Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 2820 |
|---|---|
| ensemblid | ENSG00000115159.17 |
| hgncid | 4456 |
| symbol | GPD2 |
| name | glycerol-3-phosphate dehydrogenase 2 |
| refseq_nuc | NM_000408.5 |
| refseq_prot | NP_000399.3 |
| ensembl_nuc | ENST00000438166.7 |
| ensembl_prot | ENSP00000409708.2 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 156436379 |
| end | 156586403 |
| strand | + |
| ver | v1.2 |
| region | chr2:156436379-156586403 |
| region5000 | chr2:156431379-156591403 |
| regionname0 | GPD2_chr2_156436379_156586403 |
| regionname5000 | GPD2_chr2_156431379_156591403 |
| 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 | 727 | 167 | 27 | 25 | 86 | 4 | 25 | 65 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| a0002 | 1/1 | 727 | 78 | 23 | 17 | 27 | 2 | 7 | 20 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| a0003 | 0/0 | 727 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| a0004 | 0/0 | 727 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| 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 | 2184 | 160 | 27 | 24 | 82 | 3 | 24 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| c0002 | 1/1 | 2184 | 78 | 23 | 17 | 27 | 2 | 7 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| c0003 | 0/0 | 2184 | 8 | 8 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| c0004 | 0/0 | 2184 | 3 | 0 | 1 | 0 | 1 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| c0005 | 0/0 | 2184 | 2 | 0 | 0 | 2 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| c0006 | 0/0 | 2184 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| c0007 | 0/0 | 2184 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| c0008 | 0/0 | 2184 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| 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 | 3629 | 138 | 22 | 22 | 71 | 4 | 19 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| t0002 | 0/1 | 3629 | 32 | 7 | 6 | 12 | 1 | 5 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| t0003 | 0/0 | 3627 | 18 | 2 | 2 | 9 | 0 | 5 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| t0004 | 0/0 | 3629 | 11 | 0 | 0 | 11 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| t0005 | 0/0 | 3629 | 9 | 9 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| t0006 | 0/0 | 3629 | 8 | 3 | 3 | 2 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| t0007 | 0/0 | 3629 | 7 | 7 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| t0008 | 1/0 | 3629 | 5 | 4 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| t0009 | 0/0 | 3629 | 5 | 0 | 5 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| t0010 | 0/0 | 3629 | 4 | 0 | 0 | 4 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| t0011 | 0/0 | 3629 | 3 | 0 | 1 | 0 | 0 | 2 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| t0012 | 0/0 | 3629 | 3 | 3 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| t0013 | 0/0 | 3629 | 2 | 0 | 0 | 2 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| t0014 | 0/0 | 3629 | 2 | 0 | 2 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| t0015 | 0/0 | 3629 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| t0016 | 0/0 | 3629 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| t0017 | 0/0 | 3629 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| t0018 | 0/0 | 3627 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| t0019 | 0/0 | 3629 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| t0020 | 0/0 | 3629 | 1 | 0 | 0 | 0 | 1 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| t0021 | 0/0 | 3629 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| 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 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0092 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0175 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| 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 | 2184 | 160 | 27 | 24 | 82 | 3 | 24 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| a0001c0004 | 0/0 | 2184 | 3 | 0 | 1 | 0 | 1 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| a0001c0005 | 0/0 | 2184 | 2 | 0 | 0 | 2 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| a0001c0006 | 0/0 | 2184 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| a0001c0007 | 0/0 | 2184 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| a0002c0002 | 1/1 | 2184 | 78 | 23 | 17 | 27 | 2 | 7 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| a0003c0003 | 0/0 | 2184 | 8 | 8 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| a0004c0008 | 0/0 | 2184 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5812 | 125 | 18 | 21 | 65 | 3 | 18 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| a0001c0001t0003 | 0/0 | 5810 | 18 | 2 | 2 | 9 | 0 | 5 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| a0001c0001t0005 | 0/0 | 5812 | 7 | 7 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| a0001c0001t0010 | 0/0 | 5812 | 4 | 0 | 0 | 4 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| a0001c0001t0013 | 0/0 | 5812 | 2 | 0 | 0 | 2 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| a0001c0001t0015 | 0/0 | 5812 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| a0001c0001t0016 | 0/0 | 5812 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| a0001c0001t0017 | 0/0 | 5812 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| a0001c0001t0018 | 0/0 | 5810 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| a0001c0004t0001 | 0/0 | 5812 | 3 | 0 | 1 | 0 | 1 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| a0001c0005t0001 | 0/0 | 5812 | 2 | 0 | 0 | 2 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| a0001c0006t0001 | 0/0 | 5812 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| a0001c0007t0001 | 0/0 | 5812 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| a0002c0002t0001 | 0/0 | 5812 | 5 | 4 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| a0002c0002t0002 | 0/1 | 5812 | 32 | 7 | 6 | 12 | 1 | 5 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| a0002c0002t0004 | 0/0 | 5812 | 11 | 0 | 0 | 11 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| a0002c0002t0005 | 0/0 | 5812 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| a0002c0002t0006 | 0/0 | 5812 | 8 | 3 | 3 | 2 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| a0002c0002t0008 | 1/0 | 5812 | 5 | 4 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| a0002c0002t0009 | 0/0 | 5812 | 5 | 0 | 5 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| a0002c0002t0011 | 0/0 | 5812 | 3 | 0 | 1 | 0 | 0 | 2 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| a0002c0002t0012 | 0/0 | 5812 | 3 | 3 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| a0002c0002t0014 | 0/0 | 5812 | 2 | 0 | 2 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| a0002c0002t0019 | 0/0 | 5812 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| a0002c0002t0020 | 0/0 | 5812 | 1 | 0 | 0 | 0 | 1 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| a0002c0002t0021 | 0/0 | 5812 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| a0003c0003t0005 | 0/0 | 5812 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| a0003c0003t0007 | 0/0 | 5812 | 7 | 7 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| a0004c0008t0001 | 0/0 | 5812 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | copy fasta | chr2 | 156431379 | 156591403 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0003g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0003g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0003g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0003g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0003g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0003g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0003g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0003g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0003g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0003g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0005g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0005g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0005g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0005g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0005g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0005g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0005g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0010g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0010g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0010g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0010g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0013g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0013g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0015g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0016g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0017g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0001t0018g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0004t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0004t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0004t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0005t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0005t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0006t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0001c0007t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0002g0092 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0004g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0004g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0004g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0004g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0004g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0004g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0004g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0004g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0004g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0005g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0006g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0006g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0006g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0006g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0006g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0006g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0006g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0006g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0008g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0008g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0008g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0008g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0008g0175 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0009g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0009g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0009g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0009g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0009g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0011g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0011g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0011g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0012g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0012g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0012g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0014g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0014g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0019g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0020g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0002c0002t0021g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0003c0003t0005g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0003c0003t0007g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0003c0003t0007g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0003c0003t0007g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0003c0003t0007g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0003c0003t0007g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0003c0003t0007g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0003c0003t0007g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| a0004c0008t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0142 | EUR | GBR | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG00140 | hp2 | a0001 | c0004 | t0001 | g0238 | EUR | GBR | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0207 | EUR | FIN | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG00323 | hp2 | a0002 | c0002 | t0002 | g0048 | EUR | FIN | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG00438 | hp1 | a0001 | c0001 | t0010 | g0060 | EAS | CHS | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG00438 | hp2 | a0002 | c0002 | t0004 | g0025 | EAS | CHS | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | CHS | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG00621 | hp1 | a0002 | c0002 | t0004 | g0027 | EAS | CHS | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | CHS | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0093 | AMR | PUR | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | CHS | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG00673 | hp2 | a0002 | c0002 | t0006 | g0070 | EAS | CHS | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG00735 | hp1 | a0002 | c0002 | t0006 | g0156 | AMR | PUR | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG01070 | hp2 | a0002 | c0002 | t0014 | g0123 | AMR | PUR | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG01099 | hp2 | a0002 | c0002 | t0006 | g0155 | AMR | PUR | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG01106 | hp1 | a0002 | c0002 | t0002 | g0044 | AMR | PUR | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG01167 | hp2 | a0002 | c0002 | t0002 | g0134 | AMR | PUR | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG01192 | hp2 | a0002 | c0002 | t0014 | g0089 | AMR | PUR | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG01243 | hp1 | a0002 | c0002 | t0006 | g0157 | AMR | PUR | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0068 | AMR | CLM | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG01261 | hp1 | a0002 | c0002 | t0002 | g0108 | AMR | CLM | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG01261 | hp2 | a0001 | c0001 | t0016 | g0039 | AMR | CLM | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG01346 | hp2 | a0002 | c0002 | t0009 | g0133 | AMR | CLM | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG01358 | hp1 | a0002 | c0002 | t0002 | g0145 | AMR | CLM | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG01433 | hp1 | a0001 | c0004 | t0001 | g0232 | AMR | CLM | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG01433 | hp2 | a0002 | c0002 | t0009 | g0131 | AMR | CLM | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG01496 | hp1 | a0002 | c0002 | t0009 | g0132 | AMR | CLM | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG01496 | hp2 | a0002 | c0002 | t0011 | g0076 | AMR | CLM | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0023 | EUR | IBS | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG01517 | hp2 | a0002 | c0002 | t0020 | g0020 | EUR | IBS | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0088 | AFR | ACB | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG01884 | hp2 | a0002 | c0002 | t0002 | g0118 | AFR | ACB | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG01891 | hp1 | a0003 | c0003 | t0007 | g0122 | AFR | ACB | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG01891 | hp2 | a0003 | c0003 | t0005 | g0158 | AFR | ACB | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG01928 | hp1 | a0002 | c0002 | t0009 | g0033 | AMR | PEL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG01928 | hp2 | a0002 | c0002 | t0002 | g0047 | AMR | PEL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG01975 | hp1 | a0002 | c0002 | t0009 | g0137 | AMR | PEL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | KHV | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG02040 | hp1 | a0002 | c0002 | t0002 | g0094 | EAS | KHV | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG02055 | hp1 | a0003 | c0003 | t0007 | g0012 | AFR | ACB | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG02055 | hp2 | a0002 | c0002 | t0002 | g0117 | AFR | ACB | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG02056 | hp1 | a0001 | c0001 | t0015 | g0144 | EAS | KHV | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | KHV | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0200 | EAS | KHV | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG02071 | hp2 | a0001 | c0001 | t0010 | g0030 | EAS | KHV | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG02074 | hp2 | a0002 | c0002 | t0021 | g0079 | EAS | KHV | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG02129 | hp1 | a0002 | c0002 | t0002 | g0038 | EAS | KHV | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CDX | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | CDX | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG02258 | hp1 | a0002 | c0002 | t0006 | g0154 | AFR | ACB | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG02258 | hp2 | a0002 | c0002 | t0012 | g0152 | AFR | ACB | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG02451 | hp1 | a0002 | c0002 | t0002 | g0138 | AFR | ACB | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | ACB | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG02523 | hp2 | a0001 | c0001 | t0013 | g0043 | EAS | KHV | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG02602 | hp1 | a0002 | c0002 | t0002 | g0029 | SAS | PJL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0182 | AFR | GWD | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG02630 | hp2 | a0002 | c0002 | t0005 | g0159 | AFR | GWD | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0069 | SAS | PJL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG02683 | hp2 | a0001 | c0001 | t0017 | g0065 | SAS | PJL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG02717 | hp1 | a0002 | c0002 | t0002 | g0162 | AFR | GWD | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG02717 | hp2 | a0001 | c0001 | t0005 | g0177 | AFR | GWD | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG02723 | hp1 | a0002 | c0002 | t0008 | g0136 | AFR | GWD | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG02723 | hp2 | a0001 | c0001 | t0005 | g0181 | AFR | GWD | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG02738 | hp1 | a0002 | c0002 | t0011 | g0075 | SAS | PJL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG02886 | hp2 | a0003 | c0003 | t0007 | g0169 | AFR | GWD | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0178 | AFR | GWD | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG02897 | hp1 | a0003 | c0003 | t0007 | g0183 | AFR | GWD | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG02965 | hp1 | a0002 | c0002 | t0002 | g0160 | AFR | ESN | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ESN | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0172 | AFR | ESN | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG02976 | hp2 | a0003 | c0003 | t0007 | g0180 | AFR | ESN | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | MSL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG03098 | hp2 | a0002 | c0002 | t0019 | g0171 | AFR | MSL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ESN | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0165 | AFR | ESN | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | ESN | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | ESN | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG03486 | hp1 | a0002 | c0002 | t0008 | g0167 | AFR | MSL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG03486 | hp2 | a0002 | c0002 | t0012 | g0096 | AFR | MSL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG03492 | hp1 | a0002 | c0002 | t0002 | g0080 | SAS | PJL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0166 | AFR | GWD | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG03540 | hp2 | a0001 | c0001 | t0005 | g0151 | AFR | GWD | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | MSL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG03579 | hp2 | a0003 | c0003 | t0007 | g0168 | AFR | MSL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG03654 | hp1 | a0002 | c0002 | t0002 | g0046 | SAS | PJL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG03704 | hp1 | a0001 | c0004 | t0001 | g0239 | SAS | PJL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0087 | SAS | PJL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0244 | SAS | BEB | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG03834 | hp2 | a0002 | c0002 | t0011 | g0125 | SAS | BEB | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG04115 | hp1 | a0002 | c0002 | t0002 | g0147 | SAS | STU | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | STU | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | BEB | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | BEB | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | STU | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0247 | SAS | STU | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0204 | SAS | STU | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0086 | SAS | STU | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | CHB | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | CHB | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA18906 | hp1 | a0002 | c0002 | t0001 | g0179 | AFR | YRI | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA18906 | hp2 | a0002 | c0002 | t0008 | g0173 | AFR | YRI | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA18941 | hp2 | a0002 | c0002 | t0002 | g0084 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA18943 | hp2 | a0002 | c0002 | t0002 | g0019 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA18944 | hp2 | a0002 | c0002 | t0002 | g0091 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA18948 | hp2 | a0002 | c0002 | t0004 | g0035 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA18952 | hp1 | a0001 | c0005 | t0001 | g0223 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA18952 | hp2 | a0002 | c0002 | t0004 | g0112 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA18953 | hp1 | a0002 | c0002 | t0002 | g0109 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA18959 | hp1 | a0004 | c0008 | t0001 | g0231 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA18964 | hp2 | a0002 | c0002 | t0006 | g0098 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA18969 | hp2 | a0002 | c0002 | t0002 | g0126 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA18971 | hp2 | a0002 | c0002 | t0004 | g0061 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA18975 | hp1 | a0002 | c0002 | t0002 | g0127 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA18980 | hp1 | a0002 | c0002 | t0002 | g0045 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA18984 | hp2 | a0001 | c0001 | t0013 | g0058 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA18991 | hp1 | a0002 | c0002 | t0004 | g0034 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA18999 | hp2 | a0002 | c0002 | t0004 | g0113 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA19002 | hp2 | a0002 | c0002 | t0002 | g0110 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA19007 | hp2 | a0001 | c0001 | t0010 | g0146 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA19010 | hp1 | a0002 | c0002 | t0002 | g0078 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | LWK | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA19030 | hp2 | a0002 | c0002 | t0001 | g0185 | AFR | LWK | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA19043 | hp1 | a0002 | c0002 | t0006 | g0176 | AFR | LWK | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | LWK | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA19057 | hp2 | a0002 | c0002 | t0004 | g0121 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA19060 | hp1 | a0001 | c0005 | t0001 | g0197 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA19066 | hp1 | a0001 | c0007 | t0001 | g0196 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA19067 | hp2 | a0001 | c0006 | t0001 | g0198 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA19074 | hp1 | a0002 | c0002 | t0002 | g0013 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA19076 | hp1 | a0001 | c0001 | t0010 | g0018 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA19076 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA19082 | hp1 | a0002 | c0002 | t0004 | g0097 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA19087 | hp1 | a0002 | c0002 | t0004 | g0128 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA19087 | hp2 | a0001 | c0001 | t0018 | g0011 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA19091 | hp1 | a0002 | c0002 | t0004 | g0120 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | GIH | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA20905 | hp2 | a0002 | c0002 | t0002 | g0139 | SAS | GIH | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | CLM | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG01123 | hp2 | a0002 | c0002 | t0002 | g0090 | AMR | CLM | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG02109 | hp1 | a0002 | c0002 | t0006 | g0161 | AFR | ACB | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG02559 | hp1 | a0002 | c0002 | t0002 | g0164 | AFR | ACB | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG02559 | hp2 | a0002 | c0002 | t0012 | g0073 | AFR | ACB | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG06807 | hp1 | a0003 | c0003 | t0007 | g0170 | AFR | USA | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| HG06807 | hp2 | a0002 | c0002 | t0008 | g0174 | AFR | USA | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA20300 | hp1 | a0002 | c0002 | t0002 | g0163 | AFR | USA | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0249 | AFR | USA | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0184 | AFR | LWK | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | LWK | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0002 | g0092 | REF | REF | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| homoSapiens_grch38 | hp1 | a0002 | c0002 | t0008 | g0175 | REF | REF | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:156476190
|
C | T | 1 | a0004 | 1 | NA18959.hp1 | missense_variant | MODERATE | c.85C>T | p.His29Tyr | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/17 | 228/5812 | 85/2184 | 29/727 | chr2 | 156476190 | ||
| chr2:156549737
|
G | A | 2 | a0001a0004 | 168 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
missense_variant | MODERATE | c.791G>A | p.Arg264His | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 7/17 | 934/5812 | 791/2184 | 264/727 | chr2 | 156549737 | ||
| chr2:156569419
|
A | C | 1 | a0003 | 8 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(5): Show |
missense_variant | MODERATE | c.1357A>C | p.Lys453Gln | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 11/17 | 1500/5812 | 1357/2184 | 453/727 | chr2 | 156569419 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:156513495
|
C | T | 1 | a0001c0007 | 1 | NA19066.hp1 | splice_region_variant&synonymous_variant | LOW | c.660C>T | p.Asp220Asp | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/17 | 803/5812 | 660/2184 | 220/727 | chr2 | 156513495 | ||
| chr2:156549675
|
A | G | 1 | a0001c0005 | 2 | NA18952.hp1 NA19060.hp1 |
synonymous_variant | LOW | c.729A>G | p.Thr243Thr | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 7/17 | 872/5812 | 729/2184 | 243/727 | chr2 | 156549675 | ||
| chr2:156569460
|
G | A | 1 | a0001c0004 | 3 | HG00140.hp2 HG01433.hp1 HG03704.hp1 |
synonymous_variant | LOW | c.1398G>A | p.Gly466Gly | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 11/17 | 1541/5812 | 1398/2184 | 466/727 | chr2 | 156569460 | ||
| chr2:156571286
|
G | A | 1 | a0001c0006 | 1 | NA19067.hp2 | synonymous_variant | LOW | c.1761G>A | p.Lys587Lys | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/17 | 1904/5812 | 1761/2184 | 587/727 | chr2 | 156571286 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:156436387
|
G | T | 1 | a0002c0002t0004 | 11 | HG00438.hp2 HG00621.hp1 NA18948.hp2 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-135G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/17 | 39719 | chr2 | 156436387 | |||||
| chr2:156436417
|
C | T | 1 | a0002c0002t0021 | 1 | HG02074.hp2 | 5_prime_UTR_variant | MODIFIER | c.-105C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/17 | 39689 | chr2 | 156436417 | |||||
| chr2:156583078
|
G | C | 1 | a0001c0001t0013 | 2 | HG02523.hp2 NA18984.hp2 |
3_prime_UTR_variant | MODIFIER | c.*160G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 17/17 | 160 | chr2 | 156583078 | |||||
| chr2:156583140
|
C | T | 1 | a0002c0002t0020 | 1 | HG01517.hp2 | 3_prime_UTR_variant | MODIFIER | c.*222C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 17/17 | 222 | chr2 | 156583140 | |||||
| chr2:156583345
|
A | G | 28 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(25): Show | 249 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(246): Show |
3_prime_UTR_variant | MODIFIER | c.*427A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 17/17 | 427 | chr2 | 156583345 | |||||
| chr2:156583401
|
A | G | 1 | a0002c0002t0012 | 3 | HG02258.hp2 HG02559.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*483A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 17/17 | 483 | chr2 | 156583401 | |||||
| chr2:156583657
|
C | G | 1 | a0002c0002t0011 | 3 | HG01496.hp2 HG02738.hp1 HG03834.hp2 |
3_prime_UTR_variant | MODIFIER | c.*739C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 17/17 | 739 | chr2 | 156583657 | |||||
| chr2:156584007
|
C | A | 1 | a0001c0001t0015 | 1 | HG02056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1089C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 17/17 | 1089 | chr2 | 156584007 | |||||
| chr2:156584132
|
G | C | 15 | a0001c0001t0001a0001c0001t0003a0001c0001t0010others(12): Show | 169 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(166): Show |
3_prime_UTR_variant | MODIFIER | c.*1214G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 17/17 | 1214 | chr2 | 156584132 | |||||
| chr2:156584454
|
A | G | 1 | a0002c0002t0019 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1536A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 17/17 | 1536 | chr2 | 156584454 | |||||
| chr2:156584584
|
G | T | 1 | a0001c0001t0018 | 1 | NA19087.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1666G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 17/17 | 1666 | chr2 | 156584584 | |||||
| chr2:156584597
|
C | T | 1 | a0003c0003t0007 | 7 | HG01891.hp1 HG02055.hp1 HG02886.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1679C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 17/17 | 1679 | chr2 | 156584597 | |||||
| chr2:156584789
|
A | G | 1 | a0001c0001t0010 | 4 | HG00438.hp1 HG02071.hp2 NA19007.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1871A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 17/17 | 1871 | chr2 | 156584789 | |||||
| chr2:156585152
|
G | C | 9 | a0002c0002t0002a0002c0002t0004a0002c0002t0006others(6): Show | 64 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*2234G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 17/17 | 2234 | chr2 | 156585152 | |||||
| chr2:156585158
|
A | G | 1 | a0002c0002t0014 | 2 | HG01070.hp2 HG01192.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2240A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 17/17 | 2240 | chr2 | 156585158 | |||||
| chr2:156585291
|
C | T | 2 | a0002c0002t0006a0002c0002t0019 | 9 | HG00673.hp2 HG00735.hp1 HG01099.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2373C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 17/17 | 2373 | chr2 | 156585291 | |||||
| chr2:156585613
|
G | C | 1 | a0001c0001t0016 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2695G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 17/17 | 2695 | chr2 | 156585613 | |||||
| chr2:156585725
|
G | A | 1 | a0002c0002t0009 | 5 | HG01346.hp2 HG01433.hp2 HG01496.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2807G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 17/17 | 2807 | chr2 | 156585725 | |||||
| chr2:156585741
|
G | A | 9 | a0002c0002t0002a0002c0002t0004a0002c0002t0006others(6): Show | 64 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*2823G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 17/17 | 2823 | chr2 | 156585741 | |||||
| chr2:156586242
|
CTG | C | 2 | a0001c0001t0003a0001c0001t0018 | 19 | HG00558.hp1 HG00639.hp1 HG01258.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*3328_*3329delGT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 17/17 | 3328 | INFO_REALIGN_3_PRIME | chr2 | 156586242 | ||||
| chr2:156586245
|
T | G | 1 | a0001c0001t0017 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3327T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 17/17 | 3327 | chr2 | 156586245 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:156436560
|
G | C | 11 | a0001c0001t0001g0002a0001c0001t0003g0001a0001c0001t0003g0003others(8): Show | 11 | HG00558.hp1 HG02015.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.-9+47G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156436560 | ||||||
| chr2:156436561
|
G | T | 2 | a0001c0001t0001g0253a0001c0001t0001g0254 | 2 | HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-9+48G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156436561 | ||||||
| chr2:156436627
|
C | T | 1 | a0001c0001t0001g0252 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-9+114C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156436627 | ||||||
| chr2:156437434
|
A | C | 1 | a0001c0001t0001g0251 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-9+921A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156437434 | ||||||
| chr2:156437479
|
A | G | 75 | a0001c0001t0001g0002a0001c0001t0001g0187a0001c0001t0001g0188others(72): Show | 75 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.-9+966A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156437479 | ||||||
| chr2:156437527
|
C | T | 75 | a0001c0001t0001g0002a0001c0001t0001g0187a0001c0001t0001g0188others(72): Show | 75 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.-9+1014C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156437527 | ||||||
| chr2:156437595
|
C | T | 1 | a0001c0001t0001g0186 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-9+1082C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156437595 | ||||||
| chr2:156438037
|
T | G | 1 | a0003c0003t0007g0012 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-9+1524T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156438037 | ||||||
| chr2:156438432
|
T | A | 147 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(144): Show | 147 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.-9+1919T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156438432 | ||||||
| chr2:156438915
|
G | A | 1 | a0002c0002t0002g0013 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-9+2402G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156438915 | ||||||
| chr2:156439136
|
G | A | 147 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(144): Show | 147 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.-9+2623G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156439136 | ||||||
| chr2:156439474
|
T | C | 228 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(225): Show | 228 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.-9+2961T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156439474 | ||||||
| chr2:156439513
|
G | GA | 19 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0028others(16): Show | 19 | HG00438.hp2 HG00544.hp1 HG00621.hp1 others(16): Show |
intron_variant | MODIFIER | c.-9+3026dupA | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156439513 | |||||
| chr2:156439513
|
G | GAAA | 6 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(3): Show | 6 | HG01358.hp2 HG01517.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9+3024_-9+3026dup others(3): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156439513 | |||||
| chr2:156439513
|
G | GAAAA | 5 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(2): Show | 5 | HG00735.hp2 HG00741.hp2 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+3023_-9+3026dup others(4): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156439513 | |||||
| chr2:156439517
|
AAAAAAAA others(16): Show |
A | 1 | a0001c0001t0001g0153 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-9+3018_-9+3040del others(23): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156439517 | |||||
| chr2:156439518
|
AAAAAAAA others(15): Show |
A | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-9+3019_-9+3040del others(22): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156439518 | |||||
| chr2:156439519
|
AAAAAAAA others(14): Show |
A | 1 | a0002c0002t0001g0185 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-9+3020_-9+3040del others(21): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156439519 | |||||
| chr2:156439520
|
AAAAAAAA others(13): Show |
A | 2 | a0001c0001t0005g0151a0002c0002t0012g0152 | 2 | HG02258.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-9+3021_-9+3040del others(20): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156439520 | |||||
| chr2:156439522
|
AAAAAAAA others(11): Show |
A | 2 | a0001c0001t0001g0150a0002c0002t0001g0184 | 2 | NA18950.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-9+3023_-9+3040del others(18): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156439522 | |||||
| chr2:156439523
|
AAAAAAAA others(10): Show |
A | 4 | a0002c0002t0006g0154a0002c0002t0006g0155a0002c0002t0006g0156others(1): Show | 4 | HG00735.hp1 HG01099.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+3024_-9+3040del others(17): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156439523 | |||||
| chr2:156439524
|
AAAAAAAA others(9): Show |
A | 2 | a0001c0001t0001g0148a0002c0002t0002g0147 | 2 | HG04115.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-9+3025_-9+3040del others(16): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156439524 | |||||
