| geneid | 2558 |
|---|---|
| ensemblid | ENSG00000186297.12 |
| hgncid | 4079 |
| symbol | GABRA5 |
| name | gamma-aminobutyric acid type A receptor subunit alpha5 |
| refseq_nuc | NM_000810.4 |
| refseq_prot | NP_000801.1 |
| ensembl_nuc | ENST00000335625.10 |
| ensembl_prot | ENSP00000335592.5 |
| mane_status | MANE Select |
| chr | chr15 |
| start | 26867062 |
| end | 26949208 |
| strand | + |
| ver | v1.2 |
| region | chr15:26867062-26949208 |
| region5000 | chr15:26862062-26954208 |
| regionname0 | GABRA5_chr15_26867062_26949208 |
| regionname5000 | GABRA5_chr15_26862062_26954208 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 462 | 374 | 90 | 60 | 166 | 12 | 44 | 120 | GABRA5_chr15_26862062_26954208 | GABRA5 | copy fasta | chr15 | 26862062 | 26954208 |
| a0002 | 0/0 | 462 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | copy fasta | chr15 | 26862062 | 26954208 |
| 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 | 1389 | 201 | 39 | 20 | 116 | 4 | 22 | GABRA5_chr15_26862062_26954208 | GABRA5 | copy fasta | chr15 | 26862062 | 26954208 |
| c0002 | 0/1 | 1389 | 111 | 14 | 26 | 45 | 5 | 20 | GABRA5_chr15_26862062_26954208 | GABRA5 | copy fasta | chr15 | 26862062 | 26954208 |
| c0003 | 0/0 | 1389 | 33 | 23 | 6 | 3 | 1 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | copy fasta | chr15 | 26862062 | 26954208 |
| c0004 | 0/0 | 1389 | 12 | 10 | 2 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | copy fasta | chr15 | 26862062 | 26954208 |
| c0005 | 1/0 | 1389 | 7 | 1 | 1 | 2 | 1 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | copy fasta | chr15 | 26862062 | 26954208 |
| c0006 | 0/0 | 1389 | 5 | 3 | 2 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | copy fasta | chr15 | 26862062 | 26954208 |
| c0007 | 0/0 | 1389 | 3 | 0 | 2 | 0 | 1 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | copy fasta | chr15 | 26862062 | 26954208 |
| c0008 | 0/0 | 1389 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | copy fasta | chr15 | 26862062 | 26954208 |
| c0009 | 0/0 | 1389 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | copy fasta | chr15 | 26862062 | 26954208 |
| c0010 | 0/0 | 1389 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | copy fasta | chr15 | 26862062 | 26954208 |
| c0011 | 0/0 | 1389 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | copy fasta | chr15 | 26862062 | 26954208 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1165 | 362 | 82 | 58 | 164 | 12 | 44 | GABRA5_chr15_26862062_26954208 | GABRA5 | copy fasta | chr15 | 26862062 | 26954208 |
| t0002 | 0/0 | 1165 | 5 | 3 | 2 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | copy fasta | chr15 | 26862062 | 26954208 |
| t0003 | 0/0 | 1165 | 4 | 4 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | copy fasta | chr15 | 26862062 | 26954208 |
| t0004 | 0/0 | 1165 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | copy fasta | chr15 | 26862062 | 26954208 |
| t0005 | 0/0 | 1165 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | copy fasta | chr15 | 26862062 | 26954208 |
| t0006 | 0/0 | 1165 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | copy fasta | chr15 | 26862062 | 26954208 |
| t0007 | 0/0 | 1165 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | copy fasta | chr15 | 26862062 | 26954208 |
| t0008 | 0/0 | 1165 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | copy fasta | chr15 | 26862062 | 26954208 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0006 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0089 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0342 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0358 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| 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 | 1389 | 201 | 39 | 20 | 116 | 4 | 22 | GABRA5_chr15_26862062_26954208 | GABRA5 | copy fasta | chr15 | 26862062 | 26954208 |
| a0001c0002 | 0/1 | 1389 | 111 | 14 | 26 | 45 | 5 | 20 | GABRA5_chr15_26862062_26954208 | GABRA5 | copy fasta | chr15 | 26862062 | 26954208 |
| a0001c0003 | 0/0 | 1389 | 33 | 23 | 6 | 3 | 1 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | copy fasta | chr15 | 26862062 | 26954208 |
| a0001c0004 | 0/0 | 1389 | 12 | 10 | 2 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | copy fasta | chr15 | 26862062 | 26954208 |
| a0001c0005 | 1/0 | 1389 | 7 | 1 | 1 | 2 | 1 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | copy fasta | chr15 | 26862062 | 26954208 |
| a0001c0006 | 0/0 | 1389 | 5 | 3 | 2 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | copy fasta | chr15 | 26862062 | 26954208 |
| a0001c0007 | 0/0 | 1389 | 3 | 0 | 2 | 0 | 1 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | copy fasta | chr15 | 26862062 | 26954208 |
| a0001c0010 | 0/0 | 1389 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | copy fasta | chr15 | 26862062 | 26954208 |
| a0001c0011 | 0/0 | 1389 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | copy fasta | chr15 | 26862062 | 26954208 |
| a0002c0008 | 0/0 | 1389 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | copy fasta | chr15 | 26862062 | 26954208 |
| a0002c0009 | 0/0 | 1389 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | copy fasta | chr15 | 26862062 | 26954208 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2553 | 195 | 35 | 20 | 114 | 4 | 22 | GABRA5_chr15_26862062_26954208 | GABRA5 | copy fasta | chr15 | 26862062 | 26954208 |
| a0001c0001t0003 | 0/0 | 2553 | 4 | 4 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | copy fasta | chr15 | 26862062 | 26954208 |
| a0001c0001t0004 | 0/0 | 2553 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | copy fasta | chr15 | 26862062 | 26954208 |
| a0001c0001t0006 | 0/0 | 2553 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | copy fasta | chr15 | 26862062 | 26954208 |
| a0001c0002t0001 | 0/1 | 2553 | 111 | 14 | 26 | 45 | 5 | 20 | GABRA5_chr15_26862062_26954208 | GABRA5 | copy fasta | chr15 | 26862062 | 26954208 |
| a0001c0003t0001 | 0/0 | 2553 | 31 | 21 | 6 | 3 | 1 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | copy fasta | chr15 | 26862062 | 26954208 |
| a0001c0003t0007 | 0/0 | 2553 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | copy fasta | chr15 | 26862062 | 26954208 |
| a0001c0003t0008 | 0/0 | 2553 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | copy fasta | chr15 | 26862062 | 26954208 |
| a0001c0004t0001 | 0/0 | 2553 | 7 | 7 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | copy fasta | chr15 | 26862062 | 26954208 |
| a0001c0004t0002 | 0/0 | 2553 | 5 | 3 | 2 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | copy fasta | chr15 | 26862062 | 26954208 |
| a0001c0005t0001 | 1/0 | 2553 | 7 | 1 | 1 | 2 | 1 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | copy fasta | chr15 | 26862062 | 26954208 |
| a0001c0006t0001 | 0/0 | 2553 | 4 | 2 | 2 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | copy fasta | chr15 | 26862062 | 26954208 |
| a0001c0006t0005 | 0/0 | 2553 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | copy fasta | chr15 | 26862062 | 26954208 |
| a0001c0007t0001 | 0/0 | 2553 | 3 | 0 | 2 | 0 | 1 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | copy fasta | chr15 | 26862062 | 26954208 |
| a0001c0010t0001 | 0/0 | 2553 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | copy fasta | chr15 | 26862062 | 26954208 |
| a0001c0011t0001 | 0/0 | 2553 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | copy fasta | chr15 | 26862062 | 26954208 |
| a0002c0008t0001 | 0/0 | 2553 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | copy fasta | chr15 | 26862062 | 26954208 |
| a0002c0009t0001 | 0/0 | 2553 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | copy fasta | chr15 | 26862062 | 26954208 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0001g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0003g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0003g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0004g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0001t0006g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0089 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0358 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0002t0001g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0003t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0003t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0003t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0003t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0003t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0003t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0003t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0003t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0003t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0003t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0003t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0003t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0003t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0003t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0003t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0003t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0003t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0003t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0003t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0003t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0003t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0003t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0003t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0003t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0003t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0003t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0003t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0003t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0003t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0003t0007g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0003t0008g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0004t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0004t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0004t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0004t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0004t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0004t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0004t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0004t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0004t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0004t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0004t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0004t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0005t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0005t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0005t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0005t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0005t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0005t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0005t0001g0342 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0006t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0006t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0006t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0006t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0006t0005g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0007t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0007t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0007t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0010t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0001c0011t0001g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0002c0008t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| a0002c0009t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0269 | EUR | GBR | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG00099 | hp2 | a0001 | c0007 | t0001 | g0301 | EUR | GBR | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0309 | EUR | GBR | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0358 | EUR | GBR | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG00280 | hp1 | a0001 | c0003 | t0001 | g0180 | EUR | FIN | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0324 | EUR | FIN | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | CHS | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0224 | EAS | CHS | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | CHS | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0149 | EAS | CHS | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | CHS | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | CHS | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0250 | EAS | CHS | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | CHS | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG00609 | hp2 | a0001 | c0003 | t0001 | g0217 | EAS | CHS | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0326 | EAS | CHS | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0113 | AMR | PUR | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG00642 | hp2 | a0001 | c0007 | t0001 | g0014 | AMR | PUR | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG00733 | hp1 | a0001 | c0003 | t0001 | g0242 | AMR | PUR | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG00733 | hp2 | a0001 | c0005 | t0001 | g0260 | AMR | PUR | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG00735 | hp1 | a0001 | c0003 | t0001 | g0158 | AMR | PUR | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG00735 | hp2 | a0001 | c0007 | t0001 | g0327 | AMR | PUR | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0145 | AMR | PUR | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0229 | AMR | PUR | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0259 | AMR | PUR | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG01070 | hp1 | a0001 | c0004 | t0002 | g0125 | AMR | PUR | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0138 | AMR | PUR | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG01071 | hp2 | a0001 | c0004 | t0002 | g0127 | AMR | PUR | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0245 | AMR | PUR | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0097 | AMR | PUR | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG01099 | hp2 | a0001 | c0003 | t0001 | g0166 | AMR | PUR | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG01109 | hp1 | a0001 | c0003 | t0001 | g0047 | AMR | PUR | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG01109 | hp2 | a0001 | c0006 | t0001 | g0031 | AMR | PUR | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG01192 | hp1 | a0001 | c0010 | t0001 | g0119 | AMR | PUR | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0344 | AMR | PUR | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG01243 | hp1 | a0001 | c0003 | t0001 | g0134 | AMR | PUR | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0023 | AMR | PUR | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | CLM | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG01257 | hp2 | a0001 | c0006 | t0001 | g0238 | AMR | CLM | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0291 | AMR | CLM | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | CLM | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0308 | AMR | CLM | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0124 | AMR | CLM | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | CLM | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | CLM | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0228 | AMR | CLM | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0335 | AMR | CLM | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0265 | AMR | CLM | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | CLM | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0144 | EUR | IBS | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG01884 | hp1 | a0001 | c0005 | t0001 | g0126 | AFR | ACB | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG01884 | hp2 | a0001 | c0003 | t0001 | g0140 | AFR | ACB | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0333 | AFR | ACB | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0284 | AMR | PEL | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG01943 | hp1 | a0001 | c0003 | t0001 | g0285 | AMR | PEL | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0338 | AMR | PEL | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PEL | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0253 | AMR | PEL | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0350 | AMR | PEL | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0316 | AMR | PEL | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0332 | AMR | PEL | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0143 | AMR | PEL | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0341 | EAS | KHV | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0218 | EAS | KHV | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | ACB | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0189 | EAS | KHV | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0346 | EAS | KHV | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02080 | hp1 | a0001 | c0005 | t0001 | g0212 | EAS | KHV | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | KHV | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | KHV | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0323 | EAS | KHV | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | KHV | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | KHV | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0133 | EAS | CDX | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0109 | EAS | CDX | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | CDX | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | CDX | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0121 | AFR | ACB | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02257 | hp2 | a0001 | c0003 | t0001 | g0170 | AFR | ACB | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02258 | hp1 | a0001 | c0003 | t0008 | g0009 | AFR | ACB | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0077 | AFR | ACB | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0237 | AMR | PEL | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02280 | hp1 | a0001 | c0006 | t0005 | g0015 | AFR | ACB | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02280 | hp2 | a0001 | c0002 | t0001 | g0343 | AFR | ACB | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0336 | AMR | PEL | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0258 | AMR | PEL | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0337 | AMR | PEL | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0122 | AMR | PEL | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | ACB | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02451 | hp2 | a0001 | c0004 | t0002 | g0010 | AFR | ACB | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0206 | AFR | GWD | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02572 | hp2 | a0001 | c0004 | t0001 | g0043 | AFR | GWD | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0173 | SAS | PJL | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0328 | SAS | PJL | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02615 | hp1 | a0002 | c0009 | t0001 | g0128 | AFR | GWD | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02615 | hp2 | a0001 | c0004 | t0001 | g0167 | AFR | GWD | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02647 | hp1 | a0001 | c0004 | t0001 | g0012 | AFR | GWD | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02647 | hp2 | a0001 | c0006 | t0001 | g0182 | AFR | GWD | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0244 | SAS | PJL | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0361 | SAS | PJL | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02723 | hp1 | a0001 | c0003 | t0001 | g0139 | AFR | GWD | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02723 | hp2 | a0001 | c0003 | t0001 | g0334 | AFR | GWD | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0123 | SAS | PJL | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0340 | SAS | PJL | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02809 | hp1 | a0001 | c0006 | t0001 | g0271 | AFR | GWD | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02818 | hp1 | a0001 | c0003 | t0001 | g0013 | AFR | GWD | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0209 | AFR | GWD | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02886 | hp1 | a0001 | c0004 | t0001 | g0240 | AFR | GWD | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0147 | AFR | GWD | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02895 | hp1 | a0002 | c0008 | t0001 | g0011 | AFR | GWD | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0129 | AFR | GWD | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02896 | hp2 | a0001 | c0003 | t0001 | g0056 | AFR | GWD | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0130 | AFR | GWD | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02897 | hp2 | a0001 | c0003 | t0001 | g0057 | AFR | GWD | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0051 | AFR | ESN | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ESN | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02965 | hp1 | a0001 | c0003 | t0001 | g0024 | AFR | ESN | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0366 | AFR | ESN | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02970 | hp1 | a0001 | c0003 | t0001 | g0066 | AFR | ESN | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ESN | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02976 | hp1 | a0001 | c0004 | t0002 | g0075 | AFR | ESN | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ESN | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0042 | SAS | PJL | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG03041 | hp1 | a0001 | c0003 | t0001 | g0073 | AFR | GWD | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG03041 | hp2 | a0001 | c0003 | t0001 | g0171 | AFR | GWD | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0365 | AFR | MSL | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG03098 | hp2 | a0001 | c0003 | t0001 | g0107 | AFR | MSL | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG03130 | hp1 | a0001 | c0003 | t0001 | g0025 | AFR | ESN | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | ESN | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0168 | AFR | ESN | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG03139 | hp2 | a0001 | c0004 | t0002 | g0021 | AFR | ESN | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG03195 | hp2 | a0001 | c0003 | t0001 | g0154 | AFR | ESN | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG03209 | hp1 | a0001 | c0003 | t0001 | g0192 | AFR | MSL | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0302 | AFR | MSL | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0367 | AFR | MSL | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG03453 | hp2 | a0001 | c0004 | t0001 | g0268 | AFR | MSL | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0076 | AFR | MSL | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | MSL | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0005 | SAS | PJL | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0360 | SAS | PJL | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0078 | SAS | PJL | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0137 | SAS | PJL | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0005 | SAS | PJL | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0079 | SAS | PJL | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0164 | AFR | GWD | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG03540 | hp2 | a0001 | c0004 | t0001 | g0216 | AFR | GWD | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | MSL | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG03579 | hp2 | a0001 | c0003 | t0001 | g0165 | AFR | MSL | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0339 | SAS | PJL | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0141 | SAS | STU | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0251 | SAS | STU | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0027 | SAS | PJL | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG03704 | hp2 | a0001 | c0005 | t0001 | g0280 | SAS | PJL | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0175 | SAS | PJL | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG03831 | hp1 | a0001 | c0011 | t0001 | g0359 | SAS | BEB | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0345 | SAS | BEB | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0357 | SAS | BEB | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0307 | SAS | BEB | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0136 | SAS | BEB | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | BEB | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0306 | SAS | BEB | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | BEB | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | STU | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0314 | SAS | STU | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | STU | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | STU | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0195 | SAS | STU | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0261 | SAS | STU | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | YRI | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | YRI | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0331 | EAS | CHB | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0249 | EAS | CHB | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18747 | hp1 | a0001 | c0005 | t0001 | g0222 | EAS | CHB | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | CHB | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18906 | hp1 | a0001 | c0003 | t0001 | g0111 | AFR | YRI | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18906 | hp2 | a0001 | c0003 | t0001 | g0150 | AFR | YRI | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0317 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0349 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0347 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0355 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0153 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18953 | hp2 | a0001 | c0002 | t0001 | g0273 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0283 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18957 | hp2 | a0001 | c0003 | t0001 | g0086 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0142 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0266 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0227 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0071 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0214 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0356 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0330 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0272 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0208 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0364 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0117 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0286 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18993 | hp1 | a0001 | c0002 | t0001 | g0257 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0353 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18997 | hp1 | a0001 | c0002 | t0001 | g0318 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18997 | hp2 | a0001 | c0002 | t0001 | g0363 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0310 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA19003 | hp1 | a0001 | c0002 | t0001 | g0297 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA19006 | hp1 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0348 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0200 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0351 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | LWK | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA19030 | hp2 | a0001 | c0003 | t0001 | g0115 | AFR | LWK | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | LWK | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0325 | AFR | LWK | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0368 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0354 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0321 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0300 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0190 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA19074 | hp2 | a0001 | c0003 | t0001 | g0211 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA19080 | hp1 | a0001 | c0002 | t0001 | g0235 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA19081 | hp1 | a0001 | c0002 | t0001 | g0160 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA19083 | hp2 | a0001 | c0001 | t0004 | g0092 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | YRI | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA19240 | hp2 | a0001 | c0003 | t0001 | g0090 | AFR | YRI | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0179 | AFR | ASW | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ASW | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0118 | EUR | TSI | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0159 | EUR | TSI | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0148 | EUR | TSI | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA20805 | hp2 | a0001 | c0005 | t0001 | g0183 | EUR | TSI | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0352 | SAS | GIH | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0037 | SAS | GIH | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0362 | AMR | CLM | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | CLM | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0329 | AFR | ACB | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | ACB | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02559 | hp1 | a0001 | c0003 | t0007 | g0155 | AFR | ACB | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0049 | AFR | ACB | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | MSL | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG06807 | hp1 | a0001 | c0003 | t0001 | g0239 | AFR | USA | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | USA | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18955 | hp1 | a0001 | c0001 | t0006 | g0058 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | USA | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA20300 | hp2 | a0001 | c0004 | t0001 | g0202 | AFR | USA | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | LWK | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | LWK | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0089 | REF | REF | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| homoSapiens_grch38 | hp1 | a0001 | c0005 | t0001 | g0342 | REF | REF | GABRA5_chr15_26862062_26954208 | GABRA5 | chr15 | 26862062 | 26954208 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:26937214
|
G | A | 1 | a0002 | 2 | HG02615.hp1 HG02895.hp1 |
missense_variant | MODERATE | c.610G>A | p.Val204Ile | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 8/11 | 799/2553 | 610/1389 | 204/462 | chr15 | 26937214 | ||
| chr15:26949207
|
G | A | 1 | a0001 | 1 | NA18955.hp1 | splice_region_variant | LOW | c.*974G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 11/11 | chr15 | 26949207 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:26937210
|
T | C | 8 | a0001c0001a0001c0003a0001c0004others(5): Show | 255 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(252): Show |
synonymous_variant | LOW | c.606T>C | p.Val202Val | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 8/11 | 795/2553 | 606/1389 | 202/462 | chr15 | 26937210 | ||
| chr15:26943312
|
C | T | 6 | a0001c0002a0001c0003a0001c0004others(3): Show | 165 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(162): Show |
synonymous_variant | LOW | c.975C>T | p.Ala325Ala | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 10/11 | 1164/2553 | 975/1389 | 325/462 | chr15 | 26943312 | ||
| chr15:26943354
|
C | T | 1 | a0001c0010 | 1 | HG01192.hp1 | synonymous_variant | LOW | c.1017C>T | p.Ala339Ala | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 10/11 | 1206/2553 | 1017/1389 | 339/462 | chr15 | 26943354 | ||
| chr15:26947978
|
A | G | 2 | a0001c0007a0001c0011 | 4 | HG00099.hp2 HG00642.hp2 HG00735.hp2 others(1): Show |
synonymous_variant | LOW | c.1134A>G | p.Thr378Thr | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 11/11 | 1323/2553 | 1134/1389 | 378/462 | chr15 | 26947978 | ||
| chr15:26948035
|
G | A | 2 | a0001c0004a0002c0008 | 13 | HG01070.hp1 HG01071.hp2 HG02451.hp2 others(10): Show |
synonymous_variant | LOW | c.1191G>A | p.Thr397Thr | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 11/11 | 1380/2553 | 1191/1389 | 397/462 | chr15 | 26948035 | ||
| chr15:26948185
|
G | A | 1 | a0001c0006 | 5 | HG01109.hp2 HG01257.hp2 HG02280.hp1 others(2): Show |
synonymous_variant | LOW | c.1341G>A | p.Thr447Thr | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 11/11 | 1530/2553 | 1341/1389 | 447/462 | chr15 | 26948185 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:26869240
|
T | C | 1 | a0001c0001t0004 | 1 | NA19083.hp2 | 5_prime_UTR_variant | MODIFIER | c.-9T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/11 | 9 | chr15 | 26869240 | |||||
| chr15:26948450
|
G | A | 1 | a0001c0006t0005 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*217G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 11/11 | 217 | chr15 | 26948450 | |||||
| chr15:26948652
|
C | T | 1 | a0001c0001t0003 | 4 | HG02451.hp1 HG03139.hp1 HG03209.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*419C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 11/11 | 419 | chr15 | 26948652 | |||||
