACACC others(271): Show |
2 | a0011c0023t0041g0184a0011c0023t0044g0187 | 2 | HG02280.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1477+423_1477+424i others(280): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141130 | |||||
| chr5:141130
|
C | CGCACACC others(270): Show |
3 | a0013c0020t0050g0182a0013c0020t0052g0183a0013c0067t0046g0186 | 3 | HG02451.hp1 HG03041.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1477+423_1477+424i others(279): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141130 | |||||
| chr5:141135
|
AC | A | 4 | a0019c0019t0010g0164a0019c0019t0062g0191a0039c0062t0010g0165others(1): Show | 4 | HG00323.hp2 HG01081.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.1477+424delC | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141135 | |||||
| chr5:141142
|
C | CCCCCCTC others(15): Show |
1 | a0014c0065t0038g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1477+430_1477+431i others(24): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141142 | |||||
| chr5:141142
|
C | CCCCCTCC others(13): Show |
1 | a0040c0063t0063g0189 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1477+435_1477+436i others(22): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141142 | |||||
| chr5:141142
|
C | CCCCCTCC others(14): Show |
18 | a0006c0021t0056g0199a0006c0071t0018g0202a0006c0072t0036g0206others(15): Show | 18 | HG01099.hp1 HG02109.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.1477+435_1477+436i others(23): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141142 | |||||
| chr5:141142
|
C | T | 29 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0007t0008g0143others(26): Show | 29 | HG00323.hp2 HG00597.hp2 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.1477+426C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | chr5 | 141142 | ||||||
| chr5:141144
|
C | CCCTCCCC others(14): Show |
1 | a0036c0075t0061g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1477+435_1477+436i others(23): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141144 | |||||
| chr5:141157
|
A | ACCCCCAC others(79): Show |
1 | a0002c0005t0003g0096 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1477+445_1477+446i others(88): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141157 | |||||
| chr5:141164
|
A | C | 1 | a0002c0005t0003g0096 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1477+448A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | chr5 | 141164 | ||||||
| chr5:141165
|
A | C | 1 | a0002c0005t0003g0096 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1477+449A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | chr5 | 141165 | ||||||
| chr5:141177
|
C | T | 1 | a0026c0050t0009g0141 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1477+461C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | chr5 | 141177 | ||||||
| chr5:141194
|
C | T | 1 | a0014c0065t0038g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1477+478C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | chr5 | 141194 | ||||||
| chr5:141244
|
G | C | 1 | a0036c0075t0061g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1477+528G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | chr5 | 141244 | ||||||
| chr5:141411
|
G | A | 1 | a0021c0026t0060g0169 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1477+695G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | chr5 | 141411 | ||||||
| chr5:141544
|
C | T | 27 | a0001c0001t0005g0090a0001c0001t0005g0123a0001c0001t0007g0056others(24): Show | 27 | HG00140.hp1 HG00280.hp1 HG00597.hp1 others(24): Show |
intron_variant | MODIFIER | c.1477+828C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | chr5 | 141544 | ||||||
| chr5:141560
|
G | A | 5 | a0001c0001t0092g0054a0001c0002t0001g0074a0001c0002t0007g0060others(2): Show | 5 | HG00099.hp1 HG00642.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.1477+844G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | chr5 | 141560 | ||||||
| chr5:141602
|
C | T | 1 | a0002c0005t0003g0167 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1477+886C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | chr5 | 141602 | ||||||
| chr5:141711
|
A | AT | 8 | a0001c0001t0092g0054a0001c0032t0103g0007a0002c0003t0124g0017others(5): Show | 8 | HG00323.hp2 HG01106.hp2 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.1477+1016dupT | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141711 | |||||
| chr5:141711
|
A | ATT | 11 | a0008c0024t0021g0175a0008c0024t0021g0176a0008c0025t0045g0172others(8): Show | 11 | HG00280.hp2 HG01081.hp2 HG02004.hp2 others(8): Show |
intron_variant | MODIFIER | c.1477+1015_1477+101 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141711 | |||||
| chr5:141711
|
A | ATTT | 6 | a0011c0078t0059g0185a0013c0020t0050g0182a0013c0020t0052g0183others(3): Show | 6 | HG01099.hp1 HG02451.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1477+1014_1477+101 others(7): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141711 | |||||
| chr5:141711
|
A | ATTTT | 6 | a0006c0070t0054g0207a0006c0071t0018g0202a0006c0072t0036g0206others(3): Show | 6 | HG01261.hp2 HG02280.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1477+1013_1477+101 others(8): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141711 | |||||
| chr5:141711
|
A | ATTTTT | 7 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(4): Show | 7 | HG02257.hp1 HG02451.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1477+1012_1477+101 others(9): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141711 | |||||
| chr5:141711
|
AT | A | 26 | a0001c0001t0006g0075a0001c0001t0027g0052a0001c0001t0031g0112others(23): Show | 26 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.1477+1016delT | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 141711 | |||||
| chr5:141839
|
G | C | 1 | a0037c0074t0037g0203 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1477+1123G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | chr5 | 141839 | ||||||
| chr5:141848
|
A | G | 40 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(37): Show | 40 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.1477+1132A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | chr5 | 141848 | ||||||
| chr5:141955
|
A | G | 1 | a0001c0001t0028g0046 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1478-1092A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | chr5 | 141955 | ||||||
| chr5:142273
|
G | A | 1 | a0016c0018t0003g0005 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1478-774G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | chr5 | 142273 | ||||||
| chr5:142431
|
C | T | 19 | a0001c0001t0001g0084a0001c0001t0001g0159a0001c0001t0006g0075others(16): Show | 19 | HG00438.hp1 HG00438.hp2 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.1478-616C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | chr5 | 142431 | ||||||
| chr5:142432
|
GCA | G | 8 | a0011c0023t0041g0184a0011c0023t0044g0187a0011c0078t0059g0185others(5): Show | 8 | HG01099.hp1 HG02257.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1478-612_1478-611d others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 142432 | |||||
| chr5:142472
|
C | T | 2 | a0014c0027t0049g0171a0014c0066t0051g0170 | 2 | HG02809.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1478-575C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | chr5 | 142472 | ||||||
| chr5:142483
|
A | T | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1478-564A>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | chr5 | 142483 | ||||||
| chr5:142552
|
CCA | C | 39 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(36): Show | 39 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.1478-486_1478-485d others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 142552 | |||||
| chr5:142572
|
C | G | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1478-475C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | chr5 | 142572 | ||||||
| chr5:142736
|
C | T | 2 | a0001c0036t0077g0149a0001c0051t0078g0148 | 2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1478-311C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | chr5 | 142736 | ||||||
| chr5:142926
|
T | A | 40 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(37): Show | 40 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.1478-121T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | chr5 | 142926 | ||||||
| chr5:143307
|
C | T | 1 | a0022c0046t0047g0180 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1687+51C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 4/19 | chr5 | 143307 | ||||||
| chr5:143375
|
C | T | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | splice_region_variant&intron_variant | LOW | c.1688-5C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 4/19 | chr5 | 143375 | ||||||
| chr5:143528
|
C | G | 1 | a0038c0080t0043g0177 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1811+25C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 5/19 | chr5 | 143528 | ||||||
| chr5:143950
|
AT | A | 40 | a0001c0002t0086g0104a0006c0021t0018g0198a0006c0021t0056g0199others(37): Show | 40 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.1811+458delT | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr5 | 143950 | |||||
| chr5:143970
|
G | T | 4 | a0001c0001t0005g0090a0001c0001t0005g0123a0001c0001t0099g0089others(1): Show | 4 | HG00280.hp1 HG00741.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1811+467G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 5/19 | chr5 | 143970 | ||||||
| chr5:144404
|
T | A | 1 | a0002c0005t0003g0167 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1812-423T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 5/19 | chr5 | 144404 | ||||||
| chr5:144405
|
G | A | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1812-422G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 5/19 | chr5 | 144405 | ||||||
| chr5:144409
|
T | C | 39 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(36): Show | 39 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.1812-418T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 5/19 | chr5 | 144409 | ||||||
| chr5:144532
|
G | A | 1 | a0003c0004t0001g0087 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1812-295G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 5/19 | chr5 | 144532 | ||||||
| chr5:144542
|
G | A | 39 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(36): Show | 39 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.1812-285G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 5/19 | chr5 | 144542 | ||||||
| chr5:144586
|
A | G | 2 | a0011c0023t0041g0184a0011c0078t0059g0185 | 2 | HG01099.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1812-241A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 5/19 | chr5 | 144586 | ||||||
| chr5:144661
|
C | T | 1 | a0022c0046t0047g0180 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1812-166C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 5/19 | chr5 | 144661 | ||||||
| chr5:144671
|
G | A | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1812-156G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 5/19 | chr5 | 144671 | ||||||
| chr5:144716
|
C | A | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1812-111C>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 5/19 | chr5 | 144716 | ||||||
| chr5:144759
|
T | C | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1812-68T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 5/19 | chr5 | 144759 | ||||||
| chr5:145032
|
A | G | 39 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(36): Show | 39 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.1905+112A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 145032 | ||||||
| chr5:145107
|
T | C | 40 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(37): Show | 40 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.1905+187T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 145107 | ||||||
| chr5:145261
|
C | G | 4 | a0014c0027t0049g0171a0014c0066t0051g0170a0021c0026t0060g0169others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1905+341C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 145261 | ||||||
| chr5:145347
|
A | AGGG | 6 | a0006c0068t0058g0194a0008c0024t0021g0175a0008c0024t0021g0176others(3): Show | 6 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1905+429_1905+431d others(5): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr5 | 145347 | |||||
| chr5:145428
|
A | G | 1 | a0007c0010t0080g0117 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1905+508A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 145428 | ||||||
| chr5:145521
|
C | T | 1 | a0002c0005t0129g0043 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1905+601C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 145521 | ||||||
| chr5:145600
|
G | A | 1 | a0001c0001t0007g0056 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1905+680G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 145600 | ||||||
| chr5:145707
|
C | T | 49 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0007t0008g0143others(46): Show | 49 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.1905+787C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 145707 | ||||||
| chr5:145725
|
G | T | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1905+805G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 145725 | ||||||
| chr5:145740
|
G | A | 3 | a0013c0020t0050g0182a0013c0020t0052g0183a0013c0067t0046g0186 | 3 | HG02451.hp1 HG03041.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1905+820G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 145740 | ||||||
| chr5:145779
|
G | A | 8 | a0011c0023t0041g0184a0011c0023t0044g0187a0011c0078t0059g0185others(5): Show | 8 | HG01099.hp1 HG02257.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1905+859G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 145779 | ||||||
| chr5:145836
|
C | T | 38 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(35): Show | 38 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.1905+916C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 145836 | ||||||
| chr5:145848
|
G | C | 1 | a0028c0040t0090g0127 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1905+928G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 145848 | ||||||
| chr5:145862
|
T | C | 6 | a0006c0068t0058g0194a0008c0024t0021g0175a0008c0024t0021g0176others(3): Show | 6 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1905+942T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 145862 | ||||||
| chr5:145874
|
G | A | 44 | a0001c0016t0005g0160a0001c0016t0025g0152a0001c0035t0030g0137others(41): Show | 44 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.1905+954G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 145874 | ||||||
| chr5:145897
|
C | T | 1 | a0004c0006t0065g0208 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1905+977C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 145897 | ||||||
| chr5:146053
|
C | T | 38 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(35): Show | 38 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.1905+1133C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 146053 | ||||||
| chr5:146063
|
A | G | 6 | a0006c0068t0058g0194a0008c0024t0021g0175a0008c0024t0021g0176others(3): Show | 6 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1905+1143A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 146063 | ||||||
| chr5:146087
|
T | C | 38 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(35): Show | 38 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.1905+1167T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 146087 | ||||||
| chr5:146090
|
AGTCCTCC others(45): Show |
A | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1905+1188_1905+123 others(56): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr5 | 146090 | |||||
| chr5:146132
|
C | A | 1 | a0002c0039t0009g0030 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1905+1212C>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 146132 | ||||||
| chr5:146155
|
C | G | 1 | a0014c0065t0038g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1905+1235C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 146155 | ||||||
| chr5:146162
|
A | T | 1 | a0002c0039t0009g0030 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1905+1242A>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 146162 | ||||||
| chr5:146198
|
C | G | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1905+1278C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 146198 | ||||||
| chr5:146359
|
C | A | 1 | a0002c0039t0009g0030 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1905+1439C>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 146359 | ||||||
| chr5:146372
|
G | A | 3 | a0014c0027t0049g0171a0021c0026t0060g0169a0038c0080t0043g0177 | 3 | HG02486.hp2 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1905+1452G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 146372 | ||||||
| chr5:146466
|
C | T | 6 | a0006c0068t0058g0194a0008c0024t0021g0175a0008c0024t0021g0176others(3): Show | 6 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1905+1546C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 146466 | ||||||
| chr5:146550
|
C | T | 3 | a0017c0029t0112g0155a0017c0030t0039g0140a0032c0058t0040g0158 | 3 | HG02622.hp2 HG02809.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1905+1630C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 146550 | ||||||
| chr5:146571
|
G | A | 39 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(36): Show | 39 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.1905+1651G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 146571 | ||||||
| chr5:146757
|
C | G | 38 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(35): Show | 38 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.1905+1837C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 146757 | ||||||
| chr5:146793
|
C | T | 2 | a0015c0076t0067g0192a0015c0077t0053g0181 | 2 | HG02257.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1905+1873C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 146793 | ||||||
| chr5:146812
|
C | T | 1 | a0001c0051t0078g0148 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1905+1892C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 146812 | ||||||
| chr5:146813
|
G | A | 1 | a0014c0065t0038g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1905+1893G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 146813 | ||||||
| chr5:146910
|
C | T | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1905+1990C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 146910 | ||||||
| chr5:146968
|
G | A | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1905+2048G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 146968 | ||||||
| chr5:147139
|
C | T | 1 | a0003c0004t0016g0078 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1905+2219C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 147139 | ||||||
| chr5:147140
|
T | C | 39 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(36): Show | 39 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.1905+2220T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 147140 | ||||||
| chr5:147360
|
C | T | 37 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(34): Show | 37 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.1905+2440C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 147360 | ||||||
| chr5:147489
|
G | A | 3 | a0001c0001t0014g0033a0001c0001t0098g0129a0011c0023t0044g0187 | 3 | HG02080.hp2 HG02280.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1905+2569G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 147489 | ||||||
| chr5:147684
|
C | T | 3 | a0014c0027t0049g0171a0021c0026t0060g0169a0038c0080t0043g0177 | 3 | HG02486.hp2 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1905+2764C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 147684 | ||||||
| chr5:147806
|
A | G | 10 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0007t0008g0143others(7): Show | 10 | HG02109.hp1 HG02723.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.1905+2886A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 147806 | ||||||
| chr5:147883
|
T | C | 1 | a0014c0065t0038g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1905+2963T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 147883 | ||||||
| chr5:148002
|
A | G | 37 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(34): Show | 37 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.1905+3082A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 148002 | ||||||
| chr5:148050
|
C | G | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1905+3130C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 148050 | ||||||
| chr5:148241
|
G | C | 1 | a0007c0010t0080g0117 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1906-3272G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 148241 | ||||||
| chr5:148332
|
C | T | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1906-3181C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 148332 | ||||||
| chr5:148344
|
C | CA | 17 | a0001c0001t0001g0082a0001c0001t0014g0033a0001c0001t0015g0037others(14): Show | 17 | HG00099.hp1 HG00642.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.1906-3156dupA | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr5 | 148344 | |||||
| chr5:148344
|
CA | C | 22 | a0006c0068t0058g0194a0006c0070t0054g0207a0008c0024t0021g0175others(19): Show | 22 | HG00597.hp2 HG01099.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1906-3156delA | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr5 | 148344 | |||||
| chr5:148344
|
CAA | C | 10 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0071t0018g0202others(7): Show | 10 | HG01261.hp2 HG02258.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1906-3157_1906-315 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr5 | 148344 | |||||
| chr5:148349
|
A | T | 1 | a0014c0065t0038g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1906-3164A>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 148349 | ||||||
| chr5:148352
|
A | T | 4 | a0013c0067t0046g0186a0014c0027t0049g0171a0021c0026t0060g0169others(1): Show | 4 | HG02486.hp2 HG02818.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1906-3161A>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 148352 | ||||||
| chr5:148354
|
A | T | 5 | a0019c0019t0010g0164a0019c0019t0062g0191a0039c0062t0010g0165others(2): Show | 5 | HG00280.hp2 HG00323.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.1906-3159A>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 148354 | ||||||
| chr5:148355
|
A | T | 3 | a0003c0004t0084g0041a0003c0009t0017g0093a0014c0065t0038g0166 | 3 | HG01256.hp1 HG01256.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1906-3158A>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 148355 | ||||||
| chr5:148356
|
A | T | 5 | a0001c0001t0028g0046a0002c0003t0066g0209a0002c0003t0124g0017others(2): Show | 5 | HG00099.hp2 HG00639.hp2 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.1906-3157A>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 148356 | ||||||
| chr5:148357
|
A | T | 4 | a0001c0035t0030g0137a0001c0049t0096g0063a0003c0009t0120g0013others(1): Show | 4 | HG01175.hp2 HG02717.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1906-3156A>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 148357 | ||||||
| chr5:148357
|
AT | A | 9 | a0001c0002t0001g0032a0001c0007t0008g0150a0001c0007t0110g0151others(6): Show | 9 | HG02080.hp1 HG02145.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1906-3155delT | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 148357 | ||||||
| chr5:148358
|
T | A | 145 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0142others(142): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.1906-3155T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 148358 | ||||||
| chr5:148362
|
T | A | 23 | a0001c0001t0001g0082a0001c0001t0032g0094a0001c0001t0032g0144others(20): Show | 23 | HG02109.hp1 HG02145.hp1 HG02622.hp2 others(20): Show |
intron_variant | MODIFIER | c.1906-3151T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 148362 | ||||||
| chr5:148363
|
A | T | 1 | a0001c0001t0030g0027 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1906-3150A>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 148363 | ||||||
| chr5:148412
|
A | C | 1 | a0001c0001t0005g0123 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1906-3101A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 148412 | ||||||
| chr5:148580
|
C | T | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1906-2933C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 148580 | ||||||
| chr5:148796
|
G | A | 1 | a0038c0080t0043g0177 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1906-2717G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 148796 | ||||||
| chr5:149079
|
C | T | 3 | a0003c0004t0016g0078a0003c0004t0016g0133a0003c0017t0016g0110 | 3 | NA18979.hp2 NA19066.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1906-2434C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 149079 | ||||||
| chr5:149114
|
G | A | 1 | a0014c0065t0038g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1906-2399G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 149114 | ||||||
| chr5:149136
|
A | G | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1906-2377A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 149136 | ||||||
| chr5:149162
|
A | G | 9 | a0001c0001t0004g0020a0001c0002t0087g0040a0003c0004t0004g0036others(6): Show | 9 | HG00642.hp2 HG01070.hp1 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.1906-2351A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 149162 | ||||||
| chr5:149180
|
T | C | 39 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(36): Show | 39 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.1906-2333T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 149180 | ||||||
| chr5:149211
|
G | A | 39 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(36): Show | 39 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.1906-2302G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 149211 | ||||||
| chr5:149285
|
G | T | 1 | a0004c0054t0034g0139 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1906-2228G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 149285 | ||||||
| chr5:149359
|
A | T | 1 | a0001c0001t0005g0123 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1906-2154A>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 149359 | ||||||
| chr5:149445
|
G | A | 8 | a0011c0023t0041g0184a0011c0023t0044g0187a0011c0078t0059g0185others(5): Show | 8 | HG01099.hp1 HG02257.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1906-2068G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 149445 | ||||||
| chr5:149465
|
C | T | 37 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(34): Show | 37 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.1906-2048C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 149465 | ||||||
| chr5:149509
|
C | T | 1 | a0036c0075t0061g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1906-2004C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 149509 | ||||||
| chr5:149535
|
C | T | 3 | a0014c0027t0049g0171a0021c0026t0060g0169a0038c0080t0043g0177 | 3 | HG02486.hp2 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1906-1978C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 149535 | ||||||
| chr5:149536
|
G | A | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1906-1977G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 149536 | ||||||
| chr5:149553
|
TAAG | T | 38 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(35): Show | 38 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.1906-1955_1906-195 others(7): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr5 | 149553 | |||||
| chr5:149632
|
G | T | 6 | a0006c0068t0058g0194a0008c0024t0021g0175a0008c0024t0021g0176others(3): Show | 6 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1906-1881G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 149632 | ||||||
| chr5:149924
|
A | G | 1 | a0014c0065t0038g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1906-1589A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 149924 | ||||||
| chr5:149982
|
G | A | 5 | a0019c0019t0010g0164a0019c0019t0062g0191a0039c0062t0010g0165others(2): Show | 5 | HG00280.hp2 HG00323.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.1906-1531G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 149982 | ||||||
| chr5:150000
|
A | G | 1 | a0009c0012t0115g0157 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1906-1513A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 150000 | ||||||
| chr5:150065
|
T | C | 1 | a0014c0065t0038g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1906-1448T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 150065 | ||||||
| chr5:150092
|
C | T | 1 | a0033c0028t0088g0008 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1906-1421C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 150092 | ||||||
| chr5:150126
|
A | C | 5 | a0019c0019t0010g0164a0019c0019t0062g0191a0039c0062t0010g0165others(2): Show | 5 | HG00280.hp2 HG00323.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.1906-1387A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 150126 | ||||||
| chr5:150141
|
C | A | 37 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(34): Show | 37 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.1906-1372C>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 150141 | ||||||
| chr5:150283
|
A | G | 3 | a0017c0029t0112g0155a0017c0030t0039g0140a0032c0058t0040g0158 | 3 | HG02622.hp2 HG02809.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1906-1230A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 150283 | ||||||
| chr5:150341
|
T | C | 40 | a0004c0006t0002g0119a0006c0021t0018g0198a0006c0021t0056g0199others(37): Show | 40 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.1906-1172T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 150341 | ||||||
| chr5:150351
|
A | T | 1 | a0001c0001t0102g0057 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1906-1162A>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 150351 | ||||||
| chr5:150378
|
C | T | 2 | a0016c0018t0003g0005a0016c0018t0034g0004 | 2 | HG02145.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1906-1135C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 150378 | ||||||
| chr5:150559
|
A | G | 1 | a0003c0004t0089g0014 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1906-954A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 150559 | ||||||
| chr5:150654
|
G | A | 3 | a0014c0027t0049g0171a0021c0026t0060g0169a0038c0080t0043g0177 | 3 | HG02486.hp2 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1906-859G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 150654 | ||||||
| chr5:150840
|
C | T | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1906-673C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 150840 | ||||||
| chr5:151125
|
C | T | 2 | a0014c0027t0049g0171a0038c0080t0043g0177 | 2 | HG02486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1906-388C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 151125 | ||||||
| chr5:151152
|
C | G | 13 | a0001c0001t0031g0111a0001c0001t0031g0112a0001c0001t0097g0086others(10): Show | 13 | HG00323.hp1 HG01928.hp1 HG01952.hp2 others(10): Show |
intron_variant | MODIFIER | c.1906-361C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 151152 | ||||||
| chr5:151188
|
A | G | 2 | a0014c0065t0038g0166a0035c0060t0020g0188 | 2 | HG03098.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1906-325A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 151188 | ||||||
| chr5:151318
|
C | T | 1 | a0006c0070t0054g0207 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1906-195C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 151318 | ||||||
| chr5:151410
|
G | A | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1906-103G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 151410 | ||||||
| chr5:151432
|
C | T | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1906-81C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 6/19 | chr5 | 151432 | ||||||
| chr5:151606
|
G | A | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | splice_region_variant&intron_variant | LOW | c.1992+7G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 7/19 | chr5 | 151606 | ||||||
| chr5:151986
|
T | C | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1992+387T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 7/19 | chr5 | 151986 | ||||||
| chr5:152094
|
C | T | 39 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(36): Show | 39 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.1992+495C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 7/19 | chr5 | 152094 | ||||||
| chr5:152143
|
C | CT | 39 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(36): Show | 39 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.1992+544_1992+545i others(3): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 7/19 | chr5 | 152143 | ||||||
| chr5:152171
|
C | T | 15 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0070t0054g0207others(12): Show | 15 | HG00597.hp2 HG01261.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1992+572C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 7/19 | chr5 | 152171 | ||||||
| chr5:152175
|
C | A | 39 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(36): Show | 39 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.1992+576C>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 7/19 | chr5 | 152175 | ||||||
| chr5:152205
|
C | CT | 10 | a0001c0001t0032g0144a0001c0002t0022g0015a0001c0011t0048g0179others(7): Show | 10 | HG00741.hp1 HG00741.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1992+621dupT | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr5 | 152205 | |||||
| chr5:152205
|
CT | C | 7 | a0002c0005t0003g0031a0006c0068t0058g0194a0008c0024t0021g0175others(4): Show | 7 | HG00673.hp1 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1992+621delT | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr5 | 152205 | |||||
| chr5:152377
|
CT | C | 39 | a0001c0002t0013g0109a0006c0021t0018g0198a0006c0021t0056g0199others(36): Show | 39 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.1992+793delT | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr5 | 152377 | |||||
| chr5:152403
|
T | G | 39 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(36): Show | 39 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.1992+804T>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 7/19 | chr5 | 152403 | ||||||
| chr5:152431
|
G | A | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1992+832G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 7/19 | chr5 | 152431 | ||||||
| chr5:152500
|
A | C | 1 | a0007c0010t0026g0035 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1992+901A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 7/19 | chr5 | 152500 | ||||||
| chr5:152629
|
C | T | 10 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0007t0008g0143others(7): Show | 10 | HG02109.hp1 HG02723.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.1992+1030C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 7/19 | chr5 | 152629 | ||||||
| chr5:152960
|
C | T | 8 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0007t0008g0143others(5): Show | 8 | HG02109.hp1 HG02723.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1992+1361C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 7/19 | chr5 | 152960 | ||||||
| chr5:153073
|
T | C | 43 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(40): Show | 43 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.1992+1474T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 7/19 | chr5 | 153073 | ||||||
| chr5:153152
|
A | G | 1 | a0001c0001t0102g0057 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1992+1553A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 7/19 | chr5 | 153152 | ||||||
| chr5:153209
|
T | C | 1 | a0022c0046t0047g0180 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1992+1610T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 7/19 | chr5 | 153209 | ||||||
| chr5:153275
|
G | A | 1 | a0011c0023t0044g0187 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1993-1600G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 7/19 | chr5 | 153275 | ||||||
| chr5:153315
|
C | T | 6 | a0006c0068t0058g0194a0008c0024t0021g0175a0008c0024t0021g0176others(3): Show | 6 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1993-1560C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 7/19 | chr5 | 153315 | ||||||
| chr5:153494
|
A | G | 15 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0070t0054g0207others(12): Show | 15 | HG00597.hp2 HG01261.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1993-1381A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 7/19 | chr5 | 153494 | ||||||
| chr5:153572
|
G | C | 40 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(37): Show | 40 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.1993-1303G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 7/19 | chr5 | 153572 | ||||||
| chr5:153622
|
G | A | 40 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(37): Show | 40 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.1993-1253G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 7/19 | chr5 | 153622 | ||||||
| chr5:153742
|
G | A | 39 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(36): Show | 39 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.1993-1133G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 7/19 | chr5 | 153742 | ||||||
| chr5:153774
|
C | T | 1 | a0004c0006t0003g0047 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1993-1101C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 7/19 | chr5 | 153774 | ||||||
| chr5:153801
|
C | A | 2 | a0017c0029t0112g0155a0017c0030t0039g0140 | 2 | HG02622.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1993-1074C>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 7/19 | chr5 | 153801 | ||||||
| chr5:153810
|
C | T | 3 | a0011c0023t0041g0184a0011c0023t0044g0187a0011c0078t0059g0185 | 3 | HG01099.hp1 HG02280.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1993-1065C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 7/19 | chr5 | 153810 | ||||||
| chr5:153844
|
G | A | 10 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0007t0008g0143others(7): Show | 10 | HG02109.hp1 HG02723.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.1993-1031G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 7/19 | chr5 | 153844 | ||||||
| chr5:153983
|
A | G | 40 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(37): Show | 40 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.1993-892A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 7/19 | chr5 | 153983 | ||||||
| chr5:154012
|
A | AT | 37 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(34): Show | 37 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.1993-853dupT | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr5 | 154012 | |||||
| chr5:154036
|
G | A | 1 | a0001c0001t0007g0056 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1993-839G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 7/19 | chr5 | 154036 | ||||||
| chr5:154122
|
C | T | 1 | a0017c0030t0039g0140 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1993-753C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 7/19 | chr5 | 154122 | ||||||
| chr5:154152
|
C | T | 14 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0070t0054g0207others(11): Show | 14 | HG00597.hp2 HG01261.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1993-723C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 7/19 | chr5 | 154152 | ||||||
| chr5:154359
|
A | G | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1993-516A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 7/19 | chr5 | 154359 | ||||||
| chr5:154404
|
C | T | 34 | a0001c0001t0028g0046a0006c0021t0018g0198a0006c0021t0056g0199others(31): Show | 34 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.1993-471C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 7/19 | chr5 | 154404 | ||||||
| chr5:154408
|
C | T | 1 | a0001c0002t0082g0126 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1993-467C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 7/19 | chr5 | 154408 | ||||||
| chr5:154451
|
G | A | 1 | a0004c0043t0126g0099 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1993-424G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 7/19 | chr5 | 154451 | ||||||
| chr5:154451
|
G | GC | 6 | a0006c0068t0058g0194a0008c0024t0021g0175a0008c0024t0021g0176others(3): Show | 6 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1993-423dupC | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr5 | 154451 | |||||
| chr5:154490
|
C | T | 8 | a0011c0023t0041g0184a0011c0023t0044g0187a0011c0078t0059g0185others(5): Show | 8 | HG01099.hp1 HG02257.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1993-385C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 7/19 | chr5 | 154490 | ||||||
| chr5:154535
|
G | A | 2 | a0001c0001t0001g0084a0001c0002t0007g0083 | 2 | NA19012.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.1993-340G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 7/19 | chr5 | 154535 | ||||||
| chr5:154589
|
C | T | 1 | a0030c0047t0131g0067 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1993-286C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 7/19 | chr5 | 154589 | ||||||
| chr5:154621
|
C | CT | 9 | a0001c0052t0118g0121a0003c0009t0121g0092a0006c0068t0058g0194others(6): Show | 9 | HG00741.hp1 HG01928.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1993-234dupT | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr5 | 154621 | |||||
| chr5:154621
|
CT | C | 14 | a0001c0001t0015g0131a0001c0002t0086g0104a0001c0007t0008g0143others(11): Show | 14 | HG01256.hp1 HG02723.hp1 HG02896.hp1 others(11): Show |
intron_variant | MODIFIER | c.1993-234delT | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr5 | 154621 | |||||
| chr5:154621
|
CTTT | C | 22 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0070t0054g0207others(19): Show | 22 | HG01099.hp1 HG01261.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.1993-236_1993-234d others(5): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr5 | 154621 | |||||
| chr5:154621
|
CTTTT | C | 8 | a0014c0066t0051g0170a0015c0077t0053g0181a0019c0019t0010g0164others(5): Show | 8 | HG00280.hp2 HG00323.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.1993-237_1993-234d others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr5 | 154621 | |||||
| chr5:154674
|
G | C | 52 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0007t0008g0143others(49): Show | 52 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.1993-201G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 7/19 | chr5 | 154674 | ||||||
| chr5:155022
|
G | A | 38 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(35): Show | 38 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.2109+31G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 8/19 | chr5 | 155022 | ||||||
| chr5:155040
|
T | A | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2109+49T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 8/19 | chr5 | 155040 | ||||||
| chr5:155146
|
G | A | 1 | a0010c0014t0019g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2109+155G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 8/19 | chr5 | 155146 | ||||||
| chr5:155252
|
C | T | 39 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(36): Show | 39 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.2110-93C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 8/19 | chr5 | 155252 | ||||||
| chr5:155324
|
C | T | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2110-21C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 8/19 | chr5 | 155324 | ||||||
| chr5:155514
|
C | G | 39 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(36): Show | 39 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.2208+71C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 9/19 | chr5 | 155514 | ||||||
| chr5:155516
|
T | C | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2208+73T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 9/19 | chr5 | 155516 | ||||||
| chr5:155556
|
C | T | 40 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(37): Show | 40 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.2208+113C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 9/19 | chr5 | 155556 | ||||||
| chr5:155571
|
T | G | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2208+128T>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 9/19 | chr5 | 155571 | ||||||
| chr5:155700
|
C | T | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2208+257C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 9/19 | chr5 | 155700 | ||||||
| chr5:155716
|
C | T | 39 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(36): Show | 39 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.2208+273C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 9/19 | chr5 | 155716 | ||||||
| chr5:155739
|
G | A | 14 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0070t0054g0207others(11): Show | 14 | HG00597.hp2 HG01261.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.2208+296G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 9/19 | chr5 | 155739 | ||||||
| chr5:155866
|
C | T | 1 | a0004c0006t0002g0119 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2209-205C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 9/19 | chr5 | 155866 | ||||||
| chr5:155956
|
C | T | 1 | a0031c0031t0085g0108 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2209-115C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 9/19 | chr5 | 155956 | ||||||
| chr5:156065
|
G | A | 38 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(35): Show | 38 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(35): Show |
splice_region_variant&intron_variant | LOW | c.2209-6G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 9/19 | chr5 | 156065 | ||||||
| chr5:156271
|
T | C | 1 | a0014c0065t0038g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2348+61T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 10/19 | chr5 | 156271 | ||||||
| chr5:156539
|
A | G | 2 | a0004c0006t0125g0048a0004c0043t0126g0099 | 2 | HG01261.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.2349-234A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 10/19 | chr5 | 156539 | ||||||