| chr2:156439525
|
AAAAAAAA others(8): Show |
A | 1 | a0001c0001t0010g0146 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-9+3026_-9+3040del others(15): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156439525 | |||||
| chr2:156439528
|
A | C | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-9+3015A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156439528 | ||||||
| chr2:156439529
|
AAAAAAAA others(4): Show |
A | 1 | a0001c0001t0001g0143 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-9+3027_-9+3037del others(11): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156439529 | |||||
| chr2:156439530
|
AAAAAAAA others(3): Show |
A | 1 | a0001c0001t0001g0142 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-9+3027_-9+3036del others(10): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156439530 | |||||
| chr2:156439535
|
AAAAAC | A | 8 | a0001c0001t0001g0250a0001c0001t0003g0006a0001c0001t0003g0007others(5): Show | 8 | HG00558.hp1 HG02015.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-9+3027_-9+3031del others(5): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156439535 | |||||
| chr2:156439536
|
A | C | 1 | a0001c0001t0001g0149 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-9+3023A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156439536 | ||||||
| chr2:156439536
|
AAAAC | A | 9 | a0001c0001t0001g0002a0001c0001t0001g0140a0001c0001t0001g0141others(6): Show | 9 | HG01256.hp1 HG02056.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-9+3027_-9+3030del others(4): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156439536 | |||||
| chr2:156439537
|
AAAC | A | 23 | a0001c0001t0001g0227a0001c0001t0001g0228a0001c0001t0001g0229others(20): Show | 23 | HG00140.hp2 HG00639.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.-9+3027_-9+3029del others(3): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156439537 | |||||
| chr2:156439538
|
AAC | A | 51 | a0001c0001t0001g0119a0001c0001t0001g0124a0001c0001t0001g0129others(48): Show | 51 | HG00323.hp1 HG00544.hp2 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.-9+3027_-9+3028del others(2): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156439538 | |||||
| chr2:156439539
|
AC | A | 61 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0074others(58): Show | 61 | HG00621.hp2 HG00639.hp1 HG00673.hp2 others(58): Show |
intron_variant | MODIFIER | c.-9+3027delC | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156439539 | ||||||
| chr2:156439540
|
C | A | 68 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(65): Show | 68 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.-9+3027C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156439540 | ||||||
| chr2:156439541
|
A | C | 3 | a0002c0002t0002g0145a0002c0002t0005g0159a0002c0002t0019g0171 | 3 | HG01358.hp1 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-9+3028A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156439541 | ||||||
| chr2:156439620
|
G | A | 1 | a0001c0001t0003g0069 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-9+3107G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156439620 | ||||||
| chr2:156439744
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-9+3231G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156439744 | ||||||
| chr2:156439849
|
A | AAAATAAA others(1): Show |
136 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(133): Show | 136 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.-9+3356_-9+3363dup others(8): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156439849 | |||||
| chr2:156439849
|
A | AAAATAAA others(5): Show |
20 | a0001c0001t0001g0067a0001c0001t0001g0111a0001c0001t0001g0114others(17): Show | 20 | HG01243.hp1 HG01258.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.-9+3352_-9+3363dup others(12): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156439849 | |||||
| chr2:156439849
|
A | AAAATAAA others(9): Show |
62 | a0001c0001t0001g0002a0001c0001t0001g0187a0001c0001t0001g0188others(59): Show | 62 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.-9+3348_-9+3363dup others(16): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156439849 | |||||
| chr2:156439849
|
A | AAAATAAA others(13): Show |
8 | a0001c0001t0001g0222a0001c0001t0001g0224a0001c0001t0001g0225others(5): Show | 8 | HG02698.hp1 HG02818.hp1 NA18945.hp2 others(5): Show |
intron_variant | MODIFIER | c.-9+3344_-9+3363dup others(20): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156439849 | |||||
| chr2:156439849
|
A | AAAATAAA others(17): Show |
1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-9+3340_-9+3363dup others(24): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156439849 | |||||
| chr2:156439935
|
A | G | 2 | a0001c0001t0001g0220a0001c0001t0001g0221 | 2 | NA19006.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.-9+3422A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156439935 | ||||||
| chr2:156440221
|
C | T | 1 | a0001c0001t0003g0190 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-9+3708C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156440221 | ||||||
| chr2:156440264
|
A | C | 1 | a0002c0002t0009g0137 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-9+3751A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156440264 | ||||||
| chr2:156440273
|
A | G | 9 | a0001c0001t0005g0182a0002c0002t0001g0165a0002c0002t0001g0184others(6): Show | 9 | HG02622.hp2 HG02886.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.-9+3760A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156440273 | ||||||
| chr2:156440466
|
G | A | 1 | a0001c0001t0001g0253 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-9+3953G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156440466 | ||||||
| chr2:156440647
|
A | G | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-9+4134A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156440647 | ||||||
| chr2:156440679
|
A | G | 1 | a0001c0001t0001g0219 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-9+4166A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156440679 | ||||||
| chr2:156441010
|
C | T | 242 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(239): Show | 242 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.-9+4497C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156441010 | ||||||
| chr2:156441339
|
C | T | 1 | a0001c0001t0001g0066 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-9+4826C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156441339 | ||||||
| chr2:156441414
|
C | T | 1 | a0001c0001t0017g0065 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-9+4901C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156441414 | ||||||
| chr2:156441454
|
G | C | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-9+4941G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156441454 | ||||||
| chr2:156441669
|
A | G | 147 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(144): Show | 147 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.-9+5156A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156441669 | ||||||
| chr2:156441817
|
G | T | 1 | a0001c0001t0001g0251 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-9+5304G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156441817 | ||||||
| chr2:156441919
|
A | G | 5 | a0001c0001t0001g0036a0001c0001t0001g0062a0001c0001t0001g0063others(2): Show | 5 | HG01070.hp1 HG01192.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9+5406A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156441919 | ||||||
| chr2:156441957
|
T | C | 3 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0119 | 3 | HG02895.hp1 HG02897.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-9+5444T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156441957 | ||||||
| chr2:156442075
|
G | T | 147 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(144): Show | 147 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.-9+5562G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156442075 | ||||||
| chr2:156442542
|
G | T | 223 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(220): Show | 223 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.-9+6029G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156442542 | ||||||
| chr2:156442679
|
G | A | 75 | a0001c0001t0001g0002a0001c0001t0001g0187a0001c0001t0001g0188others(72): Show | 75 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.-9+6166G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156442679 | ||||||
| chr2:156442756
|
A | G | 75 | a0001c0001t0001g0002a0001c0001t0001g0187a0001c0001t0001g0188others(72): Show | 75 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.-9+6243A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156442756 | ||||||
| chr2:156443127
|
C | G | 2 | a0001c0001t0001g0218a0001c0001t0001g0245 | 2 | NA19000.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.-9+6614C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156443127 | ||||||
| chr2:156443224
|
C | A | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-9+6711C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156443224 | ||||||
| chr2:156443433
|
C | T | 224 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(221): Show | 224 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.-9+6920C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156443433 | ||||||
| chr2:156443526
|
T | C | 3 | a0001c0001t0001g0222a0001c0001t0001g0230a0001c0001t0001g0246 | 3 | HG02698.hp1 HG02818.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-9+7013T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156443526 | ||||||
| chr2:156443650
|
T | C | 1 | a0001c0001t0001g0037 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-9+7137T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156443650 | ||||||
| chr2:156444089
|
T | C | 11 | a0001c0001t0001g0002a0001c0001t0003g0001a0001c0001t0003g0003others(8): Show | 11 | HG00558.hp1 HG02015.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.-9+7576T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156444089 | ||||||
| chr2:156444110
|
G | A | 144 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(141): Show | 144 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.-9+7597G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156444110 | ||||||
| chr2:156444133
|
G | A | 2 | a0002c0002t0001g0200a0004c0008t0001g0231 | 2 | HG02071.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.-9+7620G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156444133 | ||||||
| chr2:156444252
|
A | G | 1 | a0001c0001t0001g0189 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-9+7739A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156444252 | ||||||
| chr2:156444329
|
T | C | 2 | a0002c0002t0001g0179a0003c0003t0007g0180 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-9+7816T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156444329 | ||||||
| chr2:156444436
|
G | C | 1 | a0001c0001t0005g0182 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-9+7923G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156444436 | ||||||
| chr2:156444720
|
T | TAC | 154 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(151): Show | 154 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.-9+8226_-9+8227dup others(2): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156444720 | |||||
| chr2:156444720
|
T | TACAC | 3 | a0002c0002t0004g0120a0002c0002t0004g0121a0002c0002t0012g0073 | 3 | HG02559.hp2 NA19057.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-9+8224_-9+8227dup others(4): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156444720 | |||||
| chr2:156444720
|
T | TACACACA others(3): Show |
74 | a0001c0001t0001g0002a0001c0001t0001g0187a0001c0001t0001g0188others(71): Show | 74 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.-9+8218_-9+8227dup others(10): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156444720 | |||||
| chr2:156444720
|
T | TACACACA others(5): Show |
1 | a0001c0001t0001g0201 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-9+8216_-9+8227dup others(12): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156444720 | |||||
| chr2:156444846
|
C | T | 1 | a0002c0002t0004g0035 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-9+8333C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156444846 | ||||||
| chr2:156444925
|
A | G | 2 | a0002c0002t0004g0034a0002c0002t0004g0061 | 2 | NA18971.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.-9+8412A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156444925 | ||||||
| chr2:156445161
|
C | G | 1 | a0001c0001t0001g0248 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-9+8648C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156445161 | ||||||
| chr2:156445316
|
T | G | 2 | a0002c0002t0004g0120a0002c0002t0004g0121 | 2 | NA19057.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-9+8803T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156445316 | ||||||
| chr2:156445668
|
C | T | 5 | a0002c0002t0002g0160a0002c0002t0002g0162a0002c0002t0002g0163others(2): Show | 5 | HG02109.hp1 HG02559.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9+9155C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156445668 | ||||||
| chr2:156445679
|
A | G | 224 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(221): Show | 224 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.-9+9166A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156445679 | ||||||
| chr2:156445802
|
T | G | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-9+9289T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156445802 | ||||||
| chr2:156445879
|
A | G | 224 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(221): Show | 224 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.-9+9366A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156445879 | ||||||
| chr2:156446107
|
A | AT | 148 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(145): Show | 148 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.-9+9602dupT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156446107 | |||||
| chr2:156446159
|
G | A | 5 | a0002c0002t0002g0160a0002c0002t0002g0162a0002c0002t0002g0163others(2): Show | 5 | HG02109.hp1 HG02559.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9+9646G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156446159 | ||||||
| chr2:156446256
|
C | T | 1 | a0002c0002t0002g0109 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-9+9743C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156446256 | ||||||
| chr2:156446335
|
G | A | 224 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(221): Show | 224 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.-9+9822G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156446335 | ||||||
| chr2:156446339
|
G | A | 1 | a0001c0001t0001g0230 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-9+9826G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156446339 | ||||||
| chr2:156446531
|
A | G | 4 | a0003c0003t0007g0168a0003c0003t0007g0169a0003c0003t0007g0170others(1): Show | 4 | HG02886.hp2 HG02897.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9+10018A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156446531 | ||||||
| chr2:156446606
|
G | A | 2 | a0002c0002t0001g0179a0003c0003t0007g0180 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-9+10093G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156446606 | ||||||
| chr2:156446670
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-9+10157G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156446670 | ||||||
| chr2:156446982
|
G | A | 1 | a0002c0002t0002g0038 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-9+10469G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156446982 | ||||||
| chr2:156447233
|
C | T | 1 | a0001c0001t0005g0181 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-9+10720C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156447233 | ||||||
| chr2:156447399
|
A | G | 2 | a0001c0001t0001g0218a0001c0001t0001g0245 | 2 | NA19000.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.-9+10886A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156447399 | ||||||
| chr2:156447498
|
T | C | 1 | a0001c0001t0001g0187 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-9+10985T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156447498 | ||||||
| chr2:156447584
|
C | A | 1 | a0001c0001t0001g0191 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-9+11071C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156447584 | ||||||
| chr2:156447690
|
T | C | 242 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(239): Show | 242 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.-9+11177T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156447690 | ||||||
| chr2:156447934
|
G | A | 2 | a0001c0001t0001g0222a0001c0001t0001g0246 | 2 | HG02698.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-9+11421G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156447934 | ||||||
| chr2:156447959
|
A | G | 2 | a0001c0001t0010g0018a0001c0001t0010g0060 | 2 | HG00438.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.-9+11446A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156447959 | ||||||
| chr2:156448119
|
C | CT | 77 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0187others(74): Show | 77 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.-9+11619dupT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156448119 | |||||
| chr2:156448220
|
G | T | 1 | a0001c0001t0005g0178 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-9+11707G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156448220 | ||||||
| chr2:156448232
|
C | T | 1 | a0001c0001t0005g0177 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-9+11719C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156448232 | ||||||
| chr2:156448269
|
G | A | 147 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(144): Show | 147 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.-9+11756G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156448269 | ||||||
| chr2:156448352
|
C | A | 147 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(144): Show | 147 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.-9+11839C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156448352 | ||||||
| chr2:156448619
|
C | T | 147 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(144): Show | 147 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.-9+12106C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156448619 | ||||||
| chr2:156448675
|
A | G | 75 | a0001c0001t0001g0002a0001c0001t0001g0187a0001c0001t0001g0188others(72): Show | 75 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.-9+12162A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156448675 | ||||||
| chr2:156448742
|
T | C | 76 | a0001c0001t0001g0002a0001c0001t0001g0187a0001c0001t0001g0188others(73): Show | 76 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-9+12229T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156448742 | ||||||
| chr2:156448918
|
T | G | 1 | a0001c0001t0003g0069 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-9+12405T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156448918 | ||||||
| chr2:156449218
|
G | C | 147 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(144): Show | 147 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.-9+12705G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156449218 | ||||||
| chr2:156449251
|
T | C | 75 | a0001c0001t0001g0002a0001c0001t0001g0187a0001c0001t0001g0188others(72): Show | 75 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.-9+12738T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156449251 | ||||||
| chr2:156449376
|
T | C | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-9+12863T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156449376 | ||||||
| chr2:156449395
|
C | A | 1 | a0001c0001t0016g0039 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-9+12882C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156449395 | ||||||
| chr2:156449856
|
C | CAAAAAAA others(4): Show |
1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-9+13345_-9+13355d others(13): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156449856 | |||||
| chr2:156449856
|
C | CAAAAAAA others(5): Show |
5 | a0001c0001t0001g0135a0002c0002t0002g0118a0002c0002t0002g0138others(2): Show | 5 | HG01884.hp2 HG01891.hp2 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9+13344_-9+13355d others(14): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156449856 | |||||
| chr2:156449856
|
C | CAAAAAAA others(6): Show |
182 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(179): Show | 182 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.-9+13355_-9+13356i others(15): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156449856 | |||||
| chr2:156449856
|
C | CAAAAAAA others(7): Show |
34 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0037others(31): Show | 34 | HG00438.hp1 HG00438.hp2 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.-9+13355_-9+13356i others(16): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156449856 | |||||
| chr2:156450016
|
GA | G | 242 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(239): Show | 242 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.-9+13509delA | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156450016 | |||||
| chr2:156450176
|
A | G | 223 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(220): Show | 223 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.-9+13663A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156450176 | ||||||
| chr2:156450208
|
T | C | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-9+13695T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156450208 | ||||||
| chr2:156450368
|
A | G | 1 | a0001c0001t0016g0039 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-9+13855A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156450368 | ||||||
| chr2:156450516
|
G | C | 223 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(220): Show | 223 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.-9+14003G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156450516 | ||||||
| chr2:156450652
|
C | G | 1 | a0002c0002t0002g0134 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-9+14139C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156450652 | ||||||
| chr2:156450665
|
C | CTTT | 74 | a0001c0001t0001g0002a0001c0001t0001g0187a0001c0001t0001g0188others(71): Show | 74 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.-9+14167_-9+14169d others(5): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156450665 | |||||
| chr2:156450665
|
C | CTTTT | 17 | a0001c0001t0001g0250a0001c0001t0005g0182a0002c0002t0001g0165others(14): Show | 17 | HG02109.hp1 HG02451.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.-9+14166_-9+14169d others(6): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156450665 | |||||
| chr2:156450682
|
T | TTTA | 15 | a0001c0001t0001g0036a0001c0001t0001g0062a0001c0001t0001g0071others(12): Show | 15 | HG01070.hp1 HG01070.hp2 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.-9+14169_-9+14170i others(5): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156450682 | ||||||
| chr2:156450682
|
T | TTTTA | 135 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(132): Show | 135 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.-9+14169_-9+14170i others(6): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156450682 | ||||||
| chr2:156450687
|
C | A | 246 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(243): Show | 246 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.-9+14174C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156450687 | ||||||
| chr2:156450707
|
G | A | 75 | a0001c0001t0001g0002a0001c0001t0001g0187a0001c0001t0001g0188others(72): Show | 75 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.-9+14194G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156450707 | ||||||
| chr2:156450731
|
C | T | 228 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(225): Show | 228 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.-9+14218C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156450731 | ||||||
| chr2:156450734
|
G | T | 3 | a0002c0002t0002g0117a0002c0002t0002g0118a0002c0002t0002g0138 | 3 | HG01884.hp2 HG02055.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-9+14221G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156450734 | ||||||
| chr2:156450917
|
C | A | 1 | a0001c0001t0001g0250 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-9+14404C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156450917 | ||||||
| chr2:156451122
|
G | C | 227 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(224): Show | 227 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.-9+14609G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156451122 | ||||||
| chr2:156451158
|
C | T | 3 | a0001c0001t0001g0142a0001c0001t0005g0166a0001c0001t0005g0177 | 3 | HG00140.hp1 HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-9+14645C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156451158 | ||||||
| chr2:156451183
|
C | A | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-9+14670C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156451183 | ||||||
| chr2:156451193
|
G | T | 1 | a0002c0002t0002g0139 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-9+14680G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156451193 | ||||||
| chr2:156451233
|
G | C | 151 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(148): Show | 151 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.-9+14720G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156451233 | ||||||
| chr2:156451241
|
CGGGCAGA others(120): Show |
C | 1 | a0001c0001t0001g0201 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-9+14797_-9+14923d others(2): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156451241 | |||||
| chr2:156451296
|
A | AC | 57 | a0001c0001t0001g0037a0001c0001t0001g0187a0001c0001t0001g0188others(54): Show | 57 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.-9+14790dupC | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156451296 | |||||
| chr2:156451303
|
C | G | 1 | a0002c0002t0008g0167 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-9+14790C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156451303 | ||||||
| chr2:156451315
|
G | A | 1 | a0002c0002t0020g0020 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-9+14802G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156451315 | ||||||
| chr2:156451341
|
TGCTCCTC others(268): Show |
T | 1 | a0002c0002t0001g0179 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-9+14978_-9+15252d others(2): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156451341 | |||||
| chr2:156451393
|
G | A | 34 | a0001c0001t0001g0028a0001c0001t0001g0077a0001c0001t0001g0124others(31): Show | 34 | HG00639.hp1 HG01070.hp2 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.-9+14880G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156451393 | ||||||
| chr2:156451424
|
CCCCCCCA others(41): Show |
C | 1 | a0001c0001t0001g0042 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-9+14918_-9+14965d others(50): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156451424 | |||||
| chr2:156451442
|
G | C | 2 | a0001c0001t0001g0024a0001c0001t0001g0095 | 2 | NA18959.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.-9+14929G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156451442 | ||||||
| chr2:156451447
|
G | C | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-9+14934G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156451447 | ||||||
| chr2:156451462
|
CGGGGGGC others(43): Show |
C | 147 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(144): Show | 147 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.-9+14978_-9+15027d others(52): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156451462 | |||||
| chr2:156451473
|
CCCCCCCA others(42): Show |
C | 3 | a0001c0001t0016g0039a0002c0002t0002g0108a0002c0002t0009g0137 | 3 | HG01261.hp1 HG01261.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.-9+14967_-9+15015d others(51): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156451473 | |||||
| chr2:156451491
|
G | A | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-9+14978G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156451491 | ||||||
| chr2:156451491
|
GGAAGGGG others(43): Show |
G | 5 | a0001c0001t0001g0199a0001c0001t0001g0220a0001c0001t0001g0221others(2): Show | 5 | HG01993.hp2 NA19006.hp1 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9+14981_-9+15030d others(52): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156451491 | |||||
| chr2:156451491
|
GGAAGGGG others(268): Show |
G | 2 | a0001c0001t0001g0203a0001c0001t0001g0235 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-9+14981_-9+15255d others(2): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156451491 | |||||
| chr2:156451494
|
A | C | 76 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0187others(73): Show | 76 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-9+14981A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156451494 | ||||||
| chr2:156451509
|
A | G | 2 | a0001c0001t0001g0042a0001c0001t0001g0188 | 2 | NA19006.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.-9+14996A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156451509 | ||||||
| chr2:156451512
|
G | A | 1 | a0001c0001t0005g0181 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-9+14999G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156451512 | ||||||
| chr2:156451517
|
G | A | 5 | a0002c0002t0002g0160a0002c0002t0002g0162a0002c0002t0002g0163others(2): Show | 5 | HG02109.hp1 HG02559.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9+15004G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156451517 | ||||||
| chr2:156451572
|
C | A | 1 | a0001c0001t0001g0227 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-9+15059C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156451572 | ||||||
| chr2:156451598
|
C | T | 1 | a0001c0001t0001g0066 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-9+15085C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156451598 | ||||||
| chr2:156451717
|
GGACGGGG others(42): Show |
G | 1 | a0002c0002t0002g0139 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-9+15208_-9+15256d others(51): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156451717 | |||||
| chr2:156451721
|
G | A | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-9+15208G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156451721 | ||||||
| chr2:156451725
|
C | T | 86 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(83): Show | 86 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.-9+15212C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156451725 | ||||||
| chr2:156451731
|
GCCGGGCG others(10): Show |
G | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-9+15221_-9+15237d others(19): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156451731 | |||||
| chr2:156451766
|
A | G | 225 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(222): Show | 225 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.-9+15253A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156451766 | ||||||
| chr2:156451849
|
T | C | 2 | a0002c0002t0005g0159a0003c0003t0005g0158 | 2 | HG01891.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-9+15336T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156451849 | ||||||
| chr2:156451927
|
G | C | 3 | a0001c0001t0003g0069a0001c0001t0003g0086a0001c0001t0003g0087 | 3 | HG02683.hp1 HG03710.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-9+15414G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156451927 | ||||||
| chr2:156451933
|
A | G | 1 | a0001c0001t0001g0036 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-9+15420A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156451933 | ||||||
| chr2:156452202
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-9+15689C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156452202 | ||||||
| chr2:156452233
|
G | A | 1 | a0001c0001t0001g0049 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-9+15720G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156452233 | ||||||
| chr2:156452360
|
C | T | 1 | a0001c0001t0003g0204 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-9+15847C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156452360 | ||||||
| chr2:156452434
|
A | G | 2 | a0002c0002t0002g0080a0002c0002t0002g0147 | 2 | HG03492.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-9+15921A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156452434 | ||||||
| chr2:156452542
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-9+16029G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156452542 | ||||||
| chr2:156452565
|
G | A | 3 | a0002c0002t0002g0117a0002c0002t0002g0118a0002c0002t0002g0138 | 3 | HG01884.hp2 HG02055.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-9+16052G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156452565 | ||||||
| chr2:156453377
|
T | C | 3 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0237 | 3 | HG02735.hp1 HG03239.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-9+16864T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156453377 | ||||||
| chr2:156453833
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-9+17320C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156453833 | ||||||
| chr2:156453948
|
A | G | 228 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(225): Show | 228 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.-9+17435A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156453948 | ||||||
| chr2:156454043
|
A | G | 1 | a0002c0002t0002g0048 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-9+17530A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156454043 | ||||||
| chr2:156454150
|
G | A | 1 | a0001c0001t0001g0251 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-9+17637G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156454150 | ||||||
| chr2:156454256
|
T | C | 1 | a0001c0001t0001g0192 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-9+17743T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156454256 | ||||||
| chr2:156454493
|
G | GA | 92 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(89): Show | 92 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.-9+17991dupA | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156454493 | |||||
| chr2:156454493
|
G | GAA | 53 | a0001c0001t0001g0028a0001c0001t0001g0077a0001c0001t0001g0124others(50): Show | 53 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.-9+17990_-9+17991d others(4): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156454493 | |||||
| chr2:156454539
|
T | C | 1 | a0001c0001t0005g0151 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-9+18026T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156454539 | ||||||
| chr2:156455005
|
A | G | 1 | a0002c0002t0008g0136 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-9+18492A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156455005 | ||||||
| chr2:156455216
|
C | T | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-9+18703C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156455216 | ||||||
| chr2:156455310
|
T | C | 3 | a0001c0001t0001g0191a0001c0001t0001g0193a0001c0001t0001g0207 | 3 | HG00323.hp1 HG01106.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.-9+18797T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156455310 | ||||||
| chr2:156455337
|
G | A | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-9+18824G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156455337 | ||||||
| chr2:156455635
|
A | G | 228 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(225): Show | 228 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.-9+19122A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156455635 | ||||||
| chr2:156455713
|
G | T | 4 | a0002c0002t0002g0019a0002c0002t0002g0045a0002c0002t0002g0094others(1): Show | 4 | HG02040.hp1 NA18943.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+19200G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156455713 | ||||||
| chr2:156455759
|
GT | G | 226 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(223): Show | 226 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.-9+19249delT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156455759 | |||||
| chr2:156455892
|
T | C | 2 | a0002c0002t0001g0179a0003c0003t0007g0180 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-9+19379T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156455892 | ||||||
| chr2:156456023
|
A | G | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-9+19510A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156456023 | ||||||
| chr2:156456436
|
T | A | 226 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(223): Show | 226 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.-8-19662T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156456436 | ||||||
| chr2:156456472
|
G | A | 1 | a0003c0003t0007g0122 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-8-19626G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156456472 | ||||||
| chr2:156456586
|
A | T | 1 | a0002c0002t0004g0121 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-8-19512A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156456586 | ||||||
| chr2:156456595
|
C | CA | 5 | a0002c0002t0002g0160a0002c0002t0002g0162a0002c0002t0002g0163others(2): Show | 5 | HG02109.hp1 HG02559.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-19490dupA | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156456595 | |||||
| chr2:156457081
|
T | G | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-8-19017T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156457081 | ||||||
| chr2:156457357
|
G | A | 1 | a0002c0002t0012g0096 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-8-18741G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156457357 | ||||||
| chr2:156457674
|