| chr15:26948678
|
G | A | 1 | a0001c0004t0002 | 5 | HG01070.hp1 HG01071.hp2 HG02451.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*445G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 11/11 | 445 | chr15 | 26948678 | |||||
| chr15:26948737
|
C | T | 1 | a0001c0003t0008 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*504C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 11/11 | 504 | chr15 | 26948737 | |||||
| chr15:26948757
|
A | G | 1 | a0001c0003t0007 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*524A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 11/11 | 524 | chr15 | 26948757 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:26867123
|
C | A | 2 | a0001c0003t0008g0009a0001c0004t0002g0010 | 2 | HG02258.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-140+12C>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 1/10 | chr15 | 26867123 | ||||||
| chr15:26867171
|
G | A | 3 | a0001c0003t0001g0013a0001c0004t0001g0012a0002c0008t0001g0011 | 3 | HG02647.hp1 HG02818.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.-140+60G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 1/10 | chr15 | 26867171 | ||||||
| chr15:26867216
|
C | A | 1 | a0001c0007t0001g0014 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-140+105C>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 1/10 | chr15 | 26867216 | ||||||
| chr15:26867339
|
G | A | 1 | a0001c0006t0005g0015 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-140+228G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 1/10 | chr15 | 26867339 | ||||||
| chr15:26867375
|
G | C | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0016others(141): Show | 147 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.-140+264G>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 1/10 | chr15 | 26867375 | ||||||
| chr15:26867493
|
C | A | 5 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0002t0001g0153others(2): Show | 5 | HG02559.hp1 HG03195.hp2 NA18947.hp2 others(2): Show |
intron_variant | MODIFIER | c.-140+382C>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 1/10 | chr15 | 26867493 | ||||||
| chr15:26867596
|
G | C | 2 | a0001c0002t0001g0159a0001c0003t0001g0158 | 2 | HG00735.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-140+485G>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 1/10 | chr15 | 26867596 | ||||||
| chr15:26867597
|
C | G | 2 | a0001c0002t0001g0159a0001c0003t0001g0158 | 2 | HG00735.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-140+486C>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 1/10 | chr15 | 26867597 | ||||||
| chr15:26867880
|
A | C | 1 | a0001c0002t0001g0368 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-140+769A>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 1/10 | chr15 | 26867880 | ||||||
| chr15:26868009
|
G | C | 1 | a0001c0001t0001g0016 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-139-720G>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 1/10 | chr15 | 26868009 | ||||||
| chr15:26868109
|
T | C | 4 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(1): Show | 4 | HG01496.hp2 HG02055.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.-139-620T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 1/10 | chr15 | 26868109 | ||||||
| chr15:26868115
|
G | A | 1 | a0001c0002t0001g0160 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-139-614G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 1/10 | chr15 | 26868115 | ||||||
| chr15:26868119
|
C | T | 1 | a0001c0001t0001g0367 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-139-610C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 1/10 | chr15 | 26868119 | ||||||
| chr15:26868120
|
G | C | 11 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163others(8): Show | 11 | HG01099.hp2 HG02257.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-139-609G>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 1/10 | chr15 | 26868120 | ||||||
| chr15:26868259
|
C | T | 1 | a0001c0001t0001g0008 | 2 | HG00738.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.-139-470C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 1/10 | chr15 | 26868259 | ||||||
| chr15:26868397
|
T | C | 1 | a0001c0002t0001g0368 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-139-332T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 1/10 | chr15 | 26868397 | ||||||
| chr15:26868557
|
A | G | 1 | a0001c0001t0001g0366 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-139-172A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 1/10 | chr15 | 26868557 | ||||||
| chr15:26868639
|
TTTATAGG others(14): Show |
T | 1 | a0001c0001t0001g0367 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-139-87_-139-67del others(21): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 26868639 | |||||
| chr15:26869028
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-74-147G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 2/10 | chr15 | 26869028 | ||||||
| chr15:26869066
|
C | T | 1 | a0001c0001t0001g0365 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-74-109C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 2/10 | chr15 | 26869066 | ||||||
| chr15:26869095
|
T | C | 1 | a0001c0002t0001g0173 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-74-80T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 2/10 | chr15 | 26869095 | ||||||
| chr15:26869107
|
T | C | 1 | a0001c0004t0002g0021 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-74-68T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 2/10 | chr15 | 26869107 | ||||||
| chr15:26869528
|
G | A | 5 | a0001c0001t0001g0174a0001c0001t0001g0176a0001c0001t0001g0177others(2): Show | 5 | HG02056.hp2 HG02602.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.86+194G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26869528 | ||||||
| chr15:26869659
|
T | C | 1 | a0001c0001t0001g0367 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.86+325T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26869659 | ||||||
| chr15:26869757
|
T | C | 290 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(287): Show | 295 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.86+423T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26869757 | ||||||
| chr15:26869904
|
T | C | 158 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0016others(155): Show | 159 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.86+570T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26869904 | ||||||
| chr15:26869914
|
C | A | 1 | a0001c0001t0001g0307 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.86+580C>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26869914 | ||||||
| chr15:26869938
|
T | A | 1 | a0001c0003t0008g0009 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.86+604T>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26869938 | ||||||
| chr15:26869975
|
C | G | 4 | a0001c0003t0001g0111a0001c0003t0008g0009a0001c0004t0001g0216others(1): Show | 4 | HG02258.hp1 HG02451.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.86+641C>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26869975 | ||||||
| chr15:26870262
|
G | T | 7 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0213others(4): Show | 7 | HG02015.hp1 HG02080.hp1 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.86+928G>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26870262 | ||||||
| chr15:26870293
|
G | A | 45 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(42): Show | 45 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.86+959G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26870293 | ||||||
| chr15:26870390
|
T | C | 1 | a0001c0001t0001g0002 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.86+1056T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26870390 | ||||||
| chr15:26870418
|
G | T | 127 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(124): Show | 130 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.86+1084G>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26870418 | ||||||
| chr15:26870462
|
G | A | 51 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0018others(48): Show | 51 | HG00280.hp1 HG00609.hp1 HG01099.hp1 others(48): Show |
intron_variant | MODIFIER | c.86+1128G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26870462 | ||||||
| chr15:26870581
|
T | G | 78 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0104others(75): Show | 81 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.86+1247T>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26870581 | ||||||
| chr15:26870652
|
A | AT | 34 | a0001c0001t0001g0030a0001c0001t0001g0038a0001c0001t0001g0039others(31): Show | 34 | HG00408.hp1 HG00423.hp2 HG02040.hp1 others(31): Show |
intron_variant | MODIFIER | c.86+1327dupT | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 26870652 | |||||
| chr15:26870761
|
T | G | 1 | a0001c0001t0001g0223 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.86+1427T>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26870761 | ||||||
| chr15:26870772
|
G | A | 11 | a0001c0001t0001g0032a0001c0001t0001g0156a0001c0001t0001g0185others(8): Show | 11 | HG01109.hp2 HG01243.hp1 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.86+1438G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26870772 | ||||||
| chr15:26870838
|
T | A | 39 | a0001c0001t0001g0033a0001c0001t0001g0038a0001c0001t0001g0039others(36): Show | 39 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.86+1504T>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26870838 | ||||||
| chr15:26870892
|
T | G | 1 | a0001c0002t0001g0175 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.86+1558T>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26870892 | ||||||
| chr15:26870912
|
C | G | 1 | a0001c0001t0001g0269 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.86+1578C>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26870912 | ||||||
| chr15:26870949
|
T | C | 189 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0026others(186): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.86+1615T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26870949 | ||||||
| chr15:26870962
|
G | A | 159 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0026others(156): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.86+1628G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26870962 | ||||||
| chr15:26870969
|
G | A | 80 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0033others(77): Show | 80 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(77): Show |
intron_variant | MODIFIER | c.86+1635G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26870969 | ||||||
| chr15:26870991
|
C | T | 90 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0033others(87): Show | 90 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.86+1657C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26870991 | ||||||
| chr15:26871062
|
C | T | 236 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0017others(233): Show | 239 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.86+1728C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26871062 | ||||||
| chr15:26871167
|
T | C | 195 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0017others(192): Show | 198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.86+1833T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26871167 | ||||||
| chr15:26871209
|
C | G | 1 | a0001c0002t0001g0179 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.86+1875C>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26871209 | ||||||
| chr15:26871335
|
G | C | 2 | a0001c0001t0001g0151a0001c0003t0001g0150 | 2 | HG02970.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.86+2001G>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26871335 | ||||||
| chr15:26871415
|
T | C | 14 | a0001c0001t0001g0032a0001c0001t0001g0067a0001c0001t0001g0072others(11): Show | 14 | HG01109.hp2 HG01884.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.86+2081T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26871415 | ||||||
| chr15:26871448
|
A | G | 262 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(259): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.86+2114A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26871448 | ||||||
| chr15:26871536
|
A | C | 4 | a0001c0001t0001g0026a0001c0003t0001g0024a0001c0003t0001g0025others(1): Show | 4 | HG02965.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.86+2202A>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26871536 | ||||||
| chr15:26871571
|
G | A | 232 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(229): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.86+2237G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26871571 | ||||||
| chr15:26871641
|
C | T | 5 | a0001c0001t0001g0029a0001c0001t0001g0169a0001c0003t0001g0090others(2): Show | 5 | HG02257.hp2 HG02622.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.86+2307C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26871641 | ||||||
| chr15:26871686
|
C | G | 39 | a0001c0001t0001g0004a0001c0001t0001g0044a0001c0001t0001g0045others(36): Show | 39 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(36): Show |
intron_variant | MODIFIER | c.86+2352C>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26871686 | ||||||
| chr15:26871786
|
C | T | 1 | a0001c0003t0001g0158 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.86+2452C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26871786 | ||||||
| chr15:26871798
|
G | T | 223 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(220): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.86+2464G>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26871798 | ||||||
| chr15:26871825
|
G | C | 106 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0033others(103): Show | 106 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.86+2491G>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26871825 | ||||||
| chr15:26871828
|
G | T | 3 | a0001c0001t0001g0263a0001c0002t0001g0005a0001c0002t0001g0089 | 4 | HG03490.hp1 HG03492.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.86+2494G>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26871828 | ||||||
| chr15:26871867
|
G | A | 3 | a0001c0002t0001g0077a0001c0002t0001g0164a0002c0008t0001g0011 | 3 | HG02258.hp2 HG02895.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.86+2533G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26871867 | ||||||
| chr15:26871894
|
A | G | 2 | a0001c0001t0001g0087a0001c0001t0001g0088 | 2 | HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.86+2560A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26871894 | ||||||
| chr15:26871981
|
G | T | 4 | a0001c0001t0001g0029a0001c0001t0001g0169a0001c0003t0001g0170others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.86+2647G>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26871981 | ||||||
| chr15:26872176
|
A | T | 1 | a0001c0002t0001g0329 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.86+2842A>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26872176 | ||||||
| chr15:26872309
|
G | C | 1 | a0001c0004t0001g0167 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.86+2975G>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26872309 | ||||||
| chr15:26872314
|
G | A | 19 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0157others(16): Show | 19 | HG02056.hp1 HG02132.hp2 HG02165.hp2 others(16): Show |
intron_variant | MODIFIER | c.86+2980G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26872314 | ||||||
| chr15:26872471
|
C | T | 1 | a0001c0006t0001g0271 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.86+3137C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26872471 | ||||||
| chr15:26872556
|
G | T | 89 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0033others(86): Show | 89 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.86+3222G>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26872556 | ||||||
| chr15:26872602
|
G | C | 26 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(23): Show | 26 | HG00558.hp2 HG02040.hp2 HG02080.hp2 others(23): Show |
intron_variant | MODIFIER | c.86+3268G>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26872602 | ||||||
| chr15:26872630
|
G | T | 5 | a0001c0001t0001g0029a0001c0001t0001g0169a0001c0003t0001g0090others(2): Show | 5 | HG02257.hp2 HG02622.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.86+3296G>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26872630 | ||||||
| chr15:26872719
|
T | A | 276 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(273): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.86+3385T>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26872719 | ||||||
| chr15:26872792
|
G | A | 2 | a0001c0001t0001g0223a0001c0002t0001g0224 | 2 | HG00423.hp1 HG00597.hp2 |
intron_variant | MODIFIER | c.86+3458G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26872792 | ||||||
| chr15:26872882
|
T | C | 137 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(134): Show | 140 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.86+3548T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26872882 | ||||||
| chr15:26872890
|
A | G | 88 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0017others(85): Show | 91 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.86+3556A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26872890 | ||||||
| chr15:26872899
|
A | G | 262 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(259): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.86+3565A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26872899 | ||||||
| chr15:26873144
|
C | A | 2 | a0001c0001t0001g0178a0001c0002t0001g0190 | 2 | HG00609.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.86+3810C>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26873144 | ||||||
| chr15:26873396
|
T | TA | 94 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0033others(91): Show | 94 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(91): Show |
intron_variant | MODIFIER | c.86+4069dupA | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 26873396 | |||||
| chr15:26873542
|
T | C | 1 | a0001c0001t0001g0199 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.86+4208T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26873542 | ||||||
| chr15:26873553
|
G | T | 13 | a0001c0001t0001g0032a0001c0001t0001g0067a0001c0001t0001g0072others(10): Show | 13 | HG01109.hp2 HG02615.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.86+4219G>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26873553 | ||||||
| chr15:26873587
|
A | G | 1 | a0001c0001t0001g0308 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.86+4253A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26873587 | ||||||
| chr15:26873655
|
C | T | 223 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(220): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.86+4321C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26873655 | ||||||
| chr15:26873738
|
C | T | 89 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0033others(86): Show | 89 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.86+4404C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26873738 | ||||||
| chr15:26873753
|
C | T | 1 | a0001c0001t0001g0292 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.86+4419C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26873753 | ||||||
| chr15:26873755
|
G | C | 1 | a0001c0002t0001g0310 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.86+4421G>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26873755 | ||||||
| chr15:26873781
|
G | C | 1 | a0001c0002t0001g0329 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.86+4447G>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26873781 | ||||||
| chr15:26873816
|
C | T | 225 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(222): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.86+4482C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26873816 | ||||||
| chr15:26873962
|
T | C | 252 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(249): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.86+4628T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26873962 | ||||||
| chr15:26873972
|
G | T | 1 | a0001c0003t0008g0009 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.86+4638G>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26873972 | ||||||
| chr15:26873995
|
A | G | 146 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(143): Show | 149 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.86+4661A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26873995 | ||||||
| chr15:26874027
|
C | T | 4 | a0001c0001t0001g0029a0001c0001t0001g0169a0001c0003t0001g0170others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.86+4693C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26874027 | ||||||
| chr15:26874083
|
C | T | 4 | a0001c0001t0001g0029a0001c0001t0001g0169a0001c0003t0001g0170others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.86+4749C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26874083 | ||||||
| chr15:26874104
|
G | A | 2 | a0001c0001t0001g0296a0001c0001t0001g0308 | 2 | HG01261.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.86+4770G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26874104 | ||||||
| chr15:26874260
|
C | T | 1 | a0001c0003t0001g0090 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.86+4926C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26874260 | ||||||
| chr15:26874275
|
A | G | 1 | a0001c0002t0001g0179 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.86+4941A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26874275 | ||||||
| chr15:26874317
|
AT | A | 7 | a0001c0001t0001g0194a0001c0001t0003g0168a0001c0002t0001g0077others(4): Show | 7 | HG02258.hp2 HG02895.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.86+4993delT | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 26874317 | |||||
| chr15:26874326
|
T | TA | 169 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(166): Show | 172 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.86+4992_86+4993ins others(1): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26874326 | ||||||
| chr15:26874327
|
T | A | 169 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(166): Show | 172 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.86+4993T>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26874327 | ||||||
| chr15:26874375
|
G | C | 2 | a0001c0001t0001g0225a0001c0007t0001g0014 | 2 | HG00642.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.86+5041G>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26874375 | ||||||
| chr15:26874423
|
G | A | 171 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(168): Show | 174 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.86+5089G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26874423 | ||||||
| chr15:26874662
|
G | A | 1 | a0001c0002t0001g0101 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.86+5328G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26874662 | ||||||
| chr15:26874779
|
TA | T | 167 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(164): Show | 170 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.86+5453delA | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 26874779 | |||||
| chr15:26874847
|
T | C | 167 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(164): Show | 170 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.86+5513T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26874847 | ||||||
| chr15:26874863
|
C | T | 1 | a0001c0002t0001g0005 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.86+5529C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26874863 | ||||||
| chr15:26874985
|
C | T | 4 | a0001c0001t0001g0309a0001c0001t0001g0360a0001c0002t0001g0023others(1): Show | 4 | HG00140.hp1 HG01243.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.86+5651C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26874985 | ||||||
| chr15:26875022
|
T | G | 10 | a0001c0001t0001g0034a0001c0001t0001g0069a0001c0001t0001g0070others(7): Show | 10 | HG00408.hp1 HG02027.hp1 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.86+5688T>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26875022 | ||||||
| chr15:26875027
|
T | A | 1 | a0001c0001t0001g0306 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.86+5693T>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26875027 | ||||||
| chr15:26875129
|
C | T | 167 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(164): Show | 170 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.87-5717C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26875129 | ||||||
| chr15:26875238
|
G | A | 11 | a0001c0001t0001g0034a0001c0001t0001g0069a0001c0001t0001g0070others(8): Show | 11 | HG00408.hp1 HG01243.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.87-5608G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26875238 | ||||||
| chr15:26875263
|
T | C | 167 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(164): Show | 170 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.87-5583T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26875263 | ||||||
| chr15:26875279
|
C | G | 5 | a0001c0001t0001g0029a0001c0001t0001g0169a0001c0003t0001g0090others(2): Show | 5 | HG02257.hp2 HG02622.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.87-5567C>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26875279 | ||||||
| chr15:26875302
|
G | C | 1 | a0001c0001t0001g0017 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.87-5544G>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26875302 | ||||||
| chr15:26875345
|
T | A | 167 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(164): Show | 170 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.87-5501T>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26875345 | ||||||
| chr15:26875517
|
G | A | 84 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0017others(81): Show | 87 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.87-5329G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26875517 | ||||||
| chr15:26875551
|
T | G | 1 | a0001c0001t0001g0210 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.87-5295T>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26875551 | ||||||
| chr15:26875652
|
T | C | 182 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(179): Show | 185 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.87-5194T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26875652 | ||||||
| chr15:26875667
|
G | A | 1 | a0001c0003t0001g0134 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.87-5179G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26875667 | ||||||
| chr15:26875695
|
C | T | 1 | a0001c0001t0001g0269 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.87-5151C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26875695 | ||||||
| chr15:26875745
|
C | T | 11 | a0001c0001t0001g0034a0001c0001t0001g0069a0001c0001t0001g0070others(8): Show | 11 | HG00408.hp1 HG01358.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.87-5101C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26875745 | ||||||
| chr15:26875776
|
C | G | 14 | a0001c0001t0001g0034a0001c0001t0001g0069a0001c0001t0001g0070others(11): Show | 14 | HG00408.hp1 HG01243.hp1 HG02027.hp1 others(11): Show |
intron_variant | MODIFIER | c.87-5070C>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26875776 | ||||||
| chr15:26875833
|
A | G | 1 | a0001c0004t0001g0240 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.87-5013A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26875833 | ||||||
| chr15:26875842
|
GA | G | 14 | a0001c0001t0001g0034a0001c0001t0001g0069a0001c0001t0001g0070others(11): Show | 14 | HG00408.hp1 HG01243.hp1 HG02027.hp1 others(11): Show |
intron_variant | MODIFIER | c.87-5001delA | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 26875842 | |||||
| chr15:26876020
|
G | A | 121 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(118): Show | 124 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.87-4826G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26876020 | ||||||
| chr15:26876103
|
A | G | 169 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(166): Show | 172 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.87-4743A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26876103 | ||||||
| chr15:26876143
|
G | C | 2 | a0001c0001t0001g0054a0001c0001t0001g0055 | 2 | NA18949.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.87-4703G>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26876143 | ||||||
| chr15:26876177
|
G | A | 8 | a0001c0001t0001g0050a0001c0001t0001g0093a0001c0001t0001g0112others(5): Show | 8 | HG00558.hp2 NA18747.hp2 NA18957.hp1 others(5): Show |
intron_variant | MODIFIER | c.87-4669G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26876177 | ||||||
| chr15:26876211
|
G | A | 2 | a0001c0003t0001g0107a0001c0006t0001g0238 | 2 | HG01257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.87-4635G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26876211 | ||||||
| chr15:26876341
|
G | A | 165 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0016others(162): Show | 168 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.87-4505G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26876341 | ||||||
| chr15:26876381
|
G | A | 2 | a0001c0001t0001g0223a0001c0002t0001g0224 | 2 | HG00423.hp1 HG00597.hp2 |
intron_variant | MODIFIER | c.87-4465G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26876381 | ||||||
| chr15:26876404
|
C | T | 166 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0016others(163): Show | 169 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.87-4442C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26876404 | ||||||
| chr15:26876510
|
A | G | 1 | a0001c0001t0001g0277 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.87-4336A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26876510 | ||||||
| chr15:26876712
|
C | T | 148 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0016others(145): Show | 150 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.87-4134C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26876712 | ||||||
| chr15:26876777
|
G | A | 1 | a0001c0001t0001g0226 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.87-4069G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26876777 | ||||||
| chr15:26876793
|
A | G | 1 | a0001c0002t0001g0273 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.87-4053A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26876793 | ||||||
| chr15:26876855
|
C | T | 101 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0033others(98): Show | 102 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.87-3991C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26876855 | ||||||
| chr15:26876969
|
G | C | 24 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(21): Show | 24 | HG00558.hp2 HG02040.hp2 HG02080.hp2 others(21): Show |
intron_variant | MODIFIER | c.87-3877G>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26876969 | ||||||
| chr15:26876970
|
G | A | 1 | a0001c0001t0001g0306 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.87-3876G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26876970 | ||||||
| chr15:26877179
|
T | C | 141 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0016others(138): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.87-3667T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26877179 | ||||||
| chr15:26877266
|
C | G | 1 | a0001c0002t0001g0027 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.87-3580C>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26877266 | ||||||
| chr15:26877283
|
T | C | 2 | a0001c0002t0001g0078a0001c0002t0001g0079 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.87-3563T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26877283 | ||||||
| chr15:26877351
|
A | C | 7 | a0001c0001t0001g0029a0001c0001t0001g0169a0001c0002t0001g0129others(4): Show | 7 | HG02257.hp2 HG02615.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.87-3495A>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26877351 | ||||||
| chr15:26877356
|
A | G | 1 | a0001c0003t0001g0090 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.87-3490A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26877356 | ||||||
| chr15:26877821
|
A | G | 1 | a0001c0001t0001g0205 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.87-3025A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26877821 | ||||||
| chr15:26877877
|
T | C | 3 | a0001c0001t0001g0201a0001c0002t0001g0003a0001c0002t0001g0113 | 4 | HG00642.hp1 HG01257.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.87-2969T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26877877 | ||||||
| chr15:26877962
|
G | C | 19 | a0001c0001t0001g0034a0001c0001t0001g0069a0001c0001t0001g0070others(16): Show | 19 | HG00408.hp1 HG01243.hp1 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.87-2884G>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26877962 | ||||||
| chr15:26878033
|
T | C | 5 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(2): Show | 5 | HG01496.hp2 HG02055.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.87-2813T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26878033 | ||||||
| chr15:26878050
|
T | C | 218 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(215): Show | 222 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.87-2796T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26878050 | ||||||
| chr15:26878138
|
T | C | 3 | a0001c0001t0001g0032a0001c0001t0001g0067a0001c0006t0001g0031 | 3 | HG01109.hp2 HG02622.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.87-2708T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26878138 | ||||||
| chr15:26878140
|