| chr5:156562
|
C | T | 1 | a0001c0007t0100g0025 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2349-211C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 10/19 | chr5 | 156562 | ||||||
| chr5:156622
|
C | T | 40 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(37): Show | 40 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.2349-151C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 10/19 | chr5 | 156622 | ||||||
| chr5:157112
|
C | T | 1 | a0006c0068t0058g0194 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2487+201C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/19 | chr5 | 157112 | ||||||
| chr5:157635
|
C | T | 39 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(36): Show | 39 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.2487+724C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/19 | chr5 | 157635 | ||||||
| chr5:157741
|
C | T | 39 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(36): Show | 39 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.2487+830C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/19 | chr5 | 157741 | ||||||
| chr5:157757
|
C | T | 1 | a0017c0029t0112g0155 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2487+846C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/19 | chr5 | 157757 | ||||||
| chr5:157885
|
A | G | 8 | a0011c0023t0041g0184a0011c0023t0044g0187a0011c0078t0059g0185others(5): Show | 8 | HG01099.hp1 HG02257.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.2487+974A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/19 | chr5 | 157885 | ||||||
| chr5:157890
|
C | T | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2487+979C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/19 | chr5 | 157890 | ||||||
| chr5:158006
|
C | T | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2487+1095C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/19 | chr5 | 158006 | ||||||
| chr5:158107
|
T | G | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2487+1196T>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/19 | chr5 | 158107 | ||||||
| chr5:158121
|
A | G | 4 | a0014c0027t0049g0171a0014c0066t0051g0170a0021c0026t0060g0169others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2487+1210A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/19 | chr5 | 158121 | ||||||
| chr5:158192
|
C | T | 1 | a0028c0040t0090g0127 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2487+1281C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/19 | chr5 | 158192 | ||||||
| chr5:158243
|
CCTGCCCA others(33): Show |
C | 1 | a0014c0065t0038g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2487+1404_2487+144 others(44): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr5 | 158243 | |||||
| chr5:158281
|
C | CCTCTGCC others(113): Show |
1 | a0001c0001t0007g0056 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2487+1397_2487+151 others(124): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr5 | 158281 | |||||
| chr5:158302
|
T | A | 1 | a0001c0002t0007g0060 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2487+1391T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/19 | chr5 | 158302 | ||||||
| chr5:158308
|
A | G | 3 | a0008c0024t0021g0175a0008c0024t0021g0176a0008c0025t0045g0172 | 3 | HG02109.hp2 HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.2487+1397A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/19 | chr5 | 158308 | ||||||
| chr5:158315
|
C | G | 39 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(36): Show | 39 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.2487+1404C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/19 | chr5 | 158315 | ||||||
| chr5:158569
|
G | A | 1 | a0014c0065t0038g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2487+1658G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/19 | chr5 | 158569 | ||||||
| chr5:158600
|
C | T | 1 | a0028c0040t0090g0127 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2487+1689C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/19 | chr5 | 158600 | ||||||
| chr5:158611
|
G | A | 1 | a0014c0065t0038g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2487+1700G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/19 | chr5 | 158611 | ||||||
| chr5:158715
|
G | A | 1 | a0001c0002t0081g0034 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2487+1804G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/19 | chr5 | 158715 | ||||||
| chr5:158729
|
G | A | 2 | a0001c0001t0032g0094a0001c0001t0032g0144 | 2 | HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2487+1818G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/19 | chr5 | 158729 | ||||||
| chr5:158745
|
GGGTGTCT others(32): Show |
G | 8 | a0011c0023t0041g0184a0011c0023t0044g0187a0011c0078t0059g0185others(5): Show | 8 | HG01099.hp1 HG02257.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.2487+1837_2487+187 others(43): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr5 | 158745 | |||||
| chr5:158756
|
C | T | 5 | a0019c0019t0010g0164a0019c0019t0062g0191a0039c0062t0010g0165others(2): Show | 5 | HG00280.hp2 HG00323.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.2487+1845C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/19 | chr5 | 158756 | ||||||
| chr5:159012
|
G | A | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2487+2101G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/19 | chr5 | 159012 | ||||||
| chr5:159023
|
C | T | 1 | a0036c0075t0061g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2487+2112C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/19 | chr5 | 159023 | ||||||
| chr5:159024
|
G | A | 2 | a0001c0001t0015g0022a0001c0001t0015g0037 | 2 | HG01099.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.2487+2113G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/19 | chr5 | 159024 | ||||||
| chr5:159024
|
G | T | 3 | a0001c0001t0073g0107a0003c0009t0119g0049a0003c0017t0074g0050 | 3 | HG00738.hp2 HG01069.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.2487+2113G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/19 | chr5 | 159024 | ||||||
| chr5:159089
|
C | T | 6 | a0006c0068t0058g0194a0008c0024t0021g0175a0008c0024t0021g0176others(3): Show | 6 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2487+2178C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/19 | chr5 | 159089 | ||||||
| chr5:159097
|
C | A | 1 | a0001c0001t0028g0046 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2487+2186C>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/19 | chr5 | 159097 | ||||||
| chr5:159205
|
CCAGGTGT others(29): Show |
C | 40 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(37): Show | 40 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.2487+2361_2487+239 others(40): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr5 | 159205 | |||||
| chr5:159252
|
T | A | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2487+2341T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/19 | chr5 | 159252 | ||||||
| chr5:159379
|
C | T | 5 | a0001c0001t0092g0054a0001c0002t0001g0074a0001c0002t0007g0060others(2): Show | 5 | HG00099.hp1 HG00642.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.2488-2404C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/19 | chr5 | 159379 | ||||||
| chr5:159406
|
TC | T | 7 | a0001c0032t0103g0007a0019c0019t0010g0164a0019c0019t0062g0191others(4): Show | 7 | HG00280.hp2 HG00323.hp2 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.2488-2375delC | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr5 | 159406 | |||||
| chr5:159490
|
C | T | 4 | a0014c0027t0049g0171a0014c0066t0051g0170a0021c0026t0060g0169others(1): Show | 4 | HG02486.hp2 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2488-2293C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/19 | chr5 | 159490 | ||||||
| chr5:159571
|
A | G | 41 | a0001c0032t0103g0007a0006c0021t0018g0198a0006c0021t0056g0199others(38): Show | 41 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.2488-2212A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/19 | chr5 | 159571 | ||||||
| chr5:159946
|
C | T | 1 | a0001c0001t0001g0159 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2488-1837C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/19 | chr5 | 159946 | ||||||
| chr5:160051
|
G | A | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2488-1732G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/19 | chr5 | 160051 | ||||||
| chr5:160082
|
G | A | 9 | a0011c0023t0041g0184a0011c0023t0044g0187a0011c0078t0059g0185others(6): Show | 9 | HG01099.hp1 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.2488-1701G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/19 | chr5 | 160082 | ||||||
| chr5:160174
|
C | T | 36 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0007t0008g0143others(33): Show | 36 | HG00597.hp2 HG01261.hp2 HG02109.hp1 others(33): Show |
intron_variant | MODIFIER | c.2488-1609C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/19 | chr5 | 160174 | ||||||
| chr5:160236
|
G | A | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2488-1547G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/19 | chr5 | 160236 | ||||||
| chr5:160335
|
T | C | 1 | a0002c0003t0135g0128 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2488-1448T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/19 | chr5 | 160335 | ||||||
| chr5:160363
|
G | A | 9 | a0011c0023t0041g0184a0011c0023t0044g0187a0011c0078t0059g0185others(6): Show | 9 | HG01099.hp1 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.2488-1420G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/19 | chr5 | 160363 | ||||||
| chr5:160439
|
C | T | 1 | a0001c0001t0097g0086 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2488-1344C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/19 | chr5 | 160439 | ||||||
| chr5:160452
|
G | A | 1 | a0036c0075t0061g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2488-1331G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/19 | chr5 | 160452 | ||||||
| chr5:160482
|
C | T | 4 | a0006c0072t0036g0206a0010c0014t0019g0205a0010c0014t0055g0201others(1): Show | 4 | HG02258.hp2 HG02451.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2488-1301C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/19 | chr5 | 160482 | ||||||
| chr5:160870
|
G | C | 40 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0068t0058g0194others(37): Show | 40 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.2488-913G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/19 | chr5 | 160870 | ||||||
| chr5:160966
|
C | T | 2 | a0014c0027t0049g0171a0014c0066t0051g0170 | 2 | HG02809.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2488-817C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/19 | chr5 | 160966 | ||||||
| chr5:161076
|
G | A | 6 | a0001c0007t0008g0143a0001c0007t0008g0145a0001c0007t0008g0146others(3): Show | 6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2488-707G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/19 | chr5 | 161076 | ||||||
| chr5:161177
|
C | T | 5 | a0019c0019t0010g0164a0019c0019t0062g0191a0039c0062t0010g0165others(2): Show | 5 | HG00280.hp2 HG00323.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.2488-606C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/19 | chr5 | 161177 | ||||||
| chr5:161186
|
G | A | 9 | a0011c0023t0041g0184a0011c0023t0044g0187a0011c0078t0059g0185others(6): Show | 9 | HG01099.hp1 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.2488-597G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/19 | chr5 | 161186 | ||||||
| chr5:161428
|
C | T | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2488-355C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/19 | chr5 | 161428 | ||||||
| chr5:161477
|
C | T | 1 | a0001c0002t0087g0040 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2488-306C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/19 | chr5 | 161477 | ||||||
| chr5:161556
|
A | C | 2 | a0003c0044t0001g0116a0034c0059t0001g0114 | 2 | NA18977.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.2488-227A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/19 | chr5 | 161556 | ||||||
| chr5:161572
|
C | G | 3 | a0013c0020t0050g0182a0013c0020t0052g0183a0013c0067t0046g0186 | 3 | HG02451.hp1 HG03041.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2488-211C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/19 | chr5 | 161572 | ||||||
| chr5:161587
|
A | G | 18 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0070t0054g0207others(15): Show | 18 | HG00597.hp2 HG01261.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.2488-196A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/19 | chr5 | 161587 | ||||||
| chr5:161642
|
C | T | 1 | a0003c0004t0089g0014 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2488-141C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/19 | chr5 | 161642 | ||||||
| chr5:161643
|
G | A | 2 | a0001c0001t0001g0084a0001c0002t0007g0083 | 2 | NA19012.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.2488-140G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/19 | chr5 | 161643 | ||||||
| chr5:161679
|
G | A | 3 | a0015c0076t0067g0192a0015c0077t0053g0181a0035c0060t0020g0188 | 3 | HG02257.hp1 HG02717.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2488-104G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/19 | chr5 | 161679 | ||||||
| chr5:161749
|
G | A | 1 | a0021c0026t0060g0169 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2488-34G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 11/19 | chr5 | 161749 | ||||||
| chr5:162012
|
C | T | 1 | a0003c0004t0001g0087 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2649+68C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 12/19 | chr5 | 162012 | ||||||
| chr5:162078
|
C | G | 1 | a0032c0058t0040g0158 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2649+134C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 12/19 | chr5 | 162078 | ||||||
| chr5:162079
|
CT | C | 37 | a0001c0001t0028g0046a0001c0002t0006g0134a0001c0002t0024g0024others(34): Show | 37 | HG00597.hp2 HG01243.hp2 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.2649+136delT | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 12/19 | chr5 | 162079 | ||||||
| chr5:162211
|
C | G | 7 | a0008c0024t0021g0175a0008c0024t0021g0176a0008c0025t0045g0172others(4): Show | 7 | HG02109.hp2 HG02145.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.2649+267C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 12/19 | chr5 | 162211 | ||||||
| chr5:162246
|
GCAGACTG others(25): Show |
G | 4 | a0008c0024t0021g0175a0008c0024t0021g0176a0008c0025t0045g0172others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2649+308_2649+339d others(34): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr5 | 162246 | |||||
| chr5:162255
|
TCGCCTGC others(25): Show |
T | 82 | a0001c0001t0001g0082a0001c0001t0001g0159a0001c0001t0005g0090others(79): Show | 82 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.2649+327_2649+358d others(34): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr5 | 162255 | |||||
| chr5:162256
|
C | T | 1 | a0026c0050t0009g0141 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2649+312C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 12/19 | chr5 | 162256 | ||||||
| chr5:162262
|
C | T | 2 | a0001c0002t0082g0126a0003c0004t0108g0010 | 2 | NA18947.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.2649+318C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 12/19 | chr5 | 162262 | ||||||
| chr5:162271
|
A | C | 1 | a0006c0071t0018g0202 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2649+327A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 12/19 | chr5 | 162271 | ||||||
| chr5:162271
|
ACGCGCCC others(25): Show |
A | 1 | a0001c0001t0006g0075 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2649+334_2649+365d others(34): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr5 | 162271 | |||||
| chr5:162274
|
C | T | 1 | a0040c0063t0063g0189 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2649+330C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 12/19 | chr5 | 162274 | ||||||
| chr5:162275
|
G | A | 1 | a0001c0001t0113g0044 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2649+331G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 12/19 | chr5 | 162275 | ||||||
| chr5:162304
|
C | T | 1 | a0027c0053t0107g0009 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2649+360C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 12/19 | chr5 | 162304 | ||||||
| chr5:162314
|
A | G | 1 | a0028c0040t0090g0127 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2649+370A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 12/19 | chr5 | 162314 | ||||||
| chr5:162335
|
G | A | 31 | a0001c0001t0079g0059a0001c0001t0091g0120a0001c0002t0001g0074others(28): Show | 31 | HG00280.hp2 HG00642.hp1 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.2650-387G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 12/19 | chr5 | 162335 | ||||||
| chr5:162454
|
C | T | 3 | a0008c0024t0021g0175a0008c0024t0021g0176a0008c0025t0045g0172 | 3 | HG02109.hp2 HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.2650-268C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 12/19 | chr5 | 162454 | ||||||
| chr5:162475
|
C | T | 3 | a0003c0004t0028g0058a0003c0004t0105g0081a0023c0055t0029g0079 | 3 | HG02273.hp1 HG03710.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.2650-247C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 12/19 | chr5 | 162475 | ||||||
| chr5:162497
|
C | T | 1 | a0001c0002t0001g0074 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2650-225C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 12/19 | chr5 | 162497 | ||||||
| chr5:162516
|
G | A | 1 | a0021c0026t0060g0169 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2650-206G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 12/19 | chr5 | 162516 | ||||||
| chr5:162559
|
C | T | 14 | a0001c0002t0022g0138a0001c0002t0094g0021a0003c0004t0089g0014others(11): Show | 14 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.2650-163C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 12/19 | chr5 | 162559 | ||||||
| chr5:162566
|
C | G | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2650-156C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 12/19 | chr5 | 162566 | ||||||
| chr5:162579
|
C | T | 2 | a0002c0003t0132g0028a0004c0006t0134g0011 | 2 | HG01123.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2650-143C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 12/19 | chr5 | 162579 | ||||||
| chr5:162632
|
A | C | 7 | a0001c0001t0079g0059a0001c0001t0092g0054a0001c0007t0100g0025others(4): Show | 7 | HG01192.hp2 HG02257.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.2650-90A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 12/19 | chr5 | 162632 | ||||||
| chr5:162701
|
A | G | 1 | a0015c0077t0053g0181 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2650-21A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 12/19 | chr5 | 162701 | ||||||
| chr5:162717
|
C | T | 1 | a0017c0030t0039g0140 | 1 | HG02622.hp2 | splice_region_variant&intron_variant | LOW | c.2650-5C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 12/19 | chr5 | 162717 | ||||||
| chr5:163589
|
G | C | 1 | a0022c0046t0047g0180 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3476+41G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 163589 | ||||||
| chr5:163636
|
A | C | 1 | a0002c0005t0127g0124 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.3476+88A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 163636 | ||||||
| chr5:163654
|
G | A | 125 | a0001c0001t0004g0020a0001c0001t0005g0123a0001c0001t0012g0069others(122): Show | 125 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.3476+106G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 163654 | ||||||
| chr5:163781
|
C | A | 72 | a0001c0001t0092g0054a0001c0007t0008g0143a0001c0007t0008g0145others(69): Show | 72 | HG00099.hp2 HG00597.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.3476+233C>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 163781 | ||||||
| chr5:163950
|
G | A | 93 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(90): Show | 93 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.3476+402G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 163950 | ||||||
| chr5:163992
|
C | T | 1 | a0020c0081t0064g0200 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3476+444C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 163992 | ||||||
| chr5:164002
|
C | T | 4 | a0011c0023t0041g0184a0011c0023t0044g0187a0015c0076t0067g0192others(1): Show | 4 | HG02257.hp1 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.3476+454C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164002 | ||||||
| chr5:164028
|
C | T | 91 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(88): Show | 91 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.3476+480C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164028 | ||||||
| chr5:164050
|
C | G | 1 | a0008c0079t0068g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3476+502C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164050 | ||||||
| chr5:164078
|
C | T | 44 | a0002c0003t0066g0209a0002c0003t0071g0095a0002c0003t0124g0017others(41): Show | 44 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.3476+530C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164078 | ||||||
| chr5:164185
|
A | C | 79 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(76): Show | 79 | HG00099.hp2 HG00597.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.3476+637A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164185 | ||||||
| chr5:164287
|
T | C | 1 | a0001c0001t0014g0125 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.3476+739T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164287 | ||||||
| chr5:164319
|
C | T | 1 | a0021c0026t0060g0169 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3476+771C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164319 | ||||||
| chr5:164340
|
C | T | 72 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(69): Show | 72 | HG00099.hp2 HG00597.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.3476+792C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164340 | ||||||
| chr5:164435
|
G | T | 1 | a0025c0045t0122g0002 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3476+887G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164435 | ||||||
| chr5:164436
|
C | T | 1 | a0025c0045t0122g0002 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3476+888C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164436 | ||||||
| chr5:164442
|
CAG | C | 3 | a0002c0005t0003g0031a0002c0039t0009g0030a0004c0054t0034g0139 | 3 | HG00673.hp1 HG01928.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.3476+895_3476+896d others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164442 | ||||||
| chr5:164444
|
GGGGGCGG others(145): Show |
G | 2 | a0001c0036t0077g0149a0001c0051t0078g0148 | 2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.3476+899_3476+1050 others(3): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 164444 | |||||
| chr5:164447
|
G | A | 26 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(23): Show | 26 | HG00597.hp2 HG00735.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.3476+899G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164447 | ||||||
| chr5:164450
|
GGGGCTCA others(21): Show |
G | 1 | a0003c0004t0001g0087 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.3476+904_3476+931d others(30): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 164450 | |||||
| chr5:164450
|
GGGGCTCA others(546): Show |
G | 1 | a0019c0019t0010g0164 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.3476+918_3476+1470 others(3): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 164450 | |||||
| chr5:164452
|
G | A | 32 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(29): Show | 32 | HG00597.hp2 HG00735.hp1 HG01261.hp2 others(29): Show |
intron_variant | MODIFIER | c.3476+904G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164452 | ||||||
| chr5:164455
|
T | TCA | 4 | a0008c0024t0021g0175a0008c0024t0021g0176a0008c0025t0045g0172others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.3476+910_3476+911d others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 164455 | |||||
| chr5:164455
|
TCACAGTA others(117): Show |
T | 1 | a0019c0019t0062g0191 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.3476+918_3476+1041 others(3): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 164455 | |||||
| chr5:164457
|
ACAGTAAT others(284): Show |
A | 2 | a0014c0027t0049g0171a0021c0026t0060g0169 | 2 | HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3476+912_3476+1202 others(3): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 164457 | |||||
| chr5:164460
|
GTAATGTT others(173): Show |
G | 1 | a0041c0064t0010g0190 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3476+918_3476+1097 others(3): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 164460 | |||||
| chr5:164460
|
GTAATGTT others(200): Show |
G | 3 | a0003c0009t0120g0013a0039c0062t0010g0165a0040c0063t0063g0189 | 3 | HG00280.hp2 HG01175.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.3476+917_3476+1123 others(3): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 164460 | |||||
| chr5:164465
|
G | C | 6 | a0003c0009t0017g0088a0003c0009t0017g0093a0003c0009t0119g0049others(3): Show | 6 | HG01243.hp1 HG01256.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.3476+917G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164465 | ||||||
| chr5:164466
|
T | C | 81 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(78): Show | 81 | HG00099.hp2 HG00597.hp2 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.3476+918T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164466 | ||||||
| chr5:164466
|
T | TTGTGACG others(175): Show |
3 | a0001c0001t0006g0075a0001c0001t0030g0027a0001c0001t0093g0105 | 3 | HG00438.hp1 HG02165.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.3476+979_3476+980i others(184): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 164466 | |||||
| chr5:164468
|
G | C | 6 | a0003c0009t0017g0088a0003c0009t0017g0093a0003c0009t0119g0049others(3): Show | 6 | HG01243.hp1 HG01256.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.3476+920G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164468 | ||||||
| chr5:164472
|
C | T | 3 | a0013c0020t0050g0182a0013c0020t0052g0183a0013c0067t0046g0186 | 3 | HG02451.hp1 HG03041.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3476+924C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164472 | ||||||
| chr5:164475
|
A | G | 10 | a0003c0009t0017g0088a0003c0009t0017g0093a0003c0009t0119g0049others(7): Show | 10 | HG01243.hp1 HG01256.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.3476+927A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164475 | ||||||
| chr5:164478
|
A | G | 82 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(79): Show | 82 | HG00099.hp2 HG00597.hp2 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.3476+930A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164478 | ||||||
| chr5:164488
|
C | CTAATGCT others(25): Show |
1 | a0014c0065t0038g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3476+948_3476+979d others(34): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 164488 | |||||
| chr5:164493
|
G | GCTCTGAC others(52): Show |
1 | a0020c0081t0064g0200 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3476+952_3476+953i others(61): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 164493 | |||||
| chr5:164493
|
G | GCTCTGAC others(20): Show |
4 | a0006c0021t0018g0198a0006c0021t0056g0199a0017c0029t0112g0155others(1): Show | 4 | HG03041.hp2 HG03195.hp2 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.3476+952_3476+953i others(29): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 164493 | |||||
| chr5:164496
|
C | G | 5 | a0002c0003t0135g0128a0008c0024t0021g0175a0008c0024t0021g0176others(2): Show | 5 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.3476+948C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164496 | ||||||
| chr5:164500
|
CAG | C | 6 | a0003c0009t0017g0088a0003c0009t0017g0093a0003c0009t0119g0049others(3): Show | 6 | HG01243.hp1 HG01256.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.3476+953_3476+954d others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164500 | ||||||
| chr5:164500
|
CAGG | C | 21 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(18): Show | 21 | HG00597.hp2 HG00735.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.3476+953_3476+955d others(5): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164500 | ||||||
| chr5:164510
|
A | G | 6 | a0003c0009t0017g0088a0003c0009t0017g0093a0003c0009t0119g0049others(3): Show | 6 | HG01243.hp1 HG01256.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.3476+962A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164510 | ||||||
| chr5:164518
|
CAG | C | 22 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(19): Show | 22 | HG00597.hp2 HG00735.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.3476+971_3476+972d others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164518 | ||||||
| chr5:164518
|
CAGTAATG others(87): Show |
C | 6 | a0003c0009t0017g0088a0003c0009t0017g0093a0003c0009t0119g0049others(3): Show | 6 | HG01243.hp1 HG01256.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.3476+971_3476+1064 others(97): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164518 | ||||||
| chr5:164525
|
G | A | 21 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(18): Show | 21 | HG00597.hp2 HG00735.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.3476+977G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164525 | ||||||
| chr5:164528
|
G | C | 73 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(70): Show | 73 | HG00099.hp2 HG00597.hp2 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.3476+980G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164528 | ||||||
| chr5:164532
|
CAG | C | 24 | a0001c0001t0012g0069a0001c0001t0024g0135a0001c0002t0012g0066others(21): Show | 24 | HG00140.hp2 HG00642.hp2 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.3476+985_3476+986d others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164532 | ||||||
| chr5:164560
|
C | CTGACGGG others(51): Show |
3 | a0008c0024t0021g0175a0008c0024t0021g0176a0008c0025t0045g0172 | 3 | HG02109.hp2 HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.3476+1016_3476+101 others(62): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 164560 | |||||
| chr5:164560
|
C | G | 1 | a0014c0066t0051g0170 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3476+1012C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164560 | ||||||
| chr5:164564
|
C | CGGGGCGG others(21): Show |
7 | a0002c0057t0003g0026a0004c0006t0002g0119a0004c0006t0134g0011others(4): Show | 7 | HG01081.hp1 HG01261.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.3476+1016_3476+101 others(32): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164564 | ||||||
| chr5:164564
|
CAG | C | 61 | a0001c0001t0028g0046a0001c0001t0032g0094a0001c0001t0032g0144others(58): Show | 61 | HG00099.hp2 HG00597.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.3476+1017_3476+101 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164564 | ||||||
| chr5:164566
|
G | C | 7 | a0002c0057t0003g0026a0004c0006t0002g0119a0004c0006t0134g0011others(4): Show | 7 | HG01081.hp1 HG01261.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.3476+1018G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164566 | ||||||
| chr5:164588
|
T | C | 4 | a0001c0001t0091g0120a0001c0061t0001g0006a0014c0065t0038g0166others(1): Show | 4 | HG02273.hp2 HG02486.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.3476+1040T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164588 | ||||||
| chr5:164589
|
G | C | 1 | a0019c0019t0062g0191 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.3476+1041G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164589 | ||||||
| chr5:164589
|
GCTGTGAC others(162): Show |
G | 1 | a0014c0066t0051g0170 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3476+1044_3476+121 others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 164589 | |||||
| chr5:164592
|
G | C | 64 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(61): Show | 64 | HG00099.hp2 HG00597.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.3476+1044G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164592 | ||||||
| chr5:164596
|
C | CAG | 13 | a0002c0057t0003g0026a0004c0006t0002g0119a0004c0006t0134g0011others(10): Show | 13 | HG01081.hp1 HG01261.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.3476+1048_3476+104 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164596 | ||||||
| chr5:164599
|
A | G | 64 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(61): Show | 64 | HG00099.hp2 HG00597.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.3476+1051A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164599 | ||||||
| chr5:164607
|
T | TCA | 59 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(56): Show | 59 | HG00099.hp2 HG00597.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.3476+1062_3476+106 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 164607 | |||||
| chr5:164607
|
T | TCACACAG others(25): Show |
3 | a0002c0003t0135g0128a0022c0046t0047g0180a0024c0042t0006g0012 | 3 | HG02735.hp2 HG02818.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.3476+1063_3476+106 others(36): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 164607 | |||||
| chr5:164612
|
G | C | 2 | a0015c0077t0053g0181a0019c0019t0062g0191 | 2 | HG02004.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.3476+1064G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164612 | ||||||
| chr5:164620
|
G | C | 11 | a0003c0009t0017g0088a0003c0009t0017g0093a0003c0009t0119g0049others(8): Show | 11 | HG01243.hp1 HG01256.hp1 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.3476+1072G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164620 | ||||||
| chr5:164624
|
C | CAG | 58 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(55): Show | 58 | HG00099.hp2 HG00597.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.3476+1076_3476+107 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164624 | ||||||
| chr5:164627
|
A | AGCGGAGC others(246): Show |
1 | a0029c0033t0042g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3476+1123_3476+112 others(257): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 164627 | |||||
| chr5:164627
|
A | G | 14 | a0002c0003t0002g0098a0002c0003t0002g0101a0003c0009t0017g0088others(11): Show | 14 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.3476+1079A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164627 | ||||||
| chr5:164630
|
G | A | 13 | a0002c0003t0128g0029a0002c0057t0003g0026a0004c0006t0002g0119others(10): Show | 13 | HG00639.hp2 HG01081.hp1 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.3476+1082G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164630 | ||||||
| chr5:164632
|
A | G | 10 | a0002c0003t0002g0098a0002c0003t0002g0101a0003c0009t0017g0088others(7): Show | 10 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.3476+1084A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164632 | ||||||
| chr5:164635
|
T | TTA | 2 | a0002c0003t0002g0098a0002c0003t0002g0101 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.3476+1087_3476+108 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164635 | ||||||
| chr5:164640
|
C | CAG | 4 | a0008c0024t0021g0175a0008c0024t0021g0176a0008c0025t0045g0172others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.3476+1092_3476+109 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164640 | ||||||
| chr5:164640
|
C | G | 65 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(62): Show | 65 | HG00099.hp2 HG00597.hp2 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.3476+1092C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164640 | ||||||
| chr5:164644
|
T | C | 6 | a0003c0009t0017g0088a0003c0009t0017g0093a0003c0009t0119g0049others(3): Show | 6 | HG01243.hp1 HG01256.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.3476+1096T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164644 | ||||||
| chr5:164645
|
G | C | 1 | a0041c0064t0010g0190 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3476+1097G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164645 | ||||||
| chr5:164648
|
C | G | 57 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(54): Show | 57 | HG00099.hp2 HG00597.hp2 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.3476+1100C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164648 | ||||||
| chr5:164652
|
C | CG | 14 | a0003c0009t0017g0088a0003c0009t0017g0093a0003c0009t0119g0049others(11): Show | 14 | HG01243.hp1 HG01256.hp1 HG01515.hp1 others(11): Show |
intron_variant | MODIFIER | c.3476+1107dupG | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 164652 | |||||
| chr5:164654
|
G | GA | 60 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(57): Show | 60 | HG00099.hp2 HG00597.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.3476+1106_3476+110 others(5): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164654 | ||||||
| chr5:164657
|
G | A | 58 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(55): Show | 58 | HG00099.hp2 HG00597.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.3476+1109G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164657 | ||||||
| chr5:164659
|
A | G | 8 | a0003c0009t0017g0088a0003c0009t0017g0093a0003c0009t0119g0049others(5): Show | 8 | HG01243.hp1 HG01256.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.3476+1111A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164659 | ||||||
| chr5:164667
|
C | G | 40 | a0002c0003t0002g0098a0002c0003t0002g0101a0002c0003t0002g0132others(37): Show | 40 | HG00099.hp2 HG00639.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.3476+1119C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164667 | ||||||
| chr5:164671
|
T | C | 1 | a0019c0019t0062g0191 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.3476+1123T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164671 | ||||||
| chr5:164672
|
A | C | 9 | a0003c0009t0017g0088a0003c0009t0017g0093a0003c0009t0119g0049others(6): Show | 9 | HG00280.hp2 HG01175.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.3476+1124A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164672 | ||||||
| chr5:164672
|
A | G | 76 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(73): Show | 76 | HG00099.hp2 HG00597.hp2 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.3476+1124A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164672 | ||||||
| chr5:164675
|
C | G | 4 | a0008c0024t0021g0175a0008c0024t0021g0176a0008c0025t0045g0172others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.3476+1127C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164675 | ||||||
| chr5:164679
|
CAG | C | 14 | a0003c0004t0116g0103a0003c0004t0117g0070a0003c0009t0017g0088others(11): Show | 14 | HG00280.hp2 HG01081.hp2 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.3476+1132_3476+113 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164679 | ||||||
| chr5:164679
|
CAGG | C | 59 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(56): Show | 59 | HG00099.hp2 HG00597.hp2 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.3476+1132_3476+113 others(7): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164679 | ||||||
| chr5:164680
|
A | G | 1 | a0008c0079t0068g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3476+1132A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164680 | ||||||
| chr5:164681
|
G | T | 1 | a0015c0077t0053g0181 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3476+1133G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164681 | ||||||
| chr5:164681
|
GGGGGCGG others(21): Show |
G | 9 | a0002c0003t0128g0029a0002c0057t0003g0026a0004c0006t0002g0119others(6): Show | 9 | HG00639.hp2 HG01081.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.3476+1154_3476+118 others(32): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 164681 | |||||
| chr5:164682
|
G | GGCGGGGC others(46): Show |
1 | a0008c0079t0068g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3476+1135_3476+113 others(57): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 164682 | |||||
| chr5:164682
|
G | T | 1 | a0002c0003t0130g0130 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3476+1134G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164682 | ||||||
| chr5:164684
|
G | A | 1 | a0030c0047t0131g0067 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3476+1136G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164684 | ||||||
| chr5:164689
|
A | G | 3 | a0011c0023t0041g0184a0019c0019t0062g0191a0041c0064t0010g0190 | 3 | HG01081.hp2 HG02004.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.3476+1141A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164689 | ||||||
| chr5:164697
|
C | CAG | 3 | a0008c0024t0021g0175a0008c0024t0021g0176a0008c0025t0045g0172 | 3 | HG02109.hp2 HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.3476+1149_3476+115 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164697 | ||||||
| chr5:164697
|
C | CTAATACT others(331): Show |
2 | a0006c0021t0018g0198a0006c0021t0056g0199 | 2 | HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.3476+1153_3476+115 others(342): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 164697 | |||||
| chr5:164697
|
C | G | 2 | a0019c0019t0062g0191a0030c0047t0131g0067 | 2 | HG02004.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.3476+1149C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164697 | ||||||
| chr5:164702
|
G | A | 29 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(26): Show | 29 | HG00597.hp2 HG00735.hp1 HG01261.hp2 others(26): Show |
intron_variant | MODIFIER | c.3476+1154G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164702 | ||||||
| chr5:164702
|
G | C | 1 | a0019c0019t0062g0191 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.3476+1154G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164702 | ||||||
| chr5:164705
|
C | G | 1 | a0030c0047t0131g0067 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3476+1157C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164705 | ||||||
| chr5:164709
|
C | CAG | 54 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(51): Show | 54 | HG00099.hp2 HG00597.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.3476+1161_3476+116 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164709 | ||||||
| chr5:164709
|
C | CGGGGTGG others(138): Show |
1 | a0015c0077t0053g0181 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3476+1165_3476+116 others(149): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 164709 | |||||
| chr5:164712
|
G | A | 1 | a0030c0047t0131g0067 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3476+1164G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164712 | ||||||
| chr5:164715
|
G | A | 2 | a0019c0019t0062g0191a0030c0047t0131g0067 | 2 | HG02004.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.3476+1167G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164715 | ||||||
| chr5:164717
|
A | G | 15 | a0003c0009t0017g0088a0003c0009t0017g0093a0003c0009t0119g0049others(12): Show | 15 | HG00280.hp2 HG01081.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.3476+1169A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164717 | ||||||
| chr5:164725
|
C | CAG | 2 | a0008c0024t0021g0175a0008c0025t0045g0172 | 2 | HG02109.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.3476+1177_3476+117 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164725 | ||||||
| chr5:164725
|
C | CAGTAATG others(115): Show |
1 | a0008c0024t0021g0176 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3476+1177_3476+117 others(126): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164725 | ||||||
| chr5:164725
|
C | G | 6 | a0006c0021t0018g0198a0006c0021t0056g0199a0006c0071t0018g0202others(3): Show | 6 | HG02622.hp1 HG02922.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.3476+1177C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164725 | ||||||
| chr5:164729
|
T | C | 1 | a0041c0064t0010g0190 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3476+1181T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164729 | ||||||
| chr5:164730
|
A | C | 1 | a0020c0081t0064g0200 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3476+1182A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164730 | ||||||
| chr5:164730
|
A | G | 19 | a0003c0009t0017g0088a0003c0009t0017g0093a0003c0009t0119g0049others(16): Show | 19 | HG00280.hp2 HG01081.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.3476+1182A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164730 | ||||||
| chr5:164733
|
C | G | 2 | a0008c0024t0021g0175a0008c0025t0045g0172 | 2 | HG02109.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.3476+1185C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164733 | ||||||
| chr5:164737
|
C | T | 1 | a0011c0023t0041g0184 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3476+1189C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164737 | ||||||
| chr5:164745
|
G | A | 4 | a0008c0024t0021g0175a0008c0025t0045g0172a0020c0081t0064g0200others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.3476+1197G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164745 | ||||||
| chr5:164748
|
T | TCACACAG others(145): Show |
1 | a0008c0025t0045g0172 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3476+1204_3476+120 others(156): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 164748 | |||||
| chr5:164748
|
T | TCACACAG others(235): Show |
1 | a0008c0024t0021g0175 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3476+1204_3476+120 others(246): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 164748 | |||||
| chr5:164750
|
A | T | 2 | a0001c0001t0001g0082a0001c0001t0001g0159 | 2 | NA18947.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.3476+1202A>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164750 | ||||||
| chr5:164753
|
G | C | 10 | a0003c0009t0120g0013a0006c0021t0018g0198a0006c0021t0056g0199others(7): Show | 10 | HG00280.hp2 HG01175.hp2 HG02004.hp2 others(7): Show |
intron_variant | MODIFIER | c.3476+1205G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164753 | ||||||
| chr5:164757