C | G | 1 | a0001c0001t0005g0151 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-8-18424C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156457674 | ||||||
| chr2:156458487
|
A | G | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-8-17611A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156458487 | ||||||
| chr2:156458858
|
C | T | 1 | a0001c0001t0003g0093 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-8-17240C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156458858 | ||||||
| chr2:156458909
|
C | T | 3 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0006t0001g0198 | 3 | NA18945.hp2 NA18983.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.-8-17189C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156458909 | ||||||
| chr2:156458912
|
T | C | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-8-17186T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156458912 | ||||||
| chr2:156459006
|
A | AAT | 8 | a0002c0002t0001g0184a0002c0002t0001g0185a0002c0002t0002g0160others(5): Show | 8 | HG02109.hp1 HG02559.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-8-17072_-8-17071d others(4): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156459006 | |||||
| chr2:156459006
|
AAT | A | 74 | a0001c0001t0001g0002a0001c0001t0001g0187a0001c0001t0001g0188others(71): Show | 74 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.-8-17072_-8-17071d others(4): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156459006 | |||||
| chr2:156459006
|
AATAT | A | 3 | a0001c0001t0001g0250a0002c0002t0004g0120a0002c0002t0004g0121 | 3 | HG02451.hp2 NA19057.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-8-17074_-8-17071d others(6): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156459006 | |||||
| chr2:156459006
|
AATATAT | A | 150 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(147): Show | 150 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.-8-17076_-8-17071d others(8): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156459006 | |||||
| chr2:156459026
|
T | C | 2 | a0001c0001t0005g0182a0002c0002t0005g0159 | 2 | HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-8-17072T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156459026 | ||||||
| chr2:156459236
|
G | T | 51 | a0001c0001t0001g0028a0001c0001t0001g0077a0001c0001t0001g0124others(48): Show | 51 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.-8-16862G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156459236 | ||||||
| chr2:156459292
|
A | C | 75 | a0001c0001t0001g0002a0001c0001t0001g0187a0001c0001t0001g0188others(72): Show | 75 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.-8-16806A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156459292 | ||||||
| chr2:156459493
|
T | C | 5 | a0001c0001t0005g0182a0003c0003t0007g0168a0003c0003t0007g0169others(2): Show | 5 | HG02622.hp2 HG02886.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-16605T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156459493 | ||||||
| chr2:156459569
|
T | G | 3 | a0002c0002t0001g0179a0002c0002t0019g0171a0003c0003t0007g0180 | 3 | HG02976.hp2 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-8-16529T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156459569 | ||||||
| chr2:156459603
|
G | A | 2 | a0001c0001t0001g0002a0001c0001t0003g0006 | 2 | NA18970.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.-8-16495G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156459603 | ||||||
| chr2:156459672
|
G | C | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-8-16426G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156459672 | ||||||
| chr2:156459682
|
G | A | 2 | a0001c0001t0001g0050a0001c0001t0001g0099 | 2 | NA18941.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.-8-16416G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156459682 | ||||||
| chr2:156459686
|
C | CAAA | 11 | a0001c0001t0001g0081a0001c0001t0001g0206a0001c0001t0001g0217others(8): Show | 11 | HG00673.hp2 HG00735.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.-8-16391_-8-16389d others(5): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156459686 | |||||
| chr2:156459686
|
C | CAAAA | 60 | a0001c0001t0001g0002a0001c0001t0001g0187a0001c0001t0001g0189others(57): Show | 60 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.-8-16392_-8-16389d others(6): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156459686 | |||||
| chr2:156459686
|
C | CAAAAA | 20 | a0001c0001t0001g0188a0001c0001t0001g0194a0001c0001t0001g0195others(17): Show | 20 | HG00621.hp2 HG00741.hp1 HG02015.hp1 others(17): Show |
intron_variant | MODIFIER | c.-8-16393_-8-16389d others(7): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156459686 | |||||
| chr2:156459686
|
C | CAAAAAAA | 10 | a0001c0001t0005g0166a0001c0001t0005g0172a0001c0001t0005g0177others(7): Show | 10 | HG01891.hp2 HG02109.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8-16395_-8-16389d others(9): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156459686 | |||||
| chr2:156459686
|
C | CAAAAAAA others(2): Show |
5 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0119others(2): Show | 5 | HG00438.hp1 HG02895.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-16397_-8-16389d others(11): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156459686 | |||||
| chr2:156459686
|
C | CAAAAAAA others(3): Show |
5 | a0001c0001t0001g0032a0001c0001t0001g0059a0001c0001t0001g0107others(2): Show | 5 | HG00639.hp2 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-16398_-8-16389d others(12): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156459686 | |||||
| chr2:156459686
|
C | CAAAAAAA others(4): Show |
20 | a0001c0001t0001g0022a0001c0001t0001g0062a0001c0001t0001g0064others(17): Show | 20 | HG01070.hp1 HG01070.hp2 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.-8-16399_-8-16389d others(13): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156459686 | |||||
| chr2:156459686
|
C | CAAAAAAA others(5): Show |
46 | a0001c0001t0001g0021a0001c0001t0001g0026a0001c0001t0001g0028others(43): Show | 46 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.-8-16400_-8-16389d others(14): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156459686 | |||||
| chr2:156459686
|
C | CAAAAAAA others(6): Show |
28 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(25): Show | 28 | HG00438.hp2 HG00735.hp2 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.-8-16401_-8-16389d others(15): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156459686 | |||||
| chr2:156459686
|
C | CAAAAAAA others(7): Show |
21 | a0001c0001t0001g0024a0001c0001t0001g0040a0001c0001t0001g0049others(18): Show | 21 | HG00323.hp2 HG00639.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.-8-16402_-8-16389d others(16): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156459686 | |||||
| chr2:156459686
|
C | CAAAAAAA others(8): Show |
2 | a0001c0001t0001g0042a0002c0002t0012g0073 | 2 | HG02559.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.-8-16403_-8-16389d others(17): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156459686 | |||||
| chr2:156459686
|
C | CAAAAAAA others(9): Show |
1 | a0001c0001t0003g0088 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-8-16404_-8-16389d others(18): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156459686 | |||||
| chr2:156459686
|
C | CAAAAAAA others(10): Show |
2 | a0001c0001t0001g0143a0001c0001t0001g0150 | 2 | HG04184.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.-8-16405_-8-16389d others(19): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156459686 | |||||
| chr2:156459686
|
C | CAAAAAAA others(16): Show |
1 | a0001c0001t0003g0086 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-8-16411_-8-16389d others(25): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156459686 | |||||
| chr2:156459686
|
CAAAAAAA others(3): Show |
C | 8 | a0001c0001t0001g0036a0002c0002t0009g0033a0002c0002t0009g0131others(5): Show | 8 | HG01346.hp2 HG01433.hp2 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.-8-16398_-8-16389d others(12): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156459686 | |||||
| chr2:156460129
|
A | C | 3 | a0002c0002t0001g0179a0002c0002t0019g0171a0003c0003t0007g0180 | 3 | HG02976.hp2 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-8-15969A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156460129 | ||||||
| chr2:156460241
|
C | G | 1 | a0001c0001t0001g0216 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-8-15857C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156460241 | ||||||
| chr2:156460241
|
C | T | 1 | a0001c0001t0001g0252 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-8-15857C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156460241 | ||||||
| chr2:156460564
|
T | C | 227 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(224): Show | 227 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.-8-15534T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156460564 | ||||||
| chr2:156460574
|
G | C | 227 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(224): Show | 227 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.-8-15524G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156460574 | ||||||
| chr2:156460574
|
G | T | 1 | a0001c0001t0003g0006 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-8-15524G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156460574 | ||||||
| chr2:156460645
|
T | A | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-8-15453T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156460645 | ||||||
| chr2:156460680
|
A | G | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-8-15418A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156460680 | ||||||
| chr2:156460740
|
G | A | 1 | a0001c0001t0001g0201 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-8-15358G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156460740 | ||||||
| chr2:156460952
|
T | C | 75 | a0001c0001t0001g0002a0001c0001t0001g0187a0001c0001t0001g0188others(72): Show | 75 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.-8-15146T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156460952 | ||||||
| chr2:156461033
|
T | C | 5 | a0001c0001t0001g0032a0001c0001t0001g0059a0001c0001t0001g0071others(2): Show | 5 | HG02630.hp1 HG02886.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-15065T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156461033 | ||||||
| chr2:156461161
|
C | CT | 6 | a0001c0001t0005g0166a0002c0002t0001g0165a0002c0002t0001g0184others(3): Show | 6 | HG02886.hp2 HG02897.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-14912dupT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156461161 | |||||
| chr2:156461161
|
CT | C | 71 | a0001c0001t0001g0002a0001c0001t0001g0187a0001c0001t0001g0189others(68): Show | 71 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.-8-14912delT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156461161 | |||||
| chr2:156461161
|
CTTTTTTT others(1): Show |
C | 87 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(84): Show | 87 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.-8-14919_-8-14912d others(10): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156461161 | |||||
| chr2:156461161
|
CTTTTTTT others(2): Show |
C | 62 | a0001c0001t0001g0028a0001c0001t0001g0077a0001c0001t0001g0081others(59): Show | 62 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.-8-14920_-8-14912d others(11): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156461161 | |||||
| chr2:156461161
|
CTTTTTTT others(3): Show |
C | 1 | a0002c0002t0002g0138 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-8-14921_-8-14912d others(12): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156461161 | |||||
| chr2:156461303
|
A | G | 151 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(148): Show | 151 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.-8-14795A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156461303 | ||||||
| chr2:156461430
|
C | A | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-8-14668C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156461430 | ||||||
| chr2:156461580
|
A | C | 1 | a0001c0001t0001g0252 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-8-14518A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156461580 | ||||||
| chr2:156461646
|
C | T | 228 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(225): Show | 228 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.-8-14452C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156461646 | ||||||
| chr2:156461915
|
G | C | 1 | a0001c0001t0001g0107 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-8-14183G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156461915 | ||||||
| chr2:156462354
|
C | T | 5 | a0002c0002t0002g0160a0002c0002t0002g0162a0002c0002t0002g0163others(2): Show | 5 | HG02109.hp1 HG02559.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-13744C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156462354 | ||||||
| chr2:156462379
|
G | A | 161 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(158): Show | 161 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.-8-13719G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156462379 | ||||||
| chr2:156462386
|
A | C | 1 | a0001c0001t0001g0057 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-8-13712A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156462386 | ||||||
| chr2:156462435
|
A | G | 1 | a0002c0002t0008g0167 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-8-13663A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156462435 | ||||||
| chr2:156462453
|
A | AT | 9 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0056others(6): Show | 9 | HG00741.hp2 HG01109.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.-8-13625dupT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156462453 | |||||
| chr2:156462453
|
AT | A | 72 | a0001c0001t0001g0002a0001c0001t0001g0187a0001c0001t0001g0188others(69): Show | 72 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.-8-13625delT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156462453 | |||||
| chr2:156462674
|
G | A | 3 | a0001c0001t0001g0026a0001c0001t0001g0050a0001c0001t0001g0099 | 3 | HG02602.hp2 NA18941.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.-8-13424G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156462674 | ||||||
| chr2:156462733
|
GA | G | 4 | a0002c0002t0006g0154a0002c0002t0006g0155a0002c0002t0006g0156others(1): Show | 4 | HG00735.hp1 HG01099.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-13363delA | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156462733 | |||||
| chr2:156462748
|
G | C | 1 | a0002c0002t0006g0098 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-8-13350G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156462748 | ||||||
| chr2:156462864
|
G | C | 1 | a0001c0001t0001g0230 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-8-13234G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156462864 | ||||||
| chr2:156463416
|
A | G | 5 | a0002c0002t0002g0160a0002c0002t0002g0162a0002c0002t0002g0163others(2): Show | 5 | HG02109.hp1 HG02559.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-12682A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156463416 | ||||||
| chr2:156463421
|
A | G | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-8-12677A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156463421 | ||||||
| chr2:156463510
|
T | C | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-8-12588T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156463510 | ||||||
| chr2:156463543
|
T | G | 3 | a0002c0002t0004g0112a0002c0002t0004g0113a0002c0002t0004g0128 | 3 | NA18952.hp2 NA18999.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.-8-12555T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156463543 | ||||||
| chr2:156463580
|
C | T | 1 | a0002c0002t0009g0133 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-8-12518C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156463580 | ||||||
| chr2:156463598
|
G | A | 1 | a0002c0002t0002g0046 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-8-12500G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156463598 | ||||||
| chr2:156463646
|
G | T | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-8-12452G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156463646 | ||||||
| chr2:156463682
|
C | T | 85 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(82): Show | 85 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.-8-12416C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156463682 | ||||||
| chr2:156463692
|
C | A | 3 | a0001c0004t0001g0232a0001c0004t0001g0238a0001c0004t0001g0239 | 3 | HG00140.hp2 HG01433.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-8-12406C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156463692 | ||||||
| chr2:156463692
|
C | G | 9 | a0001c0001t0005g0182a0002c0002t0001g0165a0002c0002t0001g0184others(6): Show | 9 | HG02622.hp2 HG02886.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.-8-12406C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156463692 | ||||||
| chr2:156463749
|
A | G | 1 | a0001c0001t0001g0150 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-8-12349A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156463749 | ||||||
| chr2:156463825
|
C | T | 1 | a0001c0001t0001g0041 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-8-12273C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156463825 | ||||||
| chr2:156463904
|
A | G | 228 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(225): Show | 228 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.-8-12194A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156463904 | ||||||
| chr2:156464189
|
C | A | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-8-11909C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156464189 | ||||||
| chr2:156464262
|
T | C | 2 | a0001c0001t0001g0141a0001c0001t0001g0148 | 2 | HG04115.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-8-11836T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156464262 | ||||||
| chr2:156464380
|
T | G | 5 | a0002c0002t0002g0160a0002c0002t0002g0162a0002c0002t0002g0163others(2): Show | 5 | HG02109.hp1 HG02559.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-11718T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156464380 | ||||||
| chr2:156464486
|
A | G | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-8-11612A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156464486 | ||||||
| chr2:156464772
|
A | G | 1 | a0001c0001t0001g0050 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-8-11326A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156464772 | ||||||
| chr2:156464828
|
C | G | 75 | a0001c0001t0001g0002a0001c0001t0001g0187a0001c0001t0001g0188others(72): Show | 75 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.-8-11270C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156464828 | ||||||
| chr2:156465169
|
A | G | 228 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(225): Show | 228 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.-8-10929A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156465169 | ||||||
| chr2:156465180
|
C | T | 1 | a0001c0001t0005g0181 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-8-10918C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156465180 | ||||||
| chr2:156465272
|
TAA | T | 151 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(148): Show | 151 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.-8-10825_-8-10824d others(4): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156465272 | ||||||
| chr2:156465361
|
CT | C | 158 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(155): Show | 158 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(155): Show |
intron_variant | MODIFIER | c.-8-10719delT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156465361 | |||||
| chr2:156465361
|
CTT | C | 6 | a0001c0001t0001g0071a0001c0001t0001g0077a0001c0001t0001g0124others(3): Show | 6 | HG02523.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-10720_-8-10719d others(4): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156465361 | |||||
| chr2:156465362
|
T | TTTC | 75 | a0001c0001t0001g0002a0001c0001t0001g0099a0001c0001t0001g0187others(72): Show | 75 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.-8-10734_-8-10733i others(5): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156465362 | |||||
| chr2:156465365
|
T | C | 6 | a0001c0001t0001g0041a0001c0001t0001g0142a0001c0001t0005g0151others(3): Show | 6 | HG00140.hp1 HG01884.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-10733T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156465365 | ||||||
| chr2:156465366
|
T | C | 139 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(136): Show | 139 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.-8-10732T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156465366 | ||||||
| chr2:156465367
|
T | C | 5 | a0001c0001t0001g0071a0001c0001t0001g0077a0001c0001t0001g0124others(2): Show | 5 | HG02523.hp2 HG02897.hp2 NA19009.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-10731T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156465367 | ||||||
| chr2:156465559
|
C | G | 227 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(224): Show | 227 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.-8-10539C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156465559 | ||||||
| chr2:156465621
|
G | A | 228 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(225): Show | 228 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.-8-10477G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156465621 | ||||||
| chr2:156465759
|
A | G | 1 | a0001c0001t0001g0081 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-8-10339A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156465759 | ||||||
| chr2:156465820
|
T | C | 1 | a0001c0001t0001g0234 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-8-10278T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156465820 | ||||||
| chr2:156465867
|
A | G | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-8-10231A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156465867 | ||||||
| chr2:156466048
|
G | C | 1 | a0001c0001t0005g0181 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-8-10050G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156466048 | ||||||
| chr2:156466330
|
G | A | 3 | a0002c0002t0002g0044a0002c0002t0002g0092a0002c0002t0021g0079 | 3 | HG01106.hp1 HG02074.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-8-9768G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156466330 | ||||||
| chr2:156466460
|
G | A | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-8-9638G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156466460 | ||||||
| chr2:156466792
|
T | C | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-8-9306T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156466792 | ||||||
| chr2:156467096
|
A | C | 228 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(225): Show | 228 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.-8-9002A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156467096 | ||||||
| chr2:156467174
|
G | T | 1 | a0001c0001t0001g0119 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-8-8924G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156467174 | ||||||
| chr2:156467476
|
T | C | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-8-8622T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156467476 | ||||||
| chr2:156467494
|
T | C | 1 | a0002c0002t0001g0185 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-8-8604T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156467494 | ||||||
| chr2:156467500
|
G | C | 1 | a0002c0002t0001g0185 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-8-8598G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156467500 | ||||||
| chr2:156467640
|
C | A | 75 | a0001c0001t0001g0002a0001c0001t0001g0187a0001c0001t0001g0188others(72): Show | 75 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.-8-8458C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156467640 | ||||||
| chr2:156467654
|
G | A | 1 | a0003c0003t0007g0169 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-8-8444G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156467654 | ||||||
| chr2:156467698
|
G | A | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-8-8400G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156467698 | ||||||
| chr2:156467926
|
T | C | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-8-8172T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156467926 | ||||||
| chr2:156468313
|
T | C | 128 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0077others(125): Show | 128 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.-8-7785T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156468313 | ||||||
| chr2:156468540
|
CA | C | 3 | a0002c0002t0002g0117a0002c0002t0002g0118a0002c0002t0002g0138 | 3 | HG01884.hp2 HG02055.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-8-7554delA | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156468540 | |||||
| chr2:156468615
|
T | G | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-8-7483T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156468615 | ||||||
| chr2:156468862
|
A | C | 1 | a0001c0001t0001g0103 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-8-7236A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156468862 | ||||||
| chr2:156469478
|
T | C | 3 | a0001c0004t0001g0232a0001c0004t0001g0238a0001c0004t0001g0239 | 3 | HG00140.hp2 HG01433.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-8-6620T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156469478 | ||||||
| chr2:156469525
|
T | C | 2 | a0001c0001t0010g0018a0001c0001t0010g0060 | 2 | HG00438.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.-8-6573T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156469525 | ||||||
| chr2:156469566
|
A | G | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-8-6532A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156469566 | ||||||
| chr2:156469820
|
G | A | 2 | a0002c0002t0014g0089a0002c0002t0014g0123 | 2 | HG01070.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.-8-6278G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156469820 | ||||||
| chr2:156469858
|
A | G | 1 | a0002c0002t0002g0080 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-8-6240A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156469858 | ||||||
| chr2:156469884
|
A | C | 25 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0194others(22): Show | 25 | HG00544.hp2 HG00621.hp2 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.-8-6214A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156469884 | ||||||
| chr2:156470121
|
G | A | 9 | a0001c0001t0005g0182a0002c0002t0001g0165a0002c0002t0001g0184others(6): Show | 9 | HG02622.hp2 HG02886.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.-8-5977G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156470121 | ||||||
| chr2:156470164
|
C | T | 246 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(243): Show | 246 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.-8-5934C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156470164 | ||||||
| chr2:156470270
|
T | C | 1 | a0001c0001t0003g0204 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-8-5828T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156470270 | ||||||
| chr2:156470496
|
C | T | 5 | a0001c0001t0005g0182a0003c0003t0007g0168a0003c0003t0007g0169others(2): Show | 5 | HG02622.hp2 HG02886.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-5602C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156470496 | ||||||
| chr2:156470929
|
A | G | 1 | a0002c0002t0001g0184 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-8-5169A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156470929 | ||||||
| chr2:156471098
|
G | C | 5 | a0002c0002t0009g0033a0002c0002t0009g0131a0002c0002t0009g0132others(2): Show | 5 | HG01346.hp2 HG01433.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-5000G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156471098 | ||||||
| chr2:156471118
|
A | G | 229 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(226): Show | 229 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.-8-4980A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156471118 | ||||||
| chr2:156471125
|
A | T | 1 | a0002c0002t0002g0134 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-8-4973A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156471125 | ||||||
| chr2:156471437
|
T | C | 228 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(225): Show | 228 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.-8-4661T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156471437 | ||||||
| chr2:156471761
|
A | G | 1 | a0002c0002t0002g0047 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-8-4337A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156471761 | ||||||
| chr2:156471801
|
C | T | 5 | a0002c0002t0002g0160a0002c0002t0002g0162a0002c0002t0002g0163others(2): Show | 5 | HG02109.hp1 HG02559.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-4297C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156471801 | ||||||
| chr2:156471852
|
T | C | 1 | a0001c0001t0001g0028 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-8-4246T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156471852 | ||||||
| chr2:156471928
|
G | T | 2 | a0002c0002t0001g0179a0003c0003t0007g0180 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-8-4170G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156471928 | ||||||
| chr2:156472068
|
T | A | 1 | a0001c0001t0005g0181 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-8-4030T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156472068 | ||||||
| chr2:156472189
|
A | C | 1 | a0001c0001t0005g0181 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-8-3909A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156472189 | ||||||
| chr2:156472191
|
C | CT | 12 | a0001c0001t0005g0182a0002c0002t0001g0165a0002c0002t0001g0184others(9): Show | 12 | HG01884.hp2 HG02055.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-8-3897dupT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156472191 | |||||
| chr2:156472202
|
G | T | 1 | a0001c0001t0001g0253 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-8-3896G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156472202 | ||||||
| chr2:156472385
|
G | A | 228 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(225): Show | 228 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.-8-3713G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156472385 | ||||||
| chr2:156472435
|
C | T | 2 | a0001c0001t0005g0151a0002c0002t0012g0152 | 2 | HG02258.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-8-3663C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156472435 | ||||||
| chr2:156472448
|
G | C | 1 | a0002c0002t0006g0161 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-8-3650G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156472448 | ||||||
| chr2:156472465
|
C | T | 7 | a0001c0001t0001g0081a0002c0002t0006g0070a0002c0002t0006g0098others(4): Show | 7 | HG00673.hp2 HG00735.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8-3633C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156472465 | ||||||
| chr2:156472592
|
G | T | 4 | a0001c0001t0001g0236a0001c0001t0001g0247a0001c0001t0001g0248others(1): Show | 4 | HG04199.hp2 NA18975.hp2 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-3506G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156472592 | ||||||
| chr2:156472617
|
C | A | 75 | a0001c0001t0001g0002a0001c0001t0001g0187a0001c0001t0001g0188others(72): Show | 75 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.-8-3481C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156472617 | ||||||
| chr2:156472646
|
T | A | 2 | a0001c0001t0001g0141a0001c0001t0001g0148 | 2 | HG04115.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-8-3452T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156472646 | ||||||
| chr2:156473172
|
T | C | 246 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(243): Show | 246 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.-8-2926T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156473172 | ||||||
| chr2:156473373
|
A | G | 3 | a0002c0002t0001g0165a0002c0002t0001g0184a0002c0002t0001g0185 | 3 | HG03130.hp2 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-8-2725A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156473373 | ||||||
| chr2:156473823
|
T | C | 1 | a0001c0001t0005g0181 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-8-2275T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156473823 | ||||||
| chr2:156473961
|
CA | C | 227 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(224): Show | 227 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.-8-2134delA | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156473961 | |||||
| chr2:156474367
|
G | A | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-8-1731G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156474367 | ||||||
| chr2:156474471
|
G | A | 3 | a0002c0002t0002g0029a0002c0002t0002g0046a0002c0002t0002g0108 | 3 | HG01261.hp1 HG02602.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.-8-1627G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156474471 | ||||||
| chr2:156474626
|
G | A | 1 | a0001c0004t0001g0232 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-8-1472G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156474626 | ||||||
| chr2:156474641
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-8-1457C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156474641 | ||||||
| chr2:156474648
|
A | T | 7 | a0001c0001t0001g0217a0001c0001t0001g0224a0001c0001t0001g0225others(4): Show | 7 | NA18945.hp2 NA18952.hp1 NA18969.hp1 others(4): Show |
intron_variant | MODIFIER | c.-8-1450A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156474648 | ||||||
| chr2:156474847
|
G | T | 1 | a0001c0001t0001g0116 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-8-1251G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156474847 | ||||||
| chr2:156474870
|
C | T | 75 | a0001c0001t0001g0002a0001c0001t0001g0187a0001c0001t0001g0188others(72): Show | 75 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.-8-1228C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156474870 | ||||||
| chr2:156474891
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-8-1207G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156474891 | ||||||
| chr2:156475308
|
C | T | 7 | a0002c0002t0009g0033a0002c0002t0009g0131a0002c0002t0009g0132others(4): Show | 7 | HG01346.hp2 HG01433.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.-8-790C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156475308 | ||||||
| chr2:156475411
|
C | G | 11 | a0001c0001t0001g0002a0001c0001t0003g0001a0001c0001t0003g0003others(8): Show | 11 | HG00558.hp1 HG02015.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.-8-687C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156475411 | ||||||
| chr2:156475485
|
C | T | 1 | a0001c0001t0001g0202 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-8-613C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156475485 | ||||||
| chr2:156475539
|
T | C | 1 | a0002c0002t0006g0161 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-8-559T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156475539 | ||||||
| chr2:156475728
|
A | G | 1 | a0002c0002t0002g0108 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-8-370A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156475728 | ||||||
| chr2:156475729
|
G | A | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-8-369G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156475729 | ||||||
| chr2:156475781
|
C | A | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-8-317C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156475781 | ||||||
| chr2:156475816
|
A | T | 1 | a0001c0001t0005g0166 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-8-282A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156475816 | ||||||
| chr2:156475957
|
G | C | 3 | a0002c0002t0009g0131a0002c0002t0009g0132a0002c0002t0009g0133 | 3 | HG01346.hp2 HG01433.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.-8-141G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156475957 | ||||||
| chr2:156476387
|
C | A | 1 | a0001c0001t0001g0244 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.102+180C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156476387 | ||||||
| chr2:156476735
|
A | C | 4 | a0002c0002t0002g0019a0002c0002t0002g0045a0002c0002t0002g0094others(1): Show | 4 | HG02040.hp1 NA18943.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.102+528A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156476735 | ||||||
| chr2:156476736
|
A | G | 152 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(149): Show | 152 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.102+529A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156476736 | ||||||
| chr2:156477015
|
T | C | 1 | a0001c0001t0001g0250 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.102+808T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156477015 | ||||||
| chr2:156477417
|
A | G | 246 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(243): Show | 246 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.102+1210A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156477417 | ||||||
| chr2:156477717
|
G | A | 2 | a0002c0002t0006g0070a0002c0002t0006g0098 | 2 | HG00673.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.102+1510G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156477717 | ||||||
| chr2:156477886
|
A | G | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.102+1679A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156477886 | ||||||
| chr2:156477956
|
C | T | 1 | a0001c0001t0001g0226 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.102+1749C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156477956 | ||||||
| chr2:156478004
|