C | T | 19 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0080others(16): Show | 19 | HG02056.hp1 HG02132.hp2 HG02165.hp2 others(16): Show |
intron_variant | MODIFIER | c.87-2706C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26878140 | ||||||
| chr15:26878160
|
G | T | 1 | a0001c0001t0001g0062 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.87-2686G>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26878160 | ||||||
| chr15:26878167
|
C | T | 1 | a0002c0008t0001g0011 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.87-2679C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26878167 | ||||||
| chr15:26878230
|
G | A | 1 | a0001c0001t0001g0264 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.87-2616G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26878230 | ||||||
| chr15:26878273
|
A | C | 4 | a0001c0001t0003g0302a0001c0003t0001g0013a0001c0003t0001g0165others(1): Show | 4 | HG01099.hp2 HG02818.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.87-2573A>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26878273 | ||||||
| chr15:26878377
|
A | G | 1 | a0001c0002t0001g0142 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.87-2469A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26878377 | ||||||
| chr15:26878519
|
A | C | 2 | a0001c0001t0001g0194a0001c0001t0003g0168 | 2 | HG03139.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.87-2327A>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26878519 | ||||||
| chr15:26878525
|
C | A | 1 | a0001c0002t0001g0027 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.87-2321C>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26878525 | ||||||
| chr15:26878799
|
C | T | 1 | a0001c0003t0001g0171 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.87-2047C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26878799 | ||||||
| chr15:26878884
|
G | C | 1 | a0001c0003t0001g0139 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.87-1962G>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26878884 | ||||||
| chr15:26878934
|
G | A | 122 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0022others(119): Show | 124 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.87-1912G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26878934 | ||||||
| chr15:26878939
|
T | C | 1 | a0001c0002t0001g0257 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.87-1907T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26878939 | ||||||
| chr15:26878951
|
C | T | 2 | a0001c0001t0001g0225a0001c0007t0001g0014 | 2 | HG00642.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.87-1895C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26878951 | ||||||
| chr15:26878959
|
A | G | 51 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(48): Show | 52 | HG00558.hp2 HG00741.hp2 HG01099.hp2 others(49): Show |
intron_variant | MODIFIER | c.87-1887A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26878959 | ||||||
| chr15:26879064
|
T | C | 1 | a0001c0001t0001g0072 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.87-1782T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26879064 | ||||||
| chr15:26879297
|
T | C | 1 | a0001c0003t0001g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.87-1549T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26879297 | ||||||
| chr15:26879323
|
T | A | 1 | a0001c0001t0001g0069 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.87-1523T>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26879323 | ||||||
| chr15:26879600
|
C | A | 2 | a0001c0002t0001g0035a0001c0002t0001g0036 | 2 | NA18952.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.87-1246C>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26879600 | ||||||
| chr15:26880424
|
A | G | 1 | a0001c0001t0001g0114 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.87-422A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26880424 | ||||||
| chr15:26880564
|
G | A | 1 | a0001c0001t0001g0269 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.87-282G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26880564 | ||||||
| chr15:26880652
|
G | C | 4 | a0001c0001t0003g0302a0001c0003t0001g0013a0001c0003t0001g0165others(1): Show | 4 | HG01099.hp2 HG02818.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.87-194G>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26880652 | ||||||
| chr15:26880654
|
A | T | 4 | a0001c0001t0003g0302a0001c0003t0001g0013a0001c0003t0001g0165others(1): Show | 4 | HG01099.hp2 HG02818.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.87-192A>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26880654 | ||||||
| chr15:26880657
|
GTATC | G | 4 | a0001c0001t0003g0302a0001c0003t0001g0013a0001c0003t0001g0165others(1): Show | 4 | HG01099.hp2 HG02818.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.87-188_87-185delTA others(2): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26880657 | ||||||
| chr15:26880662
|
C | G | 4 | a0001c0001t0003g0302a0001c0003t0001g0013a0001c0003t0001g0165others(1): Show | 4 | HG01099.hp2 HG02818.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.87-184C>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26880662 | ||||||
| chr15:26880664
|
T | G | 4 | a0001c0001t0003g0302a0001c0003t0001g0013a0001c0003t0001g0165others(1): Show | 4 | HG01099.hp2 HG02818.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.87-182T>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26880664 | ||||||
| chr15:26880665
|
G | A | 4 | a0001c0001t0003g0302a0001c0003t0001g0013a0001c0003t0001g0165others(1): Show | 4 | HG01099.hp2 HG02818.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.87-181G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26880665 | ||||||
| chr15:26880669
|
G | C | 4 | a0001c0001t0003g0302a0001c0003t0001g0013a0001c0003t0001g0165others(1): Show | 4 | HG01099.hp2 HG02818.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.87-177G>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26880669 | ||||||
| chr15:26880670
|
TTG | T | 4 | a0001c0001t0003g0302a0001c0003t0001g0013a0001c0003t0001g0165others(1): Show | 4 | HG01099.hp2 HG02818.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.87-175_87-174delTG | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26880670 | ||||||
| chr15:26880768
|
C | T | 1 | a0001c0001t0001g0050 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.87-78C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26880768 | ||||||
| chr15:26880819
|
G | A | 1 | a0001c0002t0001g0332 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.87-27G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26880819 | ||||||
| chr15:26880821
|
T | A | 1 | a0001c0002t0001g0141 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.87-25T>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 3/10 | chr15 | 26880821 | ||||||
| chr15:26881062
|
A | G | 2 | a0001c0001t0001g0087a0001c0001t0001g0088 | 2 | HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.208+95A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 4/10 | chr15 | 26881062 | ||||||
| chr15:26881121
|
T | C | 1 | a0001c0001t0001g0367 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.208+154T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 4/10 | chr15 | 26881121 | ||||||
| chr15:26881137
|
G | T | 199 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0016others(196): Show | 202 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.208+170G>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 4/10 | chr15 | 26881137 | ||||||
| chr15:26881588
|
A | G | 61 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(58): Show | 62 | HG00408.hp1 HG01070.hp1 HG01071.hp2 others(59): Show |
intron_variant | MODIFIER | c.208+621A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 4/10 | chr15 | 26881588 | ||||||
| chr15:26881680
|
A | C | 4 | a0001c0001t0003g0302a0001c0003t0001g0013a0001c0003t0001g0165others(1): Show | 4 | HG01099.hp2 HG02818.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.208+713A>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 4/10 | chr15 | 26881680 | ||||||
| chr15:26881730
|
G | A | 1 | a0001c0003t0001g0090 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.208+763G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 4/10 | chr15 | 26881730 | ||||||
| chr15:26881884
|
G | A | 56 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0044others(53): Show | 56 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.208+917G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 4/10 | chr15 | 26881884 | ||||||
| chr15:26881887
|
A | G | 1 | a0001c0001t0001g0033 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.208+920A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 4/10 | chr15 | 26881887 | ||||||
| chr15:26882416
|
G | A | 5 | a0001c0001t0001g0032a0001c0001t0001g0067a0001c0001t0001g0114others(2): Show | 5 | HG01109.hp2 HG01243.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.209-750G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 4/10 | chr15 | 26882416 | ||||||
| chr15:26882678
|
C | A | 1 | a0001c0003t0001g0242 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.209-488C>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 4/10 | chr15 | 26882678 | ||||||
| chr15:26882753
|
G | C | 34 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(31): Show | 35 | HG01070.hp1 HG01071.hp2 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.209-413G>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 4/10 | chr15 | 26882753 | ||||||
| chr15:26882916
|
A | C | 1 | a0001c0002t0001g0190 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.209-250A>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 4/10 | chr15 | 26882916 | ||||||
| chr15:26883027
|
A | G | 55 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0044others(52): Show | 55 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.209-139A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 4/10 | chr15 | 26883027 | ||||||
| chr15:26883105
|
A | G | 2 | a0001c0002t0001g0121a0001c0004t0001g0202 | 2 | HG02257.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.209-61A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 4/10 | chr15 | 26883105 | ||||||
| chr15:26883107
|
A | G | 28 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0034others(25): Show | 28 | HG00408.hp1 HG01109.hp2 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.209-59A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 4/10 | chr15 | 26883107 | ||||||
| chr15:26883314
|
C | T | 56 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0044others(53): Show | 56 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.277-23C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 5/10 | chr15 | 26883314 | ||||||
| chr15:26883789
|
G | C | 3 | a0001c0001t0001g0191a0001c0003t0001g0154a0001c0003t0007g0155 | 3 | HG01346.hp2 HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.497+232G>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26883789 | ||||||
| chr15:26883845
|
AATT | A | 12 | a0001c0001t0001g0034a0001c0001t0001g0069a0001c0001t0001g0070others(9): Show | 12 | HG00408.hp1 HG02027.hp1 NA18612.hp1 others(9): Show |
intron_variant | MODIFIER | c.497+294_497+296del others(3): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26883845 | |||||
| chr15:26883945
|
T | C | 1 | a0001c0001t0001g0131 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.497+388T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26883945 | ||||||
| chr15:26883988
|
G | A | 1 | a0001c0002t0001g0173 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.497+431G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26883988 | ||||||
| chr15:26884018
|
C | CA | 124 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0022others(121): Show | 127 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.497+470dupA | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26884018 | |||||
| chr15:26884045
|
C | G | 3 | a0001c0001t0001g0262a0001c0001t0001g0346a0001c0002t0001g0345 | 3 | HG02074.hp1 HG02132.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.497+488C>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26884045 | ||||||
| chr15:26884268
|
A | G | 2 | a0001c0001t0001g0186a0001c0005t0001g0183 | 2 | HG01346.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.497+711A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26884268 | ||||||
| chr15:26884304
|
G | A | 1 | a0001c0002t0001g0122 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.497+747G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26884304 | ||||||
| chr15:26884365
|
T | C | 1 | a0001c0002t0001g0138 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.497+808T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26884365 | ||||||
| chr15:26884610
|
G | C | 68 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0034others(65): Show | 68 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.497+1053G>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26884610 | ||||||
| chr15:26884631
|
T | G | 1 | a0001c0002t0001g0206 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.497+1074T>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26884631 | ||||||
| chr15:26884816
|
G | A | 1 | a0001c0001t0001g0231 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.497+1259G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26884816 | ||||||
| chr15:26884839
|
G | T | 9 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(6): Show | 10 | HG01496.hp2 HG02055.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.497+1282G>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26884839 | ||||||
| chr15:26884881
|
T | C | 1 | a0001c0003t0001g0140 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.497+1324T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26884881 | ||||||
| chr15:26884921
|
G | A | 119 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0022others(116): Show | 121 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(118): Show |
intron_variant | MODIFIER | c.497+1364G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26884921 | ||||||
| chr15:26885023
|
A | G | 123 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017others(120): Show | 124 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.497+1466A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26885023 | ||||||
| chr15:26885167
|
C | T | 55 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0044others(52): Show | 55 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.497+1610C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26885167 | ||||||
| chr15:26885168
|
G | A | 1 | a0001c0002t0001g0206 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.497+1611G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26885168 | ||||||
| chr15:26885188
|
A | G | 1 | a0001c0002t0001g0206 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.497+1631A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26885188 | ||||||
| chr15:26885190
|
T | G | 1 | a0001c0003t0001g0024 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.497+1633T>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26885190 | ||||||
| chr15:26885215
|
C | T | 55 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0044others(52): Show | 55 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.497+1658C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26885215 | ||||||
| chr15:26885265
|
C | T | 1 | a0001c0001t0001g0247 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.497+1708C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26885265 | ||||||
| chr15:26885298
|
C | CA | 88 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(85): Show | 90 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.497+1758dupA | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26885298 | |||||
| chr15:26885298
|
CA | C | 18 | a0001c0001t0001g0034a0001c0001t0001g0069a0001c0001t0001g0070others(15): Show | 18 | HG00408.hp1 HG01243.hp1 HG02027.hp1 others(15): Show |
intron_variant | MODIFIER | c.497+1758delA | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26885298 | |||||
| chr15:26885320
|
G | A | 1 | a0001c0004t0001g0216 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.497+1763G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26885320 | ||||||
| chr15:26885355
|
C | CT | 55 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0044others(52): Show | 55 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.497+1799dupT | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26885355 | |||||
| chr15:26885358
|
T | A | 55 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0044others(52): Show | 55 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.497+1801T>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26885358 | ||||||
| chr15:26885360
|
T | A | 55 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0044others(52): Show | 55 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.497+1803T>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26885360 | ||||||
| chr15:26885361
|
C | G | 55 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0044others(52): Show | 55 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.497+1804C>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26885361 | ||||||
| chr15:26885362
|
C | A | 55 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0044others(52): Show | 55 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.497+1805C>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26885362 | ||||||
| chr15:26885380
|
A | G | 55 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0044others(52): Show | 55 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.497+1823A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26885380 | ||||||
| chr15:26885413
|
A | C | 29 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(26): Show | 29 | HG00558.hp2 HG00741.hp2 HG01361.hp2 others(26): Show |
intron_variant | MODIFIER | c.497+1856A>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26885413 | ||||||
| chr15:26885577
|
C | T | 1 | a0001c0003t0001g0192 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.497+2020C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26885577 | ||||||
| chr15:26885632
|
G | C | 25 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(22): Show | 26 | HG01070.hp1 HG01071.hp2 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.497+2075G>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26885632 | ||||||
| chr15:26885661
|
G | C | 6 | a0001c0001t0001g0007a0001c0001t0001g0054a0001c0001t0001g0055others(3): Show | 7 | NA18949.hp1 NA18966.hp1 NA18971.hp2 others(4): Show |
intron_variant | MODIFIER | c.497+2104G>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26885661 | ||||||
| chr15:26885716
|
C | T | 3 | a0001c0001t0001g0267a0001c0004t0001g0268a0001c0004t0002g0010 | 3 | HG02055.hp1 HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.497+2159C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26885716 | ||||||
| chr15:26885739
|
G | A | 1 | a0001c0001t0001g0102 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.497+2182G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26885739 | ||||||
| chr15:26885769
|
C | A | 55 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0044others(52): Show | 55 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.497+2212C>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26885769 | ||||||
| chr15:26885779
|
G | C | 1 | a0001c0006t0001g0238 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.497+2222G>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26885779 | ||||||
| chr15:26885804
|
G | A | 1 | a0001c0001t0001g0226 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.497+2247G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26885804 | ||||||
| chr15:26885832
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.497+2275C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26885832 | ||||||
| chr15:26885917
|
G | A | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG02523.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.497+2360G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26885917 | ||||||
| chr15:26886015
|
C | CTGT | 120 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0022others(117): Show | 122 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.497+2479_497+2481d others(5): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26886015 | |||||
| chr15:26886145
|
A | G | 4 | a0001c0001t0001g0215a0001c0001t0001g0294a0001c0002t0001g0214others(1): Show | 4 | HG02015.hp1 HG02080.hp1 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.497+2588A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26886145 | ||||||
| chr15:26886180
|
C | T | 2 | a0001c0001t0001g0151a0001c0003t0001g0150 | 2 | HG02970.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.497+2623C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26886180 | ||||||
| chr15:26886272
|
G | A | 1 | a0001c0001t0001g0314 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.497+2715G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26886272 | ||||||
| chr15:26886359
|
C | CTCTAT | 3 | a0001c0001t0001g0032a0001c0001t0001g0067a0001c0006t0001g0031 | 3 | HG01109.hp2 HG02622.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.497+2806_497+2810d others(7): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26886359 | |||||
| chr15:26886993
|
C | T | 209 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(206): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.497+3436C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26886993 | ||||||
| chr15:26887000
|
C | G | 1 | a0001c0003t0001g0140 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.497+3443C>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26887000 | ||||||
| chr15:26887110
|
C | T | 51 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0044others(48): Show | 51 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.497+3553C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26887110 | ||||||
| chr15:26887169
|
G | A | 2 | a0001c0003t0001g0107a0001c0006t0001g0238 | 2 | HG01257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.497+3612G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26887169 | ||||||
| chr15:26887176
|
A | G | 1 | a0001c0003t0001g0171 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.497+3619A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26887176 | ||||||
| chr15:26887395
|
T | A | 25 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(22): Show | 26 | HG01070.hp1 HG01071.hp2 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.497+3838T>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26887395 | ||||||
| chr15:26887585
|
C | CTCGGCCT others(9): Show |
1 | a0001c0001t0001g0248 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.497+4038_497+4053d others(18): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26887585 | |||||
| chr15:26887702
|
G | T | 1 | a0001c0003t0001g0192 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.497+4145G>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26887702 | ||||||
| chr15:26887767
|
A | T | 52 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0044others(49): Show | 52 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.497+4210A>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26887767 | ||||||
| chr15:26887840
|
A | G | 37 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(34): Show | 38 | HG00408.hp1 HG01070.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.497+4283A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26887840 | ||||||
| chr15:26888269
|
A | T | 8 | a0001c0001t0001g0029a0001c0001t0001g0169a0001c0002t0001g0129others(5): Show | 8 | HG02257.hp2 HG02615.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.497+4712A>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26888269 | ||||||
| chr15:26888285
|
G | A | 2 | a0001c0001t0001g0033a0001c0002t0001g0357 | 2 | HG03834.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.497+4728G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26888285 | ||||||
| chr15:26888308
|
G | T | 50 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0044others(47): Show | 50 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.497+4751G>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26888308 | ||||||
| chr15:26888322
|
C | A | 119 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0022others(116): Show | 121 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(118): Show |
intron_variant | MODIFIER | c.497+4765C>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26888322 | ||||||
| chr15:26888394
|
C | T | 88 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017others(85): Show | 89 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.497+4837C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26888394 | ||||||
| chr15:26888450
|
G | A | 37 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(34): Show | 38 | HG00408.hp1 HG01070.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.497+4893G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26888450 | ||||||
| chr15:26888643
|
C | A | 4 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(1): Show | 4 | HG02572.hp2 HG02896.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.497+5086C>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26888643 | ||||||
| chr15:26888768
|
C | T | 7 | a0001c0001t0001g0162a0001c0002t0001g0051a0001c0003t0001g0066others(4): Show | 7 | HG02258.hp1 HG02280.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.497+5211C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26888768 | ||||||
| chr15:26888880
|
T | C | 1 | a0001c0002t0001g0317 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.497+5323T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26888880 | ||||||
| chr15:26888894
|
G | T | 3 | a0001c0001t0001g0032a0001c0001t0001g0067a0001c0006t0001g0031 | 3 | HG01109.hp2 HG02622.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.497+5337G>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26888894 | ||||||
| chr15:26888935
|
C | T | 4 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0295others(1): Show | 4 | HG02056.hp1 HG02165.hp2 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.497+5378C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26888935 | ||||||
| chr15:26888960
|
C | A | 29 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(26): Show | 29 | HG00558.hp2 HG00741.hp2 HG01361.hp2 others(26): Show |
intron_variant | MODIFIER | c.497+5403C>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26888960 | ||||||
| chr15:26888988
|
G | A | 1 | a0001c0001t0001g0367 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.497+5431G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26888988 | ||||||
| chr15:26889336
|
C | T | 3 | a0001c0001t0001g0002a0001c0001t0001g0252a0001c0001t0001g0254 | 4 | HG01069.hp1 HG01071.hp1 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.497+5779C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26889336 | ||||||
| chr15:26889372
|
CT | C | 37 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(34): Show | 38 | HG00408.hp1 HG01070.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.497+5827delT | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26889372 | |||||
| chr15:26889424
|
T | C | 8 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0161others(5): Show | 8 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.497+5867T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26889424 | ||||||
| chr15:26889487
|
A | G | 245 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(242): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.497+5930A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26889487 | ||||||
| chr15:26889500
|
A | G | 268 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(265): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.497+5943A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26889500 | ||||||
| chr15:26889552
|
C | T | 7 | a0001c0001t0001g0162a0001c0002t0001g0051a0001c0003t0001g0066others(4): Show | 7 | HG02258.hp1 HG02280.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.497+5995C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26889552 | ||||||
| chr15:26889563
|
A | C | 1 | a0001c0001t0001g0191 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.497+6006A>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26889563 | ||||||
| chr15:26889630
|
G | T | 1 | a0001c0002t0001g0042 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.497+6073G>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26889630 | ||||||
| chr15:26889659
|
A | G | 25 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(22): Show | 26 | HG01070.hp1 HG01071.hp2 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.497+6102A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26889659 | ||||||
| chr15:26889679
|
C | T | 12 | a0001c0001t0001g0034a0001c0001t0001g0069a0001c0001t0001g0070others(9): Show | 12 | HG00408.hp1 HG02027.hp1 NA18612.hp1 others(9): Show |
intron_variant | MODIFIER | c.497+6122C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26889679 | ||||||
| chr15:26889730
|
T | C | 3 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0213 | 3 | NA18977.hp1 NA18989.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.497+6173T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26889730 | ||||||
| chr15:26889875
|
G | A | 1 | a0001c0002t0001g0206 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.497+6318G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26889875 | ||||||
| chr15:26889877
|
G | A | 266 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(263): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.497+6320G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26889877 | ||||||
| chr15:26890117
|
TA | T | 3 | a0001c0001t0001g0032a0001c0001t0001g0067a0001c0006t0001g0031 | 3 | HG01109.hp2 HG02622.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.497+6561delA | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26890117 | ||||||
| chr15:26890158
|
C | T | 1 | a0001c0005t0001g0222 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.497+6601C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26890158 | ||||||
| chr15:26890425
|
A | C | 1 | a0001c0001t0001g0020 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.497+6868A>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26890425 | ||||||
| chr15:26890426
|
A | AT | 10 | a0001c0001t0001g0176a0001c0001t0001g0197a0001c0001t0001g0296others(7): Show | 10 | HG00597.hp1 HG01261.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.497+6887dupT | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26890426 | |||||
| chr15:26890426
|
A | ATTTT | 6 | a0001c0001t0001g0162a0001c0002t0001g0051a0001c0003t0001g0066others(3): Show | 6 | HG02258.hp1 HG02886.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.497+6884_497+6887d others(6): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26890426 | |||||
| chr15:26890426
|
A | ATTTTTT | 6 | a0001c0001t0001g0151a0001c0001t0001g0267a0001c0003t0001g0090others(3): Show | 6 | HG02055.hp1 HG02895.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.497+6882_497+6887d others(8): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26890426 | |||||
| chr15:26890426
|
A | ATTTTTTT | 11 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0067others(8): Show | 11 | HG01109.hp2 HG01891.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.497+6881_497+6887d others(9): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26890426 | |||||
| chr15:26890426
|
A | ATTTTTTT others(1): Show |
37 | a0001c0001t0001g0034a0001c0001t0001g0038a0001c0001t0001g0039others(34): Show | 37 | HG00408.hp1 HG00558.hp2 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.497+6880_497+6887d others(10): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26890426 | |||||
| chr15:26890426
|
A | ATTTTTTT others(2): Show |
24 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(21): Show | 25 | HG01071.hp2 HG01496.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.497+6879_497+6887d others(11): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26890426 | |||||
| chr15:26890426
|
A | ATTTTTTT others(3): Show |
5 | a0001c0001t0001g0020a0001c0001t0001g0163a0001c0001t0003g0076others(2): Show | 5 | HG02615.hp2 HG03139.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.497+6878_497+6887d others(12): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26890426 | |||||
| chr15:26890426
|
A | ATTTTTTT others(5): Show |
1 | a0001c0001t0001g0367 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.497+6876_497+6887d others(14): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26890426 | |||||
| chr15:26890426
|
ATT | A | 6 | a0001c0001t0001g0304a0001c0001t0003g0302a0001c0002t0001g0100others(3): Show | 6 | HG01099.hp2 HG02818.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.497+6886_497+6887d others(4): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26890426 | |||||
| chr15:26890426
|
ATTT | A | 50 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0044others(47): Show | 50 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.497+6885_497+6887d others(5): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26890426 | |||||
| chr15:26890603
|
C | T | 13 | a0001c0001t0001g0029a0001c0001t0001g0114a0001c0001t0001g0169others(10): Show | 13 | HG01891.hp1 HG02055.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.497+7046C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26890603 | ||||||
| chr15:26890630
|
C | A | 1 | a0001c0001t0001g0053 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.497+7073C>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26890630 | ||||||
| chr15:26890693
|
A | G | 96 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(93): Show | 97 | HG00408.hp1 HG00558.hp2 HG00741.hp2 others(94): Show |
intron_variant | MODIFIER | c.497+7136A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26890693 | ||||||