|
T | C | 3 | a0003c0009t0120g0013a0039c0062t0010g0165a0040c0063t0063g0189 | 3 | HG00280.hp2 HG01175.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.3476+1209T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164757 | ||||||
| chr5:164758
|
C | G | 15 | a0003c0009t0120g0013a0006c0021t0018g0198a0006c0021t0056g0199others(12): Show | 15 | HG00280.hp2 HG01175.hp2 HG02004.hp2 others(12): Show |
intron_variant | MODIFIER | c.3476+1210C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164758 | ||||||
| chr5:164761
|
C | G | 3 | a0008c0024t0021g0176a0014c0027t0049g0171a0021c0026t0060g0169 | 3 | HG02145.hp2 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3476+1213C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164761 | ||||||
| chr5:164765
|
C | CAG | 2 | a0008c0024t0021g0176a0030c0047t0131g0067 | 2 | HG02145.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.3476+1217_3476+121 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164765 | ||||||
| chr5:164771
|
G | A | 1 | a0041c0064t0010g0190 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3476+1223G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164771 | ||||||
| chr5:164773
|
A | AGCTCACA others(621): Show |
4 | a0001c0001t0012g0069a0001c0002t0012g0066a0001c0002t0012g0072others(1): Show | 4 | HG00733.hp2 HG01074.hp2 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.3476+1349_3476+135 others(632): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 164773 | |||||
| chr5:164773
|
A | G | 5 | a0003c0009t0120g0013a0011c0023t0041g0184a0019c0019t0062g0191others(2): Show | 5 | HG00280.hp2 HG01175.hp2 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.3476+1225A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164773 | ||||||
| chr5:164781
|
C | CAG | 4 | a0008c0024t0021g0175a0008c0024t0021g0176a0008c0025t0045g0172others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.3476+1233_3476+123 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164781 | ||||||
| chr5:164781
|
C | G | 4 | a0003c0009t0120g0013a0019c0019t0062g0191a0039c0062t0010g0165others(1): Show | 4 | HG00280.hp2 HG01175.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.3476+1233C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164781 | ||||||
| chr5:164786
|
G | A | 1 | a0030c0047t0131g0067 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3476+1238G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164786 | ||||||
| chr5:164786
|
G | C | 4 | a0003c0009t0120g0013a0019c0019t0062g0191a0039c0062t0010g0165others(1): Show | 4 | HG00280.hp2 HG01175.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.3476+1238G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164786 | ||||||
| chr5:164789
|
C | G | 7 | a0008c0024t0021g0175a0008c0024t0021g0176a0008c0025t0045g0172others(4): Show | 7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.3476+1241C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164789 | ||||||
| chr5:164793
|
C | CAG | 2 | a0014c0027t0049g0171a0021c0026t0060g0169 | 2 | HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3476+1245_3476+124 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164793 | ||||||
| chr5:164793
|
C | T | 1 | a0011c0023t0041g0184 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3476+1245C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164793 | ||||||
| chr5:164796
|
G | A | 1 | a0020c0081t0064g0200 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3476+1248G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164796 | ||||||
| chr5:164796
|
GGCGGAGC others(23): Show |
G | 1 | a0041c0064t0010g0190 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3476+1262_3476+129 others(34): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 164796 | |||||
| chr5:164799
|
G | A | 1 | a0040c0063t0063g0189 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.3476+1251G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164799 | ||||||
| chr5:164801
|
A | G | 1 | a0030c0047t0131g0067 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3476+1253A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164801 | ||||||
| chr5:164801
|
AGCTCACA others(645): Show |
A | 1 | a0001c0007t0008g0150 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3476+1262_3476+191 others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 164801 | |||||
| chr5:164804
|
TCA | T | 8 | a0003c0009t0120g0013a0006c0071t0018g0202a0011c0023t0041g0184others(5): Show | 8 | HG00280.hp2 HG01175.hp2 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.3476+1262_3476+126 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 164804 | |||||
| chr5:164809
|
CACTAATG others(83): Show |
C | 6 | a0003c0009t0017g0088a0003c0009t0017g0093a0003c0009t0119g0049others(3): Show | 6 | HG01243.hp1 HG01256.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.3476+1262_3476+135 others(94): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164809 | ||||||
| chr5:164811
|
C | G | 7 | a0008c0024t0021g0175a0008c0024t0021g0176a0008c0025t0045g0172others(4): Show | 7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.3476+1263C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164811 | ||||||
| chr5:164816
|
G | C | 1 | a0030c0047t0131g0067 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3476+1268G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164816 | ||||||
| chr5:164819
|
G | C | 13 | a0003c0009t0120g0013a0006c0071t0018g0202a0008c0024t0021g0175others(10): Show | 13 | HG00280.hp2 HG01175.hp2 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.3476+1271G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164819 | ||||||
| chr5:164823
|
C | T | 2 | a0014c0066t0051g0170a0020c0081t0064g0200 | 2 | HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3476+1275C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164823 | ||||||
| chr5:164826
|
A | G | 14 | a0003c0009t0120g0013a0006c0071t0018g0202a0008c0024t0021g0175others(11): Show | 14 | HG00280.hp2 HG01175.hp2 HG02004.hp2 others(11): Show |
intron_variant | MODIFIER | c.3476+1278A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164826 | ||||||
| chr5:164831
|
A | G | 8 | a0003c0009t0120g0013a0006c0071t0018g0202a0008c0024t0021g0176others(5): Show | 8 | HG00280.hp2 HG01081.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.3476+1283A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164831 | ||||||
| chr5:164839
|
C | G | 1 | a0020c0081t0064g0200 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3476+1291C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164839 | ||||||
| chr5:164847
|
G | C | 7 | a0003c0009t0120g0013a0019c0019t0062g0191a0020c0081t0064g0200others(4): Show | 7 | HG00280.hp2 HG01081.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.3476+1299G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164847 | ||||||
| chr5:164851
|
C | CGGGGCGG others(271): Show |
1 | a0006c0021t0018g0198 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3476+1303_3476+130 others(282): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164851 | ||||||
| chr5:164851
|
CAG | C | 32 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(29): Show | 32 | HG00597.hp2 HG00639.hp2 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.3476+1304_3476+130 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164851 | ||||||
| chr5:164851
|
CAGGGGGC others(503): Show |
C | 2 | a0040c0063t0063g0189a0041c0064t0010g0190 | 2 | HG00280.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.3476+1304_3476+181 others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164851 | ||||||
| chr5:164853
|
G | C | 1 | a0006c0021t0018g0198 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3476+1305G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164853 | ||||||
| chr5:164853
|
G | T | 1 | a0019c0019t0062g0191 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.3476+1305G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164853 | ||||||
| chr5:164856
|
G | A | 1 | a0036c0075t0061g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3476+1308G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164856 | ||||||
| chr5:164857
|
G | T | 1 | a0006c0071t0018g0202 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3476+1309G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164857 | ||||||
| chr5:164861
|
G | A | 10 | a0006c0071t0018g0202a0008c0024t0021g0175a0008c0024t0021g0176others(7): Show | 10 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.3476+1313G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164861 | ||||||
| chr5:164864
|
T | TCA | 7 | a0008c0024t0021g0175a0008c0024t0021g0176a0008c0025t0045g0172others(4): Show | 7 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.3476+1319_3476+132 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 164864 | |||||
| chr5:164866
|
ACAGTAAT others(135): Show |
A | 1 | a0006c0071t0018g0202 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3476+1321_3476+146 others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 164866 | |||||
| chr5:164869
|
G | C | 3 | a0019c0019t0062g0191a0020c0081t0064g0200a0030c0047t0131g0067 | 3 | HG02004.hp2 HG03486.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.3476+1321G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164869 | ||||||
| chr5:164869
|
GTAATGCT others(81): Show |
G | 4 | a0002c0005t0129g0043a0004c0006t0002g0065a0004c0006t0002g0119others(1): Show | 4 | HG00140.hp2 HG00738.hp1 HG01081.hp1 others(1): Show |
intron_variant | MODIFIER | c.3476+1350_3476+143 others(92): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 164869 | |||||
| chr5:164874
|
G | C | 2 | a0003c0009t0120g0013a0039c0062t0010g0165 | 2 | HG01175.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.3476+1326G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164874 | ||||||
| chr5:164877
|
C | G | 2 | a0030c0047t0131g0067a0036c0075t0061g0178 | 2 | HG03225.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.3476+1329C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164877 | ||||||
| chr5:164881
|
C | T | 1 | a0001c0001t0028g0046 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3476+1333C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164881 | ||||||
| chr5:164882
|
GGGGCGGA others(137): Show |
G | 4 | a0002c0003t0002g0101a0003c0009t0120g0013a0004c0006t0123g0003others(1): Show | 4 | HG01071.hp1 HG01175.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.3476+1350_3476+149 others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 164882 | |||||
| chr5:164884
|
G | A | 2 | a0030c0047t0131g0067a0036c0075t0061g0178 | 2 | HG03225.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.3476+1336G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164884 | ||||||
| chr5:164885
|
G | GCGGAGCT others(163): Show |
3 | a0010c0014t0019g0205a0010c0014t0055g0201a0010c0069t0019g0204 | 3 | HG02258.hp2 HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.3476+1349_3476+135 others(174): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 164885 | |||||
| chr5:164886
|
C | T | 3 | a0002c0003t0002g0098a0002c0003t0002g0132a0002c0003t0011g0210 | 3 | HG00735.hp2 HG01069.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.3476+1338C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164886 | ||||||
| chr5:164887
|
G | A | 1 | a0036c0075t0061g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3476+1339G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164887 | ||||||
| chr5:164889
|
A | G | 3 | a0002c0005t0127g0124a0006c0021t0018g0198a0011c0023t0041g0184 | 3 | HG00733.hp1 HG02622.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.3476+1341A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164889 | ||||||
| chr5:164891
|
C | G | 1 | a0001c0061t0001g0006 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3476+1343C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164891 | ||||||
| chr5:164892
|
TCACACAG others(53): Show |
T | 4 | a0002c0003t0002g0132a0002c0039t0009g0030a0018c0022t0011g0195others(1): Show | 4 | HG00735.hp2 HG01928.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.3476+1350_3476+140 others(64): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 164892 | |||||
| chr5:164894
|
A | ACACTAAT others(19): Show |
9 | a0006c0070t0054g0207a0006c0073t0020g0193a0010c0014t0057g0197others(6): Show | 9 | HG01261.hp2 HG02451.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.3476+1349_3476+135 others(30): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 164894 | |||||
| chr5:164894
|
A | ACACTAAT others(299): Show |
1 | a0004c0041t0003g0077 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3476+1349_3476+135 others(310): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 164894 | |||||
| chr5:164894
|
A | ACACTAAT others(47): Show |
7 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0007t0008g0143others(4): Show | 7 | HG02109.hp1 HG02723.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.3476+1349_3476+135 others(58): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 164894 | |||||
| chr5:164894
|
A | ACACTAAT others(75): Show |
1 | a0001c0001t0113g0044 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.3476+1349_3476+135 others(86): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 164894 | |||||
| chr5:164894
|
A | ACACTAAT others(131): Show |
2 | a0018c0022t0011g0196a0037c0074t0037g0203 | 2 | HG00597.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.3476+1349_3476+135 others(142): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 164894 | |||||
| chr5:164894
|
A | ACACTAAT others(47): Show |
1 | a0011c0023t0044g0187 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3476+1349_3476+135 others(58): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 164894 | |||||
| chr5:164894
|
A | ACACTAAT others(159): Show |
1 | a0015c0076t0067g0192 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3476+1349_3476+135 others(170): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 164894 | |||||
| chr5:164894
|
A | ACACTAAT others(301): Show |
2 | a0006c0068t0058g0194a0008c0025t0069g0174 | 2 | HG02647.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3476+1349_3476+135 others(312): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 164894 | |||||
| chr5:164894
|
A | ACACTAAT others(187): Show |
1 | a0006c0021t0056g0199 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3476+1349_3476+135 others(198): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 164894 | |||||
| chr5:164897
|
CAG | C | 35 | a0002c0003t0066g0209a0002c0003t0071g0095a0002c0003t0124g0017others(32): Show | 35 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.3476+1350_3476+135 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164897 | ||||||
| chr5:164897
|
CAGTAATG others(109): Show |
C | 2 | a0002c0003t0002g0098a0002c0003t0011g0210 | 2 | HG01069.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.3476+1350_3476+146 others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164897 | ||||||
| chr5:164899
|
G | C | 12 | a0001c0001t0113g0044a0004c0041t0003g0077a0006c0021t0056g0199others(9): Show | 12 | HG00597.hp2 HG00735.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.3476+1351G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164899 | ||||||
| chr5:164907
|
G | C | 64 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(61): Show | 64 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.3476+1359G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164907 | ||||||
| chr5:164907
|
G | GTGACGGG others(257): Show |
1 | a0008c0024t0021g0176 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3476+1379_3476+138 others(268): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 164907 | |||||
| chr5:164911
|
C | CAG | 3 | a0018c0022t0011g0196a0030c0047t0131g0067a0037c0074t0037g0203 | 3 | HG00597.hp2 NA18522.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.3476+1363_3476+136 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164911 | ||||||
| chr5:164911
|
C | T | 6 | a0003c0009t0017g0088a0003c0009t0017g0093a0003c0009t0119g0049others(3): Show | 6 | HG01243.hp1 HG01256.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.3476+1363C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164911 | ||||||
| chr5:164915
|
G | T | 2 | a0018c0022t0011g0196a0037c0074t0037g0203 | 2 | HG00597.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.3476+1367G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164915 | ||||||
| chr5:164916
|
C | T | 1 | a0001c0001t0006g0075 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.3476+1368C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164916 | ||||||
| chr5:164917
|
G | A | 6 | a0006c0070t0054g0207a0006c0073t0020g0193a0010c0014t0057g0197others(3): Show | 6 | HG01261.hp2 HG02451.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.3476+1369G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164917 | ||||||
| chr5:164919
|
A | G | 43 | a0001c0001t0113g0044a0002c0003t0066g0209a0002c0003t0071g0095others(40): Show | 43 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.3476+1371A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164919 | ||||||
| chr5:164922
|
TCACACTA others(23): Show |
T | 1 | a0001c0001t0030g0027 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.3476+1387_3476+141 others(34): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 164922 | |||||
| chr5:164924
|
ACACTAAT others(77): Show |
A | 3 | a0014c0027t0049g0171a0014c0066t0051g0170a0021c0026t0060g0169 | 3 | HG02809.hp1 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3476+1380_3476+146 others(88): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 164924 | |||||
| chr5:164927
|
C | CAG | 4 | a0008c0024t0021g0175a0008c0025t0045g0172a0018c0022t0011g0196others(1): Show | 4 | HG00597.hp2 HG02109.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.3476+1379_3476+138 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164927 | ||||||
| chr5:164927
|
C | G | 11 | a0006c0070t0054g0207a0006c0073t0020g0193a0008c0079t0068g0173others(8): Show | 11 | HG01261.hp2 HG02451.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.3476+1379C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164927 | ||||||
| chr5:164932
|
G | A | 1 | a0036c0075t0061g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3476+1384G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164932 | ||||||
| chr5:164935
|
G | C | 66 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(63): Show | 66 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.3476+1387G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164935 | ||||||
| chr5:164939
|
C | CAG | 3 | a0004c0041t0003g0077a0008c0024t0021g0175a0008c0025t0045g0172 | 3 | HG02109.hp2 HG02486.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.3476+1391_3476+139 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164939 | ||||||
| chr5:164939
|
C | T | 4 | a0010c0014t0019g0205a0010c0014t0055g0201a0010c0069t0019g0204others(1): Show | 4 | HG02258.hp2 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.3476+1391C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164939 | ||||||
| chr5:164939
|
CGGGGCGG others(191): Show |
C | 1 | a0036c0075t0061g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3476+1392_3476+158 others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164939 | ||||||
| chr5:164945
|
G | A | 1 | a0017c0029t0112g0155 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3476+1397G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164945 | ||||||
| chr5:164947
|
G | A | 62 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0007t0008g0143others(59): Show | 62 | HG00099.hp2 HG00597.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.3476+1399G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164947 | ||||||
| chr5:164950
|
TTA | T | 63 | a0001c0001t0113g0044a0002c0003t0066g0209a0002c0003t0071g0095others(60): Show | 63 | HG00099.hp2 HG00597.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.3476+1403_3476+140 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164950 | ||||||
| chr5:164951
|
T | C | 9 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0007t0008g0143others(6): Show | 9 | HG02109.hp1 HG02109.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.3476+1403T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164951 | ||||||
| chr5:164952
|
A | ACACACTA others(217): Show |
1 | a0027c0053t0107g0009 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3476+1556_3476+155 others(228): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 164952 | |||||
| chr5:164952
|
A | ACACACTA others(251): Show |
1 | a0003c0004t0108g0010 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.3476+1500_3476+150 others(262): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 164952 | |||||
| chr5:164952
|
A | ACACTAAT others(19): Show |
1 | a0020c0081t0064g0200 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3476+1407_3476+140 others(30): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 164952 | |||||
| chr5:164952
|
A | ACAGTAAT others(355): Show |
1 | a0008c0024t0021g0175 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3476+1406_3476+140 others(366): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 164952 | |||||
| chr5:164952
|
A | ACAGTAAT others(19): Show |
7 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0007t0008g0143others(4): Show | 7 | HG02109.hp1 HG02723.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.3476+1406_3476+140 others(30): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 164952 | |||||
| chr5:164957
|
C | G | 6 | a0001c0001t0113g0044a0004c0041t0003g0077a0006c0068t0058g0194others(3): Show | 6 | HG00735.hp1 HG02486.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.3476+1409C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164957 | ||||||
| chr5:164961
|
T | C | 1 | a0008c0024t0021g0176 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3476+1413T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164961 | ||||||
| chr5:164962
|
G | C | 4 | a0001c0001t0113g0044a0006c0068t0058g0194a0008c0025t0045g0172others(1): Show | 4 | HG00735.hp1 HG02486.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.3476+1414G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164962 | ||||||
| chr5:164969
|
C | T | 3 | a0002c0003t0002g0132a0018c0022t0011g0196a0037c0074t0037g0203 | 3 | HG00597.hp2 HG00735.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.3476+1421C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164969 | ||||||
| chr5:164974
|
C | T | 2 | a0002c0005t0129g0043a0004c0041t0003g0077 | 2 | HG00140.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.3476+1426C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164974 | ||||||
| chr5:164977
|
A | C | 3 | a0004c0006t0003g0047a0012c0013t0133g0118a0016c0018t0034g0004 | 3 | HG02602.hp2 HG03579.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.3476+1429A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164977 | ||||||
| chr5:164977
|
A | G | 29 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(26): Show | 29 | HG00597.hp2 HG00735.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.3476+1429A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164977 | ||||||
| chr5:164985
|
C | G | 2 | a0018c0022t0011g0195a0020c0081t0064g0200 | 2 | HG03486.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.3476+1437C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164985 | ||||||
| chr5:164993
|
C | G | 3 | a0004c0006t0003g0047a0012c0013t0133g0118a0016c0018t0034g0004 | 3 | HG02602.hp2 HG03579.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.3476+1445C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164993 | ||||||
| chr5:164997
|
C | T | 1 | a0001c0001t0079g0059 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3476+1449C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 164997 | ||||||
| chr5:165003
|
A | G | 79 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(76): Show | 79 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.3476+1455A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165003 | ||||||
| chr5:165005
|
G | A | 10 | a0002c0003t0002g0132a0002c0039t0009g0030a0006c0021t0018g0198others(7): Show | 10 | HG00735.hp2 HG01928.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.3476+1457G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165005 | ||||||
| chr5:165005
|
G | C | 27 | a0002c0003t0066g0209a0002c0003t0071g0095a0002c0003t0124g0017others(24): Show | 27 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.3476+1457G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165005 | ||||||
| chr5:165008
|
T | TCACACTA others(25): Show |
1 | a0015c0076t0067g0192 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3476+1464_3476+146 others(36): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165008 | |||||
| chr5:165013
|
G | C | 47 | a0002c0003t0002g0132a0002c0003t0066g0209a0002c0003t0071g0095others(44): Show | 47 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.3476+1465G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165013 | ||||||
| chr5:165018
|
G | C | 23 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(20): Show | 23 | HG00323.hp2 HG00597.hp2 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.3476+1470G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165018 | ||||||
| chr5:165021
|
C | G | 37 | a0002c0003t0002g0132a0002c0003t0066g0209a0002c0003t0071g0095others(34): Show | 37 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.3476+1473C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165021 | ||||||
| chr5:165025
|
C | T | 16 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(13): Show | 16 | HG00597.hp2 HG00735.hp1 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.3476+1477C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165025 | ||||||
| chr5:165026
|
A | G | 80 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(77): Show | 80 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.3476+1478A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165026 | ||||||
| chr5:165029
|
G | GGT | 7 | a0006c0070t0054g0207a0006c0073t0020g0193a0008c0079t0068g0173others(4): Show | 7 | HG01261.hp2 HG02451.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.3476+1481_3476+148 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165029 | ||||||
| chr5:165030
|
C | T | 14 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(11): Show | 14 | HG00597.hp2 HG00735.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.3476+1482C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165030 | ||||||
| chr5:165031
|
G | A | 1 | a0006c0071t0018g0202 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3476+1483G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165031 | ||||||
| chr5:165033
|
A | G | 35 | a0002c0003t0002g0132a0002c0003t0066g0209a0002c0003t0071g0095others(32): Show | 35 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.3476+1485A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165033 | ||||||
| chr5:165041
|
C | CAG | 8 | a0006c0070t0054g0207a0006c0073t0020g0193a0008c0079t0068g0173others(5): Show | 8 | HG01261.hp2 HG02451.hp1 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.3476+1493_3476+149 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165041 | ||||||
| chr5:165041
|
C | G | 26 | a0002c0003t0002g0132a0002c0003t0066g0209a0002c0003t0071g0095others(23): Show | 26 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.3476+1493C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165041 | ||||||
| chr5:165045
|
T | C | 2 | a0008c0024t0021g0176a0008c0025t0045g0172 | 2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.3476+1497T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165045 | ||||||
| chr5:165049
|
C | G | 10 | a0006c0070t0054g0207a0006c0073t0020g0193a0008c0079t0068g0173others(7): Show | 10 | HG01261.hp2 HG02451.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.3476+1501C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165049 | ||||||
| chr5:165053
|
C | CAG | 3 | a0014c0027t0049g0171a0021c0026t0060g0169a0024c0042t0006g0012 | 3 | HG02735.hp2 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3476+1505_3476+150 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165053 | ||||||
| chr5:165053
|
C | T | 8 | a0002c0003t0002g0101a0004c0006t0123g0003a0006c0068t0058g0194others(5): Show | 8 | HG01071.hp1 HG02647.hp1 HG03579.hp1 others(5): Show |
intron_variant | MODIFIER | c.3476+1505C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165053 | ||||||
| chr5:165057
|
G | A | 1 | a0029c0033t0042g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3476+1509G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165057 | ||||||
| chr5:165058
|
C | T | 1 | a0002c0003t0002g0132 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.3476+1510C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165058 | ||||||
| chr5:165061
|
A | C | 2 | a0002c0039t0009g0030a0030c0047t0131g0067 | 2 | HG01928.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.3476+1513A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165061 | ||||||
| chr5:165061
|
A | G | 5 | a0006c0071t0018g0202a0011c0023t0041g0184a0011c0023t0044g0187others(2): Show | 5 | HG00323.hp2 HG02280.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.3476+1513A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165061 | ||||||
| chr5:165069
|
C | CAG | 3 | a0014c0027t0049g0171a0021c0026t0060g0169a0024c0042t0006g0012 | 3 | HG02735.hp2 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3476+1521_3476+152 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165069 | ||||||
| chr5:165069
|
C | G | 1 | a0011c0023t0041g0184 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3476+1521C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165069 | ||||||
| chr5:165073
|
T | TGCTGTGA others(301): Show |
1 | a0008c0025t0045g0172 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3476+1528_3476+152 others(312): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165073 | |||||
| chr5:165077
|
C | G | 4 | a0002c0003t0002g0098a0002c0003t0011g0210a0002c0039t0009g0030others(1): Show | 4 | HG01069.hp1 HG01074.hp1 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.3476+1529C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165077 | ||||||
| chr5:165081
|
C | CAG | 3 | a0002c0003t0002g0098a0002c0003t0011g0210a0014c0066t0051g0170 | 3 | HG01069.hp1 HG01074.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.3476+1533_3476+153 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165081 | ||||||
| chr5:165081
|
C | T | 35 | a0002c0003t0066g0209a0002c0003t0071g0095a0002c0003t0124g0017others(32): Show | 35 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.3476+1533C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165081 | ||||||
| chr5:165089
|
G | A | 36 | a0002c0003t0002g0101a0002c0003t0066g0209a0002c0003t0071g0095others(33): Show | 36 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.3476+1541G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165089 | ||||||
| chr5:165089
|
G | C | 3 | a0002c0057t0003g0026a0004c0006t0002g0119a0016c0018t0034g0004 | 3 | HG01081.hp1 HG03579.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.3476+1541G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165089 | ||||||
| chr5:165092
|
TCACACTA others(23): Show |
T | 2 | a0002c0003t0002g0098a0002c0003t0011g0210 | 2 | HG01069.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.3476+1549_3476+157 others(34): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165092 | |||||
| chr5:165097
|
C | CAG | 4 | a0014c0027t0049g0171a0014c0066t0051g0170a0021c0026t0060g0169others(1): Show | 4 | HG02735.hp2 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.3476+1549_3476+155 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165097 | ||||||
| chr5:165097
|
C | G | 5 | a0002c0003t0002g0132a0002c0039t0009g0030a0006c0071t0018g0202others(2): Show | 5 | HG00735.hp2 HG01928.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.3476+1549C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165097 | ||||||
| chr5:165100
|
A | C | 1 | a0006c0071t0018g0202 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3476+1552A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165100 | ||||||
| chr5:165101
|
T | C | 3 | a0008c0024t0021g0176a0017c0029t0112g0155a0019c0019t0010g0164 | 3 | HG00323.hp2 HG02145.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.3476+1553T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165101 | ||||||
| chr5:165102
|
G | C | 2 | a0006c0071t0018g0202a0029c0033t0042g0163 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3476+1554G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165102 | ||||||
| chr5:165103
|
C | A | 1 | a0014c0066t0051g0170 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3476+1555C>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165103 | ||||||
| chr5:165105
|
G | C | 63 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0079g0059others(60): Show | 63 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.3476+1557G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165105 | ||||||
| chr5:165109
|
C | CAG | 8 | a0002c0003t0002g0101a0002c0005t0129g0043a0004c0041t0003g0077others(5): Show | 8 | HG00140.hp2 HG01071.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.3476+1561_3476+156 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165109 | ||||||
| chr5:165109
|
C | T | 1 | a0011c0023t0041g0184 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3476+1561C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165109 | ||||||
| chr5:165109
|
CGGGGCGG others(187): Show |
C | 1 | a0004c0006t0123g0003 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3476+1562_3476+175 others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165109 | ||||||
| chr5:165113
|
G | GCGGGGCT others(221): Show |
1 | a0008c0025t0069g0174 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3476+1568_3476+156 others(232): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165113 | |||||
| chr5:165113
|
G | GT | 14 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(11): Show | 14 | HG00597.hp2 HG00735.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.3476+1565_3476+156 others(5): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165113 | ||||||
| chr5:165113
|
G | T | 7 | a0002c0005t0129g0043a0004c0041t0003g0077a0006c0021t0018g0198others(4): Show | 7 | HG00140.hp2 HG02257.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.3476+1565G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165113 | ||||||
| chr5:165117
|
A | G | 17 | a0001c0001t0079g0059a0002c0003t0002g0101a0002c0057t0003g0026others(14): Show | 17 | HG00323.hp2 HG01071.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.3476+1569A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165117 | ||||||
| chr5:165119
|
C | T | 1 | a0014c0066t0051g0170 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3476+1571C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165119 | ||||||
| chr5:165120
|
TCA | T | 7 | a0002c0003t0002g0101a0002c0057t0003g0026a0004c0006t0002g0119others(4): Show | 7 | HG00323.hp2 HG01071.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.3476+1577_3476+157 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165120 | |||||
| chr5:165122
|
A | ACACTAAT others(73): Show |
1 | a0008c0079t0068g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3476+1577_3476+157 others(84): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165122 | |||||
| chr5:165122
|
A | ACACTAAT others(215): Show |
1 | a0001c0001t0079g0059 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3476+1577_3476+157 others(226): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165122 | |||||
| chr5:165122
|
A | ACACTAAT others(19): Show |
1 | a0016c0018t0034g0004 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3476+1577_3476+157 others(30): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165122 | |||||
| chr5:165122
|
A | ACAGTAAT others(19): Show |
1 | a0006c0070t0054g0207 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.3476+1576_3476+157 others(30): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165122 | |||||
| chr5:165122
|
A | ACAGTAAT others(19): Show |
4 | a0006c0073t0020g0193a0013c0020t0050g0182a0013c0020t0052g0183others(1): Show | 4 | HG01261.hp2 HG02451.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.3476+1576_3476+157 others(30): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165122 | |||||
| chr5:165124
|
A | C | 1 | a0014c0066t0051g0170 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3476+1576A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165124 | ||||||
| chr5:165125
|
CAG | C | 46 | a0002c0003t0002g0132a0002c0003t0066g0209a0002c0003t0071g0095others(43): Show | 46 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.3476+1578_3476+157 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165125 | ||||||
| chr5:165127
|
G | C | 9 | a0001c0001t0079g0059a0006c0070t0054g0207a0006c0073t0020g0193others(6): Show | 9 | HG01261.hp2 HG02451.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.3476+1579G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165127 | ||||||
| chr5:165132
|
G | C | 2 | a0010c0014t0057g0197a0019c0019t0010g0164 | 2 | HG00323.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.3476+1584G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165132 | ||||||
| chr5:165132
|
GCTGTGAC others(49): Show |
G | 1 | a0006c0071t0018g0202 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3476+1587_3476+164 others(60): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165132 | |||||
| chr5:165135
|
G | C | 31 | a0001c0001t0079g0059a0002c0003t0002g0098a0002c0003t0002g0101others(28): Show | 31 | HG00323.hp2 HG00735.hp2 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.3476+1587G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165135 | ||||||
| chr5:165135
|
G | GTGACGGG others(77): Show |
7 | a0001c0001t0031g0111a0001c0001t0102g0057a0001c0032t0103g0007others(4): Show | 7 | HG01952.hp2 HG02132.hp2 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.3476+1637_3476+163 others(88): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165135 | |||||
| chr5:165135
|
GTGACGGG others(49): Show |
G | 1 | a0002c0005t0129g0043 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.3476+1627_3476+168 others(60): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165135 | |||||
| chr5:165139
|
C | CGGGGCAG others(21): Show |
1 | a0004c0041t0003g0077 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3476+1596_3476+159 others(32): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165139 | |||||
| chr5:165139
|
C | G | 1 | a0036c0075t0061g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3476+1591C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165139 | ||||||
| chr5:165139
|
C | T | 3 | a0002c0039t0009g0030a0010c0014t0057g0197a0030c0047t0131g0067 | 3 | HG01928.hp2 NA18747.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.3476+1591C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165139 | ||||||
| chr5:165139
|
CGGGGCGG others(103): Show |
C | 1 | a0014c0066t0051g0170 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3476+1592_3476+170 others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165139 | ||||||
| chr5:165139
|
CGGGGCGG others(157): Show |
C | 2 | a0002c0005t0002g0064a0002c0005t0003g0096 | 2 | NA18954.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.3476+1592_3476+175 others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165139 | ||||||
| chr5:165142
|
G | A | 1 | a0024c0042t0006g0012 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3476+1594G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165142 | ||||||
| chr5:165144
|
C | T | 4 | a0002c0003t0002g0098a0002c0003t0002g0101a0002c0003t0011g0210others(1): Show | 4 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.3476+1596C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165144 | ||||||
| chr5:165147
|
A | AGCTCACA others(23): Show |
1 | a0006c0072t0036g0206 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.3476+1607_3476+160 others(34): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165147 | |||||
| chr5:165147
|
A | AGCTCACA others(105): Show |
1 | a0008c0024t0021g0175 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3476+1626_3476+162 others(116): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165147 | |||||
| chr5:165147
|
A | AGCTCACA others(439): Show |
3 | a0003c0004t0016g0078a0003c0004t0016g0133a0003c0017t0016g0110 | 3 | NA18979.hp2 NA19066.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.3476+1637_3476+163 others(450): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165147 | |||||
| chr5:165147
|
A | AGCTCACA others(21): Show |
1 | a0015c0076t0067g0192 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3476+1618_3476+161 others(32): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165147 | |||||
| chr5:165147
|
A | G | 32 | a0002c0003t0066g0209a0002c0003t0071g0095a0002c0003t0124g0017others(29): Show | 32 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.3476+1599A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165147 | ||||||
| chr5:165152
|
ACACTAAT others(19): Show |
A | 4 | a0003c0009t0017g0088a0003c0009t0017g0093a0003c0009t0119g0049others(1): Show | 4 | HG01243.hp1 HG01256.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.3476+1608_3476+163 others(30): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165152 | |||||
| chr5:165152
|
ACACTAAT others(47): Show |
A | 2 | a0014c0027t0049g0171a0021c0026t0060g0169 | 2 | HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3476+1608_3476+166 others(58): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165152 | |||||
| chr5:165152
|
ACACTAAT others(325): Show |
A | 1 | a0019c0019t0062g0191 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.3476+1608_3476+193 others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165152 | |||||
| chr5:165155
|
C | G | 26 | a0002c0003t0066g0209a0002c0003t0071g0095a0002c0003t0124g0017others(23): Show | 26 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.3476+1607C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165155 | ||||||
| chr5:165159
|
T | C | 1 | a0008c0024t0021g0176 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3476+1611T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165159 | ||||||
| chr5:165159
|
T | TGCTGTGA others(77): Show |
1 | a0008c0025t0045g0172 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3476+1614_3476+161 others(88): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165159 | |||||
| chr5:165160
|
G | A | 1 | a0036c0075t0061g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3476+1612G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165160 | ||||||
| chr5:165160
|
G | GCTGTGAC others(74): Show |
1 | a0003c0056t0017g0080 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3476+1614_3476+161 others(85): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165160 | |||||
| chr5:165160
|
GCTCTGAC others(21): Show |
G | 1 | a0004c0006t0002g0119 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3476+1627_3476+165 others(32): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165160 | |||||
| chr5:165160
|
GCTCTGAC others(159): Show |
G | 2 | a0002c0039t0009g0030a0030c0047t0131g0067 | 2 | HG01928.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.3476+1627_3476+179 others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165160 | |||||
| chr5:165163
|
C | G | 3 | a0011c0023t0041g0184a0016c0018t0034g0004a0024c0042t0006g0012 | 3 | HG02622.hp1 HG02735.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.3476+1615C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165163 | ||||||
| chr5:165167
|
C | T | 17 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(14): Show | 17 | HG00597.hp2 HG00735.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.3476+1619C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165167 | ||||||
| chr5:165170
|
G | A | 1 | a0024c0042t0006g0012 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3476+1622G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165170 | ||||||
| chr5:165172
|
C | T | 1 | a0004c0041t0003g0077 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3476+1624C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165172 | ||||||
| chr5:165173
|
G | A | 1 | a0024c0042t0006g0012 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3476+1625G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165173 | ||||||
| chr5:165175
|
G | A | 34 | a0002c0003t0066g0209a0002c0003t0071g0095a0002c0003t0124g0017others(31): Show | 34 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.3476+1627G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165175 | ||||||
| chr5:165178
|
T | TCACACTA others(136): Show |
1 | a0018c0022t0011g0195 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.3476+1634_3476+163 others(147): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165178 | |||||
| chr5:165178
|
T | TCACACTA others(25): Show |
1 | a0015c0077t0053g0181 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3476+1634_3476+163 others(36): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165178 | |||||
| chr5:165183
|
G | C | 57 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(54): Show | 57 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.3476+1635G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165183 | ||||||
| chr5:165183
|
GTACTCCT others(75): Show |
G | 1 | a0017c0029t0112g0155 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3476+1638_3476+171 others(86): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165183 | |||||
| chr5:165186
|
C | A | 85 | a0001c0001t0006g0075a0001c0001t0031g0112a0001c0001t0032g0094others(82): Show | 85 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.3476+1638C>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165186 | ||||||
| chr5:165187
|
T | C | 2 | a0001c0001t0032g0094a0001c0001t0032g0144 | 2 | HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3476+1639T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165187 | ||||||
| chr5:165188
|
C | CCTCTGAT others(105): Show |
2 | a0010c0014t0055g0201a0010c0069t0019g0204 | 2 | HG02258.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.3476+1646_3476+164 others(116): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165188 | |||||
| chr5:165188
|
C | G | 68 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(65): Show | 68 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.3476+1640C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165188 | ||||||
| chr5:165191
|
C | G | 7 | a0002c0003t0002g0132a0003c0009t0017g0088a0003c0009t0017g0093others(4): Show | 7 | HG00735.hp2 HG01243.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.3476+1643C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165191 | ||||||