A | G | 1 | a0002c0002t0019g0171 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.102+1797A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156478004 | ||||||
| chr2:156478097
|
T | A | 1 | a0002c0002t0002g0134 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.102+1890T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156478097 | ||||||
| chr2:156478350
|
A | T | 151 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(148): Show | 151 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.102+2143A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156478350 | ||||||
| chr2:156478443
|
A | T | 1 | a0001c0001t0003g0249 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.102+2236A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156478443 | ||||||
| chr2:156478469
|
T | TA | 3 | a0001c0001t0001g0082a0001c0001t0001g0100a0001c0001t0001g0129 | 3 | HG02109.hp2 HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.102+2263dupA | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156478469 | |||||
| chr2:156478488
|
A | G | 1 | a0002c0002t0009g0137 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.102+2281A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156478488 | ||||||
| chr2:156478573
|
A | G | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.102+2366A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156478573 | ||||||
| chr2:156478648
|
G | A | 1 | a0001c0001t0003g0006 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.102+2441G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156478648 | ||||||
| chr2:156478777
|
G | A | 3 | a0002c0002t0001g0179a0002c0002t0019g0171a0003c0003t0007g0180 | 3 | HG02976.hp2 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.102+2570G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156478777 | ||||||
| chr2:156478785
|
A | T | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.102+2578A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156478785 | ||||||
| chr2:156478850
|
G | T | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.102+2643G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156478850 | ||||||
| chr2:156479104
|
T | G | 228 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(225): Show | 228 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.102+2897T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156479104 | ||||||
| chr2:156479114
|
G | A | 228 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(225): Show | 228 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.102+2907G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156479114 | ||||||
| chr2:156479179
|
T | C | 1 | a0001c0001t0001g0220 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.102+2972T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156479179 | ||||||
| chr2:156479224
|
A | C | 2 | a0001c0001t0001g0192a0001c0001t0001g0208 | 2 | HG00741.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.102+3017A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156479224 | ||||||
| chr2:156479227
|
A | T | 1 | a0002c0002t0002g0038 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.102+3020A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156479227 | ||||||
| chr2:156479267
|
G | A | 1 | a0001c0001t0001g0141 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.102+3060G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156479267 | ||||||
| chr2:156479568
|
A | G | 1 | a0002c0002t0008g0136 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.102+3361A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156479568 | ||||||
| chr2:156479751
|
T | C | 1 | a0001c0001t0001g0066 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.102+3544T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156479751 | ||||||
| chr2:156479864
|
G | A | 1 | a0002c0002t0012g0073 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.102+3657G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156479864 | ||||||
| chr2:156479897
|
G | A | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.102+3690G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156479897 | ||||||
| chr2:156480362
|
A | G | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.102+4155A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156480362 | ||||||
| chr2:156480429
|
G | GT | 87 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(84): Show | 87 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.102+4225dupT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156480429 | |||||
| chr2:156480631
|
TGGCTTTG | T | 227 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(224): Show | 227 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.102+4432_102+4438d others(9): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156480631 | |||||
| chr2:156480694
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.102+4487G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156480694 | ||||||
| chr2:156480774
|
C | CT | 9 | a0001c0001t0001g0077a0001c0001t0005g0182a0001c0006t0001g0198others(6): Show | 9 | HG01891.hp2 HG02622.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.102+4584dupT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156480774 | |||||
| chr2:156481079
|
C | T | 1 | a0003c0003t0007g0170 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.102+4872C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156481079 | ||||||
| chr2:156481248
|
G | A | 1 | a0001c0001t0001g0226 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.102+5041G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156481248 | ||||||
| chr2:156481385
|
T | C | 2 | a0002c0002t0006g0070a0002c0002t0006g0098 | 2 | HG00673.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.102+5178T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156481385 | ||||||
| chr2:156481486
|
C | CA | 75 | a0001c0001t0001g0002a0001c0001t0001g0187a0001c0001t0001g0188others(72): Show | 75 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.102+5281dupA | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156481486 | |||||
| chr2:156481606
|
G | C | 1 | a0001c0001t0001g0199 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.102+5399G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156481606 | ||||||
| chr2:156481650
|
T | G | 1 | a0001c0001t0001g0242 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.102+5443T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156481650 | ||||||
| chr2:156481815
|
T | G | 1 | a0001c0001t0001g0220 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.102+5608T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156481815 | ||||||
| chr2:156481874
|
G | A | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.102+5667G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156481874 | ||||||
| chr2:156481899
|
C | T | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.102+5692C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156481899 | ||||||
| chr2:156481974
|
T | C | 1 | a0001c0001t0005g0178 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.102+5767T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156481974 | ||||||
| chr2:156482054
|
T | C | 4 | a0002c0002t0006g0154a0002c0002t0006g0155a0002c0002t0006g0156others(1): Show | 4 | HG00735.hp1 HG01099.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.102+5847T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156482054 | ||||||
| chr2:156482115
|
C | T | 1 | a0001c0001t0001g0236 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.102+5908C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156482115 | ||||||
| chr2:156482140
|
T | C | 75 | a0001c0001t0001g0002a0001c0001t0001g0187a0001c0001t0001g0188others(72): Show | 75 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.102+5933T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156482140 | ||||||
| chr2:156482166
|
C | T | 1 | a0002c0002t0002g0078 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.102+5959C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156482166 | ||||||
| chr2:156482413
|
G | A | 1 | a0001c0001t0016g0039 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.102+6206G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156482413 | ||||||
| chr2:156482500
|
GGA | G | 4 | a0002c0002t0002g0019a0002c0002t0002g0045a0002c0002t0002g0094others(1): Show | 4 | HG02040.hp1 NA18943.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.102+6294_102+6295d others(4): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156482500 | ||||||
| chr2:156482658
|
G | A | 226 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(223): Show | 226 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.102+6451G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156482658 | ||||||
| chr2:156482721
|
C | G | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.102+6514C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156482721 | ||||||
| chr2:156483286
|
C | T | 1 | a0002c0002t0001g0165 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.102+7079C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156483286 | ||||||
| chr2:156483386
|
A | G | 75 | a0001c0001t0001g0002a0001c0001t0001g0187a0001c0001t0001g0188others(72): Show | 75 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.102+7179A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156483386 | ||||||
| chr2:156483460
|
C | G | 75 | a0001c0001t0001g0002a0001c0001t0001g0187a0001c0001t0001g0188others(72): Show | 75 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.102+7253C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156483460 | ||||||
| chr2:156483663
|
T | A | 54 | a0001c0001t0001g0028a0001c0001t0001g0077a0001c0001t0001g0124others(51): Show | 54 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.102+7456T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156483663 | ||||||
| chr2:156483848
|
T | A | 1 | a0001c0001t0003g0008 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.102+7641T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156483848 | ||||||
| chr2:156483987
|
CT | C | 115 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0077others(112): Show | 115 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.102+7804delT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156483987 | |||||
| chr2:156483987
|
CTT | C | 98 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(95): Show | 98 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.102+7803_102+7804d others(4): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156483987 | |||||
| chr2:156484204
|
G | A | 75 | a0001c0001t0001g0002a0001c0001t0001g0187a0001c0001t0001g0188others(72): Show | 75 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.102+7997G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156484204 | ||||||
| chr2:156484227
|
C | T | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.102+8020C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156484227 | ||||||
| chr2:156484388
|
C | T | 1 | a0001c0001t0003g0204 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.102+8181C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156484388 | ||||||
| chr2:156484407
|
G | A | 75 | a0001c0001t0001g0002a0001c0001t0001g0187a0001c0001t0001g0188others(72): Show | 75 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.102+8200G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156484407 | ||||||
| chr2:156484449
|
A | G | 226 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(223): Show | 226 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.102+8242A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156484449 | ||||||
| chr2:156484472
|
A | G | 6 | a0001c0001t0005g0182a0002c0002t0008g0167a0003c0003t0007g0168others(3): Show | 6 | HG02622.hp2 HG02886.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.102+8265A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156484472 | ||||||
| chr2:156484788
|
C | T | 1 | a0002c0002t0001g0165 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.102+8581C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156484788 | ||||||
| chr2:156484824
|
A | G | 1 | a0002c0002t0008g0136 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.102+8617A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156484824 | ||||||
| chr2:156484949
|
A | G | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.102+8742A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156484949 | ||||||
| chr2:156485043
|
C | G | 1 | a0001c0001t0001g0189 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.102+8836C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156485043 | ||||||
| chr2:156485180
|
A | G | 1 | a0002c0002t0002g0029 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.102+8973A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156485180 | ||||||
| chr2:156485217
|
T | C | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.102+9010T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156485217 | ||||||
| chr2:156485309
|
A | G | 1 | a0002c0002t0008g0136 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.102+9102A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156485309 | ||||||
| chr2:156485463
|
C | G | 231 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(228): Show | 231 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.102+9256C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156485463 | ||||||
| chr2:156485637
|
G | A | 7 | a0002c0002t0002g0110a0002c0002t0006g0070a0002c0002t0006g0098others(4): Show | 7 | HG00673.hp2 HG00735.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.102+9430G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156485637 | ||||||
| chr2:156485715
|
C | G | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.102+9508C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156485715 | ||||||
| chr2:156485795
|
T | C | 3 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0119 | 3 | HG02895.hp1 HG02897.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.102+9588T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156485795 | ||||||
| chr2:156485930
|
G | A | 75 | a0001c0001t0001g0002a0001c0001t0001g0187a0001c0001t0001g0188others(72): Show | 75 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.102+9723G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156485930 | ||||||
| chr2:156486450
|
T | C | 1 | a0001c0001t0001g0014 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.103-9594T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156486450 | ||||||
| chr2:156486677
|
G | A | 2 | a0002c0002t0001g0184a0002c0002t0001g0185 | 2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.103-9367G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156486677 | ||||||
| chr2:156487038
|
G | A | 3 | a0001c0001t0001g0191a0001c0001t0001g0193a0001c0001t0001g0207 | 3 | HG00323.hp1 HG01106.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.103-9006G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156487038 | ||||||
| chr2:156487299
|
G | A | 1 | a0001c0001t0001g0042 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.103-8745G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156487299 | ||||||
| chr2:156487450
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.103-8594G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156487450 | ||||||
| chr2:156487915
|
A | G | 1 | a0001c0001t0001g0194 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.103-8129A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156487915 | ||||||
| chr2:156488038
|
G | C | 7 | a0001c0001t0001g0081a0002c0002t0006g0070a0002c0002t0006g0098others(4): Show | 7 | HG00673.hp2 HG00735.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.103-8006G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156488038 | ||||||
| chr2:156488219
|
A | G | 1 | a0002c0002t0006g0176 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.103-7825A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156488219 | ||||||
| chr2:156488405
|
G | T | 1 | a0002c0002t0001g0165 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.103-7639G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156488405 | ||||||
| chr2:156488761
|
A | G | 3 | a0002c0002t0012g0073a0002c0002t0012g0096a0002c0002t0012g0152 | 3 | HG02258.hp2 HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.103-7283A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156488761 | ||||||
| chr2:156488946
|
A | G | 1 | a0002c0002t0002g0029 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.103-7098A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156488946 | ||||||
| chr2:156489083
|
G | A | 3 | a0001c0001t0001g0222a0001c0001t0001g0230a0001c0001t0001g0246 | 3 | HG02698.hp1 HG02818.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.103-6961G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156489083 | ||||||
| chr2:156489086
|
C | T | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.103-6958C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156489086 | ||||||
| chr2:156489114
|
C | T | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.103-6930C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156489114 | ||||||
| chr2:156489247
|
T | G | 3 | a0001c0001t0001g0217a0001c0005t0001g0197a0001c0005t0001g0223 | 3 | NA18952.hp1 NA18969.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.103-6797T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156489247 | ||||||
| chr2:156489397
|
T | C | 1 | a0001c0001t0001g0186 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.103-6647T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156489397 | ||||||
| chr2:156489474
|
A | G | 1 | a0002c0002t0001g0184 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.103-6570A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156489474 | ||||||
| chr2:156489687
|
TCTTC | T | 84 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0187others(81): Show | 84 | HG00323.hp1 HG00558.hp1 HG00621.hp2 others(81): Show |
intron_variant | MODIFIER | c.103-6322_103-6319d others(6): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156489687 | |||||
| chr2:156489687
|
TCTTCCTT others(1): Show |
T | 157 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(154): Show | 157 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.103-6326_103-6319d others(10): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156489687 | |||||
| chr2:156489687
|
TCTTCCTT others(13): Show |
T | 1 | a0001c0001t0001g0130 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.103-6338_103-6319d others(22): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156489687 | |||||
| chr2:156489714
|
TCCTTCCT others(13): Show |
T | 1 | a0002c0002t0002g0127 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.103-6326_103-6307d others(22): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156489714 | |||||
| chr2:156489722
|
T | C | 2 | a0001c0001t0003g0003a0002c0002t0008g0136 | 2 | HG02723.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.103-6322T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156489722 | ||||||
| chr2:156489722
|
TCCTCCCT others(5): Show |
T | 1 | a0001c0001t0003g0204 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.103-6305_103-6294d others(14): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156489722 | |||||
| chr2:156489730
|
C | T | 1 | a0001c0001t0003g0003 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.103-6314C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156489730 | ||||||
| chr2:156489734
|
C | T | 223 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(220): Show | 223 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.103-6310C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156489734 | ||||||
| chr2:156489760
|
T | C | 253 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(250): Show | 253 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.103-6284T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156489760 | ||||||
| chr2:156489763
|
T | C | 253 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(250): Show | 253 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.103-6281T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156489763 | ||||||
| chr2:156489765
|
G | C | 253 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(250): Show | 253 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.103-6279G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156489765 | ||||||
| chr2:156489811
|
CT | C | 253 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(250): Show | 253 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.103-6232delT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156489811 | ||||||
| chr2:156489850
|
CT | C | 253 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(250): Show | 253 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.103-6192delT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156489850 | |||||
| chr2:156489863
|
TTCCTTCC others(37): Show |
T | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.103-6170_103-6127d others(46): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156489863 | |||||
| chr2:156489949
|
A | AC | 13 | a0001c0001t0001g0077a0001c0001t0001g0095a0001c0001t0001g0253others(10): Show | 13 | HG00438.hp1 HG01099.hp2 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.103-6090dupC | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156489949 | |||||
| chr2:156490034
|
T | A | 6 | a0001c0001t0001g0031a0001c0001t0001g0054a0001c0001t0001g0057others(3): Show | 6 | HG00544.hp1 HG02015.hp2 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.103-6010T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156490034 | ||||||
| chr2:156490185
|
C | T | 1 | a0002c0002t0002g0078 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.103-5859C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156490185 | ||||||
| chr2:156490387
|
G | GA | 81 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0028others(78): Show | 81 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.103-5643dupA | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156490387 | |||||
| chr2:156490387
|
G | GAA | 6 | a0001c0001t0001g0205a0001c0001t0001g0215a0001c0001t0001g0218others(3): Show | 6 | HG04199.hp1 HG04199.hp2 NA19000.hp1 others(3): Show |
intron_variant | MODIFIER | c.103-5644_103-5643d others(4): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156490387 | |||||
| chr2:156490402
|
C | A | 5 | a0001c0001t0001g0142a0002c0002t0002g0160a0002c0002t0002g0162others(2): Show | 5 | HG00140.hp1 HG02109.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.103-5642C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156490402 | ||||||
| chr2:156490404
|
A | T | 5 | a0002c0002t0002g0160a0002c0002t0002g0162a0002c0002t0002g0163others(2): Show | 5 | HG02109.hp1 HG02559.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.103-5640A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156490404 | ||||||
| chr2:156490497
|
G | C | 2 | a0002c0002t0001g0179a0003c0003t0007g0180 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.103-5547G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156490497 | ||||||
| chr2:156490509
|
C | T | 1 | a0002c0002t0019g0171 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.103-5535C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156490509 | ||||||
| chr2:156490689
|
C | A | 6 | a0001c0001t0001g0201a0001c0001t0001g0213a0001c0001t0001g0218others(3): Show | 6 | HG00544.hp2 HG00673.hp1 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.103-5355C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156490689 | ||||||
| chr2:156490927
|
GTAAAATT others(42): Show |
G | 76 | a0001c0001t0001g0002a0001c0001t0001g0187a0001c0001t0001g0188others(73): Show | 76 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.103-5073_103-5025d others(51): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156490927 | |||||
| chr2:156490958
|
A | G | 152 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(149): Show | 152 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.103-5086A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156490958 | ||||||
| chr2:156491792
|
G | A | 1 | a0003c0003t0007g0169 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.103-4252G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156491792 | ||||||
| chr2:156492018
|
TA | T | 59 | a0001c0001t0001g0077a0001c0001t0001g0081a0001c0001t0001g0115others(56): Show | 59 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.103-4011delA | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156492018 | |||||
| chr2:156492082
|
G | A | 226 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(223): Show | 226 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.103-3962G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156492082 | ||||||
| chr2:156492117
|
T | C | 246 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(243): Show | 246 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.103-3927T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156492117 | ||||||
| chr2:156492125
|
C | G | 246 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(243): Show | 246 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.103-3919C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156492125 | ||||||
| chr2:156492147
|
C | CT | 91 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0022others(88): Show | 91 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.103-3872dupT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156492147 | |||||
| chr2:156492147
|
C | CTT | 18 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0024others(15): Show | 18 | HG00735.hp2 HG00741.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.103-3873_103-3872d others(4): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156492147 | |||||
| chr2:156492147
|
CTT | C | 15 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0217others(12): Show | 15 | HG02056.hp2 HG02698.hp1 HG02735.hp1 others(12): Show |
intron_variant | MODIFIER | c.103-3873_103-3872d others(4): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156492147 | |||||
| chr2:156492147
|
CTTT | C | 60 | a0001c0001t0001g0002a0001c0001t0001g0187a0001c0001t0001g0188others(57): Show | 60 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.103-3874_103-3872d others(5): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156492147 | |||||
| chr2:156492223
|
G | A | 1 | a0001c0001t0001g0150 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.103-3821G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156492223 | ||||||
| chr2:156492444
|
C | CT | 65 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0017others(62): Show | 65 | HG00438.hp2 HG00544.hp1 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.103-3585dupT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156492444 | |||||
| chr2:156492460
|
C | T | 1 | a0001c0001t0001g0014 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.103-3584C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156492460 | ||||||
| chr2:156492596
|
G | A | 3 | a0002c0002t0011g0075a0002c0002t0011g0076a0002c0002t0011g0125 | 3 | HG01496.hp2 HG02738.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.103-3448G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156492596 | ||||||
| chr2:156492748
|
G | A | 1 | a0001c0001t0001g0101 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.103-3296G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156492748 | ||||||
| chr2:156492926
|
G | C | 1 | a0001c0001t0005g0166 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.103-3118G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156492926 | ||||||
| chr2:156493050
|
G | A | 1 | a0002c0002t0001g0184 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.103-2994G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156493050 | ||||||
| chr2:156493356
|
A | G | 1 | a0003c0003t0007g0122 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.103-2688A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156493356 | ||||||
| chr2:156493425
|
C | T | 246 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(243): Show | 246 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.103-2619C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156493425 | ||||||
| chr2:156493700
|
C | T | 1 | a0001c0001t0017g0065 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.103-2344C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156493700 | ||||||
| chr2:156493706
|
C | T | 1 | a0001c0001t0005g0177 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.103-2338C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156493706 | ||||||
| chr2:156493813
|
A | G | 1 | a0002c0002t0006g0098 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.103-2231A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156493813 | ||||||
| chr2:156493926
|
A | ATGTATGT others(3): Show |
2 | a0001c0001t0001g0100a0001c0001t0001g0129 | 2 | HG02109.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.103-2115_103-2114i others(12): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156493926 | |||||
| chr2:156493926
|
A | ATGTGTGT others(7): Show |
1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.103-2098_103-2085d others(16): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156493926 | |||||
| chr2:156493926
|
A | ATGTGTGT others(9): Show |
3 | a0002c0002t0002g0160a0002c0002t0002g0163a0002c0002t0006g0161 | 3 | HG02109.hp1 HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.103-2100_103-2085d others(18): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156493926 | |||||
| chr2:156493926
|
A | ATGTGTGT others(11): Show |
2 | a0002c0002t0002g0162a0002c0002t0002g0164 | 2 | HG02559.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.103-2102_103-2085d others(20): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156493926 | |||||
| chr2:156493926
|
A | G | 1 | a0001c0001t0001g0143 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.103-2118A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156493926 | ||||||
| chr2:156493926
|
ATG | A | 3 | a0002c0002t0001g0165a0002c0002t0001g0179a0002c0002t0019g0171 | 3 | HG03098.hp2 HG03130.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.103-2086_103-2085d others(4): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156493926 | |||||
| chr2:156493958
|
G | A | 4 | a0001c0001t0001g0100a0001c0001t0001g0129a0001c0001t0001g0227others(1): Show | 4 | HG01993.hp2 HG02109.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.103-2086G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156493958 | ||||||
| chr2:156493958
|
G | GTA | 76 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0187others(73): Show | 76 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.103-2083_103-2082d others(4): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156493958 | |||||
| chr2:156493958
|
G | GTGTA | 7 | a0001c0001t0001g0188a0001c0001t0001g0208a0001c0001t0001g0220others(4): Show | 7 | HG00741.hp1 HG01517.hp2 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.103-2085_103-2084i others(6): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156493958 | |||||
| chr2:156493958
|
G | GTGTGTA | 40 | a0001c0001t0001g0028a0001c0001t0001g0077a0001c0001t0001g0124others(37): Show | 40 | HG00323.hp2 HG00639.hp1 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.103-2085_103-2084i others(8): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156493958 | |||||
| chr2:156493958
|
G | GTGTGTGT others(1): Show |
15 | a0001c0001t0001g0248a0002c0002t0002g0046a0002c0002t0002g0117others(12): Show | 15 | HG00438.hp2 HG00621.hp1 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.103-2085_103-2084i others(10): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156493958 | |||||
| chr2:156493958
|
G | GTGTGTGT others(3): Show |
21 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0032others(18): Show | 21 | HG00558.hp2 HG00639.hp2 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.103-2085_103-2084i others(12): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156493958 | |||||
| chr2:156493958
|
G | GTGTGTGT others(5): Show |
45 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0022others(42): Show | 45 | HG00140.hp1 HG00544.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.103-2085_103-2084i others(14): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156493958 | |||||
| chr2:156493958
|
G | GTGTGTGT others(7): Show |
11 | a0001c0001t0001g0017a0001c0001t0001g0026a0001c0001t0001g0051others(8): Show | 11 | HG00438.hp1 HG00741.hp2 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.103-2085_103-2084i others(16): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156493958 | |||||
| chr2:156493958
|
G | GTGTGTGT others(9): Show |
6 | a0001c0001t0001g0015a0001c0001t0001g0049a0001c0001t0001g0056others(3): Show | 6 | HG01243.hp2 HG03654.hp2 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.103-2085_103-2084i others(18): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156493958 | |||||
| chr2:156493958
|
G | GTGTGTGT others(11): Show |
2 | a0001c0001t0010g0030a0002c0002t0008g0136 | 2 | HG02071.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.103-2085_103-2084i others(20): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156493958 | |||||
| chr2:156494024
|
A | G | 1 | a0001c0001t0003g0010 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.103-2020A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156494024 | ||||||
| chr2:156494031
|
A | G | 76 | a0001c0001t0001g0002a0001c0001t0001g0187a0001c0001t0001g0188others(73): Show | 76 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.103-2013A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156494031 | ||||||
| chr2:156494204
|
T | C | 1 | a0003c0003t0007g0183 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.103-1840T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156494204 | ||||||
| chr2:156494336
|
T | G | 5 | a0001c0001t0003g0069a0001c0001t0003g0086a0001c0001t0003g0087others(2): Show | 5 | HG00639.hp1 HG01884.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.103-1708T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156494336 | ||||||
| chr2:156494414
|
A | G | 7 | a0001c0001t0001g0081a0002c0002t0006g0070a0002c0002t0006g0098others(4): Show | 7 | HG00673.hp2 HG00735.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.103-1630A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156494414 | ||||||
| chr2:156494555
|
T | G | 1 | a0002c0002t0004g0025 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.103-1489T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156494555 | ||||||
| chr2:156494818
|
T | A | 153 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(150): Show | 153 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.103-1226T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156494818 | ||||||
| chr2:156494855
|
G | C | 1 | a0001c0001t0001g0082 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.103-1189G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156494855 | ||||||
| chr2:156495006
|
C | T | 3 | a0001c0001t0001g0082a0001c0001t0001g0100a0001c0001t0001g0129 | 3 | HG02109.hp2 HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.103-1038C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156495006 | ||||||
| chr2:156495176
|
C | T | 76 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0187others(73): Show | 76 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.103-868C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156495176 | ||||||
| chr2:156495312
|
C | T | 1 | a0001c0001t0003g0204 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.103-732C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156495312 | ||||||
| chr2:156495892
|
A | G | 1 | a0002c0002t0006g0070 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.103-152A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156495892 | ||||||
| chr2:156495906
|
A | G | 74 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0187others(71): Show | 74 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.103-138A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156495906 | ||||||
| chr2:156496232
|
T | A | 1 | a0002c0002t0002g0091 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.274+17T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156496232 | ||||||
| chr2:156496234
|
T | A | 1 | a0002c0002t0012g0073 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.274+19T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156496234 | ||||||
| chr2:156496478
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.274+263G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156496478 | ||||||
| chr2:156496669
|
C | CTT | 151 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(148): Show | 151 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.274+455_274+456ins others(2): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 156496669 | |||||
| chr2:156496669
|
CTATATTT others(6): Show |
C | 78 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0042others(75): Show | 78 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.274+456_274+468del others(13): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 156496669 | |||||
| chr2:156496786
|
A | G | 1 | a0001c0001t0005g0182 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.274+571A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156496786 | ||||||
| chr2:156496869
|
T | TC | 229 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(226): Show | 229 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.274+655dupC | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 156496869 | |||||
| chr2:156496959
|
TTCTG | T | 73 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0116others(70): Show | 73 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.274+748_274+751del others(4): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 156496959 | |||||
| chr2:156497169
|
T | G | 248 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(245): Show | 248 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.274+954T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156497169 | ||||||
| chr2:156497991
|
C | G | 1 | a0002c0002t0001g0200 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.274+1776C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156497991 | ||||||
| chr2:156498046
|
A | G | 1 | a0002c0002t0014g0089 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.274+1831A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156498046 | ||||||