| chr15:26890700
|
G | A | 3 | a0001c0001t0001g0267a0001c0004t0001g0268a0001c0004t0002g0010 | 3 | HG02055.hp1 HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.497+7143G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26890700 | ||||||
| chr15:26891412
|
T | C | 1 | a0001c0003t0001g0090 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.497+7855T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26891412 | ||||||
| chr15:26891420
|
A | C | 1 | a0001c0001t0001g0067 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.497+7863A>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26891420 | ||||||
| chr15:26891456
|
G | T | 3 | a0001c0001t0001g0263a0001c0002t0001g0005a0001c0002t0001g0089 | 4 | HG03490.hp1 HG03492.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.497+7899G>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26891456 | ||||||
| chr15:26891574
|
A | C | 1 | a0001c0003t0001g0090 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.497+8017A>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26891574 | ||||||
| chr15:26891587
|
C | G | 1 | a0001c0002t0001g0206 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.497+8030C>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26891587 | ||||||
| chr15:26891713
|
G | C | 52 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0016others(49): Show | 53 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.497+8156G>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26891713 | ||||||
| chr15:26891777
|
C | T | 2 | a0001c0003t0001g0107a0001c0006t0001g0238 | 2 | HG01257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.497+8220C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26891777 | ||||||
| chr15:26891842
|
G | A | 1 | a0001c0005t0001g0126 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.497+8285G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26891842 | ||||||
| chr15:26891900
|
A | C | 292 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(289): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.497+8343A>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26891900 | ||||||
| chr15:26892017
|
G | C | 1 | a0001c0002t0001g0173 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.497+8460G>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26892017 | ||||||
| chr15:26892097
|
A | G | 1 | a0001c0001t0001g0223 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.497+8540A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26892097 | ||||||
| chr15:26892286
|
G | T | 4 | a0001c0001t0001g0215a0001c0001t0001g0294a0001c0002t0001g0214others(1): Show | 4 | HG02015.hp1 HG02080.hp1 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.497+8729G>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26892286 | ||||||
| chr15:26892337
|
G | A | 293 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(290): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.497+8780G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26892337 | ||||||
| chr15:26892397
|
GGGCCCTA others(47): Show |
G | 12 | a0001c0001t0001g0034a0001c0001t0001g0069a0001c0001t0001g0070others(9): Show | 12 | HG00408.hp1 HG02027.hp1 NA18612.hp1 others(9): Show |
intron_variant | MODIFIER | c.497+8845_497+8898d others(56): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26892397 | |||||
| chr15:26892404
|
A | G | 281 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(278): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.497+8847A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26892404 | ||||||
| chr15:26892434
|
G | C | 1 | a0001c0001t0001g0059 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.497+8877G>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26892434 | ||||||
| chr15:26892436
|
G | C | 280 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(277): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.497+8879G>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26892436 | ||||||
| chr15:26892570
|
A | T | 1 | a0001c0001t0001g0264 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.497+9013A>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26892570 | ||||||
| chr15:26892655
|
C | T | 292 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(289): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.497+9098C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26892655 | ||||||
| chr15:26892728
|
G | A | 2 | a0001c0001t0001g0223a0001c0002t0001g0224 | 2 | HG00423.hp1 HG00597.hp2 |
intron_variant | MODIFIER | c.497+9171G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26892728 | ||||||
| chr15:26892734
|
T | G | 284 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(281): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.497+9177T>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26892734 | ||||||
| chr15:26892781
|
A | C | 284 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(281): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.497+9224A>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26892781 | ||||||
| chr15:26892900
|
T | C | 3 | a0001c0001t0001g0267a0001c0004t0001g0268a0001c0004t0002g0010 | 3 | HG02055.hp1 HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.497+9343T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26892900 | ||||||
| chr15:26892927
|
T | C | 1 | a0001c0003t0001g0090 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.497+9370T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26892927 | ||||||
| chr15:26892942
|
G | T | 1 | a0001c0003t0001g0140 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.497+9385G>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26892942 | ||||||
| chr15:26893023
|
G | A | 1 | a0001c0002t0001g0141 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.497+9466G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26893023 | ||||||
| chr15:26893087
|
T | C | 1 | a0001c0001t0001g0070 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.497+9530T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26893087 | ||||||
| chr15:26893111
|
T | C | 1 | a0001c0004t0002g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.497+9554T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26893111 | ||||||
| chr15:26893129
|
C | T | 8 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0161others(5): Show | 8 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.497+9572C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26893129 | ||||||
| chr15:26893139
|
A | T | 297 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(294): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.497+9582A>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26893139 | ||||||
| chr15:26893205
|
G | C | 28 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(25): Show | 28 | HG00558.hp2 HG00741.hp2 HG01361.hp2 others(25): Show |
intron_variant | MODIFIER | c.497+9648G>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26893205 | ||||||
| chr15:26893206
|
G | T | 285 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(282): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.497+9649G>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26893206 | ||||||
| chr15:26893279
|
A | T | 285 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(282): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.497+9722A>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26893279 | ||||||
| chr15:26893291
|
G | A | 4 | a0001c0001t0003g0302a0001c0003t0001g0013a0001c0003t0001g0165others(1): Show | 4 | HG01099.hp2 HG02818.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.497+9734G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26893291 | ||||||
| chr15:26893414
|
T | TTGTGTGT others(579): Show |
3 | a0001c0001t0001g0068a0001c0001t0001g0146a0001c0001t0001g0184 | 3 | HG00621.hp1 HG03669.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.497+9871_497+9872i others(588): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26893414 | |||||
| chr15:26893414
|
T | TTGTGTGT others(575): Show |
1 | a0001c0001t0001g0292 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.497+9871_497+9872i others(584): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26893414 | |||||
| chr15:26893414
|
T | TTGTGTGT others(574): Show |
1 | a0001c0002t0001g0118 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.497+9871_497+9872i others(583): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26893414 | |||||
| chr15:26893414
|
T | TTGTGTGT others(574): Show |
88 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0026others(85): Show | 89 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.497+9871_497+9872i others(583): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26893414 | |||||
| chr15:26893414
|
T | TTGTGTGT others(579): Show |
149 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(146): Show | 153 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.497+9871_497+9872i others(588): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26893414 | |||||
| chr15:26893414
|
T | TTGTGTGT others(579): Show |
1 | a0001c0002t0001g0218 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.497+9871_497+9872i others(588): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26893414 | |||||
| chr15:26893414
|
T | TTGTGTGT others(579): Show |
9 | a0001c0001t0001g0028a0001c0001t0001g0225a0001c0001t0001g0251others(6): Show | 9 | HG00642.hp2 HG01123.hp2 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.497+9871_497+9872i others(588): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26893414 | |||||
| chr15:26893414
|
T | TTGTGTGT others(580): Show |
1 | a0001c0001t0001g0348 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.497+9871_497+9872i others(589): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26893414 | |||||
| chr15:26893414
|
T | TTGTGTGT others(579): Show |
3 | a0001c0002t0001g0129a0001c0002t0001g0130a0002c0009t0001g0128 | 3 | HG02615.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.497+9871_497+9872i others(588): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26893414 | |||||
| chr15:26893414
|
T | TTGTGTGT others(579): Show |
1 | a0001c0001t0001g0341 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.497+9871_497+9872i others(588): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26893414 | |||||
| chr15:26893414
|
T | TTGTGTGT others(704): Show |
1 | a0001c0002t0001g0141 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.497+9874_497+9875i others(713): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26893414 | |||||
| chr15:26893414
|
T | TTGTGTGT others(583): Show |
4 | a0001c0001t0003g0302a0001c0003t0001g0013a0001c0003t0001g0165others(1): Show | 4 | HG01099.hp2 HG02818.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.497+9874_497+9875i others(592): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26893414 | |||||
| chr15:26893414
|
T | TTGTGTGT others(704): Show |
28 | a0001c0001t0001g0002a0001c0001t0001g0059a0001c0001t0001g0177others(25): Show | 29 | HG00408.hp2 HG00738.hp2 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.497+9874_497+9875i others(713): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26893414 | |||||
| chr15:26893414
|
T | TTGTGTGT others(707): Show |
1 | a0001c0001t0001g0034 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.497+9876_497+9877i others(716): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26893414 | |||||
| chr15:26893414
|
T | TTGTGTGT others(704): Show |
1 | a0001c0001t0001g0193 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.497+9876_497+9877i others(713): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26893414 | |||||
| chr15:26893414
|
T | TTGTGTGT others(707): Show |
20 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0105others(17): Show | 20 | HG00408.hp1 HG02258.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.497+9876_497+9877i others(716): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26893414 | |||||
| chr15:26893414
|
T | TTGTGTGT others(599): Show |
27 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(24): Show | 27 | HG00558.hp2 HG00741.hp2 HG01361.hp2 others(24): Show |
intron_variant | MODIFIER | c.497+9876_497+9877i others(608): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26893414 | |||||
| chr15:26893414
|
T | TTGTGTGT others(599): Show |
1 | a0001c0002t0001g0042 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.497+9876_497+9877i others(608): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26893414 | |||||
| chr15:26893414
|
T | TTGTGTGT others(576): Show |
1 | a0001c0004t0001g0167 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.497+9876_497+9877i others(585): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26893414 | |||||
| chr15:26893414
|
T | TTGTGTGT others(577): Show |
1 | a0001c0001t0001g0367 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.497+9876_497+9877i others(586): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26893414 | |||||
| chr15:26893414
|
T | TTGTGTGT others(579): Show |
23 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(20): Show | 24 | HG01070.hp1 HG01071.hp2 HG01496.hp2 others(21): Show |
intron_variant | MODIFIER | c.497+9876_497+9877i others(588): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26893414 | |||||
| chr15:26893414
|
T | TTGTGTGT others(581): Show |
3 | a0001c0001t0001g0032a0001c0001t0001g0067a0001c0006t0001g0031 | 3 | HG01109.hp2 HG02622.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.497+9876_497+9877i others(590): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26893414 | |||||
| chr15:26893477
|
T | C | 15 | a0001c0001t0001g0072a0001c0001t0001g0074a0001c0001t0001g0163others(12): Show | 15 | HG01070.hp1 HG01071.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.497+9920T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26893477 | ||||||
| chr15:26893503
|
C | T | 4 | a0001c0001t0001g0215a0001c0001t0001g0294a0001c0002t0001g0214others(1): Show | 4 | HG02015.hp1 HG02080.hp1 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.497+9946C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26893503 | ||||||
| chr15:26893515
|
G | A | 2 | a0001c0001t0001g0063a0001c0001t0001g0064 | 2 | HG01934.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.497+9958G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26893515 | ||||||
| chr15:26893573
|
C | G | 53 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0016others(50): Show | 54 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.497+10016C>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26893573 | ||||||
| chr15:26893741
|
A | C | 289 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(286): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.497+10184A>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26893741 | ||||||
| chr15:26893801
|
G | A | 52 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0016others(49): Show | 53 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.497+10244G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26893801 | ||||||
| chr15:26894057
|
G | GTGCTCCC others(11): Show |
94 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0026others(91): Show | 95 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.497+10504_497+1052 others(22): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26894057 | |||||
| chr15:26894117
|
C | A | 1 | a0001c0001t0001g0367 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.497+10560C>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26894117 | ||||||
| chr15:26894126
|
G | A | 11 | a0001c0001t0001g0034a0001c0001t0001g0069a0001c0001t0001g0070others(8): Show | 11 | HG00408.hp1 HG02027.hp1 NA18612.hp1 others(8): Show |
intron_variant | MODIFIER | c.497+10569G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26894126 | ||||||
| chr15:26894154
|
C | A | 274 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(271): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.497+10597C>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26894154 | ||||||
| chr15:26894157
|
G | C | 12 | a0001c0001t0001g0034a0001c0001t0001g0069a0001c0001t0001g0070others(9): Show | 12 | HG00408.hp1 HG02027.hp1 NA18612.hp1 others(9): Show |
intron_variant | MODIFIER | c.497+10600G>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26894157 | ||||||
| chr15:26894229
|
C | T | 9 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(6): Show | 10 | HG01496.hp2 HG02055.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.497+10672C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26894229 | ||||||
| chr15:26894317
|
T | C | 1 | a0001c0003t0001g0134 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.497+10760T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26894317 | ||||||
| chr15:26894324
|
A | C | 288 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(285): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.497+10767A>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26894324 | ||||||
| chr15:26894435
|
C | A | 51 | a0001c0001t0001g0034a0001c0001t0001g0038a0001c0001t0001g0039others(48): Show | 51 | HG00408.hp1 HG00558.hp2 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.497+10878C>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26894435 | ||||||
| chr15:26894445
|
C | A | 51 | a0001c0001t0001g0034a0001c0001t0001g0038a0001c0001t0001g0039others(48): Show | 51 | HG00408.hp1 HG00558.hp2 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.497+10888C>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26894445 | ||||||
| chr15:26894461
|
G | A | 28 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(25): Show | 28 | HG00558.hp2 HG00741.hp2 HG01361.hp2 others(25): Show |
intron_variant | MODIFIER | c.497+10904G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26894461 | ||||||
| chr15:26894503
|
G | A | 289 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(286): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.497+10946G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26894503 | ||||||
| chr15:26894511
|
A | T | 90 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0026others(87): Show | 91 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.497+10954A>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26894511 | ||||||
| chr15:26894550
|
A | G | 101 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0028others(98): Show | 104 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.497+10993A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26894550 | ||||||
| chr15:26894566
|
TCTC | T | 5 | a0001c0001t0001g0194a0001c0002t0001g0129a0001c0002t0001g0130others(2): Show | 5 | HG02615.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.497+11012_497+1101 others(7): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26894566 | |||||
| chr15:26894609
|
A | G | 15 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0067others(12): Show | 15 | HG01099.hp2 HG01109.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.497+11052A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26894609 | ||||||
| chr15:26894631
|
T | C | 290 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(287): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.497+11074T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26894631 | ||||||
| chr15:26894753
|
G | A | 289 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(286): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.497+11196G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26894753 | ||||||
| chr15:26894760
|
A | T | 289 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(286): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.497+11203A>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26894760 | ||||||
| chr15:26894781
|
T | C | 289 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(286): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.497+11224T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26894781 | ||||||
| chr15:26894806
|
G | A | 91 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0026others(88): Show | 92 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.497+11249G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26894806 | ||||||
| chr15:26894903
|
T | C | 1 | a0001c0002t0001g0037 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.497+11346T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26894903 | ||||||
| chr15:26894908
|
A | G | 8 | a0001c0001t0001g0001a0001c0001t0001g0083a0001c0001t0001g0084others(5): Show | 9 | HG02071.hp1 HG02132.hp2 NA18957.hp2 others(6): Show |
intron_variant | MODIFIER | c.497+11351A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26894908 | ||||||
| chr15:26894909
|
T | C | 22 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(19): Show | 23 | HG01070.hp1 HG01071.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.497+11352T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26894909 | ||||||
| chr15:26894911
|
T | C | 358 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(355): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.497+11354T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26894911 | ||||||
| chr15:26894975
|
G | A | 14 | a0001c0001t0001g0072a0001c0001t0001g0074a0001c0001t0001g0163others(11): Show | 14 | HG01070.hp1 HG01071.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.497+11418G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26894975 | ||||||
| chr15:26895057
|
A | T | 290 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(287): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.497+11500A>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26895057 | ||||||
| chr15:26895106
|
C | T | 1 | a0001c0001t0001g0188 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.497+11549C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26895106 | ||||||
| chr15:26895135
|
C | T | 9 | a0001c0001t0001g0162a0001c0001t0001g0243a0001c0002t0001g0051others(6): Show | 9 | HG02258.hp1 HG02280.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.497+11578C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26895135 | ||||||
| chr15:26895193
|
C | A | 1 | a0001c0001t0001g0178 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.497+11636C>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26895193 | ||||||
| chr15:26895262
|
C | T | 12 | a0001c0001t0001g0034a0001c0001t0001g0069a0001c0001t0001g0070others(9): Show | 12 | HG00408.hp1 HG02027.hp1 NA18612.hp1 others(9): Show |
intron_variant | MODIFIER | c.497+11705C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26895262 | ||||||
| chr15:26895442
|
G | T | 3 | a0001c0001t0001g0267a0001c0004t0001g0268a0001c0004t0002g0010 | 3 | HG02055.hp1 HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.497+11885G>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26895442 | ||||||
| chr15:26895577
|
C | G | 12 | a0001c0001t0001g0034a0001c0001t0001g0069a0001c0001t0001g0070others(9): Show | 12 | HG00408.hp1 HG02027.hp1 NA18612.hp1 others(9): Show |
intron_variant | MODIFIER | c.497+12020C>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26895577 | ||||||
| chr15:26895735
|
C | G | 90 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0026others(87): Show | 91 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.497+12178C>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26895735 | ||||||
| chr15:26895792
|
G | A | 1 | a0001c0003t0001g0134 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.497+12235G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26895792 | ||||||
| chr15:26895812
|
C | CAAAAAAA others(3): Show |
1 | a0001c0002t0001g0129 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.497+12262_497+1227 others(14): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26895812 | |||||
| chr15:26895812
|
C | CAAAAAAA others(4): Show |
6 | a0001c0001t0001g0032a0001c0001t0001g0067a0001c0002t0001g0130others(3): Show | 6 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.497+12261_497+1227 others(15): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26895812 | |||||
| chr15:26895812
|
C | CAAAAAAA others(6): Show |
5 | a0001c0001t0001g0169a0001c0001t0003g0302a0001c0003t0001g0013others(2): Show | 5 | HG01099.hp2 HG02622.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.497+12259_497+1227 others(17): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26895812 | |||||
| chr15:26895812
|
C | CAAAAAAA others(7): Show |
2 | a0001c0003t0001g0165a0001c0003t0001g0170 | 2 | HG02257.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.497+12258_497+1227 others(18): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26895812 | |||||
| chr15:26895812
|
CA | C | 210 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(207): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.497+12271delA | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26895812 | |||||
| chr15:26895823
|
A | AAGAAG | 99 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0028others(96): Show | 102 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.497+12267_497+1226 others(9): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26895823 | |||||
| chr15:26895826
|
A | AAAAAAAA others(7): Show |
1 | a0001c0002t0001g0164 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.497+12271_497+1227 others(18): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26895826 | |||||
| chr15:26895826
|
A | AAAAAAAA others(6): Show |
11 | a0001c0001t0001g0072a0001c0001t0001g0074a0001c0001t0001g0163others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.497+12271_497+1227 others(17): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26895826 | |||||
| chr15:26895826
|
A | AAAAAAAA others(9): Show |
1 | a0001c0001t0001g0367 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.497+12271_497+1227 others(20): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26895826 | |||||
| chr15:26895826
|
A | AAAAAAAA others(5): Show |
7 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(4): Show | 7 | HG01496.hp2 HG02055.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.497+12271_497+1227 others(16): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26895826 | |||||
| chr15:26895826
|
A | AAAAAAAA others(4): Show |
3 | a0001c0001t0001g0263a0001c0002t0001g0005a0001c0002t0001g0089 | 4 | HG03490.hp1 HG03492.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.497+12271_497+1227 others(15): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26895826 | |||||
| chr15:26895826
|
A | G | 173 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(170): Show | 177 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.497+12269A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26895826 | ||||||
| chr15:26895847
|
A | G | 1 | a0001c0002t0001g0123 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.497+12290A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26895847 | ||||||
| chr15:26895939
|
C | T | 1 | a0001c0002t0001g0124 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.497+12382C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26895939 | ||||||
| chr15:26895982
|
T | C | 65 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(62): Show | 66 | HG00408.hp1 HG00558.hp2 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.497+12425T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26895982 | ||||||
| chr15:26896048
|
C | G | 1 | a0001c0001t0001g0074 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.497+12491C>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26896048 | ||||||
| chr15:26896107
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.497+12550C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26896107 | ||||||
| chr15:26896121
|
G | A | 12 | a0001c0001t0001g0072a0001c0001t0001g0074a0001c0001t0001g0163others(9): Show | 12 | HG01070.hp1 HG01071.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.497+12564G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26896121 | ||||||
| chr15:26896399
|
T | A | 15 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0067others(12): Show | 15 | HG01099.hp2 HG01109.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.497+12842T>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26896399 | ||||||
| chr15:26896438
|
G | T | 13 | a0001c0001t0001g0072a0001c0001t0001g0074a0001c0001t0001g0163others(10): Show | 13 | HG01070.hp1 HG01071.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.497+12881G>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26896438 | ||||||
| chr15:26896627
|
G | T | 2 | a0001c0001t0001g0033a0001c0002t0001g0357 | 2 | HG03834.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.497+13070G>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26896627 | ||||||
| chr15:26896739
|
G | A | 13 | a0001c0001t0001g0060a0001c0001t0001g0152a0001c0001t0001g0191others(10): Show | 13 | HG00140.hp1 HG00735.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.497+13182G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26896739 | ||||||
| chr15:26896838
|
A | G | 15 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0067others(12): Show | 15 | HG01099.hp2 HG01109.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.497+13281A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26896838 | ||||||
| chr15:26896925
|
T | TATGTAGA others(24): Show |
1 | a0001c0004t0002g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.497+13397_497+1342 others(35): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26896925 | |||||
| chr15:26896925
|
T | TATGTAGA others(55): Show |
2 | a0001c0002t0001g0142a0001c0002t0001g0297 | 2 | NA18959.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.497+13427_497+1342 others(66): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26896925 | |||||
| chr15:26896925
|
TATGTAGA others(24): Show |
T | 165 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(162): Show | 169 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.497+13397_497+1342 others(35): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26896925 | |||||
| chr15:26896925
|
TATGTAGA others(55): Show |
T | 2 | a0001c0001t0001g0045a0001c0003t0001g0090 | 2 | HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.497+13397_497+1345 others(66): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26896925 | |||||
| chr15:26896954
|
C | CAGATGTA others(24): Show |
4 | a0001c0001t0001g0333a0001c0004t0002g0125a0001c0004t0002g0127others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.497+13440_497+1347 others(35): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26896954 | |||||
| chr15:26896954
|
C | G | 2 | a0001c0001t0001g0065a0001c0001t0001g0091 | 2 | NA18955.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.497+13397C>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26896954 | ||||||
| chr15:26896954
|
CAGATGTA others(24): Show |
C | 133 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0018others(130): Show | 135 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.497+13440_497+1347 others(35): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26896954 | |||||
| chr15:26896985
|
G | C | 1 | a0001c0003t0001g0066 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.497+13428G>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26896985 | ||||||
| chr15:26897119
|
A | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(179): Show | 186 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.497+13562A>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26897119 | ||||||
| chr15:26897199
|
C | T | 1 | a0001c0001t0001g0306 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.497+13642C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26897199 | ||||||
| chr15:26897259
|
G | A | 4 | a0001c0001t0001g0029a0001c0001t0001g0169a0001c0003t0001g0170others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.497+13702G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26897259 | ||||||
| chr15:26897395
|
A | G | 4 | a0001c0001t0001g0201a0001c0002t0001g0003a0001c0002t0001g0113others(1): Show | 5 | HG00140.hp2 HG00642.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.497+13838A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26897395 | ||||||
| chr15:26897617
|
C | T | 1 | a0002c0008t0001g0011 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.497+14060C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26897617 | ||||||
| chr15:26897821
|
G | A | 126 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(123): Show | 130 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.497+14264G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26897821 | ||||||
| chr15:26897839
|
G | A | 14 | a0001c0001t0001g0072a0001c0001t0001g0074a0001c0001t0001g0114others(11): Show | 14 | HG01070.hp1 HG01071.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.497+14282G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26897839 | ||||||
| chr15:26898035
|
T | A | 1 | a0001c0002t0001g0206 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.497+14478T>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26898035 | ||||||
| chr15:26898235
|
T | A | 1 | a0001c0003t0001g0171 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.497+14678T>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26898235 | ||||||
| chr15:26898238
|
G | T | 1 | a0001c0001t0001g0313 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.497+14681G>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26898238 | ||||||
| chr15:26898311
|
A | AC | 196 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(193): Show | 200 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.497+14756dupC | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26898311 | |||||
| chr15:26898441
|
G | A | 4 | a0001c0002t0001g0124a0001c0002t0001g0129a0001c0002t0001g0130others(1): Show | 4 | HG01261.hp2 HG02615.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.497+14884G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26898441 | ||||||
| chr15:26898711
|
T | C | 13 | a0001c0001t0001g0072a0001c0001t0001g0074a0001c0001t0001g0163others(10): Show | 13 | HG01070.hp1 HG01071.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.497+15154T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26898711 | ||||||