| chr5:165195
|
C | T | 29 | a0002c0003t0066g0209a0002c0003t0071g0095a0002c0003t0124g0017others(26): Show | 29 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.3476+1647C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165195 | ||||||
| chr5:165199
|
G | GCGGGGCT others(106): Show |
1 | a0006c0021t0018g0198 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3476+1654_3476+165 others(117): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165199 | |||||
| chr5:165199
|
G | GT | 5 | a0006c0070t0054g0207a0006c0073t0020g0193a0013c0020t0050g0182others(2): Show | 5 | HG01261.hp2 HG02451.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.3476+1651_3476+165 others(5): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165199 | ||||||
| chr5:165199
|
G | T | 1 | a0002c0003t0002g0132 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.3476+1651G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165199 | ||||||
| chr5:165200
|
C | CGGCGCTC others(21): Show |
1 | a0004c0041t0003g0077 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3476+1654_3476+165 others(32): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165200 | |||||
| chr5:165200
|
C | T | 1 | a0010c0014t0019g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3476+1652C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165200 | ||||||
| chr5:165201
|
G | A | 1 | a0002c0005t0129g0043 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.3476+1653G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165201 | ||||||
| chr5:165203
|
A | AGCTCACA others(21): Show |
1 | a0008c0024t0021g0175 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3476+1682_3476+168 others(32): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165203 | |||||
| chr5:165203
|
A | G | 23 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(20): Show | 23 | HG00323.hp2 HG00597.hp2 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.3476+1655A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165203 | ||||||
| chr5:165211
|
C | CAG | 7 | a0002c0003t0002g0132a0006c0021t0018g0198a0006c0070t0054g0207others(4): Show | 7 | HG00735.hp2 HG01261.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.3476+1663_3476+166 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165211 | ||||||
| chr5:165211
|
C | CTAATGCT others(25): Show |
1 | a0011c0023t0044g0187 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3476+1670_3476+167 others(36): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165211 | |||||
| chr5:165211
|
C | G | 3 | a0003c0056t0017g0080a0019c0019t0010g0164a0035c0060t0020g0188 | 3 | HG00323.hp2 HG02683.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.3476+1663C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165211 | ||||||
| chr5:165214
|
A | C | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3476+1666A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165214 | ||||||
| chr5:165216
|
G | C | 3 | a0003c0056t0017g0080a0019c0019t0010g0164a0035c0060t0020g0188 | 3 | HG00323.hp2 HG02683.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.3476+1668G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165216 | ||||||
| chr5:165216
|
G | GCTCTGAC others(131): Show |
1 | a0006c0021t0056g0199 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3476+1682_3476+168 others(142): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165216 | |||||
| chr5:165219
|
C | G | 12 | a0002c0003t0002g0132a0004c0006t0003g0047a0006c0021t0018g0198others(9): Show | 12 | HG00735.hp2 HG01261.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.3476+1671C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165219 | ||||||
| chr5:165223
|
C | CAG | 2 | a0012c0013t0133g0118a0024c0042t0006g0012 | 2 | HG02735.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.3476+1675_3476+167 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165223 | ||||||
| chr5:165223
|
C | T | 10 | a0002c0005t0129g0043a0003c0009t0017g0088a0003c0009t0017g0093others(7): Show | 10 | HG00140.hp2 HG01243.hp1 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.3476+1675C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165223 | ||||||
| chr5:165223
|
CGGGGCGG others(73): Show |
C | 1 | a0004c0006t0003g0047 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3476+1676_3476+175 others(84): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165223 | ||||||
| chr5:165224
|
G | GGGGCGGA others(195): Show |
1 | a0001c0037t0006g0045 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3476+1691_3476+169 others(206): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165224 | |||||
| chr5:165228
|
C | T | 1 | a0001c0002t0001g0018 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.3476+1680C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165228 | ||||||
| chr5:165229
|
G | A | 1 | a0002c0003t0002g0132 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.3476+1681G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165229 | ||||||
| chr5:165231
|
A | G | 26 | a0001c0001t0006g0075a0001c0001t0032g0094a0001c0001t0032g0144others(23): Show | 26 | HG00597.hp2 HG00735.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.3476+1683A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165231 | ||||||
| chr5:165238
|
ACTAATGC others(17): Show |
A | 1 | a0036c0075t0061g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3476+1692_3476+171 others(28): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165238 | |||||
| chr5:165239
|
C | CAG | 2 | a0003c0009t0120g0013a0010c0014t0057g0197 | 2 | HG01175.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.3476+1691_3476+169 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165239 | ||||||
| chr5:165239
|
C | G | 2 | a0012c0013t0133g0118a0029c0033t0042g0163 | 2 | NA19030.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.3476+1691C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165239 | ||||||
| chr5:165242
|
A | C | 1 | a0029c0033t0042g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3476+1694A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165242 | ||||||
| chr5:165243
|
T | C | 11 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(8): Show | 11 | HG00597.hp2 HG00735.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.3476+1695T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165243 | ||||||
| chr5:165243
|
TGCTCTGA others(47): Show |
T | 1 | a0039c0062t0010g0165 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3476+1718_3476+177 others(58): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165243 | |||||
| chr5:165244
|
G | A | 1 | a0024c0042t0006g0012 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3476+1696G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165244 | ||||||
| chr5:165244
|
G | C | 1 | a0029c0033t0042g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3476+1696G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165244 | ||||||
| chr5:165244
|
GCTCTGAC others(75): Show |
G | 1 | a0002c0057t0003g0026 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.3476+1711_3476+179 others(86): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165244 | |||||
| chr5:165247
|
C | G | 29 | a0002c0003t0066g0209a0002c0003t0071g0095a0002c0003t0124g0017others(26): Show | 29 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.3476+1699C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165247 | ||||||
| chr5:165251
|
C | CAG | 9 | a0002c0005t0003g0031a0004c0006t0134g0011a0004c0054t0034g0139others(6): Show | 9 | HG00673.hp1 HG02145.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.3476+1703_3476+170 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165251 | ||||||
| chr5:165251
|
C | G | 1 | a0014c0066t0051g0170 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3476+1703C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165251 | ||||||
| chr5:165251
|
C | T | 12 | a0002c0003t0002g0132a0003c0009t0017g0088a0003c0009t0017g0093others(9): Show | 12 | HG00735.hp2 HG01243.hp1 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.3476+1703C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165251 | ||||||
| chr5:165251
|
CGGGGCGG others(45): Show |
C | 19 | a0002c0003t0066g0209a0002c0003t0071g0095a0002c0003t0124g0017others(16): Show | 19 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.3476+1704_3476+175 others(56): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165251 | ||||||
| chr5:165256
|
C | T | 1 | a0012c0013t0133g0118 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.3476+1708C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165256 | ||||||
| chr5:165259
|
G | A | 12 | a0001c0001t0006g0075a0001c0037t0006g0045a0003c0009t0120g0013others(9): Show | 12 | HG00323.hp2 HG01175.hp2 HG02165.hp2 others(9): Show |
intron_variant | MODIFIER | c.3476+1711G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165259 | ||||||
| chr5:165262
|
T | TCA | 31 | a0001c0037t0006g0045a0002c0003t0002g0098a0002c0003t0002g0101others(28): Show | 31 | HG00140.hp2 HG00323.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.3476+1716_3476+171 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165262 | |||||
| chr5:165262
|
T | TCACACGC others(45): Show |
1 | a0015c0076t0067g0192 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3476+1717_3476+171 others(56): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165262 | |||||
| chr5:165262
|
T | TCACACTA others(135): Show |
1 | a0008c0024t0021g0176 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3476+1717_3476+171 others(146): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165262 | |||||
| chr5:165262
|
T | TCACACTA others(165): Show |
1 | a0001c0001t0006g0075 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.3476+1717_3476+171 others(176): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165262 | |||||
| chr5:165262
|
T | TCACACTA others(109): Show |
1 | a0012c0013t0133g0118 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.3476+1717_3476+171 others(120): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165262 | |||||
| chr5:165262
|
T | TCACAGTA others(79): Show |
1 | a0022c0046t0047g0180 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3476+1717_3476+171 others(90): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165262 | |||||
| chr5:165262
|
T | TCACAGTA others(357): Show |
1 | a0010c0014t0019g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3476+1717_3476+171 others(368): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165262 | |||||
| chr5:165262
|
T | TCACAGTA others(51): Show |
1 | a0006c0068t0058g0194 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3476+1717_3476+171 others(62): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165262 | |||||
| chr5:165262
|
T | TCACAGTA others(23): Show |
6 | a0001c0001t0031g0112a0001c0001t0097g0086a0001c0001t0104g0023others(3): Show | 6 | HG00323.hp1 HG02004.hp1 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.3476+1717_3476+171 others(34): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165262 | |||||
| chr5:165262
|
T | TCAGTAAT others(21): Show |
4 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0007t0110g0151others(1): Show | 4 | HG02109.hp1 HG02723.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.3476+1716_3476+171 others(32): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165262 | |||||
| chr5:165262
|
T | TCAGTAAT others(105): Show |
1 | a0001c0007t0109g0147 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3476+1716_3476+171 others(116): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165262 | |||||
| chr5:165262
|
T | TCAGTAAT others(358): Show |
1 | a0001c0007t0008g0146 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3476+1716_3476+171 others(369): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165262 | |||||
| chr5:165265
|
C | CACAG | 2 | a0014c0027t0049g0171a0021c0026t0060g0169 | 2 | HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3476+1717_3476+171 others(8): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165265 | ||||||
| chr5:165265
|
C | CACTAACG others(419): Show |
1 | a0032c0058t0040g0158 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3476+1717_3476+171 others(430): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165265 | ||||||
| chr5:165265
|
C | CACTAATG others(193): Show |
1 | a0017c0030t0039g0140 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3476+1717_3476+171 others(204): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165265 | ||||||
| chr5:165265
|
C | CACTAATG others(79): Show |
1 | a0011c0023t0041g0184 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3476+1717_3476+171 others(90): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165265 | ||||||
| chr5:165265
|
C | CAG | 10 | a0002c0005t0003g0031a0004c0006t0002g0119a0004c0006t0134g0011others(7): Show | 10 | HG00673.hp1 HG01081.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.3476+1717_3476+171 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165265 | ||||||
| chr5:165265
|
C | G | 5 | a0001c0001t0113g0044a0001c0007t0008g0143a0001c0007t0008g0145others(2): Show | 5 | HG00597.hp2 HG00735.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.3476+1717C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165265 | ||||||
| chr5:165265
|
CT | C | 4 | a0003c0009t0017g0088a0003c0009t0017g0093a0003c0009t0119g0049others(1): Show | 4 | HG01243.hp1 HG01256.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.3476+1718delT | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165265 | ||||||
| chr5:165268
|
A | G | 4 | a0003c0009t0017g0088a0003c0009t0017g0093a0003c0009t0119g0049others(1): Show | 4 | HG01243.hp1 HG01256.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.3476+1720A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165268 | ||||||
| chr5:165269
|
T | C | 2 | a0001c0001t0015g0131a0037c0074t0037g0203 | 2 | NA18522.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.3476+1721T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165269 | ||||||
| chr5:165270
|
G | A | 4 | a0003c0009t0017g0088a0003c0009t0017g0093a0003c0009t0119g0049others(1): Show | 4 | HG01243.hp1 HG01256.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.3476+1722G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165270 | ||||||
| chr5:165270
|
G | C | 7 | a0001c0001t0113g0044a0001c0007t0008g0143a0001c0007t0008g0145others(4): Show | 7 | HG00597.hp2 HG00735.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.3476+1722G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165270 | ||||||
| chr5:165271
|
C | A | 2 | a0014c0027t0049g0171a0021c0026t0060g0169 | 2 | HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3476+1723C>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165271 | ||||||
| chr5:165273
|
C | G | 10 | a0002c0003t0002g0098a0002c0003t0002g0101a0002c0003t0011g0210others(7): Show | 10 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.3476+1725C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165273 | ||||||
| chr5:165277
|
C | CAG | 4 | a0002c0003t0002g0098a0002c0003t0002g0101a0002c0003t0011g0210others(1): Show | 4 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.3476+1729_3476+173 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165277 | ||||||
| chr5:165277
|
C | CTG | 2 | a0014c0027t0049g0171a0021c0026t0060g0169 | 2 | HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3476+1729_3476+173 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165277 | ||||||
| chr5:165277
|
C | T | 5 | a0003c0009t0120g0013a0008c0079t0068g0173a0010c0014t0057g0197others(2): Show | 5 | HG00323.hp2 HG01175.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.3476+1729C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165277 | ||||||
| chr5:165280
|
G | A | 2 | a0014c0066t0051g0170a0036c0075t0061g0178 | 2 | HG02809.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3476+1732G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165280 | ||||||
| chr5:165281
|
G | GCGGAGCT others(247): Show |
2 | a0001c0007t0008g0143a0001c0007t0008g0145 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3476+1736_3476+173 others(258): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165281 | |||||
| chr5:165281
|
G | T | 4 | a0002c0003t0002g0098a0002c0003t0002g0101a0002c0003t0011g0210others(1): Show | 4 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.3476+1733G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165281 | ||||||
| chr5:165282
|
C | T | 6 | a0002c0005t0003g0031a0004c0006t0134g0011a0004c0054t0034g0139others(3): Show | 6 | HG00673.hp1 HG02145.hp1 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.3476+1734C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165282 | ||||||
| chr5:165285
|
G | A | 43 | a0001c0001t0006g0075a0001c0001t0031g0112a0001c0001t0097g0086others(40): Show | 43 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.3476+1737G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165285 | ||||||
| chr5:165287
|
C | T | 2 | a0014c0027t0049g0171a0021c0026t0060g0169 | 2 | HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3476+1739C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165287 | ||||||
| chr5:165290
|
ACACTAAC others(19): Show |
A | 3 | a0002c0003t0002g0098a0002c0003t0002g0101a0002c0003t0011g0210 | 3 | HG01069.hp1 HG01071.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.3476+1746_3476+177 others(30): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165290 | |||||
| chr5:165293
|
C | G | 3 | a0014c0027t0049g0171a0021c0026t0060g0169a0037c0074t0037g0203 | 3 | HG02818.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3476+1745C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165293 | ||||||
| chr5:165297
|
C | T | 64 | a0001c0001t0006g0075a0001c0001t0031g0112a0001c0001t0032g0094others(61): Show | 64 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.3476+1749C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165297 | ||||||
| chr5:165298
|
G | C | 1 | a0037c0074t0037g0203 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3476+1750G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165298 | ||||||
| chr5:165301
|
C | G | 10 | a0001c0037t0006g0045a0002c0003t0002g0132a0006c0068t0058g0194others(7): Show | 10 | HG00735.hp2 HG02647.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.3476+1753C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165301 | ||||||
| chr5:165305
|
C | CAG | 6 | a0002c0003t0002g0132a0006c0068t0058g0194a0014c0027t0049g0171others(3): Show | 6 | HG00735.hp2 HG02647.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.3476+1757_3476+175 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165305 | ||||||
| chr5:165305
|
C | CGGGGCGG others(23): Show |
1 | a0006c0021t0056g0199 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3476+1764_3476+176 others(34): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165305 | |||||
| chr5:165305
|
C | CGGGGCGG others(219): Show |
1 | a0022c0046t0047g0180 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3476+1772_3476+177 others(230): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165305 | |||||
| chr5:165305
|
C | G | 23 | a0002c0003t0066g0209a0002c0003t0071g0095a0002c0003t0124g0017others(20): Show | 23 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.3476+1757C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165305 | ||||||
| chr5:165305
|
C | T | 4 | a0003c0009t0120g0013a0003c0056t0017g0080a0004c0006t0002g0119others(1): Show | 4 | HG01081.hp1 HG01175.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.3476+1757C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165305 | ||||||
| chr5:165313
|
G | A | 10 | a0001c0037t0006g0045a0002c0005t0129g0043a0004c0006t0002g0119others(7): Show | 10 | HG00140.hp2 HG00323.hp2 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.3476+1765G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165313 | ||||||
| chr5:165313
|
G | GGCTCACA others(47): Show |
5 | a0006c0070t0054g0207a0006c0073t0020g0193a0013c0020t0050g0182others(2): Show | 5 | HG01261.hp2 HG02451.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.3476+1772_3476+177 others(58): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165313 | |||||
| chr5:165313
|
GGCTCACA others(21): Show |
G | 1 | a0001c0002t0024g0024 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3476+1773_3476+180 others(32): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165313 | |||||
| chr5:165316
|
T | TCA | 2 | a0001c0037t0006g0045a0024c0042t0006g0012 | 2 | HG02647.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.3476+1771_3476+177 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165316 | |||||
| chr5:165316
|
TCA | T | 3 | a0010c0014t0055g0201a0010c0069t0019g0204a0018c0022t0011g0195 | 3 | HG02258.hp2 HG02451.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.3476+1771_3476+177 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165316 | |||||
| chr5:165318
|
A | ACACGCTC others(15): Show |
1 | a0011c0023t0044g0187 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3476+1772_3476+177 others(26): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165318 | |||||
| chr5:165319
|
CAG | C | 8 | a0001c0001t0006g0075a0001c0001t0031g0112a0001c0001t0097g0086others(5): Show | 8 | HG00323.hp1 HG01975.hp1 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.3476+1772_3476+177 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165319 | ||||||
| chr5:165321
|
G | C | 22 | a0001c0001t0113g0044a0001c0007t0109g0147a0002c0005t0129g0043others(19): Show | 22 | HG00140.hp2 HG00323.hp2 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.3476+1773G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165321 | ||||||
| chr5:165324
|
A | C | 1 | a0003c0056t0017g0080 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3476+1776A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165324 | ||||||
| chr5:165325
|
T | C | 1 | a0006c0021t0018g0198 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3476+1777T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165325 | ||||||
| chr5:165326
|
C | G | 73 | a0001c0001t0006g0075a0001c0001t0031g0112a0001c0001t0097g0086others(70): Show | 73 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.3476+1778C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165326 | ||||||
| chr5:165326
|
CCTCTGAC others(133): Show |
C | 1 | a0006c0071t0018g0202 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3476+1829_3476+196 others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165326 | |||||
| chr5:165329
|
C | G | 9 | a0001c0037t0006g0045a0002c0003t0002g0098a0002c0003t0002g0101others(6): Show | 9 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.3476+1781C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165329 | ||||||
| chr5:165333
|
C | T | 6 | a0001c0007t0109g0147a0003c0009t0017g0088a0003c0009t0017g0093others(3): Show | 6 | HG01243.hp1 HG01256.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.3476+1785C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165333 | ||||||
| chr5:165336
|
G | A | 3 | a0014c0027t0049g0171a0021c0026t0060g0169a0024c0042t0006g0012 | 3 | HG02735.hp2 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3476+1788G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165336 | ||||||
| chr5:165338
|
C | T | 27 | a0001c0001t0014g0115a0001c0001t0014g0125a0002c0003t0002g0132others(24): Show | 27 | HG00099.hp2 HG00438.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.3476+1790C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165338 | ||||||
| chr5:165339
|
G | A | 3 | a0002c0003t0002g0098a0002c0003t0002g0101a0002c0003t0011g0210 | 3 | HG01069.hp1 HG01071.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.3476+1791G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165339 | ||||||
| chr5:165341
|
A | AGCTCACA others(21): Show |
1 | a0008c0025t0045g0172 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3476+1801_3476+182 others(32): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165341 | |||||
| chr5:165341
|
A | C | 1 | a0002c0057t0003g0026 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.3476+1793A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165341 | ||||||
| chr5:165341
|
A | G | 25 | a0001c0001t0006g0075a0001c0001t0031g0112a0001c0001t0097g0086others(22): Show | 25 | HG00323.hp1 HG00323.hp2 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.3476+1793A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165341 | ||||||
| chr5:165349
|
C | G | 3 | a0001c0001t0113g0044a0008c0025t0069g0174a0018c0022t0011g0196 | 3 | HG00597.hp2 HG00735.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3476+1801C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165349 | ||||||
| chr5:165353
|
T | C | 10 | a0001c0001t0006g0075a0001c0001t0031g0112a0001c0001t0097g0086others(7): Show | 10 | HG00323.hp1 HG02004.hp1 HG02165.hp2 others(7): Show |
intron_variant | MODIFIER | c.3476+1805T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165353 | ||||||
| chr5:165353
|
T | TGCTCTGA others(159): Show |
1 | a0001c0002t0022g0015 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.3476+1818_3476+181 others(170): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165353 | |||||
| chr5:165354
|
G | C | 3 | a0001c0001t0113g0044a0008c0025t0069g0174a0018c0022t0011g0196 | 3 | HG00597.hp2 HG00735.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3476+1806G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165354 | ||||||
| chr5:165354
|
G | GCTCTGAC others(189): Show |
1 | a0001c0032t0103g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3476+1820_3476+182 others(200): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165354 | |||||
| chr5:165354
|
GCTCTGAC others(21): Show |
G | 1 | a0014c0066t0051g0170 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3476+1821_3476+184 others(32): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165354 | |||||
| chr5:165357
|
C | CTGACGGG others(191): Show |
1 | a0008c0024t0021g0176 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3476+1820_3476+182 others(202): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165357 | |||||
| chr5:165357
|
C | G | 12 | a0002c0005t0003g0031a0002c0005t0129g0043a0002c0039t0009g0030others(9): Show | 12 | HG00140.hp2 HG00673.hp1 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.3476+1809C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165357 | ||||||
| chr5:165361
|
C | CAG | 6 | a0002c0005t0003g0031a0004c0006t0002g0119a0004c0054t0034g0139others(3): Show | 6 | HG00673.hp1 HG01081.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.3476+1813_3476+181 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165361 | ||||||
| chr5:165361
|
C | CGGGGCGG others(49): Show |
1 | a0015c0076t0067g0192 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3476+1820_3476+182 others(60): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165361 | |||||
| chr5:165361
|
C | T | 6 | a0001c0007t0008g0143a0001c0007t0008g0145a0002c0003t0002g0098others(3): Show | 6 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.3476+1813C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165361 | ||||||
| chr5:165362
|
G | GGGGCGGG others(21): Show |
1 | a0010c0069t0019g0204 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3476+1828_3476+182 others(32): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165362 | |||||
| chr5:165366
|
C | CGGGGCTC others(21): Show |
1 | a0004c0041t0003g0077 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3476+1833_3476+183 others(32): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165366 | |||||
| chr5:165369
|
G | A | 17 | a0001c0001t0113g0044a0001c0007t0008g0143a0001c0007t0008g0145others(14): Show | 17 | HG00597.hp2 HG00735.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.3476+1821G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165369 | ||||||
| chr5:165369
|
G | C | 1 | a0012c0013t0133g0118 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.3476+1821G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165369 | ||||||
| chr5:165369
|
G | GGCTCACA others(49): Show |
1 | a0011c0023t0044g0187 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3476+1828_3476+182 others(60): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165369 | |||||
| chr5:165369
|
G | GGCTCACA others(221): Show |
1 | a0001c0007t0109g0147 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3476+1828_3476+182 others(232): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165369 | |||||
| chr5:165369
|
GGCTCACA others(21): Show |
G | 2 | a0002c0003t0002g0098a0002c0003t0011g0210 | 2 | HG01069.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.3476+1829_3476+185 others(32): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165369 | |||||
| chr5:165377
|
G | C | 28 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(25): Show | 28 | HG00597.hp2 HG00735.hp1 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.3476+1829G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165377 | ||||||
| chr5:165377
|
G | GTACTCCT others(243): Show |
1 | a0001c0002t0013g0109 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3476+1831_3476+183 others(254): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165377 | |||||
| chr5:165377
|
GTAATCCT others(21): Show |
G | 2 | a0002c0003t0002g0132a0030c0047t0131g0067 | 2 | HG00735.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.3476+1834_3476+186 others(32): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165377 | |||||
| chr5:165380
|
A | C | 3 | a0003c0056t0017g0080a0015c0077t0053g0181a0035c0060t0020g0188 | 3 | HG02683.hp1 HG02717.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3476+1832A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165380 | ||||||
| chr5:165382
|
C | G | 68 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(65): Show | 68 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.3476+1834C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165382 | ||||||
| chr5:165385
|
C | G | 2 | a0012c0013t0133g0118a0039c0062t0010g0165 | 2 | HG04204.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.3476+1837C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165385 | ||||||
| chr5:165389
|
C | T | 2 | a0003c0009t0120g0013a0008c0079t0068g0173 | 2 | HG01175.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3476+1841C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165389 | ||||||
| chr5:165390
|
G | A | 1 | a0010c0014t0055g0201 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3476+1842G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165390 | ||||||
| chr5:165393
|
G | GCGGAGCT others(23): Show |
1 | a0006c0021t0056g0199 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3476+1864_3476+186 others(34): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165393 | |||||
| chr5:165394
|
C | T | 5 | a0002c0003t0002g0101a0002c0005t0003g0031a0004c0006t0002g0119others(2): Show | 5 | HG00673.hp1 HG01071.hp1 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.3476+1846C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165394 | ||||||
| chr5:165397
|
A | C | 1 | a0016c0018t0034g0004 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3476+1849A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165397 | ||||||
| chr5:165397
|
A | G | 22 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(19): Show | 22 | HG00597.hp2 HG00735.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.3476+1849A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165397 | ||||||
| chr5:165405
|
C | CTAATGCT others(109): Show |
2 | a0001c0007t0008g0143a0001c0007t0008g0145 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3476+1864_3476+186 others(120): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165405 | |||||
| chr5:165405
|
C | CTAATGCT others(25): Show |
2 | a0004c0006t0134g0011a0016c0018t0003g0005 | 2 | HG02145.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.3476+1864_3476+186 others(36): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165405 | |||||
| chr5:165405
|
C | CTAATGCT others(137): Show |
1 | a0008c0024t0021g0175 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3476+1864_3476+186 others(148): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165405 | |||||
| chr5:165405
|
C | G | 7 | a0001c0002t0013g0109a0001c0007t0109g0147a0001c0032t0103g0007others(4): Show | 7 | HG01071.hp1 HG02451.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.3476+1857C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165405 | ||||||
| chr5:165408
|
A | C | 1 | a0002c0003t0002g0101 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.3476+1860A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165408 | ||||||
| chr5:165409
|
T | C | 4 | a0003c0009t0017g0088a0003c0009t0017g0093a0003c0009t0119g0049others(1): Show | 4 | HG01243.hp1 HG01256.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.3476+1861T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165409 | ||||||
| chr5:165410
|
G | C | 4 | a0001c0002t0013g0109a0001c0032t0103g0007a0002c0003t0002g0101others(1): Show | 4 | HG01071.hp1 HG02451.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.3476+1862G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165410 | ||||||
| chr5:165410
|
G | GCTCTGAC others(243): Show |
1 | a0001c0037t0006g0045 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3476+1876_3476+187 others(254): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165410 | |||||
| chr5:165410
|
G | GCTCTGAC others(103): Show |
1 | a0032c0058t0040g0158 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3476+1876_3476+187 others(114): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165410 | |||||
| chr5:165410
|
G | GCTCTGAT others(187): Show |
1 | a0017c0030t0039g0140 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3476+1868_3476+186 others(198): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165410 | |||||
| chr5:165411
|
C | G | 1 | a0011c0023t0044g0187 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3476+1863C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165411 | ||||||
| chr5:165413
|
C | G | 5 | a0004c0006t0134g0011a0008c0024t0021g0175a0010c0014t0019g0205others(2): Show | 5 | HG02109.hp2 HG02145.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.3476+1865C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165413 | ||||||
| chr5:165417
|
C | T | 11 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0007t0110g0151others(8): Show | 11 | HG01243.hp1 HG01256.hp1 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.3476+1869C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165417 | ||||||
| chr5:165417
|
CGGGGCGG others(21): Show |
C | 3 | a0001c0002t0024g0024a0003c0056t0017g0080a0014c0066t0051g0170 | 3 | HG02683.hp1 HG02809.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.3476+1897_3476+192 others(32): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165417 | |||||
| chr5:165421
|
G | T | 1 | a0010c0014t0019g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3476+1873G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165421 | ||||||
| chr5:165422
|
C | T | 3 | a0002c0003t0002g0098a0002c0003t0011g0210a0002c0005t0129g0043 | 3 | HG00140.hp2 HG01069.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.3476+1874C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165422 | ||||||
| chr5:165423
|
G | A | 2 | a0004c0006t0134g0011a0016c0018t0003g0005 | 2 | HG02145.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.3476+1875G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165423 | ||||||
| chr5:165425
|
G | A | 59 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0079g0059others(56): Show | 59 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.3476+1877G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165425 | ||||||
| chr5:165425
|
G | C | 3 | a0002c0003t0002g0101a0002c0057t0003g0026a0004c0041t0003g0077 | 3 | HG01071.hp1 HG03017.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.3476+1877G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165425 | ||||||
| chr5:165425
|
G | GGCTCACA others(129): Show |
1 | a0006c0021t0018g0198 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3476+1896_3476+189 others(140): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165425 | |||||
| chr5:165425
|
G | GGCTCACA others(21): Show |
8 | a0001c0001t0006g0075a0001c0001t0031g0112a0001c0001t0097g0086others(5): Show | 8 | HG00323.hp1 HG00741.hp2 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.3476+1884_3476+188 others(32): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165425 | |||||
| chr5:165433
|
C | G | 14 | a0002c0003t0002g0098a0002c0003t0011g0210a0002c0005t0003g0031others(11): Show | 14 | HG00140.hp2 HG00673.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.3476+1885C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165433 | ||||||
| chr5:165436
|
A | C | 8 | a0002c0003t0002g0098a0002c0003t0011g0210a0002c0005t0129g0043others(5): Show | 8 | HG00140.hp2 HG01069.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.3476+1888A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165436 | ||||||
| chr5:165438
|
G | C | 8 | a0002c0003t0002g0098a0002c0003t0011g0210a0002c0005t0129g0043others(5): Show | 8 | HG00140.hp2 HG01069.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.3476+1890G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165438 | ||||||
| chr5:165441
|
C | G | 6 | a0002c0057t0003g0026a0004c0041t0003g0077a0006c0068t0058g0194others(3): Show | 6 | HG02257.hp1 HG02280.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.3476+1893C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165441 | ||||||
| chr5:165443
|
G | GAC | 2 | a0006c0068t0058g0194a0008c0079t0068g0173 | 2 | HG02647.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3476+1896_3476+189 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165443 | |||||
| chr5:165445
|
T | C | 89 | a0001c0001t0006g0075a0001c0001t0031g0112a0001c0001t0032g0094others(86): Show | 89 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.3476+1897T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165445 | ||||||
| chr5:165445
|
T | G | 2 | a0006c0068t0058g0194a0008c0079t0068g0173 | 2 | HG02647.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3476+1897T>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165445 | ||||||
| chr5:165445
|
TGGGGCGG others(301): Show |
T | 1 | a0001c0001t0073g0107 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3476+1913_3476+222 others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165445 | |||||
| chr5:165450
|
C | T | 1 | a0002c0003t0002g0101 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.3476+1902C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165450 | ||||||
| chr5:165453
|
G | A | 24 | a0001c0001t0113g0044a0001c0007t0109g0147a0002c0003t0002g0101others(21): Show | 24 | HG00597.hp2 HG00673.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.3476+1905G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165453 | ||||||
| chr5:165453
|
G | C | 3 | a0002c0003t0002g0098a0002c0003t0011g0210a0002c0005t0129g0043 | 3 | HG00140.hp2 HG01069.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.3476+1905G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165453 | ||||||
| chr5:165453
|
G | GGCTCACA others(51): Show |
2 | a0001c0001t0032g0094a0001c0001t0032g0144 | 2 | HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3476+1920_3476+192 others(62): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165453 | |||||
| chr5:165453
|
G | GGCTCACA others(49): Show |
2 | a0017c0030t0039g0140a0032c0058t0040g0158 | 2 | HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.3476+1912_3476+191 others(60): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165453 | |||||
| chr5:165455
|
C | T | 3 | a0014c0027t0049g0171a0014c0066t0051g0170a0021c0026t0060g0169 | 3 | HG02809.hp1 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3476+1907C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165455 | ||||||
| chr5:165461
|
C | CTAATGCT others(23): Show |
1 | a0008c0024t0021g0175 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3476+1920_3476+192 others(34): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165461 | |||||
| chr5:165461
|
C | CTAATGCT others(845): Show |
1 | a0001c0007t0110g0151 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3476+1920_3476+192 others(856): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165461 | |||||
| chr5:165461
|
C | G | 17 | a0001c0002t0024g0024a0001c0007t0008g0143a0001c0007t0008g0145others(14): Show | 17 | HG02257.hp1 HG02280.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.3476+1913C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165461 | ||||||
| chr5:165463
|
AATGCTCT others(248): Show |
A | 1 | a0039c0062t0010g0165 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3476+1916_3476+217 others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165463 | ||||||
| chr5:165465
|
T | C | 1 | a0003c0009t0120g0013 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3476+1917T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165465 | ||||||
| chr5:165466
|
G | C | 7 | a0001c0002t0024g0024a0003c0056t0017g0080a0010c0014t0057g0197others(4): Show | 7 | HG02683.hp1 HG02809.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.3476+1918G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165466 | ||||||
| chr5:165466
|
G | GCTGTGAC others(529): Show |
1 | a0020c0081t0064g0200 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3476+1920_3476+192 others(540): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165466 | |||||
| chr5:165469
|
C | G | 29 | a0002c0003t0066g0209a0002c0003t0071g0095a0002c0003t0124g0017others(26): Show | 29 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.3476+1921C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165469 | ||||||
| chr5:165473
|
C | CAG | 25 | a0002c0003t0066g0209a0002c0003t0071g0095a0002c0003t0124g0017others(22): Show | 25 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.3476+1925_3476+192 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165473 | ||||||
| chr5:165473
|
C | T | 22 | a0001c0001t0006g0075a0001c0001t0031g0112a0001c0001t0097g0086others(19): Show | 22 | HG00323.hp1 HG00741.hp2 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.3476+1925C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165473 | ||||||
| chr5:165477
|
G | T | 24 | a0002c0003t0066g0209a0002c0003t0071g0095a0002c0003t0124g0017others(21): Show | 24 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.3476+1929G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165477 | ||||||
| chr5:165478
|
C | T | 6 | a0002c0003t0002g0098a0002c0003t0011g0210a0002c0005t0129g0043others(3): Show | 6 | HG00140.hp2 HG01069.hp1 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.3476+1930C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165478 | ||||||
| chr5:165481
|
A | AGCTCACA others(411): Show |
1 | a0001c0001t0079g0059 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3476+1960_3476+196 others(422): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165481 | |||||
| chr5:165481
|
A | G | 35 | a0001c0001t0006g0075a0001c0001t0031g0112a0001c0001t0032g0094others(32): Show | 35 | HG00323.hp1 HG00597.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.3476+1933A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165481 | ||||||
| chr5:165481
|
AGCTCACA others(21): Show |
A | 83 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0142others(80): Show | 83 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.3476+1997_3476+202 others(32): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165481 | |||||
| chr5:165489
|
C | CAG | 25 | a0002c0003t0066g0209a0002c0003t0071g0095a0002c0003t0124g0017others(22): Show | 25 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.3476+1941_3476+194 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165489 | ||||||
| chr5:165489
|
C | CTAATGCT others(49): Show |
1 | a0012c0013t0009g0019 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.3476+1960_3476+196 others(60): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165489 | |||||
| chr5:165489
|
C | CTAATGCT others(25): Show |
1 | a0018c0022t0011g0195 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.3476+1948_3476+194 others(36): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165489 | |||||
| chr5:165489
|
C | G | 16 | a0001c0001t0032g0094a0001c0001t0032g0144a0002c0039t0009g0030others(13): Show | 16 | HG01175.hp2 HG01243.hp1 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.3476+1941C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165489 | ||||||
| chr5:165492
|
A | C | 6 | a0003c0009t0017g0088a0003c0009t0017g0093a0003c0009t0119g0049others(3): Show | 6 | HG01243.hp1 HG01256.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.3476+1944A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165492 | ||||||
| chr5:165494
|
G | C | 9 | a0003c0009t0017g0088a0003c0009t0017g0093a0003c0009t0119g0049others(6): Show | 9 | HG01243.hp1 HG01256.hp1 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.3476+1946G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165494 | ||||||
| chr5:165497
|
C | G | 35 | a0001c0001t0113g0044a0002c0003t0066g0209a0002c0003t0071g0095others(32): Show | 35 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(32): Show |
intron_variant | MODIFIER | c.3476+1949C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165497 | ||||||
| chr5:165497
|
CTGACGGG others(382): Show |
C | 1 | a0003c0009t0120g0013 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3476+1950_3476+233 others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165497 | ||||||
| chr5:165501
|
C | CAG | 2 | a0010c0014t0019g0205a0030c0047t0131g0067 | 2 | HG03579.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.3476+1953_3476+195 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165501 | ||||||
| chr5:165501
|
C | T | 5 | a0002c0057t0003g0026a0004c0041t0003g0077a0008c0079t0068g0173others(2): Show | 5 | HG02451.hp2 HG03017.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.3476+1953C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165501 | ||||||
| chr5:165505
|
G | T | 1 | a0010c0014t0019g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3476+1957G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165505 | ||||||
| chr5:165506
|
C | T | 1 | a0002c0003t0002g0132 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.3476+1958C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165506 | ||||||
| chr5:165507
|
G | A | 23 | a0002c0003t0066g0209a0002c0003t0071g0095a0002c0003t0124g0017others(20): Show | 23 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.3476+1959G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165507 | ||||||