| chr2:156498132
|
G | C | 5 | a0002c0002t0001g0165a0002c0002t0001g0179a0002c0002t0001g0184others(2): Show | 5 | HG02630.hp2 HG03130.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.274+1917G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156498132 | ||||||
| chr2:156498279
|
A | C | 1 | a0001c0001t0001g0250 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.274+2064A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156498279 | ||||||
| chr2:156498400
|
G | C | 6 | a0003c0003t0005g0158a0003c0003t0007g0168a0003c0003t0007g0169others(3): Show | 6 | HG01891.hp2 HG02886.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.274+2185G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156498400 | ||||||
| chr2:156498405
|
A | T | 5 | a0002c0002t0002g0029a0002c0002t0002g0047a0002c0002t0002g0048others(2): Show | 5 | HG00323.hp2 HG01261.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.274+2190A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156498405 | ||||||
| chr2:156498456
|
G | A | 170 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(167): Show | 170 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.274+2241G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156498456 | ||||||
| chr2:156498566
|
G | A | 179 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(176): Show | 179 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.274+2351G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156498566 | ||||||
| chr2:156499429
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.274+3214G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156499429 | ||||||
| chr2:156499648
|
T | A | 170 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(167): Show | 170 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.274+3433T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156499648 | ||||||
| chr2:156499739
|
T | C | 1 | a0002c0002t0001g0179 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.274+3524T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156499739 | ||||||
| chr2:156499944
|
A | G | 1 | a0001c0001t0001g0186 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.274+3729A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156499944 | ||||||
| chr2:156499948
|
A | C | 175 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(172): Show | 175 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.274+3733A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156499948 | ||||||
| chr2:156500454
|
A | G | 1 | a0001c0001t0001g0244 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.274+4239A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156500454 | ||||||
| chr2:156500642
|
A | G | 1 | a0002c0002t0020g0020 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.274+4427A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156500642 | ||||||
| chr2:156500694
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.274+4479C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156500694 | ||||||
| chr2:156500779
|
T | C | 2 | a0002c0002t0001g0179a0002c0002t0005g0159 | 2 | HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.274+4564T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156500779 | ||||||
| chr2:156501291
|
T | C | 1 | a0001c0001t0001g0193 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.274+5076T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156501291 | ||||||
| chr2:156501342
|
G | A | 18 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(15): Show | 18 | HG00558.hp1 HG00639.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.274+5127G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156501342 | ||||||
| chr2:156501540
|
A | G | 183 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(180): Show | 183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.274+5325A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156501540 | ||||||
| chr2:156501696
|
A | T | 1 | a0001c0001t0005g0181 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.274+5481A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156501696 | ||||||
| chr2:156501811
|
G | A | 1 | a0001c0001t0001g0243 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.274+5596G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156501811 | ||||||
| chr2:156501874
|
T | C | 5 | a0002c0002t0001g0165a0002c0002t0001g0179a0002c0002t0001g0184others(2): Show | 5 | HG02630.hp2 HG03130.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.274+5659T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156501874 | ||||||
| chr2:156502028
|
G | A | 1 | a0002c0002t0002g0090 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.274+5813G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156502028 | ||||||
| chr2:156502057
|
T | C | 5 | a0002c0002t0001g0165a0002c0002t0001g0179a0002c0002t0001g0184others(2): Show | 5 | HG02630.hp2 HG03130.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.274+5842T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156502057 | ||||||
| chr2:156502104
|
A | ATG | 5 | a0003c0003t0007g0168a0003c0003t0007g0169a0003c0003t0007g0170others(2): Show | 5 | HG02886.hp2 HG02897.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.274+5909_274+5910d others(4): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 156502104 | |||||
| chr2:156502104
|
ATG | A | 168 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(165): Show | 168 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.274+5909_274+5910d others(4): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 156502104 | |||||
| chr2:156502111
|
T | C | 1 | a0002c0002t0001g0165 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.274+5896T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156502111 | ||||||
| chr2:156502168
|
C | T | 3 | a0002c0002t0001g0165a0002c0002t0001g0184a0002c0002t0001g0185 | 3 | HG03130.hp2 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.274+5953C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156502168 | ||||||
| chr2:156502200
|
C | T | 5 | a0003c0003t0007g0168a0003c0003t0007g0169a0003c0003t0007g0170others(2): Show | 5 | HG02886.hp2 HG02897.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.274+5985C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156502200 | ||||||
| chr2:156502237
|
T | A | 1 | a0001c0001t0001g0230 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.274+6022T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156502237 | ||||||
| chr2:156502238
|
T | A | 171 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(168): Show | 171 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.274+6023T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156502238 | ||||||
| chr2:156502245
|
T | G | 183 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(180): Show | 183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.274+6030T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156502245 | ||||||
| chr2:156502252
|
G | A | 2 | a0002c0002t0002g0019a0002c0002t0002g0127 | 2 | NA18943.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.274+6037G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156502252 | ||||||
| chr2:156502326
|
G | A | 2 | a0001c0001t0001g0041a0001c0001t0001g0105 | 2 | NA19067.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.274+6111G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156502326 | ||||||
| chr2:156502552
|
G | T | 2 | a0001c0001t0001g0199a0001c0001t0001g0227 | 2 | HG01993.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.274+6337G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156502552 | ||||||
| chr2:156502615
|
T | C | 6 | a0003c0003t0005g0158a0003c0003t0007g0168a0003c0003t0007g0169others(3): Show | 6 | HG01891.hp2 HG02886.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.274+6400T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156502615 | ||||||
| chr2:156502749
|
TTGTTA | T | 13 | a0001c0001t0001g0026a0001c0001t0001g0050a0001c0001t0001g0052others(10): Show | 13 | HG00140.hp1 HG02074.hp1 HG02523.hp2 others(10): Show |
intron_variant | MODIFIER | c.274+6541_274+6545d others(7): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 156502749 | |||||
| chr2:156502862
|
A | AT | 179 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(176): Show | 179 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.274+6655dupT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 156502862 | |||||
| chr2:156502893
|
A | T | 6 | a0003c0003t0005g0158a0003c0003t0007g0168a0003c0003t0007g0169others(3): Show | 6 | HG01891.hp2 HG02886.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.274+6678A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156502893 | ||||||
| chr2:156502963
|
T | G | 1 | a0002c0002t0001g0200 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.274+6748T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156502963 | ||||||
| chr2:156502976
|
T | C | 7 | a0002c0002t0009g0033a0002c0002t0009g0131a0002c0002t0009g0132others(4): Show | 7 | HG01346.hp2 HG01433.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.274+6761T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156502976 | ||||||
| chr2:156503014
|
A | T | 86 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(83): Show | 86 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.274+6799A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156503014 | ||||||
| chr2:156503044
|
C | A | 176 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(173): Show | 176 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.274+6829C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156503044 | ||||||
| chr2:156503125
|
T | A | 2 | a0001c0001t0005g0181a0002c0002t0001g0200 | 2 | HG02071.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.274+6910T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156503125 | ||||||
| chr2:156503168
|
G | A | 1 | a0001c0001t0001g0064 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.274+6953G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156503168 | ||||||
| chr2:156503400
|
G | A | 2 | a0002c0002t0012g0073a0002c0002t0012g0096 | 2 | HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.274+7185G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156503400 | ||||||
| chr2:156503574
|
G | T | 2 | a0001c0001t0001g0141a0001c0001t0001g0148 | 2 | HG04115.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.275-7222G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156503574 | ||||||
| chr2:156503643
|
A | G | 1 | a0001c0001t0001g0187 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.275-7153A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156503643 | ||||||
| chr2:156503657
|
A | G | 4 | a0002c0002t0009g0033a0002c0002t0009g0131a0002c0002t0009g0132others(1): Show | 4 | HG01346.hp2 HG01433.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.275-7139A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156503657 | ||||||
| chr2:156503702
|
G | C | 5 | a0002c0002t0001g0165a0002c0002t0001g0179a0002c0002t0001g0184others(2): Show | 5 | HG02630.hp2 HG03130.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.275-7094G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156503702 | ||||||
| chr2:156503748
|
TAA | T | 3 | a0001c0001t0001g0082a0001c0001t0001g0100a0001c0001t0001g0129 | 3 | HG02109.hp2 HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.275-7045_275-7044d others(4): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 156503748 | |||||
| chr2:156503764
|
G | A | 87 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(84): Show | 87 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.275-7032G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156503764 | ||||||
| chr2:156503883
|
C | T | 4 | a0002c0002t0002g0019a0002c0002t0002g0045a0002c0002t0002g0094others(1): Show | 4 | HG02040.hp1 NA18943.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.275-6913C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156503883 | ||||||
| chr2:156503935
|
A | G | 5 | a0002c0002t0001g0165a0002c0002t0001g0179a0002c0002t0001g0184others(2): Show | 5 | HG02630.hp2 HG03130.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.275-6861A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156503935 | ||||||
| chr2:156504106
|
C | G | 1 | a0002c0002t0002g0047 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.275-6690C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156504106 | ||||||
| chr2:156504122
|
A | AATAG | 183 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(180): Show | 183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.275-6671_275-6670i others(6): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 156504122 | |||||
| chr2:156504220
|
A | G | 8 | a0001c0001t0001g0032a0001c0001t0001g0059a0001c0001t0001g0071others(5): Show | 8 | HG00639.hp2 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.275-6576A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156504220 | ||||||
| chr2:156504480
|
A | T | 1 | a0002c0002t0002g0163 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.275-6316A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156504480 | ||||||
| chr2:156504590
|
G | A | 183 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(180): Show | 183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.275-6206G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156504590 | ||||||
| chr2:156504777
|
G | A | 2 | a0002c0002t0001g0179a0002c0002t0005g0159 | 2 | HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.275-6019G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156504777 | ||||||
| chr2:156504778
|
G | C | 1 | a0002c0002t0020g0020 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.275-6018G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156504778 | ||||||
| chr2:156504936
|
G | A | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.275-5860G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156504936 | ||||||
| chr2:156505200
|
A | G | 5 | a0001c0001t0001g0067a0001c0001t0001g0111a0001c0001t0001g0114others(2): Show | 5 | NA18747.hp1 NA18999.hp1 NA19001.hp2 others(2): Show |
intron_variant | MODIFIER | c.275-5596A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156505200 | ||||||
| chr2:156505287
|
A | G | 1 | a0002c0002t0001g0200 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.275-5509A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156505287 | ||||||
| chr2:156505628
|
T | C | 1 | a0001c0001t0001g0023 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.275-5168T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156505628 | ||||||
| chr2:156505688
|
T | C | 1 | a0002c0002t0001g0200 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.275-5108T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156505688 | ||||||
| chr2:156505780
|
G | A | 1 | a0001c0001t0005g0181 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.275-5016G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156505780 | ||||||
| chr2:156505782
|
A | G | 1 | a0002c0002t0001g0179 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.275-5014A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156505782 | ||||||
| chr2:156506263
|
A | G | 1 | a0002c0002t0002g0110 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.275-4533A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156506263 | ||||||
| chr2:156506763
|
C | A | 5 | a0003c0003t0007g0168a0003c0003t0007g0169a0003c0003t0007g0170others(2): Show | 5 | HG02886.hp2 HG02897.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.275-4033C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156506763 | ||||||
| chr2:156506816
|
C | T | 3 | a0001c0001t0001g0191a0001c0001t0001g0193a0001c0001t0001g0207 | 3 | HG00323.hp1 HG01106.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.275-3980C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156506816 | ||||||
| chr2:156507036
|
C | T | 3 | a0002c0002t0001g0165a0002c0002t0001g0184a0002c0002t0001g0185 | 3 | HG03130.hp2 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.275-3760C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156507036 | ||||||
| chr2:156507231
|
T | C | 183 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(180): Show | 183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.275-3565T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156507231 | ||||||
| chr2:156507326
|
CT | C | 182 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(179): Show | 182 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.275-3457delT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 156507326 | |||||
| chr2:156507427
|
A | T | 3 | a0001c0001t0001g0082a0001c0001t0001g0100a0001c0001t0001g0129 | 3 | HG02109.hp2 HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.275-3369A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156507427 | ||||||
| chr2:156507516
|
A | G | 183 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(180): Show | 183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.275-3280A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156507516 | ||||||
| chr2:156507539
|
G | C | 3 | a0001c0004t0001g0232a0001c0004t0001g0238a0001c0004t0001g0239 | 3 | HG00140.hp2 HG01433.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.275-3257G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156507539 | ||||||
| chr2:156507596
|
G | T | 5 | a0001c0001t0001g0201a0001c0001t0001g0213a0001c0001t0001g0218others(2): Show | 5 | HG00544.hp2 NA18950.hp2 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.275-3200G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156507596 | ||||||
| chr2:156507682
|
G | C | 183 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(180): Show | 183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.275-3114G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156507682 | ||||||
| chr2:156507729
|
C | A | 1 | a0002c0002t0011g0125 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.275-3067C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156507729 | ||||||
| chr2:156507876
|
C | T | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.275-2920C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156507876 | ||||||
| chr2:156508319
|
T | G | 1 | a0003c0003t0007g0122 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.275-2477T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156508319 | ||||||
| chr2:156508323
|
G | T | 2 | a0001c0001t0001g0026a0001c0001t0001g0050 | 2 | HG02602.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.275-2473G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156508323 | ||||||
| chr2:156508561
|
G | T | 1 | a0002c0002t0011g0075 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.275-2235G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156508561 | ||||||
| chr2:156508571
|
G | C | 1 | a0002c0002t0004g0027 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.275-2225G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156508571 | ||||||
| chr2:156508629
|
T | A | 1 | a0001c0001t0001g0105 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.275-2167T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156508629 | ||||||
| chr2:156509081
|
C | T | 55 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0116others(52): Show | 55 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.275-1715C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156509081 | ||||||
| chr2:156509200
|
T | C | 1 | a0002c0002t0009g0131 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.275-1596T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156509200 | ||||||
| chr2:156509528
|
T | C | 5 | a0003c0003t0007g0168a0003c0003t0007g0169a0003c0003t0007g0170others(2): Show | 5 | HG02886.hp2 HG02897.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.275-1268T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156509528 | ||||||
| chr2:156509531
|
G | T | 8 | a0001c0001t0001g0032a0001c0001t0001g0059a0001c0001t0001g0071others(5): Show | 8 | HG00639.hp2 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.275-1265G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156509531 | ||||||
| chr2:156509559
|
C | T | 2 | a0001c0001t0005g0172a0001c0001t0005g0182 | 2 | HG02622.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.275-1237C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156509559 | ||||||
| chr2:156509753
|
G | C | 1 | a0001c0001t0001g0186 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.275-1043G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156509753 | ||||||
| chr2:156509765
|
C | CTTTT | 5 | a0001c0001t0001g0052a0001c0001t0001g0054a0001c0001t0001g0072others(2): Show | 5 | HG01261.hp2 HG02895.hp1 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.275-1015_275-1012d others(6): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 156509765 | |||||
| chr2:156509765
|
C | CTTTTT | 84 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(81): Show | 84 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.275-1016_275-1012d others(7): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 156509765 | |||||
| chr2:156509765
|
C | CTTTTTT | 74 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0037others(71): Show | 74 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.275-1017_275-1012d others(8): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 156509765 | |||||
| chr2:156509765
|
C | CTTTTTTT | 11 | a0001c0001t0001g0212a0001c0001t0001g0240a0001c0001t0003g0003others(8): Show | 11 | HG02258.hp2 HG02559.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.275-1018_275-1012d others(9): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 156509765 | |||||
| chr2:156509784
|
T | TTTTTTTA | 7 | a0001c0001t0005g0181a0002c0002t0001g0200a0003c0003t0005g0158others(4): Show | 7 | HG01891.hp2 HG02071.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.275-1012_275-1011i others(9): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156509784 | ||||||
| chr2:156509804
|
C | T | 7 | a0002c0002t0009g0033a0002c0002t0009g0131a0002c0002t0009g0132others(4): Show | 7 | HG01346.hp2 HG01433.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.275-992C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156509804 | ||||||
| chr2:156509834
|
C | G | 1 | a0002c0002t0001g0200 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.275-962C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156509834 | ||||||
| chr2:156509885
|
G | T | 183 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(180): Show | 183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.275-911G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156509885 | ||||||
| chr2:156509898
|
C | T | 3 | a0001c0001t0001g0051a0001c0001t0001g0083a0001c0001t0015g0144 | 3 | HG02056.hp1 NA19004.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.275-898C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156509898 | ||||||
| chr2:156510218
|
C | CTCTT | 5 | a0002c0002t0002g0029a0002c0002t0002g0047a0002c0002t0002g0048others(2): Show | 5 | HG00323.hp2 HG01261.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.275-565_275-562dup others(4): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 156510218 | |||||
| chr2:156510259
|
C | A | 1 | a0001c0001t0001g0222 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.275-537C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156510259 | ||||||
| chr2:156510377
|
G | A | 1 | a0002c0002t0002g0046 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.275-419G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156510377 | ||||||
| chr2:156510518
|
A | G | 1 | a0002c0002t0020g0020 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.275-278A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156510518 | ||||||
| chr2:156510590
|
C | T | 1 | a0001c0001t0010g0030 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.275-206C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156510590 | ||||||
| chr2:156510599
|
C | G | 6 | a0001c0001t0001g0032a0001c0001t0001g0059a0001c0001t0001g0071others(3): Show | 6 | HG00639.hp2 HG02630.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.275-197C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156510599 | ||||||
| chr2:156510987
|
G | A | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.399+67G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 4/16 | chr2 | 156510987 | ||||||
| chr2:156511741
|
G | A | 183 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(180): Show | 183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.400-479G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 4/16 | chr2 | 156511741 | ||||||
| chr2:156511906
|
A | G | 1 | a0001c0001t0001g0130 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.400-314A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 4/16 | chr2 | 156511906 | ||||||
| chr2:156512365
|
T | C | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.497+48T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 5/16 | chr2 | 156512365 | ||||||
| chr2:156512649
|
G | T | 3 | a0001c0001t0001g0191a0001c0001t0001g0193a0001c0001t0001g0207 | 3 | HG00323.hp1 HG01106.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.497+332G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 5/16 | chr2 | 156512649 | ||||||
| chr2:156512710
|
G | C | 183 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(180): Show | 183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.497+393G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 5/16 | chr2 | 156512710 | ||||||
| chr2:156512728
|
C | T | 1 | a0001c0001t0001g0252 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.497+411C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 5/16 | chr2 | 156512728 | ||||||
| chr2:156512739
|
TA | T | 5 | a0002c0002t0001g0165a0002c0002t0001g0179a0002c0002t0001g0184others(2): Show | 5 | HG02630.hp2 HG03130.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.497+424delA | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 156512739 | |||||
| chr2:156513505
|
TG | T | 5 | a0002c0002t0001g0165a0002c0002t0001g0179a0002c0002t0001g0184others(2): Show | 5 | HG02630.hp2 HG03130.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.661+10delG | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156513505 | ||||||
| chr2:156513506
|
GT | G | 6 | a0001c0001t0003g0069a0001c0001t0003g0086a0001c0001t0003g0087others(3): Show | 6 | HG00639.hp1 HG01884.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.661+24delT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156513506 | |||||
| chr2:156513514
|
T | C | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.661+18T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156513514 | ||||||
| chr2:156513585
|
A | C | 3 | a0001c0001t0001g0141a0001c0001t0001g0148a0001c0001t0017g0065 | 3 | HG02683.hp2 HG04115.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.661+89A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156513585 | ||||||
| chr2:156513654
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.661+158G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156513654 | ||||||
| chr2:156513683
|
A | G | 1 | a0003c0003t0007g0012 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.661+187A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156513683 | ||||||
| chr2:156513802
|
A | G | 1 | a0002c0002t0002g0092 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.661+306A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156513802 | ||||||
| chr2:156514129
|
C | CT | 5 | a0003c0003t0007g0168a0003c0003t0007g0169a0003c0003t0007g0170others(2): Show | 5 | HG02886.hp2 HG02897.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.661+648dupT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156514129 | |||||
| chr2:156514129
|
CT | C | 91 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0037others(88): Show | 91 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.661+648delT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156514129 | |||||
| chr2:156514129
|
CTT | C | 87 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(84): Show | 87 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.661+647_661+648del others(2): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156514129 | |||||
| chr2:156514493
|
T | C | 2 | a0002c0002t0001g0179a0002c0002t0005g0159 | 2 | HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.661+997T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156514493 | ||||||
| chr2:156514595
|
A | G | 3 | a0002c0002t0012g0073a0002c0002t0012g0096a0002c0002t0012g0152 | 3 | HG02258.hp2 HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.661+1099A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156514595 | ||||||
| chr2:156514713
|
T | C | 248 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(245): Show | 248 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.661+1217T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156514713 | ||||||
| chr2:156514737
|
A | G | 1 | a0002c0002t0001g0165 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.661+1241A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156514737 | ||||||
| chr2:156515221
|
C | T | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.661+1725C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156515221 | ||||||
| chr2:156515345
|
C | A | 81 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0116others(78): Show | 81 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.661+1849C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156515345 | ||||||
| chr2:156515488
|
ATTG | A | 5 | a0002c0002t0001g0165a0002c0002t0001g0179a0002c0002t0001g0184others(2): Show | 5 | HG02630.hp2 HG03130.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.661+1997_661+1999d others(5): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156515488 | |||||
| chr2:156515620
|
T | A | 1 | a0001c0001t0001g0141 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.661+2124T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156515620 | ||||||
| chr2:156515922
|
A | G | 2 | a0002c0002t0001g0179a0002c0002t0005g0159 | 2 | HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.661+2426A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156515922 | ||||||
| chr2:156516001
|
T | C | 1 | a0002c0002t0001g0179 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.661+2505T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156516001 | ||||||
| chr2:156516125
|
T | C | 1 | a0002c0002t0002g0078 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.661+2629T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156516125 | ||||||
| chr2:156516411
|
C | T | 1 | a0002c0002t0008g0167 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.661+2915C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156516411 | ||||||
| chr2:156516504
|
T | C | 2 | a0001c0001t0001g0212a0001c0001t0001g0240 | 2 | NA19004.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.661+3008T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156516504 | ||||||
| chr2:156516595
|
A | G | 1 | a0001c0001t0013g0043 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.661+3099A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156516595 | ||||||
| chr2:156516813
|
CACTT | C | 5 | a0003c0003t0007g0168a0003c0003t0007g0169a0003c0003t0007g0170others(2): Show | 5 | HG02886.hp2 HG02897.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.661+3322_661+3325d others(6): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156516813 | |||||
| chr2:156517100
|
G | T | 183 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(180): Show | 183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.661+3604G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156517100 | ||||||
| chr2:156517345
|
A | G | 2 | a0003c0003t0007g0012a0003c0003t0007g0122 | 2 | HG01891.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.661+3849A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156517345 | ||||||
| chr2:156517358
|
C | T | 2 | a0001c0001t0005g0181a0002c0002t0001g0200 | 2 | HG02071.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.661+3862C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156517358 | ||||||
| chr2:156517497
|
T | C | 1 | a0002c0002t0001g0200 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.661+4001T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156517497 | ||||||
| chr2:156517780
|
A | G | 2 | a0002c0002t0001g0179a0002c0002t0005g0159 | 2 | HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.661+4284A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156517780 | ||||||
| chr2:156517895
|
G | A | 5 | a0002c0002t0001g0165a0002c0002t0001g0179a0002c0002t0001g0184others(2): Show | 5 | HG02630.hp2 HG03130.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.661+4399G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156517895 | ||||||
| chr2:156518004
|
A | G | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.661+4508A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156518004 | ||||||
| chr2:156518480
|
T | G | 1 | a0001c0001t0001g0237 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.661+4984T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156518480 | ||||||
| chr2:156518490
|
G | A | 1 | a0002c0002t0001g0200 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.661+4994G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156518490 | ||||||
| chr2:156518670
|
T | C | 2 | a0001c0001t0005g0151a0002c0002t0012g0152 | 2 | HG02258.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.661+5174T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156518670 | ||||||
| chr2:156519210
|
T | G | 4 | a0002c0002t0002g0160a0002c0002t0002g0162a0002c0002t0002g0163others(1): Show | 4 | HG02559.hp1 HG02717.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.661+5714T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156519210 | ||||||
| chr2:156519211
|
G | T | 85 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(82): Show | 85 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.661+5715G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156519211 | ||||||
| chr2:156519305
|
A | T | 7 | a0002c0002t0002g0013a0002c0002t0002g0038a0002c0002t0002g0046others(4): Show | 7 | HG02129.hp1 HG03654.hp1 NA18941.hp2 others(4): Show |
intron_variant | MODIFIER | c.661+5809A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156519305 | ||||||
| chr2:156519444
|
A | G | 1 | a0001c0001t0001g0135 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.661+5948A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156519444 | ||||||
| chr2:156519453
|
A | T | 1 | a0001c0001t0001g0021 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.661+5957A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156519453 | ||||||
| chr2:156519658
|
T | C | 183 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(180): Show | 183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.661+6162T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156519658 | ||||||
| chr2:156519659
|
G | A | 1 | a0001c0001t0001g0135 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.661+6163G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156519659 | ||||||
| chr2:156519663
|
C | G | 2 | a0002c0002t0012g0073a0002c0002t0012g0096 | 2 | HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.661+6167C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156519663 | ||||||
| chr2:156519707
|
C | T | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.661+6211C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156519707 | ||||||
| chr2:156519725
|
G | A | 2 | a0002c0002t0012g0073a0002c0002t0012g0096 | 2 | HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.661+6229G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156519725 | ||||||
| chr2:156519779
|
C | T | 3 | a0002c0002t0002g0117a0002c0002t0002g0118a0002c0002t0002g0138 | 3 | HG01884.hp2 HG02055.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.661+6283C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156519779 | ||||||
| chr2:156519960
|
G | C | 176 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(173): Show | 176 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.661+6464G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156519960 | ||||||
| chr2:156519961
|
G | A | 1 | a0001c0001t0016g0039 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.661+6465G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156519961 | ||||||
| chr2:156520207
|
G | T | 1 | a0002c0002t0011g0075 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.661+6711G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156520207 | ||||||
| chr2:156520270
|
A | G | 3 | a0002c0002t0012g0073a0002c0002t0012g0096a0002c0002t0012g0152 | 3 | HG02258.hp2 HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.661+6774A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156520270 | ||||||
| chr2:156520355
|
CA | C | 183 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(180): Show | 183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.661+6861delA | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156520355 | |||||
| chr2:156520433
|
A | G | 1 | a0001c0001t0005g0151 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.661+6937A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156520433 | ||||||
| chr2:156520560
|
G | GTTATTTA others(1): Show |
2 | a0002c0002t0001g0184a0002c0002t0001g0185 | 2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.661+7099_661+7106d others(10): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156520560 | |||||
| chr2:156520560
|
GTTAT | G | 86 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0130others(83): Show | 86 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.661+7103_661+7106d others(6): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156520560 | |||||
| chr2:156520560
|
GTTATTTA others(1): Show |
G | 143 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(140): Show | 143 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.661+7099_661+7106d others(10): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156520560 | |||||
| chr2:156520560
|
GTTATTTA others(5): Show |
G | 2 | a0001c0001t0003g0249a0001c0001t0005g0166 | 2 | HG03540.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.661+7095_661+7106d others(14): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156520560 | |||||
| chr2:156520828
|