| chr15:26898730
|
C | CT | 16 | a0001c0001t0001g0022a0001c0001t0001g0034a0001c0001t0001g0069others(13): Show | 16 | HG00408.hp1 HG01099.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.497+15187dupT | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26898730 | |||||
| chr15:26898730
|
CT | C | 154 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0018others(151): Show | 156 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.497+15187delT | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26898730 | |||||
| chr15:26899024
|
A | G | 13 | a0001c0001t0001g0072a0001c0001t0001g0074a0001c0001t0001g0163others(10): Show | 13 | HG01070.hp1 HG01071.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.497+15467A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26899024 | ||||||
| chr15:26899055
|
G | T | 13 | a0001c0001t0001g0072a0001c0001t0001g0074a0001c0001t0001g0163others(10): Show | 13 | HG01070.hp1 HG01071.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.497+15498G>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26899055 | ||||||
| chr15:26899103
|
T | C | 1 | a0001c0001t0001g0282 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.497+15546T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26899103 | ||||||
| chr15:26899558
|
T | C | 2 | a0001c0001t0001g0033a0001c0002t0001g0357 | 2 | HG03834.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.498-15245T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26899558 | ||||||
| chr15:26899627
|
G | T | 181 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(178): Show | 185 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.498-15176G>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26899627 | ||||||
| chr15:26899727
|
T | C | 107 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0026others(104): Show | 108 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.498-15076T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26899727 | ||||||
| chr15:26899781
|
T | C | 1 | a0001c0001t0001g0048 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.498-15022T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26899781 | ||||||
| chr15:26899835
|
C | G | 10 | a0001c0001t0001g0151a0001c0001t0001g0162a0001c0001t0001g0243others(7): Show | 10 | HG02258.hp1 HG02280.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.498-14968C>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26899835 | ||||||
| chr15:26899842
|
G | T | 1 | a0001c0003t0001g0066 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.498-14961G>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26899842 | ||||||
| chr15:26899961
|
C | T | 3 | a0001c0004t0002g0125a0001c0004t0002g0127a0001c0005t0001g0126 | 3 | HG01070.hp1 HG01071.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.498-14842C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26899961 | ||||||
| chr15:26899962
|
T | G | 13 | a0001c0001t0001g0072a0001c0001t0001g0074a0001c0001t0001g0163others(10): Show | 13 | HG01070.hp1 HG01071.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.498-14841T>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26899962 | ||||||
| chr15:26900007
|
G | A | 1 | a0001c0006t0001g0271 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.498-14796G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26900007 | ||||||
| chr15:26900140
|
C | T | 13 | a0001c0001t0001g0072a0001c0001t0001g0074a0001c0001t0001g0163others(10): Show | 13 | HG01070.hp1 HG01071.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.498-14663C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26900140 | ||||||
| chr15:26900202
|
G | A | 1 | a0001c0002t0001g0123 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.498-14601G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26900202 | ||||||
| chr15:26900223
|
G | A | 6 | a0001c0001t0001g0162a0001c0001t0001g0243a0001c0003t0001g0239others(3): Show | 6 | HG02258.hp1 HG02280.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.498-14580G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26900223 | ||||||
| chr15:26900307
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.498-14496C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26900307 | ||||||
| chr15:26900309
|
A | AT | 13 | a0001c0001t0001g0072a0001c0001t0001g0074a0001c0001t0001g0163others(10): Show | 13 | HG01070.hp1 HG01071.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.498-14487dupT | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26900309 | |||||
| chr15:26900309
|
AT | A | 6 | a0001c0001t0001g0007a0001c0001t0001g0054a0001c0001t0001g0055others(3): Show | 7 | NA18949.hp1 NA18966.hp1 NA18971.hp2 others(4): Show |
intron_variant | MODIFIER | c.498-14487delT | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26900309 | |||||
| chr15:26900427
|
G | A | 1 | a0001c0002t0001g0206 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.498-14376G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26900427 | ||||||
| chr15:26900578
|
A | G | 2 | a0001c0001t0001g0204a0001c0001t0001g0205 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.498-14225A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26900578 | ||||||
| chr15:26900624
|
T | C | 13 | a0001c0001t0001g0072a0001c0001t0001g0074a0001c0001t0001g0163others(10): Show | 13 | HG01070.hp1 HG01071.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.498-14179T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26900624 | ||||||
| chr15:26900752
|
C | T | 13 | a0001c0001t0001g0072a0001c0001t0001g0074a0001c0001t0001g0163others(10): Show | 13 | HG01070.hp1 HG01071.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.498-14051C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26900752 | ||||||
| chr15:26900753
|
G | A | 2 | a0001c0001t0001g0356a0001c0002t0001g0286 | 2 | NA18965.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.498-14050G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26900753 | ||||||
| chr15:26900796
|
A | T | 2 | a0001c0002t0001g0108a0001c0002t0001g0363 | 2 | NA18997.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.498-14007A>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26900796 | ||||||
| chr15:26900853
|
T | A | 1 | a0001c0001t0001g0060 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.498-13950T>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26900853 | ||||||
| chr15:26900987
|
C | G | 1 | a0001c0001t0001g0053 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.498-13816C>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26900987 | ||||||
| chr15:26901041
|
CTA | C | 4 | a0001c0001t0001g0029a0001c0001t0001g0169a0001c0003t0001g0170others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.498-13759_498-1375 others(6): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26901041 | |||||
| chr15:26901193
|
G | GGATC | 28 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0067others(25): Show | 28 | HG01070.hp1 HG01071.hp2 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.498-13610_498-1360 others(8): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26901193 | ||||||
| chr15:26901374
|
C | A | 1 | a0001c0003t0001g0134 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.498-13429C>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26901374 | ||||||
| chr15:26901416
|
G | A | 9 | a0001c0001t0001g0151a0001c0001t0001g0162a0001c0001t0001g0243others(6): Show | 9 | HG02258.hp1 HG02280.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.498-13387G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26901416 | ||||||
| chr15:26901515
|
A | C | 157 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(154): Show | 161 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.498-13288A>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26901515 | ||||||
| chr15:26901569
|
T | C | 1 | a0001c0003t0001g0171 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.498-13234T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26901569 | ||||||
| chr15:26901576
|
T | C | 8 | a0001c0001t0001g0052a0001c0001t0001g0247a0001c0001t0001g0277others(5): Show | 8 | HG00621.hp2 NA18747.hp2 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.498-13227T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26901576 | ||||||
| chr15:26901767
|
G | T | 3 | a0001c0001t0001g0232a0001c0001t0001g0356a0001c0002t0001g0286 | 3 | HG02071.hp2 NA18965.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.498-13036G>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26901767 | ||||||
| chr15:26901911
|
G | A | 12 | a0001c0001t0001g0034a0001c0001t0001g0069a0001c0001t0001g0070others(9): Show | 12 | HG00408.hp1 HG02027.hp1 NA18612.hp1 others(9): Show |
intron_variant | MODIFIER | c.498-12892G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26901911 | ||||||
| chr15:26901922
|
G | A | 183 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(180): Show | 187 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.498-12881G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26901922 | ||||||
| chr15:26902160
|
A | C | 1 | a0001c0001t0001g0072 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.498-12643A>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26902160 | ||||||
| chr15:26902184
|
C | T | 13 | a0001c0001t0001g0072a0001c0001t0001g0074a0001c0001t0001g0163others(10): Show | 13 | HG01070.hp1 HG01071.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.498-12619C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26902184 | ||||||
| chr15:26902263
|
T | C | 6 | a0001c0001t0001g0065a0001c0001t0001g0120a0001c0001t0001g0223others(3): Show | 6 | HG00423.hp1 HG00438.hp1 HG00597.hp2 others(3): Show |
intron_variant | MODIFIER | c.498-12540T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26902263 | ||||||
| chr15:26902462
|
A | T | 15 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0067others(12): Show | 15 | HG01099.hp2 HG01109.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.498-12341A>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26902462 | ||||||
| chr15:26902643
|
G | T | 10 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(7): Show | 11 | HG01496.hp2 HG02055.hp2 HG02976.hp1 others(8): Show |
intron_variant | MODIFIER | c.498-12160G>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26902643 | ||||||
| chr15:26902827
|
T | G | 12 | a0001c0001t0001g0029a0001c0001t0001g0169a0001c0001t0003g0302others(9): Show | 12 | HG01099.hp2 HG02257.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.498-11976T>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26902827 | ||||||
| chr15:26902900
|
A | G | 2 | a0001c0001t0001g0291a0001c0002t0001g0124 | 2 | HG01258.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.498-11903A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26902900 | ||||||
| chr15:26903066
|
G | C | 2 | a0001c0001t0001g0102a0001c0001t0001g0207 | 2 | HG02083.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.498-11737G>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26903066 | ||||||
| chr15:26903067
|
C | T | 1 | a0001c0001t0001g0262 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.498-11736C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26903067 | ||||||
| chr15:26903135
|
A | G | 1 | a0001c0003t0001g0090 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.498-11668A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26903135 | ||||||
| chr15:26903226
|
C | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(151): Show | 158 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.498-11577C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26903226 | ||||||
| chr15:26903346
|
T | C | 183 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(180): Show | 187 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.498-11457T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26903346 | ||||||
| chr15:26903400
|
T | C | 336 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(333): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.498-11403T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26903400 | ||||||
| chr15:26903429
|
C | T | 1 | a0001c0001t0001g0290 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.498-11374C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26903429 | ||||||
| chr15:26903569
|
C | A | 1 | a0001c0001t0001g0048 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.498-11234C>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26903569 | ||||||
| chr15:26903579
|
A | G | 127 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(124): Show | 131 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.498-11224A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26903579 | ||||||
| chr15:26903609
|
C | G | 13 | a0001c0001t0001g0072a0001c0001t0001g0074a0001c0001t0001g0163others(10): Show | 13 | HG01070.hp1 HG01071.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.498-11194C>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26903609 | ||||||
| chr15:26903688
|
C | T | 4 | a0001c0001t0001g0201a0001c0002t0001g0003a0001c0002t0001g0113others(1): Show | 5 | HG00140.hp2 HG00642.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.498-11115C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26903688 | ||||||
| chr15:26903776
|
A | G | 182 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(179): Show | 186 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.498-11027A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26903776 | ||||||
| chr15:26903787
|
G | A | 216 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(213): Show | 220 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.498-11016G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26903787 | ||||||
| chr15:26903802
|
GT | G | 22 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(19): Show | 22 | HG00558.hp2 HG00741.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.498-10997delT | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26903802 | |||||
| chr15:26903807
|
G | T | 1 | a0001c0002t0001g0250 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.498-10996G>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26903807 | ||||||
| chr15:26903899
|
T | G | 1 | a0001c0001t0001g0367 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.498-10904T>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26903899 | ||||||
| chr15:26904195
|
G | T | 1 | a0001c0004t0001g0268 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.498-10608G>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26904195 | ||||||
| chr15:26904366
|
A | C | 9 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0255others(6): Show | 9 | NA18952.hp1 NA18952.hp2 NA18960.hp2 others(6): Show |
intron_variant | MODIFIER | c.498-10437A>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26904366 | ||||||
| chr15:26904446
|
G | C | 12 | a0001c0001t0001g0074a0001c0001t0001g0163a0001c0001t0001g0367others(9): Show | 12 | HG01070.hp1 HG01071.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.498-10357G>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26904446 | ||||||
| chr15:26904526
|
C | T | 181 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(178): Show | 185 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.498-10277C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26904526 | ||||||
| chr15:26904588
|
A | G | 24 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(21): Show | 24 | HG00558.hp2 HG00741.hp2 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.498-10215A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26904588 | ||||||
| chr15:26904598
|
A | G | 1 | a0001c0001t0001g0316 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.498-10205A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26904598 | ||||||
| chr15:26905281
|
G | GT | 293 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(290): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.498-9512dupT | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26905281 | |||||
| chr15:26905478
|
A | G | 28 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0067others(25): Show | 28 | HG01070.hp1 HG01071.hp2 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.498-9325A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26905478 | ||||||
| chr15:26905670
|
AT | A | 21 | a0001c0001t0001g0029a0001c0001t0001g0072a0001c0001t0001g0074others(18): Show | 21 | HG01070.hp1 HG01071.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.498-9125delT | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26905670 | |||||
| chr15:26905672
|
T | G | 3 | a0001c0001t0001g0215a0001c0001t0001g0294a0001c0002t0001g0214 | 3 | HG02015.hp1 NA18944.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.498-9131T>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26905672 | ||||||
| chr15:26905831
|
G | A | 3 | a0001c0001t0001g0366a0001c0003t0001g0107a0001c0006t0001g0238 | 3 | HG01257.hp2 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.498-8972G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26905831 | ||||||
| chr15:26905896
|
T | C | 28 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0067others(25): Show | 28 | HG01070.hp1 HG01071.hp2 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.498-8907T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26905896 | ||||||
| chr15:26906002
|
T | C | 7 | a0001c0001t0001g0032a0001c0001t0001g0067a0001c0001t0003g0302others(4): Show | 7 | HG01099.hp2 HG01109.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.498-8801T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26906002 | ||||||
| chr15:26906127
|
T | TTTTGTTT others(1): Show |
181 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(178): Show | 185 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.498-8668_498-8661d others(10): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26906127 | |||||
| chr15:26906127
|
T | TTTTGTTT others(5): Show |
3 | a0001c0001t0001g0156a0001c0001t0001g0185a0001c0001t0001g0354 | 3 | NA18947.hp2 NA18959.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.498-8672_498-8661d others(14): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26906127 | |||||
| chr15:26906147
|
C | T | 2 | a0001c0001t0001g0194a0001c0001t0003g0168 | 2 | HG03139.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.498-8656C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26906147 | ||||||
| chr15:26906159
|
T | C | 1 | a0001c0002t0001g0206 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.498-8644T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26906159 | ||||||
| chr15:26906195
|
A | C | 1 | a0001c0001t0001g0029 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.498-8608A>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26906195 | ||||||
| chr15:26906344
|
T | C | 1 | a0001c0003t0001g0090 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.498-8459T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26906344 | ||||||
| chr15:26906462
|
C | A | 1 | a0001c0002t0001g0179 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.498-8341C>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26906462 | ||||||
| chr15:26906545
|
C | T | 1 | a0001c0002t0001g0042 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.498-8258C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26906545 | ||||||
| chr15:26906805
|
A | T | 1 | a0001c0001t0001g0223 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.498-7998A>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26906805 | ||||||
| chr15:26906981
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.498-7822A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26906981 | ||||||
| chr15:26907050
|
C | T | 27 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0067others(24): Show | 27 | HG01070.hp1 HG01071.hp2 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.498-7753C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26907050 | ||||||
| chr15:26907071
|
G | T | 23 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(20): Show | 23 | HG00558.hp2 HG00741.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.498-7732G>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26907071 | ||||||
| chr15:26907094
|
A | G | 2 | a0001c0003t0001g0056a0001c0003t0001g0057 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.498-7709A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26907094 | ||||||
| chr15:26907143
|
C | A | 4 | a0001c0001t0001g0255a0001c0001t0001g0303a0001c0001t0001g0304others(1): Show | 4 | NA18952.hp2 NA18966.hp2 NA18987.hp1 others(1): Show |
intron_variant | MODIFIER | c.498-7660C>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26907143 | ||||||
| chr15:26907433
|
C | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(151): Show | 158 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.498-7370C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26907433 | ||||||
| chr15:26907619
|
G | A | 28 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0067others(25): Show | 28 | HG01070.hp1 HG01071.hp2 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.498-7184G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26907619 | ||||||
| chr15:26907714
|
C | T | 1 | a0001c0001t0001g0248 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.498-7089C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26907714 | ||||||
| chr15:26907849
|
G | A | 182 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(179): Show | 186 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.498-6954G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26907849 | ||||||
| chr15:26907926
|
G | A | 7 | a0001c0001t0001g0032a0001c0001t0001g0067a0001c0001t0003g0302others(4): Show | 7 | HG01099.hp2 HG01109.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.498-6877G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26907926 | ||||||
| chr15:26907971
|
G | A | 23 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(20): Show | 23 | HG00558.hp2 HG00741.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.498-6832G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26907971 | ||||||
| chr15:26908135
|
T | C | 21 | a0001c0001t0001g0029a0001c0001t0001g0072a0001c0001t0001g0074others(18): Show | 21 | HG01070.hp1 HG01071.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.498-6668T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26908135 | ||||||
| chr15:26908278
|
A | G | 1 | a0001c0002t0001g0208 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.498-6525A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26908278 | ||||||
| chr15:26908392
|
A | G | 1 | a0002c0008t0001g0011 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.498-6411A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26908392 | ||||||
| chr15:26908491
|
G | C | 186 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0018others(183): Show | 188 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.498-6312G>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26908491 | ||||||
| chr15:26908626
|
G | A | 28 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0067others(25): Show | 28 | HG01070.hp1 HG01071.hp2 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.498-6177G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26908626 | ||||||
| chr15:26908640
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.498-6163G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26908640 | ||||||
| chr15:26908913
|
G | A | 1 | a0001c0002t0001g0141 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.498-5890G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26908913 | ||||||
| chr15:26909226
|
C | T | 1 | a0001c0001t0006g0058 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.498-5577C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26909226 | ||||||
| chr15:26909304
|
C | T | 128 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(125): Show | 132 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.498-5499C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26909304 | ||||||
| chr15:26909354
|
T | A | 1 | a0001c0002t0001g0049 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.498-5449T>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26909354 | ||||||
| chr15:26909418
|
A | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(152): Show | 159 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.498-5385A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26909418 | ||||||
| chr15:26909482
|
A | G | 8 | a0001c0001t0001g0001a0001c0001t0001g0083a0001c0001t0001g0084others(5): Show | 9 | HG02071.hp1 HG02132.hp2 NA18957.hp2 others(6): Show |
intron_variant | MODIFIER | c.498-5321A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26909482 | ||||||
| chr15:26909536
|
G | C | 154 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(151): Show | 158 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.498-5267G>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26909536 | ||||||
| chr15:26909688
|
C | G | 1 | a0001c0003t0001g0134 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.498-5115C>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26909688 | ||||||
| chr15:26909922
|
G | A | 2 | a0001c0001t0001g0194a0001c0001t0003g0168 | 2 | HG03139.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.498-4881G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26909922 | ||||||
| chr15:26909926
|
A | G | 334 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(331): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.498-4877A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26909926 | ||||||
| chr15:26910070
|
G | GT | 76 | a0001c0001t0001g0034a0001c0001t0001g0038a0001c0001t0001g0039others(73): Show | 76 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.498-4724dupT | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26910070 | |||||
| chr15:26910070
|
G | GTT | 80 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0018others(77): Show | 82 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.498-4725_498-4724d others(4): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26910070 | |||||
| chr15:26910122
|
G | C | 9 | a0001c0001t0001g0151a0001c0001t0001g0162a0001c0001t0001g0243others(6): Show | 9 | HG02258.hp1 HG02280.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.498-4681G>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26910122 | ||||||
| chr15:26910326
|
G | T | 3 | a0001c0001t0001g0263a0001c0002t0001g0005a0001c0002t0001g0089 | 4 | HG03490.hp1 HG03492.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.498-4477G>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26910326 | ||||||
| chr15:26910419
|
G | T | 1 | a0001c0001t0001g0367 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.498-4384G>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26910419 | ||||||
| chr15:26910522
|
C | T | 1 | a0001c0001t0001g0340 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.498-4281C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26910522 | ||||||
| chr15:26910587
|
G | A | 4 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0221others(1): Show | 4 | HG00438.hp2 HG00558.hp1 HG02027.hp2 others(1): Show |
intron_variant | MODIFIER | c.498-4216G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26910587 | ||||||
| chr15:26910597
|
C | CA | 28 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0050others(25): Show | 28 | HG00558.hp2 HG00741.hp2 HG01361.hp2 others(25): Show |
intron_variant | MODIFIER | c.498-4190dupA | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26910597 | |||||
| chr15:26910597
|
CA | C | 157 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(154): Show | 161 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.498-4190delA | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26910597 | |||||
| chr15:26910597
|
CAA | C | 17 | a0001c0001t0001g0048a0001c0001t0001g0087a0001c0001t0001g0088others(14): Show | 17 | HG01884.hp2 HG01891.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.498-4191_498-4190d others(4): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26910597 | |||||
| chr15:26910597
|
CAAA | C | 98 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0026others(95): Show | 99 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.498-4192_498-4190d others(5): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26910597 | |||||
| chr15:26910597
|
CAAAA | C | 29 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(26): Show | 30 | HG01070.hp1 HG01071.hp2 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.498-4193_498-4190d others(6): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26910597 | |||||
| chr15:26910741
|
G | A | 1 | a0002c0008t0001g0011 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.498-4062G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26910741 | ||||||
| chr15:26910792
|
C | T | 2 | a0001c0002t0001g0121a0001c0004t0001g0202 | 2 | HG02257.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.498-4011C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26910792 | ||||||
| chr15:26910905
|
A | C | 1 | a0001c0001t0001g0215 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.498-3898A>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26910905 | ||||||
| chr15:26910953
|
A | G | 25 | a0001c0001t0001g0074a0001c0001t0001g0151a0001c0001t0001g0162others(22): Show | 25 | HG01070.hp1 HG01071.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.498-3850A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26910953 | ||||||
| chr15:26911001
|
A | C | 1 | a0001c0001t0001g0114 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.498-3802A>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26911001 | ||||||
| chr15:26911060
|
A | G | 1 | a0001c0002t0001g0147 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.498-3743A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26911060 | ||||||
| chr15:26911079
|
A | G | 240 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(237): Show | 246 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.498-3724A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26911079 | ||||||
| chr15:26911171
|
G | GAATTCT | 305 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(302): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.498-3629_498-3624d others(8): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26911171 | |||||
| chr15:26911176
|
C | CTAA | 6 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0204others(3): Show | 6 | HG02451.hp1 HG02486.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.498-3626_498-3624d others(5): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26911176 | |||||
| chr15:26911357
|
C | G | 15 | a0001c0001t0001g0191a0001c0001t0001g0201a0001c0002t0001g0003others(12): Show | 16 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(13): Show |
intron_variant | MODIFIER | c.498-3446C>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26911357 | ||||||
| chr15:26911365
|
CTGCA | C | 5 | a0001c0001t0001g0018a0001c0001t0001g0061a0001c0002t0001g0129others(2): Show | 5 | HG02055.hp2 HG02615.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.498-3433_498-3430d others(6): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26911365 | |||||
| chr15:26911367
|
G | GCA | 16 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0040others(13): Show | 17 | HG01952.hp1 HG02280.hp2 HG02735.hp1 others(14): Show |
intron_variant | MODIFIER | c.498-3435_498-3434d others(4): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26911367 | |||||
| chr15:26911367
|
G | GCACA | 6 | a0001c0001t0001g0006a0001c0001t0001g0033a0001c0001t0001g0091others(3): Show | 7 | HG00099.hp2 HG00558.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.498-3434_498-3433i others(6): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26911367 | |||||
| chr15:26911367
|
G | GCACACA | 18 | a0001c0001t0001g0039a0001c0001t0001g0053a0001c0001t0001g0084others(15): Show | 18 | HG00438.hp2 HG00558.hp1 HG00621.hp2 others(15): Show |
intron_variant | MODIFIER | c.498-3434_498-3433i others(8): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26911367 | |||||
| chr15:26911367
|
G | GCACACAC others(3): Show |
1 | a0001c0002t0001g0036 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.498-3434_498-3433i others(12): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26911367 | |||||
| chr15:26911367
|
GCATGCA | G | 4 | a0001c0001t0001g0161a0001c0003t0001g0170a0001c0003t0001g0171others(1): Show | 4 | HG02257.hp2 HG02976.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.498-3433_498-3428d others(8): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26911367 | |||||
| chr15:26911367
|
GCATGCAC others(1): Show |
G | 9 | a0001c0001t0001g0106a0001c0001t0001g0131a0001c0001t0001g0176others(6): Show | 9 | HG02040.hp2 HG02080.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.498-3433_498-3426d others(10): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26911367 | |||||
| chr15:26911367
|
GCATGCAC others(3): Show |
G | 2 | a0001c0001t0001g0187a0001c0002t0001g0189 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.498-3433_498-3424d others(12): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26911367 | |||||
| chr15:26911367
|
GCATGCAC others(5): Show |
G | 1 | a0001c0001t0001g0308 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.498-3433_498-3422d others(14): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26911367 | |||||
| chr15:26911367
|
GCATGCAC others(7): Show |
G | 1 | a0001c0001t0001g0207 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.498-3433_498-3420d others(16): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26911367 | |||||
| chr15:26911367
|
GCATGCAC others(9): Show |
G | 1 | a0001c0002t0001g0321 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.498-3433_498-3418d others(18): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26911367 | |||||
| chr15:26911369
|