| chr5:165509
|
G | A | 72 | a0001c0001t0006g0075a0001c0001t0031g0112a0001c0001t0032g0094others(69): Show | 72 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.3476+1961G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165509 | ||||||
| chr5:165509
|
G | C | 4 | a0004c0006t0134g0011a0012c0013t0009g0016a0016c0018t0003g0005others(1): Show | 4 | HG02145.hp1 HG02735.hp2 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.3476+1961G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165509 | ||||||
| chr5:165509
|
G | GGCTCACA others(355): Show |
3 | a0003c0004t0016g0078a0003c0004t0016g0133a0003c0017t0016g0110 | 3 | NA18979.hp2 NA19066.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.3476+1986_3476+198 others(366): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165509 | |||||
| chr5:165509
|
G | GGCTCACA others(21): Show |
1 | a0015c0076t0067g0192 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3476+1988_3476+198 others(32): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165509 | |||||
| chr5:165509
|
G | GGCTCACA others(781): Show |
1 | a0001c0015t0076g0154 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3476+1996_3476+199 others(792): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165509 | |||||
| chr5:165509
|
G | GGCTCACA others(107): Show |
1 | a0001c0007t0008g0146 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3476+1976_3476+197 others(118): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165509 | |||||
| chr5:165509
|
G | GGCTCACA others(79): Show |
1 | a0006c0068t0058g0194 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3476+1968_3476+196 others(90): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165509 | |||||
| chr5:165517
|
C | CTAATGCT others(79): Show |
1 | a0012c0013t0009g0019 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.3476+1980_3476+198 others(90): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165517 | |||||
| chr5:165517
|
C | G | 4 | a0002c0003t0002g0132a0012c0013t0133g0118a0022c0046t0047g0180others(1): Show | 4 | HG00735.hp2 HG02818.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.3476+1969C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165517 | ||||||
| chr5:165520
|
A | C | 1 | a0002c0003t0002g0132 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.3476+1972A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165520 | ||||||
| chr5:165521
|
T | TGCTCTGA others(133): Show |
1 | a0001c0001t0099g0089 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3476+1996_3476+199 others(144): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165521 | |||||
| chr5:165522
|
G | C | 2 | a0002c0003t0002g0132a0022c0046t0047g0180 | 2 | HG00735.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.3476+1974G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165522 | ||||||
| chr5:165522
|
G | GCTGTGAC others(21): Show |
1 | a0010c0069t0019g0204 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3476+1976_3476+197 others(32): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165522 | |||||
| chr5:165525
|
C | CTGACGGG others(249): Show |
1 | a0001c0007t0109g0147 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3476+1988_3476+198 others(260): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165525 | |||||
| chr5:165525
|
C | G | 15 | a0001c0001t0113g0044a0002c0005t0003g0031a0004c0006t0002g0119others(12): Show | 15 | HG00323.hp2 HG00597.hp2 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.3476+1977C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165525 | ||||||
| chr5:165529
|
C | CAG | 5 | a0001c0001t0113g0044a0002c0005t0003g0031a0004c0006t0002g0119others(2): Show | 5 | HG00597.hp2 HG00673.hp1 HG00735.hp1 others(2): Show |
intron_variant | MODIFIER | c.3476+1981_3476+198 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165529 | ||||||
| chr5:165529
|
C | CGGGGCGG others(193): Show |
1 | a0008c0025t0069g0174 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3476+1988_3476+198 others(204): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165529 | |||||
| chr5:165529
|
C | T | 32 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0002t0024g0024others(29): Show | 32 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.3476+1981C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165529 | ||||||
| chr5:165533
|
G | GCGGGGCT others(245): Show |
6 | a0001c0001t0031g0111a0001c0001t0102g0057a0003c0004t0028g0058others(3): Show | 6 | HG01952.hp2 HG02132.hp2 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.3476+1996_3476+199 others(256): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165533 | |||||
| chr5:165533
|
G | T | 5 | a0001c0001t0113g0044a0002c0005t0003g0031a0004c0006t0002g0119others(2): Show | 5 | HG00597.hp2 HG00673.hp1 HG00735.hp1 others(2): Show |
intron_variant | MODIFIER | c.3476+1985G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165533 | ||||||
| chr5:165534
|
C | T | 7 | a0002c0003t0130g0130a0002c0003t0132g0028a0002c0003t0136g0071others(4): Show | 7 | HG00639.hp1 HG01123.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.3476+1986C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165534 | ||||||
| chr5:165537
|
G | A | 22 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(19): Show | 22 | HG00323.hp2 HG00597.hp2 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.3476+1989G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165537 | ||||||
| chr5:165537
|
G | C | 1 | a0002c0003t0002g0132 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.3476+1989G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165537 | ||||||
| chr5:165537
|
G | GGCTCACA others(51): Show |
1 | a0020c0081t0064g0200 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3476+1996_3476+199 others(62): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165537 | |||||
| chr5:165537
|
G | GGCTCACA others(79): Show |
1 | a0006c0073t0020g0193 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3476+1996_3476+199 others(90): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165537 | |||||
| chr5:165542
|
ACACTAAT others(19): Show |
A | 1 | a0004c0006t0002g0119 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3476+1998_3476+202 others(30): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165542 | |||||
| chr5:165545
|
C | CAG | 2 | a0002c0005t0003g0031a0004c0054t0034g0139 | 2 | HG00673.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.3476+1997_3476+199 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165545 | ||||||
| chr5:165545
|
C | G | 15 | a0001c0007t0100g0025a0001c0007t0109g0147a0003c0009t0017g0088others(12): Show | 15 | HG00280.hp2 HG01081.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.3476+1997C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165545 | ||||||
| chr5:165549
|
T | C | 6 | a0001c0001t0099g0089a0001c0007t0008g0143a0001c0007t0008g0145others(3): Show | 6 | HG00280.hp1 HG01071.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.3476+2001T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165549 | ||||||
| chr5:165550
|
G | C | 9 | a0001c0007t0100g0025a0003c0009t0017g0088a0003c0009t0017g0093others(6): Show | 9 | HG00280.hp2 HG01081.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.3476+2002G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165550 | ||||||
| chr5:165553
|
C | CTGACGGG others(239): Show |
1 | a0011c0023t0044g0187 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3476+2016_3476+201 others(250): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165553 | |||||
| chr5:165553
|
C | CTGACGGG others(193): Show |
1 | a0010c0069t0019g0204 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3476+2044_3476+204 others(204): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165553 | |||||
| chr5:165553
|
C | G | 13 | a0002c0005t0003g0031a0002c0057t0003g0026a0003c0056t0017g0080others(10): Show | 13 | HG00673.hp1 HG02257.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.3476+2005C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165553 | ||||||
| chr5:165557
|
C | CAG | 4 | a0006c0021t0056g0199a0006c0070t0054g0207a0016c0018t0034g0004others(1): Show | 4 | HG02896.hp2 HG03041.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.3476+2009_3476+201 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165557 | ||||||
| chr5:165557
|
C | CAGGGGTC others(83): Show |
1 | a0008c0079t0068g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3476+2009_3476+201 others(94): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165557 | ||||||
| chr5:165557
|
C | CGGGGCGG others(23): Show |
1 | a0001c0007t0008g0146 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3476+2016_3476+201 others(34): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165557 | |||||
| chr5:165557
|
C | CGGGGCGG others(109): Show |
2 | a0001c0001t0032g0094a0001c0001t0032g0144 | 2 | HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3476+2016_3476+201 others(120): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165557 | |||||
| chr5:165557
|
C | T | 4 | a0006c0071t0018g0202a0012c0013t0133g0118a0019c0019t0010g0164others(1): Show | 4 | HG00323.hp2 HG02004.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.3476+2009C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165557 | ||||||
| chr5:165561
|
G | GCGGAGCT others(137): Show |
1 | a0006c0021t0018g0198 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3476+2016_3476+201 others(148): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165561 | |||||
| chr5:165561
|
G | T | 2 | a0006c0070t0054g0207a0037c0074t0037g0203 | 2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.3476+2013G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165561 | ||||||
| chr5:165562
|
C | T | 24 | a0002c0003t0002g0132a0002c0003t0066g0209a0002c0003t0071g0095others(21): Show | 24 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.3476+2014C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165562 | ||||||
| chr5:165563
|
G | A | 2 | a0002c0005t0003g0031a0004c0054t0034g0139 | 2 | HG00673.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.3476+2015G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165563 | ||||||
| chr5:165565
|
G | A | 30 | a0001c0001t0099g0089a0001c0002t0024g0024a0001c0007t0008g0143others(27): Show | 30 | HG00280.hp1 HG00280.hp2 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.3476+2017G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165565 | ||||||
| chr5:165565
|
G | GGCTCACA others(133): Show |
1 | a0006c0072t0036g0206 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.3476+2024_3476+202 others(144): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165565 | |||||
| chr5:165565
|
GGCTCACA others(77): Show |
G | 1 | a0002c0005t0129g0043 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.3476+2025_3476+210 others(88): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165565 | |||||
| chr5:165568
|
T | TCACACAC others(165): Show |
2 | a0001c0007t0008g0143a0001c0007t0008g0145 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3476+2024_3476+202 others(176): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165568 | |||||
| chr5:165573
|
G | C | 43 | a0001c0001t0099g0089a0001c0002t0024g0024a0001c0007t0008g0143others(40): Show | 43 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.3476+2025G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165573 | ||||||
| chr5:165573
|
G | GTAATGCT others(249): Show |
1 | a0006c0021t0056g0199 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3476+2029_3476+203 others(260): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165573 | |||||
| chr5:165573
|
GTAATCCT others(77): Show |
G | 1 | a0030c0047t0131g0067 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3476+2030_3476+211 others(88): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165573 | |||||
| chr5:165576
|
A | C | 23 | a0002c0003t0066g0209a0002c0003t0071g0095a0002c0003t0124g0017others(20): Show | 23 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.3476+2028A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165576 | ||||||
| chr5:165577
|
T | C | 2 | a0002c0003t0002g0098a0002c0003t0011g0210 | 2 | HG01069.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.3476+2029T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165577 | ||||||
| chr5:165578
|
C | G | 57 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0099g0089others(54): Show | 57 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.3476+2030C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165578 | ||||||
| chr5:165578
|
CCTCTGAC others(105): Show |
C | 1 | a0002c0003t0002g0101 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.3476+2045_3476+215 others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165578 | |||||
| chr5:165581
|
C | G | 4 | a0002c0039t0009g0030a0004c0006t0002g0119a0008c0025t0045g0172others(1): Show | 4 | HG01081.hp1 HG01928.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.3476+2033C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165581 | ||||||
| chr5:165585
|
C | T | 7 | a0006c0068t0058g0194a0008c0025t0069g0174a0011c0023t0041g0184others(4): Show | 7 | HG00323.hp2 HG02622.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.3476+2037C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165585 | ||||||
| chr5:165587
|
G | GGGCGGAG others(21): Show |
1 | a0001c0007t0100g0025 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3476+2044_3476+204 others(32): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165587 | |||||
| chr5:165590
|
C | A | 1 | a0022c0046t0047g0180 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3476+2042C>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165590 | ||||||
| chr5:165590
|
C | T | 3 | a0004c0041t0003g0077a0016c0018t0034g0004a0018c0022t0011g0195 | 3 | HG03017.hp1 HG03579.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.3476+2042C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165590 | ||||||
| chr5:165591
|
G | A | 1 | a0004c0006t0002g0119 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3476+2043G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165591 | ||||||
| chr5:165593
|
G | A | 40 | a0001c0001t0031g0111a0001c0001t0032g0094a0001c0001t0032g0144others(37): Show | 40 | HG00280.hp1 HG00280.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.3476+2045G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165593 | ||||||
| chr5:165593
|
G | C | 23 | a0002c0003t0066g0209a0002c0003t0071g0095a0002c0003t0124g0017others(20): Show | 23 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.3476+2045G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165593 | ||||||
| chr5:165601
|
C | CTAATGCT others(107): Show |
1 | a0010c0014t0057g0197 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.3476+2060_3476+206 others(118): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165601 | |||||
| chr5:165601
|
C | G | 13 | a0001c0007t0109g0147a0001c0007t0110g0151a0002c0003t0002g0098others(10): Show | 13 | HG00323.hp2 HG01069.hp1 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.3476+2053C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165601 | ||||||
| chr5:165602
|
TAATGCTC others(216): Show |
T | 1 | a0036c0075t0061g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3476+2055_3476+227 others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165602 | ||||||
| chr5:165605
|
T | C | 1 | a0016c0018t0003g0005 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3476+2057T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165605 | ||||||
| chr5:165606
|
G | C | 2 | a0002c0003t0002g0098a0002c0003t0011g0210 | 2 | HG01069.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.3476+2058G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165606 | ||||||
| chr5:165609
|
C | G | 12 | a0001c0007t0008g0143a0001c0007t0008g0145a0003c0056t0017g0080others(9): Show | 12 | HG01261.hp2 HG02145.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.3476+2061C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165609 | ||||||
| chr5:165613
|
C | T | 5 | a0001c0001t0113g0044a0002c0057t0003g0026a0004c0006t0002g0119others(2): Show | 5 | HG00597.hp2 HG00735.hp1 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.3476+2065C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165613 | ||||||
| chr5:165614
|
G | A | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3476+2066G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165614 | ||||||
| chr5:165615
|
G | T | 1 | a0028c0040t0090g0127 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3476+2067G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165615 | ||||||
| chr5:165615
|
GGGCGGAG others(21): Show |
G | 4 | a0002c0003t0066g0209a0002c0003t0071g0095a0002c0005t0070g0100others(1): Show | 4 | HG00099.hp2 HG01192.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.3476+2093_3476+212 others(32): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165615 | |||||
| chr5:165618
|
C | T | 23 | a0001c0002t0025g0073a0002c0003t0124g0017a0002c0003t0128g0029others(20): Show | 23 | HG00639.hp1 HG00639.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.3476+2070C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165618 | ||||||
| chr5:165621
|
A | C | 1 | a0004c0041t0003g0077 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3476+2073A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165621 | ||||||
| chr5:165621
|
A | G | 30 | a0001c0001t0005g0123a0001c0001t0032g0094a0001c0001t0032g0144others(27): Show | 30 | HG00280.hp2 HG00673.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.3476+2073A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165621 | ||||||
| chr5:165629
|
C | CTAATGCT others(361): Show |
1 | a0010c0014t0055g0201 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3476+2092_3476+209 others(372): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165629 | |||||
| chr5:165629
|
C | G | 13 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0007t0008g0143others(10): Show | 13 | HG00673.hp1 HG02004.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.3476+2081C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165629 | ||||||
| chr5:165632
|
A | C | 2 | a0002c0005t0003g0031a0004c0054t0034g0139 | 2 | HG00673.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.3476+2084A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165632 | ||||||
| chr5:165634
|
G | C | 3 | a0002c0005t0003g0031a0004c0054t0034g0139a0019c0019t0062g0191 | 3 | HG00673.hp1 HG02004.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.3476+2086G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165634 | ||||||
| chr5:165634
|
G | GCTCTGAC others(245): Show |
6 | a0001c0001t0031g0111a0001c0001t0102g0057a0003c0004t0028g0058others(3): Show | 6 | HG01952.hp2 HG02132.hp2 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.3476+2092_3476+209 others(256): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165634 | |||||
| chr5:165635
|
C | G | 1 | a0015c0077t0053g0181 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3476+2087C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165635 | ||||||
| chr5:165637
|
C | CTGACGGG others(51): Show |
1 | a0008c0024t0021g0175 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3476+2092_3476+209 others(62): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165637 | |||||
| chr5:165637
|
C | G | 17 | a0003c0009t0017g0088a0003c0009t0017g0093a0003c0009t0119g0049others(14): Show | 17 | HG00280.hp2 HG01081.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.3476+2089C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165637 | ||||||
| chr5:165639
|
G | GAC | 3 | a0012c0013t0009g0016a0017c0029t0112g0155a0037c0074t0037g0203 | 3 | NA18522.hp1 NA18973.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3476+2092_3476+209 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165639 | |||||
| chr5:165641
|
T | C | 82 | a0001c0001t0031g0111a0001c0001t0032g0094a0001c0001t0032g0144others(79): Show | 82 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.3476+2093T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165641 | ||||||
| chr5:165641
|
T | G | 3 | a0012c0013t0009g0016a0017c0029t0112g0155a0037c0074t0037g0203 | 3 | NA18522.hp1 NA18973.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3476+2093T>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165641 | ||||||
| chr5:165641
|
T | TGGGGCGG others(193): Show |
1 | a0006c0070t0054g0207 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.3476+2094_3476+209 others(204): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165641 | |||||
| chr5:165643
|
T | G | 94 | a0001c0001t0031g0111a0001c0001t0032g0094a0001c0001t0032g0144others(91): Show | 94 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.3476+2095T>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165643 | ||||||
| chr5:165644
|
G | GGCGGGGC others(23): Show |
1 | a0013c0020t0050g0182 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3476+2100_3476+210 others(34): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165644 | |||||
| chr5:165645
|
G | T | 2 | a0017c0029t0112g0155a0037c0074t0037g0203 | 2 | NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3476+2097G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165645 | ||||||
| chr5:165646
|
C | T | 5 | a0002c0003t0066g0209a0002c0003t0071g0095a0002c0005t0070g0100others(2): Show | 5 | HG00099.hp2 HG01192.hp1 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.3476+2098C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165646 | ||||||
| chr5:165647
|
G | A | 1 | a0003c0004t0089g0014 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.3476+2099G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165647 | ||||||
| chr5:165649
|
A | AGCTCACA others(21): Show |
1 | a0001c0001t0099g0089 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3476+2129_3476+215 others(32): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165649 | |||||
| chr5:165649
|
A | C | 4 | a0002c0005t0003g0031a0004c0006t0123g0003a0004c0054t0034g0139others(1): Show | 4 | HG00673.hp1 HG03579.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.3476+2101A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165649 | ||||||
| chr5:165649
|
A | G | 25 | a0001c0007t0110g0151a0002c0003t0002g0098a0002c0003t0002g0132others(22): Show | 25 | HG00323.hp2 HG00735.hp2 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.3476+2101A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165649 | ||||||
| chr5:165649
|
AGCTCACA others(357): Show |
A | 1 | a0001c0001t0005g0123 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3476+2127_3476+249 others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165649 | |||||
| chr5:165657
|
C | G | 13 | a0002c0039t0009g0030a0003c0009t0017g0088a0003c0009t0017g0093others(10): Show | 13 | HG00323.hp2 HG01243.hp1 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.3476+2109C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165657 | ||||||
| chr5:165661
|
T | C | 5 | a0002c0003t0002g0098a0002c0003t0002g0132a0002c0003t0011g0210others(2): Show | 5 | HG00140.hp2 HG00735.hp2 HG01069.hp1 others(2): Show |
intron_variant | MODIFIER | c.3476+2113T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165661 | ||||||
| chr5:165662
|
G | C | 7 | a0003c0009t0017g0088a0003c0009t0017g0093a0003c0009t0119g0049others(4): Show | 7 | HG01243.hp1 HG01256.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.3476+2114G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165662 | ||||||
| chr5:165665
|
C | G | 11 | a0001c0001t0113g0044a0001c0007t0008g0146a0002c0057t0003g0026others(8): Show | 11 | HG00280.hp2 HG00597.hp2 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.3476+2117C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165665 | ||||||
| chr5:165669
|
C | CAG | 3 | a0001c0007t0008g0146a0002c0057t0003g0026a0004c0006t0002g0119 | 3 | HG01081.hp1 NA19088.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.3476+2121_3476+212 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165669 | ||||||
| chr5:165669
|
C | CGGGGCGG others(221): Show |
1 | a0006c0021t0018g0198 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3476+2128_3476+212 others(232): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165669 | |||||
| chr5:165669
|
C | T | 6 | a0003c0056t0017g0080a0008c0025t0069g0174a0012c0013t0133g0118others(3): Show | 6 | HG00323.hp2 HG02683.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.3476+2121C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165669 | ||||||
| chr5:165674
|
C | T | 3 | a0002c0005t0003g0031a0004c0054t0034g0139a0012c0013t0009g0016 | 3 | HG00673.hp1 NA18970.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.3476+2126C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165674 | ||||||
| chr5:165675
|
G | A | 1 | a0017c0029t0112g0155 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3476+2127G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165675 | ||||||
| chr5:165677
|
G | A | 33 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0007t0109g0147others(30): Show | 33 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.3476+2129G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165677 | ||||||
| chr5:165677
|
G | GGCTCACA others(305): Show |
1 | a0008c0024t0021g0176 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3476+2144_3476+214 others(316): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165677 | |||||
| chr5:165677
|
G | GGCTCACA others(133): Show |
1 | a0006c0068t0058g0194 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3476+2144_3476+214 others(144): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165677 | |||||
| chr5:165685
|
C | CAG | 4 | a0018c0022t0011g0195a0035c0060t0020g0188a0040c0063t0063g0189others(1): Show | 4 | HG00280.hp2 HG01081.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.3476+2137_3476+213 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165685 | ||||||
| chr5:165685
|
C | CTAATGCT others(107): Show |
1 | a0006c0021t0056g0199 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3476+2144_3476+214 others(118): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165685 | |||||
| chr5:165685
|
C | G | 31 | a0001c0001t0031g0111a0001c0001t0102g0057a0001c0001t0113g0044others(28): Show | 31 | HG00140.hp2 HG00597.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.3476+2137C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165685 | ||||||
| chr5:165688
|
A | C | 1 | a0003c0056t0017g0080 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3476+2140A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165688 | ||||||
| chr5:165690
|
G | C | 19 | a0001c0001t0031g0111a0001c0001t0102g0057a0001c0007t0008g0150others(16): Show | 19 | HG00140.hp2 HG00735.hp2 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.3476+2142G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165690 | ||||||
| chr5:165693
|
C | G | 12 | a0001c0007t0109g0147a0002c0039t0009g0030a0003c0009t0017g0088others(9): Show | 12 | HG00280.hp2 HG01081.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.3476+2145C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165693 | ||||||
| chr5:165697
|
C | CAG | 2 | a0002c0039t0009g0030a0008c0079t0068g0173 | 2 | HG01928.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3476+2149_3476+215 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165697 | ||||||
| chr5:165697
|
C | T | 6 | a0004c0041t0003g0077a0006c0068t0058g0194a0008c0025t0069g0174others(3): Show | 6 | HG02622.hp1 HG02647.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.3476+2149C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165697 | ||||||
| chr5:165699
|
G | T | 1 | a0028c0040t0090g0127 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3476+2151G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165699 | ||||||
| chr5:165701
|
GCGGAGCT others(105): Show |
G | 18 | a0002c0003t0124g0017a0002c0003t0128g0029a0002c0003t0130g0130others(15): Show | 18 | HG00639.hp1 HG00639.hp2 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.3476+2157_3476+226 others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165701 | |||||
| chr5:165702
|
C | CGGAGCTC others(165): Show |
1 | a0012c0013t0133g0118 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.3476+2172_3476+217 others(176): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165702 | |||||
| chr5:165702
|
C | T | 4 | a0001c0002t0007g0060a0002c0057t0003g0026a0004c0006t0002g0119others(1): Show | 4 | HG00099.hp1 HG01081.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.3476+2154C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165702 | ||||||
| chr5:165703
|
G | A | 1 | a0010c0014t0055g0201 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3476+2155G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165703 | ||||||
| chr5:165705
|
A | G | 28 | a0001c0001t0031g0111a0001c0001t0032g0094a0001c0001t0032g0144others(25): Show | 28 | HG00099.hp2 HG01192.hp1 HG01928.hp2 others(25): Show |
intron_variant | MODIFIER | c.3476+2157A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165705 | ||||||
| chr5:165713
|
C | CTAATGCT others(51): Show |
1 | a0001c0007t0008g0146 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3476+2184_3476+218 others(62): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165713 | |||||
| chr5:165713
|
C | CTAATGCT others(137): Show |
1 | a0020c0081t0064g0200 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3476+2172_3476+217 others(148): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165713 | |||||
| chr5:165713
|
C | G | 8 | a0001c0007t0100g0025a0001c0007t0109g0147a0002c0039t0009g0030others(5): Show | 8 | HG01928.hp2 HG02257.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.3476+2165C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165713 | ||||||
| chr5:165717
|
T | C | 4 | a0001c0001t0032g0094a0001c0001t0032g0144a0004c0006t0134g0011others(1): Show | 4 | HG02004.hp2 HG02109.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.3476+2169T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165717 | ||||||
| chr5:165718
|
G | C | 1 | a0001c0007t0100g0025 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3476+2170G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165718 | ||||||
| chr5:165721
|
C | G | 5 | a0010c0014t0057g0197a0011c0023t0044g0187a0012c0013t0009g0019others(2): Show | 5 | HG02280.hp1 HG02717.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.3476+2173C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165721 | ||||||
| chr5:165725
|
C | CAG | 3 | a0010c0014t0057g0197a0012c0013t0009g0019a0037c0074t0037g0203 | 3 | NA18522.hp1 NA18979.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.3476+2177_3476+217 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165725 | ||||||
| chr5:165725
|
C | CGGGGCGG others(363): Show |
2 | a0013c0020t0052g0183a0013c0067t0046g0186 | 2 | HG03041.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3476+2192_3476+219 others(374): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165725 | |||||
| chr5:165725
|
C | T | 10 | a0003c0009t0017g0088a0003c0009t0017g0093a0003c0009t0119g0049others(7): Show | 10 | HG00280.hp2 HG01081.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.3476+2177C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165725 | ||||||
| chr5:165729
|
G | A | 1 | a0012c0013t0133g0118 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.3476+2181G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165729 | ||||||
| chr5:165729
|
G | T | 2 | a0010c0014t0057g0197a0037c0074t0037g0203 | 2 | NA18522.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.3476+2181G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165729 | ||||||
| chr5:165729
|
GCGGGGCT others(77): Show |
G | 5 | a0009c0012t0033g0161a0009c0012t0114g0156a0009c0012t0115g0157others(2): Show | 5 | HG01099.hp1 HG02886.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.3476+2261_3476+234 others(88): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165729 | |||||
| chr5:165730
|
C | T | 1 | a0002c0039t0009g0030 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.3476+2182C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165730 | ||||||
| chr5:165733
|
G | A | 27 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(24): Show | 27 | HG00323.hp2 HG00597.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.3476+2185G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165733 | ||||||
| chr5:165736
|
T | TCACACAC others(221): Show |
1 | a0001c0001t0032g0094 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3476+2193_3476+219 others(232): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165736 | |||||
| chr5:165741
|
C | CTAATGCT others(163): Show |
1 | a0001c0001t0032g0144 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3476+2210_3476+221 others(174): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165741 | |||||
| chr5:165741
|
C | G | 12 | a0001c0007t0008g0143a0001c0007t0008g0145a0002c0057t0003g0026others(9): Show | 12 | HG01081.hp1 HG02004.hp2 HG02683.hp1 others(9): Show |
intron_variant | MODIFIER | c.3476+2193C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165741 | ||||||
| chr5:165745
|
T | C | 11 | a0002c0003t0002g0101a0002c0003t0002g0132a0002c0003t0066g0209others(8): Show | 11 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(8): Show |
intron_variant | MODIFIER | c.3476+2197T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165745 | ||||||
| chr5:165745
|
T | TGCTGTGA others(501): Show |
1 | a0008c0025t0045g0172 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3476+2200_3476+220 others(512): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165745 | |||||
| chr5:165746
|
G | C | 4 | a0003c0056t0017g0080a0004c0006t0134g0011a0006c0071t0018g0202others(1): Show | 4 | HG02683.hp1 HG02922.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.3476+2198G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165746 | ||||||
| chr5:165749
|
C | G | 7 | a0004c0041t0003g0077a0011c0023t0041g0184a0012c0013t0009g0016others(4): Show | 7 | HG02451.hp1 HG02622.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.3476+2201C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165749 | ||||||
| chr5:165749
|
CTGACGGG others(130): Show |
C | 1 | a0019c0019t0062g0191 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.3476+2202_3476+233 others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165749 | ||||||
| chr5:165753
|
C | CAG | 4 | a0011c0023t0041g0184a0012c0013t0009g0016a0024c0042t0006g0012others(1): Show | 4 | HG02622.hp1 HG02735.hp2 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.3476+2205_3476+220 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165753 | ||||||
| chr5:165753
|
C | CGGGGCGG others(23): Show |
1 | a0006c0068t0058g0194 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3476+2212_3476+221 others(34): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165753 | |||||
| chr5:165753
|
C | CGGGGCGG others(135): Show |
1 | a0015c0076t0067g0192 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3476+2220_3476+222 others(146): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165753 | |||||
| chr5:165753
|
C | T | 11 | a0001c0007t0100g0025a0003c0009t0017g0088a0003c0009t0017g0093others(8): Show | 11 | HG00280.hp2 HG00323.hp2 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.3476+2205C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165753 | ||||||
| chr5:165757
|
G | T | 1 | a0030c0047t0131g0067 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3476+2209G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165757 | ||||||
| chr5:165757
|
GCGGGGCT others(49): Show |
G | 3 | a0002c0005t0003g0031a0004c0006t0123g0003a0004c0054t0034g0139 | 3 | HG00673.hp1 HG04115.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.3476+2221_3476+227 others(60): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165757 | |||||
| chr5:165758
|
C | T | 2 | a0013c0020t0052g0183a0013c0067t0046g0186 | 2 | HG03041.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3476+2210C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165758 | ||||||
| chr5:165761
|
G | A | 12 | a0001c0001t0113g0044a0002c0057t0003g0026a0003c0056t0017g0080others(9): Show | 12 | HG00597.hp2 HG00735.hp1 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.3476+2213G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165761 | ||||||
| chr5:165761
|
GGCTCACA others(105): Show |
G | 2 | a0002c0003t0002g0098a0002c0003t0011g0210 | 2 | HG01069.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.3476+2221_3476+233 others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165761 | |||||
| chr5:165769
|
G | C | 23 | a0001c0001t0032g0144a0001c0001t0113g0044a0001c0007t0109g0147others(20): Show | 23 | HG00597.hp2 HG00735.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.3476+2221G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165769 | ||||||
| chr5:165769
|
G | GTAATGCT others(51): Show |
1 | a0006c0073t0020g0193 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3476+2225_3476+222 others(62): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165769 | |||||
| chr5:165771
|
AATC | A | 2 | a0040c0063t0063g0189a0041c0064t0010g0190 | 2 | HG00280.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.3476+2224_3476+222 others(7): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165771 | ||||||
| chr5:165772
|
A | C | 10 | a0003c0009t0017g0088a0003c0009t0017g0093a0003c0009t0119g0049others(7): Show | 10 | HG00323.hp2 HG01243.hp1 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.3476+2224A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165772 | ||||||
| chr5:165773
|
T | C | 1 | a0006c0070t0054g0207 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.3476+2225T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165773 | ||||||
| chr5:165774
|
C | CCTCTGAC others(77): Show |
1 | a0022c0046t0047g0180 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3476+2238_3476+223 others(88): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165774 | |||||
| chr5:165774
|
C | CCTCTGAT others(79): Show |
1 | a0001c0007t0110g0151 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3476+2232_3476+223 others(90): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165774 | |||||
| chr5:165774
|
C | G | 40 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(37): Show | 40 | HG00597.hp2 HG00735.hp1 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.3476+2226C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165774 | ||||||
| chr5:165777
|
C | G | 5 | a0001c0001t0113g0044a0016c0018t0034g0004a0018c0022t0011g0196others(2): Show | 5 | HG00597.hp2 HG00735.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.3476+2229C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165777 | ||||||
| chr5:165779
|
G | C | 2 | a0003c0004t0116g0103a0003c0004t0117g0070 | 2 | HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3476+2231G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165779 | ||||||
| chr5:165781
|
C | CAG | 3 | a0001c0001t0113g0044a0016c0018t0034g0004a0018c0022t0011g0196 | 3 | HG00597.hp2 HG00735.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.3476+2233_3476+223 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165781 | ||||||
| chr5:165781
|
C | T | 3 | a0012c0013t0009g0019a0015c0077t0053g0181a0039c0062t0010g0165 | 3 | HG02717.hp2 HG04204.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.3476+2233C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165781 | ||||||
| chr5:165786
|
C | T | 1 | a0024c0042t0006g0012 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3476+2238C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165786 | ||||||
| chr5:165787
|
G | A | 1 | a0030c0047t0131g0067 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3476+2239G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165787 | ||||||
| chr5:165787
|
G | GGAGCTCA others(77): Show |
1 | a0010c0014t0055g0201 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3476+2260_3476+226 others(88): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165787 | |||||
| chr5:165789
|
A | C | 1 | a0012c0013t0133g0118 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.3476+2241A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165789 | ||||||
| chr5:165789
|
A | G | 8 | a0001c0001t0113g0044a0006c0021t0018g0198a0010c0014t0019g0205others(5): Show | 8 | HG00597.hp2 HG00735.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.3476+2241A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165789 | ||||||
| chr5:165797
|
C | CACTAATG others(109): Show |
1 | a0006c0070t0054g0207 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.3476+2249_3476+225 others(120): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165797 | ||||||
| chr5:165797
|
C | CTAATGCT others(51): Show |
1 | a0008c0079t0068g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3476+2260_3476+226 others(62): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165797 | |||||
| chr5:165797
|
C | G | 4 | a0001c0001t0113g0044a0016c0018t0034g0004a0018c0022t0011g0196others(1): Show | 4 | HG00597.hp2 HG00735.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.3476+2249C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165797 | ||||||
| chr5:165801
|
T | C | 1 | a0018c0022t0011g0195 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.3476+2253T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165801 | ||||||
| chr5:165802
|
GCTCTGAT others(49): Show |
G | 1 | a0019c0019t0010g0164 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.3476+2261_3476+231 others(60): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165802 | |||||
| chr5:165802
|
GCTCTGAT others(497): Show |
G | 3 | a0014c0027t0049g0171a0014c0066t0051g0170a0021c0026t0060g0169 | 3 | HG02809.hp1 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3476+2261_3476+276 others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165802 | |||||
| chr5:165803
|
CTCTGATG others(693): Show |
C | 1 | a0001c0007t0008g0150 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3476+2261_3477-283 others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165803 | |||||
| chr5:165805
|
C | G | 2 | a0012c0013t0133g0118a0022c0046t0047g0180 | 2 | HG02818.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.3476+2257C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165805 | ||||||
| chr5:165809
|
T | C | 68 | a0001c0001t0012g0069a0001c0001t0031g0111a0001c0001t0032g0144others(65): Show | 68 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.3476+2261T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165809 | ||||||
| chr5:165809
|
T | TGGGGCGG others(49): Show |
1 | a0010c0014t0057g0197 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.3476+2264_3476+226 others(60): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165809 | |||||
| chr5:165809
|
T | TGGGGCGG others(79): Show |
1 | a0006c0068t0058g0194 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3476+2264_3476+226 others(90): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165809 | |||||
| chr5:165813
|
A | G | 72 | a0001c0001t0031g0111a0001c0001t0032g0094a0001c0001t0032g0144others(69): Show | 72 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.3476+2265A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165813 | ||||||
| chr5:165814
|
C | T | 2 | a0016c0018t0034g0004a0017c0029t0112g0155 | 2 | HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3476+2266C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165814 | ||||||
| chr5:165815
|
G | GGAGCTCA others(195): Show |
1 | a0011c0023t0041g0184 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3476+2268_3476+226 others(206): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165815 | |||||
| chr5:165817
|
G | A | 26 | a0001c0001t0032g0094a0001c0001t0113g0044a0001c0007t0008g0146others(23): Show | 26 | HG00597.hp2 HG00735.hp1 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.3476+2269G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165817 | ||||||
| chr5:165825
|
C | G | 15 | a0001c0001t0032g0144a0001c0007t0109g0147a0003c0009t0017g0088others(12): Show | 15 | HG00280.hp2 HG01081.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.3476+2277C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165825 | ||||||
| chr5:165829
|
T | C | 29 | a0001c0007t0008g0146a0002c0003t0066g0209a0002c0003t0071g0095others(26): Show | 29 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.3476+2281T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165829 | ||||||
| chr5:165830
|
G | C | 8 | a0003c0009t0017g0088a0003c0009t0017g0093a0003c0009t0119g0049others(5): Show | 8 | HG00280.hp2 HG01081.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.3476+2282G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165830 | ||||||
| chr5:165833
|
C | G | 6 | a0002c0057t0003g0026a0004c0006t0002g0119a0011c0023t0044g0187others(3): Show | 6 | HG01081.hp1 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.3476+2285C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165833 | ||||||
| chr5:165837
|
C | CAG | 3 | a0002c0057t0003g0026a0012c0013t0009g0019a0015c0077t0053g0181 | 3 | HG02717.hp2 NA18979.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.3476+2289_3476+229 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165837 | ||||||
| chr5:165837
|
C | CGGGGCGG others(195): Show |
1 | a0012c0013t0009g0016 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.3476+2296_3476+229 others(206): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165837 | |||||
| chr5:165837
|
C | T | 10 | a0001c0001t0079g0059a0003c0009t0017g0088a0003c0009t0017g0093others(7): Show | 10 | HG00280.hp2 HG01081.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.3476+2289C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165837 | ||||||
| chr5:165841
|
G | T | 1 | a0002c0057t0003g0026 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.3476+2293G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165841 | ||||||
| chr5:165842
|
C | A | 1 | a0022c0046t0047g0180 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3476+2294C>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165842 | ||||||
| chr5:165842
|
C | T | 1 | a0030c0047t0131g0067 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3476+2294C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165842 | ||||||
| chr5:165843
|
G | A | 2 | a0004c0006t0002g0119a0016c0018t0034g0004 | 2 | HG01081.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.3476+2295G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165843 | ||||||
| chr5:165845
|
G | A | 26 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0007t0008g0143others(23): Show | 26 | HG00280.hp2 HG01081.hp1 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.3476+2297G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165845 | ||||||