C | T | 1 | a0001c0001t0005g0181 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.661+7332C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156520828 | ||||||
| chr2:156520990
|
A | C | 183 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(180): Show | 183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.661+7494A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156520990 | ||||||
| chr2:156521444
|
A | G | 1 | a0001c0001t0001g0153 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.661+7948A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156521444 | ||||||
| chr2:156521687
|
A | G | 8 | a0001c0001t0005g0181a0002c0002t0001g0200a0003c0003t0005g0158others(5): Show | 8 | HG01891.hp2 HG02071.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.661+8191A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156521687 | ||||||
| chr2:156521830
|
A | G | 1 | a0001c0001t0001g0240 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.661+8334A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156521830 | ||||||
| chr2:156521957
|
C | T | 5 | a0001c0001t0001g0201a0001c0001t0001g0213a0001c0001t0001g0218others(2): Show | 5 | HG00544.hp2 NA18950.hp2 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.661+8461C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156521957 | ||||||
| chr2:156522021
|
A | G | 167 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(164): Show | 167 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.661+8525A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156522021 | ||||||
| chr2:156522105
|
G | A | 1 | a0002c0002t0004g0097 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.661+8609G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156522105 | ||||||
| chr2:156522107
|
A | G | 1 | a0001c0001t0005g0181 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.661+8611A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156522107 | ||||||
| chr2:156522311
|
C | T | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.661+8815C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156522311 | ||||||
| chr2:156522332
|
T | C | 1 | a0002c0002t0019g0171 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.661+8836T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156522332 | ||||||
| chr2:156522444
|
C | T | 3 | a0002c0002t0002g0044a0002c0002t0002g0092a0002c0002t0021g0079 | 3 | HG01106.hp1 HG02074.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.661+8948C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156522444 | ||||||
| chr2:156522528
|
A | G | 2 | a0001c0001t0001g0054a0001c0001t0001g0104 | 2 | NA19060.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.661+9032A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156522528 | ||||||
| chr2:156522683
|
CT | C | 177 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(174): Show | 177 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.661+9202delT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156522683 | |||||
| chr2:156522921
|
T | A | 4 | a0002c0002t0002g0160a0002c0002t0002g0162a0002c0002t0002g0163others(1): Show | 4 | HG02559.hp1 HG02717.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.661+9425T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156522921 | ||||||
| chr2:156522948
|
AT | A | 81 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0116others(78): Show | 81 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.661+9456delT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156522948 | |||||
| chr2:156523248
|
C | T | 1 | a0001c0001t0005g0151 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.661+9752C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156523248 | ||||||
| chr2:156523291
|
T | A | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.661+9795T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156523291 | ||||||
| chr2:156523331
|
G | C | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.661+9835G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156523331 | ||||||
| chr2:156523500
|
C | T | 1 | a0002c0002t0009g0133 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.661+10004C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156523500 | ||||||
| chr2:156523649
|
T | C | 2 | a0002c0002t0001g0179a0002c0002t0005g0159 | 2 | HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.661+10153T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156523649 | ||||||
| chr2:156523670
|
C | CTAGA | 76 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0026others(73): Show | 76 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.661+10221_661+1022 others(8): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156523670 | |||||
| chr2:156523670
|
C | CTAGATAG others(1): Show |
21 | a0001c0001t0001g0054a0001c0001t0001g0059a0001c0001t0001g0066others(18): Show | 21 | HG01346.hp1 HG01891.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.661+10217_661+1022 others(12): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156523670 | |||||
| chr2:156523670
|
C | CTAGATAG others(5): Show |
3 | a0001c0001t0001g0205a0001c0001t0001g0236a0001c0001t0003g0069 | 3 | HG02683.hp1 HG04199.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.661+10213_661+1022 others(16): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156523670 | |||||
| chr2:156523670
|
CTAGA | C | 31 | a0001c0001t0001g0024a0001c0001t0001g0064a0001c0001t0001g0081others(28): Show | 31 | HG00323.hp2 HG00558.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.661+10221_661+1022 others(8): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156523670 | |||||
| chr2:156523670
|
CTAGATAG others(1): Show |
C | 7 | a0001c0001t0001g0209a0001c0001t0001g0212a0001c0001t0001g0214others(4): Show | 7 | HG01123.hp1 HG02451.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.661+10217_661+1022 others(12): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156523670 | |||||
| chr2:156523670
|
CTAGATAG others(5): Show |
C | 5 | a0001c0001t0001g0150a0001c0001t0005g0178a0002c0002t0002g0047others(2): Show | 5 | HG01884.hp2 HG01928.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.661+10213_661+1022 others(16): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156523670 | |||||
| chr2:156523670
|
CTAGATAG others(9): Show |
C | 2 | a0002c0002t0012g0073a0002c0002t0012g0152 | 2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.661+10209_661+1022 others(20): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156523670 | |||||
| chr2:156523804
|
G | A | 5 | a0001c0001t0003g0069a0001c0001t0003g0086a0001c0001t0003g0087others(2): Show | 5 | HG00639.hp1 HG01884.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.661+10308G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156523804 | ||||||
| chr2:156524040
|
A | G | 2 | a0002c0002t0001g0184a0002c0002t0001g0185 | 2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.661+10544A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156524040 | ||||||
| chr2:156524067
|
G | A | 170 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(167): Show | 170 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.661+10571G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156524067 | ||||||
| chr2:156524560
|
T | C | 1 | a0001c0001t0001g0085 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.661+11064T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156524560 | ||||||
| chr2:156525242
|
A | G | 50 | a0002c0002t0002g0013a0002c0002t0002g0019a0002c0002t0002g0029others(47): Show | 50 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.661+11746A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156525242 | ||||||
| chr2:156525365
|
G | C | 1 | a0001c0001t0005g0172 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.661+11869G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156525365 | ||||||
| chr2:156525567
|
A | T | 1 | a0002c0002t0001g0200 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.661+12071A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156525567 | ||||||
| chr2:156525628
|
A | C | 5 | a0002c0002t0001g0165a0002c0002t0001g0179a0002c0002t0001g0184others(2): Show | 5 | HG02630.hp2 HG03130.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.661+12132A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156525628 | ||||||
| chr2:156525659
|
T | C | 1 | a0002c0002t0001g0165 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.661+12163T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156525659 | ||||||
| chr2:156525807
|
T | G | 4 | a0002c0002t0002g0160a0002c0002t0002g0162a0002c0002t0002g0163others(1): Show | 4 | HG02559.hp1 HG02717.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.661+12311T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156525807 | ||||||
| chr2:156526109
|
G | C | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.661+12613G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156526109 | ||||||
| chr2:156526296
|
C | T | 1 | a0001c0001t0001g0224 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.661+12800C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156526296 | ||||||
| chr2:156526307
|
C | A | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.661+12811C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156526307 | ||||||
| chr2:156526601
|
T | TAGTTTA | 248 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(245): Show | 248 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.661+13108_661+1311 others(10): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156526601 | |||||
| chr2:156526750
|
T | C | 1 | a0002c0002t0002g0134 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.661+13254T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156526750 | ||||||
| chr2:156527106
|
C | G | 6 | a0003c0003t0005g0158a0003c0003t0007g0168a0003c0003t0007g0169others(3): Show | 6 | HG01891.hp2 HG02886.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.661+13610C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156527106 | ||||||
| chr2:156527163
|
C | G | 1 | a0002c0002t0001g0200 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.661+13667C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156527163 | ||||||
| chr2:156527433
|
C | G | 85 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(82): Show | 85 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.661+13937C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156527433 | ||||||
| chr2:156527456
|
C | T | 2 | a0002c0002t0001g0179a0002c0002t0005g0159 | 2 | HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.661+13960C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156527456 | ||||||
| chr2:156527706
|
G | A | 2 | a0002c0002t0001g0179a0002c0002t0005g0159 | 2 | HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.661+14210G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156527706 | ||||||
| chr2:156527724
|
T | C | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.661+14228T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156527724 | ||||||
| chr2:156527849
|
G | A | 1 | a0001c0001t0005g0182 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.661+14353G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156527849 | ||||||
| chr2:156528239
|
C | T | 1 | a0002c0002t0001g0200 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.661+14743C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156528239 | ||||||
| chr2:156528536
|
C | G | 2 | a0002c0002t0001g0179a0002c0002t0005g0159 | 2 | HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.661+15040C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156528536 | ||||||
| chr2:156528587
|
C | G | 1 | a0002c0002t0001g0200 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.661+15091C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156528587 | ||||||
| chr2:156528594
|
C | G | 1 | a0003c0003t0007g0012 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.661+15098C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156528594 | ||||||
| chr2:156528633
|
C | T | 3 | a0002c0002t0001g0165a0002c0002t0001g0184a0002c0002t0001g0185 | 3 | HG03130.hp2 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.661+15137C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156528633 | ||||||
| chr2:156528773
|
A | AT | 3 | a0002c0002t0002g0117a0002c0002t0002g0118a0002c0002t0002g0138 | 3 | HG01884.hp2 HG02055.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.661+15283dupT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156528773 | |||||
| chr2:156528887
|
C | T | 3 | a0001c0001t0001g0024a0001c0001t0001g0095a0001c0001t0001g0186 | 3 | NA18959.hp2 NA19000.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.661+15391C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156528887 | ||||||
| chr2:156528900
|
G | C | 1 | a0001c0001t0016g0039 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.661+15404G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156528900 | ||||||
| chr2:156528971
|
A | T | 1 | a0002c0002t0009g0131 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.661+15475A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156528971 | ||||||
| chr2:156529062
|
A | G | 177 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(174): Show | 177 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.661+15566A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156529062 | ||||||
| chr2:156529085
|
G | C | 177 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(174): Show | 177 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.661+15589G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156529085 | ||||||
| chr2:156529093
|
G | T | 176 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(173): Show | 176 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.661+15597G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156529093 | ||||||
| chr2:156529103
|
T | C | 2 | a0001c0001t0001g0015a0001c0001t0001g0056 | 2 | HG01243.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.661+15607T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156529103 | ||||||
| chr2:156529105
|
T | C | 177 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(174): Show | 177 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.661+15609T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156529105 | ||||||
| chr2:156529134
|
C | T | 1 | a0002c0002t0001g0200 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.661+15638C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156529134 | ||||||
| chr2:156529210
|
A | G | 1 | a0002c0002t0002g0160 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.661+15714A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156529210 | ||||||
| chr2:156529212
|
G | GT | 177 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(174): Show | 177 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.661+15722dupT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156529212 | |||||
| chr2:156529265
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.661+15769G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156529265 | ||||||
| chr2:156529318
|
A | G | 2 | a0003c0003t0007g0012a0003c0003t0007g0122 | 2 | HG01891.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.661+15822A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156529318 | ||||||
| chr2:156529582
|
T | G | 7 | a0002c0002t0006g0070a0002c0002t0006g0098a0002c0002t0006g0154others(4): Show | 7 | HG00673.hp2 HG00735.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.661+16086T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156529582 | ||||||
| chr2:156529620
|
C | G | 5 | a0001c0001t0003g0069a0001c0001t0003g0086a0001c0001t0003g0087others(2): Show | 5 | HG00639.hp1 HG01884.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.661+16124C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156529620 | ||||||
| chr2:156529798
|
A | C | 3 | a0002c0002t0002g0044a0002c0002t0002g0092a0002c0002t0021g0079 | 3 | HG01106.hp1 HG02074.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.661+16302A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156529798 | ||||||
| chr2:156529810
|
G | A | 1 | a0001c0001t0005g0151 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.661+16314G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156529810 | ||||||
| chr2:156529833
|
T | G | 3 | a0002c0002t0002g0117a0002c0002t0002g0118a0002c0002t0002g0138 | 3 | HG01884.hp2 HG02055.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.661+16337T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156529833 | ||||||
| chr2:156529870
|
C | T | 5 | a0002c0002t0001g0165a0002c0002t0001g0179a0002c0002t0001g0184others(2): Show | 5 | HG02630.hp2 HG03130.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.661+16374C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156529870 | ||||||
| chr2:156529915
|
G | A | 1 | a0002c0002t0012g0096 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.661+16419G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156529915 | ||||||
| chr2:156529938
|
A | G | 3 | a0002c0002t0001g0165a0002c0002t0001g0184a0002c0002t0001g0185 | 3 | HG03130.hp2 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.661+16442A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156529938 | ||||||
| chr2:156529981
|
G | C | 5 | a0002c0002t0001g0165a0002c0002t0001g0179a0002c0002t0001g0184others(2): Show | 5 | HG02630.hp2 HG03130.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.661+16485G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156529981 | ||||||
| chr2:156529989
|
G | A | 3 | a0002c0002t0001g0165a0002c0002t0001g0184a0002c0002t0001g0185 | 3 | HG03130.hp2 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.661+16493G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156529989 | ||||||
| chr2:156530038
|
C | T | 1 | a0001c0001t0001g0067 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.661+16542C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156530038 | ||||||
| chr2:156530047
|
T | G | 1 | a0001c0001t0001g0107 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.661+16551T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156530047 | ||||||
| chr2:156530292
|
A | G | 1 | a0001c0001t0001g0021 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.661+16796A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156530292 | ||||||
| chr2:156530302
|
T | TTTGCTGA others(2): Show |
183 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(180): Show | 183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.661+16811_661+1681 others(13): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156530302 | |||||
| chr2:156530359
|
G | C | 1 | a0002c0002t0019g0171 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.661+16863G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156530359 | ||||||
| chr2:156530465
|
A | G | 3 | a0002c0002t0002g0044a0002c0002t0002g0092a0002c0002t0021g0079 | 3 | HG01106.hp1 HG02074.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.661+16969A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156530465 | ||||||
| chr2:156530574
|
G | A | 171 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(168): Show | 171 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.661+17078G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156530574 | ||||||
| chr2:156530642
|
C | G | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.661+17146C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156530642 | ||||||
| chr2:156530674
|
A | C | 2 | a0002c0002t0001g0179a0002c0002t0005g0159 | 2 | HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.661+17178A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156530674 | ||||||
| chr2:156530736
|
T | A | 176 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(173): Show | 176 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.661+17240T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156530736 | ||||||
| chr2:156531111
|
C | T | 1 | a0002c0002t0002g0038 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.661+17615C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156531111 | ||||||
| chr2:156531114
|
T | G | 3 | a0002c0002t0004g0112a0002c0002t0004g0113a0002c0002t0004g0128 | 3 | NA18952.hp2 NA18999.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.661+17618T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156531114 | ||||||
| chr2:156531136
|
A | G | 1 | a0001c0001t0001g0119 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.661+17640A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156531136 | ||||||
| chr2:156531148
|
T | G | 1 | a0002c0002t0002g0127 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.661+17652T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156531148 | ||||||
| chr2:156531207
|
T | A | 183 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(180): Show | 183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.661+17711T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156531207 | ||||||
| chr2:156531551
|
C | T | 3 | a0002c0002t0001g0165a0002c0002t0001g0184a0002c0002t0001g0185 | 3 | HG03130.hp2 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.661+18055C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156531551 | ||||||
| chr2:156531704
|
T | A | 3 | a0002c0002t0001g0165a0002c0002t0001g0184a0002c0002t0001g0185 | 3 | HG03130.hp2 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.662-17904T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156531704 | ||||||
| chr2:156531856
|
G | A | 1 | a0001c0001t0001g0246 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.662-17752G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156531856 | ||||||
| chr2:156531868
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.662-17740G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156531868 | ||||||
| chr2:156532013
|
CT | C | 171 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(168): Show | 171 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.662-17589delT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156532013 | |||||
| chr2:156532058
|
A | C | 1 | a0002c0002t0004g0097 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.662-17550A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156532058 | ||||||
| chr2:156532122
|
C | T | 1 | a0003c0003t0007g0170 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.662-17486C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156532122 | ||||||
| chr2:156532138
|
T | C | 183 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(180): Show | 183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.662-17470T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156532138 | ||||||
| chr2:156532190
|
A | G | 177 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(174): Show | 177 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.662-17418A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156532190 | ||||||
| chr2:156532236
|
G | T | 1 | a0001c0001t0001g0252 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.662-17372G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156532236 | ||||||
| chr2:156532270
|
G | A | 4 | a0002c0002t0002g0019a0002c0002t0002g0045a0002c0002t0002g0094others(1): Show | 4 | HG02040.hp1 NA18943.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.662-17338G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156532270 | ||||||
| chr2:156532475
|
A | T | 28 | a0001c0001t0001g0203a0001c0001t0001g0235a0001c0001t0003g0001others(25): Show | 28 | HG00558.hp1 HG00639.hp1 HG01256.hp2 others(25): Show |
intron_variant | MODIFIER | c.662-17133A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156532475 | ||||||
| chr2:156532515
|
A | G | 3 | a0002c0002t0011g0075a0002c0002t0011g0076a0002c0002t0011g0125 | 3 | HG01496.hp2 HG02738.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.662-17093A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156532515 | ||||||
| chr2:156532682
|
C | T | 3 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0229 | 3 | HG02735.hp2 HG03239.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.662-16926C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156532682 | ||||||
| chr2:156532699
|
G | A | 1 | a0002c0002t0001g0200 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.662-16909G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156532699 | ||||||
| chr2:156532763
|
T | C | 1 | a0002c0002t0006g0098 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.662-16845T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156532763 | ||||||
| chr2:156532949
|
T | C | 1 | a0002c0002t0001g0200 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.662-16659T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156532949 | ||||||
| chr2:156532978
|
G | T | 1 | a0002c0002t0002g0108 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.662-16630G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156532978 | ||||||
| chr2:156533505
|
A | C | 1 | a0001c0004t0001g0239 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.662-16103A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156533505 | ||||||
| chr2:156533514
|
T | A | 1 | a0002c0002t0001g0200 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.662-16094T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156533514 | ||||||
| chr2:156533532
|
G | GT | 7 | a0001c0001t0005g0151a0001c0001t0005g0166a0001c0001t0005g0172others(4): Show | 7 | HG02622.hp2 HG02717.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.662-16070dupT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156533532 | |||||
| chr2:156533538
|
T | A | 1 | a0001c0001t0001g0002 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.662-16070T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156533538 | ||||||
| chr2:156533599
|
C | T | 1 | a0002c0002t0001g0200 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.662-16009C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156533599 | ||||||
| chr2:156533790
|
C | G | 5 | a0003c0003t0007g0168a0003c0003t0007g0169a0003c0003t0007g0170others(2): Show | 5 | HG02886.hp2 HG02897.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.662-15818C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156533790 | ||||||
| chr2:156533905
|
G | A | 1 | a0002c0002t0001g0200 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.662-15703G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156533905 | ||||||
| chr2:156533940
|
T | C | 3 | a0002c0002t0001g0165a0002c0002t0001g0184a0002c0002t0001g0185 | 3 | HG03130.hp2 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.662-15668T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156533940 | ||||||
| chr2:156534111
|
A | G | 6 | a0003c0003t0005g0158a0003c0003t0007g0168a0003c0003t0007g0169others(3): Show | 6 | HG01891.hp2 HG02886.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.662-15497A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156534111 | ||||||
| chr2:156534226
|
T | C | 183 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(180): Show | 183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.662-15382T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156534226 | ||||||
| chr2:156534251
|
C | CCTT | 183 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(180): Show | 183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.662-15355_662-1535 others(7): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156534251 | |||||
| chr2:156534428
|
T | C | 1 | a0001c0001t0001g0102 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.662-15180T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156534428 | ||||||
| chr2:156534670
|
A | G | 5 | a0003c0003t0007g0168a0003c0003t0007g0169a0003c0003t0007g0170others(2): Show | 5 | HG02886.hp2 HG02897.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.662-14938A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156534670 | ||||||
| chr2:156534672
|
A | G | 2 | a0002c0002t0001g0179a0002c0002t0005g0159 | 2 | HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.662-14936A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156534672 | ||||||
| chr2:156534810
|
T | TA | 6 | a0001c0001t0001g0215a0002c0002t0001g0165a0002c0002t0001g0179others(3): Show | 6 | HG00673.hp2 HG02630.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.662-14785dupA | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156534810 | |||||
| chr2:156535064
|
G | T | 54 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0116others(51): Show | 54 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.662-14544G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156535064 | ||||||
| chr2:156535118
|
G | T | 3 | a0002c0002t0001g0165a0002c0002t0001g0184a0002c0002t0001g0185 | 3 | HG03130.hp2 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.662-14490G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156535118 | ||||||
| chr2:156535222
|
T | C | 171 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(168): Show | 171 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.662-14386T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156535222 | ||||||
| chr2:156535274
|
TGAGA | T | 7 | a0002c0002t0001g0200a0002c0002t0002g0019a0002c0002t0002g0045others(4): Show | 7 | HG02040.hp1 HG02071.hp1 NA18943.hp2 others(4): Show |
intron_variant | MODIFIER | c.662-14321_662-1431 others(8): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156535274 | |||||
| chr2:156535324
|
AAG | A | 54 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0116others(51): Show | 54 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.662-14270_662-1426 others(6): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156535324 | |||||
| chr2:156535363
|
G | T | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.662-14245G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156535363 | ||||||
| chr2:156535389
|
TG | T | 160 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(157): Show | 160 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.662-14210delG | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156535389 | |||||
| chr2:156535394
|
G | C | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.662-14214G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156535394 | ||||||
| chr2:156535437
|
G | GGAGA | 7 | a0002c0002t0008g0167a0003c0003t0005g0158a0003c0003t0007g0168others(4): Show | 7 | HG01891.hp2 HG02886.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.662-14150_662-1414 others(8): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156535437 | |||||
| chr2:156535437
|
G | GGGGA | 167 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(164): Show | 167 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.662-14170_662-1416 others(8): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156535437 | |||||
| chr2:156535437
|
GGAGAGAG others(3): Show |
G | 1 | a0001c0001t0001g0081 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.662-14156_662-1414 others(14): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156535437 | |||||
| chr2:156535439
|
A | G | 1 | a0001c0001t0003g0001 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.662-14169A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156535439 | ||||||
| chr2:156535449
|
A | G | 1 | a0001c0001t0001g0081 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.662-14159A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156535449 | ||||||
| chr2:156535462
|
A | G | 1 | a0001c0001t0001g0252 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.662-14146A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156535462 | ||||||
| chr2:156535520
|
T | G | 184 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(181): Show | 184 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.662-14088T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156535520 | ||||||
| chr2:156535546
|
A | G | 1 | a0001c0001t0005g0182 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.662-14062A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156535546 | ||||||
| chr2:156536051
|
G | A | 4 | a0001c0001t0001g0199a0001c0001t0001g0220a0001c0001t0001g0221others(1): Show | 4 | HG01993.hp2 NA19006.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.662-13557G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156536051 | ||||||
| chr2:156536112
|
C | G | 54 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0116others(51): Show | 54 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.662-13496C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156536112 | ||||||
| chr2:156536196
|
G | A | 1 | a0001c0001t0015g0144 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.662-13412G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156536196 | ||||||
| chr2:156536494
|
G | A | 1 | a0002c0002t0008g0174 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.662-13114G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156536494 | ||||||
| chr2:156536508
|
A | T | 183 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(180): Show | 183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.662-13100A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156536508 | ||||||
| chr2:156536587
|
C | A | 1 | a0001c0001t0003g0009 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.662-13021C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156536587 | ||||||
| chr2:156536652
|
C | T | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.662-12956C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156536652 | ||||||
| chr2:156536762
|
C | A | 26 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(23): Show | 26 | HG00558.hp1 HG00639.hp1 HG01258.hp1 others(23): Show |
intron_variant | MODIFIER | c.662-12846C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156536762 | ||||||
| chr2:156536775
|
C | G | 1 | a0002c0002t0001g0179 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.662-12833C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156536775 | ||||||
| chr2:156536835
|
A | G | 4 | a0002c0002t0001g0165a0002c0002t0001g0184a0002c0002t0001g0185others(1): Show | 4 | HG02630.hp2 HG03130.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.662-12773A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156536835 | ||||||
| chr2:156536916
|
A | G | 4 | a0002c0002t0001g0165a0002c0002t0001g0184a0002c0002t0001g0185others(1): Show | 4 | HG02630.hp2 HG03130.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.662-12692A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156536916 | ||||||
| chr2:156537062
|
A | G | 1 | a0001c0001t0001g0150 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.662-12546A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156537062 | ||||||
| chr2:156537092
|
T | C | 1 | a0002c0002t0002g0046 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.662-12516T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156537092 | ||||||
| chr2:156537225
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.662-12383C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156537225 | ||||||
| chr2:156537237
|
T | C | 182 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(179): Show | 182 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.662-12371T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156537237 | ||||||
| chr2:156537264
|
C | T | 3 | a0002c0002t0001g0165a0002c0002t0001g0184a0002c0002t0001g0185 | 3 | HG03130.hp2 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.662-12344C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156537264 | ||||||
| chr2:156537414
|
C | T | 1 | a0001c0001t0003g0249 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.662-12194C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156537414 | ||||||
| chr2:156537549
|
G | T | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.662-12059G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156537549 | ||||||
| chr2:156537682
|
A | C | 4 | a0002c0002t0001g0165a0002c0002t0001g0184a0002c0002t0001g0185others(1): Show | 4 | HG02630.hp2 HG03130.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.662-11926A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156537682 | ||||||
| chr2:156537688
|
A | G | 4 | a0002c0002t0001g0165a0002c0002t0001g0184a0002c0002t0001g0185others(1): Show | 4 | HG02630.hp2 HG03130.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.662-11920A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156537688 | ||||||
| chr2:156537699
|
C | A | 8 | a0001c0001t0001g0032a0001c0001t0001g0059a0001c0001t0001g0071others(5): Show | 8 | HG00639.hp2 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.662-11909C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156537699 | ||||||
| chr2:156537886
|
G | A | 3 | a0001c0001t0001g0082a0001c0001t0001g0100a0001c0001t0001g0129 | 3 | HG02109.hp2 HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.662-11722G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156537886 | ||||||
| chr2:156537931
|
G | T | 50 | a0002c0002t0002g0013a0002c0002t0002g0019a0002c0002t0002g0029others(47): Show | 50 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.662-11677G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156537931 | ||||||
| chr2:156538013
|
G | A | 183 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(180): Show | 183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.662-11595G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156538013 | ||||||
| chr2:156538016
|
A | T | 183 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(180): Show | 183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.662-11592A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156538016 | ||||||
| chr2:156538243
|
C | T | 1 | a0002c0002t0001g0179 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.662-11365C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156538243 | ||||||
| chr2:156538379
|
A | G | 1 | a0001c0001t0005g0182 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.662-11229A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156538379 | ||||||
| chr2:156538437
|
A | G | 1 | a0002c0002t0002g0046 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.662-11171A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156538437 | ||||||
| chr2:156538477
|
TA | T | 61 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0116others(58): Show | 61 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.662-11116delA | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156538477 | |||||
| chr2:156538554
|