ATG | A | 44 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0019others(41): Show | 45 | HG00140.hp1 HG01070.hp2 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.498-3433_498-3432d others(4): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26911369 | ||||||
| chr15:26911370
|
T | C | 90 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0022others(87): Show | 92 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.498-3433T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26911370 | ||||||
| chr15:26911371
|
G | A | 77 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0022others(74): Show | 79 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.498-3432G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26911371 | ||||||
| chr15:26911371
|
G | GCA | 58 | a0001c0001t0001g0004a0001c0001t0001g0034a0001c0001t0001g0048others(55): Show | 58 | HG00099.hp1 HG00621.hp1 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.498-3407_498-3406d others(4): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26911371 | |||||
| chr15:26911371
|
G | GCACA | 8 | a0001c0001t0001g0060a0001c0001t0001g0093a0001c0001t0001g0281others(5): Show | 8 | HG00738.hp2 HG02293.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.498-3409_498-3406d others(6): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26911371 | |||||
| chr15:26911371
|
G | GCACACA | 12 | a0001c0001t0001g0088a0001c0001t0001g0152a0001c0001t0001g0203others(9): Show | 12 | HG01934.hp1 HG02155.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.498-3411_498-3406d others(8): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26911371 | |||||
| chr15:26911371
|
G | GCACACAC others(1): Show |
37 | a0001c0001t0001g0016a0001c0001t0001g0052a0001c0001t0001g0059others(34): Show | 37 | HG00408.hp2 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.498-3413_498-3406d others(10): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26911371 | |||||
| chr15:26911371
|
G | GCACACAC others(3): Show |
5 | a0001c0001t0001g0225a0001c0001t0001g0350a0001c0004t0002g0125others(2): Show | 5 | HG01070.hp1 HG01071.hp2 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.498-3415_498-3406d others(12): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26911371 | |||||
| chr15:26911371
|
GCA | G | 19 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0063others(16): Show | 20 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.498-3407_498-3406d others(4): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26911371 | |||||
| chr15:26911373
|
A | G | 1 | a0001c0006t0001g0182 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.498-3430A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26911373 | ||||||
| chr15:26911388
|
C | CACAAACA others(7): Show |
1 | a0001c0002t0001g0330 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.498-3412_498-3411i others(16): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26911388 | |||||
| chr15:26911388
|
C | CACACAAA others(9): Show |
1 | a0001c0002t0001g0339 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.498-3410_498-3409i others(18): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26911388 | |||||
| chr15:26911388
|
C | CACACACA others(11): Show |
13 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0050others(10): Show | 13 | HG00423.hp1 HG00438.hp1 HG00597.hp2 others(10): Show |
intron_variant | MODIFIER | c.498-3408_498-3407i others(20): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26911388 | |||||
| chr15:26911388
|
C | CACACACA others(13): Show |
7 | a0001c0001t0001g0083a0001c0001t0001g0132a0001c0001t0001g0262others(4): Show | 7 | HG02015.hp2 HG02071.hp1 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.498-3396_498-3395i others(22): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26911388 | |||||
| chr15:26911388
|
C | CACACACA others(23): Show |
1 | a0001c0001t0001g0198 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.498-3396_498-3395i others(32): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26911388 | |||||
| chr15:26911388
|
C | CACACACA others(11): Show |
2 | a0001c0002t0001g0190a0001c0002t0001g0208 | 2 | NA18979.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.498-3406_498-3405i others(20): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26911388 | |||||
| chr15:26911392
|
CACACAA | C | 11 | a0001c0001t0001g0038a0001c0001t0001g0102a0001c0001t0001g0306others(8): Show | 11 | HG01943.hp1 HG03098.hp1 HG03942.hp1 others(8): Show |
intron_variant | MODIFIER | c.498-3405_498-3400d others(8): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26911392 | |||||
| chr15:26911394
|
CACAA | C | 22 | a0001c0001t0001g0186a0001c0001t0001g0199a0001c0001t0001g0256others(19): Show | 23 | HG00423.hp2 HG00733.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.498-3405_498-3402d others(6): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26911394 | |||||
| chr15:26911396
|
CAA | C | 16 | a0001c0001t0001g0110a0001c0001t0001g0114a0001c0001t0001g0163others(13): Show | 16 | HG00280.hp2 HG01891.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.498-3405_498-3404d others(4): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26911396 | |||||
| chr15:26911398
|
A | C | 32 | a0001c0001t0001g0001a0001c0001t0001g0029a0001c0001t0001g0048others(29): Show | 34 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(31): Show |
intron_variant | MODIFIER | c.498-3405A>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26911398 | ||||||
| chr15:26911493
|
C | T | 1 | a0001c0003t0007g0155 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.498-3310C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26911493 | ||||||
| chr15:26911685
|
T | C | 127 | a0001c0001t0001g0006a0001c0001t0001g0022a0001c0001t0001g0029others(124): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.498-3118T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26911685 | ||||||
| chr15:26911747
|
A | G | 3 | a0001c0001t0001g0001a0001c0001t0001g0085a0001c0003t0001g0086 | 4 | NA18957.hp2 NA18969.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.498-3056A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26911747 | ||||||
| chr15:26911893
|
A | G | 167 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0016others(164): Show | 168 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.498-2910A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26911893 | ||||||
| chr15:26912113
|
G | C | 1 | a0001c0001t0001g0279 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.498-2690G>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26912113 | ||||||
| chr15:26912124
|
T | G | 34 | a0001c0001t0001g0016a0001c0001t0001g0034a0001c0001t0001g0052others(31): Show | 34 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.498-2679T>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26912124 | ||||||
| chr15:26912169
|
A | G | 36 | a0001c0001t0001g0016a0001c0001t0001g0034a0001c0001t0001g0052others(33): Show | 36 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.498-2634A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26912169 | ||||||
| chr15:26912192
|
C | T | 3 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0002t0001g0218 | 3 | HG00438.hp2 HG02027.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.498-2611C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26912192 | ||||||
| chr15:26912193
|
A | C | 1 | a0001c0001t0003g0302 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.498-2610A>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26912193 | ||||||
| chr15:26912193
|
A | G | 175 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(172): Show | 178 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.498-2610A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26912193 | ||||||
| chr15:26912386
|
A | G | 1 | a0001c0001t0001g0341 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.498-2417A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26912386 | ||||||
| chr15:26912435
|
T | A | 34 | a0001c0001t0001g0029a0001c0001t0001g0067a0001c0001t0001g0072others(31): Show | 36 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(33): Show |
intron_variant | MODIFIER | c.498-2368T>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26912435 | ||||||
| chr15:26912521
|
C | A | 8 | a0001c0001t0001g0048a0001c0001t0001g0152a0001c0001t0001g0366others(5): Show | 8 | HG02257.hp2 HG02922.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.498-2282C>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26912521 | ||||||
| chr15:26912636
|
G | A | 1 | a0001c0002t0001g0326 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.498-2167G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26912636 | ||||||
| chr15:26912725
|
G | A | 317 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(314): Show | 323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.498-2078G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26912725 | ||||||
| chr15:26912740
|
A | G | 1 | a0001c0002t0001g0109 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.498-2063A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26912740 | ||||||
| chr15:26912836
|
G | A | 3 | a0001c0002t0001g0147a0001c0003t0001g0107a0001c0004t0001g0012 | 3 | HG02647.hp1 HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.498-1967G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26912836 | ||||||
| chr15:26912921
|
G | A | 114 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(111): Show | 117 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.498-1882G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26912921 | ||||||
| chr15:26912948
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.498-1855C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26912948 | ||||||
| chr15:26913105
|
AC | A | 147 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(144): Show | 150 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.498-1695delC | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26913105 | |||||
| chr15:26913109
|
G | A | 31 | a0001c0001t0001g0016a0001c0001t0001g0034a0001c0001t0001g0052others(28): Show | 31 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.498-1694G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26913109 | ||||||
| chr15:26913139
|
C | A | 1 | a0001c0002t0001g0224 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.498-1664C>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26913139 | ||||||
| chr15:26913139
|
C | T | 3 | a0001c0003t0001g0239a0001c0003t0008g0009a0001c0006t0005g0015 | 3 | HG02258.hp1 HG02280.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.498-1664C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26913139 | ||||||
| chr15:26913182
|
C | CA | 48 | a0001c0001t0001g0034a0001c0001t0001g0052a0001c0001t0001g0063others(45): Show | 48 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.498-1602dupA | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26913182 | |||||
| chr15:26913182
|
CA | C | 125 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0020others(122): Show | 128 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.498-1602delA | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26913182 | |||||
| chr15:26913182
|
CAA | C | 17 | a0001c0001t0001g0004a0001c0001t0001g0060a0001c0001t0001g0204others(14): Show | 17 | HG01109.hp2 HG02257.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.498-1603_498-1602d others(4): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26913182 | |||||
| chr15:26913286
|
G | A | 4 | a0001c0001t0001g0052a0001c0001t0001g0298a0001c0002t0001g0101others(1): Show | 4 | NA18950.hp1 NA18950.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.498-1517G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26913286 | ||||||
| chr15:26913327
|
G | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0016others(198): Show | 204 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.498-1476G>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26913327 | ||||||
| chr15:26913348
|
C | A | 4 | a0001c0001t0001g0151a0001c0001t0001g0367a0001c0001t0003g0076others(1): Show | 4 | HG02970.hp2 HG03139.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.498-1455C>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26913348 | ||||||
| chr15:26913402
|
C | A | 317 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(314): Show | 323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.498-1401C>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26913402 | ||||||
| chr15:26913635
|
C | T | 1 | a0001c0001t0001g0110 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.498-1168C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26913635 | ||||||
| chr15:26913694
|
A | G | 9 | a0001c0001t0001g0004a0001c0001t0001g0204a0001c0001t0001g0205others(6): Show | 9 | HG01109.hp2 HG02451.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.498-1109A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26913694 | ||||||
| chr15:26913750
|
G | A | 1 | a0001c0001t0001g0194 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.498-1053G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26913750 | ||||||
| chr15:26913937
|
G | T | 1 | a0001c0002t0001g0343 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.498-866G>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26913937 | ||||||
| chr15:26913942
|
G | T | 1 | a0001c0002t0001g0237 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.498-861G>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26913942 | ||||||
| chr15:26914049
|
C | T | 136 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(133): Show | 139 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.498-754C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26914049 | ||||||
| chr15:26914175
|
A | G | 20 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0048others(17): Show | 20 | HG00733.hp1 HG01496.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.498-628A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26914175 | ||||||
| chr15:26914242
|
A | AT | 30 | a0001c0001t0001g0016a0001c0001t0001g0034a0001c0001t0001g0052others(27): Show | 30 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.498-559dupT | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 26914242 | |||||
| chr15:26914268
|
C | A | 4 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0087others(1): Show | 4 | HG01496.hp2 HG02809.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.498-535C>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26914268 | ||||||
| chr15:26914316
|
T | A | 4 | a0001c0001t0001g0007a0001c0001t0001g0055a0001c0001t0001g0135others(1): Show | 5 | NA18949.hp1 NA18966.hp1 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.498-487T>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26914316 | ||||||
| chr15:26914362
|
A | G | 16 | a0001c0001t0001g0048a0001c0001t0001g0152a0001c0001t0001g0366others(13): Show | 16 | HG00733.hp1 HG02257.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.498-441A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26914362 | ||||||
| chr15:26914485
|
A | T | 1 | a0001c0002t0001g0133 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.498-318A>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26914485 | ||||||
| chr15:26914679
|
G | C | 1 | a0001c0001t0001g0114 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.498-124G>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 6/10 | chr15 | 26914679 | ||||||
| chr15:26915097
|
A | C | 1 | a0001c0001t0001g0099 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.580+212A>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26915097 | ||||||
| chr15:26915388
|
C | T | 136 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(133): Show | 139 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.580+503C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26915388 | ||||||
| chr15:26915586
|
G | T | 134 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(131): Show | 137 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.580+701G>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26915586 | ||||||
| chr15:26915653
|
T | C | 1 | a0001c0002t0001g0122 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.580+768T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26915653 | ||||||
| chr15:26915795
|
G | A | 15 | a0001c0001t0001g0050a0001c0001t0001g0054a0001c0001t0001g0083others(12): Show | 15 | HG02015.hp2 HG02027.hp1 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.580+910G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26915795 | ||||||
| chr15:26915891
|
A | G | 8 | a0001c0003t0001g0154a0001c0003t0001g0192a0001c0003t0001g0239others(5): Show | 8 | HG00733.hp1 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.580+1006A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26915891 | ||||||
| chr15:26915979
|
C | T | 180 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0019others(177): Show | 183 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.580+1094C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26915979 | ||||||
| chr15:26915990
|
G | A | 3 | a0001c0001t0001g0152a0001c0002t0001g0027a0001c0002t0001g0051 | 3 | HG02922.hp1 HG02922.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.580+1105G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26915990 | ||||||
| chr15:26916914
|
G | A | 30 | a0001c0001t0001g0016a0001c0001t0001g0034a0001c0001t0001g0052others(27): Show | 30 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.580+2029G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26916914 | ||||||
| chr15:26917053
|
C | T | 1 | a0001c0003t0001g0073 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.580+2168C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26917053 | ||||||
| chr15:26917080
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.580+2195G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26917080 | ||||||
| chr15:26917116
|
G | A | 1 | a0001c0001t0001g0006 | 2 | HG01515.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.580+2231G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26917116 | ||||||
| chr15:26917215
|
A | G | 1 | a0001c0002t0001g0265 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.580+2330A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26917215 | ||||||
| chr15:26917266
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.580+2381G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26917266 | ||||||
| chr15:26917433
|
T | C | 2 | a0001c0002t0001g0121a0001c0002t0001g0206 | 2 | HG02257.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.580+2548T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26917433 | ||||||
| chr15:26917445
|
A | C | 4 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0087others(1): Show | 4 | HG01496.hp2 HG02809.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.580+2560A>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26917445 | ||||||
| chr15:26917448
|
G | T | 1 | a0001c0001t0001g0365 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.580+2563G>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26917448 | ||||||
| chr15:26917768
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.580+2883T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26917768 | ||||||
| chr15:26918447
|
C | T | 1 | a0001c0002t0001g0352 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.580+3562C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26918447 | ||||||
| chr15:26918515
|
G | T | 8 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0046others(5): Show | 8 | HG01099.hp2 HG02055.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.580+3630G>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26918515 | ||||||
| chr15:26918530
|
C | T | 1 | a0001c0002t0001g0258 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.580+3645C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26918530 | ||||||
| chr15:26918547
|
G | T | 1 | a0001c0001t0001g0264 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.580+3662G>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26918547 | ||||||
| chr15:26918648
|
C | T | 2 | a0001c0002t0001g0121a0001c0002t0001g0206 | 2 | HG02257.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.580+3763C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26918648 | ||||||
| chr15:26918829
|
T | C | 175 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0019others(172): Show | 178 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.580+3944T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26918829 | ||||||
| chr15:26918966
|
C | A | 21 | a0001c0001t0001g0004a0001c0001t0001g0060a0001c0001t0001g0114others(18): Show | 21 | HG01109.hp2 HG01891.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.580+4081C>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26918966 | ||||||
| chr15:26918981
|
AC | A | 3 | a0001c0001t0003g0302a0001c0002t0001g0121a0001c0002t0001g0206 | 3 | HG02257.hp1 HG02572.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.580+4097delC | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26918981 | ||||||
| chr15:26918982
|
C | A | 313 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(310): Show | 319 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.580+4097C>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26918982 | ||||||
| chr15:26919032
|
A | G | 1 | a0001c0001t0001g0032 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.580+4147A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26919032 | ||||||
| chr15:26919051
|
A | T | 30 | a0001c0001t0001g0016a0001c0001t0001g0034a0001c0001t0001g0052others(27): Show | 30 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.580+4166A>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26919051 | ||||||
| chr15:26919121
|
C | T | 1 | a0001c0002t0001g0149 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.580+4236C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26919121 | ||||||
| chr15:26919126
|
G | T | 33 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0020others(30): Show | 33 | HG01109.hp2 HG01496.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.580+4241G>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26919126 | ||||||
| chr15:26919127
|
T | C | 1 | a0001c0001t0001g0055 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.580+4242T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26919127 | ||||||
| chr15:26919149
|
C | CA | 175 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0019others(172): Show | 178 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.580+4268dupA | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 26919149 | |||||
| chr15:26919154
|
C | A | 175 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0019others(172): Show | 178 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.580+4269C>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26919154 | ||||||
| chr15:26919296
|
T | C | 1 | a0001c0001t0001g0157 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.580+4411T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26919296 | ||||||
| chr15:26919353
|
A | AT | 172 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0019others(169): Show | 175 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.580+4476dupT | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 26919353 | |||||
| chr15:26919421
|
C | T | 30 | a0001c0001t0001g0016a0001c0001t0001g0034a0001c0001t0001g0052others(27): Show | 30 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.580+4536C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26919421 | ||||||
| chr15:26919498
|
A | G | 97 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(94): Show | 100 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.580+4613A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26919498 | ||||||
| chr15:26919597
|
T | TTTGCCTT others(6537): Show |
1 | a0001c0002t0001g0121 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.580+4728_580+4729i others(6546): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 26919597 | |||||
| chr15:26919650
|
C | A | 1 | a0001c0001t0001g0292 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.580+4765C>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26919650 | ||||||
| chr15:26919665
|
CTTTA | C | 3 | a0001c0002t0001g0097a0001c0002t0001g0228a0001c0002t0001g0338 | 3 | HG01099.hp1 HG01361.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.580+4784_580+4787d others(6): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 26919665 | |||||
| chr15:26919707
|
A | G | 1 | a0001c0001t0001g0196 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.580+4822A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26919707 | ||||||
| chr15:26919744
|
G | T | 8 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0046others(5): Show | 8 | HG01099.hp2 HG02055.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.580+4859G>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26919744 | ||||||
| chr15:26919769
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.580+4884C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26919769 | ||||||
| chr15:26919849
|
G | A | 30 | a0001c0001t0001g0016a0001c0001t0001g0034a0001c0001t0001g0052others(27): Show | 30 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.580+4964G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26919849 | ||||||
| chr15:26919955
|
T | TA | 111 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(108): Show | 114 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.580+5079dupA | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 26919955 | |||||
| chr15:26920032
|
T | C | 53 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0030others(50): Show | 54 | HG00140.hp1 HG00423.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.580+5147T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26920032 | ||||||
| chr15:26920155
|
CA | C | 5 | a0001c0001t0001g0163a0001c0002t0001g0129a0001c0002t0001g0130others(2): Show | 5 | HG02615.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.580+5271delA | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26920155 | ||||||
| chr15:26920180
|
T | TTTG | 4 | a0001c0001t0001g0029a0001c0001t0001g0060a0001c0006t0001g0271others(1): Show | 4 | HG02280.hp1 HG02630.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.580+5319_580+5321d others(5): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 26920180 | |||||
| chr15:26920466
|
T | C | 1 | a0001c0002t0001g0325 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.580+5581T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26920466 | ||||||
| chr15:26920484
|
T | G | 1 | a0001c0002t0001g0035 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.580+5599T>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26920484 | ||||||
| chr15:26920535
|
T | C | 6 | a0001c0001t0001g0094a0001c0001t0001g0156a0001c0001t0001g0185others(3): Show | 6 | HG00621.hp2 HG02080.hp2 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.580+5650T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26920535 | ||||||
| chr15:26921350
|
C | T | 5 | a0001c0001t0001g0048a0001c0001t0001g0366a0001c0003t0001g0066others(2): Show | 5 | HG02257.hp2 HG02965.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.580+6465C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26921350 | ||||||
| chr15:26921472
|
G | A | 1 | a0001c0002t0001g0051 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.580+6587G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26921472 | ||||||
| chr15:26921483
|
G | A | 1 | a0001c0002t0001g0339 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.580+6598G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26921483 | ||||||
| chr15:26921530
|
T | A | 189 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0019others(186): Show | 192 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.580+6645T>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26921530 | ||||||
| chr15:26921531
|
C | A | 2 | a0001c0001t0001g0030a0001c0002t0001g0352 | 2 | HG03710.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.580+6646C>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26921531 | ||||||
| chr15:26921648
|
T | C | 202 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0016others(199): Show | 205 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.580+6763T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26921648 | ||||||
| chr15:26921671
|
CA | C | 8 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0046others(5): Show | 8 | HG01099.hp2 HG02055.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.580+6788delA | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 26921671 | |||||
| chr15:26921867
|
T | C | 1 | a0001c0002t0001g0109 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.580+6982T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26921867 | ||||||
| chr15:26921951
|
G | A | 189 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0019others(186): Show | 192 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.580+7066G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26921951 | ||||||
| chr15:26921994
|
T | C | 5 | a0001c0001t0001g0048a0001c0001t0001g0366a0001c0003t0001g0066others(2): Show | 5 | HG02257.hp2 HG02965.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.580+7109T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26921994 | ||||||
| chr15:26922001
|
A | G | 41 | a0001c0001t0001g0029a0001c0001t0001g0067a0001c0001t0001g0072others(38): Show | 43 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(40): Show |
intron_variant | MODIFIER | c.580+7116A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26922001 | ||||||
| chr15:26922568
|
T | C | 328 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(325): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.580+7683T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26922568 | ||||||
| chr15:26922652
|
G | A | 1 | a0001c0005t0001g0183 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.580+7767G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26922652 | ||||||
| chr15:26922687
|
AT | A | 153 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0020others(150): Show | 156 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.580+7805delT | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 26922687 | |||||
| chr15:26922726
|
C | G | 141 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0028others(138): Show | 144 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.580+7841C>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26922726 | ||||||
| chr15:26922744
|
T | C | 1 | a0001c0002t0001g0141 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.580+7859T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26922744 | ||||||
| chr15:26922850
|
T | C | 1 | a0001c0001t0001g0203 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.580+7965T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26922850 | ||||||
| chr15:26922941
|
A | G | 21 | a0001c0001t0001g0004a0001c0001t0001g0060a0001c0001t0001g0114others(18): Show | 21 | HG01109.hp2 HG01891.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.580+8056A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26922941 | ||||||
| chr15:26922957
|
G | T | 316 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(313): Show | 322 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.580+8072G>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26922957 | ||||||
| chr15:26923078
|
T | C | 1 | a0001c0001t0001g0112 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.580+8193T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26923078 | ||||||
| chr15:26923340
|
T | C | 210 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0016others(207): Show | 213 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.580+8455T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26923340 | ||||||
| chr15:26923511
|
CT | C | 210 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0016others(207): Show | 213 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.580+8635delT | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 26923511 | |||||
| chr15:26923610
|
T | A | 1 | a0001c0001t0001g0074 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.580+8725T>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26923610 | ||||||
| chr15:26923912
|
A | AT | 31 | a0001c0001t0001g0016a0001c0001t0001g0034a0001c0001t0001g0052others(28): Show | 31 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.580+9036dupT | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 26923912 | |||||
| chr15:26923940
|
G | C | 1 | a0001c0001t0003g0302 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.580+9055G>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26923940 | ||||||
| chr15:26924108
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.580+9223C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26924108 | ||||||
| chr15:26924158
|
C | CT | 12 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0087others(9): Show | 12 | HG01071.hp2 HG01099.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.580+9290dupT | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 26924158 | |||||
| chr15:26924158
|
C | CTT | 91 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0028others(88): Show | 92 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.580+9289_580+9290d others(4): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 26924158 | |||||
| chr15:26924158
|
C | CTTTT | 6 | a0001c0001t0001g0163a0001c0001t0001g0365a0001c0002t0001g0129others(3): Show | 6 | HG02615.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.580+9287_580+9290d others(6): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 26924158 | |||||
| chr15:26924158
|
CT | C | 113 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(110): Show | 116 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.580+9290delT | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 26924158 | |||||
| chr15:26924158
|
CTT | C | 6 | a0001c0001t0001g0169a0001c0002t0001g0051a0001c0002t0001g0321others(3): Show | 6 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.580+9289_580+9290d others(4): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 26924158 | |||||