| chr5:165845
|
GGCTCACA others(21): Show |
G | 1 | a0002c0003t0002g0101 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.3476+2305_3476+233 others(32): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165845 | |||||
| chr5:165848
|
T | TCACACTA others(337): Show |
1 | a0008c0025t0069g0174 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3476+2304_3476+230 others(348): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165848 | |||||
| chr5:165853
|
G | C | 33 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0007t0008g0143others(30): Show | 33 | HG00140.hp2 HG00280.hp2 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.3476+2305G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165853 | ||||||
| chr5:165853
|
G | GTAATGCT others(23): Show |
1 | a0006c0073t0020g0193 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3476+2309_3476+231 others(34): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165853 | |||||
| chr5:165856
|
A | C | 3 | a0003c0056t0017g0080a0010c0014t0055g0201a0030c0047t0131g0067 | 3 | HG02451.hp2 HG02683.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.3476+2308A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165856 | ||||||
| chr5:165857
|
T | C | 2 | a0001c0007t0008g0146a0039c0062t0010g0165 | 2 | HG04204.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.3476+2309T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165857 | ||||||
| chr5:165858
|
C | CCTCTGAC others(21): Show |
6 | a0001c0001t0031g0111a0001c0001t0102g0057a0003c0004t0028g0058others(3): Show | 6 | HG01952.hp2 HG02132.hp2 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.3476+2353_3476+238 others(32): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165858 | |||||
| chr5:165858
|
C | CCTCTGAC others(21): Show |
1 | a0015c0076t0067g0192 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3476+2324_3476+232 others(32): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165858 | |||||
| chr5:165858
|
C | G | 51 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(48): Show | 51 | HG00140.hp2 HG00280.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.3476+2310C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165858 | ||||||
| chr5:165858
|
CCTCTGAC others(21): Show |
C | 4 | a0001c0016t0005g0160a0001c0016t0025g0152a0001c0035t0030g0137others(1): Show | 4 | HG02717.hp1 HG02922.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.3476+2353_3476+238 others(32): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165858 | |||||
| chr5:165861
|
C | G | 7 | a0001c0001t0032g0094a0002c0039t0009g0030a0002c0057t0003g0026others(4): Show | 7 | HG01928.hp2 HG02486.hp1 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.3476+2313C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165861 | ||||||
| chr5:165865
|
C | CAG | 3 | a0002c0039t0009g0030a0004c0041t0003g0077a0006c0021t0056g0199 | 3 | HG01928.hp2 HG03017.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.3476+2317_3476+231 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165865 | ||||||
| chr5:165865
|
C | T | 6 | a0001c0001t0032g0144a0002c0003t0002g0132a0002c0005t0129g0043others(3): Show | 6 | HG00140.hp2 HG00735.hp2 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.3476+2317C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165865 | ||||||
| chr5:165869
|
G | T | 1 | a0002c0039t0009g0030 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.3476+2321G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165869 | ||||||
| chr5:165870
|
C | T | 1 | a0012c0013t0009g0019 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.3476+2322C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165870 | ||||||
| chr5:165871
|
G | A | 3 | a0002c0057t0003g0026a0008c0025t0069g0174a0037c0074t0037g0203 | 3 | NA18522.hp1 NA19043.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.3476+2323G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165871 | ||||||
| chr5:165871
|
G | GGAGCTCA others(281): Show |
1 | a0006c0070t0054g0207 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.3476+2344_3476+234 others(292): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165871 | |||||
| chr5:165871
|
G | GGAGCTCA others(369): Show |
1 | a0020c0081t0064g0200 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3476+2340_3476+234 others(380): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165871 | |||||
| chr5:165873
|
A | AGCTCACA others(23): Show |
1 | a0004c0006t0134g0011 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3476+2333_3476+233 others(34): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165873 | |||||
| chr5:165873
|
A | C | 1 | a0030c0047t0131g0067 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3476+2325A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165873 | ||||||
| chr5:165873
|
A | G | 14 | a0001c0001t0032g0094a0004c0006t0002g0119a0004c0041t0003g0077others(11): Show | 14 | HG00323.hp2 HG01081.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.3476+2325A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165873 | ||||||
| chr5:165876
|
T | TCACACAC others(165): Show |
1 | a0001c0007t0008g0146 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3476+2333_3476+233 others(176): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165876 | |||||
| chr5:165881
|
C | CTAATGCT others(141): Show |
1 | a0011c0023t0041g0184 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3476+2340_3476+234 others(152): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165881 | |||||
| chr5:165881
|
C | G | 5 | a0001c0001t0032g0094a0004c0041t0003g0077a0006c0021t0056g0199others(2): Show | 5 | HG00323.hp2 HG03017.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.3476+2333C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165881 | ||||||
| chr5:165884
|
A | C | 2 | a0019c0019t0010g0164a0039c0062t0010g0165 | 2 | HG00323.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.3476+2336A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165884 | ||||||
| chr5:165885
|
T | C | 1 | a0016c0018t0003g0005 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3476+2337T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165885 | ||||||
| chr5:165886
|
G | C | 2 | a0019c0019t0010g0164a0039c0062t0010g0165 | 2 | HG00323.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.3476+2338G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165886 | ||||||
| chr5:165886
|
G | GCTCTGAT others(49): Show |
1 | a0028c0040t0090g0127 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3476+2344_3476+234 others(60): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165886 | |||||
| chr5:165886
|
GCTCTGAC others(49): Show |
G | 1 | a0002c0003t0002g0132 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.3476+2409_3476+246 others(60): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165886 | |||||
| chr5:165889
|
C | G | 3 | a0002c0039t0009g0030a0012c0013t0009g0016a0037c0074t0037g0203 | 3 | HG01928.hp2 NA18522.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.3476+2341C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165889 | ||||||
| chr5:165893
|
C | T | 5 | a0002c0003t0002g0098a0002c0003t0002g0101a0002c0003t0011g0210others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.3476+2345C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165893 | ||||||
| chr5:165897
|
GCGGAGCT others(217): Show |
G | 1 | a0002c0005t0129g0043 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.3476+2353_3476+257 others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165897 | |||||
| chr5:165898
|
C | CGGAGCTC others(163): Show |
1 | a0012c0013t0133g0118 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.3476+2368_3476+236 others(174): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165898 | |||||
| chr5:165898
|
C | T | 3 | a0004c0006t0002g0119a0004c0041t0003g0077a0030c0047t0131g0067 | 3 | HG01081.hp1 HG03017.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.3476+2350C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165898 | ||||||
| chr5:165899
|
G | A | 1 | a0002c0039t0009g0030 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.3476+2351G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165899 | ||||||
| chr5:165901
|
A | G | 41 | a0001c0007t0109g0147a0002c0003t0066g0209a0002c0003t0071g0095others(38): Show | 41 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.3476+2353A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165901 | ||||||
| chr5:165905
|
C | CACACTAA others(217): Show |
2 | a0017c0030t0039g0140a0032c0058t0040g0158 | 2 | HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.3476+2436_3476+243 others(228): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165905 | |||||
| chr5:165909
|
C | G | 4 | a0004c0006t0002g0119a0012c0013t0009g0016a0012c0013t0009g0019others(1): Show | 4 | HG01081.hp1 HG02145.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.3476+2361C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165909 | ||||||
| chr5:165912
|
A | C | 1 | a0004c0006t0002g0119 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3476+2364A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165912 | ||||||
| chr5:165913
|
T | C | 34 | a0002c0003t0124g0017a0002c0003t0128g0029a0002c0003t0130g0130others(31): Show | 34 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.3476+2365T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165913 | ||||||
| chr5:165913
|
T | TGCTCTGA others(475): Show |
1 | a0013c0020t0050g0182 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3476+2380_3476+238 others(486): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165913 | |||||
| chr5:165914
|
G | C | 2 | a0004c0006t0002g0119a0016c0018t0003g0005 | 2 | HG01081.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.3476+2366G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165914 | ||||||
| chr5:165914
|
G | GCTCTGAC others(49): Show |
1 | a0010c0014t0055g0201 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3476+2380_3476+238 others(60): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165914 | |||||
| chr5:165914
|
GCTCTGAC others(245): Show |
G | 1 | a0030c0047t0131g0067 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3476+2381_3476+263 others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165914 | |||||
| chr5:165917
|
C | G | 8 | a0001c0001t0032g0144a0001c0007t0008g0146a0006c0021t0018g0198others(5): Show | 8 | HG01261.hp2 HG02109.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.3476+2369C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165917 | ||||||
| chr5:165921
|
C | CAG | 6 | a0006c0021t0018g0198a0006c0068t0058g0194a0006c0073t0020g0193others(3): Show | 6 | HG01261.hp2 HG02647.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.3476+2373_3476+237 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165921 | ||||||
| chr5:165921
|
C | CGGGGCGG others(81): Show |
1 | a0012c0013t0009g0019 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.3476+2380_3476+238 others(92): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165921 | |||||
| chr5:165921
|
C | CGGGGCGG others(79): Show |
1 | a0022c0046t0047g0180 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3476+2388_3476+238 others(90): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165921 | |||||
| chr5:165921
|
C | CGGGGCGG others(107): Show |
2 | a0008c0024t0021g0175a0008c0024t0021g0176 | 2 | HG02109.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.3476+2388_3476+238 others(118): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165921 | |||||
| chr5:165921
|
C | T | 9 | a0001c0001t0093g0105a0003c0009t0017g0088a0003c0009t0017g0093others(6): Show | 9 | HG00280.hp2 HG01081.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.3476+2373C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165921 | ||||||
| chr5:165925
|
G | T | 1 | a0024c0042t0006g0012 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3476+2377G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165925 | ||||||
| chr5:165925
|
GCGGGGCT others(189): Show |
G | 3 | a0002c0003t0002g0098a0002c0003t0002g0101a0002c0003t0011g0210 | 3 | HG01069.hp1 HG01071.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.3476+2389_3476+258 others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165925 | |||||
| chr5:165926
|
C | T | 2 | a0002c0057t0003g0026a0015c0077t0053g0181 | 2 | HG02717.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.3476+2378C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165926 | ||||||
| chr5:165927
|
G | A | 2 | a0010c0014t0019g0205a0010c0069t0019g0204 | 2 | HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.3476+2379G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165927 | ||||||
| chr5:165929
|
G | A | 8 | a0001c0007t0109g0147a0008c0025t0045g0172a0010c0014t0019g0205others(5): Show | 8 | HG02145.hp1 HG02258.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.3476+2381G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165929 | ||||||
| chr5:165929
|
G | C | 1 | a0004c0006t0002g0119 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3476+2381G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165929 | ||||||
| chr5:165929
|
G | GGCTCACA others(165): Show |
1 | a0001c0001t0113g0044 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.3476+2388_3476+238 others(176): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165929 | |||||
| chr5:165929
|
G | GGCTCACA others(137): Show |
1 | a0018c0022t0011g0196 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3476+2388_3476+238 others(148): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165929 | |||||
| chr5:165932
|
T | TCACACTA others(25): Show |
1 | a0016c0018t0034g0004 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3476+2388_3476+238 others(36): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165932 | |||||
| chr5:165937
|
G | C | 19 | a0001c0001t0113g0044a0001c0007t0109g0147a0002c0003t0066g0209others(16): Show | 19 | HG00099.hp2 HG00597.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.3476+2389G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165937 | ||||||
| chr5:165940
|
A | C | 18 | a0001c0002t0007g0060a0002c0057t0003g0026a0003c0009t0017g0088others(15): Show | 18 | HG00099.hp1 HG00280.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.3476+2392A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165940 | ||||||
| chr5:165942
|
C | CCTCTGAC others(609): Show |
3 | a0003c0004t0016g0078a0003c0004t0016g0133a0003c0017t0016g0110 | 3 | NA18979.hp2 NA19066.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.3477-2796_3477-279 others(620): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165942 | |||||
| chr5:165942
|
C | CCTCTGAT others(871): Show |
2 | a0001c0007t0008g0143a0001c0007t0008g0145 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3476+2400_3476+240 others(882): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165942 | |||||
| chr5:165942
|
C | CCTCTGAT others(645): Show |
1 | a0001c0007t0110g0151 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3476+2400_3476+240 others(656): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165942 | |||||
| chr5:165942
|
C | CTTCTGAC others(49): Show |
6 | a0001c0001t0031g0111a0001c0001t0102g0057a0003c0004t0028g0058others(3): Show | 6 | HG01952.hp2 HG02132.hp2 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.3476+2394_3476+239 others(60): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165942 | ||||||
| chr5:165942
|
C | G | 34 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(31): Show | 34 | HG00099.hp2 HG00597.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.3476+2394C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165942 | ||||||
| chr5:165945
|
C | G | 4 | a0011c0023t0044g0187a0015c0077t0053g0181a0016c0018t0034g0004others(1): Show | 4 | HG02280.hp1 HG02717.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.3476+2397C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165945 | ||||||
| chr5:165949
|
C | CGGGGCGG others(107): Show |
1 | a0001c0007t0109g0147 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3476+2436_3476+243 others(118): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165949 | |||||
| chr5:165949
|
C | T | 4 | a0002c0003t0066g0209a0002c0003t0071g0095a0002c0005t0070g0100others(1): Show | 4 | HG00099.hp2 HG01192.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.3476+2401C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165949 | ||||||
| chr5:165954
|
C | T | 4 | a0001c0001t0113g0044a0002c0039t0009g0030a0004c0006t0002g0119others(1): Show | 4 | HG00597.hp2 HG00735.hp1 HG01081.hp1 others(1): Show |
intron_variant | MODIFIER | c.3476+2406C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165954 | ||||||
| chr5:165955
|
G | A | 2 | a0016c0018t0034g0004a0024c0042t0006g0012 | 2 | HG02735.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.3476+2407G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165955 | ||||||
| chr5:165957
|
A | AGCTCACA others(105): Show |
2 | a0001c0001t0097g0086a0001c0001t0104g0023 | 2 | HG00323.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.3476+2436_3476+243 others(116): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165957 | |||||
| chr5:165957
|
A | AGCTCACA others(137): Show |
1 | a0012c0013t0133g0118 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.3476+2424_3476+242 others(148): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165957 | |||||
| chr5:165957
|
A | C | 1 | a0002c0057t0003g0026 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.3476+2409A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165957 | ||||||
| chr5:165957
|
A | G | 12 | a0002c0003t0002g0132a0002c0039t0009g0030a0003c0056t0017g0080others(9): Show | 12 | HG00735.hp2 HG01928.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.3476+2409A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165957 | ||||||
| chr5:165957
|
AGCTCACA others(77): Show |
A | 1 | a0003c0004t0117g0070 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3476+2465_3476+254 others(88): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165957 | |||||
| chr5:165965
|
C | G | 2 | a0002c0039t0009g0030a0015c0077t0053g0181 | 2 | HG01928.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.3476+2417C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165965 | ||||||
| chr5:165968
|
A | C | 1 | a0002c0039t0009g0030 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.3476+2420A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165968 | ||||||
| chr5:165969
|
T | C | 3 | a0008c0025t0045g0172a0016c0018t0003g0005a0018c0022t0011g0195 | 3 | HG02145.hp1 HG02486.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.3476+2421T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165969 | ||||||
| chr5:165970
|
G | C | 1 | a0002c0039t0009g0030 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.3476+2422G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165970 | ||||||
| chr5:165970
|
GCTCTGAC others(21): Show |
G | 4 | a0003c0009t0017g0088a0003c0009t0017g0093a0003c0009t0119g0049others(1): Show | 4 | HG01243.hp1 HG01256.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.3476+2445_3476+247 others(32): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165970 | |||||
| chr5:165970
|
GCTCTGAC others(105): Show |
G | 2 | a0003c0056t0017g0080a0036c0075t0061g0178 | 2 | HG02683.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3476+2437_3476+254 others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165970 | |||||
| chr5:165971
|
CTCTGACG others(525): Show |
C | 1 | a0006c0071t0018g0202 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3476+2437_3477-282 others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165971 | |||||
| chr5:165973
|
C | G | 2 | a0010c0014t0055g0201a0012c0013t0009g0019 | 2 | HG02451.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.3476+2425C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165973 | ||||||
| chr5:165977
|
C | T | 3 | a0011c0023t0041g0184a0016c0018t0034g0004a0024c0042t0006g0012 | 3 | HG02622.hp1 HG02735.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.3476+2429C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165977 | ||||||
| chr5:165981
|
G | A | 1 | a0011c0023t0041g0184 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3476+2433G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165981 | ||||||
| chr5:165982
|
C | CGGAGCTC others(137): Show |
1 | a0004c0041t0003g0077 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3476+2436_3476+243 others(148): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165982 | |||||
| chr5:165982
|
C | T | 3 | a0002c0057t0003g0026a0006c0070t0054g0207a0008c0025t0069g0174 | 3 | HG02896.hp2 NA19043.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.3476+2434C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165982 | ||||||
| chr5:165983
|
GGGGCTCA others(49): Show |
G | 15 | a0002c0003t0124g0017a0002c0003t0128g0029a0002c0003t0135g0128others(12): Show | 15 | HG00639.hp2 HG00673.hp1 HG00733.hp1 others(12): Show |
intron_variant | MODIFIER | c.3476+2445_3476+250 others(60): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165983 | |||||
| chr5:165985
|
G | A | 18 | a0001c0001t0113g0044a0001c0007t0008g0143a0001c0007t0008g0145others(15): Show | 18 | HG00597.hp2 HG00735.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.3476+2437G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165985 | ||||||
| chr5:165985
|
G | C | 1 | a0002c0039t0009g0030 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.3476+2437G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165985 | ||||||
| chr5:165985
|
G | GGCTCACA others(105): Show |
1 | a0006c0021t0056g0199 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3476+2444_3476+244 others(116): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165985 | |||||
| chr5:165993
|
G | C | 38 | a0001c0001t0113g0044a0001c0007t0008g0143a0001c0007t0008g0145others(35): Show | 38 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.3476+2445G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165993 | ||||||
| chr5:165993
|
G | GTAATGCT others(333): Show |
1 | a0001c0001t0032g0144 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3476+2449_3476+245 others(344): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165993 | |||||
| chr5:165993
|
G | GTAATGCT others(361): Show |
1 | a0006c0068t0058g0194 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3476+2449_3476+245 others(372): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165993 | |||||
| chr5:165996
|
A | ATGCTCTG others(193): Show |
1 | a0001c0001t0032g0094 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3476+2449_3476+245 others(204): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165996 | |||||
| chr5:165996
|
A | C | 6 | a0004c0041t0003g0077a0010c0014t0019g0205a0010c0069t0019g0204others(3): Show | 6 | HG00280.hp2 HG01081.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.3476+2448A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165996 | ||||||
| chr5:165997
|
T | C | 1 | a0004c0006t0134g0011 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3476+2449T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165997 | ||||||
| chr5:165998
|
C | G | 48 | a0001c0001t0032g0144a0001c0001t0113g0044a0001c0007t0008g0143others(45): Show | 48 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.3476+2450C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165998 | ||||||
| chr5:165998
|
CCTCTGAC others(553): Show |
C | 1 | a0001c0001t0028g0046 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3476+2484_3477-274 others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 165998 | |||||
| chr5:165999
|
C | T | 5 | a0001c0016t0005g0160a0001c0016t0025g0152a0001c0035t0030g0137others(2): Show | 5 | HG02717.hp1 HG02922.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.3476+2451C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 165999 | ||||||
| chr5:166001
|
C | G | 1 | a0011c0023t0041g0184 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3476+2453C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166001 | ||||||
| chr5:166005
|
C | CGGGGCGG others(21): Show |
1 | a0006c0073t0020g0193 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3476+2464_3476+246 others(32): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166005 | |||||
| chr5:166005
|
C | T | 3 | a0008c0024t0021g0175a0008c0024t0021g0176a0011c0023t0044g0187 | 3 | HG02109.hp2 HG02145.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.3476+2457C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166005 | ||||||
| chr5:166010
|
C | T | 4 | a0002c0003t0002g0132a0002c0039t0009g0030a0016c0018t0034g0004others(1): Show | 4 | HG00735.hp2 HG01928.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.3476+2462C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166010 | ||||||
| chr5:166011
|
G | A | 1 | a0011c0023t0041g0184 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3476+2463G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166011 | ||||||
| chr5:166013
|
G | A | 33 | a0001c0001t0032g0094a0001c0007t0008g0146a0001c0007t0109g0147others(30): Show | 33 | HG00280.hp2 HG01081.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.3476+2465G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166013 | ||||||
| chr5:166013
|
G | AGCTCACA others(277): Show |
1 | a0010c0014t0057g0197 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.3476+2464_3476+246 others(288): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166013 | ||||||
| chr5:166013
|
G | C | 1 | a0004c0041t0003g0077 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3476+2465G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166013 | ||||||
| chr5:166021
|
C | G | 7 | a0002c0003t0066g0209a0002c0003t0071g0095a0002c0005t0072g0153others(4): Show | 7 | HG00099.hp2 HG02735.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.3476+2473C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166021 | ||||||
| chr5:166024
|
A | C | 2 | a0016c0018t0034g0004a0024c0042t0006g0012 | 2 | HG02735.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.3476+2476A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166024 | ||||||
| chr5:166025
|
T | C | 9 | a0003c0009t0017g0088a0003c0009t0017g0093a0003c0009t0119g0049others(6): Show | 9 | HG01243.hp1 HG01256.hp1 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.3476+2477T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166025 | ||||||
| chr5:166026
|
G | C | 6 | a0002c0003t0066g0209a0002c0003t0071g0095a0002c0005t0072g0153others(3): Show | 6 | HG00099.hp2 HG02735.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.3476+2478G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166026 | ||||||
| chr5:166026
|
G | GCTCTGAC others(49): Show |
1 | a0022c0046t0047g0180 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3476+2490_3476+249 others(60): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166026 | |||||
| chr5:166026
|
G | GCTGTGAC others(109): Show |
1 | a0015c0077t0053g0181 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3476+2480_3476+248 others(120): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166026 | |||||
| chr5:166029
|
C | G | 2 | a0015c0076t0067g0192a0019c0019t0010g0164 | 2 | HG00323.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.3476+2481C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166029 | ||||||
| chr5:166033
|
C | T | 14 | a0002c0003t0130g0130a0002c0003t0132g0028a0002c0005t0003g0167others(11): Show | 14 | HG00639.hp1 HG01123.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.3476+2485C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166033 | ||||||
| chr5:166037
|
GCAGGGCT others(77): Show |
G | 3 | a0002c0003t0066g0209a0002c0003t0071g0095a0002c0005t0072g0153 | 3 | HG00099.hp2 NA18971.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.3476+2491_3476+257 others(88): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166037 | |||||
| chr5:166038
|
C | T | 1 | a0004c0041t0003g0077 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3476+2490C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166038 | ||||||
| chr5:166039
|
A | G | 66 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(63): Show | 66 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.3476+2491A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166039 | ||||||
| chr5:166039
|
AGGGCTCA others(21): Show |
A | 1 | a0001c0001t0092g0054 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3476+2501_3476+252 others(32): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166039 | |||||
| chr5:166039
|
AGGGCTCA others(77): Show |
A | 2 | a0003c0004t0116g0103a0025c0045t0122g0002 | 2 | HG03540.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.3476+2573_3476+265 others(88): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166039 | |||||
| chr5:166041
|
G | A | 19 | a0001c0001t0032g0094a0001c0007t0109g0147a0002c0003t0002g0132others(16): Show | 19 | HG00639.hp1 HG00735.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.3476+2493G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166041 | ||||||
| chr5:166041
|
G | C | 4 | a0012c0013t0009g0016a0012c0013t0133g0118a0016c0018t0034g0004others(1): Show | 4 | HG02735.hp2 HG03579.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.3476+2493G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166041 | ||||||
| chr5:166049
|
C | G | 18 | a0001c0007t0008g0146a0001c0036t0077g0149a0001c0051t0078g0148others(15): Show | 18 | HG00280.hp2 HG00323.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.3476+2501C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166049 | ||||||
| chr5:166052
|
A | C | 4 | a0003c0009t0017g0088a0003c0009t0017g0093a0003c0009t0119g0049others(1): Show | 4 | HG01243.hp1 HG01256.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.3476+2504A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166052 | ||||||
| chr5:166053
|
T | C | 8 | a0001c0001t0032g0144a0001c0001t0113g0044a0001c0007t0008g0143others(5): Show | 8 | HG00597.hp2 HG00735.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.3476+2505T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166053 | ||||||
| chr5:166054
|
G | C | 15 | a0001c0036t0077g0149a0001c0051t0078g0148a0003c0009t0017g0088others(12): Show | 15 | HG00280.hp2 HG00323.hp2 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.3476+2506G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166054 | ||||||
| chr5:166054
|
GCTCTGAC others(161): Show |
G | 1 | a0002c0003t0002g0132 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.3476+2529_3476+269 others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166054 | |||||
| chr5:166057
|
C | CTGACGGG others(77): Show |
1 | a0012c0013t0009g0019 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.3476+2520_3476+252 others(88): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166057 | |||||
| chr5:166057
|
C | G | 4 | a0011c0023t0044g0187a0012c0013t0009g0016a0012c0013t0133g0118others(1): Show | 4 | HG02280.hp1 NA18522.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.3476+2509C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166057 | ||||||
| chr5:166061
|
C | CGGGGCGG others(79): Show |
1 | a0015c0076t0067g0192 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3476+2520_3476+252 others(90): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166061 | |||||
| chr5:166065
|
GCGGGGCT others(49): Show |
G | 2 | a0002c0057t0003g0026a0004c0006t0002g0051 | 2 | HG01515.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.3476+2529_3476+258 others(60): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166065 | |||||
| chr5:166066
|
C | T | 4 | a0015c0077t0053g0181a0016c0018t0003g0005a0016c0018t0034g0004others(1): Show | 4 | HG02145.hp1 HG02717.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.3476+2518C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166066 | ||||||
| chr5:166069
|
G | A | 18 | a0001c0001t0032g0094a0001c0007t0109g0147a0004c0041t0003g0077others(15): Show | 18 | HG00280.hp2 HG01081.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.3476+2521G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166069 | ||||||
| chr5:166069
|
G | GGCTCACA others(137): Show |
1 | a0008c0079t0068g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3476+2528_3476+252 others(148): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166069 | |||||
| chr5:166069
|
G | GGCTCACA others(193): Show |
1 | a0011c0023t0041g0184 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3476+2528_3476+252 others(204): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166069 | |||||
| chr5:166074
|
A | ACACTAAC others(19): Show |
1 | a0006c0073t0020g0193 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3476+2528_3476+252 others(30): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166074 | |||||
| chr5:166077
|
G | C | 59 | a0001c0001t0032g0094a0001c0007t0109g0147a0001c0036t0077g0149others(56): Show | 59 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.3476+2529G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166077 | ||||||
| chr5:166081
|
T | C | 7 | a0006c0068t0058g0194a0006c0070t0054g0207a0008c0024t0021g0175others(4): Show | 7 | HG02109.hp2 HG02145.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.3476+2533T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166081 | ||||||
| chr5:166082
|
C | G | 67 | a0001c0001t0032g0094a0001c0007t0008g0146a0001c0007t0109g0147others(64): Show | 67 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.3476+2534C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166082 | ||||||
| chr5:166085
|
C | G | 10 | a0003c0009t0017g0088a0003c0009t0017g0093a0003c0009t0119g0049others(7): Show | 10 | HG00323.hp2 HG01175.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.3476+2537C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166085 | ||||||
| chr5:166089
|
C | T | 18 | a0002c0003t0124g0017a0002c0003t0128g0029a0002c0003t0135g0128others(15): Show | 18 | HG00639.hp2 HG00673.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.3476+2541C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166089 | ||||||
| chr5:166093
|
G | T | 1 | a0037c0074t0037g0203 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3476+2545G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166093 | ||||||
| chr5:166094
|
C | T | 2 | a0002c0005t0070g0100a0008c0079t0068g0173 | 2 | HG01192.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3476+2546C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166094 | ||||||
| chr5:166095
|
G | GGGGCTCA others(77): Show |
1 | a0010c0014t0055g0201 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3476+2548_3476+254 others(88): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166095 | |||||
| chr5:166097
|
A | G | 26 | a0001c0001t0032g0094a0001c0036t0077g0149a0001c0051t0078g0148others(23): Show | 26 | HG00280.hp2 HG00639.hp1 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.3476+2549A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166097 | ||||||
| chr5:166105
|
C | G | 13 | a0002c0003t0130g0130a0002c0003t0132g0028a0002c0005t0003g0167others(10): Show | 13 | HG00639.hp1 HG01123.hp1 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.3476+2557C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166105 | ||||||
| chr5:166108
|
A | C | 2 | a0008c0024t0021g0175a0008c0024t0021g0176 | 2 | HG02109.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.3476+2560A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166108 | ||||||
| chr5:166109
|
T | C | 1 | a0002c0039t0009g0030 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.3476+2561T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166109 | ||||||
| chr5:166110
|
G | C | 13 | a0002c0003t0130g0130a0002c0003t0132g0028a0002c0005t0003g0167others(10): Show | 13 | HG00639.hp1 HG01123.hp1 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.3476+2562G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166110 | ||||||
| chr5:166110
|
G | GCTCTGAC others(331): Show |
1 | a0008c0025t0045g0172 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3476+2572_3476+257 others(342): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166110 | |||||
| chr5:166113
|
C | CTGATGGG others(455): Show |
1 | a0011c0023t0044g0187 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3476+2568_3476+256 others(466): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166113 | |||||
| chr5:166117
|
C | T | 14 | a0003c0009t0017g0088a0003c0009t0017g0093a0003c0009t0119g0049others(11): Show | 14 | HG00323.hp2 HG01175.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.3476+2569C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166117 | ||||||
| chr5:166121
|
A | G | 82 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(79): Show | 82 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.3476+2573A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166121 | ||||||
| chr5:166122
|
C | T | 9 | a0002c0003t0066g0209a0002c0003t0071g0095a0002c0003t0130g0130others(6): Show | 9 | HG00099.hp2 HG00639.hp1 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.3476+2574C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166122 | ||||||
| chr5:166125
|
G | A | 21 | a0001c0007t0109g0147a0002c0005t0070g0100a0004c0006t0134g0011others(18): Show | 21 | HG01192.hp1 HG02109.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.3476+2577G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166125 | ||||||
| chr5:166133
|
C | G | 3 | a0001c0036t0077g0149a0001c0051t0078g0148a0002c0039t0009g0030 | 3 | HG01928.hp2 HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.3476+2585C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166133 | ||||||
| chr5:166137
|
T | C | 6 | a0001c0001t0032g0094a0002c0057t0003g0026a0004c0006t0002g0119others(3): Show | 6 | HG01081.hp1 HG02258.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.3476+2589T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166137 | ||||||
| chr5:166137
|
T | TGCTCTGA others(17): Show |
1 | a0015c0077t0053g0181 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3476+2612_3476+261 others(28): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166137 | |||||
| chr5:166138
|
G | C | 3 | a0001c0036t0077g0149a0001c0051t0078g0148a0002c0039t0009g0030 | 3 | HG01928.hp2 HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.3476+2590G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166138 | ||||||
| chr5:166138
|
GCTCTGAC others(77): Show |
G | 1 | a0002c0005t0070g0100 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3476+2613_3476+269 others(88): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166138 | |||||
| chr5:166141
|
C | CTGACGGG others(133): Show |
1 | a0012c0013t0133g0118 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.3476+2604_3476+260 others(144): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166141 | |||||
| chr5:166141
|
C | G | 4 | a0035c0060t0020g0188a0037c0074t0037g0203a0040c0063t0063g0189others(1): Show | 4 | HG00280.hp2 HG01081.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.3476+2593C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166141 | ||||||
| chr5:166145
|
C | CGGGGCGG others(279): Show |
1 | a0006c0021t0018g0198 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3476+2604_3476+260 others(290): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166145 | |||||
| chr5:166145
|
C | CGGGGCGG others(335): Show |
2 | a0012c0013t0009g0016a0012c0013t0009g0019 | 2 | NA18973.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.3476+2604_3476+260 others(346): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166145 | |||||
| chr5:166145
|
C | T | 10 | a0003c0009t0017g0088a0003c0009t0017g0093a0003c0009t0119g0049others(7): Show | 10 | HG00323.hp2 HG01175.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.3476+2597C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166145 | ||||||
| chr5:166153
|
G | A | 20 | a0001c0007t0008g0146a0001c0036t0077g0149a0001c0051t0078g0148others(17): Show | 20 | HG00280.hp2 HG00639.hp1 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.3476+2605G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166153 | ||||||
| chr5:166153
|
G | GGCTCACA others(45): Show |
1 | a0011c0023t0041g0184 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3476+2612_3476+261 others(56): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166153 | |||||
| chr5:166153
|
G | GGCTCACA others(49): Show |
2 | a0016c0018t0034g0004a0024c0042t0006g0012 | 2 | HG02735.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.3476+2612_3476+261 others(60): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166153 | |||||
| chr5:166153
|
G | GGCTCACA others(49): Show |
6 | a0001c0001t0032g0144a0001c0007t0008g0143a0001c0007t0008g0145others(3): Show | 6 | HG00597.hp2 HG02109.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.3476+2612_3476+261 others(60): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166153 | |||||
| chr5:166153
|
GGCTCACA others(21): Show |
G | 2 | a0001c0001t0030g0027a0004c0006t0134g0011 | 2 | HG00438.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.3476+2613_3476+264 others(32): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166153 | |||||
| chr5:166154
|
G | T | 1 | a0002c0003t0124g0017 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.3476+2606G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166154 | ||||||
| chr5:166158
|
A | ACACGCTC others(15): Show |
1 | a0011c0023t0044g0187 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3476+2612_3476+261 others(26): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166158 | |||||
| chr5:166161
|
G | C | 40 | a0001c0001t0032g0144a0001c0001t0113g0044a0001c0007t0008g0143others(37): Show | 40 | HG00099.hp2 HG00280.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.3476+2613G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166161 | ||||||
| chr5:166163
|
AATC | A | 5 | a0003c0009t0017g0088a0003c0009t0017g0093a0003c0009t0119g0049others(2): Show | 5 | HG01243.hp1 HG01256.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.3476+2616_3476+261 others(7): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166163 | ||||||
| chr5:166164
|
A | C | 8 | a0003c0009t0120g0013a0008c0024t0021g0175a0008c0024t0021g0176others(5): Show | 8 | HG00323.hp2 HG01175.hp2 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.3476+2616A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166164 | ||||||
| chr5:166165
|
T | C | 1 | a0001c0001t0113g0044 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.3476+2617T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166165 | ||||||
| chr5:166166
|
C | CCTCTGAT others(79): Show |
1 | a0001c0007t0109g0147 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3476+2624_3476+262 others(90): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166166 | |||||
| chr5:166166
|
C | G | 44 | a0001c0001t0032g0144a0001c0001t0113g0044a0001c0007t0008g0143others(41): Show | 44 | HG00099.hp2 HG00280.hp2 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.3476+2618C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166166 | ||||||
| chr5:166169
|
C | G | 1 | a0015c0076t0067g0192 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3476+2621C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166169 | ||||||
| chr5:166173
|
C | T | 5 | a0001c0001t0113g0044a0001c0036t0077g0149a0001c0051t0078g0148others(2): Show | 5 | HG00280.hp2 HG00735.hp1 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.3476+2625C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166173 | ||||||
| chr5:166177
|
G | A | 2 | a0001c0036t0077g0149a0001c0051t0078g0148 | 2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.3476+2629G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166177 | ||||||
| chr5:166178
|
C | CGGGGCTC others(77): Show |
1 | a0022c0046t0047g0180 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3476+2632_3476+263 others(88): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166178 | |||||
| chr5:166178
|
C | T | 19 | a0002c0003t0011g0210a0002c0003t0124g0017a0002c0003t0128g0029others(16): Show | 19 | HG00140.hp2 HG00639.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.3476+2630C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166178 | ||||||
| chr5:166179
|
G | A | 1 | a0015c0076t0067g0192 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3476+2631G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166179 | ||||||
| chr5:166181
|
A | AGCTCACA others(1001): Show |
1 | a0032c0058t0040g0158 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3476+2660_3476+266 others(1012): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166181 | |||||
| chr5:166181
|
A | AGCTCACA others(1001): Show |
1 | a0017c0030t0039g0140 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3476+2660_3476+266 others(1012): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166181 | |||||
| chr5:166181
|
A | G | 40 | a0001c0001t0113g0044a0001c0036t0077g0149a0001c0051t0078g0148others(37): Show | 40 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.3476+2633A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166181 | ||||||
| chr5:166188
|
A | T | 2 | a0002c0003t0071g0095a0002c0005t0072g0153 | 2 | NA18971.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.3476+2640A>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166188 | ||||||
| chr5:166189
|
C | G | 2 | a0001c0001t0113g0044a0012c0013t0133g0118 | 2 | HG00735.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.3476+2641C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166189 | ||||||
| chr5:166193
|
T | C | 10 | a0002c0039t0009g0030a0006c0068t0058g0194a0006c0070t0054g0207others(7): Show | 10 | HG01928.hp2 HG02145.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.3476+2645T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166193 | ||||||
| chr5:166193
|
T | TGCTCTGA others(21): Show |
2 | a0002c0057t0003g0026a0004c0041t0003g0077 | 2 | HG03017.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.3476+2668_3476+266 others(32): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166193 | |||||
| chr5:166193
|
T | TGCTCTGA others(185): Show |
1 | a0015c0076t0067g0192 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3476+2652_3476+265 others(196): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166193 | |||||
| chr5:166193
|
T | TGCTGTGA others(105): Show |
1 | a0037c0074t0037g0203 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3476+2648_3476+264 others(116): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166193 | |||||
| chr5:166194
|
G | C | 1 | a0001c0001t0113g0044 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.3476+2646G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166194 | ||||||
| chr5:166197
|
C | G | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3476+2649C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166197 | ||||||