T | C | 1 | a0001c0001t0001g0099 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.662-11054T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156538554 | ||||||
| chr2:156538625
|
C | A | 1 | a0001c0001t0005g0172 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.662-10983C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156538625 | ||||||
| chr2:156538631
|
T | C | 3 | a0002c0002t0012g0073a0002c0002t0012g0096a0002c0002t0012g0152 | 3 | HG02258.hp2 HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.662-10977T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156538631 | ||||||
| chr2:156538760
|
G | A | 1 | a0002c0002t0001g0200 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.662-10848G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156538760 | ||||||
| chr2:156538820
|
C | CA | 206 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(203): Show | 206 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.662-10770dupA | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156538820 | |||||
| chr2:156538820
|
C | CAA | 34 | a0001c0001t0001g0024a0001c0001t0001g0054a0001c0001t0001g0104others(31): Show | 34 | HG00558.hp1 HG00639.hp1 HG01192.hp2 others(31): Show |
intron_variant | MODIFIER | c.662-10771_662-1077 others(6): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156538820 | |||||
| chr2:156538835
|
A | AT | 3 | a0002c0002t0002g0019a0002c0002t0002g0045a0002c0002t0002g0127 | 3 | NA18943.hp2 NA18975.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.662-10773_662-1077 others(5): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156538835 | ||||||
| chr2:156538835
|
A | T | 1 | a0002c0002t0002g0094 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.662-10773A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156538835 | ||||||
| chr2:156539192
|
T | C | 1 | a0002c0002t0002g0047 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.662-10416T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156539192 | ||||||
| chr2:156539441
|
A | G | 1 | a0002c0002t0002g0134 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.662-10167A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156539441 | ||||||
| chr2:156539856
|
G | A | 183 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(180): Show | 183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.662-9752G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156539856 | ||||||
| chr2:156539949
|
C | CT | 183 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(180): Show | 183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.662-9657dupT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156539949 | |||||
| chr2:156540085
|
A | G | 2 | a0001c0001t0001g0051a0001c0001t0001g0083 | 2 | NA19004.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.662-9523A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156540085 | ||||||
| chr2:156540123
|
A | C | 1 | a0001c0001t0001g0244 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.662-9485A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156540123 | ||||||
| chr2:156540349
|
C | T | 4 | a0002c0002t0001g0165a0002c0002t0001g0184a0002c0002t0001g0185others(1): Show | 4 | HG02630.hp2 HG03130.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.662-9259C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156540349 | ||||||
| chr2:156540596
|
C | T | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.662-9012C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156540596 | ||||||
| chr2:156540605
|
A | G | 5 | a0003c0003t0007g0168a0003c0003t0007g0169a0003c0003t0007g0170others(2): Show | 5 | HG02886.hp2 HG02897.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.662-9003A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156540605 | ||||||
| chr2:156540642
|
G | A | 4 | a0002c0002t0002g0160a0002c0002t0002g0162a0002c0002t0002g0163others(1): Show | 4 | HG02559.hp1 HG02717.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.662-8966G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156540642 | ||||||
| chr2:156540739
|
A | G | 178 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(175): Show | 178 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.662-8869A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156540739 | ||||||
| chr2:156540796
|
G | A | 2 | a0001c0001t0001g0041a0001c0001t0001g0105 | 2 | NA19067.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.662-8812G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156540796 | ||||||
| chr2:156540833
|
A | C | 1 | a0001c0001t0001g0101 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.662-8775A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156540833 | ||||||
| chr2:156540981
|
C | T | 1 | a0002c0002t0012g0096 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.662-8627C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156540981 | ||||||
| chr2:156541327
|
A | G | 178 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(175): Show | 178 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.662-8281A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156541327 | ||||||
| chr2:156541820
|
G | GTTT | 3 | a0001c0001t0001g0213a0001c0001t0001g0219a0001c0001t0001g0245 | 3 | HG00544.hp2 NA18953.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.662-7787_662-7785d others(5): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156541820 | |||||
| chr2:156541824
|
G | GT | 55 | a0002c0002t0002g0013a0002c0002t0002g0029a0002c0002t0002g0038others(52): Show | 55 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.662-7762dupT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156541824 | |||||
| chr2:156541824
|
G | GTT | 18 | a0002c0002t0001g0165a0002c0002t0001g0184a0002c0002t0001g0185others(15): Show | 18 | HG00735.hp1 HG01099.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.662-7763_662-7762d others(4): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156541824 | |||||
| chr2:156541824
|
G | GTTT | 78 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0054others(75): Show | 78 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.662-7764_662-7762d others(5): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156541824 | |||||
| chr2:156541824
|
G | GTTTT | 75 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(72): Show | 75 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.662-7765_662-7762d others(6): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156541824 | |||||
| chr2:156541824
|
G | GTTTTT | 16 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0037others(13): Show | 16 | HG01192.hp1 HG02071.hp2 HG02602.hp2 others(13): Show |
intron_variant | MODIFIER | c.662-7766_662-7762d others(7): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156541824 | |||||
| chr2:156541824
|
G | T | 5 | a0001c0001t0001g0201a0001c0001t0001g0213a0001c0001t0001g0218others(2): Show | 5 | HG00544.hp2 NA18950.hp2 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.662-7784G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156541824 | ||||||
| chr2:156541981
|
TG | T | 172 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(169): Show | 172 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.662-7625delG | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156541981 | |||||
| chr2:156542171
|
C | T | 1 | a0002c0002t0002g0038 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.662-7437C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156542171 | ||||||
| chr2:156542307
|
A | G | 2 | a0001c0001t0010g0018a0001c0001t0010g0060 | 2 | HG00438.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.662-7301A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156542307 | ||||||
| chr2:156542335
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.662-7273G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156542335 | ||||||
| chr2:156542449
|
A | C | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.662-7159A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156542449 | ||||||
| chr2:156542521
|
C | T | 5 | a0001c0001t0001g0201a0001c0001t0001g0213a0001c0001t0001g0218others(2): Show | 5 | HG00544.hp2 NA18950.hp2 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.662-7087C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156542521 | ||||||
| chr2:156542824
|
G | A | 1 | a0002c0002t0006g0070 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.662-6784G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156542824 | ||||||
| chr2:156542879
|
T | C | 1 | a0002c0002t0006g0176 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.662-6729T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156542879 | ||||||
| chr2:156543038
|
C | T | 84 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(81): Show | 84 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.662-6570C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156543038 | ||||||
| chr2:156543100
|
A | G | 2 | a0001c0001t0005g0166a0001c0001t0005g0177 | 2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.662-6508A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156543100 | ||||||
| chr2:156543206
|
C | G | 4 | a0002c0002t0002g0160a0002c0002t0002g0162a0002c0002t0002g0163others(1): Show | 4 | HG02559.hp1 HG02717.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.662-6402C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156543206 | ||||||
| chr2:156543442
|
A | C | 1 | a0001c0001t0005g0151 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.662-6166A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156543442 | ||||||
| chr2:156543784
|
C | T | 1 | a0002c0002t0002g0145 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.662-5824C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156543784 | ||||||
| chr2:156543788
|
T | C | 1 | a0002c0002t0006g0161 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.662-5820T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156543788 | ||||||
| chr2:156543855
|
C | T | 1 | a0002c0002t0004g0128 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.662-5753C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156543855 | ||||||
| chr2:156544128
|
G | A | 1 | a0002c0002t0004g0097 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.662-5480G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156544128 | ||||||
| chr2:156544188
|
G | C | 4 | a0002c0002t0001g0165a0002c0002t0001g0184a0002c0002t0001g0185others(1): Show | 4 | HG02630.hp2 HG03130.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.662-5420G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156544188 | ||||||
| chr2:156544316
|
A | C | 184 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(181): Show | 184 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.662-5292A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156544316 | ||||||
| chr2:156544370
|
C | T | 2 | a0001c0001t0001g0203a0001c0001t0001g0235 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.662-5238C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156544370 | ||||||
| chr2:156544376
|
G | A | 43 | a0002c0002t0002g0013a0002c0002t0002g0019a0002c0002t0002g0029others(40): Show | 43 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.662-5232G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156544376 | ||||||
| chr2:156544457
|
A | C | 180 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(177): Show | 180 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.662-5151A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156544457 | ||||||
| chr2:156544593
|
A | G | 1 | a0001c0001t0001g0210 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.662-5015A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156544593 | ||||||
| chr2:156544658
|
T | C | 4 | a0002c0002t0002g0019a0002c0002t0002g0045a0002c0002t0002g0094others(1): Show | 4 | HG02040.hp1 NA18943.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.662-4950T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156544658 | ||||||
| chr2:156544757
|
A | G | 180 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(177): Show | 180 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.662-4851A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156544757 | ||||||
| chr2:156544894
|
T | C | 1 | a0002c0002t0001g0179 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.662-4714T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156544894 | ||||||
| chr2:156545042
|
A | T | 1 | a0002c0002t0002g0091 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.662-4566A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156545042 | ||||||
| chr2:156545114
|
A | G | 1 | a0001c0001t0005g0178 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.662-4494A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156545114 | ||||||
| chr2:156545342
|
C | A | 184 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(181): Show | 184 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.662-4266C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156545342 | ||||||
| chr2:156546301
|
G | A | 1 | a0001c0001t0001g0252 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.662-3307G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156546301 | ||||||
| chr2:156546618
|
G | A | 86 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(83): Show | 86 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.662-2990G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156546618 | ||||||
| chr2:156546722
|
C | T | 1 | a0001c0001t0001g0129 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.662-2886C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156546722 | ||||||
| chr2:156546920
|
C | CTGTT | 250 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(247): Show | 250 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.662-2686_662-2683d others(6): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156546920 | |||||
| chr2:156547084
|
C | T | 55 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0116others(52): Show | 55 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.662-2524C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156547084 | ||||||
| chr2:156547125
|
G | A | 176 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(173): Show | 176 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.662-2483G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156547125 | ||||||
| chr2:156547236
|
A | G | 1 | a0002c0002t0002g0092 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.662-2372A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156547236 | ||||||
| chr2:156547248
|
C | A | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.662-2360C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156547248 | ||||||
| chr2:156547399
|
A | G | 1 | a0001c0001t0015g0144 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.662-2209A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156547399 | ||||||
| chr2:156547682
|
A | T | 5 | a0001c0001t0005g0166a0001c0001t0005g0172a0001c0001t0005g0177others(2): Show | 5 | HG02622.hp2 HG02717.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.662-1926A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156547682 | ||||||
| chr2:156547777
|
A | G | 1 | a0002c0002t0009g0132 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.662-1831A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156547777 | ||||||
| chr2:156548062
|
A | G | 2 | a0001c0001t0001g0024a0001c0001t0001g0095 | 2 | NA18959.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.662-1546A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156548062 | ||||||
| chr2:156548201
|
G | A | 26 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(23): Show | 26 | HG00558.hp1 HG00639.hp1 HG01258.hp1 others(23): Show |
intron_variant | MODIFIER | c.662-1407G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156548201 | ||||||
| chr2:156548309
|
C | T | 171 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(168): Show | 171 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.662-1299C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156548309 | ||||||
| chr2:156548310
|
C | T | 1 | a0001c0001t0001g0083 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.662-1298C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156548310 | ||||||
| chr2:156548456
|
G | A | 56 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0116others(53): Show | 56 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.662-1152G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156548456 | ||||||
| chr2:156548594
|
A | G | 1 | a0001c0001t0017g0065 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.662-1014A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156548594 | ||||||
| chr2:156548909
|
C | A | 183 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(180): Show | 183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.662-699C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156548909 | ||||||
| chr2:156549048
|
A | G | 3 | a0002c0002t0001g0165a0002c0002t0001g0184a0002c0002t0001g0185 | 3 | HG03130.hp2 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.662-560A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156549048 | ||||||
| chr2:156549074
|
G | A | 1 | a0002c0002t0002g0019 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.662-534G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156549074 | ||||||
| chr2:156549451
|
G | A | 1 | a0001c0001t0001g0211 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.662-157G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156549451 | ||||||
| chr2:156549784
|
A | C | 185 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(182): Show | 185 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.826+12A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 7/16 | chr2 | 156549784 | ||||||
| chr2:156549821
|
T | C | 6 | a0001c0001t0001g0032a0001c0001t0001g0059a0001c0001t0001g0071others(3): Show | 6 | HG00639.hp2 HG02630.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.826+49T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 7/16 | chr2 | 156549821 | ||||||
| chr2:156549956
|
A | G | 3 | a0002c0002t0001g0165a0002c0002t0001g0184a0002c0002t0001g0185 | 3 | HG03130.hp2 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.826+184A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 7/16 | chr2 | 156549956 | ||||||
| chr2:156550113
|
A | G | 1 | a0001c0001t0001g0202 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.826+341A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 7/16 | chr2 | 156550113 | ||||||
| chr2:156550246
|
T | C | 3 | a0002c0002t0012g0073a0002c0002t0012g0096a0002c0002t0012g0152 | 3 | HG02258.hp2 HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.827-356T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 7/16 | chr2 | 156550246 | ||||||
| chr2:156551111
|
A | T | 48 | a0002c0002t0002g0013a0002c0002t0002g0019a0002c0002t0002g0029others(45): Show | 48 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.971+365A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156551111 | ||||||
| chr2:156551127
|
C | T | 1 | a0001c0001t0001g0150 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.971+381C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156551127 | ||||||
| chr2:156551186
|
C | A | 1 | a0002c0002t0001g0200 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.971+440C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156551186 | ||||||
| chr2:156551208
|
AT | A | 172 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(169): Show | 172 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.971+463delT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156551208 | ||||||
| chr2:156551265
|
G | A | 1 | a0001c0001t0003g0204 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.971+519G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156551265 | ||||||
| chr2:156551353
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.971+607G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156551353 | ||||||
| chr2:156551355
|
C | G | 3 | a0002c0002t0012g0073a0002c0002t0012g0096a0002c0002t0012g0152 | 3 | HG02258.hp2 HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.971+609C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156551355 | ||||||
| chr2:156551539
|
A | T | 1 | a0001c0001t0005g0177 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.971+793A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156551539 | ||||||
| chr2:156551611
|
G | A | 3 | a0002c0002t0012g0073a0002c0002t0012g0096a0002c0002t0012g0152 | 3 | HG02258.hp2 HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.971+865G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156551611 | ||||||
| chr2:156552272
|
T | C | 1 | a0002c0002t0001g0184 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.971+1526T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156552272 | ||||||
| chr2:156552319
|
G | A | 184 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(181): Show | 184 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.971+1573G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156552319 | ||||||
| chr2:156552784
|
G | A | 1 | a0001c0001t0001g0247 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.971+2038G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156552784 | ||||||
| chr2:156552822
|
G | A | 3 | a0002c0002t0001g0165a0002c0002t0001g0184a0002c0002t0001g0185 | 3 | HG03130.hp2 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.971+2076G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156552822 | ||||||
| chr2:156552894
|
C | CT | 15 | a0001c0001t0001g0026a0001c0001t0001g0041a0001c0001t0001g0148others(12): Show | 15 | HG00438.hp1 HG00673.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.971+2171dupT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | 156552894 | |||||
| chr2:156552894
|
CT | C | 16 | a0001c0001t0001g0022a0001c0001t0001g0067a0001c0001t0001g0111others(13): Show | 16 | HG00639.hp2 HG01070.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.971+2171delT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | 156552894 | |||||
| chr2:156552894
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0016g0039 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.971+2160_971+2171d others(14): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | 156552894 | |||||
| chr2:156552960
|
T | C | 179 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(176): Show | 179 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.971+2214T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156552960 | ||||||
| chr2:156552986
|
A | G | 182 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(179): Show | 182 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.971+2240A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156552986 | ||||||
| chr2:156553048
|
C | T | 1 | a0002c0002t0002g0117 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.971+2302C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156553048 | ||||||
| chr2:156553439
|
A | G | 1 | a0001c0001t0005g0182 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.971+2693A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156553439 | ||||||
| chr2:156553492
|
G | C | 1 | a0001c0001t0001g0244 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.971+2746G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156553492 | ||||||
| chr2:156553595
|
C | G | 1 | a0001c0001t0001g0236 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.971+2849C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156553595 | ||||||
| chr2:156553597
|
C | G | 85 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(82): Show | 85 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.971+2851C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156553597 | ||||||
| chr2:156553616
|
C | G | 8 | a0001c0001t0001g0041a0001c0001t0001g0051a0001c0001t0001g0083others(5): Show | 8 | HG00438.hp1 HG02071.hp2 NA19004.hp1 others(5): Show |
intron_variant | MODIFIER | c.971+2870C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156553616 | ||||||
| chr2:156553671
|
T | C | 2 | a0001c0001t0001g0203a0001c0001t0001g0235 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.971+2925T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156553671 | ||||||
| chr2:156553688
|
A | T | 12 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(9): Show | 12 | HG00735.hp2 HG00741.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.971+2942A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156553688 | ||||||
| chr2:156553718
|
A | G | 1 | a0002c0002t0001g0200 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.971+2972A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156553718 | ||||||
| chr2:156553784
|
G | A | 1 | a0001c0001t0017g0065 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.971+3038G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156553784 | ||||||
| chr2:156553961
|
C | A | 2 | a0002c0002t0004g0112a0002c0002t0004g0113 | 2 | NA18952.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.971+3215C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156553961 | ||||||
| chr2:156554131
|
C | T | 1 | a0001c0001t0001g0024 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.972-3258C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156554131 | ||||||
| chr2:156554164
|
C | A | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.972-3225C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156554164 | ||||||
| chr2:156554188
|
G | C | 1 | a0002c0002t0002g0126 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.972-3201G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156554188 | ||||||
| chr2:156554378
|
T | A | 1 | a0002c0002t0001g0200 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.972-3011T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156554378 | ||||||
| chr2:156554485
|
A | G | 1 | a0002c0002t0001g0200 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.972-2904A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156554485 | ||||||
| chr2:156554486
|
C | T | 185 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(182): Show | 185 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.972-2903C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156554486 | ||||||
| chr2:156554839
|
A | G | 1 | a0001c0001t0001g0053 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.972-2550A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156554839 | ||||||
| chr2:156554953
|
G | A | 1 | a0001c0001t0013g0058 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.972-2436G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156554953 | ||||||
| chr2:156554980
|
A | T | 1 | a0001c0001t0001g0236 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.972-2409A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156554980 | ||||||
| chr2:156555031
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.972-2358C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156555031 | ||||||
| chr2:156555139
|
A | G | 1 | a0001c0001t0003g0068 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.972-2250A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156555139 | ||||||
| chr2:156555334
|
A | G | 1 | a0002c0002t0002g0164 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.972-2055A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156555334 | ||||||
| chr2:156555456
|
A | G | 184 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(181): Show | 184 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.972-1933A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156555456 | ||||||
| chr2:156555498
|
G | T | 85 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(82): Show | 85 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.972-1891G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156555498 | ||||||
| chr2:156555849
|
C | T | 1 | a0001c0001t0010g0018 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.972-1540C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156555849 | ||||||
| chr2:156556350
|
A | G | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.972-1039A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156556350 | ||||||
| chr2:156556586
|
C | A | 184 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(181): Show | 184 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.972-803C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156556586 | ||||||
| chr2:156556996
|
G | A | 1 | a0001c0001t0005g0182 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.972-393G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156556996 | ||||||
| chr2:156557009
|
T | C | 1 | a0002c0002t0002g0045 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.972-380T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156557009 | ||||||
| chr2:156557238
|
T | C | 1 | a0003c0003t0007g0012 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.972-151T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156557238 | ||||||
| chr2:156557239
|
T | C | 21 | a0001c0001t0001g0203a0001c0001t0001g0235a0001c0001t0003g0001others(18): Show | 21 | HG00558.hp1 HG00639.hp1 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.972-150T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156557239 | ||||||
| chr2:156557615
|
G | C | 8 | a0003c0003t0005g0158a0003c0003t0007g0012a0003c0003t0007g0122others(5): Show | 8 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1165+33G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156557615 | ||||||
| chr2:156557743
|
G | A | 1 | a0001c0001t0001g0220 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1165+161G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156557743 | ||||||
| chr2:156558183
|
C | T | 8 | a0003c0003t0005g0158a0003c0003t0007g0012a0003c0003t0007g0122others(5): Show | 8 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1165+601C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156558183 | ||||||
| chr2:156558277
|
C | G | 1 | a0002c0002t0008g0167 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1165+695C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156558277 | ||||||
| chr2:156558441
|
G | T | 26 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(23): Show | 26 | HG00558.hp1 HG00639.hp1 HG01258.hp1 others(23): Show |
intron_variant | MODIFIER | c.1165+859G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156558441 | ||||||
| chr2:156558568
|
A | C | 183 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(180): Show | 183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.1165+986A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156558568 | ||||||
| chr2:156558765
|
C | CT | 18 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0003g0004others(15): Show | 18 | HG00673.hp2 HG01358.hp1 HG01928.hp1 others(15): Show |
intron_variant | MODIFIER | c.1165+1214dupT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 156558765 | |||||
| chr2:156558765
|
C | CTT | 7 | a0002c0002t0012g0096a0003c0003t0005g0158a0003c0003t0007g0168others(4): Show | 7 | HG01891.hp2 HG02886.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1165+1213_1165+121 others(6): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 156558765 | |||||
| chr2:156558765
|
C | CTTTTT | 28 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0116others(25): Show | 28 | HG01109.hp1 HG01256.hp2 HG01258.hp2 others(25): Show |
intron_variant | MODIFIER | c.1165+1210_1165+121 others(9): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 156558765 | |||||
| chr2:156558765
|
C | CTTTTTT | 17 | a0001c0001t0001g0192a0001c0001t0001g0195a0001c0001t0001g0202others(14): Show | 17 | HG00140.hp2 HG00544.hp2 HG00621.hp2 others(14): Show |
intron_variant | MODIFIER | c.1165+1209_1165+121 others(10): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 156558765 | |||||
| chr2:156558765
|
C | CTTTTTTT | 8 | a0001c0001t0001g0189a0001c0001t0001g0207a0001c0001t0001g0218others(5): Show | 8 | HG00323.hp1 HG01433.hp1 NA18943.hp1 others(5): Show |
intron_variant | MODIFIER | c.1165+1208_1165+121 others(11): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 156558765 | |||||
| chr2:156558765
|
C | CTTTTTTT others(4): Show |
1 | a0001c0001t0001g0193 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1165+1204_1165+121 others(15): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 156558765 | |||||
| chr2:156558765
|
CT | C | 82 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(79): Show | 82 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.1165+1214delT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 156558765 | |||||
| chr2:156558765
|
CTTTTTTT others(4): Show |
C | 2 | a0002c0002t0006g0155a0002c0002t0006g0156 | 2 | HG00735.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.1165+1204_1165+121 others(15): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 156558765 | |||||
| chr2:156558871
|
C | T | 183 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(180): Show | 183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.1165+1289C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156558871 | ||||||
| chr2:156558962
|
C | A | 1 | a0002c0002t0001g0179 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1165+1380C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156558962 | ||||||
| chr2:156559124
|
T | C | 183 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(180): Show | 183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.1165+1542T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156559124 | ||||||
| chr2:156559203
|
T | C | 1 | a0001c0001t0001g0031 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1165+1621T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156559203 | ||||||
| chr2:156559485
|
T | A | 1 | a0003c0003t0007g0012 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1165+1903T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156559485 | ||||||
| chr2:156559523
|
C | T | 184 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(181): Show | 184 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.1165+1941C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156559523 | ||||||
| chr2:156559548
|
A | T | 2 | a0001c0001t0001g0202a0001c0001t0001g0210 | 2 | HG01109.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.1165+1966A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156559548 | ||||||
| chr2:156559641
|
T | A | 56 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0116others(53): Show | 56 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.1165+2059T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156559641 | ||||||
| chr2:156560199
|
A | G | 3 | a0001c0001t0001g0141a0001c0001t0001g0148a0001c0001t0017g0065 | 3 | HG02683.hp2 HG04115.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1165+2617A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156560199 | ||||||
| chr2:156560300
|
TG | T | 175 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(172): Show | 175 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.1165+2720delG | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 156560300 | |||||
| chr2:156560581
|
A | G | 3 | a0002c0002t0001g0165a0002c0002t0001g0184a0002c0002t0001g0185 | 3 | HG03130.hp2 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1165+2999A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156560581 | ||||||
| chr2:156560988
|
T | C | 1 | a0001c0001t0003g0249 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1165+3406T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156560988 | ||||||
| chr2:156561034
|
A | G | 1 | a0001c0001t0005g0151 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1165+3452A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156561034 | ||||||
| chr2:156561040
|
C | CT | 46 | a0002c0002t0002g0013a0002c0002t0002g0019a0002c0002t0002g0029others(43): Show | 46 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.1165+3483dupT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 156561040 | |||||
| chr2:156561040
|
C | CTT | 7 | a0002c0002t0002g0080a0002c0002t0002g0147a0002c0002t0004g0113others(4): Show | 7 | HG00735.hp1 HG01099.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1165+3482_1165+348 others(6): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 156561040 | |||||
| chr2:156561040
|
C | CTTTTTTT others(3): Show |
11 | a0001c0001t0001g0135a0001c0001t0003g0086a0001c0001t0003g0087others(8): Show | 11 | HG00639.hp1 HG01884.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.1165+3474_1165+348 others(14): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 156561040 | |||||
| chr2:156561040
|
C | CTTTTTTT others(4): Show |
30 | a0001c0001t0001g0023a0001c0001t0001g0050a0001c0001t0001g0051others(27): Show | 30 | HG00639.hp2 HG01070.hp1 HG01258.hp1 others(27): Show |
intron_variant | MODIFIER | c.1165+3473_1165+348 others(15): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 156561040 | |||||
| chr2:156561040
|
C | CTTTTTTT others(5): Show |
59 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0022others(56): Show | 59 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.1165+3472_1165+348 others(16): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 156561040 | |||||
| chr2:156561040
|
C | CTTTTTTT others(6): Show |
42 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0021others(39): Show | 42 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1165+3471_1165+348 others(17): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 156561040 | |||||
| chr2:156561040
|
C | CTTTTTTT others(7): Show |
19 | a0001c0001t0001g0017a0001c0001t0001g0049a0001c0001t0001g0085others(16): Show | 19 | HG00741.hp1 HG00741.hp2 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.1165+3470_1165+348 others(18): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 156561040 | |||||
| chr2:156561040
|
C | CTTTTTTT others(8): Show |
5 | a0001c0001t0001g0041a0001c0001t0001g0218a0001c0001t0001g0221others(2): Show | 5 | HG01261.hp2 NA19000.hp1 NA19006.hp1 others(2): Show |
intron_variant | MODIFIER | c.1165+3469_1165+348 others(19): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 156561040 | |||||
| chr2:156561040
|
C | CTTTTTTT others(9): Show |
1 | a0001c0001t0001g0253 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1165+3468_1165+348 others(20): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 156561040 | |||||
| chr2:156561040
|
C | CTTTTTTT others(10): Show |
1 | a0001c0001t0001g0234 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1165+3467_1165+348 others(21): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 156561040 | |||||