| chr15:26924309
|
T | A | 30 | a0001c0001t0001g0016a0001c0001t0001g0034a0001c0001t0001g0052others(27): Show | 30 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.580+9424T>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26924309 | ||||||
| chr15:26924554
|
C | T | 12 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0048others(9): Show | 12 | HG01496.hp2 HG02257.hp2 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.580+9669C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26924554 | ||||||
| chr15:26924609
|
C | T | 1 | a0001c0002t0001g0027 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.580+9724C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26924609 | ||||||
| chr15:26924720
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.580+9835G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26924720 | ||||||
| chr15:26924729
|
G | C | 106 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0028others(103): Show | 107 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.580+9844G>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26924729 | ||||||
| chr15:26924747
|
G | A | 1 | a0001c0002t0001g0273 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.580+9862G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26924747 | ||||||
| chr15:26924922
|
C | G | 1 | a0001c0001t0001g0110 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.580+10037C>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26924922 | ||||||
| chr15:26924927
|
C | A | 1 | a0001c0001t0001g0314 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.580+10042C>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26924927 | ||||||
| chr15:26924931
|
C | T | 2 | a0001c0001t0001g0191a0001c0003t0001g0047 | 2 | HG01109.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.580+10046C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26924931 | ||||||
| chr15:26924970
|
A | C | 6 | a0001c0001t0001g0215a0001c0001t0001g0255a0001c0001t0001g0307others(3): Show | 6 | HG02015.hp1 HG03834.hp2 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.580+10085A>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26924970 | ||||||
| chr15:26925038
|
A | G | 1 | a0001c0001t0001g0306 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.580+10153A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26925038 | ||||||
| chr15:26925114
|
T | G | 1 | a0001c0002t0001g0123 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.580+10229T>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26925114 | ||||||
| chr15:26925206
|
T | A | 189 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0019others(186): Show | 192 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.580+10321T>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26925206 | ||||||
| chr15:26925230
|
T | A | 10 | a0001c0001t0001g0060a0001c0001t0001g0114a0001c0001t0001g0151others(7): Show | 10 | HG01891.hp1 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.580+10345T>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26925230 | ||||||
| chr15:26925270
|
C | A | 1 | a0001c0002t0001g0358 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.580+10385C>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26925270 | ||||||
| chr15:26925676
|
C | T | 2 | a0001c0002t0001g0249a0001c0002t0001g0330 | 2 | NA18612.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.580+10791C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26925676 | ||||||
| chr15:26925754
|
G | T | 97 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(94): Show | 100 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.580+10869G>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26925754 | ||||||
| chr15:26925838
|
T | C | 316 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(313): Show | 322 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.580+10953T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26925838 | ||||||
| chr15:26926001
|
T | C | 316 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(313): Show | 322 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.580+11116T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26926001 | ||||||
| chr15:26926220
|
C | T | 6 | a0001c0001t0001g0163a0001c0002t0001g0129a0001c0002t0001g0130others(3): Show | 6 | HG02615.hp1 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.581-10965C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26926220 | ||||||
| chr15:26926442
|
A | G | 159 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0020others(156): Show | 162 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.581-10743A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26926442 | ||||||
| chr15:26926701
|
C | CTT | 210 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0016others(207): Show | 213 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.581-10483_581-1048 others(6): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 26926701 | |||||
| chr15:26926797
|
G | A | 189 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0019others(186): Show | 192 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.581-10388G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26926797 | ||||||
| chr15:26926869
|
C | T | 10 | a0001c0001t0001g0060a0001c0001t0001g0114a0001c0001t0001g0151others(7): Show | 10 | HG01891.hp1 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.581-10316C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26926869 | ||||||
| chr15:26926876
|
T | A | 210 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0016others(207): Show | 213 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.581-10309T>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26926876 | ||||||
| chr15:26926882
|
T | C | 30 | a0001c0001t0001g0016a0001c0001t0001g0034a0001c0001t0001g0052others(27): Show | 30 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.581-10303T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26926882 | ||||||
| chr15:26926945
|
A | G | 9 | a0001c0001t0001g0004a0001c0001t0001g0204a0001c0001t0001g0205others(6): Show | 9 | HG01109.hp2 HG02451.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.581-10240A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26926945 | ||||||
| chr15:26926982
|
C | A | 21 | a0001c0001t0001g0004a0001c0001t0001g0060a0001c0001t0001g0114others(18): Show | 21 | HG01109.hp2 HG01891.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.581-10203C>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26926982 | ||||||
| chr15:26927196
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.581-9989C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26927196 | ||||||
| chr15:26927270
|
A | AT | 150 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0026others(147): Show | 151 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.581-9900dupT | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 26927270 | |||||
| chr15:26927270
|
A | ATT | 43 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0067others(40): Show | 45 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(42): Show |
intron_variant | MODIFIER | c.581-9901_581-9900d others(4): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 26927270 | |||||
| chr15:26927270
|
AT | A | 6 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0065others(3): Show | 6 | HG02055.hp2 NA18955.hp2 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.581-9900delT | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 26927270 | |||||
| chr15:26927424
|
A | G | 98 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0028others(95): Show | 99 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.581-9761A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26927424 | ||||||
| chr15:26927553
|
G | C | 1 | a0001c0003t0001g0111 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.581-9632G>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26927553 | ||||||
| chr15:26927622
|
A | G | 1 | a0001c0004t0001g0167 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.581-9563A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26927622 | ||||||
| chr15:26927710
|
T | C | 1 | a0001c0001t0001g0050 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.581-9475T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26927710 | ||||||
| chr15:26927873
|
G | A | 12 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0048others(9): Show | 12 | HG01496.hp2 HG02257.hp2 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.581-9312G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26927873 | ||||||
| chr15:26928010
|
G | A | 5 | a0001c0001t0001g0048a0001c0001t0001g0366a0001c0003t0001g0066others(2): Show | 5 | HG02257.hp2 HG02965.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.581-9175G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26928010 | ||||||
| chr15:26928132
|
G | A | 1 | a0001c0004t0001g0268 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.581-9053G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26928132 | ||||||
| chr15:26928217
|
C | T | 5 | a0001c0001t0001g0048a0001c0001t0001g0366a0001c0003t0001g0066others(2): Show | 5 | HG02257.hp2 HG02965.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.581-8968C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26928217 | ||||||
| chr15:26928394
|
G | A | 12 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0032others(9): Show | 12 | HG01496.hp2 HG02257.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.581-8791G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26928394 | ||||||
| chr15:26928511
|
A | G | 8 | a0001c0001t0001g0114a0001c0001t0001g0151a0001c0001t0001g0367others(5): Show | 8 | HG01891.hp1 HG02615.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.581-8674A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26928511 | ||||||
| chr15:26928536
|
C | T | 25 | a0001c0001t0001g0034a0001c0001t0001g0052a0001c0001t0001g0093others(22): Show | 25 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.581-8649C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26928536 | ||||||
| chr15:26928551
|
G | A | 2 | a0001c0001t0001g0207a0001c0001t0001g0349 | 2 | HG02083.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.581-8634G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26928551 | ||||||
| chr15:26928569
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.581-8616C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26928569 | ||||||
| chr15:26928695
|
T | C | 6 | a0001c0001t0001g0163a0001c0002t0001g0129a0001c0002t0001g0130others(3): Show | 6 | HG02615.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.581-8490T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26928695 | ||||||
| chr15:26928724
|
A | C | 1 | a0001c0001t0001g0048 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.581-8461A>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26928724 | ||||||
| chr15:26928729
|
A | G | 214 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(211): Show | 218 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.581-8456A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26928729 | ||||||
| chr15:26928735
|
C | T | 314 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(311): Show | 320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.581-8450C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26928735 | ||||||
| chr15:26928744
|
G | A | 1 | a0001c0001t0001g0309 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.581-8441G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26928744 | ||||||
| chr15:26928976
|
C | T | 1 | a0001c0005t0001g0280 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.581-8209C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26928976 | ||||||
| chr15:26929034
|
G | C | 5 | a0001c0001t0001g0163a0001c0002t0001g0129a0001c0002t0001g0130others(2): Show | 5 | HG02615.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.581-8151G>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26929034 | ||||||
| chr15:26929037
|
G | A | 49 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0022others(46): Show | 51 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.581-8148G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26929037 | ||||||
| chr15:26929039
|
ACACAGTT others(11): Show |
A | 47 | a0001c0001t0001g0067a0001c0001t0001g0072a0001c0001t0001g0074others(44): Show | 49 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.581-8141_581-8124d others(20): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 26929039 | |||||
| chr15:26929394
|
G | C | 4 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0087others(1): Show | 4 | HG01496.hp2 HG02809.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.581-7791G>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26929394 | ||||||
| chr15:26929463
|
T | G | 45 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0022others(42): Show | 47 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.581-7722T>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26929463 | ||||||
| chr15:26929523
|
C | G | 1 | a0001c0003t0001g0217 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.581-7662C>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26929523 | ||||||
| chr15:26929527
|
T | G | 1 | a0001c0003t0001g0180 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.581-7658T>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26929527 | ||||||
| chr15:26929640
|
T | C | 5 | a0001c0001t0001g0060a0001c0003t0001g0239a0001c0003t0008g0009others(2): Show | 5 | HG02258.hp1 HG02280.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.581-7545T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26929640 | ||||||
| chr15:26929646
|
G | A | 6 | a0001c0001t0001g0163a0001c0001t0001g0169a0001c0002t0001g0129others(3): Show | 6 | HG02615.hp1 HG02622.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.581-7539G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26929646 | ||||||
| chr15:26929819
|
T | G | 1 | a0001c0001t0001g0162 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.581-7366T>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26929819 | ||||||
| chr15:26929951
|
G | C | 1 | a0001c0001t0001g0069 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.581-7234G>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26929951 | ||||||
| chr15:26929982
|
TTTC | T | 3 | a0001c0002t0001g0129a0001c0002t0001g0130a0001c0007t0001g0014 | 3 | HG00642.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.581-7179_581-7177d others(5): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 26929982 | |||||
| chr15:26930000
|
C | T | 60 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(57): Show | 63 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.581-7185C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26930000 | ||||||
| chr15:26930003
|
C | T | 61 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(58): Show | 64 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.581-7182C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26930003 | ||||||
| chr15:26930006
|
C | CTTCTTTT others(7): Show |
1 | a0001c0001t0001g0093 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.581-7177_581-7176i others(16): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 26930006 | |||||
| chr15:26930006
|
C | CTTTTTTT others(3): Show |
3 | a0001c0001t0001g0275a0001c0001t0001g0288a0001c0002t0001g0101 | 3 | NA19054.hp2 NA19074.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.581-7172_581-7163d others(12): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 26930006 | |||||
| chr15:26930006
|
C | CTTTTTTT others(4): Show |
22 | a0001c0001t0001g0034a0001c0001t0001g0052a0001c0001t0001g0059others(19): Show | 22 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(19): Show |
intron_variant | MODIFIER | c.581-7173_581-7163d others(13): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 26930006 | |||||
| chr15:26930006
|
C | T | 61 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(58): Show | 64 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.581-7179C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26930006 | ||||||
| chr15:26930006
|
CT | C | 109 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0019others(106): Show | 110 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.581-7163delT | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 26930006 | |||||
| chr15:26930006
|
CTT | C | 49 | a0001c0001t0001g0008a0001c0001t0001g0063a0001c0001t0001g0064others(46): Show | 52 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.581-7164_581-7163d others(4): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 26930006 | |||||
| chr15:26930007
|
T | TTC | 11 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0062others(8): Show | 11 | HG00423.hp2 HG02622.hp1 HG02735.hp2 others(8): Show |
intron_variant | MODIFIER | c.581-7177_581-7176i others(4): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 26930007 | |||||
| chr15:26930010
|
T | C | 1 | a0001c0001t0001g0313 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.581-7175T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26930010 | ||||||
| chr15:26930012
|
T | TTTTTTTT others(4): Show |
2 | a0001c0001t0001g0098a0001c0002t0001g0297 | 2 | NA18968.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.581-7166_581-7156d others(13): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 26930012 | |||||
| chr15:26930016
|
T | G | 76 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0017others(73): Show | 78 | HG00099.hp2 HG00423.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.581-7169T>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26930016 | ||||||
| chr15:26930016
|
T | TG | 5 | a0001c0001t0001g0006a0001c0001t0001g0233a0001c0001t0001g0348others(2): Show | 6 | HG01515.hp2 HG03209.hp2 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.581-7169_581-7168i others(3): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26930016 | ||||||
| chr15:26930016
|
T | TTTTTTTT others(2): Show |
6 | a0001c0001t0001g0060a0001c0003t0001g0107a0001c0003t0001g0239others(3): Show | 6 | HG02258.hp1 HG02280.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.581-7163_581-7162i others(11): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 26930016 | |||||
| chr15:26930016
|
T | TTTTTTTT others(3): Show |
12 | a0001c0001t0001g0026a0001c0001t0001g0072a0001c0001t0001g0114others(9): Show | 12 | HG01891.hp1 HG02615.hp2 HG02896.hp2 others(9): Show |
intron_variant | MODIFIER | c.581-7163_581-7162i others(12): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 26930016 | |||||
| chr15:26930016
|
T | TTTTTTTT others(4): Show |
1 | a0001c0003t0001g0285 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.581-7163_581-7162i others(13): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 26930016 | |||||
| chr15:26930126
|
C | T | 4 | a0001c0001t0001g0163a0001c0001t0001g0169a0001c0003t0001g0150others(1): Show | 4 | HG02615.hp1 HG02622.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.581-7059C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26930126 | ||||||
| chr15:26930162
|
G | A | 2 | a0001c0001t0003g0302a0001c0004t0001g0202 | 2 | HG03209.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.581-7023G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26930162 | ||||||
| chr15:26930170
|
G | T | 2 | a0001c0001t0001g0169a0002c0009t0001g0128 | 2 | HG02615.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.581-7015G>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26930170 | ||||||
| chr15:26930190
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.581-6995T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26930190 | ||||||
| chr15:26930250
|
T | C | 2 | a0001c0001t0001g0225a0001c0001t0001g0324 | 2 | HG00280.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.581-6935T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26930250 | ||||||
| chr15:26930268
|
A | G | 3 | a0001c0004t0002g0125a0001c0004t0002g0127a0001c0005t0001g0126 | 3 | HG01070.hp1 HG01071.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.581-6917A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26930268 | ||||||
| chr15:26930343
|
C | G | 1 | a0001c0003t0001g0057 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.581-6842C>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26930343 | ||||||
| chr15:26930349
|
C | T | 1 | a0001c0004t0001g0012 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.581-6836C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26930349 | ||||||
| chr15:26930360
|
A | G | 4 | a0001c0001t0001g0255a0001c0001t0001g0307a0001c0001t0001g0319others(1): Show | 4 | HG03834.hp2 NA18943.hp1 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.581-6825A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26930360 | ||||||
| chr15:26930538
|
G | T | 28 | a0001c0001t0001g0034a0001c0001t0001g0052a0001c0001t0001g0059others(25): Show | 28 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(25): Show |
intron_variant | MODIFIER | c.581-6647G>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26930538 | ||||||
| chr15:26930556
|
C | T | 1 | a0001c0002t0001g0143 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.581-6629C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26930556 | ||||||
| chr15:26930589
|
C | G | 1 | a0001c0007t0001g0014 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.581-6596C>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26930589 | ||||||
| chr15:26930623
|
T | A | 319 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(316): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.581-6562T>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26930623 | ||||||
| chr15:26930895
|
C | CT | 24 | a0001c0001t0001g0072a0001c0001t0001g0085a0001c0001t0001g0106others(21): Show | 24 | HG01891.hp1 HG01891.hp2 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.581-6272dupT | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 26930895 | |||||
| chr15:26930895
|
CT | C | 92 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(89): Show | 96 | HG00099.hp2 HG00423.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.581-6272delT | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 26930895 | |||||
| chr15:26930895
|
CTT | C | 11 | a0001c0001t0001g0080a0001c0001t0001g0163a0001c0001t0001g0169others(8): Show | 11 | HG00609.hp1 HG02451.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.581-6273_581-6272d others(4): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 26930895 | |||||
| chr15:26930912
|
T | C | 1 | a0001c0002t0001g0175 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.581-6273T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26930912 | ||||||
| chr15:26931065
|
T | A | 134 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0028others(131): Show | 135 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.581-6120T>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26931065 | ||||||
| chr15:26931070
|
A | AT | 5 | a0001c0001t0001g0060a0001c0003t0001g0239a0001c0003t0008g0009others(2): Show | 5 | HG02258.hp1 HG02280.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.581-6107dupT | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 26931070 | |||||
| chr15:26931191
|
G | A | 1 | a0001c0002t0001g0051 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.581-5994G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26931191 | ||||||
| chr15:26931192
|
C | A | 12 | a0001c0001t0001g0026a0001c0001t0001g0072a0001c0001t0001g0114others(9): Show | 12 | HG01891.hp1 HG02615.hp2 HG02896.hp2 others(9): Show |
intron_variant | MODIFIER | c.581-5993C>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26931192 | ||||||
| chr15:26931265
|
T | C | 45 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0022others(42): Show | 47 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.581-5920T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26931265 | ||||||
| chr15:26931290
|
C | T | 30 | a0001c0001t0001g0034a0001c0001t0001g0052a0001c0001t0001g0059others(27): Show | 30 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.581-5895C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26931290 | ||||||
| chr15:26931480
|
C | G | 183 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0026others(180): Show | 184 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.581-5705C>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26931480 | ||||||
| chr15:26931598
|
G | A | 3 | a0001c0001t0001g0281a0001c0001t0001g0340a0001c0002t0001g0123 | 3 | HG00738.hp2 HG02738.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.581-5587G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26931598 | ||||||
| chr15:26931636
|
G | A | 30 | a0001c0001t0001g0034a0001c0001t0001g0052a0001c0001t0001g0059others(27): Show | 30 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.581-5549G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26931636 | ||||||
| chr15:26931759
|
G | A | 9 | a0001c0001t0001g0055a0001c0001t0001g0220a0001c0001t0001g0351others(6): Show | 9 | HG01123.hp1 HG02273.hp2 NA18949.hp1 others(6): Show |
intron_variant | MODIFIER | c.581-5426G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26931759 | ||||||
| chr15:26931766
|
C | T | 2 | a0001c0006t0001g0182a0001c0006t0001g0238 | 2 | HG01257.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.581-5419C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26931766 | ||||||
| chr15:26931991
|
T | C | 1 | a0001c0001t0001g0110 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.581-5194T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26931991 | ||||||
| chr15:26932035
|
A | G | 46 | a0001c0001t0001g0008a0001c0001t0001g0063a0001c0001t0001g0064others(43): Show | 49 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.581-5150A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26932035 | ||||||
| chr15:26932089
|
C | A | 4 | a0001c0001t0001g0225a0001c0001t0001g0324a0001c0002t0001g0332others(1): Show | 4 | HG00280.hp2 HG01123.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.581-5096C>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26932089 | ||||||
| chr15:26932168
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.581-5017C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26932168 | ||||||
| chr15:26932718
|
G | A | 2 | a0001c0002t0001g0332a0001c0002t0001g0337 | 2 | HG01993.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.581-4467G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26932718 | ||||||
| chr15:26932779
|
G | A | 1 | a0001c0001t0001g0215 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.581-4406G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26932779 | ||||||
| chr15:26932821
|
C | T | 17 | a0001c0001t0001g0067a0001c0001t0001g0074a0001c0001t0001g0162others(14): Show | 17 | HG00733.hp1 HG02257.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.581-4364C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26932821 | ||||||
| chr15:26932840
|
C | T | 1 | a0001c0006t0001g0182 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.581-4345C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26932840 | ||||||
| chr15:26932956
|
C | G | 304 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(301): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.581-4229C>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26932956 | ||||||
| chr15:26933099
|
TA | T | 198 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(195): Show | 200 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.581-4070delA | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 26933099 | |||||
| chr15:26933127
|
T | C | 1 | a0001c0001t0001g0215 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.581-4058T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26933127 | ||||||
| chr15:26933216
|
A | G | 4 | a0001c0001t0001g0163a0001c0001t0001g0169a0001c0003t0001g0150others(1): Show | 4 | HG02615.hp1 HG02622.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.581-3969A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26933216 | ||||||
| chr15:26933263
|
G | A | 1 | a0001c0001t0001g0034 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.581-3922G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26933263 | ||||||
| chr15:26933284
|
G | A | 12 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0046others(9): Show | 12 | HG01099.hp2 HG02055.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.581-3901G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26933284 | ||||||
| chr15:26933288
|
C | T | 3 | a0001c0001t0001g0067a0001c0001t0001g0162a0001c0001t0001g0243 | 3 | HG02717.hp2 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.581-3897C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26933288 | ||||||
| chr15:26933328
|
C | T | 2 | a0001c0002t0001g0144a0001c0002t0001g0265 | 2 | HG01433.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.581-3857C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26933328 | ||||||
| chr15:26933404
|
T | C | 1 | a0001c0001t0001g0288 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.581-3781T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26933404 | ||||||
| chr15:26933760
|
G | A | 1 | a0001c0002t0001g0227 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.581-3425G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26933760 | ||||||
| chr15:26933803
|
A | G | 1 | a0001c0001t0001g0008 | 2 | HG00738.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.581-3382A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26933803 | ||||||
| chr15:26933869
|
T | G | 31 | a0001c0001t0001g0016a0001c0001t0001g0034a0001c0001t0001g0052others(28): Show | 31 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.581-3316T>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26933869 | ||||||
| chr15:26934018
|
T | C | 233 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(230): Show | 236 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.581-3167T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26934018 | ||||||
| chr15:26934032
|
C | T | 5 | a0001c0001t0001g0060a0001c0003t0001g0239a0001c0003t0008g0009others(2): Show | 5 | HG02258.hp1 HG02280.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.581-3153C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26934032 | ||||||
| chr15:26934056
|
C | T | 31 | a0001c0001t0001g0016a0001c0001t0001g0034a0001c0001t0001g0052others(28): Show | 31 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.581-3129C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26934056 | ||||||
| chr15:26934082
|
A | G | 234 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(231): Show | 237 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.581-3103A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26934082 | ||||||
| chr15:26934230
|
T | C | 304 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(301): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.581-2955T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26934230 | ||||||
| chr15:26934248
|
TA | T | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(188): Show | 194 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.581-2918delA | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 26934248 | |||||
| chr15:26934248
|
TAA | T | 10 | a0001c0001t0001g0161a0001c0001t0001g0308a0001c0001t0001g0341others(7): Show | 10 | HG00735.hp2 HG01070.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.581-2919_581-2918d others(4): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 26934248 | |||||
| chr15:26934264
|
A | G | 33 | a0001c0001t0001g0016a0001c0001t0001g0034a0001c0001t0001g0052others(30): Show | 33 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.581-2921A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26934264 | ||||||
| chr15:26934288
|
A | G | 184 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(181): Show | 187 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.581-2897A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26934288 | ||||||
| chr15:26934371
|
A | G | 21 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0029others(18): Show | 21 | HG00099.hp2 HG00735.hp1 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.581-2814A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26934371 | ||||||
| chr15:26934510
|
C | T | 6 | a0001c0001t0001g0001a0001c0001t0001g0084a0001c0001t0001g0085others(3): Show | 7 | NA18944.hp1 NA18957.hp2 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.581-2675C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26934510 | ||||||
| chr15:26934658
|
T | TA | 320 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(317): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.581-2527_581-2526i others(3): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26934658 | ||||||
| chr15:26934856
|
A | T | 203 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(200): Show | 206 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.581-2329A>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26934856 | ||||||
| chr15:26934874
|
G | T | 2 | a0001c0001t0003g0302a0001c0004t0001g0202 | 2 | HG03209.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.581-2311G>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26934874 | ||||||
| chr15:26934912
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.581-2273C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26934912 | ||||||
| chr15:26935015
|
A | ATGC | 233 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(230): Show | 236 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.581-2168_581-2167i others(5): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 26935015 | |||||
| chr15:26935053
|
C | A | 1 | a0001c0001t0001g0312 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.581-2132C>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26935053 | ||||||
| chr15:26935190
|