| chr5:166201
|
C | CGGGGCGG others(217): Show |
1 | a0010c0014t0055g0201 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3476+2660_3476+266 others(228): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166201 | |||||
| chr5:166201
|
C | CGGGGCGG others(1179): Show |
1 | a0001c0007t0008g0146 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3476+2660_3476+266 others(1190): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166201 | |||||
| chr5:166201
|
C | CGGGGCGG others(1089): Show |
1 | a0006c0021t0056g0199 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3476+2660_3476+266 others(1100): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166201 | |||||
| chr5:166201
|
C | CGGGGCGG others(49): Show |
2 | a0001c0001t0032g0094a0010c0069t0019g0204 | 2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3476+2668_3476+266 others(60): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166201 | |||||
| chr5:166201
|
C | T | 5 | a0006c0070t0054g0207a0020c0081t0064g0200a0037c0074t0037g0203others(2): Show | 5 | HG00280.hp2 HG01081.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.3476+2653C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166201 | ||||||
| chr5:166202
|
G | A | 1 | a0001c0049t0096g0063 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3476+2654G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166202 | ||||||
| chr5:166209
|
G | A | 24 | a0001c0001t0113g0044a0002c0003t0002g0098a0002c0003t0002g0101others(21): Show | 24 | HG00140.hp2 HG00639.hp2 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.3476+2661G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166209 | ||||||
| chr5:166209
|
GGCTCACA others(105): Show |
G | 1 | a0030c0047t0131g0067 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3476+2669_3476+278 others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166209 | |||||
| chr5:166217
|
G | C | 35 | a0001c0001t0032g0144a0001c0001t0113g0044a0001c0007t0008g0143others(32): Show | 35 | HG00140.hp2 HG00597.hp2 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.3476+2669G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166217 | ||||||
| chr5:166217
|
G | GTAATGCT others(839): Show |
1 | a0001c0007t0109g0147 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3476+2673_3476+267 others(850): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166217 | |||||
| chr5:166220
|
A | C | 2 | a0040c0063t0063g0189a0041c0064t0010g0190 | 2 | HG00280.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.3476+2672A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166220 | ||||||
| chr5:166222
|
C | G | 39 | a0001c0001t0032g0144a0001c0001t0113g0044a0001c0007t0008g0143others(36): Show | 39 | HG00140.hp2 HG00597.hp2 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.3476+2674C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166222 | ||||||
| chr5:166225
|
C | G | 1 | a0012c0013t0133g0118 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.3476+2677C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166225 | ||||||
| chr5:166229
|
C | T | 10 | a0003c0009t0017g0088a0003c0009t0017g0093a0003c0009t0119g0049others(7): Show | 10 | HG00323.hp2 HG01175.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.3476+2681C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166229 | ||||||
| chr5:166234
|
C | T | 1 | a0004c0006t0134g0011 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3476+2686C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166234 | ||||||
| chr5:166237
|
G | A | 66 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(63): Show | 66 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.3476+2689G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166237 | ||||||
| chr5:166237
|
G | GGCTCACA others(133): Show |
1 | a0010c0014t0019g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3476+2700_3476+270 others(144): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166237 | |||||
| chr5:166237
|
G | GGCTCACA others(21): Show |
1 | a0006c0073t0020g0193 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3476+2708_3476+270 others(32): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166237 | |||||
| chr5:166237
|
G | GGCTCACA others(49): Show |
1 | a0011c0023t0044g0187 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3476+2696_3476+269 others(60): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166237 | |||||
| chr5:166237
|
G | GGCTCACA others(2611): Show |
1 | a0006c0021t0018g0198 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3476+2696_3476+269 others(2622): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166237 | |||||
| chr5:166237
|
GGCTCACA others(77): Show |
G | 1 | a0001c0001t0093g0105 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.3476+2801_3476+288 others(88): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166237 | |||||
| chr5:166244
|
A | T | 1 | a0002c0005t0070g0100 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3476+2696A>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166244 | ||||||
| chr5:166245
|
C | G | 1 | a0012c0013t0133g0118 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.3476+2697C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166245 | ||||||
| chr5:166250
|
G | GCTCTGAC others(581): Show |
1 | a0001c0001t0031g0112 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.3477-2796_3477-279 others(592): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166250 | |||||
| chr5:166250
|
GCTCTGAC others(49): Show |
G | 2 | a0017c0029t0112g0155a0019c0019t0062g0191 | 2 | HG02004.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.3476+2717_3476+277 others(60): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166250 | |||||
| chr5:166251
|
C | G | 1 | a0011c0023t0044g0187 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3476+2703C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166251 | ||||||
| chr5:166257
|
C | T | 2 | a0004c0006t0002g0119a0035c0060t0020g0188 | 2 | HG01081.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.3476+2709C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166257 | ||||||
| chr5:166262
|
C | T | 3 | a0001c0036t0077g0149a0001c0051t0078g0148a0012c0013t0133g0118 | 3 | HG03139.hp1 HG06807.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.3476+2714C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166262 | ||||||
| chr5:166265
|
G | A | 40 | a0001c0001t0032g0094a0001c0007t0008g0146a0001c0036t0077g0149others(37): Show | 40 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.3476+2717G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166265 | ||||||
| chr5:166265
|
G | GGCTCACA others(163): Show |
3 | a0008c0024t0021g0175a0008c0024t0021g0176a0008c0025t0045g0172 | 3 | HG02109.hp2 HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.3476+2744_3476+274 others(174): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166265 | |||||
| chr5:166265
|
G | GGCTCACA others(105): Show |
1 | a0008c0079t0068g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3476+2752_3476+275 others(116): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166265 | |||||
| chr5:166265
|
G | GGCTCACA others(1780): Show |
1 | a0006c0073t0020g0193 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3476+2732_3476+273 others(1791): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166265 | |||||
| chr5:166265
|
G | GGCTCACA others(21): Show |
1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3476+2724_3476+272 others(32): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166265 | |||||
| chr5:166273
|
C | G | 25 | a0002c0003t0002g0098a0002c0003t0002g0101a0002c0003t0002g0132others(22): Show | 25 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.3476+2725C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166273 | ||||||
| chr5:166277
|
T | C | 1 | a0016c0018t0003g0005 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3476+2729T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166277 | ||||||
| chr5:166278
|
G | C | 25 | a0002c0003t0002g0098a0002c0003t0002g0101a0002c0003t0002g0132others(22): Show | 25 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.3476+2730G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166278 | ||||||
| chr5:166281
|
C | G | 1 | a0011c0023t0044g0187 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3476+2733C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166281 | ||||||
| chr5:166285
|
C | T | 2 | a0040c0063t0063g0189a0041c0064t0010g0190 | 2 | HG00280.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.3476+2737C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166285 | ||||||
| chr5:166290
|
C | A | 2 | a0001c0036t0077g0149a0001c0051t0078g0148 | 2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.3476+2742C>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166290 | ||||||
| chr5:166291
|
G | A | 1 | a0036c0075t0061g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3476+2743G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166291 | ||||||
| chr5:166293
|
G | A | 12 | a0001c0001t0113g0044a0003c0009t0017g0088a0003c0009t0017g0093others(9): Show | 12 | HG00280.hp2 HG00323.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.3476+2745G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166293 | ||||||
| chr5:166293
|
GGCTCACA others(21): Show |
G | 1 | a0004c0006t0002g0119 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3476+2753_3476+278 others(32): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166293 | |||||
| chr5:166296
|
T | TCACACTA others(25): Show |
2 | a0012c0013t0009g0016a0012c0013t0009g0019 | 2 | NA18973.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.3476+2752_3476+275 others(36): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166296 | |||||
| chr5:166301
|
G | C | 51 | a0001c0001t0032g0094a0001c0001t0113g0044a0001c0007t0008g0146others(48): Show | 51 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.3476+2753G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166301 | ||||||
| chr5:166305
|
T | C | 3 | a0003c0009t0120g0013a0019c0019t0010g0164a0039c0062t0010g0165 | 3 | HG00323.hp2 HG01175.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.3476+2757T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166305 | ||||||
| chr5:166306
|
C | CCTCTGAC others(105): Show |
1 | a0022c0046t0047g0180 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3476+2772_3476+277 others(116): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166306 | |||||
| chr5:166306
|
C | G | 55 | a0001c0001t0032g0094a0001c0001t0113g0044a0001c0007t0008g0146others(52): Show | 55 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.3476+2758C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166306 | ||||||
| chr5:166309
|
C | G | 2 | a0012c0013t0009g0016a0012c0013t0009g0019 | 2 | NA18973.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.3476+2761C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166309 | ||||||
| chr5:166313
|
C | CGGGGCGG others(77): Show |
1 | a0016c0018t0003g0005 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3476+2836_3476+283 others(88): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166313 | |||||
| chr5:166313
|
C | CGGGGCGG others(273): Show |
1 | a0015c0077t0053g0181 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3476+2772_3476+277 others(284): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166313 | |||||
| chr5:166313
|
C | T | 12 | a0002c0039t0009g0030a0002c0057t0003g0026a0003c0009t0120g0013others(9): Show | 12 | HG00323.hp2 HG01175.hp2 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.3476+2765C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166313 | ||||||
| chr5:166319
|
G | A | 2 | a0012c0013t0009g0016a0012c0013t0009g0019 | 2 | NA18973.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.3476+2771G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166319 | ||||||
| chr5:166321
|
A | G | 24 | a0001c0001t0032g0144a0001c0001t0113g0044a0001c0007t0008g0143others(21): Show | 24 | HG00323.hp2 HG00597.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.3476+2773A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166321 | ||||||
| chr5:166321
|
AGCTCACA others(21): Show |
A | 20 | a0002c0003t0002g0098a0002c0003t0002g0101a0002c0003t0002g0132others(17): Show | 20 | HG00140.hp2 HG00639.hp2 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.3476+2809_3476+283 others(32): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166321 | |||||
| chr5:166329
|
C | G | 8 | a0003c0009t0017g0088a0003c0009t0017g0093a0003c0009t0119g0049others(5): Show | 8 | HG00323.hp2 HG01175.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.3476+2781C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166329 | ||||||
| chr5:166332
|
A | C | 8 | a0003c0009t0017g0088a0003c0009t0017g0093a0003c0009t0119g0049others(5): Show | 8 | HG00323.hp2 HG01175.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.3476+2784A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166332 | ||||||
| chr5:166333
|
T | A | 3 | a0014c0027t0049g0171a0014c0066t0051g0170a0021c0026t0060g0169 | 3 | HG02809.hp1 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3476+2785T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166333 | ||||||
| chr5:166334
|
G | C | 8 | a0003c0009t0017g0088a0003c0009t0017g0093a0003c0009t0119g0049others(5): Show | 8 | HG00323.hp2 HG01175.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.3476+2786G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166334 | ||||||
| chr5:166335
|
CTCTGACG others(161): Show |
C | 1 | a0036c0075t0061g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3476+2801_3477-282 others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166335 | |||||
| chr5:166337
|
C | G | 1 | a0012c0013t0133g0118 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.3476+2789C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166337 | ||||||
| chr5:166341
|
C | T | 2 | a0012c0013t0009g0016a0012c0013t0009g0019 | 2 | NA18973.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.3476+2793C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166341 | ||||||
| chr5:166347
|
G | A | 2 | a0001c0001t0027g0052a0001c0001t0027g0053 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.3476+2799G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166347 | ||||||
| chr5:166349
|
G | A | 41 | a0001c0001t0032g0144a0001c0007t0008g0143a0001c0007t0008g0145others(38): Show | 41 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.3476+2801G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166349 | ||||||
| chr5:166349
|
G | GGCTCACA others(21): Show |
1 | a0012c0013t0133g0118 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.3476+2808_3476+280 others(32): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166349 | |||||
| chr5:166357
|
C | G | 4 | a0001c0001t0113g0044a0002c0005t0070g0100a0004c0006t0002g0119others(1): Show | 4 | HG00735.hp1 HG01081.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.3476+2809C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166357 | ||||||
| chr5:166361
|
T | C | 8 | a0008c0024t0021g0175a0008c0024t0021g0176a0008c0025t0045g0172others(5): Show | 8 | HG00280.hp2 HG01081.hp2 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.3476+2813T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166361 | ||||||
| chr5:166362
|
G | C | 4 | a0001c0001t0113g0044a0002c0005t0070g0100a0004c0006t0002g0119others(1): Show | 4 | HG00735.hp1 HG01081.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.3476+2814G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166362 | ||||||
| chr5:166362
|
G | GCTCTGAC others(3279): Show |
1 | a0011c0023t0044g0187 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3476+2828_3476+282 others(3290): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166362 | |||||
| chr5:166362
|
G | GCTCTGAC others(105): Show |
1 | a0015c0076t0067g0192 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3476+2836_3476+283 others(116): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166362 | |||||
| chr5:166369
|
C | T | 7 | a0008c0024t0021g0175a0008c0024t0021g0176a0008c0025t0045g0172others(4): Show | 7 | HG00280.hp2 HG01081.hp2 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.3476+2821C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166369 | ||||||
| chr5:166374
|
C | T | 3 | a0004c0006t0002g0119a0012c0013t0009g0016a0012c0013t0009g0019 | 3 | HG01081.hp1 NA18973.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.3476+2826C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166374 | ||||||
| chr5:166377
|
G | A | 10 | a0001c0001t0032g0144a0001c0007t0008g0143a0001c0007t0008g0145others(7): Show | 10 | HG00597.hp2 HG01192.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.3476+2829G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166377 | ||||||
| chr5:166385
|
G | C | 24 | a0001c0001t0032g0144a0001c0001t0113g0044a0001c0007t0008g0143others(21): Show | 24 | HG00099.hp2 HG00597.hp2 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.3476+2837G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166385 | ||||||
| chr5:166388
|
A | C | 17 | a0003c0009t0017g0088a0003c0009t0017g0093a0003c0009t0119g0049others(14): Show | 17 | HG00280.hp2 HG00323.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.3476+2840A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166388 | ||||||
| chr5:166390
|
C | CCTCTGAC others(21): Show |
2 | a0001c0001t0097g0086a0001c0001t0104g0023 | 2 | HG00323.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.3477-2879_3477-285 others(32): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166390 | |||||
| chr5:166390
|
C | CCTCTGAC others(21): Show |
5 | a0001c0001t0032g0094a0006c0070t0054g0207a0010c0069t0019g0204others(2): Show | 5 | HG02258.hp2 HG02896.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.3476+2856_3476+285 others(32): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166390 | |||||
| chr5:166390
|
C | CCTCTGAC others(49): Show |
1 | a0015c0077t0053g0181 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3476+2856_3476+285 others(60): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166390 | |||||
| chr5:166390
|
C | CCTCTGAC others(21): Show |
2 | a0002c0039t0009g0030a0004c0041t0003g0077 | 2 | HG01928.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.3476+2853_3476+285 others(32): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166390 | |||||
| chr5:166390
|
C | G | 25 | a0001c0001t0032g0144a0001c0001t0113g0044a0001c0007t0008g0143others(22): Show | 25 | HG00099.hp2 HG00597.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.3476+2842C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166390 | ||||||
| chr5:166397
|
C | T | 5 | a0001c0016t0005g0160a0001c0016t0025g0152a0001c0035t0030g0137others(2): Show | 5 | HG02717.hp1 HG02922.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.3476+2849C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166397 | ||||||
| chr5:166402
|
C | T | 3 | a0002c0057t0003g0026a0016c0018t0034g0004a0024c0042t0006g0012 | 3 | HG02735.hp2 HG03579.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.3476+2854C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166402 | ||||||
| chr5:166405
|
A | C | 2 | a0012c0013t0009g0016a0012c0013t0009g0019 | 2 | NA18973.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.3476+2857A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166405 | ||||||
| chr5:166405
|
A | G | 31 | a0001c0001t0032g0144a0001c0007t0008g0143a0001c0007t0008g0145others(28): Show | 31 | HG00099.hp2 HG00597.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.3476+2857A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166405 | ||||||
| chr5:166413
|
C | G | 9 | a0001c0001t0032g0144a0001c0007t0008g0143a0001c0007t0008g0145others(6): Show | 9 | HG00597.hp2 HG02109.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.3476+2865C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166413 | ||||||
| chr5:166418
|
G | C | 9 | a0001c0001t0032g0144a0001c0007t0008g0143a0001c0007t0008g0145others(6): Show | 9 | HG00597.hp2 HG02109.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.3476+2870G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166418 | ||||||
| chr5:166418
|
G | GCTCTGAC others(133): Show |
1 | a0022c0046t0047g0180 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3477-2859_3477-285 others(144): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166418 | |||||
| chr5:166418
|
G | GCTCTGAC others(77): Show |
2 | a0006c0021t0056g0199a0010c0014t0055g0201 | 2 | HG02451.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.3476+2871_3477-283 others(88): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166418 | |||||
| chr5:166418
|
G | GCTCTGAC others(49): Show |
6 | a0001c0001t0032g0094a0001c0001t0113g0044a0006c0070t0054g0207others(3): Show | 6 | HG00735.hp1 HG02258.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.3477-2880_3477-287 others(60): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166418 | |||||
| chr5:166418
|
G | GCTCTGAC others(77): Show |
1 | a0008c0025t0069g0174 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3477-2888_3477-288 others(88): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166418 | |||||
| chr5:166424
|
A | G | 9 | a0002c0003t0066g0209a0002c0003t0071g0095a0002c0003t0130g0130others(6): Show | 9 | HG00099.hp2 HG00639.hp1 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.3476+2876A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166424 | ||||||
| chr5:166425
|
C | T | 3 | a0014c0027t0049g0171a0014c0066t0051g0170a0021c0026t0060g0169 | 3 | HG02809.hp1 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3476+2877C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166425 | ||||||
| chr5:166425
|
C | TGGGGCGG others(49): Show |
1 | a0008c0079t0068g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3476+2876_3476+287 others(60): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166425 | ||||||
| chr5:166425
|
CGGGGCGG others(75): Show |
C | 3 | a0002c0003t0066g0209a0002c0003t0071g0095a0002c0005t0072g0153 | 3 | HG00099.hp2 NA18971.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.3476+2878_3477-283 others(86): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166425 | ||||||
| chr5:166425
|
CGGGGCGG others(103): Show |
C | 6 | a0002c0003t0130g0130a0002c0003t0132g0028a0002c0005t0003g0167others(3): Show | 6 | HG00639.hp1 HG01123.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.3476+2878_3477-280 others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166425 | ||||||
| chr5:166433
|
A | AGCTCACA others(77): Show |
1 | a0016c0018t0034g0004 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3477-2838_3477-283 others(88): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166433 | |||||
| chr5:166433
|
A | AGCTCACA others(77): Show |
2 | a0016c0018t0003g0005a0024c0042t0006g0012 | 2 | HG02145.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.3477-2838_3477-283 others(88): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166433 | |||||
| chr5:166433
|
A | AGCTCACA others(165): Show |
1 | a0012c0013t0133g0118 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.3477-2880_3477-287 others(176): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166433 | |||||
| chr5:166433
|
A | G | 19 | a0002c0005t0070g0100a0003c0009t0017g0088a0003c0009t0017g0093others(16): Show | 19 | HG00280.hp2 HG00323.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.3476+2885A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166433 | ||||||
| chr5:166441
|
C | G | 15 | a0003c0009t0017g0088a0003c0009t0017g0093a0003c0009t0119g0049others(12): Show | 15 | HG00280.hp2 HG00323.hp2 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.3476+2893C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166441 | ||||||
| chr5:166444
|
A | C | 7 | a0008c0024t0021g0175a0008c0024t0021g0176a0008c0025t0045g0172others(4): Show | 7 | HG00280.hp2 HG01081.hp2 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.3476+2896A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166444 | ||||||
| chr5:166446
|
G | C | 15 | a0003c0009t0017g0088a0003c0009t0017g0093a0003c0009t0119g0049others(12): Show | 15 | HG00280.hp2 HG00323.hp2 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.3477-2894G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166446 | ||||||
| chr5:166448
|
T | G | 1 | a0015c0077t0053g0181 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3477-2892T>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166448 | ||||||
| chr5:166453
|
C | T | 3 | a0001c0036t0077g0149a0001c0051t0078g0148a0006c0068t0058g0194 | 3 | HG02647.hp1 HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.3477-2887C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166453 | ||||||
| chr5:166459
|
G | A | 1 | a0030c0047t0131g0067 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3477-2881G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166459 | ||||||
| chr5:166461
|
A | G | 38 | a0002c0003t0002g0098a0002c0003t0002g0101a0002c0003t0002g0132others(35): Show | 38 | HG00140.hp2 HG00639.hp2 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.3477-2879A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166461 | ||||||
| chr5:166469
|
C | G | 13 | a0002c0039t0009g0030a0004c0006t0002g0119a0004c0041t0003g0077others(10): Show | 13 | HG01081.hp1 HG01928.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.3477-2871C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166469 | ||||||
| chr5:166474
|
G | C | 13 | a0002c0039t0009g0030a0004c0006t0002g0119a0004c0041t0003g0077others(10): Show | 13 | HG01081.hp1 HG01928.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.3477-2866G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166474 | ||||||
| chr5:166474
|
G | GCGCTGAC others(49): Show |
2 | a0011c0023t0044g0187a0015c0076t0067g0192 | 2 | HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.3477-2865_3477-286 others(60): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166474 | |||||
| chr5:166480
|
A | G | 2 | a0002c0005t0070g0100a0030c0047t0131g0067 | 2 | HG01192.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.3477-2860A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166480 | ||||||
| chr5:166481
|
CGGGGCGG others(19): Show |
C | 1 | a0030c0047t0131g0067 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3477-2858_3477-283 others(30): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166481 | ||||||
| chr5:166481
|
CGGGGCGG others(47): Show |
C | 1 | a0002c0005t0070g0100 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3477-2858_3477-280 others(58): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166481 | ||||||
| chr5:166489
|
G | A | 12 | a0011c0023t0044g0187a0012c0013t0009g0016a0012c0013t0009g0019others(9): Show | 12 | HG02257.hp1 HG02280.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.3477-2851G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166489 | ||||||
| chr5:166497
|
G | C | 45 | a0002c0003t0002g0098a0002c0003t0002g0101a0002c0003t0002g0132others(42): Show | 45 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.3477-2843G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166497 | ||||||
| chr5:166502
|
C | CCTCTGAC others(21): Show |
20 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(17): Show | 20 | HG00597.hp2 HG00735.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.3477-2838_3477-283 others(32): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166502 | ||||||
| chr5:166502
|
C | CCTCTGAC others(105): Show |
2 | a0001c0007t0008g0146a0006c0073t0020g0193 | 2 | HG01261.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.3477-2838_3477-283 others(116): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166502 | ||||||
| chr5:166502
|
C | CCTCTGAC others(105): Show |
1 | a0002c0057t0003g0026 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.3477-2838_3477-283 others(116): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166502 | ||||||
| chr5:166502
|
C | G | 44 | a0002c0003t0002g0098a0002c0003t0002g0101a0002c0003t0002g0132others(41): Show | 44 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.3477-2838C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166502 | ||||||
| chr5:166503
|
T | C | 80 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(77): Show | 80 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.3477-2837T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166503 | ||||||
| chr5:166503
|
T | TGACGGGG others(74): Show |
1 | a0011c0023t0041g0184 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3477-2837_3477-283 others(85): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166503 | ||||||
| chr5:166507
|
G | GGC | 21 | a0002c0003t0002g0098a0002c0003t0002g0101a0002c0003t0002g0132others(18): Show | 21 | HG00140.hp2 HG00639.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.3477-2833_3477-283 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166507 | ||||||
| chr5:166509
|
C | G | 25 | a0002c0003t0002g0098a0002c0003t0002g0101a0002c0003t0002g0132others(22): Show | 25 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.3477-2831C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166509 | ||||||
| chr5:166511
|
G | A | 25 | a0002c0003t0002g0098a0002c0003t0002g0101a0002c0003t0002g0132others(22): Show | 25 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.3477-2829G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166511 | ||||||
| chr5:166517
|
AGCTCACA others(21): Show |
A | 26 | a0002c0003t0002g0098a0002c0003t0002g0101a0002c0003t0002g0132others(23): Show | 26 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.3477-2776_3477-274 others(32): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166517 | |||||
| chr5:166531
|
C | T | 15 | a0003c0009t0017g0088a0003c0009t0017g0093a0003c0009t0119g0049others(12): Show | 15 | HG00280.hp2 HG00323.hp2 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.3477-2809C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166531 | ||||||
| chr5:166537
|
C | G | 7 | a0002c0003t0130g0130a0002c0003t0132g0028a0002c0005t0003g0167others(4): Show | 7 | HG00639.hp1 HG01123.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.3477-2803C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166537 | ||||||
| chr5:166539
|
G | A | 7 | a0002c0003t0130g0130a0002c0003t0132g0028a0002c0005t0003g0167others(4): Show | 7 | HG00639.hp1 HG01123.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.3477-2801G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166539 | ||||||
| chr5:166539
|
G | GGGCGGAG others(79): Show |
4 | a0012c0013t0133g0118a0016c0018t0003g0005a0016c0018t0034g0004others(1): Show | 4 | HG02145.hp1 HG02735.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.3477-2796_3477-279 others(90): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166539 | |||||
| chr5:166545
|
G | A | 13 | a0002c0003t0130g0130a0002c0003t0132g0028a0002c0005t0003g0167others(10): Show | 13 | HG00639.hp1 HG01123.hp1 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.3477-2795G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166545 | ||||||
| chr5:166545
|
G | GGCTCACA others(135): Show |
3 | a0002c0039t0009g0030a0004c0006t0002g0119a0004c0041t0003g0077 | 3 | HG01081.hp1 HG01928.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.3477-2788_3477-278 others(146): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166545 | |||||
| chr5:166600
|
C | CGGAGCTC others(51): Show |
3 | a0002c0057t0003g0026a0012c0013t0009g0016a0012c0013t0009g0019 | 3 | NA18973.hp1 NA18979.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.3477-2732_3477-273 others(62): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 166600 | |||||
| chr5:166600
|
C | T | 39 | a0002c0003t0002g0098a0002c0003t0002g0101a0002c0003t0002g0132others(36): Show | 39 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.3477-2740C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166600 | ||||||
| chr5:166741
|
T | C | 14 | a0003c0009t0017g0088a0003c0009t0017g0093a0003c0009t0119g0049others(11): Show | 14 | HG00280.hp2 HG00323.hp2 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.3477-2599T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166741 | ||||||
| chr5:166946
|
G | T | 1 | a0036c0075t0061g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3477-2394G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 166946 | ||||||
| chr5:167066
|
G | A | 1 | a0001c0001t0028g0046 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3477-2274G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 167066 | ||||||
| chr5:167167
|
T | C | 1 | a0038c0080t0043g0177 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3477-2173T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 167167 | ||||||
| chr5:167183
|
G | C | 1 | a0020c0081t0064g0200 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3477-2157G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 167183 | ||||||
| chr5:167250
|
G | C | 1 | a0036c0075t0061g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3477-2090G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 167250 | ||||||
| chr5:167442
|
G | GA | 77 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(74): Show | 77 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.3477-1890dupA | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 167442 | |||||
| chr5:167490
|
T | TAAGGAGG others(308): Show |
1 | a0003c0009t0120g0013 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3477-1836_3477-183 others(319): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 167490 | |||||
| chr5:167490
|
T | TAAGGAGG others(318): Show |
1 | a0003c0009t0017g0093 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.3477-1836_3477-183 others(329): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 167490 | |||||
| chr5:167490
|
T | TAAGGAGG others(319): Show |
8 | a0003c0009t0119g0049a0003c0009t0121g0092a0003c0056t0017g0080others(5): Show | 8 | HG00280.hp2 HG00323.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.3477-1836_3477-183 others(330): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 167490 | |||||
| chr5:167490
|
T | TAAGGAGG others(320): Show |
1 | a0003c0009t0017g0088 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3477-1836_3477-183 others(331): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 167490 | |||||
| chr5:167568
|
G | A | 1 | a0021c0026t0060g0169 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3477-1772G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 167568 | ||||||
| chr5:167692
|
T | C | 1 | a0021c0026t0060g0169 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3477-1648T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 167692 | ||||||
| chr5:167776
|
G | C | 2 | a0017c0030t0039g0140a0032c0058t0040g0158 | 2 | HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.3477-1564G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 167776 | ||||||
| chr5:167808
|
G | A | 15 | a0003c0009t0017g0088a0003c0009t0017g0093a0003c0009t0119g0049others(12): Show | 15 | HG00280.hp2 HG00323.hp2 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.3477-1532G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 167808 | ||||||
| chr5:167843
|
C | T | 1 | a0001c0007t0008g0146 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3477-1497C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 167843 | ||||||
| chr5:167954
|
A | G | 4 | a0011c0023t0041g0184a0011c0023t0044g0187a0015c0076t0067g0192others(1): Show | 4 | HG02257.hp1 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.3477-1386A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 167954 | ||||||
| chr5:168327
|
T | C | 1 | a0003c0004t0108g0010 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.3477-1013T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 168327 | ||||||
| chr5:168388
|
G | C | 1 | a0038c0080t0043g0177 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3477-952G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 168388 | ||||||
| chr5:168458
|
T | C | 1 | a0001c0002t0013g0109 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3477-882T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 168458 | ||||||
| chr5:168552
|
ACTG | A | 5 | a0001c0002t0006g0134a0001c0011t0029g0136a0001c0011t0106g0085others(2): Show | 5 | HG02647.hp2 HG02723.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.3477-784_3477-782d others(5): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 168552 | |||||
| chr5:168622
|
G | A | 4 | a0011c0023t0041g0184a0011c0023t0044g0187a0015c0076t0067g0192others(1): Show | 4 | HG02257.hp1 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.3477-718G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 168622 | ||||||
| chr5:168698
|
A | G | 1 | a0001c0002t0101g0068 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.3477-642A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 168698 | ||||||
| chr5:168810
|
G | A | 79 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(76): Show | 79 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.3477-530G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 168810 | ||||||
| chr5:168822
|
A | AGT | 3 | a0014c0027t0049g0171a0014c0066t0051g0170a0021c0026t0060g0169 | 3 | HG02809.hp1 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3477-517_3477-516d others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 168822 | |||||
| chr5:168834
|
CTGAGGAT others(27): Show |
C | 3 | a0008c0024t0021g0175a0008c0024t0021g0176a0008c0025t0045g0172 | 3 | HG02109.hp2 HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.3477-504_3477-471d others(36): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 168834 | |||||
| chr5:168865
|
CT | C | 9 | a0001c0001t0079g0059a0001c0001t0104g0023a0001c0036t0077g0149others(6): Show | 9 | HG00323.hp1 HG01928.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.3477-454delT | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 168865 | |||||
| chr5:168865
|
CTT | C | 84 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(81): Show | 84 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.3477-455_3477-454d others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 168865 | |||||
| chr5:168961
|
C | T | 4 | a0011c0023t0041g0184a0011c0023t0044g0187a0015c0076t0067g0192others(1): Show | 4 | HG02257.hp1 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.3477-379C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 168961 | ||||||
| chr5:169174
|
G | A | 3 | a0008c0024t0021g0175a0008c0024t0021g0176a0008c0025t0045g0172 | 3 | HG02109.hp2 HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.3477-166G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 169174 | ||||||
| chr5:169186
|
A | G | 45 | a0002c0003t0002g0098a0002c0003t0002g0101a0002c0003t0002g0132others(42): Show | 45 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.3477-154A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 169186 | ||||||
| chr5:169246
|
C | T | 62 | a0001c0001t0113g0044a0002c0003t0002g0098a0002c0003t0002g0101others(59): Show | 62 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.3477-94C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 169246 | ||||||
| chr5:169294
|
T | C | 15 | a0003c0009t0017g0088a0003c0009t0017g0093a0003c0009t0119g0049others(12): Show | 15 | HG00280.hp2 HG00323.hp2 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.3477-46T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | chr5 | 169294 | ||||||
| chr5:169593
|
G | A | 1 | a0002c0005t0075g0076 | 1 | NA18954.hp1 | splice_donor_variant&intron_variant | HIGH | c.3729+1G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 14/19 | chr5 | 169593 | ||||||
| chr5:169647
|
C | T | 1 | a0036c0075t0061g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3729+55C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 14/19 | chr5 | 169647 | ||||||
| chr5:169648
|
A | G | 76 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(73): Show | 76 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.3729+56A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 14/19 | chr5 | 169648 | ||||||
| chr5:169714
|
C | G | 33 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(30): Show | 33 | HG00597.hp2 HG00735.hp1 HG01261.hp2 others(30): Show |
intron_variant | MODIFIER | c.3729+122C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 14/19 | chr5 | 169714 | ||||||
| chr5:169787
|
T | C | 98 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(95): Show | 98 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.3729+195T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 14/19 | chr5 | 169787 | ||||||
| chr5:169887
|
T | G | 8 | a0001c0036t0077g0149a0001c0051t0078g0148a0009c0012t0033g0161others(5): Show | 8 | HG01099.hp1 HG02886.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.3729+295T>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 14/19 | chr5 | 169887 | ||||||
| chr5:169898
|
C | T | 1 | a0036c0075t0061g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3729+306C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 14/19 | chr5 | 169898 | ||||||
| chr5:170018
|
G | A | 1 | a0036c0075t0061g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3729+426G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 14/19 | chr5 | 170018 | ||||||
| chr5:170280
|
G | A | 1 | a0036c0075t0061g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3729+688G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 14/19 | chr5 | 170280 | ||||||
| chr5:170334
|
G | A | 1 | a0025c0045t0122g0002 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3730-709G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 14/19 | chr5 | 170334 | ||||||
| chr5:170343
|
C | T | 1 | a0001c0001t0014g0125 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.3730-700C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 14/19 | chr5 | 170343 | ||||||
| chr5:170374
|
C | T | 15 | a0003c0009t0017g0088a0003c0009t0017g0093a0003c0009t0119g0049others(12): Show | 15 | HG00280.hp2 HG00323.hp2 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.3730-669C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 14/19 | chr5 | 170374 | ||||||
| chr5:170451
|
G | A | 1 | a0001c0002t0022g0015 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.3730-592G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 14/19 | chr5 | 170451 | ||||||
| chr5:170499
|
A | G | 1 | a0006c0073t0020g0193 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3730-544A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 14/19 | chr5 | 170499 | ||||||
| chr5:170541
|
C | T | 1 | a0008c0024t0021g0176 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3730-502C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 14/19 | chr5 | 170541 | ||||||
| chr5:170690
|
G | A | 1 | a0001c0001t0079g0059 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3730-353G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 14/19 | chr5 | 170690 | ||||||
| chr5:170805
|
C | T | 15 | a0003c0009t0017g0088a0003c0009t0017g0093a0003c0009t0119g0049others(12): Show | 15 | HG00280.hp2 HG00323.hp2 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.3730-238C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 14/19 | chr5 | 170805 | ||||||
| chr5:171183
|
C | T | 11 | a0003c0009t0017g0088a0003c0009t0017g0093a0003c0009t0119g0049others(8): Show | 11 | HG00280.hp2 HG00323.hp2 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.3820-31C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 15/19 | chr5 | 171183 | ||||||
| chr5:171454
|
T | C | 96 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(93): Show | 96 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.4050+10T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 16/19 | chr5 | 171454 | ||||||
| chr5:171528
|
C | G | 94 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(91): Show | 94 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.4050+84C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 16/19 | chr5 | 171528 | ||||||
| chr5:171634
|
G | A | 79 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(76): Show | 79 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.4050+190G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 16/19 | chr5 | 171634 | ||||||
| chr5:171814
|
T | G | 96 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(93): Show | 96 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.4050+370T>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 16/19 | chr5 | 171814 | ||||||
| chr5:172038
|
C | T | 2 | a0001c0036t0077g0149a0001c0051t0078g0148 | 2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.4050+594C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 16/19 | chr5 | 172038 | ||||||
| chr5:172125
|
G | T | 2 | a0001c0036t0077g0149a0001c0051t0078g0148 | 2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.4050+681G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 16/19 | chr5 | 172125 | ||||||
| chr5:172147
|
A | G | 2 | a0014c0027t0049g0171a0014c0066t0051g0170 | 2 | HG02809.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.4050+703A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 16/19 | chr5 | 172147 | ||||||
| chr5:172151
|
C | T | 1 | a0006c0072t0036g0206 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.4050+707C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 16/19 | chr5 | 172151 | ||||||
| chr5:172168
|
CT | C | 3 | a0006c0068t0058g0194a0008c0025t0069g0174a0008c0079t0068g0173 | 3 | HG02647.hp1 HG03471.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.4050+726delT | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr5 | 172168 | |||||
| chr5:172203
|
C | T | 1 | a0037c0074t0037g0203 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4051-694C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 16/19 | chr5 | 172203 | ||||||
| chr5:172237
|
C | T | 15 | a0003c0009t0017g0088a0003c0009t0017g0093a0003c0009t0119g0049others(12): Show | 15 | HG00280.hp2 HG00323.hp2 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.4051-660C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 16/19 | chr5 | 172237 | ||||||
| chr5:172305
|
G | A | 88 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0073g0107others(85): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.4051-592G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 16/19 | chr5 | 172305 | ||||||
| chr5:172332
|
G | A | 71 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0073g0107others(68): Show | 71 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.4051-565G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 16/19 | chr5 | 172332 | ||||||
| chr5:172347
|
G | A | 30 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(27): Show | 30 | HG00597.hp2 HG00735.hp1 HG01261.hp2 others(27): Show |