| chr2:156561040
|
C | CTTTTTTT others(12): Show |
1 | a0001c0001t0001g0187 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1165+3465_1165+348 others(23): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 156561040 | |||||
| chr2:156561040
|
C | CTTTTTTT others(13): Show |
1 | a0001c0007t0001g0196 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1165+3464_1165+348 others(24): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 156561040 | |||||
| chr2:156561193
|
A | G | 185 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(182): Show | 185 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.1165+3611A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156561193 | ||||||
| chr2:156561209
|
G | A | 1 | a0001c0001t0001g0251 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1165+3627G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156561209 | ||||||
| chr2:156561253
|
G | T | 4 | a0002c0002t0004g0097a0002c0002t0004g0112a0002c0002t0004g0113others(1): Show | 4 | NA18952.hp2 NA18999.hp2 NA19082.hp1 others(1): Show |
intron_variant | MODIFIER | c.1165+3671G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156561253 | ||||||
| chr2:156561293
|
G | A | 84 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(81): Show | 84 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.1165+3711G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156561293 | ||||||
| chr2:156561473
|
A | G | 1 | a0001c0001t0001g0219 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1165+3891A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156561473 | ||||||
| chr2:156561601
|
G | T | 2 | a0002c0002t0014g0089a0002c0002t0014g0123 | 2 | HG01070.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.1165+4019G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156561601 | ||||||
| chr2:156562114
|
A | G | 183 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(180): Show | 183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.1165+4532A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156562114 | ||||||
| chr2:156562584
|
AC | A | 180 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(177): Show | 180 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.1165+5007delC | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 156562584 | |||||
| chr2:156562585
|
C | A | 6 | a0001c0001t0001g0083a0001c0001t0001g0115a0001c0001t0001g0234others(3): Show | 6 | HG00673.hp2 HG02630.hp2 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.1165+5003C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156562585 | ||||||
| chr2:156562627
|
G | T | 1 | a0001c0001t0001g0230 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1165+5045G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156562627 | ||||||
| chr2:156562764
|
T | C | 184 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(181): Show | 184 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.1165+5182T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156562764 | ||||||
| chr2:156563126
|
A | G | 3 | a0002c0002t0012g0073a0002c0002t0012g0096a0002c0002t0012g0152 | 3 | HG02258.hp2 HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1165+5544A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156563126 | ||||||
| chr2:156563714
|
G | A | 1 | a0001c0001t0005g0151 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1166-5111G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156563714 | ||||||
| chr2:156563962
|
C | A | 5 | a0001c0001t0001g0202a0001c0001t0001g0210a0001c0001t0001g0214others(2): Show | 5 | HG01109.hp1 HG01123.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.1166-4863C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156563962 | ||||||
| chr2:156564080
|
A | C | 184 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(181): Show | 184 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.1166-4745A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156564080 | ||||||
| chr2:156564081
|
A | G | 1 | a0002c0002t0001g0200 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1166-4744A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156564081 | ||||||
| chr2:156564226
|
T | C | 1 | a0002c0002t0019g0171 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1166-4599T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156564226 | ||||||
| chr2:156564340
|
T | C | 2 | a0002c0002t0014g0089a0002c0002t0014g0123 | 2 | HG01070.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.1166-4485T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156564340 | ||||||
| chr2:156564730
|
T | G | 3 | a0002c0002t0012g0073a0002c0002t0012g0096a0002c0002t0012g0152 | 3 | HG02258.hp2 HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1166-4095T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156564730 | ||||||
| chr2:156564829
|
G | C | 3 | a0002c0002t0012g0073a0002c0002t0012g0096a0002c0002t0012g0152 | 3 | HG02258.hp2 HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1166-3996G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156564829 | ||||||
| chr2:156564850
|
A | C | 2 | a0001c0001t0001g0203a0001c0001t0001g0235 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1166-3975A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156564850 | ||||||
| chr2:156565357
|
C | T | 3 | a0001c0001t0001g0141a0001c0001t0001g0148a0001c0001t0017g0065 | 3 | HG02683.hp2 HG04115.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1166-3468C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156565357 | ||||||
| chr2:156565400
|
C | T | 1 | a0001c0001t0001g0031 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1166-3425C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156565400 | ||||||
| chr2:156565491
|
G | A | 1 | a0002c0002t0002g0164 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1166-3334G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156565491 | ||||||
| chr2:156565552
|
A | G | 1 | a0001c0001t0016g0039 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1166-3273A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156565552 | ||||||
| chr2:156565633
|
C | T | 183 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(180): Show | 183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.1166-3192C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156565633 | ||||||
| chr2:156565659
|
T | C | 1 | a0002c0002t0002g0126 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1166-3166T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156565659 | ||||||
| chr2:156565831
|
GGTTTT | G | 84 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(81): Show | 84 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.1166-2988_1166-298 others(9): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 156565831 | |||||
| chr2:156566067
|
G | C | 1 | a0001c0001t0005g0172 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1166-2758G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156566067 | ||||||
| chr2:156566154
|
C | T | 84 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(81): Show | 84 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.1166-2671C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156566154 | ||||||
| chr2:156566295
|
A | G | 1 | a0002c0002t0019g0171 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1166-2530A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156566295 | ||||||
| chr2:156566564
|
G | A | 7 | a0003c0003t0007g0012a0003c0003t0007g0122a0003c0003t0007g0168others(4): Show | 7 | HG01891.hp1 HG02055.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1166-2261G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156566564 | ||||||
| chr2:156566658
|
G | A | 184 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(181): Show | 184 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.1166-2167G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156566658 | ||||||
| chr2:156566805
|
T | C | 8 | a0003c0003t0005g0158a0003c0003t0007g0012a0003c0003t0007g0122others(5): Show | 8 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1166-2020T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156566805 | ||||||
| chr2:156566866
|
T | C | 85 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(82): Show | 85 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.1166-1959T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156566866 | ||||||
| chr2:156567071
|
G | C | 7 | a0003c0003t0007g0012a0003c0003t0007g0122a0003c0003t0007g0168others(4): Show | 7 | HG01891.hp1 HG02055.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1166-1754G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156567071 | ||||||
| chr2:156567110
|
A | G | 1 | a0001c0001t0001g0192 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1166-1715A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156567110 | ||||||
| chr2:156567240
|
G | A | 1 | a0002c0002t0019g0171 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1166-1585G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156567240 | ||||||
| chr2:156567306
|
T | C | 1 | a0001c0001t0001g0226 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1166-1519T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156567306 | ||||||
| chr2:156567394
|
C | A | 1 | a0001c0001t0001g0229 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1166-1431C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156567394 | ||||||
| chr2:156567574
|
C | T | 7 | a0003c0003t0007g0012a0003c0003t0007g0122a0003c0003t0007g0168others(4): Show | 7 | HG01891.hp1 HG02055.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1166-1251C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156567574 | ||||||
| chr2:156567614
|
C | G | 2 | a0001c0001t0001g0054a0001c0001t0001g0104 | 2 | NA19060.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1166-1211C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156567614 | ||||||
| chr2:156567670
|
C | G | 1 | a0001c0001t0001g0222 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1166-1155C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156567670 | ||||||
| chr2:156567947
|
C | T | 1 | a0002c0002t0001g0165 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1166-878C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156567947 | ||||||
| chr2:156568025
|
T | C | 12 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(9): Show | 12 | HG00735.hp2 HG00741.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.1166-800T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156568025 | ||||||
| chr2:156568059
|
G | C | 1 | a0001c0001t0001g0066 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1166-766G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156568059 | ||||||
| chr2:156568450
|
T | C | 1 | a0001c0001t0001g0107 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1166-375T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156568450 | ||||||
| chr2:156568466
|
C | T | 5 | a0002c0002t0006g0154a0002c0002t0006g0155a0002c0002t0006g0156others(2): Show | 5 | HG00735.hp1 HG01099.hp2 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.1166-359C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156568466 | ||||||
| chr2:156568585
|
A | G | 2 | a0002c0002t0001g0184a0002c0002t0001g0185 | 2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1166-240A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156568585 | ||||||
| chr2:156568719
|
C | G | 2 | a0002c0002t0004g0120a0002c0002t0004g0121 | 2 | NA19057.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1166-106C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156568719 | ||||||
| chr2:156568990
|
C | CT | 181 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(178): Show | 181 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.1300+47dupT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr2 | 156568990 | |||||
| chr2:156569100
|
A | G | 2 | a0001c0001t0001g0041a0001c0001t0001g0105 | 2 | NA19067.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.1300+141A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 10/16 | chr2 | 156569100 | ||||||
| chr2:156569223
|
T | A | 6 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0036others(3): Show | 6 | HG00741.hp2 HG01192.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.1301-140T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 10/16 | chr2 | 156569223 | ||||||
| chr2:156569289
|
A | G | 26 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(23): Show | 26 | HG00558.hp1 HG00639.hp1 HG01258.hp1 others(23): Show |
intron_variant | MODIFIER | c.1301-74A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 10/16 | chr2 | 156569289 | ||||||
| chr2:156569306
|
A | G | 1 | a0001c0001t0001g0214 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1301-57A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 10/16 | chr2 | 156569306 | ||||||
| chr2:156569602
|
ACTGGCAG others(4): Show |
A | 19 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(16): Show | 19 | HG00558.hp1 HG00639.hp1 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.1476+66_1476+76del others(11): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr2 | 156569602 | |||||
| chr2:156569605
|
G | A | 1 | a0002c0002t0002g0160 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1476+67G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 11/16 | chr2 | 156569605 | ||||||
| chr2:156570052
|
C | T | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1477-35C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 11/16 | chr2 | 156570052 | ||||||
| chr2:156570359
|
T | C | 1 | a0002c0002t0002g0110 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1608+141T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 12/16 | chr2 | 156570359 | ||||||
| chr2:156570410
|
A | T | 1 | a0002c0002t0004g0113 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1608+192A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 12/16 | chr2 | 156570410 | ||||||
| chr2:156570486
|
A | G | 8 | a0003c0003t0005g0158a0003c0003t0007g0012a0003c0003t0007g0122others(5): Show | 8 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1608+268A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 12/16 | chr2 | 156570486 | ||||||
| chr2:156570553
|
T | G | 1 | a0002c0002t0001g0179 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1608+335T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 12/16 | chr2 | 156570553 | ||||||
| chr2:156570671
|
T | A | 1 | a0002c0002t0002g0117 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1608+453T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 12/16 | chr2 | 156570671 | ||||||
| chr2:156570775
|
G | A | 8 | a0003c0003t0005g0158a0003c0003t0007g0012a0003c0003t0007g0122others(5): Show | 8 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1609-359G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 12/16 | chr2 | 156570775 | ||||||
| chr2:156570810
|
A | T | 86 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(83): Show | 86 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.1609-324A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 12/16 | chr2 | 156570810 | ||||||
| chr2:156571081
|
T | C | 249 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(246): Show | 249 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.1609-53T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 12/16 | chr2 | 156571081 | ||||||
| chr2:156571325
|
C | A | 175 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(172): Show | 175 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.1767+33C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156571325 | ||||||
| chr2:156571338
|
G | A | 175 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(172): Show | 175 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.1767+46G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156571338 | ||||||
| chr2:156571743
|
TAC | T | 83 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(80): Show | 83 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.1767+462_1767+463d others(4): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr2 | 156571743 | |||||
| chr2:156571754
|
A | G | 1 | a0001c0001t0001g0254 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1767+462A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156571754 | ||||||
| chr2:156571756
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1767+464G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156571756 | ||||||
| chr2:156571823
|
T | A | 65 | a0002c0002t0001g0200a0002c0002t0002g0013a0002c0002t0002g0019others(62): Show | 65 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.1767+531T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156571823 | ||||||
| chr2:156571882
|
A | C | 65 | a0002c0002t0001g0200a0002c0002t0002g0013a0002c0002t0002g0019others(62): Show | 65 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.1767+590A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156571882 | ||||||
| chr2:156571963
|
C | G | 3 | a0002c0002t0012g0073a0002c0002t0012g0096a0002c0002t0012g0152 | 3 | HG02258.hp2 HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1767+671C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156571963 | ||||||
| chr2:156572095
|
C | T | 1 | a0001c0001t0005g0172 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1767+803C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156572095 | ||||||
| chr2:156572154
|
C | G | 85 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(82): Show | 85 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.1767+862C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156572154 | ||||||
| chr2:156572191
|
T | C | 8 | a0001c0001t0001g0032a0001c0001t0001g0059a0001c0001t0001g0071others(5): Show | 8 | HG00639.hp2 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1767+899T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156572191 | ||||||
| chr2:156572220
|
G | A | 1 | a0002c0002t0001g0179 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1767+928G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156572220 | ||||||
| chr2:156572253
|
C | T | 1 | a0001c0001t0001g0194 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1767+961C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156572253 | ||||||
| chr2:156572297
|
G | A | 1 | a0001c0001t0001g0216 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1767+1005G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156572297 | ||||||
| chr2:156572389
|
G | A | 8 | a0003c0003t0005g0158a0003c0003t0007g0012a0003c0003t0007g0122others(5): Show | 8 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1767+1097G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156572389 | ||||||
| chr2:156572576
|
G | C | 8 | a0003c0003t0005g0158a0003c0003t0007g0012a0003c0003t0007g0122others(5): Show | 8 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1767+1284G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156572576 | ||||||
| chr2:156572649
|
G | A | 1 | a0001c0001t0001g0052 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1767+1357G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156572649 | ||||||
| chr2:156572786
|
T | G | 6 | a0002c0002t0001g0200a0002c0002t0009g0033a0002c0002t0009g0131others(3): Show | 6 | HG01346.hp2 HG01433.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.1767+1494T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156572786 | ||||||
| chr2:156573065
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1767+1773G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156573065 | ||||||
| chr2:156573220
|
T | A | 3 | a0001c0001t0001g0141a0001c0001t0001g0148a0001c0001t0017g0065 | 3 | HG02683.hp2 HG04115.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1767+1928T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156573220 | ||||||
| chr2:156573274
|
A | G | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1767+1982A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156573274 | ||||||
| chr2:156573645
|
A | G | 43 | a0002c0002t0002g0013a0002c0002t0002g0019a0002c0002t0002g0029others(40): Show | 43 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.1767+2353A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156573645 | ||||||
| chr2:156573776
|
C | G | 1 | a0002c0002t0001g0200 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1767+2484C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156573776 | ||||||
| chr2:156573893
|
G | A | 7 | a0003c0003t0007g0012a0003c0003t0007g0122a0003c0003t0007g0168others(4): Show | 7 | HG01891.hp1 HG02055.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1767+2601G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156573893 | ||||||
| chr2:156573920
|
C | T | 249 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(246): Show | 249 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.1767+2628C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156573920 | ||||||
| chr2:156574020
|
T | A | 8 | a0003c0003t0005g0158a0003c0003t0007g0012a0003c0003t0007g0122others(5): Show | 8 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1767+2728T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156574020 | ||||||
| chr2:156574043
|
A | G | 1 | a0002c0002t0001g0200 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1767+2751A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156574043 | ||||||
| chr2:156574155
|
G | A | 19 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(16): Show | 19 | HG00558.hp1 HG00639.hp1 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.1767+2863G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156574155 | ||||||
| chr2:156574215
|
G | GA | 59 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0116others(56): Show | 59 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.1767+2934dupA | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr2 | 156574215 | |||||
| chr2:156574247
|
C | T | 3 | a0001c0004t0001g0232a0001c0004t0001g0238a0001c0004t0001g0239 | 3 | HG00140.hp2 HG01433.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1767+2955C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156574247 | ||||||
| chr2:156574338
|
T | C | 3 | a0001c0001t0001g0082a0001c0001t0001g0100a0001c0001t0001g0129 | 3 | HG02109.hp2 HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1767+3046T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156574338 | ||||||
| chr2:156574408
|
C | G | 5 | a0002c0002t0006g0154a0002c0002t0006g0155a0002c0002t0006g0156others(2): Show | 5 | HG00735.hp1 HG01099.hp2 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.1767+3116C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156574408 | ||||||
| chr2:156574557
|
A | G | 249 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(246): Show | 249 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.1767+3265A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156574557 | ||||||
| chr2:156574592
|
AT | A | 60 | a0002c0002t0002g0013a0002c0002t0002g0019a0002c0002t0002g0029others(57): Show | 60 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.1767+3311delT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr2 | 156574592 | |||||
| chr2:156574909
|
G | A | 8 | a0003c0003t0005g0158a0003c0003t0007g0012a0003c0003t0007g0122others(5): Show | 8 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1767+3617G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156574909 | ||||||
| chr2:156575031
|
A | C | 1 | a0001c0001t0001g0187 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1767+3739A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156575031 | ||||||
| chr2:156575154
|
A | C | 8 | a0003c0003t0005g0158a0003c0003t0007g0012a0003c0003t0007g0122others(5): Show | 8 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1768-3735A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156575154 | ||||||
| chr2:156575176
|
C | T | 1 | a0001c0001t0001g0199 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1768-3713C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156575176 | ||||||
| chr2:156575206
|
A | G | 1 | a0002c0002t0009g0137 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1768-3683A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156575206 | ||||||
| chr2:156575243
|
A | G | 64 | a0002c0002t0002g0013a0002c0002t0002g0019a0002c0002t0002g0029others(61): Show | 64 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.1768-3646A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156575243 | ||||||
| chr2:156575402
|
CT | C | 230 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(227): Show | 230 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(227): Show |
intron_variant | MODIFIER | c.1768-3469delT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr2 | 156575402 | |||||
| chr2:156575402
|
CTT | C | 6 | a0001c0001t0001g0062a0001c0001t0001g0207a0001c0001t0001g0219others(3): Show | 6 | HG00323.hp1 HG00323.hp2 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.1768-3470_1768-346 others(6): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr2 | 156575402 | |||||
| chr2:156575407
|
T | C | 1 | a0001c0001t0001g0056 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1768-3482T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156575407 | ||||||
| chr2:156575510
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1768-3379C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156575510 | ||||||
| chr2:156575523
|
C | T | 3 | a0002c0002t0001g0165a0002c0002t0001g0184a0002c0002t0001g0185 | 3 | HG03130.hp2 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1768-3366C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156575523 | ||||||
| chr2:156575769
|
AT | A | 7 | a0003c0003t0007g0012a0003c0003t0007g0122a0003c0003t0007g0168others(4): Show | 7 | HG01891.hp1 HG02055.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1768-3116delT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr2 | 156575769 | |||||
| chr2:156575936
|
T | G | 1 | a0001c0001t0001g0192 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1768-2953T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156575936 | ||||||
| chr2:156576162
|
G | A | 177 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(174): Show | 177 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.1768-2727G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156576162 | ||||||
| chr2:156576226
|
A | G | 9 | a0002c0002t0006g0070a0002c0002t0006g0098a0002c0002t0006g0154others(6): Show | 9 | HG00673.hp2 HG00735.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.1768-2663A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156576226 | ||||||
| chr2:156576288
|
C | T | 1 | a0001c0001t0001g0250 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1768-2601C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156576288 | ||||||
| chr2:156576466
|
T | TA | 7 | a0003c0003t0007g0012a0003c0003t0007g0122a0003c0003t0007g0168others(4): Show | 7 | HG01891.hp1 HG02055.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1768-2409dupA | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr2 | 156576466 | |||||
| chr2:156576466
|
TA | T | 157 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(154): Show | 157 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.1768-2409delA | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr2 | 156576466 | |||||
| chr2:156576466
|
TAA | T | 16 | a0001c0001t0001g0050a0001c0001t0001g0221a0001c0001t0003g0001others(13): Show | 16 | HG00558.hp1 HG01258.hp1 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.1768-2410_1768-240 others(6): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr2 | 156576466 | |||||
| chr2:156576466
|
TAAA | T | 62 | a0002c0002t0002g0013a0002c0002t0002g0019a0002c0002t0002g0029others(59): Show | 62 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.1768-2411_1768-240 others(7): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr2 | 156576466 | |||||
| chr2:156576549
|
T | C | 26 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(23): Show | 26 | HG00558.hp1 HG00639.hp1 HG01258.hp1 others(23): Show |
intron_variant | MODIFIER | c.1768-2340T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156576549 | ||||||
| chr2:156576744
|
A | C | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1768-2145A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156576744 | ||||||
| chr2:156577006
|
A | G | 249 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(246): Show | 249 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.1768-1883A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156577006 | ||||||
| chr2:156577088
|
G | A | 2 | a0002c0002t0002g0080a0002c0002t0002g0147 | 2 | HG03492.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1768-1801G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156577088 | ||||||
| chr2:156577101
|
A | T | 2 | a0001c0001t0001g0077a0001c0001t0001g0124 | 2 | NA19009.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1768-1788A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156577101 | ||||||
| chr2:156577166
|
C | G | 63 | a0002c0002t0002g0013a0002c0002t0002g0019a0002c0002t0002g0029others(60): Show | 63 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.1768-1723C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156577166 | ||||||
| chr2:156577319
|
C | T | 2 | a0001c0001t0001g0077a0001c0001t0001g0124 | 2 | NA19009.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1768-1570C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156577319 | ||||||
| chr2:156577338
|
A | T | 9 | a0002c0002t0001g0200a0003c0003t0005g0158a0003c0003t0007g0012others(6): Show | 9 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1768-1551A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156577338 | ||||||
| chr2:156577362
|
A | G | 249 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(246): Show | 249 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.1768-1527A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156577362 | ||||||
| chr2:156577522
|
A | G | 1 | a0002c0002t0001g0200 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1768-1367A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156577522 | ||||||
| chr2:156577777
|
T | A | 1 | a0002c0002t0021g0079 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1768-1112T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156577777 | ||||||
| chr2:156577779
|
A | C | 1 | a0002c0002t0021g0079 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1768-1110A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156577779 | ||||||
| chr2:156577883
|
T | G | 185 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(182): Show | 185 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.1768-1006T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156577883 | ||||||
| chr2:156578372
|
C | CTT | 8 | a0003c0003t0005g0158a0003c0003t0007g0012a0003c0003t0007g0122others(5): Show | 8 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1768-505_1768-504d others(4): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr2 | 156578372 | |||||
| chr2:156578377
|
T | C | 21 | a0001c0001t0001g0203a0001c0001t0001g0235a0001c0001t0003g0001others(18): Show | 21 | HG00558.hp1 HG00639.hp1 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.1768-512T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156578377 | ||||||
| chr2:156578455
|
T | C | 3 | a0002c0002t0001g0165a0002c0002t0001g0184a0002c0002t0001g0185 | 3 | HG03130.hp2 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1768-434T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156578455 | ||||||
| chr2:156578565
|
G | A | 8 | a0003c0003t0005g0158a0003c0003t0007g0012a0003c0003t0007g0122others(5): Show | 8 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1768-324G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156578565 | ||||||
| chr2:156578622
|
G | A | 1 | a0001c0001t0003g0249 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1768-267G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156578622 | ||||||
| chr2:156578754
|
T | C | 3 | a0002c0002t0012g0073a0002c0002t0012g0096a0002c0002t0012g0152 | 3 | HG02258.hp2 HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1768-135T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156578754 | ||||||
| chr2:156578834
|
G | GA | 8 | a0003c0003t0005g0158a0003c0003t0007g0012a0003c0003t0007g0122others(5): Show | 8 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1768-48dupA | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr2 | 156578834 | |||||
| chr2:156578834
|
GA | G | 3 | a0002c0002t0002g0160a0002c0002t0002g0162a0002c0002t0002g0164 | 3 | HG02559.hp1 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1768-48delA | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr2 | 156578834 | |||||
| chr2:156579012
|
TAA | T | 4 | a0002c0002t0001g0165a0002c0002t0001g0179a0002c0002t0001g0184others(1): Show | 4 | HG03130.hp2 NA18906.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1880+12_1880+13del others(2): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 14/16 | chr2 | 156579012 | ||||||
| chr2:156579309
|
A | T | 26 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(23): Show | 26 | HG00558.hp1 HG00639.hp1 HG01258.hp1 others(23): Show |
intron_variant | MODIFIER | c.1959+145A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 15/16 | chr2 | 156579309 | ||||||
| chr2:156579310
|
T | A | 1 | a0001c0001t0005g0181 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1959+146T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 15/16 | chr2 | 156579310 | ||||||
| chr2:156579329
|
C | CT | 7 | a0001c0001t0001g0032a0001c0001t0001g0059a0001c0001t0001g0071others(4): Show | 7 | HG00639.hp2 HG02630.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1959+180dupT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 156579329 | |||||
| chr2:156579329
|
CT | C | 27 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(24): Show | 27 | HG00558.hp1 HG00639.hp1 HG01258.hp1 others(24): Show |
intron_variant | MODIFIER | c.1959+180delT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 156579329 | |||||
| chr2:156579551
|
C | T | 1 | a0002c0002t0019g0171 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1960-139C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 15/16 | chr2 | 156579551 | ||||||
| chr2:156579967
|
G | A | 1 | a0001c0001t0001g0220 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.2058+179G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 16/16 | chr2 | 156579967 | ||||||
| chr2:156580237
|
T | C | 2 | a0001c0001t0005g0151a0001c0001t0005g0181 | 2 | HG02723.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2058+449T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 16/16 | chr2 | 156580237 | ||||||
| chr2:156580454
|
A | C | 8 | a0003c0003t0005g0158a0003c0003t0007g0012a0003c0003t0007g0122others(5): Show | 8 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.2058+666A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 16/16 | chr2 | 156580454 | ||||||
| chr2:156580702
|
C | T | 1 | a0001c0001t0001g0250 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2058+914C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 16/16 | chr2 | 156580702 | ||||||
| chr2:156580856
|
A | G | 248 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(245): Show | 248 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.2058+1068A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 16/16 | chr2 | 156580856 | ||||||
| chr2:156581071
|
T | C | 58 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0116others(55): Show | 58 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.2058+1283T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 16/16 | chr2 | 156581071 | ||||||
| chr2:156581142
|
A | T | 1 | a0001c0001t0001g0062 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2058+1354A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 16/16 | chr2 | 156581142 | ||||||
| chr2:156581260
|
C | T | 1 | a0002c0002t0008g0167 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2058+1472C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 16/16 | chr2 | 156581260 | ||||||
| chr2:156581311
|
A | AT | 4 | a0001c0001t0003g0069a0001c0001t0003g0087a0001c0001t0003g0088others(1): Show | 4 | HG00639.hp1 HG01884.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.2059-1475dupT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 156581311 | |||||
| chr2:156581500
|
C | T | 1 | a0001c0001t0001g0077 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2059-1293C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 16/16 | chr2 | 156581500 | ||||||
| chr2:156581691
|
T | C | 1 | a0002c0002t0001g0185 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2059-1102T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 16/16 | chr2 | 156581691 | ||||||
| chr2:156581692
|
C | T | 3 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0229 | 3 | HG02735.hp2 HG03239.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.2059-1101C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 16/16 | chr2 | 156581692 | ||||||
| chr2:156581847
|
A | C | 2 | a0001c0001t0003g0088a0001c0001t0003g0093 | 2 | HG00639.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.2059-946A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 16/16 | chr2 | 156581847 | ||||||
| chr2:156581988
|
GATGTGTG others(3): Show |
G | 1 | a0001c0001t0005g0181 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2059-796_2059-787d others(12): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 156581988 | |||||
| chr2:156582453
|
A | G | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2059-340A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 16/16 | chr2 | 156582453 | ||||||
| chr2:156582484
|
T | TA | 103 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(100): Show | 103 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.2059-293dupA | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 156582484 | |||||
| chr2:156582484
|
T | TAA | 81 | a0001c0001t0001g0055a0001c0001t0001g0106a0001c0001t0003g0001others(78): Show | 81 | HG00323.hp2 HG00438.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.2059-294_2059-293d others(4): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 156582484 | |||||
| chr2:156582615
|
C | T | 1 | a0001c0001t0013g0043 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2059-178C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 16/16 | chr2 | 156582615 |