G | A | 10 | a0001c0001t0001g0029a0001c0001t0001g0152a0001c0001t0001g0191others(7): Show | 10 | HG00099.hp2 HG00735.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.581-1995G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26935190 | ||||||
| chr15:26935200
|
C | G | 1 | a0001c0001t0004g0092 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.581-1985C>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26935200 | ||||||
| chr15:26935268
|
G | T | 31 | a0001c0001t0001g0016a0001c0001t0001g0034a0001c0001t0001g0052others(28): Show | 31 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.581-1917G>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26935268 | ||||||
| chr15:26935442
|
C | T | 1 | a0001c0002t0001g0109 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.581-1743C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26935442 | ||||||
| chr15:26935594
|
T | A | 1 | a0001c0001t0001g0088 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.581-1591T>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26935594 | ||||||
| chr15:26935619
|
G | A | 6 | a0001c0001t0001g0152a0001c0001t0001g0191a0001c0002t0001g0136others(3): Show | 6 | HG00099.hp2 HG00735.hp1 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.581-1566G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26935619 | ||||||
| chr15:26935653
|
A | G | 95 | a0001c0001t0001g0004a0001c0001t0001g0028a0001c0001t0001g0032others(92): Show | 95 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.581-1532A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26935653 | ||||||
| chr15:26935654
|
C | T | 1 | a0001c0001t0001g0267 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.581-1531C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26935654 | ||||||
| chr15:26935656
|
C | T | 1 | a0001c0002t0001g0352 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.581-1529C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26935656 | ||||||
| chr15:26935768
|
C | T | 171 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(168): Show | 174 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(171): Show |
intron_variant | MODIFIER | c.581-1417C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26935768 | ||||||
| chr15:26935920
|
G | A | 1 | a0002c0008t0001g0011 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.581-1265G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26935920 | ||||||
| chr15:26936154
|
G | A | 8 | a0001c0001t0001g0046a0001c0001t0001g0163a0001c0003t0001g0013others(5): Show | 8 | HG01099.hp2 HG02615.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.581-1031G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26936154 | ||||||
| chr15:26936166
|
T | A | 1 | a0001c0001t0001g0110 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.581-1019T>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26936166 | ||||||
| chr15:26936254
|
A | G | 37 | a0001c0001t0001g0016a0001c0001t0001g0034a0001c0001t0001g0052others(34): Show | 37 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.581-931A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26936254 | ||||||
| chr15:26936358
|
A | C | 40 | a0001c0001t0001g0016a0001c0001t0001g0034a0001c0001t0001g0052others(37): Show | 40 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.581-827A>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26936358 | ||||||
| chr15:26936384
|
C | T | 2 | a0001c0001t0001g0048a0001c0001t0001g0162 | 2 | HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.581-801C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26936384 | ||||||
| chr15:26936404
|
C | T | 1 | a0001c0002t0001g0071 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.581-781C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26936404 | ||||||
| chr15:26936429
|
G | T | 24 | a0001c0001t0001g0048a0001c0001t0001g0110a0001c0001t0001g0114others(21): Show | 24 | HG01070.hp1 HG01071.hp2 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.581-756G>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26936429 | ||||||
| chr15:26936434
|
G | A | 4 | a0001c0004t0001g0012a0001c0004t0001g0167a0001c0004t0001g0202others(1): Show | 4 | HG02615.hp2 HG02647.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.581-751G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26936434 | ||||||
| chr15:26936450
|
T | C | 1 | a0001c0001t0001g0230 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.581-735T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26936450 | ||||||
| chr15:26936683
|
G | A | 1 | a0001c0002t0001g0206 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.581-502G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26936683 | ||||||
| chr15:26936827
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.581-358G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26936827 | ||||||
| chr15:26936987
|
G | C | 1 | a0001c0011t0001g0359 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.581-198G>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26936987 | ||||||
| chr15:26937018
|
A | G | 1 | a0001c0002t0001g0037 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.581-167A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26937018 | ||||||
| chr15:26937047
|
A | G | 1 | a0001c0001t0001g0110 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.581-138A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26937047 | ||||||
| chr15:26937065
|
G | A | 49 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0028others(46): Show | 50 | HG00280.hp2 HG01123.hp2 HG01257.hp2 others(47): Show |
intron_variant | MODIFIER | c.581-120G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 7/10 | chr15 | 26937065 | ||||||
| chr15:26937344
|
G | A | 1 | a0001c0005t0001g0126 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.724+16G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 8/10 | chr15 | 26937344 | ||||||
| chr15:26937509
|
A | G | 246 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(243): Show | 251 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.724+181A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 8/10 | chr15 | 26937509 | ||||||
| chr15:26937651
|
T | C | 123 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(120): Show | 124 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.724+323T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 8/10 | chr15 | 26937651 | ||||||
| chr15:26937896
|
A | G | 2 | a0001c0001t0001g0223a0001c0001t0001g0276 | 2 | HG00597.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.724+568A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 8/10 | chr15 | 26937896 | ||||||
| chr15:26937935
|
G | A | 1 | a0001c0002t0001g0229 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.724+607G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 8/10 | chr15 | 26937935 | ||||||
| chr15:26938100
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.724+772C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 8/10 | chr15 | 26938100 | ||||||
| chr15:26938430
|
G | A | 1 | a0001c0001t0001g0110 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.724+1102G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 8/10 | chr15 | 26938430 | ||||||
| chr15:26938442
|
C | T | 116 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(113): Show | 120 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.724+1114C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 8/10 | chr15 | 26938442 | ||||||
| chr15:26938689
|
G | A | 172 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0044others(169): Show | 174 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.725-1236G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 8/10 | chr15 | 26938689 | ||||||
| chr15:26938712
|
G | A | 7 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(4): Show | 7 | HG01891.hp2 HG02615.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.725-1213G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 8/10 | chr15 | 26938712 | ||||||
| chr15:26938717
|
A | G | 1 | a0001c0001t0001g0366 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.725-1208A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 8/10 | chr15 | 26938717 | ||||||
| chr15:26938764
|
A | G | 39 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0110others(36): Show | 39 | HG00733.hp1 HG01070.hp1 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.725-1161A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 8/10 | chr15 | 26938764 | ||||||
| chr15:26938828
|
C | T | 1 | a0001c0002t0001g0124 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.725-1097C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 8/10 | chr15 | 26938828 | ||||||
| chr15:26938834
|
C | T | 49 | a0001c0001t0001g0052a0001c0001t0001g0054a0001c0001t0001g0055others(46): Show | 49 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.725-1091C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 8/10 | chr15 | 26938834 | ||||||
| chr15:26938839
|
T | C | 1 | a0001c0002t0001g0144 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.725-1086T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 8/10 | chr15 | 26938839 | ||||||
| chr15:26939022
|
C | A | 19 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(16): Show | 19 | HG01109.hp2 HG01891.hp2 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.725-903C>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 8/10 | chr15 | 26939022 | ||||||
| chr15:26939041
|
C | T | 1 | a0001c0002t0001g0345 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.725-884C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 8/10 | chr15 | 26939041 | ||||||
| chr15:26939194
|
G | A | 1 | a0001c0002t0001g0344 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.725-731G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 8/10 | chr15 | 26939194 | ||||||
| chr15:26939245
|
C | T | 1 | a0001c0003t0001g0139 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.725-680C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 8/10 | chr15 | 26939245 | ||||||
| chr15:26939288
|
C | T | 122 | a0001c0001t0001g0072a0001c0001t0001g0367a0001c0001t0003g0168others(119): Show | 124 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.725-637C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 8/10 | chr15 | 26939288 | ||||||
| chr15:26939335
|
C | T | 122 | a0001c0001t0001g0072a0001c0001t0001g0367a0001c0001t0003g0168others(119): Show | 124 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.725-590C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 8/10 | chr15 | 26939335 | ||||||
| chr15:26939370
|
G | A | 122 | a0001c0001t0001g0072a0001c0001t0001g0367a0001c0001t0003g0168others(119): Show | 124 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.725-555G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 8/10 | chr15 | 26939370 | ||||||
| chr15:26939405
|
G | A | 1 | a0001c0001t0001g0308 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.725-520G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 8/10 | chr15 | 26939405 | ||||||
| chr15:26939435
|
A | G | 1 | a0001c0001t0001g0081 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.725-490A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 8/10 | chr15 | 26939435 | ||||||
| chr15:26939618
|
G | A | 1 | a0001c0001t0001g0320 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.725-307G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 8/10 | chr15 | 26939618 | ||||||
| chr15:26939620
|
G | A | 2 | a0001c0001t0001g0072a0001c0001t0003g0168 | 2 | HG03139.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.725-305G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 8/10 | chr15 | 26939620 | ||||||
| chr15:26939629
|
G | C | 1 | a0001c0002t0001g0214 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.725-296G>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 8/10 | chr15 | 26939629 | ||||||
| chr15:26940159
|
C | T | 7 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(4): Show | 7 | HG01891.hp2 HG02615.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.877+82C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 9/10 | chr15 | 26940159 | ||||||
| chr15:26940210
|
C | T | 5 | a0001c0002t0001g0138a0001c0007t0001g0014a0001c0007t0001g0301others(2): Show | 5 | HG00099.hp2 HG00642.hp2 HG00735.hp2 others(2): Show |
intron_variant | MODIFIER | c.877+133C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 9/10 | chr15 | 26940210 | ||||||
| chr15:26940301
|
T | C | 1 | a0002c0009t0001g0128 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.877+224T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 9/10 | chr15 | 26940301 | ||||||
| chr15:26940346
|
C | A | 1 | a0001c0002t0001g0037 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.877+269C>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 9/10 | chr15 | 26940346 | ||||||
| chr15:26940415
|
G | C | 1 | a0001c0002t0001g0332 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.877+338G>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 9/10 | chr15 | 26940415 | ||||||
| chr15:26940495
|
C | T | 1 | a0001c0001t0001g0054 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.877+418C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 9/10 | chr15 | 26940495 | ||||||
| chr15:26940509
|
C | T | 33 | a0001c0001t0001g0032a0001c0001t0001g0110a0001c0001t0001g0163others(30): Show | 33 | HG00733.hp1 HG01070.hp1 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.877+432C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 9/10 | chr15 | 26940509 | ||||||
| chr15:26940532
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.877+455C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 9/10 | chr15 | 26940532 | ||||||
| chr15:26940542
|
C | A | 2 | a0001c0002t0001g0173a0001c0002t0001g0344 | 2 | HG01192.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.877+465C>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 9/10 | chr15 | 26940542 | ||||||
| chr15:26940548
|
GTT | G | 39 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0110others(36): Show | 39 | HG00733.hp1 HG01070.hp1 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.877+474_877+475del others(2): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr15 | 26940548 | |||||
| chr15:26940939
|
T | G | 121 | a0001c0001t0001g0038a0001c0001t0001g0313a0001c0002t0001g0003others(118): Show | 123 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.877+862T>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 9/10 | chr15 | 26940939 | ||||||
| chr15:26940953
|
A | T | 1 | a0001c0002t0001g0141 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.877+876A>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 9/10 | chr15 | 26940953 | ||||||
| chr15:26941033
|
G | A | 1 | a0001c0002t0001g0051 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.877+956G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 9/10 | chr15 | 26941033 | ||||||
| chr15:26941128
|
A | G | 1 | a0001c0001t0001g0267 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.877+1051A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 9/10 | chr15 | 26941128 | ||||||
| chr15:26941265
|
C | T | 1 | a0001c0001t0001g0194 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.877+1188C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 9/10 | chr15 | 26941265 | ||||||
| chr15:26941347
|
G | T | 33 | a0001c0001t0001g0032a0001c0001t0001g0110a0001c0001t0001g0163others(30): Show | 33 | HG00733.hp1 HG01070.hp1 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.877+1270G>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 9/10 | chr15 | 26941347 | ||||||
| chr15:26941439
|
C | A | 1 | a0001c0001t0001g0110 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.877+1362C>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 9/10 | chr15 | 26941439 | ||||||
| chr15:26941502
|
C | T | 7 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(4): Show | 7 | HG01891.hp2 HG02615.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.877+1425C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 9/10 | chr15 | 26941502 | ||||||
| chr15:26941578
|
G | C | 1 | a0001c0002t0001g0265 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.877+1501G>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 9/10 | chr15 | 26941578 | ||||||
| chr15:26941702
|
C | T | 286 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(283): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.878-1513C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 9/10 | chr15 | 26941702 | ||||||
| chr15:26941794
|
C | G | 8 | a0001c0003t0001g0056a0001c0003t0001g0057a0001c0003t0001g0090others(5): Show | 8 | HG01109.hp2 HG02572.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.878-1421C>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 9/10 | chr15 | 26941794 | ||||||
| chr15:26941827
|
A | G | 53 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0052others(50): Show | 53 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.878-1388A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 9/10 | chr15 | 26941827 | ||||||
| chr15:26941837
|
A | G | 2 | a0001c0003t0001g0056a0001c0003t0001g0057 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.878-1378A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 9/10 | chr15 | 26941837 | ||||||
| chr15:26942085
|
G | A | 37 | a0001c0001t0001g0032a0001c0001t0001g0110a0001c0001t0001g0163others(34): Show | 37 | HG00733.hp1 HG01070.hp1 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.878-1130G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 9/10 | chr15 | 26942085 | ||||||
| chr15:26942115
|
G | T | 4 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0087others(1): Show | 4 | HG01496.hp2 HG02809.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.878-1100G>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 9/10 | chr15 | 26942115 | ||||||
| chr15:26942250
|
G | A | 1 | a0001c0001t0001g0263 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.878-965G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 9/10 | chr15 | 26942250 | ||||||
| chr15:26942368
|
G | T | 1 | a0001c0001t0001g0110 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.878-847G>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 9/10 | chr15 | 26942368 | ||||||
| chr15:26942377
|
G | T | 36 | a0001c0001t0001g0032a0001c0001t0001g0110a0001c0001t0001g0163others(33): Show | 36 | HG00733.hp1 HG01070.hp1 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.878-838G>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 9/10 | chr15 | 26942377 | ||||||
| chr15:26942468
|
C | T | 1 | a0001c0002t0001g0323 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.878-747C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 9/10 | chr15 | 26942468 | ||||||
| chr15:26942560
|
A | G | 6 | a0001c0001t0001g0048a0001c0001t0001g0243a0001c0001t0001g0264others(3): Show | 6 | HG02717.hp2 HG03139.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.878-655A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 9/10 | chr15 | 26942560 | ||||||
| chr15:26942579
|
T | C | 1 | a0002c0008t0001g0011 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.878-636T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 9/10 | chr15 | 26942579 | ||||||
| chr15:26942751
|
A | G | 1 | a0001c0001t0001g0314 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.878-464A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 9/10 | chr15 | 26942751 | ||||||
| chr15:26942816
|
G | C | 1 | a0001c0001t0001g0267 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.878-399G>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 9/10 | chr15 | 26942816 | ||||||
| chr15:26942912
|
C | T | 8 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(5): Show | 8 | HG01891.hp2 HG02055.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.878-303C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 9/10 | chr15 | 26942912 | ||||||
| chr15:26943036
|
A | AT | 51 | a0001c0001t0001g0016a0001c0001t0001g0052a0001c0001t0001g0054others(48): Show | 51 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.878-177dupT | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr15 | 26943036 | |||||
| chr15:26943062
|
C | T | 1 | a0001c0002t0001g0361 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.878-153C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 9/10 | chr15 | 26943062 | ||||||
| chr15:26943077
|
C | G | 19 | a0001c0001t0001g0029a0001c0003t0001g0056a0001c0003t0001g0057others(16): Show | 19 | HG01109.hp2 HG02258.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.878-138C>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 9/10 | chr15 | 26943077 | ||||||
| chr15:26943183
|
G | A | 1 | a0001c0003t0008g0009 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.878-32G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 9/10 | chr15 | 26943183 | ||||||
| chr15:26943188
|
T | A | 89 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(86): Show | 93 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.878-27T>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 9/10 | chr15 | 26943188 | ||||||
| chr15:26943206
|
C | A | 213 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(210): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.878-9C>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 9/10 | chr15 | 26943206 | ||||||
| chr15:26943526
|
G | A | 1 | a0001c0002t0001g0250 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1089+100G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 10/10 | chr15 | 26943526 | ||||||
| chr15:26943922
|
C | G | 1 | a0001c0004t0001g0268 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1089+496C>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 10/10 | chr15 | 26943922 | ||||||
| chr15:26944015
|
G | A | 3 | a0001c0002t0001g0078a0001c0002t0001g0079a0001c0003t0008g0009 | 3 | HG02258.hp1 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1089+589G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 10/10 | chr15 | 26944015 | ||||||
| chr15:26944021
|
G | A | 261 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(258): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.1089+595G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 10/10 | chr15 | 26944021 | ||||||
| chr15:26944091
|
G | A | 10 | a0001c0003t0001g0056a0001c0003t0001g0057a0001c0003t0001g0090others(7): Show | 10 | HG01109.hp2 HG02572.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.1089+665G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 10/10 | chr15 | 26944091 | ||||||
| chr15:26944101
|
G | A | 4 | a0001c0004t0001g0012a0001c0004t0001g0167a0001c0004t0001g0202others(1): Show | 4 | HG02615.hp2 HG02647.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1089+675G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 10/10 | chr15 | 26944101 | ||||||
| chr15:26944186
|
T | C | 5 | a0001c0001t0001g0243a0001c0001t0001g0264a0001c0001t0003g0076others(2): Show | 5 | HG02717.hp2 HG03139.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1089+760T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 10/10 | chr15 | 26944186 | ||||||
| chr15:26944262
|
G | A | 2 | a0001c0001t0001g0353a0001c0001t0001g0355 | 2 | NA18949.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.1089+836G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 10/10 | chr15 | 26944262 | ||||||
| chr15:26944356
|
T | C | 322 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(319): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.1089+930T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 10/10 | chr15 | 26944356 | ||||||
| chr15:26944428
|
C | G | 4 | a0001c0002t0001g0143a0001c0002t0001g0195a0001c0002t0001g0258others(1): Show | 4 | HG01934.hp1 HG01993.hp2 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.1089+1002C>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 10/10 | chr15 | 26944428 | ||||||
| chr15:26944456
|
G | T | 1 | a0001c0002t0001g0363 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1089+1030G>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 10/10 | chr15 | 26944456 | ||||||
| chr15:26944508
|
G | A | 3 | a0001c0002t0001g0051a0001c0006t0001g0182a0001c0006t0001g0238 | 3 | HG01257.hp2 HG02647.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1089+1082G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 10/10 | chr15 | 26944508 | ||||||
| chr15:26944521
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1089+1095C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 10/10 | chr15 | 26944521 | ||||||
| chr15:26944602
|
G | C | 119 | a0001c0001t0001g0072a0001c0001t0001g0313a0001c0002t0001g0003others(116): Show | 120 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.1089+1176G>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 10/10 | chr15 | 26944602 | ||||||
| chr15:26944621
|
G | A | 59 | a0001c0001t0001g0029a0001c0001t0001g0044a0001c0001t0001g0045others(56): Show | 59 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.1089+1195G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 10/10 | chr15 | 26944621 | ||||||
| chr15:26944621
|
G | T | 1 | a0001c0010t0001g0119 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1089+1195G>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 10/10 | chr15 | 26944621 | ||||||
| chr15:26944623
|
T | C | 1 | a0001c0010t0001g0119 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1089+1197T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 10/10 | chr15 | 26944623 | ||||||
| chr15:26944706
|
G | A | 5 | a0001c0001t0001g0243a0001c0001t0001g0264a0001c0001t0003g0076others(2): Show | 5 | HG02717.hp2 HG03139.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1089+1280G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 10/10 | chr15 | 26944706 | ||||||
| chr15:26944732
|
A | T | 1 | a0001c0001t0001g0110 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1089+1306A>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 10/10 | chr15 | 26944732 | ||||||
| chr15:26944984
|
C | T | 121 | a0001c0001t0001g0018a0001c0001t0001g0060a0001c0001t0001g0072others(118): Show | 122 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.1089+1558C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 10/10 | chr15 | 26944984 | ||||||
| chr15:26944999
|
G | A | 2 | a0001c0001t0001g0270a0001c0001t0001g0319 | 2 | NA18963.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.1089+1573G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 10/10 | chr15 | 26944999 | ||||||
| chr15:26945074
|
C | T | 323 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(320): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.1089+1648C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 10/10 | chr15 | 26945074 | ||||||
| chr15:26945079
|
T | C | 4 | a0001c0003t0001g0013a0001c0003t0001g0073a0001c0003t0001g0165others(1): Show | 4 | HG01099.hp2 HG02818.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1089+1653T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 10/10 | chr15 | 26945079 | ||||||
| chr15:26945081
|
A | G | 5 | a0001c0001t0001g0018a0001c0001t0001g0060a0001c0001t0001g0072others(2): Show | 5 | HG02055.hp2 HG02630.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1089+1655A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 10/10 | chr15 | 26945081 | ||||||
| chr15:26945117
|
G | C | 1 | a0001c0002t0001g0005 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1089+1691G>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 10/10 | chr15 | 26945117 | ||||||
| chr15:26945260
|
C | G | 1 | a0001c0001t0001g0340 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1089+1834C>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 10/10 | chr15 | 26945260 | ||||||
| chr15:26945271
|
G | A | 3 | a0001c0002t0001g0206a0001c0002t0001g0272a0001c0002t0001g0368 | 3 | HG02572.hp1 NA18979.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.1089+1845G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 10/10 | chr15 | 26945271 | ||||||
| chr15:26945646
|
C | G | 1 | a0001c0002t0001g0338 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1089+2220C>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 10/10 | chr15 | 26945646 | ||||||
| chr15:26945750
|
C | T | 1 | a0001c0002t0001g0258 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1090-2184C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 10/10 | chr15 | 26945750 | ||||||
| chr15:26945822
|
C | A | 1 | a0001c0002t0001g0347 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1090-2112C>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 10/10 | chr15 | 26945822 | ||||||
| chr15:26946002
|
G | A | 2 | a0001c0002t0001g0077a0001c0002t0001g0147 | 2 | HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1090-1932G>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 10/10 | chr15 | 26946002 | ||||||
| chr15:26946102
|
TG | T | 9 | a0001c0001t0001g0034a0001c0001t0001g0081a0001c0001t0001g0174others(6): Show | 9 | HG00438.hp2 HG02056.hp2 NA18949.hp2 others(6): Show |
intron_variant | MODIFIER | c.1090-1830delG | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr15 | 26946102 | |||||
| chr15:26946114
|
A | T | 1 | a0001c0002t0001g0042 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1090-1820A>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 10/10 | chr15 | 26946114 | ||||||
| chr15:26946153
|
TG | T | 15 | a0001c0003t0001g0013a0001c0003t0001g0073a0001c0003t0001g0139others(12): Show | 15 | HG00733.hp1 HG01070.hp1 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.1090-1778delG | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr15 | 26946153 | |||||
| chr15:26946155
|
G | C | 1 | a0001c0001t0001g0104 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1090-1779G>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 10/10 | chr15 | 26946155 | ||||||
| chr15:26946233
|
A | T | 1 | a0001c0002t0001g0173 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1090-1701A>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 10/10 | chr15 | 26946233 | ||||||
| chr15:26946360
|
G | T | 4 | a0001c0004t0001g0012a0001c0004t0001g0167a0001c0004t0001g0202others(1): Show | 4 | HG02615.hp2 HG02647.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1090-1574G>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 10/10 | chr15 | 26946360 | ||||||
| chr15:26946433
|
G | GT | 85 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(82): Show | 88 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.1090-1487dupT | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr15 | 26946433 | |||||
| chr15:26946433
|
GT | G | 140 | a0001c0001t0001g0018a0001c0001t0001g0032a0001c0001t0001g0060others(137): Show | 141 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.1090-1487delT | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr15 | 26946433 | |||||
| chr15:26946433
|
GTT | G | 58 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0052others(55): Show | 58 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.1090-1488_1090-148 others(6): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr15 | 26946433 | |||||
| chr15:26946564
|
A | G | 135 | a0001c0001t0001g0018a0001c0001t0001g0038a0001c0001t0001g0060others(132): Show | 136 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.1090-1370A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 10/10 | chr15 | 26946564 | ||||||
| chr15:26946789
|
C | CA | 322 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(319): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.1090-1135dupA | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr15 | 26946789 | |||||
| chr15:26946800
|
C | A | 7 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(4): Show | 7 | HG01891.hp2 HG02615.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1090-1134C>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 10/10 | chr15 | 26946800 | ||||||
| chr15:26946801
|
T | C | 7 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(4): Show | 7 | HG01891.hp2 HG02615.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1090-1133T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 10/10 | chr15 | 26946801 | ||||||
| chr15:26946961
|
C | T | 135 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(132): Show | 136 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.1090-973C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 10/10 | chr15 | 26946961 | ||||||
| chr15:26947311
|
C | T | 4 | a0001c0001t0001g0264a0001c0001t0003g0076a0001c0001t0003g0168others(1): Show | 4 | HG03139.hp1 HG03209.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1090-623C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 10/10 | chr15 | 26947311 | ||||||
| chr15:26947393
|
CTCTT | C | 5 | a0001c0001t0001g0032a0001c0001t0001g0163a0001c0003t0001g0239others(2): Show | 5 | HG02280.hp1 HG02622.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1090-539_1090-536d others(6): Show |
GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr15 | 26947393 | |||||
| chr15:26947410
|
T | C | 8 | a0001c0001t0001g0048a0001c0001t0001g0072a0001c0001t0001g0110others(5): Show | 8 | HG02055.hp1 HG03139.hp1 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.1090-524T>C | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 10/10 | chr15 | 26947410 | ||||||
| chr15:26947429
|
C | A | 13 | a0001c0001t0001g0032a0001c0001t0001g0163a0001c0003t0001g0056others(10): Show | 13 | HG01109.hp2 HG02280.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1090-505C>A | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 10/10 | chr15 | 26947429 | ||||||
| chr15:26947565
|
C | T | 51 | a0001c0001t0001g0052a0001c0001t0001g0054a0001c0001t0001g0055others(48): Show | 51 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.1090-369C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 10/10 | chr15 | 26947565 | ||||||
| chr15:26947647
|
A | G | 1 | a0001c0001t0001g0251 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1090-287A>G | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 10/10 | chr15 | 26947647 | ||||||
| chr15:26947705
|
C | T | 299 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(296): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.1090-229C>T | GABRA5 | ENSG00000186297.12 | transcript | ENST00000335625.10 | protein_coding | 10/10 | chr15 | 26947705 |