intron_variant | MODIFIER | c.4051-550G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 16/19 | chr5 | 172347 | ||||||
| chr5:172350
|
C | T | 27 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(24): Show | 27 | HG00597.hp2 HG00735.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.4051-547C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 16/19 | chr5 | 172350 | ||||||
| chr5:172353
|
C | T | 1 | a0018c0022t0011g0195 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.4051-544C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 16/19 | chr5 | 172353 | ||||||
| chr5:172371
|
C | T | 38 | a0001c0001t0073g0107a0002c0003t0002g0098a0002c0003t0002g0101others(35): Show | 38 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.4051-526C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 16/19 | chr5 | 172371 | ||||||
| chr5:172450
|
G | C | 19 | a0002c0003t0130g0130a0003c0009t0017g0088a0003c0009t0017g0093others(16): Show | 19 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.4051-447G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 16/19 | chr5 | 172450 | ||||||
| chr5:172500
|
G | A | 1 | a0001c0002t0087g0040 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.4051-397G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 16/19 | chr5 | 172500 | ||||||
| chr5:172515
|
A | T | 98 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0079g0059others(95): Show | 98 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.4051-382A>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 16/19 | chr5 | 172515 | ||||||
| chr5:172541
|
G | T | 1 | a0025c0045t0122g0002 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.4051-356G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 16/19 | chr5 | 172541 | ||||||
| chr5:172594
|
G | T | 1 | a0011c0023t0044g0187 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.4051-303G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 16/19 | chr5 | 172594 | ||||||
| chr5:172649
|
G | T | 11 | a0003c0009t0119g0049a0003c0009t0120g0013a0003c0056t0017g0080others(8): Show | 11 | HG00280.hp2 HG00323.hp2 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.4051-248G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 16/19 | chr5 | 172649 | ||||||
| chr5:172689
|
GC | G | 2 | a0001c0036t0077g0149a0001c0051t0078g0148 | 2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.4051-207delC | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 16/19 | chr5 | 172689 | ||||||
| chr5:172795
|
C | T | 1 | a0007c0010t0005g0113 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.4051-102C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 16/19 | chr5 | 172795 | ||||||
| chr5:172847
|
A | G | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4051-50A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 16/19 | chr5 | 172847 | ||||||
| chr5:172856
|
G | A | 75 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(72): Show | 75 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.4051-41G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 16/19 | chr5 | 172856 | ||||||
| chr5:173077
|
G | A | 4 | a0008c0024t0021g0175a0008c0024t0021g0176a0008c0025t0045g0172others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.4221+10G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 17/19 | chr5 | 173077 | ||||||
| chr5:173085
|
C | T | 72 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(69): Show | 72 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.4221+18C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 17/19 | chr5 | 173085 | ||||||
| chr5:173143
|
A | G | 91 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(88): Show | 91 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.4221+76A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 17/19 | chr5 | 173143 | ||||||
| chr5:173186
|
C | T | 1 | a0001c0001t0001g0142 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.4221+119C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 17/19 | chr5 | 173186 | ||||||
| chr5:173309
|
G | A | 3 | a0014c0027t0049g0171a0014c0066t0051g0170a0021c0026t0060g0169 | 3 | HG02809.hp1 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.4221+242G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 17/19 | chr5 | 173309 | ||||||
| chr5:173503
|
G | T | 1 | a0002c0003t0128g0029 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.4222-415G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 17/19 | chr5 | 173503 | ||||||
| chr5:173597
|
G | C | 94 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(91): Show | 94 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.4222-321G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 17/19 | chr5 | 173597 | ||||||
| chr5:173619
|
T | A | 3 | a0013c0020t0050g0182a0013c0020t0052g0183a0013c0067t0046g0186 | 3 | HG02451.hp1 HG03041.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.4222-299T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 17/19 | chr5 | 173619 | ||||||
| chr5:173632
|
A | ACAC | 28 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(25): Show | 28 | HG00735.hp1 HG01261.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.4222-285_4222-283d others(5): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr5 | 173632 | |||||
| chr5:173653
|
G | C | 94 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(91): Show | 94 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.4222-265G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 17/19 | chr5 | 173653 | ||||||
| chr5:173677
|
GTCAC | G | 12 | a0001c0001t0001g0142a0001c0001t0007g0056a0001c0001t0027g0052others(9): Show | 12 | HG00597.hp1 HG00741.hp2 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.4222-236_4222-233d others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr5 | 173677 | |||||
| chr5:173726
|
C | G | 3 | a0014c0027t0049g0171a0014c0066t0051g0170a0021c0026t0060g0169 | 3 | HG02809.hp1 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.4222-192C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 17/19 | chr5 | 173726 | ||||||
| chr5:173728
|
C | T | 1 | a0001c0001t0093g0105 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.4222-190C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 17/19 | chr5 | 173728 | ||||||
| chr5:173764
|
C | T | 3 | a0014c0027t0049g0171a0014c0066t0051g0170a0021c0026t0060g0169 | 3 | HG02809.hp1 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.4222-154C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 17/19 | chr5 | 173764 | ||||||
| chr5:173812
|
A | C | 28 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(25): Show | 28 | HG00735.hp1 HG01261.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.4222-106A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 17/19 | chr5 | 173812 | ||||||
| chr5:174125
|
G | A | 91 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(88): Show | 91 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.4402+27G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 174125 | ||||||
| chr5:174126
|
C | A | 91 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(88): Show | 91 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.4402+28C>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 174126 | ||||||
| chr5:174151
|
C | T | 1 | a0018c0022t0011g0196 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.4402+53C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 174151 | ||||||
| chr5:174152
|
A | G | 91 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(88): Show | 91 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.4402+54A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 174152 | ||||||
| chr5:174211
|
G | A | 1 | a0002c0005t0129g0043 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.4402+113G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 174211 | ||||||
| chr5:174237
|
G | A | 1 | a0006c0070t0054g0207 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.4402+139G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 174237 | ||||||
| chr5:174244
|
G | T | 1 | a0002c0003t0135g0128 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.4402+146G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 174244 | ||||||
| chr5:174315
|
G | A | 6 | a0001c0007t0008g0143a0001c0007t0008g0145a0001c0007t0008g0146others(3): Show | 6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.4402+217G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 174315 | ||||||
| chr5:174319
|
C | CG | 6 | a0001c0036t0077g0149a0001c0051t0078g0148a0011c0023t0041g0184others(3): Show | 6 | HG02145.hp1 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.4402+221_4402+222i others(3): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 174319 | ||||||
| chr5:174320
|
A | G | 96 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(93): Show | 96 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.4402+222A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 174320 | ||||||
| chr5:174381
|
T | C | 93 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0079g0059others(90): Show | 93 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.4402+283T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 174381 | ||||||
| chr5:174425
|
C | T | 3 | a0008c0024t0021g0175a0008c0024t0021g0176a0008c0025t0045g0172 | 3 | HG02109.hp2 HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.4402+327C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 174425 | ||||||
| chr5:174659
|
A | G | 2 | a0017c0030t0039g0140a0032c0058t0040g0158 | 2 | HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.4402+561A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 174659 | ||||||
| chr5:174659
|
A | T | 1 | a0004c0006t0134g0011 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.4402+561A>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 174659 | ||||||
| chr5:174750
|
C | T | 1 | a0001c0007t0100g0025 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.4402+652C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 174750 | ||||||
| chr5:174760
|
G | A | 1 | a0001c0007t0008g0150 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.4402+662G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 174760 | ||||||
| chr5:174793
|
C | G | 3 | a0014c0027t0049g0171a0014c0066t0051g0170a0021c0026t0060g0169 | 3 | HG02809.hp1 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.4402+695C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 174793 | ||||||
| chr5:174825
|
G | A | 46 | a0001c0001t0007g0056a0002c0003t0002g0098a0002c0003t0002g0101others(43): Show | 46 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.4402+727G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 174825 | ||||||
| chr5:174938
|
C | G | 13 | a0001c0052t0118g0121a0003c0009t0017g0088a0003c0009t0017g0093others(10): Show | 13 | HG00323.hp2 HG00741.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.4402+840C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 174938 | ||||||
| chr5:174956
|
C | T | 79 | a0001c0001t0005g0123a0001c0001t0007g0056a0001c0002t0006g0134others(76): Show | 79 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.4402+858C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 174956 | ||||||
| chr5:175027
|
C | T | 16 | a0001c0052t0118g0121a0003c0009t0017g0088a0003c0009t0017g0093others(13): Show | 16 | HG00280.hp2 HG00323.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.4402+929C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 175027 | ||||||
| chr5:175068
|
G | A | 15 | a0001c0052t0118g0121a0003c0009t0017g0088a0003c0009t0017g0093others(12): Show | 15 | HG00280.hp2 HG00323.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.4402+970G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 175068 | ||||||
| chr5:175104
|
G | A | 1 | a0001c0007t0109g0147 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4402+1006G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 175104 | ||||||
| chr5:175116
|
C | T | 1 | a0001c0001t0014g0033 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.4402+1018C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 175116 | ||||||
| chr5:175210
|
C | T | 2 | a0006c0070t0054g0207a0017c0029t0112g0155 | 2 | HG02896.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.4402+1112C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 175210 | ||||||
| chr5:175275
|
C | T | 49 | a0001c0001t0005g0090a0001c0001t0005g0123a0001c0001t0012g0069others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.4402+1177C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 175275 | ||||||
| chr5:175321
|
C | G | 56 | a0001c0052t0118g0121a0002c0003t0002g0098a0002c0003t0002g0101others(53): Show | 56 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.4402+1223C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 175321 | ||||||
| chr5:175374
|
G | A | 7 | a0001c0052t0118g0121a0003c0009t0017g0088a0003c0009t0017g0093others(4): Show | 7 | HG00741.hp1 HG01175.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.4402+1276G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 175374 | ||||||
| chr5:175444
|
A | G | 2 | a0001c0007t0008g0150a0011c0023t0041g0184 | 2 | HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.4402+1346A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 175444 | ||||||
| chr5:175566
|
A | ACAGACAC others(51): Show |
2 | a0013c0020t0050g0182a0013c0020t0052g0183 | 2 | HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.4402+1521_4402+157 others(62): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr5 | 175566 | |||||
| chr5:175566
|
A | ACAGACAC others(51): Show |
14 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(11): Show | 14 | HG00735.hp1 HG01261.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.4402+1491_4402+149 others(62): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr5 | 175566 | |||||
| chr5:175590
|
C | T | 10 | a0001c0007t0008g0143a0001c0007t0008g0145a0001c0007t0008g0146others(7): Show | 10 | HG02647.hp1 HG02723.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.4402+1492C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 175590 | ||||||
| chr5:175594
|
T | C | 5 | a0011c0023t0041g0184a0011c0023t0044g0187a0015c0076t0067g0192others(2): Show | 5 | HG02257.hp1 HG02280.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.4402+1496T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 175594 | ||||||
| chr5:175594
|
T | TGCACCCC others(226): Show |
2 | a0001c0036t0077g0149a0001c0051t0078g0148 | 2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.4402+1553_4402+155 others(237): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr5 | 175594 | |||||
| chr5:175614
|
A | AC | 5 | a0003c0004t0007g0097a0014c0027t0049g0171a0014c0066t0051g0170others(2): Show | 5 | HG02622.hp2 HG02809.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.4402+1520dupC | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr5 | 175614 | |||||
| chr5:175614
|
A | ACCCCCTC others(230): Show |
1 | a0032c0058t0040g0158 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4402+1520_4402+152 others(241): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr5 | 175614 | |||||
| chr5:175614
|
A | ACCCCTCC others(52): Show |
1 | a0001c0001t0073g0107 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.4402+1756_4402+181 others(63): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr5 | 175614 | |||||
| chr5:175614
|
A | ACCCCTCC others(170): Show |
1 | a0001c0002t0025g0073 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.4402+1638_4402+181 others(181): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr5 | 175614 | |||||
| chr5:175614
|
ACCCCTCC others(52): Show |
A | 2 | a0001c0002t0012g0066a0001c0002t0082g0126 | 2 | HG01106.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.4402+1756_4402+181 others(63): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr5 | 175614 | |||||
| chr5:175652
|
T | C | 5 | a0001c0036t0077g0149a0001c0051t0078g0148a0017c0030t0039g0140others(2): Show | 5 | HG02622.hp2 HG02809.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.4402+1554T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 175652 | ||||||
| chr5:175672
|
AC | A | 53 | a0001c0007t0008g0143a0001c0007t0008g0145a0001c0007t0008g0146others(50): Show | 53 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.4402+1579delC | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr5 | 175672 | |||||
| chr5:175711
|
T | C | 8 | a0001c0036t0077g0149a0001c0051t0078g0148a0011c0023t0041g0184others(5): Show | 8 | HG02257.hp1 HG02280.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.4402+1613T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 175711 | ||||||
| chr5:175731
|
ACCCCCTC others(112): Show |
A | 3 | a0011c0023t0041g0184a0011c0023t0044g0187a0015c0076t0067g0192 | 3 | HG02257.hp1 HG02280.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.4402+1638_4402+175 others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr5 | 175731 | |||||
| chr5:175732
|
CCCCCTCC others(169): Show |
C | 5 | a0009c0012t0033g0161a0009c0012t0114g0156a0009c0012t0115g0157others(2): Show | 5 | HG01099.hp1 HG02886.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.4402+1697_4402+187 others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr5 | 175732 | |||||
| chr5:175770
|
T | C | 5 | a0001c0036t0077g0149a0001c0051t0078g0148a0017c0030t0039g0140others(2): Show | 5 | HG02622.hp2 HG02809.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.4402+1672T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 175770 | ||||||
| chr5:175790
|
ACCCCCTC others(53): Show |
A | 12 | a0001c0052t0118g0121a0003c0009t0017g0088a0003c0009t0017g0093others(9): Show | 12 | HG00280.hp2 HG00323.hp2 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.4402+1697_4402+175 others(64): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr5 | 175790 | |||||
| chr5:175791
|
C | CCCCCTCC others(109): Show |
2 | a0014c0027t0049g0171a0021c0026t0060g0169 | 2 | HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.4402+1755_4402+175 others(120): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr5 | 175791 | |||||
| chr5:175829
|
T | C | 4 | a0001c0036t0077g0149a0001c0051t0078g0148a0017c0030t0039g0140others(1): Show | 4 | HG02622.hp2 HG03098.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.4402+1731T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 175829 | ||||||
| chr5:175849
|
AC | A | 42 | a0002c0003t0002g0098a0002c0003t0002g0101a0002c0003t0002g0132others(39): Show | 42 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.4402+1756delC | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr5 | 175849 | |||||
| chr5:175850
|
C | CCCCCTCC others(51): Show |
1 | a0014c0027t0049g0171 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.4402+1873_4402+193 others(62): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr5 | 175850 | |||||
| chr5:175850
|
C | CCCCTCCA others(167): Show |
1 | a0014c0066t0051g0170 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.4402+1755_4402+175 others(178): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr5 | 175850 | |||||
| chr5:175868
|
G | A | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4402+1770G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 175868 | ||||||
| chr5:175888
|
T | C | 4 | a0001c0036t0077g0149a0001c0051t0078g0148a0015c0076t0067g0192others(1): Show | 4 | HG02257.hp1 HG03098.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.4402+1790T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 175888 | ||||||
| chr5:175908
|
A | AC | 33 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(30): Show | 33 | HG00735.hp1 HG01261.hp2 HG02109.hp1 others(30): Show |
intron_variant | MODIFIER | c.4402+1814dupC | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr5 | 175908 | |||||
| chr5:175908
|
A | ACCCCCTC others(53): Show |
1 | a0017c0030t0039g0140 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.4402+1814_4402+181 others(64): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr5 | 175908 | |||||
| chr5:175908
|
A | ACCCCCTC others(872): Show |
1 | a0006c0068t0058g0194 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.4402+1814_4402+181 others(883): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr5 | 175908 | |||||
| chr5:175908
|
A | ACCCCCTC others(872): Show |
1 | a0008c0025t0069g0174 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4402+1814_4402+181 others(883): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr5 | 175908 | |||||
| chr5:175908
|
A | ACCCCCTC others(872): Show |
1 | a0008c0079t0068g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4402+1814_4402+181 others(883): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr5 | 175908 | |||||
| chr5:175926
|
G | GACCAGGG others(167): Show |
1 | a0001c0001t0028g0046 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.4402+1847_4402+184 others(178): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr5 | 175926 | |||||
| chr5:175934
|
CTCCTGCA others(338): Show |
C | 1 | a0004c0006t0134g0011 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.4402+1843_4402+218 others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr5 | 175934 | |||||
| chr5:175946
|
T | C | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4402+1848T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 175946 | ||||||
| chr5:175954
|
G | A | 1 | a0036c0075t0061g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4402+1856G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 175954 | ||||||
| chr5:175966
|
A | AC | 71 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0007t0008g0143others(68): Show | 71 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.4402+1872dupC | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr5 | 175966 | |||||
| chr5:175966
|
A | ACCCCCTC others(53): Show |
1 | a0001c0001t0113g0044 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.4402+1872_4402+187 others(64): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr5 | 175966 | |||||
| chr5:175981
|
C | T | 2 | a0001c0001t0097g0086a0001c0001t0104g0023 | 2 | HG00323.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.4402+1883C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 175981 | ||||||
| chr5:175992
|
CTCCTGCA others(280): Show |
C | 44 | a0002c0003t0002g0098a0002c0003t0002g0101a0002c0003t0002g0132others(41): Show | 44 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.4402+1901_4402+218 others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr5 | 175992 | |||||
| chr5:176000
|
C | T | 2 | a0003c0044t0001g0116a0034c0059t0001g0114 | 2 | NA18977.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.4402+1902C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 176000 | ||||||
| chr5:176004
|
T | C | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4402+1906T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 176004 | ||||||
| chr5:176012
|
G | A | 1 | a0036c0075t0061g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4402+1914G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 176012 | ||||||
| chr5:176034
|
GGT | G | 3 | a0002c0005t0002g0064a0002c0005t0003g0096a0035c0060t0020g0188 | 3 | HG03098.hp2 NA18954.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.4402+1938_4402+193 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr5 | 176034 | |||||
| chr5:176038
|
A | C | 3 | a0002c0005t0002g0064a0002c0005t0003g0096a0035c0060t0020g0188 | 3 | HG03098.hp2 NA18954.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.4402+1940A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 176038 | ||||||
| chr5:176041
|
C | A | 3 | a0002c0005t0002g0064a0002c0005t0003g0096a0035c0060t0020g0188 | 3 | HG03098.hp2 NA18954.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.4402+1943C>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 176041 | ||||||
| chr5:176045
|
C | G | 3 | a0002c0005t0002g0064a0002c0005t0003g0096a0035c0060t0020g0188 | 3 | HG03098.hp2 NA18954.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.4402+1947C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 176045 | ||||||
| chr5:176046
|
ACCTCCCC others(220): Show |
A | 2 | a0002c0005t0002g0064a0002c0005t0003g0096 | 2 | NA18954.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.4402+1951_4402+217 others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr5 | 176046 | |||||
| chr5:176049
|
T | A | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4402+1951T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 176049 | ||||||
| chr5:176049
|
T | C | 1 | a0036c0075t0061g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4402+1951T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 176049 | ||||||
| chr5:176050
|
C | G | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4402+1952C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 176050 | ||||||
| chr5:176051
|
C | G | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4402+1953C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 176051 | ||||||
| chr5:176052
|
C | G | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4402+1954C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 176052 | ||||||
| chr5:176054
|
A | T | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4402+1956A>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 176054 | ||||||
| chr5:176057
|
G | T | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4402+1959G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 176057 | ||||||
| chr5:176060
|
C | A | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4402+1962C>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 176060 | ||||||
| chr5:176063
|
T | C | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4402+1965T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 176063 | ||||||
| chr5:176065
|
A | C | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4402+1967A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 176065 | ||||||
| chr5:176067
|
A | C | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4402+1969A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 176067 | ||||||
| chr5:176069
|
A | C | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4402+1971A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 176069 | ||||||
| chr5:176071
|
T | G | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4402+1973T>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 176071 | ||||||
| chr5:176074
|
G | T | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4402+1976G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 176074 | ||||||
| chr5:176081
|
G | C | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4402+1983G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 176081 | ||||||
| chr5:176083
|
T | C | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4402+1985T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 176083 | ||||||
| chr5:176085
|
T | C | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4402+1987T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 176085 | ||||||
| chr5:176086
|
G | T | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4402+1988G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 176086 | ||||||
| chr5:176087
|
T | C | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4402+1989T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 176087 | ||||||
| chr5:176091
|
A | G | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4402+1993A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 176091 | ||||||
| chr5:176094
|
C | G | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4402+1996C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 176094 | ||||||
| chr5:176096
|
G | C | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4402+1998G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 176096 | ||||||
| chr5:176097
|
G | A | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4402+1999G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 176097 | ||||||
| chr5:176098
|
G | C | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4402+2000G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 176098 | ||||||
| chr5:176102
|
C | A | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4402+2004C>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 176102 | ||||||
| chr5:176106
|
T | G | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4402+2008T>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 176106 | ||||||
| chr5:176110
|
G | T | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4402+2012G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 176110 | ||||||
| chr5:176111
|
T | C | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4402+2013T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 176111 | ||||||
| chr5:176113
|
G | T | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4402+2015G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 176113 | ||||||
| chr5:176114
|
C | G | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4402+2016C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 176114 | ||||||
| chr5:176118
|
A | G | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4402+2020A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 176118 | ||||||
| chr5:176122
|
T | A | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4402+2024T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 176122 | ||||||
| chr5:176127
|
C | G | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4402+2029C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 176127 | ||||||
| chr5:176128
|
T | C | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4402+2030T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 176128 | ||||||
| chr5:176132
|
G | A | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4402+2034G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 176132 | ||||||
| chr5:176133
|
C | G | 4 | a0014c0027t0049g0171a0014c0066t0051g0170a0021c0026t0060g0169others(1): Show | 4 | HG02809.hp1 HG02818.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.4402+2035C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 176133 | ||||||
| chr5:176138
|
A | C | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4402+2040A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 176138 | ||||||
| chr5:176139
|
G | C | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4402+2041G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 176139 | ||||||
| chr5:176145
|
T | A | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4402+2047T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 176145 | ||||||
| chr5:176149
|
T | G | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4402+2051T>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 176149 | ||||||
| chr5:176152
|
T | A | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4402+2054T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 176152 | ||||||
| chr5:176154
|
C | G | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4402+2056C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 176154 | ||||||
| chr5:176155
|
ACACCCCC others(111): Show |
A | 1 | a0035c0060t0020g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4402+2059_4402+217 others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr5 | 176155 | |||||
| chr5:176277
|
C | G | 3 | a0002c0005t0002g0064a0002c0005t0003g0096a0035c0060t0020g0188 | 3 | HG03098.hp2 NA18954.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.4402+2179C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 176277 | ||||||
| chr5:176278
|
G | A | 2 | a0001c0001t0073g0107a0001c0001t0098g0129 | 2 | HG00738.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.4402+2180G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 176278 | ||||||
| chr5:176279
|
G | GC | 3 | a0002c0005t0002g0064a0002c0005t0003g0096a0035c0060t0020g0188 | 3 | HG03098.hp2 NA18954.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.4402+2181_4402+218 others(5): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 176279 | ||||||
| chr5:176422
|
G | A | 1 | a0027c0053t0107g0009 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4402+2324G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 176422 | ||||||
| chr5:176467
|
G | A | 2 | a0001c0036t0077g0149a0001c0051t0078g0148 | 2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.4402+2369G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 176467 | ||||||
| chr5:176547
|
C | T | 1 | a0001c0001t0007g0056 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.4402+2449C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 176547 | ||||||
| chr5:176636
|
C | T | 13 | a0001c0052t0118g0121a0003c0009t0017g0088a0003c0009t0017g0093others(10): Show | 13 | HG00280.hp2 HG00323.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.4402+2538C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 176636 | ||||||
| chr5:176850
|
C | T | 1 | a0003c0009t0017g0088 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.4402+2752C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 176850 | ||||||
| chr5:176866
|
C | T | 1 | a0015c0076t0067g0192 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.4402+2768C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 176866 | ||||||
| chr5:177103
|
C | T | 3 | a0017c0030t0039g0140a0032c0058t0040g0158a0036c0075t0061g0178 | 3 | HG02622.hp2 HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.4402+3005C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 177103 | ||||||
| chr5:177106
|
T | C | 3 | a0017c0030t0039g0140a0032c0058t0040g0158a0036c0075t0061g0178 | 3 | HG02622.hp2 HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.4402+3008T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 177106 | ||||||
| chr5:177117
|
A | G | 12 | a0001c0052t0118g0121a0003c0009t0017g0088a0003c0009t0017g0093others(9): Show | 12 | HG00280.hp2 HG00323.hp2 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.4402+3019A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 177117 | ||||||
| chr5:177149
|
A | C | 40 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(37): Show | 40 | HG00735.hp1 HG01099.hp1 HG01261.hp2 others(37): Show |
intron_variant | MODIFIER | c.4402+3051A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 177149 | ||||||
| chr5:177149
|
A | T | 1 | a0036c0075t0061g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4402+3051A>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 177149 | ||||||
| chr5:177195
|
A | C | 2 | a0017c0030t0039g0140a0032c0058t0040g0158 | 2 | HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.4402+3097A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 177195 | ||||||
| chr5:177274
|
C | G | 39 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(36): Show | 39 | HG00735.hp1 HG01099.hp1 HG01261.hp2 others(36): Show |
intron_variant | MODIFIER | c.4402+3176C>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 177274 | ||||||
| chr5:177360
|
T | C | 2 | a0001c0036t0077g0149a0001c0051t0078g0148 | 2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.4402+3262T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 177360 | ||||||
| chr5:177599
|
C | T | 12 | a0001c0052t0118g0121a0003c0009t0017g0088a0003c0009t0017g0093others(9): Show | 12 | HG00280.hp2 HG00323.hp2 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.4402+3501C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 177599 | ||||||
| chr5:177628
|
G | T | 1 | a0001c0001t0006g0075 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.4402+3530G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 177628 | ||||||
| chr5:177653
|
G | A | 2 | a0001c0001t0015g0022a0001c0001t0015g0037 | 2 | HG01099.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.4402+3555G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 177653 | ||||||
| chr5:177715
|
C | T | 2 | a0017c0030t0039g0140a0032c0058t0040g0158 | 2 | HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.4402+3617C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 177715 | ||||||
| chr5:177722
|
C | T | 41 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(38): Show | 41 | HG00735.hp1 HG01099.hp1 HG01261.hp2 others(38): Show |
intron_variant | MODIFIER | c.4402+3624C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 177722 | ||||||
| chr5:177809
|
G | A | 2 | a0011c0023t0044g0187a0015c0076t0067g0192 | 2 | HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.4403-3705G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 177809 | ||||||
| chr5:177875
|
ACTTTCGT others(141): Show |
A | 6 | a0001c0007t0008g0143a0001c0007t0008g0145a0001c0007t0008g0146others(3): Show | 6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.4403-3559_4403-341 others(4): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr5 | 177875 | |||||
| chr5:177881
|
G | C | 34 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(31): Show | 34 | HG00735.hp1 HG01099.hp1 HG01261.hp2 others(31): Show |
intron_variant | MODIFIER | c.4403-3633G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 177881 | ||||||
| chr5:177917
|
T | C | 3 | a0014c0027t0049g0171a0014c0066t0051g0170a0021c0026t0060g0169 | 3 | HG02809.hp1 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.4403-3597T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 177917 | ||||||
| chr5:177988
|
G | A | 2 | a0017c0030t0039g0140a0032c0058t0040g0158 | 2 | HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.4403-3526G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 177988 | ||||||
| chr5:178047
|
G | A | 1 | a0002c0003t0071g0095 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.4403-3467G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 178047 | ||||||
| chr5:178050
|
C | T | 6 | a0011c0023t0041g0184a0011c0023t0044g0187a0014c0027t0049g0171others(3): Show | 6 | HG02257.hp1 HG02280.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.4403-3464C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 178050 | ||||||
| chr5:178207
|
G | C | 1 | a0015c0076t0067g0192 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.4403-3307G>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 178207 | ||||||
| chr5:178429
|
G | A | 2 | a0014c0027t0049g0171a0014c0066t0051g0170 | 2 | HG02809.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.4403-3085G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 178429 | ||||||
| chr5:178594
|
A | G | 5 | a0009c0012t0033g0161a0009c0012t0114g0156a0009c0012t0115g0157others(2): Show | 5 | HG01099.hp1 HG02886.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.4403-2920A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 178594 | ||||||
| chr5:178600
|
CTT | C | 4 | a0001c0036t0077g0149a0001c0051t0078g0148a0017c0030t0039g0140others(1): Show | 4 | HG02622.hp2 HG02809.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.4403-2910_4403-290 others(6): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr5 | 178600 | |||||
| chr5:178782
|
T | C | 2 | a0016c0018t0003g0005a0016c0018t0034g0004 | 2 | HG02145.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.4403-2732T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 178782 | ||||||
| chr5:178785
|
G | A | 39 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(36): Show | 39 | HG00735.hp1 HG01099.hp1 HG01261.hp2 others(36): Show |
intron_variant | MODIFIER | c.4403-2729G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 178785 | ||||||
| chr5:178831
|
C | T | 2 | a0017c0030t0039g0140a0032c0058t0040g0158 | 2 | HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.4403-2683C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 178831 | ||||||
| chr5:179014
|
G | T | 5 | a0001c0036t0077g0149a0001c0051t0078g0148a0017c0030t0039g0140others(2): Show | 5 | HG02622.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.4403-2500G>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 179014 | ||||||
| chr5:179180
|
G | A | 5 | a0003c0009t0017g0088a0003c0009t0017g0093a0003c0009t0119g0049others(2): Show | 5 | HG01243.hp1 HG01256.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.4403-2334G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 179180 | ||||||
| chr5:179383
|
G | A | 2 | a0001c0001t0113g0044a0010c0014t0057g0197 | 2 | HG00735.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.4403-2131G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 179383 | ||||||
| chr5:179556
|
C | T | 1 | a0001c0032t0103g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4403-1958C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 179556 | ||||||
| chr5:179644
|
C | T | 46 | a0002c0003t0002g0098a0002c0003t0002g0101a0002c0003t0002g0132others(43): Show | 46 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.4403-1870C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 179644 | ||||||
| chr5:179810
|
C | T | 5 | a0001c0036t0077g0149a0001c0051t0078g0148a0017c0030t0039g0140others(2): Show | 5 | HG02622.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.4403-1704C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 179810 | ||||||
| chr5:179933
|
AT | A | 3 | a0014c0027t0049g0171a0014c0066t0051g0170a0021c0026t0060g0169 | 3 | HG02809.hp1 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.4403-1578delT | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr5 | 179933 | |||||
| chr5:180027
|
G | A | 5 | a0001c0016t0005g0160a0001c0016t0025g0152a0001c0035t0030g0137others(2): Show | 5 | HG02717.hp1 HG02922.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.4403-1487G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 180027 | ||||||
| chr5:180056
|
T | A | 2 | a0006c0070t0054g0207a0017c0029t0112g0155 | 2 | HG02896.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.4403-1458T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 180056 | ||||||
| chr5:180210
|
T | G | 88 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(85): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.4403-1304T>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 180210 | ||||||
| chr5:180237
|
T | C | 63 | a0001c0036t0077g0149a0001c0051t0078g0148a0001c0052t0118g0121others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.4403-1277T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 180237 | ||||||
| chr5:180245
|
G | A | 2 | a0001c0001t0032g0094a0001c0001t0032g0144 | 2 | HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.4403-1269G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 180245 | ||||||
| chr5:180266
|
C | T | 8 | a0001c0036t0077g0149a0001c0051t0078g0148a0002c0003t0071g0095others(5): Show | 8 | HG01192.hp1 HG02622.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.4403-1248C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 180266 | ||||||
| chr5:180531
|
C | T | 34 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(31): Show | 34 | HG00735.hp1 HG01099.hp1 HG01261.hp2 others(31): Show |
intron_variant | MODIFIER | c.4403-983C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 180531 | ||||||
| chr5:180695
|
G | A | 1 | a0001c0011t0106g0085 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4403-819G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 180695 | ||||||
| chr5:180863
|
G | A | 1 | a0041c0064t0010g0190 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.4403-651G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 180863 | ||||||
| chr5:180991
|
G | A | 1 | a0038c0080t0043g0177 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.4403-523G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 180991 | ||||||
| chr5:181006
|
G | A | 203 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0142others(200): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.4403-508G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 181006 | ||||||
| chr5:181105
|
T | C | 3 | a0014c0027t0049g0171a0014c0066t0051g0170a0021c0026t0060g0169 | 3 | HG02809.hp1 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.4403-409T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 181105 | ||||||
| chr5:181335
|
C | A | 3 | a0009c0012t0114g0156a0009c0012t0115g0157a0011c0078t0059g0185 | 3 | HG01099.hp1 HG02886.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.4403-179C>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 181335 | ||||||
| chr5:181348
|
T | C | 105 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(102): Show | 105 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.4403-166T>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 181348 | ||||||
| chr5:181384
|
G | A | 24 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(21): Show | 24 | HG00735.hp1 HG01261.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.4403-130G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 181384 | ||||||
| chr5:181393
|
G | A | 1 | a0019c0019t0062g0191 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.4403-121G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 181393 | ||||||
| chr5:181451
|
G | A | 5 | a0001c0036t0077g0149a0001c0051t0078g0148a0014c0065t0038g0166others(2): Show | 5 | HG02622.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.4403-63G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 18/19 | chr5 | 181451 | ||||||
| chr5:181746
|
C | T | 7 | a0001c0015t0035g0122a0001c0015t0076g0154a0001c0036t0077g0149others(4): Show | 7 | HG02622.hp2 HG02809.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.4564+71C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 19/19 | chr5 | 181746 | ||||||
| chr5:181756
|
G | A | 2 | a0001c0001t0031g0111a0001c0001t0031g0112 | 2 | HG01952.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.4564+81G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 19/19 | chr5 | 181756 | ||||||
| chr5:181788
|
A | G | 1 | a0002c0005t0003g0167 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.4564+113A>G | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 19/19 | chr5 | 181788 | ||||||
| chr5:181839
|
A | C | 35 | a0001c0001t0032g0094a0001c0001t0032g0144a0001c0001t0113g0044others(32): Show | 35 | HG00735.hp1 HG01099.hp1 HG01261.hp2 others(32): Show |
intron_variant | MODIFIER | c.4564+164A>C | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 19/19 | chr5 | 181839 | ||||||
| chr5:181944
|
G | A | 1 | a0001c0061t0001g0006 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.4565-60G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 19/19 | chr5 | 181944 | ||||||
| chr5:181962
|
T | A | 47 | a0002c0003t0002g0098a0002c0003t0002g0101a0002c0003t0002g0132others(44): Show | 47 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.4565-42T>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 19/19 | chr5 | 181962 | ||||||
| chr5:181967
|
C | T | 1 | a0001c0001t0028g0046 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.4565-37C>T | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 19/19 | chr5 | 181967 | ||||||
| chr5:181983
|
G | A | 1 | a0012c0013t0133g0118 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.4565-21G>A | PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 19/19 | chr5 | 181983 |